DE2927807A1 - Haertbare masse - Google Patents
Haertbare masseInfo
- Publication number
- DE2927807A1 DE2927807A1 DE19792927807 DE2927807A DE2927807A1 DE 2927807 A1 DE2927807 A1 DE 2927807A1 DE 19792927807 DE19792927807 DE 19792927807 DE 2927807 A DE2927807 A DE 2927807A DE 2927807 A1 DE2927807 A1 DE 2927807A1
- Authority
- DE
- Germany
- Prior art keywords
- acid
- tin
- lead
- weight
- composition according
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims description 35
- 229920000642 polymer Polymers 0.000 claims description 20
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 12
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 claims description 10
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 claims description 8
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 6
- -1 amine compound Chemical class 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 6
- 229920000620 organic polymer Polymers 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- IUTCEZPPWBHGIX-UHFFFAOYSA-N tin(2+) Chemical class [Sn+2] IUTCEZPPWBHGIX-UHFFFAOYSA-N 0.000 claims description 6
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 claims description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
- 230000002378 acidificating effect Effects 0.000 claims description 5
- 229940070765 laurate Drugs 0.000 claims description 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 4
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 claims description 4
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 4
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 claims description 4
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 claims description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 4
- 229960002446 octanoic acid Drugs 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 claims description 3
- 239000000945 filler Substances 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 claims description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 2
- PXRFIHSUMBQIOK-CVBJKYQLSA-L (z)-octadec-9-enoate;tin(2+) Chemical compound [Sn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O PXRFIHSUMBQIOK-CVBJKYQLSA-L 0.000 claims description 2
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 claims description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 2
- AFPHTEQTJZKQAQ-UHFFFAOYSA-N 3-nitrobenzoic acid Chemical compound OC(=O)C1=CC=CC([N+]([O-])=O)=C1 AFPHTEQTJZKQAQ-UHFFFAOYSA-N 0.000 claims description 2
- OTLNPYWUJOZPPA-UHFFFAOYSA-N 4-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1 OTLNPYWUJOZPPA-UHFFFAOYSA-N 0.000 claims description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 2
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 claims description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 2
- 239000005639 Lauric acid Substances 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 2
- 239000005642 Oleic acid Substances 0.000 claims description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- 235000021355 Stearic acid Nutrition 0.000 claims description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims description 2
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 claims description 2
- 229940106681 chloroacetic acid Drugs 0.000 claims description 2
- 235000015165 citric acid Nutrition 0.000 claims description 2
- 229960002887 deanol Drugs 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 2
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 claims description 2
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 claims description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 2
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 claims description 2
- 229940049964 oleate Drugs 0.000 claims description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
- 235000006408 oxalic acid Nutrition 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 235000019260 propionic acid Nutrition 0.000 claims description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 2
- 239000008117 stearic acid Substances 0.000 claims description 2
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims 2
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- KVKFRMCSXWQSNT-UHFFFAOYSA-N n,n'-dimethylethane-1,2-diamine Chemical compound CNCCNC KVKFRMCSXWQSNT-UHFFFAOYSA-N 0.000 claims 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 10
- 230000006835 compression Effects 0.000 description 9
- 238000007906 compression Methods 0.000 description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- 238000011084 recovery Methods 0.000 description 8
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 6
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 239000003112 inhibitor Substances 0.000 description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 230000032683 aging Effects 0.000 description 4
- 239000004359 castor oil Substances 0.000 description 4
- 235000019438 castor oil Nutrition 0.000 description 4
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000000565 sealant Substances 0.000 description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000005077 polysulfide Substances 0.000 description 2
- 229920001021 polysulfide Polymers 0.000 description 2
- 150000008117 polysulfides Polymers 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- BOZRCGLDOHDZBP-UHFFFAOYSA-N 2-ethylhexanoic acid;tin Chemical compound [Sn].CCCCC(CC)C(O)=O BOZRCGLDOHDZBP-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- ICTGOBXINXNBMY-UHFFFAOYSA-L decanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCC([O-])=O.CCCCCCCCCC([O-])=O ICTGOBXINXNBMY-UHFFFAOYSA-L 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- PYBNTRWJKQJDRE-UHFFFAOYSA-L dodecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O PYBNTRWJKQJDRE-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- RRBRFYNWESTLOL-UHFFFAOYSA-L hexanoate;tin(2+) Chemical compound [Sn+2].CCCCCC([O-])=O.CCCCCC([O-])=O RRBRFYNWESTLOL-UHFFFAOYSA-L 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- SBOJXQVPLKSXOG-UHFFFAOYSA-N o-amino-hydroxylamine Chemical compound NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 description 1
- CYCFYXLDTSNTGP-UHFFFAOYSA-L octadecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CYCFYXLDTSNTGP-UHFFFAOYSA-L 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- UZRCGISJYYLJMA-UHFFFAOYSA-N phenol;styrene Chemical compound OC1=CC=CC=C1.C=CC1=CC=CC=C1 UZRCGISJYYLJMA-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/695—Polyesters containing atoms other than carbon, hydrogen and oxygen containing silicon
- C08G63/6954—Polyesters containing atoms other than carbon, hydrogen and oxygen containing silicon derived from polxycarboxylic acids and polyhydroxy compounds
- C08G63/6956—Dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/91—Polymers modified by chemical after-treatment
- C08G63/914—Polymers modified by chemical after-treatment derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/916—Dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/91—Polymers modified by chemical after-treatment
- C08G63/914—Polymers modified by chemical after-treatment derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/918—Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G85/00—General processes for preparing compounds provided for in this subclass
- C08G85/004—Modification of polymers by chemical after-treatment
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S528/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S528/901—Room temperature curable silicon-containing polymer
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)
- Compositions Of Macromolecular Compounds (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Sealing Material Composition (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8328378A JPS559669A (en) | 1978-07-07 | 1978-07-07 | Curable composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2927807A1 true DE2927807A1 (de) | 1980-01-31 |
| DE2927807C2 DE2927807C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1989-07-13 |
Family
ID=13798037
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19792927807 Granted DE2927807A1 (de) | 1978-07-07 | 1979-07-06 | Haertbare masse |
Country Status (9)
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0106330A1 (en) * | 1982-10-15 | 1984-04-25 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Pressure sensitive adhesive composition |
| EP0228087A3 (en) * | 1985-12-27 | 1988-04-06 | Toray Silicone Company Limited | Room-temperature curable silicone-modified polyether composition |
| EP0473793A4 (en) * | 1990-03-09 | 1992-09-02 | Kanegafuchi Chemical Industry Co., Ltd. | Curable composition |
| EP0532049A1 (en) * | 1991-09-12 | 1993-03-17 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Curable composition |
| EP0538881A3 (en) * | 1991-10-24 | 1993-08-04 | Kanegafuchi Chemical Industry Co., Ltd. | Curable resin composition |
| EP0538880A3 (en) * | 1991-10-24 | 1993-08-04 | Kanegafuchi Chemical Industry Co., Ltd. | Curable resin composition |
| EP0541074A3 (en) * | 1991-11-06 | 1993-09-08 | Sunrise Meisei Corporation | Non-pollution sealant compound |
Families Citing this family (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5763351A (en) * | 1980-10-03 | 1982-04-16 | Kanegafuchi Chem Ind Co Ltd | Composition having improved pot life |
| JPS57155249A (en) * | 1981-03-20 | 1982-09-25 | Kanegafuchi Chem Ind Co Ltd | Curable composition |
| JPS58136225A (ja) * | 1982-02-08 | 1983-08-13 | 株式会社日立製作所 | 地絡方向継電器 |
| FR2565413B1 (fr) * | 1984-05-29 | 1986-08-29 | Elf Aquitaine | Materiau macromoleculaire a conduction ionique pour la realisation d'electrolytes ou d'electrodes |
| US6576733B1 (en) * | 1990-03-09 | 2003-06-10 | Kanegafuchi Chemical Industry Co., Ltd. | Curable oxypropylene polymer composition |
| JP2832496B2 (ja) * | 1991-09-09 | 1998-12-09 | 鐘淵化学工業株式会社 | 硬化性組成物の作業性を改善しつつ、硬化物の表面の粘着性または埃付着性を改善する方法 |
| US5965260A (en) * | 1991-09-12 | 1999-10-12 | Kansai Research Institute (Kri) | Highly oriented polymer fiber and method for making the same |
| US5227434A (en) * | 1992-08-26 | 1993-07-13 | Olin Corporation | Moisture curable polymers |
| JP3976350B2 (ja) | 1997-03-14 | 2007-09-19 | スリーエム カンパニー | 反応性シラン官能性を有する要求に応じて硬化する、湿分硬化性組成物 |
| US6262289B1 (en) | 1997-06-11 | 2001-07-17 | Kaneka Corporation | Process for preparing cyclic oligosiloxanes |
| US6828403B2 (en) * | 1998-04-27 | 2004-12-07 | Essex Specialty Products, Inc. | Method of bonding a window to a substrate using a silane functional adhesive composition |
| EP1080126B1 (en) | 1998-04-27 | 2003-10-22 | Essex Specialty Products, Inc. | Method of bonding a window to a substrate using a silane functional adhesive composition |
| US6410640B1 (en) | 1999-03-29 | 2002-06-25 | Kaneka Corporation | One-pack type curable resin composition |
| DE60232456D1 (de) * | 2001-07-27 | 2009-07-09 | Kaneka Corp | Härtbare zusammensetzung |
| US6649016B2 (en) | 2002-03-04 | 2003-11-18 | Dow Global Technologies Inc. | Silane functional adhesive composition and method of bonding a window to a substrate without a primer |
| WO2004031300A1 (ja) * | 2002-10-02 | 2004-04-15 | Kaneka Corporation | 硬化性組成物 |
| WO2004031299A1 (ja) * | 2002-10-02 | 2004-04-15 | Kaneka Corporation | １液型硬化性組成物 |
| JP4101632B2 (ja) * | 2002-11-01 | 2008-06-18 | 株式会社カネカ | 硬化性組成物および復元性、クリープ性改善方法 |
| CN100429279C (zh) | 2003-05-12 | 2008-10-29 | 株式会社钟化 | 固化性组合物 |
| JP4533842B2 (ja) | 2003-08-01 | 2010-09-01 | セメダイン株式会社 | 硬化性組成物及び硬化性組成物の製造方法 |
| JP4874650B2 (ja) | 2003-08-25 | 2012-02-15 | 株式会社カネカ | 耐熱性の改善された硬化性組成物 |
| CA2547767A1 (en) * | 2003-12-10 | 2005-06-30 | Dow Global Technologies Inc. | System for bonding glass into a structure |
| JP4504007B2 (ja) * | 2003-12-22 | 2010-07-14 | セメダイン株式会社 | 建築用弾性シーリング材組成物 |
| WO2005097908A1 (ja) | 2004-04-01 | 2005-10-20 | Kaneka Corporation | １液型硬化性組成物 |
| WO2005097907A1 (ja) * | 2004-04-01 | 2005-10-20 | Kaneka Corporation | 硬化性組成物 |
| JPWO2005097898A1 (ja) * | 2004-04-01 | 2008-02-28 | 株式会社カネカ | 硬化性組成物 |
| US20080269405A1 (en) * | 2004-04-01 | 2008-10-30 | Toshihiko Okamoto | Single-Component Curable Composition |
| JP2005320447A (ja) * | 2004-05-10 | 2005-11-17 | Sanyo Chem Ind Ltd | 硬化性組成物 |
| US8030427B2 (en) * | 2004-06-09 | 2011-10-04 | Kaneka Corporation | Curable composition |
| US7494540B2 (en) * | 2004-12-15 | 2009-02-24 | Dow Global Technologies, Inc. | System for bonding glass into a structure |
| WO2006070637A1 (ja) | 2004-12-28 | 2006-07-06 | Kaneka Corporation | 硬化性組成物 |
| WO2006112340A1 (ja) * | 2005-04-15 | 2006-10-26 | Kaneka Corporation | 透明性に優れた硬化性組成物及び硬化物 |
| WO2007036981A1 (ja) | 2005-09-27 | 2007-04-05 | Cemedine Co., Ltd. | 硬化性組成物 |
| JP5420840B2 (ja) | 2005-09-30 | 2014-02-19 | 株式会社カネカ | 硬化性と貯蔵安定性の改善された硬化性組成物 |
| JP5243798B2 (ja) | 2005-09-30 | 2013-07-24 | 株式会社カネカ | 硬化性と接着性の改善された硬化性組成物 |
| CN101490134A (zh) * | 2006-07-25 | 2009-07-22 | 旭硝子株式会社 | 氧化烯聚合物的制造方法 |
| US8124690B2 (en) | 2006-09-13 | 2012-02-28 | Kaneka Corporation | Moisture curable polymer having SiF group, and curable composition containing the same |
| CN102443162B (zh) | 2006-11-01 | 2015-05-13 | 株式会社钟化 | 固化性有机聚合物及其制造方法以及含该聚合物的固化性组合物 |
| US7842146B2 (en) * | 2007-01-26 | 2010-11-30 | Dow Global Technologies Inc. | Ultrasonic energy for adhesive bonding |
| US7819964B2 (en) * | 2007-02-16 | 2010-10-26 | Dow Global Technologies Inc. | System for bonding glass into a structure |
| JP2010116444A (ja) * | 2008-11-11 | 2010-05-27 | Kaneka Corp | 硬化性組成物 |
| CN102834461B (zh) | 2009-10-16 | 2015-10-21 | 株式会社钟化 | 固化性组合物 |
| JP5883439B2 (ja) | 2010-11-24 | 2016-03-15 | 株式会社カネカ | 硬化性組成物 |
| US20140093679A1 (en) | 2011-04-15 | 2014-04-03 | Kaneka Corporation | Cladding material for construction |
| JP6272763B2 (ja) | 2012-09-28 | 2018-01-31 | 株式会社カネカ | 構造体 |
| CN105622926B (zh) * | 2015-12-23 | 2017-11-03 | 江苏苏博特新材料股份有限公司 | 一种高分子量双烯丙基封端聚醚的制备方法 |
| EP4407005A1 (en) | 2021-09-24 | 2024-07-31 | Kaneka Corporation | Curable composition |
| JPWO2024029615A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2022-08-04 | 2024-02-08 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3676420A (en) * | 1969-04-25 | 1972-07-11 | Michael Fulton | Room temperature vulcanizable silicone rubber composition |
| US3839280A (en) * | 1971-07-28 | 1974-10-01 | Gen Electric | Curable siloxane resin compositions |
| US3971751A (en) * | 1975-06-09 | 1976-07-27 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Vulcanizable silylether terminated polymer |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3231527A (en) * | 1966-01-25 | Curing organopolysiloxanes with a combination of trichloroacetic acid andidibutylxtin | ||
| US3109826A (en) * | 1963-11-05 | Room temperature curable organo- | ||
| US2676948A (en) * | 1952-10-21 | 1954-04-27 | Westinghouse Electric Corp | Curing catalyst for polysiloxane resins |
| US2843555A (en) * | 1956-10-01 | 1958-07-15 | Gen Electric | Room temperature curing organopolysiloxane |
| US3070559A (en) * | 1958-09-12 | 1962-12-25 | Wacker Chemie Gmbh | Silicone rubber stocks |
| US3077465A (en) * | 1959-09-28 | 1963-02-12 | Dow Corning | One component room temperature vulcanizable organopolysiloxane elastomers |
| US3408321A (en) * | 1965-06-14 | 1968-10-29 | Gen Electric | Moisture curable siloxy terminated polyethers |
| GB1154853A (en) * | 1965-08-26 | 1969-06-11 | Gen Electric | Improvements in Curable Compositions |
| GB1207594A (en) * | 1967-03-16 | 1970-10-07 | Union Carbide Corp | One component room temperature vulcanizable silicon terminated polymers |
| BE759618A (fr) * | 1969-12-01 | 1971-06-01 | Dow Corning | Procede pour promouvoir la reaction entre un radical hydroxyle lie au silicium et un radical alcoxy lie au silicium |
| JPS5273998A (en) * | 1975-12-16 | 1977-06-21 | Kanegafuchi Chem Ind Co Ltd | Room temperature curing compositions |
-
1978
- 1978-07-07 JP JP8328378A patent/JPS559669A/ja active Granted
-
1979
- 1979-07-06 FR FR7917565A patent/FR2430439B1/fr not_active Expired
- 1979-07-06 DE DE19792927807 patent/DE2927807A1/de active Granted
- 1979-07-06 CA CA331,283A patent/CA1112791A/en not_active Expired
- 1979-07-06 BE BE0/196179A patent/BE877541A/fr not_active IP Right Cessation
- 1979-07-06 GB GB7923677A patent/GB2029842B/en not_active Expired
- 1979-07-06 IT IT49676/79A patent/IT1164695B/it active
- 1979-07-06 NL NL7905314A patent/NL7905314A/nl not_active Application Discontinuation
-
1983
- 1983-11-08 US US06/524,029 patent/US4507469A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3676420A (en) * | 1969-04-25 | 1972-07-11 | Michael Fulton | Room temperature vulcanizable silicone rubber composition |
| US3839280A (en) * | 1971-07-28 | 1974-10-01 | Gen Electric | Curable siloxane resin compositions |
| US3971751A (en) * | 1975-06-09 | 1976-07-27 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Vulcanizable silylether terminated polymer |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0106330A1 (en) * | 1982-10-15 | 1984-04-25 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Pressure sensitive adhesive composition |
| EP0228087A3 (en) * | 1985-12-27 | 1988-04-06 | Toray Silicone Company Limited | Room-temperature curable silicone-modified polyether composition |
| EP0473793A4 (en) * | 1990-03-09 | 1992-09-02 | Kanegafuchi Chemical Industry Co., Ltd. | Curable composition |
| EP0532049A1 (en) * | 1991-09-12 | 1993-03-17 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Curable composition |
| EP0538881A3 (en) * | 1991-10-24 | 1993-08-04 | Kanegafuchi Chemical Industry Co., Ltd. | Curable resin composition |
| EP0538880A3 (en) * | 1991-10-24 | 1993-08-04 | Kanegafuchi Chemical Industry Co., Ltd. | Curable resin composition |
| EP0541074A3 (en) * | 1991-11-06 | 1993-09-08 | Sunrise Meisei Corporation | Non-pollution sealant compound |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS559669A (en) | 1980-01-23 |
| NL7905314A (nl) | 1980-01-09 |
| IT7949676A0 (it) | 1979-07-06 |
| FR2430439A1 (fr) | 1980-02-01 |
| FR2430439B1 (fr) | 1985-11-08 |
| DE2927807C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1989-07-13 |
| GB2029842B (en) | 1982-09-22 |
| IT1164695B (it) | 1987-04-15 |
| JPS6160867B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1986-12-23 |
| BE877541A (fr) | 1980-01-07 |
| GB2029842A (en) | 1980-03-26 |
| US4507469A (en) | 1985-03-26 |
| CA1112791A (en) | 1981-11-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2927807C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE2523224C3 (de) | Verfahren zum Verstärken des Haftens von Organopolysiloxanelastomeren | |
| EP0089066B1 (de) | Verfahren zum Verstärken des Haftens von Organopolysiloxanelastomeren | |
| EP0281936B1 (de) | Wässrige Schichtsilikatdispersionen, Verwendung dieser Dispersionen als Lackhilfsmittel und wasserverdünnbare, Schichtsilikate enthaltende Beschichtungszusammensetzungen | |
| DE2653499C3 (de) | Unter Ausschluß von Wasser lagerfähige bei Zutritt desselben bei Raumtemperatur zu Elastomeren vernetzende Organopolysiloxanformmassen | |
| DE1928129B2 (de) | Verfahren zur Herstellung von nichtzelligen Polyurethankunststoffen | |
| EP0261409A1 (de) | Verfarhen zur herstellung von Alkoxysilanterminierten, feuchtigkeitsärtenden Polyurethanen sowie ihre Verwendung für Klebe- und Dichtungsmassen | |
| DE3500979A1 (de) | Organopolysiloxanmasse und ihre verwendung | |
| DE2437889B2 (de) | Polyurethan-Elastomere und ihre Herstellung | |
| DE2051242A1 (de) | Komposition aus Kautschuk und amorphem Polybutadien 1,2, sowie Ver fahren zu deren Herstellung | |
| DE1114318B (de) | Verfahren zur Herstellung von vernetzten homogenen Elastomeren | |
| DE3424443C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| EP0603747B1 (de) | Zusammensetzungen zur Imprägnierung von mineralischen Baustoffen | |
| EP0367012B1 (de) | Unter Ausschluss von Feuchtigkeit lagerfähige RTV-1K-Massen, die überstreichbare Elastomere bilden | |
| DE69233460T2 (de) | Härtbare Zusammensetzung | |
| DE3523206A1 (de) | Verfahren zur herstellung von poly(diorganosiloxanen) mit alkoxyendgruppen | |
| DE1254344B (de) | Haertbare Dichtungs- und UEberzugsmassen | |
| DE1745498B2 (de) | Nach zutritt von feuchtigkeit bei raumtemperatur zu elastomeren haertende gemische von linearen organopolysiloxaminen und organosiliciumverbindungen | |
| DE3336135A1 (de) | Rtv-siliconpasten | |
| DE2504810A1 (de) | Bei zimmertemperatur haertbare, elastische masse | |
| DE3012369A1 (de) | Verfahren zur gewinnung von silanderivaten aus sepiolith durch reaktion mit alkoxylsilanen fuer die haertesteigerung von polymeren | |
| DE2054565A1 (de) | Verfahren zur Stabilisierung und Har tung eines organischen Polymers mit SH End gruppen und hartbare Polymermasse hierfür | |
| DE2625639C2 (de) | Verfahren zum Beschichten von vorbehandelten, vernetzten Artikeln aus Polyalkylenkautschuk | |
| DE2036661A1 (de) | Verfahren zur Herstellung elastischer Bitumenmassen | |
| DE1520305C3 (de) | Verfahren zur Herstellung von nichtzelligen Polyurethanen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition |