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排序方式: 共有4101条查询结果,搜索用时 953 毫秒
41.
CHEN Shuixia LIU Jinrong ZHANG Xiaoping ZENG Hanmin Materials Science Institute Zhongshan University Guangzhou Department of Environmental Science Engineering South China University of Technology Guangzhou P. R. China 《Chinese Journal of Reactive Polymers》2002,(2)
1. INTRODUCTION Microbial pollution will bring about various problems in industry and other vital fields, such as causing decomposing of materials, harming people抯 health. In order to reduce these problems, new antibacterial materials have been demanded. Recently, much attention has been paid to inorganic materials including zinc oxide [1~4]. These inorganic antibacterial materials are now substituting for organic materials to avoid releasing noxious organic molecules harmful to humans;… 相似文献
42.
以共沉淀法合成了硅铝系载体(AS和SA),并采用改性天然高铝石为原料合成了矿物质载体(MC-1和MC-2),采用浸渍法合成了镍负载型催化剂。用常压固定床管式反应器,考察了液化石油气水蒸气重整反应活性,通过XRD、物理吸附等手段对催化剂进行了表征。结果表明,以MC-1、MC-2和SA、AS为载体的催化剂的水蒸气重整活性明显高于目前普遍使用的Ni/α-Al2O3催化剂。以SA为载体,负载5%镍的催化剂具有最好的水蒸气重整活性。在750 ℃,水碳比为2.0的条件下转化率达100%,C1选择性达94.46%。XRD分析结果表明1 300 ℃焙烧后的SA载体中存在α-Al2O3晶型和莫来石结构。硅、铝添加次序对水蒸气重整活性影响较大,硅-铝添加次序的催化剂样品的活性高于铝-硅添加次序的样品,C1选择性提高12.7%。 相似文献
43.
Dispersion of MoO3, NiO, ZnO on rutile TiO2 with low specific surface area was studied with Mercury Porosimeter, SEM, XPS and Ammonia Extraction method. The dispersion thresholds of MoO3, NiO, ZnO on three rutile TiO2 carriers were obtained with XPS, and com-pared with those on anatase TiO2 with high specific surf are area. Ammonia Extraction method was used to identify the surface oxide species interarting with support surface in different strength and it was found that the proportions of oxides that can not be extracted by ammonia extraction are different for MoO3, NiO and ZnO which are supported on rutile TiO2. 相似文献
44.
45.
A capillary gas chromatographic method is described for the quantitative determination of liquid paraffin in blood. Paraffin is extracted from blood into n-heptane. After solvent evaporation and dissolution of the residue in 100–200 μl n-heptane one μl is injected into a gas chromatograph fitted with a fused silica capillary column (Permabond® OV-1-CB-0.1, 10 m × 0.32 mm i.d.) and flame ionization detector. Analysis is performed by using an oven program [50°C (3 min)?285°C (5 min), rise 10%min]. The sensitivity (1.5 ng hexadecane) and the reproducibility prove the applicability of the method for the determination of liquid paraffin in blood and for the study of the stability of the liquid paraffin hollow fiber membranes used in an extracorporeal liver support system. 相似文献
46.
S. Küppers 《Accreditation and quality assurance》1997,2(1):30-35
Any analytical data is used to provide information about a sample. The "possible error" of the measurement can be of extreme
importance in order to have complete information. The measurement uncertainty concept is a way to achieve quantitative information
about this "possible error" using an estimation procedure. On the basis of the analytical result, the chemist makes a decision
on the next step of the development process. If the uncertainty is unknown, the information is not complete; therefore this
decision might be impossible. The major problem for the in-process control (IPC) procedure is that not only the repeatability
but also the intermediate precision (which expresses the variations within laboratories related to different days, different
analysts, different equipment, etc.) has to be good enough to make a decision. Unfortunately, the statistical information
achieved from one single analytical run only gives information about the repeatability. This paper shows that the estimation
of the measurement uncertainty for IPC is a way to solve the problem and gives the necessary information about the quality
of the procedure. An example demonstrates that an estimate of uncertainty based on the standard deviations of an analytical
method gives a value similar to one based on the standard deviations obtained from a control chart. Therefore, the estimation
is both a very useful and also a very cost-effective tool. Though measurement uncertainty cannot replace validation in general,
it is a viable alternative to validation for all methods that will never be used routinely.
Received: 24 May 1996 Accepted: 10 August 1996 相似文献
47.
玻璃载体表面脱氧核糖核酸的固定及其化学发光检测 总被引:2,自引:0,他引:2
用硅烷化偶联剂把DNA直接共价固定在载玻片表面,将辣根过氧化物酶标记的探针与之进行核酸杂交,杂交后用增强的化学发光检测。方法的检出限为75pg。研究了DNA分子固定在玻璃载体表面的各种条件,并建立了在玻璃载体表面进行核酸杂交的体系,为研究光纤DNA生物传感器打下了基础。 相似文献
48.
STUDY ON 1-HEXENE POLYMERIZATION BASED ON ZIEGLER-NATTA CATALYSTS WITH DOPED SUPPORT 总被引:1,自引:0,他引:1
XueJiang Zhi-qiangFan 《高分子科学》2004,(4):305-308
A series of Ti/Mg supported catalysts are prepared by using ball-milled mixtures of MgCl2-ethanol adducts and NaCl as supports, and 1-hexene polymerizations catalyzed by the novel catalysts are studied. It is found that the molecular weight distribution of poly(1-hexene) becomes apparently narrower when catalysts with doped supports are used, indicating that changing the structure of the support is an effective way to regulate the active center distribution of heterogeneous Ziegler-Natta catalyst. 相似文献
49.
Yoichi M.A Yamada 《Tetrahedron》2004,60(18):4097-4105
The efficient heterogeneous Heck reaction was achieved by a new networked and supramolecular catalyst PdAS-V (1b). Employing of PdAS-V in 5.0×10−5 mol equiv. efficiently progressed the heterogeneous Heck reaction of a series of aryl iodides with acrylates, styrenes and acrylic acid. PdAS-V was successfully recycled five times without any decrease in its activity, and showed good stability in toluene and water, and hence the Heck reaction was efficiently performed in both reaction media. The use of 8.0×10−7 mol equiv. of PdAS-V resulted in the coupling product in 92% yield with the turnover number (TON) and the turnover frequency (TOF) of PdAS-V reached up to 1,150,000 and 12,000, respectively. The efficient synthesis of resveratrol was achieved via the PdAS-V-promoted Heck reaction. 相似文献
50.