气相色谱/质谱法测定水中15种酞酸酯类化合物

采用固相萃取-气相色谱/质谱法测定水中15种酞酸酯类化合物,确定方法的最优条件为:依次用10 m L正己烷和丙酮混合溶剂(V/V=5∶1)、甲醇和空白试剂水活化C18固相萃取柱后,水样以5 m L/min过柱萃取,再以8 m L正己烷:丙酮(V/V=5∶1)混合溶剂洗脱后,浓缩至1 m L,进气相色谱/质谱测定。该法的检出限为0.18~0.38μg/L,在0.50~20.0 mg/L范围内线性良好,相关系数均0.996。空白水样的加标回收率为71.8%~120%,相对标准偏差为1.73%~12.7%;实际废水水样的加标回收率为64.8%~135%,相对标准偏差为2.75%~18.0%。     

能力验证中总硬度标准品均匀性及稳定性分析

研究用氯化钙和硫酸镁配制总硬度标准品的均匀性和稳定性,根据《能力验证样品均匀性和稳定性评价指南》(CNAS-GL03:2006),随机抽取样品进行检验。结果表明,4种浓度的样品在p H值2,室温25℃时,样品内和样品间均无显著性差异,样品均匀性合格,在一年内稳定性较好。     

Effects of pH, Fe, and Cd on the uptake of Fe2+ and Cd2+ by rice

The rhizosphere plays an important role in altering cadmium (Cd) solubility in paddy soils and Cd accumulation in rice. However, more studies are needed to elucidate the mechanism controlling rice Cd solubility and bioavailability under different rhizosphere conditions to explain the discrepancy of previous studies. A rice culture with nutrient solution and vermiculite was conducted to assess the effects of pH, Eh, and iron (Fe) concentration on Cd, Fe fractions on the vermiculite/root surface and their uptake by rice. The solution pH was set from 4.5 to 7.5, with additions of Fe (30 and 50 mg L^?1) and Cd (0.5 and 0.9 mg L^?1). At pH 5.5, the Eh in the rice rhizosphere was higher whereas transpiration, Cd²⁺, and Fe²⁺ adsorption on the vermiculite/root surface and accumulation in rice were lower than the other pH treatments. Cadmium addition had no impact on pH and Eh in rice rhizosphere while Fe addition decreased pH and increased Eh significantly. Compared with control, Fe addition resulted in the decrease of rhizosphere Cd, Fe solubility and bioavailability. Higher redox potential in the rice rhizosphere resulted in the decline of transpiration, Cd, and Fe accumulation in the rice tissues, suggesting that the transfer of two elements from soil to rice was depressed when the rhizosphere was more oxidized.     

Gridded inventories of historical usage for selected organochlorine pesticides in Gansu Province, China

HCHs and DDTs were banned in 1983 in China; however, they are still remaining in various environmental media. Since endosulfan was introduced in China in 1994, it is widely used in agriculture. In this study, temporal and spatial uses of endosulfan, HCHs, and DDTs in Gansu province of China have been presented. It is estimated that the total usage is 701 tons for endosulfan between 1994 and 2007, 1,712 tons for HCHs between 1952 and 1983, and 462 tons for DDTs between 1951 and 1983, respectively. Endosulfan usage increased dramatically in 1998 due to its application on other crops except on cotton. The HCH and DDT usage displayed a rapid increase after 1972, reaching the peak in 1976 and in 1975, respectively; since then, they declined until being banned in 1983. The gridded usage inventories of these three kinds of organochlorine pesticides in Gansu province, with a 1/4° longitude by 1/6° latitude resolution, have been created by using different crops for endosulfan and the area of dry farmland for HCHs and DDTs as surrogate data. The most intensive use was in northwestern regions for endosulfan and southeastern regions for HCHs and DDTs in Gansu province.     

炼焦煤尾煤催化热解制取富氢燃料气

以炼焦煤原煤、尾煤为研究对象,采用微量热重、常量固定床实验装置对其在热解过程中的质量变化和气相产物进行了对比分析。考察了温度、6种催化剂（CaO、MgO、Fe、Ni、NaOH、A1）及其添加比例对炼焦煤尾煤热解制取富氢燃料气的影响。结果表明,尾煤中富集的无机矿物质对热解制取富氢燃料气有促进作用,单位尾煤热解H2产率要比原煤高出1．93％。温度是影响尾煤热解产气的重要参数,热解终温的上升有利于H2产量的提高,随终温800℃升高到950℃H,产量增长了32．59mL／g。在催化热解实验中,除Al和MgO对尾煤热解有抑制作用外,CaO、Fe、Ni及NaOH均对尾煤热解产H2有促进作用,以CaO和Fe效果最为明显。并且不同添加比例的CaO和Fe对热解制取富氢燃料有一定的影响。     

含砷冶炼废渣高温烧结过程砷的迁移特性

研究了烧结温度和烧结时间对含砷冶炼废渣烧结过程中砷的迁移特性的影响。烧结条件为在10 MPa下加压成型,进空气流量为2 000 mL/min,烧结温度1 000～1 350℃,烧结时间5～120 min。结果表明,烧结过程中存在砷的挥发,但烧结前后砷的总量变化不大,砷的固化率均保持在90%以上。毒性浸出实验表明,不同的烧结条件对烧结体中砷的毒性浸出有重要的影响,从烧结体的环境安全性考虑,最佳的烧结温度和时间分别为1 200℃和45 min。     

Low-cost adsorbent prepared from sewage sludge and corn stalk for the removal of COD in leachate

Sewage sludge (SS) with corn stalk (CS) was used to prepare SS-based activated carbon (SAC) by pyrolysis with ZnCl₂. The effects of mixing ratio on surface area and pore size distribution, elemental composition, surface chemistry, and morphology were investigated. The results demonstrated that the addition of CS into SS samples improved the surface area (from 92 to 902 m²/g) and the microporosity (from 1.2 to 4.1 %) of the adsorbents and, therefore, enhancing the adsorption performance. The removal of leachate chemical oxygen demand (COD) was also determined. It was found that the COD removal rate reached 85 % at pH 4 with the SAC (90 wt% CS) dosage of 2 % (g/mL) and an adsorption time of 40 min. The adsorption experimental data were fitted by both Langmuir and Freundlich adsorption isotherms. Long-chain alkanes and refractory organics were found in raw leachate, but could be removed by SAC largely.     

2种人工湿地的水力停留时间及净化效果

以复合垂直流人工湿地(IVCW)和水平潜流人工湿地(HSCW)为研究对象,研究了2种湿地运行的季节性最佳水力停留时间(HRT)参数,并监测了2种湿地在最佳HRT参数下运行时对污水的净化效果。结果显示:(1)在IVCW中,最佳HRT在春、秋季为8～10 h;夏季为6 h;冬季为12 h。在HSCW中,最佳HRT在春、秋季为10～12 h;夏季为6～8h;冬季为24～36 h。(2)2种湿地对COD的去除率均无显著的季节性差异;湿地进水中NH4+-N/TN比值与TN去除率显著负相关;不同季节下IVCW对TN的去除效果均高于HSCW。(3)水温对TN、TP去除率的影响在IVCW中比HSCW中的明显;水温高时,2种湿地中的TN去除率较高,IVCW中的TP去除率也较高,但HSCW中的TP去除率则较低,它们间均未达到显著的相关性。     

基本单分散气溶胶透过率测试中真实值的计算

通过对高效、超高效滤料透过率测试台工作原理的分析得到:利用基本单分散粒子作为气溶胶测得的透过率关系与滤料真正的透过率-粒径曲线有区别,实际上是所使用实验气溶胶的综合透过率。详细研究了真正透过率与实验透过率的关系、误差和偏离产生原因,最终提出了一种独特的计算方法,实现了根据实验得到的表观透过率-粒径关系,就可以计算出真实透过率-粒径曲线,并得到了采用较为理想的实验气溶胶测试出的真实透过率的实际验证,这将大大提高高效、超高效滤料性能测试台的精度,拓展了其应用范围,为高效滤料的过滤理论和应用研究提供了比较理想的测试手段。