corrosion

腐蚀
  • 文章类型: Journal Article
    研究了铸铁管道腐蚀对饮用水分配系统(DWDS)中水质风险和微生物生态的影响。已发现,在旧的DWDS中,三卤甲烷(THM)浓度和抗生素抗性基因(ARG)急剧增加。在相同的余氯浓度条件下,旧DWDS(Eff-old)废水中的三磷酸腺苷浓度显着高于新DWDS废水中的三磷酸腺苷浓度。此外,Eff-old的胞外聚合物中共存有较强的生物絮凝能力和较弱的疏水性,同时,铁颗粒可以很好地插入到生物膜的结构中,以增强生物膜的机械强度和稳定性,因此增强了THMs的形成。旧的DWDSs显着影响了散装水的微生物群落,并引发了更强的微生物抗氧化系统反应,导致更高的ARGs丰度。腐蚀的铸铁管诱导了独特的生物膜相互作用系统,氯,和腐蚀产物。因此,随着铸铁管年龄的增长,应重视水质和微生物生态的波动,以维护自来水的安全。
    The effects of cast iron pipe corrosion on water quality risk and microbial ecology in drinking water distribution systems (DWDSs) were investigated. It was found that trihalomethane (THMs) concentration and antibiotic resistance genes (ARGs) increased sharply in the old DWDSs. Under the same residual chlorine concentration conditions, the adenosine triphosphate concentration in the effluent of old DWDSs (Eff-old) was significantly higher than that in the effluent of new DWDSs. Moreover, stronger bioflocculation ability and weaker hydrophobicity coexisted in the extracellular polymeric substances of Eff-old, meanwhile, iron particles could be well inserted into the structure of the biofilms to enhance the mechanical strength and stability of the biofilms, hence enhancing the formation of THMs. Old DWDSs significantly influenced the microbial community of bulk water and triggered stronger microbial antioxidant systems response, resulting in higher ARGs abundance. Corroded cast iron pipes induced a unique interaction system of biofilms, chlorine, and corrosion products. Therefore, as the age of cast iron pipes increases, the fluctuation of water quality and microbial ecology should be paid more attention to maintain the safety of tap water.
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  • 文章类型: Journal Article
    本研究调查了虎杖根提取物(PCRE)在0.5MHCl酸性环境中对低碳钢的腐蚀抑制潜力。在这里,采用了各种技术,包括电化学和重量测量,随着扫描电子显微镜(SEM)和接触角(CA)测量的表面形貌分析。阻抗研究揭示了耐腐蚀性的浓度依赖性增强,将PCRE分类为混合型抑制剂(即,抑制阳极和阴极反应)。效率最高,在298K时为96.71%,在1000-ppm的PCRE浓度下观察到。Langmuir模型计算表明PCRE在电极基底上的化学吸附和物理吸附。在1000ppm下增加Rp(从28.648到174.01Ω)和Rct(185.74Ωcm2)显示出改进的耐腐蚀性。此外,SEM分析显示,保护表面,减少金属降解。理论计算强调了PCRE和低碳钢之间的强相互作用,具有低能隙(ΔE),如下:1-O-甲基大黄素(2.267eV)<大黄素(2.288eV)<大黄素-1-O-葡萄糖苷(2.343eV) This study investigates the corrosion inhibition potential of Polygonum cuspidatum root extract (PCRE) on mild steel in a 0.5 M HCl acidic environment. Herein, various techniques including electrochemical and gravimetric measurements were employed, along with scanning electron microscopy (SEM) and contact angle (CA) measurements for surface morphology analysis. The impedance study revealed a concentration-dependent enhancement in corrosion resistance, classifying PCRE as a mixed-type inhibitor (i.e., inhibits both anodic and cathodic reactions). The highest efficiency, 96.71% at 298 K, was observed at a 1000-ppm PCRE concentration. Langmuir model computations suggested chemisorption and physisorption of PCRE on the electrode substrate. Increased Rp (from 28.648 to 174.01 Ω) and Rct (185.74 Ω cm2) at 1000 ppm demonstrated improved corrosion resistance. Additionally, SEM analysis displayed a uniform, protective surface, reducing metal degradation. Theoretical calculations highlighted strong interactions between PCRE and mild steel, with a low energy gap (ΔE), as follows: 1-O-methylemodin (2.267 eV) < emodin (2.288 eV) < emodin-1-O-glucoside (2.343 eV) < piceid (2.931 eV) < resveratrol (2.952 eV), confirming PCRE\'s excellent micro-level anti-corrosion capabilities. This eco-benign corrosion inhibitor offers sustainable, low-toxicity protection, cost-effectiveness, and versatile performance, surpassing commercial counterparts while aligning with sustainability goals.
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  • 文章类型: Journal Article
    硅空气电池具有很高的能量密度,高理论电压,和长寿命,但它们在氢氧化钾电解液中的阳极利用率较低。在这项工作中,通过二次生长法制备和调制ZIF-8保护层,然后应用于保护Si-空气电池的Si平坦和Si纳米线(NW)阳极。通过调整转换比率,颗粒大小,和ZIF-8在Si表面的结晶度,控制了Si阳极与水和OH-的接触方式,从而实现长期耐腐蚀和钝化。SiNWs@ZIF-8表现出1.16V的最高平均放电电压,Si扁平@ZIF-8阳极实现了420h的最长放电时间。这项工作证实了ZIF-8作为阳极保护层来改善Si空气电池的性能,也为MOFs对Si阳极的保护提供了有价值的见解。
    Si-air batteries have a high energy density, high theoretical voltage, and long lifetime, but they present a low anode utilization rate in a potassium hydroxide electrolyte. In this work, a ZIF-8 protective layer was prepared and modulated by a secondary growth method and then applied to protect the Si flat and Si nanowire (NW) anodes of a Si-air battery. By adjusting the conversion ratio, particle size, and crystallinity of ZIF-8 on the Si surface, the contact mode of the Si anode with water and OH- was controlled, thus achieving long-term corrosion and passivation resistance. Si NWs@ZIF-8 exhibited the highest average discharge voltage of 1.16 V, and the Si flat@ZIF-8 anode achieved the longest discharge time of 420 h. This work confirms that ZIF-8 acts as an anode protective layer to improve the properties of Si-air batteries and also provides valuable insights into the protection of Si anodes by MOFs.
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  • 文章类型: Journal Article
    Ti基生物医学植入物的增材制造(AM)是一个关键的研究课题,因为它能够生产具有复杂几何形状的植入物。尽管理想的机械性能和生物相容性的钛合金,一个主要的缺点是它们缺乏固有的抗菌性能,增加术后感染的风险。因此,本文的研究重点是Ti536(Ti5Al3V6Cu)合金,通过电子束粉末床融合(EB-PBF)开发,探索生物腐蚀,抗菌特性,和细胞生物相容性。微观结构表征揭示了晶粒细化和Ti基体中不同形貌和尺寸的Ti2Cu析出物的形成。电化学测试表明,Cu含量对腐蚀电流密度的影响最小,虽然它稍微影响了稳定性,缺陷密度,和钝化膜的化学成分。根据调查结果,Ti536合金表现出增强的抗菌性能,而不损害其细胞生物相容性和腐蚀行为,由于Ti2Cu沉淀。这可以归因于Cu离子的释放和Ti2Cu沉淀物。目前的研究表明,EB-PBF制造的Ti536样品非常适合用于医疗行业的承重应用。这项研究还为使用AM方法具有优越生物学性能的新型生物医学Ti基合金提供了合金设计路线图。
    Additive manufacturing (AM) of Ti-based biomedical implants is a pivotal research topic because of its ability to produce implants with complicated geometries. Despite desirable mechanical properties and biocompatibility of Ti alloys, one major drawback is their lack of inherent antibacterial properties, increasing the risk of postoperative infections. Hence, this research focuses on the Ti536 (Ti5Al3V6Cu) alloy, developed through Electron Beam Powder Bed Fusion (EB-PBF), exploring bio-corrosion, antibacterial features, and cell biocompatibility. The microstructural characterization revealed grain refinement and the formation of Ti2Cu precipitates with different morphologies and sizes in the Ti matrix. Electrochemical tests showed that Cu content minimally influenced the corrosion current density, while it slightly affected the stability, defect density, and chemical composition of the passive film. According to the findings, the Ti536 alloy demonstrated enhanced antibacterial properties without compromising its cell biocompatibility and corrosion behavior, thanks to Ti2Cu precipitates. This can be attributed to both the release of Cu ions and the Ti2Cu precipitates. The current study suggests that the EB-PBF fabricated Ti536 sample is well-suited for use in load-bearing applications within the medical industry. This research also offers an alloy design roadmap for novel biomedical Ti-based alloys with superior biological performance using AM methods.
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  • 文章类型: Journal Article
    电化学阻抗谱(EIS)是一种用于评估涂层保护能力的现代有效方法。然而,实验数据的解释是一项艰巨的任务。本文旨在研究纳米粘土的添加效果,Cloesite30B®,在充气氯化钠溶液中通过电化学阻抗谱研究环氧基体系的阻隔性能。分析的样品的EIS光谱显示随时间的不同演变。使用等效电路对光谱进行后续处理是一种出色的分析工具,可以评估涂层的保护能力。通过分析,可以定义和理解在环氧树脂涂料中添加不同浓度的纳米粘土的影响。这项工作表明,这种类型的纳米粘土增加涂层的阻隔效果的有效性。然而,这种改进与获得纳米粒子的正确分散有关。否则,在涂层内部形成颗粒的宏观团簇。它们的外观可导致涂层性能的劣化。
    Electrochemical impedance spectroscopy (EIS) is a modern and efficient method for the evaluation of the protective abilities of coatings. However, the interpretation of the experimental data is a difficult task. This paper aims to investigate the effect of the addition of a nano clay, Cloesite 30B®, on the barrier properties of an epoxy-based system through electrochemical impedance spectroscopy in an aerated sodium chloride solution. The EIS spectra of the samples analysed showed different evolutions over time. The subsequent processing of spectra using equivalent electrical circuits is an excellent analytical tool and allows the protective capacity of coatings to be assessed. By using this analysis, it was possible to define and comprehend the impact of adding nano clay in different concentrations to the epoxy resin coating. The work has shown the effectiveness of increasing the barrier effect of the coating with this type of nano clay. However, the improvement is linked to obtaining a correct dispersion of nanoparticles. Otherwise, there is the formation of macro-clusters of particles inside the coating. Their appearance can cause a deterioration in coating performance.
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  • 文章类型: Journal Article
    铝技术合金以其出色的机械性能而闻名,特别是热处理后。然而,淬火和时效,提高了机械性能,通过形成与基体相干并阻止位错运动的富Cu区和相,导致元素在合金中的不均匀分布,从而使其易于腐蚀。一种提供令人满意的铝合金腐蚀保护的方法是阳极氧化。在工业规模上,它通常在含有铬酸盐的电解质中进行,这些铬酸盐被发现具有致癌作用和毒性。因此,已经付出了很多努力来寻找替代品。目前,有许多无Cr(VI)的替代品,如酒石酸-硫酸阳极氧化或柠檬酸-硫酸阳极氧化。尽管即使在工业规模上也使用了这种方法,Cr(VI)基阳极氧化似乎仍然是优越的;因此,有一种冲动,以寻找更复杂但更有效的方法在阳极氧化。从电解质向阳极氧化铝中引入阴离子是公知的效应。研究人员利用这种现象将各种其他阴离子和有机化合物截留到阳极氧化铝中以改变它们的性质。在这篇综述论文中,讨论了在阳极氧化铝中掺入各种缓蚀剂对合金腐蚀性能的影响。表明Mo化合物是有前途的,尤其是与有机酸结合时。
    Aluminum technical alloys are well known for their outstanding mechanical properties, especially after heat treatment. However, quenching and aging, which improve the mechanical properties, by the formation of Cu-rich zones and phases that are coherent with the matrix and block the dislocation motion, cause uneven distribution of the elements in the alloy and consequently make it prone to corrosion. One method providing satisfactory corrosion protection of aluminum alloys is anodizing. On an industrial scale, it is usually carried out in electrolytes containing chromates that were found to be cancerogenic and toxic. Therefore, much effort has been undertaken to find substitutions. Currently, there are many Cr(VI)-free substitutes like tartaric-sulfuric acid anodizing or citric-sulfuric acid anodizing. Despite using such approaches even on the industrial scale, Cr(VI)-based anodizing still seems to be superior; therefore, there is an urge to find more complex but more effective approaches in anodizing. The incorporation of anions into anodic alumina from the electrolytes is a commonly known effect. Researchers used this phenomenon to entrap various other anions and organic compounds into anodic alumina to change their properties. In this review paper, the impact of the incorporation of various corrosion inhibitors into anodic alumina on the corrosion performance of the alloys is discussed. It is shown that Mo compounds are promising, especially when combined with organic acids.
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  • 文章类型: Journal Article
    镁合金在水溶液中的快速腐蚀是其广泛应用的主要障碍之一,和涂层在其腐蚀保护中起着至关重要的作用。最近,保护和功能集成涂层在镁合金研究领域备受关注。在这项工作中,提出了一种简单的化学转化方法,通过浸入由Ca(OH)2和NaHCO3制成的水溶液中,在镁-钕合金上制备复合涂层。浸泡过程后,获得由两个自发形成的层组成的涂层。顶部的花状层由Mg5(OH)2(CO3)4·4H2O组成,Mg(OH)2和CaCO3,并猜测其内部致密层为Mg(OH)2。电化学阻抗谱,极化测试,和析氢相结合来评估模拟体液中的耐腐蚀性,模拟海水溶液,和模拟混凝土孔隙溶液,这表明涂层样品比未涂层样品具有更好的耐腐蚀性。用氟化硅烷对涂层样品进行改性后,可以实现具有151.74°的平均水接触角和约4°的滑动角的防水表面。因此,我们的结果表明,有效的腐蚀防护和潜在的自清洁能力已经集成在镁合金的表面在这项研究。此外,从基体与其外液相互作用的角度讨论了自层涂层的形成机理。
    Rapid corrosion in aqueous solutions of magnesium alloys is one of the major obstacles to their wide application, and coating plays a crucial role in their corrosion protection. Recently, protection- and function-integrated coatings have attracted much attention in the research field of magnesium alloys. In this work, a simple chemical conversion process is proposed to fabricate a composite coating on a magnesium-neodymium alloy through immersion in an aqueous solution made of Ca(OH)2 and NaHCO3. After the immersion process, a coating consisting of two spontaneously formed layers is acquired. The top flower-like layer is composed of Mg5(OH)2(CO3)4∙4H2O, Mg(OH)2 and CaCO3, and the inner dense layer is speculated to be Mg(OH)2. Electrochemical impedance spectroscopy, polarization tests, and hydrogen evolution are combined to evaluate the corrosion resistance in simulated body fluid, simulated seawater solution, and simulated concrete pore solution, which reveals that the coated sample has better corrosion resistance than the uncoated one. After the coated sample is modified with fluorinated silane, a water-repellent surface can be achieved with an average water contact angle of 151.74° and a sliding angle of about 4°. Therefore, our results indicate that effective corrosion protection and potential self-cleaning ability have been integrated on the surface of the magnesium alloy in this study. In addition, the formation mechanism of the self-layered coating is discussed from the viewpoint of the interaction between the substrate and its external solution.
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  • 文章类型: Journal Article
    这项研究的目的是通过电化学方法评估两种类型的低合金碳钢BVDH36和LRAH36在天然海水(Nāvodari地区)中的耐腐蚀性。使用的电化学方法是自由电位(OCP)的演变,电化学阻抗谱(EIS),极化电阻(Rp)和腐蚀速率(Vcorr),动电位极化(PD),和循环伏安法(CV)。这些研究是通过对腐蚀前后的研究表面进行非原位表征分析完成的,例如:光学显微镜,扫描电子显微镜和X射线衍射分析。研究结果表明,与低合金碳钢LRAH36的极化电阻相比,低合金碳钢BVDH36的极化电阻更高。还观察到,随着样品在天然海水中浸泡时间的增加,BVDH36合金的极化电阻随时间增加,最后降低,并且对于碳钢LRAH36,极化电阻增加。
    The purpose of this study is to evaluate the corrosion resistance in natural seawater (Năvodari area) of two types of low-alloy carbon steels BVDH36 and LRAH36 by electrochemical methods. The electrochemical methods used were the evolution of the free potential (OCP), electrochemical impedance spectroscopy (EIS), polarization resistance (Rp) and corrosion rate (Vcorr), potentiodynamic polarization (PD), and cyclic voltammetry (CV). The studies were completed by ex situ characterization analyzes of the studied surfaces before and after corrosion such as: optical microscopy, scanning electron microscopy and X-ray diffraction analysis. The results of the study show us that the polarization resistance of the low-alloy carbon steel BVDH36 is higher compared to the polarization resistance of the low-alloy carbon steel LRAH36. It is also observed that with the increase in the immersion time of the samples in natural seawater, the polarization resistance of the BVDH36 alloy increases over time and finally decreases, and for the carbon steel LRAH36 the polarization resistance increases.
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  • 文章类型: Journal Article
    最近2D材料的兴起扩展了调整各种属性的机会。摩擦腐蚀,机械磨损和化学腐蚀之间复杂的协同作用,在材料经受摩擦学应力和腐蚀环境的众多行业中提出了重大挑战。这种复杂的相互作用通常导致加速的材料降解和失效。这篇评论严格评估了利用2D纳米材料增强摩擦腐蚀和氧化行为的当前状态。在评估2D材料的关键贡献之前,本文总结了有关摩擦腐蚀和氧化机理的基本知识,包括石墨烯,过渡金属硫族化物,六方氮化硼,MXenes,和黑磷,关于由此产生的摩擦和磨损行为。研究了这些纳米材料对腐蚀和氧化的保护作用,突出了它们在减轻材料降解方面的潜力。此外,在摩擦腐蚀和氧化保护的二维材料的具体应用中,我们深入研究了机械和腐蚀因素之间的细微差别。关键发现的综合强调了通过集成2D纳米材料所取得的进步。对未来的研究方向进行了展望,找出未探索的途径,并提出推动该领域前进的战略。本分析旨在指导未来二维纳米材料动态交叉点的研究和发展。摩擦腐蚀,和氧化保护。
    The recent rise of 2D materials has extended the opportunities of tuning a variety of properties. Tribo-corrosion, the complex synergy between mechanical wear and chemical corrosion, poses significant challenges across numerous industries where materials are subjected to both tribological stressing and corrosive environments. This intricate interplay often leads to accelerated material degradation and failure. This review critically assesses the current state of utilizing 2D nanomaterials to enhance tribo-corrosion and -oxidation behavior. The paper summarizes the fundamental knowledge about tribo-corrosion and -oxidation mechanisms before assessing the key contributions of 2D materials, including graphene, transition metal chalcogenides, hexagonal boron nitride, MXenes, and black phosphorous, regarding the resulting friction and wear behavior. The protective roles of these nanomaterials against corrosion and oxidation are investigated, highlighting their potential in mitigating material degradation. Furthermore, we delve into the nuanced interplay between mechanical and corrosive factors in the specific application of 2D materials for tribo-corrosion and -oxidation protection. The synthesis of key findings underscores the advancements achieved through integrating 2D nanomaterials. An outlook for future research directions is provided, identifying unexplored avenues, and proposing strategies to propel the field forward. This analysis aims at guiding future investigations and developments at the dynamic intersection of 2D nanomaterials, tribo-corrosion, and -oxidation protection.
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  • 文章类型: Journal Article
    研究了20G和TP347H材料在熔融LiCl-NaCl-KCl盐中的腐蚀行为。这些材料在熔融氯化物盐中的腐蚀速率很高,并且受到合金化表面氧化物形成的强烈影响。20G显示出均匀的表面腐蚀,在表面上几乎没有形成保护性氧化物。相比之下,奥氏体钢TP347H由于其高Cr含量而在熔融氯化物盐中表现出更好的耐腐蚀性。由于熔融氯化物盐的高腐蚀性,熔盐中的Cl-可以与氧化物和合金反应,在熔融氯化物盐环境中诱导奥氏体钢的晶间腐蚀。
    The corrosion behavior of 20G and TP347H materials was investigated in molten LiCl-NaCl-KCl salt. The corrosion rates of these materials in molten chloride salt are high and are strongly affected by the alloying surface oxide formation. The 20G shows uniform surface corrosion with almost no protective oxide formation on the surface. In contrast, the austenitic steel TP347H exhibits better corrosion resistance in molten chloride salts due to its high Cr content. Owing to the highly corrosive nature of molten chloride salts, the Cl- in molten salt could react with oxides and alloy, inducing intergranular corrosion of austenitic steel in molten chloride salt environments.
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