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
  • C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
• • 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
  • C08J9/0066—Use of inorganic compounding ingredients
• • 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
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L25/00—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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
  • C08L25/02—Homopolymers or copolymers of hydrocarbons
  • C08L25/04—Homopolymers or copolymers of styrene
  • C08L25/06—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
  • 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
• • 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
• • 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
  • C08J2471/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2205/00—Polymer mixtures characterised by other features
  • C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L25/00—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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
  • C08L25/02—Homopolymers or copolymers of hydrocarbons
  • C08L25/04—Homopolymers or copolymers of styrene
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L25/00—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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
  • C08L25/02—Homopolymers or copolymers of hydrocarbons
  • C08L25/04—Homopolymers or copolymers of styrene
  • C08L25/08—Copolymers of styrene
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
  • C08L71/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
  • C08L71/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
  • C08L71/12—Polyphenylene oxides

Definitions

• the present invention relates to compositions based on vinylaromatic polymers with an improved expandability.
• the present invention relates to compositions based on polystyrene, with an improved expandability.
• Vinylaromatic polymers and among these, polystyrene in particular, are known products which have been adopted for a long time for preparing compact and/or expanded articles which can be used in various applicative sectors, among which the most important are household appliances, the transport and building industries, office machines, etc.
• a particularly interesting sector is the field of thermal insulation, where vinylaromatic polymers are essentially used in expanded form.
• the expandability of vinylaromatic polymers can be improved by adding plasticizers such as rubbers or oils, to the polymer.
• plasticizers such as rubbers or oils
• Additives contained in resins effectively cause a good, immediate expansion but, as they remain englobed in the polymeric matrix, they cause the products to collapse with a consequent deterioration in the density.
• Object of the present invention is to provide an expandable composition based on vinylaromatic polymers with an improved expandability which can be processed with technologies and operating conditions analogous to those of equivalent products available on the market.
• n is zero or an integer ranging from 1 to 5 and Y is a halogen, such as chlorine or bromine, or an alkyl or alkoxyl radical having from 1 to 4 carbon atoms .
• vinylaromatic monomers having the general formula defined above are: styrene, m thylstyrene, ethyl- styrene, butylstyrene, dimethylstyrene, mono-, di-, tri-, tetra- and penta-chlorostyrene, bromo-styrene, methoxy- styrene, acetoxy-styrene, etc.
• Styrene is the preferred vinylaromatic monomer.
• the vinylaromatic monomers having general formula (I) can be used alone or in a mixture of up to 50% by weight with other copolymerizable monomers.
• these monomers are (meth) acrylic acid; C ⁇ -C 4 : alkyl esters of
• (meth) acrylic acid such as methyl acrylate, methyl- methacrylate, ethyl acrylate, ethylmethacrylate, " - isopropyl acrylate, butyl acrylate; amides and nitriles of (meth) acrylic acid such as acrylamide, methacrylamide, ac- rylonitrile, methacrylonitrile; butadiene, ethylene, divi- nylbenzene, maleic anhydride, etc.
• Preferred copolymerizable monomers are acrylonitrile and methylmethacrylate .
• the vinylaromatic polymer or copolymer which is ob- tained has a molecular weight Mw ranging from 50,000 to 170,000, preferably from 70,000 to 150,000.
• the vinylaromatic monomers are also copolymerized with an ⁇ -alkylstyrene in quantities ranging from 0.1 to 15% by weight, preferably from 2 to 10%, to give the copolymer (a) .
• the preferred ⁇ -alkylstyrene according to the present invention is ⁇ -methylstyrene, ⁇ -ethylstyrene or ⁇ - propylstyrene. ⁇ -methylstyrene is particularly preferred.
• any expanding agent capable of being englobed in the polymeric matrix can be used in a combination with the vi- nylaromatic polymers object of the present invention.
• liquid substances can be used, with a boiling point ranging from 10 to 100°C, preferably from 20 to 80°C. Typical examples are aliphatic hydrocarbons, freon, carbon dioxide, water, etc.
• the expanding agent (c) can be added to the polymeric mixture during the polymerization phase / as described below, or, alternatively, by impregnation of the beads produced at the end of the polymerization or by injection into the molten product. At the end of the addition, a.
• polymer which can be transformed to produce expanded articles with a density ranging from 5 to 50 g/1, preferably from 8 to 25 g/1, with an excellent thermal insulation capacity.
• additives capable of forming bonds both of the weak type (for example hydrogen bridges) or strong type (for example acid-base adducts) can be used with the expanding agent. Examples of these additives are methyl alcohol, isopropyl alcohol, dioctylphthalate, di- methylcarbonate, derivatives containing an amine group.
• the compatible polymer (b) with a crystallinity degree lower than 10%, preferably equal to or lower than 5%, and a Tg higher than 100°C, is preferably used in quantities ranging from 2 to 8% by weight.
• these polymers are polyphenylethers, such as polyphenyleneoxide (PPO) and polycarbonates such as polycarbonate from tetramethyl- bisphenol A.
• additives generally used with commercial materials, such as pigments, stabilizers, flame-retardant agents, mineral fillers of athermanous materials, such as graphite or carbon black, or refracting and/or reflecting agents such as titanium dioxide, antistatic agents, detaching agents, shock-resistant agents, etc., can be added to the expandable vinylaromatic polymers, object of the present invention.
• Vinylaromatic polymers with an improved expandability can alternatively comprise those consisting of: d) a matrix obtained by polymerizing one or more vinylaromatic monomers and 0.1-14.5% by weight of an ⁇ - alkylstyrene; e) 2-10% by weight, calculated with respect to the polymer (a) , of an expanding agent englobed in the polymeric matrix; f) 0-10% by weight, preferably 2-8% calculated with respect to the polymer (a) , of a compatible polymer with a crys- tallinity lower than 10% and a glass transition temperature (Tg) higher than 100°C.
• Tg glass transition temperature
• a further object of the present invention relates to the process for the preparation of mixtures with an improved expandability based on vinylaromatic polymers .
• a further object of the present invention relates to a process for preparing expandable compositions based on vinylaromatic polymers which comprises polymerizing in aqueous suspension a composition containing one or more vinylaromatic monomers, 0-50% by weight of a copolymer (a) , obtained by polymerizing one or more vinylaromatic monomers and 0.1-15% by weight of ⁇ - alkylstyrene, and 0-10% by weight of a compatible polymer (b) with a crystallinity lower than 10% and a glass transition temperature (Tg) higher than 100°C, (a) and (b) being pre-dissolved in the monomeric mixture, in the presence of an expanding agent (c) added during or after the end of the polymerization, with the proviso that at least one of (a) or (b) is present in the reagent mixture.
• substantially spherical polymer beads are obtained, with an average diameter ranging from 0.2 to 2 mm, inside which the expanding agent is homogeneously dispersed.
• polymerization additives typically used for producing vinylaromatic polymers
• polymerization catalysts and chain transfer agents through which it is also possible to regulate the molecular weight of the end-polymer, stabilizing agents of the suspension, expanding aids, nucleating agents, plasticizers, mineral fillers, etc.
• mineral fillers of athermanous materials such as graphite, or refracting agents, such as titanium dioxide, in quantities ranging from 0.05 to 25% by weight, calculated with respect to the resulting polymer.
• the expanding agents are preferably added during the polymerization phase and are selected from aliphatic or cy- cloaliphatic hydrocarbons containing from 3 to 6 carbo atoms such as n-pentane, isopentane, cyclopentane or their mixtures; the halogenated derivatives of ' aliphatic hydro- carbons containing from 1 to 3 carbon atoms such as, for example, dichlorodifluoromethane, 1, 2, 2-trifluoroethane, 1, 1, 2-trifluoroethane; carbon dioxide and water.
• the viscosity of the reagent solution by dissolving some vinylaromatic polymer therein, in a concentration ranging from 1 to 30% by weight, preferably from 5 to 20%, calculated with respect to the polymer alone.
• the solution can be obtained either by dissolving a preformed polymer (for example fresh polymer or the waste products of previous polymerizations and/or expansions) in the reagent mixture or by pre-polymerizing the monomer, or mixture of monomers, in mass, in order to obtain the above concentrations, and then continuing the polymerization in aqueous suspension in the presence of the remaining additives, in particular (b) and (c) .
• Another object of the present invention relates to a process for preparing in continuous mass, expandable mixtures based on vinylaromatic polymers, which comprises the following steps in series: i. feeding to an extruder a vinylaromatic polymer, together with 0-50% by weight of a copolymer (a) , obtained by polymerizing one or more vinylaromatic monomers and 0.1-15% by weight of an ⁇ -alkylstyrene, and 0-10% by weight of a compatible polymer (b) with a crystallinity lower than 10% and a glass transition temperature (Tg) higher than 100°C, with the proviso that at least one of (a) or (b) is present in the mixture; ii .
• a copolymer obtained by polymerizing one or more vinylaromatic monomers and 0.1-15% by weight of an ⁇ -alkylstyrene
• Tg glass transition temperature
• the beads are subjected to pre-treatment generally applied to traditional materials and which essentially consists in: 1. coating the beads with a liquid antistatic agent such as amines, tertiary ethoxylated alkylamines, ethylene ox- ide-propylene oxide copolymers, etc.
• a liquid antistatic agent such as amines, tertiary ethoxylated alkylamines, ethylene ox- ide-propylene oxide copolymers, etc.
• This agent is to facilitate both the adhesion of the coating and also the screening of the beads prepared in suspension; 2.
• said "coat- ing” essentially consists of a mixture of mono-, di- and tri-esters of glycerin (or other alcohols) with fatty acids and of metallic stearates such as zinc and/or magnesium stearate.
• the polymer obtained containing the expanding agent is extruded through the holes of a die, cut by means of knives, baked at 60°C, dried and lubricated with 0.1% by weight of magnesium stearate and 0.3% by weight of glyc- erylmonostearate .
• Example 1 is repeated, feeding 40 parts of styrene/ ⁇ - ethyl-styrene copolymer and 60 parts of the polystyrene used in Example 1. 6.2% of a mixture of n/i-pentane 80/20 is fed to the extruder as expanding agent. The copolymer contains 6.5% of
• Example 1 (comparative) Example 1 is repeated but using 98 parts of a polystyrene having an MFI of 8 (Mw of 180,000), available on the market under the trade-name of Edistir N 1782 of ENICHEM S.p.A.
• Example 1 is repeated but using only polystyrene granules (therefore 100 parts) .
• Example 4 is repeated but using only granules of polystyrene Edistir N 1782.

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• Organic Chemistry (AREA)
• Inorganic Chemistry (AREA)
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• Graft Or Block Polymers (AREA)

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