页岩气开发压裂返排液环境监管及对策建议

水力压裂技术是目前页岩气开发广泛采用的储层改造技术,但该技术的应用产生大量的返排液,返排液如何处置和监管引起了人们的广泛关注。本文收集了国内外压裂液的成分、返排液的水量和水质等资料,从深井灌注、市政污水处理厂处理后外排、现场处理后回用、现场处理后外排四种处理方式上,分析我国返排液环境监管存在的问题,针对实际问题提出对策建议,包括对化学品进行申报登记、制订污水排放的行业标准、对页岩气开发项目进行分段验收、鼓励研发污水处理新技术等。     

重庆秀山锰矿区土壤重金属污染分析与评价

通过采样分析重庆秀山锰矿区土壤中的Mn、Pb、Zn、Cu、Cr、Cd、Ni、Co、As等9种重金属元素含量,使用单因子污染指数法、综合污染指数法、地积累指数法、潜在生态危害指数法等方法,对秀山锰矿区土壤重金属污染状况及其潜在风险程度进行了评价。结果表明,秀山锰矿区域范围内的土壤中Cr、As等重金属元素含量偏高,同时受到金属Mn的严重污染;尾矿库下游土壤的生态风险程度为中等,其余均为轻微的生态风险等级。     

全球经济一体化中的环境壁垒与我国环境和贸易政策选择

本文纵观全球经济贸易格局和环境问题特点,指出了环境壁垒是影响全球贸易和环境的重要因素,分析了环境壁垒产生的本质,提出了国际贸易的新形势下我国如何实现可持续经济发展的贸易和环境政策。     

A study on marine industry and environment of China: regarding Japan’s experience

China is facing the challenge of many marine environment problems with rapid economic growth. Japan had experienced similar marine environmental pressure during its industrialization and had been facing the problem through successful environment policy step by step. The paper reviews the lessons and experiences of Japan’s marine environment protection and analyzes the marine environment pollution in China and its causes, taking Shandong province as a case, such as GDP-oriented economic growth, heavy coal assumption, etc. The paper also analyzes the marine industry with focuses on coastal tourism and its relationship with marine environment. Suggestions on polices are provided based on the analysis on China’ marine environment and Japan’s experience.     

Rheology,Morphology, Crystallization Behaviors,Mechanical and Thermal Properties of Poly(lactic acid)/Polypropylene/Maleic Anhydride-Grafted Polypropylene Blends

The rheologies, morphologies, crystallization behaviors, mechanical and thermal properties of poly(lactic acid) (PLA)/polypropylene (PP) blends and PLA/PP/maleic anhydride-grafted PP (MAPP) blends were investigated. The results showed that the complex viscosities of PLA/PP blends were between those of neat PLA and neat PP, and MAPP had a thinning effect on those of the blends. PLA/PP blends exhibited the distinct phase separation morphologies due to the limited partial miscibility of the blend components. MAPP slightly improved the miscibility between PLA and PP. Both the cold crystallization of PLA component and melt crystallization of PP component were enhanced, probably because PLA and PP were reciprocal nucleating agents. The tensile strength and flexural modulus decreased, while the tensile strain at break and heat deflection temperature (HDT) increased with the increasing PP content. MAPP had the positive effects on the notched impact strength and HDT of PLA-rich blends and also increased the flexural modulus of the binary blends. The thermal stability of the blend was improved by PP, and the incorporation of MAPP further enhanced the thermal stability.     

5种不同晶型的纳米二氧化钛对金属铜生物积累的影响

纳米二氧化钛(nTiO_2)作为一种具有独特物理化学性质的纳米材料被广泛应用。然而,在生产、使用的过程中,nTiO_2会不可避免地进入于水环境中。重金属是水体中常见的污染物之一,nTiO_2进入水体后是否会与水体中的重金属发生相互作用,进而影响重金属的生物积累,目前相关报道还很少。本论文以大型溞为模式生物,考察了5种不同晶型nTiO_2对常见的重金属铜生物积累影响。结果表明,nTiO_2对Cu2+的吸附降低了试验液中Cu2+浓度。但5种不同晶型nTiO_2的吸附能力并不一样,其中锐钛矿晶型(A-S)的吸附能力最高,这可能是由于结构缺陷和表面羟基的存在,为Cu2+提供了更多的结合位点,从而提高了A-S的吸附能力。nTiO_2的存在降低了金属铜在大型溞体内的积累,这可能是由于nTiO_2对金属铜的吸附,降低了自由Cu2+的生物可利用性。由于nTiO_2样品之间比表面积的差异,不同晶型之间单位nTiO_2引起的铜积累有显著性差异性(P0.05),其中锐钛矿和金红石之比为4:1混合晶型(M1)最高,A-S最低。     

不同利用方式对江西省农田土壤碳氮磷生态化学计量特征的影响

根据江西省2013年采集的16582个农田耕层(0～20 cm)土壤样点数据,运用实地调查、经典统计学与地统计学等相结合方法,研究了江西省耕地土壤碳氮磷生态化学计量特征的空间变异性及不同农田利用方式对其的影响.研究结果表明:江西省耕地土壤有机碳(SOC)、全氮(TN)和全磷(TP)平均含量分别为17.90、1.58和0.52 g·kg~(-1),土壤碳氮比(C∶N)、碳磷比(C∶P)和氮磷比(N∶P)平均值分别为11.72、38.29和3.38,土壤C∶N∶P比平均值为34.44∶3.03∶1,说明P是江西省耕地土壤主要的限制因素.此外,由于碳、氮、磷三者之间并不存在显著的两两相关性,表明江西省耕地土壤中不存在稳定的"Redfield ratio";半方差函数表明,江西省土壤碳、氮、磷生态化学计量特征具有中等程度的空间变异性,其空间变异特征主要受到随机性因素的影响;经ANOVA检验显示,不同农田利用方式对土壤碳氮磷生态化学计量特征影响显著(p0.05),土壤SOC和TN平均含量依次表现为:两季水田水旱轮作一季水田一季旱地两季旱地,土壤TP平均含量依次表现为:两季旱地两季水田一季水田一季旱地水旱轮作,土壤C∶N依次表现为:两季水田两季旱地一季水田水旱轮作一季旱地,土壤C∶P平均值依次表现为:水旱轮作两季水田一季水田一季旱地两季旱地,土壤N∶P平均值依次表现为:水旱轮作一季旱地两季水田一季水田两季旱地.总体而言,土壤碳、氮、磷生态化学计量比的变化特征是农田利用方式和环境因子综合作用的结果,土壤C∶N∶P比对土壤碳、氮、磷储量及养分的限制性具有重要的指示作用.     

Altitude dependence of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in surface soil from Tibetan Plateau, China

Remote mountain areas besides high latitude regions are beginning to receive increased attention in studying the transport and behavior of persistent organic pollutants (POPs). In the present work, surface soil samples were collected from the Tibetan Plateau, the highest plateau in the world which includes the northern slope of Mt. Qomolangma, to investigate the levels and trends of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) along the altitudinal gradient. The average PCB and PBDE concentrations were 185.6 ng kg⁻¹ dry weight (dw) (range 47.1–422.6 ng kg⁻¹ dw) and 11.1 ng kg⁻¹ dw (range 4.3–34.9 ng kg⁻¹ dw), respectively. Regression analysis between the log-transformed TOC-normalized concentrations and the altitudes of the sampling sites showed two opposite trends with regard to altitude dependence: negative relationship with altitude below about 4500 m followed by a positive altitude dependence above this point. Considering minimum anthropogenic activities and very sparse precipitation in the north of Himalayas, the trends above 4500 m imply that the significant altitude dependence of these two groups of POPs were irrespective of pollution sources, but could be predicted by the global distillation effect involving cold condensation in high altitude mountain areas. Increasing levels of heavier congeners were found in higher altitude sites, although the lighter congeners were the main contributors to the total amount, suggesting that less volatile congeners seem to become enriched easier than those more volatile at higher altitudes in this region.     

Fluoride removal performance of a novel Fe-Al-Ce trimetal oxide adsorbent

A trimetal oxide was developed as a fluoride adsorbent by coprecipitation of Fe(II), Al(III) and Ce(IV) salt solutions with a molar ratio of 1:4:1 under alkaline condition. The material retained amorphous structure and maintained relatively stable fluoride adsorption performance at calcination temperatures lower than 600 degrees C. The optimum pH range for fluoride adsorption was 6.0-6.5 and the adsorbent also showed high defluoridation ability around pH 5.5-7.0, which is preferable for actual application. A high fluoride adsorption capacity of 178 mg g(-1) was acquired under an equilibrium fluoride concentration of 84.5 mg l(-1), adsorbent dose of 150 mg l(-1) and pH 7.0. The adsorption isotherm could be better described by the two-site Langmuir model than the one-site model, suggesting the existence of two types of active sites on the adsorbent surface. Coexistence of high concentrations of phosphate or arsenate only led to partial inhibition of fluoride adsorption, which further suggests the existence of heterogeneous adsorption sites. Sulfate and chloride did not affect fluoride adsorption, and nitrate influenced it only when the concentration of NO(3)(-)-N exceeded 50 mg l(-1). A high desorption efficiency of 97% was achieved by treating fluoride loaded Fe-Al-Ce oxide with NaOH solution at pH 12.2. A column experiment using the adsorbent fabricated into 1mm pellets was performed at an initial fluoride concentration of 5.5 mg l(-1), space velocity of 5h(-1) and pH of 5.8, and 2240 bed volumes were treated with the effluent fluoride under 1.0 mg l(-1).     

Determination of benzene, toluene, ethylbenzene, xylenes in water at sub-ng l-1 levels by solid-phase microextraction coupled to cryo-trap gas chromatography-mass spectrometry

A trace analytical method of benzene, toluene, ethylbenzene and xylenes (BTEX) in water has been developed by using headspace solid-phase microextraction (HS-SPME) coupled to cryo-trap gas chromatography-mass spectrometry (GC-MS). The chromatographic peak shape for BTEX was improved by using cryo-trap equipment. The HS-SPME experimental procedures to extract BTEX from water were optimized with a 75 microm carboxen/polydimethylsiloxane (CAR/PDMS)-coated fiber at a sodium chloride concentration of 267 g l(-1), extraction for 15 min at 25 degrees C and desorption at 290 degrees C for 2 min. Good linearity was verified in a range of 0.0001-50 microg l(-1) for each analyte (r(2)=0.996-0.999). The limits of detection (LODs) of BTEX in water reached at sub-ng l(-1) levels. LODs of benzene, toluene, ethylbenzene, m/p-xylene and o-xylene were 0.04, 0.02, 0.05, 0.01 and 0.02 ng l(-1), respectively. The proposed analytical method was successfully used for the quantification of trace BTEX in ground water. The results indicate that HS-SPME coupled to cryo-trap GC-MS is an effective tool for analysis of BTEX in water samples at the sub-ng l(-1) level.