CH656888A5 - Kaltvulkanisierbare kautschukzusammensetzung und gegenstaende daraus. - Google Patents

Kaltvulkanisierbare kautschukzusammensetzung und gegenstaende daraus. Download PDF

Info

Publication number: CH656888A5
Authority: CH; Switzerland
Prior art keywords: composition according; composition; weight; carbon atoms; anaerobic
Prior art date: 1979-10-19

Application number

CH7642/80A

Other languages

German (de)

English (en)

Inventor

James P Jun Moran

Barbara B Logvin

Frederick F Newberth

Original Assignee

Loctite Corp

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.)

1979-10-19

Filing date

1980-10-14

Publication date

1986-07-31

1980-10-14 Application filed by Loctite Corp filed Critical Loctite Corp

1986-07-31 Publication of CH656888A5 publication Critical patent/CH656888A5/de

Links

239000000203 mixture Substances 0.000 title claims description 77
229920001971 elastomer Polymers 0.000 title claims description 18
239000005060 rubber Substances 0.000 title claims description 17
KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 38
239000000178 monomer Substances 0.000 claims description 28
125000004432 carbon atom Chemical group C* 0.000 claims description 20
239000003999 initiator Substances 0.000 claims description 18
-1 carboxy, mercapto Chemical class 0.000 claims description 16
239000000463 material Substances 0.000 claims description 16
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 15
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 14
229920000642 polymer Polymers 0.000 claims description 13
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 8
238000000576 coating method Methods 0.000 claims description 8
229920001577 copolymer Polymers 0.000 claims description 8
239000001257 hydrogen Substances 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 8
239000011248 coating agent Substances 0.000 claims description 7
239000004408 titanium dioxide Substances 0.000 claims description 7
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 6
239000000945 filler Substances 0.000 claims description 6
125000000864 peroxy group Chemical group O(O*)* 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 5
150000001875 compounds Chemical class 0.000 claims description 5
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 5
238000006116 polymerization reaction Methods 0.000 claims description 5
239000003381 stabilizer Substances 0.000 claims description 5
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical group COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 claims description 4
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 4
239000002202 Polyethylene glycol Substances 0.000 claims description 4
125000003277 amino group Chemical group 0.000 claims description 4
239000003054 catalyst Substances 0.000 claims description 4
150000002432 hydroperoxides Chemical class 0.000 claims description 4
229920001223 polyethylene glycol Polymers 0.000 claims description 4
238000007789 sealing Methods 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical group C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 claims description 3
239000003566 sealing material Substances 0.000 claims description 3
239000007787 solid Substances 0.000 claims description 3
229920003051 synthetic elastomer Polymers 0.000 claims description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
239000004636 vulcanized rubber Substances 0.000 claims description 3
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 2
239000004215 Carbon black (E152) Substances 0.000 claims description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 2
239000005062 Polybutadiene Substances 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
150000003857 carboxamides Chemical class 0.000 claims description 2
239000012876 carrier material Substances 0.000 claims description 2
125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical group 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
239000011810 insulating material Substances 0.000 claims description 2
150000002791 naphthoquinones Chemical class 0.000 claims description 2
150000002976 peresters Chemical class 0.000 claims description 2
150000002989 phenols Chemical class 0.000 claims description 2
229920002857 polybutadiene Polymers 0.000 claims description 2
229920001195 polyisoprene Polymers 0.000 claims description 2
239000005061 synthetic rubber Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
230000001070 adhesive effect Effects 0.000 claims 3
229930192627 Naphthoquinone Natural products 0.000 claims 2
239000000853 adhesive Substances 0.000 claims 2
229920001343 polytetrafluoroethylene Polymers 0.000 claims 2
239000004810 polytetrafluoroethylene Substances 0.000 claims 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
150000003973 alkyl amines Chemical group 0.000 claims 1
125000003710 aryl alkyl group Chemical group 0.000 claims 1
NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical group C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 claims 1
FRASJONUBLZVQX-UHFFFAOYSA-N naphthoquinone group Chemical group C1(C=CC(C2=CC=CC=C12)=O)=O FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 claims 1
150000002978 peroxides Chemical class 0.000 claims 1
230000005855 radiation Effects 0.000 claims 1
239000000565 sealant Substances 0.000 claims 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
239000000047 product Substances 0.000 description 12
239000000243 solution Substances 0.000 description 11
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
150000002148 esters Chemical class 0.000 description 7
238000000034 method Methods 0.000 description 7
239000001301 oxygen Substances 0.000 description 7
229910052760 oxygen Inorganic materials 0.000 description 7
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 6
239000007795 chemical reaction product Substances 0.000 description 5
229920001778 nylon Polymers 0.000 description 5
229920013646 Hycar Polymers 0.000 description 4
239000004677 Nylon Substances 0.000 description 4
229920000572 Nylon 6/12 Polymers 0.000 description 4
239000003112 inhibitor Substances 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
239000004809 Teflon Substances 0.000 description 3
229920006362 Teflon® Polymers 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
238000003490 calendering Methods 0.000 description 3
238000009472 formulation Methods 0.000 description 3
150000002431 hydrogen Chemical class 0.000 description 3
239000007788 liquid Substances 0.000 description 3
150000003440 styrenes Chemical class 0.000 description 3
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 3
XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
238000001816 cooling Methods 0.000 description 2
230000008021 deposition Effects 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
229920000126 latex Polymers 0.000 description 2
239000004816 latex Substances 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
229920000058 polyacrylate Polymers 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
239000002002 slurry Substances 0.000 description 2
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 2
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
JIABEENURMZTTI-UHFFFAOYSA-N 1-isocyanato-2-[(2-isocyanatophenyl)methyl]benzene Chemical compound O=C=NC1=CC=CC=C1CC1=CC=CC=C1N=C=O JIABEENURMZTTI-UHFFFAOYSA-N 0.000 description 1
JFZBUNLOTDDXNY-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)propoxy]propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)OCC(C)OC(=O)C(C)=C JFZBUNLOTDDXNY-UHFFFAOYSA-N 0.000 description 1
HQKURBRFOOUSNI-UHFFFAOYSA-N 2-[2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOCCOC(=O)C(C)=C HQKURBRFOOUSNI-UHFFFAOYSA-N 0.000 description 1
SZTBMYHIYNGYIA-UHFFFAOYSA-M 2-chloroacrylate Chemical compound [O-]C(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-M 0.000 description 1
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
HTWRFCRQSLVESJ-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCOC(=O)C(C)=C HTWRFCRQSLVESJ-UHFFFAOYSA-N 0.000 description 1
KBXUTBMGSKKPFL-UHFFFAOYSA-N 3-hydroxy-2-methylprop-2-enoic acid Chemical compound OC=C(C)C(O)=O KBXUTBMGSKKPFL-UHFFFAOYSA-N 0.000 description 1
GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-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
ZADFIQOSPLTJDC-UHFFFAOYSA-N C=CC1=CC=CC=C1.C(CCCO)O Chemical compound C=CC1=CC=CC=C1.C(CCCO)O ZADFIQOSPLTJDC-UHFFFAOYSA-N 0.000 description 1
KSPIHGBHKVISFI-UHFFFAOYSA-N Diphenylcarbazide Chemical compound C=1C=CC=CC=1NNC(=O)NNC1=CC=CC=C1 KSPIHGBHKVISFI-UHFFFAOYSA-N 0.000 description 1
229920012375 Elvamide® 8061 Polymers 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
229920006099 Vestamid® Polymers 0.000 description 1
QILXPCHTWXAUHE-UHFFFAOYSA-N [Na].NCCN Chemical compound [Na].NCCN QILXPCHTWXAUHE-UHFFFAOYSA-N 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
230000001934 delay Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
239000000975 dye Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
229940071106 ethylenediaminetetraacetate Drugs 0.000 description 1
230000007717 exclusion Effects 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000011888 foil Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
229920006158 high molecular weight polymer Polymers 0.000 description 1
150000002429 hydrazines Chemical class 0.000 description 1
125000001867 hydroperoxy group Chemical group [*]OO[H] 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000010705 motor oil Substances 0.000 description 1
TXIZEHFTRRBEMY-UHFFFAOYSA-N n'-(4-bromophenyl)acetohydrazide Chemical compound CC(=O)NNC1=CC=C(Br)C=C1 TXIZEHFTRRBEMY-UHFFFAOYSA-N 0.000 description 1
BTNWTSYUNCUTSP-UHFFFAOYSA-N n'-(4-methoxyphenyl)acetohydrazide Chemical compound COC1=CC=C(NNC(C)=O)C=C1 BTNWTSYUNCUTSP-UHFFFAOYSA-N 0.000 description 1
UICBCXONCUFSOI-UHFFFAOYSA-N n'-phenylacetohydrazide Chemical compound CC(=O)NNC1=CC=CC=C1 UICBCXONCUFSOI-UHFFFAOYSA-N 0.000 description 1
CKLPECFHCLIYKN-UHFFFAOYSA-N n'-phenylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)NNC1=CC=CC=C1 CKLPECFHCLIYKN-UHFFFAOYSA-N 0.000 description 1
GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
239000003973 paint Substances 0.000 description 1
HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
238000007639 printing Methods 0.000 description 1
150000004053 quinones Chemical class 0.000 description 1
238000010526 radical polymerization reaction Methods 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
229960002317 succinimide Drugs 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
238000004073 vulcanization Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J109/00—Adhesives based on homopolymers or copolymers of conjugated diene hydrocarbons
- C09J109/02—Copolymers with acrylonitrile
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
- C09J4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09J159/00 - C09J187/00
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
- 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
- C08K5/14—Peroxides
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
- C08K5/24—Derivatives of hydrazine

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Adhesives Or Adhesive Processes (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Macromonomer-Based Addition Polymer (AREA)
Laminated Bodies (AREA)

CH7642/80A 1979-10-19 1980-10-14 Kaltvulkanisierbare kautschukzusammensetzung und gegenstaende daraus. CH656888A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US8633679A	1979-10-19	1979-10-19

Publications (1)

Publication Number	Publication Date
CH656888A5 true CH656888A5 (de)	1986-07-31

Family

ID=22197915

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH7642/80A CH656888A5 (de)	1979-10-19	1980-10-14	Kaltvulkanisierbare kautschukzusammensetzung und gegenstaende daraus.

Country Status (12)

Country	Link
JP (1)	JPS5665065A (fr)
AU (1)	AU526311B2 (fr)
BR (1)	BR8006239A (fr)
CA (1)	CA1161586A (fr)
CH (1)	CH656888A5 (fr)
DE (1)	DE3039323C2 (fr)
ES (1)	ES495958A0 (fr)
FR (1)	FR2467875A1 (fr)
GB (1)	GB2060669B (fr)
IT (1)	IT1144012B (fr)
NL (1)	NL8005771A (fr)
SE (1)	SE8007228L (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH10237420A (ja) *	1997-02-20	1998-09-08	Three Bond Co Ltd	嫌気硬化性シール剤組成物
JP5501241B2 (ja) *	2007-10-29	2014-05-21	ヘンケルコーポレイション	耐熱性、嫌気硬化性組成物
KR101612585B1 (ko)	2009-04-08	2016-04-14	헨켈 아이피 앤드 홀딩 게엠베하	필름 형태의 혐기성 접착제 및 밀봉제 조성물, 필름 형태의 이러한 조성물을 함유하는 필름 스풀 조립체 및 교합가능한 부품 상에 예비도포된 그의 변형물
GB2546320B (en) *	2016-01-15	2018-02-14	Henkel IP & Holding GmbH	Cure of anaerobic compositions
GB2548918B (en) *	2016-04-01	2020-07-15	Henkel IP & Holding GmbH	Anaerobically curable (meth)acrylate compositions

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3625875A (en) *	1968-02-29	1971-12-07	Loctite Corp	Anaerobic adhesive and sealant compositions in nonflowable form
GB1505348A (en) *	1974-05-13	1978-03-30	Avdel Adhesives	Anaerobically curable compositions
US4243791A (en) *	1978-01-25	1981-01-06	Rocol Limited	Anaerobic adhesives

1980
- 1980-09-11 CA CA000360082A patent/CA1161586A/fr not_active Expired
- 1980-09-29 BR BR8006239A patent/BR8006239A/pt unknown
- 1980-10-03 JP JP13864380A patent/JPS5665065A/ja active Pending
- 1980-10-06 AU AU62986/80A patent/AU526311B2/en not_active Ceased
- 1980-10-07 IT IT49832/80A patent/IT1144012B/it active
- 1980-10-14 CH CH7642/80A patent/CH656888A5/de not_active IP Right Cessation
- 1980-10-15 SE SE8007228A patent/SE8007228L/xx not_active Application Discontinuation
- 1980-10-15 ES ES495958A patent/ES495958A0/es active Granted
- 1980-10-16 GB GB8033376A patent/GB2060669B/en not_active Expired
- 1980-10-17 FR FR8022267A patent/FR2467875A1/fr active Granted
- 1980-10-17 DE DE3039323A patent/DE3039323C2/de not_active Expired
- 1980-10-20 NL NL8005771A patent/NL8005771A/nl not_active Application Discontinuation

Also Published As

Publication number	Publication date
AU526311B2 (en)	1983-01-06
DE3039323A1 (de)	1981-05-07
IT8049832A0 (it)	1980-10-07
AU6298680A (en)	1981-04-30
FR2467875B1 (fr)	1985-02-15
JPS5665065A (en)	1981-06-02
GB2060669B (en)	1984-02-08
DE3039323C2 (de)	1985-07-18
SE8007228L (sv)	1981-04-20
BR8006239A (pt)	1981-04-22
NL8005771A (nl)	1981-04-22
ES8202858A1 (es)	1982-03-01
GB2060669A (en)	1981-05-07
FR2467875A1 (fr)	1981-04-30
ES495958A0 (es)	1982-03-01
IT1144012B (it)	1986-10-29
CA1161586A (fr)	1984-01-31

Legal Events

Date	Code	Title	Description
1997-06-13	PL	Patent ceased

Publication	Publication Date	Title
DE19902685B4 (de)	2006-08-10	Neuartige Urethan(meth)acrylate, Verfahren zu deren Herstellung und deren Verwendung
DE1817196C2 (de)	1982-03-25	Klebstoffmasse und ihre Verwendung zum Verbinden von nichtporösen Oberflächen
DE3444186C2 (fr)	1990-04-05
CH494812A (de)	1970-08-15	Polyacrylathaltiges Abdichtungsmittel und Verfahren zu seiner Herstellung
DE69712853T2 (de)	2003-03-27	Schutzfolie für Anstrichfilme
EP0017916B1 (fr)	1983-08-31	Procédé de préparation de polymérisats
DE2507068A1 (de)	1975-10-09	Anaerobe, druckempfindliche klebezusammensetzung
DE1909990A1 (de)	1969-09-18	Klebmittel fuer Folien und UEberzuege und Verfahren zu ihrer Herstellung
DE2544901A1 (de)	1976-04-15	Anaerobes druckempfindliches klebematerial
DE2634729A1 (de)	1977-03-03	Elastomere vom aethylen-propylen- termonomer-typ und sie enthaltende vulkanisierbare mischungen und kautschukformkoerper
DE2524117A1 (de)	1975-12-18	Vernetzungsverfahren
DE3008258A1 (de)	1981-01-08	Anaerob haertende chemische zusammensetzung sowie ein verfahren zu ihrer herstellung
DE19751953A1 (de)	1999-05-27	Funktionelle Farbstoffe als Indikator in aerob härtenden Zusammensetzungen
DE3012478A1 (de)	1980-10-16	Verfahren zur herstellung eines lagerbestaendigen klebstoffs
DE2048610C3 (de)	1983-04-07	Anaerob härtende Kleb- und Haftmittel
WO1995014725A1 (fr)	1995-06-01	Composition d'adhesif pratiquement inodore comprenant des (meth)acrylates renfermant des groupements urethanne
EP1297023B1 (fr)	2010-01-13	Procede de production de substances auto-adhesives d'acrylate reticulables
DE69016406T2 (de)	1995-08-17	Klebstoffzusammensetzung.
CH656888A5 (de)	1986-07-31	Kaltvulkanisierbare kautschukzusammensetzung und gegenstaende daraus.
EP0140006B2 (fr)	1995-07-12	Matériau d'étanchéité dont le durcissement nécessite l'exclusion d'oxygène, pour l'étanchéification de surfaces et de filetages
DE3611307C2 (fr)	1989-05-24
EP0641846B1 (fr)	1996-12-27	Préparations à base de (méth)acrylate inodores durcissant par polymérisation radicalaire
DE2521172C2 (fr)	1989-05-03
EP0547504B1 (fr)	1996-02-28	Procédé pour souder à chaud avec un matériel de revêtement soudable à chaud
DE69931668T2 (de)	2006-09-28	Druckempfindlicher Klebstoff und Oberflächenschutz