Inferring suspended sediment carbon content and particle size at high frequency from the optical response of a submerged spectrometer 

Author(s):  
Dhruv Sehgal ◽  
Núria Martínez-Carreras ◽  
Christophe Hissler ◽  
Victor Bense ◽  
AJF (Ton) Hoitink

<p>Manual and unattended sampling in the field and laboratory analysis are common practices to measure suspended sediment (SS) carbon content and particle size. However, one of the major drawbacks of these ex-situ methods is that they make high frequency measurements challenging. This includes restricted data collection due to limited access to the sampling locations during turbulent conditions or high flows, when the largest amount of sediments is transported downstream, introducing uncertainty in quantification of SS properties (particle size and carbon content) and sediment loads. Knowledge on SS carbon content and particle size is also important to better understand the multi-component form of suspended sediments (i.e. flocs) that directly affect sediment transport and other sediment properties (e.g. settling velocity and density). Moreover, SS carbon content and particle size exert an impact on the optical sensor readings that are traditionally used to measure turbidity. In that respect, high frequency measurements of SS carbon content and particle size could eventually help us to move from ‘local’ calibrations towards ‘global’ dependencies based on in-situ SS characterization.</p><p>In this study, we propose to use a submerged UV-VIS spectrometer to infer SS carbon content and particle size. The sensor measures the entire light absorption spectrum of water between 200 nm and 750 nm at sampling intervals as short as 2-minutes. To this end, we first test our approach under controlled conditions with an experimental laboratory setup consisting of a cylindrical tank (40-L) with an open top. An UV-VIS spectrometer and a LISST-200X sensor (to measure particle size distribution) are installed horizontally. A stirrer facilitates the homogeneous mixing of SS and prevents the settling of heavy particles at the bottom. We use the sediments sampled from 6 sites in Luxembourg with contrasting composition and representing different land use types and geological settings. The sampled sediments were wet sieved into 3 size classes to clearly recognize the effect of particle size on absorption. In our investigation, we use specific wavelengths, chemometric techniques and carbon content specific absorbance indices to infer SS composition and particle size from the absorption spectrum. Results are then validated using in-situ field data from two instrumented field sites in Luxembourg. Amid the challenge of associating laboratory and field results, the preliminary results indicate that the absorption spectrum measured with a submerged UV-VIS spectrometer can be used to estimate SS particle size and carbon content.</p>

Metals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1201
Author(s):  
Xinghua Ji ◽  
Cheng Zhang ◽  
Shufeng Li

SiCp reinforced aluminium matrix composites (AMCs), which are widely used in the aerospace, automotive, and electronic packaging fields along with others, are usually prepared by ex situ techniques. However, interfacial contamination and poor wettability of the ex situ techniques make further improvement in their comprehensive performance difficult. In this paper, SiCp reinforced AMCs with theoretical volume fractions of 15, 20, and 30% are prepared by powder metallurgy and in situ reaction via an Al-Si-C system. Moreover, a combined method of external addition and an in situ method is used to investigate the synergistic effect of ex situ and in situ SiCp on AMCs. SiC particles can be formed by an indirect reaction: 4Al + 3C → Al4C3 and Al4C3 + 3Si → 3SiC + 4Al. This reaction is mainly through the diffusion of Si, in which Si diffuses around Al4C3 and then reacts with Al4C3 to form SiCp. The in situ SiC particles have a smooth boundary, and the particle size is approximately 1–3 μm. A core-shell structure having good bonding with an aluminium matrix was generated, which consists of an ex situ SiC core and an in situ SiC shell with a thickness of 1–5 μm. The yield strength and ultimate tensile strength of in situ SiCp reinforced AMCs can be significantly increased with a constant ductility by adding 5% ex situ SiCp for Al-28Si-7C. The graphite particle size has a significant effect on the properties of the alloy. A criterion to determine whether Al4C3 is a complete reaction is achieved, and the forming mechanism of the core-shell structure is analysed.


2020 ◽  
Vol 13 (06) ◽  
pp. 2051035
Author(s):  
Xiaoping Jiang ◽  
Ronghua Wang ◽  
Ning Hu ◽  
Chaohe Xu

Ultra-small MnCo2O4 nanocrystals/nitrogen enriched carbon nanofiber composites, with particle size as small as 2–4[Formula: see text]nm and nitrogen content as high as [Formula: see text][Formula: see text]at.%, were designed and used as oxygen cathode materials for Li-O2 batteries, with an aprotic electrolyte. Via an in-situ nucleation and growth, the morphology, size and distribution of MnCo2O4 nanocrystals were well controlled on surface of nanofibers, with strong interfacial interactions between the two components. Benefitting from the unique microstructure and high-level nitrogen doping, the MnCo2O4/NCF composite can deliver discharge and charge capacities of 4147.8 and 3842.8[Formula: see text]mAh/g as oxygen cathode materials, and columbic efficiencies are about 92.6%. More importantly, the discharge products can completely decompose in charging process as evidenced by an ex-situ FESEM investigation, while for pure NCF cathode, particle and plate-like Li2O2 were still observed on its surface, which confirmed that the MnCo2O4/NCF composite has a superior electrocatalytic activity that that of NCF.


2015 ◽  
Vol 54 (20) ◽  
pp. 6367 ◽  
Author(s):  
Yuanzhi Zhang ◽  
Zhaojun Huang ◽  
Chuqun Chen ◽  
Yijun He ◽  
Tingchen Jiang

2021 ◽  
Vol 20 (4) ◽  
pp. 215-221
Author(s):  
Chatton Eliot ◽  
Labasque Thierry ◽  
Aurélie Guillou ◽  
Floury Paul ◽  
Aquilina Luc ◽  
...  

Dissolved gases are particularly relevant tools for the investigation of environmental processes. Indeed, their solubility being a function of the variables of physical state of the medium (temperature, pressure, salinity), the dissolved noble gases are for instance good indicators of equilibrium conditions with the atmosphere and mixing of water bodies. Dissolved gases can also inform the biogeochemical functioning of natural systems by providing information on major processes such as photosynthesis, respiration or denitrification. Classical methods relying on the sampling, the storage and the ex situ analysis of water samples for the measurement of dissolved gases suffer from the difficulty of taking sufficiently frequent and representative samples as well as the analyte preservation. High-frequency in situ measurement of dissolved gases is therefore the most relevant for the study of environmental processes. The use of Membrane Inlet Mass Spectrometer (MIMS) technology provides access to high frequency measurements of a large set of dissolved gases in the field (He, Ne, Ar, Kr, Xe, N2, O2, CO2, CH4, N2O, H2) which offers a real opportunity for environmental studies.


Author(s):  
R. Szymanski ◽  
J. Lynch

TEM is routinely used to control the metallic dispersion of industrial supported metal catalysts, since in complement to the chemisorptive methods it provides unique local information about particle size distribution, i.e. about the quality of the metal dispersion. An evaluation by TEM of the mean particle size can be useful to quantify the metal dispersion assuming a simple model for the particle shape, e.g. spherical or cubic. However, except for the cases where chemisorption fails (e.g. poisonning), this evaluation is mainly considered as a mean of checking the representativity of the statistical distribution of local information in comparison with chemisorption results. Discrepancies are often observed between the two techniques and many reasons can be advanced for these such as statistics, particle shape models, electron beam induced changes, chemisorption assumptions (cf coverage), etc... In fact, we consider that in a number of cases one of the primary limitations is likely to be due to the in situ problem in TEM, which is inherent to most techniques involving an ex situ characterization.


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