CN107955352A - 一种聚乳酸复合材料及其制备方法 - Google Patents

一种聚乳酸复合材料及其制备方法 Download PDF

Info

Publication number
CN107955352A
CN107955352A CN201711340222.8A CN201711340222A CN107955352A CN 107955352 A CN107955352 A CN 107955352A CN 201711340222 A CN201711340222 A CN 201711340222A CN 107955352 A CN107955352 A CN 107955352A
Authority
CN
China
Prior art keywords
modified
fiber
composite material
lactic acid
fibre
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.)
Pending
Application number
CN201711340222.8A
Other languages
English (en)
Inventor
赫凯
敖广宇
邱凡
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shenyang Golden Bodi Ecological Environmental Protection Science And Technology Ltd Co
Original Assignee
Shenyang Golden Bodi Ecological Environmental Protection Science And Technology Ltd Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shenyang Golden Bodi Ecological Environmental Protection Science And Technology Ltd Co filed Critical Shenyang Golden Bodi Ecological Environmental Protection Science And Technology Ltd Co
Priority to CN201711340222.8A priority Critical patent/CN107955352A/zh
Publication of CN107955352A publication Critical patent/CN107955352A/zh
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/04Reinforcing macromolecular compounds with loose or coherent fibrous material
    • C08J5/06Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/04Reinforcing macromolecular compounds with loose or coherent fibrous material
    • C08J5/047Reinforcing macromolecular compounds with loose or coherent fibrous material with mixed fibrous material
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/32Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/38Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/50Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with organometallic compounds; with organic compounds containing boron, silicon, selenium or tellurium atoms
    • D06M13/51Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond
    • D06M13/513Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond with at least one carbon-silicon bond
    • D06M13/5135Unsaturated compounds containing silicon atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2367/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2367/04Polyesters derived from hydroxy carboxylic acids, e.g. lactones
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2401/00Characterised by the use of cellulose, modified cellulose or cellulose derivatives
    • C08J2401/02Cellulose; Modified cellulose
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2497/00Characterised by the use of lignin-containing materials
    • C08J2497/02Lignocellulosic material, e.g. wood, straw or bagasse
    • 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
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/02Fibres or whiskers
    • C08K7/04Fibres or whiskers inorganic
    • C08K7/06Elements
    • 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
    • C08K9/00Use of pretreated ingredients
    • C08K9/02Ingredients treated with inorganic substances
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Biological Depolymerization Polymers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

本发明公开了一种聚乳酸复合材料,由以下重量百分数的原料制成:聚乳酸60~90%,改性纤维10~30%,热稳定剂0.2~10%,交联剂0.3~8%,加工助剂0.1~10%。改性纤维由改性秸秆纤维、改性麻纤维和改性碳纤维组成;热稳定剂选自环氧大豆油、丙三醇、亚磷酸三苯酯、酒石酸、肉桂酸、三醋酸甘油脂。其制备方法为:将聚乳酸、改性纤维、热稳定剂、交联剂、加工助剂混合均匀,直接注塑成型,注塑温度为150~200℃,注塑时间2~10分钟,压力5~25MPa。本发明选用秸秆纤维为主要增强体,并加入麻纤维及碳纤维,有效地改善了聚乳酸的各类性能,避免了单一纤维改性的不稳定性和局限性,同时实现了秸秆的高效利用。

Description

一种聚乳酸复合材料及其制备方法
技术领域
本发明涉及一种聚乳酸复合材料及其制备方法,属于高分子材料技术领域。
背景技术
聚乳酸是一种常见的可完全生物降解的聚合物,其具有良好的生物相容性及加工性能。但是纯聚乳酸质硬,具有较低的冲击性能,韧性差,易弯曲变形,需要对其进行增强增韧等改性。
纤维增强能够明显的提高聚乳酸材料强度。公开号为CN 102085680 A的专利采用秸秆纤维增强聚乳酸材料,能够提高聚乳酸的强度性能。公开号为CN 107118528 A的专利申请采用黄麻纤维增强聚乳酸性能,纤维与PLA有良好的相容性和粘结性。然而单一纤维对于增强聚乳酸性能存在不稳定性和局限性,同时因麻类植物种植的地域局限性,其成本日益增高。此外,还有采用人造纤维制备聚乳酸复合材料的专利申请,可有效改善材料性能,但因其价格较贵,限制了其大规模生产应用。因此,亟需找到一种成本较低并能有效改善聚乳酸性能的复合方法。
发明内容
针对上述现有技术,本发明提供了一种聚乳酸复合材料及其制备方法。本发明选用价格低廉、来源广泛的秸秆纤维为主要增强体,并加入一定的麻纤维及碳纤维,经改性后以合理的比例混合,后制备聚乳酸复合材料。本发明以较低的生产成本制备出性能优异的聚乳酸复合材料,有效改善聚乳酸各类性能,避免了单一纤维改性的不稳定性和局限性,同时实现了秸秆的高效利用。
本发明是通过以下技术方案实现的:
一种聚乳酸复合材料,由以下重量百分数的原料制成:聚乳酸60~90%,改性纤维10~30%,热稳定剂0.2~10%,交联剂0.3~8%,加工助剂0.1~10%。
所述改性纤维,由改性秸秆纤维、改性麻纤维和改性碳纤维组成,三种纤维的质量比为: 60~80:15~30:5~10。
所述改性秸秆纤维、改性麻纤维是通过以下方法制备得到的:
a.秸秆纤维与麻纤维混合后用水洗净,常温下,在10%(质量百分数)氢氧化钠溶液中浸泡2~4小时,用蒸馏水洗涤若干次,调节PH至中性(用醋酸或硝酸调节),放入干燥箱中干燥3~10小时,干燥箱温度50~100℃;
b.上述经碱处理过的纤维,常温下,在1~5%(质量百分数)的硅烷水溶液中浸泡2~4小时,用蒸馏水洗涤若干次(比如3次),放入干燥箱中干燥3~10小时,干燥箱温度50~100℃
所述硅烷选自乙烯基三乙氧基硅烷、乙烯基三甲氧基硅烷。
所述改性碳纤维是通过以下方法制备得到的:将碳纤维在50%~60%的浓硝酸溶液中浸泡5~8小时,去离子水洗涤若干次,干燥箱中干燥3~10小时,干燥箱温度80~120℃。
所述热稳定剂选自环氧大豆油、丙三醇、亚磷酸三苯酯、酒石酸、肉桂酸、三醋酸甘油脂中的任意一种或任意两种以上的组合物。
所述交联剂选自季戊四醇、山梨醇、马来酸酐、山梨糖醇中的任意一种或任意两种以上的组合物。
所述加工助剂选自硬脂酸、金属皂、硬脂酸复合脂中的任意一种或任意两种以上的组合物。
所述聚乳酸复合材料的制备方法为:将聚乳酸、改性纤维、热稳定剂、交联剂、加工助剂混合均匀,直接注塑成型,注塑温度为150~200℃,注塑时间2~10分钟,压力5~25MPa,即得聚乳酸复合材料。
本发明的聚乳酸复合材料,具有以下优点:
(1)采用多种纤维改性后制备聚乳酸复合材料,弥补单一纤维增强聚乳酸材料性能上的不稳定性和局限性。
(2)以较低的成本制备相对性能最佳的聚乳酸复合材料。对秸秆纤维及麻纤维进行碱处理,溶解掉纤维表面的胶质,同时增大了纤维表面粗糙度,提高了界面结合力,从而使材料强度显著提高。硅烷处理后,纤维表面与PLA之间形成亲脂分子层,通过化学键与基体紧密结合,同时纤维分散均匀。改性后聚乳酸强度和耐热性明显提高。
(3)实现了秸秆的高效利用。
具体实施方式
下面结合实施例对本发明作进一步的说明。
下述实施例中所涉及的仪器、试剂、材料等,若无特别说明,均为现有技术中已有的常规仪器、试剂、材料等,可通过正规商业途径获得。下述实施例中所涉及的实验方法,检测方法等,若无特别说明,均为现有技术中已有的常规实验方法,检测方法等。
下述实施例中,所用聚乳酸,其分子量为100000。所用秸秆纤维,为玉米秸秆纤维。所用麻纤维,为黄麻纤维。
实施例1:制备聚乳酸复合材料
原料用量配比关系为:聚乳酸75%,改性纤维18%(秸秆纤维12%,麻纤维5%,碳纤维1%),环氧大豆油2%,季戊四醇2%,硬脂酸3%。
其中,改性纤维是通过以下方法制备得到的:
(1)秸秆纤维与麻纤维改性:
a.秸秆纤维与麻纤维按比例混合后用水洗净,在10%的氢氧化钠溶液常温下浸泡3小时,之后用蒸馏水洗涤若干次,再用醋酸调pH至中性后,放入干燥箱中干燥8小时,干燥箱温度80℃。
b.将上述经过碱处理过的纤维,用4%的硅烷(乙烯基三乙氧基硅烷)水溶液常温浸泡3小时,蒸馏水清洗3次,放入干燥箱中干燥8小时,干燥箱温度80℃。
(2)碳纤维改性:碳纤维浸泡在60%的浓硝酸溶液中5小时,去离子水清洗若干次,于干燥箱中干燥7小时,干燥箱温度100℃。
聚乳酸复合材料的制备方法为:将聚乳酸、改性纤维、环氧大豆油、季戊四醇、硬脂酸混合均匀,注塑成型,注塑温度为180℃,注塑时间3分钟,压力20MPa,得聚乳酸复合材料。
实施例2:制备聚乳酸复合材料
原料用量配比关系为:聚乳酸70%,改性纤维23%(秸秆纤维15%,麻纤维6%,碳纤维2%),环氧大豆油2%,季戊四醇2%,硬脂酸3%。
其中,改性纤维是通过以下方法制备得到的:
(1)秸秆纤维与黄麻纤维改性:
a.秸秆纤维与麻纤维按比例混合后用水洗净,在10%的氢氧化钠溶液常温下浸泡3小时,之后用蒸馏水洗涤若干次,再用硝酸调pH至中性后,放入干燥箱中干燥8时,干燥箱温度80℃。
b.将上述经过碱处理过的纤维,用4%的硅烷(乙烯基三甲氧基硅烷)水溶液常温浸泡3小时,蒸馏水清洗3次,放入干燥箱中干燥8小时,干燥箱温度80℃。
(2)碳纤维改性:碳纤维浸泡在50%的浓硝酸溶液中8小时,去离子水清洗若干次,于干燥箱中干燥7小时,干燥箱温度100℃。
聚乳酸复合材料的制备方法为:将聚乳酸、改性纤维、环氧大豆油、季戊四醇、硬脂酸混合均匀,注塑成型,注塑温度为180℃,注塑时间3分钟,压力20MPa,得聚乳酸复合材料。
实施例3:制备聚乳酸复合材料
原料用量配比关系为:聚乳酸79%,改性纤维14%(秸秆纤维9%,麻纤维3%,碳纤维2%),环氧大豆油2%,季戊四醇2%,硬脂酸3%。
其中,改性纤维是通过以下方法制备得到的:
(1)秸秆纤维与黄麻纤维改性:
a.秸秆纤维与黄麻纤维按比例混合后用水洗净,在10%的氢氧化钠溶液常温下浸泡3小时,之后用蒸馏水洗涤若干次,再用硝酸调pH至中性后,放入干燥箱中干燥8时,干燥箱温度80℃。
b.将上述经过碱处理过的纤维,用4%的硅烷(乙烯基三甲氧基硅烷)水溶液常温浸泡3小时,蒸馏水清洗3次,放入干燥箱中干燥8小时,干燥箱温度80℃。
(2)碳纤维改性:碳纤维浸泡在50%的浓硝酸溶液中8小时,去离子水清洗若干次,于干燥箱中干燥7小时,干燥箱温度100℃。
聚乳酸复合材料的制备方法为:将聚乳酸、改性纤维、环氧大豆油、季戊四醇、硬脂酸混合均匀,注塑成型,注塑温度为180℃,注塑时间3分钟,压力20MPa,得聚乳酸复合材料。
实施例4:制备聚乳酸复合材料
原料用量配比关系为:聚乳酸68%,改性纤维21%(秸秆纤维14%,麻纤维5%,碳纤维2%),环氧大豆油4%,季戊四醇3%,硬脂酸4%。
其中,改性纤维是通过以下方法制备得到的:
(1)秸秆纤维与黄麻纤维改性:
a.秸秆纤维与黄麻纤维按比例混合后用水洗净,在10%的氢氧化钠溶液常温下浸泡3小时,之后用蒸馏水洗涤若干次,再用硝酸调pH至中性后,放入干燥箱中干燥8时,干燥箱温度80℃。
b.将上述经过碱处理过的纤维,用4%的硅烷(乙烯基三甲氧基硅烷)水溶液常温浸泡3小时,蒸馏水清洗3次,放入干燥箱中干燥8小时,干燥箱温度80℃。
(2)碳纤维改性:碳纤维浸泡在50%的浓硝酸溶液中8小时,去离子水清洗若干次,于干燥箱中干燥7小时,干燥箱温度100℃。
聚乳酸复合材料的制备方法为:将聚乳酸、改性纤维、环氧大豆油、季戊四醇、硬脂酸混合均匀,注塑成型,注塑温度为180℃,注塑时间3分钟,压力20MPa,得聚乳酸复合材料。
实施例5:制备聚乳酸复合材料
原料用量配比关系为:聚乳酸68%,改性纤维23%(秸秆纤维15%,麻纤维6%,碳纤维2%),环氧大豆油3%,季戊四醇3%,硬脂酸3%。
其中,改性纤维是通过以下方法制备得到的:
(1)秸秆纤维与黄麻纤维改性:
a.秸秆纤维与黄麻纤维按比例混合后用水洗净,在10%的氢氧化钠溶液常温下浸泡3小时,之后用蒸馏水洗涤若干次,再用硝酸调pH至中性后,放入干燥箱中干燥8时,干燥箱温度80℃。
b.将上述经过碱处理过的纤维,用4%的硅烷(乙烯基三甲氧基硅烷)水溶液常温浸泡3小时,蒸馏水清洗3次,放入干燥箱中干燥8小时,干燥箱温度80℃。
(2)碳纤维改性:碳纤维浸泡在50%的浓硝酸溶液中8小时,去离子水清洗若干次,于干燥箱中干燥7小时,干燥箱温度100℃。
聚乳酸复合材料的制备方法为:将聚乳酸、改性纤维、环氧大豆油、季戊四醇、硬脂酸混合均匀,注塑成型,注塑温度为180℃,注塑时间3分钟,压力20MPa,得聚乳酸复合材料。
对比例1:制备纯聚乳酸材料
将聚乳酸注塑成型,注塑温度为180℃,注塑时间3分钟,压力20MPa,得聚乳酸材料。
对比例2:制备单一纤维增强聚乳酸材料
原料用量配比关系为:聚乳酸70%,改性麻纤维23%,环氧大豆油2%,季戊四醇2%,硬脂酸3%。
所述改性麻纤维是通过以下方法制备得到的:麻纤维用水洗净后,在10%的氢氧化钠溶液中常温浸泡3小时,之后用蒸馏水洗涤3次,醋酸调pH至中性后,放入100℃干燥箱中干燥5小时。再用4%的硅烷(乙烯基三乙氧基硅烷)水溶液常温浸泡3小时,蒸馏水清洗3次,放入100℃干燥箱中干燥8小时。
单一纤维增强聚乳酸材料的制备方法为:将聚乳酸、改性麻纤维、环氧大豆油、季戊四醇、硬脂酸混合均匀,注塑成型,注塑温度为180℃,注塑时间3分钟,压力20MPa,得单一纤维增强聚乳酸材料。
比较上述实施例1、2、3、4、5对比例1、2所得材料的弯曲强度、冲击强度,如表1所示。
表1
由表1可见,本发明制备的复合材料,其性能(弯曲强度、冲击强度)明显优于纯聚乳酸材料、单一纤维增强聚乳酸材料,得到了明显的提高。

Claims (7)

1.一种聚乳酸复合材料,其特征在于:由以下重量百分数的原料制成:聚乳酸60~90%,改性纤维10~30%,热稳定剂0.2~10%,交联剂0.3~8%,加工助剂0.1~10%;
所述改性纤维,由改性秸秆纤维、改性麻纤维和改性碳纤维组成,三种纤维的质量比为:改性秸秆纤维60~80:15~30:5~10;
所述热稳定剂选自环氧大豆油、丙三醇、亚磷酸三苯酯、酒石酸、肉桂酸、三醋酸甘油脂中的任意一种或任意两种以上的组合物;
所述交联剂选自季戊四醇、山梨醇、马来酸酐、山梨糖醇中的任意一种或任意两种以上的组合物;
所述加工助剂选自硬脂酸、金属皂、硬脂酸复合脂中的任意一种或任意两种以上的组合物。
2.根据权利要求1所述的聚乳酸复合材料,其特征在于:所述改性秸秆纤维、改性麻纤维和改性碳纤维的质量比为:60~80:15~30:5~10。
3.根据权利要求1所述的聚乳酸复合材料,其特征在于:所述改性秸秆纤维、改性麻纤维是通过以下方法制备得到的:
a.秸秆纤维与麻纤维混合后用水洗净,常温下,在氢氧化钠溶液中浸泡2~4小时,用水洗涤若干次,调节pH至中性,放入干燥箱中干燥3~10小时,干燥箱温度50~100℃;
b.上述经碱处理过的纤维,常温下,在1~5%的硅烷水溶液中浸泡2~4小时,用水洗涤若干次,放入干燥箱中干燥3~10小时,干燥箱温度50~100℃;
所述硅烷选自乙烯基三乙氧基硅烷、乙烯基三甲氧基硅烷。
4.根据权利要求1所述的聚乳酸复合材料,其特征在于:所述改性碳纤维是通过以下方法制备得到的:将碳纤维在50%~60%的浓硝酸溶液中浸泡5~8小时,水洗涤若干次,干燥箱中干燥3~10小时,干燥箱温度80~120℃。
5.根据权利要求1所述的聚乳酸复合材料,其特征在于:由以下重量百分数的原料制成:聚乳酸75%,秸秆纤维12%,麻纤维5%,碳纤维1%,环氧大豆油2%,季戊四醇2%,硬脂酸3%。
6.根据权利要求1所述的聚乳酸复合材料,其特征在于:由以下重量百分数的原料制成:聚乳酸70%,秸秆纤维15%,麻纤维6%,碳纤维2%,环氧大豆油2%,季戊四醇2%,硬脂酸3%。
7.权利要求1~6中任一项所述的聚乳酸复合材料的制备方法,其特征在于:将聚乳酸、改性纤维、热稳定剂、交联剂、加工助剂混合均匀,直接注塑成型,注塑温度为150~200℃,注塑时间2~10分钟,压力5~25MPa,即得聚乳酸复合材料。
CN201711340222.8A 2017-12-14 2017-12-14 一种聚乳酸复合材料及其制备方法 Pending CN107955352A (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201711340222.8A CN107955352A (zh) 2017-12-14 2017-12-14 一种聚乳酸复合材料及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711340222.8A CN107955352A (zh) 2017-12-14 2017-12-14 一种聚乳酸复合材料及其制备方法

Publications (1)

Publication Number Publication Date
CN107955352A true CN107955352A (zh) 2018-04-24

Family

ID=61958924

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201711340222.8A Pending CN107955352A (zh) 2017-12-14 2017-12-14 一种聚乳酸复合材料及其制备方法

Country Status (1)

Country Link
CN (1) CN107955352A (zh)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108728923A (zh) * 2018-06-07 2018-11-02 新沂市中诺新材料科技有限公司 一种新型再生纤维的制备方法
CN110541300A (zh) * 2018-05-28 2019-12-06 句容市华冠服帽厂 一种pla改性纤维的制备方法及改性纤维
CN111234487A (zh) * 2020-03-05 2020-06-05 温州三星环保包装有限公司 基于可降解复合包装材料的一次性餐盒

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101538401A (zh) * 2009-03-13 2009-09-23 上海大学 耐热型二元纤维/聚乳酸基复合材料及其制备方法

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101538401A (zh) * 2009-03-13 2009-09-23 上海大学 耐热型二元纤维/聚乳酸基复合材料及其制备方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
郑学晶等: "《天然高分子材料》", 31 December 2010, 化学工业出版社 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110541300A (zh) * 2018-05-28 2019-12-06 句容市华冠服帽厂 一种pla改性纤维的制备方法及改性纤维
CN108728923A (zh) * 2018-06-07 2018-11-02 新沂市中诺新材料科技有限公司 一种新型再生纤维的制备方法
CN111234487A (zh) * 2020-03-05 2020-06-05 温州三星环保包装有限公司 基于可降解复合包装材料的一次性餐盒
CN111234487B (zh) * 2020-03-05 2022-02-25 温州三星环保包装有限公司 基于可降解复合包装材料的一次性餐盒

Similar Documents

Publication Publication Date Title
Eng et al. Impact strength and flexural properties enhancement of methacrylate silane treated oil palm mesocarp fiber reinforced biodegradable hybrid composites
CN107955352A (zh) 一种聚乳酸复合材料及其制备方法
Islam et al. Characterization of Laccase-Treated Kenaf Fibre Reinforced Recycled Polypropylene Composites.
Kumar et al. Synthesis and characterization of cellulose nanocrystals/PVA based bionanocomposite
CN107033564B (zh) 经表面改性后的竹纤维长纤和聚乳酸共混复合材料的制备方法
JP2016532020A (ja) 表面修飾セルロースナノ繊維、バイオ複合樹脂組成物およびその製造方法
US11524921B2 (en) Composite materials containing hemp and nanocellulose
CN104514041A (zh) 一种可降解纤维及其制备方法
CN105885112A (zh) 一种环保塑料袋
CN1665889A (zh) 具有经提高的耐水性的生物降解性组合物及其制作工艺
Gieparda et al. Chemical modification of natural fibres to epoxy laminate for lightweight constructions
CN106009065A (zh) 一种降解后直接增加土壤活力的塑料袋
CN104562694A (zh) 一种超低收缩拒水聚酯工业丝及其制备方法
JP2015052052A (ja) 成形材料用樹脂組成物の製造方法およびその成形体
CN107602835A (zh) 一种采用高分子扩链改性制备高粘度pbt的方法
CN108456401B (zh) 一种管道复合材料及其制备方法
CN105544181B (zh) 一种亲水防缩双面呢
CN112724612A (zh) 一种异质型木质素/聚乳酸复合材料的制备方法
CN105754264A (zh) 一种高强度耐拉伸渔网
CN105133056A (zh) 一种隔音保暖性好的新型复合纤维纺织材料
Bhaskaran et al. Natural fibre reinforced vegetable-oil based polyurethane composites: A review
CN107476051A (zh) 剑麻纤维聚乙烯纤维复合材料制备钓鱼线的方法
CN106589747A (zh) 一种洗衣机内筒用耐磨抗振聚丙烯复合材料及其制备方法
CN105586676A (zh) 一种木棉和聚乳酸的混合纺纱工艺
Seo et al. Preparation and Characterization of Electrospun Composite Nanofibers from Poly (vinyl alcohol)/Lignocellulose Nanofibrils with Different Chemical Compositions

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
RJ01 Rejection of invention patent application after publication

Application publication date: 20180424

RJ01 Rejection of invention patent application after publication