山区小城镇国土空间格局优化研究

面对资源约束趋紧和生态环境破坏的严峻态势,生态文明建设中亟需通过国土空间格局优化,应对环境保护和经济发展的双重需要.本文以丹棱县顺龙乡国土空间开发格局为例,从顺龙乡生态环境和社会经济现状出发,指出了当前发展面临的问题,分别从生产空间、生活空间、生态空间三方面提出了优化顺龙乡国土空间的具体方案,探索了山区小城镇国土空间格局优化的思路.     

安徽北部农村地区地下水重金属健康风险评价

为了解安徽北部农村地区地下水重金属污染对人类健康产生危害的风险,采集了26个农村地下水样品,测试分析了Mn、Zn、Cu、Pb、Ni、Cr和Cd七种重金属,并采用美国环境保护局(USEPA)推荐的风险评价模型对健康风险进行了初步评价。结果表明:非致癌污染物Mn、Zn、Cu、Pb和Ni的平均个人年风险分别为1.21×10~(-10)a~(-1)、8.46×10~(-11)a~(-1)、2.93×10~(-10)a~(-1)、8.29×10~(-10)a~(-1)和2.89×10~(-10)a~(-1),均远低于国际辐射防护委员会(ICRP)推荐的最大可接受值(5.0×10~(-5)a~(-1))和USEPA推荐的健康风险等级标准(1×10~(-4)a~(-1)),基本不会对暴露人群构成明显危害;致癌污染物Cd和Cr饮水途径健康危害平均个人年风险分别为1.44×10~(-6)a~(-1)和1.93×10~(-5)a~(-1),超出瑞典环境保护署、荷兰建设与环境部和英国皇家协会推荐标准(1×10~(-6)a~(-1)),Cr甚至超出19倍,为研究区首要污染物,应引起环境卫生部门的重视。     

典型河谷城市儿童土壤与灰尘铅暴露风险

为定量评价河谷型城市土壤与灰尘铅对城市儿童健康的影响与风险,结合野外调查的基础上,以陕西渭河谷地典型工业城市宝鸡、西安、渭南和铜川为研究区域,以定量分析河谷型城市儿童环境铅暴露为核心,收集4个城市土壤与灰尘分析样品总计243个。利用X射线荧光光谱法测定了4个城市土壤与灰尘铅的含量;采用BCR连续形态分级法探究了城市土壤与灰尘重金属铅地球化学形态分布与迁移特征;根据US EPA污染物暴露与健康风险评价模型对城市儿童铅暴露进行了评价。研究结果表明渭河谷地典型城市宝鸡、铜川、西安和渭南城市土壤与灰尘铅浓度(X±SD)分别为(409.2±52.54)和(624.70±66.15)mg·kg-1、(357.47±41.37)和(592.60±36.78)mg·kg-1、(61.4±13.31)和(78.42±14.89)mg·kg-1、(46.71±12.11)和(64.7±13.76)mg·kg-1,均高出陕西省土壤铅背景值;污染水平依次为宝鸡铜川西安渭南。4个河谷型城市土壤与灰尘重金属铅发生整体迁移的趋势为:宝鸡城市灰尘(90.71%)西安城市灰尘(84.74%)≥宝鸡城市土壤(83.12%)渭南城市灰尘(74.89%)≥西安城市土壤(74.50%)铜川城市灰尘(72.49%)铜川城市土壤(57.50%)渭南城市土壤(53.79%)。可见,铅在均在城市灰尘中的迁移趋势远大于相应的城市土壤。4个城市土壤与灰尘均表现出较大的儿童暴露致癌风险,宝鸡和铜川城市儿童土壤与灰尘铅暴露也分别存在非致癌风险,风险程度依次为宝鸡铜川西安渭南。儿童铅暴露致癌与非致癌风险程度与其城市土壤和灰尘中铅可氧化态分布呈相似的规律,表明碱性的城市土壤与城市灰尘(p H7)中可氧化态铅可能是导致河谷型城市儿童铅暴露风险和儿童血铅污染的主要形态和因素。由此,城市燃煤排放与含铅制品的加工等活动可能是渭河谷地河谷型城市儿童血铅与铅暴露最主要的贡献源,必须采取长期有效的监测与控制措施。     

关于焦化行业CO2排放核算方法的探讨

本文分析了适用于焦化行业通用CO₂排放核算方法,在此基础上结合我国焦化行业工艺和原料的特征,采用排放因子法和物料衡算法等两种方法对10家典型焦化企业CO₂排放进行核算。结果表明:物料衡算法能很好地反映不同类型焦化企业的排放特征;排放因子法对我国独立焦化企业存在碳排放量系统性高估的可能。为此,建议我国焦化企业可借鉴德国焦化企业的碳核算经验,采用碳平衡法对不同类型的焦化企业(单元)的碳排放量进行核算,并完善相关的统计和监测技术。     

Ambient volatile organic compounds at a receptor site in the Pearl River Delta region: Variations, source apportionment and effects on ozone formation

We present the continuously measurements of volatile organic compounds（VOCs） at a receptor site（Wan Qing Sha, WQS） in the Pearl River Delta（PRD） region from September to November of 2017. The average mixing ratios of total VOCs（TVOCs） was 36.3 ± 27.9 ppbv with the dominant contribution from alkanes（55.5%）, followed by aromatics（33.3%）. The diurnal variation of TVOCs showed a strong photochemical consumption during daytime,resulting in the formation of ozone（O₃）. Five VOC sources were ...     

Extracellular polymeric substance induces biogenesis of vivianite under inorganic phosphate-free conditions

Vivianite is often found in reducing environments rich in iron and phosphorus from organic debris degradation or phosphorus mineral dissolution. The formation of vivianite is essential to the geochemical cycling of phosphorus and iron elements in natural environments. In this study, extracellular polymeric substances (EPS) were selected as the source of phosphorus. Microcosm experiments were conducted to test the evolution of mineralogy during the reduction of polyferric sulfate flocs (PFS) by Shewanella oneidensis MR-1 (S. oneidensis MR-1) at EPS concentrations of 0, 0.03, and 0.3 g/L. Vivianite was found to be the secondary mineral in EPS treatment when there was no phosphate in the media. The EPS DNA served as the phosphorus source and DNA-supplied phosphate could induce the formation of vivianite. EPS impedes PFS aggregation, contains redox proteins and stores electron shuttle, and thus greatly promotes the formation of minerals and enhances the reduction of Fe(III). At EPS concentration of 0, 0.03, and 0.3 g/L, the produced HCl-extractable Fe(II) was 107.9, 111.0, and 115.2 mg/L, respectively. However, when the microcosms remained unstirred, vivianite can be formed without the addition of EPS. In unstirred systems, the EPS secreted by S. oneidensis MR-1 could agglomerate at some areas, resulting in the formation of vivianite in the proximity of microbial cells. It was found that vivianite can be generated biogenetically by S. oneidensis MR-1 strain and EPS may play a key role in iron reduction and concentrating phosphorus in the oligotrophic ecosystems where quiescent conditions prevail.     

The role of doped-Mn on enhancing arsenic removal by MgAl-LDHs

To meet the challenges posed by global arsenic water contamination, the MgAlMn-LDHs with extraordinary efficiency of arsenate removal was developed. In order to clarify the enhancement effect of the doped-Mn on the arsenate removal performance of the LDHs, the cluster models of the MgAlMn-LDHs and MgAl-LDHs were established and calculated by using density functional theory (DFT). The results shown that the doped-Mn can significantly change the electronic structure of the LDHs and improve its chemical activity. Compared with the MgAl-LDHs that without the doped-Mn, the HOMO-LUMO gap was smaller after doping. In addition, the -OH and Al on the laminates were also activated to improve the adsorption property of the LDHs. Besides, the doped-Mn existed as a novel active site. On the other hand, the MgAlMn-LDHs with the doped-Mn, the increased of the binding energy, as well as the decreased of the ion exchange energy of interlayer Cl⁻, making the ability to arsenate removal had been considerably elevated than the MgAl-LDHs. Furthermore, there is an obvious coordination covalent bond between arsenate and the laminates of the MgAlMn-LDHs that with the doped-Mn.     

Highly efficient P uptake by Fe3O4 loaded amorphous Zr-La (carbonate) oxides: Electrostatic attraction, inner-sphere complexation and oxygen vacancies acceleration effect

Bimetallic oxides composites have received an increasing attention as promising adsorbents for aqueous phosphate (P) removal in recent years. In this study, a novel magnetic composite MZLCO was prepared by hybridizing amorphous Zr-La (carbonate) oxides (ZLCO) with nano-Fe₃O₄ through a one-pot solvothermal method for efficient phosphate adsorption. Our optimum sample of MZLCO-45 exhibited a high Langmuir maximum adsorption capacity of 96.16 mg P/g and performed well even at low phosphate concentration. The phosphate adsorption kinetics by MZLCO-45 fitted well with the pseudo-second-order model, and the adsorption capacity could reach 79% of the ultimate value within the first 60 min. The phosphate adsorption process was highly pH-dependent, and MZLCO-45 performed well over a wide pH range of 2.0-8.0. Moreover, MZLCO-45 showed a strong selectivity to phosphate in the presence of competing ions (Cl⁻, NO₃⁻, SO₄²⁻, HCO₃⁻, Ca²⁺, and Mg²⁺) and a good reusability using the eluent of NaOH/NaCl mixture, then 64% adsorption capacity remained after ten recycles. The initial 2.0 mg P/L in municipal wastewater and surface water could be efficiently reduced to below 0.1mg P/L by 0.07 g/L MZLCO-45, and the phosphate removal efficiencies were 95.7% and 96.21%, respectively. Phosphate adsorption mechanisms by MZLCO-45 could be attributed to electrostatic attraction and the inner-sphere complexation via ligand exchange forming Zr/La-O-P, -OH and CO₃²⁻ groups on MZLCO-45 surface played important roles in the ligand exchange process. The existence of oxygen vacancies could accelerate the phosphate absorption rate of the MZLCO-45 composites.     

液化石油气槽车泄漏处置专用接头套组的应用探讨

针对消防救援车辆缺乏专业堵漏和倒罐装备、应急处置受限等问题,研究采用专用注压接头套组与消防车配合,通过向事故槽车阀门注水加压或惰性气体的方式实施辅助堵漏,能够实现因地制宜、快速有效地解决现场液化石油气大量泄漏的问题,降低事故危害。     

侵彻引信用磁电传感器的输出特性仿真分析

目的 解决侵彻引信用磁电传感器在不同侵彻环境下输出特性难以预知的问题,掌握不同结构参数对传感器输出的影响。方法 基于一种新型磁电传感器的结构原理,提出一种联合仿真研究方法,研究过程分为2部分,一部分是利用ADAMS软件进行磁电传感器惯性系统的力学特性仿真,另一部分是利用COMSOL软件进行传感器机电转换元件的磁电特性仿真,仿真模型的输入是战斗部在穿靶过程中的过载信息。通过磁电传感器在多次冲击加载试验中获取的实测数据,对仿真模型的仿真结果进行验证。改变仿真模型的相关参数,模拟并分析传感器结构对仿真输出特性的影响。结果 仿真穿靶时间的平均绝对误差约为138 μs,穿靶时刻仿真电压值的平均相对误差约为5.9%。在给定力学环境的前提下,侵彻引信用磁电传感器中的线圈与磁铁的相对高度会影响输出信号的正负、幅值以及波峰出现的时间,线圈匝数、线圈与磁铁之间的间隔仅对信号的幅值产生影响。结论 仿真误差在可控范围内,验证了联合仿真模型的正确性与该研究方法的可行性。该仿真模型可以为侵彻引信用磁电传感器的设计提供指导,并为后续进一步验证侵彻引信起爆控制系统的性能工作提供了新的思路。