SE438158B - Komposition med hog halt fasta substanser och innehallande ett esterdiolalkoxylat - Google Patents

Komposition med hog halt fasta substanser och innehallande ett esterdiolalkoxylat

Info

Publication number: SE438158B
Authority: SE; Sweden
Prior art keywords: polycaprolactone; composition according; molecular weight; polyol; aminoplast crosslinker
Prior art date: 1977-09-29

Application number

SE7810206A

Other languages

English (en)

Swedish (sv)

Other versions

SE7810206L (sv

Inventor

J V Koleske

R J Knopf

O W Smith

Original Assignee

Union Carbide 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.)

1977-09-29

Filing date

1978-09-28

Publication date

1985-04-01

1978-09-28 Application filed by Union Carbide Corp filed Critical Union Carbide Corp

1979-05-17 Publication of SE7810206L publication Critical patent/SE7810206L/

1985-04-01 Publication of SE438158B publication Critical patent/SE438158B/sv

Links

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WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 1
JHNGQEIVWBCYHQ-UHFFFAOYSA-N 3,6-dihydroxy-2,2,5,5-tetramethylhexanoic acid Chemical compound OCC(C)(C)CC(O)C(C)(C)C(O)=O JHNGQEIVWBCYHQ-UHFFFAOYSA-N 0.000 description 1
SXFJDZNJHVPHPH-UHFFFAOYSA-N 3-methylpentane-1,5-diol Chemical compound OCCC(C)CCO SXFJDZNJHVPHPH-UHFFFAOYSA-N 0.000 description 1
WXQZLPFNTPKVJM-UHFFFAOYSA-N 4-[(4-hydroxycyclohexyl)methyl]cyclohexan-1-ol Chemical compound C1CC(O)CCC1CC1CCC(O)CC1 WXQZLPFNTPKVJM-UHFFFAOYSA-N 0.000 description 1
CDBAMNGURPMUTG-UHFFFAOYSA-N 4-[2-(4-hydroxycyclohexyl)propan-2-yl]cyclohexan-1-ol Chemical compound C1CC(O)CCC1C(C)(C)C1CCC(O)CC1 CDBAMNGURPMUTG-UHFFFAOYSA-N 0.000 description 1
XOGJBKWFLRETGW-UHFFFAOYSA-N 5-aminotriazine-4-carbaldehyde Chemical class NC1=CN=NN=C1C=O XOGJBKWFLRETGW-UHFFFAOYSA-N 0.000 description 1
GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
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239000004821 Contact adhesive Substances 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
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IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
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239000005977 Ethylene Substances 0.000 description 1
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239000002202 Polyethylene glycol Substances 0.000 description 1
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NIYNIOYNNFXGFN-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol;7-oxabicyclo[4.1.0]heptane-4-carboxylic acid Chemical compound OCC1CCC(CO)CC1.C1C(C(=O)O)CCC2OC21.C1C(C(=O)O)CCC2OC21 NIYNIOYNNFXGFN-UHFFFAOYSA-N 0.000 description 1
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YDPHAWREMXVRAC-UHFFFAOYSA-N acetic acid;2-aminoacetic acid Chemical compound CC([O-])=O.[NH3+]CC(O)=O YDPHAWREMXVRAC-UHFFFAOYSA-N 0.000 description 1
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238000007259 addition reaction Methods 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000001464 adherent effect Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
230000002152 alkylating effect Effects 0.000 description 1
125000005529 alkyleneoxy group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
239000012965 benzophenone Substances 0.000 description 1
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229940106691 bisphenol a Drugs 0.000 description 1
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-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
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
238000006555 catalytic reaction Methods 0.000 description 1
238000005336 cracking Methods 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
INSRQEMEVAMETL-UHFFFAOYSA-N decane-1,1-diol Chemical compound CCCCCCCCCC(O)O INSRQEMEVAMETL-UHFFFAOYSA-N 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
229940009714 erythritol Drugs 0.000 description 1
235000019414 erythritol Nutrition 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical compound C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 description 1
XVSYEJJQLZWETL-UHFFFAOYSA-N ethenyl prop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.C=COC(=O)C=C XVSYEJJQLZWETL-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
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238000011156 evaluation Methods 0.000 description 1
239000007888 film coating Substances 0.000 description 1
238000009501 film coating Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
229940051250 hexylene glycol Drugs 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
238000013035 low temperature curing Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
239000000178 monomer Substances 0.000 description 1
238000000465 moulding Methods 0.000 description 1
BYVCTYDTPSKPRM-UHFFFAOYSA-N naphthalene-1-carbonyl naphthalene-1-carboxylate Chemical compound C1=CC=C2C(C(OC(=O)C=3C4=CC=CC=C4C=CC=3)=O)=CC=CC2=C1 BYVCTYDTPSKPRM-UHFFFAOYSA-N 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000000843 powder Substances 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
239000011734 sodium Chemical class 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical class [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
229940014800 succinic anhydride Drugs 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
239000003039 volatile agent Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4887—Polyethers containing carboxylic ester groups derived from carboxylic acids other than acids of higher fatty oils or other than resin acids
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/46—Block or graft polymers prepared by polycondensation of aldehydes or ketones on to macromolecular compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3221—Polyhydroxy compounds hydroxylated esters of carboxylic acids other than higher fatty acids
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2615—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen the other compounds containing carboxylic acid, ester or anhydride groups
- 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
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Materials Engineering (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Polyurethanes Or Polyureas (AREA)
Polyesters Or Polycarbonates (AREA)
Paints Or Removers (AREA)
Adhesives Or Adhesive Processes (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Compositions Of Macromolecular Compounds (AREA)

SE7810206A 1977-09-29 1978-09-28 Komposition med hog halt fasta substanser och innehallande ett esterdiolalkoxylat SE438158B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/837,731 US4158652A (en)	1977-09-29	1977-09-29	High solids compositions containing ester diol alkoxylates

Publications (2)

Publication Number	Publication Date
SE7810206L SE7810206L (sv)	1979-05-17
SE438158B true SE438158B (sv)	1985-04-01

Family

ID=25275254

Family Applications (3)

Application Number	Title	Priority Date	Filing Date
SE7810206A SE438158B (sv)	1977-09-29	1978-09-28	Komposition med hog halt fasta substanser och innehallande ett esterdiolalkoxylat
SE8402219A SE451264B (sv)	1977-09-29	1984-04-19	Komposition med hog halt fasta substanser och innehallande en blandning av ett esterdiolalkoxylat och ett organiskt polyisocyanat
SE8402220A SE451265B (sv)	1977-09-29	1984-04-19	Komposition med hog halt fasta substanser och innehallande en blandning av ett esterdiolalkoxylat och en vattenhaltig akryllatex

Family Applications After (2)

Application Number	Title	Priority Date	Filing Date
SE8402219A SE451264B (sv)	1977-09-29	1984-04-19	Komposition med hog halt fasta substanser och innehallande en blandning av ett esterdiolalkoxylat och ett organiskt polyisocyanat
SE8402220A SE451265B (sv)	1977-09-29	1984-04-19	Komposition med hog halt fasta substanser och innehallande en blandning av ett esterdiolalkoxylat och en vattenhaltig akryllatex

Country Status (10)

Country	Link
US (1)	US4158652A (fr)
JP (1)	JPS5848591B2 (fr)
BE (1)	BE870839A (fr)
CA (1)	CA1131390A (fr)
DE (1)	DE2842272C3 (fr)
FR (1)	FR2404654A1 (fr)
GB (1)	GB2006794B (fr)
IT (1)	IT1099187B (fr)
NL (1)	NL7809839A (fr)
SE (3)	SE438158B (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4297476A (en) *	1980-05-27	1981-10-27	Union Carbide Corporation	Ester diol alkoxylate based alkyd resins
US4410668A (en) *	1982-01-29	1983-10-18	Ppg Industries, Inc.	Elastomeric coating compositions
US4410667A (en) *	1982-01-29	1983-10-18	Ppg Industries, Inc.	Elastomeric coating compositions
US4419407A (en) *	1982-01-29	1983-12-06	Ppg Industries, Inc.	Elastomeric coating compositions
US4403093A (en) *	1982-09-28	1983-09-06	Ppg Industries, Inc.	Polyesters
US4403091A (en) *	1982-09-28	1983-09-06	Ppg Industries, Inc.	Ungelled hydroxy group-containing oligomers
DE3328285A1 (de) *	1983-08-05	1985-02-21	Basf Ag, 6700 Ludwigshafen	Verfahren zur herstellung von lichtgehaerteten schichten mit definierter haerte
US4598021A (en) *	1984-08-17	1986-07-01	General Electric Company	Weatherable abrasion resistant etherified aminoplast derived coating for plastic substrates
JPS63230779A (ja) *	1987-03-20	1988-09-27	Toyo Ink Mfg Co Ltd	缶外面用水性塗料組成物
DE102010027911A1 (de)	2010-04-19	2011-11-03	Endress + Hauser Wetzer Gmbh + Co. Kg	Anschlussklemmenblock

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3267174A (en) *	1963-05-10	1966-08-16	Union Carbide Corp	Acrylic coating composition containing an adduct of a triol with an alkylene oxide
US3959201A (en) *	1972-10-26	1976-05-25	Ppg Industries, Inc.	High solids, water thinnable compositions

1977
- 1977-09-29 US US05/837,731 patent/US4158652A/en not_active Expired - Lifetime
1978
- 1978-09-18 CA CA311,490A patent/CA1131390A/fr not_active Expired
- 1978-09-28 NL NL7809839A patent/NL7809839A/xx not_active Application Discontinuation
- 1978-09-28 JP JP53118694A patent/JPS5848591B2/ja not_active Expired
- 1978-09-28 BE BE190771A patent/BE870839A/fr not_active IP Right Cessation
- 1978-09-28 SE SE7810206A patent/SE438158B/sv not_active IP Right Cessation
- 1978-09-28 IT IT28194/78A patent/IT1099187B/it active
- 1978-09-28 DE DE2842272A patent/DE2842272C3/de not_active Expired
- 1978-09-28 GB GB7838446A patent/GB2006794B/en not_active Expired
- 1978-09-28 FR FR7827782A patent/FR2404654A1/fr active Granted
1984
- 1984-04-19 SE SE8402219A patent/SE451264B/sv not_active IP Right Cessation
- 1984-04-19 SE SE8402220A patent/SE451265B/sv not_active IP Right Cessation

Also Published As

Publication number	Publication date
SE7810206L (sv)	1979-05-17
DE2842272C3 (de)	1981-06-19
JPS5848591B2 (ja)	1983-10-29
US4158652A (en)	1979-06-19
SE8402220D0 (sv)	1984-04-19
FR2404654A1 (fr)	1979-04-27
IT7828194A0 (it)	1978-09-28
SE8402219L (sv)	1984-04-19
GB2006794A (en)	1979-05-10
IT1099187B (it)	1985-09-18
SE451265B (sv)	1987-09-21
JPS5457564A (en)	1979-05-09
BE870839A (fr)	1979-03-28
SE451264B (sv)	1987-09-21
NL7809839A (nl)	1979-04-02
GB2006794B (en)	1982-03-31
DE2842272B2 (de)	1980-10-30
FR2404654B1 (fr)	1983-02-04
SE8402219D0 (sv)	1984-04-19
CA1131390A (fr)	1982-09-07
SE8402220L (sv)	1984-04-19
DE2842272A1 (de)	1979-04-05

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