CN107791535A - 生物降解薄膜制备方法 - Google Patents

生物降解薄膜制备方法 Download PDF

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CN107791535A
CN107791535A CN201710985956.5A CN201710985956A CN107791535A CN 107791535 A CN107791535 A CN 107791535A CN 201710985956 A CN201710985956 A CN 201710985956A CN 107791535 A CN107791535 A CN 107791535A
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film
parts
mass fraction
preparation
biodegradable
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CN107791535B (zh
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翁文伟
王伟
祝二斌
林速
林一速
林东山
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Fujian Hengan Household Life Article Co Ltd
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FUJIAN HENGAN HYGIENE MATERIAL Co Ltd
Hengan Fujian Holding Group Co Ltd
Fujian Hengan Sanitary Material Co Ltd
Fujian Hengan Household Life Article Co Ltd
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Priority to CN201710985956.5A priority Critical patent/CN107791535B/zh
Priority to CN201910775802.2A priority patent/CN110669239B/zh
Priority to CN201910775823.4A priority patent/CN110669240B/zh
Priority to CN201910775310.3A priority patent/CN110643153B/zh
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Abstract

本发明公开一种生物降解薄膜的制备方法。包括(1)将聚乳酸、聚丁二酸丁二醇酯和聚己二酸/对苯二甲酸丁二酯按照预定比例混合并搅拌得到混合材料A;(2)将聚羟基脂肪酸酯和聚碳酸亚丙酯按照预定比例混合并搅拌得到混合材料B;(3)将步骤(1)中获得的混合原材料A进行吹膜得到第一薄膜;将步骤(2)中得到的混合材料B进行吹膜得到第二薄膜;(4)将步骤(1)中的第一薄膜进行横向拉伸,将步骤(2)中得到的第二薄膜置于第一薄膜的上表面,将第一薄膜和第二薄膜粘合得到生物降解薄膜。

Description

生物降解薄膜制备方法
技术领域
本发明涉及一种生物降解薄膜及其制备方法。
背景技术
随着人们生活水平与卫生要求的提高,卫生用品发展迅速,已深入到每个家庭,其用量呈现快速上升的势头。然而传统的卫生用品一般选用PE、PP等材质,其缺点是该卫生用品使用后,不能降解,对环境产生较大破坏,造成“白色污染”。生物降解塑料可在自然界广泛存在的微生物或动植物体内酶的作用下最终分解成二氧化碳及水而回归环境。该类材料的应用是解决传统塑料造成的“白色污染”问题的主要途径之一。
聚乳酸使用后可完全降解,不会对环境造成污染,其技术开发成为当前研究的热点,从近几年聚乳酸相关专利的申请就可见端倪。聚乳酸有良好的生物相容性和可生物降解性,能被酸、碱、生物酶、微生物等降解;聚乳酸制品使用后能被自然界中微生物完全降解,最终变成二氧化碳和水,不污染环境,对保护环境非常有利。但聚乳酸也有一些性能有待改进,如聚乳酸的柔韧性较差,冲击强度和断裂伸长率均低于通用树脂,货架寿命较短。
发明内容
针对上述问题,本发明提供一种生物降解薄膜的制备方法。
为达到上述目的,本发明一种生物降解薄膜的制备方法,包括如下步骤:
(1)将聚乳酸、聚丁二酸丁二醇酯和聚己二酸/对苯二甲酸丁二酯按照预定比例混合并搅拌得到混合材料A;
(2)将聚羟基脂肪酸酯和聚碳酸亚丙酯素按照预定比例混合并搅拌得到混合材料B;
(3)将步骤(1)中获得的混合原材料A进行吹膜得到第一薄膜;将步骤(2)中得到的混合材料B进行吹膜得到第二薄膜;
(4)将步骤(1)中的第一薄膜进行横向拉伸,将步骤(2)中得到的第二薄膜置于第一薄膜的上表面,将第一薄膜和第二薄膜粘合得到生物降解薄膜。
进一步地,所述步骤(1)中,聚乳酸的质量份数为10-30份;
所述聚丁二酸丁二醇脂的质量份数为40-70份;
所述聚己二酸/对苯二甲酸丁二酯的质量份数为1-20份。
进一步地,所述步骤(2)中,聚羟基脂肪酸酯的质量份数为10-60份;
所述聚碳酸亚丙酯的质量份数为60-80份。
进一步地,所述步骤(3)中对混合材料A进行吹膜的温度范围为120℃~180℃。
进一步地,所述步骤(3)中对混合材料B进行吹膜的温度范围为120℃~180℃。
进一步地,所述步骤(3)中,对第一薄膜进行横向拉伸的拉伸比为2:1。
进一步地,所述步骤4的具体过程为在第一薄膜的上表面喷涂热熔胶,再将第二薄膜置于第一薄膜上进行粘合。
进一步地,所述方法还包括向步骤(3)中制得的第一薄膜的下表面喷涂纳米银抗菌剂,并在40℃-60℃的温度下对第一薄膜进行干燥处理。
进一步地,所述方法还包括向步骤(3)中制得的第二薄膜的上表面喷涂纳米银抗菌剂,并在40℃-60℃的温度下对第二薄膜进行干燥处理。
进一步地,所述抗菌剂包括纳米银、黄檗提取物、积雪草提取物、聚二甲基硅氧烷、羧甲基纤维素和聚丙烯酸钠;
所述纳米银的质量份数为0.01-3份;
所述黄檗提取物质量份数为20-30份;
所述积雪草提取物质量份数为20-30份;
所述聚二甲基硅氧烷的质量份数为1-5份;
所述羧甲基纤维素的质量份数为5-10份;
所述乙醇的质量份数为20-30份;
聚丙烯酸钠的质量份数为1-15份。
本发明通过在第一薄膜和第二薄膜的表面涂覆抗菌剂,使制得的生物降解薄膜具有抗菌、杀菌的功能;在制备第二薄膜时,通过对第一薄膜进行拉伸使得生物降解薄膜更加轻薄。
针对上述问题,本发明提供一种生物降解薄膜。
为达到上述目的,本发明提供一种生物降解薄膜,按照如上所述生物降解薄膜的制备方法制得的薄膜。
本发明生物降接薄膜通过在第一薄膜和第二薄膜的表面涂覆抗菌剂,使制得的生物降解薄膜具有抗菌、杀菌的功能;在制备第二薄膜时,通过对第一薄膜进行拉伸使得生物降解薄膜更加轻薄。
具体实施方式
实施例1
本实施例提供一种生物降解薄膜的制备方法,包括如下步骤:
(1)将聚乳酸、聚丁二酸丁二醇酯和聚己二酸/对苯二甲酸丁二酯按照预定比例混合并搅拌得到混合材料A;其中,聚乳酸的质量份数为10-30份;所述聚丁二酸丁二醇脂的质量份数为40-70份;所述聚己二酸/对苯二甲酸丁二酯的质量份数为1-20份;
(2)将聚羟基脂肪酸酯和聚碳酸亚丙酯按照预定比例混合并搅拌得到混合材料B;其中,所述聚羟基脂肪酸酯的质量份数为10-60份;所述聚碳酸亚丙酯的质量份数为60-80份;
(3)将步骤(1)中获得的混合原材料A在120℃~180℃的温度下进行吹膜得到第一薄膜,在制得的第一薄膜的下表面喷涂纳米银抗菌剂,并在40℃-60℃的温度下对第一薄膜进行干燥处理。将步骤(2)中得到的混合材料B在120℃~180℃的温度下进行吹膜得到第二薄膜;制得的第二薄膜的上的表面喷涂纳米银抗菌剂,并在40℃-60℃的温度下对第二薄膜进行干燥处理。
(4)将步骤(3)中的制得的第一薄膜进行横向拉伸后,在第一薄膜的上表面喷涂热熔胶,将步骤(3)中得到的第二薄膜的下表面对应第一薄膜的上表面放置、将二者进行粘合得到生物降解薄膜。
本实施例中所述抗菌剂包括纳米银、黄檗提取物、积雪草提取物、聚二甲基硅氧烷、羧甲基纤维素、和聚丙烯酸钠和乙醇;所述纳米银的质量份数为0.01-3份;所述黄檗提取物质量份数为20-30份;所述积雪草提取物质量份数为20-30份;所述聚二甲基硅氧烷的质量份数为1-5份;所述羧甲基纤维素的质量份数为5-10份;所述乙醇的质量份数为20-30份;聚丙烯酸钠的质量份数为1-15份。
实施例2
本实施例提供一种生物降解薄膜的制备方法,包括如下步骤:
(1)将聚乳酸、聚丁二酸丁二醇酯和聚己二酸/对苯二甲酸丁二酯按照预定比例混合并搅拌得到混合材料A;其中,聚乳酸的质量份数为15份;所述聚丁二酸丁二醇脂的质量份数为55份;所述聚己二酸/对苯二甲酸丁二酯的质量份数为10份;
(2)将聚羟基脂肪酸酯和聚碳酸亚丙酯按照预定比例混合并搅拌得到混合材料B;其中,所述聚羟基脂肪酸酯的质量份数为30份;所述聚碳酸亚丙酯的质量份数为70份。
(3)将步骤(1)中获得的混合原材料A在200℃的温度下进行吹膜得到第一薄膜,在制得的第一薄膜的下表面喷涂纳米银抗菌剂,并在20℃的温度下对第一薄膜进行干燥处理。将步骤(2)中得到的混合材料B在220℃的温度下进行吹膜得到第二薄膜;制得的第二薄膜的上的表面喷涂纳米银抗菌剂,并在15℃的温度下对第二薄膜进行干燥处理。
(4)将步骤(3)中的制得的第一薄膜进行横向拉伸后,在第一薄膜的上表面喷涂热熔胶,将步骤(2)中得到的第二薄膜的下表面对应第一薄膜放置在第一薄膜的上表面、将二者进行粘合得到生物降解薄膜。本实施例中所述抗菌剂包括纳米银、黄檗提取物、积雪草提取物、聚二甲基硅氧烷、羧甲基纤维素、和聚丙烯酸钠和乙醇;
所述纳米银的质量份数为1份;所述黄檗提取物质量份数为25份;所述积雪草提取物质量份数为23份;所述聚二甲基硅氧烷的质量份数为3份;所述羧甲基纤维素的质量份数为7份;所述乙醇的质量份数为25份;聚丙烯酸钠的质量份数为10份。
本发明通过在第一薄膜和第二薄膜的表面涂覆抗菌剂,使制得的生物降解薄膜具有抗菌、杀菌的功能;在制备第二薄膜时,通过对第一薄膜进行拉伸提高了生物降解薄膜的更加的轻薄。
以上,仅为本发明的较佳实施例,但本发明的保护范围并不局限于此,任何熟悉本技术领域的技术人员在本发明揭露的技术范围内,可轻易想到的变化或替换,都应涵盖在本的保护范围之内。因此,本发明的保护范围应该以权利要求所界定的保护范围为准。

Claims (10)

1.一种生物降解薄膜的制备方法,其特征在于,包括如下步骤:
(1)将聚乳酸、聚丁二酸丁二醇酯和聚己二酸/对苯二甲酸丁二酯按照预定比例混合并搅拌得到混合材料A;
(2)将聚羟基脂肪酸酯和聚碳酸亚丙酯按照预定比例混合并搅拌得到混合材料B;
(3)将步骤(1)中获得的混合原材料A进行吹膜得到第一薄膜;将步骤(2)中得到的混合材料B进行吹膜得到第二薄膜;
(4)将步骤(1)中的第一薄膜进行横向拉伸,将步骤(2)中得到的第二薄膜置于第一薄膜的上表面,将第一薄膜和第二薄膜粘合得到生物降解薄膜。
2.根据权利要求1所述的生物降解薄膜的制备方法,其特征在于,所述步骤(1)中,聚乳酸的质量份数为10-30份;
所述聚丁二酸丁二醇脂的质量份数为40-70份;
所述聚己二酸/对苯二甲酸丁二酯的质量份数为1-20份。
3.根据权利要求1所述的生物降解薄膜的制备方法,其特征在于,所述步骤(2)中,
所述聚羟基脂肪酸酯的质量份数为10-60份;
所述聚碳酸亚丙酯的质量份数为60-80份。
4.根据权利要求1所述的生物降解薄膜的制备方法,其特征在于,所述步骤(3)中对混合材料A进行吹膜的温度范围为120℃~180℃。
5.根据权利要求1所述的生物降解薄膜的制备方法,其特征在于,所述步骤(3)中对混合材料B进行吹膜的温度范围为120℃~180℃。
6.根据权利要求1所述的生物降解薄膜,其特征在于所述步骤(3)中,对第一薄膜进行横向拉伸的拉伸比为2:1。
7.根据权利要求1所述的生物降解薄膜的制备方法,其特征在于,所述步骤4的具体过程为在第一薄膜的上表面喷涂热熔胶,再将第二薄膜置于第一薄膜上进行粘合。
8.根据权利要求1所述的生物降解薄膜的制备方法,其特征在于,所述方法还包括向步骤(3)中制得的第一薄膜的下表面喷涂纳米银抗菌剂,并在40℃-60℃的温度下对第一薄膜进行干燥处理。
9.根据权利要求1所述的生物降解薄膜的制备方法,其特征在于,所述方法还包括向步骤(3)中制得的第二薄膜的上表面喷涂纳米银抗菌剂,并在40℃-60℃的温度下对第二薄膜进行干燥处理。
10.根据权利要求8-9所述的生物降解薄膜的制备方法,其特征在于,所述抗菌剂包括纳米银、黄檗提取物、积雪草提取物、聚二甲基硅氧烷、羧甲基纤维素和聚丙烯酸钠;
所述纳米银的质量份数为0.01-3份;
所述黄檗提取物质量份数为20-30份;
所述积雪草提取物质量份数为20-30份;
所述聚二甲基硅氧烷的质量份数为1-5份;
所述羧甲基纤维素的质量份数为5-10份;
所述乙醇的质量份数为20-30份;
聚丙烯酸钠的质量份数为1-15份。
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