GB867278A - Solvent compositions, and resin solutions and compositions comprising resins dissolved in solvent compositions - Google Patents
Solvent compositions, and resin solutions and compositions comprising resins dissolved in solvent compositionsInfo
- Publication number
- GB867278A GB867278A GB1735558A GB1735558A GB867278A GB 867278 A GB867278 A GB 867278A GB 1735558 A GB1735558 A GB 1735558A GB 1735558 A GB1735558 A GB 1735558A GB 867278 A GB867278 A GB 867278A
- Authority
- GB
- United Kingdom
- Prior art keywords
- solvent
- acetate
- vinyl chloride
- butyrolactone
- vinyl
- Prior art date
- 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
Links
- 239000000203 mixture Substances 0.000 title abstract 9
- 239000002904 solvent Substances 0.000 title abstract 8
- 239000011347 resin Substances 0.000 title 2
- 229920005989 resin Polymers 0.000 title 2
- -1 ethyl- Chemical group 0.000 abstract 8
- 229920001577 copolymer Polymers 0.000 abstract 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 6
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 abstract 6
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 abstract 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 5
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 5
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 239000008096 xylene Substances 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract 2
- 150000003997 cyclic ketones Chemical class 0.000 abstract 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 abstract 2
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 2
- 150000002596 lactones Chemical class 0.000 abstract 2
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 239000011707 mineral Substances 0.000 abstract 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 235000015096 spirit Nutrition 0.000 abstract 2
- 150000003738 xylenes Chemical class 0.000 abstract 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 239000011976 maleic acid Substances 0.000 abstract 1
- 229920003002 synthetic resin Polymers 0.000 abstract 1
- 239000000057 synthetic resin Substances 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- C09D127/00—Coating compositions based on homopolymers or 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 halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or 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 halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/04—Coating compositions based on homopolymers or 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 halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C09D127/06—Homopolymers or copolymers of vinyl chloride
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Polymerisation Methods In General (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Paints Or Removers (AREA)
Abstract
Copolymers of vinyl acetate and less than 92,6% mol of vinyl chloride are soluble in a solvent composition comprising (1) a mononuclear aromatic hydrocarbon and (ii) at least 7% (by weight of (i) and (ii) of g -butyrolactone or a C1 to C4 alkyl substituted derivative thereof or a mixture of such lactones. Aromatic hydrocarbons mentioned are benzene, toluene, the xylenes and mixtures thereof; ethyl-, propyl- and butyl-substituted benzenes; and mesitylene; the presence of up to 5% of aliphatic hydrocarbons, e.g. mineral spirits, in the aromatic hydrocarbons is tolerable. g -butyrolactone derivatives specified are those substituted by methyl, ethyl or propyl groups or one or more of the a -, b - or g -carbon atoms e.g. g -valerolactone. The solvent composition may also contain up to 30% of methyl ethyl ketone, a glycol ether acetate, dimethyl p formamide, cyclic ketones such as cyclohexanone, or isophorone. Examples contrast the effectiveness of the lactones and cyclohexanone and isophorone in combination with varying proportions of xylene as a solvent 87/13 %wt. vinyl chloride/acetate copolymer; and of g -butyrolactone/styrene in varying proportions as a solvent for 87/13 and 90/10 vinyl chloride/acetate copolymers, 86/13/1 vinyl chloride/vinyl acetate/maleic acid copolymer, 6/3/91 vinyl alcohol/vinyl acetate/vinyl chloride copolymer obtained by the hydrolysis of a 87/13 vinyl chloride/acetate copolymer, and P.V.C. Mention is also made of copolymers including a few per cent of acrylic acid. Specification 758,489 is referred to.ALSO:A composition comprising a mono-nuclear aromatic hydrocarbon and at least 7 wt. % of gamma-butyrolactone and/or one or more C1 to C4 alkyl substituted derivatives thereof is a solvent for synthetic resins (see Group IV(a)). Alkyl derivatives specified are these substituted by methyl, ethyl or propyl groups on one or more of the alpha-, beta- or gammacarbon atoms e.g. gamma-valerolactone. Aromatic hydrocarbons mentioned are benzene, toluene, the xylenes, mesitylene, and ethyl-, propyl-, and butyl-substituted benzenes. The presence of up to 5% aliphatic hydrocarbons, e.g. mineral spirits is tolerable. The solvent composition may also contain up to 30% of methyl ethyl ketone, a glycol ether acetate, dimethyl formamide, cyclic ketones such as cyclohexanone, or isophorone. Specification 758,489 is referred to.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1735558A GB867278A (en) | 1958-05-30 | 1958-05-30 | Solvent compositions, and resin solutions and compositions comprising resins dissolved in solvent compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1735558A GB867278A (en) | 1958-05-30 | 1958-05-30 | Solvent compositions, and resin solutions and compositions comprising resins dissolved in solvent compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB867278A true GB867278A (en) | 1961-05-03 |
Family
ID=10093729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1735558A Expired GB867278A (en) | 1958-05-30 | 1958-05-30 | Solvent compositions, and resin solutions and compositions comprising resins dissolved in solvent compositions |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB867278A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4675354A (en) * | 1982-12-01 | 1987-06-23 | A/S F. Heimann & Co. | Glue solution |
-
1958
- 1958-05-30 GB GB1735558A patent/GB867278A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4675354A (en) * | 1982-12-01 | 1987-06-23 | A/S F. Heimann & Co. | Glue solution |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB580911A (en) | Improvements in or relating to the manufacture of polystyrene | |
| GB1424002A (en) | Hair preparations | |
| GB1263152A (en) | Distillate petroleum oil compositions | |
| KR920002717A (en) | Powder coating composition | |
| JPS5674145A (en) | Preparation of polyamide resin composition | |
| GB980880A (en) | Electrophotographic materials | |
| GB1126208A (en) | Composition and process of preparing solid infusible resin | |
| GB867278A (en) | Solvent compositions, and resin solutions and compositions comprising resins dissolved in solvent compositions | |
| GB1164180A (en) | Hair Dressing Compositions | |
| GB1185226A (en) | Hot Melt Adhesive | |
| US3285819A (en) | Poly(n-propyl-n-vinylacetamide) in hair setting compositions | |
| GB862845A (en) | Resin solutions comprising resins dissolved in solvent compositions | |
| GB1164374A (en) | Poly-(1,4-Bis-(Hydroxymethyl)-Cyclohexane-Terephthalate) having improved Dyeability | |
| ES336958A1 (en) | PROCEDURE FOR THE PREPARATION OF NEW N, - N'DIGLICIDILIC COMPOUNDS, SOLUBLE IN WATER. | |
| JPS5738864A (en) | Preparation of coating composition | |
| KR830007725A (en) | Method for producing colored molding of thermoplastic resin | |
| GB756138A (en) | Stabilizing alkenyl aromatic resins against weathering | |
| GB1193151A (en) | Coloured Polymers | |
| GB1048863A (en) | Plasticizers and plasticized compositions | |
| SU566794A1 (en) | Polymer-concrete composition | |
| GB899667A (en) | Crystalline griseofulvin | |
| Takahashi et al. | Oligoethylenes in high pressure polyethylenes: II. Production mechanism | |
| GB996350A (en) | Improvements in or relating to cross-linking polymers | |
| JPS5491542A (en) | Pressure-sensitive adhesive composition | |
| GB835759A (en) | Polymers of branched chain ª‡-olefins and process for preparing them |