Abstract: The disclosure provides personal care compositions that comprise a compound of formula (I) wherein n is an integer from 2 to 5, R1 is independently H or C1-C3 alkyl and R2 is an unsubstituted linear or branched C1-C6 alkyl and a cosmetically acceptable vehicle. In particular, the compound of formula (I) is diglycolamine acetamide The composition may be used to moisturise skin or hair.

Abstract: The disclosure provides personal care compositions that comprise a moisturizing agent of formula (I) wherein n is an integer from 2 to 5, R1 is independently H or C1-C3 alkyl and R2 is an unsubstituted linear or branched C1-C6 alkyl, at least one additional moisturizing agent and a cosmetically acceptable vehicle. In particular, the compound of formula (I) is diglycolamine acetamide. The compositions generally improve moisturization of skin and hair.

Abstract: Disclosed are copolymers of alkyl methacrylate monomers wherein said alkyl methacrylate monomers comprise at least: a. Monomers (A) selected from C6-C10 alkyl methacrylate monomers, and b. Monomers (B) selected from C10-C18 alkyl methacrylate monomers, wherein the mass ratio of Monomers (B) in the copolymer to Monomers (A) in the copolymer is about 99:1 to about 60:40 by weight. In some cases, the copolymers are of lauryl methacrylate and C8alkyl methacrylate. Also disclosed are methods for the preparation of the copolymers.

Abstract: A hair fixative composition includes at least one carboxylated starch ester based polyglucose polymer, an alcohol based solvent system, and a cosmetically acceptable additive, wherein the polyglucose polymer is soluble in the alcohol based solvent system. The polyglucose polymer is obtained by reacting at least one starch ester with at least one anhydride.

Abstract: Methods are provided for manufacturing a cyclic urea adduct of an ethyleneamine compound, the ethyleneamine compound being selected from the group of ethyleneamines and hydroxyethylethyleneamines and comprising at least one —NH—CH2-CH2-NH— moiety and at least two ethylene moieties, wherein the ethyleneamine compound is reacted with CO2 in the presence of an auxiliary compound selected from ethylenediamine (EDA), monoethanolamine (MEA) and mixtures thereof, the molar ratio of auxiliary compound to amine compound being at least 0.02:1. It has been found that the presence of an auxiliary compound selected from ethylenediamine (EDA), monoethanolamine (MEA) and mixtures thereof leads to a substantial increase of the reaction rate as compared to a process wherein the auxiliary compound is not present.

Abstract: The present invention relates to a process to prepare a salt product containing sodium chloride (NaCl) and at least one additive, wherein the salt product has a particle size of from 50 ?m to 10 mm, which process comprises the steps of: a. optionally, crushing a sodium chloride-containing material to a particle size that is between 1,000 times smaller and 3 times smaller than the size of the final salt product; b. optionally, crushing the at least one additive starting material to a particle size that is between 0.5 and 2 times the particle size of the sodium chloride-containing material particles resulting from step a.); c. subsequently, mixing the sodium chloride-containing material particles of a particle size that is between 1,000 times smaller and 3 times smaller than the size of the final salt product, and additive particles of a particle size that is between 0.5 and 2.0 times the particle size of the sodium chloride-containing material particles; d.

Abstract: A personal care formulation comprises a dermatologically acceptable organic liquid and a cross linked (meth)acrylate copolymer, wherein the organic liquid is thickened by the cross linked (meth)acrylate copolymer, and wherein the cross linked (meth)acrylate copolymer comprises at least one alkyl (meth)acrylate and at least one of the following monomers: a bicyclic (meth)acrylate different from the alkyl (meth)acrylate, and an aromatic vinyl monomer. In one embodiment the formulation can further comprise water and be in the form of a water-in-oil emulsion. In another embodiment the formulation can comprise water and an aqueous thickener and be in the form of an oil-in-water emulsion. The personal care formulation can be a hair care formulation, a skin care formulation, or a sunscreen formulation.

Abstract: 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.

Abstract: 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 oil-in-water sunscreen formulations.

Abstract: The present disclosure generally relates to a waterproofing polymer that is a 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 water-in-oil sunscreen formulations.

Abstract: Process for preparing a powdery organic peroxide formulation, said process comprises the following steps: a) preparing a reaction mixture comprising: 40-80 wt % water 10-25 wt % of an acid chloride or chloroformate, 1-4 wt % hydrogen peroxide, 2-8 wt % alkali metal hydroxide, 1-25 wt % of a phlegmatizer selected from the group consisting of ethylene glycol dibenzoate, phenyl benzoate, trimethylol propane tribenzoate, glyceryl tribenzoate, ethylene glycol ditoluate, 1,3-propanediol ditoluate, ethylene glycol 4-tert-butylbenzoate, ethylene glycol monobenzoate monotoluate, 2,3-butanediol dibenzoate, 4-methylphenyl benzoate acid ester, trimethylolpropane dibenzoate, and combinations thereof 0.002-0.20 wt % of a surfactant, and 0.25-5.0 wt % of an inert organic solvent, all percentages based on the weight of the reaction mixture, b) heating the reaction mixture at a temperature in the range 5-50° C.

Abstract: Process for the production composite articles, comprising the steps of: a) providing a curable mixture comprising: 30-95 wt % of filler material, —5-70 wt % of resin, selected from unsaturated polyester resins, vinyl ester resins, (meth)acrylate resins, and combinations thereof, 0.5-10 phr of at least one peroxyester, 0.1-2.0 phr of at least one organic hydroperoxide, the weight ratio peroxyester/organic hydroperoxide being below 14.0, the curable mixture being essentially free of ketone peroxide, b) shaping the mixture, and c) heating the shaped mixture at a temperature in the range 60-100° C. to affect hardening of the resin and the formation of an article.

Abstract: The present disclosure relates to diesel fuel emulsions, a process to make them and the use thereof in a combustion process. The emulsions are comprise a surfactant of formula wherein R is a C5-C22 linear or branched, saturated or non-saturated, substituted or unsubstituted hydrocarbon group, A is or CH2, each X, independently, is H, COOM or SO3M, with at least one X in the molecule being COOM or SO3M, each R2, independently, is H, CH3, or C2H5, k=0-3, each m, independently, is about 2-6, each n, independently, is about 1-6 and the alkylene formed when n>1 may be substituted with alkyl groups, o=0-40, and each M, independently, is selected from H and any cation M+.

Abstract: An integrated process for manufacturing polyethyleneamine compounds selected from the group of polyethyleneamines and hydroxyethylethyleneamines is provided.

Abstract: The invention relates to specific copolymers obtainable by co-polymerizing at least the following monomers: at least one bicyclic (meth)acrylate ester at least one lower-alkyl (meth)acrylate optionally, and preferably, at least one aromatic vinyl monomer; and optionally other ethylenically unsaturated monomers, whereby the copolymer has a weight averaged molecular weight of from 100,000 to 10,000,000 D, determined using GPC-MALS techniques for a solution in THF at 40° C., as well as to the way to synthesize such copolymers and the use of such polymers to modify the rheology of a liquid in which they are soluble.

Abstract: Aqueous emulsion comprising: —25-70 wt % organic peroxide, based on the weight of the emulsion, —a cyclohexane dicarboxylate ester, and —water. This emulsion is storage stable and can be used for the production of polymers, in particular PVC, that come into contact with food products.

Abstract: A process to prepare an amine-functional ester of an amino carboxylic acid includes the step of reacting a polyol of the formula (I) HO-A-OH??(I) where A is a carbon chain with about 2 to about 36 carbon atoms that is aliphatic linear or branched, saturated or unsaturated, or aromatic, or CH2CH(OH)CH2, CH2C(CH2OH)2CH2, CH2C(CH2OH)(CH3)CH2, CH2C(CH2OH)(CH2CH3)CH2, p-tetrahydrofuran, erythritol or an ester of di- or tricarboxylic acids with ethylene or propylene glycol, and wherein A can optionally be alkoxylated or reacted with hydroxy carboxylic acids, with an aminocarboxylic acid of formula II or its cyclic amide of the formula III, where m is an integer of about 1 to about 8 in formula II and about 3 to about 8 in formula III, each R independently is hydrogen or a C1-C4 alkyl group, or CH2CH2COOH, or CH2COOH, or (CH2)4NH2, in the presence of a Brønsted-Lowry acid.

Abstract: A process to treat metal or mineral ores is disclosed. The metal or mineral ore is a metallic sulphide ore including copper, gold, platinum, silver, nickel, molybdenum, arsenic sulphides, cobalt, zinc, lead, tin, antimony, or combinations thereof with a collector composition including a dimeric fatty nitrile. The dimeric fatty nitrile is prepared by a process including reacting a dimer fatty acid with ammonia at a temperature between about 200° C. and about 400° C. to form a dimeric amide and removing water from the dimeric amide to form the dimeric nitrile. The present disclosure also provides a collector composition containing the dimeric fatty nitrile and at least one further collector or frother compound.

Abstract: A skin care formulation includes at least one polymer and at least one sunscreen active agent and provides low tack and an improved sun protection factor. The polymer is derived from at least one acid-containing monomer, at least one N-alkyl(meth)acrylamide monomer, and, optionally, at least one alkyl(meth)acrylate monomer.

Abstract: The present disclosure generally relates to herbicidal compositions, and more particularly, herbicidal compositions comprising glyphosate or a salt thereof and a surfactant comprising at least one castor oil triglycidyl ether-based (“COTE-based”) adjuvant.