NO121079B - - Google Patents
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- Publication number
- NO121079B NO121079B NO169151A NO16915167A NO121079B NO 121079 B NO121079 B NO 121079B NO 169151 A NO169151 A NO 169151A NO 16915167 A NO16915167 A NO 16915167A NO 121079 B NO121079 B NO 121079B
- Authority
- NO
- Norway
- Prior art keywords
- acid
- alcohols
- methyl
- ester
- ethyl
- Prior art date
Links
- 239000004014 plasticizer Substances 0.000 claims description 11
- 150000001298 alcohols Chemical class 0.000 claims description 9
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
- 150000007524 organic acids Chemical class 0.000 claims description 6
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 6
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 6
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 6
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 4
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 claims description 4
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 claims description 4
- 239000001361 adipic acid Substances 0.000 claims description 3
- 235000011037 adipic acid Nutrition 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 235000005985 organic acids Nutrition 0.000 claims description 3
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 2
- 229920003023 plastic Polymers 0.000 claims description 2
- 239000004033 plastic Substances 0.000 claims description 2
- 229920005992 thermoplastic resin Polymers 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000004185 ester group Chemical group 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 18
- 150000002148 esters Chemical class 0.000 description 6
- 150000001336 alkenes Chemical class 0.000 description 5
- 238000006471 dimerization reaction Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 230000006315 carbonylation Effects 0.000 description 3
- 238000005810 carbonylation reaction Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 239000012815 thermoplastic material Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 2
- -1 aluminum alkyl compound Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- KQTIIICEAUMSDG-UHFFFAOYSA-N tricarballylic acid Chemical compound OC(=O)CC(C(O)=O)CC(O)=O KQTIIICEAUMSDG-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- XTVRLCUJHGUXCP-UHFFFAOYSA-N 3-methyleneheptane Chemical compound CCCCC(=C)CC XTVRLCUJHGUXCP-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- RZKSECIXORKHQS-UHFFFAOYSA-N Heptan-3-ol Chemical compound CCCCC(O)CC RZKSECIXORKHQS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001559 benzoic acids Chemical class 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
- 238000003490 calendering Methods 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 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
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/38—Gaseous or foamed well-drilling compositions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C3/00—Tyres characterised by the transverse section
- B60C3/08—Tyres characterised by the transverse section collapsible into storage or non-use condition, e.g. space-saving spare tyres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C9/00—Reinforcements or ply arrangement of pneumatic tyres
- B60C9/02—Carcasses
- B60C9/04—Carcasses the reinforcing cords of each carcass ply arranged in a substantially parallel relationship
- B60C9/06—Carcasses the reinforcing cords of each carcass ply arranged in a substantially parallel relationship the cords extend diagonally from bead to bead and run in opposite directions in each successive carcass ply, i.e. bias angle ply
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B21/00—Methods or apparatus for flushing boreholes, e.g. by use of exhaust air from motor
- E21B21/16—Methods or apparatus for flushing boreholes, e.g. by use of exhaust air from motor using gaseous fluids
Landscapes
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Mechanical Engineering (AREA)
- Geology (AREA)
- Mining & Mineral Resources (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
- Physics & Mathematics (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Tires In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
Mykningsmiddel for termoplaster.
Foreliggende oppfinnelse vedrører nye mykningsmidler for termoplastharpikser.
I henhold til oppfinnelsen tilveiebringes mykningsmidler for termoplast, særlig vinylplast og celluloseplast, bestående av en eller flere estere av en organisk syre og en alkohol, eller alkoholer, utvalgt fra føl-gende gruppe: 3-metyll-heksanol-l, 3-etyll-heksanol-1,
3-metyll-heptanol-l, 3-etyll-heptanol-1.
Passende organiske syrer, med hvilke de ovennevnte alkoholder kan forestres omfatter f. eks. enbasiske syrer, som f. eks. maursyre, stearinsyre, laurinsyre, oleinsyre, kaprinsyre og bensolsyrer, og flerbasiske syrer, som f. eks. pftalsyre, adipinsyre, sebasinsyre, ravsyre, vinsyre, glykolsyre, si-tronsyre og trikarballylsyre. De fortrinsvis anvendte syrer er glutarsyre, adipinsyre, pimelinsyre, suberinsyre, azelainsyre og sebasinsyre, og særlig ftalsyre.
Mykningsmidlene kan anvendes i for-bindelse med en eller flere syntetiske har-pikser, omfattende f. eks. cellulosederivater som cellulosenitrat eller nitrocellulose, cel-luloseacetat, etyllcellulose, polymerer og interpolymerer av forbindelser som inneholder vinylidengruppen (d.v.s. gruppen CH, = C = ), som vinylklorid, vinylacetat, vinyliden-klorid, og akrylsyrederivater, f. eks. metyll-metakrylat og akrylnitril, og visse derivater av disse polymerer og interpolymerer, som acetaler av hydrolyserte polyvinylesterde-rivater, særlig butyraler. Det nye mykningsmiddel anvendes særlig for termo-plastisk materiale basert på polyvinylklorid.
Det er å foretrekke at alkoholene som esterne i komposisjonene i følge oppfinnelsen fremstilles av, skal bestå primært av en eller flere slike som er utvalgt fra den ovenfor angitte gruppe, men mindre mengder av andre alkoholer kan være tilstede.
De relative mengder av de termoplastiske materialer og mykningsmidlet som anvendes, kan varieres innen vide grenser, alt etter de spesielle egenskaper som kreves. Vanligvis er mengden lik de mengder som anvendes vanligvis med andre mykningsmidler, og en mengde av mykningsmidlet i produktene av fra ca. 10 til 60 vektprosent er f. eks. skikket for de fleste øyemed.
Foruten de termoplastiske materialer og esterplastiseringsmidlene ifølge oppfinnelsen kan der være til stede andre be-standdeler i komposisjonene, hvis dette er ønsket, f. eks. andre mykningsmidler, eks-tendere, stabiliseringsmidler, fyllstoffer og farvestoffer.
Komposisjonene av plastiserte materialer som tilveiebringes i henhold til foreliggende oppfinnelse, kan anvendes til et stort antall forskjellige formål. F. eks. er komposisjoner av denne art som inneholder polyvinylklorid som er plastisert med ftal-atestere av de beskrevne alkoholer meget godt skikket for fremstilling av krystall-klare kalanderte plater, gulv og veggfliser og transportbelter. De er også skikket for kabelisolering og for fremstilling av pro-dukter for utførelse av hylstre o. 1. til kab-ler. Disse komposisjoner kan også anvendes for å tilveiebringe polyvinylklorid-pastaer for slike øyemed som neddyppings-forming eller støping ved fremstilling av f. eks. hansker. Andre anvendelser for slike komposisjoner vil lett forstås av fagfolk.
Alkoholene som anvendes ved frem- 1 stillingen av esterplastiseringsmidlene og komposisjonene ifølge oppfinnelsen kan : fås ved å behandle et passende olefin eller olefinblanding i to trinn. I det første trinn fremstilles et olefin eller en blanding av olefiner ved dimerisering. Det annet trinn omfatter behandling i en karbonyliserings-prosess, hvor dimeriseringsproduktet fra det første trinn behandles med en blanding av kulloksyd og vannstoff og produktet utsettes derpå for en hydreringsbehand-ling. F. eks. kan 3-metyll-heksanol-l fremstilles ved dimerisering av propylen i nær-vær av en aluminiumalkylforbindelse så at man får 2-metyll-penten-l, som efter kar-bonylisering og hydrering gir 3-metyll-heksanol-l, som kan forestres med en organisk syre efler syrer, så at der tilveiebringes estere for anvendelse i komposisjoner ifølge oppfinnelsen. En blanding av propylen og buten-1 gir som dimeriseringsprodukt en blanding av olefiner, hvorfra kan utskilles tre fraksjoner, 2-metyll-penten-l, 2-etyll-hexen-1, og en blanding av isomerene 2-metyll-hexen-1 og 2-etyll-penten-l. Disse fraksjoner kan særskilt behandles i et kar-bonyliseringstrinn for å gi resp. 3-metyll-hexanol-1, 3-etyll-heptanol-l og en blanding bestående av isomerene 3-metyll-heptanol-1 og 3-etyll-hexanol-l. Disse alkoholer kan sluttelig forestres med en eller flere organiske syrer for å tilveiebringe estere for anvendelse i komposisjoner ifølge foreliggende oppfinnelse.
I det følgende eksempel ble den føl-gende sammensetning overalt anvendt:
Plastiseringsmidlet for hver prøve omfatter en pftalatester, og sammensetningen ble fremstilt i henhold til et vanlig arbeids-forløp. Formete prøver ble fremstilt og ut-satt for de mekaniske og elektriske prøver, som er anført i «British Standard for Flex-ible Polyvinyl Chloride Extrusion Com-pounds 2571:1955.
Eksempel.
Claims (1)
- Mykningsmiddel av estertypen for termoplastharpikser, særlig vinylplast og celluloseplast, karakterisert ved at nevnte middel er en ester av en organisk syre og i det minste én av alkoholene 3-metyllhek-sanol-1, 3-etyllheksanol-l, 3-metyllhepta-nol-1 og 3-etyllheptanol-l, og nevnte organiske syre er fortrinnsvis ftalsyre, glutarsyre, suberinsyre, adipinsyre, azelainsyre, pimelinsyre eller sebasinsyre.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US568578A US3394750A (en) | 1966-07-28 | 1966-07-28 | Pneumatic expansible tire having resilient folding sidewalls |
Publications (1)
Publication Number | Publication Date |
---|---|
NO121079B true NO121079B (no) | 1971-01-11 |
Family
ID=24271850
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO169151A NO121079B (no) | 1966-07-28 | 1967-07-22 |
Country Status (7)
Country | Link |
---|---|
US (1) | US3394750A (no) |
DE (1) | DE1605701A1 (no) |
FI (1) | FI49787C (no) |
GB (1) | GB1191736A (no) |
NL (1) | NL149443B (no) |
NO (1) | NO121079B (no) |
SE (1) | SE329349B (no) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4177851A (en) * | 1976-03-15 | 1979-12-11 | The Goodyear Tire & Rubber Company | Foldable spare tire |
JPS52126804A (en) * | 1976-04-15 | 1977-10-25 | Bridgestone Corp | Foldable tire |
FR2427916A1 (fr) * | 1978-06-05 | 1980-01-04 | Michelin & Cie | Pneumatique de secours a carcasse radiale |
US4238259A (en) * | 1979-05-21 | 1980-12-09 | The Goodyear Tire & Rubber Company | Foldable spare tire |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3347300A (en) * | 1965-07-20 | 1967-10-17 | Goodrich Co B F | Tire |
-
1966
- 1966-07-28 US US568578A patent/US3394750A/en not_active Expired - Lifetime
-
1967
- 1967-07-19 DE DE19671605701 patent/DE1605701A1/de active Pending
- 1967-07-22 NO NO169151A patent/NO121079B/no unknown
- 1967-07-26 NL NL676710311A patent/NL149443B/xx unknown
- 1967-07-27 SE SE10904/67*A patent/SE329349B/xx unknown
- 1967-07-28 FI FI672074A patent/FI49787C/fi active
- 1967-07-28 GB GB34874/67A patent/GB1191736A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB1191736A (en) | 1970-05-13 |
FI49787C (fi) | 1975-10-10 |
NL6710311A (no) | 1968-01-29 |
DE1605701A1 (de) | 1971-01-28 |
SE329349B (no) | 1970-10-05 |
NL149443B (nl) | 1976-05-17 |
US3394750A (en) | 1968-07-30 |
FI49787B (no) | 1975-06-30 |
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