CN107383636A - 一种低导热系数发泡粒子及其制备方法 - Google Patents
一种低导热系数发泡粒子及其制备方法 Download PDFInfo
- Publication number
- CN107383636A CN107383636A CN201710725928.XA CN201710725928A CN107383636A CN 107383636 A CN107383636 A CN 107383636A CN 201710725928 A CN201710725928 A CN 201710725928A CN 107383636 A CN107383636 A CN 107383636A
- Authority
- CN
- China
- Prior art keywords
- particle
- preparation
- expanded
- thermal conductivity
- expanded particle
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002245 particle Substances 0.000 title claims abstract description 112
- 238000002360 preparation method Methods 0.000 title claims abstract description 21
- 238000005187 foaming Methods 0.000 claims abstract description 21
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 19
- 239000004088 foaming agent Substances 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims abstract description 17
- 239000003063 flame retardant Substances 0.000 claims abstract description 14
- 238000002156 mixing Methods 0.000 claims abstract description 8
- 238000002844 melting Methods 0.000 claims abstract description 6
- 230000008018 melting Effects 0.000 claims abstract description 6
- 238000001125 extrusion Methods 0.000 claims abstract description 3
- 238000005453 pelletization Methods 0.000 claims abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 27
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 9
- 229910002804 graphite Inorganic materials 0.000 claims description 9
- 239000010439 graphite Substances 0.000 claims description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000004711 α-olefin Substances 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 4
- 239000003963 antioxidant agent Substances 0.000 claims description 4
- 239000000975 dye Substances 0.000 claims description 4
- 229910001872 inorganic gas Inorganic materials 0.000 claims description 4
- 239000000049 pigment Substances 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 239000003112 inhibitor Substances 0.000 claims description 3
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 claims description 3
- 235000010234 sodium benzoate Nutrition 0.000 claims description 3
- 239000004299 sodium benzoate Substances 0.000 claims description 3
- 230000003078 antioxidant effect Effects 0.000 claims description 2
- 238000000465 moulding Methods 0.000 claims description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 239000012745 toughening agent Substances 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims 2
- 238000002485 combustion reaction Methods 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000003610 charcoal Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 238000007493 shaping process Methods 0.000 claims 1
- 239000004575 stone Substances 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 19
- 238000004519 manufacturing process Methods 0.000 abstract description 6
- -1 polypropylene Polymers 0.000 description 13
- 239000004743 Polypropylene Substances 0.000 description 12
- 239000002667 nucleating agent Substances 0.000 description 11
- 229920001155 polypropylene Polymers 0.000 description 11
- 239000005977 Ethylene Substances 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000002216 antistatic agent Substances 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000012757 flame retardant agent Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical compound [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 description 2
- 238000010923 batch production Methods 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000002612 dispersion medium Substances 0.000 description 2
- 229910021389 graphene Inorganic materials 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000012796 inorganic flame retardant Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- 229920005606 polypropylene copolymer Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 229920001384 propylene homopolymer Polymers 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 229910052761 rare earth metal Inorganic materials 0.000 description 2
- 150000002910 rare earth metals Chemical class 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920005674 ethylene-propylene random copolymer Polymers 0.000 description 1
- 238000010097 foam moulding Methods 0.000 description 1
- 238000013012 foaming technology Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000013518 molded foam Substances 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000012508 resin bead Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/122—Hydrogen, oxygen, CO2, nitrogen or noble gases
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/141—Hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/143—Halogen containing compounds
- C08J9/144—Halogen containing compounds containing carbon, halogen and hydrogen only
- C08J9/146—Halogen containing compounds containing carbon, halogen and hydrogen only only fluorine as halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/06—CO2, N2 or noble gases
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
- C08J2203/142—Halogenated saturated hydrocarbons, e.g. H3C-CF3
-
- 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
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/08—Copolymers of ethene
-
- 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
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/10—Homopolymers or copolymers of propene
- C08J2323/14—Copolymers of propene
-
- 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
- C08J2353/00—Characterised by the use of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/002—Physical properties
- C08K2201/003—Additives being defined by their diameter
Landscapes
- 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)
- Materials Engineering (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
本发明提供了一种低导热系数发泡粒子的制备方法,包括以下步骤:A)将聚烯烃系树脂颗粒、绝热粒子、阻燃剂、成核剂熔融混合,然后与发泡剂混合,得到混合物料;B)将所述混合物料挤出发泡,切粒,得到初级发泡粒子;C)所述初级发泡粒子经预压‑二次发泡,得到低导热系数发泡粒子。本发明在聚烯烃系树脂颗粒中添加了绝热粒子,并采用两步发泡的方法,提高了生产效率的同时降低了生产成本,制备的发泡粒子具有较低的导热系数。
Description
技术领域
本发明涉及高分子技术领域,尤其涉及一种低导热系数发泡粒子及其制备方法,以及一种发泡成型体。
背景技术
目前生产热塑性聚合物发泡珠粒常用的方法是釜压发泡法,所谓釜压发泡是指:将混合树脂颗粒、发泡剂、表面活性剂、分散剂和分散介质加入高压釜中,搅拌(搅拌速度一般为100-900转/分)下加热至比基体树脂的熔点低5-10℃的温度,保温15-60min,然后升温至发泡温度,在恒定温度下继续保温15-60min,使发泡剂浸润树脂颗粒,打开高压釜,将树脂颗粒、发泡剂、表面活性剂、分散剂和分散介质释放到比高压釜内的压力低的环境下,一般释放到大气压环境中,发泡,得到发泡颗粒。该间歇生产工艺较复杂,成本较高。
如专利CN1271125C公开了一种发泡聚丙烯树脂珠粒及其生产工艺,该工艺使用高压釜将微造粒的聚丙烯小颗粒与分散剂、表面活性剂及气体发泡剂均匀分散在液体介质中,升温至指定温度及压力下保持一定时间,然后卸压至常压得到聚丙烯发泡粒子,发泡倍率为2~90倍,然后经洗涤烘干等处理后才可用于模压制品的原料。该间歇式生产工艺较复杂,成本较高。
1994年basell推出了高熔体强度聚丙烯,并成功应用于连续聚丙烯挤出发泡工艺。目前,世界上己商品化的连续式聚丙烯的发泡技术(制备泡沫密度100kg/m3以下的聚丙烯泡沫塑料)是利用高熔体强度聚丙烯经丙烷或丁烷发泡来实现的。CN201110260389公开了一种采用高熔体强度聚丙烯与普通PP的混合物制备挤出发泡粒子的方法,得到了23-30倍的发泡粒子。
CN 101538387公开了一种挤出发泡聚丙烯珠粒的制备方法,可以得到发泡倍率为18.2倍的发泡材料。但是一次得到高倍率(>5)的发泡倍率,不仅对原材料要求较高比如采用高熔体强度聚丙烯,并且对设备要求较高,而且不易实现稳定的控制。
发明内容
有鉴于此,本发明要解决的技术问题在于提供一种低导热系数发泡粒子及其制备方法,以及一种发泡成型体,制备的发泡粒子具有较低的导热系数。
本发明提供了一种低导热系数发泡粒子的制备方法,包括以下步骤:
A)将聚烯烃系树脂颗粒、绝热粒子、阻燃剂、成核剂熔融混合,然后与发泡剂混合,得到混合物料;
B)将所述混合物料挤出发泡,切粒,得到初级发泡粒子;
C)所述初级发泡粒子经预压-二次发泡,得到低导热系数发泡粒子。
优选的,所述绝热粒子为石墨粉。
优选的,所述石墨粉为鳞片石墨、膨胀石墨、石墨烯和可膨胀石墨中的任意一种或多种。
优选的,所述石墨粉的粒径为200~1500目,碳含量为85%~99.9%。
优选的,所述初级发泡粒子的粒径为0.5~3.0mm,密度为200~900kg/m3;所述低导热系数发泡粒子的粒径为1~5mm,密度为15~200kg/m3。
优选的,所述聚烯烃系树脂颗粒、绝热粒子、阻燃剂、成核剂、发泡剂的质量比为100:(1~40):(0~20):(0.05~1):(1~60)。
优选的,所述聚烯烃系树脂颗粒为丙烯和除丙烯外的α-烯烃的共聚物,丙烯均聚物,或乙烯和除乙烯外的α-烯烃的共聚物,乙烯均聚物。
优选的,所述发泡剂为C1~6的烷烃,氢氟烃或无机气体;所述阻燃剂为卤素阻燃剂、磷-氮类阻燃剂和无机阻燃剂中的任意一种或多种;所述成核剂为无机粉末、苯甲酸钠、稠环芳烃、有机羧酸及其盐和稀土类成核剂中的任意一种或几种。
优选的,所述混合物料中还包括增韧剂、抗氧剂、防紫外线剂、抗静电剂、颜料、染料和炭黑中的任意一种或多种。
本发明提供了上述制备方法制备的发泡粒子,所述发泡粒子的导热系数为0.03~0.04w/m.k。
本发明还提供了一种发泡成型体,为上述制备方法制备的发泡粒子或上述发泡粒子经模内发泡成型制备得到。
与现有技术相比,本发明提供了一种低导热系数发泡粒子的制备方法,包括以下步骤:A)将聚烯烃系树脂颗粒、绝热粒子、阻燃剂、成核剂熔融混合,然后与发泡剂混合,得到混合物料;B)将所述混合物料挤出发泡,切粒,得到初级发泡粒子;C)所述初级发泡粒子经预压-二次发泡,得到低导热系数发泡粒子。本发明在聚烯烃系树脂颗粒中添加了绝热粒子,并采用两步发泡的方法,提高了生产效率的同时降低了生产成本,制备的发泡粒子具有较低的导热系数。
具体实施方式
本发明提供了一种低导热系数发泡粒子的制备方法,包括以下步骤:
A)将聚烯烃系树脂颗粒、绝热粒子、阻燃剂、成核剂熔融混合,然后与发泡剂混合,得到混合物料;
B)将所述混合物料挤出发泡,切粒,得到初级发泡粒子;
C)所述初级发泡粒子经预压-二次发泡,得到低导热系数发泡粒子。
本发明优选的,首先将聚烯烃系树脂颗粒、绝热粒子、阻燃剂、成核剂在挤出机中熔融混合,然后加入发泡剂,通过螺杆挤出机的剪切混合作用使各组分物料混合均匀,使发泡剂充分溶解,得到混合物料。
所述聚烯烃系树脂颗粒优选为丙烯和除丙烯外的α-烯烃的共聚物,丙烯均聚物,或乙烯和除乙烯外的α-烯烃的共聚物,乙烯均聚物。更优选为乙烯-丙烯无规共聚物,丙烯-丁烯-1无规共聚物,乙烯-丙烯-丁烯-1无规共聚物,乙烯-辛烯嵌段共聚物,乙烯-辛烯无规共聚物中的任意一种或多种。
本发明优选的,所述聚烯烃系树脂颗粒的熔融指数为6~12g/10min。
所述绝热粒子优选为石墨粉,更优选为鳞片石墨、膨胀石墨、石墨烯和可膨胀石墨中的任意一种或多种。所述石墨粉的粒径优选为200~1500目,碳含量优选为85%~99.9%。本发明优选的,所述石墨粉为活化石墨粉,本发明对所述活化方法并无特殊限定,可以为本领域技术人员熟知的方法,本发明优选采用化学或物理方法提高其分散性。所述绝热粒子的添加量优选为聚烯烃树脂的1wt%~40wt%。
上述石墨粉可以反射红外线,进而降低发泡粒子的导热系数。
所述阻燃剂优选为卤素阻燃剂、磷-氮类阻燃剂和无机阻燃剂中的任意一种或多种。
所述成核剂优选为无机粉末、苯甲酸钠、稠环芳烃、有机羧酸及其盐和稀土类成核剂中的任意一种或几种。所述无机粉末优选为硼酸锌、滑石粉、碳酸钙和氢氧化铝中的任意一种或几种;所述稠环芳烃优选为喹吖啶酮;所述有机羧酸及其盐优选为庚二酸/硬脂酸钙复合物。
所述发泡剂优选为C1~6的烷烃,氢氟烃(HFCs)或无机气体。所述C1~6的烷烃优选为丁烷、戊烷或己烷;所述氢氟烃优选为R134a,R152,R410a,R125中的一种或多种;所述无机气体优选为CO2,N2和空气中的一种或几种的混合气体。
所述聚烯烃系树脂颗粒、绝热粒子、阻燃剂、成核剂、发泡剂的质量比优选为100:(1~40):(0~20):(0.05~1):(1~60)。
本发明优选的,所述混合物料中还包括增韧剂、抗氧剂、防紫外线剂、抗静电剂、颜料、染料和炭黑中的任意一种或多种。
上述增韧剂、抗氧剂、防紫外线剂、抗静电剂、颜料、染料和炭黑的总量优选为聚烯烃系树脂颗粒的0.1wt%~30wt%。
本发明优选的,所述混合在挤出机中进行,本发明对所述挤出机并无特殊限定,可以为本领域技术人员熟知的挤出机,本发明优选为双螺杆挤出机,单螺杆挤出机,双螺杆-串联双螺杆挤出机,双螺杆串联单螺杆挤出机,单螺杆挤出机串联双螺杆挤出机,单螺杆串联单螺杆挤出机。优选的,所述挤出机后面添加静态混合器,动态混合器提高其冷却能力;优选的,所述挤出机模头前面增加熔体泵提高熔体压力。
然后将得到的混合物料冷却后,通过多孔模头挤出发泡,并用水下切粒机将挤出的熔体切粒,得到初级发泡粒子。
得到的初级发泡粒子的粒径为0.5~3.0mm,密度为200~900kg/m3。其发泡倍率低于5倍。
本发明优选的,将切好的初级发泡粒子经过脱水烘干筛分,备用。
最后将筛分好的初级发泡粒子,经过预压-二次发泡,即可得到所述低导热系数发泡粒子。
具体的,将初级发泡粒子加入到耐压容器内,分步通入如上所述的发泡剂气体或者空气,并保持一段时间,使初级发泡粒子内部存在内压力,将存在内压力的初级发泡粒子加入到预发机内进行发泡获得高倍率的次级发泡粒子,即所述低导热系数发泡粒子。
本发明优选的,所述预压的压力为1-8kg,预压时间为8-20小时。
得到的低导热系数发泡粒子的粒径为1~5mm,密度为15~200kg/m3。其发泡倍率为5-60倍。
本发明还提供了上述制备方法制备的发泡粒子,其导热系数为0.03~0.04w/m.k。
本发明还提供了一种发泡成型体,首先采用上述制备方法制备发泡粒子,或直接以上述发泡粒子为原料,经模内发泡成型制备得到。所述发泡成型体具有较低的导热系数。
为了进一步说明本发明,下面结合实施例对本发明提供的低导热系数发泡粒子及其制备方法进行详细描述。
实施例1~5
聚烯烃系树脂以100重量份计,绝热粒子以及发泡剂的种类与份数如表1所示,阻燃剂为0份,成核剂二氧化硅0.5份。
向挤出机中加入上述聚烯烃系树脂混合物以及发泡剂,充分熔融混合冷却通过多孔模头挤出发泡,水下切粒获得发泡倍率不同的初级发泡粒子,测定初级发泡粒子的表观密度,结果如表1所示。获得的初级发泡粒子经预压-二次发泡获得二次发泡粒子,测定其表观密度如表1所示,对获得的二次发泡粒子经过成型获得发泡粒子成型体并测得其导热系数如表1所示。
比较例1~3
采用与实施例1~5相同的方法与步骤,仅仅在配方中不添加石墨粉,获得的初级粒子以及二次发泡粒子的表观密度以及成型体的导热系数结果如表1所示。
表1实施例1~5及比较例1~3的配比及检测结果
由上述实施例及比较例可知,本发明在制备发泡粒子的过程中,添加了石墨粉,并采用两步发泡的方法,降低了发泡粒子的导热系数。
以上实施例的说明只是用于帮助理解本发明的方法及其核心思想。应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以对本发明进行若干改进和修饰,这些改进和修饰也落入本发明权利要求的保护范围内。
Claims (10)
1.一种低导热系数发泡粒子的制备方法,其特征在于,包括以下步骤:
A)将聚烯烃系树脂颗粒、绝热粒子、阻燃剂、成核剂熔融混合,然后与发泡剂混合,得到混合物料;
B)将所述混合物料挤出发泡,切粒,得到初级发泡粒子;
C)所述初级发泡粒子经预压-二次发泡,得到低导热系数发泡粒子。
2.根据权利要求1所述的制备方法,其特征在于,所述绝热粒子为石墨粉。
3.根据权利要求2所述的制备方法,其特征在于,所述石墨粉为鳞片石墨、膨胀石墨、石墨烯和可膨胀石墨中的任意一种或多种。
4.根据权利要求2所述的制备方法,其特征在于,所述石墨粉的粒径为200~1500目,碳含量为85%~99.9%。
5.根据权利要求1所述的制备方法,其特征在于,所述初级发泡粒子的粒径为0.5~3.0mm,密度为200~900kg/m3;所述低导热系数发泡粒子的粒径为1~5mm,密度为15~200kg/m3。
6.根据权利要求1所述的制备方法,其特征在于,所述聚烯烃系树脂颗粒、绝热粒子、阻燃剂、成核剂、发泡剂的质量比为100:(1~40):(0~20):(0.05~1):(1~60)。
7.根据权利要求1所述的制备方法,其特征在于,所述聚烯烃系树脂颗粒为丙烯和除丙烯外的α-烯烃的共聚物,丙烯均聚物,或乙烯和除乙烯外的α-烯烃的共聚物,乙烯均聚物。
8.根据权利要求1所述的制备方法,其特征在于,所述发泡剂为C1~6的烷烃,氢氟烃或无机气体;所述阻燃剂为卤素阻燃剂、磷-氮类阻燃剂和无机阻燃剂中的任意一种或多种;所述成核剂为无机粉末、苯甲酸钠、稠环芳烃、有机羧酸及其盐和稀土类成核剂中的任意一种或几种;所述混合物料中还包括增韧剂、抗氧剂、防紫外线剂、抗静电剂、颜料、染料和炭黑中的任意一种或多种。
9.权利要求1~8任一项所述的制备方法制备的发泡粒子,其特征在于,所述发泡粒子的导热系数为0.03~0.04w/m.k。
10.一种发泡成型体,为权利要求1~8任一项所述的制备方法制备的发泡粒子或权利要求9所述的发泡粒子经模内发泡成型制备得到。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710725928.XA CN107383636B (zh) | 2017-08-22 | 2017-08-22 | 一种低导热系数发泡粒子及其制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710725928.XA CN107383636B (zh) | 2017-08-22 | 2017-08-22 | 一种低导热系数发泡粒子及其制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN107383636A true CN107383636A (zh) | 2017-11-24 |
CN107383636B CN107383636B (zh) | 2021-03-19 |
Family
ID=60353859
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710725928.XA Active CN107383636B (zh) | 2017-08-22 | 2017-08-22 | 一种低导热系数发泡粒子及其制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN107383636B (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109762201A (zh) * | 2018-11-27 | 2019-05-17 | 浙江众创材料科技有限公司 | 一种阻燃低导热的发泡聚丙烯及其制备方法 |
CN109836700A (zh) * | 2018-11-27 | 2019-06-04 | 浙江众创材料科技有限公司 | 一种阻燃低导热发泡聚丙烯的制备方法及发泡聚丙烯 |
CN110181741A (zh) * | 2019-06-05 | 2019-08-30 | 浙江众创材料科技有限公司 | 发泡聚烯烃珠粒的制备方法、发泡聚烯烃板材及其应用 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103443176A (zh) * | 2011-03-08 | 2013-12-11 | 株式会社钟化 | 聚乙烯系树脂发泡颗粒、聚乙烯系树脂模内发泡成形体、及聚乙烯系树脂发泡颗粒的制造方法 |
CN104231461A (zh) * | 2014-09-28 | 2014-12-24 | 南京法宁格节能科技有限公司 | 石墨eps珠粒及其生产工艺 |
CN104987526A (zh) * | 2015-04-27 | 2015-10-21 | 中国科学院长春应用化学研究所 | 聚丙烯系树脂复合发泡颗粒及其制备方法与应用 |
-
2017
- 2017-08-22 CN CN201710725928.XA patent/CN107383636B/zh active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103443176A (zh) * | 2011-03-08 | 2013-12-11 | 株式会社钟化 | 聚乙烯系树脂发泡颗粒、聚乙烯系树脂模内发泡成形体、及聚乙烯系树脂发泡颗粒的制造方法 |
CN104231461A (zh) * | 2014-09-28 | 2014-12-24 | 南京法宁格节能科技有限公司 | 石墨eps珠粒及其生产工艺 |
CN104987526A (zh) * | 2015-04-27 | 2015-10-21 | 中国科学院长春应用化学研究所 | 聚丙烯系树脂复合发泡颗粒及其制备方法与应用 |
Non-Patent Citations (4)
Title |
---|
丁浩: "《塑料工业实用手册 上册》", 31 May 1995, 化学工业出版社 * |
刘际泽: "《塑料制品与模具设计题案》", 30 June 2001, 中国轻工业出版社 * |
周其凤: "《高分子化学》", 31 October 2001, 化学工业出版社 * |
方少明: "《高分子材料成型工程》", 30 June 2014, 中国轻工业出版社 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109762201A (zh) * | 2018-11-27 | 2019-05-17 | 浙江众创材料科技有限公司 | 一种阻燃低导热的发泡聚丙烯及其制备方法 |
CN109836700A (zh) * | 2018-11-27 | 2019-06-04 | 浙江众创材料科技有限公司 | 一种阻燃低导热发泡聚丙烯的制备方法及发泡聚丙烯 |
CN110181741A (zh) * | 2019-06-05 | 2019-08-30 | 浙江众创材料科技有限公司 | 发泡聚烯烃珠粒的制备方法、发泡聚烯烃板材及其应用 |
Also Published As
Publication number | Publication date |
---|---|
CN107383636B (zh) | 2021-03-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111234373B (zh) | 一种无卤阻燃聚丙烯泡沫材料的制备方法 | |
CN102295807B (zh) | 挤出发泡聚丙烯珠粒及其制备方法 | |
CN102015851B (zh) | 具有提高隔热能力的可发泡乙烯基芳族聚合物的组合物、它们的制备方法和由其得到的发泡制品 | |
CN111253677B (zh) | 一种低密度聚丙烯珠粒泡沫、其制备方法及应用 | |
CN101538387A (zh) | 聚丙烯发泡材料及其生产方法 | |
CA2756693C (en) | Polymeric foam containing alumina boehmite | |
CN107674234B (zh) | 聚丙烯系树脂发泡粒子的制备方法 | |
CN101868496A (zh) | 防火的可发性苯乙烯聚合物及其制备方法 | |
CN110183713B (zh) | 一种聚丁烯发泡珠粒(epb)的制备方法 | |
CN107383636A (zh) | 一种低导热系数发泡粒子及其制备方法 | |
CN112940468B (zh) | 一种聚乳酸基发泡粒子及其制备方法 | |
CN103665583A (zh) | 丙烯乙烯高熔体强度聚丙烯发泡珠粒及其制备方法 | |
CN102391571A (zh) | 具有较低热成型压力的挤出发泡聚丙烯珠粒及其制备方法 | |
CN110105677A (zh) | 基于回收塑料的聚丙烯发泡材料及其制备方法 | |
CN110606975A (zh) | 一种高强度抗回缩微孔聚乙烯发泡珠粒(epe)的方法 | |
CN101613488A (zh) | 一种聚丙烯及其共混物粒子物理气体发泡的制备方法 | |
CN104877162B (zh) | 原位微纤化聚丙烯系树脂复合发泡颗粒及其应用 | |
CN112980098A (zh) | 一种高回弹、防静电的聚烯烃吸油泡沫及其制备方法 | |
CN106633451A (zh) | 采用co2组合发泡剂挤出聚苯乙烯发泡材料的制备方法 | |
CN107353489B (zh) | 一种聚烯烃树脂发泡材料及其制备方法 | |
JP5670816B2 (ja) | ポリオレフィン系樹脂発泡粒子の製造方法 | |
CN115895117A (zh) | 一种抗菌发泡聚丙烯珠粒及其制备方法 | |
CN104140589B (zh) | 一种聚丙烯发泡粒子及其制备方法 | |
CN113563670A (zh) | 一种高熔体强度聚丁烯珠粒及其制备方法和应用 | |
JP7194535B2 (ja) | 発泡性ポリスチレン系樹脂粒子、ポリスチレン系樹脂予備発泡粒子、およびポリスチレン系樹脂発泡成形体 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |