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Fe/N共掺杂纳米TiO_2光催化降解室内甲醛的实验研究 被引量:3

The experimental research on the degradation of formaldehyde by photocatalysis of Fe/N co-doped TiO_2
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摘要 采用溶胶—凝胶法制备了纯TiO2、Fe-TiO2、N-TiO2以及Fe-N-TiO2,并将其负载于瓷砖上,使用XRD和SEM技术对薄膜样品的晶型和表面形态进行表征,以甲醛为目标降解物,测试其光催化降解效果。结果表明,Fe-N-TiO2(500℃)光催化剂以锐钛矿结构为主,粒径分布均匀,平均粒径较小。共掺杂离子的掺杂量、掺杂配比和光催化剂的煅烧温度均影响纳米TiO2的光催化性能,当掺杂配比为n(Fe)∶n(N)∶n(TiO2)=0.1%∶1%∶1、煅烧温度为500℃时,Fe-N共掺杂样品对甲醛降解效率最高,在紫外光照射下Fe-N-TiO2在2 h内对甲醛的降解率达到53%,高于Fe-TiO2的45%、N-TiO2的43%和纯TiO2的25%。 TiO2,Fe-TiO2,N-TiO2,and Fe-N co-doped TiO2 were prepared by were prepared by sol-gel method,and then loaded on the faces of enamel tiles,the surface morpho-logies and crystalline properties were characterized by X-ray diffraction(XRD) and Scanning electron microscope(SEM),and its photocatalysis properties were studied by photocatalytical degradation of formaldehyde.The results indicated,the prepared co-doped TiO2 was mostly presented to be anatase,the diameter of particals were pretty small and well-distributed.The photocatalytic activity of the co-doped TiO2 is mainly affected by factors such as doping content、doping ratio and calcinate temperature.When the co-doping amount(in molar ratio) for Fe-N is n(Fe)∶n(N)∶n(TiO2)=0.1%∶1%∶1 and the temperature of heat treatment is 500℃,in 2 hours and under UV light,Fe-N-TiO2's degradation efficiency to formaldehyde is 53%,higher than Fe-TiO2's 45%、N-TiO2's 43% and much higher than pure TiO2's 25%.
出处 《微量元素与健康研究》 CAS 2010年第2期54-56,共3页 Studies of Trace Elements and Health
关键词 溶胶—凝胶法 降解效果 共掺杂 光催化性能 sol-gel method degradation effect co-dope activities of photochemical catalysis
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  • 1杨南如,余桂郁.溶胶-凝胶法简介第一讲——溶胶-凝胶法的基本原理与过程[J].硅酸盐通报,1993,12(2):56-63. 被引量:133
  • 2CHOI WONYONG, KO JOUNGYUN, PARK HYUNWOONG. Investigation on coated optical fibers for gas-phase Photoeatalytic oxidation of acetone[J]. Applied Catalysis B : Enviromental,2001,31 (3) :209 - 220.
  • 3HARIZANOV O, IVANOVA T, HARIZANOVA A. Study of sol-gel Ti02 and TiO2-MnO obtained from a peptized solution[ J ]. Materials Letters,2001,49(3 - 4) : 165 - 171.
  • 4PISCOPO A, ROBERT D, WEBER J V. Comparison between the reactivity of commercial and synthetic TiO2 photocatalysts[ J ]. Journal of Photochemistry and Photobiology A : Chemistry, 2001,139(2) :253 - 256.
  • 5RACHEL A, SUBBAHMANYAM M, BOULE P.Comparison of photocatalytic efficiencies of TiO2 in suspended and immobifised form for the photoeatalytic degration of nitrobenzenesulfonic acids[ J ].Applied Catalysis B : Environmental, 2002,37 (4) :301 - 308.
  • 6FUJISHIMA A. Titanium dioxide photocatalysis[J]. Journal of Photochemistry and Photobiology C : Photochemical Reviews, 2000,1 ( 1 ) : 1 - 22.
  • 7FUJISHIMA A, TATA N R, DONALD A T. TiO2 Photocatalysts and diamond electrodes [ J ]. Electrochimica Acta 2000,45:4 683 -4 690.
  • 8Fujishima A, Honda K. Electrochemical Photolysis of Water at a Semiconductor Electrode[J]. Nature,1972, 238: 37-38.
  • 9Hiramoto M. Electron transfer and photoluminescence dynamics of CdS particles deposited on porous vycor glass[J]. Chem Phys Lett, 1987,133: 440-444.
  • 10Legrini O, Oliveros E, Braun A M. Photochemical processes for water treatment [J]. Chemical Reviews,1993, 93(2): 671-699.

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