茶叶梗/BiOBr复合催化剂的制备及其光催化性能研究

康巧梅, 吴非彦

化工新型材料 ›› 2026, Vol. 54 ›› Issue (6) : 214 -219.

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化工新型材料 ›› 2026, Vol. 54 ›› Issue (6) : 214-219. DOI: 10.19817/j.cnki.issn1006-3536.2026.06.006
科学研究

茶叶梗/BiOBr复合催化剂的制备及其光催化性能研究

    康巧梅, 吴非彦
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Preparation and photocatalytic performance of tea stem/BiOBr composite catalysts

  • Kang Qiaomei, Wu Feiyan
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摘要

以茶叶梗和溴氧化铋(BiOBr)作为主要原料,制备了茶叶梗/BiOBr复合催化剂。采用X射线衍射仪、紫外-可见漫反射光谱仪、全自动比表面积及孔隙分析仪、X射线光电子能谱仪、扫描电子显微镜等对催化剂样品进行表征与分析,探究了复合催化剂的降解效果以及对不同染料的光催化降解性能。结果表明:茶叶梗/BiOBr复合催化剂比纯BiOBr具有更好的光催化降解稳定性,且具有良好的结晶度,禁带宽度为2.66eV,比表面积为628.792m2/g;当茶叶梗与BiOBr质量比为3∶1时,茶叶梗/BiOBr复合催化剂的光催化效果最佳;投加15mg复合催化剂处理100mL质量浓度20mg/L罗丹明B溶液,在250W氙灯下照射90min,罗丹明B降解率可达94.72%。

Abstract

Tea stem/BiOBr composite catalysts were prepared using tea stems and bismuth oxybromide (BiOBr) as the main raw materials.The catalyst samples were characterized and analyzed by X-ray diffraction (XRD),ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS),automatic specific surface area and porosity analyzer,X-ray photoelectron spectroscopy (XPS),and scanning electron microscopy (SEM).The degradation effects of the composite catalysts and their photocatalytic degradation performance for different dyes were investigated.The results showed that the tea stem/BiOBr composite catalyst exhibited better photocatalytic degradation stability than pure BiOBr,along with good crystallinity,an optical band gap of 2.66eV and a specific surface area of 628.792m2/g.When the mass ratio of tea stems to BiOBr was 3∶1,the tea stem/BiOBr composite catalyst achieved the optimal photocatalytic effect.When 15mg of the composite catalyst was added to treat 100mL of 20mg/L Rhodamine B solution and irradiated under a 250W xenon lamp for 90 minutes,the degradation rate of Rhodamine B reached 94.72%.

关键词

茶叶梗 / BiOBr / 光催化降解 / 罗丹明B / 光催化活性

Key words

tea stems / BiOBr / photocatalytic degradation / Rhodamine B / photocatalytic activity

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茶叶梗/BiOBr复合催化剂的制备及其光催化性能研究[J]. 化工新型材料, 2026, 54(6): 214-219 DOI:10.19817/j.cnki.issn1006-3536.2026.06.006

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基金资助

环境科学省级一流专业建设(SJZY-2022-02)

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