不同类型天然碳酸盐矿物对风化煤矸石污染物释放的影响

为评价喀斯特背景条件下天然碳酸盐矿物对风化煤矸石典型污染物释放的控制效果,在风化煤矸石中分别添加纯品碳酸钙及3种典型天然碳酸盐矿物(石灰石、白云石、方解石),对混合物浸出液特征污染组分进行分析。结果表明,纯品碳酸钙及3种天然碳酸盐矿物均能有效缓冲风化煤矸石的酸度,并显著抑制Fe2+、Mn2+、Cu2+、SO2-4等多种特征污染物的溶出,但天然碳酸盐矿物对Zn2+释放的控制效果不明显,特别是方解石在一定程度上甚至促进了Zn2+的释放。在污染控制效果上,纯品碳酸钙的控制效果最优,其次是石灰石,而白云石和方解石对污染物的控制效果相对较差,两者处理后风化煤矸石浸出液中溶出组分没有明显差异。     

Modeling soil and plant phosphorus within DSSAT

The crop models in the Decision Support System for Agrotechnology Transfer (DSSAT) have served worldwide as a research tool for improving predictions of relationships between soil and plant nitrogen (N) and crop yield. However, without a phosphorus (P) simulation option, the applicability of the DSSAT crop models in P-deficient environments is limited. In this study, a soil-plant P model integrated to DSSAT was described, and results showing the ability of the model to mimic wide differences in maize responses to P in Ghana are presented as preliminary attempts to testing the model on highly weathered soils. The model simulates P transformations between soil inorganic labile, active and stable pools and soil organic microbial and stable pools. Plant growth is limited by P between two concentration thresholds that are species-specific optimum and minimum concentrations of P defined at different stages of plant growth. Phosphorus stress factors are computed to reduce photosynthesis, dry matter accumulation and dry matter partitioning. Testing on two highly weathered soils from Ghana over a wide range of N and P fertilizer application rates indicated that the P model achieved good predictability skill at one site (Kpeve) with a final grain yield root mean squared error (RMSE) of 535 kg ha⁻¹and a final biomass RMSE of 507 kg ha⁻¹. At the other site (Wa), the RMSE was 474 kg ha⁻¹ for final grain yield and 1675 kg ha⁻¹ for final biomass. A local sensitivity analysis indicated that under P-limiting conditions and no P fertilizer application, crop biomass, grain yield, and P uptake could be increased by over 0.10% due to organic P mineralization resulting from a 1% increase in organic carbon. It was also shown that the modeling philosophy that makes P in a root-free zone unavailable to plants resulted in a better agreement of simulated crop biomass and grain yield with field measurements. Because the complex soil P chemistry makes the availability of P to plants extremely variable, testing under a wider range of agro-ecological conditions is needed to complement the initial evaluation presented here, and extend the use of the DSSAT-P model to other P-deficient environments.     

川东地区气田水水质特性研究

气田水是天然气开采过程中采出的地层水,因其来源广泛、类型众多以及成分复杂等原因导致其很难达标处理,且容易对土壤、地表水以及地下水造成污染。因此,本文以川东地区气田水为研究对象,通过常规水质分析和GC-MS等技术手段对其进行全面分析,结果表明：①川东地区气田水特征污染物为氯化物、COD、SS、阴离子表面活性剂以及硫化物等物质;②根据其水质特性可以将川东地区气田水分为两类,一类是高矿化度、高含有机物气田水;另一类是高含硫、高含有机物气田水;③川东地区气田水中共有17种有机污染物,主要为烷烃类、醇类、酯类以及少量酸类等物质。     

Sustainable wood-based nanotechnologies for photocatalytic degradation of organic contaminants in aquatic environment

•Wood and its reassemblies are ideal substrates to develop novel photocatalysts. •Synthetic methods and mechanisms of wood-derived photocatalysts are summarized. •Advances in wood-derived photocatalysts for organic pollutant removal are summed up. •Metal doping, morphology control and semiconductor coupling methods are highlighted. •Structure-activity relationship and catalytic mechanism of photocatalysts are given. Wood-based nanotechnologies have received much attention in the area of photocatalytic degradation of organic contaminants in aquatic environment in recent years, because of the high abundance and renewability of wood as well as the high reaction activity and unique structural features of these materials. Herein, we present a comprehensive review of the current research activities centering on the development of wood-based nanocatalysts for photodegradation of organic pollutants. This review begins with a brief introduction of the development of photocatalysts and hierarchical structure of wood. The review then focuses on strategies of designing novel photocatalysts based on wood or its recombinants (such as 1D fiber, 2D films and 3D porous gels) using advanced nanotechnology including sol-gel method, hydrothermal method, magnetron sputtering method, dipping method and so on. Next, we highlight typical approaches that improve the photocatalytic property, including metal element doping, morphology control and semiconductor coupling. Also, the structure-activity relationship of photocatalysts is emphasized. Finally, a brief summary and prospect of wood-derived photocatalysts is provided.     

Rapid method for on-site determination of phenolic contaminants in water using a disposable biosensor

A disposable biosensor was fabricated using single-walled carbon nanotubes, gold nanoparticles and tyrosinase (SWCNTs-AuNPs-Tyr) modified screen-printed electrodes. The prepared biosensor was applied to the rapid determination of phenolic contaminants within 15 minutes. The SWCNTs-AuNPs-Tyr bionanocomposite sensing layer was characterized with scanning electron microscopy, electrochemical impedance spectroscopy and cyclic voltammetry methods. The characterization results revealed that SWCNTs could lead to a high loading of tyrosinase (Tyr) with the large surface area and the porous morphology, while AuNPs could retain the bioactivity of Tyr and enhance the sensitivity. The detection conditions, including working potential, pH of supporting electrolyte and the amount of Tyr were optimumed. As an example, the biosensor for catechol determination displayed a linear range of 8.0 × 10^-8 to 2.0 × 10^-5 mol·L^-1 with a detection limit of 4.5 × 10^-8 mol·L^-1 (S/N = 3). This method has a rapid response time within 10 s, and shows excellent repeatability and stability. Moreover, the resulting biosensor could be disposable, low-cost, reliable and easy to carry. This kind of new Tyr biosensor provides great potential for rapid, on-site and cost-effective analysis of phenolic contaminants in environmental water samples.     

Role of organic and black carbon in the chemical composition of atmospheric aerosol at European background sites

The mass concentrations of inorganic ions, water-soluble organic carbon, water-insoluble organic carbon and black carbon were determined in atmospheric aerosol collected at three European background sites: (i) the Jungfraujoch, Switzerland (high-alpine, PM_2.5 aerosol); (ii) K-puszta, Hungary (rural, PM_1.0 aerosol); (iii) Mace Head, Ireland (marine, total particulate matter). At the Jungfraujoch and K-puszta the contribution of carbonaceous compounds to the aerosol mass was higher than that of inorganic ions by 33% and 94%, respectively. At these continental sites about 60% of the organic carbon was water soluble, 55–75% of the total carbon proved to be refractory and a considerable portion of the water soluble, refractory organic matter was composed of humic-like substances. At Mace Head the mass concentration of organic matter was found to be about twice than that of nonsea-salt ions, 40% of the organic carbon was water soluble and the amount of highly refractory carbon was low. Humic-like substances were not detected but instead low molecular weight carboxylic acids were responsible for about one-fifth of the water-soluble organic mass. These results imply that the influence of carbonaceous compounds on aerosol properties (e.g. hygroscopic, optical) might be significant.     

微生物选育技术在废水生物处理中的应用进展

通过对微生物特别是细菌进行筛选和培育 ,可以得到降解能力强的高效菌株 ,将这些菌株应用于废水生物处理 ,能够增强废水处理工艺去除难降解有机污染物及削减其毒性的能力 ,本文对此进行了评述与展望。     

松针燃烧排放物的热重桥/质谱在线监测方法

森林火灾排放物主要包含气体、挥发性有机化合物(VOCs)、和半挥发性有机化合物(SVOCs),这些物质会严重威胁消防队员和居民的健康。森林火灾烟气是一种包含固体颗粒、液体和气体化合物的复杂混合物。在火前锋附近(靠近消防队员)或者离火前锋很远(但靠近居民)的地方,当苯、甲苯、烯烃等有机化合物的浓度超过各健康安全组织规定的极限值,就可能对健康产生影响。本文给出了一种使用室内热重桥一质谱联用对炉内松针燃烧实验进行火前锋排放物在线监测的新方法。该燃烧实验被认为含氧量较低,这是真实森林火灾中通常的情形。使用这种方法测量得到的苯和甲苯的最大浓度分别是1050和2050ppm。CO2的最大浓度超过10．000ppm。     

Effect of cationic and anionic surfactants on the sorption and desorption of perfluorooctane sulfonate (PFOS) on natural sediments

Sorption and desorption of PFOS at water-sediment interfaces were investigated in the presence of a cationic surfactant, cetyltrimethylammonium bromide (CTAB), and an anionic surfactant, sodium dodecylbenzene sulfonate (SDBS). CTAB remarkably enhanced the sorption of PFOS on the sediment. In contrast, the influence of SDBS to the sorption of PFOS was concentration dependent. Two contrasting factors were responsible for the phenomenon. One was the sorption of the surfactant itself to the sediment, which enhanced the sorption of PFOS. The other was the increase in solubility of PFOS caused by the adding of surfactants, which decreased the sorption of PFOS. SDBS had a much lower sorption capacity, but rather strong ability to increase the solubility of PFOS. High levels of SDBS remarkably reduced the sorption of PFOS on the sediment. These results imply that cationic and anionic surfactants may have contrast impacts on the distribution and transport of PFOS in the environment.     

Selenium fractions in organic matter from Se-rich soils and weathered stone coal in selenosis areas of China

A high degree of association between Selenium (Se) and organic matter has been demonstrated in natural environments, but Se fractions and speciation in organic matter is unclear. In this study, a method for quantifying organic matter associated with Se (OM-Se) was developed to investigate Se fractions in organic matter in Se-rich soils and weathered stone coal from Enshi, China, where Se poisoning of humans and livestock has been documented. Initially, Se was extracted using water and a phosphate buffer. Subsequently, OM-Se was extracted using NaOH, and then speciated into Se associated with fulvic acids (FA-Se) and humic acids (HA-Se). Both FA-Se and HA-Se were further speciated into the weakly bound and strongly bound fractions using a customized hydride generation reactor. The results show that FA-Se (1.91-479 mg kg⁻¹) is the predominant form of Se in all Se-rich soils and the weathered stone coal samples, accounting for more than 62% of OM-Se (3.07-484 mg kg⁻¹). Weakly bound FA-Se (1.33-450 mg kg⁻¹) was prevalent in the total FA-Se, while weakly bound HA-Se (0.62-26.2 mg kg⁻¹) was variable in the total HA-Se (1.15-32.5 mg kg⁻¹). These data indicate that OM-Se could play a significant source and sink role in the biogeochemical cycling of Se in the supergene environment. Weakly bound FA-Se seems to act as a potential source for bioavailable Se, whereas strongly bound HA-Se is a possible OM-Se sink which is not readily transformed into bioavailable Se.