Production of water-expandable styrene polymers

Details Production of water-expandable styrene polymers Production of water-expandable styrene polymers

2001-12-28

2003-04-29

Teskin, Fred (Department: 1713)

Synthetic resins or natural rubbers -- part of the class 520 ser

Synthetic resins

Polymers from only ethylenic monomers or processes of...

C526S213000, C526S214000, C526S225000, C521S056000, C521S082000, C521S146000

Reexamination Certificate

active

06555638

ABSTRACT:

DESCRIPTION
The invention relates to a process for the production of water-expandable styrene polymers (WEPS) by polymerization of styrene in aqueous suspension, the suspended styrene droplets comprising an emulsion of finely divided water.
Particulate expandable styrene polymers (EPS) are normally prepared by polymerization of styrene in aqueous suspension in the presence of a volatile organic expanding agent. Commonly used expanding agents are hydrocarbons, particularly pentane. For environmental reasons, pentane emitted during production and processing of EPS must be re-collected. This is an elaborate and cost-intensive procedure. Thus it is expedient to replace these organic substances in the long run by more acceptable expanding agents, for example water.
A dissertation of the University of Eindhoven “Water Expandable Polystyrene” by J. J. Crevecoeur dating from 1997 describes a process for the production of WEPS, in which water, finely distributed in styrene, is first of all emulsified by means of surface-active substances, after which the styrene is polymerized up to a conversion of 50%, the mixture is suspended in water with phase inversion and the styrene is finally polymerized to completion by means of peroxide initiators. The surface-active substances used are amphiphilic emulsifiers, eg sodium bis(2-ethylhexyl)sulfosuccinate or sodium styrenesulfonate or block copolymers comprising polystyrene blocks and poly(styrene sulfonate) blocks. All of these substances exhibit both a hydrophilic and a hydrophobic radical and are thus capable of emulsifying water in styrene.
In addition, Patent Applications WO 98/01489 and WO 98/01501 describe two-stage processes for the production of WEPS in which amphiphilic organic substances or water-miscible polar polymers are used as emulsifiers. Express mention is made of the fact that good results are only obtained when prepolymerization in substance is carried out in an initial step.
These processes suffer from the drawback, however, that they are carried out in a complicated manner in two stages: water is first emulsified in the styrene/polystyrene mixture and the organic phase is then suspended in water with phase inversion.
It is thus an object of the invention to provide a simpler, single-stage process for the production of WEPS.
This object is achieved in the present invention in that the emulsifying auxiliary added at the commencement of or during the suspension polymerization is an amphiphilic organic emulsifier, which carries both hydrophilic and hydrophobic groups, or a polar group-containing, water-miscible polymer, and that polymerization is carried out in aqueous suspension right from the start.
The amphiphilic emulsifiers are added in amounts of from 0.1 to 5 wt % and preferably from 0.2 to 3 wt %, based on the monomers. Suitable emulsifiers may be selected from a wide range of compounds. Preferably, the emulsifier is of the type which gives water-in-oil emulsions. The emulsifier can be a non-ionic, an anionic or a cationic surfactant.
Suitable emulsifiers include nonionic surfactants such as sorbitan carboxylates, sorbitol or mannitol carboxylates, glycol or glycerol carboxylates, alkanolamides, alkyl phenols and dialkyl ethers. Any of these emulsifiers may contain a polyalkoxy chain with 1 to 20 oxyalkylene groups, such as oxyethylene or oxypropylene moieties. Suitable anionic emulsifiers include salts of long chain (C
8
-C
30
) carboxylic acids, long chain (C
8-30
) alkyl sulphonic acid, alkylarylsulphonic acid, sulphosuccinic acid. The cation of these emulsifiers may suitably be an ammonium moiety or an alkali or alkaline earth metal ion. Suitable cationic surfactants can be selected from high-molecular-weight fatty amines, ammonium or other nitrogen derivatives of long chain carboxylic acids. The anionic and cationic emulsifiers may contain a polyoxyalkyl group. Good results have been obtained with bisalkylsulphosuccinates, sorbitol-C
8-20
-carboxylates and/or C
8-20
-alkylxylene sulphonates. Preferred are the metal salts of bis(2-ethylhexyl)-sulphosuccinic acid. Preference is given to bisalkylsulfosuccinates, sorbitol (C
6
-C
20
) carboxylates and C
8
-C
20
alkylxylene sulfonates.
The polar polymers are added in amounts of from 2 to 20 wt % and preferably from 3 to 10 wt %, based on the monomers. Suitable polymers are defined as being capable of absorbing at least 0.5 g of water per gram of dry polymer. The absorption capacity is determined according to ASTM method F 716-82. Suitable absorption capacities range from 0.5 g water/g polar polymer to more than 200 g water/g polar polymer. Although any polar polymer can be used, it is suitably selected from polyvinyl alcohol, polyvinyl acetate, polyacrylic acid, polyethylene glycols and cellulose derivatives. Polyvinylpyrrolidone (PVP) is a preferred polar polymer. This polar polymer is completely miscible with water within the temperature range of 0 to 120° C. The absorption capacity is therefore taken to be higher than 200 g water/g of dry polymer.
Another preferred class of polar polymer is constituted by starch and modified starches. The modification of starch is suitably conducted by esterification or etherification. The water absorption of starch can be increased by gelatinisation. Starch may also be modified by etherification of part of the hydroxyl groups, e.g. from 0.1 to 10%, with an alkyl group, e.g. a C
1
-C
6
alkyl group. Part of the hydroxyl groups may also be esterified. It is possible to make esters with a mono- or a dicarboxylic acid. Suitable acids include acetic, propionic and butyric acid, and malonic, maleic and succinic acid. Preferred acids are succinic acids which contain an alkyl or alkenyl substituent. The alkyl or alkenyl substituent has suitably from 1 to 16 carbon atoms. The dicarboxylic acids may be used in such amounts that from 0.1 to 10% of the hydroxyl groups are esterified. Preferably the mono-ester is formed; the remaining carboxylic group may be left acidic or be converted to a salt, e.g. an alkali metal or ammonium salt.
The polar polymer may have molecular weights which can vary within wide limits such as from 50 to 500,000,000. Suitable molecular weights (weight average molecular weight) range from 50,000 to 750,000.
Preference is given to polyvinylpyrrolidone, which at the same time acts as suspension stabilizer.
In the suspension polymerization of the invention the monomer used is preferably styrene alone. However, up to 20% of its weight can be replaced by other ethylenically unsaturated monomers, such as alkyl styrenes, divinyl benzene, acrylonitrile, 1,1-diphenylethylene or &agr;-methylstyrene.
When carrying out the suspension polymerization, conventional auxiliaries, such as suspension stabilizers, free radical initiators, flameproofing agents, chain-transfer agents, expanding agents, nucleation agents and plasticizers, can be added. It is advantageous to add, as suspension stabilizers, organic protective colloids, preferably in amounts of from 0.1 to 1 wt %, based on the monomers. Examples of suitable protective colloids are polyvinyl alcohol, hydroxyethylcellulose and polyvinylpyrrolidone. So-called pickering stabilizers, such as tricalcium orthophosphate and magnesium diphosphate are less suitable because when they are used together with major amounts of polar polymers, the suspension might coagulate. Preferred flameproofing agents are organic bromine compounds, such as hexabromocyclododecane, which are added in amounts of from 0.1 to 2 wt %, based on the monomers.
It is advantageous to carry out polymerization in the presence of from 1 to 30 wt % and preferably from 3 to 15 wt % of polystyrene, which is advantageously used in the form of a styrenic solution. Instead of pure polystyrene, polystyrene recyclate may alternatively be used.
The solid matter is preferably added at the very start of the suspension polymerization; alternatively, it can be metered in during polymerization until a conversion of 90% has been reached.
The suspension polymerization is advantageously carried out at two temperature levels, use being

Affiliated with

Also associated with

Rating

Production of water-expandable styrene polymers does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Production of water-expandable styrene polymers, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Production of water-expandable styrene polymers will most certainly appreciate the feedback.

Rate now

Comments { 0 }

Profile ID: LFUS-PAI-O-3069119