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原位复TiN/O‘—sialon在空气中的氧化行为 总被引:4,自引:1,他引:3
通过对不同气孔率和TiN含量的原位复合TiN/O’-sialon材料在空气中的氧化行为研究,得出了不同材料的不同温度下的氧化结果,提出了不同材料在不同温度下的氧化机理和模。 相似文献
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《超硬材料工程》2014,(5):4-4
硬质涂层材料中,工艺最成熟、应用最广泛的是TiN。目前,工业发达国家TiN涂层高速钢刀具的使用率已占高速钢刀具的50%~70%,有的不可重磨的复杂刀具的使用率已超过90%。由于现代金属切削对刀具有很高的技术要求,TiN涂层日益不能适应。TiN涂层的耐氧化性较差,使用温度达500℃时,膜层明显氧化而被烧蚀,而且它的硬度也满足不了需要。TiC有较高的显微硬度,因而该材料的耐磨性能较好。同时它与基体的附着牢固,在制备多层耐磨涂层时,常将TiC作为与基体接触的底层膜,在涂层刀具中它是十分常用的涂层材料。TiCN和TiAlN的开发,又使涂层刀具的性能上了一个台阶。TiCN可降低涂层的内应力, 相似文献
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碳热还原氮化合成TiN的研究 总被引:2,自引:1,他引:1
以锐钛矿(中位径0.38μm)、金红石(中位径4.58μm)和鳞片石墨(粒度<0.15mm)、炭黑(平均粒度0.02μm)、可膨胀石墨(粒度<0.15mm)为原料,固定配比nC∶nTiO2为5∶1时分别组成不同的原料组合,并以锐钛矿和鳞片石墨为原料,改变配比nC∶nTiO2分别为3∶1、4∶1、5∶1、6∶1、7∶1和8∶1进行配料,在管式电炉、流动N2中分别于1300℃和1400℃制备了TiN,并进行了合成产物的氧化脱碳试验;采用XRD测定TiN的特征峰(d200=0.212nm)强度,以表征TiN的合成率,研究了原料粒度、反应物活性、反应温度等因素对TiN合成率的影响。结果表明:选用粒度较细或晶格活性大的原料,提高反应温度,均有利于提高TiN粉末的合成率;合成TiN粉末的最佳原料组合是可膨胀石墨和锐钛矿;以鳞片石墨和锐钛矿为原料时,其配比为nC∶nTiO2=6∶1时TiN合成率最高;合成产物中均含有一定量的碳,采用普通的加热氧化法不能除碳,其原因是TiN的氧化温度低于石墨的。 相似文献
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氮化硅-氮化钛陶瓷的氧化行为是建立在对其微观结构的观察,对这种氧化模型现象进行了描述,并对其氧化动力学模型进行研究。当温度<1 000℃,只有TiN相被氧化。此氧化过程是由氧气通过TiO2扩散来控制的,由氧化动力学抛物线方程来描述。超过1 000℃的过程是非常复杂的,那是因为同时发生Si3N4和TiN相的两种氧化反应。三种氧化模型都被清晰的扩散机理所控制,是接连发生的。第1步,Si3N4和TiN相被独立的氧化,它们分别被氧化为SiO2和TiO2相。Si3N4的氧化是由氧通过SiO2扩散控制的,而TiN的氧化由钛通过TiO2扩散所控制。第2步,TiN的氧化被氧通过TiO2扩散控制,而通过SiO2被氧化形成Si3N4。第3步,TiN和Si3N4的氧化由氧通过二氧化硅层扩散控制。动力学方程可以由这三种氧化模型的任意一种决定。 相似文献
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通过对不同Si3N4含量、不同温度下Si3N4-SiC材料的氧化实验,分析氧化后的氧化增重率,得出Si3N4含量越高,材料氧化越严重;氧化温度越高,材料氧化越严重;且氧化增重率与氧化时间呈直线-抛物线规律。 相似文献
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ONACCURACYOFANALYSISOFOFHYDROGEN1前言我公司目前应用的氢气纯度分析方法有两种,一种是爆炸反应法,另一种是焦性没食子酸吸收法。几年来,人们对两种分析方法的准确性曾有过褒贬不一的评论。这里我们也谈谈自己粗浅的观点。2爆炸法测定氢气纯度一定量的氢气样品与适量的空气之均匀混合物因反应后生成液体水而引起气体体积减少,减少的体积等于参加反应气体体积之和。其中l/3为氧气,2/3为氢气。根据氢气取样量和反应前后混气体体积之差,以及氢气在反应中的体积比例关系,可计算出样品的氢气纯度。计算公式式中:A一混… 相似文献
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P. P. Budnikoff 《Journal of the American Ceramic Society》1924,7(11):817-820
The different analytical methods proposed for the evaluation of gypsum have been subjected to an experimental test. A combination method, consisting of a fusion with KHCO3 and determination of CaO by KMnO4 titration, the SO3 by Andrews method of titration of BaCrO4 has been found to give very reliable results with the least consumption of time. 相似文献
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A model is developed for the sedimentation from a suspension of two particle species of unequal densities and of different sizes. The composition and the thickness of various layers in the sediments are predicted using graphical and analytical methods. The model predictions were in excellent agreement with experimental results, when the particle size ratio was ≥ 108. When size ratio of the particles was 2.60 and 4.31 the agreement occurred in about 50 percent of the cases. 相似文献
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A novel technique serves to monitor instantaneous rates of loss of a volatile solute from a suspended drop during drying. A highly sensitive electron capture detector is used to monitor concentrations of SF6 released into a flowing gas stream from a suspended, drying drop. Simultaneously, the appearance and morphological development of the drop are monitored with a video camera. This provides the wherewithal of relating instantaneous rates of loss of the volatile solute to particular events during the development of particle morphology.
Initial experiments have been carried out with drops of aqueous solutions of glucose, sucrose, maltodextrin and coffee extract. The results clearly display the onset of the volatiles-retentive selective diffusion phenomenon. There is also substantial loss of the volatile component later in the drying process, when the drops undergo repeated ex ansion, bursting and cratering due to the formation of internaf bubbles. These experiments appear to be the first quantitative demonstration of major losses accompanying changes in drop morphology. 相似文献
Initial experiments have been carried out with drops of aqueous solutions of glucose, sucrose, maltodextrin and coffee extract. The results clearly display the onset of the volatiles-retentive selective diffusion phenomenon. There is also substantial loss of the volatile component later in the drying process, when the drops undergo repeated ex ansion, bursting and cratering due to the formation of internaf bubbles. These experiments appear to be the first quantitative demonstration of major losses accompanying changes in drop morphology. 相似文献
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ANALYSIS OF RECENT MEASUREMENTS OF THE VISCOSITY OF GLASSES 总被引:5,自引:0,他引:5
Viscosity of Simple Soda-Silicate 500° to 1400°C Comparison of the results given by English with those of Washburn, Shelton and Libman, indicates a discrepancy in the absolute values of log10 viscosity amounting to 0.6, those of Washburn et al., being relatively too high. If correction for this is made, the isothermal curves of log10 viscosity as a function of soda content are smooth up to 50% Na2O, showing no inflection. The observations as a function of temperature T are all represented within accidental error by an equation of the type where all three constants vary regularly with the composition. Change of Viscosity of Glass (6SiO2, 2Na2O) due to Molecular Substitution of CaO, MgO and Al2O3 for Na2O The effect is clearly brought out by plotting (from the results of English) the change of log10η due to the substitution as a function of temperature. The curves each show a sharp bend at a temperature between 840° and 1050°C, which is designated the aggregation temperature Ta. If we divide these curves by the corresponding percentage substituted, we get curves for each oxide which are straight and parallel below the aggregation temperatures, the slopes (increase of change of log10η per 100°C) being −0.056 (CaO), −0.055 (MgO), −0.018 (A12O3) per per cent oxide substituted. For substitution of 1/2 molecule the slopes are −0.325 (CaO), −0.23 (MgO) and −0.18 (Al2O3) per 100°. At the aggregation temperature the change of log10η per per cent is a minimum, 0.03 to 0.06 for CaO, 0.12 for MgO, 0.07 for Al2O3. Evidence of Aggregation in Glasses, from viscosity Measurements The sharp bends in the plots of change of log10η due to substitution of an oxide for Na2O, suggest the beginning of molecular aggregation at these temperatures. These aggregation temperatures are close to the devitrification temperatures, but the effect on the viscosity curves cannot be due to actual devitrification since it does not change with time. Taking the aggregation temperatures as equal to devitrification temperatures, additional isotherms are roughly sketched into the equilibrium triangle of the system Na2O-CaO-SiO2. Change of Viscosity of Glass (4SiO2, 2Na2O) due to of Substitution of B2O3 for SiO2 The change of log10η (from the results of English) is plotted as a function of temperature, and also the change of log10η per per cent B2O3. The curves are more complex than for the substitution for Na2O. 相似文献
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面对日益激烈的市场竞争,摩托车油箱外观质量越来越成为影响销售的因素之一。文章介绍了改进工艺后的油箱涂装,该涂装体系提高了油箱外观的丰满度,降低了油箱涂装的生产成本。 相似文献