Mg2+ improves biomass production from soybean wastewater using purple non-sulfur bacteria

Soybean wastewater was used to generate biomass resource by use of purple non-sulfur bacteria(PNSB). This study investigated the enhancement of PNSB cell accumulation in wastewater by Mg2+under the light-anaerobic condition. Results showed that with the optimal Mg2+dosage of 10 mg/L, biomass production was improved by 70% to 3630 mg/L,and biomass yield also was improved by 60%. Chemical Oxygen Demand(COD) removal reached above 86% and hydraulic retention time was shortened from 96 to 72 hr. The mechanism analysis indicated that Mg2+could promote the content of bacteriochlorophyll in photosynthesis because Mg2+is the bacteriochlorophyll active center, and thus improved adenosine triphosphate(ATP) production. An increase of ATP production enhanced the conversion of organic matter in wastewater into PNSB cell materials(biomass yield) and COD removal, leading to more biomass production. With 10 mg/L Mg2+, bacteriochlorophyll content and ATP production were improved by 60% and 33% respectively.     

人工湿地应用于富营养化景观水体修复

以某会议中心1号和2号人工湿地为研究对象,研究了人工湿地对富营养化景观水体的净化效果。结果表明:1号和2号人工湿地对COD、TN和TP均具有较好的处理效果,植物的差异对湿地污染物去除效果的影响不明显。TP的去除主要依靠基质的作用。湿地的前段和中段是整个湿地COD和TN去除的主体,且前段的去除率高于中段。     

Toward rational design of amines for CO2 capture: Substituent effect on kinetic process for the reaction of monoethanolamine with CO2

Amines have been considered as promising candidates for post-combustion CO₂ capture. A mechanistic understanding for the chemical processes involved in the capture and release of CO₂ is important for the rational design of amines. In this study, the structural effects of amines on the kinetic competition among three typical products (carbamates, carbamic acids and bicarbonate) from amines + CO₂ were investigated, in contrast to previous thermodynamic studies to tune the reaction of amines with CO₂ based on desirable reaction enthalpy and reaction stoichiometry. We used a quantum chemical method to calculate the activation energies (E_a) for the reactions of a range of substituted monoethanolamines with CO₂ covering three pathways to the three products. The results indicate that the formation of carbamates is the most favorable, among the three considered products. In addition, we found that the E_a values for all pathways linearly correlate with pK_a of amines, and more importantly, the kinetic competition between carbamate and bicarbonate absorption pathways varies with pK_a of the amines, i.e. stronger basicity results in less difference in E_a. These results highlight the importance of the consideration of kinetic competition among different reaction pathways in amine design.     

Removal of formaldehyde over MnxCe1-xO2 catalysts: Thermal catalytic oxidation versus ozone catalytic oxidation

MnxCe1- xO2（x： 0.3–0.9） prepared by Pechini method was used as a catalyst for the thermal catalytic oxidation of formaldehyde（HCHO）. At x = 0.3 and 0.5, most of the manganese was incorporated in the fluorite structure of Ce O2 to form a solid solution. The catalytic activity was best at x = 0.5, at which the temperature of 100% removal rate is the lowest（270°C）. The temperature for 100% removal of HCHO oxidation is reduced by approximately 40°C by loading 5 wt.% Cu Oxinto Mn0.5Ce0.5O2. With ozone catalytic oxidation, HCHO（61 ppm） in gas stream was completely oxidized by adding 506 ppm O3 over Mn0.5Ce0.5O2 catalyst with a GHSV（gas hourly space velocity） of 10,000 hr-1at 25°C. The effect of the molar ratio of O3 to HCHO was also investigated. As O3/HCHO ratio was increased from 3 to 8, the removal efficiency of HCHO was increased from 83.3% to 100%. With O3/HCHO ratio of 8, the mineralization efficiency of HCHO to CO2 was 86.1%. At 25°C, the p-type oxide semiconductor（Mn0.5Ce0.5O2） exhibited an excellent ozone decomposition efficiency of 99.2%,which significantly exceeded that of n-type oxide semiconductors such as Ti O2, which had a low ozone decomposition efficiency（9.81%）. At a GHSV of 10,000 hr-1, [O3]/[HCHO] = 3 and temperature of 25°C, a high HCHO removal efficiency（≥ 81.2%） was maintained throughout the durability test of 80 hr, indicating the long-term stability of the catalyst for HCHO removal.     

溶藻细菌L7代谢物对水华鱼腥藻的溶藻效应

从等体积不同密度的溶藻细菌L7菌液中提取胞内、胞外代谢物,分别加入等体积等密度的水华鱼腥藻中连续培养7d,研究L7代谢物对水华鱼腥藻的溶藻效应。2.78×105~2.78×10 7cfu/mL的L7胞内代谢物能显著促进藻生长和异形胞分化,到培养结束藻密度为对照组的1.7~1.98倍;异形胞数最大可为对照组的2.31倍。2.78×10 8、2.78×10 9cfu/mL的L7胞内代谢物能抑制藻生长,藻密度最低为对照组的58%;能极显著抑制异形胞分化,可不形成异形胞。2.78×10 5~2.78×109 cfu/mL的L7胞外代谢物能极显著抑制藻生长和异形胞分化,藻密度最低为对照组的0.63%,不形成异形胞;藻丝的藻细胞间隔变模糊,藻细胞变大变形,并有大量的单个球形藻体散落。L7主要通过分泌胞外代谢物溶藻,菌胞内代谢物对藻生长有"低促高抑"的作用。     

沈阳辉山水库水质污染现状分析及评价

根据《地表水环境质量评价办法》中规定的方法,对沈阳辉山水库进行了水质和富营养化状态评价,并对污染源和水质污染特性进行了分析。结果显示:水库水质类别为劣Ⅴ类,水质状况为重度污染。富营养化综合营养状态指数为34.44,辉山水库水质为中营养化水平,水库没有藻类水华的产生。水库主要污染指标为总磷、总氮和悬浮物,分别超出国家地表水Ⅲ类标准的14.2倍、5.85倍和2.72倍。整个库区水质变化不均匀,水质变化受库区沿岸污染物排放影响较大,辉山明渠上游和某工厂暗渠排污口输入是水库主要污染源,库区周围动迁后的荒地和蚯蚓养殖,是辉山水库地面径流和农业污染污染源。     

城市建筑垃圾的资源化利用

随着建设项目的增多,建筑垃圾也日益增多。本文对建筑垃圾资源化利用进行了初步分析,重点通过对建筑垃圾的分类研究,提出我国建筑垃圾资源化存在问题及建议。     

超声波萃取-毛细管气相色谱法测定土壤和底质中的25种有机氯农药研究

建立了超声波萃取、Florisil柱净化,SPB-5毛细管柱分离,ECD检测器测定土壤和底质中25种有机氯农药的方法.该方法的检出限为0.079 μg/kg ～1.2 μg/kg,加标回收率为73.1％ ～ 126.5％,相对标准偏差为3.3％ ～9.7％.实验结果证明,该方法灵敏度高、精密度高,操作快速简便,满足土壤和底质中有机氯农药的测定要求.     

新旧微孔曝气器氧转移速率试验研究

以某污水处理厂运行4年多的旧盘式曝气器和同型号的新盘式曝气器为试验对象,对其氧转移速率进行了对比试验,结果表明新旧曝气盘氧转移速率均明显分为两个阶段,运行了4年的旧曝气盘微孔数量减少、微孔孔径增大、气泡数量减少、气泡尺寸增大,氧转移速率比新曝气盘降低了29.2%。因此,污水处理厂在日常运行管理中要做好曝气器的保养工作,及时清洗更换破损、堵塞的曝气器避免能耗浪费。     

Antimony(V) removal from water by hydrated ferric oxides supported by calcite sand and polymeric anion exchanger

We fabricated and characterized two hybrid adsorbents originated from hydrated ferric oxides(HFOs) using a polymeric anion exchanger D201 and calcite as host. The resultant adsorbents(denoted as HFO-201 and IOCCS) were employed for Sb(V) removal from water. Increasing solution pH from 3 to 9 apparently weakened Sb(V) removal by both composites, while increasing temperature from 293 to 313 K only improved Sb(V) uptake by IOCCS. HFO-201 exhibited much higher capacity for Sb(V) than for IOCCS in the absence of other anions in solution. Increasing ionic strength from 0.01 to 0.1 mol/L NaNO3would result in a significant drop of the capacity of HFO-201 in the studied pH ranges; however, negligible effect was observed for IOCCS under similar conditions. Similarly, the competing chloride and sulfate pose more negative effect on Sb(V) adsorption by HFO-201 than by IOCCS, and the presence of silicate greatly decreased their adsorption simultaneously, while calcium ions were found to promote the adsorption of both adsorbents. XPS analysis further demonstrated that preferable Sb(V) adsorption by both hybrids was attributed to the inner sphere complexation of Sb(V) and HFO, and Ca(II) induced adsorption enhancement possibly resulted from the formation of HFO-Ca-Sb complexes. Column adsorption runs proved that Sb(V) in the synthetic water could be effectively removed from 30 μg/L to below 5 μg/L(the drinking water standard regulated by China), and the effective treatable volume of IOCCS was around 6 times as that of HFO-201, implying that HFO coatings onto calcite might be a more effective approach than immobilization inside D201.