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Photophoretictrapping-Raman spectroscopy for single pollens and fungal spores trapped in air

机译:用于单个花粉的photophoretictrapping-Raman光谱 和真菌孢子被困在空气中

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摘要

Photophoretic trapping-Raman spectroscopy (PTRS) is a new technique for measuring Raman spectra of particles that are held in air using photophoretic forces. It was initially demonstrated with Raman spectra of stro ly-absorbing carbon nanoparticles (Pan et al. [44] (Opt Express 2012 )). In the present paper we report the first demonstration of the use ofPTRS to measure Raman spectra of absorbing and weakly-absorbing bioaerosol particles (pollens and spores ). Raman spectra of three pollens and one smut spore in a size range of 6.2- 41.8 11m illuminated at 488 nm are shown. Quality spectra were obtained in the Raman s hift range of 1600- 3400 cm- I in this exploratory stud y. Distinguis hable Raman scattering signals with one or a few clear Raman peaks for all four aerosol particles were observed within the wavenumber region 2940- 3030 cm- I. Peaks in this region are consistent with previous reports of Raman peaks in the 1600- 3400 cm- I range for pollens and spores excited at 514 nm measured by a conventional Raman spectrometer. Noise in the spectra, the fluorescence background, and the weak Raman signals in most of the 1600- 3400 cm - I region make some of the spectral features barely discernable or not discernable for these bioaerosols except the strong signal within 2940- 3030 cm- I . Up to five bands are identified in the three pollens and only two bands appear in the fungal spore, but this may be because the fungal spore is so much smaller than any of the pollens. The fungal spore signal relative to the air-nitrogen Raman band is approximately 10 times smaller than that ratio for the pollens. The five bands are tentatively assigned to the CH2 symmetric stretch at 2948 cm - I, CH2 Fermi resonance stretch at 2970 cm- I, CH) symmetric stretch at 2990 cm - I, CH3 out-of-plane end asymmetric stretch at 3010 cm - I, and unsaturated = CH stretch at 3028 cm - I . The two dominant bands of the up-to-five Raman bands in the 2940- 3030 cm - I region have a consistent band spacing of 25 cm- I in all four aerosols. Finally we discuss improvements to the PTRS that should provide a system which can trap a hig her fraction of particle types and obtain Raman spectra over a larger range (e.g., 200- 3600 cm - I ) than those achieved here.
机译:光电捕获-拉曼光谱法(PTRS)是一种新技术,可利用电泳力测量保留在空气中的颗粒的拉曼光谱。最初是用吸收性碳纳米粒子的拉曼光谱证明的(Pan等人[44](Opt Express 2012)。在本文中,我们报告了使用PTRS来测量吸收和弱吸收生物气溶胶颗粒(花粉和孢子)的拉曼光谱的首次演示。显示了在488 nm照射下大小为6.2-41.8 11m的三个花粉和一个黑穗病孢子的拉曼光谱。在该研究性研究中,在1600-3400 cm-1的拉曼分离范围内获得了质量光谱。在波数区域2940-3030 cm-I内观察到所有四个气溶胶颗粒具有一个或几个清晰的拉曼峰的可分辨拉曼散射信号。该区域的峰与先前报道的1600-3400 cm-内的拉曼峰一致。 I范围是用常规拉曼光谱仪测得的在514nm激发的花粉和孢子。在1600-3400 cm-I区域的大部分区域中,光谱中的噪声,荧光背景和微弱的拉曼信号使这些生物气溶胶的光谱特征几乎无法辨别或无法辨别,除了2940-3030 cm- I范围内的强信号。在三个花粉中最多识别出五个条带,而在真菌孢子中仅出现两个条带,但这可能是因为真菌孢子比任何花粉都小得多。相对于空气氮拉曼谱带,真菌孢子信号比花粉的比率小约10倍。暂时将这五个频段分配给2948 cm处的CH2对称拉伸-I,2970 cm-1处的CH2费米共振拉伸-I,2990 cm处的CH2对称拉伸-I,3010 cm处的CH3面外端不对称拉伸- I,不饱和= CH在3028 cm处拉伸-I。在所有4个气溶胶中,在2940-3030 cm-I区域中最多五个拉曼带的两个主要带具有一致的25 cm-1的带间距。最后,我们讨论了对PTRS的改进,该改进应该提供一个系统,该系统可以捕获比其所实现的更大的范围(例如200- 3600 cm-I)的粒子类型的一部分,并获得拉曼光谱。

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