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HCHO is ubiquitous and important chemical constitutes in the troposphere. The concentrations of the HCHO (aq) in the rainwater were measured in the Guiyang city, southeastern of China from May 2006 to April 2007 and 153 discrete samples were collected. Rainwater (N = 151) HCHO (aq) concentrations ranged from lower than method detection limit (MDL) to 40.2 µmol/L with a volume weighted mean value of 7.4 ± 8.8 µmol/L. The strong correlations between HCHO (aq) and HCOO? (r = 0.69, n = 137), HCHO (aq) and nss‐ (r = 0.74, n = 137), HCHO (aq) and (r = 0.67, n = 137), HCHO (aq) and (r = 0.74, n = 133) suggest the significant influence of the anthropogenic input for the HCHO (aq) levels. The concentration levels of rainwater HCHO (aq) was inversely proportional to the amount of rainfall, indicating the below‐cloud process is the most important mechanism for rainwater HCHO (aq) scavenging processes. More than 70% of the HCHO (aq) wet deposition took place during the early stage of the rainfall. According to the air mass back‐trajectory analysis, the rainwater with industrial back‐trajectories coming from the north had the highest levels of HCHO (aq) while the rainwater with the green‐covered or marine back‐trajectories from the southeast had the lowest concentrations, and this indicate the HCHO (aq) originated from urban or industrial regions served as an important source of the rainwater. The annual HCHO (aq) wet deposition flux was calculated as 6.96 mmol/m2 per year and the total deposition flux was estimated as 24.35 mmol/m2 per year, 71.4% of which was dominated by dry deposition. 相似文献
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利用Aura/OMI月均甲醛对流层垂直柱浓度数据对2005年—2016年中国广东省和江苏省的大气甲醛的时空变化规律、不同排放源的前体物的潜在贡献进行了分析。甲醛在广东省主要集中在珠三角地区,在江苏省分布则相对较为均匀。2005年—2010年,随着经济发展,在两省都发现了大面积的甲醛增加趋势;相应的,在2011年—2016年,由于减排等治理措施的实施,在两省都有大面积的甲醛减少现象。广东省的甲醛主要呈现出春季、秋季高于冬季再高于夏季的特征;而江苏地区夏季甲醛浓度远高于其他季节,并与光照强度的季节性特征较为一致。此外,由于广东省甲醛分布的均一性较差,因此区域性因素(如地形等)对广东省甲醛分布可能有着较大的影响。各个排放源中,工业源、交通源对珠三角潜在贡献可能较大;自然源对梅州等林地覆盖地区可能有相对较高的影响;在江苏省,各个排放源对甲醛的贡献相对均衡,但夏季较为频繁的生物质燃烧可能对夏季高值甲醛有着相对较高的贡献。 相似文献
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基于美国宇航局NASA/AURA卫星臭氧监测仪OMI数据,分析了2005—2014年长三角地区及其典型城市对流层O_3、NO_2柱浓度和HCHO大气总柱浓度的时空分布特征。结果表明:10 a间,长三角地区对流层O_3柱浓度和HCHO总柱浓度呈现增长趋势,O_3增量为0.23ppbv/10 a,HCHO增量为0.07×10~(16) mol/(cm~2·10 a),对流层NO_2柱浓度呈现降低趋势,减量为0.06×10~(15)mol/(cm~2·10 a);长三角地区对流层O_3柱浓度最大值出现在3、4、5月,而对流层NO_2柱浓度最大值出现在1、12月,HCHO总柱浓度最大值出现在6、7月;对流层O_3柱浓度的高值区分布在长三角中部、北部区域,对流层NO_2柱浓度高值区分布于长三角中部,HCHO总柱浓度高值区相对分散,且四季的分布各不相同。O_3与NO_2和HCHO在时间和空间上呈现一定的相关性。 相似文献
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大气痕量气体差分吸收光谱仪EMI( Environmental trace gases Monitoring Instrument)是搭载在“高分五号”(GF-5)卫星上的覆盖紫外—可见光波段的光谱仪,用于测量240—710 nm波长范围内的地球后向散射和太阳辐射,旨在量化全球对流层和平流层痕量气体的分布,如臭氧、二氧化氮等。本文关注EMI载荷对大气弱痕量气体甲醛(HCHO)的探测能力,并基于实测数据初步评估EMI HCHO产品的探测能力与精度。研究结果表明EMI的辐照度波长校准精度高,但在不同行之间存在较大的不均匀性,其波长校正的精度与仪器的狭缝函数高度依赖行位置的变化。基于EMI的HCHO反演的结果表明,EMI UV2频段的标称信噪比较低,使得利用差分吸收光谱技术(DOAS)得到的HCHO斜柱浓度SCD(Slant Column Density)存在较大的随机误差和拟合残差。现阶段,评估得到的EMI HCHO斜柱浓度的不确定性为1.2×1016 molec./cm2。与国际同类载荷TROPOMI(TROPospheric Ozone Monitoring Instrument)、OMI(Ozone Monitoring Instrument)的交叉对比验证结果表明,EMI可以捕捉到中国地区夏季HCHO的空间分布特征。EMI & TROPOMI与EMI & OMI的相关系数均大于0.8。但是在华东地区EMI HCHO普遍高于OMI和TROPOMI,其原因需要进一步研究。本文的研究证明了EMI对夏季HCHO的探测潜力及不足,可为后续类似载荷的指标设计和算法研发提供参考。 相似文献
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Formic acid is the major contributor to acid rain in some regions but its sources are not fully understood. We investigated the aqueous‐phase reactions of HCHO (aq) and OH . radicals at enlarged rainwater pH values (2.49–5.89) in Guiyang, China from May 2006 to April 2007. Our results show that there were no significant correlation between the [HCOOH]t/[HCHO] (aq) and the rainwater pH. The ratio did not appear to vary consistently as a function of rainwater pH as predicted by theoretical model. In addition, we saw no clear evidence that oxidation of HCHO (aq) would produce significant HCOOH (aq) which indicates this reaction may be only a minor contribution to the budget of HCOOH (g) in atmosphere. Further investigation is strongly suggested to be carried out in field cloud water, fog water, or rainwater because the ratios would be diverged from equilibrium value as a result of other chemical or physical processes. 相似文献
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为克服海泡石吸附甲醛达到饱和后失去吸附功能的缺陷,利用静态吸附实验研究热处理温度对海泡石吸附微量甲醛的影响,并运用扫描电镜、X射线衍射、红外吸收光谱、热重和BET比表面检测等方法研究相关机理。结果表明,硅胶干燥剂的存在明显提高了海泡石对空气中微量甲醛的吸附能力,并能降低甲醛含量至法定安全上限以下,在≤400℃的温度热处理后海泡石仍能保持良好的甲醛吸附性能,但经≥500℃热处理后甲醛吸附性能显著降低。结合表征研究,认为海泡石相的结晶水对甲醛形成化学吸附,而其以沸石孔洞为主的结构微孔有利于物理吸附的甲醛占位,≥450℃的热处理使结晶水不可逆脱出,沸石孔坍塌,从而吸附性能显著降低。该研究表明海泡石的吸附性能可以在低于450℃的温度下热再生,脱出的甲醛也可以通过燃烧消除。间歇性热再生海泡石的吸附性能可持续脱除空气中的微量甲醛。 相似文献
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