NL8005771A - Koud vulcaniseerbare rubbersamenstelling. - Google Patents

Koud vulcaniseerbare rubbersamenstelling. Download PDF

Info

Publication number: NL8005771A
Authority: NL; Netherlands
Prior art keywords: composition according; weight; composition; group; butadiene
Prior art date: 1979-10-19

Application number

NL8005771A

Other languages

English (en)

Dutch (nl)

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

1980-10-20

Publication date

1981-04-22

1980-10-20 Application filed by Loctite Corp filed Critical Loctite Corp

1981-04-22 Publication of NL8005771A publication Critical patent/NL8005771A/nl

Links

239000000203 mixture Substances 0.000 title claims description 79
229920001971 elastomer Polymers 0.000 title claims description 24
239000005060 rubber Substances 0.000 title claims description 24
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 39
239000000178 monomer Substances 0.000 claims description 30
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 18
229920001577 copolymer Polymers 0.000 claims description 18
125000004432 carbon atom Chemical group C* 0.000 claims description 17
239000000463 material Substances 0.000 claims description 17
239000003999 initiator Substances 0.000 claims description 16
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 15
-1 carboxy, mercapto Chemical class 0.000 claims description 14
229920001778 nylon Polymers 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
239000000945 filler Substances 0.000 claims description 9
239000004408 titanium dioxide Substances 0.000 claims description 9
238000000576 coating method Methods 0.000 claims description 8
150000003254 radicals Chemical class 0.000 claims description 8
239000004677 Nylon Substances 0.000 claims description 7
239000004809 Teflon Substances 0.000 claims description 7
229920006362 Teflon® Polymers 0.000 claims description 7
239000011248 coating agent Substances 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
229920001223 polyethylene glycol Polymers 0.000 claims description 6
239000002202 Polyethylene glycol Substances 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
239000003381 stabilizer Substances 0.000 claims description 5
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound 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
150000002432 hydroperoxides Chemical class 0.000 claims description 4
229920000642 polymer Polymers 0.000 claims description 4
125000003277 amino group Chemical group 0.000 claims description 3
239000003054 catalyst Substances 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
150000002791 naphthoquinones Chemical class 0.000 claims description 3
125000000864 peroxy group Chemical group O(O*)* 0.000 claims description 3
239000007787 solid Substances 0.000 claims description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical group O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 2
239000004215 Carbon black (E152) Substances 0.000 claims description 2
239000005062 Polybutadiene Substances 0.000 claims description 2
150000003857 carboxamides Chemical group 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
150000002429 hydrazines Chemical class 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
230000000977 initiatory effect Effects 0.000 claims description 2
UICBCXONCUFSOI-UHFFFAOYSA-N n'-phenylacetohydrazide Chemical group CC(=O)NNC1=CC=CC=C1 UICBCXONCUFSOI-UHFFFAOYSA-N 0.000 claims description 2
238000012856 packing Methods 0.000 claims description 2
150000002976 peresters Chemical class 0.000 claims description 2
229920002857 polybutadiene Polymers 0.000 claims description 2
238000010526 radical polymerization reaction Methods 0.000 claims description 2
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical group C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 claims description 2
235000019204 saccharin Nutrition 0.000 claims description 2
229920002554 vinyl polymer Polymers 0.000 claims description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims 4
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
150000002978 peroxides Chemical class 0.000 claims 2
239000000565 sealant Substances 0.000 claims 2
150000003440 styrenes Chemical class 0.000 claims 2
150000003973 alkyl amines Chemical group 0.000 claims 1
125000002877 alkyl aryl group Chemical group 0.000 claims 1
125000003710 aryl alkyl group Chemical group 0.000 claims 1
150000002989 phenols Chemical class 0.000 claims 1
229920001195 polyisoprene Polymers 0.000 claims 1
238000002360 preparation method Methods 0.000 claims 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
239000000047 product Substances 0.000 description 15
229920003051 synthetic elastomer Polymers 0.000 description 12
239000005061 synthetic rubber Substances 0.000 description 12
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
150000001875 compounds 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
150000002148 esters Chemical class 0.000 description 6
239000003112 inhibitor Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
229920013646 Hycar Polymers 0.000 description 5
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 5
239000007795 chemical reaction product Substances 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
229920000572 Nylon 6/12 Polymers 0.000 description 4
230000000694 effects Effects 0.000 description 4
239000004615 ingredient Substances 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
230000001070 adhesive effect Effects 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
230000009975 flexible effect Effects 0.000 description 3
238000009472 formulation Methods 0.000 description 3
239000011521 glass Substances 0.000 description 3
150000002431 hydrogen Chemical class 0.000 description 3
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
239000007788 liquid Substances 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 2
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
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
238000007792 addition Methods 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
238000000151 deposition Methods 0.000 description 2
230000008021 deposition Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
229920000126 latex Polymers 0.000 description 2
239000004816 latex Substances 0.000 description 2
238000002156 mixing Methods 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
229920000058 polyacrylate Polymers 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
238000007789 sealing Methods 0.000 description 2
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
238000012360 testing method Methods 0.000 description 2
239000004636 vulcanized rubber Substances 0.000 description 2
150000005208 1,4-dihydroxybenzenes Chemical class 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
HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-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
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
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-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
CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-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
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
RMUCZJUITONUFY-UHFFFAOYSA-N Phenelzine Chemical compound NNCCC1=CC=CC=C1 RMUCZJUITONUFY-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
229910000754 Wrought iron Inorganic materials 0.000 description 1
UFMIJARKFNAIOI-UHFFFAOYSA-N [SH2]=N.C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 Chemical compound [SH2]=N.C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 UFMIJARKFNAIOI-UHFFFAOYSA-N 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
125000003342 alkenyl group Chemical group 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
238000003490 calendering Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000004386 diacrylate group Chemical group 0.000 description 1
GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
FDPIMTJIUBPUKL-UHFFFAOYSA-N dimethylacetone Natural products CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
238000004090 dissolution Methods 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
238000001035 drying Methods 0.000 description 1
ZMJOQTILTVQJJE-UHFFFAOYSA-N ethenol;2-methylprop-2-enoic acid Chemical compound OC=C.CC(=C)C(O)=O ZMJOQTILTVQJJE-UHFFFAOYSA-N 0.000 description 1
DOMLXBPXLNDFAB-UHFFFAOYSA-N ethoxyethane;methyl prop-2-enoate Chemical compound CCOCC.COC(=O)C=C DOMLXBPXLNDFAB-UHFFFAOYSA-N 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
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 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
239000004519 grease Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
210000003141 lower extremity Anatomy 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
239000010705 motor oil Substances 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
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
QIWOKEQEGOOGGH-UHFFFAOYSA-N n-anilinoformamide Chemical compound O=CNNC1=CC=CC=C1 QIWOKEQEGOOGGH-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
229940067157 phenylhydrazine Drugs 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
238000007639 printing Methods 0.000 description 1
150000004053 quinones Chemical class 0.000 description 1
239000002002 slurry Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
229960002317 succinimide Drugs 0.000 description 1
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
239000000725 suspension Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
229940096522 trimethylolpropane triacrylate Drugs 0.000 description 1
238000011179 visual inspection Methods 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)

NL8005771A 1979-10-19 1980-10-20 Koud vulcaniseerbare rubbersamenstelling. NL8005771A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US8633679A	1979-10-19	1979-10-19
US8633679		1979-10-19

Publications (1)

Publication Number	Publication Date
NL8005771A true NL8005771A (nl)	1981-04-22

Family

ID=22197915

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8005771A NL8005771A (nl)	1979-10-19	1980-10-20	Koud vulcaniseerbare rubbersamenstelling.

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

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* Cited by examiner, † Cited by third party
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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
CH656888A5 (de)	1986-07-31
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
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
1985-01-01	A85	Still pending on 85-01-01
1987-12-01	BV	The patent application has lapsed

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