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91.
An ordering of magnesium is observed in the as-synthesized MAPO-36 molecular sieve. Upon calcination, part of the magnesium is removed from the sample and part occupies extraframework positions thus rendering a random distribution of magnesium in the lattice. The shoulder observed in the31P spectrum of the calcined sample is assigned to P(3Al, 1Mg) sites in conflict with the earlier assignment to P-OH groups. The bridging hydroxyl groups located at these sites are detected in the1H MAS spectrum at 3.6 ppm. Further, MAPO-36 catalyzed acetone conversion to mesityloxide that cracked at elevated temperature to yield acetic acid and aliphatics. 相似文献
92.
Heat-shock induction of heat-shock protein genes is due to a specific promoter element (the heat-shock element, HSE). This study used lacZ under HSE control (HSE-lacZ) to characterize HSE activity in Saccharomyces cerevisiae cells of different physiological states and differing genetic backgrounds. In batch fermentations HSE-lacZ induction by heat shock was maximal in exponential growth, and showed marked decline with the approach to stationary phase. Expression in the absence of heat shock was unaffected by growth phase, indicating that the growth-dependent expression of many yeast heat-shock genes uses promoter elements in addition to the HSE. Heat-induced expression was strongly influenced by the temperature at which cultures were grown. While basal, uninduced expression was constant during growth at different temperatures to 30 degrees C, induction by transfer to 39 degrees C was reduced by increases in growth temperature as low as 18-24 degrees C. Maximal HSE-lacZ induction (30- to 50-fold) was in cultures grown at low temperatures (18-24 degrees C), then heat shocked at 39 degrees C. Ethanol was a poor inducer. Mutations having little effect on HSE-lacZ expression included a respiratory petite; ubi4 (which inactivates the poly-ubiquitin gene); also ubc4 and ubc5 (which each inactivate one of the ubiquitin ligases involved in degradation of aberrant protein). pep4-3 increased both basal and induced beta-galactosidase about two-fold, probably because of slower turnover of this enzyme in pep4-3 strains. 相似文献
93.
双噁唑啉化合物对PBT的增粘作用 总被引:1,自引:0,他引:1
以2.2'-双(2-唑啉)和双(2-唑啉基)苯作扩链剂,用焙融挤出的方法,对聚对苯二甲酸丁二酯(PBT)进行扩链,考察扩链剂的用量、反应时间和反应温度对PBT的特性粘度及端羧基含量(CV)的影响。结果表明,当用2,2'-双(2-唑啉)作扩链剂时,PBT的特性粘度[η]从0.799提高到0.926dL/g,CV降至5eq/10 ̄6g以下;当用双(2- 唑啉基)苯作扩链剂,[η]从0.763增至0.925dL/g,CV降至10eq/10 ̄6g以下,达到了较满意的扩链效果。 相似文献
94.
Journal of Electronic Materials - Low pressure chemical vapor deposition (LPCVD) of tungsten (W) by SiH4 reduction of WF6 on Si(100) surfaces was studied in a single-wafer, cold-wall reactor over a... 相似文献
95.
分别以94%品位高钛渣和90%品位高钛渣为原料,采用沸腾氯化工艺制备粗TiCl4,分析了两种品位高钛渣对沸腾氯化工艺的影响。结果表明:94%品位高钛渣由于其活性低而对沸腾氯化工艺的影响较大。 相似文献
96.
VNS反应合成LLM-116 总被引:2,自引:0,他引:2
以1,3-二硝基吡唑为原料,经热重排、氨气中和得到3,5-二硝基吡唑铵盐,然后酸化得到3,5-二硝基吡唑。以三甲基肼碘化物(TMHI)作为异常亲核取代氢(VNS)反应试剂,与3,5-二硝基吡唑在叔丁醇钾为催化剂,利用VNS反应合成4-氨基-3,5-二硝基吡唑(LLM-116)。采用红外分析、核磁共振、元素分析等仪器鉴定了其结构,讨论了VNS反应机理及影响因素。通过实验,得出最佳VNS反应试剂为TMHI,反应时间为4h,反应温度为25℃,收率达到60%。 相似文献
97.
F. H. Sam Froes 《Powder Metallurgy and Metal Ceramics》2007,46(5-6):303-310
The approaches to production of titanium powder injection molded parts are reviewed. Historically, oxygen levels have been
too high for structural use (particularly with the Ti-6Al-4V alloy). However, recent advances in starting powders, binders
and sintering facilities now allow oxygen levels in the Ti-6Al-4V alloy to be controlled to about 0.2 wt.% oxygen. This should
result in significant expansion of the titanium PIM market place into aerospace, automobiles, surgical instruments, dentistry,
communication devices (such as computers and cell phones), knives and guns.
__________
Translated from Poroshkovaya Metallurgiya, Vol. 46, No. 5–6 (455), pp. 118–125, 2007. 相似文献
98.
99.
研制成用LD泵浦的声光调Q的Nd:YVO4-KTP腔内倍频激光器,得到了TEM00模、频率高达100kHz的稳定的532um绿激光脉冲系列输出,阈值泵浦功率为27mW;在连续570mW的泵浦功率下,绿激光脉冲的峰值功率达1100W,脉宽为4.6us;输出功率稳定,在±5℃的工作温度变化下,输出功率变化小于±2%。此种器件可望得到广泛的应用。 相似文献
100.
Maciej Winiewski Artur Jakubiak Jan Szymanowski 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1995,63(3):209-214
Decyl isonicotiniate and decyl nicotiniate permit a rapid extraction of palladium(II) from its hydrochloride solutions. Decyl picoliniate is not a suitable extractant. 4-Octylphenylamine can act as a phase transfer catalyst when its concentration in the organic phase is at least 2·5 × 10?4 M . It seems that the interfacial adsorption of pyridine carboxylates and of 4-octylphenylamine is not the decisive phenomenon in palladium(II) extraction. The negligible protonation of the pyridine-type extractants and the phase transfer catalysis explains well the quick extraction of palladium(II) with the commercial and highly hydrophobic extractant ACORGA CLX-50. 相似文献