Modeling the Hydrology of Climate Change in California’s Sierra Nevada for Subwatershed Scale Adaptation1

Young, Charles A., Marisa I. Escobar‐Arias, Martha Fernandes, Brian Joyce, Michael Kiparsky, Jeffrey F. Mount, Vishal K. Mehta, David Purkey, Joshua H. Viers, and David Yates, 2009. Modeling the Hydrology of Climate Change in California’s Sierra Nevada for Subwatershed Scale Adaptation. Journal of the American Water Resources Association (JAWRA) 45(6):1409‐1423. Abstract: The rainfall‐runoff model presented in this study represents the hydrology of 15 major watersheds of the Sierra Nevada in California as the backbone of a planning tool for water resources analysis including climate change studies. Our model implementation documents potential changes in hydrologic metrics such as snowpack and the initiation of snowmelt at a finer resolution than previous studies, in accordance with the needs of watershed‐level planning decisions. Calibration was performed with a sequence of steps focusing sequentially on parameters of land cover, snow accumulation and melt, and water capacity and hydraulic conductivity of soil horizons. An assessment of the calibrated streamflows using goodness of fit statistics indicate that the model robustly represents major features of weekly average flows of the historical 1980‐2001 time series. Runs of the model for climate warming scenarios with fixed increases of 2°C, 4°C, and 6°C for the spatial domain were used to analyze changes in snow accumulation and runoff timing. The results indicated a reduction in snowmelt volume that was largest in the 1,750‐2,750 m elevation range. In addition, the runoff center of mass shifted to earlier dates and this shift was non‐uniformly distributed throughout the Sierra Nevada. Because the hydrologic model presented here is nested within a water resources planning system, future research can focus on the management and adaptation of the water resources system in the context of climate change.     

TiO2催化高压脉冲放电等离子体降解2，4-二硝基苯酚

采用TiO2催化高压脉冲放电等离子体降解废水中的2,4-二硝基苯酚,对反应进行了动力学研究.研究结果表明,在高压脉冲放电等离子体及TiO2催化高压脉冲放电等离子体反应中,2,4-二硝基苯酚的降解过程均符合表观一级反应动力学方程.加入TiO2催化剂、提高放电电压均可提高2,4-二硝基苯酚的降解反应速率常数.在TiO2加入量为0.15%、放电电压为16 kV时,2,4-二硝基苯酚的降解率为87.4%,TiO2的催化效应增强因子为1.55.     

Biofiltration treatment of odors from municipal solid waste treatment plants

An in situ compost biofilter was established for the treatment of odors from biostabilization processing of municipal solid waste. The concentrations of total volatile organic compounds (VOCs) in odors and their components were measured. Biofilter media was characterized in terms of total carbon (TC), total nitrogen (TN), total phosphorus (TP), organic matter (OM), pH value and determination of bacterial colony structure. Gas chromatography–mass spectrometry (GC–MS) analysis showed that the main components of the produced gas were benzene, toluene, ethylbenzene and xylene (BTEX) along with other alkanes, alkenes, terpenes, and sulphur compounds. The compost biofilter had remarkable removal ability for alkylated benzenes (>80%), but poor removal for terpenes (～30%). Total VOC concentrations in odors during the biostabilization process period ranged from 0.7 to 87 ppmv, and the VOC removal efficiency of the biofilter varied from 20% to 95%. After about 140 days operation, TN, TC, TP and OM in compost were kept almost stable, but the dissolved N, NH₄–N and NO₃–N experienced an increase of 44.5%, 56.2% and 76.3%, respectively. Dissolved P decreased by 27.3%. The pH value experienced an increase in the early period and finally varied from 7.38 to 8.08. Results of bacterial colony in packing material indicated that bacteria and mold colony counts increased, but yeasts and actinomyces decreased along with biofilter operation, which were respectively, 3.7, 3.4, 0.04 and 0.07 times of their initial values.     

Ru/γ-Al_2O_3和Ru/AC催化剂的制备及其对氨氧化反应的催化性能

分别以γ-Al_2O_3和活性炭(AC)为载体,采用浸渍法制备了Ru质量分数均为2.0%的Ru/γ-Al_2O_3和Ru/AC催化剂,并用X射线衍射仪和透射电子显微镜等方法对催化剂结构进行了表征.实验结果表明:Ru/AC中Ru沉积在AC表面,分散度较低;而Ru/γ-Al_2O_3中Ru进入到γ-Al_2O_3内部,形成了一种高度分散体系.Ru/γ-Al_2O_3对氨的催化活性高于Ru/AC,氨在Ru/γ-Al_2O_3和Ru/AC上的起活温度分别为200 ℃和266 ℃,T_(90)(氨去除率达90%时的反应温度)分别为267℃和320 ℃.随混合气体空速增大,Ru/γ-Al_2O_3催化剂的T_(90)逐渐升高,气体空速分别为3 600,4 800,5 400 h~(-1)时,T_(90)分别为235,266,303 ℃.随反应前混合气体中氨质量分数增加,氨的去除率降低.     

煤粉锅炉飞灰份额影响因素分析

通过对10个电厂22台机组36组实测数据的分析,论述了燃煤挥发分、灰分及过剩空气系数对煤粉锅炉飞灰份额的影响趋势。     

LEHR superfund stormwater runoff and putah creek mercury issues

Stormwater runoff from the University of California, Davis/U.S. Department of Energy Laboratory for Energy‐Related Health Research (UCD/US DOE LEHR) Superfund site located on the University of California campus in Davis, California, has been found to contain over 500 ng/L of total recoverable mercury, which is about ten times the California Toxics Rule criterion. This stormwater runoff is discharged to Putah Creek, which is Clean Water Act Section 303(d) listed as impaired for excessive mercury bioaccumulation in edible fish. A discussion is presented on the potential impact of the mercury in stormwater runoff from LEHR leading to excessive bioaccumulation of mercury in Putah Creek fish. The mercury in the stormwater runoff is derived from former flooding of the soils near the creek, which contains mercury derived from abandoned upstream mercury mines located in the Coast Range Vaca Hills to the west of LEHR. The implications of this situation for implementing a Total Maximum Daily Load (TMDL) to control mercury in stormwater runoff to Putah Creek are presented. © 2009 Wiley Periodicals, Inc.     

日本城市废弃物处理和综合利用技术简介

应日本新技术促进机构邀请,对日本城市废弃物处理和综合利用技术进行考察.简要介绍日本新技术促进机构以及日本企业对于城市垃圾、废塑料和电子废弃物的处置和再利用技术,为中日再生资源行业深入合作,推动我国再生资源行业技术发展提供借鉴.     

复合材料静态处理煤矿高浓度含锰废水的研究

针对目前云南省某煤矿排放废水中Mn~(2+)超标的问题,利用一种新型复合材料进行除锰试验.该复合材料是纳米分子筛与硅藻土经合理复配后,掺入复配絮凝荆形成的.试验中优化了不同材料的复合方式、絮凝剂的复配比例与用量.利用复配的多孔材料,对云南某煤矿含有大量悬浮物、Mn~(2+)质量浓度为5.32 mg/L的黑色废水及Mn~(2+)质量浓度为42.mg/L的红褐色废水进行了Mn~(2+)去除效果研究.结果表明,黑色废水中Mn~(2+)去除率达到70%,出水pH值为7.9;红褐色废水中Mn~(2+)去除率达到91.0%,出水pH值为7.1.与此同时,还研究了废水中Fe~(3+)、固体悬浮物(SS)对Mn~(2+)去除效果的影响,废水中Fe~(3+)的存在使pH降低,并与Mn~(2+)产生竞争吸附,对复合材料除锰有不利影响,而SS的存在对Mn~(2+)的去除效果没有显著的影响.     

公路路侧安全等级评价与分级路侧防护

为降低路侧事故率,提高路侧安全设计水平,综合分析影响交通安全的因素及其影响程度,提出了路侧危险度的概念,建立了基于灰色聚类理论的4级路侧安全等级评价方法.对评价对象的路侧安全状况及其变化趋势进行客观描述,进而提出了不同危险级别情况下应设置的防护设施.本研究对部分案例进行简要剖析,为工程技术人员和决策者识别公路安全整治的备选路段、确定安全改善项目实施的优先级、合理设置公路安全防护设施提供了理论依据.