由1,4-萘醌催化合成1,4-二烷氧基萘-2,3-二甲腈

研究了以 1 ,4-萘醌为原料 ,通过溴代、氰化和 O-烷基化三步合成 1 ,4-二烷氧基萘 -2 ,3 -二甲腈。在溴代反应中以溴化试剂代替液溴 ;在氰化和 O-烷基化反应中以溴化十二烷基三甲基铵 (DTMAB)和聚乙二醇(PEG)作为相转移催化剂 ,并采用正交设计法考察了相转移催化剂、固体碱、反应温度等因素对反应的影响 ,其中氰化产物收率达 88.7%。     

C5/C6异构化催化剂的首次工业应用

采用中石化金陵分公司研究院研制的CI-50(Pd/丝光沸石)作C5/C6烷烃异构化催化剂.详细介绍了该催化剂的工业放大试验装置的工艺流程、首次开工过程中技术问题及处理方法.     

3961连续重整催化剂性能考察

新一代高活性，高水热稳定性3961（PS－Ⅳ）型连续重整催化剂于1996年在上海石化芳烃厂400kt/a连续重整装置上首次进行工业应用试验。开工5a，催化剂跟踪分析结果表明，该剂保持了良好的物化性质和反应性能，表现为良好的比表面积稳定性和持氯能力，经过200个以上再生周期的催化剂未发现有明显的相变和金属分散度的变化。     

国产CN—31催化剂与ICI65—2催化剂工业应用的比较

国产轻油预转化催化剂与进口催化剂相比,具有性能相当、价格低廉、供应方便等优势。国产预转化催化剂需在较高的液空速、温度较低的条件下实现烃类转化反应,生成含甲烷60%以上的富气。采用国产催化剂能明显反映性能价格比。文章对两种催化剂进行了工业应用比较和分析。     

苯部分加氢催化剂失活原因的研究

探讨了环己醇装置苯部分加氢催化剂失活的原因，分析了失活机理，并结合实例——母液置换法解决催化剂的氮化物中毒。     

卤素置换反应用氯化锌催化剂的再生

研究了用于催化卤素置换反应后的氯化锌催化剂的再生方法。其过程包括：用石灰乳中和，沉淀出氢氧化锌，用氢氧化锌中和氯化锌废液至pH值为5—6，通入氯气氧化氯化锌废液中的有机物，蒸发至必要的浓度。     

固载于SBA-15分子筛中的同双核金属配合物催化剂

合成了3种同双核金属配合物[M2LCl3]Cl(L代表配体三亚乙基四胺,M代表Co,Cu,Cr),采用微波加热法合成了SBA-15分子筛,采用浸渍法将3种同双核金属配合物分别固载在表面官能化的SBA-15分子筛(SBA-15-NH2分子筛)中制得负载型催化剂。傅里叶变换红外光谱、X射线衍射、紫外可见光谱和热分析表征结果表明,同双核金属配合物被固载后,其结构仍保持完整。以环己烷氧化反应为探针反应,考察了[Co2LCl3]Cl/SBA-15-NH2,[Cu2LCl3]Cl/SBA-15-NH2,[Cr2LCl3]Cl/SBA-15-NH2催化剂的活性,环己烷转化率分别为11.0%,49.5%,57.9%;对于[Cr2LCl3]Cl/SBA-15-NH2催化剂,当分别以乙睛、丙酮和冰醋酸为溶剂时,环己烷转化率分别为57.9%,52.1%,34.2%,3次重复实验的环己烷转化率分别为57.9%,47.8%,46.5%,表明该催化剂具有较好的活性和重复使用性。     

Ti-silicalite as catalyst for gas-phase ammoximation of cyclohexanone with molecular oxygen

The catalyst behaviour of titanium silicalite, which was found the most active and selective catalyst for liquid-phase ammoximation of cyclohexanone to the corresponding oxime with hydrogen peroxide, was investigated in the gas-phase ammoximation with molecular oxygen in and compared with those of pure silicalite and samples of vanadium and chromium silicalites. The results showed that Ti-silicalite is a selective catalyst not only in the reaction with hydrogen peroxide but also in the reaction with molecular oxygen. However, a big limitation was found in the poor activity of the silicalites which do not allow to reach high oxime yields.     

Crystalline and viscoelastic properties of branched polyethylenes synthesized using bidentate nickel (II) catalyst

In this work, five branched polyethylenes with different branching units were synthesized using bidentate nickel (II) catalyst containing -diimine ligands. For comparison, one linear polyethylene was also prepared using tridentate iron (II) catalyst containing -diimine ligand. The crystalline structure of the polyethylenes was investigated using X-ray diffraction (XRD) and polarized optical microscope. The crystalline properties were also measured by differential scanning calorimeter (DSC). Viscoelastic properties of the polyethylenes were investigated using rheometric dynamic analyzer. The DSC and XRD results showed that highly branched polyethylenes exhibit no melting points and no predominating crystalline forms, while the linear polyethylene exhibits clear orthorhombic (110) and (200) reflections on XRD pattern and a clear melting point at 118 °C. The viscoelastic properties of the branched polyethylenes were very complicated due to the combined effect of the molecular weight difference and the degree of chain branching as well as the branching structure.     

La-OMS-2催化剂催化甲苯氧化制苯甲醛

合成了氧化锰八面体(OMS-2)分子筛,采用离子交换法和浸渍法制备了稀土金属La改性的OMS-2分子筛(La-OMS-2)催化剂,并用于甲苯液相选择性氧化制苯甲醛,考察了催化剂用量、反应温度、反应时间、氧气流量及溶剂种类对甲苯转化率和苯甲醛选择性的影响,对La-OMS-2催化剂进行了X射线衍射表征和BET比表面积测定。实验结果表明,离子交换法制备的La-OMS-2-A催化剂的活性高于浸渍法制备的La-OMS-2-B催化剂,在甲苯0.1mol、溶剂冰乙酸10mL、氧气流量60mL/min、La-OMS-2-A催化剂用量0.10g、反应温度353K、反应时间1.0h的条件下,甲苯转化率达61%,苯甲醛收率为56%。加入La对OMS-2分子筛中的MnO晶格结构产生了影响,提高了苯甲醛的收率。