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Influence of the target material on secondary plasma formation underwater and its laser induced breakdown spectroscopy (LIBS) signal

机译:目标材料对水下二次等离子体形成的影响及其激光诱导击穿光谱(LIBS)信号

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The goal of this study was to investigate whether a secondary plasma can be formed on a non-metallic target under water and to give insight into the related processes. The material of choice here was alumina, since its physical, thermal and mechanical properties are substantially different from those of pure Al, only for which secondary plasma formation was recently demonstrated. To achieve this, plasma and bubble formation on alumina under water after single pulse laser excitation were studied using fast photography, shadowgraphy, Schlieren and LIBS techniques. The results show that the secondary plasma caused by backward heating of the target and successive slow target evaporation into the growing vapour bubble also occurs for alumina. The secondary plasma formed on alumina involves only a narrow interaction region on the target resulting in an almost spherical plume shape. In contrast, on thermally conductive and easily melting/evaporating aluminium, the secondary plasma is intense, with a large volume which is flattened on the target surface. Inside the expanded bubble above the alumina target, glowing particles were not observed. Due to less efficient secondary plasma formation on alumina compared to aluminium, its optical emission only slightly increases at a delay of 400 ns from the laser pulse but emission persists during three bubble cycles with a total duration of about 650 us. The LIBS spectra related to the secondary plasma are almost free from any continuum component and show narrow emission lines from low excited states. Here we discuss the observed differences in the plasma's spatial, temporal and spectral evolution on the two considered target materials. The obtained results indicate that under water a secondary plasma might be formed on very different materials and that its detection produces a good quality LIBS signal from single pulse excitation using a commercial nanosecond laser source.
机译:这项研究的目的是调查是否可以在水下的非金属靶上形成二次等离子体,并深入了解相关过程。此处选择的材料是氧化铝,因为它的物理,热和机械性能与纯铝的性能有很大不同,只有最近才证明可形成二次等离子体。为了达到这个目的,使用快速摄影,阴影照相法,Schlieren和LIBS技术研究了单脉冲激光激发后在水下氧化铝上的等离子体和气泡的形成。结果表明,对于氧化铝,还会发生由靶材向后加热和连续缓慢的靶材蒸发进入不断增长的蒸汽泡所引起的次级等离子体。在氧化铝上形成的次级等离子体仅涉及靶材上的狭窄相互作用区域,从而产生近乎球形的羽状形状。相反,在导热且易于熔化/蒸发的铝上,次级等离子体强度大,在目标表面变平。在氧化铝靶上方的膨胀气泡内部,未观察到发光颗粒。由于与氧化铝相比,氧化铝上次生等离子体的形成效率较低,因此其光发射仅在距激光脉冲400 ns的延迟处略有增加,但在三个气泡循环中持续存在,总持续时间约为650 us。与次级等离子体相关的LIBS光谱几乎没有任何连续谱成分,并且显示出来自低激发态的窄发射线。在这里,我们讨论了在两种考虑的目标材料上,等离子体在空间,时间和光谱演化方面观察到的差异。获得的结果表明,在水下,次级等离子体可能在非常不同的材料上形成,并且其检测通过使用商用纳秒激光源的单脉冲激发产生了高质量的LIBS信号。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2017年第2期|345-353|共9页
  • 作者单位

    Institute of Physics, University of Belgrade, P.O. Box 68, 11081 Belgrade, Serbia;

    ESEA (FSN-TECFIS-DIM), Via E. Fermi 45, 00044 Frascati, RM, Italy;

    Institute of Physics, University of Belgrade, P.O. Box 68, 11081 Belgrade, Serbia;

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