改性TiO2催化剂光催化降解盐酸四环素

IF 3 4区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES
Xiaoliang Yang, Hengcan Dai, Kangtao Yuan, Hao Tang, Zirui Luo
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引用次数: 0

摘要

结果表明,摩尔比为1:6的Ag₂S/TiO₂复合催化剂具有优异的颗粒分散性和均匀性,从而提高了光生载流子的迁移效率。XRD分析表明,Ag₂S和TiO₂催化剂分别为单斜晶型和锐钛矿型晶体结构,没有检测到额外的杂质峰。此外,不同摩尔比的催化剂对可见光的吸收发生了明显的红移,提高了催化剂的可见光响应能力。在最佳条件下,摩尔比为1:6,催化剂用量为1.0 g/L, pH为7,在可见光下反应210 min。当初始浓度为30 mg/L时,对TCH的去除率达90.72%。值得注意的是,在相同的最优条件下,即使经过5次重复使用,TCH的去除率仍保持在77.00%,具有良好的光催化稳定性。TCH的降解主要通过脱氨、去甲基和氢化途径进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Photocatalytic Degradation of Tetracycline Hydrochloride by Modified TiO2 Catalyst

Photocatalytic Degradation of Tetracycline Hydrochloride by Modified TiO2 Catalyst

The results demonstrated that the Ag₂S/TiO₂ composite catalyst with a molar ratio of 1:6 exhibited superior particle dispersion and uniformity, thereby enhancing the migration efficiency of photogenerated carriers. XRD analysis revealed that the Ag₂S and TiO₂ catalysts exhibited a monoclinic and anatase crystal structure, respectively, with no additional impurity peaks detected. Furthermore, the visible light absorption of the catalysts with different molar ratios underwent a significant redshift, which improved their visible light response capability. Under optimal conditions, where the molar ratio was 1:6, the catalyst dosage was 1.0 g/L, and the pH was 7, the reaction was conducted under visible light for 210 min. The removal efficiency of TCH reached 90.72% for an initial concentration of 30 mg/L. Notably, under the same optimal conditions, the removal efficiency of TCH remained at 77.00% even after five reuse cycles, indicating excellent photocatalytic stability. The degradation of TCH primarily occurred through deamination, demethylation, and hydrogenation pathways.

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来源期刊
Water, Air, & Soil Pollution
Water, Air, & Soil Pollution 环境科学-环境科学
CiteScore
4.50
自引率
6.90%
发文量
448
审稿时长
2.6 months
期刊介绍: Water, Air, & Soil Pollution is an international, interdisciplinary journal on all aspects of pollution and solutions to pollution in the biosphere. This includes chemical, physical and biological processes affecting flora, fauna, water, air and soil in relation to environmental pollution. Because of its scope, the subject areas are diverse and include all aspects of pollution sources, transport, deposition, accumulation, acid precipitation, atmospheric pollution, metals, aquatic pollution including marine pollution and ground water, waste water, pesticides, soil pollution, sewage, sediment pollution, forestry pollution, effects of pollutants on humans, vegetation, fish, aquatic species, micro-organisms, and animals, environmental and molecular toxicology applied to pollution research, biosensors, global and climate change, ecological implications of pollution and pollution models. Water, Air, & Soil Pollution also publishes manuscripts on novel methods used in the study of environmental pollutants, environmental toxicology, environmental biology, novel environmental engineering related to pollution, biodiversity as influenced by pollution, novel environmental biotechnology as applied to pollution (e.g. bioremediation), environmental modelling and biorestoration of polluted environments. Articles should not be submitted that are of local interest only and do not advance international knowledge in environmental pollution and solutions to pollution. Articles that simply replicate known knowledge or techniques while researching a local pollution problem will normally be rejected without review. Submitted articles must have up-to-date references, employ the correct experimental replication and statistical analysis, where needed and contain a significant contribution to new knowledge. The publishing and editorial team sincerely appreciate your cooperation. Water, Air, & Soil Pollution publishes research papers; review articles; mini-reviews; and book reviews.
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