首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到19条相似文献,搜索用时 171 毫秒
1.
由椴木木粉和酚醛树脂制备木材陶瓷的研究   总被引:16,自引:0,他引:16  
以椴木木粉和酚醛树脂为原料制成一种新的木材陶瓷.用TGA、XRlD和SEM技术分别对木材陶瓷的形成机理、物相构成和微观结构进行了表征与研究.详细讨论了碳化温度和酚醛树脂用量对木材陶瓷显气孔率、体积电阻率和弯曲强度的影响.结果表明,木材陶瓷是由酚醛树脂生成的玻璃态的硬碳和由木粉生成的无定形的软碳组成的多孔性碳复合材料;随碳化温度升高或酚醛树脂用量的增加,木材陶瓷的显气孔率和弯曲强度增大,体积电阻率下降;碳化温度升高可以使(002)衍射峰逐渐变窄,强度增大,并且向高角度移动,晶面间距d(002)减小,而酚醛树脂用量的增加对(002)衍射峰和晶面间距d(002)基本没有影响;当碳化温度为1350℃,酚醛树脂用量为160wt%时,木材陶瓷的显气孔率、体积电阻率和弯曲强度分别达到了50%、2.0×10-2Ω·cm和25MPa.  相似文献   

2.
20062021 木陶瓷/SiC复合的电磁波吸收特性通过烧结酚醛树脂粉、木粉和SiC粉的压密混合物制备的木陶瓷/SiC复合材料的电磁波吸收特性采用测量S-参数(综合反射系数)装置进行网络结构分析,并且同堆积密度,X-射线分析,电阻率和电子显微镜微相结构分析相结合进行了分析讨论。将30%质量分数的酚醛树脂粉和70%的木粉压密混合物进行碳化制备的木陶瓷在2GHz频率下有大的吸收峰(50db)。而SiC粉的加入在高频区9GHz含47%SiC的烧结复合材料样出现了漂移混合吸收峰。SiC的加入促进了基体木陶瓷的石墨化,增加了渗透性和堆积密度,且降低了电阻率。(CAl38:110760)  相似文献   

3.
通过配位反应,将镍离子引入酚醛树脂结构中,在惰性气氛保护下制备镍改性酚醛树脂,并将其分别在600、800、1000℃下进行碳化处理。XRD检测结果表明:600℃时热解碳出现明显的C(002)晶面衍射峰;当温度升高(800、1000℃)时,半峰宽增大,峰位左移,峰强度减小。SEM和TEM的检测结果表明,即使在1000℃下,普通酚醛树脂热解碳仍为无定形碳,而温度高于800℃后镍改性酚醛树脂热解碳中生成石墨烯,且升温和增大催化剂用量均有利于石墨烯生成。镍改性酚醛树脂炭化形成石墨烯的过程遵循"溶碳析碳机制"。  相似文献   

4.
原位反应烧结法制备SiC多孔木材陶瓷   总被引:1,自引:0,他引:1  
以香杉木粉、硅粉和环氧树脂为原料,先低温制成木材陶瓷,然后利用高温原位反应烧结工艺制成了具有原木微观结构的SiC多孔木材陶瓷。TGA研究了木粉和环氧树脂的热分解行为,用XRD和SEM研究SiC多孔木材陶瓷的物相组成和微观结构,用阿基米德法测定SiC多孔木材陶瓷的显气孔率,系统研究了烧结温度和成分配比对SiC多孔木材陶瓷的摩擦学性能的影响。结果显示:SiC多孔木材陶瓷具有类似于原始木材的微观管胞结构;显气孔率随着烧结温度的升高而降低,但随着Si含量的升高而升高;在1600℃下制备的SiC多孔木材陶瓷具有良好的摩擦学性能,后期析出的碳颗粒可以有效降低磨损量。  相似文献   

5.
以甘油为相容剂,利用木粉、马来酸酐酯化淀粉和聚乳酸(PLA)进行熔融挤出制备了木粉/酯化淀粉/聚乳酸复合材料。利用XRD和SEM对复合材料的结晶度和断面形貌进行分析表征,以研究木粉含量对复合材料界面相容性的影响;并对复合材料的热稳定性、力学性能、流变性能以及吸水率进行表征。实验结果表明,随着木粉含量的增加,复合材料的界面相容性下降,拉伸强度和弯曲强度增大,断裂伸长率下降,吸水率逐渐增大;TGA测试结果表明木粉的加入使材料的热稳定性下降;流变测试表明木粉用量的增加,使复合材料的储能模量、损耗模量和复数粘度逐渐增加。  相似文献   

6.
阚小清  丁军  余超  邓承继  祝洪喜  樊国栋  冷光辉 《材料导报》2018,32(10):1602-1605, 1627
以碳化后的梧桐木块作为碳模板,采用金属锆作为锆源,在KCl和KF的混合熔盐体系中制备了多孔ZrC/C复合陶瓷材料。研究了不同碳化温度对碳模板的显微形貌、显气孔率和体积密度的影响。并采用X射线光电子能谱(XPS)、傅里叶变换红外光谱(FTIR)、X射线衍射仪(XRD)和扫描电子显微镜(SEM)表征了梧桐木的碳化过程以及复合材料的物相组成和显微形貌。结果表明:梧桐木的碳化分为有机物的热分解和石墨化两个过程;碳化后的梧桐木保留了多孔的特征结构,随着碳化温度的升高,碳模板显气孔率变大,体积密度减小;反应时间的延长有利于增强ZrC层与碳模板基体表面的结合力;KF的加入量需要严格控制,过量的KF会破坏复合材料的结构。  相似文献   

7.
以杉木粉为原料、硼酚醛预聚体为前驱体,采用溶胶-凝胶法制备了硼酚醛/杉木粉复合材料。采用红外光谱、X射线衍射、扫描电镜、热失重等分析方法,研究了该复合材料的结构和相关性能。结果表明,木材中的羟基与硼酚醛预聚体上的羟基发生了缩合反应,形成了比较稳定的B-O-C键,木材纤维素的结晶被破坏,介观空隙消失;木粉用量的增加会导致复合材料缩合反应程度下降,木材纤维素结晶遭破坏程度降低。缩合反应生成的强化学键显著提高了复合材料的耐热性能,使失重10%时的热分解温度从270℃(木粉)提高到547℃。复合材料的吸水率远小于木材,而冲击强度、拉伸强度均呈现随木粉用量的增加先增大后降低的趋势。  相似文献   

8.
采用固体废弃物甘蔗渣为原料,与环氧树脂混合后真空烧结制备碳木材陶瓷。利用TG-DSC分析了木材陶瓷的热分解行为。利用XRD、SEM表征了木材陶瓷的相组成和微观结构,研究了碳化温度对木材陶瓷的残炭率、体积收缩率、平面尺寸收缩率、厚度收缩率和体积电阻率的影响。结果表明:甘蔗渣制备的木材陶瓷是一种多孔碳材料,随着碳化温度升高,石墨化程度提高;烧结温度每升高100℃,残炭率降低约1%~2%,体积收缩率升高0.5%~1%。平面尺寸和厚度收缩率与烧结温度正相关。体积电阻率随温度升高而降低。  相似文献   

9.
一种新型多孔SiC的制备与性能研究   总被引:1,自引:0,他引:1  
以滤纸和酚醛树脂为原料, 通过模压成型、固化、碳化和渗硅制备出微观结构均匀的多孔碳化硅. 碳化的温度固定时, 多孔碳的气孔率随酚醛树脂用量的增大而减少, 弯曲强度随着酚醛树脂用量的增大而增大. 酚醛树脂/滤纸两种成分的质量比固定时, 气孔率随着碳化温度的升高而减小, 弯曲强度随着碳化温度的升高而增大, 从SEM照片可以看出, 由滤纸纤维的杂乱排列和碳化时不同的收缩率产生了相互连通不规则的孔, 在多孔碳化硅结构中也得以保留. 多孔碳化硅的气孔率随着排硅时间的增加而增大, 强度和韧性随着排硅时间的增加而减小. 在1650℃, 并经过30min排Si, 较大孔隙中的Si就可以排掉, 此时得到的多孔SiC具有较高的强度和韧性.  相似文献   

10.
近年来,生物质碳因成本低廉、易制备、理化性能优异和具有多孔结构被广泛应用于吸波领域。然而,其吸波性能仍然受较高电导率引发的不良阻抗限制。在此,使用镍(Ni)改性木棉纤维,并使用不同的碳化温度获得镍/木棉纤维衍生碳(Ni/C)复合材料。扫描电镜结果表明,随着碳化温度的升高,Ni颗粒的尺寸增加,且木棉纤维表面出现更多的缺陷结构。XRD和XPS结果证明了Ni和木棉纤维衍生碳的成功复合。Raman结果表明碳化温度的升高导致碳组分石墨化程度增加,提高了复合材料的传导损耗能力。最后,我们将复合材料与石蜡以5∶95的超低填充比例混合,Ni/C-800展现出-52.6 dB的反射损耗值和8.32 GHz的有效吸收带宽。复合材料优异的吸波性能取决于衰减能力和阻抗匹配的协同、介电损耗和磁损耗的共同作用以及大比表面积和中空多孔结构造成的多重散射能力的增强。  相似文献   

11.
木质陶瓷的X射线衍射和喇曼光谱研究   总被引:6,自引:0,他引:6  
采用X射线衍射和激光喇曼光谱, 研究了以烟杆和酚醛树脂为原料制备木质陶瓷炭化过程中结构的变化特征. 研究结果表明, 炭化温度的升高可以使木质陶瓷XRD谱图中衍射峰增加, 强度增大, 同时木质陶瓷中石墨微晶的平均层间距d002减小, 堆积厚度L c增加, 微晶直径 L a在973K出现转折点; 木质陶瓷的喇曼光谱图为典型的类石墨炭材料的喇曼谱图, 只出现了表征无序结构的D线和表征石墨结构的G线, 且表征无序化度的二者积分强度比R值随炭化温度的升高先增后减, 而根据Tuinstra-Koenig 经验式计算得到的微晶直径L a值表现出与R值相反的规律; 两种分析方法的结果较为一致, 均表明木质陶瓷结构在973K发生根本改变, 说明喇曼光谱有望成为木质陶瓷结构的快速测试方法.  相似文献   

12.
In this paper, a new woodceramics from carbonized bamboo fiber and liquefied wood was developed and the effects of carbonization temperature on the dimension shrinkage, weight loss, density, compressive strength, and volume electrical resistivity of the woodceramics were investigated. The results show that, with the increase in the carbonization temperature, liquefied wood decompose and then combine with carbonized bamboo fiber, the dimension of sample almost keep constant, but its compressive strength was improved, and its electrical resistivity was reduced.  相似文献   

13.
Woodceramics samples derived from carbonized tobacco stems and different contents of phenolic resin, using different carbonization temperatures have been investigated by Raman spectroscopy. It was found that the full width at half maximum (FWHM) and the R-value decreased with an increase of the carbonization temperature and the content of phenolic resin. And the crystallite size La of these samples show low microcrystalline size, i.e. La varying between 1.85 and 5.40 nm. The results obtained indicate that 973 K is the turning point temperature for the preparation of woodceramics. The results of Raman spectra were confirmed by SEM results of the woodceramics.  相似文献   

14.
The effect of carbonization temperature on the electrical resistivity and physical properties of solid (ash) wood, plywood, and particleboard carbonized in a vacuum furnace under a gas flow of nitrogen (200 ml/min) between 400 and 1100 °C was investigated. The electrical resistivity, dimension shrinkage and weight loss of the carbonized specimens were extensively investigated. The electrical resistivity of specimens significantly decreased with increasing carbonization temperature. The rates of the volumetric shrinkage and weight loss of the specimens significantly increased with increasing the temperature. At the carbonization temperature of 1100 °C, the particleboard had the highest electrical conductivity property, followed by the plywood and solid wood, respectively. The electrical resistivities of wood, plywood, and particleboard carbonized at 1100 °C were less than about 1 ohm-cm, thereby making them suitable for use as an electrode in a fuel cell, battery or electrolyzer.  相似文献   

15.
Acacia andEucalyptus wood chars, prepared at various temperatures in the range 400–1200°C, have been studied by X-ray diffractometry. The objective was to investigate the changes in structural ordering in relation to carbonization temperature and time. For both theAcacia andEucalyptus wood chars, the apparent interlayer spacing (d 002) decreased slightly while the apparent microcrystallite diameter,L a, increased markedly with increasing carbonization temperature. The trend was, in general, similar with increased soaking time at carbonization temperatures of 800 and 1000°C, but these X-ray properties (i.e.d 002 andL a) were found to be more susceptible to carbonization temperature than to time. The results also showed that both the wood species, when carbonized under identical conditions, yielded chars with practically similar diffraction profiles.  相似文献   

16.
Three-dimensionally (3D) well-ordered carbon microparticle assemblies with different particle morphologies were fabricated by infiltration of phenolic resin solution into SiO2 inverse opal structures and subsequent carbonization. The effect of the phenolic resin solution concentration and the carbonization temperature on the morphology of the fabricated carbon microparticles was investigated. At a carbonization temperature of 1000 °C, carbon microparticles with interlocked bridges were obtained when the concentration of phenolic resin solution is 40 wt% and hollow carbon microparticles with opened window channels were obtained at a concentration of 30–35 wt%. When the carbonization temperature was decreased to 500 °C, carbon microparticles with interlocked bridges also were observed, even when the phenolic resin concentration was 30 wt%. The structures and properties of the carbon microparticles and their assemblies were characterized using SEM, XRD, and N2 adsorption.  相似文献   

17.
Si-B-C ceramic composites were synthesized using SiB6, B4C, and phenolic resin as a carbon source by pressureless sintering in an Ar atmosphere. Then, the Si-B-C ceramic composites were fabricated to determine their potential for applications as high hardness and high temperature composites. The X-ray diffraction patterns of sintered bodies of SiB6-B4C with carbonized phenolic resin can be seen that SiB6 and C changed to B4C and SiC. In this study, it is obtained that carbonized phenolic resin is good addition material as a reaction material comparing to carbon powder at 1683 K for 1 h by pressureless sintering in an Ar atmosphere.  相似文献   

18.
凹凸棒石-针铁矿改性麦秸木质陶瓷的微观结构   总被引:1,自引:0,他引:1       下载免费PDF全文
以凹凸棒石、针铁矿和小麦秸秆为原料,添加少量的环氧树脂作为黏结剂,在适宜的温度和气氛下煅烧,同步完成了生物质碳化、凹凸棒石热活化及针铁矿的还原,获得了具有高气孔率和强磁性的凹凸棒石-针铁矿改性麦秸木质陶瓷,利用XRD和SEM分析了原料质量比及焙烧温度对其物相及微观结构的影响。结果表明:凹凸棒石-针铁矿改性麦秸木质陶瓷是一种非晶态多孔质碳素材料,在相同温度下,原料的质量比对其物相几乎无影响;随着焙烧温度的升高,凹凸棒石的特征衍射峰逐渐消失,凹凸棒石-针铁矿改性麦秸木质陶瓷中有新的物相产生。  相似文献   

19.
以硅粉和酚醛树脂为原料, 硝酸镍为催化剂前驱体, 采用微波加热催化反应法, 在流通氩气气氛中1150℃/0.5 h反应后合成了β-SiC粉体。研究了反应温度、催化剂用量和保温时间等对合成β-SiC的影响。采用XRD、SEM和TEM对产物的物相组成及显微结构进行了表征。结果表明: 微波加热条件下, 无催化剂存在时, β-SiC的完全合成温度为1250℃; 而添加1.0wt%的Ni作催化剂时, 1150℃/0.5 h反应后即可合成纯相的β-SiC。所合成的试样中都存在着颗粒状和晶须状两种SiC, 加入催化剂后会使试样中β-SiC晶须的长径比变大。密度泛函理论(DFT)计算结果表明, Ni-Si合金纳米颗粒的形成使Si原子之间的键长拉长, 弱化了Si原子之间的结合强度, 进而促进了Si粉在低温下的碳化反应。  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号