DD154986A5 - Sauerstoffhaertbare massen auf basis mercaptofunktioneller organischer verbindungen und ihre verwendung zur herstellung hoehermolekularer produkte - Google Patents

Sauerstoffhaertbare massen auf basis mercaptofunktioneller organischer verbindungen und ihre verwendung zur herstellung hoehermolekularer produkte Download PDF

Info

Publication number: DD154986A5
Authority: DD; German Democratic Republic
Prior art keywords: mercapto; weight; oxygen; parts; item
Prior art date: 1979-12-03

Application number

DD80225689A

Other languages

German (de)

English (en)

Inventor

Gary R Homan

Chi-Long Lee

Original Assignee

Dow Corning

Priority date (The priority date 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 date listed.)

1979-12-03

Filing date

1980-12-03

Publication date

1982-05-05

1980-12-03 Application filed by Dow Corning filed Critical Dow Corning

1982-05-05 Publication of DD154986A5 publication Critical patent/DD154986A5/de

Links

238000004519 manufacturing process Methods 0.000 title 1
239000000203 mixture Substances 0.000 claims abstract description 57
150000002894 organic compounds Chemical class 0.000 claims abstract description 46
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 44
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 40
229910052760 oxygen Inorganic materials 0.000 claims abstract description 40
239000001301 oxygen Substances 0.000 claims abstract description 40
125000003396 thiol group Chemical group [H]S* 0.000 claims abstract description 32
229910052751 metal Inorganic materials 0.000 claims abstract description 22
239000002184 metal Substances 0.000 claims abstract description 22
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 20
239000000945 filler Substances 0.000 claims abstract description 13
238000002156 mixing Methods 0.000 claims abstract description 7
230000003197 catalytic effect Effects 0.000 claims abstract description 6
ANHQLUBMNSSPBV-UHFFFAOYSA-N 4h-pyrido[3,2-b][1,4]oxazin-3-one Chemical group C1=CN=C2NC(=O)COC2=C1 ANHQLUBMNSSPBV-UHFFFAOYSA-N 0.000 claims abstract description 4
NBFCJULAAWWTBL-UHFFFAOYSA-N buta-1,3-diene;carbon monoxide;iron Chemical group [Fe].[O+]#[C-].[O+]#[C-].[O+]#[C-].C=CC=C NBFCJULAAWWTBL-UHFFFAOYSA-N 0.000 claims abstract description 3
229920000642 polymer Polymers 0.000 claims description 35
239000003054 catalyst Substances 0.000 claims description 17
150000001875 compounds Chemical class 0.000 claims description 16
238000000034 method Methods 0.000 claims description 13
125000004432 carbon atom Chemical group C* 0.000 claims description 9
239000007788 liquid Substances 0.000 claims description 8
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
125000001931 aliphatic group Chemical group 0.000 claims description 6
125000002947 alkylene group Chemical group 0.000 claims description 6
238000002360 preparation method Methods 0.000 claims description 6
239000011572 manganese Substances 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 3
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 3
230000007717 exclusion Effects 0.000 claims description 2
101100345589 Mus musculus Mical1 gene Proteins 0.000 claims 1
238000000576 coating method Methods 0.000 abstract description 8
GXQCGPVEDZFCGW-UHFFFAOYSA-N 2,3-dihydro-1h-pyrrolo[3,4-c]pyridine;dihydrochloride Chemical group Cl.Cl.N1=CC=C2CNCC2=C1 GXQCGPVEDZFCGW-UHFFFAOYSA-N 0.000 abstract 1
239000004615 ingredient Substances 0.000 abstract 1
229940087654 iron carbonyl Drugs 0.000 abstract 1
239000000463 material Substances 0.000 description 10
229920000620 organic polymer Polymers 0.000 description 9
229910052742 iron Inorganic materials 0.000 description 8
238000006116 polymerization reaction Methods 0.000 description 8
238000009472 formulation Methods 0.000 description 7
239000010410 layer Substances 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000000243 solution Substances 0.000 description 6
238000003860 storage Methods 0.000 description 6
-1 alkylene sulfide Chemical compound 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
150000003384 small molecules Chemical class 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
239000012763 reinforcing filler Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
YAAUVJUJVBJRSQ-UHFFFAOYSA-N [3-(3-sulfanylpropanoyloxy)-2-[[3-(3-sulfanylpropanoyloxy)-2,2-bis(3-sulfanylpropanoyloxymethyl)propoxy]methyl]-2-(3-sulfanylpropanoyloxymethyl)propyl] 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(COC(=O)CCS)(COC(=O)CCS)COCC(COC(=O)CCS)(COC(=O)CCS)COC(=O)CCS YAAUVJUJVBJRSQ-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
239000003431 cross linking reagent Substances 0.000 description 3
239000002480 mineral oil Substances 0.000 description 3
235000010446 mineral oil Nutrition 0.000 description 3
PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
239000000049 pigment Substances 0.000 description 3
229920001021 polysulfide Polymers 0.000 description 3
239000011148 porous material Substances 0.000 description 3
238000007789 sealing Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
229910052717 sulfur Inorganic materials 0.000 description 3
239000011593 sulfur Substances 0.000 description 3
239000002344 surface layer Substances 0.000 description 3
VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 2
239000004593 Epoxy Substances 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000001569 carbon dioxide Substances 0.000 description 2
229910002092 carbon dioxide Inorganic materials 0.000 description 2
150000001728 carbonyl compounds Chemical class 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
239000010941 cobalt Substances 0.000 description 2
229910017052 cobalt Inorganic materials 0.000 description 2
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
239000000470 constituent Substances 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
239000000806 elastomer Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
150000002816 nickel compounds Chemical class 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
150000002902 organometallic compounds Chemical class 0.000 description 2
125000005702 oxyalkylene group Chemical group 0.000 description 2
238000004806 packaging method and process Methods 0.000 description 2
239000003973 paint Substances 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
239000011253 protective coating Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000565 sealant Substances 0.000 description 2
JRNVQLOKVMWBFR-UHFFFAOYSA-N 1,2-benzenedithiol Chemical compound SC1=CC=CC=C1S JRNVQLOKVMWBFR-UHFFFAOYSA-N 0.000 description 1
SRZXCOWFGPICGA-UHFFFAOYSA-N 1,6-Hexanedithiol Chemical compound SCCCCCCS SRZXCOWFGPICGA-UHFFFAOYSA-N 0.000 description 1
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
CSDZDBQCGPJRDC-UHFFFAOYSA-N 2-[bis(2-sulfanylethyl)amino]ethanethiol Chemical compound SCCN(CCS)CCS CSDZDBQCGPJRDC-UHFFFAOYSA-N 0.000 description 1
PIWWUZJXXNOVQY-UHFFFAOYSA-N 2-methylbutane-1,2,3-trithiol Chemical compound CC(S)C(C)(S)CS PIWWUZJXXNOVQY-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
HCDLDZCJYMCKQH-UHFFFAOYSA-N 4-chlorobenzene-1,3-dithiol Chemical compound SC1=CC=C(Cl)C(S)=C1 HCDLDZCJYMCKQH-UHFFFAOYSA-N 0.000 description 1
NIAAGQAEVGMHPM-UHFFFAOYSA-N 4-methylbenzene-1,2-dithiol Chemical compound CC1=CC=C(S)C(S)=C1 NIAAGQAEVGMHPM-UHFFFAOYSA-N 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
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000007824 aliphatic compounds Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
235000008429 bread Nutrition 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
QAEKNCDIHIGLFI-UHFFFAOYSA-L cobalt(2+);2-ethylhexanoate Chemical compound [Co+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O QAEKNCDIHIGLFI-UHFFFAOYSA-L 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000005336 cracking Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
HSKXLONFPAHGJD-UHFFFAOYSA-N cycloheptane-1,2-dithiol Chemical compound SC1CCCCCC1S HSKXLONFPAHGJD-UHFFFAOYSA-N 0.000 description 1
JVHVWOGHQHGPEV-UHFFFAOYSA-N cyclohexane-1,2,3-trithiol Chemical compound SC1CCCC(S)C1S JVHVWOGHQHGPEV-UHFFFAOYSA-N 0.000 description 1
239000000539 dimer Substances 0.000 description 1
YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 1
229910001882 dioxygen Inorganic materials 0.000 description 1
235000021186 dishes Nutrition 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
NVUDVUDVVXAWGV-UHFFFAOYSA-N dodecane-1,12-dithiol Chemical compound SCCCCCCCCCCCCS NVUDVUDVVXAWGV-UHFFFAOYSA-N 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000012765 fibrous filler Substances 0.000 description 1
238000011049 filling Methods 0.000 description 1
239000010408 film Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
238000001879 gelation Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229910001385 heavy metal Inorganic materials 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
238000011835 investigation Methods 0.000 description 1
GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
239000010985 leather Substances 0.000 description 1
229920001684 low density polyethylene Polymers 0.000 description 1
239000004702 low-density polyethylene Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
239000000178 monomer Substances 0.000 description 1
229940094933 n-dodecane Drugs 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
150000003961 organosilicon compounds Chemical class 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001228 polyisocyanate Polymers 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
230000002028 premature Effects 0.000 description 1
UIVPQCZZDVPHOJ-UHFFFAOYSA-N pyridine-3,5-dithiol Chemical compound SC1=CN=CC(S)=C1 UIVPQCZZDVPHOJ-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
229910052895 riebeckite Inorganic materials 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
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
PXLIDIMHPNPGMH-UHFFFAOYSA-N sodium chromate Chemical compound [Na+].[Na+].[O-][Cr]([O-])(=O)=O PXLIDIMHPNPGMH-UHFFFAOYSA-N 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000005979 thermal decomposition reaction Methods 0.000 description 1
239000010409 thin film Substances 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
229940034610 toothpaste Drugs 0.000 description 1
239000000606 toothpaste Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000009423 ventilation Methods 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 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
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/04—Polysulfides
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/14—Polysulfides
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
- C09K3/1012—Sulfur-containing polymers, e.g. polysulfides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Compositions Of Macromolecular Compounds (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Sealing Material Composition (AREA)

DD80225689A 1979-12-03 1980-12-03 Sauerstoffhaertbare massen auf basis mercaptofunktioneller organischer verbindungen und ihre verwendung zur herstellung hoehermolekularer produkte DD154986A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/099,282 US4271289A (en)	1979-12-03	1979-12-03	Oxygen-curable mercapto-functional organic compound compositions catalyzed by metal carbonyl compounds and method of forming higher molecular weight products therefrom

Publications (1)

Publication Number	Publication Date
DD154986A5 true DD154986A5 (de)	1982-05-05

Family

ID=22274175

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD80225689A DD154986A5 (de)	1979-12-03	1980-12-03	Sauerstoffhaertbare massen auf basis mercaptofunktioneller organischer verbindungen und ihre verwendung zur herstellung hoehermolekularer produkte

Country Status (12)

Country	Link
US (1)	US4271289A (fr)
EP (1)	EP0041544B1 (fr)
JP (1)	JPS5942008B2 (fr)
BE (1)	BE886455A (fr)
BR (1)	BR8008944A (fr)
CA (1)	CA1177999A (fr)
DD (1)	DD154986A5 (fr)
DE (1)	DE3067492D1 (fr)
ES (1)	ES8302030A1 (fr)
IT (1)	IT1209286B (fr)
WO (1)	WO1981001558A1 (fr)
ZA (1)	ZA807409B (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS60214509A (ja) *	1984-04-11	1985-10-26	Matsushita Electric Ind Co Ltd	小型コイル
JPS60187509U (ja) *	1984-05-24	1985-12-12	東北金属工業株式会社	小型インダクタ
JPS6219718U (fr) *	1985-07-22	1987-02-05
JPS62213214A (ja) *	1986-03-14	1987-09-19	Matsushita Electric Ind Co Ltd	インダクタ
EP0265373B1 (fr) *	1986-09-19	1991-03-13	Ciba-Geigy Ag	Procédé de durcissement de revêtements de polyisocyanates
AU2280888A (en) *	1987-10-12	1989-04-13	Takeda Chemical Industries Ltd.	Polyurethane resins having mercapto groups, use in magnetic recording medium
US6632674B1 (en)	1999-03-31	2003-10-14	Industrial Scientific Corporation	Method of testing gas detection instruments and associated apparatus
CN112225839B (zh) *	2020-09-22	2022-05-24	浙江工业大学	一种超高分子量聚甲基丙烯酸甲酯的合成方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2466963A (en) *	1945-06-16	1949-04-12	Thiokol Corp	Polysulfide polymer
US2964503A (en) *	1957-03-29	1960-12-13	Products Res Company	Polysulfide compositions and cure
US3402155A (en) *	1966-08-22	1968-09-17	Thiokol Chemical Corp	Storable, one-part polythiol compositions with amine-loaded molecular sieves

1979
- 1979-12-03 US US06/099,282 patent/US4271289A/en not_active Expired - Lifetime
1980
- 1980-11-17 BR BR8008944A patent/BR8008944A/pt unknown
- 1980-11-17 WO PCT/US1980/001547 patent/WO1981001558A1/fr not_active Ceased
- 1980-11-17 EP EP81900115A patent/EP0041544B1/fr not_active Expired
- 1980-11-17 DE DE8181900115T patent/DE3067492D1/de not_active Expired
- 1980-11-17 JP JP56500272A patent/JPS5942008B2/ja not_active Expired
- 1980-11-18 CA CA000364864A patent/CA1177999A/fr not_active Expired
- 1980-11-27 ZA ZA00807409A patent/ZA807409B/xx unknown
- 1980-12-02 ES ES497373A patent/ES8302030A1/es not_active Expired
- 1980-12-02 BE BE0/203013A patent/BE886455A/fr not_active IP Right Cessation
- 1980-12-02 IT IT8026356A patent/IT1209286B/it active
- 1980-12-03 DD DD80225689A patent/DD154986A5/de unknown

Also Published As

Publication number	Publication date
BE886455A (fr)	1981-06-02
JPS5942008B2 (ja)	1984-10-12
ZA807409B (en)	1981-12-30
ES497373A0 (es)	1982-12-16
CA1177999A (fr)	1984-11-13
EP0041544A1 (fr)	1981-12-16
EP0041544A4 (fr)	1982-05-10
IT8026356A0 (it)	1980-12-02
IT1209286B (it)	1989-07-16
US4271289A (en)	1981-06-02
JPS56501605A (fr)	1981-11-05
EP0041544B1 (fr)	1984-04-11
DE3067492D1 (en)	1984-05-17
ES8302030A1 (es)	1982-12-16
BR8008944A (pt)	1981-10-20
WO1981001558A1 (fr)	1981-06-11

Publication	Publication Date	Title
DE3650283T2 (de)	1995-09-28	Modifizierte Disulfidpolymerzusammensetzungen und Verfahren zu ihrer Herstellung.
DE2453173C2 (de)	1986-06-12	Polymerisate mit endständigen Mercaptangruppen und Verfahren zu ihrer Herstellung
DE69307890T2 (de)	1997-06-05	Polythiole mit niedriger viskosität und anwendungen
DE69207808T2 (de)	1996-08-08	Feuchtigkeitshartbare Polyurethanzusammensetzung
DE69815662T2 (de)	2004-04-08	Zusammensetzung und verfahren zur herstellung von flüssiger, treibstoffbeständiger polymere mit hoher biegsamkeit bei tiefer temperatur
DE2627879A1 (de)	1977-12-29	Verfahren zur herstellung von polyurethan-zusammensetzungen
DE1519432A1 (de)	1970-02-19	Polyurethanbeschichtungsmassen
CH493584A (de)	1970-07-15	Verfahren zur Herstellung einer Polysulfid enthaltenden härtbaren Zusammensetzung und deren Verwendung
EP0619355B1 (fr)	1999-09-01	Masses d'étancheité
DE2702046A1 (de)	1977-09-08	Zu einem elastomer haertbare siliconmasse und verfahren zu ihrer herstellung
DE1645500A1 (de)	1970-02-26	Verfahren zur Herstellung haertbarer Polymercaptanaddukte
EP0043501B1 (fr)	1983-11-30	Masses de moulage plastiques à base d'organopolysiloxanes stables à l'abri de l'eau
EP0194361B1 (fr)	1988-03-16	Masse d'adhérence ou d'étanchéité thermodurcissable, procédé de préparation et utilisation
DD154986A5 (de)	1982-05-05	Sauerstoffhaertbare massen auf basis mercaptofunktioneller organischer verbindungen und ihre verwendung zur herstellung hoehermolekularer produkte
EP0066167B1 (fr)	1985-03-27	Procédé de préparation d'oligouréthanes contenant des groupes mercapto, leur utilisation comme liant pour des masses de revêtement ou de calfatage durcissables par oxydation ou comme additif pour des résines époxydes
DE2000658A1 (de)	1971-07-15	Neue Polyaether-Verbindungen und Verfahren zur Herstellung dieser Polyaether
DE1719217A1 (de)	1970-11-12	Durch Feuchtigkeit haertbare Polythiolpolymermasse
DE2119550B2 (de)	1973-03-15	Verfahren zur herstellung eines fluessigen polymerproduktes
DE2533041A1 (de)	1976-02-26	Plastifizierte schwefelgemische und verfahren zum plastifizieren von schwefel
DE1494530A1 (de)	1969-11-13	An der Luft haertbare UEberzugs- und Abdichtungsmasse
DD154996A5 (de)	1982-05-05	Sauerstoffhaertbare massenauf basis mercaptofunktioneller organischer verbindungen und ihre verwendung zur herstellung hoehermolekularer produkte
DE2635176C2 (de)	1982-05-06	Härtbare Formmassen auf der Basis chlorsulfonierter Polyolefine
DD154997A5 (de)	1982-05-05	Sauerstoffhaertbare mercaptoorganopolysiloxanmasse und ihre verwendung zur herstellung hoehermolekularer produkte
DE3601189A1 (de)	1987-07-23	Verfahren zur herstellung von mercaptoendgruppen aufweisenden oligourethanen und deren verwendung in dichtungsmassen bzw. als zusatz zu vernetzbaren epoxidharzsystemen
DD154995A5 (de)	1982-05-05	Sauerstoffhaertbare mercaptoorganosiloxanmasse und ihre verwendung zur herstellung hoehermolekularer produkte