GB654477A - Improvements in or relating to non-rubbery, free-flowing pulverulent vinyl chloride compositions and method of producing same - Google Patents
Improvements in or relating to non-rubbery, free-flowing pulverulent vinyl chloride compositions and method of producing sameInfo
- Publication number
- GB654477A GB654477A GB9336/48A GB933648A GB654477A GB 654477 A GB654477 A GB 654477A GB 9336/48 A GB9336/48 A GB 9336/48A GB 933648 A GB933648 A GB 933648A GB 654477 A GB654477 A GB 654477A
- Authority
- GB
- United Kingdom
- Prior art keywords
- butyl
- polymer
- vinyl
- methyl
- ketone
- 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 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title abstract 2
- 229920000642 polymer Polymers 0.000 abstract 5
- 229920001577 copolymer Polymers 0.000 abstract 4
- -1 lithopone Chemical compound 0.000 abstract 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 3
- 239000004615 ingredient Substances 0.000 abstract 3
- 239000004014 plasticizer Substances 0.000 abstract 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 abstract 3
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 abstract 2
- 238000013329 compounding Methods 0.000 abstract 2
- 150000005690 diesters Chemical class 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- 239000000843 powder Substances 0.000 abstract 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 abstract 2
- FZDRTKCXVAUHJB-UHFFFAOYSA-N (2-methylnaphthalen-1-yl)-phenylmethanone Chemical compound CC1=CC=C2C=CC=CC2=C1C(=O)C1=CC=CC=C1 FZDRTKCXVAUHJB-UHFFFAOYSA-N 0.000 abstract 1
- SNDGLCYYBKJSOT-UHFFFAOYSA-N 1,1,3,3-tetrabutylurea Chemical compound CCCCN(CCCC)C(=O)N(CCCC)CCCC SNDGLCYYBKJSOT-UHFFFAOYSA-N 0.000 abstract 1
- MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 abstract 1
- PMDHMYFSRFZGIO-UHFFFAOYSA-N 1,4,7-trioxacyclotridecane-8,13-dione Chemical compound O=C1CCCCC(=O)OCCOCCO1 PMDHMYFSRFZGIO-UHFFFAOYSA-N 0.000 abstract 1
- MAIQOOYTTWNDGG-UHFFFAOYSA-N 1-O-butyl 4-O-octadecyl butanedioate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC(=O)OCCCC MAIQOOYTTWNDGG-UHFFFAOYSA-N 0.000 abstract 1
- KTHUKEZOIFYPEH-UHFFFAOYSA-N 1-benzylnaphthalene Chemical compound C=1C=CC2=CC=CC=C2C=1CC1=CC=CC=C1 KTHUKEZOIFYPEH-UHFFFAOYSA-N 0.000 abstract 1
- YBVRNZTWGYQFKN-UHFFFAOYSA-N 1-naphthalen-1-yldodecan-1-one Chemical compound C1=CC=C2C(C(=O)CCCCCCCCCCC)=CC=CC2=C1 YBVRNZTWGYQFKN-UHFFFAOYSA-N 0.000 abstract 1
- FDHDUXOBMHHFFJ-UHFFFAOYSA-N 1-pentylnaphthalene Chemical compound C1=CC=C2C(CCCCC)=CC=CC2=C1 FDHDUXOBMHHFFJ-UHFFFAOYSA-N 0.000 abstract 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- YEVQZPWSVWZAOB-UHFFFAOYSA-N 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(I)C(CBr)=C1 YEVQZPWSVWZAOB-UHFFFAOYSA-N 0.000 abstract 1
- XXUNIGZDNWWYED-UHFFFAOYSA-N 2-methylbenzamide Chemical compound CC1=CC=CC=C1C(N)=O XXUNIGZDNWWYED-UHFFFAOYSA-N 0.000 abstract 1
- JBQKDXQJSYBVEN-UHFFFAOYSA-N 6-dodecoxy-6-oxohexanoic acid Chemical compound CCCCCCCCCCCCOC(=O)CCCCC(O)=O JBQKDXQJSYBVEN-UHFFFAOYSA-N 0.000 abstract 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 abstract 1
- HTIRHQRTDBPHNZ-UHFFFAOYSA-N Dibutyl sulfide Chemical group CCCCSCCCC HTIRHQRTDBPHNZ-UHFFFAOYSA-N 0.000 abstract 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 abstract 1
- OXPCWUWUWIWSGI-MSUUIHNZSA-N Lauryl oleate Chemical compound CCCCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC OXPCWUWUWIWSGI-MSUUIHNZSA-N 0.000 abstract 1
- 229910000003 Lead carbonate Inorganic materials 0.000 abstract 1
- 241000276489 Merlangius merlangus Species 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 abstract 1
- NKSOSPOXQKNIKJ-CLFAGFIQSA-N Polyoxyethylene dioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCOC(=O)CCCCCCC\C=C/CCCCCCCC NKSOSPOXQKNIKJ-CLFAGFIQSA-N 0.000 abstract 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 abstract 1
- 229920001800 Shellac Polymers 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 abstract 1
- 239000010425 asbestos Substances 0.000 abstract 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 abstract 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 abstract 1
- BEWFIPLBFJGWSR-UHFFFAOYSA-N butyl 12-acetyloxyoctadec-9-enoate Chemical compound CCCCCCC(OC(C)=O)CC=CCCCCCCCC(=O)OCCCC BEWFIPLBFJGWSR-UHFFFAOYSA-N 0.000 abstract 1
- VFGRALUHHHDIQI-UHFFFAOYSA-N butyl 2-hydroxyacetate Chemical compound CCCCOC(=O)CO VFGRALUHHHDIQI-UHFFFAOYSA-N 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 239000000378 calcium silicate Substances 0.000 abstract 1
- 229910052918 calcium silicate Inorganic materials 0.000 abstract 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 abstract 1
- 238000003490 calendering Methods 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000006229 carbon black Substances 0.000 abstract 1
- 239000004359 castor oil Substances 0.000 abstract 1
- 235000019438 castor oil Nutrition 0.000 abstract 1
- 239000004568 cement Substances 0.000 abstract 1
- 239000006231 channel black Substances 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- AMFIJXSMYBKJQV-UHFFFAOYSA-L cobalt(2+);octadecanoate Chemical compound [Co+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AMFIJXSMYBKJQV-UHFFFAOYSA-L 0.000 abstract 1
- 239000003240 coconut oil Substances 0.000 abstract 1
- 235000019864 coconut oil Nutrition 0.000 abstract 1
- 238000004040 coloring Methods 0.000 abstract 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 abstract 1
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 abstract 1
- KYBDAUNESKLXAZ-UHFFFAOYSA-N didodecyl oxalate Chemical compound CCCCCCCCCCCCOC(=O)C(=O)OCCCCCCCCCCCC KYBDAUNESKLXAZ-UHFFFAOYSA-N 0.000 abstract 1
- VOEQTGMCAHZUNJ-AATRIKPKSA-N diethyl (e)-2-chlorobut-2-enedioate Chemical compound CCOC(=O)\C=C(\Cl)C(=O)OCC VOEQTGMCAHZUNJ-AATRIKPKSA-N 0.000 abstract 1
- BQHDXNZNSPVVKB-UHFFFAOYSA-N diethyl 2-methylidenepropanedioate Chemical compound CCOC(=O)C(=C)C(=O)OCC BQHDXNZNSPVVKB-UHFFFAOYSA-N 0.000 abstract 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 abstract 1
- 229940106012 diethylene glycol adipate Drugs 0.000 abstract 1
- ZWWQRMFIZFPUAA-UHFFFAOYSA-N dimethyl 2-methylidenebutanedioate Chemical compound COC(=O)CC(=C)C(=O)OC ZWWQRMFIZFPUAA-UHFFFAOYSA-N 0.000 abstract 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 abstract 1
- 238000001125 extrusion Methods 0.000 abstract 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 238000001746 injection moulding Methods 0.000 abstract 1
- 239000011133 lead Substances 0.000 abstract 1
- HTUMBQDCCIXGCV-UHFFFAOYSA-N lead oxide Chemical compound [O-2].[Pb+2] HTUMBQDCCIXGCV-UHFFFAOYSA-N 0.000 abstract 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N lead(II) oxide Inorganic materials [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 abstract 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 abstract 1
- 239000001095 magnesium carbonate Substances 0.000 abstract 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 abstract 1
- 239000000395 magnesium oxide Substances 0.000 abstract 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- OBPFYQODGYGZPG-UHFFFAOYSA-N n,n-dibutyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)N(CCCC)CCCC OBPFYQODGYGZPG-UHFFFAOYSA-N 0.000 abstract 1
- GIPDEPRRXIBGNF-KTKRTIGZSA-N oxolan-2-ylmethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC1CCCO1 GIPDEPRRXIBGNF-KTKRTIGZSA-N 0.000 abstract 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 abstract 1
- PBOUTGGNTILOQZ-UHFFFAOYSA-N phenyl(1,2,3,4-tetrahydronaphthalen-1-yl)methanone Chemical compound C1CCC2=CC=CC=C2C1C(=O)C1=CC=CC=C1 PBOUTGGNTILOQZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 abstract 1
- 229910052895 riebeckite Inorganic materials 0.000 abstract 1
- 229940113147 shellac Drugs 0.000 abstract 1
- 239000004208 shellac Substances 0.000 abstract 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 abstract 1
- 235000013874 shellac Nutrition 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- 229940072958 tetrahydrofurfuryl oleate Drugs 0.000 abstract 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 abstract 1
- BANLNYYTSYHBAP-SQFISAMPSA-N tributyl (z)-prop-1-ene-1,2,3-tricarboxylate Chemical compound CCCCOC(=O)C\C(C(=O)OCCCC)=C\C(=O)OCCCC BANLNYYTSYHBAP-SQFISAMPSA-N 0.000 abstract 1
- 239000001993 wax Substances 0.000 abstract 1
- 239000011667 zinc carbonate Substances 0.000 abstract 1
- 229910000010 zinc carbonate Inorganic materials 0.000 abstract 1
- 235000004416 zinc carbonate Nutrition 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/18—Plasticising macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of 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; Derivatives of such polymers
- C08J2327/02—Characterised by the use of 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; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/04—Characterised by the use of 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; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08J2327/06—Homopolymers or copolymers of vinyl chloride
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Free-flowing pulverulent plasticized vinyl chloride polymer or copolymer compositions are made by mixing the finely-divided polymer or copolymer, without solid ingredients save a minor proportion of stabilizer or colouring materials, if desired, with a plasticizer for the polymer, whereby a damp mixture containing discrete particles of polymer is formed and heating and agitating the mixture at a temperature in the range of 200 DEG to 250 DEG F. for a period of from 10 to 30 minutes until the polymer or copolymer has completely absorbed the plasticizer. Optionally, the plasticized particles either while hot or cooled may be mixed with powdered compounding ingredients until a free-flowing powder results. The other component of the vinyl chloride copolymer may be vinylidene chloride, methyl acrylate, ethyl acrylate, methyl methacrylate, vinyl acetate, vinyl butyrate, vinyl naphthalene, acrylonitrile, ethyl methylene malonate, styrene, methyl vinyl ketone, dimethylitaconate, diethyl fumarate, diethyl chloromaleate. Specified compounding ingredients are lead carbonate, calcined clay, carbon and channel black, lead stearate, organic dyes, zinc oxide, magnesium oxide, aluminium oxide, magnesium carbonate, lead silicate, calcium silicate, ground whiting, barytes, lithopone, litharge, zinc carbonate, asbestos powder, waxes, diatomaceous earths, cobalt stearate, rosin and shellac. The plasticizers may be di-2-ethyl hexyl-, di-butoxyethyl-di-(n)-butyl-, dilauryl-, dimethyl glycol-, octadecyl butyl-, dihexyl-, didodecyl-di - 1 - methylheptyl -, dioctyl - phthalate, tricresyl-, tributyl-, tris-(beta-butoxyethyl)-, trioctyl-phosphate, dodecyl adipate, diethylene glycol adipate, dodecyloleate, tetrahydrofurfuryl oleate, ethylene glycol dioleate, butyl acetyl ricinoleate, di-2-ethylhexyl sebacate, octadecyl butyl succinate, 1,10-decamethylene glycol dicaprylate, tributyl aconitate, butyl phthalyl butyl glycollate, diesters of triethylene glycol and aliphatic acids of 8 to 14 carbon atoms, acetylated castor oil, dilauryl oxalate, tetraethyl adipamide, N,N-dibutyl stearamide, methyl benzamide, N-mon-butyl benzene sulphonamide, N,N,N1,N1-tetraethyl adipamide, tetrahydronaphthyl phenyl ketone, methyl naphthyl phenyl ketone, undecyl naphthyl ketone, xylyl undecyl ketone, amyl naphthalene, tetrabutyl urea, benzylnaphthalene, betaphenoxymethyl tetralin, dibutyl thio diglycollate, methylene bis-butyl thioglycollate, aliphatic acids, diesters from triethylene glycol and coconut oil, and mixtures. The compositions may be used for extrusion or injection moulding, in coating and calendering operations and dissolved in solvents for use in cements. Specification 564,127 is referred to.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US96422147A | 1947-04-30 | 1947-04-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB654477A true GB654477A (en) | 1951-06-20 |
Family
ID=22062779
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB9336/48A Expired GB654477A (en) | 1947-04-30 | 1948-04-02 | Improvements in or relating to non-rubbery, free-flowing pulverulent vinyl chloride compositions and method of producing same |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB654477A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE953119C (en) * | 1952-01-30 | 1956-11-29 | Ici Ltd | Process for the preparation of vinyl chloride polymers |
| US3287309A (en) * | 1963-03-13 | 1966-11-22 | Monsanto Co | Process for incorporating additives |
| US11597859B2 (en) | 2020-01-24 | 2023-03-07 | Oatey Co. | Solvent cement formulations having extended shelf life |
-
1948
- 1948-04-02 GB GB9336/48A patent/GB654477A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE953119C (en) * | 1952-01-30 | 1956-11-29 | Ici Ltd | Process for the preparation of vinyl chloride polymers |
| US3287309A (en) * | 1963-03-13 | 1966-11-22 | Monsanto Co | Process for incorporating additives |
| US11597859B2 (en) | 2020-01-24 | 2023-03-07 | Oatey Co. | Solvent cement formulations having extended shelf life |
| US11976222B2 (en) | 2020-01-24 | 2024-05-07 | Oatey Co. | Solvent cement formulations having extended shelf life |
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