Corrosion performance of zinc coated steel in seawater environment

Considering the continuous exploitation of marine resources,it is very important to study the anticorrosion performance and durability of zinc coated streel(ZCS) because its increasing use as reinforcements in seawater.Tafel polarization curves and linear polarization curves combined with electrochemical impedance spectroscopy(EIS) were employed to evaluate the corrosion performance of ZCS at Qingdao test station during long-term immersion in seawater.The results indicated that the corrosion rate of the ZCS increased obviously with immersion time in seawater.The corrosion products that formed on the zinc coated steel were loose and porous,and were mainly composed of Zn_5(OH)_8Cl_2,Zns(OH)_6(CO_3)_2,and ZnO.Pitting corrosion occurred on the steel surface in neutral seawater,and the rate of ZCS corrosion decreased with increasing pH.     

Embeddable reference electrode for reinforced concrete

Laboratory and field tests on our newly developed embeddable reference electrode for reinforced concrete show it can be embedded into reinforced concrete structures and be used for measuring the potentials of the rebar or other metal elements in the outer structural part exposed to seawater. Its potential varies little with the change of Cl⁻ concentration of the electrolyte and is stable over a time range of 260 days. The electrode can be used for monitoring corrosion and cathodic protection of reinforced concrete structures in seawater. Contribution No. 1605 from the Institute of Oceanology, Academia Sinica.     

D_（001）树脂在酸性硫脲溶液中吸附、分离金银研究

本文研究了Ｄ_００１大孔阳离子强酸树脂从Ｈ_２ＳＯ_４－ＣＳ（ＮＨ_２）_２溶液中，富集及分离Ａｕ（Ｉ）、Ａｇ（Ｉ）的性能。表明在ｐＨ＝２．０左右，树脂对Ａｕ（Ｔｕ）￣＋_２、Ａｇ（Ｔｕ）￣＋_２（Ｔｕ＝硫脲）有良好的吸附性能，Ａｕ和Ａｇ的吸附容量分别为６１．１８ｍｇ／ｇ－Ｒｅｓｉｎ和９９．１１ｍｇ／ｇ—Ｒｅｓｉｎ。负载柱上的Ａｕ、Ａｇ可分别用ＮａＣＮ—ＮａＯＨ和Ｈ_３ＢＯ_３－ＮａＯＨ－Ｎａ_２Ｓ_２Ｏ_３定量洗脱。可进行一定程度的Ａｕ、Ａｇ分离。     

Study of the Corrosion Resistance of Electroless Ni-P Deposits in a Sodium Chloride Medium

The corrosion resistance of electroless Ni-P deposits with phosphorous contents from 12% to 14% in sodium chloride solutions was studied. The deposits were immersed in 3.5% NaCl solutions for 29 d to obtain the electrochemical parameters and were examined in a standard salt spray test for 15 d respectively. The corrosion resistance of the deposits was studied by poten- tio-dynamic scan, electrochemical impedance spectroscopy (EIS), X-ray diffraction (XRD) and cold-field emission scanning electron microscopy (FE-SEM) equipped with an energy dispersive X-ray detector (EDX). The patterns of XRD and the results of FE-SEM showed that the prepared deposits were amorphous. But after a 15 d standard salt spray test, a few pinholes appeared on the surface of the deposit and the weight content of phosphorus on the surface of the deposit was higher (which was beneficial to the formation of the passivation films) than that before the standard salt spray test when the nickel content was lower because the dissolved weight of nickel was greater than that of phosphorus. The results from potentio-dynamic scan and EIS showed that passivation films formed on the Ni-P deposit after immersion in the NaCl solutions, which decreased the corrosion rate of Ni-P samples. The results of this work show their potential applications in marine corrosion.     

鄂尔多斯盆地东胜铀矿成矿作用研究

对东胜铀矿提出了物源、地层、古气候等3种成矿因素。岩相学与成矿矿物学研究表明,铀矿石中含有大量的方解石,并且长石与高岭石含量呈正相关,铀矿化与有机质也有一定的联系。结合铀矿地质特征初步分析认为,东胜铀矿是在氧化带铀元素以碳酸铀酰络合物搬运,在酸性介质条件下,还原带长石碎屑蚀变为高岭石,并有钙离子析出。当碳酸铀酰络合物从氧化带迁移到还原带,遇有大量钙离子时发生分解,出现铀矿石与方解石同时沉淀现象,有机质的还原作用也是铀矿沉淀的主要因素,经漫长的地质作用富集成工业矿体。     

西宁盆地泥质型钙芒硝资源的开发利用

西宁盆地蕴藏着极为丰富的钙芒硝资源,80年代即已探明硫酸钠(Na_2SO_4)地质储量20亿吨,远景储量100亿吨以上。矿床所在地距西宁市区2～10余km,水、电、路“三通”良好,且无水硫酸钠及其深加工产品市场颇为广阔。80年代以来,这种“城市矿”曾几次建厂开发。至今未能开发成功的直接原因是,矿石含泥质物较高,用常规方法脱除困难。笔者以新的工艺流程进行的日产10吨芒硝的脱泥除杂中试试验表明,以这种泥质型矿为原料,完全可以以低的成本生产出高纯度的硫酸钠产品,可以取得可观的经济效益。西宁盆地具备形成一个硫酸钠盐型盐化工工业基地的基本条件。     

Study on kinetics of cathodic reduction of dissolved oxygen in 3.5% sodium chloride solution

Electrochemical reduction of dissolved oxygen in seawater on metals is of great importance for corrosion studies. The present paper studied cathodic reduction of dissolved oxygen on Q235 carbon steel in 3. 5% sodium chloride(NaCl)solutions by cyclic voltammetry(CV), electrochemical impedance spectroscopy(EIS), rotating disk electrode(RDE)and rotating ring-disk electrode(RRDE). The cyclic voltammetric results demonstrated the cathodic process on Q235 carbon steel in O2-saturated 3. 5% NaCl solution contains three reactions:dissolved oxygen reduction, iron oxides reduction and hydrogen evolution. The peak potential of oxygen reduction reaction(ORR)is-0. 85 V vs Ag/AgCl, 3 molL-1 KCl. The E1S results indicated that the ORR occurring on Q235 carbon steel is a 4-electron process and that no finite diffusion is caused by the intermediate of H2O2 produced by ORR. The RDE and RRDE voltammograms confirmed the EIS results and it was found that the number of transferred electrons for ORR was nearly 4, I. E. , dissolved oxygen reduced to water.     

Effect of Fe2+ ions on polarization behavior of X60 steel in CO2 saturated salty water

The effects of ferrous ions on cathodic and anodic polarization behavior of the X60 steel in CO₂ saturated salty water were studied by potentio-dynamic polarization method. The results show that the reducing current peak of cathodic polarization is affected significantly if FeCl₂ is added to the salty solution of controlled pH, but not the anodic polarization. It is considered that the ferrous ions accelerate the formation of a protective ferrous carbonate film. Films formed by addition of ferrous ions and those formed by ferrous ions produced from steel corrosion have the same forming mechanism. The former can fully meet the formative condition of the film and can play the role of inhibitor.     

Surface modification of ZrO2 nanoparticles with styrene coupling agent and its effect on the corrosion behaviour of epoxy coating

The surface of ZrO2 nanoparticles was modified by styrene coupling grafting method to improve the dispersion and interaction of the nanoparticles with the epoxy coating in which the modified ZrO2 nanoparticles were used as an additive. The grafting performance and microstructure of the nano- ZrO2/epoxy coating were analyzed by Fourier transformation infrared spectroscopy, X-ray diffraction, and scanning electron microscopy. The corrosion behavior of the nano-ZrO2/epoxy coating on mild steel was evaluated in neutral 3.5 wt% NaC1 solution using electrochemical impedance spectroscopy （EIS）. Both the coating capacitance and coating resistance fitted by the equivalent circuit from EIS were used to evaluate the protective performance of the coating towards the mild steel. The results show a superior stability and efficient corrosion protection by the modified ZrO2 nanoparticles. The epoxy coating containing 2 wt% modified ZrO2 nanoparticles exhibited the best corrosion performance among all the coating specimens. This research may provide an insight into the protection of mild steel using modified epoxy coatings.     

三元复合驱采油污水阻垢缓蚀剂电化学分析

研制适用于三元复合驱采油污水工况条件下的MPM固体缓蚀阻垢剂,分析三元复合驱采油污水中MPM的电化学特性.结果表明:随着温度增加,20#钢在采油污水的腐蚀速率呈增加趋势,极化曲线显示钝化区表面材料在表面高温下处于钝化状态,产生的钝化膜能够降低腐蚀速度.在阻垢缓蚀剂质量浓度相同的情况下,不同温度的电化学阻抗谱在高频区出现容抗弧,显示优良的缓蚀性能.不同质量浓度MPM极化曲线表明,缓蚀率随MPM质量浓度的增加而增大,MPM极值质量浓度为80mg/L.污水体系中的Ca2+、Cl-对缓蚀率产生影响.MPM适用于高质量浓度Ca2+的三元复合驱采油污水处理.     

一种新型光纤光栅锈蚀传感器及其对混凝土结构钢筋锈蚀监测实验研究

设计一种新型光纤光栅锈蚀传感器,主要由锈蚀体、不锈钢体和2段串联的光纤布拉格光栅（FBG）组成。缠绕于锈蚀体表面的FBG监测钢筋的锈胀应变,缠绕于不锈钢体表面的FBG用作温度补偿器,消除温度变化对锈胀应变监测的影响。此外,设计电化学加速腐蚀实验,探究该传感器在不同强度等级混凝土中的工作性能。结果表明,该传感器监测质量腐蚀率的灵敏度为0.02%,监测范围大于1%,可实时监测混凝土中钢筋的锈蚀过程及特征,为预警钢筋锈蚀引起的钢筋混凝土结构耐久性损失提供阈值,在结构健康监测领域具有较大的应用价值。     

Effect of Carbonation and Drying-Wetting Cycles on Chloride Diffusion Behavior of Coral Aggregate Seawater Concrete

Based on seawater immersion,drying-wetting cycles,carbonation and drying-wetting cycles for coral aggregate sea-water concrete(CASC)with different strength grades,the effect of carbonation and drying-wetting cycles on chloride diffusion be-havior of CASC is studied.The results show that the free surface chloride concentration(Cs),free chloride diffusion coefficient(Df)and time-dependent index(m)of CASC in the drying-wetting cycles is obviously higher than that in seawater immersion.The Df and m of CASC of carbonation and drying-wetting cycles is higher than that in the drying-wetting cycles.Carbonation increases the Df and m of CASC,which is against CASC to resist chloride corrosion.The corrosion possibility of CASC structures in different ex-posed areas is as follows:splash zone(carbonation and drying-wetting cycles)>tidal zone(drying-wetting cycles)>underwater zone(seawater immersion).Besides,the chloride diffusion rate of C65-CASC is 17.8%-63.4%higher than that of C65-ordinary aggre-gate concrete(OAC)in seawater immersion(underwater zone).Therefore,anti-corrosion measures should be adopted to improve the service life of CASC structure in the oceanic environment.     

改进重铬酸钾法快速测定水样CODcr

研究了用硫酸锰代替贵金属硫酸银作催化剂,在H2SO4-H3PO4介质中,重铬酸钾回流法测定水样中CODcr的新方法.通过实验,确定了最佳测定条件:MnSO4浓度为1×10-1mol.L-1;混酸溶液(H2SO4:H3PO4)=5:1(体积比);回流时间10min.并与标准方法进行了对比,准确度和精密度同标准法相近,大大节约了分析时间.     

Deposition of atmospheric pollutant and their chemical characterization in snow pit profile at Dokriani Glacier,Central Himalaya

The uncertainty in assessing the numerous atmospheric pollutants transported via wind from arid and semi-arid regions is affecting the glacial ecosystem. In our study area due to the complexity of the system, a prominent seasonal difference noticed among major ions(Ca~(2+), Mg~(2+), SO_4~(2-), and NO_3~-). There is a need for understanding the ions cycling as a whole and the directionality of the feedback loops in the system. Therefore, we provide an appraisal of our current hypothesis for seasonal difference in major ion concentration from snow samples for two corresponding years(2013 and 2015) at Dokriani Glacier. A systematic study of chemical compositionsin the shallow snow pit from Dokriani Glacier was undertaken for the pre-monsoon season to understand the cycling of major ions from atmosphere to solute acquisition process. The intimating connections of ions cycling in snow and its temporal behavior was observed and analyzed through various statistical tests. Among major ions, the SO_4~(2-)has the highest concentration among anions on an average considered as 14.21% in 2013 and 29.46% in 2015. On the other side Ca~(2+) is the dominant cation contributing 28.22% in 2013 and 15.3% in 2015 on average. The average ratio of Na+/Cl-was higher in 2013 whereas lower in 2015. The backward trajectory analysis suggests the possible sources of the ions transported from Central Asia through the Western Disturbance(WD) as a prominent source of winter precipitation mainly in the Central Himalaya. Ionicconcentration of Ca~(2+) in cations was highly dominated while in anion SO_4~(2-)played the major role. Factor analysis and correlation matrix suggested that, the precipitation chemistry is mostly influenced by anthropogenic, crustal, and sea salt sources over the studied region. The elemental cycling through ocean, atmosphere and biosphere opens up new ways to understand the geochemical processes operating at the glacierized catchments of the Himalaya. Moreover, increasing the field-based studies in the coming decades would also have the certain advantage in overcoming the conceptual and computational geochemical modelling difficulties.     

Effects of composition and structure of alginates on adsorption of divalent metals

Results of a series of experiments (on the adsorption of divalent metal ions by dried alginic acid, Na and Ca alginates of different composition and block structure) conducted in this systematic study of the effects of the composition and structure of alginates on the static adsorption equilibrium of divalent metal ions indicate that the properties of alginate adsorption to divalent metal ions are highly different, depending not only on the cations used, but also on the form and structure of the alginates. There is close correlation between the adsorption properties and the structure of the alginates. The selectivity coefficient of Na alginate for Cd-Sr ion exchange tends to increase with the increase of theM/G ratio in alginate, whereas the adsorption capacity of Ca alginate for Cu²⁺ ion decrease with the increase of the G-block or the average length of the G-block and the total adsorption capacity of alginic acid is found to vary in the same order as theF _MM(diad frequency) in alginate in the mixed solution of Sr²⁺, Ba²⁺ and Cd²⁺. Contribution No. 2166 from the Institute of Oceanology, Chinese Academy of Sciences.     

Interception of sulfate deposition from a closed canopy to a forest gap edge canopy in a subalpine dragon spruce plantation

Reducing the threats of sulfate ion(SO_4~(2-))deposition to terrestrial ecosystems is a great challenge.The canopy interception effect on SO_4~(2-)deposition has been well documented,but the interception efficiency of the gap edge remains unknown.Therefore,a subalpine dragon spruce(Picea asperata) plantation was evaluated in the upper reaches of the Yangtze River.The dynamics of the SO_4~(2-) concentration in the throughfall were investigated from the gap edge to the closed canopy during the rainfall and snowfall periods from August 2015 to July 2016.The annual input of SO_4~(2-) totaled 2.56 kg/ha through rainfall and 0.69 kg/ha through snowfall.The total annual net interception fluxes(NIFs) of SO_4~(2-) at the gap edge and in the closed canopy were 1.48 kg/ha and 0.66 kg/ha,respectively,and the net interception ratios(NIRs) accounted for 45.40% and 20.25%,respectively.The NIF and the NIR of SO_4~(2-) at the gap edge were higher than those in the closed canopy.Therefore,the results suggested that a significant amount of SO_4~(2-) deposition was intercepted by the tree canopy in the subalpine plantation,with more SO_4~(2-) deposition at the gap edge than in the closed canopy,which is beneficial for improving the water quality in the upper reaches of the Yangtze River via forest management.     

EFFECT OF SULPHATE-REDUCING BACTERIA ON ELECTRO-CHEMICAL CORROSION BEHAVIOR OF 16Mn STEEL IN SEA MUD

ＩＮＴＲＯＤＵＣＴＩＯＮＩｔｗａｓｇｅｎｅｒａｌｌｙｃｏｎｓｉｄｅｒｅｄｐｒｅｖｉｏｕｓｌｙｔｈａｔｔｈｅｃｏｒｒｏｓｉｏｎｏｆｓｔｅｅｌｉｎｓｅａｍｕｄｗａｓｎｏｔｓｅｒｉｏｕｓ.Ｈｏｗｅｖｅｒ,ｉｔｗａｓｌａｔｅｒｆｏｕｎｄｔｈａｔｔｈｅｃｏｒｒｏｓｉｏｎｒａｔｅｏｆｓｔｅｅｌｉｎｓｏｍｅｓｅａｍｕｄｗａｓｈｉｇｈｅｒｔｈａｎｔｈａｔｉｎｓｅａｗａｔｅｒ(Ｋｉｎｇ,1980;Ｓｅｈｍｉｄｅ,1982;Ｇｕｏｅｔａｌ.,1997;Ｈｏｕ,1998).Ｔｈｅｒｅａｒｅｓｏｍｅｒｅｐｏｒｔｓｔｈａｔｔｈｅｃｏｒｒｏｓｉｏｎｒ…     

Research on Corrosion Effect of Sulfate Ions on Concrete Under Wetting-Drying Cycle

Saline soil is widely distributed in the marine sediments along the coast of the world and the arid-semi-arid areas of the Middle East and Iraq,and calcium sulfate erosion has become one of the important factors affecting the durability of concrete in this area.In order to clarify the mechanism of sulfate ion damage to concrete,this paper mainly takes saline soil with high sulfate content in coastal area as well as arid-semi-arid area as the research object,and uses indoor geotechnical test,field test and numerical simulation to study the influence of different dry-wet cycle times on the unconfined compressive strength of concrete test blocks,and puts forward the relationship between the erosion arrival depth and time of sulfate ion in concrete,so as to predict the long-term erosion depth by using the erosion depth of sulfate ion in concrete in short time.The results show that the shorter the erosion time when the erosion reaches a certain depth,and the larger the erosion reaches when the erosion time is the same,the faster the erosion reaches the depth with the increase of erosion time.Compared with rectangular section concrete,circular section concrete penetrates faster.The results of this study can provide a reference for the durability design of concrete in saline soil sites containing sulfate.     

Inhibitor-concentration-induced extreme behaviour in electrochemical parameters

ImODUcrIONIngeneral,fOrmosttypesofinhibitorstheperformancecanbecontinuouslyheight-enedbyincreasingtheconeentration.Thehighertheinhibitorconcentration,thestrongertheinhibitionbomes.However,nantobservationsshowedthatsometypesofinhibitorsexhibitedbotperformanceonlywithinashortediumrangeofinhibitorconcentrationinsulfuricaddso1ution,whichistheso-cailedphenornenonofinhibitorconcenhation-indutalextreminhibition.EpelbOin(l979)reportedthattheinhibitingeffidenCyrnaxdrindataroundlmml4ofpropargylalcoh…     

The Study of the Varying Characteristics of Cathodic Regions for Defective Coating in 3.5% Sodium Chloride Solution by EIS and WBE

The current distributions over carbon steel under iron red alkyd primer exposed to 3.5% sodium chloride solution were mapped using the wire beam electrode(WBE). The electrochemical impedance spectroscopy(EIS) of the WBE was carried out to analyze the performance of coating delamination and corrosion behavior of carbon steel beneath defective coating. The EIS data revealed that protective capability of coating decreased with immersion time and the degree of cathodic delamination showed a rapid rise. The current density distribution of WBE indicated that cathodic sites was located at the defect at the beginning of immersion and gradually spread into the intact coating. The cathodic regions were distinguished from the anodic area and distributed over the WBE. The changes of cathodic sites could reflect the deterioration process of defective coating. The cathodic area ratio was a more useful parameter than the cathodic delamination degree to evaluate the coating cathodic delamination. The polarity reversals of electrodes at the defect and beneath coating were observed. A simple discussion of relationship between the blister and the polarity reversal was made from a standpoint of electrochemical distribution. WBE method was able to map and record the changes of local cathodic sites beneath defective coating in real time, which could provide more detailed information about the local degradation of coating.