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291.
对间二甲苯氨氧化制备间苯二腈新型m-509催化剂,及其在工业流化床反应器上进行试验后的下床催化剂,进行了宏观物理性质、X光电子能谱、等离子发射光谱等表征分析,发现催化剂在工业安装上使用6个月后,其表面存在大量积炭,催化剂活性组分流失较严重,活性组分流失是催化剂活性下的主要原因,而积炭对催化剂的活性影响不大。 相似文献
292.
Luiza P. V. Calsavara Flávio F. De Moraes Gisella M. Zanin 《Applied biochemistry and biotechnology》1999,79(1-3):789-806
The enzyme cellobiase Novozym 188, which is used for improving hydrolysis of bagasse with cellulase, was characterized in
its commercial available form and integrated kinetic models were applied to the hydrolysis of cellobiose. The specific activity
of this enzyme was determined for pH values from 3.0–7.0, and temperatures from 40–75°C, with cellobiose at 2 g/L. Thermal
stability was measured at pH 4.8 and temperatures from 40–70°C. Substrate inhibition was studied at the same pH, 50°C, and
cellobiose concentrations from 0.4–20 g/L. Product inhibition was determined at 50°C, pH 4.8, cellobiose concentrations of
2 and 20 g/L, and initial glucose concentration nearly zero or 1.8 g/L. The enzyme has shown the greatest specific activity,
17.8 U/mg, at pH 4.5 and 65°C. Thermal activation of the enzyme followed Arrhenius equation with the Energy of Activation
being equal to 11 kcal/mol for pH values 4 and 5. Thermal deactivation was adequately modeled by the exponential decay model
with Energy of Deactivation giving 81.6 kcal/mol. Kinetics parameters for substrate uncompetitive inhibition were: Km=2.42 mM, V
max=16.31 U/mg, Ks=54.2 mM. Substrate inhibition was clearly observed above 10 mM cellobiose. Product inhibition at the concentration studied has usually doubled the time necessary to reach the same conversion
at the lower temperature tested. 相似文献
293.
在加压条件下(0.1~1.1MPa)考察了MgO/BaCO_3催化剂在甲烷氧化偶联反应中的性能,以及加压后该催化剂的失活。XRD谱图表明,在加压失活的MgO/BaCO_3催化剂表面有部分MgCO_3牛成,这是由于部分活性相MgO发生了转变:XPS表征结果表明,在加压失活后的MgO/BaCO_3催化剂中B3CO_3向表面富积,致使催化剂的表面活性相MgO的浓度相对降低和催化剂表面积降低。另外,在加压失活后的MgO/B3CO_3催化剂上表面活性氧物种的离子浓度大大降低,表面晶格氧的流动性及晶格氧参与甲烷转化的能力也大大减弱;另外,由于该失活催化剂表面结构的变化,由MgO和BaCO_3共同作用形成的强碱中心也消失了。 相似文献
294.
Jiaqi An Zongye Wang Shouhua Hui Ziyu Wang Yanwu Zhang 《Journal of polymer science. Part A, Polymer chemistry》2024,62(9):1890-1901
Dispersants play a significant role in the formulation of positive battery slurry. Adding a small amount of dispersant can effectively reduce the viscosity of the slurry, which is beneficial for the production of positive batteries. A series of copolymers of N-vinylpyrrolidone (NVP) and 2-ethylhexyl acrylate (2-EHA) with different molar ratios of NVP to 2-EHA, different polymer molecular weights and different polymer structures are synthesized by dl -methionine-mediated reversible deactivation radical polymerization. The ability of these copolymers to disperse LiFePO4 battery positive slurry with a high solid content (57.08%) as dispersants has been evaluated. Research shows that when the ratio of NVP to 2-EHA is 20 and the polymer molecular weight is 6000, poly(N-vinylpyrrolidone-ran-2-ethylhexyl acrylate) (NVP-ran-2-EHA) exhibits the strongest dispersing ability to the slurry. This polymer can reduce the viscosity of the slurry by 43.925% and has the longest stabilization time of 3 h, which is better than poly(N-vinylpyrrolidone) (PVP) and poly(N-vinylpyrrolidone)-block-poly(2-ethylhexyl acrylate) (PVP-b-PEHA) with the same molecular weight. 相似文献
295.
制备了KNO3/Al2O3负载型固体碱催化剂,通过XRD、DRIFT、低温氮吸附、ICP和碱度滴定等手段对催化剂表面性质进行了表征,研究了其对大豆油与甲醇酯交换制备生物柴油的催化性能,剖析了在反应过程中该催化剂的催化本质以及失活原因。结果表明,高温焙烧后Al2O3表面KNO3完全分解,形成了大量偏铝酸钾分散在载体表面;在酯交换反应时Al2O3表面的偏铝酸盐等活性组分不断溶出并参与反应,这是该催化剂表现出高活性的主要原因。在反应过程中生成的产物生物柴油和甘油对催化剂的活性有很大影响,其中,生物柴油与活性物种发生的皂化反应是造成催化剂失活的主要原因。 相似文献
296.
《Journal of polymer science. Part A, Polymer chemistry》2018,56(18):2072-2079
A photoinduced electron transfer‐reversible addition‐fragmentation chain transfer (PET‐RAFT) polymerization of p‐methylstyrene (p‐MS) and styrene (St) with 2‐(dodecylthiocarbonothioylthio)‐2‐methylpropionic acid as the chain transfer agent (CTA) and aromatic aldehydes, including 4‐cyanobenzaldehyde (PC1), 2,4‐dimethoxy benzaldehyde, and 4‐methoxy benzaldehyde, as organic photocatalysts has been demonstrated via irradiation with 23 W compact fluorescent lamps. The kinetics of the polymerizations shows first order with respect to monomer conversions. Linear evolution of the Mn of the produced polymers with the monomer conversion is observed. Meanwhile, the as‐prepared polymers are of relatively narrow polydispersity (PDI = Mw/Mn). For instance, the polymerization of p‐MS shows living polymerization features using PC1 within a range of solvents. Especially, the Mn of PpMS increased from about 2100 to 12,700 g/mol with the monomer conversion from 8% to 52% in tetrahydrofuran. The controlled polymerization of St is also observed under optimal reaction conditions. However, the Mn discrepancy between the experimental readings and theoretical calculations is greater at the monomer conversions greater than 40% and the PDI increased gradually over the monomer conversion. This is probably because that CTA is strongly sensitive to the light irradiation with wave range around its characteristic absorption wavelength, leading to significant decomposition of CTA moieties during the RAFT polymerization. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 2072–2079 相似文献
297.
Marianna Gambino Martin Veselý Matthias Filez Ramon Oord Dario Ferreira Sanchez Daniel Grolimund Nikolai Nesterenko Delphine Minoux Marianne Maquet Florian Meirer Bert M. Weckhuysen 《Angewandte Chemie (International ed. in English)》2020,59(10):3922-3927
Ni contamination from crude oil in the fluid catalytic cracking (FCC) process is one of the primary sources of catalyst deactivation, thereby promoting dehydrogenation–hydrogenation and speeding up coke growth. Herein, single‐particle X‐ray fluorescence, diffraction and absorption (μXRF‐μXRD‐μXAS) tomography is used in combination with confocal fluorescence microscopy (CFM) after thiophene staining to spatially resolve Ni interaction with catalyst components and study zeolite degradation, including the processes of dealumination and Brønsted acid sites distribution changes. The comparison between a Ni‐lean particle, exposed to hydrotreated feedstock, and a Ni‐rich one, exposed to non‐hydrotreated feedstock, reveals a preferential interaction of Ni, found in co‐localization with Fe, with the γ‐Al2O3 matrix, leading to the formation of spinel‐type hotspots. Although both particles show similar surface zeolite degradation, the Ni‐rich particle displays higher dealumination and a clear Brønsted acidity drop. 相似文献
298.
Francesca D'Acunzo Giancarlo Masci 《Journal of polymer science. Part A, Polymer chemistry》2021,59(24):3059-3083
In this review article, we survey the 2016–June 2021 scientific literature on the synthesis of multi-stimuli responsive (MSR) polymers, the main focus being on reversible deactivation radical polymerization techniques (RDRPs, also known as controlled radical polymerizations). In fact, along more than 40 years of extensive research, RDRPs have boosted the synthesis of stimuli-responsive polymers. RDRPs are now robust, versatile, relatively user-friendly and even interconvertible, thus allowing control over composition, sequence, and topology of polymers. Such control can afford materials with well-defined responses to physical, chemical, and biological external stimuli. Furthermore, “click” reactions are used to combine macromolecular precursors or to introduce specific functional groups in the target structure. As a result, MSR polymers are obtained from diverse combinations of commercial or specially synthesized building blocks arranged at will into desired sequences and architectures. Thanks to this versatility, self-assembling polymeric structures are designed either to respond to triggers and perform specific applicative tasks, or to investigate the influence of structural variables on the responsivity of polymers. The “green” trend emerging in the field of responsive polymers and RDRPs is also briefly discussed. 相似文献
299.
Dr. Saskia Möller Nora Jannsen Dr. Julia Rüger Dr. Hans-Joachim Drexler Moritz Horstmann Dr. Felix Bauer Prof. Dr. Bernhard Breit Prof. Dr. Detlef Heller 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(56):14034-14041
Detailed mechanistic investigations on our previously reported synthesis of branched allylic esters by the rhodium complex-catalyzed propargylic C−H activation have been carried out. Based on initial mechanistic studies, we present herein more detailed investigations of the reaction mechanism. For this, various analytical (NMR, X-ray crystal structure analysis, Raman) and kinetic methods were used to characterize the formation of intermediates under the reaction conditions. The knowledge obtained by this was used to further optimize the previous conditions and generate a more active catalytic system. 相似文献
300.
催化裂化是石油化工的核心单元之一.从催化裂化尾气中分离出来的碳四馏分富含许多的不饱和烯烃,如1-丁烯、顺、反式-2-丁烯以及少量的1,3-丁二烯,这些不饱和烯烃可以通过后续聚合反应,生成合成橡胶和工程塑料的重要原料,具有重要的应用价值.上述工艺过程对原料中1,3-丁二烯的含量(<100~200 ppm)有严苛的要求.采用选择性加氢技术对碳四馏分中的1,3-丁二烯进行选择性加氢,将其转化为更高附加值的单烯烃是一个理想的解决方案.然而,1,3-丁二烯加氢反应得到的单烯烃可能发生深度加氢得到副产物丁烷.因此,开发高效选择性加氢催化剂对碳四资源的利用具有重要的现实意义.另一方面,1,3-丁二烯加氢反应可以作为模型反应,用来考察选择性加氢催化剂的性能.基于此,该反应无论在工业界还是学术界均受到广泛关注.尽管如此,有关1,3-丁二烯加氢催化剂研究进展方面的综述极少.仅有关于1,3-丁二烯加氢作为模型反应的综述报道.本文对过去半个世纪以来1,3-丁二烯加氢反应中不同催化剂的发展历程进行系统综述,特别是包括Pd,Pt和Au等的单一贵金属催化剂.重点介绍以下内容:(1)固体催化剂构效关系,包括活性金属尺寸效应、晶面和形貌效应以及载体效应(晶相、孔道和酸碱性);(2)高性能催化剂的设计新策略,如单原子催化剂、核壳结构催化剂、金属-离子液复合催化体系以及载体的形貌调控;(3)催化剂的反应机理和失活机理.提出了1,3-丁二烯选择性加氢高性能催化剂开发面临的挑战,并对潜在的发展方向进行了展望.本文认为随着纳米技术和金属纳米材料合成方法的快速发展,对贵金属活性组分进行原子层面上的调控(包括形貌、尺寸以及单原子配位环境等)已成为可能.这将有助于研制出一类新型高性能选择性加氢催化材料,从而实现高转化率条件下高附加值单烯烃的定向转化.此外,载体的酸碱性和孔道结构的调控有助于进一步调节催化剂的抗积炭性能,也是未来发展的一个重要方向. 相似文献