GB866038A - Polyvinyl acetate powder and method of making the same - Google Patents

Polyvinyl acetate powder and method of making the same

Info

Publication number
GB866038A
GB866038A GB30426/58A GB3042658A GB866038A GB 866038 A GB866038 A GB 866038A GB 30426/58 A GB30426/58 A GB 30426/58A GB 3042658 A GB3042658 A GB 3042658A GB 866038 A GB866038 A GB 866038A
Authority
GB
United Kingdom
Prior art keywords
polyvinyl acetate
spray
drying
emulsion
inert material
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
GB30426/58A
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.)
Airco Inc
Original Assignee
Air Reduction Co Inc
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 Air Reduction Co Inc filed Critical Air Reduction Co Inc
Publication of GB866038A publication Critical patent/GB866038A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/12Powdering or granulating
    • C08J3/16Powdering or granulating by coagulating dispersions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D1/00Evaporating
    • B01D1/16Evaporating by spraying
    • B01D1/18Evaporating by spraying to obtain dry solids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • C08J3/205Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase
    • C08J3/21Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase
    • C08J3/212Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase and solid additives
    • 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
    • C08K3/01Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013Fillers, pigments or reinforcing additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2331/00Characterised by the use of 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 acyloxy radical of a saturated carboxylic acid, or carbonic acid, or of a haloformic acid
    • C08J2331/02Characterised by the use of omopolymers or copolymers of esters of monocarboxylic acids
    • C08J2331/04Homopolymers or copolymers of vinyl acetate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A dry polyvinyl acetate powder, which can be reconstituted upon the addition of water to form an emulsion having substantially the properties of the original aqueous emulsion from which it is obtained, is prepared by spray-drying the aqueous emulsion and, before the polyvinyl acetate is completely dried, adding thereto an inert material, the drying of the polyvinyl acetate being completed in the presence of the inert material. Inert materials are exemplified by pigments and fillers such as clay, talc, calcium carbonate, silica, diatomaceous earth and titanium dioxide. Not less than 5% of inert material, based on the weight of the dried polyvinyl acetate powder, is employed. Preferred polyvinyl acetate emulsions are those in which the polyvinyl acetate particles have an average grain size of 2-8 microns and provide a solids content of 15-35%. Polyvinyl alcohol of low viscosity may be added as a stabilizer to the emulsion before spray-drying, the alcohol content being at least 10% by weight of the total solids present in the emulsion. A plasticizer may be incorporated into the dry polyvinyl acetate powder by mixing the plasticizer with an inert carrier and adding the mix to the polyvinyl acetate after the latter has been spray-dried or before the latter is completely dried by the spray-drying process. In either case inert material is also employed. Plasticizers exemplified are dipropylene glycol dibenzoate, dibutyl phthalate, and the mono-ethyl ether of diethylene glycol acetate. Inert carriers are preferred which have high absorptive capacity for the plasticizer, e.g. calcium silicate. Spray-drying is effected with maximum air inlet and outlet temperatures of 300 DEG F. and 130 DEG F.ALSO:<PICT:0866038/III/1> A dry polyvinyl acetate powder, which can be reconstituted upon the addition of water to form an emulsion having substantially the properties of the original aqueous emulsion from which it is obtained, is prepared by spray-drying the aqueous emulsion and, before the polyvinyl acetate is completely dried, adding thereto an inert material, the drying of the polyvinyl acetate being completed in the presence of the inert material. In Fig. 1 emulsion to be dried is fed into an atomizing device and hot air at a temperature not exceeding 300 DEG F. forces the spray into a vortex. Inert material is fed through a cold air inlet 4 which admits cooling air to control the drying temperature. The dried emulsion is removed through an outlet 3 at a temperature not greater than 130 DEG F. In another apparatus the spray chamber is wholly cylindrical and a vibrator hopper feeds inert material into the top of the chamber. In addition to inert materials (e.g. clay, talc, calcium carbonate, silica, diatomaceous earth and titanium dioxide) plasticizers mixed with or absorbed upon an inert carrier, and also polyvinyl alcohol, may be incorporated in the polyvinyl acetate powder.
GB30426/58A 1957-10-18 1958-09-23 Polyvinyl acetate powder and method of making the same Expired GB866038A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US866038XA 1957-10-18 1957-10-18

Publications (1)

Publication Number Publication Date
GB866038A true GB866038A (en) 1961-04-26

Family

ID=22199667

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30426/58A Expired GB866038A (en) 1957-10-18 1958-09-23 Polyvinyl acetate powder and method of making the same

Country Status (2)

Country Link
FR (1) FR1211157A (en)
GB (1) GB866038A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0841364A1 (en) * 1996-11-06 1998-05-13 Basf Aktiengesellschaft Powdery polymercompositions
DE102006053375A1 (en) * 2006-11-10 2008-05-15 Boehringer Ingelheim Pharma Gmbh & Co. Kg Process for mixing powders
EP1811008A3 (en) * 2006-01-18 2009-12-16 Joseph Iannicelli Method and composition for controlled heat release and disposable chemical heater utilizing same

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2214410C3 (en) * 1972-03-24 1978-10-12 Hoechst Ag, 6000 Frankfurt Process for the production of a redispersible vinyl acetate / ethylene polymer dispersion powder
DE4422438A1 (en) * 1994-06-29 1996-01-04 Hoechst Ag Device and method for adding aggregates to disk atomizing dryers

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0841364A1 (en) * 1996-11-06 1998-05-13 Basf Aktiengesellschaft Powdery polymercompositions
US6143808A (en) * 1996-11-06 2000-11-07 Basf Aktiengesellschaft Polymer compositions in powder form
AU743886B2 (en) * 1996-11-06 2002-02-07 Basf Aktiengesellschaft Polymer compositions in powder form
EP1811008A3 (en) * 2006-01-18 2009-12-16 Joseph Iannicelli Method and composition for controlled heat release and disposable chemical heater utilizing same
US8080172B2 (en) 2006-01-18 2011-12-20 J.I. Enterprises, Inc. Method and composition for controlled heat release and disposable chemical heater utilizing same
DE102006053375A1 (en) * 2006-11-10 2008-05-15 Boehringer Ingelheim Pharma Gmbh & Co. Kg Process for mixing powders
WO2008055951A1 (en) 2006-11-10 2008-05-15 Boehringer Ingelheim Pharma Gmbh & Co. Kg Method for mixing powders

Also Published As

Publication number Publication date
FR1211157A (en) 1960-03-14

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