GB1057044A - Improved release of curing agents from molecular sieves - Google Patents
Improved release of curing agents from molecular sievesInfo
- Publication number
- GB1057044A GB1057044A GB22718/63A GB2271863A GB1057044A GB 1057044 A GB1057044 A GB 1057044A GB 22718/63 A GB22718/63 A GB 22718/63A GB 2271863 A GB2271863 A GB 2271863A GB 1057044 A GB1057044 A GB 1057044A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cured
- zeolite
- curing
- glycol
- bis
- 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.)
- Expired
Links
- 239000003795 chemical substances by application Substances 0.000 title abstract 18
- 239000002808 molecular sieve Substances 0.000 title abstract 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 title abstract 3
- 239000010457 zeolite Substances 0.000 abstract 12
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract 11
- 229910021536 Zeolite Inorganic materials 0.000 abstract 10
- -1 carboxy compound Chemical class 0.000 abstract 10
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 abstract 10
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 abstract 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 6
- 229920001971 elastomer Polymers 0.000 abstract 6
- 239000000203 mixture Substances 0.000 abstract 6
- 229920005989 resin Polymers 0.000 abstract 6
- 239000011347 resin Substances 0.000 abstract 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 5
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 5
- 239000000806 elastomer Substances 0.000 abstract 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 4
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 abstract 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 4
- 239000003822 epoxy resin Substances 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 4
- 238000010438 heat treatment Methods 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 150000007524 organic acids Chemical class 0.000 abstract 4
- 235000005985 organic acids Nutrition 0.000 abstract 4
- 229920000647 polyepoxide Polymers 0.000 abstract 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- 229940051250 hexylene glycol Drugs 0.000 abstract 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 abstract 3
- 150000002989 phenols Chemical class 0.000 abstract 3
- 229920000768 polyamine Polymers 0.000 abstract 3
- 229920001223 polyethylene glycol Polymers 0.000 abstract 3
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 abstract 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 abstract 2
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000002202 Polyethylene glycol Substances 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 239000005864 Sulphur Substances 0.000 abstract 2
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 abstract 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 abstract 2
- 150000002576 ketones Chemical class 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N methyl pentane Natural products CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 2
- 238000002156 mixing Methods 0.000 abstract 2
- 150000002978 peroxides Chemical class 0.000 abstract 2
- 239000011148 porous material Substances 0.000 abstract 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 2
- 238000010058 rubber compounding Methods 0.000 abstract 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 abstract 2
- 150000005846 sugar alcohols Polymers 0.000 abstract 2
- 150000003585 thioureas Chemical class 0.000 abstract 2
- 229960001124 trientine Drugs 0.000 abstract 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract 2
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 abstract 1
- FNAVFEIPRKSZFP-UHFFFAOYSA-N 1-(oxiran-2-yl)-2-[2,3,4-tris[2-hydroxy-2-(oxiran-2-yl)ethoxy]butoxy]ethanol Chemical compound C1OC1C(O)COCC(C(COCC(O)C1OC1)OCC(O)C1OC1)OCC(O)C1CO1 FNAVFEIPRKSZFP-UHFFFAOYSA-N 0.000 abstract 1
- XUOYFIIIMAZPTR-UHFFFAOYSA-N 1-[4-[2-hydroxy-3-(oxiran-2-yl)propoxy]phenoxy]-3-(oxiran-2-yl)propan-2-ol Chemical compound C1OC1CC(O)COC(C=C1)=CC=C1OCC(O)CC1CO1 XUOYFIIIMAZPTR-UHFFFAOYSA-N 0.000 abstract 1
- HTJFSXYVAKSPNF-UHFFFAOYSA-N 2-[2-(oxiran-2-yl)ethyl]oxirane Chemical compound C1OC1CCC1CO1 HTJFSXYVAKSPNF-UHFFFAOYSA-N 0.000 abstract 1
- DDNLLYYWFSTMHR-UHFFFAOYSA-N 2-[2-[2-chloro-4-[2-(oxiran-2-yl)ethoxy]cyclohexyl]oxyethyl]oxirane Chemical compound ClC1CC(OCCC2OC2)CCC1OCCC1CO1 DDNLLYYWFSTMHR-UHFFFAOYSA-N 0.000 abstract 1
- IQROXMUHJFAJIQ-UHFFFAOYSA-N 2-[3-[2-hydroxy-2-(oxiran-2-yl)ethoxy]phenoxy]-1-(oxiran-2-yl)ethanol Chemical compound C1OC1C(O)COC(C=1)=CC=CC=1OCC(O)C1CO1 IQROXMUHJFAJIQ-UHFFFAOYSA-N 0.000 abstract 1
- FADZHHSLTCASRS-UHFFFAOYSA-N 2-[3-[3-chloro-5-[3-(oxiran-2-yl)propoxy]phenoxy]propyl]oxirane Chemical compound C=1C(OCCCC2OC2)=CC(Cl)=CC=1OCCCC1CO1 FADZHHSLTCASRS-UHFFFAOYSA-N 0.000 abstract 1
- GHKUPRJIYGBNRL-UHFFFAOYSA-N 2-[[3-(oxiran-2-ylmethoxy)cyclohexyl]oxymethyl]oxirane Chemical compound C1OC1COC(C1)CCCC1OCC1CO1 GHKUPRJIYGBNRL-UHFFFAOYSA-N 0.000 abstract 1
- FSYPIGPPWAJCJG-UHFFFAOYSA-N 2-[[4-(oxiran-2-ylmethoxy)phenoxy]methyl]oxirane Chemical compound C1OC1COC(C=C1)=CC=C1OCC1CO1 FSYPIGPPWAJCJG-UHFFFAOYSA-N 0.000 abstract 1
- PHMRPWPDDRGGGF-UHFFFAOYSA-N 2-bromoprop-1-ene Chemical compound CC(Br)=C PHMRPWPDDRGGGF-UHFFFAOYSA-N 0.000 abstract 1
- PNLQPWWBHXMFCA-UHFFFAOYSA-N 2-chloroprop-1-ene Chemical compound CC(Cl)=C PNLQPWWBHXMFCA-UHFFFAOYSA-N 0.000 abstract 1
- DWVXFVWWARTDCQ-UHFFFAOYSA-N 2-ethylbenzene-1,3-diol Chemical compound CCC1=C(O)C=CC=C1O DWVXFVWWARTDCQ-UHFFFAOYSA-N 0.000 abstract 1
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical group CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 abstract 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 abstract 1
- ZFIVKAOQEXOYFY-UHFFFAOYSA-N Diepoxybutane Chemical compound C1OC1C1OC1 ZFIVKAOQEXOYFY-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- 244000043261 Hevea brasiliensis Species 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 abstract 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-O N-dimethylethanolamine Chemical compound C[NH+](C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-O 0.000 abstract 1
- 229920000459 Nitrile rubber Polymers 0.000 abstract 1
- 239000005062 Polybutadiene Substances 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 150000001266 acyl halides Chemical class 0.000 abstract 1
- 150000004996 alkyl benzenes Chemical class 0.000 abstract 1
- JYIBXUUINYLWLR-UHFFFAOYSA-N aluminum;calcium;potassium;silicon;sodium;trihydrate Chemical compound O.O.O.[Na].[Al].[Si].[K].[Ca] JYIBXUUINYLWLR-UHFFFAOYSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000004982 aromatic amines Chemical class 0.000 abstract 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 abstract 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 abstract 1
- 229920005549 butyl rubber Polymers 0.000 abstract 1
- UNYSKUBLZGJSLV-UHFFFAOYSA-L calcium;1,3,5,2,4,6$l^{2}-trioxadisilaluminane 2,4-dioxide;dihydroxide;hexahydrate Chemical compound O.O.O.O.O.O.[OH-].[OH-].[Ca+2].O=[Si]1O[Al]O[Si](=O)O1.O=[Si]1O[Al]O[Si](=O)O1 UNYSKUBLZGJSLV-UHFFFAOYSA-L 0.000 abstract 1
- 239000004359 castor oil Substances 0.000 abstract 1
- 235000019438 castor oil Nutrition 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 229910052676 chabazite Inorganic materials 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 229910001603 clinoptilolite Inorganic materials 0.000 abstract 1
- 239000011280 coal tar Substances 0.000 abstract 1
- 239000000470 constituent Substances 0.000 abstract 1
- 229960002887 deanol Drugs 0.000 abstract 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 abstract 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 abstract 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 1
- 150000005205 dihydroxybenzenes Chemical class 0.000 abstract 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 abstract 1
- 239000012972 dimethylethanolamine Substances 0.000 abstract 1
- 238000007598 dipping method Methods 0.000 abstract 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052675 erionite Inorganic materials 0.000 abstract 1
- LDLDYFCCDKENPD-UHFFFAOYSA-N ethenylcyclohexane Chemical compound C=CC1CCCCC1 LDLDYFCCDKENPD-UHFFFAOYSA-N 0.000 abstract 1
- HFLGBNBLMBSXEM-UHFFFAOYSA-N ethyl catechol Natural products CCC1=CC=C(O)C(O)=C1 HFLGBNBLMBSXEM-UHFFFAOYSA-N 0.000 abstract 1
- 229940012017 ethylenediamine Drugs 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 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 abstract 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 239000004312 hexamethylene tetramine Substances 0.000 abstract 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 abstract 1
- 229940018564 m-phenylenediamine Drugs 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- 239000011976 maleic acid Substances 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 229960004011 methenamine Drugs 0.000 abstract 1
- 229910052680 mordenite Inorganic materials 0.000 abstract 1
- 229920003052 natural elastomer Polymers 0.000 abstract 1
- 229920001194 natural rubber Polymers 0.000 abstract 1
- 150000001451 organic peroxides Chemical class 0.000 abstract 1
- 229920001084 poly(chloroprene) Polymers 0.000 abstract 1
- 229920000058 polyacrylate Polymers 0.000 abstract 1
- 229920002857 polybutadiene Polymers 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- 229920001195 polyisoprene Polymers 0.000 abstract 1
- 229920001451 polypropylene glycol Polymers 0.000 abstract 1
- 150000007519 polyprotic acids Polymers 0.000 abstract 1
- 229920001296 polysiloxane Polymers 0.000 abstract 1
- 229920000915 polyvinyl chloride Polymers 0.000 abstract 1
- 239000004800 polyvinyl chloride Substances 0.000 abstract 1
- 229960001755 resorcinol Drugs 0.000 abstract 1
- 239000005060 rubber Substances 0.000 abstract 1
- 229960004889 salicylic acid Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920002379 silicone rubber Polymers 0.000 abstract 1
- 239000004945 silicone rubber Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000003549 soybean oil Substances 0.000 abstract 1
- 235000012424 soybean oil Nutrition 0.000 abstract 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- 229960004418 trolamine Drugs 0.000 abstract 1
- 229920006337 unsaturated polyester resin Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- 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
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
- C08J3/241—Preventing premature crosslinking by physical separation of components, e.g. encapsulation
-
- 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
- C08K9/00—Use of pretreated ingredients
- C08K9/12—Adsorbed ingredients, e.g. ingredients on carriers
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201334A US3417046A (en) | 1962-06-11 | 1962-06-11 | Release of curing agents for vicinal epoxides from molecular sieves using a polyalkylene glycol as release agent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1057044A true GB1057044A (en) | 1967-02-01 |
Family
ID=22745421
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB22718/63A Expired GB1057044A (en) | 1962-06-11 | 1963-06-07 | Improved release of curing agents from molecular sieves |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3417046A (https=) |
| AT (1) | AT272655B (https=) |
| BE (1) | BE633338A (https=) |
| CH (1) | CH497494A (https=) |
| DE (1) | DE1569479B2 (https=) |
| GB (1) | GB1057044A (https=) |
| NL (2) | NL293896A (https=) |
| SE (1) | SE321805B (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT413484B (de) * | 2002-02-26 | 2006-03-15 | Hraschan Jakob | Verwendung von zeolithen zur senkung der anteile von lactaten im menschlichen und tierischen organismus |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5177117A (en) * | 1989-05-01 | 1993-01-05 | Air Products And Chemicals, Inc. | Controlled release catalysts and curing agents for making polyurethane and/or polyisocyanurate product |
| DE102008006614A1 (de) * | 2008-01-29 | 2009-07-30 | Riepe, Angelika | Trennmittel |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3036980A (en) * | 1956-12-31 | 1962-05-29 | Union Carbide Corp | Rubber composition containing zeolitic molecular sieve and process for curing |
| US3018264A (en) * | 1957-11-25 | 1962-01-23 | Union Carbide Corp | Polyepoxide compositions |
-
0
- BE BE633338D patent/BE633338A/xx unknown
- NL NL128925D patent/NL128925C/xx active
- NL NL293896D patent/NL293896A/xx unknown
-
1962
- 1962-06-11 US US201334A patent/US3417046A/en not_active Expired - Lifetime
-
1963
- 1963-06-07 GB GB22718/63A patent/GB1057044A/en not_active Expired
- 1963-06-10 CH CH720563A patent/CH497494A/de not_active IP Right Cessation
- 1963-06-10 DE DE19631569479 patent/DE1569479B2/de not_active Withdrawn
- 1963-06-10 SE SE6381/63A patent/SE321805B/xx unknown
- 1963-06-11 AT AT469763A patent/AT272655B/de active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT413484B (de) * | 2002-02-26 | 2006-03-15 | Hraschan Jakob | Verwendung von zeolithen zur senkung der anteile von lactaten im menschlichen und tierischen organismus |
Also Published As
| Publication number | Publication date |
|---|---|
| NL293896A (https=) | |
| DE1569479A1 (de) | 1969-08-14 |
| SE321805B (https=) | 1970-03-16 |
| BE633338A (https=) | |
| NL128925C (https=) | |
| DE1569479B2 (de) | 1972-02-10 |
| AT272655B (de) | 1969-07-10 |
| US3417046A (en) | 1968-12-17 |
| CH497494A (de) | 1970-10-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH02281025A (ja) | 低密度、自己消火性エポキシド組成物 | |
| CA2755854A1 (en) | Curable compositions containing cyclic diamine and cured products therefrom | |
| JP5200805B2 (ja) | 一液型熱硬化性エポキシ樹脂組成物 | |
| SG87685G (en) | Epoxide moulding compositions, moulded articles produced therefrom and their use | |
| GB1416361A (en) | Epoxy adhesive composition | |
| GB1057044A (en) | Improved release of curing agents from molecular sieves | |
| GB1105496A (en) | Epoxy resin-liquid rubber sealing compositions | |
| GB855205A (en) | Improvements in curing of polyepoxides | |
| GB857958A (en) | An improved process for treating surfaces | |
| US4195153A (en) | Non-crystallizing epoxy resin accelerator | |
| US3875072A (en) | Piperazine and alkanolamine accelerator for epoxy curing | |
| US3341488A (en) | Release of agents from adsorbate-containing molecular sieves | |
| ES336490A1 (es) | Mejoras introducidas en la preparacion de composiciones de resinas epoxidicas. | |
| GB831836A (en) | Improvements in or relating to elastomeric material | |
| JP2010090329A (ja) | 一液型熱硬化性エポキシ樹脂組成物 | |
| GB1361614A (en) | Plastics compositions | |
| GB952842A (en) | Epoxy resin compositions, and articles formed therewith adapted for surgical use | |
| GB1029732A (en) | Improved release of agents from adsorbate-containing molecular sieves | |
| US3554967A (en) | Accelerated epoxy-amine resinous compositions catalyzed with -sh yielding material | |
| KR900016303A (ko) | 도료 배합물 성분으로 적합한 사슬연장된 에폭시 수지 및 그의 제조방법 | |
| GB2226029A (en) | Two part epoxy resin composition | |
| GB997001A (en) | Terrazzo repair process | |
| JP5375011B2 (ja) | 一液型熱硬化性エポキシ樹脂組成物 | |
| JP4171160B2 (ja) | 速硬化１液樹脂組成物 | |
| US3355306A (en) | Epoxy foams prepared by the reaction of a polyepoxide with a boroxine and an amine borane |