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1.
2.
Raymond Mackay Jie Zhang Qi Wu Yuzhuo Li 《Colloids and surfaces. A, Physicochemical and engineering aspects》2004,250(1-3):343-348
The longitudinal relaxation times (T1) of water in concentrated silica and alumina slurries were measured as a function of solids content. It was shown that the results could be fit very well with a two-phase fast-exchange model between free and surface-bound water. As expected, values of T1 for bound water were in the order of 20–2000 times lower than that for free water, indicating a higher effective viscosity of the surface-bound water. The strength of the interaction depended on the particular surface, and all of the aluminas examined interacted more strongly with water than the two silicas studied, which themselves differed considerably. The chemical mechanical polishing (CMP) removal rate of tantalum by silica slurries was shown to be directly correlated with the interaction parameters, derived from the NMR relation times rather than with total surface hydroxyl group concentration. 相似文献
3.
Ozao R. Yoshida H. Inada T. Ochiai M. 《Journal of Thermal Analysis and Calorimetry》2003,72(1):113-118
Nanoporous alumina membrane prepared by anodic oxidation using sulfuric acid electrolyte was subjected to TG-DTA and X-ray
Photoelectron Spectroscopy (XPS or ESCA) to further study the distribution of sulfur. In XPS study, Ar+ ion bombardment was performed on the sample to etch the surface at a rate of 3 nm min-1. As a result, sulfur was found to be concentrated within a depth of 3nm from the surface. The S content of the surface was
found to be 2.7±0.5 wt%, and that at a depth of ca. 3 nm and ca. 10 nm was found to be as low as about 0.6±0.11 wt% (5.37±1.0
wt%→ 1.26±0.2wt% SO2). In TG-DTA, the mass loss of 7.3% was in fair agreement with that calculated on XPS results (7.1±1.2%).
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
4.
Chunlin Li Yilu Fu Guozhu Bian Tiandou Hu Yaning Xie Jing ZhanDepartment of Chemical Physics University of Science and Technology of China Hefei China Institute of High Energy Physics Chinese Academy of Sciences Beijing China 《天然气化学杂志》2003,12(3)
The Ni/CeO2-ZrO2-Al2O3 catalyst with different Al2O3 and NiO contents were prepared by hydrothermal synthesis method. The catalytic performance for CO2 reforming of CH4 reaction, the interaction among components and the relation between Ni content and catalyst surface basicity were investigated. Results show that the interaction between NiO and Al2O3 is stronger than that between NiO and CeO2-ZrO2.The addition of Al2O3 can prevent the formation of large metallic Ni ensembles, increase the dispersion of Ni, and improve catalytic activity, but excess Al2O3 causes the catalyst to deactivate easily. The interaction between NiO and CeO2 results in more facile reduction of surface CeO2. The existence of a small amount of metallic Ni can increase the number of basic sites. As metallic Ni may preferentially reside on the strong basic sites, increasing Ni content can weaken the catalyst basicity. 相似文献
5.
6.
采用聚乙烯醇对碳纳米管表面进行改性,通过化学沉淀法将Al(OH)3均匀沉积在碳纳米管表面,然后在氮气气氛下于500 ℃煅烧2 h,制备出氧化铝/碳纳米管复合材料。采用TEM、TG、DTA、XRD、IR、氮吸附脱附(比表面积及孔结构分析)等对氧化铝/碳纳米管复合材料进行表征,结果表明:未经聚乙烯醇改性的碳纳米管,氧化铝与碳纳米管相互分离;经聚乙烯醇改性的碳纳米管,氧化铝与碳纳米管结合良好。经聚乙烯醇改性的碳纳米管表面均匀覆盖一层聚乙烯醇膜,通过聚乙烯醇的吸附作用, Al(OH)3沉积在碳纳米管表面形成一层连续的覆盖层。 相似文献
7.
氧化铝具有许多重要的工业用途,而制备高热稳定活性氧化铝的技术也在不断地发展[1,2],因此,研究其高温烧结下的相变过程很有意义.离子深法作为新型测试手段,已成功地用于生物大分子结构与功能研究方面[‘],而在固体材料测试中的应用尚未见报道.我们以EU’“作为荧光探针,并结合**D和*nR研究了川对。在不同烧结温度下的相变过程.1实验部分样品的制备采用复盐分解法.先将Elf刀s用高纯硝酸溶解定容.以占AlzO。重量1%的量加入到硫酸铝锭溶液中,进行超声处理,冷冻干燥.再依次登于900”C、1000C、1100C、1200C的高温炉… 相似文献
8.
A. V. Fionov M. V. Burova E. A. Tveritinova I. V. Krylova 《Russian Chemical Bulletin》2006,55(4):639-644
Donor-acceptor properties of alumina modified with lithium cations were studied by ESR of paramagnetic complexes of adsorbed
anthraquinone. The results were compared with the data on negative ion emission (exoemission) accompanying the decomposition
of isopropyl alcohol in the adsorption layer. The data on the activity measured by the pulse microcatalytic technique in isopropyl
alcohol decomposition are discussed. Small additives of lithium were found to promote catalytic activity of the samples. The
role of acid and basic sites in isopropyl alcohol decomposition was discussed.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 616–621, April, 2006. 相似文献
9.
V. B. Vol'eva A. I. Prokofev A. Yu. Karmilov N. L. Komissarova I. S. Belostotskaya T. I. Prokofeva V. V. Ershov 《Russian Chemical Bulletin》1998,47(10):1920-1923
The formation of semiquinone and phenoxazyl radicals and metallocomplexes with semiquinone ligands was observed by ESR during
the interaction of di-tert-butylpyrocatechol with Al2O3, ZnO, SiO2, and TiO2. In the case of different modifications of SiO2, admixtures of TiO2 exhibit a higher reactivity in complex formation with the organic substrate.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1975–1978, October, 1998. 相似文献
10.
催化裂化USY/ZnO/Al2O3脱硫添加剂的高温水热失活 总被引:3,自引:0,他引:3
对USY/ZnO/Al2O3汽油催化裂化脱硫添加剂经高温水热老化处理前后的脱硫性能进行了考察,发现老化后添加剂的脱硫性能大幅度下降.采用XRD和IR等技术对USY/ZnO/Al2O3添加剂在高温和高温水热条件下失活的原因进行了研究.结果表明,在高温下,ZnO可与USY沸石中的铝发生固相反应生成ZnAl2O4尖晶石,从而造成USY晶体结构崩塌,转变成无定形状态.在ZnO含量较高的条件下,ZnO可继续与USY晶体结构崩塌后生成的无定形的硅和铝的氧化物反应,生成Zn2SiO4硅锌矿和ZnAl2O4尖晶石结构.这一方面使添加剂失去了可形成硫化物吸附中心的ZnO,另一方面破坏了硫化物的裂化活性组分USY,从而造成添加剂脱硫性能下降甚至失去脱硫活性.ZnO对USY的破坏作用主要与温度有关.在USY/ZnO/Al2O3体系中,ZnO被ZnO与Al2O3之间形成的锌铝尖晶石膜固定并与USY隔离,单纯的高温条件对添加剂的破坏不显著,而水蒸气可以促进ZnO的移动,有利于ZnO与USY的接触,因此在高温和有水蒸气存
在的条件下添加剂的结构易遭到破坏. 相似文献