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41.
Z. J. Pei S. Kassir Milind Bhagavat Graham R. Fisher 《International Journal of Machine Tools and Manufacture》2004,44(2-3):299-306
Silicon is the primary semiconductor material used to fabricate microchips. A series of processes are required to manufacture high-quality silicon wafers. Surface grinding is one of the processes used to flatten wire-sawn wafers. A major issue in grinding of wire-sawn wafers is reduction and elimination of wire-sawing induced waviness. Results of finite element analysis have shown that soft-pad grinding is very effective in reducing the waviness. This paper presents an experimental investigation into soft-pad grinding of wire-sawn silicon wafers. Wire-sawn wafers from a same silicon ingot were used for the study to ensure that these wafers have similar waviness. These wafers were ground using two different soft pads. As a comparison, some wafers were also ground on a rigid chuck. Effectiveness of soft-pad grinding in removing waviness has been clearly demonstrated. 相似文献
42.
Bradley James C.; Richards W.Graham 《Protein engineering, design & selection : PEDS》1994,7(7):859-862
Model structures for the pore of the potassium channels Shakerand ROMK1 are predicted. The models arise from computer simulationsand suggest reasons for the striking selectivity of these channelsfor K+ and the blocking of ROMK1 by internal Mg2+. The modelledstructure of the Shaker pore is supported by mutagenesis data.The mutagenesis experiments indicate the side chains responsiblefor binding to blocking agents [tetraethylammonium (TEA) andcharybdotoxin (CTX)] and the model has these side chains suitablyoriented for binding. An aromatic K+ binding site part way downthe pore is also predicted by the Shaker pore model. 相似文献
43.
A remarkably high inferred initial rate of NO oxidation by O2 has been observed over Ba–Y, FAU zeolite at 25 °C in simple flow-reactor experiments. The rate of reaction at steady state
was found to be lower, but still an order of magnitude greater than over alumina-supported Pt, also at 25 °C. 相似文献
44.
Gang Li Dan I. Enache Jennifer Edwards Albert F. Carley David W. Knight Graham J. Hutchings 《Catalysis Letters》2006,110(1-2):7-13
The oxidation of benzyl alcohol to benzaldehyde has been investigated in the absence of solvent using zeolite-supported Au
and Au–Pd catalysts. Three zeolites were investigated, ZSM-5, zeolite β and zeolite Y, and these were contrasted with the
titanoslicalite TS-1 and TiO2 as supports. For the Au catalysts the best results are obtained with zeolite β as the support and the conversions were comparable
or better than those observed with TiO2 in terms of turn over frequencies. However, the selectivities observed with the acidic zeolites were lower than the non-acidic
TS-1 and TiO2. This is due to the subsequent reaction of benzaldehyde via acid catalysed reactions to give benzyl benzoate and its dibenzyl
acetal, and, in some cases dibenzylether. Initial catalysts were evaluated with a gold loading of 2 wt% and increasing this
to 4 wt% showed the expected increase in activity, indicating that there is scope to improve the performance of these catalysts.
The most active catalysts were prepared by impregnation and catalysts prepared by deposition precipitation were considerably
less active. Introduction of Pd into the catalyst improved the activity without significantly affecting the selectivity. 相似文献
45.
Esmail O. Elakesh T. Richard Hull Dennis Price Graham J. Milnes Peter Carty 《乙烯基与添加剂工艺杂志》2005,11(1):21-27
Plasticized samples of chlorinated polyvinylchloride (CPVC) were investigated by using thermogravimetric (TG) analysis and differential scanning calorimetry (DSC). Three different plasticizers were studied, namely, dioctyl phthalate (DOP), alkyldiaryl phosphate ester (Santiciser 2148), and triaryl phosphate ester (Reofos 50). TG experiments in nitrogen showed one major decomposition stage, involving dehydrochlorination, and minor pyrolysis reaction of the hydrocarbon residue. In contrast to the three stages previously reported to occur in the nonplasticized‐stabilized CPVC, TG analyses in air showed two distinctive decomposition stages for the plasticized CPVC samples. The DOP system provided a suggestion of a third stage. The first decomposition stage was due not only to the loss of all the chlorine present, but also to loss of the plasticizer or its decomposition products. The second decomposition stage was mostly due to char oxidation, the char being formed almost exclusively from the DCE and VDC units in CPVC polymer. DSC results showed that in the presence of nitrogen, there was no significant plasticizer effect on the thermal decomposition behavior of CPVC up to about 330°C, while in air the DSC traces also show no significant differences below 400°C. The two phosphate plasticizers showed no significant differences in their effect on the thermal decomposition behavior of CPVC under the same experimental conditions. It is believed that P2O5 and polyphosphoric acid are among the main constituents of the residua. These would impart a protective glassy surface to the char. This will facilitate effective flame retardant action. This preliminary conclusion is based on the premise that the more stable the char layers are, the more resilient will be the protective layer, and consequently, the better the flame retardant effect. J. VINYL ADDIT. TECHNOL., 11:21–27, 2005. © 2005 Society of Plastics Engineers 相似文献
46.
Saleh Al-Sayari Albert F. Carley Stuart H. Taylor Graham J. Hutchings 《Topics in Catalysis》2007,44(1-2):123-128
The preparation of Au/ZnO and Au/Fe2O3 catalysts using two coprecipitation methods is investigated to determine the important factors that control the synthesis
of high activity catalysts for the oxidation of carbon monoxide at ambient temperature. In particular, the factors involved
in the preparation of catalysts that are active without the need for a calcination step are evaluated. The two preparation
methods differ in the manner in which the pH is controlled during the precipitation, either constant pH throughout or variable
pH in which the pH is raised from an initial low value to a defined end point. Non-calcined Au/ZnO catalysts prepared using
both methods are very sensitive to pH and ageing time, and catalysts prepared at a maximum pH = 5 with a short ageing time
(ca. 0–3 h) exhibit high activity. Catalysts prepared at higher pH give lower activity. However, all catalysts require a short
operation period during which the oxidation activity increases. In contrast, the calcined catalysts are not particularly sensitive
to the preparation conditions. Non-calcined Au/Fe2O3 catalysts exhibit high activity when prepared at pH ≥ 5. Calcined Au/Fe2O3 prepared using the controlled pH method retain high activity, whereas calcined catalysts prepared using the variable pH method
are inactive. The study shows the immense sensitivity of the catalyst performance to the preparation methods. It is therefore
not surprising that marked differences in the performance of supported Au catalysts for CO oxidation that are apparent in
the extensive literature on this subject, particularly the effect of calcination, can be expected if the preparation parameters
are not carefully controlled and reported. 相似文献
47.
Graham M. Carter John L. Henshall Robert M. Hooper 《Journal of the American Ceramic Society》1988,71(5):270-C
Indentation creep of yttria- and calcia-fully-stabilized single-crystal zirconia has been observed at room temperature. The Knoop hardnesses decreased by 15% and 12% of their conventional short-time values, respectively, for indentation times of 100000 s. 相似文献
48.
Zoran D. Zujovic Marija R. Gizdavic-Nikolaidis Paul A. Kilmartin Hicham Idriss Sanjaya D. Senanayake Graham A. Bowmaker 《Polymer》2006,47(4):1166-1171
The quantitative investigation of the radical scavenging properties of polyaniline (PANI) upon reaction with excess of the stable DPPH radical (a 4:1 ratio of DPPH to aniline units in the polymer) was carried out using 15N and 13C solid state NMR spectroscopy. During the process the polyaniline was oxidised so that the imine content increased from 45 to 65%. The extent of oxidation measured by NMR was confirmed by N1s XPS analysis. However, within a 30 min reaction time, about 85% of the DPPH radicals were scavenged as monitored by the decay in its EPR signal. This is about 20 times greater than the fraction of DPPH required to oxidize PANI from an imine content of 45-65%. An identification of further redox processes is required to explain the high degree of radical scavenging. At the same time, there was no evidence of significant chemical binding or trapping of DPPH in the PANI structure. 相似文献
49.
Xiaobao Li Richard P. K. Wells Peter B. Wells Graham J. Hutchings 《Catalysis Letters》2003,89(3-4):163-167
The premodification of a 5 wt% Pt/-Al2O3 catalyst with cinchonidine (0.01 and 0.2 g g-1
catalyst) is described and discussed. Premodification is carried out by treating the catalyst with a solution of cinchonidine followed by solvent removal. Catalysts premodified in this way give the same ee and initial rate of reaction for the enantioselective hydrogenation of ethyl pyruvate as those using the standard in situ modification procedure. Investigations of different solvents for premodification and reaction (dichloromethane, ethanol) show that it is the solvent used for the reaction that controls the observed enantioselection. Premodified catalysts also display the initial transient behavior typically observed with in situ modified catalysts in which the ee increases with conversion in the early part of the reaction. Premodified catalysts show an enhanced rate of reaction when ethanol is used as the reaction solvent compared with in situ modified catalysts under the same conditions. Premodification using aerobic conditions gives the best results and premodified catalysts can be stored prior to use for up to a week without loss of catalytic performance. 相似文献
50.
In the ceramic technology the first step to produce sintered bodies is the manufacturing of powders which then are densified. The adhesion mechanisms between the single particles and the agglomerates produced from them determine the densification process. Starting from theoretical considerations adhesion mechanisms, such as solid bridge formation, adhesive bonding and glide-promoting effects, are discussed in principle. Subsequently, the effects of surface-active substances on the densification behaviour of clay-ceramics and oxide-ceramic bodies are discussed. Further, the evaluation of the action of additives to the powder mixtures on the microstructure of the compacts, such as porsity and texture, leads to a compaction equation which describes the transition from the powder pile to a densified green body. 相似文献