城市酒店业的碳排放核算及低碳指标分析

随着中国的快速城市化和服务业的发展,旅游业逐渐成为主要的温室气体排放者之一,酒店面临节能减排的压力并缺乏相关的评价标准.本文建立了生命周期的酒店业碳排放核算框架和低碳指标,并以宁波市为案例城市,对其3种类型的酒店进行碳排放核算和低碳指标的分析.结果表明,能源消费是酒店业最大的碳排放源,占93.5%~94.1%;各类酒店的碳排放量在2013—2015年间有约8.2%~9.2%的减少;从低碳指标看,五星级酒店的单位建筑面积的碳排放最小,单位出租间天数和单位旅客的碳排放最大,而四星级酒店的单位营业额碳排放最小.优化区域电力碳排放水平和酒店的软硬件设施是减少酒店碳排放的有效措施,碳标签是有效的酒店业低碳管理的政策工具.     

南昌市移动源排放清单研究

根据收集的南昌市移动源活动水平数据,采用合适的估算方法、排放因子和GIS技术,建立了南昌市2007—2014年移动源排放清单,并对2014年移动源清单进行了空间化处理与分析,空间分辨率为1 km×1 km.结果表明,2007—2014年南昌市移动源共向大气排放CO、HC、NO_x、PM_(2.5)、PM_(10)、SO_2分别为18.26×10~4、5.07×10~4、18.46×10~4、0.99×10~4、1.08×10~4、3.31×10~4t.其中,2014年移动源向大气中排放的这6种污染物总量分别为2.14×10~4、0.76×10~4、1.97×10~4、0.08×10~4、0.09×10~4、0.55×10~4t.道路移动源中,汽油小型客车是CO、HC和SO_2最大的贡献源,排放量分别占机动车排放总量的55.1%、78.5%和56.1%;柴油重型货车是NO_x、PM_(2.5)和PM_(10)排放贡献率最大的车型,分别占43.2%、40%和40%.非道路移动源中,小型拖拉机对CO、HC、NO_x、PM_(2.5)和PM_(10)的贡献率均较大,分别占非道路移动源排放总量的29.9%、26.9%、23.4%、29.5%和29.8%;SO_2排放主要来源于船舶,占非道路移动源SO_2排放总量的45.1%.高污染排放集中的区域,主要是青山湖区、西湖区和东湖区.     

我国人为源气态活性氮排放时空变动特征分析

随着粮食和能源需求的增加,农业生产和化石燃料燃烧带来的活性氮污染越来越成为影响我国环境和人民健康的重要因素之一.通过对2000、2005及2010年全国31个省(直辖市、自治区)的人为源气态活性氮排放总量、单位GDP及单位人均排放量的Moran's I指数和GetisOrd G*i指数进行空间分析,探讨了气态活性氮排放及其强度的时空变动特征.结果表明,全国的气态活性氮排放及其强度呈现明显的空间集聚特征.在空间分布特征上,全国活性氮排放表现为高值集聚分布,其热点主要位于华北平原和长江中下游平原地区;排放强度方面则为高值聚集和低值聚集兼备.通过对3个年份的冷热点比较分析发现,排放强度的冷点地区变化较小,热点地区变化较大.其中,单位GDP排放强度方面,冷点地区处于东南沿海地区,热点地区则由西北地区缩小到四川、甘肃两省;而单位人口排放强度方面,冷点地区范围有所缩减,热点地区则由分散转变为集中分布于京津冀及周边的山西、内蒙古和辽宁等.分析人为源气态活性氮时空分布格局和特征及其形成原因,可为评估和减缓气态活性氮排放对生态环境的影响提供科学基础.     

基于本地污染源调查的杭州市大气污染物排放清单研究

基于实地调查数据并辅以统计数据,采用物料衡算法和排放因子法,估算了杭州市2015年大气污染物排放清单,并选取经纬度坐标、路网、航道、土地类型和人口等数据作为权重因子,研究了该地区各类排放源污染物排放空间分布特征.结果表明,杭州市2015年SO_2、NO_x、CO、VOCs、PM_(10)、PM_(2.5)和NH_3年排放总量分别为22.20×10~3、108.17×10~3、192.10×10~3、134.94×10~3、78.12×10~3、27.65×10~3和59.75×10~3t.工业源是杭州市SO_2排放的主要来源,移动源对NO_x和CO的排放贡献最为显著,扬尘源是杭州市PM_(10)和PM_(2.5)排放的最主要来源,其次为工业源;VOCs排放的主要来源依次为工业源、天然源和移动源;NH_3排放主要来自农业源.从空间分布来看,排放主要集中在中心城区及其周边的萧山、下沙、大江东、余杭和富阳等工业企业相对密集的区域.本研究建立的排放清单在污染源覆盖范围和排放因子方面仍然存在一定的不确定性,建议在后续研究中重点开展低、小、散企业及本地化排放因子调查研究工作,进一步提升大气污染物排放清单的准确度.     

G20峰会期间杭州地区空气质量特征及气象条件分析

利用空气质量和气象要素的监测资料与再分析资料,分析了2016年G20峰会期间(2016年8月10日—9月20日)杭州及周边地区空气质量演变及区域特征,探讨了气象条件对G20峰会期间杭州空气质量的影响.结果表明:G20峰会管控期间,由于机动车排放大幅度降低,杭州NO_2浓度较管控前有所下降,对比周边城市降幅居于首位;而由于不利气象条件的影响,PM_(2.5)、PM_(10)、SO_2、CO和O_3浓度比管控前有不同程度的增长,但增幅相比周边城市较小,说明管控措施对杭州空气质量有一定的改善效果.9月7日管控措施结束后污染反弹现象明显.气象条件对杭州的空气质量有重要影响:在管控前,杭州晴热高温天气有利于O3的生成,偏东风相对洁净,污染传输较少;在管控期,杭州虽受到静稳天气和外来污染传输的影响,但得益于减排应急管控措施的有效实施,NO_2浓度下降幅度最大,其他污染物的增幅也较周边城市偏小;在管控后,气象条件不利于污染物的垂直扩散,受静稳天气和污染源恢复常态的影响,PM_(2.5)、PM_(10)、NO_2、SO_2和CO出现了整个研究时段的最大值,而台风"莫兰蒂"使得杭州PM_(2.5)、PM_(10)和O_3浓度出现了整个研究时段的最低值.     

重型柴油车实测排放因子和MOBILE6预测值的对比分析

利用车载尾气检测技术(PEMS)可以获得实时的机动车排放数据.笔者利用PEMS实测了重型柴油车的排放数据,在此基础上分析了CO、HC、NOx和PM的排放因子与速度、加速度的关系,同时使用MOBILE6模型,经过模型参数的校正,从而得到相应的预测排放因子,最终对排放因子的实测值、MOBILE6模型预测值以及欧Ⅱ的排放标准估测值进行了对比分析.     

北京地区PM10与秸秆燃烧排放单颗粒对比分析

采用场发射带能谱扫描电镜(FESEM/EDS)法分析北京怀柔地区PM10与秸秆燃烧排放颗粒的形貌特征和成分差异.结果显示:秸秆燃烧后排放颗粒物多为大粒径颗粒,成分上都含S、Cl和K元素.含有生物质燃烧标志元素K的PM10颗粒物多为含Si、Al和Na元素的燃煤飞灰和矿物颗粒,与秸秆燃烧排放颗粒组成化学元素差异明显.据此推...     

Concentrations of cadmium and lead heavy metals in Dardanelles seawater

Cadmium and lead were determined simultaneously in seawater by differential pulse stripping voltammetry (DPSV) preceded by adsoptive collection of complexes with 8-hydroxyquinoline (oxine) on to a hanging mercury drop electrode (HMDE). In preliminary experiments the optimal analytical condition for oxine concentration was found to be 2.10⁻⁵ M, at pH 7.7, the accumulation potential was −1.1 V, and the initial scannig potential was −0.8 V. The peak potentials were found −0.652 V for Cd and −0.463 V for Pb At the 60 s accumalation time. The limit of detection (LOD) and limit of quantitatification (LOQ) were found to be by voltammetry as 0.588 and 1.959 μg l⁻¹ (RSD, 5.50%) for Cd and 0.931 and 3.104 μg l⁻¹ (RSD, 4.10%) for Pb at 60 s stirred accumulation time respectively. In these conditions the most of the seawater samples are amenable for direct voltammetric determination of cadmium and lead using a HMDE. An adsorptive stripping mechanism of the electrode reaction was proposed. For the comparison, seawater samples were also analysed by ICP-atomic emission spectrometry method (ICP-AES). The applied voltammetric technique was validated and good recoveries were obtained.     

Spectroscopic Distribution of Dissolved Organic Matter in a Dam Reservoir Impacted by Turbid Storm Runoff

Spectroscopic characteristics of dissolved organic matter (DOM) in a large dam reservoir were determined using ultraviolet absorbance and fluorescence spectroscopy to investigate spatial distribution of DOM composition after turbid storm runoff. Water samples were collected along a longitudinal axis of the reservoir at three to four depths after a severe storm runoff. Vertical profiles of turbidity data showed that a turbid water layer was located at a middle depth of the entire reservoir. The spectroscopic characteristics of DOM samples in the turbid water layer were similar to those of terrestrial DOM, as demonstrated by the higher specific UV absorbance (SUVA) and the lower fluorescence emission intensity ratio (F ₄₅₀/F ₅₀₀) compared to other surrounding DOM samples in the reservoir. Synchronous fluorescence spectroscopy revealed that higher content of humic-like DOM composition was contained in the turbid water. Fluorescence excitation–emission matrix (EEM) showed that lower content of protein-like aromatic amino acids was present in the turbid water DOM. The highest protein-like fluorescence was typically observed at a bottom layer of each sampling location. The bottom water DOM exhibited extremely high protein-like florescence near the dam site. The particular observation was attributed to the low water temperature and the isolation of the local bottom water due to the upper location of the withdrawal outlet near the dam. Our results suggest that the distribution of DOM composition in a dam reservoir is strongly influenced by the outflow operation, such as selective withdrawal, as well as terrestrial-origin DOM inputs from storm runoff.     

Evaluation of ogawa passive sampling devices as an alternative measurement method for the nitrogen dioxide annual standard in El Paso, Texas

Nitrogen Dioxide (NO₂) is a common urban air pollutant that results from the combustion of fossil fuels. It causes serious human health effects, is a precursor to the formation of ground level ozone, another serious air pollutant, and is one of the six criteria air pollutants established by the United States (U.S.) Clean Air Act (CAA). Ogawa Passive Sampling Devices (PSDs) for NO₂ were collocated and operated at six NO₂ Federal Reference Method (FRM) monitor locations in the El Paso, Texas area for the 2004 calendar year. Passive samples were taken at 2-week, 3-week, and 4-week intervals and compared against the continuously operating FRM monitors. Results showed that the collective NO₂ annual arithmetic mean for all passive monitors was identical to the NO₂ mean for all FRM monitors. Of the individual locations, three passive annual NO₂ means were identical to their corresponding FRM means, and three passive annual NO₂ means differed from their corresponding FRM means by only one part per billion (ppb). Linear correlation analysis between all readings of the individual NO₂ PSDs and FRM values showed an average absolute difference of 1.2 ppb with an r ² of 0.95. Paired comparison between high and low concentration annual NO₂ sites, seasonal considerations, and interlab quality control comparisons all showed excellent results. The ease of deployment, reliability, and the cost-savings that can be realized with NO₂ PSDs could make them an attractive alternative to FRM monitors for screening purposes, and even possibly an equivalent method for annual NO₂ monitoring. More tests of the Ogawa NO₂ PSD are recommended for different ecosystem and climate regimes.