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Abrasion-corrosion of downhole drill tool components

机译:井下钻具部件的磨损腐蚀

摘要

The present work is a Schlumberger funded PhD project entitled ‘Abrasion-corrosion of downhole drilltool components’. The objective of this project was to replicate the wear-corrosion mechanisms oftungsten carbide (WC)-based hardmetals and coatings occurring in downhole environments (pH 9-11)under controlled laboratory conditions, to identify and establish a better understanding thesemechanisms and the factors influencing them so as to minimise the material wastage during service.The presence of hard and soft phases within WC-based hardmetals and coatings results in complex wearmechanisms. In addition, the presence of a corrosive environment downhole further complicates thecontact conditions and can lead to accelerated surface degradation and even catastrophic failures. AScanning Electron Microscope (SEM) investigation of worn drill-tool components revealed thepresence of micro-scale (by abrasives similar size to the carbide grains i.e. less than 5 ?m) and macroscaleabrasion (by abrasives orders of magnitude larger in size compared to the carbide grains). Thewear-corrosion testing of candidate materials was investigated using a micro-macro dual approachcomprising of micro-scale abrasion testing (University of Southampton) and the modified ASTM G65tester (National Physical Laboratories, Teddington). To mimic exposure to alkaline drilling fluids forlong durations, selected samples were exposed to pH 11 NaOH solution / drilling fluid for 168 h prior towear testing. Screening of candidate materials on the basis of their wear-corrosion performance usingmicro-abrasion tester was performed and WC-10Co-4Cr coating along with sintered WC-5.7Co-0.3Crwere selected for in-depth analysis and the micro-macro dual test programme.The WC-10Co-4Cr coating exposed to pH 11 and pH 7 distilled water (for comparison), revealed thepresence of an intense localised corrosion in the form of ‘corrosion trenches’ due to the preferentialdissolution of decarburised metallic tungsten (W), which occurred around the periphery of the carbidegrains. These ‘corrosion trenches’ were found to be one-carbide deep and resulted in the carbide beingheld loose in the corrosion trenches. Alternatively, for the sintered WC-5.7Co-0.3Cr, exposure to pH 11did not show any evidence of localised corrosion. However, exposure to pH 7 distilled water resulted inthe preferential dissolution of the binder phase.For the first time, a modified micro-abrasion tester capable of in situ electrochemical measurements wasdeveloped to monitor the corrosion kinetics during micro-scale wear-corrosion. Interestingly, the lowestwear occurred under pH 11 conditions. It was proposed that the presence of Co(OH)2 based passivefilms, also detected by XPS analysis, appears to influence the rate of binder-phase removal by alteringthe stiffness of the abrasive-surface contact and lowering the friction between abrasives and the surfaceand in turn lowers the overall wear rates. This was also corroborated by the observed wear mechanismof preferential removal of the binder-phase leading to the undermining of carbides. Conversely, for thesintered WC-5.7Co-0.3Cr, despite the lack of surface passivation under similar test conditions, the wearrates were found to be independent of pH.The influence of abrasive size on the wear-corrosion performance of sprayed WC-10Co-4Cr coatingwas investigated using the modified ASTM G65 test. It was revealed that in addition to the size ofabrasives, the wear rates are dependent on the overall wear mechanisms. In general, severe damage tothe coating was caused by delamination due to the propagation of sub-surface cracks resulting in thedoubling of wear rates. The sub-surface cracking of the coating increases with an increase in theabrasive size. Alternatively, for the sintered WC-5.7Co-0.3Cr, an increase in the extent of cracking inthe carbide grains increased with the abrasive size. An order of magnitude increase in wear resultedfrom the extensive carbide cracking and the subsequent removal of the carbide grains. The dualapproach successfully replicated the wear in downhole conditions by examining the influence of contactconditions and abrasive size on the wear-corrosion of WC-based sintered hardmetals and sprayedcoatings to inform a better design / selection of surfaces subjected to downhole environments.
机译:目前的工作是由斯伦贝谢(Schlumberger)资助的博士项目,题为“井下钻具部件的磨损腐蚀”。该项目的目的是复制在受控实验室条件下在井下环境(pH 9-11)中发生的碳化钨(WC)基硬质合金和涂层的磨损腐蚀机理,以识别并建立对这些机理和影响因素的更好的理解WC基硬质合金和涂层中存在硬相和软相会导致复杂的磨损机制。另外,井下腐蚀性环境的存在进一步使接触条件复杂化,并且可以导致加速的表面退化甚至是灾难性的故障。扫描电镜(SEM)对磨损的钻具部件的研究表明,存在微米级(通过与碳化物晶粒大小相似的磨料,即小于5μm)和宏观磨损(通过尺寸比碳化物大几个数量级的磨料)的存在谷物)。使用包括微观磨损测试(南安普敦大学)和改良的ASTM G65测试仪(国家物理实验室,泰丁顿)在内的微型双宏观方法研究了候选材料的磨损腐蚀测试。为了模拟长时间暴露在碱性钻井液中,在磨损测试之前,将选定的样品暴露于pH 11 NaOH溶液/钻井液中168小时。使用微磨损测试仪根据其耐磨性能对候选材料进行了筛选,并选择了WC-10Co-4Cr涂层以及烧结的WC-5.7Co-0.3Cr进行了深入分析和微宏观双重测试程序暴露于pH 11和pH 7的蒸馏水中的WC-10Co-4Cr涂层(用于比较)表明,由于脱碳金属钨(W)的优先溶解,以'腐蚀沟槽'的形式存在强烈的局部腐蚀。发生在碳化物颗粒的周围。这些“腐蚀沟槽”的深度为一碳化物,导致碳化物在腐蚀沟槽中被松散。或者,对于烧结的WC-5.7Co-0.3Cr,暴露于pH 11不会显示出任何局部腐蚀的迹象。然而,暴露于pH 7蒸馏水导致粘合剂相优先溶解。首次开发了一种能够在原位进行电化学测量的改进型微磨损测试仪,以监测微观磨损腐蚀过程中的腐蚀动力学。有趣的是,最低磨损发生在pH 11条件下。有人提出,还可以通过XPS分析检测到的基于Co(OH)2的钝化膜的存在,似乎会通过改变磨料表面接触的刚度和降低磨料与表面之间的摩擦来影响粘结剂相的去除速率。转降低整体磨损率。观察到的优先去除粘结剂相导致碳化物破坏的磨损机理也证实了这一点。相反,对于烧结的WC-5.7Co-0.3Cr,尽管在相似的测试条件下没有表面钝化,但磨损率却不受pH的影响。磨料尺寸对喷涂WC-10Co-的磨损腐蚀性能的影响使用改进的ASTM G65测试对4Cr涂层进行了研究。结果表明,除磨料的尺寸外,磨损率还取决于整体磨损机理。通常,由于次表面裂纹的传播导致脱层,导致磨损率加倍,从而对涂层造成严重损坏。涂层的亚表面裂纹随着磨料尺寸的增加而增加。或者,对于烧结的WC-5.7Co-0.3Cr,碳化物晶粒的裂纹程度的增加随磨料尺寸的增加而增加。磨损的数量级增加是由于广泛的碳化物开裂和随后的碳化物晶粒的去除引起的。通过检查接触条件和磨料尺寸对WC基烧结硬质合金和喷涂层的磨损腐蚀的影响,双重方法成功地复制了井下条件下的磨损,从而更好地设计/选择了受井下环境影响的表面。

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    Thakare Mandar Rajiv;

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  • 年度 2008
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  • 正文语种 {"code":"en","name":"English","id":9}
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