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981.
Pil Kim Younghun Kim Taewook Kang In Kyu Song Jongheop Yi 《Catalysis Surveys from Asia》2007,11(1-2):49-58
Mesoporous materials have attracted considerable attention for use as a catalyst or a catalyst support due to their remarkable
textural properties such as high surface area and large pore volume with a narrow pore size distribution. Many efforts have
been made to design mesoporous materials for use in heterogeneous catalyst systems. Recent progress and results regarding
the preparation of nickel-mesoporous materials and their application to the hydrodechlorination of chlorinated organic compounds
were discussed in this review. Mesoporous materials were used as a support for nickel catalyst or a nickel-incorporated mesoporous
catalytic material in this work. Two research areas were described and discussed in this review. One is the preparation of
mesoporous alumina-supported nickel catalysts and their application to the hydrodechlorination of 1,2-dichloropropane and
o-dichlorobenzene. The other is the preparation of mesoporous silica-supported nickel catalysts and their application to the
hydrodechlorination of 1,1,2-trichloroethane and chlorobenzene. 相似文献
982.
983.
Yoshitsugu Kojima Takaaki Matsuoka Norio Sato Hideroh Takahashi 《Journal of polymer science. Part A, Polymer chemistry》1995,33(17):2935-2940
New conjugated oligomers were prepared by reacting phenylacetylene under high pressure of 0.11 to 0.92 GPa at 100–200°C for 0–5 h. The number-average molecular weight M?n, the weight-average molecular weight M?w, and the oligomer yield increased with pressure, tem-perature, and time. The average molecular weight of the oligomer showed the maximum value (M?n: 830, M?w: 2400) under 0.92 GPa, the maximum pressure, where phenylacetylene was oligomerized at a constant temperature. The structure of the oligomer was investigated from ESR, infrared, UV–VIS, field desorption mass (FDMS) spectra, and 13C NMR spec-trum. Analysis of the FDMS spectrum revealed that the molecular weight of the oligomer was multiple of the monomer. 13C NMR spectrum of the oligomer showed the absence of sp-carbon (? C?). We found that the oligomer had a cyclic structure. The cyclic oligomers of pentamer or more were new compounds. © 1995 John Wiley & Sons, Inc. 相似文献
984.
Fabrizio Casarini Luigi Marcheselli Andrea Marchetti Lorenzo Tassi Giuseppe Tosi 《Journal of solution chemistry》1993,22(10):895-905
The relative permittivities for the ternary 1,2-ethanediol (component 1) + 2-methoxyethanol (2) + water (3) solvent system have been measured for 66 mixtures covering the whole mole fraction composition 0X1/X2/X3 1 range at –10, –5 and 0 °C. The experimental data were used to test some empirical relations stating the dependence of = (X1, X2, X3). A comparison between the calculated and experimental data show that these equations can be usefully employed to predict values in correspondence of the experimental data gaps. 相似文献
985.
This paper reports a first approach on the kinetics parameters of terbium-activated magnesium orthosilicate using various methods. A deconvolution has also used for taking into account a more complex glow-curve structure.
Zusammenfassung Mittels verschiedener Methoden werden in erster Näherung die kinetischen Parameter von terbiumaktiviertem Magnesiumorthosilikat ermittelt Zur Berücksichtigung einer komplexeren Thermolumineszenzkurve wurde auch eine Dekonvolution angewendet.相似文献
986.
987.
988.
D. F. Grant-Taylor 《Journal of solution chemistry》1981,10(9):621-630
High precision densities of sodium chloride solutions at a constant pressure of 200 bar and temperatures between 175°C and 350°C have been measured by a mercury displacement technique. The densities have been converted to apparent molar volumes. The apparent molar volumes decrease with increasing temperature and decreasing concentration whereas the concentration effect increases with temperature. Standard partial molar volumes range from 8.0 cm3-mol–1 at 175°C to –600 cm3-mol–1 at 350°C. The results indicate the applicability of the unextended Debye-Hückel limiting law up to concentrations of 0.02 mol-kg–1. 相似文献
989.
《Arabian Journal of Chemistry》2022,15(12):104368
Protein hydrolysates have the potential to be natural and safer sources of bioactive peptides. In this study, two proteases were used to hydrolyze Chinese sturgeon (Acipenser sinensis) protein, and the hydrolysates were then purified to yield antioxidant peptides. The degree of hydrolysis of 23.56 % and 18.14 % was obtained using papain and alcalase 2.4L, respectivly, and hydrolysates had 96.80 % and 87.24 % total amino acid content, respectivly. The papain hydrolysate (PH) and alcalase 2.4L hydrolysate (AH) showed good antioxidant activity against DPPH? (IC50 of 3.64 and 3.15 mg/mL) and ABTS?+ (IC50 of 1.92 and 1.58 mg/mL), respectively. The low-molecular-weight (<1000 Da) fraction of both hydrolysates demonstrated the highest antiradical activity (IC50 of 2.59 and 2.31 mg/mL, DPPH) and (IC50 of 1.54 and 1.36 mg/mL, ABTS), respectively. Nine peptides were separated from both hydrolysates using reverse phase high performance liquid chromatography (RP-HPLC). The IC50 for ABTS?+ scavenging activity of peptide P5 with valine, glycine and asparagine (MW of 282.13 Da) from PH, and peptide P3 with histidine, glycine and alanine (MW of 302.74 Da) from AH was 0.89 and 0.72 mg/mL, respectively. The fractions and purified peptides obtained from Chinese sturgeon hydrolysates could be utilized as natural antioxidant substitutes in pharmaceuticals and food products. 相似文献
990.
建立了分散固相萃取净化-超高效液相色谱-串联质谱法快速测定鱼和虾中3类(磺胺类、喹诺酮类、氯霉素类)18种抗生素及2种三苯甲烷类(孔雀石绿、隐色孔雀石绿)兽药残留。样品经磷酸氢二钾溶液水解分散,乙腈提取,提取液经氯化钠脱水、盐析后取乙腈层,经旋转蒸发仪浓缩至近干,残留物用甲醇定容至1.0 mL,C18和PSA(N-丙基乙二胺)填料分散固相萃取净化,过滤膜后经ZORBAX C18色谱柱(50 mm×2.1 mm,1.8 μm)分离,正、负离子多反应监测模式采集数据,同位素内标法定量。实验结果表明,20种兽药在0.2~300 μg/L范围内具有良好的线性关系,检出限为0.1~0.6 μg/kg,定量限为0.3~1.8 μg/kg,相关系数均大于0.99。在1、5和20倍定量限加标浓度水平下,平均回收率为72.5%~118%,相对标准偏差(RSD)为1.9%~9.8%。该方法具有前处理简单、检测效率高、成本低等优点,适用于鱼和虾中多类兽药残留的同时测定。 相似文献