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PBT/PET共混切片结晶性质的研究 总被引:1,自引:0,他引:1
本研究采用JJY-Ⅰ型光学检偏振仪测试不同配比PBT/PET共混切片的等温结晶性质,用电子计算机处理数据,获得了PBT/PET共混切片的等温结晶动力学参数。并采用准等温处理方法,将等温结晶动力学参数用于非等温过程中,得到不同配比PBT/PET共混切片一系列结晶动力学特性参数。从其中的动力学结晶能力G,可判断在同一稳态纺丝条件下,不同配比PBT/PET卷绕丝的相对结晶度大小;采用PEDSC-Ⅱ型测试了不同共混配比的PBT/PET切片的非等温结晶性质,其结果和用JJY-Ⅰ型测试结果一致;本研究还探讨了添加剂(成核剂)对PBT/PET共混切片结晶性质的影响。 相似文献
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<正>尼龙66为一种结晶型聚合物,在实际生产过程中,如熔融纺丝、挤出、模压、吹塑等,常常是在动态、非等温条件下完成的,所以其结晶过程为一非等温结晶过程。为了选择合适的加工工艺条件,定量地研究非等温结晶动力学日益受到重视。非等温结晶过程要综合考虑温度(T)与结晶时间(t)的关系,其 相似文献
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用差示扫描量热法(DSC)和X-射线衍射法研究了染色剂对锦纶-6(PA-6)热性能和品态结构的影响。其结果表明,可溶性染料影响染色PA-6的熔点,促进PA-6品态结构中γ晶态的成长。染色PA-6拉伸丝,总结晶指数不变,(γ+h)晶态中h部分转变为α晶态。松弛热处理能使染色PA-6丝中无定型结构直接转变为α晶态结构,h晶态全部转化为α晶态,因此热处理的PA-6丝α晶态和总结晶指数明显增加。 相似文献
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通过熔融共混法制备了尼龙11/碳化硅(PA11/SiC)复合材料,利用差示扫描量热仪(DSC)研究了该复合材料的非等温结晶过程,且采用Avrami方程修正的Jeziorny法和Mo法对其非等温结晶动力学进行了研究,并计算得到相关非等温结晶动力学参数。结果表明:Jeziorny法和Mo法都适用于处理PA11及PA11/SiC复合材料的非等温结晶过程,其分析结果均显示,SiC的加入影响了PA11复合材料的非等温结晶行为,少量(1%)SiC的加入促进了PA11复合材料的成核及晶体生长,提高了结晶速率;由Jeziorny法可知,PA11及其复合材料的非等温过程可分为初期结晶和二次结晶两个阶段,在二次结晶阶段,结晶方式为一维线性、二维盘状和三维球晶生长并存。 相似文献
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采用单热电偶在线观察系统(SHTT)、图像分析程序等研究等温过程中温度和连续冷却过程中冷却速率对于人工配制灰渣结晶行为的影响,通过计算结晶动力学参数分析其析晶机理,并采用Fact Sage软件预测晶体类型。实验结果表明,等温过程中,温度降低,结晶所需时间先减小后增大,晶体尺寸减小,结晶比例先增大再稳定最后减小,不同温度区间生成晶体类型不同,导致结晶比例在某些温度出现较大的变化。连续冷却过程中,冷却速率增大,初始结晶温度降低,晶体由块状向颗粒状转变,结晶比例先稳定后减小,由于析出的晶体类型不同,结晶比例出现多个稳定区间,达到临界冷却速率后熔渣全部凝固为玻璃态,无晶体析出。由DSC得到的熔渣结晶放热曲线与SHTT得到的结果吻合较好。 相似文献
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采用单热电偶在线观察系统(SHTT)、图像分析程序等研究等温过程中温度和连续冷却过程中冷却速率对于人工配制灰渣结晶行为的影响,通过计算结晶动力学参数分析其析晶机理,并采用FactSage软件预测晶体类型。实验结果表明,等温过程中,温度降低,结晶所需时间先减小后增大,晶体尺寸减小,结晶比例先增大再稳定最后减小,不同温度区间生成晶体类型不同,导致结晶比例在某些温度出现较大的变化。连续冷却过程中,冷却速率增大,初始结晶温度降低,晶体由块状向颗粒状转变,结晶比例先稳定后减小,由于析出的晶体类型不同,结晶比例出现多个稳定区间,达到临界冷却速率后熔渣全部凝固为玻璃态,无晶体析出。由DSC得到的熔渣结晶放热曲线与SHTT得到的结果吻合较好。 相似文献
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硅灰石填充尼龙-6复合体系的非等温结晶行为及动力学研究 总被引:1,自引:0,他引:1
用差示扫描量热法(DSC)考察了硅灰石填充尼龙-6复合体系的非等温结晶行为,并用Avrami以及Mo法研究了其非等温结晶动力学。结果表明,随着降温速率的增加,复合体系的结晶峰变宽并向低温方向移动,结晶速率增加。通过对比,Mo法能很好地描述硅灰石填充尼龙-6复合体系的非等温过程。 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