覆膜与降雨类型对土壤水分及NO3--N淋失的影响

在丹江口库区青塘河五龙池小流域,以黄棕壤横垄种植玉米为例,设置覆膜与无覆膜两种处理,采用田间小区实验研究覆膜与降雨类型对0~30 cm土壤水分和NO-3-N淋失的影响.结果表明:两处理土壤含水量均随土层加深而增加,与无覆膜相比覆膜可降低0~10、10~20、20~30cm土层中的含水量.不同降雨类型对覆膜土壤含水量的影响有区别,小雨时3层土壤间差异显著,含水量随土层加深急剧增加;中雨时10~20cm比0~10 cm、20~30 cm比10~20 cm分别高50.80%、6.62%,0~10 cm土壤含水量显著低于10~20 cm和20~30 cm;暴雨时含水量随土层加深增幅变小;覆膜土壤土层越深土壤含水量受降雨的影响越小.覆膜可降低0~10、10~20 cm土层中的NO-3-N淋失量,分别降低40.74%、24.48%,但会增加20~30 cm的淋失;两处理土壤NO-3-N淋失量均随土层加深而增加.不同降雨类型对覆膜土壤NO-3-N淋失的影响也有区别,小雨时随土壤深度的增加淋失量增多;中雨时,0~10、20~30 cm NO-3-N淋失量分别为10~20 cm的1.75、8.41倍;暴雨时,0~10、20~30 cm分别比10~20 cm低18.97%和60.69%.土壤中NO-3-N淋失受土壤含水量的影响,且随土层加深含水量对NO-3-N淋失的影响减弱.     

基于ANN的土壤重金属分布和污染评价研究

农田土壤重金属污染与备受关注的农产品安全问题有密切联系,因此对其进行研究意义重大。以江苏省南通市为研究区,利用采样点实测数据,借助神经网络模型(ANN)并结合3S技术对问题进行研究,从而对土壤重金属的空间动态分布进行描述,并对各个空间位点重金属的污染状况进行评价。结果表明,神经网络模型能够智能地学习各个样点的空间位置与该点各重金属含量之间的映射关系和预先设计好的分类评价模式,并能够稳健地对各个空间插值点处的重金属含量和各个位点的重金属污染状况进行预测和评价。结论显示,南通市大部分农田土壤重金属污染较轻,但也存在局部地区的严重污染。结论与实际情况相符,表明神经网络模型可以为农田土壤重金属的研究提供一个新的思路和方法。     

Effects of cerium on growth and physiological mechanism in plants under enhanced ultraviolet-B radiation

Effect of cerium （Ce^3＋） on the growth, photosynthesis and antioxidant enzyme system in rape seedlings （Brassica juncea L.） exposed to two levels of UV-B radiation （T1： 0.15 W/m^2 and T2：0.35 W/m^2） was studied by hydroponics under laboratory conditions. After 5 d of UV-B treatment, the aboveground growth indices were obviously decreased by 13.2%-44. 1%（T1） and 21.4%-49.3% （T2）, compared to CK, and except active absorption area of roots, the belowground indices by 14.1%-35.6%（T1） and 20.3%-42.6% （T2）. For Ce＋UV-B treatments, the aboveground and belowground growth indices were decreased respectively by 4.1%-23.6%, 5.2% -23.3%（Ce＋T1） and 10.8%-28.4%, 7.0%-27.8%（Ce＋T2）, lower than those of UV-B treatments. The decrease of growth indices appeared to be the result of changes of physiological processes. Two levels of UV-B radiation induced the decrease in chlorophyll content, net photosynthesis rate, transpiration rate, stomatal conductance and water use efficiency by 11.2%-25.9%（T1） and 20.9%- 56.9%（T2）, whereas increase in membrane permeability and activities of antioxidant enzymes including superoxide dismutase（SOD）, catalase （CAT） and peroxidase （POD） by 6.9%, 22.8%, 21.5%, 9.5%（T1） and 36.6%, 122.3%, 103.5%, 208.9%（T2）, respectively. The reduction of the photosynthetic parameters in Ce＋UV-B treatments was lessened to 3.2%-13.8%（Ce＋T1） and 4.9%-27.6%（Ce＋T2）, and the increase of membrane permeability and activities of antioxidant enzymes except POD in the same treatments were lessened to 2.4%, 8.4%, 6.6%（Ce＋T1） and 30.1%, 116.7%, 75.4%（Ce＋T2）. These results indicate that the regulative effect of Ce on photosynthesis and antioxidant enzymatic function is the ecophysiological basis of alleviating the suppression of UV-B radiation on growth of seedlings. Furthermore, the protective effect of Ce on seedlings exposed to TI level of UV-B radiation is superior to T2 level.     

Enhanced triallyl isocyanurate (TAIC) degradation through application of an O3/UV process: Performance optimization and degradation pathways

• UV/O₃ process had higher TAIC mineralization rate than O₃ process. • Four possible degradation pathways were proposed during TAIC degradation. • pH impacted oxidation processes with pH of 9 achieving maximum efficiency. • CO₃^2– negatively impacted TAIC degradation while HCO₃^– not. • Cl^– can be radicals scavenger only at high concentration (over 500 mg/L Cl^–). Triallyl isocyanurate (TAIC, C₁₂H₁₅N₃O₃) has featured in wastewater treatment as a refractory organic compound due to the significant production capability and negative environmental impact. TAIC degradation was enhanced when an ozone(O₃)/ultraviolet(UV) process was applied compared with the application of an independent O₃ process. Although 99% of TAIC could be degraded in 5 min during both processes, the O₃/UV process had a 70%mineralization rate that was much higher than that of the independent O₃ process (9%) in 30 min. Four possible degradation pathways were proposed based on the organic compounds of intermediate products identified during TAIC degradation through the application of independent O₃ and O₃/UV processes. pH impacted both the direct and indirect oxidation processes. Acidic and alkaline conditions preferred direct and indirect reactions respectively, with a pH of 9 achieving maximum Total Organic Carbon (TOC) removal. Both CO₃^2– and HCO₃^– decreased TOC removal, however only CO₃^2– negatively impacted TAIC degradation. Effects of Cl^– as a radical scavenger became more marked only at high concentrations (over 500 mg/L Cl^–). Particulate and suspended matter could hinder the transmission of ultraviolet light and reduce the production of HO· accordingly.     

基于3S技术对太湖底质及水质总磷的研究

应用3S技术研究了太湖底质与水质总磷(TP)的分布情况,并结合水华频次分析了其相关性。结果表明:2016—2018年,太湖底质TP年均值在433~537 mg/kg波动,水质TP年均值从0.064 mg/L上升至0.087 mg/L。从空间分布来看,底质TP、水质TP和水华频次均呈现“西高东低”的规律,太湖西部区尤其是竺山湖区是需要开展治理的重点区域。3年间,太湖西部区水质TP上升,而底质TP与入湖河流TP下降,说明内源磷污染是太湖西部区水质TP升高的主要原因,须加强科学清淤。     

Determination of Steroid Estrogens in Wastewater Treatment Plant of A Controceptives Producing Factory

Steroid estrogens such as estrone (E1), 17β-estradiol (E2), estriol (E3), and 17α-ethynylestradiol (EE2) have been suspected to be the main contaminants, which can affect the endocrine system of animals. Many authors have investigated these chemicals in the domestic wastewater treatment plants (WTP). However, wastewater from industries producing steroid contraceptives has not got ample attention. From the environmental point of view, the four steroids are very significant because even very low concentrations (ng/L) can cause reproductive disturbances in human, livestock and wildlife. The main purpose of the present investigation was to develop an analytical method for the determination of the four steroid estrogens present in WTP of a pharmacy factory, mainly producing contraceptive medicine in Beijing, China. Analysis was performed by solid-phase extraction (SPE) system and liquid chromatography combined with tandem mass spectrometry (LC/MS/MS). The average recoveries from effluent samples ranged from 88% to 103% and the precision of the method ranged from 9% to 4%. Based on 0.5-L wastewater samples, the limit of quantification (LOQ) was determined at 0.7 ng/L for E1, 0.8 for E2, 0.9 ng/L for E3, and 0.5 ng/L for EE2 in influent, and 1.0 ng/L for E2 and EE2, and 2.0 ng/L for E1 and E3 in effluent. In the influent samples, average concentrations of 80, 85, 73 and 155 ng/L were determined for E1, E2, E3 and EE2, respectively, showing that they were removed in this WTP to the extent of 79, 73, 85 and 67%, respectively.     

高压微波络合消解石墨炉原子吸收分光光度法测定环境空气中锡

用有机滤膜采集空气中颗粒物样品,用HNO3-HCl-HClO4-EDTA微波络合消解后制成样品溶液。用石墨炉原子吸收分光光度法可确定样品溶液中锡的浓度。该方法具有消解完全,无损失,灵敏度高,准确度、精密度好等特点。     

化学解耦联剂对活性污泥产率的控制作用

采用3,3',4',5-四氯水杨酰苯胺(TCS)作为代谢解耦联剂添加到活性污泥工艺中,进行连续曝气分批培养实验.结果表明:在TCS总投加量相同的情况下,采用一次性大剂量投加的污泥减量化效果好于分次小剂量投加.每d投加 12 mg TCS,污泥产量比对照下降了33%,而每2 d一次性投加24 mg TCS,污泥产量比对照下降了55%.污泥的CODCr去除能力有所下降,当一次性投加12 mg时,CODCr去除率比对照下降了12%,但出水氨氮及总氮质量浓度均未受影响.污泥的SVI有所上升,但沉降性能未见有明显变化.      

污染物零排放的化石燃料燃烧系统

介绍了熔融盐循环热载体无烟燃烧技术(nonflame combustion technology usingthermal cyclic carrier of molten salt,简称NFCT).利用沉淀法制备了Fe2O3粉末,并通过机械法加工成氧载体.XRD分析表明所制备的Fe2O3粉末为单一的α-Fe2O3相在固定床反应器中表征了氧载体得失晶格氧的过程,随循环次数的增多,氧载体被CH4还原的速率会有所增加,氧载体在CH4和空气气氛中得失晶格氧是可逆过程,反应后,氧载体内部形成了蜂窝状结构.氧载体的转化度最大为82%,占氧载体总质量18%的晶格氧可以用来氧化CH4.在熔融盐反应器中用CH4作为燃料和所制备的氧载体进行了燃料燃烧和氧载体复原的实验研究在燃料燃烧反应的开始阶段,CH4大部分被氧化成了CO2,CO2的体积分数最高可以达到85%,随着反应时间的增加,氧载体的氧化能力下降,不完全氧化产物CO和未反应的CH4的体积分数逐渐升高,3000s时,CO2的体积分数只有50%在氧载体恢复晶格氧的过程中,在1500s以前,空气中的O2都被氧载体所吸收,1500s以后,该过程排出气体中的O2体积分数开始上升,至2000s气体成分与空气的成分相同.在实验中没有检测出NOx的生成.     

Fe3+掺杂TiO2薄膜的制备及光催化降解甲醛的研究

采用溶胶-凝胶法制备Fe3+掺杂的TiO2薄膜光催化剂,进行甲醛的光催化实验,考察Fe3+掺杂量、薄膜焙烧温度及溶胶体系pH值对光催化性能的影响。结果表明,Fe3+掺杂量为1.0%,焙烧温度500℃1h,加硝酸溶胶体系pH=4时,Fe3+掺杂TiO2薄膜光催化活性最高。