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211.
212.
This study analyzes the stability of an initially sharp interface between two miscible fluids in a porous medium. Linear stability equations are first derived using the similarity variable of the basic state, and then transformed into a system of ordinary differential equations using a spectral expansion with and without quasi-steady-state approximation (QSSA). These transformed equations are solved using the eigenanalysis and initial value problem approach. The initial growth rate analysis shows that initially the system is unconditionally stable. The stability characteristics obtained under the present QSSA are quantitatively same as those obtained without the QSSA. To support these theoretical results, numerical simulations are conducted using the Fourier-spectral method. The results of theoretical linear stability analyses and the numerical simulations validate to each other. 相似文献
213.
Polar groups in the skeletons of conjugated microporous polymers (CMPs) play an important role in determining their porosity and gas sorption performance. Understanding the effect of the polar group on the properties of CMPs is essential for further advances in this field. To address this fundamental issue, we used benzene, the simplest aromatic system, as a monomer for the construction of two novel CMPs with multi-carboxylic acid groups in their skeletons (CMP-COOH@1 and CMP-COOH@2). We then explored the profound effect the amount of free carboxylic acid in each polymer had on their porosity, isosteric heat, gas adsorption, and gas selectivity. CMP-COOH@1 and CMP-COOH@2 showed Brunauer-Emmett-Teller (BET) surface areas of 835 and 765 m2·g-1, respectively, displaying high potential for carbon dioxide storage applications. CMP-COOH@1 and CMP-COOH@2 exhibited CO2 capture capabilities of 2.17 and 2.63 mmol·g-1 (at 273 K and 1.05 × 105 Pa), respectively, which were higher than those of their counterpart polymers, CMP-1 and CMP-2, which showed CO2 capture capabilities of 1.66 and 2.28 mmol·g-1, respectively. Our results revealed that increasing the number of carboxylic acid groups in polymers could improve their adsorption capacity and selectivity. 相似文献
214.
Chang‐Ching Chan Mark S. Bolgar Dilusha Dalpathado David K. Lloyd 《Rapid communications in mass spectrometry : RCM》2012,26(12):1507-1514
A method has been developed to reduce the mass spectrometric ion signal suppression associated with the use of TFA as an additive in LC mobile phases. Through post‐column infusion of diluted NH4OH solution to LC eluents, the ammonium ion introduced causes the neutral analyte‐TFA ion pair to dissociate which consequently releases the protonated analyte as free ions into the gas phase (through regular electrospray ionization mechanisms). An ion signal improvement from 1.2 to 20 times for a variety of compounds had been achieved through the application of this method. The molar ratios of NH4OH:TFA which result in a reduction of signal suppression were determined to be between 0.5:1 and 50:1. In addition, it was shown that this NH4OH infusion method could reduce the level of doubly‐charged species and the product ions formed via in‐source collision. The use of diluted NH4OH solution is favorable since it is compatible with mass spectrometry analysis, and it is applicable in both positive and negative‐ion generation mode. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
215.
Alex H. F. Lee Jian Chen Albert S. C. Chan Tianhu Li 《Phosphorus, sulfur, and silicon and the related elements》2013,188(5):1163-1174
5-(7-Hydroxyheptyl)-1,2-dithiolan-3-one 1-oxide was designed and synthesized in our laboratories that contain the heterocycle of 1,2-dithiolan-3-one 1-oxide, a reactive core of antibiotic leinamycin. In addition, the activated ester of 5-(7-hydroxyheptyl)-1,2-dithiolan-3-one 1-oxide was prepared, which presumably is useful for coupling this DNA-cleaving functionality to certain DNA-binding agents. 相似文献
216.
The effect of p-toluenesulfonic acid and phosphoric acid on the cyclodehydration of quinazolone prepolymers has been investigated. Isothermal weight loss during the curing process was monitored closely to follow the extent of cyclization. The optimum weight loss corresponding to 2 mol water is used as an indication of the formation of a fully cyclized quinazolone structure without concurrent decarboxylation. This can be achieved by incorporating the catalyst at 2 wt% concentration, which permits a lower curing temperature than those previously reported. The polymers formed in the presence of catalyst have thermal stability superior to those prepared without catalyst. The glass transition temperature is also raised. This we conclude to be a direct result of the decrease in the amount of incomplete quinazolone rings along the polymer backbone as a result of more efficient cyclization catalyzed by the acids. 相似文献
217.
218.
Symmetrical and cyclic alkyl trithiocarbonates were synthesized by reacting CS2 and 33% aqueous NaOH with alkyl hal-ides under phase transfer catalysis conditions 相似文献
219.
Hee-Man Yang Chan Woo Park Kune Woo Lee Byung-Sik Lee Ilgook Kim In-Ho Yoon 《Journal of Radioanalytical and Nuclear Chemistry》2018,316(3):955-962
A polyvinyl alcohol (PVA)-borate hydrogel-based strippable surface decontaminant containing an ammonium salt and Prussian blue (PB) was developed for the removal of 137Cs from various surfaces. This surface decontaminant can be easily prepared by the simple mixing of commercially available materials, such as PVA, borax, NH4Cl and PB, in water, and the decontaminant can be peeled off surfaces due to its high elastic property after surface decontamination. The hydrogel displayed an effective removal performance for Cs from painted cement, aluminum, stainless steel, and cement surfaces and a potential for reusability. Therefore, the PB/PVA-borate hydrogel has good potential as a new surface decontaminant. 相似文献
220.
Yi Yuan Zong-Lin Jiang Jia-Ming Yan Ge Gao Albert S. C. Chan Ru-Gang Xie 《合成通讯》2013,43(24):4555-4561
Two new macrobicyclic imidazolium and benzimidazolium phanes were synthesized by direct quaternization of the corresponding tripodal azacycles with tribromide under high dilution condition in excellent yields. The cyclophanes were identified by 1H-NMR, 13C-NMR, FAB-MS, IR, elemental analysis and X-ray diffraction analysis. 相似文献