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61.
Ion exchange of HZSM-5 samples with alkali metal cations, using metal chloride solutions, results in partially exchanged zeolites, MHZSM-5, M = Li, Na, K or Cs. The degree of exchange is found to increase with increasing ionic radius of the cations. The catalytic properties of the alkalized zeolites were evaluated using the reaction conditions under which the catalytic activity of the HZSM-5 samples in terms of n-hexane cracking is proportional to the aluminium content. From the residual catalytic activity exhibited by the Na-, K- and CsHZSM-5 samples it is concluded that each of the larger Na+, K+ and Cs+ ions is influencing more than one AlO
4
–
tetrahedron, implying that the aluminium sites in ZSM-5 are not isolated. The ion-exchange results are then interpreted in terms of non-isolated aluminium sites. The ion-exchange and catalytic properties of the zeolites as a function of aluminium content are also discussed. 相似文献
62.
Consuelo Montes de Correa H. Ai´da Luz Villa 《Applied catalysis. B, Environmental》1996,10(4):313-323
The effect of Pd-loading on Pd-NaZSM-5 and Pd-NaMordenite catalysts prepared by ion exchange was studied for methane combustion with excess oxygen (1% CH4, 18% O2, balance N2) in the temperature range 40–500°C. Fresh and calcined samples (3 h, 450°C) showed methane conversions proportional to Pd-loading on Pd-NaZSM-5 catalysts, while conversions decreased with Pd-loading on calcined Pd-NaMordenite catalysts. TOF (number of methane molecules converted per second per Pd2+ ion) for over exchanged Pd-NaZSM5-116 was low as compared to under exchanged Pd-NaZSM5-80 and Pd-NaZSM5-58 samples. Close TOF's were found for the last two samples at 330°C. TOF differences in Pd-NaMordenite catalysts demonstrate the heterogeneity of Pd+2 sites due to structurally nonidentical locations of cations. TOF's appear to be related to Na/Pd ratios in both catalyst types. Apparent activation energies for Pd-NaZSM-5 materials are higher than those for Pd-NaMordenite catalysts. 相似文献
63.
J. H. Bordon J. R. Handley J. A. McLean R. M. Silverstein L. Chong K. N. Slessor B. D. Johnston H. R. Schuler 《Journal of chemical ecology》1980,6(2):445-456
The aggregation pheromone ofGnathotrichus retusus was isolated and identified as (S)-(+)-sulcatol (6-methyl-5-hepten-2-ol). In laboratory and field experiments,G. retusus responded to (S)-(+)-sulcatol, but not to (±)-sulcatol, which was attractive to the sympatric species,G. sulcatus. G. sulcatus did not respond to optically pure (S)-(+)-sulcatol, but began to respond when 1% (R)-(–)-sulcatol was present in an enantiomeric mixture.Research supported by the National Science Foundation, U.S.A. (Grant BMS-74-13643), and the Natural Sciences and Engineering Research Council of Canada (Co-op grant A0243 and Operating Grant A3881 and A3785). 相似文献
64.
介绍了基于IPv6视频资源服务平台的工作原理和关键技术,设计并开发了基于IPv6的视频资源服务平台,该平台能实现视频教学、影视娱乐、交流答疑、视频直播、视频点播等功能。 相似文献
65.
66.
67.
D. Miceli F. Arena A. Parmaliana M. S. Scurrell V. Sokolovskii 《Catalysis Letters》1993,18(3):283-288
Precipitated silica catalysts loaded with either MoO3 (0.2–4.0 wt%) or V2O5 (0.2–5.3 wt%) have been studied in the selective partial oxidation of methane to formaldehyde with molecular oxygen at 520 °C. The functionality of the SiO2 surface towards the formation of HCHO is significantly promoted by V2O5, while it is depressed by the MoO3. 相似文献
68.
69.
为减少和延缓旧水泥板沥青加铺层反射裂缝的产生,在分析研究各种夹层材料应用效果和SMA-5作为应力吸收层性能要求的基础上,设计了SMA-5应力吸收层的配合比,采用搓揉成型的方法改进了马歇尔试件,并对SMA-5沥青混合料的各项路用性能进行了试验研究,且成功的铺筑了试验路.结果表明:SMA-5沥青混合料可以作为夹层材料,并起到了很好的应力吸收效果.此项研究成果对于旧水泥混凝土路面加铺改造具有重要的工程实用价值,SMA-5应力吸收层具有广阔的应用前景. 相似文献
70.
Noemí de-los-Santos-Álvarez 《Electrochimica acta》2007,53(2):829-836
We have studied the potential electrocatalytic activity towards the oxidation of NADH of several oxidation products of guanine and its derivative guanosine-5′-monophosphate (5′-GMP) on pyrolytic graphite electrodes (PGE). The distribution of products generated strongly depends on the experimental conditions. Our investigations focused on the oxidation products that are adsorbed on the electrode surface, are redox active and, exhibited electrocatalytic activity toward the oxidation of NADH. These compounds were electrochemically and kinetically characterized in terms of dependence of the formal potential on pH and electron transfer rate constant (ks). The voltammetric and catalytic behavior of both guanine and 5′-GMP oxidation products was compared with that of other guanine derivatives we have previously studied. Some mechanistic aspects concerning the generation of the catalysts are also discussed. 相似文献