Ru/MCM-41催化剂上苯的液相加氢反应

 以Si-MCM-41、Al-MCM-41(1) (n(Si)/n(Al)=15)、Al-MCM-41(2) (n(Si)/n(Al)=10)以及用NH4NO3或HAc的醇溶液分别与Si-MCM-41离子交换所得的H-MCM-41(N)和H-MCM-41(H)为载体制备了系列Ru/MCM-41催化剂。采用N2吸附、XRD和H2-TPR表征了负载Ru前后催化剂的结构及Ru在各种载体表面上的分散状态。以0.5%（质量分数）苯的环己烷溶液为模型化合物，在298K、3.0MPa反应条件下，考察了上述催化剂的苯液相加氢反应性能，并与Ru/HY、Ru/H和Pt/MCM-41催化剂进行了比较。结果表明，载体MCM-41的n(Si)/n(Al)和表面化学组成等性质对Ru在其表面上的分散状态、还原性及催化性能均有影响。对苯的转化率与反应时间的关系曲线进行拟合，发现其遵循一级动力学方程，加氢反应速率常数按照Ru/Al-MCM-41(2)相似文献   

RuO4对尼龙6的染色机理研究

四氧化钌作为用透射电镜观察高分子材料时对聚合物多相体系进行选择性染色的染色剂之一，克服了四氧化锇染色的局限性，能对多种聚合物进行染色。四氧化钉对大多数聚合物都能染色，但人们至今对其染色的反应机理还不十分清楚，而关于此方面的报道也较少。前人曾就四氧化钉对聚苯乙烯（PS）、聚对苯二甲酸乙二醇酯（PET）、聚对苯二甲酸丁二醇酯（PBT）、聚碳酸酯（PC）的染色机理进行过研究，本文探讨了四氧化钌对尼龙6的染色机理。     

掺杂VO2的特性、制备方法及应用

VO2在68℃时发生从低温的单斜相向高温四方相转变，同时伴随着光、电、磁性能的突变。通过掺入其它杂质元素，能有效改变其相变温度和光、电性能，这些优异特性使其具有更好的应用前案。本文综述了掺杂的原理，掺杂对VO2相变影响、常用的掺杂方法及目前的应用情况，这对其进一步的研发应用具有重要的意义。     

预计钌价将攀升至10,000美元/公斤

随着更环保飞机的普及，钌的需求快速增长。一些贸易商认为，由于全球供应短缺的恶化，未来数月，钉价将达到10，000美元／公斤。     

德意科学家破解二氧化镎奇异磁性之谜

长期以来，二氧化镎（Np02）的奇异磁性一直未能得到科学的解释。德国和意大利的科研人员通过理论计算得出，二氧化镎的奇异磁性可能源于原子间形成的磁32极矩。     

Kelogg合成氨工艺进展

综述了以先进合成氨工艺和转化换热系统技术为代表的Ｋｅｌｏｇｇ第二代合成氨工艺。较详细介绍了钌基催化剂和转化换热器     

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.     

Mid-Temperature Synthesis of CeO2-TiO2 Complex Compound and Its XRD Structure Study

TiO2 andCeO2 aresemiconductormaterials .TiO2hasthepropertiesofphoto catalysis[1] whileCeO2 hastheabilityofoxygenstorageandcanpromotethedispersionofprecionsmetalsonthesupporter[2 ] .CeO2 TiO2 com plexcompoundwasusedascatalystandspecialfunction almaterial[3～ 5] .ThetraditionalsynthesisofCeO2 TiO2complexcompoundisbyceramicmethodthatusesoxidesasrawmaterialsanditiscalcinedabove 130 0℃[6～ 8] .However ,thestructureandmicrostructureofthecomplexcompoundarenotsuitableforcatalystandfunctionalm…