中国城镇碳排放的区域差异和影响因素

修正了IPCC关于电力碳排放系数的计算方法,根据中国(省市)能源平衡表估算了1995-2008年中国30个省市的城镇碳排放,划分了高、中、低三个不同排放区域,分析城镇碳排放的区域差异,采用STIRPAT模型分析城镇碳排放及区域差异的影响因素.结果表明,城镇碳排放是中国碳排放的主体;城镇碳排放总体快速增长趋势,2001年后表现尤为明显;中国城镇碳排放存在很强的区域差异,2008年高排放区域的八个省市城镇碳排放总量占全国城镇碳排放总量的50％以上;城镇居民人均收入对城镇碳排放影响最大,然后是城镇化率和能源强度,人口总量对碳排放影响较小;城镇居民人均收入增加、城市化进程不断推进、能源强度降低对城镇碳排放的影响存在区域差异,这种影响强度的差异是导致城镇碳排放存在区域差异的主要原因.一方面,我国城镇居民收入的不断提高和城市化进程的推进决定了城镇发展需要一定的碳排放空间,另一方面,城镇需要走可持续的低碳发展道路.     

人工湿地新型内电解基质的研究

对内电解技术在人工湿地中的应用进行了初步研究,通过静态实验对铁屑/炉渣、铁屑/粉煤灰、铁屑/活性炭组成的内电解基质进行了比选,确定铁屑/炉渣为最佳组合,其对COD、NH3-N、TP去除率高,对出水的pH值影响较小.通过单因素实验确定其最佳反应条件,即铁/炉渣投加比为1∶1,每100 mL废水投加量为20 g,反应时间6...     

Degradation of phenol in mists by a non-thermal plasma reactor

A link tooth wheel-cylinder non-thermal plasma reactor was set up to investigate the degradation of phenol in the mists. In addition, the decomposition efficiency of phenol, TOC removal, and byproduct formation were investigated. The stable discharge was achieved in both air and the mist condition. The decomposition efficiency and TOC removal increased with increasing the input power. For the input power of 3.6 W, the phenol decomposition and TOC removal reached 90% and 47%, respectively. Phenol degradation byproducts were identified as small molecular organic acids, including formic acid, acetic acid, and oxalic acid. Their masses in the trapped solutions first increased and then decreased slightly with increasing the input power. Therefore, the biodegradation capacity of the phenol degradation byproducts can be improved.     

Time-resolved measurements of PM2.5 carbonaceous aerosols at Gosan, Korea

In order to better understand the characteristics of atmospheric carbonaceous aerosol at a background site in Northeast Asia, semicontinuous organic carbon (OC) and elemental carbon (EC), and time-resolved water-soluble organic carbon (WSOC) were measured by a Sunset OC/ EC and a PILS-TOC (particle-into-liquid sampler coupled with an online total organic carbon) analyzer, respectively, at the Gosan supersite on Jeju Island, Korea, in the summer (May 28-June 17) and fall (August 24-September 30) of 2009. Hourly average OC concentration varied in the range of approximately 0.87-28.38 microgC m-3, with a mean of 4.07+/- 2.60 microgC m-3, while the hourly average EC concentration ranged approximately from 0.04 to 8.19 .microgC m-3, with a mean of 1.35 +/- 0.71 microgC m-3, from May 28 to June 17, 2009. During the fall season, OC varied in the approximate range 0.9-9.6 microgC m-3, with a mean of 2.30 +/-0.80 microgC m-3, whereas EC ranged approximately from 0.01 to 5.40 microgC m-3, with a mean of 0.66 +/- 0.38 microgC m-3. Average contributions of EC to TC and WSOC to OC were 26.0% +/- 9.7% and 20.6% +/-7.4%, and 37.6% +/- 23.5% and 57.2% +/- 22.2% during summer and fall seasons, respectively. As expected, clear diurnal variation of WSOC/OC was found in summer, varying from 0.22 during the nighttime up to 0.72 during the daytime, mainly due to the photo-oxidation process. In order to investigate the effect of air mass pathway on the characteristics of carbonaceous aerosol, 5-day back-trajectory analysis was conducted using the HYSPLIT model. The air mass pathways were classified into four types: Continental (CC), Marine (M), East Sea (ES) and Korean Peninsula (KP). The highest OC/EC ratio of 3.63 was observed when air mass originated from the Continental area (CC). The lowest OC/EC ratio of 0.79 was measured when air mass originated from the Marine area (M). A high OC concentration was occasionally observed at Gosan due to local biomass burning activities. The contribution of secondary OC to total OC varied approximately between 8.4% and 32.2% and depended on air mass type.     

Correlation between PM concentrations and aerosol optical depth in eastern China

Using one year of Aerosol Optical Depth (AOD) derived from Moderate Resolution Imaging Spectroradiometer (MODIS) on the Terra satellite and particular matter (PM) contents measured at eleven sites located mostly in the eastern China in 2007, the relationship between columnar AOD and hourly and daily average (DA) PM were established. The peak AOD observed from MODIS was generally consistent with the surface PM measurements in eastern China, where Zhengzhou had the maximum annual mean PM₁₀ of 182.1 μg m^?3, while Longfengshan had the minimum annual mean of 38.1 μg m^?3. Ground level observations indicated that PM concentration varies widely across different regions, which was mainly due to the difference in weather conditions and anthropogenic emissions. The coarse particles accounted for the main air pollution in Zhengzhou and Benxi whiles the fine particles, however, were the main constituents in other sites. Results showed that MODIS AOD (averaged over the box of 5 × 5 and 3 × 3 pixels) had a better positive correlation with the coincident hourly average (HA) PM concentration than with DA due to diurnal variation in PM mass measurements. After correcting AOD for relative humidity (RH), the correlation did not improve significantly, suggesting that the RH was not the main factor affecting the correlation of PM with AOD. The statistical regression analysis between MODIS AOD and PM mass suggested that the satellite-derived AOD is a useful tool for mapping PM distribution over large spatial domains.     

Fenton试剂催化氧化嘧啶废水的特性

研究了Fenton催化氧化法对废水中嘧啶的去除效能,优化了处理体系中的反应条件,分析了各影响因子的作用机理;并用一元线性回归方程对不同温度下,嘧啶相对残余浓度对反应时间的相关性进行了定量分析。结果表明:温度为25℃,pH为3.5,Fe²⁺的投加量64 mmol/L,H₂O₂投加量为300 mmol/L时,反应2 h,Fenton试剂对嘧啶和COD的去除率分别达90%和50%以上;同时发现Fenton试剂对嘧啶的氧化降解具有相对优先性,且符合一级反应动力学模式,并计算表观反应速率常数和活化能。     

PCBs in sediments of the Great Lakes--distribution and trends, homolog and chlorine patterns, and in situ degradation

A region-wide data analysis on polychlorinated biphenyls (PCBs) in the sediment of the Great Lakes reveals a total accumulation of approximately 300 ± 50 tonnes, representing a >30% reduction from the 1980s. Evidence of in situ degradation of sediment PCB was found, with estimated t_1/2 of 11 and 17 years, at two open water locations in Lake Ontario. The relative abundance of heavy homologs as well as para-chlorines decreases with increasing depth, while the opposite is true for medium and light homologs and ortho-chlorines. In Lake Michigan, the vertical pattern features enrichment of heavier congeners and reduction of ortho-chlorines in deeper sediment layers, opposite to the trend in Lake Ontario. PCBs decrease log-linearly with increasing latitude and longitude. Air deposition of PCBs to lake sediment decreases at about 0.077 ng cm⁻² yr⁻¹ per degree latitude (N) for the geographic region extending from the Great Lakes to within the Arctic Circle.     

Impacts of a strong cold front on concentrations of HONO,HCHO, O3, and NO2 in the heavy traffic urban area of Beijing

Much rain and strong winds caused by a cold front occurred in Beijing during the period of Sep. 27 to Oct. 4, 2004 and led to sharp drops in maximum and mean concentrations of HONO, HCHO, O₃, and NO₂, i.e., the maximum concentrations were reduced by 5.9, 21.3, 45.6, and 44.4 ppb, respectively, and the mean concentrations were decreased by 4.0, 5.5, 30.3, and 32.3 ppb, respectively. For daily HO_x production rates HONO photolysis was the largest contributor and over 90% contributions were from photolysis of HONO and HCHO. Large number and area percentages of soot aggregate from PM10, and high correlations between concentrations of PM10 and chemical formation of HONO suggested that heterogeneous reactions of NO₂ on surfaces of soot aggregate could be a key source of HONO in the heavy traffic areas of Beijing during the night and should be considered in air quality simulations for such areas.     

生物制剂对MBR中无纺布膜组件过滤性能的影响

研究了生物制剂对浸渍式膜生物反应器(submerged membrane bioreactor,SMBR)中聚丙烯无纺布(non-wov-en fabric,NWF)膜组件过滤性能的影响。结果表明,能减少膜组件表面附着污泥胞外聚合物(extra-cellular polymeric sub-stances,EPS)的含量及污泥的沉积,减缓膜通量的衰减速率和膜污染,无纺布膜组件的过滤性能得到明显改善,表现出一定的耐污染性。生物制剂能改善污泥的沉降性能,有效防止污泥膨胀;对MBR的COD去除率基本没有影响,但略微增大了处理水的浊度。     

试压堵塞器在降低井控安全风险中的应用

文章结合大港油田井下作业现场特点,通过研究井控装置FZ18-35防喷器在试压过程中存在的"原试压堵塞器不适合350型采油树井口四通"的具体问题,改进研制适合FZ18-35防喷器与350型采油树井口四通配套的ST18-35试压堵塞器来解决井控装置的现场试压问题,确保现场井控装置的完好,有效降低井控风险以及井喷事故污染环境的风险。