中国县域能源消费碳排放估算及其空间分布

将传统的碳排放因子法与人口权重分配法相结合,估算了2015年中国2 170个县域的碳排放量,并将县域分为高/低碳排放量-高/低碳排放强度的4种类型。分析表明:(1)县域的平均碳排放量为1 287×103 t,但差异较大,空间分布上整体呈现东高西低;81.58%的县域的碳排放强度在0.01～1.05t/万元,空间分布上呈现西部及西北高、东部及东南低。(2)低碳排放量-低碳排放强度类县域数量最多(占45.81%),在全国除东南沿海区域均有分布;高碳排放量-低碳排放强度类县域分布在中国部分华北地区及东部、东南沿海地区,中部也有少量分布;高碳排放量-高碳排放强度类县域主要分布在东北三省;低碳排放量-高碳排放强度类县域主要分布在中国西北的西藏自治区、新疆维吾尔自治区和青海省,同时山西省境内也有较多分布。(3)整体看,中低收入、处于发展提速的中西部县域发展仍需预留一定的碳排放空间;对于高收入的东部县域,则要提出更高的减排要求。     

Estimating and analyzing the spatial distribution of soil organic carbon in China

Research on the terrestrial carbon cycle is an important component in the study of global change. Soil organic carbon, as the main part of the terrestrial carbon reservoir, plays an important role in the Earth's carbon cycle. To accurately estimate soil organic carbon storage, its composition and dynamic change must be determined. This presents a challenge to research on the soil carbon cycle, especially in China where the nationwide soil organic carbon reservoir largely remains unknown. This paper reports a research project that attempts to estimate the nationwide soil organic carbon reservoir. Data from 2473 soil profiles from the second national soil survey were collected and GIS technology was employed to quantify the national soil carbon reservoir. The analytical results show that the total amount of soil organic carbon is about 92.4 Pg (Pg = 10(15) g) and that the average carbon density is about 10.53 kg C m(-2). The spatial distribution of soil organic carbon was also analyzed and mapped. This study presents basic data and an analysis method for carbon-cycle studies and also provides scientific support for policy-making efforts to control CO2 emissions in China.     

长江下游湖泊中可溶性有机碳的时空分布

2001年7月至2003年1月对长江下游的太湖、巢湖和龙感湖水体中可溶性有机碳(DOC)的时空分布进行了研究。结果显示．太湖水体中DOC的平均浓度最高．巢湖次之,龙感湖最低;秋季水体中的DOC浓度较冬季高;藻型湖泊水体中DOC浓度较草型湖泊高;下午水体中DOC的浓度较上午高。水体中DOC浓度的垂直分布无明显的规律性。从周年来看．DOC的浓度随温度的升高而升高。     

Modeling of gas-phase photodegradation of chloroform and carbon tetrachloride

The relationship between the irradiance in a photoreactor and the rate of photodegradation of organics is essential in the scaling-up of photoreactors to treat large volumes of air contaminated with organic pollutants. In this study, the analysis is adopted to compare results obtained from two different photoreactors. Initially, the applicability of two light models in calculating the irradiance in two photoreactors was evaluated. Thereafter, kinetic models of ultraviolet (UV) photooxidation of chloroform (CHCl3) and carbon tetrachloride (CCl4) from the archived literature were tested using experimental data under various operating conditions and different irradiances. Sensitivity analyses were conducted using different values of model parameters to determine the significance of each parameter on the photodegradation of the two chlorinated organics. For compounds that undergo photolysis as a primary mode of degradation, the rate of photodegradation at low initial concentrations can be predicted easily by the following equation: d[C]/dt = -2.303Iave, lambdaepsilonlambdaphilambda[C]. Although the photodegradation of chlorinated organic compounds in dry and humid air can be predicted well, it is difficult to predict the Cl* sensitized oxidation occurring at high initial concentrations. A good agreement between the simulated and experimental data provides a sound basis for the design of large-scale reactors.     

四氯化碳的生产与应用及其淘汰策略

四氯化碳是一种消耗臭氧层物质,其生产和消费都面临着严峻的淘汰形势.简要叙述了四氯化碳的生产技术,以四氯化碳为原料生产大宗化学品和精细化学品的转化技术,四氯化碳作为化工助剂在我国的应用情况以及相应的淘汰方法和技术进展.     

四氯化碳的生产与应用及其淘汰策略

四氯化碳是一种消耗臭氧层物质，其生产和消费都面临着严峻的淘汰形势。简要叙述了四氯化碳的生产技术，以四氯化碳为原料生产大宗化学品和精细化学品的转化技术，四氯化碳作为化工助剂在我国的应用情况以及相应的淘汰方法和技术进展。     

Formation of chloroform and carbon tetrachloride in foods treated with sodium hypochlorite

The formation of chloroform and carbon tetrachloride during the treatment of fresh vegetable homogenate with sodium hypochlorite was studied.When a n-hexane extract of the reaction mixture of fresh vegetables and sodium hypochlorite was analysed by gas chromatography, chloroform and carbon tetrachloride were detected, and many unidentified peaks were also observed. The formation conditions of chloroform and carbon tetrachloride were studied. The mechanism of chloroform formation may be different from that of carbon tetrachloride according to the study of pH on the formation of both compounds. The formation of chloroform is much greater than that of carbon tetrachoride.     

Degradation of carbon tetrachloride in the presence of iron and sulphur containing compounds

The effect of several sulphur compounds: sodium sulphate, sodium sulphide, ferrous sulphide,pyrite and an organosulphonic acid on the kinetics of the iron (Fe °) induced degradation of carbon tetrachloride was examined under aerobic conditions. It was observed that all of the sulphur compounds investigated significantly accelerated the reaction. The mechanisms of the processes studied as well as their possible influence on the efficiency of the iron-induced dehalogenation of pollutants, both in situ and in above-ground treatment are discussed.     

Removal of sulfamethoxazole and sulfapyridine by carbon nanotubes in fixed-bed columns

Sulfamethoxazole (SMX) and sulfapyridine (SPY), two representative sulfonamide antibiotics, have gained increasing attention because of the ecological risks these substances pose to plants, animals, and humans. This work systematically investigated the removal of SMX and SPY by carbon nanotubes (CNTs) in fixed-bed columns under a broad range of conditions including: CNT incorporation method, solution pH, bed depth, adsorbent dosage, adsorbate initial concentration, and flow rate. Fixed-bed experiments showed that pH is a key factor that affects the adsorption capacity of antibiotics to CNTs. The Bed Depth Service Time model describes well the relationship between service time and bed depth and can be used to design appropriate column parameters. During fixed-bed regeneration, small amounts of SMX (3%) and SPY (9%) were irreversibly bonded to the CNT/sand porous media, thus reducing the column capacity for subsequent reuse from 67.9 to 50.4 mg g^?1 for SMX and from 91.9 to 72.9 mg g^?1 for SPY. The reduced column capacity resulted from the decrease in available adsorption sites and resulting repulsion (i.e., blocking) of incoming antibiotics from those previously adsorbed. Findings from this study demonstrate that fixed-bed columns packed with CNTs can be efficiently used and regenerated to remove antibiotics from water.     

The influence of iron and sulfur mineral fractions on carbon tetrachloride transformation in model anaerobic soils and sediments

The objective of this research was to identify the dissolved species or solid phase mineral fraction(s) best correlated with rates of carbon tetrachloride (CT) reductive transformation in systems modeling sulfate-reducing and iron oxide-rich soils and sediments. We used sulfide (S(-II))-treated goethite as our model system, but also studied Fe(II) and S(-II)-treated goethite, Fe(II)-treated goethite, pure FeS, and Fe(II)-treated FeS in order to isolate and evaluate the influence of different mineral fractions on reaction rates. Initial rates of CT transformation were measured for different pH values and concentrations of added Fe(II), as well as different aging times and conditions. The following dissolved species and iron and sulfur mineral fractions were quantified and compared with CT transformation rates: aqueous Fe(2+) and S(-II), surface associated Fe(II) (including weakly and strongly bound Fe(II)), FeS(s), and Cr(II) reducible solid phase S. Over the pH range of 6-10, CT transformation rates were correlated with surface associated Fe(II), while at pH 8, rates were correlated with weakly bound Fe(II). Aging of S(-II)-treated goethite led to oxidation of surface sulfur and a change in the concentration of weakly bound Fe(II), but did not change the relationship between initial rates and weakly bound Fe(II). The results of this research suggest that surface associated Fe(II) and weakly bound Fe(II) could serve as indicators of the potential for abiotic CT dechlorination in natural soils under sulfate-reducing conditions.     

Effect of carbon tetrachloride on sonochemical decomposition of methyl orange in water

Two types of sonicators were used for the sonochemical decomposition of methyl orange (MO) in the presence and absence of carbon tetrachloride (CCl4): One is a 45kHz ultrasonic cleaning bath (a low intensity sonicator) and the other is a 200kHz ultrasonic reactor (a high intensity sonicator). It was clearly confirmed that the rates of the sonochemical decomposition of MO increased with increasing the concentration of CCl4 in both sonicators. The enhancement effect of CCl4 was much higher in the high intensity sonicator than in the low intensity one: by the addition of 100ppm of CCl4, the decomposition ratio of MO with the high intensity sonicator became 41 times larger, while that with the low intensity sonicator became 4.8 times larger. Based on the obtained results, it was suggested that the formed cavitation phenomenon was different between sonicators. It was also suggested that the sonochemical decomposition of MO in the presence of CCl4 would be useful to evaluate the sonochemical efficiency, because the rate of MO decomposition can be effectively enhanced by the sonolysis of CCl4.     

某市南郊水源地土壤四氯化碳污染特征

含四氯化碳废水在排放的过程中沿排污渠侧壁和底部的渗漏对土壤造成污染.在对某市南郊受四氯化碳污染的水源地进行钻孔检测的过程中发现,土壤四氯化碳污染的特征:靠近排污沟的钻孔均检测出四氯化碳,而远离排污沟的钻孔则未检出;四氯化碳的垂向分布存在不连续性,且受降雨影响较大;大部分钻孔浅层土壤中基本未检测到四氯化碳,而在3 m以下的土层和基岩中检测到四氯化碳;抽水井的抽水行为导致抽水井附近土壤中四氯化碳明显高于其他钻孔点位检测结果.     

Protective effects of seaweeds against liver injury caused by carbon tetrachloride in rats

Three species of seaweeds collected from Tung Ping Chau, Hong Kong, were screened for their hepatoprotective activity using carbon tetrachloride (CCl4)-induced liver injury in the rat as a model of chemical hepatitis. A single oral dose of 1.25 ml/kg of CCl4 was able to produce significantly elevated levels of serum glutamic pyruvic transaminase (GPT) and glutamic oxaloacetic transminase (GOT). Administration of 150, 300 and 600 mg/kg of aqueous extracts from Myagropsis myagroides, Sargassum henslowianum and S. siliquastrum, respectively, significantly reduced the CCl4-induced acute elevation in the levels of GPT and GOT in rats. The same result was also seen in the histopathological study of liver tissue. The seaweed crude extracts probably acted to protect against CCl4-induced liver injury through their antioxidant properties.     

Seasonal and spatial variations of carbon and nitrogen distribution in the surface sediments of the Gulf of Riga, Baltic Sea

The variations in concentrations of carbon and nitrogen in surface sediments of the Gulf of Riga were investigated between December 1993 and January 1995. The sediment samples were taken nine times during this period at two sampling sites. One sampling site, G5, exhibited high abundance of burrowing amphipods, whereas at the second site, T3, the number of macrozoobenthic organisms was comparatively small. Similar vertical profiles of mean sediment dry-weight concentrations of total carbon (TC) and total nitrogen (TN) were obtained at both sites G5 and T3. However, during autumn winter considerable differences of TC and TN concentrations in surface sediments (0-2 cm) between sites were observed. This was probably the effect of differences in the bioturbation level. During summer, when decline in numbers of amphipods were recorded, the vertical profiles of TC and TN at site G5 were similar to those at site T3. Significant differences between months were detected for TN at site T3 reflecting sedimentation of spring and autumn blooms in April and late October-early November, respectively. This was supported also by lower atomic C/N ratios in surface sediments during corresponding sampling events.     

Flow behavior and residual saturation formation of liquid carbon tetrachloride in unsaturated heterogeneous porous media

The formation of residual, discontinuous nonaqueous phase liquids (NAPLs) in the vadose zone is a process that is not well understood. To obtain data that can be used to study the development of a residual NAPL saturation in the vadose zone and to test current corresponding models, detailed transient experiments were conducted in intermediate-scale columns and flow cell. The column experiments were conducted to determine residual carbon tetrachloride (CCl(4)) saturations of two sands and to evaluate the effect of CCl(4) vapors on the water distribution. In the intermediate-scale flow cell experiment, a rectangular zone of the fine-grained sand was packed in an otherwise medium-grained matrix. A limited amount of CCl(4) was injected from a small source and allowed to redistribute until a pseudo steady state situation had developed. A dual-energy gamma radiation system was used to determine fluid saturations at numerous locations. The experiments clearly demonstrated the formation of residual CCl(4) saturations in both sands. Simulations with an established multifluid flow simulator show the shortcomings of current relative permeability-saturation-capillary pressure (k-S-P) models. The results indicate that nonspreading behavior of NAPLs should be implemented in simulators to account for the formation of residual saturations.     

Chlorination of p-cymene by chlorine in carbon tetrachloride: Model compounds for environmental analyses

p-Cymene was chlorinated by chlorine in CCl₄. The products of the chlorination were separated by distillation and purified by preparative gas chromatography. The structures of chlorocompounds were confirmed by means of their NMR and mass spectra. The distillation gave as the main compounds: (2) 2-chloro-, (4) 2,3-dichloro-, (5) 2,5-dichloro-, (6) 2,3,6-trichloro-, (7) 2,3,5,6-tetrachloro-p-cymenes and as by-products: (8) 2,5,7-trichloro-p-cymene, (9) 2,6-dichloro-1-methyl-4-(1-methylethenyl)benzene (cymenene), and (10) 2,3,6-trichloro-1-methyl-4-(1-methylethenyl)benzene (cymenene).     

Mechanism for the destruction of carbon tetrachloride and chloroform DNAPLs by modified Fenton's reagent

The destruction of a carbon tetrachloride DNAPL and a chloroform DNAPL was investigated in reactions containing 0.5 mL of DNAPL and a solution of modified Fenton's reagent (2M H2O2 and 5mM iron(III)-chelate). Carbon tetrachloride and chloroform masses were followed in the DNAPLs, the aqueous phases, and the off gasses. In addition, the rate of DNAPL destruction was compared to the rate of gas-purge dissolution. Carbon tetrachloride DNAPLs were rapidly destroyed by modified Fenton's reagent at 6.5 times the rate of gas purge dissolution, with 74% of the DNAPL destroyed within 24h. Use of reactions in which a single reactive oxygen species (hydroxyl radical, hydroperoxide anion, or superoxide radical anion) was generated showed that superoxide is the reactive species in modified Fenton's reagent responsible for carbon tetrachloride DNAPL destruction. Chloroform DNAPLs were also destroyed by modified Fenton's reagent, but at a rate slower than the rate of gas purge dissolution. Reactions generating a single reactive oxygen species demonstrated that chloroform destruction was the result of both superoxide and hydroxyl radical activity. Such a mechanism of chloroform DNAPL destruction is in agreement with the slow but relatively equal reactivity of chloroform with both superoxide and hydroxyl radical. The results of this research demonstrate that modified Fenton's reagent can rapidly and effectively destroy DNAPLs of contaminants characterized by minimal reactivity with hydroxyl radical, and should receive more consideration as a DNAPL cleanup technology.     

Effects of residence time distribution and packing on methanol oxidation in biotrickling filter

The effects of residence time distribution (RTD) on biotrickling filter systems and the comparison of the maximum elimination capacity (EC) and poisoning limits as functions of loadings of two packing media, Celite Biocatalyst Carrier R-635 and a subituminous coal, were studied. To alter the RTD patterns in the two reactor columns, two baffle designs were chosen. The RTD tests were done under dry conditions, over a range of airflow rates, with zero baffle, one baffle, and two baffles added into each column. Mixed culture from compost was used to acclimate the bed for the methanol removal efficiency study. No nutrients were added in the coal column. To study the poisoning limit, the inlet methanol concentration was randomly increased until a severe drop in removal efficiency occurred. From the RTD tests and the removal efficiency runs, which did not result in 100% conversion, number of tank-in-series (N) values, maximum EC values, and rate constants of each column with different baffle configurations could be obtained. Results from duplicate runs showed that addition of baffles decreased the N values of the columns and increased the back mixing in both systems. Maximum EC values, critical loadings, and poisoning limits also increased with increasing back mixing. Coal was superior to Celite Biocatalyst Carrier R-635 because it gave good conversions without additional nutrients. In all runs, the rate of methanol removal was controlled by a zero order process.     

Removal of low concentrations of carbon tetrachloride in compost-based biofilters operated under methanogenic conditions.

Research was performed to demonstrate the removal of carbon tetrachloride (CT) using compost biofilters operated under methanogenic conditions. Biofilters were operated at an empty-bed residence time of 2.8 minutes using nitrogen as the atmosphere. Hydrogen and carbon dioxide were supplied as an electron donor and carbon source, respectively, during acclimation of the bed medium microbes. Once methanogenesis was demonstrated, CT flow to the biofilter was established. Biofilters were operated over a CT concentration range from 20 to 700 ppbv for 6 months. Bed medium microbes were able to remove up to 75% of the inlet CT. At excessively high CT concentrations (> 500 ppmv), methane production and hydrogen utilization by the bed medium microbes appeared to be inhibited. CT removal by the biofilter decreased when the hydrogen supply was removed from the biofilter inlet, indicating that hydrogen acted as the electron donor for reductive dechlorination. The removal efficiency and relatively low empty bed residence times demonstrated by these laboratory-scale biofilters indicate that anaerobic biofiltration of CT may be a feasible full-scale process.