采用浸渍法制备了表面键联型TiO2/SiO2固定化光催化剂.XRD,FT-IR,XPS和BET比表面积测定结果表明,TiO2通过Ti-O-Si联结载于多孔硅胶的表面,由此提出TiO2/SiO2的结构模型.考察了多孔硅胶的粒度及氧化钛负载量对催化剂活性的影响.对活性艳红K-2G(R15)的光催化脱色反应,最佳的光催化剂30%TiO2/SiO2(Ims30)比B-TiO2粉末的催化速率快3倍.随着载体粒度的减小,催化剂的比表面积增大,催化活性升高;多孔硅胶不仅起着支持体的作用,而且具有分散的作用;多孔硅胶具有很好的透光性.经ξ-电位测定,所制备催化剂的等电点为3.0pH单位,表明催化剂表面呈酸性.
Surface bond-conjugated TiO2/SiO2 catalyst was prepared by m eansof impregnation method with cyclohexane solution of tetrabutyl titanate. The catalyst overcomes the difficulty of liquid-solid separation owing to the formation of milky dispersion after mixing the powdered TiO2 in water. Based on the results of XRD, FT-IR, XPS and BET measurements, the growth of TiO2 (predominantly anatase) on the SiO2 support seems to occur by anchoring the TiO2 phase through Ti-O-Si cross-linking bonds. The struct ure model of TiO2/SiO2 was proposed. Compared with B-TiO2, the most efficient catalyst is 30%TiO2/SiO2 (Ims 30), which showed three times higher pho toactivity for degradation of reactive brilliant red K-2G(R15). In addition, the catalyst had higher photoactivity and bigger specific surface area on SiO2 with smaller particle size than on that with larger particle size. SiO2 gel plays the basic roles of dispersion and support for powder TiO-. Meanwhile, SiO2 gel ha s better tra nsmission for light. The isoelectronic point of the catalyst was3.0 pH units by measurement of zeta-potential, indicating the presence of acidity on the catalyst surface.
参考文献
[1] | 朱永法,张利,姚文清,曹立礼.溶胶-凝胶法制备薄膜型TiO2光催化剂[J].催化学报,1999(03):362-364. |
[2] | Xu Y M;Zheng W;Liu W P .[J].Journal of Photochemistry and Photobiology A:Chemistry,1999,122(01):57. |
[3] | Haarstrick A;Kut O M;Heinzle E .[J].Environmental Science and Technology,1996,30(03):817. |
[4] | Torimoto T;Ito S;Kuwabata S .[J].Environmental Science and Technology,1996,30(04):1275. |
[5] | Takeda N;Ohtani M;Torimoto T .[J].Journal of Physical Chemistry B,1997,101(14):2644. |
[6] | Xu Y M;Langford C H .[J].Journal of Physical Chemistry,1995,99(29):11501. |
[7] | Green K J;Rudham R .[J].Journal of the Chemical Society,Faraday Transactions,1993,89(11):1867. |
[8] | Lassaletta G;Fernandez A;Espinos J P .[J].Journal of Physical Chemistry,1995,99(05):1484. |
[9] | acsa R R;Kiwi J .[J].Applied Catalysis B:Environmental,1998,16(01):19. |
- 下载量()
- 访问量()
- 您的评分:
-
10%
-
20%
-
30%
-
40%
-
50%