Enhancement of glass-ceramic performance by TiO2 doping: In vitro cell viability,proliferation, and differentiation

A new TiO₂-containing bioactive glass and glass-ceramics based on 50SiO₂-(45-X)CaO-(XTiO₂)-5P₂O₅ system was designed using a sol–gel technique (where X = 5, 7.5 and 10 wt %). The roles of the crystallization behavior and physicochemical characteristics of the designed glass and glass-ceramics which were played in the introduction of TiO₂ substitutions were investigated. Moreover, cell proliferation and differentiation were evaluated against human osteosarcoma cells (Saos-2). The TiO₂/CaO replacements led to the formation of a stronger glass structure and thus increased thermal parameters and the chemical stabilization of the designed materials. The FTIR data confirmed the existence of Ti within the glass and glass-ceramics samples, and no remarkable effect on their chemical integrity was observed. The XRD patterns indicated that calcium-containing minerals, including Ca₂SiO₄,Ca₃(PO₄)₂, Ca(Ti,Si)O₅, CaTiSiO₅, and Ca₁₅(PO₄)₂·(SiO₄)₆ phases were developed as a role of structure/texture under the applied heat-treatment. The results of the cytotoxicity test proved that a safe sample dose is 12–50 μg/ml, at which cell viability is ≥ 85%. The cell differentiation determined by ALP test proved the superiority of glass-ceramics compared with their native glasses. Therefore, the obtained materials could be safely used as novel biocompatible materials for the regeneration of bone tissue.     

The dielectric,thermal properties and crystallization mechanism of Li–Al – B–Si – O glass – Ceramic systems as a new ULTCC material

Li–Al–B–Si–O (LABS) glass-ceramics with a sintering temperature of 600 °C were studied for ultra-low temperature co-fired ceramics (ULTCC) applications. The crystal phase of LABS glass-ceramics is dendritic β-spodumene. The permittivity and dielectric loss of LABS glass-ceramics are ε_r = 5.8 and tgδ = 1.3 × 10⁻³ at 10 MHz, respectively. The coefficient of thermal expansion (CTE) of LABS glass-ceramics is 3.23 ppm/°C, which is close to that of silicon. The dielectric and thermal properties of LABS glass-ceramics are closely correlated to the degree of its crystallization. The permittivity decreases continually while the dielectric loss decreases first and slightly increases with the increasing of crystallization of β-spodumene. The CTE of LABS glass-ceramics decreases as β-spodumene crystallized from LABS glass. The crystallization kinetic and mechanism of LABS glass-ceramics indicate that the β-spodumene crystallizes in a two-dimensional interfacial growth mechanism due to the migration of Li-ions. The diffusion coefficients derived from energy-dispersive X-ray spectroscopy (EDS) results indicated that both Al and Ag electrodes have good compatibilities with ULTCC tapes, which could reduce the cost of multilayer electro-ceramic devices dramatically by using the ULTCC and base metallization.     

Preliminary<Emphasis Type="Italic">in vitro</Emphasis> and<Emphasis Type="Italic">in vivo</Emphasis> characterizations of a sol-gel derived bioactive glass-ceramic system

This study investigates quantitatively and qualitatively the sol-gel derived bioactive glass-ceramic system (BGS)—apatite-wollastonite (AW) type granules in the size range of 0.5–1 mm, as an effective graft material for bone augmentation and restoration. Scanning electron micrographs (SEM) of the sintered granules revealed the rough material surface with micropores in the range 10–30 μm. X-ray diffraction (XRD) pattern of the granules revealed the presence of crystalline phases of the hydroxyapatite and wollastonite, and the functional groups of the silicate and phosphates were identified by Fourier transform infrared spectroscopy (FT-IR). Thein vitro cell culture studies with L929 mouse fibroblast cell line showed very few cells adhered on the BGS disc after 24 h. This could be due to the highly reactive surface of the disc concomitant with the crystallization but not due to the cytotoxicity of the material, since the cellular viability (MTT assay) with the material was 80‰ Cytotoxicity and cytocompatibility studies proved that the material was non-toxic and biocompatible. After 12 weeks of implantation of the BGS granules in the tibia bone of New Zealand white rabbits, the granules were found to be well osteointegrated, as observed in the radiographs. Angiogram with barium sulphate and Indian ink after 12 weeks showed the presence of microcapillaries in the vicinity of the implant site implicating high vascularity. Gross observation of the implant site did not show any inflammation or necrosis. SEM of the implanted site after 24 weeks revealed good osteointegration of the material with the newly formed bone and host bone. New bone was also observed within the material, which was degrading. Histological evaluation of the bone healing with the BGS granules in the tibial defect at all time intervals was without inflammation or fibrous tissue encapsulation. After 2 weeks the new bone was observed as a trabeculae network around the granules, and by 6 weeks the defect was completely closed with immature woven bone. By 12 weeks mature woven bone was observed, and new immature woven bone was seen within the cracks of the granules. After 24 weeks the defect was completely healed with lamellar bone and the size of the granules decreased. Histomorphometrically the area percentage of new bone formed was 67.77% after 12 weeks and 63.37% after 24 weeks. Less bone formation after 24 weeks was due to an increased implant surface area contributed by the material degradation and active bone remodeling. The osteostimulative and osteoconductive potential of the BGS granules was established by tetracycline labelling of the mineralizing areas by 2 and 6 weeks. This sol-gel derived BGS granules proved to be bioactive and resorbable which in turn encouraged active bone formation.     

一种可切削玻璃陶瓷的压痕断裂特性

将断裂韧性测试的压痕方法与压痕弯曲方法相结合，独立地分离出了压痕残余应力因子ｘ，使其成为可测参量，并建立了压痕一压痕弯曲的断裂韧性测试方法．将这种方法应用于一种可切削玻璃陶瓷的测试，获得的Ｋ１ｃ值为Ｋ１ｃ＝２．０３ＭＰａ·ｍ１／２，与单边切口法（ＳＥＮＢ）获得的Ｋ１ｃ值有较好的一致性．测得的残余应力因子Ｘ＝０．０９３，符合Ａｎｓｔｉｓ经验公式的预测．     

纳米晶镁铝尖晶石透明微晶玻璃的晶化行为研究

利用DTA、XRD和TEM研究了制备工艺对微晶玻璃晶化行为的影响，并制备出具有纳米镁铝尖晶石为晶相的微晶玻璃。     

泡沫微晶玻璃的研究进展

概述了泡沫微晶玻璃的性能及应用,综述了泡沫微晶玻璃的研究进展,并对泡沫微晶玻璃的发展方向进行了展望。     

尾矿和Na_2O对包钢稀选尾矿微晶玻璃的影响

利用熔融浇注法对包钢稀选尾矿微晶玻璃在生产过程中的流动性进行了研究,利用DSC,XRD,SEM等手段研究了尾矿和Na2O含量对微晶玻璃的析晶特性及其他物理性能的影响.结果表明,当其它成分不变时,随着尾矿含量的增加,流动性增强;当其它成分不变时,随着Na2O含量的增加,流动性增强;在本实验条件下,尾矿加入量较佳范围为40%~50%;Na2O较佳范围为3%~6%.     

AP40生物活性玻璃陶瓷HVOF喷涂层的结构和性能

采用高速火焰(HVOF)喷涂技术,在Ti6Al4v基体上制备了AP40玻璃陶瓷涂层.利用光学显微镜、SEM和XRD对喷涂层形貌、显微组织结构和相组成进行了研究.探讨了热处理工艺对涂层组织结构及其性能的影响.按德国DIN EN 582—1994标准进行涂层的拉伸强度试验.结果表明:HVOF喷涂AP40玻璃陶瓷涂层具有层状结构,含有少量孔隙和未熔化的颗粒;涂层主要由羟基磷灰石、氟磷灰石、硅灰石、方石英及部分玻璃相组成,喷涂工艺对涂层的孔隙率有较大的影响;合适的热处理工艺可提高涂层的结晶度,使涂层变得致密,使孔隙明显减少,使涂层结合强度得到明显提高.     

利用正交实验方法探讨微晶玻璃的耐腐蚀性

采用正交实验方法对CaO-Al2O3-SiO2系微晶玻璃的热处理工艺进行探讨,通过分析各热处理工艺参数对微晶玻璃烧结耐酸性和耐碱性的影响,找出其最佳热处理工艺参数,并采用XRD和SEM对热处理后的微晶玻璃的物相和形貌进行分析.结果表明：热处理工艺参数对微晶玻璃的耐腐蚀性能影响明显.     

Valorization of Al slag in the production of green ceramic tiles: Effect of experimental conditions on microstructure and crystalline phase composition

This work reports the results of an investigation aimed at the development of sintered glass-ceramic tiles by the sinter-crystallization of mixtures composed of aluminum slag and reclaimed packaging glass. The thermal behaviors of mixtures incorporating 50 and 60 wt% Al slag were established by differential thermal analysis (DTA). Green compacts were sintered in a temperature range of 800°C-1050°C and then soaked for 10-60 minutes. The mineralogical characterizations of the sintered materials were obtained by X-ray diffraction (XRD). The achieved results indicated that the sintering of aluminum slag and packaging glass reclaimed led to a glass-ceramic material composed mainly of needle-like crystals of wollastonite (CaSiO₃). The bloating of samples during firing was evaluated according to a Cougny predictive diagram. After initial observations and according to bending strength characterizations, sintered tiles prepared from aluminum slag and glassy sand are appropriate for floor pavement and wall covering.