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机构地区:[1]许昌学院化学化工学院,河南许昌461000 [2]厦门大学化学化工学院,固体表面物理化学国家重点实验室,福建厦门361005
出 处:《贵金属》2010年第3期1-6,共6页Precious Metals
基 金:国家重点基础研究发展规划“973”项目(2005CB221400);国家自然科学基金项目(20473063和20590364)
摘 要:通过乙二醇液相还原法将少量金属Ru沉积在碳纳米管(简称CNTs)上,TEM、XRD表征结果表明,该法明显提高了Ru在CNTs上的分散度,Ru微晶的粒径在3~4 nm。氨分解反应结果表明,采用乙二醇液相还原法在降低Ru负载量的同时还明显提高了Ru/CNTs的催化氨分解活性。在0.4 MPa、773 K、空速GHSV100%NH3=30 000 mL/(h.g)反应条件下,在液相还原法制备的4.2%Ru/CNTs催化剂上氨分解转化率可达48.5%,约为同条件下浸渍法所得5%Ru/CNTs的1.3倍,液相还原最佳配比5.7%Ru/γ-Al2O3的1.2倍。表观活化能测试结果显示用CNTs代替γ-Al2O3作为载体或分散相并不引起所负载Ru催化剂上NH3分解制H2反应的表观活化能发生明显变化。Nowadays catalytic decomposition of ammonia is regarded as a method to obtain COfree hydrogen for its application in proton exchange membrane fuel cell.In this paper,with carbon nano-tubes(as CNTs) as substrate,a series of metallic Ru/CNTs were prepared using glycol reduction-deposition method which enhanced markedly dispersion of Ru on CNTs with the Rux0-crystallite size at 3~4 nm characterized through TEM and XRD.Under reaction conditions of 0.4 MPa,773 K and GHSV100%NH3 = 30 000 mL/(h·g),the observed NH3-decomposition conversion over the 4.2%Ru/CNTs catalyst(prepared through ethylene-glycol reduction-deposition) reached 48.5%,which was about 1.2 times as high as that of the 5.7%Ru/γ-Al2O3 catalyst prepared by the same method,and about 1.3 times as high as that of the 5%Ru/CNTs catalyst prepared by conventional incipient wetness method.Over the 4%Ru/CNTs catalyst,100% of NH3-decomposition was attained at 870 K;while over 5%Ru/CNTs prepared by conventional incipient wetness method,the reaction temperature as high as 900 K was required for the same(100%) conversion.At 870 K,the observed NH3-decomposition conversion was only 81.7% over the 5.7%Ru/γ-Al2O3 catalyst.It was experimentally also found that using the CNTs in place of γ-Al2O3 as support of the metal Ru-catalyst did not cause a marked change in the apparent activation energy(Ea) for the reaction of NH3-decomposition to yield H2.
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