Cias Pawel, Wang Chuji, Dibble Theodore S
Institute for Clean Energy Technology, Mississippi State University, 205 Research Boulevard, Starkville, Mississippi 39759, USA.
Appl Spectrosc. 2007 Feb;61(2):230-6. doi: 10.1366/000370207779947440.
Many molecules or transient radicals have well-documented absorption cross-sections in the ultraviolet (UV) region, but their absorption cross-sections in the near-infrared (NIR) region are much less often known and are difficult to measure. We propose a method to determine the unknown NIR absorption cross-sections using the known absorption cross-sections in the UV region, in which single-path UV absorption spectroscopy and NIR continuous wave cavity ringdown spectroscopy (cw-CRDS) are employed in a cross-arm reaction chamber for simultaneous measurements. Without knowing the actual sample partial pressures (or concentrations), the NIR absorption cross-sections can be accurately determined through the two sets of measurements. The method is demonstrated by measuring the NIR absorption cross-section of the first overtone of the asymmetric C-H stretch of 2-methyl-1,3-butadiene (isoprene) (3.24 (+/-0.16) x 10(-22) cm(2) molecule(-1)) at 1651.52 nm using the known value of the absorption cross-section at 220 nm. The diode laser wavelength was calibrated by atmospheric cavity ringdown spectra of CH(4), CO(2), and H(2)O. By comparison with sample pressure measurements, this method can also be used as a pressure calibration means for the reaction chamber, and this has been demonstrated with two additional measurements of the absorption cross-sections of 1,3-butadiene and 2,3-dimethyl-1,3-butadiene (2.50 (+/- 0.08) x 10(-22) and 2.82 (+/-0.16) x 10(-22) cm(2) molecule(-1), respectively) at 1651.52 nm. The applicability of the method to determining absorption cross-sections using the simultaneous measurements of cw-CRDS and single-path absorption spectroscopy is discussed.
许多分子或瞬态自由基在紫外(UV)区域具有记录详实的吸收截面,但它们在近红外(NIR)区域的吸收截面却鲜为人知且难以测量。我们提出了一种利用UV区域已知的吸收截面来确定未知的NIR吸收截面的方法,该方法在一个交叉臂反应腔中采用单路径UV吸收光谱法和NIR连续波腔衰荡光谱法(cw-CRDS)进行同步测量。在不知道实际样品分压(或浓度)的情况下,通过这两组测量可以准确确定NIR吸收截面。通过使用220nm处已知的吸收截面值,在1651.52nm处测量2-甲基-1,3-丁二烯(异戊二烯)不对称C-H伸缩振动的第一泛频的NIR吸收截面(3.24(±0.16)×10⁻²² cm² 分子⁻¹),证明了该方法的有效性。二极管激光波长通过CH₄、CO₂和H₂O的大气腔衰荡光谱进行校准。通过与样品压力测量结果相比较,该方法还可以用作反应腔的压力校准手段,这已通过在1651.52nm处对1,3-丁二烯和2,3-二甲基-1,3-丁二烯的吸收截面进行的另外两次测量(分别为2.50(±0.08)×10⁻²²和2.82(±0.16)×10⁻²² cm² 分子⁻¹)得到了验证。讨论了该方法在利用cw-CRDS和单路径吸收光谱同步测量来确定吸收截面方面的适用性。