Ecotoxicity evaluation of Cu- and Fe-CNT complexes based on the activity of bacterial bioluminescence and seed germination

The toxic effects of the composites of Fe~0 and Cu~0 with different percentages of CNTs were examined based on the activity of bacterial bioluminescence and seed germination. In terms of the EC_50 values, the toxic effects of Cu~0 on bacterial bioluminescence and seed germination were approximately 2 and 180 times greater than that of Fe~0, respectively. The toxicity increased with increasing CNT content in the Cu-CNT mixtures for both organisms,whereas opposite results were observed with Fe-CNT mixtures. The mean toxic effects of Cu-CNT(6%) were approximately 1.3–1.4 times greater than that of Cu-CNT(0%), whereas the toxic effects of Fe-CNT(6%) were approximately 2.1–2.5 times lower than that of Fe-CNT(0%) for both the bioluminescence activity and seed germination. The causes of this phenomenon are unclear at this point. More research will be needed to elucidate the mechanism of the toxicity of nano-mixture materials and the causes of the different patterns of toxicity with Cu-and Fe-CNT mixtures.     

一种硫离子响应杀菌材料的制备及应用研究

目的制备硫离子响应杀菌材料,研究它在不同浓度铜离子条件下的封装效果,以及在不同浓度硫离子条件下的释放行为。方法选择埃洛石纳米管为载体并用透射电镜进行表征、采用真空负载的方式,将甲硝唑和苯骈三氮唑(BTA)分步填充到埃洛石纳米管内部,使用紫外分光光度法测试不同浓度铜离子对纳米管中甲硝唑的封堵效果,以及材料在不同浓度硫离子条件下的释放情况。结果实验中通过调整铜离子浓度发现,铜离子浓度越大对甲硝唑的封堵效果越好,当铜离子浓度达到160 mmol/L时,对甲硝唑的封堵效果最好。杀菌材料在外界硫离子达到0.1mmol/L后,甲硝唑的释放浓度迅速提高,进一步提高硫离子浓度,释放情况改变不明显。结论铜离子浓度达到160 mmol/L时,材料的封装效果是最好的。材料能够对硫离子实现响应释放,且对应的临界浓度为0.1 mmol/L。     

石墨炉原子吸收光谱法测定海河下游水中痕量镉

原子吸收光谱法直接测定高盐水中痕量镉时，有很大背景吸收和误差。本文采用络合—萃取技术使共存元素与待测元素分离，既消除了基体干扰，又达到了富集作用，使测定结果准确可靠。     

雨天硫酸盐化速率样品扩散分析

选择采样期不同降雨天数的碱片，测定余边的硫酸盐化速率含量，其结果为：采样期全月无雨时，余边上的硫酸盐均未检出；半月以上至全月有雨时检出率为１００％，检出量占样品量的２．７０～１５．９５％。经扩散试验，查清了余边上的硫酸盐主要是有效面积上采集的样品的扩散，并提出了相应的修正方法。     

Effect of Humic Acid on the Bioavailability of γ-Hexachlorocyclohexane in Marsilea Minuta (L.)

Effect of various concentrations of humic acid (0.2 to 1%) on thebioavailability of -HCH in vegetative clones of theaquatic fern Marsilea minuta was studied in a staticexperimental bioassay system on different photoperiods. Additionof humic acid showed the reduction in the bioavailability of-HCH in all the photoperiods (72 hr light to 144 hrlight) at the interval of 16 hr light (L) and 8 hr dark (D) inboth aerial and submerged portion as compared to controlindicating its protective role in toxicity.     

Application of a systemic approach to the study of pollution of the Tinto and Odiel rivers (Spain)

The province of Huelva in the SW of Spain presents high environmental contrasts: together with the great abundance of natural spaces, it shows the impacts of historical natural resources exploitation processes. In the Ria of Huelva, the effluents of the chemical industries must be added to the contaminating inputs of the Tinto and Odiel rivers, coming from the acid drainage of the mines located in the Iberian Pyrite Belt. This forced the Environmental Agency (AMA) to elaborate in 1987 an Effluent Remediation Plan in order to negate unacceptable environmental impacts. The application of a grey box systemic analysis to the AMD pollution, undergone by the Tinto and Odiel rivers has allowed to set a conclusive explanation of the sampling results observed for a period of 11 years, thus making available an overall view of the polluting process and, above all, an explanation of its partial aspects.     

天青石及锶矿中硫酸锶的测定

通过实验，解决了测定天青石中硫酸锶时的不足，结果令人满意。     

微波高压络合消解石墨炉原子吸收分光光度法测定环境空气中锑

用有机滤膜采集空气中颗粒物样品,用微波高压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锑的浓度。该方法具有对有机滤膜和样品消解完全,省时,无损失,灵敏度高,准确度、精密度好等特点。     

工作场所空气中硫酸雾（SO3）的分析

采用碘量法测定工作场所空气中的三氧化硫及硫酸雾，三氧化硫及硫酸雾经中性水吸收后与碘化钾和碘酸钾反应，析出的碘与淀粉指示剂作用产生蓝色，进行比色测定。     

气相色谱-质谱法测定废酸油渣中的16种多环芳烃

建立了废酸油渣中16种多环芳烃超声萃取、Florisil萃取柱净化、气相色谱-质谱测定的方法。笔者对提取方式、提取剂类型和体积、提取时间和次数、净化方式等进行研究,采用无水硫酸钠分散,二氯甲烷作为提取剂超声40 min,提取液经纯水清洗、离心后取适量有机相经过3 g Florisil萃取柱净化,采用气相色谱-质谱选择离子模式(SIM),加入内标进行定量分析。结果表明:二氯甲烷提取效率比正己烷好,丙酮可能引起酸性样品中多环芳烃的降解,丙酮超声萃取时加入无水硫酸钠能在一定程度上防止目标物降解,但萃取效率不可控制,宜采用二氯甲烷作为萃取剂。分散提取能有效减少提取时间,超声清洗仪超声40 min提取效率为86.2%～104%。3g Florisil萃取柱净化比1 g Florisil萃取柱净化和GPC净化效果略好。方法检出限为0.4～1.3 mg/kg,6次空白加标的相对标准偏差为2.3%～15.3%,6个实际样品测定结果的相对标准偏差为1.2%～27.3%,基体加标回收率为51.3%～126%,连续校准稳定。该方法适用于废酸油渣样品中16种多环芳烃的检测,比直接溶解有效,比加速溶剂萃取、索氏提取、微波萃取和超声探头萃取简单、快捷,能有效减少设备污染和腐蚀,净化方法有效,测定结果准确可靠,是实现大批量样品检测的可行方法。