High Cl Research Articles

The influence Cl− on stress corrosion of 7xxx series aluminium alloys studied by experimental and simulation technology

The stress corrosion behavior of 7xxx series aluminium alloys in different concentrations NaCl solution was studied, and numerical simulation was conducted in COMSOL Multiphysics based on experimental results. Different stresses were applied on the experiment pieces, the pitting crater deepened with the change of stress level. The corrosion rate increased with the raising stress. There is no positive correlation between stress corrosion degree and chloride ion concentration. The most severe corrosion occurs in 5.0 wt% NaCl solution instead of 6.0 wt% NaCl solution due to the increase of water film conductivity and decrease of solubility of oxygen under high Cl− environment. The finite element model was used to analyze the stress distribution on aluminium alloy surface, to describe the dynamic equation of anodic dissolution of metal due to elastic and plastic deformation. Corrosion occurs mainly in stress concentrated areas. When the stress loading exceeds a certain threshold, plastic strain occurs on the surface of both the specimen and the structural part, the corrosion current density increases instantaneously, and the corrosion behavior in the stress concentration area gradually intensifies. The survey can provide practical theoretical guidance for predicting stress corrosion and extending the service life of equipment in (harsh) marine environments.

A regional examination of the footprint of agriculture and urban cover on stream water quality

Freshwater systems in cold regions, including the Laurentian Great Lakes, are threatened by both eutrophication and salinization, due to excess nitrogen (N), phosphorus (P) and chloride (Cl−) delivered in agricultural and urban runoff. However, identifying the relative contribution of urban vs. agricultural development to water quality impairment is challenging in watersheds with mixed land cover, which typify most developed regions. In this study, a self-organizing map (SOM) analysis was used to evaluate the contributions of various forms of land cover to water quality impairment in southern Ontario, a population-dense, yet highly agricultural region in the Laurentian Great Lakes basin where urban expansion and agricultural intensification have been associated with continued water quality impairment. Watersheds were classified into eight spatial clusters, representing four categories of agriculture, one urban, one natural, and two mixed land use clusters. All four agricultural clusters had high nitrate-N concentrations, but levels were especially high in watersheds with extensive corn and soybean cultivation, where exceedances of the 3 mg L−1 water quality objective dramatically increased above a threshold of ‍∼30 % watershed row crop cover. Maximum P concentrations also occurred in the most heavily tile-drained cash crop watersheds, but associations between P and land use were not as clear as for N. The most urbanized watersheds had the highest Cl− concentrations and expansions in urban area were mostly at the expense of surrounding agricultural land cover, which may drive intensification of remaining agricultural lands. Expansions in tile-drained corn and soybean area, often at the expense of mixed, lower intensity agriculture are not unique to this area and suggest that river nitrate-N levels will continue to increase in the future. The SOM approach provides a powerful means of simplifying heterogeneous land cover characteristics that can be associated with water quality patterns and identify problem areas to target management.

Degradation of organic pollutants by the Cl-/PMS process.

The viewpoints on whether high concentrations of chloride ion (Cl-) promote or inhibit the oxidation activity of activated persulfates are still inconclusive. Furthermore, the degradation of organic pollutants by the persulfates in the presence of high Cl- concentrations without any activation medium has not yet been studied. In this work, the efficiency and mechanism of degradation of organic pollutants such as carbamazepine (CBZ), sulfadiazine (SDZ), and phenol (PN) by Cl--activated PMS (denoted as Cl-/PMS) were investigated. Results showed that Cl- could effectively activate PMS for the complete removal of CBZ, SDZ, and PN with reaction kinetic constants of 0.4516min-1, 0.01753min-1, and 0.06805min-1, respectively. Parameters such as PMS dose, Cl- concentration, solution pH, and initial concentrations of organic pollutants that affect the degradation efficiencies of the Cl-/PMS process were optimized. Unlike conventional activated persulfates, it was confirmed that the free chlorine was the main active species in the Cl-/PMS process. Finally, the degradation by-products of CBZ and SDZ as well as their toxicity were detected, and a possible degradation pathway for CBZ and SDZ was proposed. Though higher toxic chlorinated by-products were generated, the Cl-/PMS process was still an efficient oxidation method for the removal of organic pollutants in aqueous solutions which contain high concentrations of Cl-.

A non-aqueous Li+/Cl− dual-ion battery with layered double hydroxide cathode

Dual-ion batteries (DIBs) have unique advantages in energy storage, such as high energy density and low cost. However, most studies on organic DIBs use anions with a large ionic radius (PF6−, TFSI−, etc.). Here, we propose a Li+/Cl− dual-ion battery (DIB) through using CoFe-Cl layered double hydroxides (LDHs) and non-aqueous LiCl electrolytes, with a mechanism involving anionic insertion into the LDHs cathode and lithium plating/stripping on the anode. Coupled X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) techniques indicate reversible expansion/extraction of (003) crystal planes of LDHs and valence state changes of Co and Fe, enabling high Cl− storage capacities of 145 mAh/g and 137 mAh/g at 200 mA/g and 1 A/g, respectively. Furthermore, this DIB demonstrates an impressive power density of 1770 W/kg with an energy density of 240 Wh/kg. This work provides a reference for developing high performance DIBs and expands the electrochemical application field of LDHs.

Upcycling of cellulosic textile waste with bacterial cellulose via Ioncell® technology

Currently the textile industry relies strongly on synthetic fibres and cotton, which contribute to many environmental problems. Man-made cellulosic fibres (MMCF) can offer sustainable alternatives. Herein, the development of Lyocell-type MMCF using bacterial cellulose (BC) as alternative raw material in the Ioncell® spinning process was investigated. BC, known for its high degree of polymerization (DP), crystallinity and strength was successfully dissolved in the ionic liquid (IL) 1,5-diazabicyclo[4.3.0]non-5-enium acetate [DBNH][OAc] to produce solutions with excellent spinnability. BC staple fibres displayed good mechanical properties and crystallinity (CI) and were spun into a yarn which was knitted into garments, demonstrating the potential of BC as suitable cellulose source for textile production. BC is also a valuable additive when recycling waste cellulose textiles (viscose fibres). The high DP and Cl of BC enhanced the spinnability in a viscose/BC blend, consequently improving the mechanical performance of the resulting fibres, as compared to neat viscose fibres.

Physiological and transcriptomic profiles of tobacco seedling leaves in response to high chloride accumulation

ABSTRACT Tobacco is a special commercial crop that prefers potassium but not chlorine, and excessive chloride (Cl–) accumulation can cause toxicity. Here, we revealed that the structural characteristics of chloroplasts in tobacco leaves were significantly destroyed under high Cl– salinity, but not mitochondria. Large differences in leaf structure, MDA content, and antioxidant enzyme activities were observed for the treatment with highest chloride accumulation at the 14th day. Moreover, RNA-seq analysis of tobacco leaves exposed to high Cl– salinity revealed global changes in gene transcription levels. A total of 1360 DEGs involved in cell wall, lipid, starch, and secondary metabolism processes were unevenly distributed on chromosomes, and were mainly enriched for starch and sucrose metabolism, phenylpropanoid biosynthesis, ribosome and ribosome biogenesis, protein processing in the endoplasmic reticulum, and plant hormone signal transduction pathways. Overall, our study provides valuable insights for further research on the mechanism underlying Cl– salinity and salt-tolerant tobacco development.

Anti-corrosive superhydrophobic coatings for reinforcement protection: recycling of concrete garbage

PurposeThe purpose of this paper was to prepare a ternary hierarchical rough particle to accelerate the anti-corrosive design for coastal concrete infrastructures.Design/methodology/approachA kind of micro-nano hydrophobic ternary microparticles was fabricated from SiO2/halloysite nanotubes (HNTs) and recycled concrete powders (RCPs), which was then mixed with sodium silicate and silane to form an inorganic slurry. The slurry was further sprayed on the concrete surface to construct a superhydrophobic coating (SHC). Transmission electron microscopy and energy-dispersive X-ray spectroscopy mappings demonstrate that the nano-sized SiO2 has been grafted on the sub-micron HNTs and then further adhered to the surface of micro-sized RCP, forming a kind of superhydrophobic particles (SiO2/HNTs@RCP) featured of abundant micro-nano hierarchical structures.FindingsThe SHC surface presents excellent superhydrophobicity with the water contact angle >156°. Electrochemical tests indicate that the corrosion rate of mild steel rebar in coated concrete reduces three-order magnitudes relative to the uncoated one in 3.5% NaCl solution. Water uptake and chloride ion (Cl-) diffusion tests show that the SHC exhibits high H2O and Cl- ions barrier properties thanks to the pore-sealing and water-repellence properties of SiO2/HNTs@RCP particles. Furthermore, the SHC possesses considerable mechanical durability and outstanding self-cleaning ability.Originality/valueSHC inhibits water uptake, Cl- diffusion and rebar corrosion of concrete, which will promote the sustainable application of concrete waste in anti-corrosive concrete projects.

Magmatic evolution and metallogenic diversity of the late Cretaceous granites in the Yidun terrane: Constraints from zircon and apatite geochemistry

Porphyry-hydrothermal type Cu-Mo(−W) deposits in the southern Yidun terrane (SYT) and hydrothermal-skarn type Sn-Pb-Zn-Ag deposits in the northern Yidun terrane (NYT) are closely related to late Cretaceous granitic intrusions in time and space. However, the genetic mechanisms and controlling factors responsible for the metallogenic diversity remain unclear. We investigated zircon and apatite compositions of the Sn-Pb-Zn-Ag-associated granites in northern Yidun terrane and the Mo-W-Cu and Mo-Cu-associated granites in southern Yidun terrane. The Cretaceous granites are distributed along a N–S-trending belt having ages ranging from 106 to 73 Ma, with a transition from predominant plagioclase crystallization to amphibole-dominated crystallization. Our data show that the granites from the NYT have lower zircon Eu/Eu* (0.06 ± 0.04), Ce4+/Ce3+, and ΔFMQ (FMQ is fayalite-magnetite-quartz) values compared to the granites in the SYT, indicating that the granites from the NYT are relatively reduced (ΔFMQ = -1.03 ± 1.02) in contrast to the oxidized granites in the SYT (ΔFMQ = 1.10 ± 1.05). Furthermore, apatite can record the volatile compositions of magma before fluid exsolution. Apatites in granites from the NYT with low XF/XCl ratios (≤120) are interpreted to have crystallized from volatile-undersaturated magma. These apatites are characterized by low Cl contents ranging from 0.04 to 0.12 wt% (0.07 ± 0.02 wt%; n = 21) and low SO3 contents of 0.01–0.06 wt%. In contrast, apatites in granite from the SYT with low XF/XCl ratios (≤80) have high Cl contents of 0.05 to 0.34 wt% (0.16 ± 0.07 wt%; n = 52) and SO3 contents of 0.01–0.46 wt%. The chemical compositions of zircon and apatite indicate that the Mo-W-Cu and Mo-Cu-associated granites in the SYT have higher fO2 and melt S contents before fluid exsolution than the Sn-Pb-Zn-Ag-associated granites in the NYT. Therefore, the contrasting magmatic oxidation states and S contents are critical in controlling the metallogenic diversity of the Cretaceous granites in the Yidun terrane. The Xingguolongba and Cuopu granites, first reported in this article, have U-Pb ages consistent with the Rongyicuo and Cuomolong granites. Furthermore, they exhibit similar geochemical properties, such as oxygen fugacity and volatiles, suggesting the possibility of forming Sn-Pb-Zn-Ag deposits.

Focusing on the corrosion resistance enhancement of HRB400 rebar by Cr addition in the marine environment

The corrosion resistance of Cr reinforced HRB400 rebar in the marine environment was investigated. The addition of Cr increases the amount of Cr(OH)3 and α-FeOOH in the passivate film, resulting in a denser passivate film structure. This enhanced passivation film inhibits localized corrosion. The pitting potential and critical chloride concentration (CTL) of the steel increased with the increase in chromium content, indicating improved corrosion resistance of the steel. On the other hand, an increase in the concentration of Cl- in solution leads to a decrease in the pitting potential and resistance of the steel, which reduces the corrosion resistance. At higher Cl- concentrations, the Cl- ions form an electrochemical interface with the steel surface, resulting in a sharp decrease in the Rf value. In addition, the gradual decrease in solution pH leads to a decrease in the pitting potential and CTL of HRB400 and 1.5Cr steel. The corrosion resistance was also found to be reduced, pH reduction accelerated the intrusion of chloride ions, which led to a severe breakdown of the passivation film.

Evidence for Two Subpopulations of Cerebrospinal Fluid-Contacting Neurons with Opposite GABAergic Signaling in Adult Mouse Spinal Cord.

Spinal cerebrospinal fluid-contacting neurons (CSF-cNs) form an evolutionary conserved bipolar cell population localized around the central canal of all vertebrates. CSF-cNs were shown to express molecular markers of neuronal immaturity into adulthood; however, the impact of their incomplete maturation on the chloride (Cl-) homeostasis as well as GABAergic signaling remains unknown. Using adult mice from both sexes, in situ hybridization revealed that a proportion of spinal CSF-cNs (18.3%) express the Na+-K+-Cl- cotransporter 1 (NKCC1) allowing intracellular Cl- accumulation. However, we did not find expression of the K+-Cl- cotransporter 2 (KCC2) responsible for Cl- efflux in any CSF-cNs. The lack of KCC2 expression results in low Cl- extrusion capacity in CSF-cNs under high Cl- load in whole-cell patch clamp. Using cell-attached patch clamp allowing recordings with intact intracellular Cl- concentration, we found that the activation of ionotropic GABAA receptors (GABAA-Rs) induced both depolarizing and hyperpolarizing responses in CSF-cNs. Moreover, depolarizing GABA responses can drive action potentials as well as intracellular calcium elevations by activating voltage-gated calcium channels. Blocking NKCC1 with bumetanide inhibited the GABA-induced calcium transients in CSF-cNs. Finally, we show that metabotropic GABAB receptors have no hyperpolarizing action on spinal CSF-cNs as their activation with baclofen did not mediate outward K+ currents, presumably due to the lack of expression of G-protein-coupled inwardly rectifying potassium (GIRK) channels. Together, these findings outline subpopulations of spinal CSF-cNs expressing inhibitory or excitatory GABAA-R signaling. Excitatory GABA may promote the maturation and integration of young CSF-cNs into the existing spinal circuit.

Internal Electric Field Facilitates Facet-Dependent Photocatalytic Cl- Utilization on BiOCl in High-Salinity Wastewater for Ammonium Removal.

High Cl- concentration in saline wastewater (e.g., landfill leachate) limits wastewater purification. Catalytic Cl- conversion into reactive chlorine species (RCS) arises as a sustainable strategy, making the salinity profitable for efficient wastewater treatment. Herein, aiming to reveal the structure-property relationship in Cl- utilization, bismuth oxychloride (BiOCl) photocatalysts with coexposed {001} and {110} facets are synthesized. With an increasing {001} ratio, the RCS production efficiency increases from 75.64 to 96.89 μg L-1 min-1. Mechanism investigation demonstrates the fast release of lattice Cl- as an RCS and the compensation of ambient Cl-. Correlation analysis between the internal electric field (IEF, parallel to [001]) and normalized efficiency on {110} (kRCS/S{110}, perpendicular to [001]) displays a coefficient of 0.86, validating that the promoted carrier dynamics eventually affects Cl- conversion on the open layered structure. The BiOCl photocatalyst is well behaved in ammonium (NH4+-N) degradation ranging from 20 to 800 mg N L-1 with different chlorinity (3-12 g L-1 NaCl). The sustainable Cl- conversion into RCS also realizes 85.4% of NH4+-N removal in the treatment of realistic landfill leachate (662 mg of N L-1 NH4+-N). The structure-property relationship provides insights into the design of efficient catalysts for environment remediation using ambient Cl-.

Genetic mechanism of geothermal water in the sandstone reservoir of western Sichuan, SW China: Evidence from hydrochemistry and δD − δ18O isotopes

Geothermal energy is the vital clean and renewable energy in the world. In China, most of high−temperature sedimentary − type geothermal waters are developed in western Sichuan, such as geothermal springs in the Litang county. In this study, hydrochemistry and δD − δ18O isotopes were investigated to clarify the genetic mechanism of high−temperature sedimentary − type geothermal waters in the Litang county. The self-organized map and Piper diagram showed three hydrochemical types of geothermal waters: (1) HCO3 − SO4 − Na, (2) HCO3 − Na with low Cl− concentration, (3) HCO3 − Na with high Cl− concentration. Cluster 1 geothermal water of Na − HCO3 − SO4 was dominated by dissolution of silicate and sulfate minerals. Cluster 2 geothermal water of HCO3 − Na with low Cl− concentration was affected by dissolution of silicate and CO2 degassing and mixed by large amounts of shallow cold water. Cluster 3 geothermal water of HCO3 − Na with high Cl− concentration was affected by dissolution of sandstone silicate and CO2 degassing and mixed by less shallow cold water. The recharge elevation of geothermal water in Litang ranges from 4799 to 4972 m, with an average of 4915 m. This suggests that the recharge sources of geothermal water are snow melt water and magmatic water. Cluster 3 geothermal water displayed the largest contribution of magmatic water. The temperature of HCO3 − SO4 − Na geothermal water after mixing is 92−102 °C, with an average of 97 °C; the initial temperature of HCO3 − Na with low Cl− geothermal water is 60−72 °C, with an average of 65 °C; the initial temperature of HCO3 − Na with high Cl− geothermal water is 74−91 °C, with an average of 81 °C. The temperature of geothermal water after mixing is Class 1 > Class 3 > Class 2. From the perspective of reservoir temperature, the Class 3 of geothermal water had the highest values, followed by Class 1 and Class 2 of geothermal water. From the perspective of cold − water mixing ratio, Class 2 and Class 3 of geothermal water had a similar mixing ratio, slightly higher than that of Class 1 of geothermal water. Therefore, the class 3 geothermal water with HCO3 − Na with high Cl− concentration possess the great potential for exploitation.

The corrosion and tribological behaviors of DLC film in CO2 saturated NaCl solution with high Cl− concentration

The failure of pipelines during oil and gas exploitation is a pressing issue in the oil and gas industry. The high permeability of chloride ions (Cl−) alters the corrosion morphology of the N80 substrate and diminishes its ability to impede the penetration of corrosive substances. This study aims to deposit DLC films on the inner surface of N80 pipeline using plasma enhanced chemical vapor deposition (PECVD), and investigate the corrosion and friction behavior of DLC films in CO2 saturated NaCl solutions with varying Cl− concentrations. The results indicate that the change in Cl− concentration possess minimal impact on the DLC film. The corrosion current density of DLC films in CO2 saturated NaCl solution with three different Cl− concentrations is one order of magnitude lower than that of the N80 substrate. Moreover, a transfer film can still form in high-concentration CO2-saturated NaCl solutions, reducing wear. DLC film demonstrates exceptional stability, corrosion resistance, and wear resistance, making it an ideal material for safeguarding pipelines during oil and gas exploitation.

WITHDRAWN: Investigation on corrosion behaviors of 316 stainless steel in deep-sea water/sediments of the South China Sea via manned deep diving

As observed in a 3404-meter-deep field test via manned diving, 316 SS mainly occurs pitting corrosion in deep-sea water/sediments and corrodes 3-4 times faster than that in shallow sea. In water, due to the synergistic effect of high hydrostatic pressure and Cl− ions, the passive film becomes loose and nonuniform, and the pits expand laterally, leading to wide and shallow pits. In sediments, S2− ions inhibit the re-passivation process and make the passive film thinner, causing numerous pits initiate. Because of the poor Cl− ions transfer efficiency, the pits expand slowly in lateral direction, resulting in vertical pits.

Impact of Combined Action of Chloride and Carbonation on Cement-Based Materials with Fly Ash

Integrating waste and industrial by-products into concrete is an alternative way to reduce global cement consumption, enhancing its eco-friendliness. In this context, residues with fly ash have been increasingly utilised. Considering the vulnerability of concrete with fly ash to carbonation and, at the same time, its high resistance to chlorides, it is important to investigate the behaviour of these concretes under their combined actions. For this purpose, an experimental investigation was conducted, studying mortar and concrete specimens with 40% replacement of cement with fly ash. These specimens were subjected to a combination of actions (Cl− and CO2) in two phases: initially through immersion and drying tests, and subsequently through a combination of accelerated tests. Concerning the chloride impact study, free and total chloride profiles were studied. Concerning the impact of carbonation, colourimetric and chemical tests were used. The results demonstrate a significant influence of combined action not only on chloride penetration in cement-based materials with fly ash but also on the development of a carbonation front. Exposure of cement-based materials with fly ash to environments with high Cl− and CO2 content sequentially may lead, on the one hand, to an increase in carbonation resistance. However, on the other hand, it may result in a substantial reduction in chloride penetration resistance.

High temperature chlorine corrosion resistance of gradient high entropy alloy coatings prepared by high-velocity-oxygen-fuel spraying

The effect of different gradient structures on the high temperature chlorine corrosion resistance of gradient high entropy alloy coating was studied to improve the service life of the heating surface of a waste-incinerated boiler. NiCrAl ceramic composite coating (NC), high entropy ceramic composite coating (HC), and gradient high entropy alloy coating (TC) were prepared on 12Cr1MoV substrate by high-velocity-oxygen-fuel spraying. The effects of morphology and microstructure of different coatings on thermal shock resistance and high temperature chlorine corrosion resistance were studied. The results indicate that the porosity of NC coating, HC coating, and TC coating decreased in turn. In the thermal shock resistance test from 800°C to room temperature, the average number of thermal shock of TC coating can reach 21. The mass change of TC coating in 650°C high temperature Cl corrosion resistance test is less than 30 mg/cm2 after 50 hours. In summary, the gradient high entropy alloy coating with HEA as the metal bonding phase can improve the density of thermal spraying gradient coating, and enhance the thermal shock resistance and high temperature Cl corrosion resistance of the coating. Based on the comprehensive on-site application results, it can be concluded that the use of high velocity oxygen flame gradient high entropy alloy coating can effectively improve the density, thermal shock resistance, and high temperature Cl corrosion resistance of the thermal spraying gradient coating on the heating surface of the boiler, and has broad application prospects.

Neurohormonal Activation and Renal Chloride Avidity in Acute Heart Failure: Clinical Evidence Supporting the “Chloride Theory”

Introduction: Heart failure (HF) progression according to changes in the serum chloride concentration ([sCl−]) was recently proposed as the “chloride (Cl) theory” for HF pathophysiology. The present study examined the association of neurohormones and renal Cl avidity to determine their contribution to acute HF and their involvement to the “Cl theory.” Methods: Data from 29 patients with acute HF (48% men; 80.3 ± 12 years) were analyzed. Blood and urine samples were obtained before decongestive therapy. Clinical tests included peripheral blood, serum and spot urinary electrolytes, b-type natriuretic peptide (BNP), and plasma neurohormones. Results: In the 29 patients, urinary Cl concentrations ([uCl−]) inversely correlated with log (plasma renin activity [PRA]) (r = −0.64, p = 0.0002) and log (plasma aldosterone concentration) (r = −0.50, p = 0.006). The [sCl−]‒[uCl−] difference positively correlated with log PRA (r = 0.63, p = 0.0002) and log (plasma aldosterone concentration) (r = 0.49, p = 0.008). Patients were divided into 2 groups according to the [sCl−]‒[uCl−] difference, an excretion (low renal Cl avidity) group and an absorption (high renal Cl avidity) group. Compared with the excretion group (−77 to ‒5 mEq/L; n = 14), the absorption group (1–84 mEq/L; n = 15) exhibited greater renal impairment (serum creatinine; 1.45 ± 0.63 vs. 1.00 ± 0.38 mg/d, p = 0.029) and cardiac burden (log BNP; 2.99 ± 0.3 vs. 2.66 ± 0.32 pg/mL, p = 0.008), higher log PRA (0.20 ± 0.58 vs. −0.25 ± 0.35 ng/mL/h, p = 0.018), and lower fractional urinary Cl excretion (1.34 ± 1.3 vs. 5.33 ± 4.1%, p < 0.001). Conclusion: Renal Cl avidity differs in acute HF, i.e., excretion (low renal Cl avidity) versus absorption (high renal Cl avidity) types, involving renin-aldosterone-angiotensin activity as the underlying mechanism, which provides the neurohormonal background for the “Cl theory.” A version of this study was presented in part at the annual international scientific assembly (ACC.23) of the American College of Cardiology, March 4–6, 2023.

Evaluation of Corrosion Impeding Concretion Layers Formed on Shipwreck Steel in the Belgian North Sea

Evaluation of Corrosion Impeding Concretion Layers Formed on Shipwreck Steel in the Belgian North Sea

Electrochemical corrosion behavior of industrial pure zirconium in high Cl- containing solutions

The effects of different Cl- concentrations on the corrosion behavior of pure zirconium and its welded joint were studied by electrochemical test and numerical fitting, and the mechanism was discussed. The results showed that：In the solution containing Cl-, the potentiodynamic polarization curves of industrial pure zirconium base metal and its welded joint show certain passivation behavior, and with the increase of Cl- concentration, the corrosion tendency of the base metal and welded joint increases, the potentiodynamic polarization curves move to the lower right, the polarization resistance of the material decreases, the corrosion current density increases, and the corrosion resistance deteriorates. Compared with the base metal, the corrosion current of the welded joint is larger and the pitting potential is lower under the same Cl- concentration, and the difference in microstructure is the main reason for the poor corrosion resistance.

Investigating the Corrosive Influence of Chloride Ions on Slag Recovery Machine Inner Guide Wheel in Power Plants.

An important method that coal-fired power plants use to realise low-cost zero discharge of desulfurisation wastewater (FGD wastewater) is to utilise wet slag removal systems. However, the high Cl- content of FGD wastewater in wet slag removal systems causes environmental damage. In this study, the corrosion behaviour of the inner guide wheel material, 20CrMnTi, was studied using dynamic weight loss and electrochemical methods. X-ray diffraction, scanning electron microscopy, and energy spectroscopy were used to analyse the organisational and phase changes on the surfaces and cross sections of the samples at different Cl- concentrations. The corrosion rate increased with the Cl- concentration up to 20 g/L, but it decreased slightly when the Cl- concentration exceeded 20 g/L. In all the cases, the corrosion rate exceeded 0.8 mm/a. The corrosion product film density initially increased and then decreased as the Cl- concentration increased. The corrosion products comprised mainly α-FeOOH, γ-FeOOH, β-FeOOH, Fe3O4, and γ-Fe2O3.