生物炭改良盐碱地研究与应用进展

盐碱地作为21世纪严重威胁粮食产量的农田问题土壤之一,分布广泛,具有极大的开发潜力.生物炭作为高效的新型土壤改良剂,在缓解土壤酸碱障碍、土壤污染治理、碳封存和肥料缓释等方面发挥了重要作用,有力地推动了盐碱地农业的可持续发展.近年来,关于生物炭改良盐碱地的研究和应用备受关注.但由于生物炭来源、结构和组分的复杂性和非均质性,其对盐碱地的改良效果存在极大的不确定,也缺乏关键机制的系统总结和深度探讨,这限制了生物炭技术在盐碱地改良中的进一步推广和应用.通过综合分析生物炭对盐碱地土壤理化性质、养分有效性和生物特征的影响,归纳总结生物炭和改性生物炭对盐碱地的改良效果及其提质增效作用,阐明生物炭在盐碱地改良中存在的可能机制,并对未来研究方向进行了展望,可为进一步研发绿色高效精准的盐碱地生物炭改良技术及其推广应用提供参考.     

Effect of Reprocessing and Accelerated Weathering on ABS Properties

The feasibility of reprocessing has been investigated as a possible alternative for acrylonitrile–butadiene–styrene terpolymer (ABS) recycling. Up to 10 reprocessing cycles have been performed by both extrusion and injection techniques and their effect on thermal and mechanical properties have been studied. Moreover, the effect of the combined reprocessing and accelerated weathering has been analyzed. Measurements collected after each molding cycle indicated virtually complete retention of thermal properties. The same behaviour has been observed from accelerated weathering tests. With respect to the mechanical properties, neither the flow index nor the tensile strength were affected by the number of reprocessing cycles though the impact strength decreased slightly. However, the studies based on the accelerated weathering show that there is an important influence of the number of reprocessing cycles on the tensile strength.     

A follow up of the decrease of non exchangeable organically bound tritium levels in the surroundings of a nuclear research center

In the past decades limited amounts of tritium were handled on the CEA site of Bruyères le Châtel with authorised atmospheric releases. A small fraction of the tritium released entered into environmental samples under three forms: (i) as part of free water (TFWT - Tissue Free Water Tritium), or associated with organic matter in two ways; either (ii) bound to the oxygen and nitrogen atoms of the material as exchangeable organically bound tritium (E-OBT), or (iii) bound to carbon atoms as non exchangeable organically bound tritium (NE-OBT). The first two components provide only a picture of atmospheric tritium concentrations at the sampling time as they are in equilibrium with atmospheric moisture and soil humidity. Unlike these exchangeable forms, however, NE-OBT is tightly bound to the organic matter and provides an integrated record of atmospheric tritium during the growing phase of the vegetation. We mapped NE-OBT in tree leaf samples in an area of about 25 × 30 km² around the centre of the CEA site and compared the results with those obtained during a previous sampling exercise in 1989. At this time, the activity levels were almost ten times higher than those observed presently in a similar area almost 20 years later which is consistent with the decrease of atmospheric releases issued from the centre. As the activity levels are now close to environmental background specific attention was also paid to the analytical procedure to ensure reliable low level NE-OBT detection.     

Evaluating the longevity of a PFAS in situ colloidal activated carbon remedy

The remediation of per‐ and polyfluoroalkyl substances by injection of colloidal activated carbon (CAC) at a contaminated site in Central Canada was evaluated using various visualization and modeling methods. Radial diagrams were used to illustrate spatial and temporal trends in perfluoroalkyl acid (PFAA) concentrations, as well as various redox indicators. To assess the CAC adsorption capacity for perfluorooctane sulfonate (PFOS), laboratory Freundlich isotherms were derived for PFOS mixed with CAC in two solutions: (1) PFOS in a pH 7.5 synthetic water that was buffered by 1 millimolar NaHCO₃ (K_f = 142,800 mg^1‐a L^a/kg and a = 0.59); and (2) a groundwater sample (pH = 7.4) containing PFOS among other PFAS from a former fire‐training area in the United States (K_f = 4,900 mg^1‐a L^a/kg and a = 0.24). A mass balance approach was derived to facilitate the numerical modeling of mass redistribution after CAC injection, when mass transitions from a two‐phase system (aqueous and sorbed to organic matter) to a three‐phase system that also includes mass sorbed to CAC. An equilibrium mixing model of mass accumulation over time was developed using a finite‐difference solution and was verified by intermodel comparison for prediction of CAC longevity in the center of a source area. A three‐dimensional reactive transport model (ISR‐MT3DMS) was used to indicate that the CAC remedy implemented at the site is likely to be effective for PFOS remediation for decades. Model results are used to recommend remedial design and monitoring alternatives that account for the uncertainty in long‐term performance predictions.     

三峡库区建坝前后森林生态系统服务动态

基于六期Landsat TM/ETM+/OLI影像数据,利用生态系统服务功能评估规范及GIS空间统计方法,对三峡库区1990~2015年间森林生态系统服务价值动态变化进行分析。结果表明：三峡库区森林面积与森林覆盖率逐年增加,森林面积增长率71.04%,森林覆盖率由31.27%增加到53.48%。库区整体的森林类型结构比较稳定,表现为针叶林>混交林>灌木林>阔叶林。时间上,三峡库区森林生态系统服务价值呈上升趋势,具体表现为快-慢-快的增长特征。三峡库区单位面积森林生态系统服务价值在总体增长趋势下出现局部负增长趋势,各森林类型的单位面积价值与三峡库区整体的单位面积价值有着相同的变化趋势,均表现为增加-减少-增加的变化特征。三峡库区各类型服务价值的贡献表现为：涵养水源>固碳释氧>生物多样性保护>保育土壤>净化大气环境>积累营养物质>森林防护。空间上,1990~2015年,三峡库区森林生态系统服务价值的地域分布大致以巫溪至武隆一线为界,呈现出东南高、西北低的特征。1990~2015年三峡库区森林生态系统服务价值变化幅度呈现出“西增加快,东增趋缓”的格局特点。     

几种模拟处理方式污泥淋出液重金属与养分特征

为了减少城市污泥重金属对农田的污染,更好地实现污泥农业资源化利用,通过盆栽实验研究不同处理(对照、黑网、附Fe黑网、附Fe黑网+K2SO4及附Fe黑网+玉米)对城市污泥淋出液重金属和养分含量等的影响。结果表明,黑网可降低污泥淋出液的Zn﹑Cd总量,且没有减少污泥淋出液中氮、磷和钾的总量。Fe(OH)3可使淋出液中Zn总量降低,但同时也显著减少了淋出液中的磷总量。K2SO4可降低淋出液中的Cu总量,且促进Fe结合磷的释放。玉米的种植可使污泥的总重降低,同时玉米籽粒和茎叶重金属含量达到饲料标准。综合来看,任何处理每次淋出液的Cu、Zn、Pb、Cd浓度均符合农田灌溉水标准,淋出液氮、磷、钾量占原污泥中氮、磷、钾总量的比例(0.98%～9.88%)远远大于重金属元素(Cu,Zn,Pb,Cd)占原污泥对应重金属总量的比例(0.04%～0.41%),污泥淋出液作为农田灌溉水进行肥水利用将是污泥农业资源化利用的适合途径,同时黑网+玉米处理可能是较理想的污泥综合处理利用方式。     

离子液体R_3NANR_3的制备及其脱硫性能

以二元酸和短链叔胺为原料,合成了已二酸三乙胺盐离子液体———R3NANR3。对该离子液体进行SO2气体的循环吸收和解吸行为的研究。实验结果表明,R3NANR3离子液体能对SO2气体进行有效的化学吸收。该吸收过程分二步进行,以第一步吸收为主。室温下（20℃）该离子液体在3 h以内吸收速率较快,3 h后吸收速率减慢并逐渐达到平衡。R3NANR3离子液体与SO2气体饱和吸收量的物质的量之比为1.08。较高温度将导致SO2气体的解吸,在90℃时饱和吸收液能较充分地解吸,残留量为0.0010 mol/L。多次吸收和解吸测试表明,R3NANR3离子液体能实现对SO2气体的循环吸收和分离,将成为烟气中SO2气体的脱除和利用的重要循环吸收剂。     

Accumulation and leaching potential of some pharmaceuticals and potential endocrine disruptors in soils irrigated with wastewater in the Tula Valley, Mexico

The reuse of wastewater for irrigation of agricultural land is a well established practice but introduces many contaminants into the terrestrial environment including pharmaceuticals and personal care products. This study reports the persistence and leaching potential of a group of acidic pharmaceuticals, carbamazepine, and three endocrine disruptors in soils from the Tula Valley in Mexico, one of the largest irrigation districts in the world that uses untreated wastewater. After irrigation of soil columns with fortified wastewater over the equivalent of one crop cycle, between 0% and 7% of the total added amounts of ibuprofen, naproxen, and diclofenac and between 0% and 25% of 4-nonylphenol, triclosan, and bisphenol-A were recovered from the soil profiles. Carbamazepine was more persistent, between 55% and 107% being recovered. Amounts in leachates suggested that movement through the soil was possible for all of the analytes, particularly in profiles of low organic matter and clay content. Analysis of soil samples from the Tula Valley confirmed the general lack of accumulation of the acidic pharmaceuticals (concentrations from below the limit of detection to 0.61 μgkg(-1)) and endocrine disruptors (concentrations from below the limit of detection to 109 μgkg(-1)) despite continual addition through regular irrigation with untreated wastewater; there was little evidence of movement through the soil profiles. In contrast, carbamazepine was present in horizon A of the soil at concentrations equivalent to several years of additions by irrigation (2.6-7.5 μgkg(-1)) and was also present in the deeper horizons. The persistence and mobility of carbamazepine suggested a potential to contaminate groundwater.     

Synthesis of chromium-doped malayaite pigments from wastewater containing low chromium(VI)

A malayaite pigment was synthesized with wastewater containing low chromium (Cr)(VI) by a novel liquid-phase reaction method. The effects of the particle size of the precursor and calcination temperature on the final product are examined. The result of scanning electron microscopy shows that the obtained precursor is amorphous and the particle size is approximately 250 nm. The results of X-ray diffraction and differential scanning calorimetry show that the complete transformation temperature was approximately 1050 degrees C. Furthermore, the Commission International de l'Eclairage laboratory shows that the red color of as-prepared pigments is more saturated with a high a* value at 34.1. This process of malayaite pigment preparation via reuse of the Cr(VI)-containing wastewater is quite simple, economical, and energy-saving for the industry, and the products have a saturated red color. There is considerable foreground for the industrial application of this work.