碳源及电子受体对厌氧微生物降解对氯硝基苯的影响

为考察氯代硝基苯的共代谢降解过程中,有机碳源类型和电子受体对氯代硝基苯厌氧降解过程的影响,以对氯硝基苯(p-CNB,para-chloronitrobenzene)为目标污染物,通过间歇试验考察了葡萄糖、乙醇、乙酸钠等有机碳源及SO2--4、NO3等竞争性电子受体对厌氧微生物降解对氯硝基苯的影响。结果显示,葡萄糖、乙醇和乙酸钠作为碳源时,菌种获得的还原能力大小依次为:乙醇葡萄糖乙酸钠。SO2-4对菌种降解对氯硝基苯过程不产生竞争性抑制。NO-3对对氯硝基苯降解过程的影响与碳源的量有关,当乙醇-COD为100 mg/L时,硝酸盐产生竞争性抑制,且抑制作用随着NO-3浓度升高而增强;当乙醇-COD为600 mg/L时,硝酸盐对菌种降解对氯硝基苯过程不产生竞争性抑制作用。     

Accelerated anaerobic dechlorination of DDT in slurry with Hydragric Acrisols using citric acid and anthraquinone-2,6-disulfonate (AQDS)

The application of electron donor and electron shuttle substances has a vital influence on electron transfer,thus may affect the reductive dechlorination of 1,1,1-trichoro-2,2-bis(p-chlorophenyl)ethane(DDT) in anaerobic reaction systems.To evaluate the roles of citric acid and anthraquinone-2,6-disulfonate(AQDS) in accelerating the reductive dechlorination of DDT in Hydragric Acrisols that contain abundant iron oxide,a batch anaerobic incubation experiment was conducted in a slurry system with four treatments of(1) control,(2) citric acid,(3) AQDS,and(4) citric acid + AQDS.Results showed that DDT residues decreased by 78.93%–92.11% of the initial quantities after 20 days of incubation,and 1,1-dichloro-2,2-bis(4-chlorophenyl)-ethane(DDD) was the dominant metabolite.The application of citric acid accelerated DDT dechlorination slightly in the first 8 days,while the methanogenesis rate increased quickly,and then the acceleration effect improved after the 8th day while the methanogenesis rate decreased.The amendment by AQDS decreased the Eh value of the reaction system and accelerated microbial reduction of Fe(III) oxides to generate Fe(II),which was an efficient electron donor,thus enhancing the reductive dechlorination rate of DDT.The addition of citric acid + AQDS was most efficient in stimulating DDT dechlorination,but no significant interaction between citric acid and AQDS on DDT dechlorination was observed.The results will be of great significance for developing an efficient in situ remediation strategy for DDT-contaminated sites.     

Effect of cooling rate and laser process parameters on additive manufactured Fe–Ti–C metal matrix composites microstructure and carbide morphology

In this paper, laser additive manufacturing (LAM) of Fe–TiC composite coating on AISI 1030 carbon steel is investigated using a numerical and experimental method. In order to have a desired result using LAM, it is crucial to understand the effects of the process parameters’ values on the TiC morphology and microstructure. For this purpose, the LAM process is numerically simulated in order to calculate cooling rate and peak temperature. Experimental data and numerical results are in good agreement in terms of the phase development. Results show that cooling rate plays a crucial role in phase transformation in the clad, however, final microstructure strongly depends on the cooling rate and powder's chemical composition. Two main carbide morphologies (i.e. dendritic and particulate) are studied and relevant cooling rates are detected. Based on this paper and developed map, it is possible to control the cooling rate in order to achieve specific carbide morphologies in the clad. In this study, scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) are used to characterize clads’ microstructure.     

辽宁省地质灾害遥感调查电子地图的制作

通过辽宁省地质构造解译图和辽宁省地质灾害遥感解译图这两个电子地图的制作，说明了电子地图制作的工具选择、制作方法、关键技术以及地图应用等。体现了地理信息系统这一现代化科技手段在防灾、减灾和地质环境的整治与保护方面的价值。     

Analysis of Heavy Metals in the Endometrial Tissue Using Electron Microscope

Objective This study was done to estimate whether heavy metals in the air may affect endometrial chemical composition. Materials and Methods A total of 30 albino Wistar rats were employed and randomly divided into three groups. The rats of Group 1 and 2 were acutely and sub-chronically exposed to the gas form of heavy metals, respectively. Group 3 was used as a control group. Endometrial tissue worth of heavy metals of the groups was measured in through using scanning electron microscope. Results A statistically no significant difference was found for endometrial chemical composition of all of the heavy metals (chrome, manganese, iron, cobalt, nickel, zinc and lead) between group 1 and 2 (p > 0.05). On the other hand, there was statistically significant difference for all of the heavy metals between group 1 and group 3 (p < 0.05), while there was statistically significant difference for chrome, manganese, iron, cobalt and nickel (p < 0.05), but zinc and lead (p > 0.05) between group 2 and 3. Conclusion Air pollutants of Pb and Zn resulting mostly from combustion of fossil fuels and certain special industrial process in Kirikkale may be a risk factor for the high pregnancy loses by changing endometrial homeostasis.     

氧化还原介体催化强化Paracoccus versutus菌株GW1反硝化特性研究

考察了Paracoccus versutus菌株GW1的醌呼吸特性及4种结构相似的醌类介体(AQS,α-AQS,AQDS和1,5-AQDS)催化强化Paracoccus versutus菌株GW1的反硝化过程.结果表明,Paracoccus versutus菌株GW1能利用醌类介体作为其电子传递链中的电子受体进行呼吸,使醌类介体还原为相应的氢醌形式;在35℃条件下,采用间歇试验法,4种介体浓度均为0.24mmol.L-1时,可分别提高硝酸盐氮降解速率1.14～1.63倍、总氮去除速率1.12～2.02倍,其从大到小顺序为:AQDS>1,5-AQDS>AQS>α-AQS;介体可降低Paracoccus versutus菌株GW1硝酸盐降解过程中氧化还原电位约33～75 mV;介体催化强化硝酸盐降解过程中pH变化趋势与空白对照组类似,最终pH稳定在9.0左右;在0～0.32 mmol.L-1AQDS浓度范围内,体系硝酸盐氮降解零级反应速率常数K与介体的浓度cAQDS呈线性关系.本研究为解决生物脱氮技术存在降解速率低的问题提供了有效途径.     

石英ESR法在河流沉积物源示踪中的探讨及应用

使用石英ESR法示踪河流沉积物源是一种新方法和新理论的探索。本文从拟解决的科学问题出发,在着重分析石英ESR信号强度和CI值物源示踪理论基础之上,讨论了该方法在亚洲现代沙尘沉降物源示踪和地质历史时期风尘堆积物源示踪研究中的有效性,结合ESR测年可覆盖整个第四纪时期的特性,认为石英ESR法不仅可以为物源示踪提供良好的年代框架约束,而且还可以较好的反映地质历史时期沉积物质来源在不同时空尺度上的变化特征。随后,通过对指导思想、研究思路以及长江流域不同河段和主要支流的地质地貌背景、岩石类型分布、水系组合特征以及"源-汇"系统之间物质剥蚀-堆积过程的可通达性等方面的综合论述与分析,讨论了石英ESR法在河流沉积物源示踪上的有效性及其在研究长江流域水系发育历史和沉积演化过程中的可行性。     

氧化还原介体调控亚硝酸盐反硝化特性研究

采用实验室驯化的亚硝酸盐反硝化菌群作为菌种,优化亚硝酸盐降解条件,探究在氧化还原介体蒽醌-2-磺酸钠(AQS)存在条件下亚硝酸盐反硝化的特性.结果表明,反硝化菌群降解亚硝酸盐的最适条件为:温度35℃,pH为8,丁二酸钠为碳源,碳氮比4∶1,初始亚硝酸盐浓度100 mg.L-1;AQS的最佳投加量为0.16 mmol.L-1,介体调控的反硝化体系氧化还原电位略有降低,维持在-400～-500 mV之间,pH随亚硝酸盐降解速率增加而增大,最终稳定到9～10之间;通过分析反硝化中间代谢产物,推测AQS在亚硝酸盐反硝化过程中不仅起到辅酶CoQ的作用而且加速了细胞色素传递电子的全过程.本研究可为氧化还原介体调控亚硝酸盐反硝化实际应用提供理论基础和优化参数.     

A simple method to harness DC (direct current) electrical energy generated by bacterial activity

We developed a new system for collecting electrons generated by bacterial activity to supply DC (direct current) electrical energy. This system used eight titanium sub-electrodes (surface area of each sub-electrode: 189 cm²) connected to one central main titanium electrode (surface area of electrode: 1571 cm²). The distance between each sub-electrode and the main electrode was 30 cm. In an initial experiment, we collected electrons during composting cattle excreta, which was mixed with a commercially available microbial compost activator/starter. We analysed the relationships between the composting temperature and electrical current and voltage. Electrons were effectively collected and used successfully to obtain DC electrical energy. Generation of a stable voltage of approximately 0.5 V was clearly observed. This voltage was not related to compost temperature; however, the generated electrical current increased and decreased with compost temperature. The method was then used in a second experiment to collect electrons generated by bacterial activity in an agricultural field (area: 48 m²). Electrons in the field were effectively collected, and we measured a stable voltage of approximately 1.1 V and a stable current of approximately 0.7 mA. The system has the advantages of being simple, easily maintained, inexpensive, and applicable to large-scale agricultural fields.     

Effect of Fe（Ⅲ） on the bromate reduction by humic substances in aqueous solution

Humic substances are ubiquitous redox-active organic compounds of environment. In this study, experiments were conducted to determine the reduction capacity of humic acid in the man-ix of bromate and Fe（Ⅲ） solutions and the role of Fe（Ⅲ） in this redox process. The results showed that the humic acid regenerated Fe（Ⅱ） and reduced bromate abiotically. The addition of Fe（Ⅲ） could accelerate the bromate reduction rate by forming humic acid-Fe（Ⅲ） complexes. Iron species acts as electron mediator and catalyst for the bromate reduction by humic acid, in which humic acid transfers electrons to the complexed Fe（Ⅲ） to form Fe（Ⅱ）, and the regenerated Fe（Ⅱ） donate the electrons to bromate. The kinetics study on bromate reduction further indicated that bromate reduction by humic acid-Fe（Ⅲ） complexes is pH dependent. The rate decreased by 2-fold with the increase in solution pH by one unit. The reduction capacity of Aldrich humic acid was observed to be lower than that of humic acid or natural organic matter of Suwanne River, indicating that such redox process is expected to occur in the environment.