沉积物对菲和五氯酚的吸附性能

研究了菲和五氯酚（PCP）在五种沉积物的吸附解吸行为，菲和PCP在各沉积物上的吸附和解吸都是较快的过程。均能在8h内达到平衡，吸附和解吸结果表明，高有机质含量的沉积物对菲和PCP的吸附和持留能力都较强，菲和PCP在各沉积物中的吸附系数跟沉积物的有机质含量呈线性正相关。等温吸附结果表明，低有机质含量的三种沉积物比有机质含量较高的两种沉积物呈更好的线性关系。不同沉积物对菲和PCP的吸附性能差异跟沉积物的有机质含量密切相关。     

不同基质条件对生物膜细胞外聚合物组成和含量的影响

对比研究了处于胶体和溶解状态的有机物对生物膜胞外聚合物组成和含量的影响，研究发现，不同基质条件对胞外聚合物的总量、多糖和蛋白质含量产生影响，另外，基质条件与会对生物膜的表面结构造成一定的影响。     

Metal immobilization by sludge-derived biochar: roles of mineral oxides and carbonized organic compartment

Pyrolyzing sludge into biochar is a potentially promising recycling/disposal solution for municipal wastewater sludge, and the sludge-derived biochar (SDBC) presents an excellent sorbent for metal immobilization. As SDBC is composed of both mineral oxides and carbonized organic compartment, this study therefore compared the sorption behaviour of Pb and Zn on SDBC to those of individual and mixture of activated carbon (AC) and amorphous aluminium oxide (Al₂O₃). Batch experiments were conducted at 25 and 45 °C, and the metal-loaded sorbents were artificially aged in the atmosphere for 1–60 days followed by additional sorption experiments. The Pb sorption was generally higher than Zn sorption, and the co-presence of Pb reduced Zn sorption on each studied sorbent. Higher sorption capacities were observed at 45 °C than 25 °C for SDBC and AC, while the opposite was shown for Al₂O₃, indicating the significance of temperature-dependent diffusion processes in SDBC and AC. Nevertheless, metal sorption was more selective on Al₂O₃ that showed a greater affinity towards Pb over Zn under competition, correlating with the reducible fraction of sequential extraction. Furthermore, significant amounts of Pb and Zn were additionally sorbed on SDBC following 30-day ageing. The X-ray diffraction revealed the formation of metal-phosphate precipitates, while the X-ray photoelectron spectroscopy showed a larger quantity of metal–oxygen bonding after 30-day ageing of metal-loaded SDBC. The results may imply favourable long-term transformation and additional sorption capacity of SDBC. In conclusion, SDBC resembles the sorption characteristics of both organic and mineral sorbents in different aspects, presenting an appropriate material for metal immobilization during soil amendment.     

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.     

Coexisting sediments and suspended particles change the sorption of lindane and ciprofloxacin in waters

The real behavior of water organic contaminants such as pesticides and pharmaceuticals is not well known because research experiments usually simplify the conditions by studying the sorption of a pure compound on a single solid. However, in natural waters, biofilms, suspended particles, and sediments are solid substances that coexist, and thus may change the contaminant fate. Therefore, we studied here the sorption of lindane and ciprofloxacin by three single-solid and three double-solid sorbents using batch experiments. We also compared the effect of dissolved organic matter (DOM) between single- and double-solid sorption systems. Results show that the sorption quantity of lindane to the double-solid system of suspended particles and sediments is lower, of 0.99 L/g, than the sum of sorption quantity in the single-solid system, of 1.39 L/g. The sorption quantity of ciprofloxacin is higher, of 2.70 L/g, than the sum of sorption quantity in the single-solid system, of 1.90 L/g. These findings are explained by changes in DOM that suppress or promote sorption. To our best knowledge, this is the first study to present evidence that coexisting river solids modify lindane and ciprofloxacin sorption.     

A comparative study of modified and unmodified maize tassels for removal of selected trace metals in contaminated water

Powdered maize tassels were studied and found to exhibit metal sorption properties due to the availability of functional groups. The tassels have a high amount of soluble organic substances that can dissolve in aqueous media, contributing to secondary pollution during a water treatment process. A chelating agent was chemically attached on the maize tassels with a view to increase the sorption capacity, minimize leaching, and enhance the tassels’ stability. Thermogravimetric analysis confirmed that modification improved their thermal stability to withstand temperatures above 600°C as well as reduced the “secondary pollution”. The modified sorbent was employed for the sorption of lead, copper, and cadmium ions in both the model solutions and the real samples. The contact time and pH were optimized after which Langmuir and Freundlich isotherms were applied to the data. The sorption capacities for Cu²⁺, Cd²⁺, and Pb²⁺ improved from 3.4, 0.8, and 1.7?g?kg^?1, respectively, to 6.3, 2.6, and 2.6?g?kg^?1 in the same order. The sorbent was shown to remove up to 95% of the metals in less than 10 min. This study has a potential application for the remediation of polluted waters.     

Chemically modified biochar produced from conocarpus waste increases NO<Subscript>3</Subscript> removal from aqueous solutions

Biochar has emerged as a universal sorbent for the removal of contaminants from water and soil. However, its efficiency is lower than that of commercially available sorbents. Engineering biochar by chemical modification may improve its sorption efficiency. In this study, conocarpus green waste was chemically modified with magnesium and iron oxides and then subjected to thermal pyrolysis to produce biochar. These chemically modified biochars were tested for NO₃ removal efficiency from aqueous solutions in batch sorption isothermal and kinetic experiments. The results revealed that MgO-biochar outperformed other biochars with a maximum NO₃ sorption capacity of 45.36 mmol kg^?1 predicted by the Langmuir sorption model. The kinetics data were well described by the Type 1 pseudo-second-order model, indicating chemisorption as the dominating mechanism of NO₃ sorption onto biochars. Greater efficiency of MgO-biochar was related to its high specific surface area (391.8 m² g^?1) and formation of strong ionic complexes with NO₃. At an initial pH of 2, more than 89 % NO₃ removal efficiency was observed for all of the biochars. We conclude that chemical modification can alter the surface chemistry of biochar, thereby leading to enhanced sorption capacity compared with simple biochar.     

The influences of different organic fractions in refuse on the sorption and bioavailability of dibutyl phthalate

The structure and composition of the organic matter in landfilled refuse might have an influence on the migration and transformation of dibutyl phthalate (DBP). Humic acid (HA) and humin (HU) were separated from aged-refuse to determine the influences of different organic fractions in the refuse on the sorption and bioavailability of DBP. The sorption kinetics and isotherms for the sorption of DBP to HA, HU, and whole refuse were determined. The results showed that the sorption constants (K) and nonlinearities decreased in the order HU?>?whole refuse?>?HA. The HA had lower K values than did the other refuse fractions, and it retarded the biodegradation of DBP over a short degradation period (48?h). Increasing the amount of HA present caused the amount of DBP that was biodegraded to decrease significantly, 81.3% of the DBP sorbed to HA being degraded in the original experiments after 48?h but 21.8% of the DBP being degraded when three times as much HA was used. Similar results were not observed when the amount of HU used was changed. These findings suggest that HA plays an important role in the biodegradation of DBP adsorbed by refuse.     

Arsenic content and distribution pattern in Chinese coals

About 500 samples of coal, pyritic coal balls, pyritic gangue and coal seam gangue were collected from different coal basins and geologic periods of coal formation to determine the arsenic (As) content and distribution pattern in China. The Permian-Carboniferous and Jurassic coals in the North China Plate and Northwest China account for nearly 85% of total Chinese coal reserves and data showed that As content ranged from 0.1 to 94?mg?kg^?1, with the majority between 1 and 14.9?mg?kg^?1. The As content of some Late Permian coals in Southwest Guizhou Province and stone coal in the South Qinling Mountain area were exceedingly high (30–534?mg?kg^?1), but the majority of coal in the Southwest Guizhou Province contained low to medium amounts. Only the coals, which are situated in or near igneous rocks and are not considered a part of Chinese coal reserves, possessed unusually high As content (>30?mg?kg^?1). Arsenic was also concentrated in pyritic coal balls and the pyritic gangue of the coal seam with values ranging from 21.5 to 142.46?mg?kg^?1 and an average of 69?mg?kg^?1 in Shaanxi and 78?mg?kg^?1 in Shandong. Arsenic contents in coal gangue in the Northwest and North China Plate is about 0.2–15?mg?kg^?1, a little lower than coals in the same seam. Washing gangue (waste from coal washing) generally contained more As than coal, because the washed gangue has more pyrite than the natural gangue (black shale). Washing coal reduced the content of the pyritic sulfur, heavy metals and As. Based on amounts of coal used with different As content in Chinese coal reserves, the average As content of Chinese coals is about 4.5?mg?kg^?1.     

Evidence for a mutual effect of biofilms, suspended particles and sediments on DDT sorption

This report shows that biofilms and suspended particles double DDT sorption capacity on surface sediments. Sorption of pollutants by solid materials, such as biofilms, suspended particles and sediments, is a major process controlling the fate of hydrophobic pollutants in natural waters. Most previous studies focused on the sorption of hydrophobic pollutants by single-solid material, whereas few studies considered the mutual effect of different solids on the sorption. Various solid materials often interact with each other when they coexist in the same system. Therefore, pollutants sorption could be different from that in the single-solid sorption system. Here we studied the mutual effect of biofilms, suspended particles and surface sediments on the sorption of dichlorodiphenyltrichloroethane (DDT). Results showed that biofilms and suspended particles double DDT sorption capacity on surface sediments. The different effects were mainly determined by distinct components and structures of the three solid materials, particularly by organic components. Here we show the mutual effect of biofilms, suspended particles and sediments on DDT sorption.     

Kinetic and mechanism studies of the adsorption of lead onto waste cow bone powder (WCBP) surfaces

This study examines the adsorption isotherms, kinetics and mechanisms of Pb²⁺ sorption onto waste cow bone powder (WCBP) surfaces. The concentrations of Pb²⁺ in the study range from 10 to 90 mg/L. Although the sorption data follow the Langmuir and Freundlich isotherm, a detailed examination reveals that surface sorption or complexation and co-precipitation are the most important mechanisms, along with possibly ion exchange and solid diffusion also contributing to the overall sorption process. The co-precipitation of Pb²⁺ with the calcium hydroxyapatite (Ca-HAP) is implied by significant changes in Ca²⁺ and PO₄ ^3? concentrations during the metal sorption processes. The Pb²⁺ sorption onto the WCBP surface by metal complexation with surface functional groups such as ≡ POH. The major metal surface species are likely to be ≡ POPb⁺. The sorption isotherm results indicated that Pb²⁺ sorption onto the Langmuir and Freundlich constant q _max and K _F is 9.52 and 8.18 mg g^?1, respectively. Sorption kinetics results indicated that Pb²⁺ sorption onto WCBP was pseudo-second-order rate constants K ₂ was 1.12 g mg^?1 h^?1. The main mechanism is adsorption or surface complexation (≡POPb⁺: 61.6%), co-precipitation or ion exchange [Ca_3.93 Pb_1.07 (PO₄)₃ (OH): 21.4%] and other precipitation [Pb 50 mg L^?1 and natural pH: 17%). Sorption isotherms showed that WCBP has a much higher Pb²⁺ removal rate in an aqueous solution; the greater capability of WCBP to remove aqueous Pb²⁺ indicates its potential as another promising way to remediate Pb²⁺-contaminated media.     

Sorption of DDTs on biofilms, suspended particles and river sediments: effects of heavy metals

The sorption by solid materials is one of the most important processes that affect the fate of hydrophobic organic pollutants in aquatic systems. Current studies focus on the sorption of hydrophobic pollutants by single natural solid material, whereas few studies compared the sorption behaviors of different solids. Furthermore, natural aquatic environment is a complex system where hydrophobic pollutants coexist with many other pollutants, but only limited studies reported the effects of coexisting components on the sorption. Here we studied the sorption of dichlorodiphenyltrichloroethanes (DDTs) by three common solids in natural water, i.e., biofilms, suspended particles and sediments. The effects of typical coexisting heavy metals on the sorption were also examined. The results show that the sorption is described by a dual-mode sorption model. Compared with sediments, more DDTs were sorbed by biofilms and suspended particles. Coexisting Pb, Cd and Cu increased the sorption of DDTs on sediments while decreasing the sorption on biofilms slightly, with little effect on the sorption on suspended particles. The different sorption behaviors of the solids were mainly determined by the composition of the solids: more organics were observed in biofilms and suspended particles.     

多环芳烃在全土及其碱提残余物上的吸附行为

以菲和芘为代表性化合物,采用8种有机质含量不同的天然全土样品及其碱提残余物进行吸附实验,并利用不同吸附模型进行数据拟合,藉以探讨有机质含量对土壤吸附行为的影响.结果表明,Freundlich吸附模型的非线性指数n都小于1,显示全土和碱提残余物在多环芳烃的吸附过程中表现出非线性特征.菲和芘的吸附行为随土壤有机质含量不同而变化,碱提残余物的吸附能力强于全土,两者吸附行为的差异主要归因于土壤有机质含量和性状的区别.     

生物炭吸附有机污染物的研究进展

生物炭(biochar)是指生物质在缺氧条件下热裂解产生的一种产物.由于其精致的孔隙结构和独特的表面化学性质,对环境介质中的有机污染物有超强的吸附能力,进而影响污染物的迁移与归宿.近年来生物炭对有机污染物的吸附特性及机理研究已成为环境科学领域的研究热点之一.本文从生物炭的典型性状、吸附有机污染物的机理、影响因素以及对土壤中有机污染物生物可给性的影响等方面进行了综述,并提出生物炭吸附有机污染物未来的研究方向.     

有机膨润土对苯胺的吸附性能及应用研究

以溴化十六烷基三甲铵为改性剂制备有机膨润土，利用正交实验研究了有机膨润土吸附垃圾渗滤液中极性有机污染物苯胺的性能、条件及改性条件对吸附效果的影响。结果表明，有机改性膨润土对苯胺有很好的吸附效果，实验条件下对苯胺的去除率可达90％以上，绘制了有机膨润土吸附苯胺的吸附等温线，通过与吸附苯酚效果的比较，总结了有机膨润土吸附极性有机污染物的一般规律。     

Sorption of 1,1,1-trichloro-2,2-bis(p-chlorophenyl) ethane (DDT) by clays and organoclays

This study focused on the sorption isotherms of 1,1,1-trichloro-2,2-bis(p-chlorophenyl) ethane (p,p'-DDT) and 1,1-dichloro-2,2-bis(p-chlorophenyl) ethylene (p,p'-DDE) on different original clays (i.e., zeolite, montmorillonite and attapulgite) and organoclay complexes. Sorption of organic pollutants was determined using gas chromatographic (GC) techniques to investigate the sorption behavior, and characterize the effect of, different organic cations. The original clays only sorbed low amounts of p,p'-DDT and p,p'-DDE, and the sorptive curves can be classified as L-shaped. Organoclays exhibited higher amounts of p,p'-DDT and p,p'-DDE sorption. The p,p'-DDT and p,p'-DDE sorption increased with increasing total organic carbon (OC) content of the organoclays. For hexadecyltrimethylammonium (HDTMA)-modified organoclays, the dominant adsorptive medium showed the partitioning sorption of hydrophobic-hydrophobic interaction, indicating no competitive sorption. The sorptive curves can be classified as C-shaped of constant partition (CP). However, benzyltrimethylammonium (BTMA)-modified organoclays exhibited competitive sorption. The sorption isotherm curves can be classified as S-shaped. The sorptive capacity of the HDTMA-modified organoclays for p,p'-DDT were higher than those for p,p'-DDE, but the BTMA-modified organoclays showed a reverse trend. This can be attributed to the different structures and shapes of organic cations, giving different sorptive mechanisms. The p,p'-DDT and p,p'-DDE sorption onto HDTMA-modified organoclays were caused by chemical interaction, with the BTMA modified organoclays occuring due to physical sorption.     

Reactivity of sulfate radicals with natural organic matters

Advanced oxidation processes based on sulfate radicals (SO ₄ ^·? ) are capable of efficiently degrade organic pollutants from ground, surface and wastewaters. However, this degradation may be limited by aqueous natural organic matter (NOM). Here we measured the absolute rate constants of reaction of SO ₄ ^·? with four types of organic matter: two fulvic acids and two lake organic matter. We used laser flash photolysis technique to monitor the SO ₄ ^·? decay and the formation of the transients from organic matters. Reaction rate constants comprised between 1530 and 3500 s^?1 mgC^?1 L were obtained by numerical analysis of differential equations and the weighted average of the extinction coefficient of the generated organic matters radicals between 400 and 800 M^?1 cm^?1.     

全氟辛烷磺酸盐(PFOS)对其它有机污染物在沉积物上吸附的影响

采用平衡振荡实验方法,研究了不同浓度的全氟辛烷磺酸盐(PFOS)对两种有机污染物(硝基苯和菲)在沉积物上吸附的影响.结果表明,单组分PFOS在沉积物上是非线性吸附;与其它有机污染物共存时,随着PFOS浓度的升高,硝基苯的吸附量先减少后增加,而菲的吸附量则先增加后减少.PFOS对其它有机污染物吸附的影响规律与有机污染物的...     

Distribution and behaviour of polycyclic aromatic hydrocarbons in subtropical river estuary,Okinawa, Japan

Surface water samples were collected along the salinity gradient of Manko estuary in Okinawa, Japan, between January and November 2012, to examine spatial and temporal variability in the distribution, composition, behaviour, and sources of particulate polycyclic aromatic hydrocarbons (PAHs). Concentrations of total particulate PAHs ranged from 169.7?ng?g^?1 at riverine station (N1) in November 2012 to 922?ng?g^?1 at another riverine station (K3) in May 2012. Based on observed environmental behaviour, particularly relationships to organic matter, the PAHs appear divisible into two groups: group I (low molecular weight) PAHs were characterised by low particles affinity and strong correlations with a pool of autochthonous organic matter (e.g. high concentrations of polyunsaturated fatty acids), reflecting processes controlling their delivery to the estuary; and, in contrast, group II (high molecular weight) PAHs were characterised by high particles affinity and exhibited estuarine distribution primarily controlled by suspended solid load and inputs from terrigenous sources through river inflows. This relationship, coupled with isomer ratios indicative of combined mixed sources from petroleum and petroleum combustions, indicates that terrestrial run-off is the dominant mode of delivery of particulate PAHs in the estuary. The relationships between distinct groups of PAHs and lipid biomarkers demonstrated in this study suggest that very specific pools of particulate organic matter, as opposed to concentrations of particulate organic carbon alone, can be important in the transport and fate of hydrophobic contaminants.