Evaluation of photolysis and hydrolysis of pyraclostrobin in aqueous solutions and its degradation products in paddy water

This study evaluated the hydrolysis and photolysis kinetics of pyraclostrobin in an aqueous solution using ultra-high-performance liquid chromatography–photodiode array detection and identified the resulting metabolites of pyraclostrobin by hydrolysis and photolysis in paddy water using high-resolution mass spectrometry coupled with liquid chromatography. The effect of solution pH, metal ions and surfactants on the hydrolysis of pyraclostrobin was explored. The hydrolysis half-lives of pyraclostrobin were 23.1–115.5?days and were stable in buffer solution at pH 5.0. The degradation rate of pyraclostrobin in an aqueous solution under sunlight was slower than that under UV photolysis reaction. The half-lives of pyraclostrobin in a buffer solution at pH 5.0, 7.0, 9.0 and in paddy water were less than 12?h under the two light irradiation types. The metabolites of the two processes were identified and compared to further understand the mechanisms underlying hydrolysis and photolysis of pyraclostrobin in natural water. The extracted ions obtained from paddy water were automatically annotated by Compound Discoverer software with manual confirmation of their fragments. Two metabolites were detected and identified in the pyraclostrobin hydrolysis, whereas three metabolites were detected and identified in the photolysis in paddy water.     

加速溶剂同时萃取和净化-气相色谱-三重四极杆串联质谱测定土壤和沉积物中8种多溴联苯醚

建立了土壤和沉积物中8种多溴联苯醚(PBDEs,BDE-28、BDE-47、BDE-99、BDE-100、BDE-153、BDE-154、BDE-183和BDE-209)加速溶剂同时萃取和净化-气相色谱-三重四极杆串联质谱(ASE-GC-MS-MS)的分析方法。通过优化加速溶剂萃取与弗罗里硅土在线净化和串联质谱多反应监测模式的条件,较好地去除基质干扰,并提高了三重四极杆串联质谱定性的准确性及定量的灵敏性。该方法采用改进的色谱柱能同时分析包括高溴代联苯醚BDE-209在内的8种PBDEs,其浓度范围为1～100 ng/mL(BDE-209为10～1 000 ng/mL),线性良好,线性回归系数均大于0.997。方法检出限为0.004～0.1 ng/g,方法回收率为75%～110%,方法精密度为2.4%～15.6%。适于批量处理土壤和沉积物中含有多组分痕量PBDEs的样品。     

不同雨强条件下太湖流域典型蔬菜地土壤磷素的径流特征

以太湖流域典型区域无锡市近郊区鸿声镇的蔬菜地为研究对象,采用人工模拟降雨的方法,通过野外径流小区试验,研究了不同雨强对菜地土壤磷素径流流失的影响.结果表明,初始产流时间随雨强的增大呈幂函数减小(R²=0.99),径流量在雨强较小时,缓慢上升,但随着雨强的增大急剧上升,在雨强0.83、1.17和1.67 mm·min^-1时,总磷(TP)和颗粒态磷(PP)都表现为初始流失浓度较高,随降雨历时延长略有下降,最终趋于稳定,而在大雨强2.50 mm·min^-1时,TP和PP呈现波浪式起伏,没有明显的变化趋势;在整个降雨-径流过程中,溶解态磷(DP)变化比较平缓,占TP的比例为20%～32%,而PP占TP的比例为68%～80%,其变化规律与TP相一致,由此可见,PP是土壤磷素流失的主要形态;通过对比不同雨强下不同形态磷素的流失率,发现TP的流失率,大雨强2.50 mm·min^-1是小雨强0.83 mm·min^-1的20倍,而DP的流失率,却是33倍,这表明随着雨强的增加,加速土壤PP流失的同时,也大大促进了DP的流失,主要原因是降雨前表施磷肥,使得磷肥中大量的无机态磷溶解释放到水环境中,增加了DP的流失,从而会加重受纳水体富营养化的程度.     

液体旋流分离器分离效率的研究

液体旋流分离器是水环境污染治理的主要设备之一.分离效率是衡量液体旋流分离器分离过程进行完善程度的最重要的技术指标,它能从质与量两方面反映出设备性能的优劣.当前液体旋流分离器设计过程还缺少具体量化的理论依据,为了给液体旋流分离器的设计提供理论依据,通过液体旋流分离器从水中分离固体粒子的性能实验,得出了液体旋流分离器各部结构尺寸、形状、相对比例对分离效率的不同影响程度,提出了结构参数的最佳取值范围.按照本研究提出的设计原则和方法,可以制造出性能优良的液体旋流分离器.     

胶州湾入海污染物总量控制研究

在胶州湾水质数值模拟的基础上,建立了污染物总量控制模型.计算了各个点源的响应系数,分担率及环境容量.结果表明,胶州湾内COD各入海污染源均有余量,不需要削减.胶州湾东北部N、P污染较严重,污染物入海总量已经超过海域的环境容量.研究结果将为胶州湾污水排海、海域水质管理、总量控制规划编制提供科学依据.     

海洋四水团混合的定量化分析和方法比较及其在东海西南海区的应用

通过构造理想的四水团混合模型,对传统温-盐二指标图解和三指标钜阵求解分析水团混合的方法进行比较,认为三指标估算结果更接近真实值.但温、盐数据因为易得且准确性好,所以传统方法仍具有一定的实用价值.在东海西南海区的应用中,检验了天然放射性226Ra核素作为第三个指标的可行性,并对实际水团混合情况进行了评估.证实黑潮次表层水在夏季顺陆坡边缘爬升后沿底部向岸运移,并在近岸涌升,是东海陆架区营养盐外源补充的一个重要动力.     

固相萃取-UPLC-MS/MS法测定环境水体中多种抗生素

采用固相萃取-超高效液相色谱串联质谱法测定环境水样中25种磺胺类和喹诺酮类抗生素,通过优化试验条件,使方法在2.00μg/L～200μg/L范围内线性良好,方法检出限为1.01ng/L～2.85ng/L,7次测定结果的RSD为2.3%～8.0%。将该方法用于自来水和地表水测定,结果均为未检出,高、低质量浓度水平的加标回收率为61.2%～102%。     

HPLC-三重四级杆质谱法测定医疗废水中抗生素残留

采用固相萃取/高效液相色谱-三重四级杆质谱法同时测定医疗废水中的20种超痕量抗生素残留,通过优化试验条件,使方法在100μg/L～100μg/L范围内线性良好,方法检出限为024ng/L～122ng/L。空白水样和实际水样3个质量浓度水平的加标回收率分别为80.2%～108%和75.8%～114%,6次测定结果的RSD分别为2.4%～8.4%和1.7%～8.1%。将该方法用于测定重庆市2家三甲医院医疗废水中的超痕量抗生素残留,结果有11种抗生素检出,其余均为未检出。     

粮食基础设施震后恢复重建关键问题研究

在对汶川8.0级地震后绵阳市粮食基础设施破坏情况调研的基础上,提出恢复与发展并重、粮食基础设施节点与网络并行、推进行业整合和信息化的建设思路,规划了绵阳市灾后恢复重建的维修保障和重建发展项目,并对规划实施效果进行了经济和社会效益分析。     

Imazaquin degradation and metabolism in a sandy loam soil amended with farm litters

Irnazaquin applied in legume crops has a long residual time in soil, which often impacts safety of the susceptible crops. To increase safety of imazaquin application, two composted litters, bovine manure （BM） and chicken manure （CM）, were used to determine their effects on imazaquin environmental behavior by incorporating each kind of manure into the tested sandy loam soil at 10% （w/w）. The degradation of imazaquin in BM- and CM-amended soil was about 2.4 and 1.5 times, respectively, faster than that in unamended soil. The half-lives of imazaquin in BM-amended soil varied between 6.7 and 15.4 d over the temperature range of 20 to 40℃, and the degradation rate constant （k） increased by a factor of about 1.5 for every 10℃ change. Higher mix ratio did not significantly increase the degradation, and the optimal active degradation of imazaquin was observed approximately at the mix ratio of 10：1 of soil to BM. The different moisture levels had negligible effect on imazaquin degradation. In both unamended and BM-amended treatments, two metabolites were observed at 5, 10 and 30 d after treatment. One metabolite at retention time （RT） of 8.4 rain was identified as 2-（4- hydroxyl-5-oxo-2-imidazolin-2-yl） quinoline acid, originating from the loss of isopropyl group and hydroxylation at the 4-position of imidazolinone ring. The other at RT of 12.9 rain was identified as quinoline-2,3-dicarboxylic anhydride, resulting from detachment of imidazolinone ring and the forming of dicarboxylic anhydride. This finding suggested that the addition of farm litters into soil might be a good management option since it can not only increase soil fertility but also contribute to increase safety of imazaquin application to the following susceptible crops.