SU559655A3 - Клей - Google Patents
КлейInfo
- Publication number
- SU559655A3 SU559655A3 SU1930103A SU1930103A SU559655A3 SU 559655 A3 SU559655 A3 SU 559655A3 SU 1930103 A SU1930103 A SU 1930103A SU 1930103 A SU1930103 A SU 1930103A SU 559655 A3 SU559655 A3 SU 559655A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- glue
- stabilizer
- tetrafluoroborate
- compound
- oxonium
- Prior art date
Links
- 239000003292 glue Substances 0.000 title claims description 7
- -1 oxonium compound Chemical class 0.000 claims description 17
- 239000002253 acid Substances 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 5
- 229920001651 Cyanoacrylate Polymers 0.000 claims 2
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 claims 2
- 239000000178 monomer Substances 0.000 claims 2
- 239000004826 Synthetic adhesive Substances 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-O oxonium Chemical compound [OH3+] XLYOFNOQVPJJNP-UHFFFAOYSA-O 0.000 claims 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 14
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- OURVIAHGSIYRHG-UHFFFAOYSA-N 4-[2-[4-[[4,6-bis[4-[2-(4-hydroxyphenyl)propan-2-yl]phenoxy]-1,3,5-triazin-2-yl]oxy]phenyl]propan-2-yl]phenol Chemical compound C=1C=C(OC=2N=C(OC=3C=CC(=CC=3)C(C)(C)C=3C=CC(O)=CC=3)N=C(OC=3C=CC(=CC=3)C(C)(C)C=3C=CC(O)=CC=3)N=2)C=CC=1C(C)(C)C1=CC=C(O)C=C1 OURVIAHGSIYRHG-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 108010068370 Glutens Proteins 0.000 description 1
- RLAHWVDQYNDAGG-UHFFFAOYSA-N Methanetriol Chemical compound OC(O)O RLAHWVDQYNDAGG-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 125000006232 ethoxy propyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000021312 gluten Nutrition 0.000 description 1
- 230000003993 interaction Effects 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
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- DWCSXQCXXITVKE-UHFFFAOYSA-N triethyloxidanium Chemical compound CC[O+](CC)CC DWCSXQCXXITVKE-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F22/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
- C08F22/30—Nitriles
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2228379A DE2228379C3 (de) | 1972-06-10 | 1972-06-10 | Stabilisierte Klebstoffe auf Basis von a -Cyanacrylsäureestern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU559655A3 true SU559655A3 (ru) | 1977-05-25 |
Family
ID=5847410
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1930103A SU559655A3 (ru) | 1972-06-10 | 1973-06-08 | Клей |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3836565A (enExample) |
| JP (1) | JPS5653593B2 (enExample) |
| AT (1) | AT323864B (enExample) |
| BE (1) | BE800714A (enExample) |
| CH (1) | CH584751A5 (enExample) |
| DE (1) | DE2228379C3 (enExample) |
| FR (1) | FR2187870B1 (enExample) |
| GB (1) | GB1422186A (enExample) |
| IT (1) | IT990627B (enExample) |
| NL (1) | NL179132B (enExample) |
| SU (1) | SU559655A3 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4980086A (en) * | 1985-10-16 | 1990-12-25 | Toagosei Chemical Industry, Co., Ltd. | Curable composition |
| US5196401A (en) * | 1988-06-27 | 1993-03-23 | The United State Of America As Represented By The Secretary Of The Interior | Method of enhancing rock fragmentation and extending drill bit life |
| US4959164A (en) * | 1988-06-27 | 1990-09-25 | The United States Of America As Represented By The Secretary Of The Interior | Rock fragmentation method |
| KR0133659B1 (ko) * | 1989-03-24 | 1998-04-20 | 히로세 유끼하루 | 접착제 조성물 |
| WO1998007801A1 (en) * | 1996-08-16 | 1998-02-26 | Loctite (Ireland) Limited | Cyanoacrylate compositions with improved thermal and glass bonding performance |
| US20080003196A1 (en) * | 2006-06-30 | 2008-01-03 | Jonn Jerry Y | Absorbable cyanoacrylate compositions |
| US8173722B2 (en) | 2008-07-10 | 2012-05-08 | Aesculap Ag | Adhesive compositions for use in surgical therapy |
| WO2015137153A1 (ja) * | 2014-03-11 | 2015-09-17 | 東亞合成株式会社 | ２－シアノアクリレート系接着剤組成物 |
-
1972
- 1972-06-10 DE DE2228379A patent/DE2228379C3/de not_active Expired
-
1973
- 1973-05-31 US US00365796A patent/US3836565A/en not_active Expired - Lifetime
- 1973-06-08 FR FR7320953A patent/FR2187870B1/fr not_active Expired
- 1973-06-08 SU SU1930103A patent/SU559655A3/ru active
- 1973-06-08 CH CH836873A patent/CH584751A5/xx not_active IP Right Cessation
- 1973-06-08 NL NLAANVRAGE7308076,A patent/NL179132B/xx active Search and Examination
- 1973-06-08 GB GB2740773A patent/GB1422186A/en not_active Expired
- 1973-06-08 AT AT508873A patent/AT323864B/de not_active IP Right Cessation
- 1973-06-08 BE BE132099A patent/BE800714A/xx not_active IP Right Cessation
- 1973-06-11 JP JP6573773A patent/JPS5653593B2/ja not_active Expired
- 1973-06-12 IT IT25212/73A patent/IT990627B/it active
Also Published As
| Publication number | Publication date |
|---|---|
| FR2187870A1 (enExample) | 1974-01-18 |
| BE800714A (fr) | 1973-12-10 |
| NL179132B (nl) | 1973-12-12 |
| GB1422186A (en) | 1976-01-21 |
| IT990627B (it) | 1975-07-10 |
| JPS4992158A (enExample) | 1974-09-03 |
| DE2228379C3 (de) | 1980-08-28 |
| US3836565A (en) | 1974-09-17 |
| JPS5653593B2 (enExample) | 1981-12-19 |
| NL7308076A (enExample) | 1973-12-12 |
| DE2228379B2 (de) | 1979-12-13 |
| DE2228379A1 (de) | 1973-12-20 |
| CH584751A5 (enExample) | 1977-02-15 |
| FR2187870B1 (enExample) | 1976-11-12 |
| AT323864B (de) | 1975-08-11 |
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