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101.
Sulfonated carbon as a strong and stable solid acid catalyst exhibited excellent catalytic performance in various acid-catalyzed reactions. Here, sulfonated carbon, as catalyst for oxidation reaction, was prepared via the carbonization of starch followed by sulfonation with concentrated sulfuric acid. N2 physisorption, X-ray diffraction, Fourier transform infrared spectroscopy, X-ray fluorescence and acid-base titration were used to characterize the obtained materials. The catalytic activity of sulfonated carbon was studied in the oxidation of aldehydes to carboxylic acids using 30 wt% H2O2 as oxidant. This oxidation protocol works well for various aldehydes including aromatic and aliphatic aldehydes. The sulfonated carbon can be recycled for three times without obvious loss of activity.  相似文献   
102.
The structure and activity of RNase A in sodium dodecyl sulphate solutions were investigated at 25.0±0.1 and pH 7.00. The results show that with increasing sodium dodecyl sulphate concentration, the structure of RNase A is collapsed gradually, however, the activity of RNase A is first increased and then decreased. This is mainly due to the different effect of SDS at different SDS concentration.  相似文献   
103.
Highly intrinsic conductive polypyrrole/cellulose fiber composites (CF) were successfully prepared through in situ chemical oxidation polymerization simply by increasing fiber concentration at the same dosage of pyrrole, oxidant and dopant (based on the weight of dry fiber). FeCl3 and anthraquinone-2-sulfonic acid sodium salt (AQSNa) were utilized as oxidant and dopant. As fiber concentration increased from 1 % (CF1) to 20 % (CF20), N and S content increased from 0.24 and 0.25 % to 1.24 and 0.89 %, and great increase in the retention of PPy and AQSNa was confirmed by elemental analysis. In addition, on the surface of conductive fiber, PPy of compact fibroid structure was detected instead of interconnected globular structure at higher fiber concentration. Furthermore, scanning transmission electron microscope and X-ray photoelectron spectroscopy (XPS)-depth profile analysis demonstrated denser and more uniformly distributed PPy inside fiber wall for CF20, while PPy tended to deposit on the surface of fiber for CF1. Fourier transform infrared spectroscopy, together with XPS certified that the PPy with longer conjugation length and higher doping level across the conductive fiber was obtained at higher fiber concentration. The doping level for CF10 decreased from 21.55 to 16.39 % with increasing fiber wall thickness, while that of CF20 decreased slightly from 30.73 to 24.10 %. The resulting CF20 showed lowest surface resistivity of 0.433 KΩ/square, as well as improved electro-conductivity stability. The incorporation of more PPy in CF improved the thermal stability.  相似文献   
104.
The paper studies a codimension-4 resonant homoclinic bifurcation with one orbit flip and two inclination flips, where the resonance takes place in the tangent direction of homoclinic orbit.Local active coordinate system is introduced to construct the Poincar′e returning map, and also the associated successor functions. We prove the existence of the saddle-node bifurcation, the perioddoubling bifurcation and the homoclinic-doubling bifurcation, and also locate the corresponding 1-periodic orbit, 1-homoclinic orbit, double periodic orbits and some 2n-homoclinic orbits.  相似文献   
105.
A general and efficient P(V)–N activation method for the preparation of symmetrical and asymmetrical dinucleoside polyphosphates (NpnN′s, n=2–4) and P2,P3-CX2-dinucleoside tetraphosphates (X=H, F, and Cl) has been established. Twenty-two dinucleoside polyphosphates and their phosphonate analogs were synthesized from nucleoside 5′-phosphoropiperidates with 4,5-dicyanoimidazole as the activator in good to high yields.  相似文献   
106.
This article discusses the effect of water fraction on the rheological properties of waxy crude oil emulsions including gel point, yield stress, viscosity, and thixotropy. The experimental results reveal that the rheological behaviors of the w/o emulsion samples all intensify with the increase of water volume fraction within 60%. Of more significance is that a correlation for w/o emulsions between yield stress and water volume fraction is put forward with an average relative error of 6.75%. In addition, some mainstream viscosity prediction models of w/o emulsions are evaluated, and Elgibaly model is the best-fit for the emulsions in this study.  相似文献   
107.
骨架环肽是线性肽的C端和N端通过酰胺键进行首尾环合而形成的环状分子.研究者从细菌、真菌、植物和动物中发现了大量的骨架环肽.这种首尾环合的结构,使得骨架环肽具有很好的酶稳定性、热稳定性和化学稳定性,部分骨架环肽具有细胞膜通透性.骨架环肽分子异常的稳定性和高效的生物活性,使得其成为目前药物领域的研究热点.为了更深入地研究它们的结构和功能,骨架环肽的制备成为一个重要问题.概述了化学合成骨架环肽的一些方法,包括:(1)固相环合策略;(2)液相环合策略;(3)分子内自然化学连接策略,并对这些方法的特点和效率进行了讨论比较.  相似文献   
108.
Selective polymer wrapping is a promising approach to obtain high‐chiral‐purity single‐walled carbon nanotubes (SWCNTs) needed in technical applications and scientific studies. We showed that among three fluorene‐based polymers with different side‐chain lengths and backbones, poly[(9,9‐dihexylfluorenyl‐2,7‐diyl)‐co‐(9,10‐anthracene)] (PFH‐A) can selectively extract SWCNTs synthesized from the CoSO4/SiO2 catalyst, which results in enrichment of 78.3 % (9,8) and 12.2 % (9,7) nanotubes among all semiconducting species. These high‐chiral‐purity SWCNTs may find potential applications in electronics, optoelectronics, and photovoltaics. Furthermore, molecular dynamics simulations suggest that the extraction selectivity of PFH‐A relates to the bending and alignment of its alkyl chains and the twisting of its two aromatic backbone units (biphenyl and anthracene) relative to SWCNTs. The strong π–π interaction between polymers and SWCNTs would increase the extraction yield, but it is not beneficial for chiral selectivity. Our findings suggest that the matching between the curvature of SWCNTs and the flexibility of the polymer side chains and the aromatic backbone units is essential in designing novel polymers for selective extraction of (n,m) species.  相似文献   
109.
A family of energetic salts with high thermal stability and low impact sensitivity based on an oxygen‐containing cation, 2,4‐diamino‐1,3,5‐triazine‐6‐one, were synthesized and fully characterized by IR and multinuclear (1H, 13C) NMR spectroscopy, elemental analysis, and differential scanning calorimetry. Insights into their sensitivities towards impact, friction, and electrostatics were gained by submitting the materials to standard tests. The structures of 2,4‐diamino‐1,3,5‐triazine‐6‐one nitrate, 2,4‐diamino‐1,3,5‐triazine‐6‐one sulfate, 2,4‐diamino‐1,3,5‐triazine‐6‐one perchlorate, 2,4‐diamino‐1,3,5‐triazine‐6‐one 5‐nitrotetrazolate were determined by single‐crystal X‐ray diffraction; their densities are 1.691, 1.776, 1.854, and 1.636 g cm?3, respectively. Most of the salts decompose at temperatures over 180 °C; in particular, the salts 2,4‐diamino‐1,3,5‐triazine‐6‐one nitrate and 2,4‐diamino‐1,3,5‐triazine‐6‐one perchlorate, which decompose at 303.3 and 336.4 °C, respectively, are fairly stable. Furthermore, most of the salts exhibit excellent impact sensitivities (>40 J), friction sensitivities (>360 N), and are insensitive to electrostatics. The measured densities of these energetic salts range from 1.64 to 2.01 g cm?3. The detonation pressure values calculated for these salts range from 14.6 to 29.2 GPa, and the detonation velocities range from 6536 to 8275 m s?1; these values make the salts potential candidates for thermally stable and insensitive energetic materials.  相似文献   
110.
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