Abstract:
The presently claimed invention relates to a process for preparing urea urethane polymer, liquid compositions comprising the urea urethane polymer and the use of the urea urethane polymer as a thickening and thixotropic agent for water based and solvent based paint and coating formulations, lacquer, varnish, paper coating, wood coating, adhesive, ink, cosmetic formulation, detergent formulation, textile and drilling muds plaster formulations, PVC plastisol and cement formulations.
Abstract:
The presently claimed invention relates to polymer with branched structure, in particular, hydrophobically modified alkali-soluble (or alkali-swellable) emulsion (HASE) copolymers which are effective thickeners at high shear rates and at the same time offer a Newtonian rheology profile and their use in aqueous compositions, particularly in aqueous coating formulations as well as a method for preparing hydrophobically modified alkali-soluble (or alkali-swellable) emulsion copolymers.
Abstract:
The presently claimed invention relates to novel monomers which can be used for preparing polymers which are useful as dispersants for pigments and fillers, as wetting agent and as thickening agents in liquid compositions.
Abstract:
The present invention relates to polyalkylene imine based polymers, which have aliphatic polyester groups attached to the polyalkylenimine backbone via an carboxamide group. The novel polymers are particularly useful as dispersants for pigments, in particular as dispersants for pigments in non-aqueous compositions. The polyalkylene imine based polymers are characterized by having a) a polyalkylene imine backbone; b) at least one aromatic moiety P.1, which is bound to a nitrogen atom of the polyalkylene imine backbone via an carboxamide or carboximide group; and c) at least one aliphatic polyester moiety P.2, which is bound to a nitrogen atom of the polyalkylene imine backbone via an carboxamide group.
Abstract:
This invention relates to end-functionalized living polymers or copolymers having a structure represented by the general formula 1 or 2, wherein R 1 is a hydrogen atom, a methyl group, or a radically non-polymerizable organic group containing 1 to 20 carbon atoms. R 2 is a functional end group of a vinyl hetero monomer selected from the group con- sisting of hydroxy, epoxy, silyl, NH 2 , NH(C 1 -C 6 alkyl), N(C 1 -C 6 alkyl) 2 , -CH=CH 2 , -C≡CH, -C(CH 3 )=CH 2 , -0-CH=CH 2 , (-O-CH 2 -CH 2 ) 1-10 -OH, -OR 20 , -COOR 20 , -CONHR 20 , -OCONHR 20 , -OCOR 20 and -NH-CO-R 20 , wherein R 20 is linear or branched C 1 -C 20 alkyl or linear or branched C 1- C 20 alkyl substituted with hydroxy, epoxy, silyl, NH 2 or N(C 1- C 6 alkyl) 2 ; or R 20 is phenyl, benzyl, -CH=CH 2 , -C≡CH or -C(CH 3 )=CH 2 , or R 2 is a residue of an acrylic acid (CH 2 =CH-COO-*), methacrylic acid, (CH 2 =C(CH 3 )-COO-*) or CH(CH 3 )=CH-COO-* or R 2 is a residue of a dicarboxylic acid HOOC-R c -COO-* or C 1 -C 6 alkyl-OOC-R c -COO-* wherein R c is C 1 -C 20 alkylene, C 1 -C 20 alkenylene or phenylene; or R 2 is a residue derived from the reaction of an isocyanate R a -NCO with the hydroxy group or with the amine group of the vinyl hetero monomer, said residue being R a -NHCOO-* or R a -NHCO-NH-* wherein R a is unsubstituted C 1 -C 20 alkyl, C 1 -C 20 cycloalkyl or C 1 -C 20 alkyl substituted with hydroxy, epoxy, silyl, NH 2 , NH(C 1 -C 6 alkyl) or N(C 1 -C 6 alkyl) 2 ; or R 2 is a residue derived from the reaction of a diisocyanate residue OCN-R b -NCO with the hydroxy group or with the amine group of the vinyl hetero monomer, said residue being *-OOC-NH-R b -NCO or *-HNOC-NH-R b -NCO or *-OOC-NH-R b -NHCOR 30 wherein R b is C 1 -C 20 alkylene or C 1 -C 20 cycloalkylene or phenylene and R 30 is a residue of hydroxyethylacrylate (CH 2 =CH-COO-(CH 2 ) 2 -0*), hydroxyethylmethacrylate (CH 2 =C(CH 3 )-COO-(CH 2 ) 2 -0*), hydroxybutylacrylate (CH 2 =CH-COO-(CH 2 ) 4 -0*) or hydroxybutylmethacrylate (CH 2 =C(CH 3 )-COO-(CH 2 ) 4 -0*), A is the hetero atom of the vinyl hetero monomer selected from the group consisting of oxygen, nitrogen, sulfur and silicon; and if R 2 is silyl and M is a direct bond, A is a direct bond; M is a bond or a divalent group linking the heteroatom of the vinyl hetero monomer and the functional end group of the vinyl hetero monomer said M being selected from the group consisting of C 1-50 alkylene, C 1-50 (hetero)alkylene, arylene and heteroarylene; X is a halogen atom, a nitroxide group or a sulphide group, Z n is a polymer or copolymer segment of random-, gradient- or block-type structure, which is built up from vinylic monomers selected from the group consisting of iso- prene, 1,3-butadiene, α-C 5-18 alkene, 4-vinyl-pyridine, 2-vinyl-pyridine, vinyl-imidazole, N-vinylpyrrolidone, dimethylacrylamide, 3-dimethylamino-propylmethacrylamide, styrene, substituted styrene and a compound of formula CH 2 =C(R 3 )-C(=R 4 )-R 5 , wherein R 3 is a hydrogen atom or a methyl group, R 4 is oxygen atom or sulfur atom; R 5 is N H 2 , hydroxy, unsubstituted C 1-18 alkoxy, C 2-100 alkoxy interrupted by at least one N and/or O atom, hydroxy-substituted C 1-18 alkoxy, unsubstituted C 1-18 alkylamino, di(C 1-18 alkyl) amino, hydroxy-substituted C 1-18 alkylamino, hydroxy-substituted di(C 1-18 alkyl)amino or -0-CH 2 -CH 2 -N(CH 3 ) 2 ; Y is the chain terminus of the polymer/copolymer Z n and Y represents the fragment of a polymerization initiator capable of initiating polymerization; Y1 represents a di-, tri- or polyvalent fragment of a di-, tri-, or polyfunctional NMP initiator; m is 2, 3 or 4, preferably 2; n is the number of monomer units Z and is between 10 and 5000.
Abstract:
The use of a polymer having a) a polyalkyleneimine backbone; b) at least one aromatic moiety P1
wherein # indicates the point of attachment to a nitrogen atom of the polyalkyleneimine backbone, Ar independently for each aromatic moiety P1 is 1,2-phenylene, 1,2-naphthylene, 2,3-naphthylene, or 1,8-naphthylene, wherein phenylene or naphthylene are unsubsituted or carry 1, 2, 3, 4, or 5 radicals which are selected from the group consisting of halogen, OH, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, COOH, CONH 2 , NO 2 , NH 2 , NH-CHO, NH- C 1 -C 4 -alkyl, and NH-(C=O)- C 1 -C 4 -alkyl;
c) at least one moiety P2,
wherein # indicates the point of attachment to a nitrogen atom of the polyalkyleneimine-backbone, n is an integer from 0 to 100, A 1 is independently selected from linear or branched alkylenes having 2 to 18 carbon atoms, A 2 for each individual repetition unit n A 2 is independently selected from linear or branched alkylenes having 2 to 18 carbon atoms,
Abstract:
The present invention relates to novel polymer compositions, to a process for their manufacturing, to the use of said polymer compositions for modifying the viscosity of aqueous compositions,and to water-borne coating compositions containing the novel polymer compositions as thickeners. The polymer compositions comprise a polymer material which is obtainable by reacting: a) a polymer P1 having at least one functional group of the formula (I), where k is an integer from 0 to 4; n is 0 or 1 p is an integer from 1 to 10, the number average of p being from 1.5 to 10; Q is a divalent moiety selected from the group consisting of -O-and -NH-; P is a p-valent hydrophilic neutral polymer radical;and R1 is as defined in the claims; with b) a succinic anhydride of the formula (II) where R is C4-C24-alkyl or C4-C24-alkenyl.