The coal to ethylene glycol (CTEG) process has drawn much attention due to the serious conflict between supply and demand of ethylene glycol in China. However, it is inevitably accompanied by the problem of high CO₂ emissions. Carbon capture is one of the most promising potential effective ways to address this issue. However, the CTEG process, integrated with carbon capture technology, will lead to energy and economic penalties. Thus, a comprehensive evaluation of CTEG process with different CO₂ capture technologies is urgently needed. This study analyzed the technoeconomic performance of four CO₂ capture alternatives for the CTEG process: Rectisol, mono-ethanol amine (MEA), chilled ammonia process (CAP) and dimethyl carbonate (DMC) technologies. Results show the energy consumption of CO₂ capture of the Rectisol process is the lowest, 1.88 GJ/tCO₂, followed by the DMC process, 2.10 GJ/tCO₂, the CAP process, 3.64 GJ/tCO₂, and the MEA process, 5.20 GJ/tCO₂. The CO₂ capture cost of the Rectisol process is lowest, CNY 169.5/tCO₂, followed by the DMC process, CNY 193.2/tCO₂, the CAP process CNY 232.6/tCO₂, and the MEA process CNY 250.5/tCO₂. As the Rectisol technology has the best comprehensive performance, it is the best option for CTEG industry in comparison with the MEA, CAP, and DMC technologies.

Palladium (Pd) nanostructures are highly active non-platinum anodic electrocatalysts in alkaline direct methanol fuel cells (DMFCs), and their electrocatalytic performance relies highly on their morphology and composition. This study reports the preparation, characterizations, and electrocatalytic properties of palladium-copper alloys loaded on the carbon support. XC-72 was used as a support, and hydrazine hydrate served as a reducing agent. Pd_xCu_y/XC-72 nanoalloy catalysts were prepared in a one-step chemical reduction process with different ratios of Pd and Cu. A range of analytical techniques was used to characterize the microstructure and electronic properties of the catalysts, including transmission electron microscopy (TEM), X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma emission spectroscopy (ICP-OES). Benefiting from excellent electronic structure, Pd₃Cu₂/XC-72 achieves higher mass activity enhancement and improves durability for MOR. Considering the simple synthesis, excellent activity, and long-term stability, Pd_xCu_y/XC-72 anodic electrocatalysts will be highly promising in alkaline DMFCs.

High-efficiency production of xylene/trimethylbenzene from benzene/toluene with methanol is a potential way to promote the implementation on the coupled cycle development strategy of petrochemical and coal chemical industry and optimize the resource structure. At the same time, relying on the innovation of catalytic new materials, physical chemistry, intelligent capture technology, process engineering, and other principles and methods, p-xylene (PX) and trimethylbenzene (TMB) with higher added value were prepared by C_6-8~arene methylation, which could elevate the level of methylation field and improve the competitiveness of the industry. This paper focuses on the one-step methylation reaction of benzene with methanol or toluene with methanol to obtain high-purity p-xylene (BM-PX/TM-PX), and the one-step methylation reaction of xylene with methanol to obtain mesitylene (XM-TMB). The methylation reaction mechanism and the preparation strategy of a high-performance catalyst were reviewed. The high selectivity of PX obtained by precisely controlling the pore size and acid site distribution of zeolites was emphasized. Meanwhile, the current research progress of TMB, the kinetic/thermodynamics of the BM-PX/TM-PX, and XM-TMB methylation reaction were described. Based on a literature research and the conclusion of our research group, the mechanism of methylation reaction process was expounded. Finally, the new research direction of catalysts used and reaction process in methylation reaction were prospected in order to guide the rapid development of this field.

The issues of feedstocks, product markets, and environmental emissions have continuously proposed a number of challenges for industrial evaluation of fresh fluid catalytic cracking (FCC) catalyst before its application in commercial units. In this work, a convenient method was proposed by comparing with the existing commercial equilibrium catalyst. A series of laboratory experiments for steam treatments and microactivity tests were established to collect reliable data, and the standalone catalyst or co-catalysts were assessed to show the evaluation process and the predicted unit performance. The results had deviation, but a consistent yield distribution than that of a commercial equilibrium catalyst. These evaluations and predictions would provide us with not only the view of hydrothermal stability and yield distribution at the unit level, but also the economic potential for fresh catalyst based on the existing industrial catalyst, which will provide refiners with industrial basis for further decisions.

Qualitative and quantitative description are key to solving the problem of heavy metal contamination on fluid catalytic cracking (FCC) catalysts. The loading efficiencies for different metals were compared for the two lab simulation methods of Multi-Cyclic Deactivation (MCD) and Advanced Catalyst Evaluation (ACE), and the microcatalytic performance of metal-contaminated catalysts was evaluated using an ACE Model C device. The results show that the MCD and ACE methods both obtain extremely high data accuracy, indicating that they can be used to ensure the parallel reliability of experimental results. The typical operating parameters for hydrothermal aging and metals loading can be adjusted to suit different metal types and content targets for either of these two simulation methods. Compared with an equilibrium catalyst from an industrial unit, the MCD method has the advantages of basic hydrothermal aging treatment with less metal loading efficiency, while the ACE method has an accurate metal amount and high loading efficiency for metal contamination, with a metal balance recovery rate above 99.5% at similar activation to the equilibrium catalyst. When used with a reasonable and effective metal pretreatment scheme, these two laboratory simulation methods can be used to evaluate new commercial catalysts and in fundamental experiments for the improvement of FCC catalysts for removal of metal contamination.