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91.
A molecular level mechanism is proposed for the highly selective 14-e– oxidative transformation ofn-butane to maleic anhydride on the surface of vanadyl pyrophosphate. The mechanism suggests that the dimeric active sites assume at any given time, one of four possible interconvertible states which differ from each other in the number of available oxygen atoms and the formal oxidation states of the individual vanadium atoms. The relative ratios of active sites in each of the four possible states are dictated by the reaction conditions, the redox properties of the reacting gases and the structure of the vanadyl pyrophosphate active surface. A crucial feature of the mechanism is a pseudo-ozonide surface species formed by the interaction of a chemisorbed dioxygen molecule and an adjacent metal-oxo group. This unusual species is responsible for the initial activation of then-butane, which occurs when the chemisorbed dioxygen abstracts an H-atom from the alkane and the adjacent metal-oxo group reacts with the incipient alkyl radical to form an alkoxy group. The proposed mechanism is entirely consistent with literature reports describing the behaviour of (VO)2P2O7 in flow, pulse and TAP reactors. 相似文献
92.
A number of targeted cytotoxic agents have been developed that selectively kill malignant or otherwise pathological cells. These engineered proteins consist of a potent cytotoxic element connected to a ligand domain that binds to specific molecules on the surface of the target cell. Several of these agents have shown promise in clinical trials and one is currently administered to patients. A significant technical obstacle that has impeded the development of some of these toxins is the difficulty of preparing certain recombinant proteins in properly folded forms. These fusion proteins have generally been produced in bacteria requiring them to be denatured and renatured in vitro. For some proteins this is an efficient process whereas for others it is not. We describe here a system to produce fusion toxins rapidly and efficiently by engineering mammalian cells to secrete them as properly folded molecules which can be purified in native form from cell culture medium. We have used this system to produce highly active preparations of DAB(389)-IL7, a molecule consisting of the catalytic and transmembrane domains of diphtheria toxin fused to interleukin 7. This system is generalizable and can be used to produce and evaluate rapidly fusion toxins incorporating novel or uncharacterized ligands. 相似文献
93.
94.
This paper describes the application of SwRI’s cold-start PO
x
catalyst technology to reduce cold-start hydrocarbon emissions from a US Tier 2 vehicle at −7 °C. A reduction in −7 °C (20
°F) cold-start hydrocarbons will help US Tier 2 vehicles meet the proposed EPA NMOG standards. Improvements in cold temperature
hydrocarbon emissions would also be beneficial in many parts of Europe during the winter months. In this work, a total hydrocarbon
reduction of 19% was realized at 24 °C, in line with previous results, but only up to 3% at −7 °C. Insufficient oxygen in
the engine-out exhaust gas at −7 °C was determined to be the reason why the PO
x
catalyst failed to significantly reduce HC emissions. Addition of supplemental oxygen to the exhaust during the cold-start,
to simulate an adjustment in the engine calibration to less rich operation, resulted in a total hydrocarbon reduction of 18%
with the PO
x
catalysts in place, but no benefit when the PO
x
catalysts were removed. Hence, the PO
x
catalyst approach can be used to good effect, even under sub-ambient cold-start conditions. 相似文献
95.
96.
以4-羟基-3-硝基苯甲酸为原料,经酯化、醚化、还原合环、硝化、水解等5步反应,合成了两个未见文献报导的化合物7-硝基-3-氧-3,4-二氢-2H-[1,4]苯并噁嗪-6-羧酸和8-硝基-3-氧-3,4-二氢-2H-[1,4]苯并嗪-6-羧酸,其结构经IR、LC/MS、1HNMR和元素分析确证。 相似文献
97.
98.
Flaky monoclinic La2Ti2O7 was prepared via a hydrothermal method based on the reaction of Ti(SO4)2 and La(NO3)3. Relative to the solid-state reaction sample, the flaky La2Ti2O7 showed higher surface areas, much smaller crystal size and more efficient light absorption. All these factors led to the
higher photoactivity to produce H2 from water splitting under UV irradiation. 相似文献
99.
100.
Stabilization of -alumina phase by silica was studied in nanocomposite (diphasic) alumina-silica gels by XRD and BET surface areas measurements. Five wt.% of silica (22 nm particles) increased the crystallization temperature of to -alumina by about 100°C from boehmite (10 nm particles) derived alumina. Stabilization of -alumina was caused by the formation of intimate contact (Al-O-Si) between components by diffusion of silica into the defect alumina structure.Also with the Department of Agronomy. 相似文献