胶州湾水体中的二氧化碳体系

采用库仑滴定法测定了胶州湾海域４个航次的总二氧化碳,根据测定的总二氧化碳的数据计算了二氧化碳各分量的含量及二氧化碳分压,得到了胶州湾水体中二氧化碳体系的平面分布、垂直分布及周日变化规律,并对结果进行了初步探讨 。     

The influence of island generated eddies on the carbon dioxide system, south of the Canary Islands

Measurements of surface partial pressure of CO₂ and water column alkalinity, pH_T, nutrients, oxygen, fluorescence and hydrography were carried out, south of the Canary Islands during September 1998. Cyclonic and anticyclonic eddies were alternatively observed from the northwestern area to the central area of the Canary Islands. Nutrient pumping and vertical uplifting of the deep chlorophyll maximum by cyclonic eddies were also ascertained by upward displacement of dissolved inorganic carbon. A model was applied to determine the net inorganic carbon balance in the cyclonic eddy. The fluxes were determined considering both the diffusive and convective contributions from the upward pumping and the corresponding horizontal transport of water outside the area. An increase in the total inorganic carbon concentration in the upper layers inside the eddy field of 133 mmol C m^− 2 d^− 1 was determined. The upward flux of inorganic carbon decreased the effect of the increased primary production on the carbon dioxide chemistry. The reduced fCO₂ inside the cyclonic eddy, 15 μatm lower than that observed in non-affected surface water, was explained by thermodynamic aspects, biological activity, eddy upward pumping and diffusion and air–sea water exchange effects.     

深海热液区主要成分的高温高压拉曼光谱分析

模拟深海热液口环境(最高压力40 MPa,最高温度350℃),对深海热液区的主要成分CO2、CH4及其混合物的水溶液在不同压力和温度条件下的拉曼光谱进行探测和分析,结果显示:常温低压下CO2水溶液的Fermi双峰分别位于1 384.9 cm-1和1 278.3 cm-1处,CH4的水溶液拉曼峰υ1位于2 912.1 cm-1处,均比其气相的拉曼频移小;常温下CO2和CH4水溶液的拉曼特征峰随压力(≤40 MPa)的变化均不明显;在40 MPa的压力下随着温度的升高(≤350℃),CO2水溶液的Fermi双峰分别向高波数区移动了约3.4 cm-1和7.0 cm-1,而CH4水溶液的拉曼峰υ1向低波数区移动了约3.1cm-1;混合后升温过程中CO2的双峰分别向高波数区移动了约4.3 cm-1和3.8 cm-1,CH4的特征峰υ1向低波数区移动了4.5 cm-1。说明在室温到350℃范围内温度的变化对CO2和CH4水溶液拉曼频移有影响,频移量与温度线性相关,而压力在≤40 MPa范围内的改变对拉曼频移影响不明显。     

二氧化氯控制欧洲鳗细菌性疾病

以二氧化氯作为一种新型的消毒剂和杀菌剂 ,以传统含氯制剂 (如漂白粉、二氯异氰尿酸钠、三氯异氰尿酸 )作为对照 ,比较其在治疗欧洲鳗细菌性疾病及改善养殖水质方面的显著特性 ,其作用活性与环境 (如 p H、温度、氨及有机物 )因子的关系。结果表明 ,二氧化氯 (Cl O2 )对爱德华氏菌、嗜水气单胞菌和柱状屈挠杆菌有很好的杀灭效果 ,能迅速治愈欧洲鳗的赤鳍病和肝肾病 ,且能有效改善养殖水体 ,水中生化需氧量比对照组下降 10 %～ 30 % ,化学耗氧量下降 5% ,溶氧量提高 8%～ 10 %。当二氧化氯体积分数为 8m L/m3时 ,其杀菌率均高达 90 %以上 ,为氯制剂的 1.8倍 ,且活性不受环境因子的影响     

山东济宁许厂煤矿下组煤瓦斯与二氧化碳开发利用前景及存在的问题

许厂煤矿下组煤中蕴藏着较为丰富的瓦斯、二氧化碳资源。下组煤位于瓦斯风化带内,含瓦斯、二氧化碳和氮气等气体,瓦斯含量与埋藏深度呈正相关关系,主要存在低含量瓦斯、二氧化碳抽采率、二氧化碳资源化转换等技术方面的问题。从国家相关优惠政策、资源优势、煤与煤层气一体化开发技术、近水平长钻孔定向钻进技术、煤层压裂造缝技术、煤层注气增产技术和瓦斯、二氧化碳气体提纯技术等关键技术的发展程度,结合煤矿的下组煤层的开采方案,认为许厂煤矿有着较好的煤炭与瓦斯、二氧化碳一体化开发利用前景。     

Targeting carbon dioxide removal in the European Union

In principle, many climate policymakers have accepted that large-scale carbon dioxide removal (CDR) is necessary to meet the Paris Agreement’s mitigation targets, but they have avoided proposing by whom CDR might be delivered. Given its role in international climate policy, the European Union (EU) might be expected to lead the way. But among EU climate policymakers so far there is little talk on CDR, let alone action. Here we assess how best to ‘target’ CDR to motivate EU policymakers exploring which CDR target strategy may work best to start dealing with CDR on a meaningful scale. A comprehensive CDR approach would focus on delivering the CDR volumes required from the EU by 2100, approximately at least 50 Gigatonnes (Gt) CO₂, according to global model simulations aiming to keep warming below 2°C. A limited CDR approach would focus on an intermediate target to deliver the CDR needed to reach ‘net zero emissions’ (i.e. the gross negative emissions needed to offset residual positive emissions that are too expensive or even impossible to mitigate). We argue that a comprehensive CDR approach may be too intimidating for EU policymakers. A limited CDR approach that only addresses the necessary steps to reach the (intermediate) target of ‘net zero emissions’ is arguably more achievable, since it is a better match to the existing policy paradigm and would allow for a pragmatic phase-in of CDR while avoiding outright resistance by environmental NGOs and the broader public.

Key policy insights

• Making CDR an integral part of EU climate policy has the potential to significantly reshape the policy landscape.

• Burden sharing considerations would probably play a major role, with comprehensive CDR prolonging the disparity and tensions between progressives and laggards.

• Introducing limited CDR in the context of ‘net zero’ pathways would retain a visible primary focus on decarbonization but acknowledge the need for a significant enhancement of removals via ‘natural’ and/or ‘engineered’ sinks.

• A decarbonization approach that intends to lead to a low level of ‘residual emissions’ (to be tackled by a pragmatic phase-in of CDR) should be the priority of EU climate policy.

     

pCO2 and carbon fluxes across sea-air interface in the Changjiang Estuary and Hangzhou Bay

Partial pressure of CO2(pCO2) was investigated in the Changjiang(Yangtze River) Estuary,Hangzhou Bay and their adjacent areas during a cruise in August 2004,China.The data show that pCO2 in surface waters of the studied area was higher than that in the atmosphere with only exception of a patch east of Zhoushan Archipelago.The pCO2 varied from 168 to 2 264 μatm,which fell in the low range compared with those of other estuaries in the world.The calculated sea-air CO2 fluxes decreased offshore and varied from -10.0 to 88.1 mmol m-2 d-1 in average of 24.4 ± 16.5 mmol m-2 d-1.Although the area studied was estimated only 2 × 104 km2,it emitted(5.9 ± 4.0) × 103 tons of carbon to the atmosphere every day.The estuaries and their plumes must be further studied for better understanding the role of coastal seas playing in the global oceanic carbon cycle.     

On the pH-dependent formation constants of iron(III)-sulfur(IV) transient complexes

An experimental study is described of Fe(III)-S(IV) formation constants measured as a function of pH (1–3), ionic strength (0.2–0.5 M) and [Fe(III)] _T (2.5–5.0×10^–4 M) using a continuous-flow spectrophotometric technique to make observations 160 ms after mixing. Preliminary experiments using pulse-accelerated-flow (PAF) spectrophotometry to measure rate constants on a microsecond timescale are also described. The conditional formation constant at 25 °C can be modeled with the following equation: {ie307-1} where {ie307-2}K ₇ andK ₈ can be interpreted as intrinsic constants for the coordination of HSO ₃ ^– by FeOH²⁺ and Fe³⁺, respectively, but until further evidence is obtained they should be regarded as fitting constants. PAF spectrophotometry showed that the initial reaction of Fe(III) with S(IV) (pH 2.0) is characterized by a second-order rate constant of 4×10⁶ M^–1 s^–1 which is comparable to rate of reaction of FeOH²⁺ with SO ₄ ^2– . However, the PAF results should be regarded as preliminary since unexpected features in the initial data indicate that the reaction may be more complex than expected.     

Measurements of Reaction Coefficients of NO2 and HONO on Aerosol Particles

The reaction coefficients of nitrogen dioxide and nitrous acid with monodisperse sodium chloride and ammonium sulphate aerosols have been measured in a flow reactor at atmospheric pressure. These experiments were performed at relative humidities above and below the deliquescence points of both aerosols (r.h. 50 and 85%) at 279 K. The results for NO₂ afford a reaction coefficient in the range (2.8–10) × 10^-4 and for HONO, (2.8–4.6) × 10^-3. For both species, there appears to be an enhancement of the reaction coefficient on sodium chloride aerosol at 50% r.h. The results are compared with reaction coefficients determined by other experimental methods. A good agreement is found for both gases between this method and the coated denuder method previously developed in our research laboratories (Msibi et al., 1993) and with the majority of other published data for NO₂. In the case of HONO, our estimate of reaction coefficient is smaller than, or at the lower limits of the ranges reported by other published studies.     

阿尔泰东南缘布尔根地区造山带型金矿床硫铅同位素特征及地质意义

阿尔泰东南缘布尔根地区造山带型金矿床受韧性剪切带控制,有两种矿化类型：一为石英脉型,另一种为糜棱岩型。糜棱岩型金矿硫化物的δ^34S值变化于-10.009‰～-2.819‰,平均值为-5.29‰,石英脉型金矿硫化物的δ^34S值变化于-0.062‰～-1.688‰,平均值为-1.0575‰。布尔根地区金矿床的金属硫化物样品具有较窄的^207Pb／^204Pb比值,变化于17.71～18.35;相对较高的^207Pb／^204Pb比值为15.31～15.64和^208Pb／^204Pb比值为37.13～38.07,铅同位素分析结果表明,该区金矿床成矿物质铅来源于地幔及下地壳。硫、铅同位素特征反映了布尔根地区金矿床成矿物质具有多来源特征。