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
  • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
  • C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
  • C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
  • C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
  • C08J9/141—Hydrocarbons
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F12/00—Homopolymers and 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
  • C08F12/02—Monomers containing only one unsaturated aliphatic radical
  • C08F12/04—Monomers containing only one unsaturated aliphatic radical containing one ring
  • C08F12/06—Hydrocarbons
  • C08F12/08—Styrene
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F2/00—Processes of polymerisation
  • C08F2/12—Polymerisation in non-solvents
  • C08F2/16—Aqueous medium
  • C08F2/18—Suspension polymerisation
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F2/00—Processes of polymerisation
  • C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
• • 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
  • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
  • C08J9/16—Making expandable particles
  • C08J9/20—Making expandable particles by suspension polymerisation in the presence of the blowing agent
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/02—Elements
  • C08K3/04—Carbon
• • 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
  • C08J2203/00—Foams characterized by the expanding agent
  • C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
• • 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
  • C08J2325/00—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 an aromatic carbocyclic ring; Derivatives of such polymers
  • C08J2325/02—Homopolymers or copolymers of hydrocarbons
  • C08J2325/04—Homopolymers or copolymers of styrene
  • C08J2325/06—Polystyrene
• • 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
  • C08J2400/00—Characterised by the use of unspecified polymers
  • C08J2400/30—Polymeric waste or recycled polymer
• • 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
  • C08J2425/00—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 an aromatic carbocyclic ring; Derivatives of such polymers
  • C08J2425/02—Homopolymers or copolymers of hydrocarbons
  • C08J2425/04—Homopolymers or copolymers of styrene
• • 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
  • C08J2425/00—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 an aromatic carbocyclic ring; Derivatives of such polymers
  • C08J2425/02—Homopolymers or copolymers of hydrocarbons
  • C08J2425/04—Homopolymers or copolymers of styrene
  • C08J2425/08—Copolymers of styrene
  • C08J2425/10—Copolymers of styrene with conjugated dienes

Definitions

• the present invention relates to a process for the preparation of expandable, low-water content, graphite- and flame retardant-containing styrene polymers by aqueous suspension polymerization.
• Flame retardant polymer foam finishing is important for a variety of applications, such as expandable polystyrene (EPS) or expanded polystyrene (XPS) expanded polystyrene foam for building insulation.
• EPS expandable polystyrene
• XPS expanded polystyrene
• halo-containing, in particular brominated, organic compounds have been used for polystyrene homopolymers and copolymers.
• HBCD hexabromocyclododecane
• Halogen-free flame retardants generally have to be used in significantly higher amounts in order to achieve the same flame retardancy of halogen-containing flame retardants. Therefore, halogen-containing flame retardants which can be used in thermoplastic polymers, such as polystyrene, often not be used in polymer foams, since they either interfere with the foaming process or affect the mechanical and thermal properties of the polymer foam. Moreover, in the production of expandable polystyrene by suspension polymerization, the high levels of flame retardant can reduce the stability of the suspension.
• WO 2007/058736 describes thermally stable, brominated butadiene-styrene copolymers as an alternative flame retardant to hexabromocyclodocecane (HBCD) in styrene polymers and extruded polystyrene foam boards (XPS).
• HBCD hexabromocyclodocecane
• WO 201 1/073141 describes flame-retardant polymer foams which have at least one halogenated polymer as flame retardant, for example brominated polystyrene or styrene-butadiene block copolymers having a bromine content in the range from 40 to 80% by weight and infrared absorbers, such as graphite, for reducing the thermal conductivity. can contain.
• halogenated polymer for example brominated polystyrene or styrene-butadiene block copolymers having a bromine content in the range from 40 to 80% by weight and infrared absorbers, such as graphite, for reducing the thermal conductivity. can contain.
• 03/033579 therefore propose, in the suspension polymerization in the presence of graphite particles, special peroxide initiators, such as tert-butyl peroxy-2-ethylhexanoate, which do not form benzoyl or benzyl radicals or use different peroxides with different decomposition temperatures and, at the beginning of the suspension polymerization, a solution of Use polystyrene in styrene.
• special peroxide initiators such as tert-butyl peroxy-2-ethylhexanoate
• WO 2007/101805 discloses a process for the preparation of expandable styrene polymers having a narrow bead size distribution by polymerization in aqueous suspension in the presence of a volatile blowing agent and 0.1 to 30 ppm, based on the organic phase of a hydroxyalkylamine. This could be processed into foams with a homogeneous cell structure.
• WO 02/055594 describes expandable polystyrene particles containing graphite or carbon black particles and, as propellant, from 2.2 to 6% by weight of pentane and from 1 to 10% by weight of water. These show a good expandability at a relatively low pentane content.
• WO 201 1/133035 describes foam moldings made of expandable polystyrene and recycled polystyrene particles from already foamed moldings.
• the foam moldings of expandable polystyrene and the recycled polystyrene particles can i.a.
• Additives such as graphite as an IR absorber and brominated polymers, in particular brominated polystyrene flame retardants included.
• Object of the present invention was to remedy the disadvantages mentioned and a process for the preparation of expandable, graphite and flame retardant-containing Styrolpo- lymerisaten low water content by polymerization in aqueous suspension to find. Due to the low water content, long and energy-intensive drying steps can be avoided.
• Expandable styrene polymers are understood as meaning blowing agents containing styrene polymers.
• Suitable styrenic polymers are homopolymers or copolymers of styrene, styrene derivatives or copolymerizable ethylenically unsaturated monomers. These are formed by suspension polymerization of styrene and the corresponding copolymerizable monomers, for example alkylstyrenes, divinylbenzene, 1, 4-butanediol dimethacrylate, para-methyl-methylstyrene, ⁇ -methylstyrene or acrylonitrile, butadiene, acrylic acid esters or methacrylic acid esters.
• the vinylaromatic monomer used is preferably styrene.
• styrene The suspension polymerization of styrene is known per se. It is described in detail in the Plastics Handbook, Volume V, "Polystyrene", Carl Hanser Verlag, 1969, pages 679 to 688. In this case, in general styrene, optionally together with the above-mentioned comonomers, suspended in water and in the presence of polymerized organic or inorganic suspension stabilizers.
• the volume ratio of water to organic phase is preferably between 0.5 and 1, 6, in particular between 1, 0 and 1, 4.
• carbon particles various natural or synthetic carbon blacks or graphites can be used.
• the carbon particles preferably contain at least 1, preferably at least 5,% by weight of graphitic structures.
• the carbon particles have an ash content, determined according to DIN 51903 of 0.005 to 15 wt .-%, preferably 0.01 to 10% by weight.
• Particular preference is given to using graphite particles having an average particle size in the range from 1 to 50 ⁇ m.
• the preferably used graphite preferably has an average particle size of from 1 to 50 ⁇ m, in particular from 2.5 to 12 ⁇ m, a bulk density of from 100 to 500 g / l and a specific surface area of from 5 to 20 m 2 / g. It can be used natural graphite or ground synthetic graphite.
• the proportion of the sum of all carbon particles is preferably in the range of 0.1 to 10 weight percent, in particular 1 to 6 weight percent, based on styrene polymer.
• Silane-modified carbon particles which are, for example, modified with silane at 0.01 to 1% by weight, preferably at 0.1 to 0.5% by weight, based on the carbon particles, can also be used as carbon particles.
• the silane-modified carbon particles preferably have on their surface C 3 -C 16 -alkylsilane or arylsilane groups, in particular C 6 -C 12 -alkylsilane groups or phenylsilane groups.
• alkyl or aryl silanes having 1 to 3 halogen atoms or methoxy groups on the silicon atom are suitable for modifying the carbon particles.
• the modification with silanes leads to a hydrophobization of the surface of the carbon particles by silyl groups, so that the interfacial activity of the carbon particles which disturbs the suspension process is markedly reduced.
• the method known per se for hydrophobicizing hydrophilic surfaces by silane in the gas phase or in solvents, such as toluene surprisingly also works in the case of relatively hydrophobic graphite in order to mask the remaining polar group.
• the surface modification of the carbon particles allows better compatibility with or even a connection to the polymer matrix.
• the usual additives for example flame retardants, nucleating agents, UV stabilizers, chain transfer agents, plasticizers, pigments and antioxidants can be added in step a).
• the usual additives for example flame retardants, nucleating agents, UV stabilizers, chain transfer agents, plasticizers, pigments and antioxidants can be added.
• the halogenated polymers are generally used in an amount in the range of 0.2 to 25 wt .-%, preferably in the range of 1 to 15 wt .-%, based on the monomers. Quantities of 5-10% by weight, based on the polymer foam, ensure sufficient flame retardancy, in particular in the case of foams made from expandable polystyrene.
• Halogen-containing or halogen-free flame retardants are preferably used as additives.
• Particularly suitable are organic, in particular aliphatic, cycloaliphatic and aromatic bromine compounds, such as hexabromocyclododecane (HBCD), Pentabrommonoch- lorcyclohexan, Pentabromphenylallylether or brominated styrenic polymers, such as styrene-butadiene block copolymers, which can be used alone or as a mixture.
• the flame retardants used are preferably exclusively brominated styrene polymers or brominated styrene-butadiene block copolymers.
• the halogenated polymer used as flame retardant preferably has an average molecular weight in the range from 5,000 to 300,000, in particular 30,000 to 150,000, determined by gel permeation chromatography (GPC).
• the halogenated polymer has a weight loss of 5 wt .-% at a temperature of 250 ° C or higher, preferably in the range of 270 to 370 ° C in the thermogravimetric analysis (TGA).
• TGA thermogravimetric analysis
• Preferred halogenated polymers as flame retardants are brominated polystyrene or styrene-butadiene block copolymer having a bromine content in the range from 40 to 80% by weight.
• the effect of the bromine-containing flame retardants can be improved by adding C-C or O-O-labile organic compounds.
• suitable flame retardant synergists are dicumyl and dicumyl peroxide.
• a preferred combination consists of 0.6 to 5 wt .-% of organic bromine compound and 0.1 to 1, 0 wt .-% of the C-C or O-O-labile organic compound.
• the blowing agents used are usually aliphatic hydrocarbons having 3 to 10, preferably 4 to 6 carbon atoms, for example n-pentane, iso-pentane or mixtures thereof.
• the blowing agent is added in the usual amounts of about 1 to 10 wt .-%, preferably 3 to 8 wt .-%, based on the weight of the present in the expandable styrene polymers styrene polymers.
• customary peroxide initiators and suspension stabilizers such as protective colloids, inorganic pickering salts and anionic and nonionic surfactants, are particularly suitable for the suspension polymerization.
• a plasticizer usually 0.1 -10% white oil or hexamole Dinch can be used to improve the expandability of the final product.
• a phosphate preferably magnesium pyrophosphate or tricalcium phosphate, in amounts of from 0.3 to 5 wt .-%, based on water, are used.
• a phosphate particularly preferably magnesium pyrophosphate or tricalcium phosphate.
• magnesium pyrophosphate particularly preferably magnesium pyrophosphate or tricalcium phosphate.
• Magnesium pyrophosphate is usually initially charged at the beginning of polymerization and generally in a concentration between 0.03 and 2.0, preferably between 0.05 and 0.5 and particularly preferably between 0.1 and 0.2 wt .-%, based on the aqueous phase used.
• the magnesium pyrophosphate is preferably prepared immediately prior to the polymerization by combining highly concentrated solutions of pyrophosphate and magnesium ions, using the stoichiometric amount of a magnesium salt required for the precipitation of Mg2P2Ü7.
• the magnesium salt may be in solid form or in aqueous solution.
• the magnesium pyrophosphate is prepared by combining aqueous solutions of sodium pyrophosphate (Na 4 P 2 O 7) and magnesium sulfate (MgSO 4 7H 2 O).
• the magnesium salt is added in at least the stoichiometrically required amount, preferably in a stoichiometric amount. For the process according to the invention, it is favorable if there is no excess of alkali pyrophosphate.
• Emulsifiers called extender used. These extenders include, for example, sodium dodecyl benzene sulfonate, long chain alkyl sulfonates, vinyl sulfonate, diisobutyl naphthalene sulfonate.
• the extenders used are preferably alkali metal salts of dodecylbenzenesulfonic acid and / or alkali metal salts of a mixture of C 12 -C 17 -alkylsulfonic acids.
• a particularly suitable mixture of C 12 -C 17 -alkyl sulfonates consists predominantly of secondary sodium alkyl sulfonates having the average chain length C 15. Such a mixture is marketed under the name Mersolat® K 30 by Bayer AG.
• the extenders increase the ability of sparingly soluble inorganic compounds to stabilize the suspension.
• the extenders are usually in amounts between 0.5 and 15, preferably 2 to
• the polymerization is initiated by customary styrene-soluble initiators, for example dibenzoyl peroxide, tert. Butyl perbenzoate, dicumyl peroxide, di-tert-butyl peroxide and mixtures thereof, preferably in amounts of from 0.05 to 1 wt .-%, based on the monomers.
• the polymerization is preferably carried out in the presence of from 0.01 to 0.5% by weight, based on the monomers, of a peroxydicarbonate. Particular preference is given to using dicetyl peroxy carbonate.
• 0.1 to 2% by weight, preferably 0.5 to 1% by weight, based on the monomers, of at least one hydroxyalkylamine are metered in during the polymerization.
• 0.1 to 30 ppm, preferably 1 to 10 ppm, based on the organic phase, of a hydroxyalkylamine are sufficient to obtain a sufficiently homogeneous foam structure and, associated therewith, a reduced thermal conductivity of up to 2 mW / mK.
• the hydroxyalkylamine can be added in the preparation of the aqueous suspension or during the heating phase, preferably before reaching a temperature of 100 ° C.
• the hydroxyalkylamine is particularly preferably metered in during the polymerization.
• hydroxyalkylamines are preferably alkyl-di (2-hydroxyethyl) amines, more preferably Ci2 / Ci4-alkyl-di (2-hydroxyethyl) amine, which is commercially available under the name Armostat® 400 Akzo, used.
• Particularly preferred method is the polymerization in the presence of
• styrene polymer containing
• the expandable styrene polymer particles obtained by the processes according to the invention can be coated with the usual coating agents, for example metal stearates, glyceryl esters and finely divided silicates.
• the propellant-containing styrene polymer particles produced according to the invention generally have a diameter between 0.2 and 4 mm. You can use standard methods, For example, with steam, foamed foam particles with a diameter between 0.1 and 2 cm and a bulk density between 5 and 100 kg / m 3 .
• the prefoamed particles can then be foamed by conventional methods to foam moldings having a density of 5 to 100 kg / m 3 .
• the foams produced from the expandable styrene polymers according to the invention are distinguished by excellent thermal insulation. This effect is particularly evident at low densities.
• the thermal conductivity is so low that it meets the requirements of the heat conductivity class 035 (according to DIN 18164), Part 1. Tab. 4, is sufficient.
• the method according to the invention has numerous advantages.
• the particle diameter of the expandable peribular styrene polymers can be controlled well and precisely.
• the blowing agent-containing expandable bead polymers have low internal water contents, high expandability and good and constant processing properties.
• Mg2P207 amorphous magnesium pyrophosphate precipitation
• Na 4 P207, Giulini Co. sodium pyrophosphate
• MgS0 4 x 7 H2O magnesium sulfate heptahydrate
• the suspension was heated to 95 ° C. within 1.5 hours and then to 131 ° C. within 4.2 hours. 1 10 minutes after reaching 80 ° C were 43.8 g of a 2% solution of the emulsifier E30 (prepared from E30-40 Fa. Leuna surfactants GmbH, mixture of Ci2-Ci7-Sodiumalkylsulfonaten) and 190 minutes after reaching 80 ° C. 222 g of pentane S (from Haltermann / Exxon) were metered in. Finally, it was polymerized at a final temperature of 131 ° C.
• E30 prepared from E30-40 Fa. Leuna surfactants GmbH, mixture of Ci2-Ci7-Sodiumalkylsulfonaten
• pentane S from Garrmann / Exxon
• the polymer obtained was decanted off and dried for 7 minutes in a stream of air at 60 ° C. for removal of the surface water and then exposed for 30 minutes at room temperature.
• a sieve cut typical for EPS between 0.8 and 1.4 mm was sieved out and coated with a coating of glycerol monostearate, glycerol tristearate and precipitated silica.
• An inner water content of 7.0% was determined on the pretreated EPS beads and the B2 flame test according to DIN 4102 was passed.
• Example 1 was repeated with the difference that the organic phase additionally contained 4.16 g of dicetyl peroxydicarbonate (Perkadox 24-FL, AkzoNobel).
• the 2% solution of the emulsifier E30 was metered in 100 minutes after reaching 80 ° C.
• the internal water content was 5.0%.
• the B2 flame test according to DIN 4102 was passed.
• Example 2 was repeated with the difference that 225 minutes after reaching 80 ° C, 43.1 g of a 2% solution of alkyl (Ci 2 -Ci 4 ) bis (2-hydroxyethyl) amine (Armostat 400, Fa. AkzoNobel) were metered into the reactor.
• the internal water content was 2.1%.
• the B2 flame test according to DIN 4102 was passed.

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• 2012
  • 2012-12-12 CN CN201280063539.0A patent/CN104011119B/zh not_active Expired - Fee Related
  • 2012-12-12 EP EP12808760.8A patent/EP2794740A2/de not_active Withdrawn
  • 2012-12-12 WO PCT/EP2012/075150 patent/WO2013092322A2/de active Application Filing
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