首页> 外文OA文献 >Obtaining triple layer polycrystalline diamond compact by HPHT method
【2h】

Obtaining triple layer polycrystalline diamond compact by HPHT method

机译:HPHT法制备三层多晶金刚石复合片

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The primary objective of this thesis was to obtain a triple layer polycrystalline diamond compact (PDC) containing a polycrystalline diamond as top layer, a WC 10 wt% Co substrate, and a WC 20 wt% Nb/Ni interface to bond these two layers via high pressure high temperature (HPHT) sintering. To achieve this objective, the project has been done in three different stages. The first stage was producing diamond sintered body with a suitable binder, and finding the best sintering parameters. The second stage of project was done to study the WC 10 wt% Co hardmetal substrate at different sintering conditions, and the third and last stage was done according to the results achieved from previous stages to obtain a triple layer PDC. At the first stage, four different binders were used to sinter diamond under HPHT condition. Binders were Nb/Fe, Nb/Co, Nb/Ni and pure Nb and 10 wt% binder was used. Sintering was carried out at different temperature and under different pressure and holding time. Obtained samples were studies according to relative density, microstructure, and hardness to find the optimum binder and sintering parameters. Studies at this stage showed that Nb is the best binder and T=1750 °C, 7.7 GPa with holding time more than 6 minutes are the best sintering parameters. At the second stage a powder mixture of WC 10 wt% Co was sintered via HPHT at 1500, 1600, 1700, 1800, and 1900°C under 7.7 GPa pressure for 2 and 3 minutes. Microstructural/structural analyses were performed by SEM/EDS and XRD and hardness, Indentation Fracture Toughness (ITF) and compression tests were also carried out to understand effects of different sintering parameters. At this stage, it was found that full density can achieved for high sintering temperature along with abnormal grain growth. High hardness was observed in range starting from 1250 up to 1650 HV. At the third stage, to obtain PDC, a thin layer of WC 20 wt% Nb/Ni was used as an interface between top layer of diamond with pure Nb binder and WC 10 wt% Co substrate. Sintering was done via HPHT method at 1750°C under 7.7 GPa of pressure. Two different holding time of 6 (three successive 2 minutes) and 9 (three successive 3 minutes) were used. Hardness was measured and microstructural/structural studies were done via SEM/EDS. The overall results showed that this new kind of PDC can successfully produce using a new pure Niobium binder for diamond without any graphitization. It was also found that using an interface having the resemblance to both substrate and sintered diamond body caused good adhesion between layers that can results in enhanced performance and improving durability of PDC.
机译:本论文的主要目的是获得一种三层多晶金刚石复合片(PDC),其中包含多晶金刚石作为顶层,WC 10 wt%的Co基体和WC 20 wt%的Nb / Ni界面以通过高压高温(HPHT)烧结。为了实现这一目标,该项目分三个不同阶段完成。第一阶段是生产具有合适粘合剂的金刚石烧结体,并找到最佳的烧结参数。完成了项目的第二阶段,以研究不同烧结条件下的WC 10 wt%Co硬质合金基材,第三阶段和最后阶段是根据前一阶段获得的结果进行的,以获得了三层PDC。在第一阶段,使用四种不同的粘结剂在HPHT条件下烧结金刚石。粘合剂为Nb / Fe,Nb / Co,Nb / Ni和纯Nb,并使用10 wt%的粘合剂。烧结是在不同温度,不同压力和保持时间下进行的。根据相对密度,微观结构和硬度研究获得的样品,以找到最佳的粘合剂和烧结参数。在这一阶段的研究表明,Nb是最佳的粘合剂,T = 1750°C,7.7 GPa的保持时间超过6分钟是最佳的烧结参数。在第二阶段,通过HPHT在7.7GPa压力下在1500、1600、1700、1800和1900℃下将WC 10wt%Co的粉末混合物烧结2分钟和3分钟。通过SEM / EDS和XRD进行显微组织/结构分析,并进行硬度,压痕断裂韧性(ITF)和压缩试验,以了解不同烧结参数的影响。在此阶段,发现在高烧结温度下伴随异常晶粒生长可以达到全密度。在从1250 HV至1650 HV的范围内观察到高硬度。在第三阶段,为了获得PDC,将一层含20%(重量)Nb / Ni的WC薄层用作具有纯Nb粘结剂的金刚石顶层和WC(10%)的Co基体之间的界面。通过HPHT方法在1750℃和7.7GPa的压力下进行烧结。使用了两种不同的保持时间:6(连续3分钟2分钟)和9(连续3分钟3分钟)。测量硬度,并通过SEM / EDS进行微观结构/结构研究。总体结果表明,这种新型的PDC可以使用新型的纯铌金刚石粘合剂成功地生产,而无需进行任何石墨化处理。还发现使用与基材和烧结金刚石体都相似的界面可引起层之间的良好粘合,这可导致增强的性能并改善PDC的耐久性。

著录项

  • 作者

    Mashhadikarimi Meysam;

  • 作者单位
  • 年度 2017
  • 总页数
  • 原文格式 PDF
  • 正文语种 por
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号