NO135159B - - Google Patents
Download PDFInfo
- Publication number
- NO135159B NO135159B NO1402/73A NO140273A NO135159B NO 135159 B NO135159 B NO 135159B NO 1402/73 A NO1402/73 A NO 1402/73A NO 140273 A NO140273 A NO 140273A NO 135159 B NO135159 B NO 135159B
- Authority
- NO
- Norway
- Prior art keywords
- monomers
- reaction
- maleic anhydride
- temperature
- reaction mixture
- Prior art date
Links
- 239000000178 monomer Substances 0.000 claims description 66
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 38
- 239000002904 solvent Substances 0.000 claims description 36
- 229920001577 copolymer Polymers 0.000 claims description 29
- 239000011541 reaction mixture Substances 0.000 claims description 15
- 238000007334 copolymerization reaction Methods 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 9
- 238000004880 explosion Methods 0.000 claims description 8
- 239000003960 organic solvent Substances 0.000 claims description 8
- 239000002685 polymerization catalyst Substances 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 5
- 230000001105 regulatory effect Effects 0.000 claims description 5
- 239000002244 precipitate Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 51
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 33
- 239000003054 catalyst Substances 0.000 description 32
- 238000006116 polymerization reaction Methods 0.000 description 20
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 18
- 239000000047 product Substances 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 13
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- -1 ethylene, propylene Chemical group 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 150000002978 peroxides Chemical class 0.000 description 6
- 239000004342 Benzoyl peroxide Substances 0.000 description 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 description 5
- 239000002360 explosive Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 4
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 4
- 230000004927 fusion Effects 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 150000001555 benzenes Chemical class 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000012295 chemical reaction liquid Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920000140 heteropolymer Polymers 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 150000002932 p-cymene derivatives Chemical class 0.000 description 2
- CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- FAMJUFMHYAFYNU-JTQLQIEISA-N (4r)-1-methyl-4-propan-2-ylcyclohexene Chemical compound CC(C)[C@@H]1CCC(C)=CC1 FAMJUFMHYAFYNU-JTQLQIEISA-N 0.000 description 1
- LGXAANYJEHLUEM-UHFFFAOYSA-N 1,2,3-tri(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC(C(C)C)=C1C(C)C LGXAANYJEHLUEM-UHFFFAOYSA-N 0.000 description 1
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 description 1
- QXXWBUHIGXKTAK-UHFFFAOYSA-N 1-(2-bromopropan-2-yl)-4-methylbenzene Chemical compound BrC(C1=CC=C(C=C1)C)(C)C QXXWBUHIGXKTAK-UHFFFAOYSA-N 0.000 description 1
- ITTZHNHXCRWVKL-UHFFFAOYSA-N 1-(2-chloropropan-2-yl)-4-methylbenzene Chemical compound CC1=CC=C(C(C)(C)Cl)C=C1 ITTZHNHXCRWVKL-UHFFFAOYSA-N 0.000 description 1
- ITLWKLGDTIXLKM-UHFFFAOYSA-N 1-(2-fluoropropan-2-yl)-4-methylbenzene Chemical compound CC1=CC=C(C(C)(C)F)C=C1 ITLWKLGDTIXLKM-UHFFFAOYSA-N 0.000 description 1
- ZWBXGMNUQKYQSF-UHFFFAOYSA-N 1-butoxy-4-propan-2-ylbenzene Chemical compound CCCCOC1=CC=C(C(C)C)C=C1 ZWBXGMNUQKYQSF-UHFFFAOYSA-N 0.000 description 1
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
- KBTYSDMXRXDGGC-UHFFFAOYSA-N 1-hydroperoxycyclohexan-1-ol Chemical compound OOC1(O)CCCCC1 KBTYSDMXRXDGGC-UHFFFAOYSA-N 0.000 description 1
- JULZQKLZSNOEEJ-UHFFFAOYSA-N 1-methoxy-4-propan-2-ylbenzene Chemical compound COC1=CC=C(C(C)C)C=C1 JULZQKLZSNOEEJ-UHFFFAOYSA-N 0.000 description 1
- DRKFWQDBPGTSOO-UHFFFAOYSA-N 1-methyl-2-nitro-4-propan-2-ylbenzene Chemical compound CC(C)C1=CC=C(C)C([N+]([O-])=O)=C1 DRKFWQDBPGTSOO-UHFFFAOYSA-N 0.000 description 1
- BSZXAFXFTLXUFV-UHFFFAOYSA-N 1-phenylethylbenzene Chemical compound C=1C=CC=CC=1C(C)C1=CC=CC=C1 BSZXAFXFTLXUFV-UHFFFAOYSA-N 0.000 description 1
- 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 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical class COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 239000000011 acetone peroxide Substances 0.000 description 1
- 235000019401 acetone peroxide Nutrition 0.000 description 1
- PDAVOLCVHOKLEO-UHFFFAOYSA-N acetyl benzenecarboperoxoate Chemical compound CC(=O)OOC(=O)C1=CC=CC=C1 PDAVOLCVHOKLEO-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-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
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229930007927 cymene Natural products 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 150000002828 nitro derivatives Chemical group 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229930004008 p-menthane Natural products 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41H—APPLIANCES OR METHODS FOR MAKING CLOTHES, e.g. FOR DRESS-MAKING OR FOR TAILORING, NOT OTHERWISE PROVIDED FOR
- A41H37/00—Machines, appliances or methods for setting fastener-elements on garments
- A41H37/001—Methods
- A41H37/003—Methods for attaching slide or glide fasteners to garments
-
- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41D—OUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
- A41D27/00—Details of garments or of their making
- A41D27/20—Pockets; Making or setting-in pockets
- A41D27/201—Pocket closures
- A41D27/202—Pocket closures with flap-sealed slide fastener
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T24/00—Buckles, buttons, clasps, etc.
- Y10T24/25—Zipper or required component thereof
- Y10T24/2539—Interlocking surface constructed from plural elements in series
- Y10T24/2548—Preattached to mounting cord
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Details Of Garments (AREA)
- Slide Fasteners (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Professional, Industrial, Or Sporting Protective Garments (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00241741A US3827085A (en) | 1972-04-06 | 1972-04-06 | Zipper stringer for fly systems and system employing same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO135159B true NO135159B (sv) | 1976-11-15 |
| NO135159C NO135159C (sv) | 1977-02-23 |
Family
ID=22911986
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO1402/73A NO135159C (sv) | 1972-04-06 | 1973-04-05 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US3827085A (sv) |
| JP (2) | JPS498350A (sv) |
| AU (1) | AU465549B2 (sv) |
| BE (1) | BE797355A (sv) |
| BR (1) | BR7302309D0 (sv) |
| CA (1) | CA994953A (sv) |
| CH (1) | CH568032A5 (sv) |
| DE (1) | DE2317121C3 (sv) |
| DK (1) | DK143585C (sv) |
| ES (1) | ES413386A1 (sv) |
| FR (1) | FR2178896B1 (sv) |
| GB (1) | GB1422168A (sv) |
| IT (1) | IT981988B (sv) |
| NL (1) | NL7304417A (sv) |
| NO (1) | NO135159C (sv) |
| SE (1) | SE407329B (sv) |
| ZA (1) | ZA731768B (sv) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2248054B2 (de) * | 1972-09-30 | 1974-12-12 | Licentia Patent-Verwaltungs-Gmbh, 6000 Frankfurt | Elektrophotographisches Aufzeichnungsmaterial |
| US3962729A (en) * | 1973-03-19 | 1976-06-15 | The H. D. Lee Company, Inc. | Zipper fly construction for garments |
| JPS50142036A (sv) * | 1974-05-01 | 1975-11-15 | ||
| US4534067A (en) * | 1983-05-05 | 1985-08-13 | The Reece Corporation | Fly construction and method of forming it |
| US4904559A (en) * | 1988-10-24 | 1990-02-27 | Xerox Corporation | Processes for suppressing the fractionation of chalcogenide alloys |
| JPH0811153B2 (ja) * | 1988-11-30 | 1996-02-07 | ジューキ株式会社 | ファスナー縫着構造 |
| AUPN000194A0 (en) * | 1994-12-12 | 1995-01-12 | Portessa Pty Ltd | A pair of pants |
| US5924172A (en) * | 1996-06-03 | 1999-07-20 | Cascade Designs, Inc. | Weather resistant structures for conventional slide fasteners and methods for making the same |
| US6434753B2 (en) * | 2000-03-01 | 2002-08-20 | Koji Kato | Hook assembly used for waist-adjusting mechanism of garment and garment having waist-adjusting mechanism |
| DE20110132U1 (de) * | 2001-06-19 | 2001-08-16 | Texplorer GmbH, 41334 Nettetal | Bekleidungsstück zum Schutz gegen chemische und/oder biologische Substanzen |
| JP4342841B2 (ja) * | 2003-06-10 | 2009-10-14 | 有限会社アライウエビング | スライドファスナー用テープ |
| USD759348S1 (en) | 2014-10-17 | 2016-06-21 | Jordache Enterprises, Inc. | Double flap fly with decorative buttons |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE553145C (de) * | 1932-06-22 | Bandfabrik | Reissverschluss | |
| GB301613A (en) * | 1927-10-28 | 1928-12-06 | John Henry Jackson | Improvements to trousers, breeches, and the like |
| US2021098A (en) * | 1934-03-19 | 1935-11-12 | Hookless Fastener Co | Garment |
| US2084499A (en) * | 1935-01-26 | 1937-06-22 | Newman Victor | Slide fastener |
| CH182383A (de) * | 1935-04-01 | 1936-02-15 | Sarasin & Co A G W | Mit Randwulst versehener bandartiger Träger für Ziehverschlüsse. |
| US3187346A (en) * | 1961-07-10 | 1965-06-08 | Jacobson Harry | Adjustable garment closure |
-
1972
- 1972-04-06 US US00241741A patent/US3827085A/en not_active Expired - Lifetime
-
1973
- 1973-03-13 CA CA165,979A patent/CA994953A/en not_active Expired
- 1973-03-14 ZA ZA731768A patent/ZA731768B/xx unknown
- 1973-03-15 GB GB1264173A patent/GB1422168A/en not_active Expired
- 1973-03-19 AU AU53453/73A patent/AU465549B2/en not_active Expired
- 1973-03-22 IT IT22021/73A patent/IT981988B/it active
- 1973-03-26 FR FR7310772A patent/FR2178896B1/fr not_active Expired
- 1973-03-26 BE BE129287A patent/BE797355A/xx not_active IP Right Cessation
- 1973-03-28 CH CH447273A patent/CH568032A5/xx not_active IP Right Cessation
- 1973-03-29 SE SE7304440A patent/SE407329B/sv unknown
- 1973-03-29 NL NL7304417A patent/NL7304417A/xx not_active Application Discontinuation
- 1973-03-30 BR BR732309A patent/BR7302309D0/pt unknown
- 1973-04-05 ES ES413386A patent/ES413386A1/es not_active Expired
- 1973-04-05 NO NO1402/73A patent/NO135159C/no unknown
- 1973-04-05 DE DE2317121A patent/DE2317121C3/de not_active Expired
- 1973-04-05 DK DK184073A patent/DK143585C/da active
- 1973-04-06 JP JP48038831A patent/JPS498350A/ja active Pending
-
1977
- 1977-06-13 JP JP1977076084U patent/JPS5324408Y2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CA994953A (en) | 1976-08-17 |
| SE407329B (sv) | 1979-03-26 |
| DE2317121B2 (de) | 1980-10-16 |
| AU465549B2 (en) | 1975-10-02 |
| BE797355A (fr) | 1973-09-26 |
| IT981988B (it) | 1974-10-10 |
| NL7304417A (sv) | 1973-10-09 |
| ES413386A1 (es) | 1975-12-16 |
| AU5345373A (en) | 1974-09-19 |
| BR7302309D0 (pt) | 1974-07-25 |
| NO135159C (sv) | 1977-02-23 |
| JPS52168615U (sv) | 1977-12-21 |
| DE2317121C3 (de) | 1981-06-04 |
| US3827085A (en) | 1974-08-06 |
| JPS5324408Y2 (sv) | 1978-06-23 |
| FR2178896A1 (sv) | 1973-11-16 |
| DK143585C (da) | 1982-02-01 |
| ZA731768B (en) | 1973-12-19 |
| JPS498350A (sv) | 1974-01-24 |
| FR2178896B1 (sv) | 1979-06-22 |
| GB1422168A (en) | 1976-01-21 |
| CH568032A5 (sv) | 1975-10-31 |
| DE2317121A1 (de) | 1973-10-18 |
| DK143585B (da) | 1981-09-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3085994A (en) | Chain terminated copolymer of styrene and maleic anhydride of low solution viscosity | |
| US3560457A (en) | Process of forming copolymers of maleic anhydride and an aliphatic olefin having from 12 to 14 carbon atoms | |
| US3560455A (en) | Process of forming copolymers of maleic anhydride and an aliphatic olefin having from 20 to 30 carbon atoms | |
| US4414370A (en) | Process for continuous bulk copolymerization of vinyl monomers | |
| NO135159B (sv) | ||
| US3957739A (en) | Process of production of water-soluble linear polymers of very high molecular weight | |
| US3461108A (en) | Process of forming copolymers of maleic anhydride and an aliphatic olefin having six carbon atoms | |
| EP0068024B1 (en) | Process for continuous bulk copolymerization of vinyl monomers | |
| US4833221A (en) | Method for polymerizing a methyl methacrylate molding composition | |
| US3553177A (en) | Process of forming copolymers of maleic anhydride and an aliphatic olefin having at least 30 carbon atoms | |
| US2706181A (en) | Catalysts for the polymerization of olefin oxides | |
| US3178395A (en) | Method for polymerizing vinyl monomers and maleic anhydride | |
| GB477843A (en) | The manufacture of new polymerisation products | |
| EP0087165B1 (en) | Production of copolymers of alpha-methylstyrene | |
| NO771790L (no) | Fremgangsm}te for fremstilling av en polymerisasjonskatalysator | |
| US2430313A (en) | Processes for copolymerizing monoethylenic hydrocarbons with compounds of the maleic anhydride type | |
| US2739142A (en) | Method of preparation of moldable copolymers of styrene and acrylonitrile | |
| US3799913A (en) | Production of hydrocarbon resin compositions from alpha-methyl styrene,indene and vinyl toluene | |
| Oliveira et al. | Reversible Addition–F ragmentation Chain Transfer Polymerization of Vinyl Acetate in Bulk and Suspension Systems | |
| JPH0233041B2 (ja) | Binirutanryotainorenzokukaijokyojugohooyobisonoseiseibutsu | |
| US3418292A (en) | Polymerization process | |
| BE545968A (sv) | ||
| US3640981A (en) | Vinyl toluene-alpha methyl styrene co-polymers and method of preparing the same | |
| US3423355A (en) | Catalytic ketone solution process for preparing high bulk density,high molecular weight styrene-maleic anhydride polymers | |
| US3077467A (en) | Polymerization process and copolymers of alkylene oxides with butadiene and methyl methacrylate |