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31.
Sevda Dehghani Ahad Hanifpour Mehdi Nekoomanesh-Haghighi Samahe Sadjadi Seyed Amin Mirmohammadi Ali Farhadi Naeimeh Bahri-Laleh 《应用聚合物科学杂志》2020,137(22):49018
The main aim of this research is to decrease the amount of AlCl3 content that is very corrosive and hazardous in the catalytic system, required for the α-olefin oligomerization without substantial change of final oil features. This was successfully achieved by supporting AlCl3 on different carriers. More precisely, a series of supported bimetallic catalysts was synthesized by immobilization of AlCl3 and TiCl4 onto Al2O3, SiO2, and mixed supports, that is, Al2O3/FeCl3 and SiO2/FeCl3. It was found that silica and alumina-based catalysts had higher catalytic activities compared to support free AlCl3; however, this enhancement for silica-based supports was more significant. According to gel permeation chromatography (GPC) results, the use of single supports, that is, Al2O3 and SiO2, increased oligomer's molecular weight, while the application of mixed supports resulted in the decrease of molecular weight of the oligomers. Viscosity characteristics of the synthesized oligomers have also been studied at two different temperatures of 40 and 100°C (KV40 and KV100). The viscosity index (VI) values, derived from KV40 and KV100, of the prepared oligomers were in the range of 126–145. The molecular weight and termination mechanisms of the oligomers were studied by 1H-NMR spectroscopy. The obtained results disclosed that the employed reaction conditions led to the production of oligomer chains with various structures including vinylidene (Vd), and di and three-substituted vinylene (2Vn, 3Vn) structures. 相似文献
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以碱式碳酸镍、碱式碳酸锌、碱式碳酸铜和水泥为原料制备水泥负载的Cu-Ni,Cu-Zn,Cu-Ni-Zn催化剂,考察了合成催化剂的甲醇裂解反应性能。结果表明:在常压、质量空速为3.39 h-1、温度为380~420 ℃的条件下,Cu-Ni/水泥催化剂作用下的甲醇转化率均在96%以上;Cu-Zn/水泥催化剂作用下的甲醇转化率较低,但对H2和CO选择性较高;Cu-Ni-Zn/水泥催化剂经1 600 h运转,甲醇转化率和产物分布变化不大,甲醇转化率基本维持在81%以上,(H2+CO)摩尔分数大于98%,说明Cu-Ni-Zn/水泥催化剂具有良好的高温稳定性。 相似文献
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35.
Xiuhui Huang Junfeng Li Jun Wang Zeqiu Li Jiayin Xu 《Frontiers of Chemical Science and Engineering》2020,14(4):534
In the last decades, many reports dealing with technology for the catalytic combustion of methane (CH4) have been published. Recently, attention has increasingly focused on the synthesis and catalytic activity of nickel oxides. In this paper, a NiO/CeO2 catalyst with high catalytic performance in methane combustion was synthesized via a facile impregnation method, and its catalytic activity, stability, and water-resistance during CH4 combustion were investigated. X-ray diffraction, low-temperature N2 adsorption, thermogravimetric analysis, Fourier transform infrared spectroscopy, hydrogen temperature programmed reduction, methane temperature programmed surface reaction, Raman spectroscopy, electron paramagnetic resonance, and transmission electron microscope characterization of the catalyst were conducted to determine the origin of its high catalytic activity and stability in detail. The incorporation of NiO was found to enhance the concentration of oxygen vacancies, as well as the activity and amount of surface oxygen. As a result, the mobility of bulk oxygen in CeO2 was increased. The presence of CeO2 prevented the aggregation of NiO, enhanced reduction by NiO, and provided more oxygen species for the combustion of CH4. The results of a kinetics study indicated that the reaction order was about 1.07 for CH4 and about 0.10 for O2 over the NiO/CeO2 catalyst. 相似文献
36.
Yifei Wang Shouying Huang Xinsheng Teng Hongyu Wang Jian Wang Qiao Zhao Yue Wang Xinbin Ma 《Frontiers of Chemical Science and Engineering》2020,14(5):802
The Fischer–Tropsch synthesis (FTS) continues to be an attractive alternative for producing a broad range of fuels and chemicals through the conversion of syngas (H2 and CO), which can be derived from various sources, such as coal, natural gas, and biomass. Among iron carbides, Fe2C, as an active phase, has barely been studied due to its thermodynamic instability. Here, we fabricated a series of Fe2C embedded in hollow carbon sphere (HCS) catalysts. By varying the crystallization time, the shell thickness of the HCS was manipulated, which significantly influenced the catalytic performance in the FTS. To investigate the relationship between the geometric structure of the HCS and the physic-chemical properties of Fe species, transmission electron microscopy, X-ray diffraction, N2 physical adsorption, X-ray photoelectron spectroscopy, hydrogen temperature-programmed reduction, Raman spectroscopy, and Mössbauer spectroscopy techniques were employed to characterize the catalysts before and after the reaction. Evidently, a suitable thickness of the carbon layer was beneficial for enhancing the catalytic activity in the FTS due to its high porosity, appropriate electronic environment, and relatively high Fe2C content. 相似文献
37.
氢能所具有的清洁、高能量密度特点,使其成为一种未来的理想能源。相较于石油、天然气等的热解制氢技术,利用可再生清洁能源进行电催化分解水制氢具有高效和清洁无污染的特点,且获得氢气产物纯度高,具备大规模发展的潜力。而在大规模水电解过程中,电催化剂是不可或缺的元素之一。它能有效地加速电解水在阴阳两极反应的动力学过程。传统的贵金属基催化剂具有良好的电催化析氢、析氧活性,但成本高昂、储量稀缺,从而限制了其规模化地推广及应用。开发新型高效廉价的非贵金属基电催化剂已成为时下研究热点。中空碳基纳米材料集成了中空材料和碳基材料的优势,作为电催化剂,在电解水方面有着潜在的应用价值。本文总结了近年来微纳米结构碳基中空材料作为新型电解水催化剂的研究进展,介绍了高效碳基中空析氧/析氢催化剂的设计原则和相应的设计策略,并对开发持久高效的中空碳基电解水催化剂进行了总结和展望。 相似文献
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39.
Carina Heisig Jelka Diedenhoven Christopher Jensen Helmut Gehrke Thomas Turek 《化学工程与技术》2020,43(3):484-492
The conversion of bio-based succinic acid (SA) to the value-added chemicals 1,4-butanediol (BDO), γ-butyrolactone (GBL), and tetrahydrofuran (THF) can replace the corresponding petrochemical production routes to achieve a sustainable process. The reaction network for aqueous-phase catalytic hydrogenation of succinic acid over a supported Re-Pd catalyst was identified and the reaction kinetics was determined. With the developed kinetic model, the composition of the product mixture regarding the desired products (BDO, GBL, THF) can be described as a function of educt concentration, temperature, and pressure. The maximum BDO yield was achieved at high pressure and low temperature, while low pressure and high temperature favored GBL and THF production. 相似文献
40.
负载型金属催化剂在水处理中起着重要的作用,浸渍法是制备负载型催化剂的重要方法。为了克服传统浸渍方法的缺点,本文通过使用甘氨酸/盐酸作为缓冲溶液,严格控制pH,获得高分散的活性组分并以此方法制备了铁基类芬顿催化剂。对苯酚催化降解的实验表明,使用缓冲溶液法制备的催化剂比未使用的样品可以更高效地去除苯酚,1h内对苯酚的降解可达89.3%。此外,通过调节浸渍温度、浸渍时间和缓冲溶液的pH等参数来精确控制活性组分的量和催化活性。更重要的是,此催化剂制备方法可以用于其他负载型金属催化剂的制备,比如过硫酸盐催化剂,并取得了良好的催化效果。 相似文献