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光敏树脂是光固化3D打印的材料基础,也是光固化3D打印陶瓷的成型媒介。光敏树脂体系影响光固化3D打印陶瓷构件成型过程的收缩率与脱脂过程的应力,本文设计了含环状结构的单官能度树脂、三官能度树脂及引入预聚物及稀释剂的多组分树脂三个树脂体系,测试了三个树脂体系的收缩率,研究表明引入预聚物及稀释剂的树脂体系具有最低的固化收缩率,有效缓解了因固化反应收缩造成的3D打印氧化铝陶瓷素坯开裂的问题。采用热失重分析和热处理实验研究了三个树脂体系的热分解行为,多组分树脂体系具有分阶段热解的特性,采用该树脂体系制备了光敏性氧化铝浆料,优化了光固化打印参数及脱脂气氛,3D打印厚壁实心(12 mm×12 mm×12 mm)样件与大尺寸(?80 mm×50 mm)的氧化铝陶瓷素坯脱脂后均无裂纹等缺陷。 相似文献
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主要研究了分散剂、pH、颗粒级配等因素对SiC水基浆料流变性能的影响,并分析了其原因。结果表明,各分散剂对SiC浆料粘度影响效果的大小顺序依次为:四甲基氢氧化铵(TMAH)>六偏磷酸钠(SHMP)>聚乙二醇(PEG)。TMAH、SHMP、PEG三种分散剂的最佳用量分别为0.8wt.%、0.6wt.%、1.0wt.%,最佳pH为13,最佳颗粒级配(F220/F1200,下同)为1.5,当固相体积分数超过50%后SiC浆料的粘度急剧增加。通过优化工艺参数,制备出了流动性较好,固相体积分数为50%、粘度为500mPa.s的SiC陶瓷浆料。 相似文献
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本文选择陶瓷含量固定,以pH值、粘结剂、分散剂这三个因素做正交实验,通过粘度测试、粒度、密度分析和扫描电镜观察,对氧化铝陶瓷膏体浆料的配制进行研究,结果表明,注射成型用氧化铝陶瓷膏体浆料,固相粉末的粒度要小于10μm,粘度要不大于1Pa·s,混合要均匀,浆料里不能存在可见的气泡和固体添加剂.采用成分为氧化铝粉末50%,聚乙二醇1%,丙三醇4%,六偏磷酸钠0.175%,卡拉胶6%,去离子水38.825%的酸性浆料,能够获得良好的挤压成型性,且得到的生坯组织均匀. 相似文献
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利用光固化技术制备的生物玻璃陶瓷骨植入物在骨修复领域具有许多优势,然而生物玻璃陶瓷受粉体粒度的影响,在光固化打印工艺、结构、力学性能和生物性能等方面存在较大的差异。本文以光固化3D打印过程中粒度的变化为切入点,制备了两种不同粒度粉体的生物玻璃陶瓷浆料,分别对生物玻璃陶瓷浆料的稳定性、流变特性和固化特性进行了表征,根据TG-DSC曲线绘制了脱脂烧结曲线并对骨支架的表面质量、结构和力学性能进行了评价,最后通过颅骨修复试验对降解性能进行了分析。结果表明:小粒度粉体的浆料稳定性较好,黏度较高,对应的固化厚度和过固化宽度也较小;小粒度粉体制备的骨支架表面质量、结构致密化程度和弯曲强度均优于大粒度粉体制备的骨支架,但降解速率较低,植入体内2个月后有新骨长入骨支架孔隙。本研究对不同粒度粉体的生物玻璃陶瓷骨支架制备具有指导意义,有助于推动基于粒度分布的梯度可控降解骨支架的开发和应用。 相似文献
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模版晶粒生长技术制备织构化铌酸钾钠无铅压电陶瓷是提高其压电性能的重要途径,为了获得较高的织构度,水系流延浆料的制备是关键技术.本研究以固相法合成的铌酸钾钠粉体和片状Nb2O5模板晶粒为固含量,以去离子水为溶剂,研究不同含量的分散剂、粘结剂和增塑剂对流延浆料性能的影响.研究结果表明,当粉体固含量为55wt%,分散剂PVP含量为5.5wt%,粘结剂苯丙乳液含量13.5wt%,增塑剂丙三醇含量为5.5wt%时,制备的流延浆料粘度适中,流延后可制得表面光滑、质地均匀、塑性较好、可任意卷曲的流延膜片. 相似文献
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苯乙烯是重要的石油化工原料。本文介绍了国内外苯乙烯生产的发展概况,合成乙苯,苯乙烯所用的催化剂种类,并就苯乙烯生产及催化剂的发展趋势提出了自己的观点。 相似文献
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Synthesis and characterization of homopolymers and copolymers of various acrylates and acrylonitrile
Various homopolymers and copolymers of methyl acrylate, ethyl acrylate, butyl acrylate, and acrylonitrile in different feed ratios were synthesized. These were characterized by IR, 13C-NMR, DSC, DTA, and TGA. Spectroscopic characterization helped in differentiating copolymers of different mol ratios. Thermal analysis revealed different degradation patterns for homopolymers and copolymers. The temperature and energy changes associated with various phase transitions were dependent on the chemical composition of homo- and copolymers, as expected. © 1993 John Wiley & Sons, Inc. 相似文献
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The variation of the Au 4f binding energy of Au clusters with the cluster size has been established by measuring the binding energies of clusters whose size distributions were independently determined by HREM and STM. The binding energy increases significantly when the cluster size is less than 2 nm. Au-Cu bimetallic clusters of the composition Cu3Au have been deposited for the first time on carbon substrates. The shifts in the core level binding energies of the bimetallic clusters show the effect of alloying in the case of large clusters, but show effects of both alloying and cluster size in the case of the small clusters. The interaction of CO with Cu3Au clusters is stronger than with a bulk Cu metal. The interaction of CO with small Cu clusters also seems to be stronger than with bulk Cu or with large Cu clusters. 相似文献
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《国际聚合物材料杂志》2012,61(1-4):113-122
Abstract Kinetics and mechanisms of oxidation of 6 acetals by molecular oxygen and ozone in liquid phase have been studied. Reaction with molecular oxygen (70°C, 15–16 hr) leads to the formation monoethers of the corresponding glycols with 68–90% selectivity. Salts of metals and complexes with crown-ethers have increased the reaction rate significally. Ozone have reacted with acetals with formation similar products. The mechanisms of intermediate stages have been proposed. 相似文献
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G. R. Hamed 《The Journal of Adhesion》1983,16(1):31-39
A substantially greater detachment energy is required to strip a polyethylene tereph-thalate (Mylar) film from a styrene-butadiene-styrene (SBS) triblock copolymer compared to that for peeling from a random styrene-butadiene (SBR) copolymer. This is true even though the intrinsic interaction between the Mylar and each elastomer is expected to be similar because of their virtually identical chemical composition. It is proposed that this difference in peel strength (between the SBS and SBR) is a consequence of the much higher dissipative capacity of the former elastomer. Another manifestation of this is the higher cohesive tear strength of the SBS compared to the SBR. Extents of energy dissipation within each elastomer during detachment of the Mylar adherend are consistent with the hypothesis that the average maximum stress experience before detachment is some similar fraction of each elastomer's tensile strength. 相似文献
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Polypentafluorostyrene (PPFS), polymethylacrylate (PMA), and poly(pentafluorostyrene-co-methylacrylate), poly(PFS-co-MA) were prepared and the wetting characteristics of polymer blends of PPFS and PMA were compared with that of poly(PFS-co-MA) via contact angle measurements. The critical surface tension of polypentafluorostyrene was found to be 22.6 dyne/cm, which is comparable to the value reported for polytrifluoroethylene (22 dyne/cm). The critical surface tension of poly(PFS-co-MA) is not linearly related to its composition. The polymer blends of PPFS and PMA exhibit significant surface enrichment of the fluoropolymer. The harmonic-mean method1 was employed to determine surface tensions of these polymers and many known polymers. It is found that the method produces useful surface tension data provided the contact angle values are derived from testing liquids of dissimilar polarity. 相似文献
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