不同温度下西安汉城湖沉积物吸附、释放特性和磷形态

以西安汉城湖为研究对象,2015年4月对湖体沉积物进行现场调查和采样分析,共设4个采样点,研究不同温度下沉积物磷的吸附释放特性及沉积物磷形态的分布。结果表明,沉积物磷等温吸附随着温度的升高而增大,吸附特征符合修正的Langmuir模型,最大吸附容量Qmax的范围为507.21~786.77 mg·kg-1。磷动力学吸附主要发生在实验进行前12 h之内,吸附量基本达到或超过72 h吸附平衡时吸附总量的85%。磷动力学释放量范围为2.02~11.058 mg·kg-1,且在6 h达到最大值。沉积物总磷的含量范围为655.37~1.809.38 mg·kg-1,以无机磷为主,沉积物不同形态磷含量为TP > IP > HCl-P > OP > NaOH-P。沉积物富营养化风险指数ERI的范围为5.92~11.86,在10℃和20℃时,4个采样点的ERI均在10以下,属于低风险,在30℃时,4个采样点的ERI均在10以上,属于中等富营养化风险。     

受污染城市河道沉积物磷吸附特征及其影响因素

采集了典型受污染城市河道——陕西省新河不同季节的沉积物,研究其磷吸附特征及影响因素,并考察其缓冲外源污染的能力,评估其磷释放风险。结果显示,沉积物平均粒径在秋季小于夏季和春季,pH为7.64~8.88;沉积物总磷 (TP) 为870~2 173 mg·kg⁻¹;计算了沉积物磷富集系数,明确了新河部分点位为重度污染类型。吸附动力学研究结果表明：0~2 h沉积物对磷的吸附量在正负之间波动;2~4 h吸附量迅速增加,吸附速率也达到了峰值;之后吸附量增加趋势变缓,并在48 h达到平衡。绘制吸附等温线,可知沉积物的磷吸附-解吸平衡质量浓度 (EPC₀) 为0.39~2.21 mg·L⁻¹,高于同时段上覆水中磷的质量浓度,具有释放风险;磷最大缓冲容量MBC和Freundlich常数K_F呈现秋季>>夏季>春季的规律;经D-R模型拟合,绝大多数样品的吸附能为8.45~11.18 kJ·mol⁻¹,说明吸附机制为离子交换。相关性分析结果表明,沉积物的磷吸附速率常数与钙的相对含量呈显著相关 (P<0.05) 。EPC₀与沉积物的总磷和易释放态磷含量呈显著相关 (P<0.01) ,与沉积物平均粒径和有机质显著相关 (P<0.05) ,与pH显著相关 (P<0.05) 。本研究结果可为受污染城市河道治理提供参考。     

赤泥在控制沉积物磷释放中的应用研究

利用烧结法赤泥中富含Ca、Fe等金属元素的氧化物而具有吸附性的特点,通过室内模拟研究赤泥投加对沉积物中各种磷形态含量及分布比例的影响,进而探讨利用赤泥控制沉积物中磷释放的可行性。对经过处理后的沉积物磷形态分析后表明,投加赤泥能促使沉积物中铁铝磷向钙磷转化（Pearson相关分析,r=-0.892,P<0.01,n=9）,且赤泥的强碱性使沉积物pH值逐渐升高。确定了赤泥最佳投加比例为5%,此时沉积物的pH为9.03,铁铝磷含量由初始的148 mg/kg降至107 mg/kg,占总磷比例也由18.1%降至13.4%,钙磷含量由486 mg/kg升至546 mg/kg,其占总磷比例则由60%增至68.7%,铁铝磷和钙磷之间的转化已基本完成,继续增加赤泥投加量对沉积物中磷形态间的相互转化影响甚微。由于铁铝磷较钙磷活性高而易释放,可见投加赤泥能降低沉积物中磷的释放风险。赤泥可以作为吸附材料被应用于沉积物磷污染控制技术中,为有效控制水体内源磷负荷提供一种新思路和廉价材料。     

赤泥投加控制河道底泥磷释放的影响因素

通过对不同赤泥投加比例下河道底泥磷释放作用的研究,发现底泥中铁铝磷与钙磷的比值(Fe/Al-P∶Ca-P)、铁磷比(Fe∶TP)及有机质含量(OM)是赤泥能否应用于河道底泥磷释放控制中的决定性因素。实验结果表明,只有当河道底泥中Fe/Al-P∶Ca-P小于0.88,Fe∶TP小于16.1,且有机质含量低于1.87%时,投加适量赤泥才能起到抑制河道底泥内源磷释放的作用;反之,赤泥的投加则有可能促进底泥内源磷的释放。在实际工程应用中,推荐赤泥与底泥的接触时间不低于7d,从而使赤泥的效能发挥到最佳状态。     

桂林会仙湿地沉积物中磷形态及分布特征

沉积物中磷的含量及其形态是影响水体营养化进程的重要因素,对研究湿地水体富营养化具有重要意义。应用蒋柏藩等石灰性土壤无机磷提取方法,调查了桂林会仙岩溶湿地5个典型区域柱状沉积物中的磷形态分布、垂向上的变化特征,分析了各形态磷之前的相关性。结果表明,桂林会仙湿地柱状沉积物中w(TP)为161.14~555.48 mg/kg,活性较高的Ca2-P(5.27~51.45 mg/kg)、Ca8-P(7.76~37.57 mg/kg)均较低。沉积物中的磷以Ca-P(42.92%)为主,Ca-P中的Ca10-P所占比例较高(>70.3%),导致内源磷不易释放,有利于减缓桂林会仙湿地水体富营养化进程。在空间分布上,Ca2-P、Ca8-P、Al-P、Fe-P与TP分布趋势相似,从沉积物表层至底层逐渐降低并趋于稳定。Pearson相关系数表明,TP与总氮(TN)、有机质(OM)、Ca2-P、Ca8-P、Al-P、Fe-P极显著相关,与Ca10-P显著相关。     

水丝蚓生物扰动对沉积物磷释放的影响

研究了不同投放密度和不同环境条件下水丝蚓的生物扰动对沉积物磷释放的影响.研究表明,水丝蚓的生物扰动作用对沉积物磷释放有明显的促进作用,与未投放水丝蚓的空白组相比,当水丝蚓密度为1 ind./cm2和2 ind./cm2时,上覆水中总磷的平均浓度分别提高了190%和230%.温度的提高,会加大水丝蚓生物扰动对磷释放的影响...     

黄河甘宁蒙段表层沉积物中磷的释放风险评估

预测表层沉积物中磷释放风险对水环境的治理和磷负荷的调控具有重要意义.基于磷释放风险指数(ERI)的两种计算方法,评估了黄河甘宁蒙段不同水期表层沉积物中的磷释放风险.结果表明:通过磷吸附指数(PSI)和磷吸附饱和度(DPS)得到的ERI表明,研究区域除S5、K3、K11和K12具有中度磷释放风险外,其余各采样点均为高度磷...     

瑶湖沉积物中磷的赋存形态及其空间分布特征

利用磷的分级提取分析方法,首先对瑶湖沉积物磷赋存形态进行了分析;其次将瑶湖分成A、B和C 3个区段(其营养状态指数TLI值的大小为:B区>A区>C区),在此基础上,探讨了铁结合态磷(Fe-P)、铝结合态磷(Al-P)、钙结合态磷(Ca-P)和有机磷(OP)的空间分布特征。研究结果表明:在沉积物磷赋存形态中,无机磷形态(IP)占总磷(TP)的平均比重为75%以上,Fe-P是IP的主要成分,Fe-P占TP比重范围为40.55%~67.63%;各种形态磷的平均含量(或占TP比重)大小为Fe-P >Al-P> OP>Ca-P >DP。Fe-P、Al-P和OP的水平分布特征的结果表明:对于相同的区段,不同磷赋存形态的含量变化具有相同的变化规律,其含量大小为Fe-P >Al-P >OP,而Ca-P含量变化相对稳定;对于不同的区段,相同磷的赋存形态含量的极值变化具有一定的差异,其中Fe-P、Al-P和OP的最大值均出现在B区段,而Fe-P和Al-P最小值出现在A区段,OP则出现在C区段。Fe-P、Al-P、Ca-P 和OP的垂直分布特征的结果显示:对于相同的区段,Fe-P、Al-P、Ca-P和OP的含量均随深度呈现递减趋势,当达到25 cm深度时其含量基本稳定;而对于不同的区段,Fe-P、Al-P和OP的含量随深度的变化趋势具有一定的差异性,A区段随深度的变化趋势比B区段和C区段缓慢,而Ca-P变化趋势则没有明显的区分,这一研究结果为揭示瑶湖富营养化发生的机制提供了数据和理论支撑。     

pH对活化前后废弃铁铝泥吸附不同种磷动力学的影响

实验研究了300℃热活化前后的给水厂废弃铁铝泥（R-FARs和H300-FARs）对正磷酸盐、聚磷酸盐和有机磷酸盐的吸附动力学特性,并考察pH对不同磷吸附动力学的影响。结果表明,pH对不同磷吸附动力学过程的影响趋势相似,即低pH有利于吸附。准二级动力学模型能够更真实地反映不同磷在R-FARs和H300-FARs的吸附动力学行为,由拟合结果可知焦磷酸盐和六肌醇磷酸盐的初始吸附速率相对较大,而甘油磷酸盐最小;且活化作用明显提高了不同磷的初始吸附速率,并减弱了pH对初始吸附速率的影响。不同磷的吸附速率受到液膜扩散、颗粒内扩散和吸附反应三者共同控制,其中吸附反应是主要的控制步骤。     

Pressure-assisted ozonation of PCB and PAH contaminated sediments

Sediment contamination by recalcitrant organics such as polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) is prevalent and of a great concern. Remediation efforts are hampered by the hydrophobic nature of the contaminants that limits their availability as well as by the sediment matrix that limits their exposure to treatment agents. Using contaminated sediment samples from the Passaic River, St. Louis River, Waukegan Harbor, and Wells National Estuarine Research Reserve, this research demonstrated a new ozonation technique that incorporates rapid, successive cycles of pressurization (690 kPa) and depressurization, enabling more effective treatment than conventional ozonation would. Conventional ozonation reached maximum 60% and 40% removal of PAHs from the Passaic River (40 mg kg(-1) initially) and St. Louis River sediment (520 mg kg(-1) initially), respectively, in 1h; however, removals ceased despite prolonged treatment for 2h. The pressure-assisted technique removed 96% of PAHs from both river sediments within 1h; it completely removed both PAHs (16 mg kg(-1) initially) and PCBs (5.1 mg kg(-1) initially) from the Waukegan Harbor sediment in 0.5 h. The heightened treatment is explained by soil aggregate fracturing upon pressure cycles that exposes the contaminants as well as by the confluence of hydrophobic contaminants and O(3) at the gas-liquid interface in the presence of microbubbles. The technique is expected to accelerate O(3) treatment of a wide range of organic contaminants, and it may provide treatment to dredged and stored contaminated sediment.     

铜在沉积物不同稳定性组分上的吸附特征

沉积物中不同成分的稳定性对重金属的迁移转化有重要影响。按照在自然条件下不同成分的稳定性将沉积物分为3个组分(轻组(LF)、腐殖质(HS)、去除HS的重组(HFRHS))。研究了铜在沉积物及其不同组分上的吸附动力学、吸附等温线以及pH对吸附的影响。结果表明,在沉积物中,LF与HS对吸附铜的速率起控制作用,而HFRHS是主要的吸附组分,pH对铜的吸附有较大影响。在自然环境中,控制LF和HS的迁移转化,可以有效降低铜的迁移能力,减小对环境的影响。     

Distribution and sources of polycyclic aromatic hydrocarbons in surface sediments of rivers and an estuary in Shanghai, China

Concentrations, spatial distribution and sources of 17 polycyclic aromatic hydrocarbons (PAHs) and methylnaphthalene were investigated in surface sediments of rivers and an estuary in Shanghai, China. Total PAH concentrations, excluding perylene, ranged from 107 to 1707 ng/g-dw. Sedimentary PAH concentrations of the Huangpu River were higher than those of the Yangtze Estuary. The concentration of the Suzhou River was close to the average concentration of the Huangpu River. PAHs source analysis suggested that, in the Yangtze Estuary, PAHs at locations far away from cities were mainly from petrogenic sources. At other locations, both petrogenic and pyrogenic inputs were significant. In the Huangpu and Suzhou Rivers, pyrogenic input outweighed other sources. The pyrogenic PAHs in the upper reaches of the Huangpu River were mainly from the incomplete combustion of grass, wood and coal, and those in the middle and lower reaches were from vehicle and vessel exhaust.     

腐殖酸、细颗粒泥沙对粉末活性炭吸附苯酚特性影响的研究

通过一系列实验,探讨了粉末活性炭吸附水中苯酚时,腐殖酸(HA)浓度和细颗粒泥沙用量对苯酚吸附量和去除率的影响.实验结果表明:在中性条件下,随着HA浓度的增加,粉末活性炭对苯酚的吸附量减少;在不同质量细颗粒泥沙的影响下,苯酚的去除率基本不变;在未加HA时,粉末活性炭对苯酚的吸附行为用Langmuir吸附等温式拟合效果最好,对苯酚的最大吸附量为150.60 mg/g,而在有HA存在时,粉末活性炭对苯酚的吸附行为用Freundlich吸附等温式拟合效果最好,对苯酚的最大吸附量为28.49 mg/g.     

多孔硅酸钙滤料吸附床除磷试验研究

以多孔硅酸钙滤料为吸附载体处理含磷的二沉池出水.通过静态吸附试验和动态吸附试验,研究了滤料粒径及投加量、初始pH、反应时间、温度以及滤料填充高度对除磷效果的影响.在静态吸附试验中,取初始磷质量浓度为4.98 mg/L的含磷废水100 mL,当多孔硅酸钙滤料粒径为4～14目,投加量为1.0g,吸附时间为2.5h,温度为25℃,溶液初始pH为7.0～9.0时,磷的去除率可达95％以上,出水磷满足《城镇污水处理厂污染物排放标准》(GB 18918-2002)的一级A标准(≤0.5 mg/L).动态吸附试验表明,在长期运行条件下,多孔硅酸钙滤料吸附床能持续有效地去除污水中的磷,综合考虑吸附率和运行费用,选择水力停留时间为30 min,滤料填充高度为60 cm为宜.     

Assessment of DDT and mercury levels in fish and sediments in the Iriri River,Brazil: Distribution and ecological risk

Abstract

In order to assess the risk of exposure of human populations to dichlorodiphenyltrichloroethane (DDT) and mercury, muscles of five fish species were analysed, along with the surface sediment of 14 Iriri River sampling sites. The fish specimens were sacrificed by the spinal section, prior to sex identification, body weight determination and total length. Considering the fish specimens studied, 11% of them showed concentrations of mercury higher than the maximum established by the World Health Organization for safe human consumption. A positive correlation between fish body weight and mercury concentration was observed, besides a positive correlation between the fish size and Hg concentration. Significant differences (P?<?0.05) were found between mean concentrations of DDT and metabolites among species of fish studied. In the Plagioscion squamossissimus species, the highest concentration of total DDT (151.4?ng/g) was found, while in Eugerres Brasilianus species, the lowest. However, the DDT levels in fish muscle of studied species are below the maximum set by FAO-Alimentarius CODEX. In the sediments, total DDT ranged from 11.58?ng/g to 48.4?ng/g, which is associated with the historical DDT use in the Amazon. According to sediment quality guidelines, these levels have a moderate toxic effect in almost all of the studied region.     

Distribution coefficients (Kd) and desorption rates of 137Cs and 241Am in Black Sea sediments

The distribution coefficients (K_d) and desorption rates of ¹³⁷Cs and ²⁴¹Am radionuclides in bottom sediments at different locations in the Black Sea were studied under laboratory conditions. The K_d values were found to be 500 for ¹³⁷Cs and 3800 for ²⁴¹Am at the steady state and described exponential curves. Rapid uptake of the radionuclides occurred during the initial period and little accumulation happened after four days. The desorption rates for ¹³⁷Cs in different bottom sediments were best described by a three-component exponential model. The desorption half-times of ¹³⁷Cs ranged from 26 to 50 d at the slow components. However, the desorption rate of ²⁴¹Am described one component for all sediment samples and desorption half-time was found to be 75 d. In general, the results showed that the ²⁴¹Am radionuclide is more effectively transferred to bottom sediment and has longer turnover time than ¹³⁷Cs under Black Sea conditions.     

Degradation of terbutryn in sediments and water under various redox conditions

Abstract

A laboratory study was conducted to examine the degradation of terbutryn [2‐(t‐butylamino)‐4‐(ethylamino)‐6‐(methylthio)‐s‐triazine] in sediment and water under different redox conditions. Terbutryn degraded slowly in static aerobic systems (loosely capped flask, 25°C) with half‐lives of 240 and 180 days in pond and river sediment, respectively. Degradation products, identified by co‐chromatography on TLC and HPLC systems, included hydroxy‐terbutryn, terbutryn‐sulfoxide and N‐deethyl terbutryn. Hydroxyterbutryn was the major degradation product in sediments and water representing 60–70% of the extractable radioactivity after 515 days incubation. Under nitrogen aeration in respirometer flasks (redox potential ‐46 to +210 mv) degradation of terbutryn was very slow with half lives greater than 650 days.     

Distribution and ecotoxicological concerns of persistent organic pollutants in sediment from creek ecosystem

In order to study the distribution and ecotoxicological concerns of persistent organic pollutants, grab sediment samples were collected from different locations across Thane creek, India. Analyses of samples were carried out using gas chromatography (GC)–electron capture detector and GC–mass spectrometry techniques. In organochlorine pesticides (OCPs), DDT (1,1,1,-trichloro-2,2-bis(p-chlorophenyl) ethane), DDE (1,1-dichloro-2,2-bis(p-chlorophenyl) ethylene), DDD (1-chloro-4-(2,2-dichloro-1-(4-chlorophenyl)ethyl) benzene) and α, β, and γ conformer of hexachlorocyclohexane (HCH), and 9 polychlorinated biphenyls (PCBs) congeners were analyzed in surface sediment samples. Concentrations of these pollutants in grab sediment samples may indicate their current use and impact on marine ecosystem. Average concentrations of total DDT (including DDD and DDE), HCH, and Σ₉PCBs were found to be 4.9, 12.5, and 2.9 µg kg^?1(dry weight) respectively. High concentrations of OCPs and PCBs were found at discharge locations in creek compared to other locations. Location-wise distribution of OCPs and PCBs indicates their high concentrations at the waste water receiving point. Data were compared for ecotoxicological impacts based on the levels specified in the sediment quality standards of the US Environmental Protection Agency and the Canadian Council of Ministers of the Environment. γ-HCH was found to have maximum potential to induce ecotoxicological impacts.