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In situ monitoring of powder blending by non-invasive Raman spectrometry with wide area illumination

机译:原位监测非侵入式拉曼光谱法与广域照明的非侵入式拉曼光谱法

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A 785nm diode laser and probe with a 6mm spot size were used to obtain spectra of stationary powders and powders mixing at 50rpm in a high shear convective blender. Two methods of assessing the effect of particle characteristics on the Raman sampling depth for microcrystalline cellulose (Avicel), aspirin or sodium nitrate were compared: (i) the information depth, based on the diminishing Raman signal of TiO2 in a reference plate as the depth of powder prior to the plate was increased, and (ii) the depth at which a sample became infinitely thick, based on the depth of powder at which the Raman signal of the compound became constant. The particle size, shape, density and/or light absorption capability of the compounds were shown to affect the " information" and " infinitely thick" depths of individual compounds. However, when different sized fractions of aspirin were added to Avicel as the main component, the depth values of aspirin were the same and matched that of the Avicel: 1.7mm for the " information" depth and 3.5mm for the " infinitely thick" depth. This latter value was considered to be the minimum Raman sampling depth when monitoring the addition of aspirin to Avicel in the blender. Mixing profiles for aspirin were obtained non-invasively through the glass wall of the vessel and could be used to assess how the aspirin blended into the main component, identify the end point of the mixing process (which varied with the particle size of the aspirin), and determine the concentration of aspirin in real time. The Raman procedure was compared to two other non-invasive monitoring techniques, near infrared (NIR) spectrometry and broadband acoustic emission spectrometry. The features of the mixing profiles generated by the three techniques were similar for addition of aspirin to Avicel. Although Raman was less sensitive than NIR spectrometry, Raman allowed compound specific mixing profiles to be generated by studying the mixing behaviour of an aspirin-aspartame-Avicel mixture. ? 2012.
机译:使用6mm光斑尺寸的785nm二极管激光和探针用于在高剪切对流混合器中获得50rpm的固定粉末和粉末混合的粉末。比较了两种评估颗粒特性对微晶纤维素(Avicel),阿司匹林或硝酸钠的拉曼采样深度的影响:(i)信息深度,基于作为深度的参考板中的TiO2中的拉曼信号递减在板之前的粉末增加,并且(ii)基于化合物的拉曼信号变得恒定的粉末的深度,样品变厚的深度。显示化合物的粒度,形状,密度和/或光吸收能力,从而影响各种化合物的“信息”和“无限厚”深度。然而,当将不同尺寸的阿司匹林的级分添加到Avicel作为主要成分中时,阿司匹林的深度值与Avicel的深度值相同并匹配“信息”深度和3.5毫米的“无限厚”深度为3.5mm 。当监测搅拌器中的Aspirin加入Aspirin时,后一个值被认为是最小拉曼采样深度。非侵入性地通过容器的玻璃壁获得阿司匹林的混合型材,可用于评估将阿司匹林混合到主要成分中的方式,鉴定混合过程的终点(与阿司匹林的粒度变化) ,并实时确定阿司匹林的浓度。将拉曼程序与另外两种非侵入性监测技术进行比较,近红外(NIR)光谱和宽带声发射光谱法。由三种技术产生的混合型材的特征类似于加入阿司匹林到Avicel。虽然拉曼比NIR光谱法敏感,但拉曼允许通过研究阿司匹林 - 阿斯巴甘氨胶混合物的混合行为来产生化合物特异性混合型材。还是2012年。

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