Concurrency control algorithm of dynamic adjustment of serialization order for distributed database based on transactions

针对分布式数据库中发生待处理的事务流提出一种动态可串行调度算法。通过执行此算法,能够高效地处理源源不断的事务流,使之尽可能串行调度地执行,从而提高并发度,以及分布式数据库各站点的并行处理度。This paper presents an algorithm of dynamic adjustment of serialization order for distributed database on real-time transactions.Running this algorithm can process continual real-time transactions and carry out with an adjustment of serialization order,so the concurrency degree can be improved simultaneously,and the parallel degree of every site of distributed database can be raised too

Studies on degradation mechanism of niclosamide ethanolamine salt Ⅰ Determination of niclosamide ethanolamine salt in photolysis solution

目的了解氯硝柳胺乙醇胺盐(nES)在水体中的光解规律。方法实验室配置PH5的0.05μg/Ml、PH7的0.5μg/Ml和PH9的2.5μg/MlnES溶液,采用氙灯光源作为模拟日光照射,照射后0、0.5、1、2、4、8、16、24、48、72、96H采集光解液,高效液相色谱法测定光解液中nES含量,同时设无光照对照试验,计算其半衰期。结果在氙灯光光照条件下,nES快速降解,8H3种PH值的nES溶液下降率分别为83.4%、78.8%和41.3%,24H下降率分别为92.1%、88.5%和95.8%。nESPH5半衰期为8.98H,PH7为10.34H,PH9为9.16H;无光照条件下放置12d溶液浓度稳定。结论nES可在水中快速光解。Objective To understand the photolysis mechanism of niclosamide ethanolamine salt(NES) in water body.Methods NES was formulated into solutions of pH 5(0.05 μg/ml),7(0.5 μg/ml) and 9(2.5 μg/ml),respectively.The xenon gas lamp was used as the simulated sunlight.After 0,0.5,1,2,4,8,16,24,48,72,96 h of the illumination,the photolysis solutions were collected to determine the amount of NES by using the high-performance liquid chromatography method(HPLC),and the experiment without illumination was also set as the control.The half-life was calculated.Results Under the illumination of xenon gas lamp,the NES degraded rapidly.The degradation rates were 83.4%,78.8% and 41.3%,respectively for 8 h,and 92.1%,88.5% and 95.8%,respectively for 24 h.The half-life of NES was 8.98 h for pH 5,10.34 h for pH 7,9.16 h for pH 9.The solution could keep stable for 12 d without illumination.Conclusion Photolysis of NES can occur quickly in water.江苏省自然科学基金(BK200602

Studies on degradation mechanism of niclosamide ethanolamine salt Ⅱ Isotopic tracing and determination of photolysis end-product

目的观察同位素示踪技术解析氯硝柳胺乙醇胺盐(nES)在水体中的稳定性及测定光解终产物CO2的变化。方法实验室配制PH5的0.05μg/Ml、PH7的0.5μg/Ml和PH9的2.5μg/MlnES溶液,采用氙灯光源作为模拟日光照射上述nES溶液,照射8、16、24、32、40、48H和72H后,分别测定nES溶液在光解管顶的气态样品,采用gASbEnCHⅡ进样针插入直接分析;液体样品则取2.5Ml注入用高纯氦吹过的密封顶空样品瓶中,用加酸泵滴加无水磷酸,30℃超声反应1H,再插入gASbEnCHⅡ进样针进行分析;与dElTAPluS/XP稳定同位素质谱仪联用测定光解产物CO2的量及碳稳定同位素。结果在氙灯光光照条件下,PH70.5μg/Ml和PH92.5μg/MlnES溶液的光解,随光照时间的增加,CO2的量也增加,并呈线性增长,72H时其产量接近nES的实际产量。同位素结果显示,随光照时间的增加,CO2的碳同位素值逐渐变负,72H时接近nES原药的碳同位素值,为-25.36±0.11,光降解已接近完全。而PH50.05μg/MlnES溶液的光解,随光照时间的增加,CO2的量也在增加,但其产量超出了nES的实际产量;同位素结果显示,随光照时间的增加,产出CO2的碳同位素值逐渐变负,但在光照16H后其产CO2的碳同位素值比nES的碳同位素值偏负。结论 nES能够在水中快速光解,终产物为CO2。Objective To analyze the stability of niclosamide ethanolamine salt(NES)in water and determine the changes of CO2,the photolysis end-product,by using the isotopic tracing technique.Methods NES was formulated into the solutions of pH 5(0.05 μg/ml),pH 7(0.5 μg/ml)and pH 9(2.5 μg/ml),respectively.The xenon gas lamp was used as the simulated sunlight.After 8,16,24,32,40,48,72 h of the illumination,the gas samples of the NES solution on the top of photolysis tube were determined by using direct insertion of GasBenchII needle.For liquid samples,2.5 ml NES solution was added into a sealed empty bottle,which was treated with high pure helium,and then anhydrous phosphoric acid was added.After ultrasonic reaction at 30 ℃ for 1 h,the GasBenchII needle was inserted for analysis.The amount of CO2 and carbon isotopic value were determined by using the GasBenchII needle combined with isotopic mass spectrometer.Results Under the illumination of xenon gas lamp,the NES solutions of pH 7 and pH 9 occurred photolysis,with the increase of illumination time,the amount of CO2 increased,showing a linear increase.At 72 h,its yield approximated to the active output of NES.The isotopic tracing results showed,with the increase of illumination time,the carbon isotope value of CO2 turned to be negative gradually,and approximately reached to the carbon isotope value(-25.36±0.11‰)of NES active ingredient at 72 h when the photolysis approximated to be completely finished.For the photolysis of pH 5 NES solution,with the increase of illumination time,the amount of CO2 increased,however,its output was more than the active output of NES.The isotopic tracing results showed,with the increase of illumination time,the carbon isotope value of CO2 turned to be negative gradually.However,after illumination for 16 h,the carbon isotope value of CO2 was more negative than that of NES.Conclusions The photolysis of NES can occur rapidly in water,and the end product is CO2.江苏省自然科学基金(BK200602);江苏省卫生厅项目(X200504

Combustion Synthesis and Electrochemical Properties of the Small Hydrofullerene C50H10

通讯作者地址: Xie, SY (通讯作者),Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China 地址: 1. Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China 2. Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China 3. Xiamen Univ, Sch Life Sci, Xiamen 361005, Peoples R China 电子邮件地址: [email protected]; [email protected] hydrofullerene C50H10 is synthesized by low-pressure benzeneoxygen diffusion combustion. The structure of C50H10 is identified through NMR, mass spectrometry, and IR and Raman spectroscopy as a D5h symmetric closed-cage molecule with five pairs of fused pentagons stabilized by ten hydrogen atoms. UV/Vis and fluorescence spectrometric analyses disclose its optical properties as comparable with those of its chloride cousin (C50Cl10). Cyclic and square-wave voltammograms reveal that the first reduction potential of C50H10 is more negative than that of C50Cl10 as well as C60, with implications for the utilization of C50H10 as a promising electron acceptor for photovoltaic applications.973 projects 2011CB935901 NSFC 21031004 21021061 2077310

半导体材料与器体生产工艺尾气中砷、磷、硫的治理及检测

研究了化合物半导体材料、器件生产工艺中排出的有毒物质砷、磷、硫及其化合物的治理方法。还研究了这些有毒物质的低温富集取样及快速、灵敏的分析监测方法,并与其它经典的方法作了对比

煅烧菱镁矿在氯化铵乙二醇溶液中的浸取动力学

　系统地研究了菱镁矿的煅烧条件以及煅烧粉在氯化铵乙二醇溶液中的浸取动力学．菱镁矿在750℃下煅烧2h左右能使MgCO3分解完全而CaCO3不分解，过烧会使晶粒长大，从而降低浸取速率．在消除外扩散影响的前提下，浸取过程在反应物（NH4Cl与MgO）以化学计量比反应、氯化铵的初始浓度为0～1．23mol／L时符合未反应收缩核模型（Unreacted shrinking core model），且浓度为1．23mol／L时浸取速率达到最大；浸取速率受表面化学反应控制，活化能为44．74kJ／mol

煅烧菱镁矿在氯化铵乙二醇溶液中的浸取动力学

系统地研究了菱镁矿的煅烧条件以及煅烧粉在氯化铵乙二醇溶液中的浸取动力学.菱镁矿在750℃下煅烧2h左右能使MgCO3分解完全而CaCO3不分解,过烧会使晶粒长大,从而降低浸取速率.在消除外扩散影响的前提下,浸取过程在反应物(NH4Cl与MgO)以化学计量比反应、氯化铵的初始浓度为0～1.23mol/L时符合未反应收缩核模型(Unreacted shrinking coremodel),且浓度为1.23mol/L时浸取速率达到最大;浸取速率受表面化学反应控制,活化能为44.74kJ/mol

The change of amino acids in leaves of maize seedlings under alternative split-root osmotic stress

用Hoagland溶液培养玉米幼苗,研究分根交替渗透胁迫对其叶片水势、可溶性糖、NH4+和游离氨基酸的影响。实验表明,当玉米根系一半处于高水势,另一半处于低水势溶液时,在24h间隔交替过程中,叶片的可溶性糖、NH4+和游离氨基酸的含量都比同浓度聚乙二醇(PEG)不分根胁迫下的处理低,但叶水势则相反。说明分根交替渗透胁迫能够发挥根系吸水的补偿效应,提高叶水势