土壤中4-溴苯胺降解动力学及其生态毒性追踪

秀谷隆是一种被广泛应用的取代脲类除草剂,其主要降解产物为４－溴苯胺（４－ＢＡ）,研究４－溴苯胺在不同土壤中的降解动力学规律,并用土壤环境指示动物弹尾目跳虫Ｃｏｌｌｅｍｂｏｌａ（Ｆｏｌｓｏｍｉａ ｃａｎｄｉｄａ）跟踪指示该化合物在进一步降解过程中的毒性,结果表明：４－溴苯胺在土壤中的降解行为可用一级反应动力学方程来较好地描述,其生态毒性明显高于母体化合物秀谷隆,该化合物在粘土中的残留量低于砂土,但毒     

单甲脒饱和蒸气压的测定和估算

用气体的法测单甲脒在１５,２５,３５和４５℃时的饱和蒸气分别为０．２０２,０．５５４６,１．９５,６．２９Ｐａ;亨利常数计算值分别为６．３０×１０＾－４,１．６７×１０＾－３,５．６８×１０＾０－３和１．７８×１０＆－２,根据Ｃｌａｕｓｉｕｓ Ｃｌａｐｅｙｒｏｎ方程求出单甲脒在常温下气化热为８９．２ｋＪ．ｍｏｌ＾－１。     

Extent and causes of 3D spatial variations in potential N mineralization and the risk of ammonium and nitrate leaching from an N-impacted permanent grassland near York, UK

Changes in the dynamics of inorganic N species transformations with depth have been investigated for seven soil profiles from a nitrogen-impacted ancient grassland on a nature reserve outside York in the UK, using incubation experiments. In five of the profiles, both ammonification and nitrification are occurring below the rooting zone, probably partly in response to the low C:N ratio in the soils. This contributes to elevated nitrate concentrations found in an adjacent stream. Accumulation of ammonium during incubation in the sub-soils of these five profiles suggests a high probability of ammonium leaching down the profiles as ammonium inputs and outputs at a given depth approach equilibrium. This ammonium may also be nitrified at depth. However, in the two profiles with the most acidic surface horizons, net mineralization was negligible or negative; some initial ammonium-N and ammonium-N produced during incubation were nitrified, so the loss in ammonium-N was closely balanced by nitrate-N production.     

Fe3O4纳米磁性微粒对全氟辛烷磺酸盐的吸附

采用共沉淀法合成Fe3O4纳米磁性颗粒,用透射电子显微镜(TEM)、X射线衍射仪(XRD)以及振动样品磁强计(VSM)对Fe3O4纳米磁性颗粒的粒径、形貌和磁性进行表征并研究Fe3O4纳米磁性微粒对全氟辛磺酸盐的吸附。结果表明:在PFOS初始浓度4 mg/L,pH为3,反应时间24 h,Fe3O4纳米磁性微粒投加量1.25 g/L,对全氟辛磺酸盐去除率达到90%。Fe3O4纳米磁性微粒对PFOS的吸附符合Freundlich吸附方程。     

纯种氨氧化菌短程反硝化特性

以Comamonas aquatica LNL3为研究对象,根据其既能短程硝化又能短程反硝化的特性,采用好氧方式富集和固定化菌种,再以厌氧方式驯化,得到具有高效短程反硝化特性的纯种氨氧化菌。采用扫描电镜对固定化前后的载体进行表征,且用正交试验考察了不同环境因子(温度、pH、碳氮比、溶解氧)对Comamonas aquatica LNL3短程反硝化的影响。结果表明,所用载体与Comamonas aquatica LNL3有良好的亲和性,适于微生物的固定化;环境因子对Comamonas aquatica LNL3短程反硝化影响大小顺序为:温度>pH>DO>C/N;在环境条件改变过程中当温度为35℃,pH=8,C/N=3,DO=2.5 mg/L时,Comamonas aquatica LNL3短程反硝化速率达到最大,为32.63 mg/(L.h);研究结果还表明,Comamonas aquatica LNL3具有好氧反硝化特性,适宜处理低碳氮比废水。     

Green and efficient degradation of cefoperazone sodium by Bi4O5Br2 leading to the production of non-toxic products: Performance and degradation pathway

Photocatalytic process represents a promising approach to overcome the pollution challenge associated with the antibiotics-containing wastewater. This study provides a green, efficient and novel approach to remove cephalosporins, particularly cefoperazone sodium (CFP). Bi₄O₅Br₂ was chosen for the first time to systematically study its degradation for CFP, including the analysis of material structure, degradation performance, the structure and toxicity of the transformation products, etc. The degradation rate results indicated that Bi₄O₅Br₂ had an excellent catalytic activity leading to 78% CFP removal compared with the pure BiOBr (38%) within 120 min of visible light irradiation. In addition, the Bi₄O₅Br₂ presents high stability and good organic carbon removal efficiency. The effects of the solution pH (3.12 - 8.75) on catalytic activity revealed that CFP was mainly photocatalyzed under acidic conditions and hydrolyzed under alkaline conditions. Combined with active species and degradation product identification, the photocatalytic degradation pathways of CFP by Bi₄O₅Br₂ was proposed, including hydrolysis, oxidation, reduction and decarboxylation. Most importantly, the identified products were all hydrolysis rather than oxidation byproducts transformed from the intermediate of β-lactam bond cleavage in CFP molecule, quite different from the mostly previous studies. Furthermore, the final products were demonstrated to be less toxic through the toxicity analysis. Overall, this study illustrates the detailed mechanism of CFP degradation by Bi₄O₅Br₂ and confirms Bi₄O₅Br₂ to be a promising material for the photodegradation of CFP.     

油菜地CO2、N2O排放及其影响因素

2005年11月至2006年5月采用静态箱法对成都平原典型水稻 - 油菜轮作区油菜地CO2、N2O排放通量进行原位测定.结果表明,CO2排放通量为121.4～1 585.8 mg·m-2·h-1,平均656.8 mg·m-2·h-1;N2O排放通量为18.0～521.0 μg·m-2·h-1,平均168.0 μg·m-2·h-1.在整个油菜生长期内,地下5 cm土壤温度与CO2、N2O排放通量之间呈指数函数关系.3种不同处理油菜地CO2、N2O排放通量均为常规处理＞无氮处理＞裸地处理.土壤温度、施氮和植物生长是影响油菜地CO2、N2O排放的主要因素.     

种稻土壤CH4排放规律的研究

通过盆栽试验研究了水稻生长期CH4排放的规律。结果表明,CH4排放存在明显的日变化,最大值出现在下午4点左右,最小值出现在凌晨4点左右。土壤温度的变化是导致CH4排放日变化的主要因素。水稻生长期CH4排放的季节变化受前茬季节作物种植及稻草还田时间的显著影响。前茬季节种植紫云英及休闲且水稻移栽前施用稻草处理在水稻生长初期即有大量CH4排放,且在水稻生长的前期、中期和后期分别出现3个CH4排放峰;前茬季节种植小麦和休闲且在前茬季节前施用稻草处理的,直至水稻生长的中期才有少量CH4排放。烤田期间CH4的排放峰值出现在土壤呈微于松软状态时;烤田至土壤干裂时,CH4排放通量降至零。     

炭化秸秆吸磷剂的制备及吸附性能研究

以水稻秸秆为原料,经炭化、KMnO4预氧化和FeSO4溶液改性后,制备得到低成本的改性炭化水稻秸秆（modified carbonized rice straw,MCRS）.采用Zeta电位分析仪、扫描电镜、能谱仪、比表面积分析仪、红外光谱分析仪和X射线衍射分析仪多种手段,分析了炭化水稻秸秆和MCRS的理化性能.通过静态吸附试验研究了吸附剂投加量、pH值和温度对MCRS除磷效果的影响.结果表明：MCRS对磷的吸附是一个吸热过程,其吸附等温线可用Langmuir方程进行拟合.当投加量为4g·L^-1、pH值为7时,MCRS对水溶液中磷的去除率最高可达96％;依据Langmuir方程计算得到,30℃条件下,MCRS对磷的最大吸附量为5.49 mg·g^-1.     

植物对沼泽湿地生态系统N2O排放的影响

利用静态暗箱/气相色谱法连续3个生长季(2003-2005年)对三江平原小叶章草甸和毛果苔草沼泽N2O排放通量进行野外对比观测试验.结果表明,植物不同生长阶段对湿地生态系统N2O排放通量的影响不尽相同.植物的参与促进了湿地生态系统N2O的排放,2003-2005年生长季小叶章草甸土壤-植物系统N2O排放通量分别是土壤表观N2O排放通量的1.58倍、2.09倍和2.34倍,同期毛果苔草沼泽土壤-植物系统N2O排放通量分别是土壤表观N2O排放通量的1.86倍、1.50倍和1.33倍.3个生长季小叶章草甸N2O排放通量均大于毛果苔草沼泽,这主要是由土壤理化性质的空间变异性以及水文情况的差异造成的.