CN107857978A - 抗静电可生物降解泡沫材料及其制备方法 - Google Patents
抗静电可生物降解泡沫材料及其制备方法 Download PDFInfo
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Abstract
本发明涉及一种抗静电可生物降解泡沫材料及其制备方法,属于泡沫材料技术领域。解决了现有技术中改善聚对苯二甲酸‑己二酸丁二醇酯发泡材料抗静电性能的方法需要添加很大比例的抗静电剂,引起材料力学性能下降的问题。本发明的抗静电可生物降解泡沫材料,由60‑100重量份聚己二酸‑对苯二甲酸丁二醇酯、0‑40重量份可生物降解聚合物、1‑15重量份抗静电剂、1‑5重量份无机填料、0.5‑15重量份发泡剂、0.01‑5重量份助发泡剂和0.1‑5重量份交联剂组成。该泡沫材料具备抗静电性能优异、物理性能优异、耐水性好、耐久性好、发泡倍率较高的优点,且可以在很宽的范围内调控力学性能。
Description
技术领域
本发明涉及一种抗静电可生物降解泡沫材料及其制备方法,属于泡沫材料技术领域。
背景技术
不论是以聚乙烯、聚苯乙烯,还是以聚氨酯为原料制得的泡沫塑料都具有质轻、省料、热导率低、隔热性能好、吸收冲击载荷、隔音性能好、比强度高等性能,在包装行业发挥着巨大的作用。然而,这些泡沫塑料被使用后,很难回收处理再次循环使用,丢弃到环境中,不能与环境同化,对环境造成巨大危害。如漂浮在海洋中被海洋生物吞服,致使海洋生物死亡。因此,大力开发和推广可降解泡沫材料受到世界范围的学术界和工业界的关注。
聚对苯二甲酸-己二酸丁二醇酯是对苯二甲酸、己二酸和1,4-丁二醇的三元共聚酯,属完全生物降解塑料。由于聚对苯二甲酸-己二酸丁二醇酯中含柔性的脂肪链和刚性的芳香键,因而具有高韧性和耐高温性,将其制备成发泡材料后,可以有效解决传统发泡材料带来的污染问题。
但是将聚对苯二甲酸-己二酸丁二醇酯制成发泡材料后,由于材料本身具有良好的电绝缘性,使得发泡材料也具有良好的电绝缘性,在成型加工或使用时,因摩擦而带静电。静电往往能吸附尘埃,从而影响产品的表观质量,在一些特殊环境中使用时,甚至会因放电而招致爆炸或燃烧事故。近年来,随着我国电子行业的迅速发展,对于一些敏感的电子元件、芯片、仪器仪表等电子产品对包装材料的要求非常严格,如果采用了非抗静电包装材料,材料会因电磁感应和摩擦产生静电积累而进行高压放电,进而破坏包装内容物的电子产品,造成极大地经济损失。要获得较好的抗静电效果,往往要在聚合物中添加导电填料,或是添加抗静电剂,利用在高聚物中形成导电通道起到抗静电的作用。但是对于单一聚合物而言,要获得较好的抗静电效果,往往要添加很大比例的抗静电剂,引起材料力学性能下降。引入另一聚合物组分,由于两相界面的存在,抗静电剂可以优先分散在一相或是界面处,可以大大减少抗静电剂的用量,提高材料的力学性能。
发明内容
本发明的目的是解决现有技术中改善聚对苯二甲酸-己二酸丁二醇酯发泡材料性能的方法需要添加很大比例的抗静电剂,引起材料力学性能下降的问题。
本发明的抗静电可生物降解泡沫材料,组成及重量份为:
所述可降解聚合物为聚乳酸、二氧化碳-环氧丙烷共聚物、聚丁二酸丁二醇酯中的一种或多种按任意比例的混合。
优选的是,所述抗静电剂为导电炭黑、碳纳米管、石墨烯、非离子型抗静电剂和阳离子型抗静电剂中的一种或多种按任意比例的混合。
优选的是,所述发泡剂为偶氮二甲酰胺、偶氮二甲酸钡、偶氮二甲酸二异丙酯、N,N-二亚硝基五次甲基四胺、4,4’-氧代双苯磺酰肼中的一种或多种按任意比例的混合。
优选的是,所述无机填料为二氧化硅、滑石粉、碳酸钙、蒙脱土中的一种或多种按任意比例的混合。
优选的是,所述助发泡剂为氧化锌、硬脂酸锌、硬脂酸钙中的一种或多种按任意比例的混合。
优选的是,所述交联剂为三烯丙基异氰脲酸酯、三羟甲基丙烷三丙烯酸酯、三羟甲基丙烷三甲基丙烯酸酯中的一种或多种按任意比例的混合,或者为乙烯基三甲基硅烷、乙烯基三乙氧基硅烷、乙烯基三(β-甲氧基乙氧基)硅烷中的一种或多种按任意比例的混合。
上述抗静电可生物降解泡沫材料的制备方法,步骤如下:
步骤一、按组成及重量份称取各原料,加入挤出机中进行混炼造粒,混炼造粒温度为80-170℃,得到的混炼造粒料在片材挤出机上挤出片材,片材厚度为0.5-3.0mm,挤出温度为100-170℃;
步骤二、室温下空气中,对共混物片材进行电离辐照,辐照剂量为2-100KGy,得到交联物料;
或者,室温下空气中,对步骤一得到的片材进行电离辐照,辐照剂量为0.5-9KGy,得到预交联物料;将预交联物料,在50-80℃的热水浴中进一步交联2-48h,得到交联物料;
步骤三、将交联物料进行发泡,温度为190-250℃,时间为1-20min,得到可生物降解聚己二酸-对苯二甲酸丁二醇酯泡沫材料。
优选的是,混炼造粒在双螺杆挤出机中完成,挤出片材的设备为单螺杆片材挤出机。
优选的是,电离辐射源为60Co源或电子加速器。
优选的是,交联物料在立式发泡炉或水平发泡炉中进行发泡。
与现有技术相比,本发明的有益效果:
本发明的抗静电可生物降解泡沫材料具有抗静电性能优异、物理性能优异、耐水性好、耐久性好、发泡倍率较高等优点,且通过与其他生物可降解高分子,如聚乳酸、二氧化碳-环氧丙烷共聚物、聚丁二酸丁二醇酯等进行共混发泡,可以有效减少添加的抗静电剂含量,使其可以应用于电子领域等的包装,还可以提高发泡材料的力学性能,并可以在很宽的范围内调控发泡材料的力学性能,如压缩强度,压缩模量,使其可以满足更多的应用领域,经试验检测,本发明的泡沫材料的表观密度为50-500Kg/m3,表面电阻率为2.6×1055.10×106Ω,断裂伸长率为100-450%,压缩强度为0.50-1.57MPa。
本发明的抗静电可生物降解泡沫材料的制备方法可采用含有乙烯基的硅烷作为交联剂,实现在低辐射剂量下对聚己二酸-对苯二甲酸丁二醇酯及其共混物进行辐照交联,降低辐射加工成本,同时,在分子链间引入硅氧化学键后可以加快这些生物降解发泡材料的生物降解速率;
本发明的抗静电可生物降解泡沫材料的制备方法可采用辐照交联和水热交联结合,保证材料满足发泡的需要,制得物理性能优异、耐水性好、耐久性好、发泡倍率较高的泡沫塑料,且进一步降低辐射剂量;
本发明的抗静电可生物降解泡沫材料的制备方法采用常温下辐照交联,操作简单。
具体实施方式
为了进一步了解本发明,下面结合具体实施方式对本发明的优选实施方案进行描述,但是应当理解,这些描述只是为了进一步说明本发明的特正和优点而不是对本发明权利要求的限制。
本发明的抗静电可生物降解泡沫材料,由60-100重量份聚己二酸-对苯二甲酸丁二醇酯、0-40重量份可生物降解聚合物、1-15重量份的抗静电剂,0.5-15重量份发泡剂、1-5重量份无机填料、0.01-5重量份助发泡剂和0.1-5重量份交联剂组成。
其中,聚己二酸-对苯二甲酸丁二醇酯重量份优选为65-80,更优选为70-75。可生物降解聚合物为聚乳酸、二氧化碳-环氧丙烷共聚物、聚丁二酸丁二醇酯中的一种或多种按任意比例的混合,重量份优选为10-35,更优选为15-30,尤其优选为18-25。抗静电剂为导电炭黑、碳纳米管、石墨烯、非离子型抗静电剂、阳离子型抗静电剂中一种或多种按任意比例的混合,重量份优选为3-12,更优选为5-10,尤其优选为6-8。无机填料为二氧化硅、滑石粉、碳酸钙、蒙脱土中的一种或多种按任意比例的混合,重量份优选为2-4,更优选为3-3.5。发泡剂为偶氮二甲酰胺、偶氮二甲酸钡、偶氮二甲酸二异丙酯、N,N-二亚硝基五次甲基四胺、4,4’-氧代双苯磺酰肼中的一种或多种按任意比例的混合,重量份优选为5-13,更优选为8-12,尤其优选为9-10。助发泡剂为氧化锌、硬脂酸锌、硬脂酸钙中的一种或多种按任意比例的混合,重量份优选为1-4,更优选为2-3.5,尤其优选为2.5-3。交联剂为乙烯基三甲基硅烷、乙烯基三乙氧基硅烷、乙烯基三(β-甲氧基乙氧基)硅烷中的一种或多种按任意比例的混合,重量份优选为2-4,更优选为3-3.5。
本发明的抗静电可生物降解泡沫材料的制备方法,步骤如下:
步骤一、按组成及重量份称取各原料,加入双螺杆挤出机中进行混炼造粒,混炼造粒温度为80-170℃,得到的混炼造粒料在单螺杆片材挤出机上挤出片材,片材厚度为0.5-3.0mm,优选1mm,挤出温度为100-170℃;
步骤二、室温下空气中,使用电子加速器或钴(60Co)源电离辐射对共混物片材进行电离辐照,辐照剂量为2-100KGy,优选为80-90KGy,得到交联物料;
或者,室温下空气中,对步骤一得到的片材进行电离辐照,辐照剂量为0.5-9KGy,得到预交联物料;将预交联物料,在50-80℃的热水浴中进一步交联2-48h,得到交联物料;
步骤三、将交联物料在立式或水平发泡炉进行发泡,温度为190-250℃,时间为1-20min,优选温度为210-240℃,时间为4-8min,得到抗静电可生物降解泡沫材料。
以下将通过实施例进一步详细的说明本发明。但是,本发明并不局限于这些例子。
实施例1
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯100重量份、导电炭黑15重量份、偶氮二甲酰胺5重量份、碳酸钙5重量份、氧化锌1重量份、三烯丙基异氰脲酸酯0.5重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用电子加速器,在室温下空气中对片材进行辐照,辐照剂量为100KGy。在立式发泡炉中发泡,发泡温度为220℃,发泡时间为4min。
对实施例1得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例2
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯70重量份、聚乳酸30重量份、导电炭黑7重量份、偶氮二甲酰胺5重量份、碳酸钙5重量份、氧化锌1重量份和三烯丙基异氰脲酸酯0.5重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用60Co源,在室温下空气中对片材进行辐照,辐照剂量为100KGy。在立式发泡炉中发泡,发泡温度为220℃,发泡时间为4min。
对实施例2得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例3
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯60重量份、聚乳酸40重量份、偶氮二甲酰胺5重量份、导电炭黑8重量份、碳酸钙5重量份、氧化锌1重量份和三烯丙基异氰脲酸酯0.5重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用电子加速器,在室温下空气中对片材进行辐照,辐照剂量为100KGy。在立式发泡炉中发泡,发泡温度为220℃,发泡时间为4min。
对实施例3得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例4
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯80重量份、二氧化碳-环氧丙烷共聚物20重量份、导电炭黑7重量份、偶氮二甲酰胺5重量份、碳酸钙5重量份、氧化锌1重量份和三烯丙基异氰脲酸酯0.5重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用电子加速器,在室温下空气中对片材进行辐照,辐照剂量为100KGy。在立式发泡炉中发泡,发泡温度为220℃,发泡时间为4min。
对实施例4得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例5
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯70重量份、聚丁二酸丁二醇酯30重量份、导电炭黑7重量份、偶氮二甲酰胺5重量份、碳酸钙5重量份、氧化锌1重量份和三烯丙基异氰脲酸酯0.5重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用电子加速器,在室温下空气中对片材进行辐照,辐照剂量为100KGy。在立式发泡炉中发泡,发泡温度为220℃,发泡时间为4min。
对实施例5得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例6
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯60重量份、聚丁二酸丁二醇酯40重量份、碳纳米管5重量份、偶氮二甲酸钡0.1重量份、二氧化硅1重量份、硬脂酸锌0.01重量份和三羟甲基丙烷三丙烯酸酯0.1重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为3.0mm。采用电子加速器,在室温下空气中对片材进行辐照,辐照剂量为2KGy。在水平发泡炉中发泡,发泡温度为250℃,发泡时间为1min。
对实施例6得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例7
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯60重量份、聚丁二酸丁二醇酯40重量份、石墨烯1重量份、偶氮二甲酸二异丙酯15重量份、蒙脱土1重量份、硬脂酸钙5重量份和三羟甲基丙烷三甲基丙烯酸酯5重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为0.5mm。采用电子加速器,在室温下空气中对片材进行辐照,辐照剂量为100KGy。在水平发泡炉中发泡,发泡温度为220℃,发泡时间为1min。
对实施例7得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例8
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯80重量份、聚丁二酸丁二醇酯20重量份、阳离子型抗静电剂6重量份、N,N-二亚硝基五次甲基四胺15重量份、蒙脱土5重量份、硬脂酸钙5重量份和三羟甲基丙烷三甲基丙烯酸酯2重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.5mm。采用电子加速器,在室温下空气中对片材进行辐照,辐照剂量为100KGy。在水平发泡炉中发泡,发泡温度为220℃,发泡时间为1min。
对实施例8得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例9
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯70重量份、聚乳酸30重量份、非离子型抗静电剂7重量份、4,4’-氧代双苯磺酰肼15重量份、滑石粉5重量份、硬脂酸5重量份、三羟甲基丙烷三甲基丙烯酸酯1重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用电子加速器,在室温下空气中对片材进行辐照,辐照剂量为150KGy。在水平发泡炉中发泡,发泡温度为190℃,发泡时间为20min。
对实施例9得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例10
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯70重量份、聚乳酸30重量份、非离子型抗静电剂7重量份、4,4’-氧代双苯磺酰肼15重量份、滑石粉5重量份、硬脂酸5重量份、乙烯基三甲基硅烷0.5重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用电子加速器,在室温下空气中对片材进行预辐照,辐照剂量为0.5KGy,将预辐射交联后的片材,在70℃的热水浴中进一步交联24h。在水平发泡炉中发泡,发泡温度为190℃,发泡时间为20min。
对实施例10得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例11
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯70重量份、聚乳酸30重量份、非离子型抗静电剂7重量份、4,4’-氧代双苯磺酰肼15重量份、滑石粉5重量份、硬脂酸5重量份、乙烯基三乙氧基硅烷3重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用电子加速器,在室温下空气中对片材进行预辐照,辐照剂量为5KGy,将预辐射交联后的片材,在80℃的热水浴中进一步交联24h。在水平发泡炉中发泡,发泡温度为190℃,发泡时间为20min。
对实施例11得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
实施例12
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯70重量份、聚乳酸30重量份、非离子型抗静电剂7重量份、4,4’-氧代双苯磺酰肼15重量份、滑石粉5重量份、硬脂酸5重量份、乙烯基三(β-甲氧基乙氧基)硅烷5重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用电子加速器,在室温下空气中对片材进行预辐照,辐照剂量为9KGy,将预辐射交联后的片材,在70℃的热水浴中进一步交联48h。在水平发泡炉中发泡,发泡温度为190℃,发泡时间为20min。
对实施例12得到的抗静电可生物降解泡沫材料进行性能检测,检测结果如表1所示。
对比例1
抗静电可生物降解泡沫材料,由聚己二酸-对苯二甲酸丁二醇酯70重量份、聚乳酸30重量份、非离子型抗静电剂7重量份、4,4’-氧代双苯磺酰肼15重量份、滑石粉5重量份、硬脂酸5重量份、三羟甲基丙烷三甲基丙烯酸酯1重量份组成。
上述抗静电可生物降解泡沫材料的制备方法:先按组成和重量份称取上述原料,然后采用双螺杆挤出机进行混炼造粒,混炼造粒温度为80-170℃,然后采用单螺杆挤出机挤成片材,挤出温度为100-170℃,片材厚度为1.0mm。采用电子加速器,在室温下空气中对片材进行预辐照,辐照剂量为9KGy,将预辐射交联后的片材,在70℃的热水浴中进一步交联48h。在水平发泡炉中发泡,发泡温度为190℃,发泡时间为20min,无法制备抗静电可生物降解泡沫材料。
对比例1说明,只有采用特定的交联剂,才能两步交联制备性能优异的泡沫材料。
对实施例1-12和对比例1的生物降解辐射交联泡沫材料的表观密度、发泡倍率、拉伸强度、断裂伸长率、压缩强度和耐久性进行检测。其中,表观密度通过GB-T-6343-2009进行检测;拉伸强度和断裂伸长率采用GB/T6344-1996中的方法进行检测;压缩强度采用GB/T8813-2008中的方法进行检测;耐久性采用的方法进行检测。检测结果如表1所示。
表1实施例1-12和对比例1的抗静电生物降解抗静电泡沫材料的性能
从表1可以看出,本发明的泡沫材料具备物理性能优异、耐久性好、发泡倍率较高、抗静电性好的优点,且通过与其他生物可降解高分子,如聚乳酸、二氧化碳-环氧丙烷共聚物、聚丁二酸丁二醇酯等进行共混发泡,可以在很宽的范围内调控发泡材料的力学性能。
对实施例1-12的泡沫材料的耐水性进行检测,检测方法为:将辐射交联可生物降解泡沫材料于80摄氏度水中浸泡15天。经检测,浸泡30天后,本发明的泡沫材料的表观良好,没有明显变化,拉伸强度无明显降低。说明本发明的泡沫材料耐水性好。
Claims (10)
1.抗静电可生物降解泡沫材料,其特征在于,组成及重量份为:
所述可降解聚合物为聚乳酸、二氧化碳-环氧丙烷共聚物、聚丁二酸丁二醇酯中的一种或多种按任意比例的混合。
2.根据权利要求1所述的抗静电可生物降解泡沫材料,其特征在于,所述抗静电剂为导电炭黑、碳纳米管、石墨烯、非离子型抗静电剂和阳离子型抗静电剂中的一种或多种按任意比例的混合。
3.根据权利要求1所述的抗静电可生物降解泡沫材料,其特征在于,所述发泡剂为偶氮二甲酰胺、偶氮二甲酸钡、偶氮二甲酸二异丙酯、N,N-二亚硝基五次甲基四胺、4,4’-氧代双苯磺酰肼中的一种或多种按任意比例的混合。
4.根据权利要求1所述的抗静电可生物降解泡沫材料,其特征在于,所述无机填料为二氧化硅、滑石粉、碳酸钙、蒙脱土中的一种或多种按任意比例的混合。
5.根据权利要求1所述的抗静电可生物降解泡沫材料,其特征在于,所述助发泡剂为氧化锌、硬脂酸锌、硬脂酸钙中的一种或多种按任意比例的混合。
6.根据权利要求1所述的抗静电可生物降解泡沫材料,其特征在于,所述交联剂为三烯丙基异氰脲酸酯、三羟甲基丙烷三丙烯酸酯、三羟甲基丙烷三甲基丙烯酸酯中的一种或多种按任意比例的混合,或者为乙烯基三甲基硅烷、乙烯基三乙氧基硅烷、乙烯基三(β-甲氧基乙氧基)硅烷中的一种或多种按任意比例的混合。
7.权利要求1-6任何一项所述的抗静电可生物降解泡沫材料的制备方法,其特征在于,步骤如下:
步骤一、按组成及重量份称取各原料,加入挤出机中进行混炼造粒,混炼造粒温度为80-170℃,得到的混炼造粒料在片材挤出机上挤出片材,片材厚度为0.5-3.0mm,挤出温度为100-170℃;
步骤二、室温下空气中,对共混物片材进行电离辐照,辐照剂量为2-100KGy,得到交联物料;
或者,室温下空气中,对步骤一得到的片材进行电离辐照,辐照剂量为0.5-9KGy,得到预交联物料;将预交联物料,在50-80℃的热水浴中进一步交联2-48h,得到交联物料;
步骤三、将交联物料进行发泡,温度为190-250℃,时间为1-20min,得到可生物降解聚己二酸-对苯二甲酸丁二醇酯泡沫材料。
8.根据权利要求7所述的抗静电可生物降解泡沫材料的制备方法,其特征在于,混炼造粒在双螺杆挤出机中完成,挤出片材的设备为单螺杆片材挤出机。
9.根据权利要求7所述的抗静电可生物降解泡沫材料的制备方法,其特征在于,电离辐射源为60Co源或电子加速器。
10.根据权利要求7所述的抗静电可生物降解泡沫材料的制备方法,其特征在于,交联物料在立式发泡炉或水平发泡炉中进行发泡。
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