首页|原位聚合法制备无机盐掺杂聚苯胺棉织物及其光电热性能研究

原位聚合法制备无机盐掺杂聚苯胺棉织物及其光电热性能研究

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掺杂氯化锌、氯化锂、二水合氯化铜、氯化铁、氯化镁等无机盐,采用原位聚合法制备了无机盐掺杂聚苯胺棉织物,通过场发射扫描电子显微镜、超快速显微拉曼成像光谱仪、X射线衍射仪、热重分析仪等对棉织物的微观形貌、结构和热稳定性进行分析并研究了其光电热性能。结果表明:聚苯胺在棉织物上发生聚合反应,赋予棉织物出色的导电性,电导率可达15。7S/m;氯化锂掺杂聚苯胺棉织物的光热性能最佳;在电热性能方面,氯化铜掺杂聚苯胺棉织物电导率最高,可达57。4S/m。发热织物能够根据人体需求调节温度,氯化锂掺杂聚苯胺棉织物在600W/m2光照强度下温度可达65。0℃,氯化铜掺杂聚苯胺棉织物在9。0V电压下表面平均温度可达40。1℃,与聚苯胺棉织物相比,光热和电热性能分别提高了 8。2%和45。8%。
Preparation of inorganic salt-doped polyaniline cotton fabrics by in-situ polymerization and their photoelectric thermal properties
Inorganic salt-doped polyaniline(PANI)cotton fabric was prepared by in-situ polymerization using inorganic salts such as zinc chloride,lithium chloride,copper chloride dihydrate,iron chloride,and magnesium chloride.The microscopic morphology,structure,and thermal stability of the cotton fabric were analyzed by field emission scanning electron microscopy,ultrafast micro-Raman imaging spectroscopy,X-ray diffraction,and thermogravimetric analysis.Additionally,its photoelectric thermal properties were studied.The results indicated that PANI underwent polymerization on the cotton fabric,imparting excellent electrical conductivity,with a conductivity of up to 15.7S/m.The lithium chloride-doped PANI cotton fabric exhibited the best photothermal performance.In terms of electrothermal performance,the copper chloride-doped PANI cotton fabric demonstrated the highest conductivity,achieving up to 57.4S/m.The heating fabric had the ability to adjust controllably its temperature according to human body's needs.The lithium chloride-doped fabric reached 65.0℃ under 600W/m2 irradiance,and the copper chloride-doped fabric reached 40.1℃ under 9.0V.The doped fabric showed an improvement of 8.2%in photothermal properties and 45.8%in electrothermal properties compared to undoped polyaniline cotton fabric.

inorganic saltin-situ polymerizationpolyanilinecotton fabricsphotoelectric thermal properties

吴涛、缪东校、祁冠杰、彭军、王潮霞

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江南大学纺织科学与工程学院,无锡 214122

无机盐 原位聚合法 聚苯胺 棉织物 光电热性能

2025

化工新型材料
中国化工信息中心

化工新型材料

北大核心
影响因子:0.357
ISSN:1006-3536
年,卷(期):2025.53(1)