GB786796A - Wax modified polystyrene compositions and process of manufacture - Google Patents

Wax modified polystyrene compositions and process of manufacture

Info

Publication number
GB786796A
GB786796A GB16511/55A GB1651155A GB786796A GB 786796 A GB786796 A GB 786796A GB 16511/55 A GB16511/55 A GB 16511/55A GB 1651155 A GB1651155 A GB 1651155A GB 786796 A GB786796 A GB 786796A
Authority
GB
United Kingdom
Prior art keywords
wax
emulsions
aqueous
polystyrene
sodium
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
Application number
GB16511/55A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Union Carbide Corp
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.)
Filing date
Publication date
Application filed by Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB786796A publication Critical patent/GB786796A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/10Metal compounds
    • C08K3/14Carbides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions 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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/06Polystyrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06Waxes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

In the process for making round records of the parent Specification, the wax and additional polystyrene which is added is obtained by precipitating a mixture of aqueous wax and polystyrene emulsions, drying, and mechanically working at between 160 DEG and 225 DEG C., before incorporating in the basic polystyrenecarbide composition. The wax emulsions may be prepared from carnauba, candelilla, montan, esparto, oricury, beeswax, cotton wax, insect wax, japan wax; a synthetic wax made by hydrogenating vegetable, marine or animal oils; or mineral waxes such as paraffin and microcrystalline waxes, ozokerite, or ceresin. The emulsions may contain zinc stearate and polyethylene glycol oleyl ether. The polystyrene emulsions may be prepared by polymerizing styrene by heating in aqueous emulsion with a potassium persulphate catalyst, a sodium soap of dehydrogenated rosin, t-dodecyl mercaptan and sodium hydroxide under nitrogen, preferably to give Standinger molecular weights of 40,000 to 150,000. The mixed emulsions may be precipitated by aqueous sodium chloridehydrochloric acid solution, aqueous isopropanol or aqueous acetic acid, and the coagulum dehydrated by exposure to air or heat. The mechanical working is carried out in a heated screw extrusion, Banbury or multi-parallel roller mixer. The product is diced and blended with fillers, e.g. diatomaceous silica, slate flour and calcium carbonate, pigments, e.g. carbon black and soaps such as zinc and calcium stearates, and moulded.
GB16511/55A 1952-10-21 1955-06-08 Wax modified polystyrene compositions and process of manufacture Expired GB786796A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US747030XA 1952-10-21 1952-10-21
US786796XA 1954-06-14 1954-06-14

Publications (1)

Publication Number Publication Date
GB786796A true GB786796A (en) 1957-11-27

Family

ID=26755958

Family Applications (2)

Application Number Title Priority Date Filing Date
GB28987/53A Expired GB747030A (en) 1952-10-21 1953-10-20 Sound record
GB16511/55A Expired GB786796A (en) 1952-10-21 1955-06-08 Wax modified polystyrene compositions and process of manufacture

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB28987/53A Expired GB747030A (en) 1952-10-21 1953-10-20 Sound record

Country Status (1)

Country Link
GB (2) GB747030A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1584662A1 (en) * 2004-04-06 2005-10-12 Clariant GmbH Use of waxes as lubricant in filled polymers.

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1584662A1 (en) * 2004-04-06 2005-10-12 Clariant GmbH Use of waxes as lubricant in filled polymers.

Also Published As

Publication number Publication date
GB747030A (en) 1956-03-28

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