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11.
Inhibition effect of imidazole derivative 1,7′-dimethyl-2′-propyl-1H,3′H-2,5′-bibenzo[d]imidazole (DPBI) against mild steel corrosion in 1 M HCl solutions was evaluated using the conventional mass loss method,
potentiodynamic polarization, linear polarization, and electrochemical impedance spectroscopy. The mass loss results showed
that DPBI is an excellent corrosion inhibitor; electrochemical polarizations data revealed the mixed mode of inhibition; and
the results of electrochemical impedance spectroscopy showed that the change in the impedance parameters, charge transfer
resistance, and double layer capacitance with the change in the concentration of the inhibitor is due to the adsorption of
the molecule leading to the formation of a protective layer on the surface of mild steel. The inhibition action of this compound
was assumed to occur via adsorption on the steel surface through the active centers of the molecule. 相似文献
12.
Tetrazolo[1,5‐a]quinoline‐4‐carbaldehyde and its Schiff base on mild steel as corrosion inhibitor in 1 M HCl solution: electrochemistry,theoretical and SEM surface analysis
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Bhupendra M Mistry Suban K Sahoo Doo Hwan Kim Smita Jauhari 《Surface and interface analysis : SIA》2015,47(6):706-718
The corrosion inhibition impact of two quinoline derivatives, viz tetrazolo [1,5‐a] quinoline‐4‐carbaldehyde ( TQC ) and (Z) ?5‐methyl‐N‐(tetrazolo [1,5‐a] quinolin‐4‐ylmethylene) thiazol‐2‐amine ( MTQT ), has been examined against mild steel in 1 M HCl solution using conventional weight loss, potentiodynamic polarization, linear polarization, electrochemical impedance spectroscopy, quantum chemical, and scanning electron microscopic studies. The experimental results have showed that TQC and MTQT revealed a good corrosion inhibition and that the inhibition efficiency increases with the increase of concentration of inhibitor to attain 94.54% for TQC and 99.25% for MTQT at 25 ppm. Polarization measurements suggest that TQC and MTQT act as a mixed‐type inhibitor. A synergism between inhibitors can be observed by polarization measurements. Electrochemical impedance spectroscopy measurements show an increase of the transfer resistance with the inhibitor concentration. Adsorption of TQC and MTQT on the mild steel surfaces in 1 N HCl solution follows the Langmuir adsorption isotherm model. Furthermore, quantum chemical calculations have been conducted using B3LYP functional and 6‐31G(d,p) basis set to complement the experimental evidences. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
13.
Rausaria S Kamadulski A Rath NP Bryant L Chen Z Salvemini D Neumann WL 《Journal of the American Chemical Society》2011,133(12):4200-4203
We report a new series of biscyclohexano-fused Mn(III) complexes of bis(hydroxyphenyl)dipyrromethenes, 4a-c, as potent and orally active peroxynitrite scavengers. Complexes 4a-c are shown to reduce peroxynitrite through a two-electron mechanism, thereby forming the corresponding Mn(V)O species, which were characterized by UV, NMR, and LC-MS methods. Mn(III) complex 4b and its strained BODIPY analogue 9b were analyzed by X-ray crystallography. Finally, complex 4a is shown to be an orally active and potent analgesic in a model carrageenan-induced hyperalgesia known to be driven by the overproduction of peroxynitrite. 相似文献
14.
Superconductivity in ternary metallic glasses has been investigated using the model pseudopotential approach, which has been
found quite successful in explaining superconductivity in metals, binary alloys and binary glasses. It is observed that this
simple methodology successfully explains superconducting behaviour of ternary glasses without requiring the solution of Dirac
equation for a many body problem or estimation of various interactions as required in ab-initio pseudopotential theory. In
the present work superconducting state parameters of fourteen metallic glasses of (Ni-Zr)-M system (M=Ti, V, Co, Cu) have
been determined in the BCS-Eliashberg-McMillan framework. It is observed that addition of V, Co, and Cu as the third element
(M) to a binary metallic glass (Ni33 Zr67) causes the parameters λ,T
c, α, andN
0
V to decrease, and Coulomb pseudopotential (μ*) to increase with concentration of M, showing that the presence of third element (M) causes suppression of superconducting
behaviour of the alloy. The decrease inT
c with increasing concentration of third element (M) may be attributed to the modifications in density of states at the Fermi
levelN(E
F), and probable changes in the band structure of the alloy due to addition of the third element (M). Slight difference is
noticed when Ti is added to the Ni33 Zr67 alloy. In this caseT
c rises initially and then decreases with concentration of M, showing a peak at aboutx=0.05. This indicates that on addition of Ti, 3d states grow near the Fermi level and hence contribute substantially toN(E
F), favouring superconducting behaviour in this case. The present results forT
c show an excellent agreement with the experimental data. QuadraticT
c equations have been proposed, which provide successfully theT
c values of ternary metallic glasses under consideration.
Paper presented at National Conference on Current Trends in Condensed Matter Research, Warangal, India, September 20–22, 2004. 相似文献
15.
Summary The complex Pt(bpyMe)Cl3 (bpyMe = N-methyl-2,2-bipyridylium cation) reacts with pyridine(py) to give cis-[Pt(bpy-Me) (py)Cl2]+, which on heating cyclometallates with loss of py to give Pt(bpyMe-H)Cl2; some Pt(py)2Cl2 is also formed. Pt(bpyMe)Cl3 reacts with 2,2-bipyridyl (bpy) to yield a mixture of [Pt(bpyMe-H)(bpy)]2+ and [Pt(bpy)2]2+. The analogous reactions with Pd(bpyMe)Cl3 proceed under very mild conditions to afford PdL2Cl2 (L2 = 2py, bpy). 相似文献
16.
3,3′-Dicarbomethoxy-2,2′-bipyridyl(DCMB)reacts with K2MCl4(M = Pd,Pt) to give M(DCMB)Cl2 and with RhCl3 to give the cis-[Rh(DCMB)2Cl2]+ ion. Attempts to prepare the tris (DCMB) complex with Rh(III) and analogous Co(III) complexes were unsuccessful. 相似文献
17.
18.
Vijai K. Rai Suhasini Mahata Smita R. Bhardiya Prashant Shukla Ankita Rai Manorama Singh 《Tetrahedron letters》2019,60(7):524-529
Reduced graphene oxide (rGO)–NaBH4 is reported as mild and efficient catalyst-system for chemo-/regioselective reduction of structurally different aliphatic, aromatic as well as α,β-unsaturated aldehydes and ketones in water. The rGO was prepared by reducing graphene oxide using Tulsi leaf extract as bio-reductant. Operational simplicity, ambient reaction condition, high yield of pure products (80–97%), no by-product formation, no use of column chromatography for purification are the salient features of the envisaged protocol. Furthermore, the recovered TRGO was recycled and reused for subsequent reductions up to five times without any loss in activity. 相似文献
19.
Rikarani R. Choudhury Smita Mohanty Sanjay Kumar Nayak 《International Journal of Polymer Analysis and Characterization》2019,24(4):334-345
This paper first time reports the preparation of random anionic copolymers from vinyl acetate (VAc) bearing electro-donating substituent and sodium 4-vinylbenzenesulfonate (SSA) having electro-withdrawing substituent. Copolymers (PVA-co-SSA) of different composition have been successfully prepared by a simple free radical solution polymerization technique. Resulting final copolymer contained neutral hydrophilic as well as ionizable ion exchange sites. Evaluation of spectral data obtained from Fourier transform Infrared spectroscopy, Raman spectroscopy, and 1H Nuclear magnetic resonance helped in identifying and confirming the chemical structure of copolymers. Characterization of copolymers by gel permeation chromatography revealed high molecular weight with moderate polydispersity index. Analysis of thermal stability and glass transition temperature of copolymers by thermogravimetric analysis and differential scanning calorimetry were found in between corresponding homopolymers. Physicochemical properties of PVA-co-SSA can be beneficial for prospective advanced application in the niche area of smart membrane technology for energy and environment. 相似文献
20.
ABSTRACTWe study the structural, energetic and electronic properties of the structured water chain clusters within the density functional theory. We refer the structured water chains to those water clusters that have specific geometric patterns stretched along one direction. External electric field required to keep the structures open chain, thereby preventing them to form closed structures, is applied along the length of the chain. The structures are essentially periodic with basic repeating unit consisting of the corner- or edge-sharing 4-, 5- or 6-membered ring water clusters. Our calculations underscore the possible existence of such structured water clusters in the electrostatic environments, which we simulate in its simplicity employing a dipolar, uniform and static electric field. Analysis reveals that the 5-membered ring water chain clusters, i.e. the pentamer chain clusters have the lowest average dipole moment per water molecule while the threshold field, that marks the onset of the field-induced closure of the HOMO (highest occupied molecular orbital)-LUMO (lowest unoccupied molecular orbital) energy gap, is highest, followed by that for the tetramer and hexamer chains. The results suggest that the pentamer chains are the most stable clusters over a wide range of electric fields. 相似文献