地下水环境影响评价导则执行过程中遇到的问题及建议

对中国各地区地下水的水质情况进行了调查,分析了地下水环境管理和保护工作中的问题,指出地下水污染防治工作的重要性、迫切性。对《环境影响评价技术导则地下水环境》(HJ 610-2011)的工作等级划分、环境影响识别、环境现状调查、影响评价及污染防治等内容进行了简要介绍,汇总了评价导则执行后,对各类项目进行地下水评价过程中遇到的困难和问题,并在对各种问题进行分析的基础上,提出了有针对性的解决方法和建议。     

制浆造纸工业废水达标可行性研究

2008年6月颁布的《制浆造纸工业水污染物排放标准》(GB 3544-2008)与原标准(GB 3544-2001)相比,增加了控制排放的污染物项目,污染物排放控制要求也大幅提高,传统的废水二级生化处理工艺已不能满足新标准要求。文章通过梳理和分析调研及现场监测的资料和数据,提出目前制浆造纸企业通过有效的技术改造和升级,增加废水三级深度处理流程,在加强管理的情况下可以实现废水稳定达标排放。但不可避免会增加企业建设和运营成本,大中型制浆造纸企业尚可接受,对小型企业的冲击则相对较大。同时提出目前制浆造纸企业废水处理仍存在一些技术和管理方面的问题,尚需通过制定技术规范、强化环境监管、深入开展相关基础研究等多方面对策,优化制浆造纸行业结构调整,确保行业污染物减排。     

四川红层浅层风化带裂隙水水化学特征的聚类分析

四川红层盆地浅层风化带裂隙水是区内分布最为广泛和目前开采最多的浅层地下水类型,本文通过对大量控制性水样分析结果进行聚类分析,探讨了该地区浅层风化带裂隙水的水化学成分特征及其分布规律,结果表明区内91%以上的浅层风化带裂隙水为HCO3-型淡水,主要分布在中部方山丘陵小区、南部台状低山丘陵小区和东部侵蚀构造平行岭谷低山丘陵小区。该研究可为开发利用浅层地下水提供地学依据。     

海岸带含水层咸淡水界面随潮汐波动的数值模拟

在分析、研究了滨海地带含水层和不透水层的水文地质特性及含水层内的咸淡水渗流运动特征的基础上,运用数学推理的手法,建立了一种较为简单适用的模拟海岸带含水层咸淡水界面和天然地下水面变动规律的二维数学模型,通过该模型的计算值与实验值的比较,证明该模型的计算结果与实验结果有着非常好的拟合度,即该模型能较客观地揭示海水入侵引起的咸淡水界面的变化规律.其后,运用该模型系统的探讨了含水层以下为非平坦的不透水层的滨海地带天然地下水面、咸淡水界面伴随着潮汐的波动而变化的规律.即伴随着潮汐的波动,一方面天然地下水面和咸淡水界面与潮汐具有相似的振动波形,波动的幅度随离海岸距离的增加而减小.在海岸附近咸淡水界面的振幅大于天然地下水面的振幅,而在离开海岸一定距离后天然地下水面的振幅超过咸淡水界面的振幅.总体上天然地下水面的振幅呈负指数衰减,而咸淡水界面的振幅几乎呈直线衰减(其衰减直线的倾角在135～150 °之间变动),且潮汐波动对天然地下水面影响的范围远大于其对咸淡水界面的影响;另一方面天然地下水面和咸淡水界面波动的振幅及它们之间的相位差的大小还与天然地下水面的水力坡度、含水层的渗透系数、有效孔隙率、不透水层形状及其变动的幅度有关,但它们之间的相位差的大小与潮汐波动的幅度无关,其振幅与潮汐的振幅成比例增减.当不透水层的形状一定时,不论天然地下水面的水力坡度、含水层的渗透系数、有效孔隙率及潮汐波动的幅度怎么变动,天然地下水面、咸淡水界面振动的相位差的变化趋势及其峰值出现的位置几乎不变,即不透水层的形状决定着天然地下水面、咸淡水界面振动的相位差的变化趋势,而其大小与含水层的水文地质参数(水力坡度、渗透系数及有效孔隙率)密切相关.此外,当天然地下水面和咸淡水界面的振动存在相位和振幅的较大差异时,可以断定含水层以下存在非平坦的不透水层,且这种差异越大,不透水层凸凹不平的程度越高.     

Spatial and temporal variations in groundwater nitrate at an intensive dairy farm in south-east Ireland: Insights from stable isotope data

Achievement of at least “good ecological status” in all waterbodies under the EU Water Framework Directive by 2015 will in some cases be a challenge. The twin challenge is to manage expectations of policy makers for such waterbodies as to a realistic length of time required for improvement in water quality. Hence, understanding the source, transformation processes and residence time of nitrate in a hydrological system is an essential part of meeting such challenges. On a dairy farm with 24 shallow groundwater wells, the dual isotopic composition of nitrate (δ¹⁵N and δ¹⁸O) was used to clarify nitrate sources, to assess spatial and temporal variability in nitrate concentrations and to determine if and where denitrification was occurring. Vertical travel time was estimated to correlate nitrate concentrations with management practices. Organically derived nitrogen was the predominant source contributing to groundwater nitrate concentrations. Denitrification was identified as prevalent within specific regions of the study site. The distinct low temporal variability in the isotopic data suggests constancy among nitrate sources and processes over time across the study site. Vertical travel times of up to 3 years were estimated on site indicating the influence of recent management practices on nitrate concentrations. Very slow horizontal migration of groundwater (decades) indicates a legacy of older management practices. Stable isotope techniques, together with an understanding of time lag, provide an extra mechanism to test the efficacy of monitoring and mitigation programmes.     

城镇污水处理排放标准改革的费效分析

从费用效果角度对提高城镇污水处理排放标准的科学性和可实施性进行探讨,利用污染源普查数据,通过城镇污水治理投资和运行函数的构建,计算不同处理规模和排放标准下的污水处理投资和运行费用,在全国层面上计算提高污水处理排放标准所需费用和污染物的减排效果.研究表明：污水处理厂的投资和运行费用的增加随着污水处理规模的增加而递减.以污...     

开放源类物料中微粒子排放估算模型的建立

利用实验室微粒子控制模拟试验装置,采用开放源类粉体物料自由下落溢出随机粉尘的实验研究方法,研究了济南市开放源类粉体物料自由下落过程中微粒子排放规律;在一定动力因素条件下,探讨了物料种类、粒度组成,物料含水率,环境空气湿度,自由下落中质量流量等因素对物料排放率的影响;通过数学归纳和模型化处理,建立了开放源类粉体物料自由下落过程中大气微粒子排放估算的数学模型;通过对实验数据进行回归分析后认为,粒径、含水率是对排放率影响最大的因素,质量流量是对排放率影响最小的因素。经试验验证,计算值与试验值基本一致。所获结论,对开放源类物料在转运、装卸、堆放等操作过程中大气微粒子的排放估算和综合防治具有重要的参考价值。     

榆神矿区矿井水零排放可行性分析

针对榆神矿区给排水现状,分析矿区给排水关系和矿井水的利用途径,并提出矿井水零排放的技术、管理对策,达到减少新水索取,实现零排放.     

Efficient dechlorination of chlorinated solvent pollutants under UV irradiation by using the synthesized TiO2 nano-sheets in aqueous phase

Titanium dioxide(TiO2), which is the widely used photo-catalyst, has been synthesized by simple hydrothermal solution containing tetrabutyl titanate and hydrofluoric acid. The synthesized product has been applied to photo-degradation in aqueous phase of chlorinated solvents, namely tetrachloroethene(PCE), trichloroethene(TCE) and 1,1,1-trichloroethane(TCA). The photo-degradation results revealed that the degradation of these harmful chemicals was better in UV/synthesized TiO2 system compared to UV/commercial P25 system and UV only system. The photo-catalytic efficiency of the synthesized TiO2 was 1.4, 1.8 and 3.0 folds higher compared to the commercial P25 for TCA, TCE and PCE degradation, respectively. Moreover, using nitrobenzene(NB) as a probe of hydroxyl radical(.OH), the degradation rate was better over UV/synthesized TiO2, suggesting the high concentration of.OH generated in UV/synthesized TiO2system. In addition,.OH concentration was confirmed by the strong peak displayed in EPR analysis over UV/synthesized TiO2system. The characterization result using XRD and TEM showed that the synthesized TiO2 was in anatase form and consisted of well-defined sheet-shaped structures having a rectangular outline with a thickness of 4 nm, side length of 50 nm and width of 33 nm and a surface 90.3 m2/g. XPS analysis revealed that ≡Ti-F bond was formed on the surface of the synthesized TiO2. The above results on both photocatalytic activity and the surface analysis demonstrated the good applicability of the synthesized TiO2 nano-sheets for the remediation of chlorinated solvent contaminated groundwater.     

Arsenic removal from groundwater by acclimated sludge under autohydrogenotrophic conditions

Arsenic in the environment is attracting increasing attention due to its chronic health effects. Although arsenite(As(III)) is generally more mobile and more toxic than arsenate(As(V)), reducing As(V) to As(III) may still be a means for decontamination, because As(III) can be removed from solution by precipitation with sulfide or by adsorption or complexation with other metal sulfides. The performance of As(V) bio-reduction under autohydrogenotrophic conditions was investigated with batch experiments. The results showed that As(V) reduction was a biochemical process while both acclimated sludge and hydrogen were essential. Most of the reduced arsenic remained in a soluble form, although 20% was removed with no addition of sulfate, while 82% was removed when sulfate was reduced to sulfide. The results demonstrated that the reduced arsenic was re-sequestered in the precipitates, probably as arsenic sulfides. Kinetic analysis showed that pseudo first-order kinetics described the bio-reduction process better than pseudo second-order. In particular, the influences of pH and temperature on As(V) reduction by acclimated sludge under autohydrogenotrophic conditions and total soluble As removal were examined. The reduction process was highly sensitive to both pH and temperature, with the optimum ranges of pH 6.5–7.0 and 30–40°C respectively. Furthermore, Arrhenius modeling results for the temperature effect indicated that the As(V) reduction trend was systematic. Total soluble As removal was consistent with the trend of As(V) reduction.