Spatial Distribution Of Chemical Components Research Articles

Diffusion zone evolution around growing crystals in combeite glass

AbstractThe precipitation of nonstoichiometric crystals (of different composition from the parent glass) motivated us to study the stoichiometric Na2O·2CaO·3SiO2 ( N2CS3) glass‐forming system comprehensively. The concentration profiles of Na and Ca in the diffusion zone around Na4+2xCa4−x[Si6O18], , crystals in an N2C3S glass were characterized by energy‐dispersive spectroscopy and were then theoretically described. We show that the diffusion zone is formed because of the rejection of part of calcium by the growing crystal. The radial variation of the Ca concentrations and the crystal nucleation rate through the diffusion zone were analyzed simultaneously. We found that the nucleation rate in the diffusion zone near the crystal–glass interface drastically decreases due to the increase in the work of critical cluster formation resulting from the composition change. In contrast, the diffusion activation barrier remains practically constant. Moreover, the Ca diffusion coefficients, DCa, in Na2O·2CaO·3SiO2 and CaO·SiO2 glasses show the same Arrhenius dependence, demonstrating that (surprisingly) DCa does not depend on the glass composition in the CaO·SiO2–Na2O·SiO2 metasilicate joint. This work provides the quantitative spatial distribution of chemical components in a partially crystallized glass, shedding light on solid solution crystallization in a glass‐forming liquid and its consequences.

Studies of Coins of Medieval Volga Bulgaria by Neutron Diffraction and Tomography

The phase composition and spatial distribution of chemical components in the volume of coins of medieval Volga Bulgaria are studied using the neutron-diffraction- and neutron-tomography methods. Two coins belonging to different time periods of this medieval state are studied: a Samanid multidirham dating from the first half of the 10th Century and a silver dirham dating from the period of the reign of the Bulgarian emir Bulat-Timur. It is established that both coins consist of a copper-silver alloy. In the Samanid multidirham, the average volume contents of copper and silver are found to be about 50%. Minor spatial variations in the chemical composition are found in the volume of the multidirham under study. It is established that the volume average silver content in the Bulat-Timur dirham is about 95%.

In Situ Chemical Monitoring and Imaging of Contents within Microfluidic Devices Having a Porous Membrane Wall Using Liquid Microjunction Surface Sampling Probe Mass Spectrometry.

The ability to observe dynamic chemical processes (e.g., signaling, transport, etc.) in vivo or in situ using nondestructive chemical imaging opens a new door to understanding the complex dynamics of developing biological systems. With the advent of "biology-on-a-chip" devices has come the ability to monitor dynamic chemical processes in a controlled environment, using these engineered habitats to capture key features of natural systems while allowing visual observation of system development. Having the capability to spatially and temporally map the chemical signals within these devices may yield new insights into the forces that drive biosystem development. Here, a porous membrane sealed microfluidic device was designed to allow normal microfluidic operation while enabling continuous, location specific sampling and chemical characterization by liquid microjunction surface sampling probe mass spectrometry (LMJ-SSP MS). LMJ-SSP was used to extract fluids with nL-to-μL/min flow rates directly from selected areas of the microfluidic device without negatively impacting the device function. These extracts were subsequently characterized using MS. This technique was used to acquire MS images of the entirety of several multi-input microfluidic devices having different degrees of fluid mixing. LMJ-SSP MS imaging visualized the spatial distribution of chemical components within the microfluidic channels and could visualize chemical reactions occurring in the device. These microfluidic devices with a porous membrane wall are wholly compatible with the construction of biology-on-a-chip devices. This ultimately would enable correlation of biosystem physical structure with an evolving chemical environment.

Revealing the Elemental Distribution within Latent Fingermarks Using Synchrotron Sourced X-ray Fluorescence Microscopy.

Fingermarks are an important form of crime-scene trace evidence; however, their usefulness may be hampered by a variation in response or a lack of robustness in detection methods. Understanding the chemical composition and distribution within fingermarks may help explain variation in latent fingermark detection with existing methods and identify new strategies to increase detection capabilities. The majority of research in the literature describes investigation of organic components of fingermark residue, leaving the elemental distribution less well understood. The relative scarcity of information regarding the elemental distribution within fingermarks is in part due to previous unavailability of direct, micron resolution elemental mapping techniques. This capability is now provided at third generation synchrotron light sources, where X-ray fluorescence microscopy (XFM) provides micron or submicron spatial resolution and direct detection with sub-μM detection limits. XFM has been applied in this study to reveal the distribution of inorganic components within fingermark residue, including endogenous trace metals (Fe, Cu, Zn), diffusible ions (Cl-, K+, Ca2+), and exogeneous metals (Ni, Ti, Bi). This study incorporated a multimodal approach using XFM and infrared microspectroscopy analyses to demonstrate colocalization of endogenous metals within the hydrophilic organic components of fingermark residue. Additional experiments were then undertaken to investigate how sources of exogenous metals (e.g., coins and cosmetics) may be transferred to, and distributed within, latent fingermarks. Lastly, this study reports a preliminary assessment of how environmental factors such as exposure to aqueous environments may affect elemental distribution within fingermarks. Taken together, the results of this study advance our current understanding of fingermark composition and its spatial distribution of chemical components and may help explain detection variation observed during detection of fingermarks using standard forensic protocols.

PAT: From Western solid dosage forms to Chinese materia medica preparations using NIR-CI.

Near-infrared chemical imaging (NIR-CI) is an emerging technology that combines traditional near-infrared spectroscopy with chemical imaging. Therefore, NIR-CI can extract spectral information from pharmaceutical products and simultaneously visualize the spatial distribution of chemical components. The rapid and non-destructive features of NIR-CI make it an attractive process analytical technology (PAT) for identifying and monitoring critical control parameters during the pharmaceutical manufacturing process. This review mainly focuses on the pharmaceutical applications of NIR-CI in each unit operation during the manufacturing processes, from the Western solid dosage forms to the Chinese materia medica preparations. Finally, future applications of chemical imaging in the pharmaceutical industry are discussed.

Studies on paint cross sections of a glass painting by using FT‐IR and Raman microspectroscopy supported by univariate and hierarchical cluster analyses

Fourier transform infrared (FT‐IR) and Raman spectroscopy is used for the non‐destructive analysis of painting materials and ageing compounds in micrometric cross sections of a glass painting. The combination of both techniques in conjunction with imaging/mapping function provides the spatial distribution of chemical components identified in vibrational spectra. The aim of our work is to show the applicability of the FT‐Raman mapping technique in the detection of painting materials. We also compare Raman information gained by using two laser excitations at 532 and 1064 nm implemented in microspectrometers with different confocality and spatial resolution. In turn among FT‐IR imaging techniques, we compare chemical images recorded in external reflection and attenuated total reflection modes that give chemical images of different size and spatial resolution. Our FT‐IR and Raman imaging characterize a number of painting materials such as pigments, binders, fillers as well as degradation products. Raman maps are constructed by using the univariate analysis. In turn, a profile of IR images requires the use of a more complex methodology. Here, we compare FT‐IR images of the painting cross sections obtained by using the univariate and hierarchical cluster analysis. We clearly show that the multivariate approach is a powerful tool for the credible construction of IR images, providing the relevant chemical information on the multicomponent stratigraphy of the samples. Moreover, the combination of all the methods allows us to demonstrate their degree of utility for the study on the paint cross sections of the works of art. Copyright © 2013 John Wiley & Sons, Ltd.

中部山岳地域の降雪に含まれる化学成分濃度の空間分布

中部山岳地域の降雪に含まれる化学成分濃度の空間分布

Evaluation of Mixing Process of Magnesium Stearate as Lubricant and the Spatial Distribution of Chemical Components in a Tablet by Vibrational Spectroscopic Imaging

In the work presented in this paper, a mixing procedure for a tableting process was evaluated using a simple formulation with Magnesium Stearate as the lubricant. Assessment of the spatial distribution of chemical components in a tablet can be effectively accomplished by Vibrational Spectroscopic Imaging techniques that employ Raman spectroscopy and NIR spectroscopy.We show that, by selecting the proper rotation speed for the high speed mixer selected, similar drug release and tablet hardness parameters can be achieved between a tumbling type mixer and a twin shell mixer. Additionally by changing the time of mixing we can produce samples from both mixing methods with similar drug release rates. We relate these release rates to the hardness of the tablets, the tablet and, ultimately, to the distribution and particle size of the drug and lubricant on the surface of the tablets evaluated using the spectroscopic imaging techniques cited above.

Spatial Distribution of Chemical Components in Aerosol Particles as Determined from Secondary Electron Yield Measurements: Implications for Mechanisms of Multicomponent Aerosol Crystallization

Secondary electron yield measurements were used to determine the distribution of chemical components in multicomponent aerosol particles formed by crystallization from aqueous solution droplets. Yield measurements were made by measuring the charge acquired by a beam of particles as they passed through an electron beam (100–600 eV energy) inside a high-vacuum apparatus. Yields were sufficiently different for certain compounds that measurements made on two-component particles could be used to obtain information on the spatial distribution of components. Variations in chemical composition as a function of depth beneath the particle surface were ascertained from the energy dependence of the measured yields, since the electron penetration depth, and therefore the probe depth, increases with electron energy. The results for mixed NaCl–NH4Cl particles indicate that the distribution of components within these particles is relatively homogeneous, while measurements made on mixed NaCl–NaNO3particles are indicative of particles having a heterogeneous core–shell morphology. Results for mixed Na2SO4–(NH4)2SO4particles are ambiguous, probably because of the complexity of the phase diagram of this system. It appears that the mechanism by which aerosol particles crystallize, and therefore the resulting distribution of chemical components within particles, is strongly dependent on particle composition and environmental variables.

Chemical characteristics of snow in the region along the Sea of Japan

The amount of acidity in precipitation has been measured in heavy-snowfall regions facing the Sea of Japan. The average pH value of precipitation measured throughout the year at Nagaoka was 4.80 during 4.5 years, 1987–92. During winter the pH value is lower and electric conductivity higher. The spatial distribution of chemical components in new-fallen snow was studied along a 55 km-long sampling route. Results from four surveys showed that acidic snows have average pH values of 4.63–4.90. From the distribution of anion and cation concentration in new-fallen snow, it is concluded that strong northwest monsoons during winter bring an abundance of snow with salt components and many non-salt components from the Sea of Japan and also, possibly, from the Asian continent.

Chemical characteristics of snow in the region along the Sea of Japan

The amount of acidity in precipitation has been measured in heavy-snowfall regions facing the Sea of Japan. The average pH value of precipitation measured throughout the year at Nagaoka was 4.80 during 4.5 years, 1987–92. During winter the pH value is lower and electric conductivity higher. The spatial distribution of chemical components in new-fallen snow was studied along a 55 km-long sampling route. Results from four surveys showed that acidic snows have average pH values of 4.63–4.90. From the distribution of anion and cation concentration in new-fallen snow, it is concluded that strong northwest monsoons during winter bring an abundance of snow with salt components and many non-salt components from the Sea of Japan and also, possibly, from the Asian continent.