SU576962A3 - Способ получени пигментированных пористых гранул - Google Patents
Способ получени пигментированных пористых гранулInfo
- Publication number
- SU576962A3 SU576962A3 SU7402070755A SU2070755A SU576962A3 SU 576962 A3 SU576962 A3 SU 576962A3 SU 7402070755 A SU7402070755 A SU 7402070755A SU 2070755 A SU2070755 A SU 2070755A SU 576962 A3 SU576962 A3 SU 576962A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- granules
- water
- weight
- polyester resin
- monomer
- Prior art date
Links
- 239000008187 granular material Substances 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 9
- 239000000203 mixture Substances 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 12
- 239000000178 monomer Substances 0.000 claims description 12
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 9
- 239000011148 porous material Substances 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- 239000000049 pigment Substances 0.000 claims description 7
- 229920001225 polyester resin Polymers 0.000 claims description 7
- 239000004645 polyester resin Substances 0.000 claims description 7
- 238000006116 polymerization reaction Methods 0.000 claims description 6
- 229920006337 unsaturated polyester resin Polymers 0.000 claims description 5
- 239000006185 dispersion Substances 0.000 claims description 3
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 238000010494 dissociation reaction Methods 0.000 claims description 2
- 230000005593 dissociations Effects 0.000 claims description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 2
- 229920000768 polyamine Polymers 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical group OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 238000004132 cross linking Methods 0.000 claims 1
- 238000004945 emulsification Methods 0.000 claims 1
- 230000001804 emulsifying effect Effects 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 238000010907 mechanical stirring Methods 0.000 claims 1
- 229920000570 polyether Polymers 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 238000005245 sintering Methods 0.000 claims 1
- 238000009736 wetting Methods 0.000 claims 1
- 238000002156 mixing Methods 0.000 description 9
- 238000003756 stirring Methods 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N butyl alcohol Substances CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- -1 malonic Chemical class 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- CKFGINPQOCXMAZ-UHFFFAOYSA-N methanediol Chemical compound OCO CKFGINPQOCXMAZ-UHFFFAOYSA-N 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- SMNNDVUKAKPGDD-UHFFFAOYSA-N 2-butylbenzoic acid Chemical group CCCCC1=CC=CC=C1C(O)=O SMNNDVUKAKPGDD-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 235000010523 Cicer arietinum Nutrition 0.000 description 1
- 244000045195 Cicer arietinum Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- LHGJTWLUIMCSNN-UHFFFAOYSA-L disodium;sulfate;heptahydrate Chemical compound O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O LHGJTWLUIMCSNN-UHFFFAOYSA-L 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000008202 granule composition Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940005740 hexametaphosphate Drugs 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- CABDFQZZWFMZOD-UHFFFAOYSA-N hydrogen peroxide;hydrochloride Chemical compound Cl.OO CABDFQZZWFMZOD-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical class OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/28—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by elimination of a liquid phase from a macromolecular composition or article, e.g. drying of coagulum
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/205—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase
- C08J3/21—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase
- C08J3/215—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase at least one additive being also premixed with a liquid phase
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0004—Use of compounding ingredients, the chemical constitution of which is unknown, broadly defined, or irrelevant
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/28—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by elimination of a liquid phase from a macromolecular composition or article, e.g. drying of coagulum
- C08J9/283—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by elimination of a liquid phase from a macromolecular composition or article, e.g. drying of coagulum a discontinuous liquid phase emulsified in a continuous macromolecular phase
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/42—Gloss-reducing agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2367/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2367/06—Unsaturated polyesters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPB510173 | 1973-10-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU576962A3 true SU576962A3 (ru) | 1977-10-15 |
Family
ID=3765778
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU7402070755A SU576962A3 (ru) | 1973-10-04 | 1974-10-03 | Способ получени пигментированных пористых гранул |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US3923704A (enExample) |
| JP (1) | JPS5226917B2 (enExample) |
| AR (1) | AR218599A1 (enExample) |
| AT (1) | AT345560B (enExample) |
| AU (1) | AU481144B2 (enExample) |
| BE (1) | BE820679A (enExample) |
| BR (1) | BR7408226D0 (enExample) |
| CA (1) | CA1033900A (enExample) |
| CH (1) | CH588520A5 (enExample) |
| DE (1) | DE2447518A1 (enExample) |
| DK (1) | DK512474A (enExample) |
| ES (1) | ES430710A1 (enExample) |
| FR (1) | FR2246584B1 (enExample) |
| GB (1) | GB1491011A (enExample) |
| IE (1) | IE40033B1 (enExample) |
| IN (1) | IN142573B (enExample) |
| IT (1) | IT1022624B (enExample) |
| NL (1) | NL7413060A (enExample) |
| NO (1) | NO139224C (enExample) |
| SE (1) | SE415073B (enExample) |
| SU (1) | SU576962A3 (enExample) |
| ZA (1) | ZA746266B (enExample) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4049609A (en) * | 1974-10-25 | 1977-09-20 | Sintetica Americana, Inc. | Process for modifying unsaturated polyester systems |
| US4089819A (en) * | 1975-04-21 | 1978-05-16 | Dulux Australia Limited | Process of preparing vesiculated polyester resin granules |
| US4134810A (en) * | 1976-04-08 | 1979-01-16 | Japan Atomic Energy Research Institute | Process for preparing a heat-curable polymer emulsion using high energy radiation |
| ZA782493B (en) * | 1978-05-01 | 1979-12-27 | Anglo Amer Corp South Africa | Rate of change detection |
| AU5002279A (en) * | 1978-09-12 | 1980-03-20 | Dulux Australia Ltd. | Cross-linked polyester |
| US4398003A (en) * | 1980-08-28 | 1983-08-09 | The Dow Chemical Company | Process for preparing thermoset polymer spheres |
| ZW17683A1 (en) * | 1982-08-10 | 1985-03-06 | Dulux Australia Ltd | Process of preparing vesiculated polyester granules |
| US4399237A (en) * | 1982-11-15 | 1983-08-16 | E. I. Du Pont De Nemours & Co. | Vesiculated polymer granules containing TiO2 |
| US5800861A (en) * | 1985-08-15 | 1998-09-01 | The Sherwin-Williams Company | High solid infrared absorbing compositions |
| US4654083A (en) * | 1985-10-18 | 1987-03-31 | Desoto, Inc. | Light weight concrete and cementitious masonry products |
| GB8709688D0 (en) * | 1987-04-24 | 1987-05-28 | Unilever Plc | Porous material |
| NZ224284A (en) * | 1987-04-24 | 1990-11-27 | Unilever Plc | Porous substrate containing gel for use in chemical synthesis, separation etc |
| GB8712074D0 (en) * | 1987-05-21 | 1987-06-24 | Tioxide Group Plc | Drying process |
| GB9014689D0 (en) * | 1990-07-02 | 1990-08-22 | Tioxide Group Services Ltd | Supports for active entities |
| US5635764A (en) * | 1992-12-10 | 1997-06-03 | Nippondenso Co., Ltd. | Surface treated structure for solder joint |
| US5464887A (en) * | 1994-04-08 | 1995-11-07 | Ppg Industries, Inc. | Crosslinked unsaturated polyesters as flatting agents in aqueous electrocoating compositions |
| US5583162A (en) * | 1994-06-06 | 1996-12-10 | Biopore Corporation | Polymeric microbeads and method of preparation |
| US6048908A (en) * | 1997-06-27 | 2000-04-11 | Biopore Corporation | Hydrophilic polymeric material |
| AUPR604001A0 (en) * | 2001-06-29 | 2001-07-26 | Orica Australia Pty Ltd | Vesiculated polyester granules |
| US6780942B2 (en) * | 2001-12-20 | 2004-08-24 | Eastman Kodak Company | Method of preparation of porous polyester particles |
| NZ548792A (en) * | 2004-01-30 | 2009-10-30 | Orica Australia Pty Ltd | Suspension polymerisation process utilising a combination of peroxide initiators |
| US7887984B2 (en) * | 2007-01-18 | 2011-02-15 | Eastman Kodak Company | Toner porous particles containing hydrocolloids |
| US7754409B2 (en) * | 2007-01-18 | 2010-07-13 | Eastman Kodak Company | Toner manufacturing method |
| US7867679B2 (en) * | 2007-04-24 | 2011-01-11 | Eastman Kodak Company | Porous particles |
| US7888410B2 (en) * | 2007-04-24 | 2011-02-15 | Eastman Kodak Company | Method of making porous particles |
| US8252414B2 (en) | 2008-07-24 | 2012-08-28 | Eastman Kodak Company | Polymer particles with additives encapsulated in microvoids |
| US8241828B2 (en) * | 2009-04-30 | 2012-08-14 | Eastman Kodak Company | Method of filtering porous particles |
| US8142976B2 (en) * | 2009-12-03 | 2012-03-27 | Eastman Kodak Company | Method for preparing multiple emulsion and porous polymer particles therefrom |
| DE102016002221A1 (de) | 2016-02-26 | 2017-08-31 | Brillux Gmbh & Co. Kg | Dispersionsfarbe |
| US10241457B1 (en) | 2018-01-19 | 2019-03-26 | Eastman Kodak Company | Process control sensing of toner coverage |
| DE102019103273A1 (de) | 2019-02-11 | 2020-08-13 | Brillux Gmbh & Co. Kg | Verfahren zur Vermeidung des mikrobiellen Befalls einer Reinigungsvorrichtung für eine Dosieranlage |
| DE102019118429A1 (de) * | 2019-04-18 | 2020-10-22 | Brillux Gmbh & Co. Kg | Granulat und daraus hergestelltes Anstrichmittel |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1137554B (de) * | 1961-06-21 | 1962-10-04 | Bayer Ag | Verfahren zur Polymerisation von wasserunloeslichen Monomeren |
| US3692724A (en) * | 1970-07-06 | 1972-09-19 | Woods Res & Dev | Water extendible polyester resins |
-
1974
- 1974-09-23 AU AU73606/74A patent/AU481144B2/en not_active Expired
- 1974-09-24 US US508993A patent/US3923704A/en not_active Expired - Lifetime
- 1974-09-24 IE IE1977/74A patent/IE40033B1/xx unknown
- 1974-09-27 DK DK512474A patent/DK512474A/da not_active Application Discontinuation
- 1974-09-30 NO NO74743550A patent/NO139224C/no unknown
- 1974-10-02 ZA ZA00746266A patent/ZA746266B/xx unknown
- 1974-10-03 CA CA210640A patent/CA1033900A/en not_active Expired
- 1974-10-03 BE BE149192A patent/BE820679A/xx not_active IP Right Cessation
- 1974-10-03 GB GB42928/74A patent/GB1491011A/en not_active Expired
- 1974-10-03 FR FR7433349A patent/FR2246584B1/fr not_active Expired
- 1974-10-03 BR BR8226/74A patent/BR7408226D0/pt unknown
- 1974-10-03 SU SU7402070755A patent/SU576962A3/ru active
- 1974-10-03 SE SE7412473A patent/SE415073B/xx not_active IP Right Cessation
- 1974-10-03 CH CH1329474A patent/CH588520A5/xx not_active IP Right Cessation
- 1974-10-03 NL NL7413060A patent/NL7413060A/xx not_active Application Discontinuation
- 1974-10-04 AT AT801374A patent/AT345560B/de not_active IP Right Cessation
- 1974-10-04 DE DE19742447518 patent/DE2447518A1/de not_active Ceased
- 1974-10-04 JP JP49113965A patent/JPS5226917B2/ja not_active Expired
- 1974-10-04 AR AR255925A patent/AR218599A1/es active
- 1974-10-04 ES ES430710A patent/ES430710A1/es not_active Expired
- 1974-10-04 IN IN2219/CAL/1974A patent/IN142573B/en unknown
- 1974-10-04 IT IT28100/74A patent/IT1022624B/it active
Also Published As
| Publication number | Publication date |
|---|---|
| ES430710A1 (es) | 1976-09-01 |
| FR2246584B1 (enExample) | 1978-12-01 |
| SE415073B (sv) | 1980-09-08 |
| AU7360674A (en) | 1976-03-25 |
| NO139224C (no) | 1979-01-24 |
| NO743550L (enExample) | 1975-04-07 |
| ZA746266B (en) | 1976-05-26 |
| IN142573B (enExample) | 1977-07-30 |
| SE7412473L (enExample) | 1975-04-07 |
| IT1022624B (it) | 1978-04-20 |
| BE820679A (fr) | 1975-02-03 |
| ATA801374A (de) | 1978-01-15 |
| AR218599A1 (es) | 1980-06-30 |
| NO139224B (no) | 1978-10-16 |
| DE2447518A1 (de) | 1975-04-17 |
| AT345560B (de) | 1978-09-25 |
| JPS5065591A (enExample) | 1975-06-03 |
| FR2246584A1 (enExample) | 1975-05-02 |
| BR7408226D0 (pt) | 1975-07-22 |
| IE40033B1 (en) | 1979-02-28 |
| DK512474A (enExample) | 1975-06-09 |
| CH588520A5 (enExample) | 1977-06-15 |
| CA1033900A (en) | 1978-06-27 |
| AU481144B2 (en) | 1977-02-21 |
| JPS5226917B2 (enExample) | 1977-07-16 |
| GB1491011A (en) | 1977-11-09 |
| IE40033L (en) | 1975-04-04 |
| US3923704A (en) | 1975-12-02 |
| NL7413060A (nl) | 1975-04-08 |
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