甲酸在鈀基催化劑下的脫氫性能研究
發(fā)布時間:2018-10-31 09:27
【摘要】:本文主要是通過浸漬法將已改性好的NH_2-SBA-15載體分別負載不同比例的Ag-Pd和Au-Pd,分別得到了Ag-Pd/NH_2-SBA-15體系和Au-Pd/NH_2-SBA-15體系的兩個體系的催化劑。在Ag-Pd/NH_2-SBA-15體系中,催化劑催化活性最好是Ag1Pd9/NH_2-SBA-15,在323 K時,Ag1Pd9/NH_2-SBA-15催化劑的TOF的值高達964 h-1。在Au-Pd/NH_2-SBA-15體系中,催化活性最好的是Au2Pd8/NH_2-SBA-15,在323 K時,Au2Pd8/NH_2-SBA-15催化劑的TOF非常高,達到了1786 h-1,催化效果極好。兩個的體系催化劑在經(jīng)過五次循環(huán)使用后,催化性能依然良好。催化劑的催化性能符合工業(yè)催化的基本規(guī)律,即隨著溫度升高,催化劑的的催化活性越高。甲酸鈉的量會對甲酸脫氫的催化劑影響很大,甲酸鈉的濃度越大,會提高甲酸脫氫的催化劑的性能。進一步通過XRD、TEM、XPS、GC等表征手段對制備的催化劑的內(nèi)部結(jié)構(gòu)進行分析和探究,Ag-Pd/NH_2-SBA-15體系和Au-Pd/NH_2-SBA-15兩個體系的催化劑均形成納米顆粒合金結(jié)構(gòu),化學性質(zhì)穩(wěn)定,且Ag1Pd9/NH_2-SBA-15和Au2Pd8/NH_2-SBA-15脫氫選擇性均是100%。
[Abstract]:In this paper, the modified NH_2-SBA-15 carrier was loaded with different proportion of Ag-Pd and Au-Pd, by impregnation method. The catalysts of Ag-Pd/NH_2-SBA-15 system and Au-Pd/NH_2-SBA-15 system were obtained respectively. In Ag-Pd/NH_2-SBA-15 system, the best catalytic activity of the catalyst is when Ag1Pd9/NH_2-SBA-15, is 323K, the value of TOF of Ag1Pd9/NH_2-SBA-15 catalyst is as high as 964h-1. In the Au-Pd/NH_2-SBA-15 system, the best catalytic activity is that when Au2Pd8/NH_2-SBA-15, is 323K, the TOF of Au2Pd8/NH_2-SBA-15 catalyst is very high, reaching 1786 h-1, and the catalytic effect is excellent. After five cycles, the catalytic performance of the two catalysts is still good. The catalytic activity of the catalyst accords with the basic law of industrial catalysis, that is, the higher the temperature, the higher the catalytic activity of the catalyst. The amount of sodium formate will have a great influence on the catalyst for the dehydrogenation of formic acid. The higher the concentration of sodium formate, the better the performance of the catalyst for dehydrogenation of formic acid. The internal structure of the prepared catalyst was further analyzed and explored by means of XRD,TEM,XPS,GC and other characterization methods. The catalysts of Ag-Pd/NH_2-SBA-15 system and Au-Pd/NH_2-SBA-15 system both formed nanocrystalline alloy structure and their chemical properties were stable. The dehydrogenation selectivity of both Ag1Pd9/NH_2-SBA-15 and Au2Pd8/NH_2-SBA-15 is 100.
【學位授予單位】:安徽工業(yè)大學
【學位級別】:碩士
【學位授予年份】:2017
【分類號】:O621.251
本文編號:2301664
[Abstract]:In this paper, the modified NH_2-SBA-15 carrier was loaded with different proportion of Ag-Pd and Au-Pd, by impregnation method. The catalysts of Ag-Pd/NH_2-SBA-15 system and Au-Pd/NH_2-SBA-15 system were obtained respectively. In Ag-Pd/NH_2-SBA-15 system, the best catalytic activity of the catalyst is when Ag1Pd9/NH_2-SBA-15, is 323K, the value of TOF of Ag1Pd9/NH_2-SBA-15 catalyst is as high as 964h-1. In the Au-Pd/NH_2-SBA-15 system, the best catalytic activity is that when Au2Pd8/NH_2-SBA-15, is 323K, the TOF of Au2Pd8/NH_2-SBA-15 catalyst is very high, reaching 1786 h-1, and the catalytic effect is excellent. After five cycles, the catalytic performance of the two catalysts is still good. The catalytic activity of the catalyst accords with the basic law of industrial catalysis, that is, the higher the temperature, the higher the catalytic activity of the catalyst. The amount of sodium formate will have a great influence on the catalyst for the dehydrogenation of formic acid. The higher the concentration of sodium formate, the better the performance of the catalyst for dehydrogenation of formic acid. The internal structure of the prepared catalyst was further analyzed and explored by means of XRD,TEM,XPS,GC and other characterization methods. The catalysts of Ag-Pd/NH_2-SBA-15 system and Au-Pd/NH_2-SBA-15 system both formed nanocrystalline alloy structure and their chemical properties were stable. The dehydrogenation selectivity of both Ag1Pd9/NH_2-SBA-15 and Au2Pd8/NH_2-SBA-15 is 100.
【學位授予單位】:安徽工業(yè)大學
【學位級別】:碩士
【學位授予年份】:2017
【分類號】:O621.251
【參考文獻】
相關(guān)期刊論文 前10條
1 閆國慶;;甲酸生產(chǎn)工藝技術(shù)及其市場應(yīng)用探討[J];企業(yè)技術(shù)開發(fā);2014年03期
2 張敏;周婧斐;沈崢;周雪飛;張亞雷;陳杰;;甲酸用途與生產(chǎn)的研究進展[J];安徽農(nóng)業(yè)科學;2012年01期
3 楊明;王圣平;張運豐;韓波;吳金平;程寒松;;儲氫材料的研究現(xiàn)狀與發(fā)展趨勢[J];硅酸鹽學報;2011年07期
4 余瑞萍;;用作儲氫材料的碳納米管[J];科技創(chuàng)新導報;2011年20期
5 周素芹;程曉春;居學海;朱小紅;;儲氫材料研究進展[J];材料科學與工程學報;2010年05期
6 賴文忠;戈芳;李星國;;儲氫材料的新載體——金屬有機框架材料[J];大學化學;2010年03期
7 郭麗霞;李海華;郭紅霞;;碳納米管儲氫的研究[J];河北工業(yè)科技;2010年03期
8 范士鋒;;金屬儲氫材料研究進展[J];化學推進劑與高分子材料;2010年02期
9 陶占良;彭博;梁靜;程方益;陳軍;;高密度儲氫材料研究進展[J];中國材料進展;2009年Z1期
10 陳軍;朱敏;;高容量儲氫材料的研究進展[J];中國材料進展;2009年05期
相關(guān)碩士學位論文 前1條
1 洪兵;負載型Ni-Pt納米催化劑的制備及用于水合肼催化性能的研究[D];安徽工業(yè)大學;2016年
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