scholarly journals CREATION A SORPTION MATERIAL FOR THE EXTRACTION OF METAL IONS FROM AQUEOUS SOLUTIONS

2021 ◽  
Vol 3 ◽  
pp. 97-107
Author(s):  
N.М. Zhunusbekova ◽  
◽  
Т.К. Iskakova ◽  
N.S. Chinibayeva ◽  
G.К. Kussainova ◽  
...  
Keyword(s):  
Acrylic Acid ◽  
Metal Ions ◽  
Polymer Composites ◽  
Contact Lenses ◽  
Specific Binding ◽  
Ion Pairs ◽  
Three Dimensional ◽  
Transition Metal Ions ◽  
Interpenetrating Networks ◽  
Soft Contact Lenses

The presence of a three-dimensional hydrophilic network structure ensures the uniqueness and wide practical application of hydrogels in industry, medicine, agriculture, etc. On their basis, soft contact lenses, dressings, superabsorbents, catalysts, soil structuring agents, preventing root drying and improving plant survival, have been created. The aimof this work is to synthesize new water-swellable polymer composites by combining monomer units of various natures based on acrylic acid and agar-agar with imidazole, differing in hydrophilic-hydrophobic balance. Results and discussion: The synthesis of new double and ternary polymer composites based on acrylic acid and agar-agar with imidazole was carried out, their physicochemical and complex-forming properties with transition metal ions in an aqueous medium were investigated. Comparative analysis showed that the complexation of interpenetrating networks with FeCl3 is more pronounced than with CoCl2. This fact can be associated with the difficulty of introducing a cobalt ion into the ligand plane during the formation of a metal complex, which further affects the binding to the functional groups of the network. The specific binding of the obtained polymer composites with metal salts was shown, which is carried out through the formation of ion pairs with the participation of counterions and coordination-unsaturated metals, which make the main contribution to the formation of extracomplexes and are responsible for the coordination of oxygen-containing ligands.

Metallo-oxidase Enzymes: Design of their Active Sites

2011 ◽  
Vol 64 (3) ◽  
pp. 231 ◽  
Author(s):  
Zhiguang Xiao ◽  
Anthony G. Wedd
Keyword(s):  
Metal Ions ◽  
Active Sites ◽  
Specific Binding ◽  
Large Family ◽  
Outer Sphere ◽  
Transition Metal Ions ◽  
Substrate Oxidation ◽  
Cellular Functions ◽  
Domains Of Life ◽  
Low Valent

Multi-copper oxidases are a large family of enzymes prevalent in all three domains of life. They couple the one-electron oxidation of substrate to the four-electron reduction of dioxygen to water and feature at least four Cu atoms, traditionally divided into three sites: T1, T2, and (binuclear) T3. The T1 site catalyzes substrate oxidation while a trinuclear cluster (comprising combined T2 and T3 centres) catalyzes the reduction of dioxygen. Substrate oxidation at the T1 Cu site occurs via an outer-sphere mechanism and consequently substrate specificities are determined primarily by the nature of a substrate docking/oxidation (SDO) site associated with the T1 Cu centre. Many of these enzymes ‘moonlight’, i.e. display broad specificities towards many different substrates and may have multiple cellular functions. A sub-set are robust catalysts for the oxidation of low-valent transition metal ions such as FeII, CuI, and MnII and are termed ‘metallo-oxidases’. They play essential roles in nutrient metal uptake and homeostasis, with the ferroxidase ceruloplasmin being a prominent member. Their SDO sites are tailored to facilitate specific binding and facile oxidation of these low-valent metal ions and this is the focus of this review.

scholarly journals Metallo-Supramolecular Hydrogels from the Copolymers of Acrylic Acid and 4-(2,2′:6′,2″-terpyridin-4′-yl)styrene

Polymers ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 1152 ◽  
Author(s):  
Huiqin Zhang ◽  
Pan Liu ◽  
Zheng Chi ◽  
Xuegang Chen
Keyword(s):  
Transition Metal ◽  
Acrylic Acid ◽  
Metal Ions ◽  
Self Assembly ◽  
Wavelength Region ◽  
Transition Metal Ions ◽  
Ion Concentration ◽  
Iron Ions ◽  
Absorption Intensity ◽  
Dilute Aqueous Solution

Hydrophilic copolymers containing 2,2′:6′,2″-terpyridine moieties and acrylic acid (AA) units poly (acrylic acid-co-4-(2,2′:6′,2″-terpyridin-4′-yl)styrene) (P(AA-co-TPY)) were synthesized and characterized. Coordinated with different transition metal ions, the dilute aqueous solution of the copolymers exhibited red-shifted UV-vis absorption peaks of π-π* transition from 317 to 340 nm. Further, interacting with iron ions, the copolymer showed new absorption peaks at a longer wavelength region (570 nm) and the absorption intensity enhanced with increase of the ion concentration. When enough ions were added to coordinate with the 2,2′:6′,2″-terpyridine moieties, novel metallo-supramolecular hydrogels were obtained due to the formation of metal coordination bonds between polymer back bones and transition metal ions (Ni2+, Zn2+, Cd2+, Fe2+ and Cu2+), which acted as self-assembly crosslinking structures. The mechanical strength and morphology of the resulting metallo-supramolecular hydrogels have been investigated.

scholarly journals Active transport of transition metal ions through poly(vinyl alcohol) and poly(acrylic acid) blend membrans.

MEMBRANE ◽  
1987 ◽  
Vol 12 (6) ◽  
pp. 351-356
Author(s):  
Reizo DOHNO ◽  
Junji TAKESHITA ◽  
Masayoshi KINUGASA ◽  
Tadao HAKUSHI
Keyword(s):  
Transition Metal ◽  
Acrylic Acid ◽  
Metal Ions ◽  
Active Transport ◽  
Vinyl Alcohol ◽  
Transition Metal Ions ◽  
Poly Vinyl Alcohol ◽  
Poly Acrylic Acid

HREM Study of electron-induced surface radiation damage in ReO3

1991 ◽  
Vol 49 ◽  
pp. 636-637
Author(s):  
R. Ai ◽  
H.-J. Fan ◽  
L. D. Marks
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Metal Oxides ◽  
Electron Irradiation ◽  
Transition Metal Oxides ◽  
Carbon Film ◽  
Transition Metal Ions ◽  
Surface Radiation ◽  
Valence Transition ◽  
Electron Microscopes

It has been known for a long time that electron irradiation induces damage in maximal valence transition metal oxides such as TiO2, V2O5, and WO3, of which transition metal ions have an empty d-shell. This type of damage is excited by electronic transition and can be explained by the Knoteck-Feibelman mechanism (K-F mechanism). Although the K-F mechanism predicts that no damage should occur in transition metal oxides of which the transition metal ions have a partially filled d-shell, namely submaximal valence transition metal oxides, our recent study on ReO3 shows that submaximal valence transition metal oxides undergo damage during electron irradiation.ReO3 has a nearly cubic structure and contains a single unit in its cell: a = 3.73 Å, and α = 89°34'. TEM specimens were prepared by depositing dry powders onto a holey carbon film supported on a copper grid. Specimens were examined in Hitachi H-9000 and UHV H-9000 electron microscopes both operated at 300 keV accelerating voltage. The electron beam flux was maintained at about 10 A/cm2 during the observation.

Synthesis, Spectral and Antimicrobial Investigation of 2-(Naphthalenel-ylamino)-2- Phenylacetonitrile and 1, 10-Phenanthroline with Five Divalent Transition Metal Ions

2019 ◽  
Vol 10 (01) ◽  
Author(s):  
Mohammed Al-Amery1 ◽  
Ashraf Saad Rasheed ◽  
Dina A. Najeeb
Keyword(s):  
Transition Metal ◽  
Metal Ions ◽  
Transition Metal Ions ◽  
Molar Conductance ◽  
Octahedral Geometry ◽  
Mixed Ligand ◽  
Gram Negative Bacteria ◽  
Magnetic Studies ◽  
Gram Positive Bacteria

Five new mixed ligand metal complexes have been synthesized by the reaction of divalent transition metal ions (Hg, Ni, Zn, Cu and Cd) with 2-(naphthalen-l-ylamino)-2-phenylacetonitrile (L1 ) and 1,10-phenanthroline (L2). The coordination likelihood of the two ligands toward metal ions has been suggested in the light of elemental analysis, UV-Vis spectra, FTIR, 1H-NMR, flam atomic absorption, molar conductance and magnetic studies. Results data suggest that the octahedral geometry for all the prepared complexes. Antibacterial examination of synthesized complexes in vitro was performed against four bacterias. Firstly, Gram-negative bacteria namely, Pseudomonas aerugin and Escherichia. Secondly, Gram-positive bacteria namely, Bacillus subtilis, Staphylococcuaurouss. Results data exhibit that the synthesized complexes exhibited more biological activity than tetracycline pharmaceutical.

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