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11.
The various metal ratios of PdCoNi/G nanocomposites (PdCoNi/G 6:1:1, 6:3:3, 6:4.5:1.5, 6:1.5:4.5, and 6:9:9) supported on graphene were synthesized using a chemical reduction of metal compounds and graphite oxide with a strong reducing agent under N2 conditions without calcinations to improve the electrocatalytic performance for methanol electrooxidation. SEM, EDX, XRD, XPS, and XANES were used to study the physical and chemical properties of all electrocatalysts. The composition of PdCoNi/G electrocatalysts was in the form of palladium metal, cobalt oxides, and nickel oxide. The electrocatalysis activity of methanol oxidation in 1 M KOH was investigated by cyclic voltammetry and chronoamperometry. It was found that PdCoNi/G (6:1:1) nanocomposite enhanced the catalytic activity. The relative potential showed the highest current density (17.27 mA/cm2) and negative potential (??0.065 V) in the catalyst studies. In addition, PdCoNi/G (6:1:1) nanoncomposite presented the best intermediate poisoning tolerance for the methanol oxidation of all synthesized electrocatalysts. These confirmed that PdCoNi/G (6:1:1) is very promising for applications in direct methanol fuel cell (DMFC).

Graphical Abstract

Schematic illustration of the synthesis of PdCoNi metal nanocomposites (various metal ratios) supported on graphene (a) oxidation of graphite to GO and (b) reduction between GO and metal compounds with NaBH4 as a reducing agent.
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12.
The direct coating of a nano-porous alumina layer on the inner surface of micro-porous alumina tubes was performed by electrophoretic deposition (EPD). A thin layer of polypyrrole (Ppy) was synthesized on the inside wall of the porous tubes by the chemical polymerization of pyrrole (Py) to give the wall electric conduction for the EPD electrode. The bimodal suspension of alumina powders with 0.6 μm and 30 nm average particle sizes was selected to control the nano-porous structure. The thickness of the coating layer was controlled by altering the applied voltage and deposition time. The interfacial connection of the coated layer and the substrate was observed by SEM before and after sintering. The pore size of the coated layer was characterized by its pore size distribution.  相似文献   
13.
A catholyte is a key factor to hydrogen production in microbial electrolysis cells (MECs). Among the four groups of catholytes investigated in this study, a 100 mM phosphate buffer solution (PBS) resulted in the highest hydrogen production rate of 0.237 ± 0.031 m3H2/m3/d, followed by 0.171 ± 0.012 m3H2/m3/d with a 134 mM NaCl solution and 0.171 ± 0.004 m3H2/m3/d with the acidified water adjusted with sulfuric acid. The MEC with all catholytes achieved good organic removal efficiency, but the removal rate varied following the trend of the hydrogen production rate. The reuse of the catholyte for an extended period led to a decreasing hydrogen production rate, affected by the elevated pH. The cost of both the acidified water and the NaCl solution was much lower than the PBS, and therefore, they could be a better choice as an MEC catholyte with further consideration of cost reduction and chemical reuse/disposal.  相似文献   
14.
Physical properties and the microstructure of Som-fug, a Thai-style fermented fish sausage, with seven different commercial brands were determined. The released water contents of Som-fug samples ranged from 5.81 to 15.81% and expressible water contents were different among the samples tested (p<0.05). Differences in hardness, fracturability, adhesiveness, springiness, cohesiveness and resilience were also observed. L*, a*, b* and whiteness varied with the samples. Overall, the samples had different acceptability in texture and color. Microstructural study revealed that Som-fug had a three-dimensional network. A more void and open structure correlated well with greater released water and was associated with lower hardness and cohesiveness. Therefore, the different physical properties and microstructure of Som-fug could be influenced by the differences in raw materials, ingredients, processing, and fermentation characteristics, and determined the acceptability of products.  相似文献   
15.
Curcumin, a major active compound in the turmeric rhizome, has many biological properties, especially anti-leukemia activity. The overexpression of FMS-like tyrosine kinase 3 protein with internal tandem duplication (FLT3-ITD) mutation protein was related to the poor prognosis and disease progression of leukemia. In this study, the cytotoxicity and inhibitory effect of curcumin on cell cycle of FLT3-ITD overexpressing MV4-11 leukemic cells were evaluated. Moreover, curcumin polymeric micelles conjugated with FLT3-specific peptide (FLT3-Cur-micelles) were prepared using a film hydration method to increase curcumin solubility and the inhibitory effect on MV4-11 cells was evaluated. Cytotoxicity and cell cycle analysis were performed using an MTT assay and flow cytometry, respectively. Physical properties of FLT3-Cur-micelles, including particle size, size distribution, morphology, and entrapment efficiency (EE), were evaluated. Cellular uptake of the micelles on MV4-11 cells was determined by flow cytometry and fluorescence microscopy. FLT3-Cur-micelles were observed with size less than 50?nm and high EE of >75%. In addition, FLT3-Cur-micelles demonstrated excellent internalization and increased curcumin accumulation in leukemic cells when compared to free curcumin. Furthermore, FLT3-Cur-micelles exhibited a strong cytotoxic effect on MV4-11 cells with IC50 value of 1.1?µM, whereas the blank micelles showed no effect. Furthermore, FLT3-Cur-micelles showed no significant effect on normal human PBMCs with IC50 value >25?µM. In summary, FLT3-Cur-micelles are a promising nanocarrier system for enhancing anti-leukemic activity of curcumin and suitable for further preclinical studies.  相似文献   
16.
Different Pt/KL catalysts containing rare earth (RE; Ce and Yb) promoters were prepared by two techniques, incipient wetness impregnation (IWI) and vapor phase impregnation (VPI). The catalysts were tested for the activity and the selectivity of n-hexane aromatization to benzene under clean, sulfur-containing, and water-containing feeds at 500 °C. It was observed that the catalysts prepared by the VPI technique exhibited much higher activity and selectivity than those prepared by IWI. It was also found that although under clean conditions, the addition of Ce or Yb caused a decrease in activity, in the presence of sulfur the addition of Ce and to a lesser extent Yb, significantly inhibited catalyst deactivation.

The influence of water in the feed was investigated by contacting the catalysts for 1 h to a feed containing 3 mol.% water. After this treatment, all the catalysts exhibited a significant activity loss. This loss was more pronounced for the catalyst prepared by the VPI method. The catalyst prepared by IWI already had suffered a significant deactivation before the water treatment, so the activity drop was not so pronounced. The sample prepared by VPI not only showed a drop in activity immediately after the water treatment but it became more susceptible to deactivation afterwards. By contrast, the Ce-promoted catalyst showed a more stable activity after the water treatment.

All catalysts were characterized before and after reaction by a number of techniques. In agreement with previous studies, FT-IR of adsorbed CO and chemisorption results indicated that the VPI method resulted in higher Pt dispersion than that obtained by the IWI method. After reaction in the presence of sulfur, the Ce-promoted Pt/KL catalyst showed a higher resistance to metal agglomeration and a lower rate of coke formation than the unpromoted Pt/KL. On all the catalysts, the amount of carbon deposits was greater in the presence of sulfur and after exposure to water vapor than under the reaction with clean feeds. This difference is explained in terms of metal particle growth and location in the zeolite.  相似文献   

17.
Short-oil alkyd resins were prepared by using five different oil types: corn oil, rice bran oil, sunflower oil, soya bean oil and dehydrated castor oil (DCO). Among these, soya bean oil gave alkyd resin with the darkest color because oxidation occurred. Auto air-dried coating films were developed and it was shown that film prepared from rice bran oil-based alkyd exhibited the longest drying time due to the low number of double bonds compared to other and the extra natural antioxidant in rice bran oil. DCO alkyd-based film revealed the shortest drying time, the greatest hardness but the poorest alkali and sea-water resistance. This is caused by the differences in the type of fatty acid and double bonds, the high amount of double bonds being in DCO. In addition, an increase in the reaction temperature only had an influence on darkening the alkyd color and decreasing the drying time of coating films. In terms of technical properties and cost competitiveness, soya bean oil-based film is the best. Coating films derived from all oil-based alkyds, except DCO, look promising for use in surfboard manufacturing.  相似文献   
18.
Platinum catalysts supported on the potassium-form of different large-pore zeolites (i.e. K-LTL, K-BEA, K-MAZ, and K-FAU) have been tested for n-octane aromatization at 500 °C. All catalysts were prepared by the vapor phase impregnation (VPI) method. It was found that the Pt/K-LTL catalyst exhibit a better aromatization performance than the other zeolite catalysts. However, due to secondary hydrogenolysis, the C8 aromatics produced inside the zeolite are converted to benzene and toluene. By contrast, a non-microporous Pt/SiO2 catalyst did not present the secondary hydrogenolysis. Therefore, despite a lower initial aromatization activity, Pt/SiO2 results in higher selectivity to C8 aromatics than any of the other zeolite catalysts. All fresh catalysts were characterized by hydrogen chemisorption and FT-IR of adsorbed CO. In addition, the residual acidity of the supports was analyzed by temperature programmed desorption (TPD) of ammonia. In agreement with previous studies, it was found that after reduction at either 350 or 500 °C, the Pt/K-LTL showed much higher Pt dispersion than other catalysts. It is known that the structure of L zeolite can stabilize the small Pt clusters inside the zeolite channel. By contrast, FT-IR indicated that a large fraction of platinum clusters were located outside the zeolite channels in the case of Pt/K-BEA and Pt/K-MAZ catalysts.  相似文献   
19.
The hydrogenation of tetralin in the vapor phase has been investigated over Ni, Pt, and Pd catalysts to determine the evolution of the trans- and cis-decalin products as a function of conversion over the different catalysts. The concentration of each isomer in the product may be important in subsequent ring opening steps if cetane number improvement is desired. The cis-decalin isomer is preferred to open the naphthenic ring in a selective way instead of multiple cracking. However, thermodynamically, this isomer is the least favored; so, kinetic control is the only solution. By selecting the proper catalyst and operating conditions, one could keep the trans/cis-decalin ratio low. In this study, we have prepared a series of supported metal catalysts and tested them in a flow reactor at 3540 kPa and 548 K. Kinetic parameters for the hydrogenation of tetralin and the cis-to-trans-decalin isomerization over the various catalysts investigated were obtained by fitting the data with a generalized Langmuir–Hinshelwood model.

The kinetic analysis revealed that the relative rates of tetralin hydrogenation, as well as the cis-to-trans isomerization are greatly affected by adsorption site competition of decalin and tetralin, which in turn has different magnitudes over the different catalysts. At tetralin conversions above 30%, the Ni catalyst yields the lowest trans/cis-decalin ratio. In contrast, the trans/cis ratio on Pd catalyst remains constant at all conversion levels and is highest at low tetralin conversion. It is concluded that the trans/cis ratio is a combination of the intrinsic selectivity of each isomer and the isomerization reaction.  相似文献   

20.
The effect of iced storage of bigeye snapper (Priacanthus tayenus) on the chemical composition, properties and acceptability of Som-fug was investigated. During 15 days of iced storage, total volatile base (TVB), trimethylamine (TMA) and TCA-soluble peptide contents as well as thiobarbituric reactive substances (TBARS) of fish muscle increased continuously after 3 days of storage (p < 0.05). It was suggested that deterioration, protein degradation and lipid oxidation proceeded with increasing storage time. Som-fug prepared from surimi of bigeye snapper stored in ice for different times had similar pH, acidity and lactic acid bacteria count at the end of the fermentation (30 °C, 48 h). Generally, higher content of TCA-soluble peptides and higher TBARS were found in fermented Som-fug produced from bigeye snapper stored in ice for a longer time (p < 0.05). Hardness, adhesiveness, springiness, cohesiveness, and resilience of fermented Som-fug decreased with a concomitant increase in weight loss, released water and expressible water contents when fish kept for a longer time were used (p < 0.05). L, a, b, whiteness and the likeness for appearance, colour, texture and flavour of Som-fug decreased when fish kept in ice for an extended time were used (p < 0.05). However, the taste likeness was not affected by iced storage time (p > 0.05). No differences in overall liking were noticeable when fish kept in ice for up to 12 days were used for Som-fug production (p > 0.05). Therefore, the quality of fish used as raw material should be an important factor in determining the characteristics of Som-fug.  相似文献   
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