Structural Description of Polyaromatic Nucleus in Residue

The proton nuclear magnetic resonance spectroscopy （1H-NMR）, the synchronous fluorescence spectrometry （SFS） and the ruthenium ions catalyzed oxidation （RICO） method were used to determine the chemical structure of polyaromatic nucleus in Oman residue fractions. The results of 1H-NMR analyses showed that the average numbers of aromatic rings in the aromatics, resins and asphaltenes units were 3.2, 5.6 and 8.2, respectively. SFS was used to investigate the distribution of aromatic rings in residue fractions, the main distribution range of aromatic rings in aromatics, resins and asphaltenes were 3 4 rings, 3--5 rings and more than 5 rings, respectively. The aromatic network in residue fractions was oxidized to produce numerous carboxylic acids. The types and content of benzenepolycarboxylic acids, such as phthalic acid, benzenetricarboxylic acids, benzenetetracarboxylic acids, benzenepentacarboxylic acid and benzenehexacarboxylic acid disclosed the condensed types of aromatic nuclei in the core. The biphenyl fraction （BIPH）, the cata-condensed fraction （CATA）, the peri-condensed fraction （PERI） and the condensed index （BCI） were calculated based on the benzenepolycarboxylic acids formed. The results implied that there was less biphenyl type structures in all residue fractions. The aromatics fraction was almost composed of the cata-condensed type system, and the asphaltenes fraction was wholly composed of the peri-condensed type system, while in the resins fraction co-existed the two types, herein the peri-con- densed type was predominant over the cata-condensed type. Based on the analytical results obtained in the study, the components --aromatics, resins and asphaltenes -- were given the likely structural models.     

The role of carbon deposition on precious metal catalyst activity during dry reforming of biogas

Gold and palladium were supported on a mesoporous TiO₂ for total oxidation of volatile organic compounds (VOCs). Mesoporous high surface area titania support was synthesised using of Ti(OC₂H₅)₂ in the presence of CTMABr surfactant. After removing the surfactant molecules, 0.5 or 1.5 wt% of palladium and 1 wt% of gold were precipitated on the support by, respectively, wet impregnation and deposition–precipitation methods. The activity for toluene and propene total oxidation of the prereduced samples follows the same order: 0.5%Pd-1%Au/TiO₂ > 1.5%Pd/TiO₂ > 0.5%Pd/TiO₂ > 1%Au-0.5%Pd/TiO₂ > 1%Au/TiO₂ > TiO₂. Moreover, a catalytic comparison with samples based on a conventional TiO₂, shows the catalytic advantage of the mesoporous TiO₂ support. The promotional effect of gold added to palladium could be partly explained by small metallic particles (TEM), but meanly by metallic particles made up of Au-rich core with a Pd-rich shell. Moreover, the hydrogen TPR profile of 0.5%Pd-1%Au/TiO₂ shows only the signal attributed to small PdO particles. Gold also implies a protecting effect of the support under reduction atmosphere. Operando diffuse reflectance infrared fourier transform (DRIFT) spectroscopy was carried on and allowed to follow the VOCs oxidation and the formation of coke molecules, but also a metallic electrodonor effect to the adsorbed molecule which increases in the same order as the activity for oxidation reaction. The presence of coke after test was also shown by DTA–TGA by exothermic signals between 300 and 500 °C and by EPR (g = 2.003).     

FY-14吸附剂用于大庆减三线润滑油基础油精制

采用有机酸改性活性白土FY—14吸附剂对大庆减三线润滑油基础油的脱氮效果进行详细考察，并与活性白土进行对比。研究结果表明，白土精制温度较高，在150℃时5．0％白土用量的碱性脱氯事为88．3％，而在100℃时2．5％FY-14吸附剂用量的碱性氮脱除率为95．6％，硫脱除率为13．2％，旋转氧弹值为268min。随着碱性氯脱除率提高，精制油折光率呈不断下降趋势。上述实验结果表明，采用FY—14吸附荆精制基础油可达到节能降耗、提高基础油收率和氧化安定性的效果。     

软锰矿湿法脱硫工艺的研究

介绍了工业除硫的基本方法，对软锰矿浆湿法脱硫工艺进行了试验研究，得出了较佳脱硫工艺条件。采用吸收液回流催化氧化二氧化硫，降低体系的pH值，有效地抑制了副反应地发生；对二氧化硫气体进行两步吸收，使其脱除率达到近96%；通过对吸收液氧化转化，调整pH值沉降等多步骤净化工艺，得到了符合一级标准的硫酸锰副产品。     

Ti-45Al-10Nb合金的高温氧化行为

研究了Ti—45A1—10Nb(原子分数，％)合金在800-960℃在氧气和空气中的氧化行为．结果表明，该合金具有较好的高温抗氧化性能，其氧化增重速率与铁基耐热不锈钢相似或略优．与Ti—50A1合金相反，Ti-45A1-10Nb合金在空气中的氧化增重速率明显低于在纯氧中的氧化增重速率．X射线衍射与能谱分析表明，Ti-45Al一10Nb合金在氧气中的氧化产物主要有TiO2和Al2O3，但在空气中的氧化产物中有TiN相．这是降低氧化速率的主要原因，同时，合金元素Nb稳定了氧化层中的TiN相，因而提高了合金在空气中的抗氧化性能．     

钼酸铵溶液深度净化工艺探索

对传统的钼酸铵溶液净化工艺及文献介绍工艺进行了较为详细的分析 ,并与实验数据对比分析 ,找到了较为合理的工艺方案     

湿法停炉保护优点多 建议采用YZ—101防腐阻垢剂作为湿法炉保护剂

介绍了湿法炉保护的作用原理,YZ—101防腐阻垢剂的使用方法、注意事项以及使用后所带来的经济效益。     

甲烷催化部分氧化催化剂研究进展

综述了国内外甲烷催化部分氧化催化剂在载体、助剂、活性组分及制备方法等方面的研究进展，以对改善催化剂的抗积碳性、提高催化剂的稳定性和选择性提供参考。     

辽河催化裂化澄清油中间馏分热反应研究

采用先加入絮凝剂脱灰，再经减压蒸馏切割420～500℃馏分的方法，将辽河催化裂化澄清油预处理，考察了澄清油、加入絮凝剂脱灰后的澄清油以及脱灰后再减压蒸馏所得的中间馏分这3种原料在热转化过程中中间相的转化历程，并采用偏光显微镜观察热转化产物。结果表明，澄清油预处理效果明显，所得中间馏分具有较低的H／C原子比（nH／nC）和适宜的组成分布，是生产针状焦的理想原料。热转化产物的光学组织结构属于各向异性发达的广域-流线型结构。     

Al/SiO_2/Si表面Al_2O_3纳米图形的AFM阳极氧化制备方法

采用AFM阳极氧化方法,在控制AFM探针尖端电压和扫描方式的条件下,在Al/SiO2/Si表面制备了Al2O3纳米图形,图形最小尺寸为70nm.研究了表面吸附水层存在下AFM阳极氧化机理.实验结果表明AFM阳极氧化是制备金属氧化物半导体纳米器件的较好方法