中国生活源固体垃圾产生和处理及其N2O排放

核算和评估固体垃圾产生和处理及其N₂O排放具有重要的现实和指导意义.本研究以中国为例（2008—2017年）,建立了固体垃圾产生、处理和N₂O排放核算框架.结果表明,10年间中国固体垃圾产生量上升了34.6%,年均6.13亿t,生活垃圾（48.6%）和工业日用品垃圾（24.6%）是主要贡献源;处理格局仍以填埋为主（占53.0%）,焚烧为辅（25.5%）;堆弃（42.5%）和焚烧（31.2%）是固体垃圾处理中N₂O气体的主要排放源,堆肥占21.9%,填埋处理排放最少（4.4%）;固体垃圾处理产生的渗滤液逐年增加,渗滤液排放的N₂O占固体垃圾处理N₂O排放总量的41.7%,生活垃圾产生的渗滤液是其主要排放源.加大垃圾分类处理和资源化利用力度,加强农村生活垃圾处理处置能力、减少垃圾堆弃量及提高垃圾处理技术对固体垃圾的产生及其N₂O排放减排至关重要.     

Efficient degradation of Rhodamine B by magnetically recoverable Fe3O4-modified ternary CoFeCu-layered double hydroxides via activating peroxymonosulfate

Environment-friendly nano-catalysts capable of activating peroxymonosulfate (PMS) have received increasing attention recently. Nevertheless, traditional nano-catalysts are generally well dispersed and difficult to be separated from reaction system, so it is particularly important to develop nano-catalysts with both good catalytic activity and excellent recycling efficiency. In this work, magnetically recoverable Fe₃O₄-modified ternary CoFeCu-layered double hydroxides (Fe₃O₄/CoFeCu-LDHs) was prepared by a simple co-precipitation method and initially applied to activate PMS for the degradation of Rhodamine B (RhB). X-ray diffraction (XRD), fourier transform infrared spectrometer (FT-IR), scanning electron microscope (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller method (BET), and vibrating sample magnetometer (VSM) were applied to characterize morphology, structure, specific surface area and magnetism. In addition, the effects of several key parameters were evaluated. The Fe₃O₄/CoFeCu-LDHs exhibited high catalytic activity, and RhB degradation efficiency could reach 100% within 20 min by adding 0.2 g/L of catalyst and 1 mmol/L of PMS into 50 mg/L of RhB solution under a wide pH condition (3.0-7.0). Notably, the Fe₃O₄/CoFeCu-LDHs showed good super-paramagnetism and excellent stability, which could be effectively and quickly recovered under magnetic condition, and the degradation efficiency after ten cycles could still maintain 98.95%. Both radicals quenching tests and electron spin resonance (ESR) identified both HO? and SO₄^?? were involved and SO₄^?? played a dominant role on the RhB degradation. Finally, the chemical states of the sample's surface elements were measured by X-ray photoelectron spectroscopy (XPS), and the possible activation mechanism in Fe₃O₄/CoFeCu-LDHs/PMS system was proposed according to comprehensive analysis.     

An unusual high ozone event over the North and Northeast China during the record-breaking summer in 2018

Under the background of global warming, the summer temperature of the North and Northeast China (NNEC) has significantly increased since 2017, which was accompanied by the aggravated ozone (O₃) pollution. In 2018, the NNEC experienced a record-breaking summer of the past 40 years. Influenced by the abnormal high temperatures, a regional ozone event occurred on 2-3 August, over 63% of 79 selected cities in the NNEC were exposed to O₃ pollution, and the maximum value of MDA8 O₃ reached 268 μg/m³. Observations indicated that ozone concentrations agree well with the maximum temperature at 2 meters (MT2M) over NNEC with a correlation coefficient of 0.69. During the pollution episode, strong downdraft in the local high (35°N-42.5°N, 112.5°E-132.5°E; LH) over the NNEC created the favourable meteorological conditions for O₃ formation. By analyzing the horizontal wind and wave activity fluxes (WAFs) at 200 hPa, we found that the LH formation was resulted from the Rossby wave propagation from upstream along the mid-latitude Asian jet. The split polar vortex intrusion further strengthened the amplitude of the Rossby wave and reinforced the LH. Moreover, a secondary circulation between Typhoon Jongdari and the LH contributed to the enhanced LH with strong subsidence. On the other hand, the stratospheric intrusions under the deep subsidence also contributed to the enhanced surface O₃. In this study, the deep-seated meteorological dynamical mechanisms contributing to the abnormal high temperatures were investigated, which can lead to a better understanding of the regional O₃ pollution over NNEC under the global-warming background.     

Removal of antibiotic-resistant genes during drinking water treatment: A review

Once contaminate the drinking water source, antibiotic resistance genes (ARGs) will propagate in drinking water systems and pose a serious risk to human health. Therefore, the drinking water treatment processes (DWTPs) are critical to manage the risks posed by ARGs. This study summarizes the prevalence of ARGs in raw water sources and treated drinking water worldwide. In addition, the removal efficiency of ARGs and related mechanisms by different DWTPs are reviewed. Abiotic and biotic factors that affect ARGs elimination are also discussed. The data on presence of ARGs in drinking water help come to the conclusion that ARGs pollution is prevalent and deserves a high priority. Generally, DWTPs indeed achieve ARGs removal, but some biological treatment processes such as biological activated carbon filtration may promote antibiotic resistance due to the enrichment of ARGs in the biofilm. The finding that disinfection and membrane filtration are superior to other DWTPs adds weight to the advice that DWTPs should adopt multiple disinfection barriers, as well as keep sufficient chlorine residuals to inhibit re-growth of ARGs during subsequent distribution. Mechanistically, DWTPs obtain direct and inderect ARGs reduction through DNA damage and interception of host bacterias of ARGs. Thus, escaping of intracellular ARGs to extracellular environment, induced by DWTPs, should be advoided. This review provides the theoretical support for developping efficient reduction technologies of ARGs. Future study should focus on ARGs controlling in terms of transmissibility or persistence through DWTPs due to their biological related nature and ubiquitous presence of biofilm in the treatment unit.     

二氧化锰改性沸石对废水中Pb2+的吸附性能及其影响因素研究

改性后的沸石材料,可大幅度提高其对金属离子的吸附量,在治理环境污染方面具有巨大的潜力。高锰酸钾和硫酸锰反应生成的二氧化锰包裹在沸石表面,可大大提高其吸附性能,最终达到吸附废水中重金属的目的。研究了二氧化锰改性沸石对废水中Pb²⁺吸附性能的影响因素,如沸石与二氧化锰投料比、反应时间、溶液pH值、反应温度、Pb²⁺初始浓度等,并探讨了其吸附机理。试验结果表明:二氧化锰改性沸石对废水中Pb²⁺的吸附效果随着沸石与二氧化锰投料比的增加而提高,平衡吸附时间为12 h,吸附反应的最佳溶液pH值为5~6;二氧化锰改性沸石对废水中Pb²⁺的吸附为自发的吸热反应,吸附过程符合Langmuir等温吸附模型,说明为单配体吸附模式;红外光谱分析发现,-OH是影响二氧化锰改性沸石吸附废水中Pb²⁺的主要官能团;低浓度腐殖酸对二氧化锰改性沸石吸附废水中Pb²⁺的影响较小,不产生竞争吸附。     

Product identification and toxicity change during oxidation of methotrexate by ferrate and permanganate in water

• Oxidation of methotrexate by high-valent metal-oxo species was first explored. • Fe(VI) presented a higher reactivity to MTX than Mn(VII) at pH 8.0. • Ketonization and cleavage of peptide bond were two initial reaction pathways. • Products of MTX were not genotoxic, neurotoxic, or endocrine-disrupting chemicals. • The less biodegradable products exhibited developmental and acute/chronic toxicity. Accompanying an annual increase in cancer incidence, the global use of anticancer drugs has remarkably increased with their worldwide environmental prevalence and ecological risks. In this study, the oxidation of methotrexate (MTX), a typical anticancer drug with ubiquitous occurrence and multi-endpoint toxicity, by ferrate(VI) (Fe(VI)) and permanganate (Mn(VII))) was investigated in water. Fe(VI) exhibited a higher reactivity with MTX (93.34 M⁻¹ s⁻¹) than Mn(VII) (3.01 M⁻¹ s⁻¹) at pH 8.0. The introduction of Cu(II) and Fe(III) at 1.0 mM improved the removal efficiency of 5.0 μM MTX by 100.0 μM Fe(VI) from 80% to 95% and 100% after 4 min, respectively. Seven oxidized products (OPs) were identified during oxidative treatments, while OP-191 and OP-205 were characterized as specific products for Fe(VI) oxidation. Initial ketonization of the L-glutamic acid moiety and cleavage of the peptide bond of MTX were proposed. Additionally, a multi-endpoint toxicity evaluation indicated no genotoxicity, neurotoxicity, or endocrine-disrupting effects of MTX and its OPs. Particularly, serious developmental toxicity in zebrafish larvae was observed in the treated MTX solutions. Based on the acute and chronic aquatic toxicity prediction, OP-190, OP-192, OP-206, and OP-208 were deemed toxic or very toxic compared to harmful MTX. Furthermore, the reduced biodegradability index from 0.15 (MTX) to −0.5 to −0.2 (OP-192, OP-206, and OP-468) indicated the formation of lower biodegradable OPs. Overall, this study suggests that Fe(VI) and Mn(VII) oxidation are promising treatments for remediating anticancer drug-contaminated water. However, the environmental risks associated with these treatments should be considered in the evaluation of water safety.     

Fluoride contamination,spatial variation,and health risk assessment of groundwater using GIS: a high-density survey sampling in Weifang City,North China

Environmental Science and Pollution Research - The present study, with the aid of GIS, utilizes high-density groundwater (GW) sampling data (1398 samples) to analyze the spatial variation...     

基于GIS的地震构造信息系统

本文讨论了地震构造信息系统的建造和信息管理。系统是以GIS工具软件ARC/INFO为开发平台建造的,原始资料复盖华北地区的大部,约北纬35～41度,东经109～120度。系统包括活动断裂、破坏性地震、仪器记录地震等信息。本文深入研究了GIS做为信息管理工具的能力,探讨了GIS在地震区划图编制中可能起到的作用。系统能使地震危险分析中信息管理方式、信息管理效率和利用率有质的改进,在某种程度上减小资料利用不充分和人为任意性引起的不确定性。作为一种探索,本文进行了一系列的空间操作和分析,以研究空间特征之间的相关性,并产生新的数据集合。     

不同种植制度土壤氧化还原酶活性和动力学特征

土壤质量与土壤的生物学性质密切相关,种植制度对土壤生物学特性的影响研究对土壤质量管理具有重要的意义.以黑龙江853农场不同种植制度土壤为研究对象,探讨种植制度对土壤理化性质,过氧化氢酶、脱氢酶活性和动力学特征的影响.主要研究结果:农作物轮作有利于提高土壤全碳含量,而大豆连作和玉米-大豆轮作使土壤有效氮和全氮含量提高,大豆连作土壤pH显著低于其它作物连作及轮作处理,全磷含量显著高于其它处理;2种轮作体系均提高土壤过氧化氢酶活性和催化能力,且催化能力的提高源于酶的Km降低(即酶-底物亲合力提高);玉米-小麦-大豆轮作提高土壤脱氢酶活性及催化能力,其催化能力的提高由2个动力学参数的变化共同决定,禾本科作物连作土壤动力学参数与豆科作物种植(大豆连作及与禾本科轮作)具有显著差异.本文的研究表明,合理的轮作方式是提高土壤生物学活性的有效手段.     

地震动作用下隧道洞口段破坏特征试验研究∗

为研究山岭隧道洞口段在地震动力作用下对边坡变形特征及其二者之间的相互影响,以宝兰客专某黄土隧道为工程背景,开展了大比例尺的黄土隧道洞口段大型振动台模型试验,输入不同类型的地震动参数,分析在地震动力作用下黄土隧道洞口段的动力响应及变形破坏特征。结果表明：(1)随着地震动强度的增大,模型表观和内部经历了弹性阶段、弹塑性阶段和破坏阶段;(2)阿里亚斯强度(Arias Intensity)的水平与垂直分量的放大系数云图呈现颜色区域互补状态,能量衰减区集中在洞口拱顶附近的围岩,仰拱底部 1~4.50 倍洞径和拱顶 2.50~4 倍洞径围岩范围则为能量加强区;(3)不同地震波形、相同加载方向,加速度水平、垂直分量的峰值连线线形相似,个别测点的加速度峰值突出到线形之外,峰值出现时刻明显提前或滞后,说明围岩发生较大的塑性变形或破坏;(4)单向加载时,拱顶、仰拱底部围岩沿隧道进深方向的加速度放大效应基本一样,沿垂直方向的放大系数连线的台阶式变化更为明显。双向耦合加载时,拱顶、仰拱底部围岩的放大系数连线的台阶式变化都较为明显。