Preliminary comparison of trace metals in coastal aerosols between Qingdao and Liverpool

Aerosol samples were collected at two coastal suburban stations, Qingdao （China） in 1995-1996 and Liverpool （U.K.） in 1995, respectively. The samples were analyzed to determine the concentrations of trace metals （Cr, Zn, Cu, Co, Ni, Pb, V, and Cd） as well as A1, Fe and Mn. Data were examined to understand the difference of trace metals in aerosols between coastal zones downwind the developing area （near the Yellow Sea） and developed region （near the Irish Sea）. The results show that most elements at Qingdao have levels 4-5 times higher than those at Liverpool, particularly for the crust-dominated elements （e.g. Al, Fe and Mn）. Moreover, the aerosol composition at Qingdao is higher in spring than in summer, underlying the influence of westerlies and local emissions in combination, whereas seasonal change of aerosol composition is not significant at Liverpool. The enrichment factors for the crustal source elements （EFcrust） at Liverpool are much higher than those at Qingdao. The contributions from the pollutant source （Rp） for some trace metals like Cu, Pb, Zn and Cd are 〉90% at Qingdao and Liverpool, suggesting overwhelming anthropogenic contributions to these metals. The contributions from crustal source （Re） for trace metals tend to increase with higher aerosol levels and Al concentration at Qingdao, indicating a good correlation between the crust-dominated component and the air mass. At Liverpool, the Rc values for trace metals are positively correlated with Al concentrations instead of with aerosol mass, suggesting that Al in aerosols represents the crustal component even though the aerosols come from different sources.     

热化学硫酸盐还原作用对碳酸盐岩气藏的化学改造——以川东北地区长兴组-飞仙关组气藏为例

目前在川东北地区长兴组—飞仙关组已发现普光、渡口河、铁山坡、罗家寨等多个高含H2S的大、中型气田。通过天然气地球化学特征、流体包裹体盐度和岩心及薄片的镜下详细观察后认为,川东北地区长兴组—飞仙关组的大多数气藏遭受了热化学硫酸盐还原作用(TSR)的化学改造,TSR的改造主要表现在3个方面:1使C2 重烃相对于CH4、12C相对于13C优先被消耗,造成天然气干燥系数变大和碳同位素变重;2由于TSR产生的大量淡水的加入,使气藏的原生地层水被稀释,造成地层水盐度降低;3TSR相关流体(烃类和H2S等)与储层岩石之间的相互作用使储层被溶蚀和硬石膏发生蚀变,造成储层孔隙度增大,从而对改善其物性具有重要意义。     

用硫酸镁和造纸草浆黑液制备吸附剂及其对活性黄ST-4RFN吸附研究

利用硫酸镁和造纸草浆黑液制备含镁氧化合物的吸附剂,通过化学分析、表面性质分析、X射线衍射和红外光谱等对吸附剂进行了表征.考察了吸附剂焙烧温度、投加量、吸附时间以及pH值等因素对活性黄ST-4RFN吸附性能的影响,吸附过程可用Freundlich模型来描述.     

新型珊瑚海水混凝土力学性能试验研究

为了解决全珊瑚海水混凝土(coral aggregate seawater concrete,简称CASC)的脆性问题,采用碱式硫酸镁水泥(basic magnesium sulfate cement,简称BMSC)为胶凝材料和剑麻纤维为增韧材料制备了一种新型全珊瑚海水混凝土(NCASC),系统测定了基本力学性能,并与普通硅酸盐水泥制备的CASC、碱式硫酸镁水泥砂石混凝土(basic magnesium sulfate cement concrete,简称BMSCC)、普通砂石混凝土(ordinary portland cement concrete,简称OPC)以及普通轻骨料混凝土(lightweight aggregate concrete,简称LAC)的力学性能进行对比。结果表明:立方体抗压强度(f_(cu),m)在15~35 MPa范围内的NCASC的轴心抗压强度(f_c,m)、劈裂抗拉强度(f_(sp),m)与f_(cu),m之间具有较显著的线性关系;对于f_(cu),m为15~35 MPa的混凝土,相同强度NCASC的f_c,m高于OPC、LAC及BMSCC,其f_c,m与f_(cu),m比值最大,大致在0.85~0.96之间,NCASC的f_(sp),m比OPC和LAC高,但比BMSCC低,且随着强度的提高,OPC与NCASC的f_(sp),m间的差距在增大,而LAC和BMSCC与NCASC的f_(sp),m间的差距在缩小;在强度等级C15~C55的范围中,NCASC和CASC的f_(sp),m、f_c,m与f_(cu),m之间的关系基本可以采用相同的线性回归方程来描述,利用这两个回归线性方程得到对应于标准强度等级的CASC和NCASC的f_(sp),m和f_c,m数据,为CASC力学性能研究与结构设计提供参考依据。     

离子色谱法测定海水中氯离子和硫酸根离子

氯离子和硫酸根离子是海水中重要的无机阴离子,在研究海洋生态变化、海洋循环作用过程与海洋全球气候变化等领域具有重要的指示意义。其测定方法较多,但缺少相应的测试方法。本文对测定海水中Cl^-,SO₄^2-的离子色谱方法进行了优化,选用IonPacAS14碳酸盐选择性离子色谱柱,以3.5 mmol/L Na₂CO₃+1 mmol/L NaHCO₃为流动相,可消除海水样品中碳酸盐及其他阴离子的干扰。该方法对Cl^-检出限为0.29 mg/L,线性相关系数r²=0.999 2,对SO₄^2-检出限为0.42 mg/L,线性相关系数r²=0.997 9。样品的加标回收率在95%~102%,Cl^-和SO₄^2-的相对标准偏差分别为1.92%和4.18%。该方法简便、迅速、灵敏、准确度高,可满足批量海水样品中Cl^-与SO₄^2-的准确测试。     

塔克拉玛干沙漠腹地气溶胶不同波段散射系数比较

利用2010年塔克拉玛干沙漠腹地塔克拉玛干沙漠大气环境观测试验站(下文简称"塔中")多波段(450、525、635 nm)积分浊度计和PM_(10)自动监测仪观测资料,并结合塔中地面气象观测资料,分析了沙漠腹地不同波段气溶胶散射系数的变化特征。分析结果显示:(1)塔中气溶胶对635 nm太阳辐射的散射作用最大,其次是525 nm,最小为450 nm。三波段(450、525、635 nm)散射系数平均值分别为:288.0、318.4、443.8 Mm~(-1)。(2)三波段散射系数日变化与PM_(10)质量浓度一致,都呈单峰变化:夜间高、白天低。在日变化中,散射系数始终保持635 nm最大,525 nm次之,450 nm最小。(3)三波段散射系数年变化基本一致,都与PM_(10)变化接近。1—5月中,除3月散射系数是450 nm最大外,另外4个月均是635 nm最大,450 nm次之,525 nm最小。6—12月散射系数都是635 nm最大,525 nm次之,450 nm最小。(4)三波段散射系数均是沙尘暴下最大,扬沙次之,浮尘最小。不同沙尘天气下,塔中气溶胶对635 nm散射作用都是最明显的,对450 nm和525nm散射作用不同:沙尘暴时,对525 nm的散射强于450 nm,在扬沙和浮尘时,对450 nm的散射强于525 nm,尤其在浮尘时。(5)三波段散射系数与PM_(10)质量浓度都呈显著正相关,PM_(10)质量浓度与525 nm散射系数相关程度最大,450 nm次之,635 nm最小。但是季节内相关程度略有差异:春、冬季PM_(10)浓度与450 nm散射系数相关程度最大,525 nm次之,635 nm最小。夏、秋季则是525nm最大。     

Response of the Tropical Indian Ocean to Greenhouse Gases and Aerosol Forcing in the GFDL CM3 Coupled Climate Model

The response of the tropical Indian Ocean (TIO) to greenhouse gases (GHGs) and aerosols are investigated based on historical single-forcing and all-forcing simulations using the Geophysical Fluid Dynamics Laboratory Climate Model, version 3 (GFDL CM3). Results reveal a positive Indian Ocean Dipole (pIOD)-like pattern in GHG forcing but a negative Indian Ocean Dipole (nIOD)-like pattern in aerosol forcing. The GHG-induced pIOD-like pattern features less (more) sea surface temperature (SST) warming over the southeastern (western) TIO, accompanied by equatorial easterly anomalies, as well as a shallower thermocline off Sumatra. The aerosol-induced nIOD-like pattern displays the reverse features, characterized by less (more) SST cooling over the southeastern (western) TIO, anomalous equatorial westerlies, and a deeper thermocline off Sumatra. Although the aerosol-induced pattern appears to resemble a reversal of the GHG-induced pattern, there is a strong asymmetry in the SST changes over the southeastern TIO, where the cooling responding to aerosol forcing exceeds the warming in response to GHG forcing, and a negative SST residual is thus produced. A mixed-layer heat budget analysis suggests that the negative SST residual results mainly from asymmetric responses of shortwave radiation, zonal advection, and diffusion to GHGs and aerosols. For comparison, the formation processes for the negative SST skewness over the southeastern TIO between the internal pIOD and nIOD are also discussed.     

Why Is the Climate Forcing of Sulfate Aerosols So Uncertain?

l. IntroductionAlthough the aerosol has been recognized as an important factor which has innuence onthe past, present and future climate for a long time, it still has much uncertainty in assessingits climate forcing. The direct radiative forcing of sulfate aerosols has been estimated rangingfrom --0.3 W/ m2 to --0.9 W/ m2 in recent publications (Charlson et al., l992, Kiehl andBriegleb l993; Taylor and Penner 1994, Boucher and Anderson l995, Kieh1 and Rodhe l995;Chuang et al., l997, Penne…     

Atmospheric nuclei in the remote free-troposphere

During May-June of 1990 an extensive flight series to survey aerosol present in the upper-troposphere was undertaken aboard the NASA DC-8 as part of the CLObal Backscatter Experiment (GLOBE). About 50,000 km were characterized between 8–12 km altitude and between 70°N and 58°S. Aerosol with diameters greater than 3nm were counted and sized with a combination of condensation nuclei counters and optical particle counters. Aerosol number and mass concentrations were separately identified with regard to both refractory and volatile components. Regions of the free-troposphere with the lowest mass concentrations were generally found to have the highest number concentrations and appeared to be effective regions for new particle production. These new particle concentrations appear inversely related to available aerosol surface area and their volatility suggests a sulfuric acid composition. The long lifetime of these new particles aloft can result in their growth to sizes effective as CN and CCN that can be mixed throughout the troposphere.     

离子色谱法同时测定地质样品中氟氯磷硫

本文研究了离子色谱同时测定地质样品中F~-、Cl~-、PO_4~(3-)、SO_4~(2-)的前处理过程,选择了色谱测定最佳条件。在Na_2CO_3全熔的样品溶液中,加入(NH_4)_2CO_3使Si、Al随大多数金属离子同时沉淀;再用预处理柱除去熔剂引入的大量Na~+及CO_3~(2-)消除其干扰;并在流出液中补加相应试剂与淋洗液相匹配,实现了多种地质样品中F~-、Cl~-、PO_4~(3-)和SO_4~(2-)的测定。方法检出限(3s,μg/ml)分别为F~-0.05、Cl~-0.1、PO_4~(3-)0.3、SO_4~(2-)0.5。测定范围为F~-0.05—3μg/ml,Cl~-0.1—6μg/ml,PO_4~(3-)0.3 —30μg/ml,SO_4~(2-)0.5—30μg/ml。