GB1462851A - Method of preparing pulverulent compositions of polymers and copolymers based on vinyl chloride - Google Patents
Method of preparing pulverulent compositions of polymers and copolymers based on vinyl chlorideInfo
- Publication number
- GB1462851A GB1462851A GB375874A GB375874A GB1462851A GB 1462851 A GB1462851 A GB 1462851A GB 375874 A GB375874 A GB 375874A GB 375874 A GB375874 A GB 375874A GB 1462851 A GB1462851 A GB 1462851A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyethylene wax
- aqueous
- graft polymer
- polyvinyl chloride
- homogeneous phase
- 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 7
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title abstract 4
- 229920001577 copolymer Polymers 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 2
- 229920000642 polymer Polymers 0.000 title abstract 2
- 229920000578 graft copolymer Polymers 0.000 abstract 5
- 229920000915 polyvinyl chloride Polymers 0.000 abstract 5
- 239000004800 polyvinyl chloride Substances 0.000 abstract 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 abstract 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 4
- 239000004698 Polyethylene Substances 0.000 abstract 4
- 239000000654 additive Substances 0.000 abstract 4
- 229920000573 polyethylene Polymers 0.000 abstract 4
- 239000006185 dispersion Substances 0.000 abstract 3
- 238000002156 mixing Methods 0.000 abstract 3
- 239000004209 oxidized polyethylene wax Substances 0.000 abstract 3
- 235000013873 oxidized polyethylene wax Nutrition 0.000 abstract 3
- -1 polyethylene Polymers 0.000 abstract 3
- KEQXNNJHMWSZHK-UHFFFAOYSA-L 1,3,2,4$l^{2}-dioxathiaplumbetane 2,2-dioxide Chemical compound [Pb+2].[O-]S([O-])(=O)=O KEQXNNJHMWSZHK-UHFFFAOYSA-L 0.000 abstract 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 239000001110 calcium chloride Substances 0.000 abstract 2
- 229910001628 calcium chloride Inorganic materials 0.000 abstract 2
- 239000002270 dispersing agent Substances 0.000 abstract 2
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 abstract 2
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 abstract 2
- 239000004816 latex Substances 0.000 abstract 2
- 229920000126 latex Polymers 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- FLPJVCMIKUWSDR-UHFFFAOYSA-N 2-(4-formylphenoxy)acetamide Chemical compound NC(=O)COC1=CC=C(C=O)C=C1 FLPJVCMIKUWSDR-UHFFFAOYSA-N 0.000 abstract 1
- KLLLJCACIRKBDT-UHFFFAOYSA-N 2-phenyl-1H-indole Chemical compound N1C2=CC=CC=C2C=C1C1=CC=CC=C1 KLLLJCACIRKBDT-UHFFFAOYSA-N 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- MTUBBMSQXXJFQP-UHFFFAOYSA-N OC(CCCCCCCCCCCCCCCCC(=O)OCC(O)CO)(O)O Chemical compound OC(CCCCCCCCCCCCCCCCC(=O)OCC(O)CO)(O)O MTUBBMSQXXJFQP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005062 Polybutadiene Substances 0.000 abstract 1
- 235000021355 Stearic acid Nutrition 0.000 abstract 1
- 229910010413 TiO 2 Inorganic materials 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- HUTDDBSSHVOYJR-UHFFFAOYSA-H bis[(2-oxo-1,3,2$l^{5},4$l^{2}-dioxaphosphaplumbetan-2-yl)oxy]lead Chemical compound [Pb+2].[Pb+2].[Pb+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O HUTDDBSSHVOYJR-UHFFFAOYSA-H 0.000 abstract 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 abstract 1
- 239000008116 calcium stearate Substances 0.000 abstract 1
- 235000013539 calcium stearate Nutrition 0.000 abstract 1
- 229940074979 cetyl palmitate Drugs 0.000 abstract 1
- 238000004040 coloring Methods 0.000 abstract 1
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 abstract 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 238000000605 extraction Methods 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- PXDJXZJSCPSGGI-UHFFFAOYSA-N hexadecanoic acid hexadecyl ester Natural products CCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC PXDJXZJSCPSGGI-UHFFFAOYSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 229920000609 methyl cellulose Polymers 0.000 abstract 1
- 239000001923 methylcellulose Substances 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 1
- 229920002857 polybutadiene Polymers 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 235000012424 soybean oil Nutrition 0.000 abstract 1
- 239000008117 stearic acid Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 235000016804 zinc Nutrition 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions 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; Compositions of derivatives of such polymers
- C08L27/02—Compositions 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; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions 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; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—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)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7303661A FR2216311B1 (enExample) | 1973-02-02 | 1973-02-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1462851A true GB1462851A (en) | 1977-01-26 |
Family
ID=9114218
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB375874A Expired GB1462851A (en) | 1973-02-02 | 1974-01-28 | Method of preparing pulverulent compositions of polymers and copolymers based on vinyl chloride |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US3898189A (enExample) |
| JP (1) | JPS5133181A (enExample) |
| AR (1) | AR197539A1 (enExample) |
| BE (1) | BE810537A (enExample) |
| DE (1) | DE2404619C3 (enExample) |
| ES (1) | ES422776A1 (enExample) |
| FR (1) | FR2216311B1 (enExample) |
| GB (1) | GB1462851A (enExample) |
| IT (1) | IT1008788B (enExample) |
| NL (1) | NL168535C (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2433562A1 (de) * | 1974-07-12 | 1976-01-29 | Degussa | Verfahren zur herstellung von pigment/ kunststoff-konzentraten |
| US3965039A (en) * | 1974-11-19 | 1976-06-22 | Chaplits Donat N | Ion-exchange molded catalyst and method of its preparation |
| FR2334706A2 (fr) * | 1975-12-11 | 1977-07-08 | Rhone Poulenc Ind | Procede de preparation en milieu aqueux de compositions pulverulentes polymeres et copolymeres a base de chlorure de vinyle directement pretes a l'emploi |
| DE2650331C3 (de) * | 1976-11-03 | 1981-05-07 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur Herstellung von zur Plastisolbereitung geeigneten Pulvern auf der Grundlage von Polyvinylchlorid |
| FR2413928A1 (fr) * | 1978-01-05 | 1979-08-03 | Rhone Poulenc Ind | Procede continu de mise en dispersion aqueuse finement divisee d'une phase homogene d'au moins un ingredient solide fusible |
| EP0005514B1 (de) * | 1978-05-19 | 1982-11-10 | Ciba-Geigy Ag | Additivsystem für die Verwendung in Polymeren |
| FR2670792B1 (fr) * | 1990-12-21 | 1993-04-16 | Rhone Poulenc Chimie | Poudres redispersables de polymeres vinyliques. |
| DE4117034A1 (de) * | 1991-05-24 | 1992-11-26 | Henkel Kgaa | Kationische schichtverbindungen modifiziert mit polymeren |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1569988A1 (de) * | 1964-06-09 | 1969-08-28 | Feldmuehle Ag | Verfahren zur Herstellung von Heissklebepraeparationen |
| FR1449669A (fr) * | 1965-04-30 | 1966-05-06 | Pechiney Saint Gobain | Procédé de préparation de composés polymères et copolymères à base de chlorure de vinyle et compositions sèches résultantes, aptes à subir directement des opérations de transformation |
| US3637571A (en) * | 1968-04-15 | 1972-01-25 | Rexall Drug Chemical | Process for preparing thermoplastic resin-additive compositions |
| GB1219352A (en) * | 1968-04-19 | 1971-01-13 | Ici Ltd | Compositions containing vinyl chloride polymers |
| DE1802471A1 (de) * | 1968-10-11 | 1970-05-14 | Bayer Ag | Verfahren zur Herstellung von homogenen,thermoplastischen und hochelastischen Kunststoffen aus Vinylchlorid-Polymerisaten und Polyurethanen |
| US3664978A (en) * | 1970-06-22 | 1972-05-23 | Phillips Petroleum Co | Agglomeration of fine rubber particles |
-
1973
- 1973-02-02 FR FR7303661A patent/FR2216311B1/fr not_active Expired
-
1974
- 1974-01-28 GB GB375874A patent/GB1462851A/en not_active Expired
- 1974-01-29 NL NLAANVRAGE7401196,A patent/NL168535C/xx not_active IP Right Cessation
- 1974-01-30 ES ES422776A patent/ES422776A1/es not_active Expired
- 1974-01-31 JP JP49012338A patent/JPS5133181A/ja active Granted
- 1974-01-31 DE DE2404619A patent/DE2404619C3/de not_active Expired
- 1974-01-31 AR AR252160A patent/AR197539A1/es active
- 1974-02-01 IT IT48098/74A patent/IT1008788B/it active
- 1974-02-01 US US438748A patent/US3898189A/en not_active Expired - Lifetime
- 1974-02-01 BE BE140494A patent/BE810537A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE2404619A1 (de) | 1974-08-22 |
| FR2216311A1 (enExample) | 1974-08-30 |
| DE2404619B2 (de) | 1975-07-17 |
| DE2404619C3 (de) | 1982-03-25 |
| US3898189A (en) | 1975-08-05 |
| AR197539A1 (es) | 1974-04-15 |
| IT1008788B (it) | 1976-11-30 |
| JPS543690B2 (enExample) | 1979-02-26 |
| FR2216311B1 (enExample) | 1976-05-14 |
| NL168535B (nl) | 1981-11-16 |
| ES422776A1 (es) | 1976-05-01 |
| NL168535C (nl) | 1984-05-16 |
| BE810537A (fr) | 1974-08-01 |
| NL7401196A (enExample) | 1974-08-06 |
| JPS5133181A (en) | 1976-03-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| 732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
| 732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
| PE20 | Patent expired after termination of 20 years |
Effective date: 19940127 |