CN107793772A - 纳米线增强复合塑料的制备方法及其产品和应用 - Google Patents
纳米线增强复合塑料的制备方法及其产品和应用 Download PDFInfo
- Publication number
- CN107793772A CN107793772A CN201711099473.1A CN201711099473A CN107793772A CN 107793772 A CN107793772 A CN 107793772A CN 201711099473 A CN201711099473 A CN 201711099473A CN 107793772 A CN107793772 A CN 107793772A
- Authority
- CN
- China
- Prior art keywords
- nano wire
- composite plastic
- aramid fiber
- reagent
- preparation
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/005—Reinforced macromolecular compounds with nanosized materials, e.g. nanoparticles, nanofibres, nanotubes, nanowires, nanorods or nanolayered materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2377/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
- C08J2377/10—Polyamides derived from aromatically bound amino and carboxyl groups of amino carboxylic acids or of polyamines and polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2381/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen, or carbon only; Polysulfones; Derivatives of such polymers
- C08J2381/06—Polysulfones; Polyethersulfones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2477/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
- C08J2477/10—Polyamides derived from aromatically bound amino and carboxyl groups of amino carboxylic acids or of polyamines and polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2481/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen, or carbon only; Polysulfones; Derivatives of such polymers
- C08J2481/06—Polysulfones; Polyethersulfones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/16—Halogen-containing compounds
- C08K2003/166—Magnesium halide, e.g. magnesium chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
- C08K2003/3009—Sulfides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/16—Halogen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Nanotechnology (AREA)
- Manufacturing & Machinery (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Reinforced Plastic Materials (AREA)
Abstract
本发明主要提供了一种纳米线增强复合塑料的制备方法及其产品和应用,将试剂A、试剂B和芳纶板置于水热釜中,制得纳米线复合芳纶板;将制得的复合芳纶板材与试剂C水热制得增强型纳米线复合芳纶板;将添加剂A与聚醚砜树脂共混制得改性聚醚砜;将增强型纳米线复合芳纶板与改性聚醚砜用真空辅助树脂灌注成型模塑技术制备为复合塑料。该方法以有序高强纳米线为核心材料将两种材料进行复合,制备出具有良好物理性能的复合塑料,且兼具不错的导热效果。
Description
技术领域
本发明涉及一种聚酯母粒的制备方法,尤其是涉及一种纳米线增强复合塑料的制备方法及其产品和应用。
背景资料
芳纶全称为"聚苯二甲酰苯二胺",英文为Aramid fiber,是一种新型高科技合成纤维,具有超高强度、高模量和耐高温、耐酸耐碱、重量轻等优良性能,其强度是钢丝的 5~6倍,模量为钢丝或玻璃纤维的2~3倍,韧性是钢丝的2倍,而重量仅为钢丝的1/5左右,在560度的温度下,不分解,不融化。它具有良好的绝缘性和抗老化性能,具有很长的生命周期。芳纶的发现,被认为是材料界一个非常重要的历史进程。
聚醚砜树脂(PES)是英国ICI公司在1972年开发的一种综合性能优异的热塑性高分子材料,是得到应用的为数不多的特种工程塑料之一。它具有优良的耐热性能、物理机械性能、绝缘性能等,特别是具有可以在高温下连续使用和在温度急剧变化的环境中仍能保持性能稳定等突出优点,在许多领域已经得到广泛应用。
特种塑料因为分子链较长,链活性较差,因此并不能较好的混合。而随着科技的发展,越来越多的领域,如飞机、汽车、风机叶片开始追求轻质高强的材料,与金属材料相比,特种塑料的质量方面具有无以伦比的优势,但是单一特种塑料及其改性产品的性能往往难以满足极端条件下的需求。
发明内容
为克服现有技术的不足,本发明目的在于:提供一种纳米线增强复合塑料的制备方法。
本发明再一目的在于:提供一种上述方法制备的产品。
本发明又一目的在于:提供一种上述方法制得产品的应用。
本发明目的通过下述方案实现:一种纳米线增强复合塑料的制备方法,包括下述步骤:
1)将试剂A、试剂B和芳纶板置于水热釜中水热反应,制得纳米线复合芳纶板,其中,所用试剂A为氯化镍、四氯化铂、二氯化钯中的一种或几种,所用试剂B为氯化钴、氯化铁、氯化镁中的一种或几种;
2)将制得的复合芳纶板材与试剂C水热反应制得增强型纳米线复合芳纶板,所用试剂C为硫化钠、硫化钾、硫化锂中的一种或几种,其中,试剂A、B和C的摩尔浓度相同;
3)将添加剂A与聚醚砜树脂共混制得改性聚醚砜,所用的添加剂A为单壁碳纳米管、氧化石墨烯、富勒烯中的一种或几种;
4)将增强型纳米线复合芳纶板与改性聚醚砜用真空辅助树脂灌注成型模塑技术制备为复合塑料。
本发明方法以纳米线为核心,将两种特种塑料均匀混合,制备出具有较好物理性能的复合塑料,同时该材料也具有良好的导热性能,有利于其在多种环境下使用。
所用试剂A的浓度为0.1~0.4 mol/L。
所用试剂B浓度为0.1~0.4 mol/L。
所用试剂C浓度为0.1~0.4 mol/L。
所用的添加剂A用量为1~3份。
1)中的水热反应的条件为:温度100~130℃,时间4~6 h;2)中的水热反应的条件为:温度150~180℃,时间12~16 h。
本发明提供一种纳米线增强复合塑料,根据上述任一所述方法制备得到。产品在拉伸强度、冲击强度和导热性能都得到极大提高。
本发明提供一种纳米线增强复合塑料的在导热材料中的应用。
本发明优越性在于:以纳米线为核心,将两种特种塑料均匀混合,制备出具有较好物理性能的复合塑料,同时该材料也具有良好的导热性能,有利于其在多种环境下使用。
具体实施方式
实施例1
1)将芳纶板材置于水热釜中,加入0.1mol/L氯化镍溶液和0.1mol/L氯化钴溶液,100℃水热4 h;
2)将板材取出,用去离子水洗净,再放入水热釜中,加入0.1mol/L的硫化钠溶液,150℃水热12 h,取出洗净,烘干后即得到纳米线改性芳纶板;
3)取1份单壁碳纳米管与100份聚醚砜树脂,熔融共混制得改性聚醚砜树脂;
4)将两种塑料置于设备中,采用真空辅助树脂灌注成型模塑法制备为纳米线增强复合塑料。测试其拉伸强度,如表1。
实施例2
1)将芳纶板材置于水热釜中,加入0.2mol/L四氯化铂溶液和0.2mol/L氯化铁溶液,120℃水热5 h;
2)将板材取出,用去离子水洗净,再放入水热釜中,加入0.2mol/L的硫化钾溶液,160℃水热14 h,取出洗净,烘干后即得到纳米线改性芳纶板;
3)取2份氧化石墨烯与100份聚醚砜树脂,熔融共混制得改性聚醚砜树脂;
4)将两种塑料置于设备中,采用真空辅助树脂灌注成型模塑法制备为纳米线增强复合塑料。测试其冲击强度,如表2。
实施例3
1)将芳纶板材置于水热釜中,加入0.4mol/L二氯化钯溶液和0.4mol/L氯化镁溶液,130℃水热6 h;
2)将板材取出,用去离子水洗净,再放入水热釜中,加入0.4mol/L的硫化锂溶液,180℃水热16 h,取出洗净,烘干后即得到纳米线改性芳纶板;
3) 取3份氧化富勒烯与100份聚醚砜树脂,熔融共混制得改性聚醚砜树脂;
将两种塑料置于设备中,采用真空辅助树脂灌注成型模塑法制备为纳米线增强复合塑料。测试其导热系数,如表3。
。
Claims (8)
1.一种纳米线增强复合塑料的制备方法,其特征在于,制备过程为:
1)将试剂A、试剂B和芳纶板置于水热釜中进行水热反应,制得纳米线复合芳纶板,其中,所述的试剂A为氯化镍、四氯化铂、二氯化钯中的一种或几种,所述的试剂B为氯化钴、氯化铁、氯化镁中的一种或几种;
2)将制得的复合芳纶板材与试剂C水热反应制得增强型纳米线复合芳纶板,所述的试剂C为硫化钠、硫化钾、硫化锂中的一种或几种,其中,试剂A、B和C的摩尔浓度相同;
3)将添加剂A与聚醚砜树脂共混制得改性聚醚砜,所述的添加剂A为单壁碳纳米管、氧化石墨烯、富勒烯中的一种或几种;
4)将2)制得的增强型纳米线复合芳纶板与3)制得的改性聚醚砜用真空辅助树脂灌注成型模塑技术制备为复合塑料。
2.如权利要求1所述纳米线增强复合塑料的制备方法,其特征在于:所用试剂A浓度为0.1~0.4 mol/L。
3.如权利要求1所述纳米线增强复合塑料的制备方法,其特征在于:所用试剂B浓度为0.1~0.4 mol/L。
4.如权利要求1所述纳米线增强复合塑料的制备方法,其特征在于:所用试剂C浓度为0.1~0.4 mol/L。
5.如权利要求1所述纳米线增强复合塑料的制备方法,其特征在于:所用的添加剂A用量为1~3份。
6.如权利要求1所述纳米线增强复合塑料的制备方法,其特征在于:1)中的水热反应的条件为:温度100~130℃,时间4~6 h;2)中的水热反应的条件为:温度150~180℃,时间12~16 h。
7.一种纳米线增强复合塑料,其特征在于根据权利要求1-6任一所述方法制备得到。
8.根据权利要求7所述纳米线增强复合塑料在导热材料中的应用。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201711099473.1A CN107793772A (zh) | 2017-11-09 | 2017-11-09 | 纳米线增强复合塑料的制备方法及其产品和应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201711099473.1A CN107793772A (zh) | 2017-11-09 | 2017-11-09 | 纳米线增强复合塑料的制备方法及其产品和应用 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN107793772A true CN107793772A (zh) | 2018-03-13 |
Family
ID=61549393
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201711099473.1A Pending CN107793772A (zh) | 2017-11-09 | 2017-11-09 | 纳米线增强复合塑料的制备方法及其产品和应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN107793772A (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113114064A (zh) * | 2021-03-17 | 2021-07-13 | 华南理工大学 | 一种摩擦纳米发电机及其制备方法 |
KR20220144674A (ko) * | 2021-04-20 | 2022-10-27 | 울산과학기술원 | 복합재, 이의 제조방법, 및 이를 포함하는 개인 체온 조절 장치 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004143625A (ja) * | 2002-10-24 | 2004-05-20 | Du Pont Toray Co Ltd | 特殊樹脂で加工した高強度繊維複合材料 |
CN101200552A (zh) * | 2007-11-27 | 2008-06-18 | 信义集团公司 | 聚醚砜酮改性树脂基摩擦材料 |
CN103552357A (zh) * | 2013-10-25 | 2014-02-05 | 中航复合材料有限责任公司 | 一种复合材料增强纤维织物的制备方法 |
CN105331081A (zh) * | 2015-11-30 | 2016-02-17 | 江门市优巨新材料有限公司 | 一种高性能改性聚醚砜树脂的制备方法 |
-
2017
- 2017-11-09 CN CN201711099473.1A patent/CN107793772A/zh active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004143625A (ja) * | 2002-10-24 | 2004-05-20 | Du Pont Toray Co Ltd | 特殊樹脂で加工した高強度繊維複合材料 |
CN101200552A (zh) * | 2007-11-27 | 2008-06-18 | 信义集团公司 | 聚醚砜酮改性树脂基摩擦材料 |
CN103552357A (zh) * | 2013-10-25 | 2014-02-05 | 中航复合材料有限责任公司 | 一种复合材料增强纤维织物的制备方法 |
CN105331081A (zh) * | 2015-11-30 | 2016-02-17 | 江门市优巨新材料有限公司 | 一种高性能改性聚醚砜树脂的制备方法 |
Non-Patent Citations (1)
Title |
---|
ANKITA HAZARIKA等: "Fabrication and synthesis of highly ordered nickel cobalt sulfide nanowire-grown woven kevlar fiber/reduced graphene oxide/polyester composites", 《APPLIED MATERIALS》 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113114064A (zh) * | 2021-03-17 | 2021-07-13 | 华南理工大学 | 一种摩擦纳米发电机及其制备方法 |
KR20220144674A (ko) * | 2021-04-20 | 2022-10-27 | 울산과학기술원 | 복합재, 이의 제조방법, 및 이를 포함하는 개인 체온 조절 장치 |
KR102486916B1 (ko) * | 2021-04-20 | 2023-01-11 | 울산과학기술원 | 복합재, 이의 제조방법, 및 이를 포함하는 개인 체온 조절 장치 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Yao et al. | Comparison of carbon nanotubes and graphene oxide coated carbon fiber for improving the interfacial properties of carbon fiber/epoxy composites | |
Liu et al. | Scratch-resistant, highly conductive, and high-strength carbon nanotube-based composite yarns | |
CN101250770B (zh) | 一种碳纳米管增强的聚丙烯腈基碳纤维的制备方法 | |
Wang et al. | Mechanical and electrical property improvement in CNT/Nylon composites through drawing and stretching | |
Mahltig et al. | Inorganic and composite fibers: production, properties, and applications | |
CN104357941A (zh) | 石墨烯和多壁碳纳米管协同增强型聚合物纤维及其制备方法 | |
CN102719092B (zh) | 一种复合增强尼龙组合物及其制备方法 | |
CN106702722A (zh) | 一种高电导率的石墨烯基导电纤维的制备方法 | |
Wang et al. | Multi‐scale hybrid composites‐based carbon nanotubes | |
CN107059403B (zh) | 一种石墨烯/碳纳米管增强增韧碳纤维复合材料的制备方法 | |
CN107793772A (zh) | 纳米线增强复合塑料的制备方法及其产品和应用 | |
Zhang et al. | Surface decoration of short-cut polyimide fibers with multi-walled carbon nanotubes and their application for reinforcement of lightweight PC/ABS composites | |
Irisawa et al. | Effects of carbon nanofibers on carbon fiber reinforced thermoplastics made with in situ polymerizable polyamide 6 | |
CN109401276A (zh) | 一种石墨烯增强聚氨酯复合材料及其制备方法 | |
CN109777101A (zh) | 一种改性聚醚酰亚胺树脂复合物及其制备方法 | |
CN102660097B (zh) | 一种增强聚乙烯醇复合物的制备方法 | |
CN106189151B (zh) | 一种复合玻璃纤维增强聚酯玻璃钢材料及其制备方法 | |
CN101457019A (zh) | 碳纳米管/聚砜酰胺纳米复合材料及其制备方法 | |
Xian et al. | Hydrogen bonds leading nanodiamonds performing different thermal conductance enhancement in different MWCNTs epoxy-based nanocomposites | |
CN107722595A (zh) | 一种纤维‑石墨烯‑热塑性聚芳醚多尺度复合材料的制备方法 | |
Cao et al. | In situ polymerized poly (amide imide)/multiwalled carbon nanotube composite: structural, mechanical, and electrical studies | |
Li et al. | Prescribed morphology and interface correlation of MWNTs-EP/PSF hybrid nanofibers reinforced and toughened epoxy matrix | |
Kim et al. | Unidirectional spread‐tow carbon fiber/polypropylene composites reinforced with mechanically aligned multi‐walled carbon nanotubes and exfoliated graphite nanoplatelets | |
CN109575405B (zh) | 一种改性超高分子量聚乙烯及其制备方法、聚乙烯复合材料及其制备方法 | |
CN103450557B (zh) | 一种聚丙烯pp纳米级增强改性颗粒的制备方法 |
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 | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20180313 |