pH Dependence of Arsenic Oxidation by Rice-Husk-Derived Biochar: Roles of Redox-Active Moieties

2019 ◽  
Vol 53 (15) ◽  
pp. 9034-9044 ◽  
Author(s):  
Delai Zhong ◽  
Yi Jiang ◽  
Zezhou Zhao ◽  
Linling Wang ◽  
Jing Chen ◽  
...  
Keyword(s):  
Rice Husk ◽  
Ph Dependence ◽  
Redox Active ◽  
Arsenic Oxidation

Arsenic Oxidation by Flavin-Derived Reactive Species under Oxic and Anoxic Conditions: Oxidant Formation and pH Dependence

2019 ◽  
Vol 53 (18) ◽  
pp. 10897-10905 ◽  
Author(s):  
Kunfu Pi ◽  
Ekaterina Markelova ◽  
Peng Zhang ◽  
Philippe Van Cappellen
Keyword(s):  
Ph Dependence ◽  
Reactive Species ◽  
Anoxic Conditions ◽  
Arsenic Oxidation

Common modifications of selenocysteine in selenoproteins

2019 ◽  
Vol 64 (1) ◽  
pp. 45-53 ◽  
Author(s):  
Elias S.J. Arnér
Keyword(s):  
Amino Acids ◽  
Covalent Binding ◽  
Physicochemical Characteristics ◽  
Redox Active

Abstract Selenocysteine (Sec), the sulfur-to-selenium substituted variant of cysteine (Cys), is the defining entity of selenoproteins. These are naturally expressed in many diverse organisms and constitute a unique class of proteins. As a result of the physicochemical characteristics of selenium when compared with sulfur, Sec is typically more reactive than Cys while participating in similar reactions, and there are also some qualitative differences in the reactivities between the two amino acids. This minireview discusses the types of modifications of Sec in selenoproteins that have thus far been experimentally validated. These modifications include direct covalent binding through the Se atom of Sec to other chalcogen atoms (S, O and Se) as present in redox active molecular motifs, derivatization of Sec via the direct covalent binding to non-chalcogen elements (Ni, Mb, N, Au and C), and the loss of Se from Sec resulting in formation of dehydroalanine. To understand the nature of these Sec modifications is crucial for an understanding of selenoprotein reactivities in biological, physiological and pathophysiological contexts.

Mechanoactivation Of Rice Husk Ash In Laboratory Conditions

2019 ◽  
pp. 20-26
Keyword(s):  
Mechanical Activation ◽  
Rice Husk ◽  
Amorphous Silica ◽  
Silicon Oxide ◽  
Rice Husk Ash ◽  
Pozzolanic Activity ◽  
Maximum Solubility ◽  
Laboratory Conditions ◽  
Before And After ◽  
Mineral Additive

In many rice producing countries of the world, including in Vietnam, various research aimed at using rice husk ash (RHA) as a finely dispersed active mineral additive in cements, concrete and mortars are being conducted. The effect of the duration of the mechanoactivation of the RHA, produced under laboratory conditions in Vietnam, on its pozzolanic activity were investigated in this study. The composition of ash was investigated by laser granulometry and the values of indicators characterizing the dispersion of its particles before and after mechanical activation were established. The content of soluble amorphous silicon oxide in rice husk ash samples was determined by photocolorimetric analysis. The pizzolanic activity of the RHA, fly ash and the silica fume was also compared according to the method of absorption of the solution of the active mineral additive. It is established that the duration of the mechanical activation of rice husk ash by grinding in a vibratory mill is optimal for increasing its pozzolanic activity, since it simultaneously results in the production of the most dispersed ash particles with the highest specific surface area and maximum solubility of the amorphous silica contained in it. Longer grinding does not lead to further reduction in the size of ash particles, which can be explained by their aggregation, and also reduces the solubility of amorphous silica in an aqueous alkaline medium.

Desalination Technology of Water by using Rice Husk Ash

2014 ◽  
Vol 27 (2) ◽  
pp. 148-160
Author(s):  
Hassan K. Hassan ◽  
Najla J. Al-Amiri ◽  
Mohammed M. Yassen
Keyword(s):  
Rice Husk ◽  
Rice Husk Ash ◽  
Desalination Technology

MATERIAL DEVELOPMENT FROM RICE HUSK FOR CO2 CAPTURE

2018 ◽  
Author(s):  
Premanath Murge ◽  
Srikanta Dinda ◽  
Bipin Chakravarthy ◽  
Sounak Roy
Keyword(s):  
Rice Husk ◽  
Co2 Capture ◽  
Material Development

Self-association of insulin. Its pH dependence and effect of plasma

Diabetes ◽  
1987 ◽  
Vol 36 (3) ◽  
pp. 261-264 ◽  
Author(s):  
E. Helmerhorst ◽  
G. B. Stokes
Keyword(s):  
Ph Dependence ◽  
Self Association

On the Crystal Chemistry of Inorganic Nitrides: Crystal-Chemical Parameters and Opportunities in the Exploration of Their Compositional Space

2020 ◽  
Author(s):  
Olivier Charles Gagné
Keyword(s):  
Functional Properties ◽  
A Priori ◽  
Lone Pair ◽  
Length Variation ◽  
Electronic Effects ◽  
Statistical Knowledge ◽  
Redox Active ◽  
Multiply Bonded ◽  
Jahn Teller ◽  
Compositional Space

The scarcity of nitrogen in Earth’s crust, combined with challenging synthesis, have made inorganic nitrides a relatively-unexplored class of compounds compared to their naturally-abundant oxide counterparts. To facilitate exploration of their compositional space via <i>a priori</i> modeling, and to help <i>a posteriori</i> structure verification not limited to inferring the oxidation state of redox-active cations, we derive a suite of bond-valence parameters and Lewis-acid strength values for 76 cations observed bonding to N<sup>3-</sup>, and further outline a baseline statistical knowledge of bond lengths for these compounds. We examine structural and electronic effects responsible for the functional properties and anomalous bonding behavior of inorganic nitrides, and identify promising venues for exploring uncharted compositional spaces beyond the reach of high-throughput computational methods. We find that many mechanisms of bond-length variation ubiquitous to oxide and oxysalt compounds (e.g., lone-pair stereoactivity, the Jahn-Teller and pseudo Jahn-Teller effects) are similarly pervasive in inorganic nitrides, and are occasionally observed to result in greater distortion magnitude than their oxide counterparts. We identify inorganic nitrides with multiply-bonded metal ions as a promising venue in heterogeneous catalysis, e.g. in the development of a post-Haber-Bosch process proceeding at milder reaction conditions, thus representing further opportunity in the thriving exploration of the functional properties of this emerging class of materials.<br>

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