J. Du
,
G.Y.Yang and S. Hagegege(General Research Institute for Non-ferrous Metals
,
Beijing 100088
,
China)(CECM-CNRS
,
15 rue G. Urbain
,
94407 Vitry/Seine
,
France Manuscript received 25 September 1995)
金属学报(英文版)
A model Cu-AlN composite has been prepared by ion implantation technique and annealing. The atomic configuration and lattice relationship of a low-energy inherent interface(11)Cn//(0001)AlN were studied by using transmission electron microscopy and geometrical modelling. By analysing the dichromatic pattern of the composite,a primary structural unit of the interface atomic configuration was determined for purpose of HREM image simulations and of studying the structurul relaxation state in the near-interface region.
关键词:
: Cu-AlN
,
null
,
null
,
null
Electrochimica Acta
To investigate the corrosion protection mechanism of polyaniline (PANI) films on ferrous metals, this work presents preparation method of a separate protonated PANI film electrode and results of its open-circuit potential (OCP) in 0.5 M NaClO4 and 0.5 M Na2SO4 solutions with different pH and the galvanic interaction between the PANI film electrode and ferrous metals. X-ray photoelectron spectroscopy (XPS) shows the lower pH corresponds to higher protonation level of H+ in the film, and a more positive OCP of PANI film. The PANI film accelerated the corrosion of 20A carbon steel slightly with a PANI to steel area ratio less than 25: 1, while the PANI films maintained passivity for a ratio above to 25:1 for the 20A steel. For the coupling of 2Cr13 stainless steel/PANI, an equal area PANI film could maintain 2Cr13 in a passive state. The results suggest that corrosion protection of 20A carbon steel and 2Cr13 stainless steel by PANI film in the acid solution is due to passivity protection. The excess oxidative charge stored in the PANI and the equilibrium activity of protonated PANI with the acid environment provide a persistent driving force for carbon steel and 2Cr13 stainless steel passivity. (C) 2004 Elsevier Ltd. All rights reserved.
关键词:
protonated polyaniline;ferrous metals;open-circuit potential;galvanic;coupling;passivity;corrosion protection;mild-steel;coatings;behavior
Materials and Corrosion-Werkstoffe Und Korrosion
In order to investigate the galvanic anodic protection (GAP) of ferrous metals (such as 410, 304 and 316 stainless steels) in acid solutions by doped polyaniline (PANi), separate doped PANi powder-pressed electrodes with different surface areas (the area ratio of the PANi electrode to stainless steel is between 1:1 and 1:2) have been prepared. These were coupled with ferrous metal in the following solutions: 5 M sulphuric acid, 5 M phosphoric acid and industrial phosphoric acid (containing 5 M phosphoric acid and 0.05% chloride ion) to construct a galvanic cell, in which PANi is cathode while ferrous metal is anode. The results indicate that a PANi electrode with sufficient area can provide corrosion protection to stainless steel in these acidic solutions. A pilot scale coupling experiment was carried out. The results indicate that PANi is a promising material as an electrode for the anodic protection of ferrous metals in acidic solutions in industrial situations.
关键词:
conducting polymer-coatings;corrosion protection;stainless-steel;spectroscopy;passivation;performance;mechanism;behavior;primers;films
LIU Chengjun
,
SHI Peiyang
,
ZHANG Dayong
,
JIANG Maofa
钢铁研究学报(英文版)
A great amount of ferrous tailings and slag cause severe damage to the ecological environment, which must be reclaimed and utilized. The composition, type, and characteristics of ferrous tailings and slag in China were introduced. The research status and the application outlook of glass ceramics made from ferrous tailings and slag were discussed. Glass ceramics made from ferrous tailings and slag can be applied to various fields, and it will be environmentally conscious materials in the 21st century.
关键词:
glass ceramics;ferrous tailings;slag
Yan NIU
,
Weitao WU and Chaoliu ZENG (State Key Lab. for Corrosion and Protection
,
Institute of Corrosion and Protection of Metals
,
Chinese Academy of Sciences
,
Shenyang 110015
,
China)F. Gesmundo and F. Viani (Instituto di Chimica
,
Facolta di Ingegneria
,
Un
材料科学技术(英文)
The corrosion of an Fe-based alloy containing 15 wt pct Y in H2-H2S mixtures under 10-3 Pa S2 was studied at 600~800℃ in an attempt to find materials with improved sulphidation resistance with respect to pure Fe. The presence of Y has been shown to be beneflcial, but not sufficient to the level expected. In fact, the alloy is able to form at all tested temperatures an external FeS layer, beneath which a zone containing a mixture of the two sulphides is also present. Thus,Fe can still diffuse through this region to form the outer FeS layer with non-negligible rate. The corrosion rate of Fe is considerably reduced by the Y addition. but the alloy corrodes still much more rapidly than Y. The sulphidation kinetics is generally rather irregular for both the pure metals, while the corrosion rate of the alloy decreases with time and tends to become parabolic after an initial period of 12~17 h. The sulphidation behaviour of the alloys is discussed by taking into account the presence of an intermetallic compound Fe17Y2 and the limited solubility of Y in Fe
关键词:
材料科学技术(英文)
The corrosion of an Fe-based alloy containing 15 wt pet Y in H-2-H2S mixtures under 10(-3) Pa S-2 was studied at 600 similar to 800 degrees C in an attempt to find materials with improved sulphidation resistance with respect to pure Fe. The presence of Y has been shown to be beneficial, but not sufficient to the level expected. In fact, the alloy is able to form at all tested temperatures an external FeS layer, beneath which a zone containing a mixture of the two sulphides is also present. Thus, Fe can still diffuse through this region to form the outer FeS layer with non-negligible rate. The corrosion rate of Fe is considerably reduced by the Y addition, but the alloy corrodes still much more rapidly than Y. The sulphidation kinetics is generally rather irregular for both the pure metals, while the corrosion rate of the alloy decreases with time and tends to become parabolic after an initial period of 12 similar to 17 h. The sulphidation behaviour of the alloys is discussed by taking into account the presence of an intermetallic compound Fe17Y2 and the limited solubility of Y in Fe.
关键词:
high-temperature sulfidation;most-reactive component;ni-nb alloys;h2-h2s mixtures;behavior;600-degrees-c-800-degrees-c;oxidation
Acta Materialia
In a first report [Jin ZH.. Gumbsch P, Ma E, Albe K, Lu K, Hahn H, et al. Scripta Mater 2006;54:1163], interactions between screw dislocation and coherent twin boundary (CTB) were studied via molecular dynamics simulations for three face-centered cubic (fcc) metals, Cu, Ni and Al. To complement those preliminary results, purely stress-driven interactions between 60 degrees non-screw lattice dislocation and CTB are considered in this paper. Depending on the material and the applied strain, slip has been observed to interact with the boundary in different ways. If a 60 degrees dislocation is forced by an external stress into a CTB, it dissociates into different partial dislocations gliding into the twin as well as along the twin boundary. A sessile dislocation lock may be generated at the CTB if the transited slip is incomplete. The details of the interaction are controlled by the material-dependent energy barriers for the formation of Shockley partial dislocations from the site where the lattice dislocation impinges upon the boundary. (c) 2007 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
关键词:
dislocation;slip;twinning;twin grain boundary;molecular dynamics;molecular-dynamics simulation;grain-boundaries;nanocrystalline;materials;cross-slip;rate sensitivity;deformation;copper;strength;aluminum;fcc
王龙妹
,
杜挺
金属学报
用直接平衡法研究了1500,1550,1600℃Ni液中Y-S平衡关系,测定了钇的脱硫常数lgK_(YS)及Y,S的一阶活度相互作用系数e_S~Y与温度的关系,并进行了有关的热力学计算。由测得的数据算出Ni液中YS的标准生成自由能△G_((Y)S),钇的标准溶解自由能△G_((Y)(l)→[Y]Ni),活度系数γ_Y~o,以及钇的克原子分数自相互作用系数∑_Y~Y和百分浓度自相互作用系数e_Y~Y与温度的关系。 对于反应[Y]_(Ni)+[S]_(Ni)=YS_(s) △G_((Y)S)=-215000+95.53T(cal/mol)脱硫常数: lgK_(YS)=-47000/T+20.86 e_S~Y=-350200/T+179 △G_((Y)(l)→[Y]Ni)=126200-79.31T(cal/mol) lgγ_(Y)=27584/T-15.151 ∑_Y~Y=-127T05/T+69.79 e_Y~Y=-364.8/T+0.2018
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