DE2756774A1 - Mischung aus ammoniak und oxalkylierten polysiloxanen und deren verwendung als waermesensibilisierungsmittel - Google Patents
Mischung aus ammoniak und oxalkylierten polysiloxanen und deren verwendung als waermesensibilisierungsmittelInfo
- Publication number
- DE2756774A1 DE2756774A1 DE19772756774 DE2756774A DE2756774A1 DE 2756774 A1 DE2756774 A1 DE 2756774A1 DE 19772756774 DE19772756774 DE 19772756774 DE 2756774 A DE2756774 A DE 2756774A DE 2756774 A1 DE2756774 A1 DE 2756774A1
- Authority
- DE
- Germany
- Prior art keywords
- numbers
- mixture
- stands
- ammonia
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims description 52
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 title claims description 47
- 229920001296 polysiloxane Polymers 0.000 title claims description 37
- 229910021529 ammonia Inorganic materials 0.000 title claims description 20
- -1 polysiloxanes Polymers 0.000 claims description 45
- 229920000126 latex Polymers 0.000 claims description 29
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 claims description 7
- 150000005840 aryl radicals Chemical class 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical group 0.000 claims description 5
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 229920001971 elastomer Polymers 0.000 claims description 3
- 150000003254 radicals Chemical class 0.000 claims description 3
- 239000005060 rubber Substances 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 22
- 238000005345 coagulation Methods 0.000 description 21
- 230000015271 coagulation Effects 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 239000004816 latex Substances 0.000 description 16
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 15
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 10
- 239000003995 emulsifying agent Substances 0.000 description 10
- 239000000178 monomer Substances 0.000 description 10
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 9
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 8
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 7
- 235000011114 ammonium hydroxide Nutrition 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 7
- 238000006555 catalytic reaction Methods 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000008346 aqueous phase Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 229910015900 BF3 Inorganic materials 0.000 description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
- 229910018557 Si O Inorganic materials 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 239000012230 colorless oil Substances 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000007720 emulsion polymerization reaction Methods 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 229920001521 polyalkylene glycol ether Polymers 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000004073 vulcanization Methods 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-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
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- HXBPYFMVGFDZFT-UHFFFAOYSA-N allyl isocyanate Chemical compound C=CCN=C=O HXBPYFMVGFDZFT-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 150000002924 oxiranes Chemical class 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- BHMLFPOTZYRDKA-IRXDYDNUSA-N (2s)-2-[(s)-(2-iodophenoxy)-phenylmethyl]morpholine Chemical compound IC1=CC=CC=C1O[C@@H](C=1C=CC=CC=1)[C@H]1OCCNC1 BHMLFPOTZYRDKA-IRXDYDNUSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical compound [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- GXBYFVGCMPJVJX-UHFFFAOYSA-N Epoxybutene Chemical compound C=CC1CO1 GXBYFVGCMPJVJX-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 206010057040 Temperature intolerance Diseases 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 230000008543 heat sensitivity Effects 0.000 description 1
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical class CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- OCAAZRFBJBEVPS-UHFFFAOYSA-N prop-2-enyl carbamate Chemical compound NC(=O)OCC=C OCAAZRFBJBEVPS-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- RKQOSDAEEGPRER-UHFFFAOYSA-L zinc diethyldithiocarbamate Chemical compound [Zn+2].CCN(CC)C([S-])=S.CCN(CC)C([S-])=S RKQOSDAEEGPRER-UHFFFAOYSA-L 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C1/00—Treatment of rubber latex
- C08C1/14—Coagulation
- C08C1/145—Heat-sensitising agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/28—Nitrogen-containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Silicon Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772756774 DE2756774A1 (de) | 1977-12-20 | 1977-12-20 | Mischung aus ammoniak und oxalkylierten polysiloxanen und deren verwendung als waermesensibilisierungsmittel |
| US05/969,100 US4250071A (en) | 1977-12-20 | 1978-12-13 | Mixture of ammonia and alkoxylated poly-siloxanes and its use as a heat sensitizer |
| DE7878101652T DE2861662D1 (en) | 1977-12-20 | 1978-12-13 | Mixture of ammoniac and a polyoxyalkylene siloxane; application as heat-sensitising agent in latices and process for making heat-sensitised rubber latices |
| EP78101652A EP0002720B1 (de) | 1977-12-20 | 1978-12-13 | Mischung aus Ammoniak und oxalkylierten Polysiloxanen, deren Verwendung als Wärmesensibilisierungsmittel und Verfahren zur Herstellung wärmesensibilisierter Kautschuklatices |
| JP15504878A JPS5490352A (en) | 1977-12-20 | 1978-12-18 | Mixture of ammonia and alkoxylated polysiloxane * and use as heattsensitive |
| CA318,133A CA1108109A (en) | 1977-12-20 | 1978-12-18 | Mixture of ammonia and alkoxylated polysiloxanes and its use as a heat sensitiser |
| BR7808334A BR7808334A (pt) | 1977-12-20 | 1978-12-19 | Composicao de amoniaco e polissiloxanos alcoxilados e seu emprego como sensibilizante ao calor |
| ES476137A ES476137A1 (es) | 1977-12-20 | 1978-12-19 | Procedimiento para la obtencion de un latex polimero termo- sensible. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772756774 DE2756774A1 (de) | 1977-12-20 | 1977-12-20 | Mischung aus ammoniak und oxalkylierten polysiloxanen und deren verwendung als waermesensibilisierungsmittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2756774A1 true DE2756774A1 (de) | 1979-06-28 |
Family
ID=6026644
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19772756774 Withdrawn DE2756774A1 (de) | 1977-12-20 | 1977-12-20 | Mischung aus ammoniak und oxalkylierten polysiloxanen und deren verwendung als waermesensibilisierungsmittel |
| DE7878101652T Expired DE2861662D1 (en) | 1977-12-20 | 1978-12-13 | Mixture of ammoniac and a polyoxyalkylene siloxane; application as heat-sensitising agent in latices and process for making heat-sensitised rubber latices |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE7878101652T Expired DE2861662D1 (en) | 1977-12-20 | 1978-12-13 | Mixture of ammoniac and a polyoxyalkylene siloxane; application as heat-sensitising agent in latices and process for making heat-sensitised rubber latices |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4250071A (enExample) |
| EP (1) | EP0002720B1 (enExample) |
| JP (1) | JPS5490352A (enExample) |
| BR (1) | BR7808334A (enExample) |
| CA (1) | CA1108109A (enExample) |
| DE (2) | DE2756774A1 (enExample) |
| ES (1) | ES476137A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12163027B2 (en) | 2022-07-20 | 2024-12-10 | Karex Holdings Sdn. Bhd. | Nitrile rubber condoms and methods of making them |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3038982A1 (de) * | 1980-10-15 | 1982-05-27 | Bayer Ag, 5090 Leverkusen | Entschaeumer fuer kunststoffdispersionen und disperionsbeschichtungsstoffe sowie verfahren zu dessen herstellung |
| US4535113A (en) * | 1984-03-13 | 1985-08-13 | Union Carbide Corporation | Olefin polymer compositions containing silicone additives and the use thereof in the production of film material |
| US5984929A (en) * | 1997-08-29 | 1999-11-16 | Target Therapeutics, Inc. | Fast detaching electronically isolated implant |
| US7638091B2 (en) * | 2004-07-02 | 2009-12-29 | Sabic Innovative Plastics Ip B. V. | Methods of sterilizing polycarbonate articles and methods of manufacture |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3246339A (en) * | 1961-10-17 | 1966-04-19 | Bayer Ag | Process for preventing the formation of web fingers in gloves made from latex by immersion |
| US3255140A (en) * | 1961-10-17 | 1966-06-07 | Bayer Ag | Siloxane heat sensitizing agents for latex mixtures |
| NL295018A (enExample) * | 1962-07-06 | |||
| US3341338A (en) * | 1965-05-28 | 1967-09-12 | Union Carbide Corp | Polysiloxane polish formulations |
| US3306869A (en) * | 1965-09-22 | 1967-02-28 | Union Carbide Corp | Floor polishes containing siloxane-oxyalkylene block copolymer leveling agents |
| DE1243394B (de) * | 1966-03-09 | 1967-06-29 | Bayer Ag | Verfahren zur Herstellung eines waermesensibilisierbaren Synthesekautschuk-Latex |
| US3484394A (en) * | 1967-06-07 | 1969-12-16 | Gen Electric | Heat-sensitive latex |
| DE2005974B2 (de) * | 1969-02-11 | 1979-09-20 | Goodrich Co B F | Wärmesensibilisierte Latices |
| US3629310A (en) * | 1969-08-28 | 1971-12-21 | Union Carbide Corp | Organo-siloxane-oxyalkylene block copolymers |
| US3702315A (en) * | 1970-10-21 | 1972-11-07 | Goodrich Co B F | Heat sensitive latices |
| US3969289A (en) * | 1971-03-15 | 1976-07-13 | General Latex And Chemical Corporation | One-part foamable latex composition |
| DE2232526A1 (de) * | 1972-07-03 | 1974-01-31 | Bayer Ag | Waermesensibilisierte latexmischungen |
-
1977
- 1977-12-20 DE DE19772756774 patent/DE2756774A1/de not_active Withdrawn
-
1978
- 1978-12-13 EP EP78101652A patent/EP0002720B1/de not_active Expired
- 1978-12-13 DE DE7878101652T patent/DE2861662D1/de not_active Expired
- 1978-12-13 US US05/969,100 patent/US4250071A/en not_active Expired - Lifetime
- 1978-12-18 CA CA318,133A patent/CA1108109A/en not_active Expired
- 1978-12-18 JP JP15504878A patent/JPS5490352A/ja active Granted
- 1978-12-19 ES ES476137A patent/ES476137A1/es not_active Expired
- 1978-12-19 BR BR7808334A patent/BR7808334A/pt unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12163027B2 (en) | 2022-07-20 | 2024-12-10 | Karex Holdings Sdn. Bhd. | Nitrile rubber condoms and methods of making them |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2861662D1 (en) | 1982-04-08 |
| EP0002720A1 (de) | 1979-07-11 |
| JPS5490352A (en) | 1979-07-18 |
| BR7808334A (pt) | 1979-08-07 |
| US4250071A (en) | 1981-02-10 |
| EP0002720B1 (de) | 1982-03-10 |
| ES476137A1 (es) | 1979-04-16 |
| JPS6123814B2 (enExample) | 1986-06-07 |
| CA1108109A (en) | 1981-09-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1894961B1 (de) | Silicon-Blockcopolymere gepfropft mit ungesättigten Monomeren | |
| DE60114177T2 (de) | Verfahren zur kondensation von verbindungen, die siliciumgebundene hydroxyl-oder alkoxygruppen enthalten | |
| EP0143877A1 (de) | Stabile Siliconemulsionen | |
| DE1205699B (de) | Verfahren zur Herstellung waessriger Dispersionen von AEthylen-Mischpolymerisaten | |
| DE2902528A1 (de) | Textilschlichtmittel | |
| DE1947268B2 (de) | Siloxan-polyoxyalkylen-blockcopolymerisate und deren verwendung | |
| DE2534304C2 (de) | Wärmeempfindliche Latexzubereitung | |
| DE69111163T2 (de) | Verfahren zur Herstellung von stabilem Latex. | |
| DE2756774A1 (de) | Mischung aus ammoniak und oxalkylierten polysiloxanen und deren verwendung als waermesensibilisierungsmittel | |
| EP0025979B1 (de) | Wässrige Lösung oder Dispersion eines Styrol/Maleinsäureanhydrid-Copolymers, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE671378C (de) | Verfahren zur Herstellung von Mischpolymerisaten | |
| EP0121184B1 (de) | Verwendung von Bis-Halbestern der Sulfobernsteinsäure mit Polyetherdiolen aud Basis Ethylenoxid/Propylenoxid bzw. ihrer Salze als Polymerisationsemulgatoren | |
| EP0002519B1 (de) | Oxalkylierte Polysiloxane, deren Herstellung und Verwendung als Wärmesensibilisierungsmittel | |
| DE2742234A1 (de) | Emulgator zur emulsionspolimerisation | |
| EP0234416B1 (de) | Zitronensäurederivate als Emulgatoren für die Emulsationspolymerisation | |
| DE1470927A1 (de) | Verfahren zur Erhoehung der durchschnittlichen Teilchengroesse synthetischer Latices | |
| DE3701579C2 (enExample) | ||
| DE2402165A1 (de) | Verfahren zum polymerisieren von chloropren | |
| DE973985C (de) | Verfahren zur Herstellung von als Dispergiermittel dienenden esterartigen Produkten | |
| EP3583196B1 (de) | Emulsionen von beta-ketocarbonyl-funktionellen organosiliciumverbindungen | |
| DE2237584A1 (de) | Polymere pentaerythrit-phosphite, verfahren zu ihrer herstellung und ihre verwendung fuer die polyurethanherstellung | |
| EP0209774B1 (de) | Verfahren zur Herstellung von verpastbaren Vinylchlorid-Polymerisaten | |
| DE2301789A1 (de) | Siloxan-polyoxyalkylen-blockmischpolymer, verfahren zu dessen herstellung und zwischenprodukt in form eines polyoxyalkylenpolymeren | |
| US2433831A (en) | Aqueous dispersions of vulcanized fatty oils | |
| DE3541515C2 (enExample) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8130 | Withdrawal |