湖南理工学院学报(自然科学版)
湖南理工學院學報(自然科學版)
호남리공학원학보(자연과학판)
JOURNAL OF HUNAN INSTITUTE OF SCIENCE AND TECHNOLOGY(NATURAL SCIENCE)
2015年
1期
66-71
,共6页
严彬彬%金献华%谭广华%陈燕%张丽
嚴彬彬%金獻華%譚廣華%陳燕%張麗
엄빈빈%금헌화%담엄화%진연%장려
水滑石%光催化剂%二氧化碳
水滑石%光催化劑%二氧化碳
수활석%광최화제%이양화탄
hydrotalcite%photocatalyst%CO2
采用水热法制备ZnMnAl-CO3类水滑石,再经焙烧制备纳米锌锰铝三元复合金属氧化物光催化剂.采用X射线衍射表征了催化剂的组成结构.在模拟太阳光下,通过光催化降解甲基橙和还原CO2来考察样品的光催化活性,并探讨论了各种金属离子比、焙烧前后及焙烧温度对光催化活性的影响.结果表明:当锌、锰和铝的摩尔比为3:1:1、400℃焙烧时所得的样品,具有很强的CO2还原活性,明显优于对甲基橙的降解.当NaOH与Na2SO3的质量比为1.6:5.04时,催化剂加入量为1g/L,反应6h所得CO2的主要还原产物甲醇最多,峰面积达89.7%,说明该样品对减排温室气体具有潜在的应用前景.
採用水熱法製備ZnMnAl-CO3類水滑石,再經焙燒製備納米鋅錳鋁三元複閤金屬氧化物光催化劑.採用X射線衍射錶徵瞭催化劑的組成結構.在模擬太暘光下,通過光催化降解甲基橙和還原CO2來攷察樣品的光催化活性,併探討論瞭各種金屬離子比、焙燒前後及焙燒溫度對光催化活性的影響.結果錶明:噹鋅、錳和鋁的摩爾比為3:1:1、400℃焙燒時所得的樣品,具有很彊的CO2還原活性,明顯優于對甲基橙的降解.噹NaOH與Na2SO3的質量比為1.6:5.04時,催化劑加入量為1g/L,反應6h所得CO2的主要還原產物甲醇最多,峰麵積達89.7%,說明該樣品對減排溫室氣體具有潛在的應用前景.
채용수열법제비ZnMnAl-CO3류수활석,재경배소제비납미자맹려삼원복합금속양화물광최화제.채용X사선연사표정료최화제적조성결구.재모의태양광하,통과광최화강해갑기등화환원CO2래고찰양품적광최화활성,병탐토론료각충금속리자비、배소전후급배소온도대광최화활성적영향.결과표명:당자、맹화려적마이비위3:1:1、400℃배소시소득적양품,구유흔강적CO2환원활성,명현우우대갑기등적강해.당NaOH여Na2SO3적질량비위1.6:5.04시,최화제가입량위1g/L,반응6h소득CO2적주요환원산물갑순최다,봉면적체89.7%,설명해양품대감배온실기체구유잠재적응용전경.
ZnMnAl-LDHs have been prepared via hydrothermal method. ZnMnAl mixed-metal oxide photocatalyst was derived from a ternary hydrotalcite-like precursor followed by controllable calcination temperature. The as-prepared samples were characterized by X-ray diffraction (XRD). The effects of the molar ratio of metal ion in the material, calcination before and after and calcination temperature on the structure and morphology of the as-prepared samples were investigated in detail. The results indicated that a single layered double hydroxide (LDH) precursor leads to a well-crystalline ternary oxide photocatalyst. The photocatalyst shows superior photocatalytic reduction of CO2 compared to the photodegradation of methyl orange (MO) under simulated sunlight irradiation. When the mass ratio of NaOH to NaCO3 is 1.6:5.04, the amount of photocatalyst is 1 g/L, the highest methanol yield can be obtained in 6 hours, most chromatographic area reached 89.7%. The present work demonstrated their potential as photocatalysts for photocatalytic CO2 reduction.