Peculiarities of Ion-Exchange Adsorption of Ca2+ and HPO 4 2 − $$ {\mathrm{HPO}}_4^{2-} $$ as Main Factor of Self-Assembly of Apatite in the Surface Layer of Biomineralization Initiators

2018 ◽  
Vol 54 (5) ◽  
pp. 339-348
Author(s):  
V. V. Strelko ◽  
O. V. Strelko
Author(s):  
Abdul Sattar Jatoi ◽  
Humair Ahmed Baloch ◽  
Shaukat Ali Mazari ◽  
N. M. Mubarak ◽  
Nizamuddin Sabzoi ◽  
...  

Molecules ◽  
2019 ◽  
Vol 24 (9) ◽  
pp. 1772 ◽  
Author(s):  
Maria de los Angeles Cortes ◽  
Raquel de la Campa ◽  
Maria Luisa Valenzuela ◽  
Carlos Díaz ◽  
Gabino A. Carriedo ◽  
...  

During the last number of years a variety of crystallization-driven self-assembly (CDSA) processes based on semicrystalline block copolymers have been developed to prepare a number of different nanomorphologies in solution (micelles). We herein present a convenient synthetic methodology combining: (i) The anionic polymerization of 2-vinylpyridine initiated by organolithium functionalized phosphane initiators; (ii) the cationic polymerization of iminophosphoranes initiated by –PR2Cl2; and (iii) a macromolecular nucleophilic substitution step, to prepare the novel block copolymers poly(bistrifluoroethoxy phosphazene)-b-poly(2-vinylpyridine) (PTFEP-b-P2VP), having semicrystalline PTFEP core forming blocks. The self-assembly of these materials in mixtures of THF (tetrahydrofuran) and 2-propanol (selective solvent to P2VP), lead to a variety of cylindrical micelles of different lengths depending on the amount of 2-propanol added. We demonstrated that the crystallization of the PTFEP at the core of the micelles is the main factor controlling the self-assembly processes. The presence of pyridinyl moieties at the corona of the micelles was exploited to stabilize gold nanoparticles (AuNPs).


2012 ◽  
Vol 9 (4) ◽  
pp. 1823-1834 ◽  
Author(s):  
P. N. Palanisamy ◽  
A. Agalya ◽  
P. Sivakumar

Poly Pyrrle saw dust composite was prepared by reinforcement of natural wood saw dust (obtained fromEuphorbia Tirucalli Lwood) and Poly Pyrrole matrix phase. The present study investigates the adsorption behaviour of Poly Pyrrole Saw dust Composite towards reactive dye. The batch adsorption studies were carried out by varying solution pH, initial dye concentration, contact time and temperature. The kinetic study showed that adsorption of Reactive Red by PPC was best represented by pseudo-second order kinetics with ion exchange adsorption. The equilibrium data were analyzed by Freundlich and Langmuir isotherm model. The equilibrium isotherm data were fitted well with Langmuir isotherm model. The maximum monolayer adsorption capacities calculated by Langmuir model were 204.08 mg/g for Reactive Red at 303 K. The thermodynamic parameters suggest the spontaneous, endothermic nature of ion exchange adsorption with weak Vader walls force of attraction. Activation energy for the adsorption of Reactive by Poly Pyrrole Composite was 11.6387 kJ/mole, Isosteric Heat of adsorption was 48.5454 kJ/mole also supported the ion exchange adsorption process in which forces of attraction between dye molecules and PPC is weak.


2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Lucie Zarybnicka ◽  
Eliska Stranska ◽  
Jana Machotova ◽  
Gabriela Lencova

The present work deals with the surface modification of a commercial microfiltration poly(ethersulfone) membrane by graft polymerization technique. Poly(styrene-co-divinylbenzene-co-4-vinylbenzylchloride) surface layer was covalently attached onto the poly(ethersulfone) support layer to improve the membrane electrochemical properties. Followed by amination, a two-layer anion-exchange membrane was prepared. The effect of surface layer treatment using the extraction in various solvents on membrane morphological and electrochemical characteristics was studied. The membranes were tested from the point of view of water content, ion-exchange capacity, specific resistance, permselectivity, FT-IR spectroscopy, and SEM analysis. It was found that the two-layer anion-exchange membranes after the extraction using tetrahydrofuran or toluene exhibited smooth and porous surface layer, which resulted in improved ion-exchange capacity, electrical resistance, and permselectivity of the membranes.


2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Xiaomin Zhang ◽  
Jie Sun

Chitosan sulfate was prepared and characterized as a new chromatography media for protein separation. The degree of sulfonation of chitosan could be well controlled and impacted under conditions in the synthesis process. The prepared chitosan sulfate shows improved binding capacity with proteins. Sulfonated chitosan shows improved ion-exchange adsorption properties with proteins, which could have good potential in protein purification.


2020 ◽  
Vol 15 (3) ◽  
pp. 551-570
Author(s):  
Eric Mutegoa ◽  
Askwar Hilonga ◽  
Karoli N. Njau

Abstract The digestion process of organic waste rich in high ammonia content has always been a gridlock during the methanogenesis process. The free ammonia may increase inhibition/toxicity, which in turn affects the microbial community in the digester and eventually leads to process failures. Substantial methods have been proposed and assessed for curtailing ammonia emissions in anaerobic digesters to attain a safe and steady process so that, along with high methane production, high quality effluents can also be recovered. There are several means for lowering the erratic ammonia in organic wastes that are in use currently, such as decrease of pH, which favours the formation of ammonium over ammonia in the equilibrium; for example, the use of chemical additives that attach ammonium-N. Ammonia can also be removed from nitrogen-rich substrates during anaerobic digestion through other methods such as struvite precipitation, membrane distillation, air stripping, ion exchange, and adsorption. A thorough survey of different articles has shown that ion exchange, adsorption and changing of the C/N ratio through the co-digestion technique are the most commonly studied methods for mitigating ammonia inhibition in wastewater during anaerobic digestion. A detailed review of these methods in the context of nitrogen-rich substrates will be discussed in this paper.


2012 ◽  
Vol 35 (5) ◽  
pp. 811-818 ◽  
Author(s):  
J. Zhang ◽  
X. L. Zhang ◽  
H. Li ◽  
B. Zhao

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