WO2017215574A1 - 自增强异型材及其制备方法和应用 - Google Patents

自增强异型材及其制备方法和应用 Download PDF

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WO2017215574A1
WO2017215574A1 PCT/CN2017/087967 CN2017087967W WO2017215574A1 WO 2017215574 A1 WO2017215574 A1 WO 2017215574A1 CN 2017087967 W CN2017087967 W CN 2017087967W WO 2017215574 A1 WO2017215574 A1 WO 2017215574A1
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reinforcing
self
reinforced
styrene
parts
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PCT/CN2017/087967
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English (en)
French (fr)
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陈平绪
叶南飚
肖鹏
李玉虎
官焕祥
魏金刚
陶四平
刘建中
何超雄
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金发科技股份有限公司
广东金发科技有限公司
天津金发新材料有限公司
四川金发科技发展有限公司
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Publication of WO2017215574A1 publication Critical patent/WO2017215574A1/zh

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions 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 a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/002Physical properties
    • C08K2201/003Additives being defined by their diameter
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/08Polymer mixtures characterised by other features containing additives to improve the compatibility between two polymers

Definitions

  • the invention relates to the technical field of plastic profiles, in particular to a self-reinforced profile material and a preparation method and application thereof.
  • PVC profiles are widely used in building doors and windows, wood-plastic flooring, furniture panels, etc.
  • PVC materials themselves have low rigidity and poor resistance to deformation
  • steel linings are required when used as door and window materials.
  • the traditional metal steel lining can effectively improve the deformation resistance of PVC profiles
  • the steel lining has the disadvantages of high production energy consumption, poor corrosion resistance, thermal insulation, poor sound insulation, high material density and low welding angle strength.
  • the installer needs to fix the steel lining and the steel profile at the construction site, and the assembly process of the door and window installation is added. Based on this situation, related companies have introduced plastic-based materials to replace traditional steel.
  • the plastic itself has the advantages of good heat insulation, corrosion resistance and light weight.
  • the unmodified plastic rigidity is too far from the steel to meet the deformation resistance requirements of the profile.
  • glass fiber reinforced means can greatly increase the rigidity of the plastic, and provides a solution for this purpose, such as CN 102817529 B, CN 203066745 U, CN 202227876 U, CN 103075071 B and the like, a glass fiber reinforced PBT is disclosed. Any one of carbon fiber reinforced PBT and modified PBT is a reinforcing strip, and a self-reinforced profile material based on PVC material is used instead of the conventional steel lining reinforcing profile.
  • Another object of the present invention is to provide a process for the preparation of the above self-reinforced profile.
  • a self-reinforcing profile comprising a PVC profile and a reinforced lining material disposed within the cavity of the PVC profile, the weight fractions of which are as follows:
  • the reinforcing lining material comprises, in parts by weight, the following components:
  • the adhesion between the PVC profile and the reinforced lining material is 400-600 N.
  • the adhesion test is carried out by injection molding a PVC profile into a 2 mm ⁇ 10 mm ⁇ 100 mm spline, and then placing the PVC spline in the same manner.
  • the 4mm ⁇ 10mm ⁇ 100mm mold was over-molded to enhance the lining material, and the adhesion between the PVC profile and the reinforced lining material was obtained. Finally, the adhesion force was tested by Zwick's tensile tester.
  • the lining material has an extrusion temperature range of 160-215 °C.
  • the styrene-based copolymer resin has a melt flow rate of from 1 g/10 min to 80 g/10 min at 220 ° C under a load of 10 kg, which is more easily extruded, preferably from 5 g/10 min to 20 g/10 min, more preferably 10 g/ 10min-15g/10min.
  • the styrene-based copolymer is selected from the group consisting of styrene-acrylonitrile copolymer, styrene-butadiene-acrylonitrile copolymer ABS, methyl methacrylate-styrene-butadiene-acrylonitrile copolymer MABS, propylene.
  • Nitrile-styrene-acrylate copolymer ASA acrylonitrile-ethylene propylene diene monomer-styrene copolymer AES, acrylonitrile-silicone rubber-styrene copolymer SAS, methyl methacrylate-styrene copolymer MS One or several of them.
  • the reinforcing agent A is selected from one or more of glass fibers, basalt fibers, talc, wollastonite, whiskers, and glass microspheres, preferably glass fibers, which have a diameter of 6-20 ⁇ m.
  • the reinforcing agent B is selected from one or more of carbon fiber, carbon nanotube, graphite, graphene or carbon black, preferably carbon fiber;
  • the reinforcing lining material of the present invention further comprises 0.5-10 parts of a compatibilizer, 0.1-5.0 parts of a coupling agent, and 0.1-5.0 parts of a processing aid in parts by weight.
  • the compatibilizer is selected from the group consisting of styrene-butadiene-acrylonitrile-maleic anhydride copolymer, styrene-butadiene-acrylonitrile-glycidyl methacrylate copolymer, styrene-acrylonitrile-Malay One or more of an acid anhydride copolymer, a styrene-acrylonitrile-glycidyl methacrylate copolymer, an acrylate resin, a methyl methacrylate-styrene copolymer resin, a styrene-maleic anhydride copolymer ;
  • the coupling agent is selected from one or more of a silane coupling agent, a titanate coupling agent, an aluminate coupling agent, and a zirconate coupling agent; the processing aid includes a lubricant or an anti- One or several of the oxygen agents.
  • the lubricant is selected from the group consisting of a fatty acid salt, a fatty acid amide, pentaerythritol stearate, a solid paraffin, a liquid paraffin, a stearate, a silicone, an N, N'-ethylene bis stearic acid amide or Several.
  • the antioxidant is tetrakis[ ⁇ -(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid] quaternary tetraol and tris[2,4-di-tert-butylphenyl]phosphite a mixture of esters.
  • the method for preparing a self-reinforced profile according to the present invention comprises the following steps:
  • reinforcing lining material In addition to the reinforcing agent A, the raw materials of the reinforcing lining material are added to the high-mixing machine according to the mixing ratio to be uniformly mixed; the above mixed material is fed into the twin-screw extruder, wherein the reinforcing agent A is added through the first vent or side feed system, melt extrusion granulation, that is, the lining material is reinforced;
  • Co-extrusion preparation is carried out by using the main machine and the auxiliary machine vertically designed by the main machine.
  • the main machine is used for extruding PVC profiles
  • the auxiliary machine is used for extrusion and reinforcing lining materials
  • the main machine and auxiliary machine are simultaneously extruded and formed.
  • Post-cooling shaping results in a self-reinforced profile.
  • the mixing temperature is 20-50 ° C, the rotation speed is 100-800 rpm, and the mixing time is 2-5 minutes; the temperature of each section of the twin-screw extruder is 200-240 ° C, double The screw extruder has a length to diameter ratio of 36-48 and a screw speed of 300-500 rpm.
  • the main machine is a twin-screw extruder, and the temperature of each section of the twin-screw extruder is 150-200 ° C;
  • the auxiliary machine is a single-screw extruder, and the temperature of each section of the single-screw extruder is 160-215 ° C.
  • the main machine is a twin-screw extruder
  • the head temperature is 175-195 ° C
  • the temperature of the fuselage one zone is 155-165 ° C
  • the temperature of the fuselage two zone is 165-175 ° C
  • the temperature of the fuselage three zones is 175-185 ° C
  • the temperature of the four fuselage of the fuselage is 175-185 ° C
  • the screw speed is 18-22 rpm
  • the auxiliary machine is a single screw extruder
  • the head temperature is 175-195 ° C
  • the temperature of the fuselage area is 160 -165 ° C
  • the fuselage two zone temperature is 160-175 ° C
  • the fuselage three zone temperature is 175-185 ° C
  • the fuselage four zone temperature is 175-185 ° C
  • the screw speed is 18-22rpm.
  • the invention also provides the use of the above self-reinforced profile in building doors and windows, wood-plastic flooring or furniture panels.
  • the present invention has the following advantages:
  • the reinforcing lining material used in the present invention is an amorphous material, and because of its better compatibility with the PVC substrate, the reinforcing lining of the self-reinforced profile material during transportation, installation and use is avoided.
  • the peeling problem of PVC substrate can be widely used in building doors and windows, wood plastic flooring or furniture panels;
  • the reinforced lining material used in the invention can be stably extruded in the temperature range of 160-215 ° C, has a wider processing window, and the extrusion molding temperature at 160 ° C is almost the same as that of the PVC material, and is solved from the root cause.
  • the decomposition and foaming, carbonization, discoloration and odor of the PVC profile due to high-temperature extrusion greatly improve the production stability of the co-extruded profile.
  • the lower molding temperature will greatly reduce energy consumption and be more environmentally friendly;
  • the reinforced lining material used in the invention has higher melt strength and more excellent processing and forming properties, thereby greatly improving the stability of molding;
  • the reinforced lining material of the invention has lower density, and the self-reinforced co-extruded profile is lighter in weight, conforming to the light weight and low carbon environmental protection trend advocated by the state;
  • the reinforced lining material of the present invention has excellent electrical conductivity and can greatly reduce the risk of lightning strikes in tall buildings during thunderstorms.
  • Figure 1 is a photograph of the adhesion of a PVC profile to a reinforced liner during the adhesion test.
  • the raw materials used are as follows:
  • ABS resin ABS AG10NP, Taiwan; melt flow rate 6g/10min;
  • PBT resin PBT 1200-211M, Changchun, Taiwan;
  • ASA styrene-acrylonitrile-acrylate copolymer ASA PW-997, Taiwan Chi Mei; melt flow rate 5g/10min;
  • the raw materials of the reinforcing lining are added to the high-mixing machine to be uniformly mixed according to the ratio of Table 1; It is fed into a twin-screw extruder in which the reinforcing agent A is fed through a first vent or side feed system, melt extrusion granulation, i.e., the inner liner is reinforced.
  • the mixing temperature is 20-50 ° C
  • the rotation speed is 100-800 rpm
  • the mixing time is 2-5 minutes
  • the temperature of each section of the twin-screw extruder is 200-240 ° C
  • the twin-screw extruder The aspect ratio is 36-48 and the screw speed is 300-500 rpm.
  • the obtained lining material was dried in a blast oven at 90 ° C for 4 hours, and then sampled with a Ningbo Haitian injection molding machine BS650-III, and the injection temperature was set to 230-240-240-250 ° C, and the obtained reinforcing lining was obtained.
  • the properties of the physical property test results of the materials are shown in Table 1.
  • the tensile strength was tested according to the ISO 527 standard.
  • the sample was a type I specimen and the test equipment was a tensile tester Z020 from Zwick, Germany.
  • the bending strength was tested according to the ISO 178 standard, the sample size was 4 mm ⁇ 10 mm ⁇ 80 mm, and the test equipment was the bending test machine Z005 of Zwick Roell, Germany.
  • the IZOD notched impact strength was tested in accordance with the ISO 180 standard, and the sample size was 4 mm ⁇ 10 mm ⁇ 80 mm, and the notch depth was 2 mm.
  • the test equipment is the impact tester HIT5.5P from Zwick Roell, Germany.
  • the density was tested according to the ISO 1183 standard, and the test equipment was a digital liquid density meter MD-300S of Japan ALFA MIRAGE.
  • the surface resistivity is tested according to the IEC60093-1980 standard.
  • the test equipment is the surface resistivity tester BDAT-A of Beijing Beiguang Jingyi Company.
  • Adhesion test PVC resin is injected into 2mm ⁇ 10mm ⁇ 100mm spline, then PVC spline is placed in 4mm ⁇ 10mm ⁇ 100mm mold to re-inject the reinforced lining material to obtain PVC profile and reinforcement. The adherent of the lining material is shown in Figure 1. Finally, Zwick's tensile tester was used to test the bond strength to characterize the bond between the reinforced liner and the PVC profile.
  • Table 1 reinforced lining each group distribution ratio (parts by weight) and physical properties
  • the reinforcing lining material of the present invention has more excellent mechanical properties in the case of the same fiber content, and in particular, the rigidity is better than that of the reinforced PBT material, and the advantage in plastic-forming steel is more obvious.
  • the reinforced lining material of the invention has lower density, and the prepared self-reinforced co-extruded profile has a lighter weight, which is in line with the nationally advocated lightweight and low carbon environmental protection trend.
  • the reinforced lining material of the present invention has excellent electrical conductivity and can greatly reduce the risk of lightning strikes in tall buildings during thunderstorms.
  • the main machine and the auxiliary machine vertically designed by the main machine are used for co-extrusion preparation.
  • the main machine is used for extruding PVC profiles
  • the auxiliary machine is used for extrusion and reinforcing lining materials
  • the main machine and auxiliary machine are simultaneously extruded. Cooling and setting to obtain a self-reinforced profile
  • the main machine is a twin-screw extruder
  • the head temperature is 175-195 ° C
  • the temperature of the fuselage one zone is 155 ° C-165 ° C
  • the temperature of the fuselage two zone is 165-175 ° C
  • the temperature of the fuselage three zones is 175-185 ° C
  • the temperature of the four fuselage is 175-185 ° C
  • the screw speed is 18 ⁇ 22 rpm
  • the auxiliary machine is a single screw extruder
  • the head temperature is 175-195 ° C
  • the temperature of the fuselage area is 160 -165 ° C
  • the fuselage two zone temperature is 160-175 ° C
  • the fuselage three zone temperature is 175-185 ° C
  • the fuselage four zone temperature is 175-185 ° C
  • the screw speed is 18-22rpm.
  • the adhesion of the reinforced PBT material to the PVC profile is only about 140N, and the reinforcing lining material of the present invention is improved in adhesion to the PVC profile to 400-600N, which is an enhanced PBT.
  • the reinforced lining material of the present invention has better compatibility with the PVC profile, and no peeling occurs during the transportation, installation and use of the profile.
  • the reinforced PBT material can be plasticized and stabilized in the temperature range of 220-250 ° C, the processing window is narrow and the processing temperature is high, and the reinforced lining material of the invention is plasticized within a wide range of 160-215 ° C.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)

Abstract

一种自增强异型材及其制备方法和应用,包括PVC型材以及设置在PVC型材型腔内的增强内衬材料,其重量份数如下:PVC型材100份,增强内衬材料5份-120份;其中,所述增强内衬材料按重量份数计,包括组分:苯乙烯基共聚物25-65份,PBT或PMMA5-30份,增强剂A20-40份,增强剂B10-25份。其制备方法是先制备增强内衬材料,然后采用主机与该主机垂直设计的辅机进行共挤,主机用于挤出PVC型材,辅机用于挤出增强内衬材料,主机、辅机同时挤出,成型后冷却定型得到自增强异型材。

Description

[根据细则37.2由ISA制定的发明名称] 自增强异型材及其制备方法和应用 技术领域
本发明涉及塑料型材技术领域,具体涉及一种自增强异型材及其制备方法和应用。
背景技术
PVC异型材广泛应用在建筑门窗,木塑地板,家具板材等方面,然而PVC材料本身刚度较低,抗变形能力差,在用作门窗材料时需加装钢衬。传统的金属钢衬虽能有效提高PVC异型材的抗变形能力,但是钢衬存在生产能耗高,耐腐蚀效果差,保温隔热,隔音效果差,材料密度大,焊角强度低的缺点,而且在型材安装时,工艺复杂,需要安装人员在施工现场将钢衬和塑钢型材固定,增加了门窗安装的装配工序。基于此种情况,相关企业推出以塑代钢的材料,取代传统钢材。塑料本身有着良好的隔热,耐腐蚀,轻量化的优点,然而未改性的塑料刚度与钢材差距太大,不能满足异型材抗变形的要求。
采用玻纤增强的手段,能大幅提高塑料的刚度,为此提供了一种解决方案,如CN 102817529 B,CN 203066745 U,CN 202227876 U,CN 103075071 B等专利公开了一种以玻纤增强PBT,碳纤增强PBT,改性PBT中的任意一种为增强条,以PVC材料为基材的自增强型材,以替代常规的钢衬增强型材。但是在这些方案中,存在以下不足之处:(1)基材PVC与增强条PBT高温共挤容易造成PVC基材的分解发泡,碳化,从而产生型材变色,气味大;(2)增强条PBT与基材PVC的界面结合力差,在型材运输,安装和使用的过程中,由于碰撞和弯曲容易导致基材PVC和增强条PBT的剥离,这样就会大大降低增强条的增强作用,大大限制了其应用。
另外,随着现在城市化进程的加速,高楼大厦的建筑越来越多,对建筑材料的防雷击要求越来越高,而常用的自增强共挤型材都属于绝缘材料,不利于雷电天气电荷的传输,在雷雨天气很容易遭受雷击,造成不可避免的破坏。
发明内容
为了克服上述现有技术的不足,本发明的目的在于提供一种自增强异型材,该自增强异型材可避免在运输,安装和使用过程中增强内衬材料与PVC型材的剥离问题,且可避免高温共挤造成PVC型材的碳化分解问题,具有优异的导电性能,可大大降低雷雨天气高层建筑被雷击的风险。
本发明的另一个目的是在于提供上述自增强异型材的制备方法。
本发明通过下述技术方案来实现:
一种自增强异型材,包括PVC型材以及设置在PVC型材型腔内的增强内衬材料,其重量份数如下:
PVC型材  100份
增强内衬材料  5份-120份
其中,所述增强内衬材料按重量份数计,包括如下组分:
苯乙烯基共聚物  25-65份;
PBT或PMMA  5-30份;
增强剂A  20-40份;
增强剂B  10-25份。
所述PVC型材与增强内衬材料的粘结力为400-600N,所述粘结力测试采用如下方法:将PVC型材注塑成2mm×10mm×100mm的样条,然后再把PVC样条放置在4mm×10mm×100mm的模具中二次注塑增强内衬材料,得到PVC型材与增强内衬材料的粘附体,最后通过Zwick公司的拉伸试验机来测试粘结力的大小。
所述增强内衬材料的挤出温度区间为160-215℃。
所述苯乙烯基共聚物树脂在220℃,10kg载荷条件下的熔体流动速率为1g/10min-80g/10min,为更易挤出成型,优选5g/10min-20g/10min,更优选为10g/10min-15g/10min。
所述苯乙烯基共聚物选自苯乙烯-丙烯腈共聚物、苯乙烯-丁二烯-丙烯腈共聚物ABS、甲基丙烯酸甲酯-苯乙烯-丁二烯-丙烯腈共聚物MABS、丙烯腈-苯乙烯-丙烯酸酯共聚物ASA、丙烯腈-三元乙丙橡胶-苯乙烯共聚物AES、丙烯腈-硅丙橡胶-苯乙烯共聚物SAS、甲基丙烯酸甲酯-苯乙烯共聚物MS中的一种或几种。
所述增强剂A选自玻璃纤维、玄武岩纤维、滑石粉、硅灰石、晶须、玻璃微珠中的一种或几种,优选玻璃纤维,所述玻璃纤维的直径为6-20μm。
所述增强剂B选自碳纤维、碳纳米管、石墨、石墨烯或炭黑中的一种或几种,优选碳纤维;
本发明所述增强内衬材料,按重量份数计,还包括相容剂0.5-10份、偶联剂0.1-5.0份、加工助剂0.1-5.0份。
所述相容剂选自苯乙烯-丁二烯-丙烯腈-马来酸酐共聚物、苯乙烯-丁二烯-丙烯腈-甲基丙烯酸缩水甘油酯共聚物、苯乙烯-丙烯腈-马来酸酐共聚物、苯乙烯-丙烯腈-甲基丙烯酸缩水甘油酯共聚物、丙烯酸酯树脂、甲基丙烯酸甲酯-苯乙烯共聚物树脂、苯乙烯-马来酸酐共聚物中的一种或几种;
所述偶联剂选自硅烷偶联剂、钛酸酯偶联剂、铝酸酯偶联剂、锆酸酯偶联剂中的一种或几种;所述加工助剂包括润滑剂或抗氧剂中的一种或几种。
所述润滑剂选自脂肪酸盐、脂肪酸酰胺、季戊四醇硬脂酸酯、固体石蜡、液体石蜡、硬脂酸盐、硅酮、N,N'-乙撑双硬脂酸酰胺中的一种或几种。
所述抗氧剂为四[β-(3,5-二叔丁基-4-羟基苯基)丙酸]季茂四醇脂和三[2,4-二叔丁基苯基]亚磷酸酯的混合物。
本发明所述的自增强异型材的制备方法,包括以下步骤:
(1)增强内衬材料的制备:除增强剂A外,按配比将增强内衬材料的各原料加入高混机中混合均匀;将上述混合物料送入双螺杆挤出机中,其中增强剂A通过第一排气孔或侧喂系统加入,熔融挤出造粒,即得增强内衬材料;
(2)共挤成型:采用主机与该主机垂直设计的辅机进行共挤制备,主机用于挤出PVC型材,辅机用于挤出增强内衬材料,主机、辅机同时挤出,成型后冷却定型得到自增强异型材。
步骤(1)中,所述混合温度为20-50℃,转速为100-800转/分钟,混合时间为2-5分钟;所述双螺杆挤出机各段温度为200-240℃,双螺杆挤出机的长径比为36-48,螺杆转速为300-500转/分钟。
步骤(2)中,所述主机为双螺杆挤出机,双螺杆挤出机各段温度为150-200℃;所述辅机为单螺杆挤出机,单螺杆挤出机各段温度为160-215℃。
优选的,所述主机为双螺杆挤出机,机头温度为175-195℃,机身一区温度为155-165℃,机身二区温度为165-175℃,机身三区温度为175-185℃,机身四区温度为175-185℃,螺杆转速为18-22rpm;所述辅机为单螺杆挤出机,机头温度为175-195℃,机身一区温度为160-165℃,机身二区温度为160-175℃,机身三区温度为175-185℃,机身四区温度为175-185℃,螺杆转速为18-22rpm。
本发明还提供了上述自增强异型材在建筑门窗、木塑地板或家具板材中的应用。
相对于现有技术,本发明具有如下优点:
(1)本发明采用的增强内衬材料为无定形材料,由于其与PVC基材具有更好的相容性,避免了自增强异型材在运输,安装和使用的过程中出现增强内衬与PVC基材的剥离问题,可广泛应用于建筑门窗、木塑地板或家具板材中;
(2)本发明采用的增强内衬材料能在160-215℃温度范围内稳定的挤出,具有更宽的加工窗口,且160℃的挤出成型温度与PVC材料相差无几,从根源解决了在共挤过程中PVC型材因高温挤出造成的分解发泡,碳化,变色,气味大问题,大大提高了共挤型材的生产稳定性, 同时较低的成型温度也会大大降低能耗,更加环保;
(3)本发明采用的增强内衬材料具有更高的熔体强度,具有更优异的加工成型性能,从而大大提高成型的稳定性;
(4)在提供同样刚性的条件下,本发明的增强内衬材料密度更低,自增强共挤型材重量更轻,符合国家提倡的轻量化,低碳环保趋势;
(5)本发明的增强内衬材料具有优异的导电性能,可大大降低雷雨天气高层建筑被雷击的风险。
附图说明:
图1为粘结力测试时,PVC型材与增强内衬的粘附体照片。
具体实施方式
为更好地理解本发明,下面通过实施例对本发明作进一步的说明,需要说明的是实施例并不构成对本发明保护范围的限制。
所用原材料如下:
PVC型材,PVC-EX23,金发科技自制;
AS苯乙烯-丙烯腈树脂,SAN PN-137H,台湾奇美,熔体流动速率12g/10min;
AS苯乙烯-丙烯腈树脂,SAN NF-5台化定制;熔体流动速率5g/10min;
AS苯乙烯-丙烯腈树脂,SAN NF2200,台化,熔体流动速率35g/10min;
ABS树脂,ABS AG10NP,台化;熔体流动速率6g/10min;
PBT树脂,PBT 1200-211M,台湾长春;
PMMA树脂,PMMA CM-205,台湾奇美;
ASA苯乙烯-丙烯腈-丙烯酸酯共聚物,ASA PW-997,台湾奇美;熔体流动速率5g/10min;
玻璃纤维,ECS13-4.5-534A,桐乡巨石,直径为13μm。
碳纳米管,Graphistrength,法国阿科玛;
碳纤维,PX35CA0250-65,日本东丽;
马来酸酐苯乙烯共聚物,SMA-700,上海华雯公司;
偶联剂,KH560,沸点化工;
润滑剂,N,N'-亚乙基双硬脂酰胺,上海宁成;
抗氧剂,168和1010,瑞士汽巴精化公司。
增强内衬材料的制备:
除增强剂A外,按表1配比将增强内衬的各原料加入高混机中混合均匀;将上述混合物料 送入双螺杆挤出机中,其中增强剂A通过第一排气孔或侧喂系统加入,熔融挤出造粒,即得增强内衬。其中,所述混合温度为20-50℃,转速为100-800转/分钟,混合时间为2-5分钟;所述双螺杆挤出机各段温度为200-240℃,双螺杆挤出机的长径比为36-48,螺杆转速为300-500转/分钟。
将得到的增强内衬材料在90℃的鼓风烘箱中干燥4小时后,用宁波海天注射成型机BS650-Ⅲ制样,注塑温度设定为230-240-240-250℃,所得增强内衬材料的物性测试结果性能见表1。
拉伸强度按ISO 527标准进行测试,试样为Ⅰ型试样,测试设备为德国Zwick公司的拉伸试验机Z020。
弯曲强度按ISO 178标准进行测试,试样尺寸为4mm×10mm×80mm,测试设备为德国Zwick Roell公司的弯曲试验机Z005。
IZOD缺口冲击强度按照ISO 180标准进行测试,试样尺寸为4mm×10mm×80mm,缺口深度为2mm。测试设备为德国Zwick Roell公司的冲击试验机HIT5.5P。
密度按ISO 1183标准进行测试,测试设备为日本ALFA MIRAGE的数显液体密度计MD-300S。
表面电阻率按IEC60093-1980标准测试,测试设备为是北京北广精仪公司的表面电阻率测试仪BDAT-A。
粘结力测试:现将PVC树脂注塑成2mm×10mm×100mm的样条,然后再把PVC样条放置在4mm×10mm×100mm的模具中二次注塑增强内衬材料,得到PVC型材与增强内衬材料的粘附体,如图1所示。最后通过Zwick公司的拉伸试验机来测试粘结力的大小,从而表征增强内衬与PVC型材的粘结性能。
表1增强内衬各组分配比(重量份)及物性
Figure PCTCN2017087967-appb-000001
Figure PCTCN2017087967-appb-000002
续表1:
Figure PCTCN2017087967-appb-000003
从表1可以看出同样纤维含量的情况下,本发明的增强内衬材料具有更加优异的力学性能,尤其是刚性更要优于增强PBT材料,在以塑代钢方面的优势更加明显。其次,在提供相同刚性的条件下,本发明的增强内衬材料密度更低,所制备的自增强共挤型材重量更轻,符合国家提倡的轻量化,低碳环保趋势。最后,本发明的增强内衬材料具有优异的导电性能,可大大降低雷雨天气高层建筑被雷击的风险。
自增强异型材的制备:
采用主机与该主机垂直设计的辅机进行共挤制备,按表2配比,主机用于挤出PVC型材,辅机用于挤出增强内衬材料,主机、辅机同时挤出,成型后冷却定型得到自增强异型材;
其中,所述主机为双螺杆挤出机,机头温度为175-195℃,机身一区温度为155℃-165℃,机身二区温度为165-175℃,机身三区温度为175-185℃,机身四区温度为175-185℃,螺杆转速为18~22rpm;所述辅机为单螺杆挤出机,机头温度为175-195℃,机身一区温度为160-165℃,机身二区温度为160-175℃,机身三区温度为175-185℃,机身四区温度为175-185℃,螺杆转速为18-22rpm。
表2自增强异型材的各组分配比及性能结果(重量份)
Figure PCTCN2017087967-appb-000004
续表2:
Figure PCTCN2017087967-appb-000005
从表2的数据可以看出,增强PBT材料与PVC型材的粘结力只有140N左右,而采用本发明的增强内衬材料,其与PVC型材的粘结力提高到400-600N,是增强PBT材料的3倍,这说明本发明的增强内衬材料与PVC型材具有更好的相容性,在型材的运输,安装和使用过程中不会出现剥离现象。其次,增强PBT材料在220-250℃的温度区间才可以塑化稳定挤出,加工窗口窄且加工温度高,而本发明的增强内衬材料在160-215℃较宽的范围之内塑化都很好,且可以稳定挤出,这说明本发明的增强内衬材料具有更宽的加工窗口,且160℃的挤出成型温度与PVC型材相差无几,从根源上避免了高温共挤造成PVC型材的分解发泡,碳化,变色,气味大等问题,同时较低的成型温度也会大大降低能耗,更加环保。

Claims (14)

  1. 一种自增强异型材,其特征在于,包括PVC型材以及设置在PVC型材型腔内的增强内衬材料,其重量份数如下:
    PVC型材      100份
    增强内衬材料 5份-120份
    其中,所述增强内衬材料按重量份数计,包括如下组分:
    苯乙烯基共聚物  25-65份;
    PBT或PMMA       5-30份;
    增强剂A         20-40份;
    增强剂B         10-25份。
  2. 根据权利要求1所述的自增强异型材,其特征在于,所述PVC型材与增强内衬材料的粘结力为400-600N,所述粘结力测试采用如下方法:将PVC型材注塑成2mm×10mm×100mm的样条,然后再把PVC样条放置在4mm×10mm×100mm的模具中二次注塑增强内衬材料,得到PVC型材与增强内衬材料的粘附体,最后通过Zwick公司的拉伸试验机来测试粘结力的大小。
  3. 根据权利要求1所述的自增强异型材,其特征在于,所述增强内衬材料的挤出温度区间为160-215℃。
  4. 根据权利要求1所述的自增强异型材,其特征在于,所述苯乙烯基共聚物在220℃,10kg载荷条件下的熔体流动速率为1g/10min-80g/10min,优选为5g/10min-20g/10min,更优选为10g/10min-15g/10min。
  5. 根据权利要求4所述的自增强异型材,其特征在于,所述苯乙烯基共聚物选自苯乙烯-丙烯腈共聚物AS、丙烯腈-丁二烯-苯乙烯共聚物ABS、甲基丙烯酸甲酯-丙烯腈-丁二烯-苯乙烯共聚物MABS、丙烯腈-苯乙烯-丙烯酸酯共聚物ASA、丙烯腈-三元乙丙橡胶-苯乙烯共聚物AES、丙烯腈-硅丙橡胶-苯乙烯共聚物SAS、甲基丙烯酸甲酯-苯乙烯共聚物MS中的一种或几种。
  6. 根据权利要求1所述的自增强异型材,其特征在于,所述增强剂A选自玻璃纤维、玄武岩纤维、滑石粉、硅灰石、晶须、玻璃微珠中的一种或几种,优选玻璃纤维。
  7. 根据权利要求6所述的自增强异型材,其特征在于,所述玻璃纤维的直径为6-20μm。
  8. 根据权利要求1所述的自增强异型材,其特征在于,所述增强剂B选自碳纤维、碳纳米管、石墨、石墨烯或炭黑中的一种或几种,优选碳纤维。
  9. 根据权利要求1所述的自增强异型材,其特征在于,按重量份数计,所述增强内衬材料 还包括相容剂0.5-10份、偶联剂0.1-5.0份、加工助剂0.1-5.0份。
  10. 根据权利要求7所述的自增强异型材,其特征在于,所述相容剂选自苯乙烯-丁二烯-丙烯腈-马来酸酐共聚物、苯乙烯-丁二烯-丙烯腈-甲基丙烯酸缩水甘油酯共聚物、苯乙烯-丙烯腈-马来酸酐共聚物、苯乙烯-丙烯腈-甲基丙烯酸缩水甘油酯共聚物、丙烯酸酯树脂、甲基丙烯酸甲酯-苯乙烯共聚物、苯乙烯-马来酸酐共聚物中的一种或几种;所述偶联剂选自硅烷偶联剂、钛酸酯偶联剂、铝酸酯偶联剂、锆酸酯偶联剂中的一种或几种;所述加工助剂包括润滑剂或抗氧剂中的一种或几种。
  11. 根据权利要求1-10任一项所述的自增强异型材的制备方法,其特征在于,包括以下步骤:
    (1)增强内衬材料的制备:除增强剂A外,按配比将增强内衬材料的各原料加入高混机中混合均匀;将上述混合物料送入双螺杆挤出机中,其中增强剂A通过第一排气孔或侧喂系统加入,熔融挤出造粒,即得增强内衬材料;
    (2)共挤成型:采用主机与该主机垂直设计的辅机进行共挤制备,主机用于挤出PVC型材,辅机用于挤出增强内衬材料,主机、辅机同时挤出,成型后冷却定型得到自增强异型材。
  12. 根据权利要求11所述的增强异型材的制备方法,其特征在于,步骤(1)中,所述混合温度为20-50℃,转速为100-800转/分钟,混合时间为2-5分钟;所述双螺杆挤出机各段温度为200-240℃,双螺杆挤出机的长径比为36-48,螺杆转速为300-500转/分钟。
  13. 根据权利要求11所述的自增强异型材的制备方法,其特征在于,步骤(2)中,所述主机为双螺杆挤出机,双螺杆挤出机各段温度为150-200℃,所述辅机为单螺杆挤出机,单螺杆挤出机各段温度为160-215℃;优选的,所述主机为双螺杆挤出机,机头温度为175-195℃,机身一区温度为155-165℃,机身二区温度为165-175℃,机身三区温度为175-185℃,机身四区温度为175-185℃,螺杆转速为18-22rpm;所述辅机为单螺杆挤出机,机头温度为175-195℃,机身一区温度为160-165℃,机身二区温度为160-175℃,机身三区温度为175-185℃,机身四区温度为175-185℃,螺杆转速为18-22rpm。
  14. 权利要求1-10任一项所述的自增强异型材在建筑门窗、木塑地板或家具板材中的应用。
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