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We present H2CO observations of young protostar candidates in the Serpens Cloud Core. We find evidence for dense molecular gas in the cores of these objects that is warmer than the surrounding dust. The strong emission and gas properties support the premise that many of these sources may be very young protostars. 相似文献
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D. W. Arlander D. Brüning U. Schmidt D. H. Ehhalt 《Journal of Atmospheric Chemistry》1995,22(3):251-269
A series of 149 measurements of the HCHO mixing ratio were made between 0 and 10 km altitude and 70° N to 60° S latitude during TROPOZ II. The data show a vertical decrease of the HCHO mixing ratio with altitude at all latitudes and a broad latitudinal maximum in the HCHO mixing ratio between 30° N and 30° S at all altitudes. The measured mixing ratios of HCHO are considerably higher than those expected from CH4 oxidation alone, but agree broadly with the average latitude by altitude distribution of HCHO derived by a 2D model including emissions of C1–C7 hydrocarbons. A number of the regional scale deviations of the measured HCHO distribution from the average modelled one can be explained in terms of the local wind field. 相似文献
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D. Perner U. Platt M. Trainer G. Hübler J. Drummond W. Junkermann J. Rudolph B. Schubert A. Volz D. H. Ehhalt K. J. Rumpel G. Helas 《Journal of Atmospheric Chemistry》1987,5(2):185-216
Using long path UV absorption spectroscopy we have measured OH concentrations close to the earth's surface. The OH values observed at two locations in Germany during 1980 through 1983 range from 0.7×106 to 3.2×106 cm-3. Simultaneously we measured the concentrations of O3, H2O, NO, NO2, CH4, CO, and the light non methane hydrocarbons. We also determined the photolysis rates of O3 and NO2. This allows calculations of OH using a zero dimensional time depdendent model. The modelled OH concentrations significantly exceed the measured values for low NO
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concentrations. It is argued that additional, so far unidentified. HO
x
loss reactions must be responsible for that discrepancy. 相似文献
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Sol-gel法制备SiO2-TiO2复合薄膜，进行甲醛的光催化降解实验，研究了SiO2掺杂量、薄膜焙烧温度、甲醛溶液pH值及初始浓度对光催化性能的影响。结果表明，500℃焙烧1h，掺杂质量SiO2：TiO2=12：100时，SiO2-TiO2薄膜的光催化活性最高，150min后甲醛降解率达76％，是单纯TiO2薄膜的1．3倍，该薄膜稳定性较好，经重复8次使用，最大降解率只下降4％。 相似文献
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The effects of Fe2+ on the trimethylamine N-oxide (TMAO) demethylating activity of the Harpadon nehereus kidney extract were studied in this research.The activity of the kidney extract was presumably inhibited by ethylene diamine tetra-acetic acid (EDTA),which indicates that the kidney extract contains an enzyme or enzyme system with metal cations as activator.Activity of the kidney extract was enhanced significantly when Fe2+ was added into the model system in vitro.As the concentration of Fe2+ increased,the decomposing rate of TMAO increased rapidly until TMAO decomposed completely.The activity of the kidney extract was also enhanced by reductant such as ascorbic acid.Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) was employed to determine the content of total iron in a number of fishery products.Significant positive correlation between the contents of total iron and endogenous formaldehyde (FA) was found,especially in marine products. 相似文献
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J. Kesselmeier 《Journal of Atmospheric Chemistry》2001,39(3):219-233
Field and laboratory investigations of the exchange of the short-chain organic acids – formic acid and acetic acid – as well as their homologous aldehydes are discussed. Both acids are substantially released from several plant species. Emission measurements under field conditions are compiled to give an overview of three years of measurements. Emission rates from several tree species were found in the range between zero and 60 nmoles m–2 min–1 for acetic acid and between zero and 90 nmoles m–2 min–1 for formic acid though also a deposition has been observed to orange trees. Investigations under laboratory conditions showed an order of magnitude lower emission rates with significant differences under light and dark conditions, and a deposition was observed under certain conditions. Hence, low emission rates or even a bi-directional exchange, emission as well as deposition have to be taken into account. Further differences between field and laboratory studies are discussed considering age of trees, stress effects and a potential production of acids by photochemical conversion of precursors inside enclosures during sampling. Field data on the exchange of form- and acetaldehyde show a complex behavior. We found emission as well as uptake. The bi-directional exchange is significantly triggered by the ambient mixing ratios of both aldehyde species and exhibits a compensation point. Further studies are needed for generalization of the exchange of these and potentially also for other compounds. 相似文献
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G. W. Harris D. Klemp T. Zenker J. P. Burrows B. Mathieu 《Journal of Atmospheric Chemistry》1992,15(3-4):315-326
Measurements of NO2, HCHO, and H2O2 were made by the highly specific method of mid infra-red absorption spectroscopy using tunable diode lasers (TDLAS) during the 1988 Polarstern expedition. The TDLAS data are compared to those obtained during the cruise using less direct methods. Southern Hemisphere NO2 levels suggest nett photochemical destruction of O3 in the boundary layer. Northern Hemisphere HCHO averaged 0.47±0.2 ppbv; the HCHO measurements are used in a simple calculation to estimate OH noontime maxima of 3–6×106 cm-3. 相似文献
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Howard B. Ross Christer Johansson Claes de Serves John Lind 《Journal of Atmospheric Chemistry》1992,14(1-4):411-423
Atmospheric peroxides and formaldehyde were measured at two sites in Sweden; inside a Scots pine stand (Jädraås) and on top of Mt. Åreskutan (1250 msl). Peroxide levels at Jädraås were highest during the day and lowest during the night. Mid-day concentrations of H2O2 varied between 0.05 and 2 ppbv. Isentropic trajectories together with local O3 measurements indicated the importance of long range transport on surface H2O2 lévels. Large diurnal variations and vertical profiles showed the importance of turbulent mixing processes and dry deposition. A comparison of H2O2 and O3 diurnal variations indicated a more rapid dry deposition of H2O2 to the forest. It would appear that terpenes emitted from the forest play a minor role in controlling the H2O2 levels. Formaldehyde at Jädraås had a different diurnal variation than peroxides; highest levels were observed in the early evening indicating chemical production of CH2O. Diurnal variations of peroxides on Mt Åreskutan were opposite to those at Jädraås, highest concentrations were observed during the night. This result is to be expected if during the day air from inside the valley, with lower peroxide levels relative to the free troposphere, rises to the mountain top. In the evening, subsidence brings free tropospheric air with higher peroxides levels to the mountain. 相似文献