Nano-phases and corrosion resistance of C+Mo dual implanted steel

The corrosion resistance of C + Mo dual-implanted HI3 steel was studied using multi-sweep cyclic voltammetry. The phase formation conditions for corrosion resistance and its effects were researched. The super-saturation solid station solution of Mo+ and C+ atoms was formed in Mo + C dual implanted steel. Precipitate phase with nanometer size Fe2Mo, FeMo, MoC, Fe5C3 and Fe7C3 were formed in dual implanted layer. The passivation layer consisted of these nanometer phases. The corrosion resistance of the dual implanted layer was better than that of single Mo implantation. Jp of the Mo implanted sample is 0.55 times that of H13 steel. The corrosion resistance of the dual implantation was enhanced when ion dose increased. When the Mo+ ion dose was 6 × 1017/cm2 in the dual implantation, Jp of the dual implanted sample was only 0.11 times that in H13 steel. What is important is that pitting corrosion properties of dual implanted steel were improved obviously.     

The influence of Ce(NO3)3·6H2O on the inhibitive effect of Ca(NO2)2 in simulated concrete pore solution

The effects of cerium nitrite on corrosion behaviors of carbon steel in simulated concrete pore solutions were studied with the methods of linear polarization, electrochemical impedance spectroscopy and surface analysis. In pore solutions in the presence of Ce(NO3)3?6H2O, the corrosion potential, polarization resistance and impedance of carbon steel obviously increased in contrast to the situation in the absence of cerium salts. The pore solution with [NO2-] / [Cl-] = 0.3 and 0.1% Ce(NO3)3?6H2O, carbon steel shows better corrosion resistance than that in the pore solution with [NO2-] / [Cl-] = 0.6, which indicates that a small amount of Ce(NO3)3?6H2O in pore solutions can effectively promote passivation of the steel and reduce the threshold [NO2-] / [Cl-] ratio for corrosion control. The surface layer formed in cerium salt containing pore solutions is more compact and smooth and 1.36%Ce is examined on the sample surface. The addition of 0.1% Ce(NO3)3?6H2O in pore solutions can decrease the corrosion rate of steel in pore solutions and has little influence on pH change of the solutions. However, more cerium nitrate addition above 0.1% may result in pH decrease of the solution.     

Preparation of calcium phosphate coating on pure titanium substrate by electrodeposition method

The influences of pH value, electrolyte temperature and loading time on depositing calcium phosphate coating on pure titanium substrate by electrodeposition process were investigated. The process was carried out with an electrochemical work-station supplying a direct current power at potential of -0.8V (vs SCE). The electrolyte consists of 7 mmol·L-1 CaCl2·2H2O, 3 mmol·L-1 Ca(H2PO4)2·H2O and 2.5% H2O2. NaOH and HCl solutions were used to adjust pH value. The deposited samples were characterized by X-ray diffraction and scanning electron microscope. The comparison of the deposits obtained at lower and higher pH values demonstrates that the crystallization process at the interface is favoured by high pH value. With temperature increasing, the deposited hydroxyapatite is occasionally of plate-like shape, and the width and the length of the deposited calcium phosphates at 65 ℃ are larger than those at 55 ℃. Therefore, it is confirmed that the morphology and microstructure of electrochemically deposited calcium phosphates can be regulated. Additionally, the coating formed in electrolyte with H2O2 additive is homogeneous and the evolution of H2 bubble can be eliminated.     

Insights into the adsorption performance and mechanism of hydrated Ca ion on talc (0 0 1) basal surface from DFT calculation

The utilization of Ca ion as assistant depressant of CMC on talc has been widely reported. Thus, the study on the adsorption mechanism of Ca ion on talc surface is very crucial for understanding the performance of CMC on talc depression. In this paper, mechanism insights into hydrated Ca ion adsorption on talc (0 0 1) basal surface were creatively provided using DFT calculation. [Ca(H₂O)₆]²⁺ and [Ca(OH)(H₂O)₃]⁺ were determined as the effective hydrate components for Ca ion adsorption, and the top O site was the most favorable position for their adsorptions on talc surface. Furthermore, the adsorption mechanisms of [Ca(H₂O)₆]²⁺ and [Ca(OH)(H₂O)₃]⁺ on talc surface were found to be not the Ca—O chemical bond, but the hydrogen bonding formed by the H atom of the H₂O ligand and the surface O atom. H₂O acted like a bridge to connect them to the talc surface. Moreover, the hydrogen bonding was formed due to the hybridization of H 1s orbital with the O 2s, O 2p orbitals. Simultaneously, electrons transferred between the H atom and the surface O atom. This work provides theoretical insights into the Ca ion adsorption on talc surface, which can help deeply understand the talc flotation using CMC as depression.     

Effect of pozzolanic reaction products on alkali-silica reaction

1 IntroductionThe use of fly ashto control the expansion dueto al-kali-silica reaction (ASR) is well established and a num-ber of reviews have been published recently[1-4]. Howflyash brings about this reductionin expansionis not yet un-derstood although a number of theories have been put for-ward to explain its action. For controlling mechanism,they put more emphasis onthe adsorption andresort of al-kali by supplementary cementing material (SCM) , formore acidity oxide in SCM,and the secon…     

RC梁钢筋锈蚀监测与概率成像定位

为评估RC结构内钢筋的锈蚀损伤状态,开展了基于压电传感的RC梁钢筋锈蚀监测与定位技术研究.首先,在钢筋表面布设3组压电陶瓷(PZT)传感器,随后对监控到的信号进行基4FFT变换和提取频谱特征,刻画了钢筋锈蚀发展过程,并验证了基于PZT的监控方法对钢筋锈蚀全过程监测的适用性;其次,通过对概率成像方法中的权重函数进行修正,...     

Preparation and electrochemical properties of Pb-0.3wt%Ag/Pb-WC composite inert anodes

We prepared Pb-0.3wt%Ag/Pb-WC(WC stands for tungsten carbide,the same below) composite inert anodes by double-pulse electrodeposition on the surface of Pb-0.3wt%Ag substrates,and investigated the electrochemical properties of the composite inert anodes,which were obtained under different forward pulse average current densities from 2 A/dm~2 to 5 A/dm~2 and WC concentrations from 0 g/L to 40 g/L in bath.The kinetic parameters of oxygen evolution,corrosion potential and corrosion current of the composite inert anodes were obtained in a synthetic zinc electrowinning electrolyte of 50 g/L Zn~(2+) and 150 g/L H_2SO_4 at 35 ℃,by measuring the anodic polarization curves,Tafel polarization curves and cyclic voltammetry curves.The results show that Pb-0.3wt% Ag/Pb-WC composite inert anodes obtained under forward pulse average current density of 3 A/dm~2 and WC concentration of 30 g/L in an original acid plating bath,possess higher electrocatalytic activity of oxygen evolution,lower overpotential of oxygen evolution,better reversibility of electrode reaction and corrosion resistance in [ZnSO_4+H_2SO_4] solution.The overpotential of oxygen evolution of the composite inert anode is 0.926 V under 500 A/m~2 in [ZnSO_4+H_2SO_4] solution,and 245 mV lower than that of Pb-1% Ag alloy;the corrosion current of the composite inert anode is 0.95×10~(-4)A which is distinctly lower than that of Pb-1%Ag alloy,showing the excellent corrosion resistance.     

水热辅助溶胶凝胶法制备纳米钛酸锌及其光催化性能

采用水热辅助的溶胶凝胶法制备纳米钛酸锌（ZnTiO₃）光催化剂,以罗丹明B为目标降解物,运用动力学模型分析罗丹明B（RhB）初始浓度对降解效果的影响。通过SEM、XRD、XPS、UV-Vis DRS对ZnTiO₃进行表征,并使用自由基捕获试验分析其降解机理。结果表明,ZnTiO₃为纯六方相,形貌为类球形,粒径50 nm左右。在催化剂用量为1 g/L、RhB初始浓度为5 mg/L、pH值为3的条件下,光催化反应150 min后,RhB降解率为93.2%。其动力学方程为k=0.132C₀^-1.253。ZnTiO₃光催化剂降解过程中,·OH、h⁺、·O₂^-均起到催化作用,产生·OH、h⁺的量相近且多于·O₂^-,说明·OH、h⁺在催化反应中起主要作用。     

The mechanism of ground granulated blastfurnace slag preventing alkali aggregate reaction

Three different methods were applied to study the alkali content of gelpores in cement. In the closed system, the concentration of K⁺, Na⁺ and OH⁻ have not reduced with the increase of age. In the open system, the diffusion and transferring of K⁺ and Na⁺ towards free space leads to the decrease of total alkali content. In the micro-analysis system, the contents of K⁺ and Na⁺ in the first hydrated layer of ground granulated blastfurnace slag (GBFS) are very low, while the contents of calcium and magnesium are relatively high. This phenomenon shows that the mechanism of GBFS preventing alkali aggregate reaction (AAR) is: when GBFS is dissolved by alkali medium, SiO₂ and Al₂O₃ are dissolved into the cement matrix, then around GBFS particles form reaction rings rich in Ca²⁺ and Mg²⁺, and the C-S-H gel of positive charges formed in the area repulses K⁺ and Na⁺, which are forced to transfer to the mortar’s matrix, pore or mortar sample surface. The transferred K⁺ and Na⁺ form alkali gel products with other dissolved ions, then become evenly distributed in the mortar sample and react with Ca(OH)₂ in pore solutions to form (Na,K) _x−2z ·zCa·(SiO₂)_y·(OH)_x gel products; and thus changes the AAR gel products’ structure. The gel products will not expand, and so they can delay expansion destruction.     

Preparation of AgSnO2 composite powders by hydrothermal process

Silver-tin oxide powders were synthesized by the hydrothermal method with Ag（NH3）2^＋ solution and Na2SnO3 solution as raw materials and Na2SO3 as reductant. The precipitation conditions of Na2SnO3 solution and the reduction conditions of Ag（NH3）2^＋ were also investigated. The powders prepared were characterized by differential thermal analysis （DTA）, X-ray diffraction analysis （XRD）, scanning electron microscope （SEM） and energy spectrum analysis, The results show that pH value of the solution is a key parameter in the formation of Sn（OH）4 precipitate and the reduction reaction of Ag（NH3）2^＋ can release H^＋ ions, which results in synchronous precipitation of Sn（OH）6^2- as Sn（OH）4. The reduction of Ag（NH3）2^＋ and precipitation of Na2SnO3 occur simultaneously and the coprecipitation of silver and tin oxide is reached by the hydrothermal method. The silver-tin oxide composite powders have mainly flake shape of about 0.3 μm in thickness and there exists homogeneous distribution of tin oxide and silver in the powder synthesized.     

Kinetics of Fe3O4 formation by air oxidation

The kinetics of Fe₃O₄ formation by air oxidation of slightly acidic suspension of Fe(OH)₂ was studied. The effects of initial concentration of Fe(II), temperature, partial pressure of oxygen, air flow rate and stirring rate on the oxidation rate were investigated. The results show that Fe₃O₄ formation is composed of two-step reaction, the first step is the formation of Fe(OH) ₂ ⁺ by oxidation of Fe(OH)⁺ complex ions, the second step is the formation of magnetite by dehydration and deprotonation of Fe(OH)⁺ and Fe(OH) ₂ ⁺ . The oxidation reaction is zero-order with respect to the concentration of Fe(II) and around 0.5-order with respect to partial pressure of oxygen, and oxygen transfer process is rate-limiting step of oxidation reaction with apparent activation energy of 2.74 kJ · mol⁻¹.     

Effects of C,N-codoped on the corrosion resistance of TiO<Subscript>2</Subscript> films prepared by plasma surface alloying and thermal oxidation duplex process

C,N-codoped TiO 2 films have been deposited onto stainless steel substrates using plasma surface alloying and thermal oxidation duplex process.Composition analysis shows that the films shield the substrates entirely.The TiO 2 films are anatase in structure as characterized by X-ray diffraction.The electrochemical measurements show that the equilibrium corrosion potential positively shifts from-0.275 eV for bare stainless steel to-0.267 eV for C,N-codoped TiO 2 coated stainless steel,and the corrosion current density decreases from 1.3×10-5 A/cm2 to 4.1×10-6 A/cm2.The corrosion resistance obtained by electrochemistry noise also reveals that the C,N-codoped TiO 2 films provide good protection for stainless steel against corrosion in stimulated body fluid.The above results indicate that C,N-codoped TiO 2 films deposited by plasma surface alloying and thermal oxidation duplex process are effective in protecting stainless steel from corrosion.     

Exploration of amino trimethylene phosphonic acid to eliminate the adverse effect of seawater in molybdenite flotation

In this investigation, a chelating agent of amino trimethylene phosphonic acid (ATMP) was introduced to eliminate the adverse effect of seawater in molybdenite flotation. Microflotation results presented that high flotation recovery of molybdenite was achieved in freshwater using kerosene as the collector, but it was significantly decreased in the presence of seawater when pH > 9.5. Among the main ions in seawater, magnesium and calcium ions played a more detrimental role than others. After the addition of ATMP, molybdenite floatability can restore in seawater. Zeta potential distribution and solution chemistry calculation results illustrated that the decreased molybdenite floatability was attributed to the interaction of positive Mg(OH)_2(s) (major) and CaOH⁺ (minor) components with the molybdenite surface. The magnesium/calcium ions of positive components of Mg(OH)_2(s) and CaOH⁺ interacted with the ionized species of ATMP and then produced ATMP-calcium/magnesium complex, leading to the electrostatic repulsion between molybdenite and ATMP-calcium/magnesium complex that was restoring the molybdenite flotation. Hence, the ATMP can be utilized as an appropriate reagent to improve molybdenite flotation in seawater.     

硝酸侵蚀衬砌喷射混凝土中性化过程及机理

以一般大气环境喷射混凝土永久衬砌长大公路隧道为工程背景,开展汽车尾气中氮氧化物对喷射混凝土衬砌结构中性化过程及机理研究。以pH值为2的硝酸溶液为侵蚀介质,对喷射混凝土开展浸泡试验。以侵蚀喷射混凝土的物理力学性能及离子含量为表征指标,分析喷射混凝土中性化过程。采用X射线衍射、热分析及扫描电镜,分析及表征喷射混凝土中性化区的物相组成及微观形貌,研究喷射混凝土中性化发展过程及机理。结果表明,硝酸侵蚀喷射混凝土中性化演化过程可分为中和反应阶段、水化产物分解阶段、混凝土表面剥蚀等3个阶段。期间,喷射混凝土pH值逐渐下降,NO₃^-含量升高。随着侵蚀的进行,水化硅酸钙及氢氧化钙的含量降低,硝酸钙、硝酸型水化氮铝酸钙及高岭石的相对含量增大,微观结构被破坏,中性化速度加快,物理力学性能降低。     

Ce~(3+)-聚苯胺/蒙脱土复合材料掺杂环氧涂层的制备及耐腐蚀性能

采用原位插层聚合法合成了聚苯胺/蒙脱土复合材料(PANI/MMT),通过阳离子交换吸附制得了Ce~(3+)-聚苯胺/蒙脱土复合材料(Ce~(3+)-PANI/MMT).随后对所制备的样品进行表征.将PANI,PANL/MMT,Ce~(3+)-PANI/MMT粉末添加到环氧树脂中(质量分数为5%),涂覆在碳钢表面,干燥.将4种涂层浸泡在3.5%NaCl溶液中,通过电化学实验来比较4种涂层的耐蚀性能.研究结果表明,Ce~(3+)-PANI/MMT复合材料掺杂的环氧涂层的耐腐蚀性能最好,且具有一定的自修复性能.     

Mechanical property and microstructure of alkali-activated Yellow River sediment-coal slime ash composites

This work focuses on the production of a new composite material using Yellow River sediment and coal slime ash via alkali-activating method. XRD, FTIR and SEM/EDS were used to characterize the alkali-activated products and microstructure of the composite material. Compressive strength was tested to characterize the mechanical property of the composite material. It is found that the compressive strength of the Yellow River sediment-coal slime ash composites increases as the added Ca(OH)₂ content grows. The compressive strength increases fast in the early stage but slowly after 28 days. The strength of the composites can be significantly improved via the addition of small amount of NaOH and gypsum. The products (C-S-H, ettringite and CaCO₃), especially C-S-H, make much contribution to the enhancement of strength. The highest strength of the composites can reach 14.4 MPa after 90 days curing with 5% Ca(OH)₂, 0.2% NaOH and 7.5% gypsum. The improved properties of the composites show great potential of utilizing Yellow River sediment for inexpensive construction materials.     

X70钢在模拟酸雨溶液中及其液膜下的腐蚀行为研究

采用交流阻抗法和极化曲线法研究了X70钢在模拟酸雨溶液中及其薄层液膜下的腐蚀行为.研究结果表明:在pH值为2.40³.50的模拟酸雨溶液中,X70钢的阻抗谱表现为一个时间常数,X70钢的腐蚀受电荷传递过程控制.X70钢的腐蚀速率和腐蚀电位随着溶液pH值升高而降低.在薄层液膜下,液膜厚度的减薄抑制了腐蚀的阴、阳极过程.液膜厚度的减薄,电荷传递电阻增大,X70钢的腐蚀速率降低.     

The corrosion behavior of nano-meter embedded phase in Ti implanted H13 steel

On the SEM micrographs of Ti implanted H13 steel, a tree-branch-like structure can be observed. Further investigation with TEM shows that the newly tormed composition is a formation of nann-meter FeTi_2 phase in Ti implanted layer. The layer with a relatively high corrosion resistance has been formed in Ti implanted H13 steel with this structure.The results of electrochemical measurement show that the corrosion current density decreases obviously with an increase of ion dose. The corrosion current density in Ti implanted steel with a dose of 1.3×10~(18)/cm~2 is 8-20 times less than that of Ti implanted steel with a dose of 6×10~(17)/cm~2. The corrosion behavior of Ti implanted steel with a dose of 6×10~(17)/cm~2 could be further improved as the sample was annealed at 500℃ for 20 min and the corrosion current density decreases by 48-80 times compared to that of non-implanted samples. The corrosion trace was not observed on the annealing sample by SEM, after multi-sweep cyclic voltammetry of 40 cycles     

Corrosion resistance of plasma sprayed NiCrAl+(ZrO2+Y2O3) thermal barrier coating on 18-8 steel surface

The corrosion resistance of NiCrAl+(ZrO₂+Y₂O₃) thermal barrier coating, formed with the plasma spraying technique, on the 18 - 8 steel surface was investigated. The phase structure and morphology of the coating were analyzed by means of X-ray diffraction (XRD) and scanning electron microscopy (SEM). The electrochemical corrosion behavior of the coating in 1.0 mol/L H₂SO₄ solution was studied by using electrochemical measurement methods. The results show that the gradient plasma spraying coating is composed of the NiCrAlY coating and the (ZrO₂+Y₂O₃) top coating, and the coating thickness is 360 μm. The microhardness of coating reaches 1 100 HV. The corrosion resistance of the plasma sprayed coating of the 18 - 8 steel surface is about 5 times as great as that of the original pattern. The corrosion resistance of the coating is enhanced notably. Foundation item: Project (5040202140) supported by Scientific Research Common Program of Beijing Municipal Commission of Education     

Morphology and conductivity of in-situ PEO-LiClO4-TiO2 composite polymer electrolyte

PEO-LiClO4-TiO2 composite polymer electrolyte films were prepared. TiO2 was formed directly in matrix by hydrolysis and condensation reaction of tetrabutyl titanate. The crystallinity, morphology and ionic conductivity of composite polymer electrolyte films were examined by differential scanning calorimetry, scanning electron microscopy, atom force microscopy and alternating current impedance spectroscopy, respectively. The glass transition temperature and the crystallinity of composite polymer electrolytes are decreased compared with those of PEO-LiClO4 polymer electrolyte film. The results show that TiO2 particles are uniformly dispersed in PEO-LiClO4-5%TiO2 composite polymer electrolyte film. The maximal conductivity of 5.5×10^-5 S/cm at 20℃ of PEO-LiClO4-TiO2 film is obtained at 5% mass fraction of TiO2.