Growth of fundamental group for Finsler manifolds with integral Ricci curvature bound

In this paper, an upper bound on the growth of fundamental group for a class of Finsler manifolds with integral Ricci curvature bound is given. This generalizes the corresponding results with pointwise Ricci curvature in literature.     

载银sod基纳米分子筛的合成及抗菌性能

采用两步法合成了sod基系列分子筛(EMT、FAU、SOD),并通过离子交换法引入Ag⁺得到载银分子筛,通过X射线衍射(XRD)、扫描电子显微镜(SEM)证明离子交换前后分子筛骨架结构和晶粒尺寸没有发生明显变化;通过红外光谱(IR)、热重(TG)证明制得的载银分子筛具有良好的稳定性;对获得的载银分子筛进行了Ag⁺释放实验与抗菌能力测试,考察了分子筛种类和晶粒尺寸对抗菌性能的影响。结果表明具有笼状结构的FAU与EMT分子筛因可储存更多的Ag⁺而具有更好的抗菌性能,而具有超笼结构的FAU分子筛抗菌性能最优。通过对比不同晶粒尺寸载银FAU分子筛抗菌数据发现,晶粒尺寸为100 nm的载银FAU分子筛因外表面丰富的抗菌活性位点以及其内部可以储存并不断释放Ag⁺而具有最优的抗菌性能和抗菌寿命。而晶粒尺寸为10 nm的载银FAU分子筛由于晶粒尺寸较小、外比表面积大、扩散路径短,Ag⁺的释放速率最快,抗菌效率最高。     

翻白草中熊果酸的微波提取工艺研究

采用单因素实验与正交实验法结合,以提取剂浓度、固液比、微波功率、微波提取时间为考察因素,以熊果酸提取率作为评价指标,优化了熊果酸的微波提取工艺。最优微波提取条件为:90 % 乙醇作为提取剂、料液比1∶20 g/mL、微波功率250 W、微波提取时间120 s。     

有机橡胶助剂的全分析

橡胶产品中橡胶助剂的分析有重要现实意义。由于橡胶产品中添加的助剂种类较多,添加量差别较大,部分助剂又已发生反应,因此进行橡胶助剂的全分析是一项有较高难度的工作。通过中压色谱分离,红外光谱定性的方法,鉴定了乙丙橡胶助剂中的矿物油、邻苯二甲酸酯、植物油等3种软化剂,以及残余的硫化促进剂M和防老化剂苯乙烯化苯酚; 采用固相萃取去除助剂中主量成分矿物油,以减少对其他少量助剂成分的干扰,通过气质联用法,推测出橡胶助剂中的2,6-二叔丁基-4-甲基苯酚防老剂、残余的秋兰姆类硫化促进剂,同时利用气质联用仪,直接测定乙丙橡胶抽提液,鉴定了残余的活泼性物质过氧化苯甲酰类硫化剂。文章研究结果可供其他橡胶体系有机助剂全分析的借鉴。     

1-乙基-3-甲基咪唑L-乳酸盐作为手性配体用于氨基酸的手性拆分

基于手性配体交换机理,研究了以手性离子液体1-乙基-3-甲基咪唑L-乳酸盐([EMIM][L-Lac])为手性配体拆分色氨酸对映体(Trys)、苯丙氨酸对映体(Phes)和酪氨酸对映体(Tyrs)的方法。实验考察了背景电解质和中心离子种类、手性配体与中心离子的浓度及比例、运行缓冲液pH等因素对Trys、Phes和Tyrs手性拆分的影响。研究发现,当运行缓冲液为40.0 mmol/L [EMIM][L-Lac]、20.0 mmol/L氯化铜(pH 4.5)时,3对对映体均能得到良好的手性拆分。为了验证[EMIM][L-Lac]的良好性能,实验进一步将L-乳酸(L-Lac)作为手性配体用于Trys的手性拆分。对比实验发现,单独使用L-乳酸,DL-Try只能得到部分拆分,加入离子液体1-乙基-3-甲基咪唑醋酸盐(EMIM-Ace)后,DL-Try分离情况得到了很大改善,但出峰时间延长至30 min以上。而使用[EMIM][L-Lac]时,Trys的出峰时间均在15 min以内。实验最后还对手性拆分机理做了进一步讨论。实验结果表明:在EMIM-Ace辅助L-Lac体系中,EMIM-Ace仅被用于抑制电渗流,并未参与手性配体交换反应;而在[EMIM][L-Lac]体系中,参与手性配体交换反应的主要是未解离的[EMIM][L-Lac],而不是解离后的L-乳酸根离子形成的L-乳酸。     

带有GARCH误差的单位根过程的估计

单位根过程在时间序列理论中占有重要地位.单位根过程能较好地刻画经济数据中经常呈现的非平稳状态,因此其在经济理论与实证中都有广泛的应用.在更新项只有二阶矩存在的条件下,讨论了带有GARCH(p,q)误差项与趋势项的单位根过程的最小二乘估计.并推导了基于最小二乘估计的Dickey-Fuller检验统计量的渐近分布.该结果在单位根检验中具有重要作用.     

Tandem Solid-Phase Extraction Columns for Simultaneous Aroma Extraction and Fractionation of Wuliangye and Other Baijiu

Wuliangye baijiu is one of the most famous baijiu in China, with a rich, harmonic aroma profile highly appreciated by consumers. Thousands of volatiles have been identified for the unique aroma profile. Among them, fatty acid esters have been identified as the main contributors to the aroma profile. In addition, many non-ester minor compounds, many of which are more polar than the esters, have been identified to contribute to the characteristic aroma unique to Wuliangye baijiu. The analysis of these minor compounds has been challenging due to the dominance of esters in the sample. Thus, it is desirable to fractionate the aroma extract into subgroups based on functional group or polarity to simplify the analysis. This study attempts a new approach to achieve simultaneous volatile extraction and fractionation using tandem LiChrolut EN and silica gel solid-phase extraction (SPE) columns. A baijiu sample (10 mL, diluted in 40 mL of water) was first passed through the LiChrolut EN (1.0 g) column. The loaded LiChrolut EN column was then dried with air and coupled with a silica gel (5.0 g) SPE column with anhydrous Na₂SO₄ (10.0 g) in between. The volatile compounds were eluted from the LiChrolut EN column and simultaneously fractionated on the silica gel column based on polarity. The simultaneous extraction and fractionation technique enabled the fractionations of all fatty acid esters into less polar fractions. Fatty acids, alcohols, pyrazines, furans, phenols, hydroxy esters, and other polar compounds were collected in more polar fractions. This technique was used to study the volatile compounds in Wuliangye, Moutai, and Fengjiu baijiu. In addition to fatty acid esters, many minor polar compounds, including 2,6-dimethylpyrazine, 2-ethyl-6-methylpyrazine, 2-ethyl-3,5-dimethylpyrazine, p-cresol, and 2-acetylpyrrole, were unequivocally identified in the samples. The procedure is fast and straightforward, with low solvent consumption.     

Generation of Maximally Entangled States of Two Nonidentical Atoms in Cavity QED

We have discussed the system which consists of two nonidentical two-level atoms trapped simultaneously in a large-detuned single-mode cavity field in this paper. The results show that it is possible to generate maximally entangled states for two nonidentical two-level atoms only if the cavity frequency and difference of two nonidentical atoms transition frequency are selected and the cavity-atom interacation time is controlled.