Sedimentary record of polycyclic aromatic hydrocarbons in Lake Erhai, Southwest China

The temporal distribution of polycyclic aromatic hydrocarbons (PAHs) was investigated in a sediment core from Lake Erhal in Southwest China using gas-chromatography/mass spectrometry (GC/MS) method.The total organic carbon (TOC) normalized total PAHs concentrations (sum of US Environmental Protection Agency proposed 16 priority PAHs) ranged from 31.9 to 269 μg/g dry weight (dw),and were characterized by a slowly increasing stage in the deeper sediments and a sharp increasing stage in the upper sediments.The PAHs in the sediments were dominated by low molecular weight (LMW) PAHs,suggesting that the primary source of PAHs was low- and moderate temperature combustion processes.However,both the significant increase in high molecular weight (HMW) PAHs in the upper sediments and the vertical profile of diagnostic ratios pointed out a change in the sources of PAHs from low-temperature combustion to high-temperature combustion.The ecotoxicological assessment based on consensus-based sediment quality guidelines implied that potential adverse biological impacts were possible for benzo(ghi)perylenelene and most LMW PAHs.In addition,the total BaP equivalent quotient of seven carcinogenic polycyclic aromatic hydrocarbons (BaA,CHr,BbF,BkF,BaP,DBA and INP) was 106.1 ng/g,according to the toxic equivalency factors.Although there was no great biological impact associated with the HMW PAlls,great attention should be paid to these PAH components based on their rapid increase in the upper sediments.     

Improved blending strategy for membrane modification by virtue of surface segregation using surface-tailored amphiphilic nanoparticles

Membrane modification is one of the most feasible and effective solutions to membrane fouling problem which tenaciously hampers the further augmentation of membrane separation technology. Blending modification with nanoparticles (NPs), owing to the convenience of being incorporated in established membrane production lines, possesses an advantageous viability in practical applications. However, the existing blending strategy suffers from a low utilization efficiency due to NP encasement by membrane matrix. The current study proposed an improved blending modification approach with amphiphilic NPs (aNPs), which were prepared through silanization using 3-(Trimethoxysilyl)propyl methacrylate (TMSPMA) as coupling agents and ZnO or SiO₂ as pristine NPs (pNPs), respectively. The Fourier transform infrared and X-ray photoelectron spectroscopy analyses revealed the presence of appropriate organic components in both the ZnO and SiO₂ aNPs, which verified the success of the silanization process. As compared with the pristine and conventional pNP-blended membranes, both the ZnO aNP-blended and SiO₂ aNP-blended membranes with proper silanization (100% and 200%w/w) achieved a significantly increased blending efficiency with more NPs scattering on the internal and external membrane surfaces under scanning electron microscope observation. This improvement contributed to the increase of membrane hydrophilicity. Nevertheless, an extra dosage of the TMSPMA led to an encasement of NPs, thereby adversely affecting the properties of the resultant membranes. On the basis of all the tests, 100% (w/w) was selected as the optimum TMSPMA dosage for blending modification for both the ZnO and SiO₂ types.

Open image in new window

     

Using regression models to evaluate the formation of trihalomethanes and haloacetonitriles via chlorination of source water with low SUVA values in the Yangtze River Delta region,China

The purpose of this study was to develop the multiple regression models to evaluate the formation of trihalomethanes (THMs) and haloacetonitriles (HANs) during chlorination of source water with low specific ultraviolet absorbance (SUVA) in Yangtze River Delta, China. The results showed that the regression models of THMs exhibited good accuracy and precision, and 86–97 % of the calculated values fell within ±25 % of the measured values. While the HANs models showed relatively weak evaluation ability, as only 75–83 % of the calculated values were within ±25 % of the measured values. The organic matter [dissolved organic carbon (DOC) or UV absorbance at 254 nm] and bromide exerted the most important influence on the formation of HANs. While for THMs, besides the organic matter and bromide, reaction time was also a key factor. Comparing the models for total THMs (T-THMs) in this study with others revealed that the regression models from the low SUVA waters may have low DOC coefficients, but high bromide coefficients as compared with those from the high SUVA waters.     

河流型饮用水水源保护区划分比较

比较分析了国内外河流型水源保护区划分的原则、方法和标准,例证了我国不同省份的划分实践。指出,我国各省多采用经验值划分水源保护区范围,部分省份划分方案久未更新,没有充分发挥保护区的作用。提出,应进一步细化水源保护区划分规范指导要求,及时修订省级水源保护区划分方案,并借鉴国外水源保护区划分经验,通过调整水质标准、重视公众参与、利用地理信息系统等方式划分水源保护区,从源头上预防水源污染,降低饮用水公共风险,保障饮用水安全。     

灰霾污染和清洁过程中污染物垂直结构特征

针对无锡地区2013年11月6—13日经历的灰霾污染和清洁过程,采用地基遥感激光雷达对空气中的气溶胶颗粒物垂直分布进行垂直探测,发现污染时段气溶胶颗粒物主要积聚在1.8 km以下,消光系数的日均值统计表明,从近地面至高空1.5 km,颗粒物产生的峰值消光系数稳定在0.2 km~(-1);而清洁时段,由于垂直扩散条件改善,颗粒物随高度增加明显减少,1.5 km处的消光系数不足0.05 km~(-1)。同时发现污染时段中,近地面PM_(10)、PM_(2.5)、碳黑(BC)的平均浓度分别是清洁时段的2.48、2.76、3.66倍;大气氧化剂(O3和NO_x的总和)平均值水平是清洁时段的1.73倍。气象条件分析发现,锋面的移动使大气水平、垂直对流运动加剧,污染物得以迅速扩散,空气质量转好,这也是此次污染清除的主要原因。     

Fluctuating asymmetry rather than oxidative stress in <Emphasis Type="Italic">Bufo raddei</Emphasis> can be an accurate indicator of environmental pollution induced by heavy metals

Oxidative stress (OS) and fluctuating asymmetry (FA) as risk markers for environmental stress are widely used to predict changes in the health and fitness of many animals exposed to pollutants. However, from the perspective of protecting declining amphibians, it remains to be verified which one would be a reliable indicator for amphibians exposed to long-term heavy metal pollution under natural conditions. In this study, the OS and FA of Bufo raddei exposed to natural heavy metal pollution were analyzed to determine which marker is more accurate for indicating heavy metal-induced stress. Three years of data were collected during the breeding season of B. raddei from Baiyin (BY), which has been mainly contaminated with Cu, Zn, Pb, and Cd compounds for a long period, and from Liujiaxia (LJX), which is a relatively unpolluted area. Unexpectedly, although significant accumulation of the four heavy metals was found in the kidney and liver of B. raddei from BY, the levels of superoxide dismutase, glutathione peroxidase, and malondialdehyde in these two organs were found to be irregular, with low repeatability in both BY and LJX. However, significant differences in the levels of FA were observed in B. raddei populations from these two areas over the past 3 years (P < 0.01). The degrees of FA in B. raddei populations from BY and LJX were assessed as degree 4 and 1, respectively. In short, this study suggested that FA was a more reliable and effective indicator than OS to monitor and predict long-term environmental stress on anuran amphibians.     

深度平均的应力-通量代数全场模型及其验证

提出了深度平均的应力—通量代数全场模型，用来模拟热水侧向排入大水体的各向异性的输移扩散规律。应用有限体积法对控制方程进行离散，利用ＳＩＭＰＬＥ法进行数值模拟。通过该模式的模拟计算给出了速度场、温度场的分布。所得的回流区形状及温度场分布与深度平均的ｋ－ε模型及实验资料对比，本文的计算结果与实测值符合得较好     

武汉地区水环境中全氟化合物污染水平及其分布特征

武汉作为中国氟化工行业的主要生产基地之一,其水环境中全氟及多氟类化合物(PFASs)污染情况对评估该地区水环境生态安全至关重要。采集了武汉城区10个污水处理厂进、出口污水和19个地表水样品,利用HPLC-ESI-MS/MS技术分析研究该区域水环境中PFASs污染水平及其分布特征。结果发现,武汉地区的污水和地表水样品中,PFASs污染均以短链同系物全氟丁酸(PFBA)和全氟丁基磺酸(PFBS)为主。污水处理厂进、出口污水中PFASs总浓度分别为11.8~12 700 ng·L~(-1)和19.1~9 970 ng·L~(-1)。在城区15个湖水样品中,PFASs总浓度为21.0~10 900 ng·L~(-1);在流经城区的4个江水样品中,PFASs总浓度为4.11~4.77 ng·L~(-1),比湖水样品中PFASs浓度水平低1~2个数量级。与污水中PFASs空间分布趋势一致,各湖泊水样中PFASs总体水平呈现汉口汉阳武昌的趋势,表明城市工业布局与人口密度程度直接影响城市PFASs污染空间分布。值得注意的是,与以往水环境中PFASs污染以全氟辛酸(PFOA)和全氟辛基磺酸(PFOS)为主不同,武汉地区水环境中PFASs污染以短链同系物为主,表明短链替代效应已经渐渐在中国化工领域出现,中国全氟行业在响应国际组织规范和建议的基础上做出了实质性进展。然而,对于短链PFASs的污染特征、迁移运输以及生态风险等科学问题,还需要更进一步的研究。     

Chemical additives affect sulfate reducing bacteria biofilm properties adsorbed on stainless steel 316L surface in circulating cooling water system

This paper studied the biofilm properties and corrosion behavior of sulfate reducing bacteria (SRB) on stainless steel 316L (SS316L) surface in circulating cooling water system with and without additives including hydroxy ethyl fork phosphonic acid (HEDP), dodecyl dimethyl benzyl ammonium chlotide (1227) and NaClO. Biochemical technique, electrochemical technology, X-ray photoelectron spectroscopy (XPS) and scanning electron microscope (SEM) were used. The results show that the extracellular polymeric substance (EPS) in biofilm attached on the SS316L surface mainly contain proteins and polysaccharides, the contents are 98 ug·cm^-2 and 635ug·cm^-2, respectively. The polysaccharides were cut by 1227 about 80%, while 55% by NaClO. The proteins were reduced by NaClO about 53%, while only 30% by 1227. The potentiodynamic polarization shows that the corrosion potential of SS316L was enhanced from -0.495 V to -0.390 V by the chemical additives, delaying the occurrence of the corrosion. And the corrosion rate was also reduced from 5.19 × 10^-3 mm·a^-1 to 2.42 × 10^-3 mm·a^-1. But NaClO still caused pitting corrosion after sterilizing the bacteria, while 1227 can form a protective film on the surface of SS316L. Though HEDP contribute to the bacteria activity, it can enhance the breakdown potential. XPS results confirmed that 1227 can change the value of C:O in the biofilm attached on metal surface, and NaClO can eliminate the existence of amidogen. This study would provide some recommendations for the selection of chemical additives in the thermal power plant.

Open image in new window