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Infrared water vapor continuum absorption at atmospheric temperatures

机译:大气温度下红外水蒸气的连续吸收

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We have used a continuous-wave carbon dioxide laser in a single-mode realization of cavity ring-down spectroscopy to measure absorption coefficients of water vapor at 944 cm(-1) for several temperatures in the range 270-315 K. The conventional description of water vapor infrared absorption is applied, in which the absorption is modeled in two parts consisting of local line absorption and the remaining residual absorption, which has become known as the water vapor continuum. This water vapor continuum consists of distinct water-water, water-nitrogen, and water-oxygen continua. The water-water continuum absorption coefficient is found to have a magnitude of C-s(296 K)=(1.82 +/- 0.02) X 10(-22) cm(2) molecule(-1) atm(-1), and the water-nitrogen coefficient has a magnitude of C-n(296 K)=(7.3 +/- 0.4) X 10(-25) cm(2) molecule(-1) atm(-1). The temperature dependences of both the water-water and the water-nitrogen continua are shown to be well represented by a model describing the expected behavior of weakly bound binary complexes. Using this model, our data yield dissociation energies of D-e=(-15.9 +/- 0.3) kJ/mole for the water dimer and D-e=(-3.2 +/- 1.7) kJ/mole for the water-nitrogen complex. These values are in excellent agreement with recent theoretical predictions of D-e=-15.7 kJ/mole (water dimer) and D-e=-2.9 kJ/mole (water-nitrogen complex), as well as the experimentally determined value of D-e=(-15.3 +/- 2.1) kJ/mole for the water dimer obtained by investigators employing a thermal conductivity technique. Although there is reasonably good agreement with the magnitude of the continuum absorption coefficients, the agreement on temperature dependence is less satisfactory. While our results are suggestive of the role played by water dimers and water complexes in producing the infrared continuum, the uncertain spectroscopy of the water dimer in this spectral region prevents us from making a firm conclusion. In the meantime, empirical models of water vapor continuum absorption, essential for atmospheric radiative transfer calculations, should be refined to give. better agreement with our low-uncertainty continuum absorption data. (c) 2005 American Institute of Physics.
机译:我们在腔衰荡光谱的单模实现中使用了连续波二氧化碳激光器,以测量270-315 K范围内几个温度下944 cm(-1)处水蒸气的吸收系数。常规描述应用水蒸气红外吸收法,其中吸收被建模为由局部线吸收和剩余的残留吸收两部分组成,这被称为水蒸气连续体。该水蒸气连续体由不同的水-水,水-氮和水-氧连续体组成。发现水-水连续体吸收系数的大小为Cs(296 K)=(1.82 +/- 0.02)X 10(-22)cm(2)分子(-1)atm(-1),并且水氮系数的大小为Cn(296 K)=(7.3 +/- 0.4)X 10(-25)cm(2)分子(-1)atm(-1)。通过描述弱结合的二元配合物的预期行为的模型可以很好地表示水-水和水-氮连续体的温度依赖性。使用该模型,我们的数据对水二聚体的解离能为D-e =(-15.9 +/- 0.3)kJ / mol,对水氮络合物的解离能为D-e =(-3.2 +/- 1.7)kJ / mol。这些值与De = -15.7 kJ / mol(水二聚体)和De = -2.9 kJ / mol(水-氮络合物)的最新理论预测以及De =(-15.3)的实验确定值非常吻合+/- 2.1)kJ /摩尔,由研究人员采用热导率技术获得。尽管与连续吸收系数的大小有相当好的一致性,但是对温度依赖性的一致性不太令人满意。虽然我们的结果表明水二聚体和水络合物在产生红外连续体中所发挥的作用,但在该光谱区域中水二聚体的不确定光谱阻止了我们做出可靠的结论。同时,应完善水蒸气连续吸收的经验模型,这对于大气辐射传递计算至关重要。与我们的低不确定连续性吸收数据更好地达成了一致。 (c)2005年美国物理研究所。

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