Processing, Morphology, and Water Uptake of Nafion/Ex situ Stöber Silica Nanocomposite Membranes As a Function of Particle Size

2012 ◽  
Vol 4 (12) ◽  
pp. 6766-6773 ◽  
Author(s):  
Beatrice Muriithi ◽  
Douglas A. Loy
Keyword(s):  
Particle Size ◽  
Water Uptake ◽  
Ex Situ ◽  
Nanocomposite Membranes ◽  
Silica Nanocomposite

scholarly journals In Situ Synthesis of Core-Shell-Structured SiCp Reinforcements in Aluminium Matrix Composites by Powder Metallurgy

Metals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1201
Author(s):  
Xinghua Ji ◽  
Cheng Zhang ◽  
Shufeng Li
Keyword(s):  
Particle Size ◽  
Powder Metallurgy ◽  
Shell Structure ◽  
Ex Situ ◽  
Aluminium Matrix ◽  
Core Shell ◽  
Matrix Composites ◽  
Aluminium Matrix Composites ◽  
Core Shell Structure

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.

scholarly journals Effects of Different Pretreatments and Seed Coat on Dormancy and Germination of Seeds of Senna obtusifolia (L.) H.S. Irwin & Barneby (Fabaceae)

2016 ◽  
Vol 8 (2) ◽  
pp. 77
Author(s):  
Stephen I. Mensah ◽  
Chimezie Ekeke
Keyword(s):  
Sulfuric Acid ◽  
Seed Dormancy ◽  
Water Uptake ◽  
Seed Coat ◽  
Critical Factor ◽  
Potassium Nitrate ◽  
Ex Situ ◽  
Mechanical Resistance ◽  
Physical Dormancy ◽  
Senna Obtusifolia

<p class="1Body">The seed dormancy of <em>Senna obtusifolia</em> was investigated through various methods, namely pretreatments in concentrated sulfuric acid, 2% potassium nitrate (KNO<sub>3</sub>), 99% ethanol, 99% methanol, and in hydrogen perioxide; examination of the seed coverings; and the determination of water uptake by the seeds in order to ascertain the most effective technique for breaking dormancy and also determine the dormancy type. The results showed that sulfuric acid treatment recorded the highest germination (100%); followed by 2% hydrogen peroxide treatment (24%) in 15minutes immersion. The methanol and ethanol pretreatments gave 18.33% and 16.5% germinations respectively. Pretreatment in 2% potassium nitrate gave the lowest germination (8.50%), while the intact seeds of <em>S. obtusifiolia</em> (control) gave 0% germination. The anatomy of the seed coat indicated the presence of hard, thickened and specialized cells of cuticle, macrosclereids, osteoscereids, and disintegrated parenchyma layers. The water uptake of intact seeds was low (13.5%) after 24 hr imbibitions. These findings revealed that the seed coat acts as barrier to germination by preventing water absorption, possibly gaseous diffusion in and out of the seed and conferring mechanical resistance to the protrusion of embryo. Pretreatments, such as immersion in H<sub>2</sub>SO<sub>4 </sub>will soften the seed coat and permit germination. Seed dormancy in <em>S. obtusifolia </em>can be considered of physical nature and classified as physical dormancy. The results obtained in this study may serve as useful information in the production and improvement of <em>S. obtusifolia </em>seedlings, as knowledge on seed dormancy and germination is a critical factor and requirements to the understanding of the propagation of this plant either in situ or ex-situ, in view of the economic potentials/attributes of this species.</p>

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

2021 ◽  
Author(s):  
Dhruv Sehgal ◽  
Núria Martínez-Carreras ◽  
Christophe Hissler ◽  
Victor Bense ◽  
AJF (Ton) Hoitink
Keyword(s):  
Particle Size ◽  
Absorption Spectrum ◽  
Carbon Content ◽  
Suspended Sediment ◽  
High Frequency ◽  
Suspended Sediments ◽  
Ex Situ ◽  
Frequency Measurements ◽  
Component Form

&lt;p&gt;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 &amp;#8216;local&amp;#8217; calibrations towards &amp;#8216;global&amp;#8217; dependencies based on in-situ SS characterization.&lt;/p&gt;&lt;p&gt;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.&lt;/p&gt;

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