Compositions and sources of organic acids in fine particles (PM2.5) over the Pearl River Delta region, south China

Organic acids as important constituents of organic aerosols not only influence the aerosols' hygroscopic property, but also enhance the formation of new particles and secondary organic aerosols. This study reported organic acids including C14–C32fatty acids, C4–C9dicarboxylic acids and aromatic acids in PM2.5collected during winter 2009 at six typical urban, suburban and rural sites in the Pearl River Delta region. Averaged concentrations of C14–C32fatty acids, aromatic acids and C4– C9 dicarboxylic acids were 157, 72.5 and 50.7 ng/m3, respectively. They totally accounted for 1.7% of measured organic carbon. C20–C32fatty acids mainly deriving from higher plant wax showed the highest concentration at the upwind rural site with more vegetation around, while C14–C18fatty acids were more abundant at urban and suburban sites, and dicarboxylic acids and aromatic acids except 1,4-phthalic acid peaked at the downwind rural site. Succinic and azelaic acid were the most abundant among C4–C9dicarboxylic acids, and 1,2-phthalic and 1,4-phthalic acid were dominant aromatic acids. Dicarboxylic acids and aromatic acids exhibited significant mutual correlations except for 1,4-phthalic acid, which was probably primarily emitted from combustion of solid wastes containing polyethylene terephthalate plastics. Spatial patterns and correlations with typical source tracers suggested that C14–C32fatty acids were mainly primary while dicarboxylic and aromatic acids were largely secondary. Principal component analysis resolved six sources including biomass burning, natural higher plant wax, two mixed anthropogenic and two secondary sources; further multiple linear regression revealed their contributions to individual organic acids. It turned out that more than 70% of C14–C18fatty acids were attributed to anthropogenic sources, about 50%–85% of the C20–C32fatty acids were attributed to natural sources, 80%–95% of dicarboxylic acids and 1,2-phthalic acid were secondary in contrast with that 81% of 1,4-phthalic acid was primary.     

氟化铵制备氟化钙最优条件研究

试验采用氟化铵与石灰石粉、石灰乳反应制取氟化钙,研究了反应温度、物料浓度、物料过量系数等各主要参数变化对氟化钙结晶、过滤速度、氟收率及其含量的影响,摸索出最优反应条件。     

碳酸钙中的碳能被微藻利用吗

碳酸钙中的碳能否被微藻利用这一问题一直处于争论中。本文在开放与隔离空气CO2环境下用含有碳酸钙粉末和不同浓度乙酰唑胺的培养液培养衣藻和小球藻。通过双向同位素示踪技术,定量描述出不同条件下微藻对碳酸钙碳源的利用份额。在隔离空气CO2的环境下,微藻对碳酸钙碳源的利用份额明显大于开放环境下。在开放环境下,随着培养液中乙酰唑胺浓度增加,生物量减少,微藻对固有无机碳源的利用份额减少,对碳酸钙碳源的利用份额增加。在隔离空气CO2的环境下,随着培养液中乙酰唑胺浓度增加,微藻生物量增加,衣藻对固有无机碳源的利用份额增加,对碳酸钙碳源的利用份额减少,而小球藻反之。微藻主要是通过利用碳酸钙溶蚀的可溶性无机碳(DIC)这种间接方式来利用碳酸钙碳源。而外界大气CO2浓度和胞外碳酸酐酶是影响碳酸钙溶解的重要因素,因此其也明显的影响着微藻对碳酸钙碳源的利用。     

重庆市主城区大气细颗粒物污染特征与来源解析

重庆市主城区大气细颗粒物(PM_(2.5))浓度从1990s的100μg·m~(-3)下降至当前的约70μg·m~(-3),但仍高于环境标准限值.为探讨重庆市主城区PM_(2.5)化学组成与来源特征,于2012—2013年在渝北区大气超级站利用四通道采样仪连续采集了颗粒物样品,分析了其中水溶性离子、碳质组分和无机元素含量.采样期间,重庆市主城区大气PM_(10)和PM_(2.5)的年日均浓度分别为103.9和75.3μg·m~(-3),扩散条件不利的冬季,细颗粒物污染较为严重.受静稳天气影响的1月和2月,受沙尘影响的3月,及二次转化显著的6月是重庆市细颗粒物污染较重的月份.重庆市PM_(2.5)组成以有机物(OM,30.8%)为主,其次为硫酸盐(SO_4~(2-),23.0%)、硝酸盐(NO_3~-,11.7%)、铵盐(NH_4~+,10.9%)、地壳物质(Soil,8.2%)、元素碳(EC,5.2%)、K~+(1.1%)、Cl~-(1.0%)和微量元素(Trace,0.6%).较高的SO_4~(2-)浓度和逐步上升的[NO_3~-]/[SO_4~(2-)]比值反映了重庆市燃煤污染较重,同时机动车污染比例逐步增加.采用主因子分析/绝对主因子得分法解析了重庆城区细颗粒物5类主要来源是:二次粒子(41.7%)、燃煤(15.6%)、建筑/道路尘(12.4%)、土壤尘(11.0%)和工业尘(10.4%),通过各污染源季节变化及与其他结果对比,该源解析结果能够较可靠反映重庆市细颗粒物的来源信息.     

Modeling the impacts of calcite precipitation on the epilimnion of an ultraoligotrophic, hard-water lake

A mass-balance model of calcite precipitation was developed to investigate the interactions of the varied processes governing the generation and fate of calcite in lakes. The model was used in conjunction with data to assess the evolution and impact of calcite precipitation for calcareous, ultraoligotrophic Torch Lake, Michigan (USA). This lake is an ideal setting for implementation of a baseline modeling study of calcite precipitation where the physical drivers could be evaluated without being dominated, as in many systems, by biological processes. The model provides a representation of calcite precipitation with particulate surface area changing over time, and demonstrates that it is possible for the change in water clarity to be explained by calcite precipitation employing standard optical models. Using the mass balance model to quantify the roles of the various chemical, biological and physical processes interacting in the lake's epilimnion, it was shown that the seasonal temperature rise and air-water CO₂ exchange drive calcite precipitation much more than primary production for this ultraoligotrophic system.     

DRY STREAM REACHES IN CARBONATE TERRANES: SURFACE INDICATORS OF GROUND-WATER RESERVOIRS1

ABSTRACT: The method of identifying dry stream reaches in carbonate terrane as surface indicators of potential ground-water reservoirs offers a valuable exploration technique that is more rapid and less expensive than traditional exploration methods involving random test drilling. In areas where dry stream reaches occur, subsurface drainage successfully competes with surface drainage, and sheet-like dissolution openings have developed parallel to bedding creating the ground-water reservoir. The occurrence and hydraulic characteristics of such reservoirs are highly variable, as attested to by the wide range of well yields. Union Hollow in south-central Tennessee is the setting for a case study that illustrates the application of the dry stream reach technique. In this technique, dry stream reach identification is based on two types of readily acquired information: (1) remotely sensed black and white infrared aerial photography; and (2) surface reconnaissance of stream channel characteristics. Test drilling in Union Hollow subsequent to identification of the dry reach proved that a localized ground-water reservoir was present.     

南京粉质粘土与粉砂互层土及粉细砂的抗液化性能试验研究

南京粉质粘土与粉砂互层土为粉质粘土与粉细砂交互沉积,呈现“千层饼”状外貌;南京粉细砂是一种以片状颗粒成分为主的粉细砂,与通常的圆形颗粒石英砂有一定区别,片状颗粒成分使得南京粉细砂具有各向异性的性质。通过南京粉质粘土与粉砂互层土及粉细砂对比液化试验,对其试验成果进行分析,从中发现:无论是偏压固结还是均压团结,当固结压力α_2=100 kPa时,南京粉质粘土与粉砂互层土的液化剪应力比比南京粉细砂的大得多;而当固结压力α_2=200kPa时,两种土的液化剪应力比相当接近。因而,对于重大工程应该慎重考虑它们的液化可能性。     

Nitrogen Budget of a Spruce Forest Ecosystem After Six-year Addition of Ammonium Sulphate in Southwest Sweden

A nitrogen (N) budget was constructed for a period of 6 years (1988–1993) in a Norway spruce stand with current deposition of 19 kg N and 22 kg S ha⁻¹ year⁻¹. The stand was fertilized annually by addition of 100 kg N and 114 kg S ha⁻¹ (NS). Above and below ground biomass, litterfall, fine- root litter production, soil solution and net mineralization were measured to estimate pools, fluxes and accumulation of nitrogen. The average needle litterfall in control (C) and NS plots in 1993 was 2.2 and 2.5 ton ha⁻¹ year⁻¹, respectively. The fine root litter production prior to treatment (1987) was 4.4 ton ha⁻¹ year⁻¹ and after treatment (1993) it was 4.5 and 3.9 ton ha⁻¹ year⁻¹ in C and NS plots, respectively. Net N mineralization in the soil profile down to 50 cm was estimated to be 86 and 115 kg ha⁻¹ year⁻¹ in C and NS plots, respectively in 1992. During the treatment period the uptake of N in the needle biomass in C and NS plots was 29 and 77 kg ha⁻¹ year⁻¹, respectively. No N was accumulated in needles of C plot where the NS plots accumulated 34 kg ha⁻¹ year⁻¹. Of the annually added inorganic N to NS plots 47% was accumulated in the above and below ground biomass and 37% in the soil. N fluxes via fine-root litter production in the C plots were much higher (54 kg ha⁻¹ year⁻¹) than that via litterfall (29 kg ha⁻¹ year⁻¹). The corresponding values in the NS plots were 65 and 43 kg ha⁻¹ year⁻¹, respectively. Most of the net N mineralization occurred in the FH layer and upper mineral soil. It is concluded that fine root litter and litterfall play an important role in the cycling of N. Despite a high N uptake the losses of N in litterfall and fine root litter resulted in an incorporation of N in soil organic matter.     

漂粉精生产过程中危险有害因素分析

通过对天津市漂粉精生产企业进行研究,分析了漂粉精生产过程可能存在的危险有害因素是尘毒、火灾、爆炸、灼伤、机械伤害等,并针对上述危险有害因素提出相应的防毒,防火防爆,防灼伤,防机械伤害等安全技术措施及安全管理措施.     

THE USE OF MAGNESIUM CARBONATE IN CHLOROPHYLL DETERMINATIONS1

Abstract: Chlorophyll analyses of both laboratory cultures and natural aquatic samples were unaffected by the use of magnesium carbonate. Equal volumes of the samples (at various pH values) were pipetted onto 0.45 micrometer filters with and without magnesium carbonate. Chlorophyll concentrations were determined for each filtered sample and those frozen for specified times. In all samples tested there was no difference either in the retention of algae or in the stability of chlorophyll over the time period and pH range tested.