CN106120322A - 一种聚乳酸纤维的亲水改性方法 - Google Patents

一种聚乳酸纤维的亲水改性方法 Download PDF

Info

Publication number
CN106120322A
CN106120322A CN201610611480.4A CN201610611480A CN106120322A CN 106120322 A CN106120322 A CN 106120322A CN 201610611480 A CN201610611480 A CN 201610611480A CN 106120322 A CN106120322 A CN 106120322A
Authority
CN
China
Prior art keywords
polylactic
parts
acid fiber
acid
fiber
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
CN201610611480.4A
Other languages
English (en)
Inventor
徐卫忠
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.)
Changxin Weifeng Textile Co Ltd
Original Assignee
Changxin Weifeng Textile Co Ltd
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 Changxin Weifeng Textile Co Ltd filed Critical Changxin Weifeng Textile Co Ltd
Priority to CN201610611480.4A priority Critical patent/CN106120322A/zh
Publication of CN106120322A publication Critical patent/CN106120322A/zh
Pending legal-status Critical Current

Links

Classifications

    • 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
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/184Carboxylic acids; Anhydrides, halides or salts thereof
    • D06M13/207Substituted carboxylic acids, e.g. by hydroxy or keto groups; Anhydrides, halides or salts thereof
    • 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
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03Polysaccharides or derivatives thereof
    • 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
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03Polysaccharides or derivatives thereof
    • D06M15/05Cellulose or derivatives thereof
    • D06M15/09Cellulose ethers
    • 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
    • D06M2101/16Synthetic fibres, other than mineral fibres
    • D06M2101/30Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/32Polyesters

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

本发明公开了一种聚乳酸纤维的亲水改性方法,可以很大程度改善聚乳酸纤维的亲水性,使得其服用性能大幅提高:(1)制备聚乳酸纤维预处理液:按下列重量份数配备溶液:羟丙基甲基纤维素2份;苹果酸5‑8份;海藻糖0.2‑0.5份;水100份;(2)将聚乳酸纤维投入预处理液中恒温50‑55℃处理5‑8min,洗净,常温干燥;(3)制备聚乳酸纤维处理液:按下列重量份数配备溶液:羟丙基甲基纤维素1份;柠檬酸10份;水100份;(4)将聚乳酸纤维投入处理液中恒温50℃处理15‑20min;(5)将处理后的聚乳酸纤维洗净,40℃烘干。

Description

一种聚乳酸纤维的亲水改性方法
技术领域
本发明涉及一种聚乳酸纤维的亲水改性方法,属于纺织领域。
背景技术
聚乳酸的主要特性是:源于自然资源、可完全生物降解性和低环境负载性。然而聚乳酸在物性上与传统材料做比较时却不占优势,特别是热力学性能,聚乳酸的玻璃环转变温度约为左右,耐热性较差,是阻碍其更广泛应用的主要原因。同时聚乳酸的结晶速度慢,结晶度不高,导致聚乳酸制品在加工成型后是一种半结晶状态或非晶态,常温下是一种硬而脆的热塑性材料,抗冲击性能差。从宏观上看,聚乳酸的缺点是铜性差和耐热变形温度低,作为医用材料时还要考虑其降解性能和使用寿命两者之间的平衡。从微观上看,聚乳酸的微观结构也限制了它的应用,聚乳酸中存在大量疏水的酷键,降低了聚乳酸的生物相容性,降解周期难以控制。同时聚乳酸聚合过程产生的分子量分布过宽,这使材料的强度往往不符合要求。其中高分子量的聚乳酸是热塑性聚合物,无色、有光泽、硬度较大,物性与聚苯乙稀相似,而无定形聚乳酸能被大多数有机溶剂溶解,如四氧呋喃、氯化物溶剂、苯、二氧杂环己焼。乳酸单体具有型和型两种立体异构形式,由于每个重复单元均有一个手性中心,大分子或多或少地具有立体规整性,这对其形态、性能有着强烈地影响,溶点、结晶度等均随立体规整性降低而迅速下降。
聚乳酸在不同的成型加工方法下可制备成薄膜、片材、棒材等。其纤维经过热成型、纺丝等二次加工后在纺织、包装、农业、医疗卫生、日常生活用品等领域也日益广泛的被应用。
本发明旨在提供一种聚乳酸纤维的亲水改性方法,其工艺简单易操作,可以很大程度改善聚乳酸纤维的亲水性,使得其服用性能大幅提高。
发明内容
本发明针对现有技术中的缺点,本发明旨在提供一种聚乳酸纤维的亲水改性方法,其工艺简单易操作,可以很大程度改善聚乳酸纤维的亲水性,使得其服用性能大幅提高。
本发明的目的可以通过以下技术方案实现:
一种聚乳酸纤维的亲水改性方法,其步骤如下:
(1)制备聚乳酸纤维预处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素2份;
苹果酸5-8份;
海藻糖0.2-0.5份;
水100份;
(2)将聚乳酸纤维投入预处理液中恒温50-55℃处理5-8min,洗净,常温干燥;
(3)制备聚乳酸纤维处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素1份;
柠檬酸10份;
水100份;
(4)将聚乳酸纤维投入处理液中恒温50℃处理15-20min;
(5)将处理后的聚乳酸纤维洗净,40℃烘干。
本发明实施例选用市售得到的PLA纤维,其强力为15.2CN,水接触角为83°。
接触角测定方法:将试样粘贴于接触角测试仪的样品台上,使用喷雾器皿向纤维表面喷水,利用显微镜观察纤维表面的水滴形态,采用量高法计算纤维的水接触角。
力学性能测定方法:在规定的降解时间点取出试样,用去离子水冲洗干净,真空干燥至恒重.使用LLY06E型电子单纤强力测试仪,在恒温条件下,选取隔距长度为10mm,拉伸速度为20mm/min,对试样纤维的拉伸断裂强力进行测试。
本发明的有益之处在于:
(1)本发明工艺简单,易于产业化操作,所用原料安全环保,对环境友好。
(2)本发明的工艺可以很大程度改善聚乳酸纤维的亲水性,使得其服用性能大幅提高,几乎不损伤力学性能。
具体实施方式
实施例1:
一种聚乳酸纤维的亲水改性方法,其步骤如下:
(1)制备聚乳酸纤维预处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素2份;
苹果酸5份;
海藻糖0.5份;
水100份;
(2)将聚乳酸纤维投入预处理液中恒温50℃处理8min,洗净,常温干燥;
(3)制备聚乳酸纤维处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素1份;
柠檬酸10份;
水100份;
(4)将聚乳酸纤维投入处理液中恒温50℃处理15min;
(5)将处理后的聚乳酸纤维洗净,40℃烘干。
结果:处理后的PLA纤维,其强力为15.1CN,水接触角为51.8°。可见,亲水性大幅度提高,而力学性能几乎不变。
实施例2:
一种聚乳酸纤维的亲水改性方法,其步骤如下:
(1)制备聚乳酸纤维预处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素2份;
苹果酸8份;
海藻糖0.2份;
水100份;
(2)将聚乳酸纤维投入预处理液中恒温55℃处理5min,洗净,常温干燥;
(3)制备聚乳酸纤维处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素1份;
柠檬酸10份;
水100份;
(4)将聚乳酸纤维投入处理液中恒温50℃处理20min;
(5)将处理后的聚乳酸纤维洗净,40℃烘干。
结果:处理后的PLA纤维,其强力为15.0CN,水接触角为62.3°。可见,亲水性大幅度提高,而力学性能几乎不变。
实施例3:
一种聚乳酸纤维的亲水改性方法,其步骤如下:
(1)制备聚乳酸纤维预处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素2份;
苹果酸6份;
海藻糖0.4份;
水100份;
(2)将聚乳酸纤维投入预处理液中恒温51℃处理7min,洗净,常温干燥;
(3)制备聚乳酸纤维处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素1份;
柠檬酸10份;
水100份;
(4)将聚乳酸纤维投入处理液中恒温50℃处理16min;
(5)将处理后的聚乳酸纤维洗净,40℃烘干。
结果:处理后的PLA纤维,其强力为15.1CN,水接触角为53.7°。可见,亲水性大幅度提高,而力学性能几乎不变。
实施例4:
一种聚乳酸纤维的亲水改性方法,其步骤如下:
(1)制备聚乳酸纤维预处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素2份;
苹果酸7份;
海藻糖0.3份;
水100份;
(2)将聚乳酸纤维投入预处理液中恒温54℃处理6min,洗净,常温干燥;
(3)制备聚乳酸纤维处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素1份;
柠檬酸10份;
水100份;
(4)将聚乳酸纤维投入处理液中恒温50℃处理19min;
(5)将处理后的聚乳酸纤维洗净,40℃烘干。
结果:处理后的PLA纤维,其强力为15.0CN,水接触角为60.4°。可见,亲水性大幅度提高,而力学性能几乎不变。
实施例5:
一种聚乳酸纤维的亲水改性方法,其步骤如下:
(1)制备聚乳酸纤维预处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素2份;
苹果酸5份;
海藻糖0.5份;
水100份;
(2)将聚乳酸纤维投入预处理液中恒温52℃处理5min,洗净,常温干燥;
(3)制备聚乳酸纤维处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素1份;
柠檬酸10份;
水100份;
(4)将聚乳酸纤维投入处理液中恒温50℃处理17min;
(5)将处理后的聚乳酸纤维洗净,40℃烘干。
结果:处理后的PLA纤维,其强力为15.1CN,水接触角为58.6°。可见,亲水性大幅度提高,而力学性能几乎不变。
由此可见,本发明工艺简单,易于产业化操作,所用原料安全环保,对环境友好。本发明的工艺可以很大程度改善聚乳酸纤维的亲水性,使得其服用性能大幅提高,几乎不损伤力学性能。
以上所述,仅为本发明较佳的具体实施方式,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,根据本发明的技术方案及其发明构思加以等同替换或改变,都应涵盖在本发明的保护范围之内。

Claims (2)

1.一种聚乳酸纤维的亲水改性方法,其步骤如下:
(1)制备聚乳酸纤维预处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素2份;
苹果酸5-8份;
海藻糖0.2-0.5份;
水100份;
(2)将聚乳酸纤维投入预处理液中恒温50-55℃处理5-8min,洗净,常温干燥;
(3)制备聚乳酸纤维处理液:
按下列重量份数配备溶液:
羟丙基甲基纤维素1份;
柠檬酸10份;
水100份;
(4)将聚乳酸纤维投入处理液中恒温50℃处理15-20min;
(5)将处理后的聚乳酸纤维洗净,40℃烘干。
2.权利要求1所述改性方法制得的改性聚乳酸纤维。
CN201610611480.4A 2016-07-29 2016-07-29 一种聚乳酸纤维的亲水改性方法 Pending CN106120322A (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610611480.4A CN106120322A (zh) 2016-07-29 2016-07-29 一种聚乳酸纤维的亲水改性方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610611480.4A CN106120322A (zh) 2016-07-29 2016-07-29 一种聚乳酸纤维的亲水改性方法

Publications (1)

Publication Number Publication Date
CN106120322A true CN106120322A (zh) 2016-11-16

Family

ID=57254921

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610611480.4A Pending CN106120322A (zh) 2016-07-29 2016-07-29 一种聚乳酸纤维的亲水改性方法

Country Status (1)

Country Link
CN (1) CN106120322A (zh)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108660609A (zh) * 2018-05-23 2018-10-16 阳光卫生医疗新材料江阴有限公司 一种抗菌非织造布的制备方法及抗菌非织造布
WO2019053074A1 (de) * 2017-09-14 2019-03-21 Trevira Gmbh Polymerfaser mit verbesserter langzeit-dispergierbarkeit
CN112553901A (zh) * 2020-11-25 2021-03-26 武汉纺织大学 一种高效热交换调温纤维材料和制备方法及其在香烟中的应用
CN112962308A (zh) * 2021-02-08 2021-06-15 安徽工程大学 一种亲水聚乳酸纤维的加工工艺及应用

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103316600A (zh) * 2013-05-14 2013-09-25 中国科学院宁波材料技术与工程研究所 一种在聚乳酸血透膜表面固定肝素的方法
CN105646887A (zh) * 2016-01-05 2016-06-08 湖北大学 一种两亲性高分子聚合物及其制备方法、应用

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103316600A (zh) * 2013-05-14 2013-09-25 中国科学院宁波材料技术与工程研究所 一种在聚乳酸血透膜表面固定肝素的方法
CN105646887A (zh) * 2016-01-05 2016-06-08 湖北大学 一种两亲性高分子聚合物及其制备方法、应用

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
陈袁曦: "明胶改性聚乳酸纤维性能的研究", 《工程塑料应用》 *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019053074A1 (de) * 2017-09-14 2019-03-21 Trevira Gmbh Polymerfaser mit verbesserter langzeit-dispergierbarkeit
CN111094647A (zh) * 2017-09-14 2020-05-01 特雷维拉股份有限公司 具有改善的长期可分散性的聚合物纤维
JP2020536178A (ja) * 2017-09-14 2020-12-10 トレヴィラ ゲーエムベーハー 改善された長期分散性を有するポリマー繊維
JP7234217B2 (ja) 2017-09-14 2023-03-07 トレヴィラ ゲーエムベーハー 改善された長期分散性を有するポリマー繊維
JP7459223B2 (ja) 2017-09-14 2024-04-01 トレヴィラ ゲーエムベーハー 改善された長期分散性を有するポリマー繊維
CN108660609A (zh) * 2018-05-23 2018-10-16 阳光卫生医疗新材料江阴有限公司 一种抗菌非织造布的制备方法及抗菌非织造布
CN112553901A (zh) * 2020-11-25 2021-03-26 武汉纺织大学 一种高效热交换调温纤维材料和制备方法及其在香烟中的应用
CN112962308A (zh) * 2021-02-08 2021-06-15 安徽工程大学 一种亲水聚乳酸纤维的加工工艺及应用
CN112962308B (zh) * 2021-02-08 2023-03-28 安徽工程大学 一种亲水聚乳酸纤维的加工工艺及应用

Similar Documents

Publication Publication Date Title
CN106120322A (zh) 一种聚乳酸纤维的亲水改性方法
Cvelbar et al. White paper on the future of plasma science and technology in plastics and textiles
Cai et al. Facile and versatile modification of cotton fibers for persistent antibacterial activity and enhanced hygroscopicity
CN101787582B (zh) 一种高强高模杂环芳纶的制备方法
Das et al. Surface modification of electrospun PVA/chitosan nanofibers by dielectric barrier discharge plasma at atmospheric pressure and studies of their mechanical properties and biocompatibility
Zhao et al. Preparation of nanofibers with renewable polymers and their application in wound dressing
CN104499294B (zh) 一种具有抗静电、抗菌和亲水性涤纶织物的整理方法
da Silva Parize et al. Poly (lactic acid) fibers obtained by solution blow spinning: Effect of a greener solvent on the fiber diameter
Roozbahani et al. Effects of chitosan alkali pretreatment on the preparation of electrospun PCL/chitosan blend nanofibrous scaffolds for tissue engineering application
CN104937150B (zh) 涂上浆剂碳纤维束、碳纤维束的制造方法及预浸料坯
Simbara et al. Comparative study of aligned and nonaligned poly (ε‐caprolactone) fibrous scaffolds prepared by solution blow spinning
CA2496655A1 (en) A method for producing cellulose fiber
Cooper et al. Electrospinning process and structure relationship of biobased poly (butylene succinate) for nanoporous fibers
Pezeshki‐Modaress et al. Fabrication of gelatin/chitosan nanofibrous scaffold: process optimization and empirical modeling
Khadka et al. Insoluble synthetic polypeptide mats from aqueous solution by electrospinning
CN108265346A (zh) 一种织物
Ravishankar et al. Using Dimensionless Numbers to Predict Centrifugal Jet‐Spun Nanofiber Morphology
Grimmelsmann et al. Electrospinning and stabilization of chitosan nanofiber mats
Bradner et al. Fabrication of elastomeric silk fibers
Kumar et al. Soy protein films with the hydrophobic surface created through non-covalent interactions
Saeed et al. A simple, green chemistry technology for fabrication of tissue-engineered scaffolds based on mussel-inspired 3D centrifugal spun
Zhang et al. Polyvinyl alcohol composite hydrogels/epoxidized natural rubber composites (CMCS/PVA/CS-ENR) with core-shell structure as biomass coating material for slow-release nitrogen fertilizer
Liu et al. Electrospun core–sheath fibers for integrating the biocompatibility of silk fibroin and the mechanical properties of PLCL
Wu et al. A silver nanoparticles-polylactic acid microspheres/polylactic acid-thermoplastic polyurethane nanofibers hierarchical antibacterial film
Bahrami et al. Layer‐by‐layer self‐assembly of collagen and chitosan biomolecules on polyurethane films

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20161116