首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到19条相似文献,搜索用时 140 毫秒
1.
Significance of nitrous oxide in atmospheric chemistry is reviewed briefly. Background concentration of N2O at Wudaoliang in Qinghai Province of Western China has been measured by collecting gas samples and analysing them with electron capture-gas chromatography. The atmospheric concentration fluctuates in the range of 303-315 ppb with the mean value of 308 ppb. The emission rate of N2O in agriculture region of Northern China has been studied primarily. Fertilization, rain and temperature of soil appear conductible to N2O emission. The interactions between greenhouse effect and N2O emission have been discussed. The catalytic action of N2O in stratospheric ozone depletion processes and the effect of high N2O concentration on ozone depletion in stratosphere have been considered and discussed.  相似文献   

2.
The emission of N2 is important to remove excess N from lakes, ponds, and wetlands. To investigate the gas emission from water, Gao et al.(2013) developed a new method using a bubble trap device to collect gas samples from waters. However, the determination accuracy of sampling volume and gas component concentration was still debatable. In this study, the method was optimized for in situ sampling, accurate volume measurement and direct injection to a gas chromatograph for the analysis of N2 and other gases. By the optimized new method, the recovery rate for N2 was 100.28% on average; the mean coefficient of determination(R2) was 0.9997; the limit of detection was 0.02%. We further assessed the effects of the new method, bottle full of water, vs. vacuum bag and vacuum vial methods, on variations of N2 concentration as influenced by sample storage times of 1,2, 3, 5, and 7 days at constant temperature of 15°C, using indices of averaged relative peak area(%) in comparison with the averaged relative peak area of each method at 0 day.The indices of the bottle full of water method were the lowest(99.5%–108.5%) compared to the indices of vacuum bag and vacuum vial methods(119%–217%). Meanwhile, the gas chromatograph determination of other gas components(O2, CH4, and N2O) was also accurate. The new method was an alternative way to investigate N2 released from various kinds of aquatic ecosystems.  相似文献   

3.
CH4 and N2O fluxes from soil under a tropical seasonal rain forest in Xishuangbanna, Southwest China were measured for one year using closed static chamber technique and gas chromatography method. Three treatments were set in the studied field: (A) litter-free,(B) with litter, and (C) with litter and seedling. The results showed that the soil in our study was a sink of atmospheric CH4 and source of atmospheric N2O. The observed mean CH4 fluxes from treatments A, B, and C were -50.0±4.0, -35.9±2.8,-31.6±2.8 μgC/(m2·h),respectively,and calculated annual fluxes in2003 were -4.1,-3.1,and -2.9kgC/hm2,respectively.The observed mean N2O fluxes from treatments A,B,and C were 30.9±3.1,28.2±3.5,50.2±3.7μgN/(m2·h),respectively,and calculated annual fluxes in 2003 were 2.8, 2.6, and 3.7 kgN/hm2, respectively. Seasonal variations in CH4 and N2O fluxes were significant among all the three treatments. The presence of litter decreased CH4 uptake during wet season (P < 0.05), but not during dry season. There was a similar increase in seedlings-mediated N2O emissions during wet and dry seasons, indicating that seedlings increased N2O emission in both seasons. A strong positive relationship existed between CH4 fluxes and soil moisture for all the three treatments, and weak relationship between CH4 fluxes and soil temperature for treatment B and treatment C. The N2O fluxes correlated with soil temperature for all the three treatments.  相似文献   

4.
The hydroxyl radical (·OH) plays a central role in the oxidation and removal of many atmospheric compounds. Measurement of atmospheric·OH is very difficult because of its high reactivity and low atmospheric abundance. In this article, a simple and highly sensitive method, high performance liquid chromatography coupled with coulometric detection (HPLC-CD), was developed to determine·OH indirectly by determining its reaction products with salicylic acid (SAL), 2,3-dihydroxybenzoic acid (2,3-DHBA), and 2,5-dihydroxybenzoic acid (2,5-DHBA). Under the optimum conditions for its determination, 2,3-DHBA and 2,5-DHBA could be well separated and the detection limits for 2,3-DHBA were 3×10~(-10) mol/L and for 2,5-DHBA were 1.5×10~(-10) mol/L, which were lower than most previous reports. This method was also applied to measure atmospheric hydroxyl radical levels and demonstrated the feasibility in clean and polluted air.  相似文献   

5.
A new instrument for measuring atmospheric nitrous acid(HONO) was developed,consisting of a double-wall glass stripping coil sampler coupled with ion chromatography(SC-IC).SC-IC is featured by small size(50 × 35 × 25 cm) and modular construction,including three independent parts:the sampling unit,the transfer and supporting unit,and the detection unit.High collection efficiency(> 99%) was achieved with 25 μmol/L Na2CO3 as absorption solution even in the presence of highly acidic compounds.This instrument has a detection limit of 8 pptv at 15 min time resolution,with a measurement uncertainty of 7%.Potential interferences from NOx,NO2+SO2,NO2+VOCs,HONO+O3,HNO3,peroxyacetyl nitrite(PAN) and particle nitrite were quantified in laboratory studies and were found to be insignificant under typical atmospheric conditions.Within the framework of the 3C-STAR project,inter-comparison between the SC-IC and LOPAP(long path liquid absorption photometer) was conducted at a rural site in the Pearl River Delta.Good agreement was achieved between the two instruments over three weeks.Both instruments determined a clear diurnal profile of ambient HONO concentrations from 0.1 to 2.5 ppbv.However,deviations were found for low ambient HONO concentrations(i.e.< 0.3 ppbv),which cannot be explained by previous investigated interference species.To accurately determine the HONO budget under illuminated conditions,more intercomparison of HONO measurement techniques is still needed in future studies,especially at low HONO concentrations.  相似文献   

6.
Degradation of the Indigo Carmine (IC) by the bipolar pulsed DBD in water-air mixture was studied. Effects of vadous parameters such as gas flow rate, solution conductivity, pulse repetitive rate and ect., on color removal efficiency of dying wastewater were investigated. Concentrations of gas phase O3 and aqueous phase H2O2 under various conditions were measured. Experimental results showed that air bubbling facil~tates the breakdown of water and promotes generation of chemically active species. Color removal efficiency of IC solution can be greatly improved by the air aeration under various solution conductivities. Decolorization efficiency increases with the increase of the gas flow rate, and decreases with the increase of the initial solution conductivity. A higher pulse repetitive rate and a larger pulse capacitor Cp are favorable for the decolorization process. Ozone and hydrogen peroxide formed decreases with the increase of initial solution conductivity. In addition, preliminary analysis of the decolorization mechanisms is given.  相似文献   

7.
Peroxyacetyl nitrate(PAN), as a major secondary pollutant, has gained increasing worldwide attentions, but relevant studies in China are still quite limited. During winter of 2015 to summer of 2016, the ambient levels of PAN were measured continuously by an automatic gas chromatograph equipped with an electron capture detector(GC–ECD) analyzer at an urban site in Jinan(China), with related parameters including concentrations of O3, NO, NO_2, PM_(2.5), HONO,the photolysis rate constant of NO_2 and meteorological factors observed concurrently. The mean and maximum values of PAN concentration were(1.89 ± 1.42) and 9.61 ppbv respectively in winter, and(2.54 ± 1.44) and 13.47 ppbv respectively in summer. Unusually high levels of PAN were observed during severe haze episodes in winter, and the formation mechanisms of them were emphatically discussed. Study showed that high levels of PAN in winter were mainly caused by local accumulation and strong photochemical reactions during haze episodes, while mass transport played only a minor role. Accelerated photochemical reactions(compared to winter days without haze) during haze episodes were deduced by the higher concentrations but shorter lifetimes of PAN, which was further supported by the sufficient solar radiation in the photolysis band along with the high concentrations of precursors(NO_2, VOCs) and HONO during haze episodes. In addition, significant PAN accumulation during calm weather of haze episodes was verified by meteorological data.  相似文献   

8.
At present,continuous observation data for atmospheric nitrous oxide(N_2O) concentrations are still lacking,especially in east Antarctica.In this paper,nitrous oxide background concentrations were measured at Zhongshan Station(69°22′25″S,76°22′14″E),east Antarctica during the period of 2008–2012,and their interannual and seasonal characteristics were analyzed and discussed.The mean N_2O concentration was 321.9 n L/L with the range of 320.5–324.8 n L/L during the five years,and it has been increasing at a rate of 0.29% year-1.Atmospheric N_2O concentrations showed a strong seasonal fluctuation during these five years.The concentrations appeared to follow a downtrend from spring to autumn,and then increased in winter.Generally the highest concentrations occurred in spring.This trend was very similar to that observed at other global observation sites.The overall N_2O concentration at the selected global sites showed an increasing annual trend,and the mean N_2O concentration in the Northern Hemisphere was slightly higher than that in the Southern Hemisphere.Our result could be representative of atmospheric N_2O background levels at the global scale.This study provided valuable data for atmospheric N_2O concentrations in east Antarctica,which is important to study on the relationships between N2 O emissions and climate change.  相似文献   

9.
Carbon dioxide (CO2) adsorption on a standard metal-organic framework Mg2(dobdc) (Mg/DOBDC or Mg-MOF-74) and a tetraethylenepentamine (TEPA) modified Mgz(dobdc) (TEPA-Mg/DOBDC) were investigated and compared. The structural information, surface chemistry and thermal behavior of the adsorbent samples were characterized by X-ray powder diffraction (XRD), infrared spectroscopy (IR), thermogravimetric analysis (TGA) and nitrogen adsorption-desorption isotherm analysis. CO2 adsorption capacity was measured by dynamic adsorption experiments with N2-CO2 mixed gases at 60℃. Results showed that the CO2 adsorption capacity of Mg/DOBDC was significantly improved after amine modification, with an increase from 2.67 to 6.06 mmol CO2/g adsorbent. Moreover, CO2 adsorption on the TEPA-Mg/DOBDC adsorbent was promoted by water vapor, and the adsorption capacity was enhanced to 8.31 mmol CO2/g absorbent. The adsorption capacity of the TEPA-Mg/DOBDC adsorbent dropped only 3% after 5 consecutive adsorption]desorption cycles. Therefore, this kind of adsorbent can be considered as a promising material for the capture of CO2 from flue gas.  相似文献   

10.
TiO2 supports doped with different amounts of Si were prepared by a sol-gel method, and 1 wt% vanadia (V2O5) loaded on Si-doped TiO2 was obtained by an impregnation method. The mole ratio of Si/Ti was 0.2, NOx conversion exceeds 94% at 300℃ and GHSV of 41,324 hr-1 , which is about 20% higher than pure V2O5/TiO2 . The catalysts were characterized by XRD, BET, TEM, FT-IR, NH3-TPD, XPS, H2-TPR, Raman and in situ DRIFTS. The results of FT-IR and XPS indicated that Si was doped into the TiO2 lattice successfully and a solid solution was obtained. V2O5 active component could be dispersed well on the support with the increasing of surface area of the catalyst, which was confirmed by Raman and XRD results. Above all, the numbers of acid sites (especially the Br nsted-acid) and oxidation properties were enhanced for Si-doped V2O5/TiO2 catalysts, which improved the deNOx catalytic activity.  相似文献   

11.
半干旱草原地-气温室气体交换速率测定   总被引:2,自引:1,他引:2  
重点介绍采用静态箱 -气相色谱法测定低交换速率的半干旱草原地 -气间温室气体交换速率的采样分析系统的配置及操作 .将静态采样箱置于采样点 ,用 50 cm3或 100 cm3的塑料注射器现场取样 ,转存于气袋中并送到实验室分析 .用改进了的进样系统并装有 FID和 ECD的气相色谱仪 ( GC)分析其中的 CH4、CO2 和 N2O浓度 ,计算出地 -气痕量温室气体的交换速率 .对内蒙古羊草草原、草甸草原 N2O、CO2 和 CH4交换速率日变化规律实测结果分析表明 ,该方法简便易行、准确可靠 .  相似文献   

12.
Nitrous oxide emissions from black soils with different pH   总被引:1,自引:0,他引:1  
N2O fluxes as a function of incubation time from soil with different available N contents and pH were determined. Cumulative carbon dioxide (CO2) emissions were measured to indicate soil respiration. A 144-hr incubation experiment was conducted in a slightly acidic agricultural soil (pHH2O 5.33) after the pH was adjusted to four different values (3.65, 5.00, 6.90 and 8.55). The experiments consisted of a control without added N, and with NH4+-N and NO3--N fertilization. The results showed that soil pH contributed significantly to N2O flux from the soils. There were higher N2O emissions in the period 0-12 hr in the four pH treatments, especially those enhanced with N-fertilization. The cumulative N2O-N emission reached a maximum at pH 8.55 and was stimulated by NO3--N fertilization (70.4 μg/kg). The minimum emissions appeared at pH 3.65 and were not stimulated by NO3--N or NH4+-N fertilization. Soil respiration increased significantly due to N-fertilization. Soil respiration increased positively with soil pH (R2 = 0.98, P < 0.01). The lowest CO2-C emission (30.2 mg/kg) was presented in pH 3.65 soils without N-fertilization. The highest CO2-C emissions appeared in the pH 8.55 soils for NH4+-N fertilization (199 mg/kg). These findings suggested that N2O emissions and soil respiration were significantly influenced by low pH, which strongly inhibits soil microbial nitrification and denitrification activities. The content of NO3--N in soil significantly and positively affected the N2O emissions through denitrification.  相似文献   

13.
厌氧条件下砂壤水稻土N2、N2O、NO、CO2和CH4排放特征   总被引:1,自引:0,他引:1       下载免费PDF全文
了解厌氧条件土壤反硝化气体(N2、N2O和NO)、CO2和CH4排放特征,是认识反硝化过程机制的基础,并有助于制定合理的温室气体减排措施.定量反硝化产物组成,可为氮转化过程模型研发制定正确的关键过程参数选取方法或参数化方案.本研究选取质地相同(砂壤土)的两个水稻土为研究对象,通过添加KNO3和葡萄糖的混合溶液,将培养土壤的初始NO-3和DOC含量分别调节到50 mg·kg-1和300 mg·kg-1,采用氦环境培养-气体及碳氮底物直接同步测定方法,研究完全厌氧条件下土壤N2、N2O、NO、CO2和CH4的排放特征,并获得反硝化气态产物中各组分的比率.结果表明,在整个培养过程中,两个供试土壤的N2、N2O和NO累积排放量分别为6~8、20和15~18 mg·kg-1,这些气体排放量测定结果可回收土壤NO-3变化量的95%~98%,反硝化气态产物以N2O和NO为主,其中3种组分的比率分别为15%~19%(N2)、47%~49%(N2O)和34%~36%(NO);但反硝化气体产物组成的逐日动态均显现为从以NO为主逐渐过渡到以N2O为主,最后才发展到以N2为主.以上结果说明,反硝化气体产物组成是随反硝化进程而变化的,在以气体产物组成比率作为关键参数计算各种反硝化气体产生率或排放率的模型中,很有必要重视这一点.  相似文献   

14.
The delafossite CuCrO2 elaborated by sol-gel from 40 nm diameter colloid is optically active in the visible region. It is characterized physically and photoelectrochemically. The microstructure is fairly homogenous with a mean crystallite size of ca. 2 μm. The optical gap (1.30 eV), determined from the diffuse reflectance, is well suited to the sunlight spectrum. The Mott Schottky plot is characteristic of P-type conductivity with a flat band potential of -0.26 VSCE. As application, the photoreduction of chromate is successfully achieved in air-equilibrated suspension CuCrO2/ZnO (1/1). CuCrO2 is photoactivated by visible light and the electrons in the conduction band (-1.34 VSCE) are injected to ZnO. In the presence of salicylic acid, a conversion of Cr(VI) to Cr(III) of 57% is obtained under optimal conditions (pH 3 at 25℃, 5×10-4 mol/L) because of the HCrO4- dark adsorption onto ZnO (4HCrO4- + 3C7H6O3 + 18O2 + 16H+ → 4Cr3+ + 21CO2 + 19H2O, ΔG0 = -557 kcal/mol). Prolonged illumination is accompanied by a deceleration in the photoactivity owing to the competitive water reduction, an issue of energetic concern. The hetero-system exhibits self sensitization for hydrogen production with an evolution rate of 149 μmol/(hr·g).  相似文献   

15.
利用气相色谱-电子捕获检测器法(GC-ECD)测量大气中氧化亚氮(N_2O)浓度是目前广泛使用的方法,但ECD分析N_2O时存在线性范围较窄的缺点,因此,标气数量和定量方式是决定分析结果的关键因素.基于此,本文对比分析了单点线性校正法(S)、多点线性拟合法(D)、单瓶标气近似校正法(SA)、单瓶标气比值校正法(SC)对N_2O检测分析结果的差异.结果表明,SA定量相对误差最小,对测试使用的6瓶标气定值平均误差为0.09×10~(-9).根据本底大气N_2O观测精度要求,以及我国大气N_2O浓度变化范围较大的特征,推荐选用SA法对大气中N_2O浓度进行定值.依据所选方法对黑龙江龙凤山本底站大气N_2O浓度进行观测(2015年1—12月),结果显示,黑龙江龙凤山站大气N_2O浓度最高值出现在4—5月,平均值超过330×10~(-9).该站大气N_2O浓度主要受人为活动排放的影响.  相似文献   

16.
The visible light photo-Fenton-like catalytic performance of BiFeO3 nanoparticles was investigated using Methyl Violet (MV), Rhodamine B (RhB) and phenol as probes. Under optimum conditions, the pseudo first-order rate constant (k) was determined to be 2.21×10-2, 5.56×10-2 and 2.01×10-2 min-1 for the degradation of MV (30 μmol/L), RhB (10 μmol/L) and phenol (3 mmol/L), respectively, in the BiFeO3-H2O2-visible light (Vis) system. The introduction of visible light irradiation increased the k values of MV, RhB and phenol degradation 3.47, 1.95 and 2.07 times in comparison with those in dark. Generally, the k values in the BiFeO3-H2O2-Vis system were accelerated by increasing BiFeO3 load and H2O2 concentration, but decreased with increasing initial pollutant concentration. To further enhance the degradation of pollutants at high concentrations, BiFeO3 was modified with the addition of surface modifiers. The addition of ethylenediamineteraacetic acid (EDTA, 0.4 mmol/L) increased the k value of MV degradation (60 μmol/L) from 1.01×10-2 min-1 in the BiFeO3-H2O2-Vis system to 1.30 min-1 in the EDTA-BiFeO3-H2O2-Vis system by a factor of 128. This suggests that in situ surface modification can enable BiFeO3 nano-particles to be a promising visible light photo-Fenton-like catalyst for the degradation of organic pollutants.  相似文献   

17.
2010年中国机动车CH4和N2O排放清单   总被引:5,自引:0,他引:5  
中国大部分机动车温室气体排放研究都集中于CO2排放,对于CH4和N2O等排放的研究鲜见. 以中国机动车污染防治年报(2011年)、中国汽车工业年鉴(2011年)、中国统计年鉴(2011年)以及交通运输部发布的相关信息和数据(2011年)等为基础,结合文献调研和2008─2010年对北京、广州等国内10余座典型城市的实地调查结果,获得2010年我国机动车活动水平及排放特征. 基于上述基础信息,解析得到按不同车型、燃料和车龄分布的机动车保有量、年均行驶里程及排放因子,建立2010年中国机动车CH4和N2O排放清单. 结果表明:2010年中国机动车CH4和N2O排放量分别为23.90×104和6.01×104t,折算成CO2分别为501.99×104和1862.51×104t. 不确定性分析则显示,中国CH4排放量在18.21×104~27.52×104t之间,N2O排放量在4.32×104~7.62×104t之间. 在机动车中,汽车CH4和N2O排放量最大,分担率(某车型污染物排放量占机动车排放总量的比例)分别为77.99%和94.22%,而摩托车和农用车排放分担率较小. 在各类汽车中,CH4排放主要来源于轻型汽油车和天然气出租车,二者的排放分担率分别为47.98%和23.42%;N2O排放则主要源于轻型汽油车,其分担率为73.09%. 因此,轻型汽油车是削减机动车CH4和N2O排放的重点车型,同时天然气出租车也应作为控制CH4排放的主要车型.  相似文献   

18.
理解底物碳氮对厌氧条件下水稻土排放氮素气体——氮气(N2)、氧化亚氮(N2O)和一氧化氮(NO)以及二氧化碳(CO2)和甲烷(CH4)的影响,有助于制定合理的温室气体减排措施,定量了解反硝化产物组成对碳底物水平的依赖性,也有助于氮转化过程模型研发中制定正确的关键过程参数选取方法或参数化方案.本研究采用粉砂壤质水稻土为研究对象,设置对照(CK)和加碳(C+)两个处理,前者的初始硝态氮和可溶性有机碳(DOC)含量分别为~50 mg·kg-1和~28 mg·kg-1,后者的分别为~50 mg·kg-1和~300 mg·kg-1.采用氦环境培养-气体及碳氮底物直接同步测定系统,研究了完全厌氧条件下碳底物水平对上述气体排放的影响.结果表明,CK处理无CH4排放,而C+处理可观测到CH4排放;C+处理的综合增温潜势显著高于CK处理(P<0.01);NO、N2O和N2排放量占这3种氮素气体排放总量的比重,在CK处理分别约为9%、35%和56%,在C+处理分别约为31%、50%和19%,处理间差异显著(P<0.01).由此表明,碳底物水平可显著改变所排放氮素气体的组成;对于旱地阶段硝态氮比较丰富的水稻土,避免在淹水前或淹水期间施用有机肥,有利于削减温室气体排放.  相似文献   

19.
农垦与放牧对内蒙古草原N2O、CO2排放和CH4吸收的影响   总被引:16,自引:3,他引:16  
利用优选静态箱/气相色谱法(GC),首次对我国内蒙古草原典型地区进行了人类活动对N2O、CO2和CH4交换通量影响的实验观测结果表明,农垦麦田N2O平均排放通量比原始草原高出3倍,并改变了草甸草原为CO2汇的性质,使其季节排放净通量以C计增加14.3 mg·(m2·h).随放牧强度的增加CO2排放通量呈线性增长,轻牧会引起草原对CH4吸收的大幅增加,而随着放牧压力的增大,增加值迅速回落.农垦麦田与草甸草原相比地-气间CH4交换无显著变化,放牧强度对N2O排放影响无显著规律.土壤湿度和温度是影响草原排放N2O和CO2、吸收CH4季节变化形式的关键因子,而人类活动仅影响排放强度.排放和吸收量年际间差异很大,但主要受降水的影响.N2O和CO2排放与CH4吸收峰值相反现象普遍存在.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号