An observational study of the HONO–NO2 coupling at an urban site in Guangzhou City,South China

The temporal behavior of HONO and NO₂ was investigated at an urban site in Guangzhou city, China, by means of a DOAS system during the Pearl River Delta 2006 intensive campaign from 10 to 24 July 2006. Within the whole measurement period, unexpected high HONO mixing ratios up to 2 ppb were observed even during the day. A nocturnal maximum concentration of about 8.43 ± 0.4 ppb was detected on the night of 24 July 2006. Combining the data simultaneously observed by different instruments, the coupling of HONO–NO₂ and the possible formation sources of HONO are discussed. During the measurement period, concentration ratios of HONO to NO₂ ranged from (0.03 ± 0.1) to (0.37 ± 0.09), which is significantly higher than previously reported values (0.01–0.1). Surprisingly, in most cases a strong daytime correlation between HONO and NO₂ was found, contrary to previous observations in China. Aerosol was found to have a minor impact on HONO formation during the whole measurement period. Using a pseudo steady state approach for interpreting the nocturnal conversion of NO₂ to HONO suggests a non-negligible role of the relative humidity for the heterogeneous HONO formation from NO₂.     

用蚕豆叶尖微核技术筛选对环境污染物敏感品种

为了筛选蚕豆叶尖微核监测技术敏感材料,以二甲苯为污染物,对甘肃产的10个蚕豆品种进行了测试。结果表明,蚕引8号微核出现率与二甲苯诱变剂浓度成正比,平均微核率差异极显著,是监测评价二甲苯污染的敏感品种。     

南运河重金属污染状况及生态风险评价

采集南运河的水样和沉积物样品,对其重金属污染状况和生态风险进行了分析评价。利用电感耦合等离子体质谱仪(ICP-MS)对水、沉积物中铅(Pb)、铬(Cr)、砷(As)、铜(Cu)和镉(Cd)浓度进行分析。结果显示南运河水样中这5种重金属浓度均低于地表水环境质量标准I类水质标准,虽然运河上游沉积物中As和Cd浓度较高,但沉积物中重金属浓度总体上均处于较低水平。地累积指数法计算显示:As和Cd在部分河段达到重度和中度污染水平,Cu、Cr、Pb均处于无污染水平。各种重金属的潜在生态风险指数(Eir)从大到小的顺序为:CdAsCuPbCr,与地累积指数法结果相似。南运河总的潜在生态风险指数(RI)均值为128.85,潜在生态风险程度为"中",沉积物中Cd和As是南运河需要优先控制的重金属污染物。     

Effects of molecular weight and concentration of carboxymethyl cellulose on morphology of hydroxyapatite nanoparticles as prepared with one-step wet chemical method

Nano-sized apatite particles (nAP) synthesized with carboxymethyl cellulose (CMC) have shown great application potentials in in situ heavy metal remediation. However, differences in CMC’s properties effects on the size of nAP produced are not well understood. In this paper, two types of CMC, with respective molecular weights (MW) of ～120000 and ～240000 Dalton or respective polymerization degrees of 500 (CMC-500) and 1050 (CMC-1050), were studied in a concentration range of 0.05%–0.5% (w/w) for nAP synthesis. Morphology of the particles was characterized with transmission electron microscopy (TEM). Results showed that 0.05% CMC-500 solution gave an average particle size of 148.7±134.9 nm, 0.25% CMC-500 solution produced particles of 21.8±20.4 nm, and, 0.5% CMC-500 solution contained particles of 15.8±7.7 nm. In comparison, 0.05% CMC-1050 solution produced nanoparticles of 6.8±3.2 nm, 0.25% CMC-1050 produced smaller nAP of 4.3±3.2 nm, and 0.5% CMC-1050 synthesized the smallest nanoparticles in this study, with an average diameter of 3.0±2.1 nm. Chemical composition of the products was identified with X-ray diffraction (XRD) as pure hydroxyapatite. Interactions between nAP and CMC were discussed with help of attenuated total reflection Fourier transform infrared (ATRFTIR) spectroscopic data. This study showed that CMC at higher concentration as well as higher MW facilitated to produce finer nanoparticles, showing that nAP size could be manipulated by selecting appropriate CMC MW and/or applying appropriate CMC concentration.     

The sorption of selenite from aqueous solutions by pyrite

Selenium (Se) is an essential trace nutrient for mammals; however, the range between deficit and toxic levels is narrow. In this study, the potential sorption of selenite onto pyrite particles from an aqueous solution was investigated. An intraparticle diffusion model was used to describe kinetic data of sorption, yielding diffusivity values of 5 × 10^?7 cm²/s. The Langmuir isotherm equation could be used to describe the experimental data. The fitting results indicated that b and {Se(IV)}_max have values of 0.37 L/mg and 3.49 mg/g, respectively. The sorption of selenite onto the surface of pyrite particles was dependent on a pH range of 2–12, and the quantity of sorption onto pyrite was negatively correlated with pH; that is, the amount of sorption onto pyrite increased with a decrease in pH. In addition, organic matter did not exert a significant effect on removal of selenite. With a reaction time greater than 1 week, sorption of selenite onto pyrite particles was found to partially reduce the amount of elemental Se.     

Fecal DDA as a biomarker of DDT exposure in chickens

Despite the largely theoretical risks for human morbidity from exposure to DDT (p, p′-dichlorodiphenyltrichloroethane), the reality that it is inexpensive and highly effective in reducing morbidity and mortality from malaria vectors has encouraged its continued use. Here we present data indicating that domestic fowl are potentially excellent sentinel species for detecting possible human exposures to DDT. In addition to measuring residues of DDT in chicken blood or eggs, a potential alternate analyte indicative of recent DDT exposure is the definitive metabolic product DDA (2,2-bis(4-chlorophenyl)acetic acid) in feces.     

炼金区土壤中汞形态分布及其生物有效性

采用修正的Tessier方法和回归、偏相关等分析技术,研究了某金矿附近土壤中汞的赋存状态及其相互转化关系和生物可利用性.结果显示该区土壤中各形态汞的含量趋势为:有机结合态残渣态可交换态铁锰氧化态碳酸盐结合态,其中有机结合态汞所占比重最大在60%以上,是最重要的赋存形态;土壤中各形态汞不是独立存在的,内部存在一定的转化关系,如碳酸盐结合态汞可以转化成铁锰氧化态、残渣态的汞,而铁锰氧化态的汞与残渣态的汞之间却存在着一定的竞争关系,这种转化关系在外界条件的影响下处于一种动态平衡状态;土壤中的可交换态和有机结合态是较容易被植物吸收利用有效态的汞,其他形态汞被植物吸收较少.