氯化氢浸渍活性炭净化汞蒸气的研究

用氯化氢对吸附汞热气用的活性炭进行浸渍处理是一种新的偿试。用氯化氢浸渍后的活性炭，对汞的吸附效率和吸附容量与没有浸渍的活性炭相比，均有很大的提高，同时，与其它吸附汞用的浸渍剂相比，具有价格低，来源广的优点，对汞的吸附效率平均在９５％以上。     

铸造用CO2硬化冷芯盒材料及工艺的发展

铸造用CO2硬化粘结剂系统具有气硬冷芯盒的优点,同时又具有环保方面的优势。主要介绍了水玻璃-CO2法、聚丙烯酸钠-CO2法、酚醛树脂-CO2法三种工艺。这些工艺方法近年来国内外研究较多,并且取得了很大进展。     

含钼废渣冶炼钼铁的优化试验

利用含钼废料钼酸钙为原料,采用碳还原法冶炼钼铁,通过单因素分析试验及正交试验优化得出最佳的试验条件,钼酸钙加入量应低于10%,熔炼温度为1 525 ℃,保温时间为25 min,碱度为1.3。通过XRD、SEM、EDS分析得出用此方法生产得到的钼铁合金中,钼以Mo₂C、Fe₃Mo以及Fe₃Mo₃C的形式存在,渣系为二元玻璃渣系,具有与普通玻璃相似的成分系统。经测定合金中钼的回收率大于99%,钼资源回收效益可观。     

碳纳米管及稀土元素钇(Y)对高Ni含量Ti(C,N)基金属陶瓷组织与性能的影响

研究了不同含量的碳纳米管及0.8%稀土Y对高Ni含量Ti(C,N)基金属陶瓷组织性能的影响.将不同成分的试样分别于1400℃、1410 ℃、1420℃真空烧结,测试抗弯强度、洛氏硬度,观察背散射电子形貌、断口形貌并做能谱分析.结果表明,加入质量分数(下同)为0.8%Y及0.3%～1.0%的碳纳米管时,碳纳米管含量为0.5%的组织较均匀,芯壳结构明显,抗弯强度及硬度均较高.     

不同活化剂对石油焦基活性炭孔结构的影响

以石油焦为原料 ,Na OH,KOH和 Na2 CO3 为活化剂制备活性炭 ,采用氮气吸附考察了不同活化剂对活性炭的比表面积、中孔和微孔孔径分布、孔容积及平均孔径等孔结构的影响 .结果表明 :KOH活化制备的活性炭包含 1 nm的微孔和 4nm的中孔 ,总孔容 0 .648cm3 /g,比表面积大 ;Na OH制备的活性炭以 1 nm的微孔为主 ,占总孔容 ( 0 .1 65 cm3 /g)的 98% ,平均孔径 1 .83nm;Na2 CO3 制备的活性炭以 4nm的中孔为主 ,占总孔容 ( 0 .1 43cm3 /g)的 68.5 % ,平均孔径 3.42 nm,比表面积小 .3种样品的孔径都呈现出多峰分布特征 .KOH和 Na2 CO3 活化制备的活性炭的 N2 吸附脱附曲线属于 型 ,Na OH活化制备的活性炭吸附脱附曲线属于 型 .     

Influence of volatile matter and deposited carbon on coke yield from coals

The relations between coke yields and the volatile matter content of 30 individual and 30 blended coals were investigated. Coke yields and deposited carbon related to volatile matter content can be expressed in the following equations: CY (%) = 97.89?0.86 VMch+VMc; and DC (%)= ?2.24+0.16 VMch; where: CY=real coke yield; VMch = volatile matter content of charging coal; VMc=volatile matter content of coke, and in the case of <2%; DC = deposited carbon. The test results show excellent correlation with practice.     

High resolution XPS characterization of chemical functionalised MWCNTs and SWCNTs

High resolution XPS analysis of chemical functionalised multi-wall carbon nanotubes (MWCNTs) and single wall carbon nanotubes (SWCNT) was done with ESCA300 (overall instrument resolution of 0.35 eV). Information to the degree of functionalisation was ascertained by argon ion bombardment of the samples followed by XPS analysis to detect the functional groups, the percentage atomic concentration of various elements present and whether or not the detected functional groups imposed a chemical shift on the CNT atoms. The results show that true chemical functionalisation was achieved and by argon ion bombardment these functional groups can be altered relative to the C 1s carbon atoms of the CNT. The choice of chemicals used for functionalisation, the techniques employed and the types of nanotubes treated are important factors in chemical characterisation. The carbon atom on the nanotube ring to which the functional group (atom) is bonded, the chirality of the CNT, the electronegativity of the functional group, the bond type and whether the CNT is single-wall or multi-wall, or cut (short) could play a role in determining the chemical shift on the CNTs atoms. These investigations are relevant to chemical functionalisation of carbon nanotubes for various applications for example DNA sensors and other biomedical sensors.     

Kinetics of the methanation of carbon dioxide over a supported Ni-La2O3 catalyst

The kinetics of the methanation of carbon dioxide was investigated using an alumina supported Ni-La₂O₂ catalyst in a differential and integral reactor. In the differential reactor the molar ratio of H₂ to CO₂ was varied from 0.6 to 30. In the integral reactor the rates were measured with up to 90% conversion. Both reactor tests were carried out at temperatures between 513 and 593 K. The experimental results were described by a Langmuir-Hinshelwood type equation. The kinetics can be explained by assuming equilibrium of dissociative carbon dioxide and hydrogen adsorption, and assuming hydrogenation of surface carbon as the rate determining step.     

Carbon Aerogels as Electrode Material in Supercapacitors

Due to their large specific surface area and their high electrical conductivity carbon aerogels are promising materials for electrodes in electrochemical double-layer capacitors (supercapacitor). The carbon aerogels were made via pyrolysis of resorcinol formaldehyde aerogels. The latter were prepared by supercritical and subcritical drying as well. The important findings of our investigation were, that the highest capacities of 46 F/cm³ were measured for samples with a density of about 800 kg/m³ pyrolyzed at 800°C. Also it was shown that RF-gels with molar resorcinol/catalyst ratios 1000 or higher can be dried subcritically without cracking or significant shrinkage. Carbon aerogels derived from these RF-aerogels have a small mesopore surface area, however an especially large micropore area. They provide electrical capacities which are most suitable for their use in supercapacitors.     

PVA-based activated carbon fibers with lotus root-like axially porous structure

A novel method was developed for the fabrication of activated carbon fiber (ACF) with wet spinning polyvinyl alcohol (PVA) fibers as the precursors. Through a combination of preoxidation, dehydration, carbonization and activation under a certain tension, PVA-based ACFs (PVA-ACFs) with high yields and good mechanical properties were obtained. The surface and cross-section morphologies, pore structures, surface geometries, surface functional groups and crystal structures of the PVA-ACFs were characterized using field emission scanning electron microscopy, low temperature nitrogen adsorption, Fourier transformed infrared spectrophotometry, X-ray photoelectron spectroscopy and X-ray power diffraction. All the PVA-ACF samples prepared had lotus root-like axially meso- and macroporous structures with the domination of micropores. Fractal geometries of PVA-ACFs deduced from nitrogen adsorption isotherms indicates that capillary force dominated in the interactions between nitrogen and the PVA-ACFs. The surface functional groups of the PVA-ACFs depend on the activating agents. Graphitoidal crystal structures were observed for the PVA-ACFs. The small crystal size and short range ordering between the crystallites ensured a high specific surface area of the PVA-ACFs.