CA1224183A - Faconnage d'un joint par prise partielle par irradiation d'un enduit a base d'acrylate avant la mise en oeuvre definitive - Google Patents

Faconnage d'un joint par prise partielle par irradiation d'un enduit a base d'acrylate avant la mise en oeuvre definitive

Info

Publication number: CA1224183A
Authority: CA; Canada
Prior art keywords: recited; group; initiator; radical; alkyl
Prior art date: 1981-11-23
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

Application number

CA000390666A

Other languages

English (en)

Inventor

Bernard J. Bolger

Francis R. Martin

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Henkel Loctite Corp

Original Assignee

Henkel 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.)

1981-11-23

Filing date

1981-11-23

Publication date

1987-07-14

1981-11-23 Application filed by Henkel Loctite Corp filed Critical Henkel Loctite Corp

1981-11-23 Priority to CA000390666A priority Critical patent/CA1224183A/fr

1987-07-14 Application granted granted Critical

1987-07-14 Publication of CA1224183A publication Critical patent/CA1224183A/fr

Status Expired legal-status Critical Current

Links

NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 title description 5
239000011248 coating agent Substances 0.000 title description 2
238000000576 coating method Methods 0.000 title description 2
238000003475 lamination Methods 0.000 title 1
238000000034 method Methods 0.000 claims abstract description 64
239000000203 mixture Substances 0.000 claims abstract description 54
-1 acry-late ester Chemical class 0.000 claims abstract description 52
239000000178 monomer Substances 0.000 claims abstract description 37
239000003999 initiator Substances 0.000 claims abstract description 30
125000000864 peroxy group Chemical group O(O*)* 0.000 claims abstract description 16
150000003254 radicals Chemical class 0.000 claims description 21
125000004432 carbon atom Chemical group C* 0.000 claims description 18
239000012530 fluid Substances 0.000 claims description 18
125000000217 alkyl group Chemical group 0.000 claims description 17
125000003118 aryl group Chemical group 0.000 claims description 15
239000002184 metal Substances 0.000 claims description 15
239000003112 inhibitor Substances 0.000 claims description 12
238000007789 sealing Methods 0.000 claims description 12
125000001424 substituent group Chemical group 0.000 claims description 12
229920005862 polyol Polymers 0.000 claims description 11
239000000460 chlorine Substances 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 9
125000000623 heterocyclic group Chemical group 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 9
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 8
229910052760 oxygen Inorganic materials 0.000 claims description 8
230000005855 radiation Effects 0.000 claims description 8
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 7
125000003710 aryl alkyl group Chemical group 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
150000002976 peresters Chemical group 0.000 claims description 7
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 6
150000007945 N-acyl ureas Chemical class 0.000 claims description 6
125000002947 alkylene group Chemical group 0.000 claims description 6
229920001577 copolymer Polymers 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
239000004721 Polyphenylene oxide Substances 0.000 claims description 5
229910052801 chlorine Inorganic materials 0.000 claims description 5
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 5
230000013011 mating Effects 0.000 claims description 5
229920000570 polyether Polymers 0.000 claims description 5
229920001228 polyisocyanate Polymers 0.000 claims description 5
239000005056 polyisocyanate Substances 0.000 claims description 5
239000003505 polymerization initiator Substances 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
241000551547 Dione <red algae> Species 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
229930192627 Naphthoquinone Natural products 0.000 claims description 4
125000002877 alkyl aryl group Chemical group 0.000 claims description 4
150000001412 amines Chemical group 0.000 claims description 4
150000004056 anthraquinones Chemical class 0.000 claims description 4
150000004982 aromatic amines Chemical class 0.000 claims description 4
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 4
239000012965 benzophenone Substances 0.000 claims description 4
150000004054 benzoquinones Chemical class 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
150000002791 naphthoquinones Chemical class 0.000 claims description 4
125000004957 naphthylene group Chemical group 0.000 claims description 4
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 4
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical group C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 3
150000002009 diols Chemical class 0.000 claims description 3
SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical group C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 claims description 3
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 3
238000010526 radical polymerization reaction Methods 0.000 claims description 3
125000003107 substituted aryl group Chemical group 0.000 claims description 3
238000005304 joining Methods 0.000 claims description 2
235000013350 formula milk Nutrition 0.000 claims 13
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 6
125000004429 atom Chemical group 0.000 claims 6
150000001728 carbonyl compounds Chemical class 0.000 claims 3
239000007795 chemical reaction product Substances 0.000 claims 3
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 3
150000002432 hydroperoxides Chemical group 0.000 claims 3
150000003077 polyols Chemical class 0.000 claims 3
235000019204 saccharin Nutrition 0.000 claims 3
150000001875 compounds Chemical class 0.000 claims 2
229920000768 polyamine Polymers 0.000 claims 2
229920001730 Moisture cure polyurethane Polymers 0.000 claims 1
229910052757 nitrogen Inorganic materials 0.000 claims 1
SONNWYBIRXJNDC-VIFPVBQESA-N phenylephrine Chemical compound CNC[C@H](O)C1=CC=CC(O)=C1 SONNWYBIRXJNDC-VIFPVBQESA-N 0.000 claims 1
239000000463 material Substances 0.000 abstract description 26
239000007788 liquid Substances 0.000 abstract description 15
238000013023 gasketing Methods 0.000 abstract description 10
238000011065 in-situ storage Methods 0.000 abstract description 2
229940048053 acrylate Drugs 0.000 abstract 1
239000000565 sealant Substances 0.000 abstract 1
238000009472 formulation Methods 0.000 description 8
239000000853 adhesive Substances 0.000 description 7
230000001070 adhesive effect Effects 0.000 description 7
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
239000011324 bead Substances 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
230000000694 effects Effects 0.000 description 7
239000001301 oxygen Substances 0.000 description 7
238000006116 polymerization reaction Methods 0.000 description 7
239000000126 substance Substances 0.000 description 7
229910000831 Steel Inorganic materials 0.000 description 6
239000000047 product Substances 0.000 description 6
238000007650 screen-printing Methods 0.000 description 6
239000010959 steel Substances 0.000 description 6
150000002148 esters Chemical class 0.000 description 5
230000000977 initiatory effect Effects 0.000 description 5
239000011521 glass Substances 0.000 description 4
229920001296 polysiloxane Polymers 0.000 description 4
239000007787 solid Substances 0.000 description 4
125000006850 spacer group Chemical group 0.000 description 4
229920001187 thermosetting polymer Polymers 0.000 description 4
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 3
125000001309 chloro group Chemical group Cl* 0.000 description 3
238000007906 compression Methods 0.000 description 3
230000006835 compression Effects 0.000 description 3
238000010276 construction Methods 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
229940024463 silicone emollient and protective product Drugs 0.000 description 3
238000003860 storage Methods 0.000 description 3
230000002459 sustained effect Effects 0.000 description 3
229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 2
HXVNBWAKAOHACI-UHFFFAOYSA-N 2,4-dimethyl-3-pentanone Chemical compound CC(C)C(=O)C(C)C HXVNBWAKAOHACI-UHFFFAOYSA-N 0.000 description 2
XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
QKTWWGYCVXCKOJ-UHFFFAOYSA-N 2-methoxy-1-(2-methoxyphenyl)-2-phenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1OC QKTWWGYCVXCKOJ-UHFFFAOYSA-N 0.000 description 2
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 2
QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 2
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
LCXXNKZQVOXMEH-UHFFFAOYSA-N Tetrahydrofurfuryl methacrylate Chemical compound CC(=C)C(=O)OCC1CCCO1 LCXXNKZQVOXMEH-UHFFFAOYSA-N 0.000 description 2
125000003282 alkyl amino group Chemical group 0.000 description 2
239000000470 constituent Substances 0.000 description 2
230000007717 exclusion Effects 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
239000002904 solvent Substances 0.000 description 2
JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 description 2
DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
QQLIGMASAVJVON-UHFFFAOYSA-N 1-naphthalen-1-ylethanone Chemical compound C1=CC=C2C(C(=O)C)=CC=CC2=C1 QQLIGMASAVJVON-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
BEWCNXNIQCLWHP-UHFFFAOYSA-N 2-(tert-butylamino)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCNC(C)(C)C BEWCNXNIQCLWHP-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 description 1
AEPWOCLBLLCOGZ-UHFFFAOYSA-N 2-cyanoethyl prop-2-enoate Chemical compound C=CC(=O)OCCC#N AEPWOCLBLLCOGZ-UHFFFAOYSA-N 0.000 description 1
229940044192 2-hydroxyethyl methacrylate Drugs 0.000 description 1
PJKVFARRVXDXAD-UHFFFAOYSA-N 2-naphthaldehyde Chemical compound C1=CC=CC2=CC(C=O)=CC=C21 PJKVFARRVXDXAD-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
VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 1
FJNCXZZQNBKEJT-UHFFFAOYSA-N 8beta-hydroxymarrubiin Natural products O1C(=O)C2(C)CCCC3(C)C2C1CC(C)(O)C3(O)CCC=1C=COC=1 FJNCXZZQNBKEJT-UHFFFAOYSA-N 0.000 description 1
229910017147 Fe(CO)5 Inorganic materials 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
229920002396 Polyurea Polymers 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
239000002253 acid Substances 0.000 description 1
230000003213 activating effect Effects 0.000 description 1
230000001464 adherent effect Effects 0.000 description 1
239000002318 adhesion promoter Substances 0.000 description 1
239000013466 adhesive and sealant Substances 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
125000004450 alkenylene group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
125000004103 aminoalkyl group Chemical group 0.000 description 1
150000005840 aryl radicals Chemical class 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
239000002738 chelating agent Substances 0.000 description 1
238000010382 chemical cross-linking Methods 0.000 description 1
FCSHDIVRCWTZOX-DVTGEIKXSA-N clobetasol Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)CCl)(O)[C@@]1(C)C[C@@H]2O FCSHDIVRCWTZOX-DVTGEIKXSA-N 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
239000007799 cork Substances 0.000 description 1
229920006037 cross link polymer Polymers 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
230000008021 deposition Effects 0.000 description 1
125000004663 dialkyl amino 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
239000003085 diluting agent Substances 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000005357 flat glass Substances 0.000 description 1
YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
239000010720 hydraulic oil Substances 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
125000004464 hydroxyphenyl group Chemical group 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
150000002484 inorganic compounds Chemical class 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
239000011344 liquid material Substances 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
239000003921 oil Substances 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
230000035515 penetration Effects 0.000 description 1
238000006303 photolysis reaction Methods 0.000 description 1
230000015843 photosynthesis, light reaction Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000003825 pressing Methods 0.000 description 1
239000013615 primer Substances 0.000 description 1
239000002987 primer (paints) Substances 0.000 description 1
239000000700 radioactive tracer Substances 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000007779 soft material Substances 0.000 description 1
238000003892 spreading Methods 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
229940096522 trimethylolpropane triacrylate Drugs 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Landscapes

Sealing Material Composition (AREA)

CA000390666A 1981-11-23 1981-11-23 Faconnage d'un joint par prise partielle par irradiation d'un enduit a base d'acrylate avant la mise en oeuvre definitive Expired CA1224183A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000390666A CA1224183A (fr)	1981-11-23	1981-11-23	Faconnage d'un joint par prise partielle par irradiation d'un enduit a base d'acrylate avant la mise en oeuvre definitive

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000390666A CA1224183A (fr)	1981-11-23	1981-11-23	Faconnage d'un joint par prise partielle par irradiation d'un enduit a base d'acrylate avant la mise en oeuvre definitive

Publications (1)

Publication Number	Publication Date
CA1224183A true CA1224183A (fr)	1987-07-14

Family

ID=4121476

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000390666A Expired CA1224183A (fr)	1981-11-23	1981-11-23	Faconnage d'un joint par prise partielle par irradiation d'un enduit a base d'acrylate avant la mise en oeuvre definitive

Country Status (1)

Country	Link
CA (1)	CA1224183A (fr)

1981
- 1981-11-23 CA CA000390666A patent/CA1224183A/fr not_active Expired

Legal Events

Date	Code	Title	Description
2004-07-14	MKEX	Expiry

Publication	Publication Date	Title
CA1243142A (fr)	1988-10-11	Colles anaerobies activees par rayonnement
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US5116558A (en)	1992-05-26	Method of forming gaskets by injection and compositions for use therein
US4414275A (en)	1983-11-08	UV Curable adhesive tape
KR970011339B1 (ko)	1997-07-09	방사선 경화 가능한 조성물을 이용한 코팅 방법
DE2507068A1 (de)	1975-10-09	Anaerobe, druckempfindliche klebezusammensetzung
JPH0233049B2 (fr)	1990-07-25
EP0738286B1 (fr)	1998-08-12	Formulation d'activateur et composition l'utilisant
CA1283992C (fr)	1991-05-07	Compositions adhesives
GB2111515A (en)	1983-07-06	Method of forming gaskets using a UV-and anaerobically- curable gasketing composition
JP2023519427A (ja)	2023-05-10	嫌気硬化性組成物
US4937118A (en)	1990-06-26	Active energy ray-curable composition
JPH02232283A (ja)	1990-09-14	低臭気接着剤組成物
EP0659859B1 (fr)	1999-03-31	Adhésifs structurels acryliques
CA1224183A (fr)	1987-07-14	Faconnage d'un joint par prise partielle par irradiation d'un enduit a base d'acrylate avant la mise en oeuvre definitive
EP0154819B1 (fr)	1988-07-06	Procédé de collage et composition pour la mise en oeuvre de ce procédé
IE51982B1 (en)	1987-05-13	Method of forming gaskets using anaerobically curable materials
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KR20250056213A (ko)	2025-04-25	혐기 경화성 조성물
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GB1566820A (en)	1980-05-08	Anaerobic pressure sensitive adhesive stocks
GB2121064A (en)	1983-12-14	Bonding a polymer film with a polymerizable adhesive