间苯二酚-甲醛树脂和十二烷基硫酸钠共辅助介孔TiO2负载Ni3Sn2金属间化合物催化剂在水中甲醇作为氢供体原位加氢脱氧棕榈酸甲酯

IF 2.3 4区 化学 Q3 CHEMISTRY, PHYSICAL
Huanjin Jiang, Jie Yang, Wenhao Wang, Hailong Fang, Jixiang Chen
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引用次数: 0

摘要

以间苯二酚-甲醛树脂(RF)和十二烷基硫酸钠(SDS)为模板,采用共沉淀法制备了负载TiO2的Ni3Sn2金属间化合物(IMC)催化剂,并对其在水相中以甲醇为供氢剂的棕榈酸甲酯进行了原位加氢脱氧(HDO)测试。研究发现,SDS和RF的引入提高了Ni3Sn2 IMC粒子的比表面积、孔体积和孔径,降低了Ni3Sn2 IMC粒子与TiO2的电子相互作用。在棕榈酸甲酯的原位HDO中,共引入RF和SDS制备的催化剂比不引入模板和单独引入RF和SDS制备的催化剂表现出更高的活性。催化剂活性主要与Ni3Sn2 IMCs的粒径大小以及Ni3Sn2与TiO2之间的电子相互作用程度有关。在330℃下,加入适量RF和SDS的催化剂的正戊烷产率为87.3%,反应5次后由于积碳和Ni3Sn2 IMC颗粒的烧结而发生轻微失活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resorcinol–Formaldehyde Resin and Sodium Dodecyl Sulfate Co-assisted Mesoporous TiO2 Supported Ni3Sn2 Intermetallic Compound Catalysts for In-Situ Hydrodeoxygenation of Methyl Palmitate with Methanol as the Hydrogen Donor in Water

TiO2 supported Ni3Sn2 intermetallic compound (IMC) catalysts were prepared by the coprecipitation method using resorcinol–formaldehyde resin (RF) and sodium dodecyl sulfate (SDS) as templates, and they were tested for in situ hydrodeoxygenation (HDO) of methyl palmitate using methanol as the hydrogen donor in the aqueous phase. It has been found that introducing SDS and RF enhances specific surface area, pore volume and pore diameter and reduces the Ni3Sn2 IMC particles and their electronic interaction with TiO2. In in situ HDO of methyl palmitate, the catalysts prepared with co-introducing RF and SDS exhibit higher activity than that without templates and those separately introducing RF and SDS. The catalyst activity is mainly related to the Ni3Sn2 IMCs particles size and the degree of the electronic interaction between Ni3Sn2 and TiO2. The catalyst with introducing a suitable amount of RF and SDS gives the n-pentadecane yield of 87.3% at 330 °C, and it is slightly deactivated after reaction for five times due to carbon deposition and the sintering of Ni3Sn2 IMC particles.

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来源期刊
Catalysis Surveys from Asia
Catalysis Surveys from Asia 化学-物理化学
CiteScore
4.80
自引率
0.00%
发文量
29
审稿时长
>12 weeks
期刊介绍: Early dissemination of important findings from Asia which may lead to new concepts in catalyst design is the main aim of this journal. Rapid, invited, short reviews and perspectives from academia and industry will constitute the major part of Catalysis Surveys from Asia . Surveys of recent progress and activities in catalytic science and technology and related areas in Asia will be covered regularly as well. We would appreciate critical comments from colleagues throughout the world about articles in Catalysis Surveys from Asia . If requested and thought appropriate, the comments will be included in the journal. We will be very happy if this journal stimulates global communication between scientists and engineers in the world of catalysis.
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