CN107793618A - 一种发泡聚乙烯材料及其制备方法 - Google Patents

一种发泡聚乙烯材料及其制备方法 Download PDF

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CN107793618A
CN107793618A CN201710979004.2A CN201710979004A CN107793618A CN 107793618 A CN107793618 A CN 107793618A CN 201710979004 A CN201710979004 A CN 201710979004A CN 107793618 A CN107793618 A CN 107793618A
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汪锋
王龙珑
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Anhui Yong Feng protection Polytron Technologies Inc
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Abstract

本发明提供了一种发泡聚乙烯材料,由如下重量份的组分组成,低密度聚乙烯70份,高密度聚乙烯15份,乙烯‑醋酸乙烯共聚物10份,钛酸酯改性碳酸钙5份,交联剂0.5份,偶氮二甲酰胺8份,氧化锌0.5份,二氧化硅3份,硬脂酸锌0.2份和抗氧剂0.2份。本发明所述的发泡聚乙烯材料,通过适量的加入高密度聚乙烯和乙烯‑醋酸乙烯共聚物,减少了减少的聚乙烯的使用,在保持发泡材料弹性的基础上,提高该材料的刚性、硬度和压缩强度,同时降低材料密度,成本低。本发明还提供了所述发泡聚乙烯材料的制备方法,生产工艺简单,可降低成本,经济实用。

Description

一种发泡聚乙烯材料及其制备方法
技术领域
本发明属于聚乙烯发泡材料技术领域,特别是涉及一种发泡聚乙烯材料及其制备方法。
背景技术
发泡聚乙烯材料(EPE)是一种新型环保材料,非交联闭孔结构,它由低密度聚乙烯脂加入超细滑石料和抗缩剂单甘油脂采用丁烷经物理发泡成形的,具有高强缓冲能力的新型环保包装材料,具有保温、防潮、耐腐蚀、重量轻、缓冲性能好、耐摩擦等性能特点,广泛适用于电子产品、仪表仪器、家具、玻璃、陶瓷、酒类、工艺品等产品的内包装和特殊包装,在物流行业车辆运输和快递包装中也运用极广,成为运输包装最重要的缓冲与保护材料之一。现有技术中,发泡聚乙烯材料的缓冲性能,韧性和强度有待改进。
发明内容
针对上述技术问题,本发明的目的在于提供一种发泡聚乙烯材料;本发明还提供了所述发泡聚乙烯材料的制备方法,
本发明采用的技术方案是:
一种发泡聚乙烯材料,由如下重量份的组分组成,低密度聚乙烯60-70份,高密度聚乙烯15-20份,乙烯-醋酸乙烯共聚物10-15份,钛酸酯改性碳酸钙4-5份,交联剂0.5-1份,偶氮二甲酰胺8-12份,氧化锌0.1-0.5份,二氧化硅1-3份,硬脂酸锌0.2-0.8份和抗氧剂0.2-0.4份。
本发明所述发泡聚乙烯材料,其中,由如下重量份的组分组成,低密度聚乙烯65份,高密度聚乙烯16份,乙烯-醋酸乙烯共聚物12份,钛酸酯改性碳酸钙4份,交联剂0.6份,偶氮二甲酰胺10份,氧化锌0.3份,二氧化硅2份,硬脂酸锌0.5份和抗氧剂0.3份。
本发明所述发泡聚乙烯材料,其中,所述交联剂为过氧化二异丙苯、过氧化苯甲酰中的一种或两种。
本发明所述发泡聚乙烯材料,其中,所述抗氧剂为4,4’-硫代双(6-叔丁基-3-甲基苯酚)和抗氧剂1010中的一种或两种。
本发明所述发泡聚乙烯材料的制备方法,包括以下步骤:
(1)将低密度聚乙烯、高密度聚乙烯和乙烯-醋酸乙烯共聚物置于开炼机中进行塑炼,塑炼温度110-120℃,塑炼时间2-5min,得到聚乙烯混炼物;
(2)然后依次将钛酸酯改性碳酸钙、氧化锌、二氧化硅、硬脂酸锌、偶氮二甲酰胺、交联剂和抗氧剂加入步骤(1)中所述聚乙烯混炼物中进行混炼,混炼温度120-130℃,混炼时间10-15min;
(3)然后将混炼后的物料放在模具中,将模具置于平板硫化机中,在160-180℃,5-15MPa条件下热压发泡5-15min,开模取出,轻压定型即可制得发泡聚乙烯材料。
本发明有益效果:
本发明所述的发泡聚乙烯材料,通过适量的加入高密度聚乙烯和乙烯-醋酸乙烯共聚物,减少了聚乙烯的使用,在保持发泡材料弹性的基础上,提高该材料的刚性、硬度和压缩强度,同时降低材料密度,成本低。
本发明所述的发泡聚乙烯材料的制备方法,生产工艺简单,可降低成本,经济实用。
具体实施方式
实施例1
一种发泡聚乙烯材料,由如下重量份的组分组成,低密度聚乙烯65份,高密度聚乙烯16份,乙烯-醋酸乙烯共聚物12份,钛酸酯改性碳酸钙4份,交联剂0.6份,偶氮二甲酰胺10份,氧化锌0.3份,二氧化硅2份,硬脂酸锌0.5份和抗氧剂0.3份,所述交联剂为过氧化二异丙苯;所述抗氧剂为抗氧剂1010。
本实施例所述发泡聚乙烯材料的制备方法,包括以下步骤:
(1)将低密度聚乙烯、高密度聚乙烯和乙烯-醋酸乙烯共聚物置于开炼机中进行塑炼,塑炼温度110℃,塑炼时间3min,得到聚乙烯混炼物;
(2)然后依次将钛酸酯改性碳酸钙、氧化锌、二氧化硅、硬脂酸锌、偶氮二甲酰胺、交联剂和抗氧剂加入步骤(1)中所述聚乙烯混炼物中进行混炼,混炼温度125℃,混炼时间12min;
(3)然后将混炼后的物料放在模具中,将模具置于平板硫化机中,在1170℃,10MPa条件下热压发泡10min,开模取出,轻压定型即可制得发泡聚乙烯材料。
实施例2
一种发泡聚乙烯材料,由如下重量份的组分组成,低密度聚乙烯60份,高密度聚乙烯20份,乙烯-醋酸乙烯共聚物15份,钛酸酯改性碳酸钙4份,交联剂1份,偶氮二甲酰胺12份,氧化锌0.1份,二氧化硅1份,硬脂酸锌0.8份和抗氧剂0.4份,所述交联剂为过氧化二异丙苯;所述抗氧剂为4,4’-硫代双(6-叔丁基-3-甲基苯酚)。
本发明所述发泡聚乙烯材料的制备方法,包括以下步骤:
(1)将低密度聚乙烯、高密度聚乙烯和乙烯-醋酸乙烯共聚物置于开炼机中进行塑炼,塑炼温度120℃,塑炼时间2min,得到聚乙烯混炼物;
(2)然后依次将钛酸酯改性碳酸钙、氧化锌、二氧化硅、硬脂酸锌、偶氮二甲酰胺、交联剂和抗氧剂加入步骤(1)中所述聚乙烯混炼物中进行混炼,混炼温度120℃,混炼时间10min;
(3)然后将混炼后的物料放在模具中,将模具置于平板硫化机中,在160℃,5MPa条件下热压发泡15min,开模取出,轻压定型即可制得发泡聚乙烯材料。
实施例3
一种发泡聚乙烯材料,由如下重量份的组分组成,低密度聚乙烯70份,高密度聚乙烯15份,乙烯-醋酸乙烯共聚物10份,钛酸酯改性碳酸钙5份,交联剂0.5份,偶氮二甲酰胺8份,氧化锌0.5份,二氧化硅3份,硬脂酸锌0.2份和抗氧剂0.2份,所述交联剂为过氧化苯甲酰;所述抗氧剂为4,4’-硫代双(6-叔丁基-3-甲基苯酚)和抗氧剂1010。
本实施例所述发泡聚乙烯材料的制备方法,包括以下步骤:
(1)将低密度聚乙烯、高密度聚乙烯和乙烯-醋酸乙烯共聚物置于开炼机中进行塑炼,塑炼温度110℃,塑炼时间5min,得到聚乙烯混炼物;
(2)然后依次将钛酸酯改性碳酸钙、氧化锌、二氧化硅、硬脂酸锌、偶氮二甲酰胺、交联剂和抗氧剂加入步骤(1)中所述聚乙烯混炼物中进行混炼,混炼温度130℃,混炼时间15min;
(3)然后将混炼后的物料放在模具中,将模具置于平板硫化机中,在180℃,15MPa条件下热压发泡5min,开模取出,轻压定型即可制得发泡聚乙烯材料。
对实施例1-3制备的产品进行常规性能测试,本发明所的发泡聚乙烯材料的发泡倍率大于7倍。将所得发泡材料制成标准样条,压缩强度按照GB/T18942-1于常温下100mm/min的速率进行测试。经过测试,所得的发泡材料压缩强度≥0.1MP,压缩永久变形≤7%。
以上所述的实施例仅仅是对本发明的优选实施方式进行描述,并非对本发明的范围进行限定,在不脱离本发明设计精神的前提下,本领域普通技术人员对本发明的技术方案作出的各种变形和改进,均应落入本发明权利要求书确定的保护范围内。

Claims (5)

1.一种发泡聚乙烯材料,其特征在于:由如下重量份的组分组成,低密度聚乙烯60-70份,高密度聚乙烯15-20份,乙烯-醋酸乙烯共聚物10-15份,钛酸酯改性碳酸钙4-5份,交联剂0.5-1份,偶氮二甲酰胺8-12份,氧化锌0.1-0.5份,二氧化硅1-3份,硬脂酸锌0.2-0.8份和抗氧剂0.2-0.4份。
2.根据权利要求1所述的发泡聚乙烯材料,其特征在于:由如下重量份的组分组成,低密度聚乙烯65份,高密度聚乙烯16份,乙烯-醋酸乙烯共聚物12份,钛酸酯改性碳酸钙4份,交联剂0.6份,偶氮二甲酰胺10份,氧化锌0.3份,二氧化硅2份,硬脂酸锌0.5份和抗氧剂0.3份。
3.根据权利要求1所述的发泡聚乙烯材料,其特征在于:所述交联剂为过氧化二异丙苯、过氧化苯甲酰中的一种或两种。
4.根据权利要求1-3任意一项所述的发泡聚乙烯材料,其特征在于:所述抗氧剂为4,4’-硫代双(6-叔丁基-3-甲基苯酚)和抗氧剂1010中的一种或两种。
5.权利要求1-4任意一项所述的发泡聚乙烯材料的制备方法,其特征在于:包括以下步骤:
(1)将低密度聚乙烯、高密度聚乙烯和乙烯-醋酸乙烯共聚物置于开炼机中进行塑炼,塑炼温度110-120℃,塑炼时间2-5min,得到聚乙烯混炼物;
(2)然后依次将钛酸酯改性碳酸钙、氧化锌、二氧化硅、硬脂酸锌、偶氮二甲酰胺、交联剂和抗氧剂加入步骤(1)中所述聚乙烯混炼物中进行混炼,混炼温度120-130℃,混炼时间10-15min;
(3)然后将混炼后的物料放在模具中,将模具置于平板硫化机中,在160-180℃,5-15MPa条件下热压发泡5-15min,开模取出,轻压定型即可制得发泡聚乙烯材料。
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