Ni/W比对NiWCx催化剂加氢性能的影响

过渡金属碳化物具有类似贵金属的电子结构和加氢性能。采用等体积浸渍法制备了不同Ni/W比的NiW/γ-Al₂O₃催化剂,以程序升温碳化法转化为NiW碳化物后对芳烃模型化合物和低温煤焦油中分离所得芳烃组分进行加氢处理。催化剂的N₂吸附、XRD、H₂-TPR和SEM表征表明,Ni的添加促进了载体表面WO₃物种的分散和还原,抑制了WO₃晶体的团聚和大晶粒的生成。萘的加氢实验表明,Ni/W原子比为0.6时催化剂的活性最佳,而添加苯酚和吡啶后的模型油加氢过程中萘的转化率和十氢萘的产率均明显下降,Ni/W原子比为0.47和0.6的催化剂性能相近,煤焦油中芳烃组分加氢后Ni/W原子比为0.47的催化剂性能更优。结果表明,Ni和W均具有良好的加氢活性,但Ni耐杂原子性能较差,二者存在一个最佳的配比以使加氢性能更优。有杂原子化合物存在时,如煤基芳烃组分的加氢,Ni/W原子比为0.47的NiW碳化物催化剂具有更好的加氢性能。     

氢处理技术在钛合金中的应用

氢处理工艺是钛合金的一种特有的热处理方式，用于改善铸造、锻造钛合金件以及粉末冶金件的组织和性能。本文综述了氢处理在钛合金中的一些应用，主要介绍了国外的研究动向。     

不饱和油脂加氢催化剂的研究

以Al₂O₃、硅藻土为载体，NiO或甲酸镍为活性组分前驱体，采用不同的沉淀法工艺制备了负载型单元镍催化剂，在相同的条件下进行活性评价。研究表明，以NiO为活性组分前驱体要优于甲酸镍，沉淀过程中反加中和优于正加中和。     

白油加氢装置技术改造

对抚顺石油化工分公司石化三厂白油加氢装置进行技术改造，通过调整加氢工艺，采用一段加氢工艺生产高品级的加氢尾油，再经分馏系统生产出多种优级品的白油，满足了市场需求，并创造了可观的经济效益和社会效益。     

Interpretation of hydrogenation kinetics of spent oil distillate from u.v. spectroscopy

Hydrotreatment of spent oil distillate was carried out on a commercial Ni-Mo-alumina catalyst in the temperature range 260–340 °C, with a liquid hourly space velocity (LHSV) of 0.7–2.0 h^?1, pressure of 4.5 MPa and $\text{H}{}_2\text{oil}$ ratio of 300 NL L^?1 (normal litre of H₂ per litre of feedstock). U.v. spectra of hydrogenated and original spent oil distillates (measured in normal hexane) gave a band with a maximum at 230 nm. The change in absorbance at three selected wavelengths for original oil distillate and hydrotreated oil at different operating conditions was taken as a guide for the determination of hydrogenation reaction rates (including partial saturation of aromatics and sulphur compound hydrogenolysis). The rate constants of hydrogenation reactions (k) using a second-order equation and a model of two parallel first-order reactions (k₁ and k₂) were calculated. Finally, the apparent activation energy (E_a), enthalpy of activation ($\text{ΔH}{}^1$) and entropy ($\text{ΔS}{}^1$) were calculated based on the values of k, k₁, and k₂. The calculated values of E_a based on k, k₁ and k₂ were 81.479, 71.188 and 62.882 kJ mol^?1, respectively. The values of $\text{ΔH}{}^1$ based on the same rate constants were 76.670, 66.564 and 58.433 kJ mol^?1, while the values of $\text{ΔS}{}^1$ were ?117.150, ?133.779 and ?150.823 J mol^?1 K^?1, respectively.     

对叔丁基苯甲酸甲酯加氢合成对叔丁基苯甲醛

以对叔丁基苯甲酸甲酯为原料,二氧化锰负载氧化物为催化剂,在常压固定床反应器上考察了加氢还原催化剂对制备对叔丁基苯甲醛的影响因素,并获得了最佳反应条件为:反应温度为 380~400℃,酯的液时空速为 5mL/h,氢气的气时空速约为1050h-1及合适的催化剂:15%~20%MnO2 /γ Al2O3。     

Reactant induced restructuring and corrosion of germanium-palladium catalysts during hydrogenation reactions

An anomalous rate enhancement with increasing conversion has been observed during the liquid phase hydrogenation of nitrobenzene and crotonaldehyde over Ge/Pd/C catalysts at ambient temperature and atmospheric pressure. Inductive coupled plasma atomic emission spectroscopy and electrochemical measurement of the oxidation state of catalysts during reaction revealed that the bimetallic particles were partially oxidized by the reactants, which resulted in Ge-dissolution and increased exposure of Pd on the surface. It is proposed that the surface and bulk composition of Ge/Pd catalysts are a function of their oxidation state. This behaviour is due to the unusually high mobility of Ge in the Pd lattice and to the good solubility of GeO₂ in polar solvents. The influence of hydrogen transport on the corrosion process and the stability of other X/Pd type bimetallic catalysts during liquid phase hydrogenation are also discussed.     

γ-丁内酯的合成及应用

介绍了 γ—丁内酯的主要用途,评述了其主要合成工艺,并推荐氯碱行业采用顺酐加氢法生产 γ—丁内酯。     

Supported Molybdenum Carbides Lie Between Metallic and Sulfided Catalysts for Deep HDS

Hydrodesulfurization (HDS) of 4,6-dimethyldibenzothiophene on alumina-supported Mo₂C has been studied. These catalysts are stable and active under deep HDS conditions (0-250 wt ppm S). However, although they are well known to have hydrogenation properties, they lead preferentially to a non-hydrogenated product of the HDS reaction: dimethylbiphenyl. For the same reaction, supported platinum and sulfided molybdenum oxide lead to the hydrogenated products dimethyldicyclohexyl and methylcyclohexyltoluene, respectively. The ranking of HDS activity is as follows: MoS₂/Al₂O₃ < Mo₂C/Al₂O₃ < Pt/SiO₂.     

室温离子液体在石油化工中的应用

介绍了室温离子液体的制备及物理性质,详细说明了室温离子液体在石油化工中的应用,如在烷基化、氢化、脱硫、C-C偶联等反应中的应用;分析了室温离子液体现存的缺点.最后,提出室温离子液体工业应用的方向及可能存在的问题.