A study on the catalytic performance of Pd/γ-Al2O3, prepared by microwave calcination, in the direct synthesis of dimethylether

A series of Pd/γ-Al₂O₃ hybrid catalysts were prepared by impregnation and subsequent calcination under microwave irradiation. The catalysts were used for direct synthesis of dimethylether (DME) from syngas. The results show that calcination under microwave irradiation improved both the activity and selectivity of the catalysts for DME synthesis. The optimum power of the microwave was determined to be 420 W. Under such optimum conditions, CO conversion, DME selectivity and time space yield of DME were 60.1%, 67.0%, and 21.5 mmol·mL⁻¹·h⁻¹, respectively. Based on various characterizations such as nitrogen physisorption, X-ray diffraction, CO-temperature- programmed desorption, and Fourier transform infrared spectral analysis, the promotional effect of the microwave irradiation on the catalytic property was mainly attributed to both the higher dispersion of Pd and the significant increase in the adsorption on the CO-bridge of Pd. Microwave irradiation with very high power led to the increase in CO-bridge adsorption and thereby decreased the catalytic activity, whereas the coverage by metallic Pd of the active sites on acidic γ-Al₂O₃ significantly occurred under microwave irradiation with very low power, resulting in a decrease in the selectivity to DME.     

聚合物水泥防水浆料及标准解读

本文介绍了聚合物水泥防水浆料行业标准的立项背景、标准制定原则、标准的技术要求及检验方法。     

轻钢加层厂房的地震反应分析

结合实例,利用ANSYS有限元软件,采用三维空间有限元模型,对钢筋混凝土框架结构、门式刚架及加层后的整体结构进行了模态分析和谱分析,获得了结构的动力特性和地震作用效应的变化规律,为轻钢加层厂房的应用提供了一定参考。     

鳜鱼消化酶活性的研究

本试验测定了鳜胃、肠道、肝脏和幽门盲囊中蛋白酶、淀粉酶主要消化酶的活性及pH对这些酶活性的影响。结果表明:从鳜的胃、肠、肝脏和幽门盲囊中均可检测出蛋白酶、淀粉酶的活性,各消化器官淀粉酶活性最适pH值分别为:肝胰脏7.0、胃6.6、幽门盲囊7.4、前肠6.6、中肠6.2、后肠6.6;且最适pH条件下淀粉酶活性大小为肝胰脏胃前肠中肠幽门盲囊后肠。蛋白酶活性最适pH值分别为:肝胰脏6.6、胃2.6、幽门盲囊4.2、前肠3.0、中肠6.6、后肠5.4。在最适pH条件下,各消化器官蛋白酶活力大小为:后肠〉中肠〉肝胰脏〉幽门〉胃〉前肠。     

Do existing ecological classifications characterize the spatial variability of stream temperatures in the Great Lakes Basin,Ontario?

Ecological classifications of stream ecosystems have been used to develop monitoring programs, identify reference and impacted systems, and focus conservation efforts. One of the most influential, but highly variable, components of stream ecosystems is water temperature but few geographically broad-scale and long-term programs exist to assess and monitor temperatures. This study evaluated if existing ecological classifications could be used to categorize the similarities and differences in stream temperatures across the Ontario portion of the Great Lakes Basin. Concordance between the spatial variability in temperatures and an existing ecological classification would support the use of that classification to define areas with similar temperatures, guide the development of a monitoring program, and inform management programs. The five classifications evaluated were the ecoregions and ecodistricts defined in the National Ecological Framework for Canada, the ecoregions and ecodistricts defined in the Ecological Land Classification of Ontario, and the aquatic ecosystem units defined in the Aquatic Ecosystem Classification (AEC) for the Ontario portion of the Great Lakes Basin. Hierarchical linear modelling and corrected Akaike Information Criterion indicated that the ecodistrict classifications characterized more of the spatial variability in temperatures than the ecoregion and AEC classification but temperatures were more variable among sites within classes than between classes. Therefore, none of the existing ecological classifications could be used to characterize thermal variability. Future research should examine if the inability of the existing classifications to capture the thermal variability translates into inaccurate classification of other ecosystem components such as water quality, and macroinvertebrate and fish assemblages.     

Densification kinetics and sintering behavior of UO2 and 0.5 wt.%MnO-doped UO2

In this work, the sintering kinetics of pure UO₂ and 0.5 wt.%MnO-doped UO₂ was studied by a high-temperature dilatometer heated up to 1500°C. In addition, the sintering behavior of pure UO₂ and 0.5 wt.%MnO-doped UO₂ was studied by pressureless sintering technique. The results showed that MnO doping enhanced the grain boundary diffusion of UO₂, which can effectively decrease the densification temperature and promote grain growth. The sintering temperature of UO₂ was significantly reduced by about 200°C with the addition of 0.5 wt.%MnO. The microscopic morphology studies showed that there were still fine particles agglomerated, forming sintered spheres in the matrix even if no severe agglomeration and bimodal size distribution were observed in raw UO₂ powder. The microstructure evolution of the sintered sphere and UO₂ matrix during the densification process was studied by isothermal sintering. Finally, the present analyses indicated that the densification of UO₂ matrix can be accelerated by adding MnO or increasing the sintering temperature, thus improving the densification inhomogeneity of UO₂ matrix.     

Effects of storage conditions on oxidative stability of soybean oil

Soybean oil in the presence or absence of 200 µg g^?1 tert‐butyl hydroquinone (TBHQ) was subjected to accelerated oxidative storage at 60 °C for 10 days or stored at room temperature for 12 months. Tocopherol contents of the oil decreased, whereas the headspace volatiles and peroxide values (PV) increased as the storage time increased. During accelerated storage, TBHQ was effective in retarding the formation of hydroperoxides and headspace volatiles in the oil. TBHQ also protected tocopherols, especially α‐tocopherol, from oxidation. During long‐term room‐temperature (LTRT) storage, the changes in PV between the oils with and without TBHQ were similar, but the oil with TBHQ had lower headspace volatile contents than that without TBHQ. Headspace volatile analysis was more suitable than PV measurement for predicting the oxidative stability of soybean oil during LTRT storage. The contents of hexanal or (E)‐2‐heptenal in the oil at 1–5 days of accelerated storage could be used to predict those of the corresponding compound in the oil at 0–4 weeks of LTRT storage. Copyright © 2005 Society of Chemical Industry     

Analysis of "total toxaphene" and selected single congeners in biota by ion trap HRGC-EI-MS/MS using congener-optimized parent ion dissociations

A method for the quantification of selected toxaphene congeners as well as "total toxaphene" was developed based on electron ionization (EI) tandem (MS/MS) ion trap mass spectrometry (MS) and a combination of fragment ion dissociations. Congeners were separated by high-resolution gas chromatography. Compared to conventional EI low-resolution MS, a 5-20-fold gain in sensitivity could be obtained for octa- or nonachlorinated compounds such as toxaphene #26 and #62 (according to Parlar nomenclature), allowing for their detection in the low picogram range in biota. In addition, response factors for important congeners such as #26, #32, #40/41, #42, #44, #50, and #62 deviated not more than a factor of 2, which is much less as compared to negative ion chemical ionization. This reduces the risk for systematic errors when determining total toxaphene on the basis of a limited number of reference compounds or the technical mixture. Furthermore, chlordanes and polychlorinated biphenyls did not interfere when applying the proposed MS/MS technique. The applicability of the method was tested by determining both total toxaphene and levels of selected congeners in six Arctic wildlife samples collected from Nunavut, Canada, as well as by repetitive analyses of the SRM 1588 certified reference material.     

The aqueous degradation of butylated hydroxyanisole by UV/S2O8(2-): study of reaction mechanisms via dimerization and mineralization

Three distinctive phases of BHA reactivity toward UV/ S2O8(2-) at acidic, neutral, and basic pH range were examined, where 80-100% mineralization has been observed within an hour of irradiation under 254 nm. A reduction in solution pH during the reaction was observed mainly due to the complete conversion of S2O8(2-) to sulfate ion together with proton generation. Seven measurable intermediates were found via an oxidation and dimerization process at all tested pH levels. The BHA decay mechanisms are quite different in acidic condition and at other pH levels. There are three unique intermediates that are only detectable at pH 3 via two additional pathways. This is due to the generation of weaker oxidants or radicals which results in a slower degradation of the BHA, and therefore, the accumulation of these intermediates to detectable levels. The rate of BHA decay generally increases from low to high pH levels; however, the corresponding mineralization at higher pH is retarded due to the futile process of recombining radicals and involvement of intermediates. Therefore, neutral pH was suggested to be the optimum condition in terms of mineralization and moderate efficiency in removing BHA.     

Use of oligonucleotide array for identification of six foodborne pathogens and Pseudomonas aeruginosa grown on selective media

Identification of presumptive foodborne pathogens grown on selective media may take one to several days and requires a different battery of biochemical tests for each microorganism. A molecular identification method was developed in which universal primers were used to amplify the 16S to 23S rDNA intergenic spacer of target microorganisms, and PCR products were hybridized to a panel of species-specific oligonucleotides that were immobilized on a nylon membrane. The seven target microorganisms were Bacillus cereus, Escherichia coli, Listeria monocytogenes, Pseudomonas aeruginosa, Salmonella, Staphylococcus aureus, and Vibrio parahaemolyticus. After testing a large collection of target bacteria (29 to 51 strains) and nontarget bacteria (> 500 strains), the performances (sensitivity and specificity) of the oligonucleotide array were as follows: B. cereus (100 and 77%), E. coli (100 and 100%), L. monocytogenes (100 and 90%), P. aeruginosa (100 and 100%), Salmonella (100 and 100%), S. aureus (100 and 100%), and V. parahaemolyticus (100 and 94.2%). Other species in the B. cereus group cross-hybridized to the probes used for identification of B. cereus, and positive results should be confirmed by additional morphological observation of colonies. Listeria innocua cross-reacted with probes used to identify L. monocytogenes, but a simple hemolysis test was used to differentiate the two species. Some strains of Vibrio harveyi and Vibrio mimicus cross-hybridized with probes used for identification of V. parahaemolyticus and caused false-positive reactions. The advantage of the array is that a common protocol was used to identify the seven target microorganisms and multiple different microorganisms could be simultaneously identified on a single array.