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在Pt-TiO上通过丁酸光重整制氢和丙烷

Hydrogen and Propane Production From Butyric Acid Photoreforming Over Pt-TiO.

作者信息

Scandura Gabriele, Rodríguez Jorge, Palmisano Giovanni

机构信息

Department of Chemical Engineering, Masdar Institute Campus, Khalifa University, Abu Dhabi, United Arab Emirates.

Research and Innovation Center on CO2 and H2 (RICH), Khalifa University, Abu Dhabi, United Arab Emirates.

出版信息

Front Chem. 2019 Aug 7;7:563. doi: 10.3389/fchem.2019.00563. eCollection 2019.

Abstract

Photocatalysis is a promising technology from economic, energetic, and ecological points of view because it takes advantage of solar light. Hence, it is one of the investigated green routes to produce hydrogen from renewable energy resources. Butyric acid (BA) is largely present in wastewater and as an intermediate product in anaerobic digestion and therefore it is an inexpensive resource, which can be converted to valuable chemicals. In this work, photoreforming of butyric acid (BAPR) under UV light in aqueous suspensions of platinum-modified titanium dioxide-based catalysts is reported for the first time. Titania nanotubes (TNT) synthesized and calcined at different temperatures (300, 400, 500°C) and commercial TiO (P25), decorated with platinum nanoparticles, have been tested and characterized through different techniques including X-ray powder diffraction, UV-vis diffuse reflectance and photoluminescence spectroscopy, transmission electron microscopy, BET and porosimetry analysis. The main identified products of the BAPR were H, propane, CO and several organic acids (e.g., pentanoic and 3-methylhexanoic acid). It has been found that the morphology and crystallinity of the photocatalysts affected dramatically their optical properties and, consequently, the reaction rate and the product distribution. Specifically, the highest conversion of BA (X) and selectivity toward H (S) was recorded with P25-Pt (X = 26.9%, S = 47.2% after 8 h of irradiation). TNT-400-Pt showed the highest selectivity toward propane (S = 16.1%) with X = 23.4% and S = 36.2%. The activity results in conjunction with the characterization of the catalysts highlighted that the main factor affecting the activity in terms of X and generation of H was the crystallinity, and in particular the presence of rutile phase in TiO, whereas S appears to increase when the electron-holes recombination is lower.

摘要

从经济、能源和生态角度来看,光催化是一项很有前景的技术,因为它利用太阳光。因此,它是从可再生能源资源生产氢气的研究中的绿色途径之一。丁酸(BA)大量存在于废水中,并且是厌氧消化的中间产物,因此它是一种廉价的资源,可以转化为有价值的化学品。在这项工作中,首次报道了在铂改性的二氧化钛基催化剂的水悬浮液中,紫外光下丁酸的光重整(BAPR)。合成并在不同温度(300、400、500°C)下煅烧的二氧化钛纳米管(TNT)以及负载铂纳米颗粒的商用TiO₂(P25),已通过不同技术进行了测试和表征,包括X射线粉末衍射、紫外可见漫反射和光致发光光谱、透射电子显微镜、BET和孔隙率分析。BAPR的主要鉴定产物是H₂、丙烷、CO和几种有机酸(例如戊酸和3 - 甲基己酸)。已经发现,光催化剂的形态和结晶度极大地影响了它们的光学性质,因此也影响了反应速率和产物分布。具体而言,P25 - Pt记录到最高的BA转化率(X)和对H₂的选择性(S)(照射8小时后,X = 26.9%,S = 47.2%)。TNT - 400 - Pt对丙烷的选择性最高(S = 16.1%),X = 23.4%,S = 36.2%。活性结果与催化剂的表征相结合,突出表明就X和H₂生成而言,影响活性的主要因素是结晶度,特别是TiO₂中金红石相的存在,而当电子 - 空穴复合较低时,S似乎会增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b81/6692698/81ee67eb4219/fchem-07-00563-g0001.jpg

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