首页|多孔型TiO2微粒的制备及其对离子型染料的吸附

多孔型TiO2微粒的制备及其对离子型染料的吸附

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针对印染废水中离子型染料的处理问题,提出以多孔型二氧化钛(TiO2)微粒为吸附剂对染料进行吸附处理.以钛酸丁酯为钛源,通过改变模板剂的种类,采用水热法制备带有不同电位的多孔型TiO2 微粒.借助固体表面Zeta电位测试仪、场发射扫描电子显微镜、透射电子显微镜以及X射线衍射仪对TiO2 的电位、形貌和晶型进行分析,通过吸附实验优化染料质量浓度和吸附剂用量,并探究TiO2 微粒的重复利用性能.结果表明:带正电的TiO2 微粒(G-TiO2)和带负电的TiO2 微粒(Y-TiO2)分别只对阴离子型和阳离子型染料进行吸附,遵从静电吸附机制;2 种TiO2 微粒经过煅烧后的晶型均为锐钛矿型;在同等实验条件下,100 mg的G-TiO2 对100 mg/L刚果红染料的吸附率高达 99.5%,100 mg的Y-TiO2 对 20 mg/L亚甲基蓝染料的吸附率可达93.5%;在循环实验中,G-TiO2 对刚果红染料循环吸附 4 次后吸附率降低约 12.6%,而Y-TiO2 对亚甲基蓝染料循环吸附 5 次后吸附率降低约 17%.
Preparation of porous TiO2 particles and their adsorption for ionic dyes
Objective The utilization rate of dyes is unable to reach 100%in practical situations,which inevitably leads to residual dyes in the water discharged after dyeing,causing serious water pollution.Therefore,it is necessary to develop a water treatment technology that can effectively treat dye wastewater.Aiming at the treatment of ionic dyes in printing and dyeing wastewater,porous titana(TiO2)particles were used as adsorbent to adsorb dyes.Method In addition to the characteristics of stable chemical properties,low price,easy availability,and no toxicity,TiO2 particles also have the unique characteristic of photocatalysis.Therefore,TiO2 particles are often adopted to adsorb and catalyze dyes in wastewater.Through photocatalysis,the dye can be degraded,so that the TiO2 particles can be reused.With tetrabutyl orthotitanate as titanium source,porous TiO2 particles with different potentials were prepared by hydrothermal method using different templates,and then the crystal form of TiO2 particles was controlled by high-temperature calcination.The potential,morphology and crystal form of TiO2 were analyzed by solid surface Zeta potential test,field emission scanning electron microscopy(FETEM),transmission electron microscopy(TEM)and X-ray diffraction(XRD).The dye concentration and adsorbent dosage were optimized by adsorption test,and the reuse performance of TiO2 particles was explored.Results Positively charged TiO2 particles(G-TiO2)adsorb anionic dyes only other than cationic dyes at all,while the negatively charged TiO2 particles(Y-TiO2)only adsorb cationic dyes other than anionic dyes(Fig.3 and Fig.4).The adsorption mechanism follows the electrostatic adsorption mechanism.G-TiO2 has a porous spherical structure formed by the aggregation of numerous particles,about 93%of which are microspheres with a particle size of 200-500 nm.Y-TiO2 is in the state of fine particle aggregation,and about 91%of which are microspheres with a particle size of 50-100 nm(Fig.6 and Fig.7).The crystal forms of the two kinds of TiO2 particles after calcination are anatase,which have photocatalytic properties(Fig.9).Under the same experimental conditions,the adsorption rate of 100 mg/L Congo Red dye by 100 mg G-TiO2 can reach 99.5%,and that of 20 mg/L Methylene Blue dye by 100 mg Y-TiO2 can reach 93.5%(Fig.11).In the cycle experiment,the adsorption rate of Congo Red dye by G-TiO2 decreased by about 12.6%after four cycles,while that of Methylene Blue dye by Y-TiO2 decreased by about 17%after five cycles(Fig.13).Conclusion Two kinds of porous TiO2 particles adsorbents were prepared by changing the type of template in the hydrothermal reaction.The adsorbents not only retain the capillary adsorption of conventional porous TiO2 particles on dyes,but also increase the electrostatic adsorption,which can realize the rapid adsorption of ionic dyes in printing and dyeing wastewater.The adsorbents can be chemically modified subsequently to have improved photocatalytic performance,and can also be loaded on polymer films or nonwovens for specific applications.This study will provide strategic support for the treatment of ionic dye wastewater.

printing and dyeing wastewaterionic dyeadsorption treatmentporoustitania microspherereuse

黄彪、郑莉娜、秦妍、程羽君、李成才、朱海霖、刘国金

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浙江理工大学 浙江省纤维材料和加工技术研究重点实验室,浙江 杭州 310018

绍兴市质量技术监督检测院,浙江 绍兴 312000

浙江省现代纺织技术创新中心,浙江 绍兴 312000

印染废水 离子型染料 吸附处理 多孔 TiO2微粒 重复利用性能

浙江理工大学青年创新专项项目

22202303-Y

2023

纺织学报
中国纺织工程学会

纺织学报

CSTPCDCSCD北大核心
影响因子:0.699
ISSN:0253-9721
年,卷(期):2023.44(11)
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