This disclosure provides a personal care composition including a) a solvent; b) water present in an amount of from 0 to about 5 wt % based on a total weight of the composition; and c) a polyvinyl alcohol (PVOH) acetal including the reaction product of i. a copolymer having at least two repeating units wherein a first repeating unit is a vinyl alcohol residue and a second repeating unit is a vinyl acetate residue; and ii. an aldehyde; wherein the PV OH acetal has an acetal content of about 30 mol % or less.
A61K 8/81 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques macromoléculaires obtenus par des réactions faisant intervenir uniquement des liaisons insaturées carbone-carbone
A61Q 17/04 - Préparations topiques pour faire écran au soleil ou aux radiationsPréparations topiques pour bronzer
C08F 216/34 - Copolymères de composés contenant un ou plusieurs radicaux aliphatiques non saturés, chaque radical ne contenant qu'une seule liaison double carbone-carbone et l'un au moins étant terminé par un radical alcool, éther, aldéhyde, cétone, acétal ou cétal par un radical aldéhyde
22n222OH, wherein R is a branched alcohol moiety having from about 8 to about 12 carbon atoms and a degree of branching of from about 0.8 to about 2.5 and n is a number of from about 2 to about 6; a water soluble hydrotrope present in the composition in an amount of from about 0.01 to about 40 weight percent actives based on a total weight of the composition; a chelating agent present in the composition in an amount of from about 1 to about 50 weight percent actives based on a total weight of the composition; and water.
Thermally expandable microspheres comprise a polymeric shell surrounding a hollow core, wherein the hollow core comprises a blowing agent, and the polymeric shell comprises isolated lignin.
B01J 13/04 - Fabrication de microcapsules ou de microbilles par des procédés physiques, p. ex. séchage, pulvérisation
B01J 13/00 - Chimie des colloïdes, p. ex. production de substances colloïdales ou de leurs solutions, non prévue ailleursFabrication de microcapsules ou de microbilles
C08J 9/18 - Fabrication de particules expansibles par imprégnation des particules du polymère avec l'agent de gonflage
Expanded microspheres include a polymeric shell surrounding a hollow core, wherein the exterior surface of the polymeric shell is free from particulate deposits originating from a solid suspending agent.
A process for producing cationic colloidal silica which is surface-modified by at least one aminoalkoxysilane having an amino group in cationic form, comprises: (i) under alkaline conditions, reacting a negatively charged colloidal silica with at least one aminoalkoxysilane having an amino group in cationic form at above 20° C. to produce a surface-modified colloidal silica with a net negative surface charge; and (ii) reversing the surface charge of the net negatively charged surface-modified colloidal silica by contacting the net negatively charged surface-modified colloidal silica with an ion exchange resin to obtain a positively charged surface-modified colloidal silica.
C09C 3/00 - Traitement, en général, de substances inorganiques, autres que des charges fibreuses, pour améliorer leurs propriétés de pigmentation ou de charge
C09C 3/10 - Traitement par des composés organiques macromoléculaires
C09C 3/12 - Traitement par des composés organiques du silicium
09 - Appareils et instruments scientifiques et électriques
42 - Services scientifiques, technologiques et industriels, recherche et conception
Produits et services
Downloadable cloud-based software for accessing, managing,
analyzing, and customizing personal care formulations. Software as a service (SAAS) services featuring software for
accessing, analyzing, managing, retrieving, customizing, and
optimizing consumer-end personal care formulations.
A herbicidal composition includes glyphosate and first and second surfactants. The first surfactant has the structure:
A herbicidal composition includes glyphosate and first and second surfactants. The first surfactant has the structure:
wherein R1 is a linear or branched, saturated or unsaturated alkyl group having from 5 to 22 carbon atoms, each of R2, R3 and R4 is independently an alkylene oxide group, a is from 0 to 10, each of b and c is independently from about 1 to about 10; and n is 0 to about 3. The second surfactant has the structure:
A herbicidal composition includes glyphosate and first and second surfactants. The first surfactant has the structure:
wherein R1 is a linear or branched, saturated or unsaturated alkyl group having from 5 to 22 carbon atoms, each of R2, R3 and R4 is independently an alkylene oxide group, a is from 0 to 10, each of b and c is independently from about 1 to about 10; and n is 0 to about 3. The second surfactant has the structure:
A herbicidal composition includes glyphosate and first and second surfactants. The first surfactant has the structure:
wherein R1 is a linear or branched, saturated or unsaturated alkyl group having from 5 to 22 carbon atoms, each of R2, R3 and R4 is independently an alkylene oxide group, a is from 0 to 10, each of b and c is independently from about 1 to about 10; and n is 0 to about 3. The second surfactant has the structure:
wherein R5 is a linear or branched, saturated or unsaturated alkyl group having from 8 to 18 carbon atoms, each of R6 and R7 is independently an alkylene oxide group, and each of d and e is independently from about 1 to about 5.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
A herbicidal composition includes glyphosate or a derivative thereof, a phosphate ester, and a surfactant component. The phosphate ester is present in an amount of from about 1 to about 15 weight percent actives based on a total weight of the composition. The surfactant component includes at least one of a first surfactant, a second surfactant, and a third surfactant. Each of the first, second, and third surfactants, if utilized, is independently present in an amount of from about 1 to about 15 weight percent actives based on a total weight of the composition.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
The present disclosure relates to the use of 50-515 ppm of at least one polymerization inhibitor as an additive in a suspension radical polymerization comprising styrene monomer and polystyrene for improving the cell structure of expanded polystyrene produced from expandable polystyrene beads obtained from said suspension polymerization, wherein said 50-515 ppm is the total amount of polymerization inhibitor added relative to the initial amount of styrene monomer in the suspension polymerization.
C08J 9/14 - Mise en œuvre de substances macromoléculaires pour produire des matériaux ou objets poreux ou alvéolairesLeur post-traitement utilisant des gaz de gonflage produits par un agent de gonflage introduit au préalable par un agent physique de gonflage organique
The present disclosure generally relates to a waterproofing polymer that is a substantially non-sequential reaction product of the following components: (i) at least one polyglycerol; (ii) at least one dimer acid; and (iii) at least one fatty acid having 8-30 carbon atoms, wherein (iii) and (i) are in a molar ratio of less than 2:1. The components are charged to a reaction vessel and subsequently reacted to produce a polyester polymer having excellent waterproofing properties. The polymers impart high static and water-resistant SPF to anhydrous sunscreen formulations.
A61Q 17/04 - Préparations topiques pour faire écran au soleil ou aux radiationsPréparations topiques pour bronzer
C08G 63/199 - Acides ou composés hydroxylés contenant des cycles cycloaliphatiques
C08G 63/21 - Polyesters préparés en présence de composés ayant un groupe réactif ou plus de deux groupes réactifs en présence d'acides monocarboxyliques non saturés ou d'alcools monohydriques non saturés ou de leurs dérivés réactifs
12.
POLYVINYL ALCOHOL FILM-FORMING POLYMERS FOR ALCOHOL-BASED HAIR FIXING FORMULATIONS AND METHODS OF USING SAME
The present disclosure relates to a hair fixing formulation comprising: (a) a volatile solvent; and (b) at least one film-forming polymer comprising at least one of: (i) polyvinyl alcohol or (ii) polyvinyl alcohol ester said polyvinyl alcohol ester having ester functionality other than solely acetate, and (i) and (ii) being soluble in the volatile solvent, provided that if the at least one film-forming polymer comprises polyvinyl alcohol, then the polyvinyl alcohol has a degree of hydrolysis less than about 60%. Methods of using the hair fixing formulations to fix hair are also disclosed.
A61K 8/81 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques macromoléculaires obtenus par des réactions faisant intervenir uniquement des liaisons insaturées carbone-carbone
A61K 8/33 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant de l'oxygène
A61Q 5/06 - Préparations pour mettre les cheveux en forme, p. ex. pour mettre en forme ou colorer temporairement
A demulsifier includes the reaction product of a) a combination of a monoglyceride and polyethylene glycol (PEG), b) an acid having at least two carboxyl groups, a full or partial ester thereof, an anhydride thereof and combinations thereof, and c) optionally, a fatty acid, a fatty alcohol and combinations thereof. A method of demulsifying a water-in-oil or oil-in-water emulsion includes adding the demulsifier to the emulsion and separating the emulsion into an oil phase and a water phase.
The present disclosure provides a device and methods for expanding thermally expandable microspheres whilst reducing black-spot formation and preventing clogging of the device at higher product throughput rates.
B01J 13/04 - Fabrication de microcapsules ou de microbilles par des procédés physiques, p. ex. séchage, pulvérisation
B29C 44/34 - Éléments constitutifs, détails ou accessoiresOpérations auxiliaires
C08J 9/32 - Mise en œuvre de substances macromoléculaires pour produire des matériaux ou objets poreux ou alvéolairesLeur post-traitement à partir de compositions contenant des microbilles, p. ex. mousses syntactiques
A personal care composition consists essentially of the reaction product of a hydrogenated fatty oil and a dialkyl aminoalkylamine and/or salts of the reaction product along with glycerol, monoglyceride, and diglyceride. The hydrogenated fatty oil has from about 14 to about 22 carbon atoms, the dialkyl moiety has 1 to 18 carbon atoms, and the aminoalkyl moiety has 2 to 4 carbon atoms.
A continuous process produces aqueous organic peroxide emulsions comprising organic peroxides that have a low self-accelerating decomposition temperature. An associated system can perform the continuous process.
A method includes the step of using an aqueous organic peroxide emulsion comprising from 0 to 0.17 wt. % of at least one emulsifier, to prepare polyvinyl chloride with an increased rate of drying. An emulsion includes from 30 to 45 wt. % of diisobutyryl peroxide; from 2.0 to 6.0 wt. % of at least one protective colloid; from 0 to 0.17 wt. % of at least one emulsifier; and at least one anti-freeze agent. A process for preparing a polyvinyl chloride polymer with a normalized drying rate of greater than 0.840 at time t* of 0.5 includes polymerizing monovinyl chloride monomer using an aqueous organic peroxide emulsion, wherein the aqueous organic peroxide emulsion comprises from 0 to 0.17 wt. % emulsifier.
The present disclosure relates to methods and compositions for controlling the formation of scale in hydrocarbon extraction and/or geothermal applications. The anti-scaling composition that inhibits the formation of scale in oil fields and/or geoengineering applications consists essentially of: a polymer that is the reaction product of (i) an acrylate monomer and (ii) 2-acrylamido-2-methyl-1-propanesulfonicacid (AMPS) and/or monomethyl maleate (MMM); and methylglycine N, N- diacetic acid and/or salts thereof.
C09K 8/528 - Compositions pour éviter, limiter ou éliminer les dépôts, p. ex. pour le nettoyage les dépôts inorganiques, p. ex. sulfates ou carbonates
C02F 5/12 - Traitement de l'eau avec des produits chimiques complexants ou des agents solubilisants pour l'adoucissement, la prévention ou l'élimination de l'entartrage, p. ex. par addition d'agents séquestrants en utilisant des substances organiques contenant de l'azote
C02F 5/14 - Traitement de l'eau avec des produits chimiques complexants ou des agents solubilisants pour l'adoucissement, la prévention ou l'élimination de l'entartrage, p. ex. par addition d'agents séquestrants en utilisant des substances organiques contenant du phosphore
C09K 8/54 - Compositions pour inhiber in situ la corrosion dans les puits ou les trous de forage
A process for sintering iron ore includes the steps of providing iron ore, colloidal silica, and water, combining the iron ore, the colloidal silica, and the water to form a mixture, granulating the mixture to form granules, and sintering the granules to form sintered ore. The present disclosure is further directed to the use of colloidal silica for reducing the amount of dust produced by a sintering process. The present disclosure is further directed to the use of colloidal silica for increasing the strength of sinter in a sintering process. The present disclosure is further directed to the use of colloidal silica for increasing productivity in a sintering process.
An agricultural composition includes (A) an adjuvant component (B) water, and (C) an agrochemical. The (A) adjuvant component includes a sol and/or a surfactant component comprising a first surfactant and/or a second surfactant. The sol includes colloidal silica present in an amount of from about 1 to about 50 weight percent SiO2 based on a total weight of the component. The first surfactant includes an alcohol alkoxylate having from 6 to 20 carbon atoms and an average degree of alkoxylation of from about 0.5 to about 12 moles of alkylene oxide. The first surfactant, if present, is present in an amount of from about 1 to about 50 weight percent actives. The second, if present, surfactant includes a linear or branched alkyl glucoside having 6 to 12 carbon atoms and is present in an amount of from about 1 to about 50 weight percent actives.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
09 - Appareils et instruments scientifiques et électriques
42 - Services scientifiques, technologiques et industriels, recherche et conception
Produits et services
Downloadable and cloud-based software for providing customer access to personal care consumer-end formulations; online software platform for managing, viewing, and selecting formulations; AI-based software for retrieving and analyzing ingredients for customizing consumer-end new formulations in personal care applications. Providing an online, customer-facing platform for accessing, and analyzing learning about consumer-end personal care formulations; software as a service (SaaS) featuring a platform for formulation retrieval and customization; scientific and technological services related to the development and optimization of consumer-end formulations.
09 - Appareils et instruments scientifiques et électriques
42 - Services scientifiques, technologiques et industriels, recherche et conception
Produits et services
Downloadable cloud-based software for for accessing, managing, analyzing, and customizing personal care formulations. Software as a service (SAAS) services featuring software for accessing, analyzing, managing, retrieving, customizing, and optimizing consumer-end personal care formulations.
23.
METHOD OF FORMING A READY-TO-USE AGRICULTURAL COMPOSITION COMPRISING GLUFOSINATE
A method of forming a ready-to-use agricultural composition comprising glufosinate includes the step of:
combining: (1) water, (2) at least one linear or branched C6-13 alcohol or alkoxylate thereof, (3) a salt of glufosinate, and (4) at least one linear or branched C8-13 alkyl ether sulfate, to form the ready-to-use agricultural composition,
wherein the concentration of each of (2), (3), and (4) is independently from about 0.05 to about 1, weight percent, based on a total weight of the ready-to-use agricultural composition.
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
A compound has the formula (I):
A compound has the formula (I):
A compound has the formula (I):
wherein R represents a fatty linear or branched, saturated or unsaturated alkyl group having 8-30 carbon atoms; and x+y is greater than about 5. This compound can be utilized in cleaning compositions.
C07C 207/04 - Composés contenant des groupes nitroso liés à un squelette carboné le squelette carboné étant substitué de plus par des atomes d'oxygène liés par des liaisons simples
A polyglycerol quaternary compound has the formula (I): wherein R represents a C8-30 aliphatic group; each R1independently represents a C1-8 aliphatic group; each Gly independently represents a polyglyceryl moiety having 7 to 20 glyceryl units; m represents 1 or 2; n represents 1 or 2; m + n = 3; and X- represents a counteranion. Also disclosed are processes for making the compound of formula (I), aqueous cleaning compositions containing the compound of formula (I), and methods of using the cleaning compositions to clean an object to be cleaned.
C11D 17/00 - Détergents ou savons caractérisés par leur forme ou leurs propriétés physiques
C07C 215/40 - Composés contenant des groupes amino et hydroxy liés au même squelette carboné ayant des groupes hydroxy et des groupes amino liés à des atomes de carbone acycliques du même squelette carboné avec des atomes d'azote quaternisés liés à des atomes de carbone du squelette carboné
26.
OIL-IN-WATER EMULSIONS THAT EXHIBIT STABILITY OVER TIME
An oil-in-water emulsion exhibits stability over time and includes (I) an oil phase present in the emulsion as droplets, (II) an aqueous phase, and (III) a polymer component. The polymer component includes (A) a starch component which includes a particular hydrophobically modified amphoteric starch, (B) a non-starch polysaccharide, and (C) a cross-linked starch. The emulsion exhibits a stability of at least 4 weeks at room temperature.
An oil-in-water emulsion exhibits stability over time and includes (I) an oil phase present in the emulsion as droplets, (II) an aqueous phase, and (III) a polymer component. The polymer component includes (A) a starch component which includes a particular hydrophobically modified starch, (B) a non-starch polysaccharide, and (C) a cross-linked starch. The emulsion exhibits a stability of at least 4 weeks at room temperature.
An oil-in-water emulsion that exhibits stability over time and comprises an oil phase present in an amount of from about 5 to about 60 weight percent actives wherein the oil phase is present in the emulsion as droplets; an aqueous phase present in an amount of from about 30 to about 94.5 weight percent actives; and a polymer component present in an amount of from about 0.5 to about 10 weight percent actives. The polymer component includes a non-starch polysaccharide present in an amount of from about 10 to about 60 weight percent actives based on a total weight of the polymer component; and a cross-linked starch present in an amount of from about 40 to about 90 weight percent actives based on a total weight of the polymer component. The emulsion exhibits a stability of at least 4 weeks at room temperature.
A hydrophobically modified starch has the structure (I), wherein R131919 branched or linear alkyl or alkenyl group, R2is H or an alkyl group having 1 to 10 carbons, R333, or COOH, R433, n is 2 or 3, and M is H, an alkali metal, an alkaline earth metal, or ammonium; and wherein Starch represents a starch moiety.
A surfactant composition includes a first surfactant and a second surfactant. The first surfactant has the following structure (I):
A surfactant composition includes a first surfactant and a second surfactant. The first surfactant has the following structure (I):
A surfactant composition includes a first surfactant and a second surfactant. The first surfactant has the following structure (I):
The second surfactant has the following structure (II):
A surfactant composition includes a first surfactant and a second surfactant. The first surfactant has the following structure (I):
The second surfactant has the following structure (II):
A process for preparing a peroxyester or peroxycarbonate comprises the steps of:
reacting an organic hydroperoxide with an acid halide, an acid anhydride, or a haloformate, in the presence of a base to form an aqueous layer and an organic layer,
separating the aqueous layer from the organic layer after completion of step a),
adding a reducing agent to the organic layer after the aqueous layer has been separated from the organic layer in step b), wherein the reducing agent reduces the organic hydroperoxide to a corresponding alcohol and forms a mixture,
maintaining or adjusting the pH of the mixture of step c) to greater than about 6.8, and
maintaining the pH of the mixture of greater than about 6.8 for at least 5 seconds.
C07C 67/31 - Préparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester par introduction de groupes fonctionnels avec de l'oxygène lié uniquement par liaison simple
C07C 67/36 - Préparation d'esters d'acides carboxyliques par réaction avec du monoxyde de carbone ou des formiates
C07C 67/58 - SéparationPurificationStabilisationEmploi d'additifs par traitement liquide-liquide
C07C 69/28 - Esters d'acides acycliques monocarboxyliques saturés dont le groupe carboxyle est lié à un atome de carbone acyclique ou à l'hydrogène avec au moins trois atomes de carbone dans la partie acide estérifiés par des composés dihydroxylés
32.
EXPANDED MICROSPHERES WITH EXCELLENT BARRIER PROPERTIES
Thermoplastic thermally expandable microspheres comprise a polymer shell and a propellant, wherein the polymer shell is formed from ethylenically unsaturated monomers and encapsulates the propellant, and wherein the ethylenically unsaturated monomers comprise acrylonitrile in an amount from 45 to 80 weight %, methacrylonitrile in an amount of from 10 to 45 weight %, and methyl acrylate and/or methyl methacrylate in an amount of 5 to 35 weight %, each based on the total weight of ethylenically unsaturated monomers, and wherein the thermoplastic thermally expandable microspheres comprise the propellant in an amount of 5 to 17 weight %, based on the total weight of the thermoplastic thermally expandable microspheres. The thermoplastic thermally expandable microspheres are formed in a process of the disclosure and may be present in an aqueous slurry.
C08J 9/32 - Mise en œuvre de substances macromoléculaires pour produire des matériaux ou objets poreux ou alvéolairesLeur post-traitement à partir de compositions contenant des microbilles, p. ex. mousses syntactiques
C08J 9/14 - Mise en œuvre de substances macromoléculaires pour produire des matériaux ou objets poreux ou alvéolairesLeur post-traitement utilisant des gaz de gonflage produits par un agent de gonflage introduit au préalable par un agent physique de gonflage organique
C08J 9/20 - Fabrication de particules expansibles par polymérisation en suspension en présence de l'agent de gonflage
33.
LUBRICANT COMPOSITION INCLUDING A PHOSPHATE ESTER AMINE SALT
A lubricant composition is ashless, metal free, and sulfur free and includes an oil of lubricating viscosity and about 0.05 to about 3 wt% actives of a phosphate ester amine salt based on a total weight of the composition. The phosphate ester amine salt is the reaction product of a particular phosphate ester and a particular amine.
C10M 153/04 - Composés macromoléculaires obtenus par des réactions autres que celles faisant intervenir uniquement des liaisons non saturées carbone-carbone
C10N 30/00 - Propriétés physiques ou chimiques particulières améliorées par l'additif caractérisant la composition lubrifiante, p. ex. additifs multifonctionnels
C10N 30/06 - OnctuositéRésistance du filmAnti-usureRésistance aux pressions extrêmes
An emulsion includes:
a) 25-70 wt. % di-n-butyl peroxydicarbonate or di-sec-butyl peroxydicarbonate,
b) a polyvinyl acetate having a degree of hydrolysis of 50-90 mole %,
c) at least one emulsifier,
d) at least one cyclohexane dicarboxylate ester,
e) ethanol,
f) at least one C2-C6 monohydric or polyhydric alcohol different to e), and
g) water.
An aqueous composition includes water, a binder, an optional pigment, and a particle. The particle itself includes at least one core polymer and at least one shell polymer. Each of the at least one core polymer and the at least one shell polymer is the polymerization reaction product of first and second monomer mixtures, respectively. Each of the first and second monomer mixtures includes a1)/a2) optionally one or more anionic ethylenically unsaturated monomers; b1)/b2) optionally one or more short chain hydrophobic ethylenically unsaturated monomers having a side chain comprising a hydrophobe that has 7 or fewer carbon atoms; c1)/c2) optionally one or more associative monomers; d1)/d2) optionally one or more cross-linking monomers; e1)/e2) optionally one or more nonionic ethylenically unsaturated monomers; and f1)/f2) optionally one or more long chain hydrophobic ethylenically unsaturated monomers having a side chain comprising a hydrophobe that has 8 or greater carbon atoms.
Silica particles have a fine pore size of 1 to 250 Angstrom (Å) and comprise a silane group which comprises two groups which are each independently chosen from alkyl, aryl, alkylaryl, heteroalkyl, heteroaryl, and heteroalkylaryl groups. The silica particles are prepared by a method. The silica particles can be used as a stationary phase for purifying a modified conjugated peptide, such as a GLP-1 agonist or a GLP-2 analog.
B01D 15/32 - Chromatographie en phase liée, p. ex. avec une phase normale liée, une phase inverse ou une interaction hydrophobe
B01J 20/10 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation contenant une substance inorganique contenant de la silice ou un silicate
B01J 20/22 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation contenant une substance organique
B01J 20/28 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation caractérisées par leur forme ou leurs propriétés physiques
The present disclosure relates to a liquid concentrate useful for cleaning applications, wherein the liquid concentrate comprises (a) one or more chelates selected from aminocarboxylate chelates and non-aminocarboxylate chelates; and (b) one or more amphoteric surfactants selected from amphoteric surfactants having the formula (I):
The present disclosure relates to a liquid concentrate useful for cleaning applications, wherein the liquid concentrate comprises (a) one or more chelates selected from aminocarboxylate chelates and non-aminocarboxylate chelates; and (b) one or more amphoteric surfactants selected from amphoteric surfactants having the formula (I):
The present disclosure relates to a liquid concentrate useful for cleaning applications, wherein the liquid concentrate comprises (a) one or more chelates selected from aminocarboxylate chelates and non-aminocarboxylate chelates; and (b) one or more amphoteric surfactants selected from amphoteric surfactants having the formula (I):
wherein R, A, X, k, m, and n are as described herein. Methods of preparing the liquid concentrate are also disclosed, as are cleaning pods and pouches containing the liquid concentrate, and methods of using the liquid concentrate or the cleaning pods and pouches in a method of cleaning a surface, for example, laundry, kitchenware, and hard surfaces.
An organic peroxide composition in solid form comprises
a) at least one organic peroxide of the formula
An organic peroxide composition in solid form comprises
a) at least one organic peroxide of the formula
An organic peroxide composition in solid form comprises
a) at least one organic peroxide of the formula
wherein each R is individually chosen from Cis alkyl groups;
b) at least one water retaining agent that is a solid at room temperature; and
c) water.
B01F 101/00 - Mélange caractérisé par la nature des matières mélangées ou par le domaine d'application
B29C 48/78 - Traitement thermique de la matière à mouler par extrusion ou des pièces ou des couches préformées, p. ex. par chauffage ou refroidissement
C08J 3/20 - Formation de mélanges de polymères avec des additifs, p. ex. coloration
C08J 3/205 - Formation de mélanges de polymères avec des additifs, p. ex. coloration en présence d'une phase liquide
40.
A PACKAGE MATERIAL AND A METHOD FOR MAKING SUCH MATERIAL
The present invention relates to an expandable granule comprising lignocellulosic material and one or more expandable particles and/or pre-expanded particles, and optionally light weight particles, optionally also containing one or more binding agents, wherein the expandable granule has a bulk density from about 0.05 to about 0.8 g/cm3, the expandable granule being suitable for use in a package. The present further relates to a method for manufacture of said granule and the use of said granule e.g. in package applications.
C08J 9/22 - Post-traitement de particules expansiblesFaçonnage d'articles en mousse
C08J 9/232 - Façonnage d'articles en mousse par frittage de particules expansibles
C08J 9/236 - Façonnage d'articles en mousse à l'aide de liants
C08J 9/32 - Mise en œuvre de substances macromoléculaires pour produire des matériaux ou objets poreux ou alvéolairesLeur post-traitement à partir de compositions contenant des microbilles, p. ex. mousses syntactiques
B32B 5/00 - Produits stratifiés caractérisés par l'hétérogénéité ou la structure physique d'une des couches
C08L 97/02 - Matériau lignocellulosique, p. ex. bois, paille ou bagasse
The present disclosure relates to a method of cleaning a surface to be cleaned, wherein said surface is selected from a household item or a vehicle, said method comprising contacting said surface with an aqueous solution comprising a polyester polyquaternary (PEPQ) compound. Formulations useful for this purpose are also disclosed.
A liquid agrochemical composition includes an agrochemical including a fungicide and/or an herbicide chosen from dicamba, 2,4-D, glufosinate, and combinations thereof and in an amount of from about 0.05 to about 60 weight percent based on a total weight of the composition; and
a surfactant in an amount of from about 0.05 to about 50 weight percent based on a total weight of the composition and consisting of;
(i) at least one alkoxylated monoglyceride in an amount of from about 30 to about 45 weight percent,
(ii) at least one alkoxylated diglyceride in an amount of from about 40 to about 50 weight percent,
(iii) at least one alkoxylated triglyceride in an amount of from about 8 to about 10 weight percent, and
(iv) at least one alkoxylated glycerin in an amount of from about 6 to about 8 weight percent, each based on a total weight of the surfactant.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
A01N 37/38 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone possédant trois liaisons à des hétéro-atomes, avec au plus deux liaisons à un halogène, p. ex. acides carboxyliques contenant au moins un groupe carboxylique ou un thio-analogue, ou d'un de leurs dérivés, et un atome d'oxygène ou de soufre lié par une liaison simple, liés au même squelette carboné, cet atome d'oxygène ou de soufre ne faisant pas partie d'un groupe carboxylique ou d'un thio-analogue, ou d'une de leurs dérivés, p. ex. acides hydroxycarboxyliques contenant au moins un atome d'oxygène ou de soufre lié à un système cyclique aromatique
A01N 37/40 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone possédant trois liaisons à des hétéro-atomes, avec au plus deux liaisons à un halogène, p. ex. acides carboxyliques contenant au moins un groupe carboxylique ou un thio-analogue, ou d'un de leurs dérivés, et un atome d'oxygène ou de soufre lié par une liaison simple, liés au même squelette carboné, cet atome d'oxygène ou de soufre ne faisant pas partie d'un groupe carboxylique ou d'un thio-analogue, ou d'une de leurs dérivés, p. ex. acides hydroxycarboxyliques contenant au moins un atome d'oxygène ou de soufre lié à un système cyclique aromatique contenant au moins un groupe carboxylique ou un thio-analogue, ou un de leurs dérivés, et un atome d'oxygène ou de soufre liés au même système cyclique aromatique
A01N 43/84 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant des cycles avec des atomes d'azote et des atomes d'oxygène ou de soufre, comme hétéro-atomes du cycle des cycles à six chaînons avec un atome d'azote et soit un atome d'oxygène, soit un atome de soufre, en positions 1,4
A01N 47/34 - Urées ou thiourées contenant les groupes N—CO—N ou N—CS—N contenant les groupes p. ex. biuretLeurs thio-analoguesProduits de condensation urée-aldéhyde
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
An agrochemical composition includes:
a linear fatty acid having a C8 to C10 alkyl chain; and
an additive chosen from a diluent, an alkoxylated phosphate ester surfactant, and combinations thereof,
wherein the alkoxylated phosphate ester surfactant has a degree of alkoxylation of from about 10 to about 100 and is chosen from alkoxylated C12-C22 alkyl phosphate esters, alkoxylated phosphate esters formed from an alkoxylated triglyceride having at least one pendant hydroxyl group, an alkoxylated phosphate ester formed from an alkoxylated alkylamine, and combinations thereof; and
wherein the diluent is chosen from C4-C10 linear or branched alcohols and their propoxylates, branched C5-C10 monocarboxylic acids, methyl and ethyl esters of linear or branched C8-C10 fatty acids, tall oil fatty acid, trialkyl C2-C8 linear or branched phosphates, aromatic solvents, mineral oils, methyl benzoate, methyl salicylate, octyl acetates, octyl lactate, alkylnitriles, and combinations thereof.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
A01N 35/06 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone possédant deux liaisons à des hétéro-atomes, avec au plus une liaison à un halogène, p. ex. un radical aldéhyde contenant des groupes cétone ou thiocétone faisant partie d'un cycle, p. ex. cyclohexanone, quinoneLeurs dérivés, p. ex. cétals
A01N 37/26 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone possédant trois liaisons à des hétéro-atomes, avec au plus deux liaisons à un halogène, p. ex. acides carboxyliques contenant le groupe —CO—N, p. ex. amides ou imides d'acide carboxyliqueLeurs thio-analogues contenant le groupe Leurs thio-analogues
A01N 37/40 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone possédant trois liaisons à des hétéro-atomes, avec au plus deux liaisons à un halogène, p. ex. acides carboxyliques contenant au moins un groupe carboxylique ou un thio-analogue, ou d'un de leurs dérivés, et un atome d'oxygène ou de soufre lié par une liaison simple, liés au même squelette carboné, cet atome d'oxygène ou de soufre ne faisant pas partie d'un groupe carboxylique ou d'un thio-analogue, ou d'une de leurs dérivés, p. ex. acides hydroxycarboxyliques contenant au moins un atome d'oxygène ou de soufre lié à un système cyclique aromatique contenant au moins un groupe carboxylique ou un thio-analogue, ou un de leurs dérivés, et un atome d'oxygène ou de soufre liés au même système cyclique aromatique
A01N 43/82 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant des cycles avec des atomes d'azote et des atomes d'oxygène ou de soufre, comme hétéro-atomes du cycle des cycles à cinq chaînons avec trois hétéro-atomes
A01N 57/12 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-oxygène ou des liaisons phosphore-soufre contenant des radicaux acycliques ou cycloaliphatiques
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
The present disclosure relates to a process for crosslinking rubber, the process comprising: a) obtaining a composition comprising: i) at least one unsaturated rubber selected from: ia) an unsaturated rubber having a number average molecular weight of at least 3000 g/mol and a polydispersity value (Mw/Mn) of less than 1.7 (Mw and Mn determined by GPC, polybutadiene standards); or ib) an unsaturated rubber having a number average molecular weight of at least 10,000 g/mol (Mw and Mn determined by GPC, polybutadiene standards); ii) at least one radical initiator that forms at least one alkyl radical upon thermal decomposition; and iii) at least one polythiol, wherein the weight ratio of ii) to iii) is from 10:1 to 1 :10; and b) curing the composition of step a) at a temperature of less than 150°C, optionally in an open-air curing environment.
The present disclosure relates to a process for preparing a tertiary alkyl organic peroxides comprising: a) in a first condensation stage, reacting a component containing at least one tertiary alcohol group with a compound containing at least one tertiary hydroperoxide function, in the presence of a catalyst and optional co-catalyst, to form a mixture comprising an organic phase comprising the tertiary alkyl organic peroxide and an aqueous phase, b) in a dewatering stage, separating the aqueous phase from the organic phase, and c) in a second condensation stage, continuing reacting the component containing at least one tertiary alcohol group with the compound containing at least one tertiary hydroperoxide group, in the presence of a catalyst and optional co-catalyst, wherein, in the first condensation stage, the mole ratio between the compound containing at least one tertiary hydroperoxide function and the component containing at least one tertiary alcohol group is at least 3:1, and wherein no dewatering takes place during the first condensation stage.
C07C 409/16 - Composés peroxy le groupe —O—O— étant lié à deux atomes de carbone, qui ne sont pas substitués de plus par des atomes d'oxygène, c.-à-d. peroxydes
46.
A METHOD OF IMPROVING WASHING EFFICIENCY OF A TEXTILE IN COLD WATER
A method of improving washing efficiency of a textile in cold water includes providing a washing composition comprising water, an anionic surfactant, and a surfactant component present in an amount of from about 1 to about 95 weight percent actives based on a total weight of the washing composition and comprising specific first and second alkoxylated tertiary amines in particular ranges of weight percent actives. The method also includes the step of contacting the washing composition and the textile in water at a temperature of less than or equal to about 30°C for a time of at least 15 minutes, thereby resulting in the textile having a delta whiteness of at least 0.5 as determined by ASTM D3050 when compared to a comparative washing composition that is free of the surfactant component.
C11D 1/44 - Éthers de polyoxyalkylènes avec des aminoalcoolsProduits de condensation d'époxyalcanes avec des amines
47.
MANUFACTURED POLYMERS HAVING ALTERED OLIGOSACCHARIDE OR POLYSACCHARIDE FUNCTIONALITY OR NARROWED OLIGOSACCHARIDE DISTRIBUTION, PROCESSES FOR PREPARING THEM, COMPOSITIONS CONTAINING THEM, AND METHODS OF USING THEM
A manufactured polymer comprises (A) a synthetic component covalently bonded to (B) a natural component, wherein the natural component comprises oligosaccharide or polysaccharide, and wherein an end group of said oligosaccharide or polysaccharide is when in an open-chain form substantially devoid of aldehyde functionality.
C08F 251/02 - Composés macromoléculaires obtenus par polymérisation de monomères sur des polysaccharides ou leurs dérivés sur la cellulose ou ses dérivés
A cleaning composition includes: A. a chelating agent present in an amount of from about 0.1 to about 25 weight percent actives based on a total weight of the cleaning composition; B. a biopolymer chosen from starch polycarboxylates, carboxymethyl celluloses, and combinations thereof and present in an amount of from about 0.1 to about 15 weight percent actives based on a total weight of the cleaning composition; C. a surfactant present in an amount of from about 1 to about 30 weight percent actives based on a total weight of the cleaning composition; D. an enzyme optionally present in an amount of from about 0.2 to about 4 weight percent actives based on a total weight of the cleaning composition; and E. a phosphorous-containing compound; wherein the cleaning composition has a phosphorous content of less than about 1 weight percent actives based on a total weight of the cleaning composition.
The present disclosure is directed to collector compositions derived from cashew nutshell liquid for use in the beneficiation of non-sulfidic minerals or non-sulfidic ores.
Thermally expandable microspheres include a polymeric shell surrounding a hollow core, wherein the hollow core comprises a blowing agent, and the polymeric shell comprises an acetate-functionalised cellulose having a glass transition temperature of from about 150 to about 250° C. and a hydrogen bond donor chosen from alcohols, urea, and carboxylic acids. The microspheres are formed using a process including the step of mixing an acetate-functionalised cellulose, an organic solvent, a blowing agent and a hydrogen bond donor to form a mixture and then spraying the mixture into drying equipment to produce the thermally expandable microspheres.
The invention relates to storage stable thermally expandable microspheres comprising a polymeric shell surrounding a hollow core, wherein the hollow core comprises a blowing agent, and the polymeric shell comprises a carboxylate-functionalised cellulose, wherein the microspheres retain at least 80 % of the original weight of blowing agent encapsulated in the microspheres after six months of storage under ambient conditions. The invention further relates to a process for preparing storage stable thermally expandable microspheres comprising a polymeric shell surrounding a hollow core, wherein the hollow core comprises a blowing agent, and the polymeric shell comprises a carboxylate-functionalised cellulose, the method comprising the following steps: (i) preparing thermally expandable microspheres comprising a polymeric shell surrounding a hollow core, wherein the hollow core comprises a blowing agent, and the polymeric shell comprises a carboxylate-functionalised cellulose; and (ii) subjecting the thermally expandable microspheres obtained in step (i) to a post heating treatment by heating the thermally expandable microspheres to a temperature of at least 40°C.
A process for manufacturing a nitrile compound through chain elongation of an alkylene amine compound containing three or more amine units in which at least two amine units are protected by a cyclic urea unit and at least one amine unit is not protected, includes reacting the at least one amine unit that is not protected with glycolonitrile or with the combination of formaldehyde and a cyanide compound selected from HCN and inorganic cyanide salts, to add at least one acetonitrile group to the at least one amine unit that is not protected.
C07C 253/30 - Préparation de nitriles d'acides carboxyliques par des réactions n'impliquant pas la formation de groupes cyano
C07C 253/12 - Préparation de nitriles d'acides carboxyliques par addition d'acide cyanhydrique ou de ses sels à des composés non saturés à des composés contenant des liaisons triples carbone-carbone
C07D 233/02 - Composés hétérocycliques contenant des cycles diazole-1, 3 ou diazole-1, 3 hydrogéné, non condensés avec d'autres cycles ne comportant pas de liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques
C09D 5/14 - Peintures contenant des biocides, p. ex. fongicides, insecticides ou pesticides
C09D 133/12 - Homopolymères ou copolymères du méthacrylate de méthyle
C09D 151/08 - Compositions de revêtement à base de polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions de revêtement à base de dérivés de tels polymères greffés sur des composés macromoléculaires obtenus autrement que par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone
Alkali-swellable rheology modifier comprising a core-shell polymer comprising a core polymer and a shell comprising at least one shell copolymer layer at least partially cross-linked and containing a mole percent of crosslinking agent greater than the mole percent of crosslinking agent in the core polymer, provided if the mole percent of crosslinking agent in the core polymer is zero, then either the core polymer is greater than 60 wt % of the core-shell polymer; the core polymer comprises at least one associative monomer; at least one shell copolymer layer copolymer comprises at least one associative monomer; and/or the at least one shell copolymer layer that is at least partially cross-linked comprises greater than 3 mole% crosslinking agent. Aqueous compositions comprising the alkali-swellable rheology modifier include personal care formulations, healthcare formulations, agricultural formulations, paint formulations, coating formulations, laundry and fabric care formulations, household cleaning formulations, and industrial and institutional cleaning formulations.
A61K 8/02 - Cosmétiques ou préparations similaires pour la toilette caractérisés par une forme physique particulière
A61K 8/81 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques macromoléculaires obtenus par des réactions faisant intervenir uniquement des liaisons insaturées carbone-carbone
A61Q 5/06 - Préparations pour mettre les cheveux en forme, p. ex. pour mettre en forme ou colorer temporairement
C08F 265/06 - Polymérisation d'esters acryliques ou méthacryliques sur des polymères de ces esters
56.
POLYESTER FILM-FORMING POLYMERS FOR ALCOHOL-BASED SUNSCREEN FORMULATIONS
A sunscreen formulation includes (a) a volatile solvent; and (b) at least one film-forming polymer that is the reaction product of (i) at least one polyglycerol; (ii) at least one diacid having 4-30 carbon atoms; and (iii) at least one fatty acid having 8-30 carbon atoms. The sunscreen formulation is used in a method of protecting skin against damaging effects of the sun.
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
Produits et services
Industrial chemicals other than industrial cleaning products; chemicals for use in batteries, namely, block copolymers, polyethylene glycol; salts for industrial purposes; salts for use in galvanic batteries; cellulose; cellulose derivatives, namely, cellulose ethers, carboxyalkyl. carboxymethyl cellulose
Provided are compositions for producing magnesia-containing refractories comprising (i) magnesia, and (ii) a modified colloidal silica, in which the colloidal silica is modified with at least one organosilane moiety comprising a silicon atom bound to the carbon atom of an organic group. The composition may optionally further comprise alumina and/or water.
Method for isolating carboxylic acid from an aqueous alkali metal carboxylate-containing side stream, e.g., the aqueous side stream of an organic peroxide production process, with co-production of alkali metal salt, involving adding an acid, or an anhydride, ketene or acid salt, to the aqueous side stream, thereby forming carboxylic acid and alkali metal salt within the aqueous side stream, and separation of the carboxylic acid from the aqueous side stream.
This invention relates to oil-in-water (water continuous) emulsions that can be used as fuels, in particular oil-in-water emulsions comprising glycerol. The invention also relates to a process for their preparation and to fuel compositions comprising such emulsions.
The present invention refers to macroinitiators of general formula (HO)x—Ra—(O—C(═O)—Rb—C(═O)—O—O—Rc)y, a process for obtaining them, as well as their use in the synthesis of polymer polyols. It also relates to the resulting polymer polyol, as well as to a dispersant obtainable in the process for preparing the polymer polyol, said dispersant being obtained by reacting said macroinitiator with at least one ethylenically unsaturated monomer.
C08G 65/332 - Polymères modifiés par post-traitement chimique avec des composés organiques contenant de l'oxygène contenant des groupes carboxyle, ou leurs halogénures ou esters
Disclosed are fluorescent water-soluble water treatment polymers suitable for use in scale inhibition or suppression of corrosion in industrial water systems, the water treatment polymers especially comprising fluorescent coumarin, fluorescein, rhodamine, and Nile blue derivative monomers. Also disclosed are methods of making the monomers, methods of making the polymers, methods of inhibiting scale in an industrial water system, methods of suppressing corrosion in an industrial water system, and methods of using the polymers in coagulation and flocculation, and in cleaning applications.
C08F 220/58 - Amides contenant de l'oxygène en plus de l'oxygène de la fonction carbonamide
C09K 15/28 - Compositions anti-oxydantesCompositions inhibant les modifications chimiques contenant des composés organiques contenant de l'azote, de l'oxygène et du soufre
C07D 311/16 - Benzo [b] pyrannes non hydrogénés dans le carbocycle avec des atomes d'oxygène ou de soufre liés directement en position 2 non hydrogénés dans l'hétérocycle substitués en position 7
B08B 3/08 - Nettoyage impliquant le contact avec un liquide le liquide ayant un effet chimique ou dissolvant
C02F 5/10 - Traitement de l'eau avec des produits chimiques complexants ou des agents solubilisants pour l'adoucissement, la prévention ou l'élimination de l'entartrage, p. ex. par addition d'agents séquestrants en utilisant des substances organiques
The present invention relates to a method for producing a carboxymethylcellulose (CMC) solution, the method comprising the following steps: a) obtaining an aqueous solution comprising at least one low molecular weight CMC having a weight average molecular weight of less than 30kDa; and b) dissolving at least one high molecular weight CMC having a weight average molecular weight of at least 30kDa into the solution of step a), wherein the at least one high molecular weight CMC is added as a solid (preferably as a powder) to the solution of step a), wherein the amount of low and high molecular weight CMC added in steps a) and b), respectively, is such that the total amount of CMC in the solution is at least 18 wt.% (relative to the total weight of the CMC solution).
C08J 3/05 - Production de solutions, dispersions, latex ou gel par d'autres procédés que ceux utilisant les techniques de polymérisation en solution, en émulsion ou en suspension dans un milieux aqueux à partir de polymères solides
An N-oxide compound has the formula (I), wherein R represents a fatty linear or branched, saturated or unsaturated alkyl group having 8-30 carbon atoms; R1 represents a linear or branched, saturated or unsaturated lower alkyl group having 1-8 carbon atoms; and n represents at least 8 and at most 25. The compound of formula (I) acts as a hydrotrope and is useful for cleaning applications. Processes of preparing the compound, cleaning compositions containing the compound, and methods of using the compound to clean an object are also disclosed.
C07C 291/04 - Composés contenant du carbone et de l'azote et comportant des groupes fonctionnels non couverts par les groupes contenant des liaisons oxyde d'azote contenant des liaisons oxyde d'amine
The present disclosure relates to a hair fixing formulation comprising: (a) a volatile solvent; and (b) at least one film-forming polymer comprising at least one of: (i) polyvinyl alcohol or (ii) polyvinyl alcohol ester said polyvinyl alcohol ester having ester functionality other than solely acetate, and (i) and (ii) being soluble in the volatile solvent, provided that if the at least one film-forming polymer comprises polyvinyl alcohol, then the polyvinyl alcohol has a degree of hydrolysis less than about 60%. Methods of using the hair fixing formulations to fix hair are also disclosed.
A61K 8/81 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques macromoléculaires obtenus par des réactions faisant intervenir uniquement des liaisons insaturées carbone-carbone
66.
POLYVINYL ALCOHOL FILM-FORMING POLYMERS FOR ALCOHOL-BASED SUNSCREEN FORMULATIONS AND METHODS OF USING SAME
The present disclosure relates to a sunscreen formulation comprising: (a) a volatile solvent; and (b) at least one film-forming polymer comprising at least one of: (i) polyvinyl alcohol or (ii) polyvinyl alcohol ester said polyvinyl alcohol ester having ester functionality other than solely acetate, and (i) and (ii) being soluble in the volatile solvent, provided that if the at least one film-forming polymer comprises polyvinyl alcohol, then the polyvinyl alcohol has a degree of hydrolysis less than about 60%. Methods of using the sunscreen formulations to protect skin against the damaging effects of sun are also disclosed.
A61K 8/81 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques macromoléculaires obtenus par des réactions faisant intervenir uniquement des liaisons insaturées carbone-carbone
A61Q 17/04 - Préparations topiques pour faire écran au soleil ou aux radiationsPréparations topiques pour bronzer
The present invention relates to water treatment formulations tailored for different water treatment systems and to the use of the water treatment formulations to treat water.
C02F 5/08 - Traitement de l'eau avec des produits chimiques complexants ou des agents solubilisants pour l'adoucissement, la prévention ou l'élimination de l'entartrage, p. ex. par addition d'agents séquestrants
C02F 5/10 - Traitement de l'eau avec des produits chimiques complexants ou des agents solubilisants pour l'adoucissement, la prévention ou l'élimination de l'entartrage, p. ex. par addition d'agents séquestrants en utilisant des substances organiques
C02F 5/14 - Traitement de l'eau avec des produits chimiques complexants ou des agents solubilisants pour l'adoucissement, la prévention ou l'élimination de l'entartrage, p. ex. par addition d'agents séquestrants en utilisant des substances organiques contenant du phosphore
68.
PROCESS TO PREPARE A CO GRANULE OF METHYLGLYCINE N,N DIACETIC ACID SALTS EMPLOYING A CRUMBLY PHASE COMPOSITION OF METHYLGLYCINE N,N DIACETIC ACID SALTS
The present disclosure relates to a process to prepare a crystalline co granule of MGDA-Nax, x being 2,5-3, containing a step of drying a crumbly phase composition containing on total weight of the composition
(i) 70-87 wt % of organic compounds and salts thereof containing 85 to 100 wt % on total organic compounds and salts thereof of MGDA-Nax, wherein at least 60 wt % of the MGDA-Nax is crystalline, and
(ii) 13-30 wt % of water
in the presence of a second composition containing at least one second component selected from the group of scale inhibitors, crystal inhibitors, film or spot preventing polymers, glass-corrosion inhibiting agents, pH modifiers, chelating agents, builders, bleaching agents, and surfactants. It also relates to the co granules obtainable by the process.
This disclosure provides a chelating composition having a pH of at least about 9 and comprising: water; and the tetrasodium salt of glutamic acid N,N-diacetic acid present in an amount of at least about 50 weight percent based on a total weight of the chelating composition as determined using an Fe-Total Sequestering Value, wherein the chelating composition has a viscosity of less than about 1350 mPa·s measured at about 5° C., or less than about 350 mPa·s measured at about 20° C., each using a Brookfield DV II plus viscometer with spindle S18 and a temperature controlled bath.
C07C 227/16 - Préparation de composés contenant des groupes amino et carboxyle liés au même squelette carboné à partir de composés contenant déjà des groupes amino et carboxyle ou leurs dérivés par des réactions n'impliquant pas les groupes amino ou carboxyle
A method of forming a chelating composition includes the steps of: providing a first mixture comprising water and a tetrasodium salt of glutamic acid N,N-diacetic acid and having a pH of greater than about 10; and acidifying the first mixture via ion exchange and/or bipolar membrane electrodialysis to reduce a pH of the chelating composition to a pH of at least about 9; wherein the chelating composition comprises the tetrasodium salt of glutamic acid N,N-diacetic acid in an amount of at least about 50 weight percent based on a total weight of the chelating composition as determined using an Fe-Total Sequestering Value; and wherein the chelating composition has a viscosity of less than about 1350 mPa·s measured at about 5° C., or less than about 350 mPa·s measured at about 20° C., each using a Brookfield DV II plus viscometer with spindle S18 and a temperature controlled bath.
C07C 227/16 - Préparation de composés contenant des groupes amino et carboxyle liés au même squelette carboné à partir de composés contenant déjà des groupes amino et carboxyle ou leurs dérivés par des réactions n'impliquant pas les groupes amino ou carboxyle
A method includes combining monosodium glutamate and/or glutamic acid with formaldehyde to form a first combination; adding hydrogen cyanide to form a second combination comprising a monosodium salt of glutamic acid diacetonitrile, a cyclic GLMN, and a sodium salt of glutamic acid N-monoacetonitrile, maintaining a temperature of the second combination at less than about 16° C. and a pH of less than about 7; converting nitrile groups to carboxylate groups thereby forming a third combination comprising water and at least about 47 weight percent of the tetrasodium salt of GLDA, wherein a reaction yield is at least about 91%; providing a fourth combination comprising water and the tetrasodium salt of GLDA and having a pH of less than about 7; and combining the third and fourth combinations to form the chelating composition.
C07C 227/16 - Préparation de composés contenant des groupes amino et carboxyle liés au même squelette carboné à partir de composés contenant déjà des groupes amino et carboxyle ou leurs dérivés par des réactions n'impliquant pas les groupes amino ou carboxyle
The present invention relates to methods for processing plant and/or micro-organism derived cellulose materials into rheology/structuring agents. More in particular, the present invention relates to methods wherein plant and/or micro-organism derived cellulose material is co-processed with carboxycellulose. The methods of the present invention provide a variety of benefits, in terms of process efficiency and scalability as well as in relation to the properties of the materials that are obtainable using these methods. For instance, it has been found that (highly) concentrated products produced using the method of the invention are easily (re)dispersible in water and aqueous systems to regain much of the cellulose component's original rheological performance.
A61K 31/7048 - Composés ayant des radicaux saccharide et des hétérocycles ayant l'oxygène comme hétéro-atome d'un cycle, p. ex. leucoglucosane, hespéridine, érythromycine, nystatine
A system for producing an oil-in-water emulsion; the system comprising: a first input for coupling to a source of fuel (10) on a vehicle; a second input for coupling to a source of water (20); a third input for coupling to a source of first additive (30); a mixing section (50) for mixing the water and the first additive to form an aqueous phase; and a blender (70) for blending the aqueous phase with the fuel to form the oil-in-water emulsion; wherein the first input is coupled to the blender; the second input and the third input are coupled to the mixing section; and the mixing section is coupled to the blender.
The present disclosure relates to the production of bis-thiol compounds, preferably DMDH/DMDH oligomer mixtures, and their use in the production of liquid polysulfide polymers
A process for treating a subterranean earth formation includes the step of introducing an acidizing treatment fluid comprising a monovalent salt of monochloroacetic acid into the subterranean earth formation in the presence of at least one bromide or iodide salt or salt precursor, wherein the at least one bromide or iodide salt or salt precursor is introduced into the subterranean earth formation in an amount of from about 0.3 to about 10 wt %, based on the total weight of the acidizing treatment fluid. The acidizing treatment fluid itself includes the monovalent salt of monochloroacetic acid, the at least one bromide or iodide salt or salt precursor, and optionally an element to suppress precipitation of calcium glycolate and/or at least one acid.
C09K 8/74 - Produits chimiques érosifs, p. ex. acides combinés avec des additifs ajoutés à des fins spécifiques
E21B 43/27 - Procédés pour activer la production par formation de crevasses ou de fractures par emploi de produits chimiques érosifs, p. ex. d'acides
C09K 8/524 - Compositions pour éviter, limiter ou éliminer les dépôts, p. ex. pour le nettoyage les dépôts organiques, p. ex. paraffines ou asphaltènes
76.
THERMALLY EXPANDABLE CELLULOSE-BASED MICROSPHERES HAVING LOW EXPANSION TEMPERATURES
The present disclosure relates to thermally expandable microspheres comprising a polymeric shell surrounding a hollow core, wherein the hollow core comprises a blowing agent, and the polymeric shell comprises a carboxylate-functionalised cellulose, wherein the thermally expandable microspheres have a temperature at which expansion starts, TStart, of from 80° C. to less than 135° C. The present disclosure further relates to a process for preparing expandable microspheres as well as to thermally expandable microspheres obtained by such process, the process comprising mixing a carboxylate-functionalised cellulose, an organic solvent, a blowing agent and, optionally, a polymer shell enhancer and then spraying the thus obtained mixture into a drying equipment to produce the thermally expandable microspheres having a polymeric shell surrounding a hollow core, in which the polymeric shell comprises the carboxylate-functionalised cellulose, and the hollow core comprises the blowing agent.
C08J 9/18 - Fabrication de particules expansibles par imprégnation des particules du polymère avec l'agent de gonflage
C08J 9/00 - Mise en œuvre de substances macromoléculaires pour produire des matériaux ou objets poreux ou alvéolairesLeur post-traitement
C08J 9/14 - Mise en œuvre de substances macromoléculaires pour produire des matériaux ou objets poreux ou alvéolairesLeur post-traitement utilisant des gaz de gonflage produits par un agent de gonflage introduit au préalable par un agent physique de gonflage organique
B01J 13/04 - Fabrication de microcapsules ou de microbilles par des procédés physiques, p. ex. séchage, pulvérisation
1231233 independently represent a negative charge or a counterion. The compound of formula (I) acts as a hydrotrope and is useful for cleaning applications. Processes of preparing the compound, cleaning compositions containing the compound, and methods of using the compound to clean an object are also disclosed.
C07C 229/24 - Composés contenant des groupes amino et carboxyle liés au même squelette carboné ayant des groupes amino et carboxyle liés à des atomes de carbone acycliques du même squelette carboné le squelette carboné étant acyclique et saturé ayant plus d'un groupe carboxyle lié au squelette carboné, p. ex. acide aspartique
A process for treating a subterranean earth formation by includes the step of introducing a buffered acidizing treatment fluid comprising a monovalent salt of monochloroacetic acid and at least one acid into the subterranean earth formation, wherein the pH of the buffered acidizing treatment fluid is from about 1.2 to about 5. The buffered acidizing treatment fluid itself includes the monovalent salt of monochloroacetic acid, the at least one acid and optionally an element to suppress salt precipitation.
E21B 43/27 - Procédés pour activer la production par formation de crevasses ou de fractures par emploi de produits chimiques érosifs, p. ex. d'acides
C09K 8/74 - Produits chimiques érosifs, p. ex. acides combinés avec des additifs ajoutés à des fins spécifiques
C09K 8/524 - Compositions pour éviter, limiter ou éliminer les dépôts, p. ex. pour le nettoyage les dépôts organiques, p. ex. paraffines ou asphaltènes
79.
METHOD OF FORMING A READY-TO-USE AGRICULTURAL COMPOSITION COMPRISING GLUFOSINATE
This disclosure provides a method of forming a ready-to-use agricultural composition comprising glufosinate, said method comprising the step of: combining: (1) water, (2) at least one linear or branched C6-13 alcohol or alkoxylate thereof, (3) a salt of glufosinate, and (4) at least one linear or branched C8-13 alkyl ether sulfate, to form the ready-to-use agricultural composition, wherein the concentration of each of (2), (3), and (4) is independently from about 0.05 to about 1, weight percent, based on a total weight of the ready-to-use agricultural composition.
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
The present disclosure relates to thermoplastic polymeric microspheres comprising a thermoplastic polymer shell surrounding a hollow core, in which the thermoplastic polymer shell comprises a copolymer of a monomer of Formula 1:
The present disclosure relates to thermoplastic polymeric microspheres comprising a thermoplastic polymer shell surrounding a hollow core, in which the thermoplastic polymer shell comprises a copolymer of a monomer of Formula 1:
The present disclosure relates to thermoplastic polymeric microspheres comprising a thermoplastic polymer shell surrounding a hollow core, in which the thermoplastic polymer shell comprises a copolymer of a monomer of Formula 1:
wherein:
each of A1 to A11 are independently selected from H and C1 to C4 alkyl, in which each C1-4 alkyl group can optionally be substituted with one or more substituents selected from halogen, hydroxy and C1-4 alkoxy;
A12 is selected from C1 to C4 alkyl, in which the C1-4 alkyl group can optionally be substituted with one or more substituents selected from halogen, hydroxy and C1-4 alkoxy
X is a linking group selected from —O—, —NR″—, —S—, —OC(O)—, —NR″C(O)—, —SC(O)—, —C(O)O—, —C(O)NR″—, and —C(O)S—; and
R″ is H or C1-2 alkyl optionally substituted with one or more substituents selected from halogen and hydroxyl.
C08J 9/14 - Mise en œuvre de substances macromoléculaires pour produire des matériaux ou objets poreux ou alvéolairesLeur post-traitement utilisant des gaz de gonflage produits par un agent de gonflage introduit au préalable par un agent physique de gonflage organique
C08J 9/18 - Fabrication de particules expansibles par imprégnation des particules du polymère avec l'agent de gonflage
C08J 3/03 - Production de solutions, dispersions, latex ou gel par d'autres procédés que ceux utilisant les techniques de polymérisation en solution, en émulsion ou en suspension dans un milieux aqueux
A surfactant composition includes a first surfactant and a second surfactant. The first surfactant has the following structure (I): (I). The second surfactant has the following structure (II): (II).
A surfactant has a structure (I)-(VI) and may be used in an agrochemical composition that includes at least one surfactant of this disclosure and an agrochemical. The surfactant may be further defined as alkyl amine polyglycerol or alkyl polyamine polyglycerol, or alkyl polyglycerylamine. In another embodiment, the surfactant may be further defined as an amine oxide, as also described above. In another embodiment, the surfactant may be further defined as a quat or quaternary ammonium compound.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
An agrochemical composition includes an agrochemical and a surfactant that has a structure (I)-(III). The surfactant may be further defined as an alkyl etheramine polyglycerol surfactant. In another embodiment, the surfactant may be further defined as an amine oxide, as also described above. In another embodiment, the surfactant may be further defined as a quat or quaternary ammonium compound.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
An agrochemical composition includes an agrochemical and a surfactant that has a structure (I)-(VI). The surfactant may be described as an alkyl amidoamine glycerol surfactant, an oxide thereof, or as a quaternary ammonium compound thereof.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
85.
THERMALLY EXPANDABLE MICROSPHERES PREPARED FROM BIO-BASED MONOMERS
The present disclosure relates to thermoplastic polymeric microspheres comprising a thermoplastic polymer shell surrounding a hollow core, in which the thermoplastic polymer shell comprises a homopolymer or copolymer of a monomer of Formula 1
The present disclosure relates to thermoplastic polymeric microspheres comprising a thermoplastic polymer shell surrounding a hollow core, in which the thermoplastic polymer shell comprises a homopolymer or copolymer of a monomer of Formula 1
wherein:
each of A1 to A11 are independently selected from H and C1 to C4 alkyl, in which each C1-4 alkyl group can optionally be substituted with one or more substituents selected from halogen, hydroxy and C1-4 alkoxy;
X is a linking group selected from —O—, —NR″—, —S—, —OC(O)—, —NR″C(O)—, —SC(O)—, —C(O)O—, —C(O)NR″—, and —C(O)S—; and
R″ is H or C1-2 alkyl optionally substituted with one or more substituents selected from halogen and hydroxy.
A liquid fabric softener composition in accordance with an exemplary embodiment comprises a fabric softener active agent, a hydroxypropyl starch phosphate, and water.
Process for preparing a reinforced rubber composition, said process comprising the step mixing, at a temperature of at least 120° C., at least the following compounds: (i) a rubber, (ii) at least one inorganic filler, (iii) at least one organic peroxide, and (iv) at least one anti-oxidant selected from phenolics, para-phenylidene diamines, and nitroxides.
An epoxidized oil-based surfactant is the reaction product of an epoxidized compound and a primary and/or secondary alkanolamine, wherein the epoxidized compound is chosen from an epoxidized oil, an epoxidized fatty acid, an epoxidized fatty acid ester, and combinations thereof. An herbicidal composition includes glyphosate or a salt thereof and at least one epoxidized oil-based surfactant. The herbicidal composition is used in a method of controlling unwanted vegetation wherein the method includes the step of applying to the unwanted vegetation a herbicidally effective amount of the aforementioned herbicidal composition. The epoxidized oil-based surfactant is prepared using a method that includes reacting the epoxidized compound and the primary and/or secondary alkanolamine. The epoxidized oil-based surfactant is also utilized in a cleaning composition for the cleaning of hard surfaces, wherein the cleaning composition includes the epoxidized oil-based surfactant and an additional component chosen from an additional surfactant and/or a chelating agent.
A01N 43/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant des cycles avec un ou plusieurs atomes d'oxygène ou de soufre comme uniques hétéro-atomes du cycle avec un hétéro-atome des cycles à trois ou quatre chaînons
A01N 37/38 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone possédant trois liaisons à des hétéro-atomes, avec au plus deux liaisons à un halogène, p. ex. acides carboxyliques contenant au moins un groupe carboxylique ou un thio-analogue, ou d'un de leurs dérivés, et un atome d'oxygène ou de soufre lié par une liaison simple, liés au même squelette carboné, cet atome d'oxygène ou de soufre ne faisant pas partie d'un groupe carboxylique ou d'un thio-analogue, ou d'une de leurs dérivés, p. ex. acides hydroxycarboxyliques contenant au moins un atome d'oxygène ou de soufre lié à un système cyclique aromatique
A01N 37/40 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone possédant trois liaisons à des hétéro-atomes, avec au plus deux liaisons à un halogène, p. ex. acides carboxyliques contenant au moins un groupe carboxylique ou un thio-analogue, ou d'un de leurs dérivés, et un atome d'oxygène ou de soufre lié par une liaison simple, liés au même squelette carboné, cet atome d'oxygène ou de soufre ne faisant pas partie d'un groupe carboxylique ou d'un thio-analogue, ou d'une de leurs dérivés, p. ex. acides hydroxycarboxyliques contenant au moins un atome d'oxygène ou de soufre lié à un système cyclique aromatique contenant au moins un groupe carboxylique ou un thio-analogue, ou un de leurs dérivés, et un atome d'oxygène ou de soufre liés au même système cyclique aromatique
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
This disclosure provides a composition comprising a mixture of molecules of Formula (I): {RO-[CH(CH3)CH2O)]b[CH2-CH2O]a}mP(=O)(O−X+)n(I), wherein R is chosen from linear or branched C10-C18 alkyl or alkenyl groups; a is 0 to 50, b is 0-30, and a+b >0; X+ is potassium, triethanolamine, or H, and m and n are each equal to 1 or 2, such that when m=1 then n=2, and when m=2 then n=1. Moreover, in the mixture some of the molecules have m=1 and n=2 and some of the molecules have m=2 and n=1, wherein the mole ratio of compounds where m=1 to compounds where m=2 is of from 1:1 to 3:1.
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
C08G 65/26 - Composés macromoléculaires obtenus par des réactions créant une liaison éther dans la chaîne principale de la macromolécule à partir d'éthers cycliques par ouverture d'un hétérocycle à partir d'éthers cycliques et d'autres composés
C08G 65/327 - Polymères modifiés par post-traitement chimique avec des composés inorganiques contenant du phosphore
A01N 43/38 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant des cycles avec un atome d'azote comme unique hétéro-atome du cycle des cycles à cinq chaînons condensés avec des carbocycles
A01N 43/70 - Diamino-triazines-1,3,5 avec un seul atome d'oxygène, de soufre ou d'halogène ou un seul groupe cyano, thiocyano (—SCN), cyanato (—OCN) ou azido (—N3) lié directement à un atome de carbone du cycle
A01N 47/30 - Dérivés contenant le groupe N—CO—N—aryle ou N—CS—N—aryle
The present disclosure relates to a liquid concentrate useful for cleaning applications, wherein the liquid concentrate comprises (a) one or more chelates selected from aminocarboxylate chelates and non-ami- nocarboxylate chelates; and (b) one or more amphoteric surfactants selected from amphoteric surfactants having the formula (I) wherein R, A, X, k, m, and n are as described herein. Methods of preparing the liquid concentrate are also disclosed, as are cleaning pods and pouches containing the liquid concentrate, and methods of using the liquid concentrate or the cleaning pods and pouches in a method of cleaning a surface, for example, laundry, kitchenware, and hard surfaces.
A demulsifier includes the reaction product of a) a combination of a monoglyceride and polyethylene glycol (PEG), b) an acid having at least two carboxyl groups, a full or partial ester thereof, an anhydride thereof and combinations thereof, and c) optionally, a fatty acid, a fatty alcohol and combinations thereof. A method of demulsifying a water-in-oil or oil-in-water emulsion includes adding the demulsifier to the emulsion and separating the emulsion into an oil phase and a water phase.
A package comprises a powder composition comprising from about 97.0 to about 99.7 weight % of sodium chlorate and from about 0.3 to about 2.0 weight % of an anti-caking agent, wherein the anticaking agent is anhydrous sodium carbonate, anhydrous sodium hydrogen carbonate, sodium carbonate monohydrate or a mixture of any of the foregoing.
The present disclosure relates to a method of cleaning a surface to be cleaned, wherein said surface is selected from a household item or a vehicle, said method comprising contacting said surface with an aqueous solution comprising a polyester polyquaternary (PEPQ) compound. Formulations useful for this purpose are also disclosed.
C11D 7/32 - Composés organiques contenant de l'azote
94.
MANUFACTURED POLYMERS HAVING ALTERED OLIGOSACCHARIDE OR POLYSACCHARIDE FUNCTIONALITY OR NARROWED OLIGOSACCHARIDE DISTRIBUTION, PROCESSES FOR PREPARING THEM, COMPOSITIONS CONTAINING THEM, AND METHODS OF USING THEM
The present disclosure relates to a manufactured polymer comprising (A) a synthetic component covalently bonded to (B) a natural component, wherein the natural component comprises oligosaccharide or polysaccharide, and wherein an end group of said oligosaccharide or polysaccharide is when in an open-chain form substantially devoid of aldehyde functionality. The present disclosure also relates to a manufactured polymer comprising (A) a synthetic component covalently bonded to (B) a natural component, wherein the natural component comprises a narrowed oligosaccharide distribution prepared by enzyme degradation of polysaccharide. The manufactured polymers described herein find use in a variety of end use applications, including cleaning, automatic dishwashing, detergents, minimizing scale, water treatment, as binders, as superabsorbents, as rheology modifiers, and in personal care.
The disclosure relates to thermally expandable microspheres comprising a polymeric shell surrounding a blowing agent-containing hollow core, the polymer shell comprising a carboxylate-functionalised cellulose having a glass transition temperature (Tg) of at least about 125° C. The disclosure also relates to a method for preparing such thermally expandable microspheres, comprising mixing an aqueous phase that optionally comprises an emulsifier with an organic phase that comprises an organic solvent, a blowing agent and a carboxylate-functionalised cellulose having a Tg of at about least 125° C., to form a microsphere dispersion.
C08J 9/14 - Mise en œuvre de substances macromoléculaires pour produire des matériaux ou objets poreux ou alvéolairesLeur post-traitement utilisant des gaz de gonflage produits par un agent de gonflage introduit au préalable par un agent physique de gonflage organique
96.
METHOD FOR ISOLATING CARBOXYLIC ACID FROM AN AQUEOUS SIDE STREAM
Method for isolating carboxylic acid from an aqueous metal carboxylate-containing side stream of an organic peroxide production process, involving the protonation of the carboxylate, separation of liquid and organic phases, and the removal of residual peroxides.
C02F 1/26 - Traitement de l'eau, des eaux résiduaires ou des eaux d'égout par extraction
C02F 1/469 - Traitement de l'eau, des eaux résiduaires ou des eaux d'égout par des procédés électrochimiques par séparation électrochimique, p. ex. par électro-osmose, électrodialyse, électrophorèse
C07C 51/487 - SéparationPurificationStabilisationEmploi d'additifs par traitement donnant lieu à une modification chimique
C02F 1/04 - Traitement de l'eau, des eaux résiduaires ou des eaux d'égout par chauffage par distillation ou évaporation
C02F 1/70 - Traitement de l'eau, des eaux résiduaires ou des eaux d'égout par réduction
An agrochemical composition includes: a linear fatty acid having a C8 to C10 alkyl chain; and an additive chosen from a diluent, an alkoxylated phosphate ester surfactant, and combinations thereof, wherein the alkoxylated phosphate ester surfactant has a degree of alkoxylation of from about 10 to about 100 and is chosen from alkoxylated C12-C22 alkyl phosphate esters, alkoxylated phosphate esters formed from an alkoxylated triglyceride having at least one pendant hydroxyl group, an alkoxylated phosphate ester formed from an alkoxylated alkylamine, and combinations thereof; and wherein the diluent is chosen from C4-C10 linear or branched alcohols and their propoxylates, branched C5-C10 monocarboxylic acids, methyl and ethyl esters of linear or branched C8-C10 fatty acids, tall oil fatty acid, trialkyl C2-C8 linear or branched phosphates, aromatic solvents, mineral oils, methyl benzoate, methyl salicylate, octyl acetates, octyl lactate, alkylnitriles, and combinations thereof.
A01N 25/02 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles contenant des liquides comme supports, diluants ou solvants
A01N 25/30 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, caractérisés par leurs formes, ingrédients inactifs ou modes d'applicationSubstances réduisant les effets nocifs des ingrédients actifs vis-à-vis d'organismes autres que les animaux nuisibles caractérisés par les agents tensio-actifs
A01N 37/02 - Acides carboxyliques saturés ou leurs thio-analoguesLeurs dérivés
A01N 57/12 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-oxygène ou des liaisons phosphore-soufre contenant des radicaux acycliques ou cycloaliphatiques
98.
Thickened organic liquid compositions with polymeric rheology modifiers
Disclosed are thickened organic liquid compositions comprising an organic liquid and a polymeric rheology modifier wherein the polymeric rheology modifier is obtainable by co-polymerizing at least two of a bicyclic (meth)acrylate ester, an alkyl (meth)acrylate, and an aromatic vinyl monomer. Also disclosed are thickened organic liquid dispersions with suspended solids and methods of stabilizing dispersions using polymeric rheology modifiers.
C08F 220/18 - Esters des alcools ou des phénols monohydriques des phénols ou des alcools contenant plusieurs atomes de carbone avec l'acide acrylique ou l'acide méthacrylique
The invention relates to thermally expandable microspheres comprising a polymeric shell surrounding a hollow core, wherein the hollow core comprises a blowing agent, and the polymeric shell comprises an acetate-functionalised cellulose having a glass transition temperature within the range of from 150 to 250°C and a hydrogen bond donor selected from the group of alcohols, urea, and carboxylic acids, preferably a hydrogen bond donor in the form of a carboxylic acid. The invention further relates to a process for preparing expandable microspheres as well as to thermally expandable microspheres obtained by such process, the process comprising mixing an acetate-functionalised cellulose, an organic solvent, a blowing agent and a hydrogen bond donor selected from the group of alcohols, urea, and carboxylic acids, preferably a hydrogen bond donor in the form of a carboxylic acid, and then spraying the thus obtained mixture into a drying equipment to produce the thermally expandable microspheres having a polymeric shell surrounding a hollow core, in which the polymeric shell comprises the acetate-functionalised cellulose, and the hollow core comprises the blowing agent.
Process for the production of a diacyl peroxide involving the reaction of an anhydride with hydrogen peroxide, removal of the formed carboxylic acid, production of an anhydride from said carboxylic acid, and recycling of the anhydride within the process.