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The statistical aspects of thermal shock damage were addressed by examining the strength distributions of quenched specimens. It was observed that slow crack growth effects were minor, and that severe damage commenced near K Ic . The increased range of retained strengths observed after thermal shock occurs because the low-strength portion of the distribution experiences the initial thermal shock damage. Crack arrest in the damaged specimens, examined by an energy balance, indicated that a large number of surface flaws actively extend during the initial stages of thermal shock damage. 相似文献
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以C和Sb2O3组合作为发泡剂,通过粉末烧结发泡工艺制备了硼硅酸盐泡沫玻璃,采用SEM观察了试样的微观结构形貌,并研究了试样的耐酸腐蚀性能.结果表明:当发泡剂C的质量分数为0.9%、Sb2O3的质量分数为8.1%时,在1200 ℃、保温30 min条件下,可以制备出平均孔径为0.2~1.0 mm、气孔分布较均匀的硼硅酸盐泡沫玻璃.试样中气孔结构主要与气泡内的气体压力、玻璃的表面张力和粘度有关.将试样浸泡在0.1 mol/L的稀硫酸中做耐酸腐蚀性实验,60 d内试样的质量先有微量增加后保持不变,这主要是由于稀硫酸进入试样的气孔结构中后形成了一层保护膜,从而阻碍了进一步的侵蚀. 相似文献
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无机抗菌硼酸盐玻璃材料的研究 总被引:5,自引:0,他引:5
采用高温熔融法,在硼酸盐玻璃的配合料中引入抗菌剂磷酸银,一次烧制而成制得抗菌玻璃材料,并对硼酸盐玻璃的抗菌性能和缓释性能进行了分析。结果表明:制备抗菌硼酸盐玻璃时,合适的银含量为1.5%-2.0%,处理温度在1100~1400℃即获得良好的抗菌效果和缓释性。 相似文献
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Pranesh Sengupta Krishna K. Dey Rumu Halder Thalasseril G. Ajithkumar Geogy Abraham Raman K. Mishra Chetan P. Kaushik Goutam K. Dey 《Journal of the American Ceramic Society》2015,98(1):88-96
Understanding the role of V2O5 within borosilicate glass matrices is important for the development of novel matrices toward immobilization of sulfate containing high‐level nuclear wastes. Present investigation shows, within sodium barium borosilicate glass matrix V2O5 can be homogeneously added up to 5 mol% and beyond which it separates out into three phases, for example, (i) silica (ii) Barium (Ba) – Vanadium (V) oxide, and (iii) glass matrix. 29Si MAS NMR (Nuclear Magnetic Resonance) studies of the samples show that below 5 mol% V2O5 addition, silicate network is dominantly constituted of Q2 and Q3 structural units, whereas above this, the network gets more polymerized through formation of Q3 and Q4 units. In case of borate network, 11B MAS NMR investigations revealed that the concentration of BO4 [(0B, 4Si)] unit increases gradually up to 5 mol% and then it decreases at the cost of BO4 [(1B, 3Si)], BO3 (symmetric) and BO3 (asymmetric) units. Micro‐Raman analyses of the samples showed that with additions of V2O5 in diluted concentrations, amorphous silicate network remained unaltered, whereas some amplification in signals corresponding to ring‐type metaborate and VO5 units exists. It is therefore apparent from both MAS‐NMR and micro‐Raman studies that with V2O5 additions within the solubility limit (≤5 mol%), borate network gets depolymerized leading to decrease in hardness from an average value of 5.0–4.2 GPa. 相似文献
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研究了硼硅酸盐玻璃主要成分(SiO2、Na2O、B2O3)对硫酸钡(BaSO4)热稳定性的影响,分析BaSO4分别与SiO2、Na2O、B2O3的混合物在不同温度(800~1 200℃)煅烧后的物相组成、显微结构、硫含量和拉曼光谱。结果表明:当BaSO4:SiO2摩尔比为7.5:92.5 (样品A)时,在温度低于1 200℃煅烧后其物相均为BaSO4和SiO2,温度达到1 200℃时出现了少量硅钡石(BaSi2O5)相;当BaSO4:SiO2:Na2O为7:86:7 (样品B)时,在800℃煅烧后即出现了少量BaSi2O5相,当温度... 相似文献
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以硼硅酸盐玻璃为原料 ,采用水热热压 (HHP)工艺制备了具有高电导性的含水玻璃 ,制得玻璃的电导率在 2 5℃时达 1.7× 10 -4 S.cm-1,在 15 0℃时达 1.2×10 -2 S .cm-1,已达到日本超导电玻璃电导率的数量级。并用IR、XRD、LCR等手段分析了玻璃的水化产物、水化过程中的物相和水化机理。同时研究了所制得含水玻璃固化体的导电机理及水化温度对固化体导电性影响。结果表明水在固化体中以分子水和结晶水为存在形式 ,≡SiOLi+H2 O ≡SiOH +Li+ +OH-,H2 O +≡Si-O -Si≡ ≡SiOH +≡SiO-,OH-+≡Si-O -Si≡ SiOH +≡SiO-为其水化机理反应式。该含水玻璃以离子导电为主 ,并且增大 -OH浓度或升高水化温度都有利于提高含水玻璃导电性 相似文献
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D. G. KARRAKER 《Journal of the American Ceramic Society》1982,65(1):53-55
Optical and Mössbauer spectra show that actinide ions are incorporated in a borosilicate glass matrix as U(VI), Np(IV), P(IV), and Am(III). Uranium was reduced by graphite to U(V) and U(IV), but Pu(IV) remained unchanged. It is inferred from their valences that Np, Pu, and Am are part of the borosilicate network and U is probably a network-modifier. 相似文献
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本研究以硼硅酸盐系统的玻璃作为基础玻璃,考察基础玻璃粉末在水热热压条件下的反应过程,制备出一种水化玻璃固化体。利用IR,DTA,TG和DTG等分析方法讨论了水在水化玻璃固化体的存在形式,得出水在水化玻璃固化体是以硅烷醇基=Si-OH和分子水两种形式存在的结论。并根据对水化过程中固化体的收缩量以及硅烷醇基=Si-OH含量的分析,探讨了水化反应的基本机理,揭示出水热热压条件下玻璃的水化过程是由两个阶段的构成的;第1阶段主要是以离子交换为主的释碱过程,第2阶段是以水分子的扩散以及碱蚀为主的破坏玻璃网络的溶蚀过程。 相似文献
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根据高硼硅酸盐玻璃的特性,阐述了高硼硅酸盐玻璃在生产实践的全过程中,影响玻璃产品质量的原料选用、配合料制备工艺、熔制工艺等环节的各种因素,控制要求和采取的各种调整方法等一系列技术管理措施. 相似文献
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Estelle Molières Frédéric Angeli Patrick Jollivet Stephane Gin Thibault Charpentier Odile Majérus Philippe Barboux Dominique de Ligny Olivier Spalla 《International Journal of Applied Glass Science》2013,4(4):383-394
The role of lanthanum in the alteration kinetics at different degrees of reaction progress was investigated at 90°C and pH 7 by complementary chemical (SIMS), morphological (SAXS), and structural (NMR, Raman, and EXAFS spectroscopy) approaches. In the first step of alteration, the forward dissolution rate diminishes with the addition of lanthanum, resembling to the behavior previously observed for zirconium. Over longer alteration time, the glasses with the highest lanthanum concentrations reach silicon saturation more slowly, but unlike zirconium, do not result in larger quantities of altered glass. Lanthanum is entirely retained in the alteration layer and is uniformly distributed; it undergoes hydrolysis and recondensation mechanisms, and its coordination number increases from 6 to 9 during leaching. Reconstruction of the alteration layer occurred more slowly at higher REE concentrations, with a slowdown in repolymerization of the silicate network and structuring of its porosity. 相似文献
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Ashutosh Goel John S. McCloy Charles F. Windisch Jr Brian J. Riley Michael J. Schweiger Carmen P. Rodriguez José M.F. Ferreira 《International Journal of Applied Glass Science》2013,4(1):42-52
A series of sodium borosilicate glasses were synthesized with KReO4 or Re2O7, to 10,000 ppm (1 mass%) target Re, to assess effects of large concentrations of rhenium on glass structure and fto estimate solubility of 99Tc, a radioactive component in low active waste nuclear glasses. Rhenium was used as a surrogate for 99Tc for laboratory testing, due to similarities in chemistry, ionic size, and redox. Magic angle spinning nuclear magnetic resonance, Fourier transform infrared spectroscopy, and Raman spectroscopy were performed to characterize the glasses. Si was coordinated in Q2 and Q3 units, Al was four-coordinated, and B was mostly three-coordinated. The rhenium additions did not have significant effects on the glass structure up to approximately 3000 ppm Re by mass, the maximum concentration that remained dissolved in glass. Rhenium likely exists in isolated anions in the interstices of the glass network, as evidenced by polarized Raman spectrum of the Re glass in the absence of sulfate. Analogous to in similar glasses, is a network modifier and above solubility forms alkali salt phases on the surface and in the bulk. Comparisons of phase separation and crystallization in containing borosilicate glasses can also be made to containing glasses. 相似文献
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Charles E. Anderson Jr. Timothy J. Holmquist Dennis L. Orphal Thilo Behner 《International Journal of Applied Ceramic Technology》2010,7(6):776-786
We have conducted impact experiments using gold long rods into borosilicate glass and the measured the penetration velocity as a function of impact velocity. At sufficiently low-impact velocities, the glass target resists penetration and there is dwell; dwell is observed to approximately 450 m/s for bare glass. If a copper buffer is placed over the glass to eliminate the impact shock, significant dwell can be seen at impact velocities as high as 890 m/s. These impact velocities correspond to Bernoulli stresses of approximately 2.0 and 7.6 GPa, respectively. The paper describes the experimental data, and summarizes the results and our findings. 相似文献
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R.F. Cook B.R. Lawn T. P. Dabbs K. D. Reeve E. J. Ramm J. L. Woolfrey 《Journal of the American Ceramic Society》1982,65(10):c172-c173
Comparative measurements have been made of the dynamic fatigue response of synroc and borosilicate glass specimens in water, using an indentation flaw technique. The results are presented in terms of a universal plotting scheme which allows for simple appraisal of the "lifetime" capabilities of the materials. Synroc is intrinsically stronger than borosilicate glass, but the fatigue susceptibilities are similar. 相似文献
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Yu. V. Larichev D. A. Shlyapin P. G. Tsyrul’nikov V. I. Bukhtiyarov 《Catalysis Letters》2008,120(3-4):204-209
Sibunit-supported Ru-catalysts promoted with cesium or rubidium compounds have been comparatively studied with XPS. The cesium promoter interacts both with support and with active component. The absence of the promoter–support interaction in the case of rubidium provides a stronger interaction between promoter and active component compared to the cesium-based catalysts. These differences in the promoter–support and promoter–metal interactions are exhibited when a sequence of ruthenium and alkali introduction are changed. 相似文献