基于转运站满负荷的北京市新东西城区生活垃圾物流优化方案研究

北京市新东城和新西城成立后迫切需要对现有生活垃圾物流方案进行优化,实现生活垃圾资源化处理.以北京市东西城区生活垃圾为研究对象,利用统计预测模型和GIS空间分析技术与方法,在分析了4个老城区生活垃圾产生量及所属密闭清洁站垃圾流向和流量基础上,提出了基于满负荷运行的三大转运站(马家楼、小武基和大屯)生活垃圾等距离收集运输优化物流模式,分析了现状及新物流模式下生活垃圾物料平衡.结果表明,与现状收集模式相比,等距离优化物流模式可使清运距离减少约9.3×105km.a-1,与现状相比减少10%;同时,基于三大转运站满负荷运转的,部分考虑海淀、丰台和朝阳区跨区运行的生活垃圾优化物流模式下,且充分利用现有的处理处置设施,可减少原生垃圾填埋量约28.3%.在优化模式的基础上若北京市正筹建的3座垃圾焚烧厂建成后,可使新东西城区生活垃圾焚烧、生化、填埋比例由现状1∶4.8∶4.2,达到3.8∶4.5∶1.7,可基本接近北京市2015年生活垃圾焚烧、堆肥和填埋比例达到4∶3∶3规划目标.     

河套灌区土壤水和地下水动态变化及水平衡研究

为探究田间土壤水及地下水在不同作物种植区、不同灌期等情况下的动态变化规律与水平衡特征,以春小麦、玉米、向日葵为典型作物,在河套灌区选取4块2亩的试验田,于2009年4-11月采集田间土壤及地下水样品进行研究.结果表明,不同作物地块间土壤含水率的变化差别主要集中在5-9月的作物生长期.夏灌灌水量不足,土壤含水率呈下降趋势,田间土壤水分变化属于“蒸腾蒸发消耗型”;秋浇期内水量充足,各地块各土层含水率均明显增加,田间土壤水分呈“入渗补给型”.各地块地下水埋深月均变化趋势基本一致,由于优先流的存在,地下水对灌溉降水响应快.本文定量研究了区域土壤水和地下水的变化规律,揭示了灌区水平衡要素间的相互转换关系,可为灌区科学合理的水资源管理提供理论依据.     

温度与pH对生物合成施氏矿物在酸性环境中溶解行为及对Cu2+吸附效果的影响

探析施氏矿物在不同温度、pH下的溶解行为,对其在酸性煤矿废水(ACMD)重金属去除领域的应用具有重要的工程指导意义.本研究通过摇瓶实验,在0.16mol·L-1FeSO4·7H2O,初始pH为2.5的酸性体系中,采用氧化亚铁硫杆菌A.ferrooxidans催化合成施氏矿物.考察了15℃与30℃,pH为2.0$6.0环境条件下矿物的溶解行为,及生物合成施氏矿物对酸性体系Cu2+的吸附去除效果.研究结果表明,经过24h反应,施氏矿物合成体系pH从原始2.50降低至2.18,体系Fe2+氧化完全,27.3%的铁离子参与矿物的合成,矿物分子式可表示为Fe8O8(OH)4.22(SO4)1.89.生物合成施氏矿物在温度为15℃,pH分别为3.2、3.0、2.8、2.6、2.4、2.2与2.0液态体系中振荡72h,矿物溶解率分别为1.92%、3.34%、5.90%、13.09%、28.74%、44.53%与61.46%.在温度为30℃的上述酸度体系中,矿物溶解率在相应时间却达到2.04%、3.98%、8.34%、20.53%、43.50%、96.74%与99.92%.在pH≥3.5的不同温度液态体系中该矿物无溶解迹象.在15℃,pH为6.0、5.0、4.5、4.0与3.5,Cu2+浓度为40mg·g-1的液态体系中,生物合成施氏矿物对Cu2+的吸附量为(50.9±2.2)、(47.3±13.3)、(40.5±4.7)、(31.1±5.0)及(16.9±6.5)mg·g-1.体系酸度一定,施氏矿物在15℃与30℃条件下对Cu2+的吸附效果无显著差异.本研究结果对生物合成施氏矿物在ACMD重金属去除工程应用提供必要的参数支撑.     

Influence of dissolved organic matter character on mercury incorporation by planktonic organisms：An experimental study using oligotrophic water from Patagonian lakes

Ligands present in dissolved organic matter （DOM） form complexes with inorganic divalent mercury （Hg^2＋） affecting its bioavailability in pelagic food webs. This investigation addresses the influence of a natural gradient of DOM present in Patagonian lakes on the bioaccumulation of Hg^2＋ （the prevailing mercury species in the water column of these lakes） by the algae Cryptomonas erosa and the zooplankters Brachionus calyciflorus and Boeckella antiqua. Hg^2＋ accumulation was studied through laboratory experiments using natural water of four oligotrophic Patagonian lakes amended with^197Hg^2＋. The bioavailability of Hg^2＋ was affected by the concentration and character of DOM. The entrance of Hg^2＋ into pelagic food webs occurs mostly through passive and active accumulation. The incorporation of Hg^2＋ by Cryptomonas, up to 27% of the Hg^2＋ amended, was found to be rapid and dominated by passive adsorption, and was greatest when low molecular weight compounds with protein-like or small phenolic signatures prevailed in the DOM. Conversely, high molecular weight compounds with a humic or fulvic signature kept Hg^2＋ in the dissolved phase, resulting in the lowest Hg^2＋ accumulation in this algae. In Brachionus and Boeckella the direct incorporation of Hg from the aqueous phase was up to 3% of the Hg^2＋ amended. The dietary incorporation of Hg^2＋ by Boeckella exceeded the direct absorption of this metal in natural water, and was remarkably similar to the Hg^2＋ adsorbed in their prey. Overall, DOM concentration and character affected the adsorption of Hg^2＋ by algae through competitive binding, while the incorporation of Hg^2＋ into the zooplankton was dominated by trophic or dietary transfer.     

Electrochemical and spectroscopic characteristics of dissolved organic matter in a forest soil profile

Dissolved organic matter （DOM） represents one of the most mobile and reactive organic compounds in ecosystem and plays an important role in the fate and transport of soil organic pollutants, nutrient cycling and more importantly global climate change. Electrochemical methods were first employed to evaluate DOM redox properties, and spectroscopic approaches were utilized to obtain information concerning its composition and structure. DOM was extracted from a forest soil profile with five horizons. Differential pulse voltammetry indicated that there were more redox-active moieties in the DOM from upper horizons than in that from lower horizons. Cyclic voltammetry further showed that these moieties were reversible in electron transfer. Chronoamperometry was employed to quantify the electron transfer capacity of DOM, including electron acceptor capacity and electron donor capacity, both of which decreased sharply with increasing depth. FT-IR, UV-Vis and fluorescence spectra results suggested that DOM from the upper horizons was enriched with aromatic and humic structures while that from the lower horizons was rich in aliphatic carbon, which supported the findings obtained by electrochemical approaches. Electrochemical approaches combined with spectroscopic methods were applied to evaluate the characteristics of DOM extracted along a forest soil profile. The electrochemical properties of DOM, which can be rapidly and simply obtained, provide insight into the migration and transformation of DOM along a soil profile and will aid in better understanding of the biogeochemical role of DOM in natural environments.     

地下水位变化对边坡稳定性影响的模拟分析

降雨引起边坡地下水位变化、降低岩土体抗剪强度进而引起边坡失稳产生滑坡是电网工程灾害中最常见的地质灾害之一。文章在现场详细工程地质勘察的基础上,基于恢复山体极限平衡法和强度折减法,利用数值分析方法对降雨引起地下水位变化条件下某电网工程边坡稳定性进行了分析。模拟结果表明,现今地下水位条件下,该边坡整体处于极限平衡状态;在最高洪水位条件下边坡则处于失稳状态。边坡的最大变形位于边坡中上部,并呈现出由上部逐渐向下部扩展的趋势。边坡潜在破坏模式为边坡后缘张拉破坏和中下部剪切破坏的复合破坏模式。最后基于数值分析结果,对该边坡的工程治理提出了建议。     

顶空气相色谱法测定水中苯系物实验研究

采用顶空气相色谱法对水中苯系物的测定方法进行了研究。在研究过程中讨论了盐,顶空平衡温度和平衡时间等因素对测定结果的影响。实验结果表明无机盐的加入可以提高苯系物的响应值,顶空平衡温度和平衡时间分别为60℃和50 min时为最优的实验分析条件。在此实验条件下,苯系物各组分回归方程的线性相关性较为显著。方法的检出限在2.5~5.9μg/L,加标回收率为93.8%～96.8%,相对标准偏差小于14.7%。该方法对于水中苯系物的测定准确、快捷、重现性好。     

北运河中游沉积物对磷的吸附特性研究

研究了位于北京郊区的北运河中游9个断面的沉积物对磷的吸附行为,分析了沉积物组成及其理化性质与磷吸附特征的关系.实验结果表明,不同断面沉积物对磷的最大吸附量在0.11 ～9.45 mg/g之间,而各断面沉积物的临界平衡磷浓度(EPC0)范围在0.33～ 1.85 mg/L之间,统计分析显示EPC0与河水中的总磷和可溶性无机磷呈显著负相关,但与沉积物中的金属和有机质含量相关性较差;根据临界平衡磷浓度定义的推断,新华大街桥、玉带桥、运河大街桥、六环路桥、宋梁路桥、湿地和甘棠橡胶坝7个断面的沉积物表现为磷的“汇”,而丰子沟和减运沟2个点表现为磷的“源”,并且各点沉积物释放和吸附磷的趋势较大.     

清洁生产审核中物料平衡的难点及应用实例

建立物料平衡是清洁生产审核第3阶段（即“审核”阶段）最核心的工作内容,其目的是为了准确分析物料流失和废物产生的原因,建立物料平衡也是产生清洁生产方案（尤其是中高费方案）最主要的方法之一。本文在介绍清洁生产审核中物料平衡的完整工作步骤的基础上,归纳了几点在实际工作中应用物料平衡遇到的难点及要点,实例介绍了物料平衡、能源平衡和水平衡三种常用平衡,为审核工作者提供些许思路参考。     

有机质分解对青海湖湖水溶解无机碳同位素（δ13CDIC）的影响及其指示意义——来自沉积物捕获器的研究

青海湖沉积物稳定碳同位素常常被用来指示古环境的变化,然而准确地解译其信号需要充分认识溶解无机碳同位素比值（δ¹³C_DIC）变化及其控制因素。本文利用沉积物捕获器连续一年收集的青海湖湖水及颗粒物,通过其中湖水的δ¹³C_DIC和细颗粒沉积物中碳酸盐稳定碳同位素（δ¹³C_carb）的同步分析,结合湖水δ¹³C_DIC的垂直分布和表层沉积物δ13Ccarb及有机碳同位素（δ¹³C_org）,探讨了有机质分解在δ¹³C_DIC和δ¹³C_carb中的调节作用。结果表明,从沉积物捕获器中获得的湖水δ¹³C_DIC的变化主要受控于与外界隔绝后（微）生物对有机质的分解作用,但这种（微）生物分解作用并不会影响到δ¹³C_carb比值。这些现象反映了（1）还原环境下（微）生物对有机质的分解作用对水体δ¹³C_DIC有重要影响和（2）青海湖自生碳酸盐主要从上层湖水沉淀,且形成后不再与周围水体发生交换作用。