CN110293728A - A kind of high temperature resistant co-extrusion type foamed polystyrene composite material and preparation method - Google Patents

A kind of high temperature resistant co-extrusion type foamed polystyrene composite material and preparation method Download PDF

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Publication number
CN110293728A
CN110293728A CN201910586105.2A CN201910586105A CN110293728A CN 110293728 A CN110293728 A CN 110293728A CN 201910586105 A CN201910586105 A CN 201910586105A CN 110293728 A CN110293728 A CN 110293728A
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high temperature
temperature resistant
weight
composite material
foamed polystyrene
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CN110293728B (en
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盛岳金
赵小亮
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HUANGSHAN MEISEN NEW MATERIAL TECHNOLOGY Co Ltd
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HUANGSHAN MEISEN NEW MATERIAL TECHNOLOGY Co Ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/36Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
    • B29C48/395Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
    • B29C48/40Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/92Measuring, controlling or regulating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/065Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of foam
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/18Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/38Layered products comprising a layer of synthetic resin comprising epoxy resins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/18Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • C08G59/4215Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof cycloaliphatic
    • 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
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0061Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
    • 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
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/06Working-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 chemical blowing agent
    • C08J9/08Working-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 chemical blowing agent developing carbon dioxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • C08L63/04Epoxynovolacs
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C2948/00Indexing scheme relating to extrusion moulding
    • B29C2948/92Measuring, controlling or regulating
    • B29C2948/92504Controlled parameter
    • B29C2948/9258Velocity
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C2948/00Indexing scheme relating to extrusion moulding
    • B29C2948/92Measuring, controlling or regulating
    • B29C2948/92504Controlled parameter
    • B29C2948/92704Temperature
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2266/00Composition of foam
    • B32B2266/02Organic
    • B32B2266/0214Materials belonging to B32B27/00
    • B32B2266/0221Vinyl resin
    • B32B2266/0228Aromatic vinyl resin, e.g. styrenic (co)polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/30Properties of the layers or laminate having particular thermal properties
    • B32B2307/306Resistant to heat
    • 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
    • C08J2203/00Foams characterized by the expanding agent
    • C08J2203/02CO2-releasing, e.g. NaHCO3 and citric acid
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    • 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
    • C08J2325/00Characterised 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
    • C08J2325/02Homopolymers or copolymers of hydrocarbons
    • C08J2325/04Homopolymers or copolymers of styrene
    • C08J2325/06Polystyrene
    • 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
    • C08J2447/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds; Derivatives of such polymers
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    • C08J2459/00Characterised by the use of polyacetals containing polyoxymethylene sequences only
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
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    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • C08L2205/025Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure

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  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Laminated Bodies (AREA)

Abstract

The invention belongs to building material technical fields, and in particular to a kind of high temperature resistant co-extrusion type foamed polystyrene composite material and preparation method.Composite material of the present invention, the surface layer processed including coextrusion mold mode and sandwich layer;The surface layer mainly uses special thermohardening type high temperature resistant ingredient, including o-cresol formaldehyde epoxy resin, E-20 epoxy resin, 1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride, ceramic powder and antioxidant are made, and the film heat-resisting ability formed after heat cure is strong, can long-time high temperature resistant without change;The sandwich layer then carries out extruding pelletization molding as raw material by polystyrene, polydicyclopentadiene, acetal resin, titanium dioxide, foaming agent, coupling agent lubricant and is made.In the hot environment of 180 DEG C/6h, the surface of foamed polystyrene composite material of the present invention hardly happens variation, illustrates that product of the present invention has excellent high temperature resistance, is applicable to the more demanding field of high temperature resistant.

Description

A kind of high temperature resistant co-extrusion type foamed polystyrene composite material and preparation method
Technical field
The invention belongs to building material technical fields, and in particular to a kind of high temperature resistant co-extrusion type foamed polystyrene composite wood Material, and preparation method is further disclosed.
Background technique
Overall plastic imitated wood material is a kind of imitated wood material prepared completely by plastics, does not use any wood substance component, passes through The processing technologys such as fretting map, injection or extrusion molding are prepared that appearance is similar to timber, product of satisfactory mechanical property.With modeling Wood material is compared, and ail-plastic materials have many advantages, such as that water resistance, mildew resistance are strong, and overall plastic imitated wood material becomes the heat of Recent study Point, wherein expanded polystyrene (EPS) imitated wood material is more one of the direction of research.
Traditional foamed polystyrene Wood-like composite material, be substantially using general polystyrene arrange in pairs or groups foaming agent into Row preparation, but since the glass transition temperature of General Purpose Polystyrenre itself is lower and high temperature resistance is poor, generally on 100 DEG C of left sides Slight deformation and surfaces of tacky can occur for the right side, easily leave trace on surface when contacting 100 DEG C or more high-temperature mediums.For The high temperature resistance for improving traditional foamed polystyrene composite material, it is sub- to generally use additional such as polyamides in the prior art The mode that the heat-resisting materials such as amine, carbon fiber are blended prepares foaming imitated wood material, can improve material to a certain extent High temperature resistance substantially may be implemented the surface 150 DEG C/2h and significant change do not occur.But since each raw material component is to use Blending method carries out extrusion molding preparation again, and the low polystyrene of high temperature resistance can be partially dispersed in surface, with temperature into One step improves (such as 165 DEG C) or the time further extends (such as 150 DEG C/6h), then the surface that will lead to obtained composite material goes out It now shrinks or cracks, micro-wave oven can not be applied to, higher to temperature requirement (180 DEG C are not or not inside lining material etc. of baking oven, drying chamber Deformation occurs) field application.As it can be seen that developing a kind of high temperature resistant type foamed polystyrene composite material for extending its application Field has positive meaning.
Summary of the invention
For this purpose, compound technical problem to be solved by the present invention lies in a kind of high temperature resistant co-extrusion type foamed polystyrene is provided Material, to solve the problems, such as that foamed polystyrene composite material high temperature resistance is poor in the prior art;
Second technical problem to be solved by this invention is to provide the preparation of above-mentioned foamed polystyrene composite material Method.
In order to solve the above technical problems, a kind of high temperature resistant co-extrusion type foamed polystyrene composite material of the present invention, The composite material includes surface layer and sandwich layer through coextrusion mold;
The surface layer prepares the component that raw material includes following parts by weight:
O-cresol formaldehyde epoxy resin 20-40 parts by weight;
E-20 epoxy resin 20-35 parts by weight;
1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride 7-15 parts by weight;
Ceramic powder 5-8 parts by weight;
Antioxidant 1-3 parts by weight;
The sandwich layer prepares the component that raw material includes following parts by weight:
General Purpose Polystyrenre 30-55 parts by weight;
Polydicyclopentadiene 15-30 parts by weight;
Acetal resin 12-25 parts by weight;
Foaming agent 2-5 parts by weight;
Lubricant 1-3 parts by weight;
Compatilizer 2-5 parts by weight.
Preferably, the high temperature resistant co-extrusion type foamed polystyrene composite material, controls the original of the surface layer and sandwich layer Material mass ratio is 0.5-0.8:10.
Specifically, the compatilizer includes the polymer of acrylonitrile and methacrylic acid.
Specifically, the lubricant includes solid paraffin and/or palmitinic acid.
Specifically, the foaming agent includes sodium carbonate and/or sodium bicarbonate.
Specifically, the antioxidant includes antioxidant 1010.
The invention also discloses a kind of methods for preparing the high temperature resistant co-extrusion type foamed polystyrene imitated wood material, including Following steps:
(1) a selected amount of o-cresol formaldehyde epoxy resin, E-20 epoxy resin, 1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride, pottery are taken Porcelain powder and antioxidant are mixed and are discharged, and obtain required surface layer premix;And gained surface layer premix is added to parallel double-screw Extruding pelletization is carried out in extruder, obtains surface layer pellet, it is spare;
(2) a selected amount of polystyrene, polydicyclopentadiene, acetal resin, foaming agent, lubricant and compatible are taken Agent is mixed and is discharged, and obtains required sandwich layer premix;And by gained sandwich layer premix be added into parallel double-screw extruder into Row extruding pelletization obtains sandwich layer pellet, spare;
(3) according to selected mass ratio, the sandwich layer pellet and surface layer pellet are melted through extruder respectively, and sets respectively In in the core cavity and surface layer cavity of co-extruding mould, through melting, coextrusion mold, shaper sizing, it is cooled and shaped and fixed length Cutting, obtains required high temperature resistant co-extrusion type foamed polystyrene composite material.
Specifically, in the step (1), the mixing and the step of discharging specifically includes each raw material component in 70-80 The step of DEG C mixed, be cooled to 40 DEG C then with bottom discharge.
Specifically, in the step (2), the mixing and the step of discharging specifically includes each raw material component in 90-110 The step of DEG C mixed, be cooled to 50 DEG C then with bottom discharge.
Specifically, the barrel temperature for controlling the parallel double-screw extruder is 110-140 in the step (1) and (2) DEG C, screw speed 100-180rpm.
Specifically, in the step (3):
The melting temperature for controlling the surface layer pellet is 120-140 DEG C;
The melting temperature for controlling the sandwich layer pellet is 150-170 DEG C;
The temperature for controlling the coextrusion mold step is 170-200 DEG C.
High temperature resistant co-extrusion type foamed polystyrene imitated wood material of the present invention, the face processed including coextrusion mold mode Layer and sandwich layer;The surface layer mainly uses special thermohardening type high temperature resistant ingredient, including o-cresol formaldehyde epoxy resin, E-20 ring Oxygen resin, 1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride and fine ceramic powder are made, and cresol novolac epoxy resins have excellent high temperature resistance, Be mainly used for high-temperature electronic encapsulating material, and the adhesive property of E-20 epoxy resin is good, the two cooperation arrange in pairs or groups fine ceramic powder and Antioxidant 1010 and 1, the surface layer that 2- cyclohexane cyclohexanedimethanodibasic acid anhydride is solidified has excellent heat-resisting ability, after heat cure The surface layer film heat-resisting ability of formation is strong, can for a long time resistance to 180 DEG C of high temperature without significant change;The sandwich layer is then By General Purpose Polystyrenre, polydicyclopentadiene, acetal resin, titanium dioxide, foaming agent, coupling agent, lubricant as raw material Extruding pelletization molding is carried out to be made.Foamed polystyrene composite material of the present invention on the whole then can be continuously in 180 DEG C/6h Without any variation in hot environment, there is excellent high temperature resistance, be applicable to the more demanding field of high temperature resistant.
Specific embodiment
In the following embodiments of the present invention:
The epoxide equivalent 195-205g/eq of the o-cresol formaldehyde epoxy resin, it is limited purchased from Shandong holy well new material share The SQCN700 series of company;
The epoxide equivalent 470-530g/eq of the E-20 epoxy resin is purchased from hundred occasion insulating materials Co., Ltd, Laizhou City;
1, the 2- cyclohexane cyclohexanedimethanodibasic acid anhydride is common commercially available, purchased from Shanghai Aladdin biochemical technology limited liability company;
The ceramic powder selects superfine powder, and granularity is 800-850 mesh, is purchased from Lingshou County Bang Sheng mineral products processing factory;
The antioxidant is antioxidant 1010;
The General Purpose Polystyrenre is common commercially available, purchased from Dushanzi petrochemical industry Co., Ltd;
The polydicyclopentadiene product is purchased from Changsha special glass steel Co., Ltd;
The acetal resin is injection grade product, DuPont Corporation's product;
The polymer of compatilizer the selection acrylonitrile and methacrylic acid, No. CAS: 25749-57-9;Purchased from Jin Jin Happy (Hunan) Chemical Co., Ltd..
Embodiment 1
High temperature resistant co-extrusion type foamed polystyrene imitated wood material described in the present embodiment, including surface layer and core through coextrusion mold Layer;
The surface layer prepares the component that raw material includes following parts by weight:
O-cresol formaldehyde epoxy resin 20kg;
E-20 epoxy resin 35kg;
1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride 7kg;
Ceramic powder 8kg;
Antioxidant 1kg;
The sandwich layer prepares the component that raw material includes following parts by weight:
General Purpose Polystyrenre 30kg;
Polydicyclopentadiene 30kg;
Acetal resin 12kg;
Sodium carbonate 5kg;
Solid paraffin 1kg;
Compatilizer 5kg.
The preparation method of high temperature resistant co-extrusion type foamed polystyrene composite material, includes the following steps: described in the present embodiment
(1) a selected amount of o-cresol formaldehyde epoxy resin, E-20 epoxy resin, 1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride, pottery are taken Porcelain powder and antioxidant are mixed well in 70-80 DEG C of stirring 1h and are discharged into chilling roller, are cooled to 40 DEG C with bottom discharge, are obtained institute Need surface layer premix;Gained surface layer premix is added into double screw extruder, the machine barrel of the double screw extruder is controlled Temperature is 110 DEG C, screw speed 180rpm, carries out extruding pelletization, obtains surface layer pellet, spare;
(2) a selected amount of polystyrene, polydicyclopentadiene, acetal resin, foaming agent, lubricant and compatible are taken Agent is mixed well in 90-110 DEG C of stirring 2h and is discharged into chilling roller, is cooled to 50 DEG C with bottom discharge, is obtained required sandwich layer premix Material;And gained sandwich layer premix is added into double screw extruder, the barrel temperature for controlling the double screw extruder is 110 DEG C, screw speed 180rpm carries out extruding pelletization, obtains sandwich layer pellet, spare;
(3) the surface layer pellet and sandwich layer pellet are taken according to the ratio of mass ratio 0.5:10;
The surface layer pellet is melted in 120-140 DEG C through extruder, by the sandwich layer pellet in 150-170 DEG C through squeezing out Machine melting, and be respectively placed in the core cavity and surface layer cavity of co-extruding mould, be formed through 170 DEG C of coextrusion molds, shaper, Cooling and shaping and fixed length cutting, obtain required high temperature resistant co-extrusion type foamed polystyrene composite material.
Embodiment 2
High temperature resistant co-extrusion type foamed polystyrene imitated wood material described in the present embodiment, including surface layer and core through coextrusion mold Layer;
The surface layer prepares the component that raw material includes following parts by weight:
25 parts by weight of o-cresol formaldehyde epoxy resin;
32 parts by weight of E-20 epoxy resin;
9 parts by weight of 1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride;
7 parts by weight of ceramic powder;
2 parts by weight of antioxidant;
The sandwich layer prepares the component that raw material includes following parts by weight:
38 parts by weight of General Purpose Polystyrenre;
25 parts by weight of polydicyclopentadiene;
15 parts by weight of acetal resin;
4 parts by weight of sodium bicarbonate;
2 parts by weight of palmitinic acid;
4 parts by weight of compatilizer.
The preparation method of high temperature resistant co-extrusion type foamed polystyrene composite material, includes the following steps: described in the present embodiment
(1) a selected amount of o-cresol formaldehyde epoxy resin, E-20 epoxy resin, 1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride, pottery are taken Porcelain powder and antioxidant are mixed well in 70-80 DEG C of stirring 1h and are discharged into chilling roller, are cooled to 40 DEG C with bottom discharge, are obtained institute Need surface layer premix;Gained surface layer premix is added into double screw extruder, the machine barrel of the double screw extruder is controlled Temperature is 130 DEG C, screw speed 1500rpm, carries out extruding pelletization, obtains surface layer pellet, spare;
(2) a selected amount of polystyrene, polydicyclopentadiene, acetal resin, foaming agent, lubricant and compatible are taken Agent is mixed well in 90-110 DEG C of stirring 2h and is discharged into chilling roller, is cooled to 50 DEG C with bottom discharge, is obtained required sandwich layer premix Material;And gained sandwich layer premix is added into double screw extruder, the barrel temperature for controlling the double screw extruder is 130 DEG C, screw speed 150rpm carries out extruding pelletization, obtains sandwich layer pellet, spare;
(3) the surface layer pellet and sandwich layer pellet are taken according to the ratio of mass ratio 0.6:10;
The surface layer pellet is melted in 120-140 DEG C through extruder, by the sandwich layer pellet in 150-170 DEG C through squeezing out Machine melting, and be respectively placed in the core cavity and surface layer cavity of co-extruding mould, be formed through 180 DEG C of coextrusion molds, shaper, Cooling and shaping and fixed length cutting, obtain required high temperature resistant co-extrusion type foamed polystyrene composite material.
Embodiment 3
High temperature resistant co-extrusion type foamed polystyrene imitated wood material described in the present embodiment, including surface layer and core through coextrusion mold Layer;
The surface layer prepares the component that raw material includes following parts by weight:
O-cresol formaldehyde epoxy resin 40kg;
E-20 epoxy resin 20kg;
1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride 15kg;
Ceramic powder 5kg;
Antioxidant 3kg;
The sandwich layer prepares the component that raw material includes following parts by weight:
General Purpose Polystyrenre 55kg;
Polydicyclopentadiene 15kg;
Acetal resin 25kg;
Sodium bicarbonate 2kg;
Solid paraffin 3kg;
Compatilizer 2kg.
The preparation method of high temperature resistant co-extrusion type foamed polystyrene composite material, includes the following steps: described in the present embodiment
(1) a selected amount of o-cresol formaldehyde epoxy resin, E-20 epoxy resin, 1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride, pottery are taken Porcelain powder and antioxidant are mixed well in 70-80 DEG C of stirring 1h and are discharged into chilling roller, are cooled to 40 DEG C with bottom discharge, are obtained institute Need surface layer premix;Gained surface layer premix is added into double screw extruder, the machine barrel of the double screw extruder is controlled Temperature is 120 DEG C, screw speed 150rpm, carries out extruding pelletization, obtains surface layer pellet, spare;
(2) a selected amount of polystyrene, polydicyclopentadiene, acetal resin, foaming agent, lubricant and compatible are taken Agent is mixed well in 90-110 DEG C of stirring 2h and is discharged into chilling roller, is cooled to 50 DEG C with bottom discharge, is obtained required sandwich layer premix Material;And gained sandwich layer premix is added into double screw extruder, the barrel temperature for controlling the double screw extruder is 120 DEG C, screw speed 150rpm carries out extruding pelletization, obtains sandwich layer pellet, spare;
(3) the surface layer pellet and sandwich layer pellet are taken according to the ratio of mass ratio 0.8:10;
The surface layer pellet is melted in 120-140 DEG C through extruder, by the sandwich layer pellet in 150-170 DEG C through squeezing out Machine melting, and be respectively placed in the core cavity and surface layer cavity of co-extruding mould, be formed through 190 DEG C of coextrusion molds, shaper, Cooling and shaping and fixed length cutting, obtain required high temperature resistant co-extrusion type foamed polystyrene composite material.
Embodiment 4
High temperature resistant co-extrusion type foamed polystyrene imitated wood material described in the present embodiment, including surface layer and core through coextrusion mold Layer;
The surface layer prepares the component that raw material includes following parts by weight:
O-cresol formaldehyde epoxy resin 35kg;
25 parts by weight of E-20 epoxy resin;
13 parts by weight of 1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride;
6 parts by weight of ceramic powder;
2 parts by weight of antioxidant;
The sandwich layer prepares the component that raw material includes following parts by weight:
48 parts by weight of General Purpose Polystyrenre;
20 parts by weight of polydicyclopentadiene;
21 parts by weight of acetal resin;
3 parts by weight of sodium carbonate;
2 parts by weight of palmitinic acid;
3 parts by weight of compatilizer.
The preparation method of high temperature resistant co-extrusion type foamed polystyrene composite material is the same as embodiment 2 described in the present embodiment.
Comparative example 1
Foamed polystyrene composite material described in the present embodiment prepares raw material, with when preparation method and 2 phase of embodiment Together, difference is only that, the surface layer prepares raw material without containing the o-cresol formaldehyde epoxy resin.
Comparative example 2
Foamed polystyrene composite material described in the present embodiment prepares raw material, with when preparation method and 2 phase of embodiment Together, difference is only that, the surface layer prepares raw material without containing the E-20 epoxy resin.
Comparative example 3
Foamed polystyrene composite material described in the present embodiment prepares raw material, with when preparation method and 2 phase of embodiment Together, difference is only that, the surface layer prepares raw material without containing 1, the 2- cyclohexane cyclohexanedimethanodibasic acid anhydride.
Comparative example 4
Foamed polystyrene composite material described in the present embodiment prepares raw material, with when preparation method and 2 phase of embodiment Together, difference is only that, the surface layer prepares raw material without containing the ceramic powder.
Comparative example 5
Foamed polystyrene imitated wood material described in the present embodiment prepares raw material, with when preparation method and 2 phase of embodiment Together, difference is only that, the sandwich layer prepares raw material without containing the polydicyclopentadiene.
Comparative example 6
Foamed polystyrene imitated wood material described in the present embodiment prepares raw material, with when preparation method and 2 phase of embodiment Together, difference is only that, the sandwich layer prepares raw material without containing the acetal resin.
Comparative example 7
Composite material described in this comparative example is to be prepared according to scheme in embodiment 1 in Chinese patent CN108084625A Composite material.
Comparative example 8
The overall plastic composite material of ordinary polystyrene described in this comparative example, according to Chinese patent CN102336977B embodiment 1 Preparation.
Experimental example
The foamed polystyrene composite material prepared in above-described embodiment 1-4 and comparative example 1-8 is subjected to boiling water resistance, is resisted Tensile strength and high temperature resistance (150 DEG C/2h, 150 DEG C/6h, 165 DEG C/6h, 180 DEG C/6h, 180 DEG C/12h, 200 DEG C/6h) Test, test method and standard are detected according to the standard of GB17657-2013, and specific structure of testing see the table below 1.
1 foamed polystyrene composite property test result of table
From upper 1 data of table it is found that high temperature resistant co-extrusion type foamed polystyrene composite material of the present invention is with excellent Water boiling resistance, tensile resistance, and variation can be hardly happened on 180 DEG C/6h, the surface 180 DEG C/12h on the whole, had There is the performance used for a long time in 180 DEG C and its following high temperature, the surface of composite material can be had by being continuously heating to 200 DEG C/6h Slight influence has excellent high temperature resistance on the whole.
And lack in the surface layer formula of co-extrusion in comparative example scheme related raw material will lead to final composite material surface it is resistance to Warm nature decline is obvious, is specifically shown in comparative example 1-4.O-cresol formaldehyde epoxy resin in comparative example 1 can mention after hardening for surface layer For the performance of resistance to 200 DEG C or more excellent high temperature;E-20 epoxy resin can not only improve temperature tolerance after hardening in comparative example 2, And since its cementitiousness is outstanding, the binding force of surface layer and sandwich layer can be improved, reduce product table under the environment such as boiling, high temperature The cracking behavior in face;And 1 in comparative example 3,2- cyclohexane cyclohexanedimethanodibasic acid anhydride is the curing agent of epoxy resin, and having lacked it will lead to Surface layer can not solidify, and entire surface layer is thermoplastic film layer, and high temperature resistance is poor, easily shrink, crack at high temperature;Comparison In the surface layer film of fine ceramic powder mixing after hardening used in example 4, due to being inorganic material, high temperature resistant is outstanding, centainly Improve the high temperature resistance of surface layer in degree, but dosage is not easy excessive, the surface layer water boiling resistance performance after otherwise solidifying is poor, easily Dusting.
The foamed polystyrene composite material of existing common non-refractory is mainly polystyrene content, 150 DEG C/2h environment Middle variation less, but can not be resistant to the high temperature of longer time, such as the hot environment of 150 DEG C/6h, it may occur that obvious shrink causes Surface is destroyed, and sees comparative example 8.Comparative example 7 is to prepare high temperature resistant polystyrene by the way of addition fire resistant resin is blended Composite material improves the high temperature resistance of product compared with comparative example 8 to a certain extent, can make material 150/2h, Variation is hardly happened in 150/6h environment, but is dispersed in again since polystyrene blend will lead to part polystyrene resin Is there is obvious shrinkage phenomenon by higher temperature, can not be resistant to higher temperature requirement (>=165 in the surface of condensation material DEG C), special dimension higher for temperature requirement is not available (comparative example 7).
Obviously, the above embodiments are merely examples for clarifying the description, and does not limit the embodiments.It is right For those of ordinary skill in the art, can also make on the basis of the above description it is other it is various forms of variation or It changes.There is no necessity and possibility to exhaust all the enbodiments.And it is extended from this it is obvious variation or It changes still within the protection scope of the invention.

Claims (10)

1. a kind of high temperature resistant co-extrusion type foamed polystyrene composite material, which is characterized in that the composite material includes through co-extrusion Molding surface layer and sandwich layer;
The surface layer prepares the component that raw material includes following parts by weight:
O-cresol formaldehyde epoxy resin 20-40 parts by weight;
E-20 epoxy resin 20-35 parts by weight;
1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride 7-15 parts by weight;
Ceramic powder 5-8 parts by weight;
Antioxidant 1-3 parts by weight;
The sandwich layer prepares the component that raw material includes following parts by weight:
General Purpose Polystyrenre 30-55 parts by weight;
Polydicyclopentadiene 15-30 parts by weight;
Acetal resin 12-25 parts by weight;
Foaming agent 2-5 parts by weight;
Lubricant 1-3 parts by weight;
Compatilizer 2-5 parts by weight.
2. high temperature resistant co-extrusion type foamed polystyrene composite material according to claim 1, which is characterized in that described in control The material quality of surface layer and sandwich layer ratio is 0.5-0.8:10.
3. high temperature resistant co-extrusion type foamed polystyrene composite material according to claim 1 or 2, which is characterized in that described Compatilizer includes the polymer of acrylonitrile and methacrylic acid.
4. high temperature resistant co-extrusion type foamed polystyrene composite material according to claim 1-3, which is characterized in that The lubricant includes solid paraffin and/or palmitinic acid.
5. high temperature resistant co-extrusion type foamed polystyrene composite material according to claim 1-4, which is characterized in that The foaming agent includes sodium carbonate and/or sodium bicarbonate.
6. a kind of method for preparing any one of claim 1-5 high temperature resistant co-extrusion type foamed polystyrene composite material, It is characterized in that, includes the following steps:
(1) a selected amount of o-cresol formaldehyde epoxy resin, E-20 epoxy resin, 1,2- cyclohexane cyclohexanedimethanodibasic acid anhydride, ceramic powder are taken It mixes and discharges with antioxidant, obtain required surface layer premix;And gained surface layer premix is added to parallel double-screw and is squeezed out Extruding pelletization is carried out in machine, obtains surface layer pellet, it is spare;
(2) take a selected amount of polystyrene, polydicyclopentadiene, acetal resin, foaming agent, lubricant and compatilizer mixed It is even and discharge, obtain required sandwich layer premix;And gained sandwich layer premix is added and is squeezed into parallel double-screw extruder It is granulated out, obtains sandwich layer pellet, it is spare;
(3) according to selected mass ratio, the sandwich layer pellet and surface layer pellet are melted respectively through extruder, and are respectively placed in altogether In the core cavity and surface layer cavity of extruding mold, through melting, coextrusion mold, shaper sizing, be cooled and shaped and fixed length cutting, Obtain required high temperature resistant co-extrusion type foamed polystyrene composite material.
7. the preparation method of high temperature resistant co-extrusion type foamed polystyrene composite material according to claim 6, which is characterized in that In the step (1), the mixing and the step of discharging specifically includes and mixes each raw material component in 70-80 DEG C, then The step of 40 DEG C are cooled to bottom discharge.
8. the preparation method of high temperature resistant co-extrusion type foamed polystyrene imitated wood material, feature described according to claim 6 or 7 exist In, in the step (2), the mixing and the step of discharging specifically includes and mixes each raw material component in 90-110 DEG C, Then the step of being cooled to 50 DEG C with bottom discharge.
9. according to the preparation method of any one of the claim 6-8 high temperature resistant co-extrusion type foamed polystyrene composite material, It is characterized in that, in the step (1) and (2), the barrel temperature for controlling the parallel double-screw extruder is 110-140 DEG C, spiral shell Bar revolving speed is 100-180rpm.
10. according to the preparation method of any one of the claim 6-9 high temperature resistant co-extrusion type foamed polystyrene imitated wood material, It is characterized in that, in the step (3):
The melting temperature for controlling the surface layer pellet is 120-140 DEG C;
The melting temperature for controlling the sandwich layer pellet is 150-170 DEG C;
The temperature for controlling the coextrusion mold step is 170-200 DEG C.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111424910A (en) * 2020-03-04 2020-07-17 江苏福瑞森塑木科技股份有限公司 Three-layer co-extrusion high-elastic anti-aging plastic-wood composite material plate and preparation method thereof
CN113292797A (en) * 2021-05-25 2021-08-24 黄山美森新材料科技股份有限公司 High-strength low-thermal-expansion high-low-temperature-resistant excellent polystyrene micro-foaming material
CN114228287A (en) * 2021-12-29 2022-03-25 黄山美森新材料科技股份有限公司 Weather-proof and high-bending-resistance polystyrene foaming co-extrusion composite material and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1464839A (en) * 2000-09-22 2003-12-31 巴塞尔聚烯烃有限公司 Layered composite material comprising various pre-hardened resin layers
CN101913281A (en) * 2010-08-12 2010-12-15 淄博英科框业有限公司 Polystyrene dual-layer coextrusion section with soft surface and manufacturing method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1464839A (en) * 2000-09-22 2003-12-31 巴塞尔聚烯烃有限公司 Layered composite material comprising various pre-hardened resin layers
CN101913281A (en) * 2010-08-12 2010-12-15 淄博英科框业有限公司 Polystyrene dual-layer coextrusion section with soft surface and manufacturing method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
黄九林: "《电缆的安装与维修》", 30 September 1983, 内蒙古人民出版社 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111424910A (en) * 2020-03-04 2020-07-17 江苏福瑞森塑木科技股份有限公司 Three-layer co-extrusion high-elastic anti-aging plastic-wood composite material plate and preparation method thereof
CN113292797A (en) * 2021-05-25 2021-08-24 黄山美森新材料科技股份有限公司 High-strength low-thermal-expansion high-low-temperature-resistant excellent polystyrene micro-foaming material
CN113292797B (en) * 2021-05-25 2023-10-03 黄山美森新材料科技股份有限公司 Polystyrene micro-foaming material with high strength, low thermal expansion and high and low temperature resistance
CN114228287A (en) * 2021-12-29 2022-03-25 黄山美森新材料科技股份有限公司 Weather-proof and high-bending-resistance polystyrene foaming co-extrusion composite material and preparation method thereof
CN114228287B (en) * 2021-12-29 2023-10-03 黄山美森新材料科技股份有限公司 Weather-resistant and high-bending-resistance polystyrene foaming co-extrusion composite material and preparation method thereof

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