Fusible glazes based on calcium borate

1966 ◽  
Vol 23 (2) ◽  
pp. 68-69 ◽  
Author(s):  
V. A. Krapivin ◽  
G. A. Demidova
Keyword(s):  
2021 ◽  
Vol 32 (7) ◽  
pp. 9392-9399
Author(s):  
Hosam M. Gomaa ◽  
I. S. Yahia ◽  
B. M. A. Makram ◽  
Ahmed H. El-Dosokey ◽  
Saeid M. Elkatlawy

2013 ◽  
Vol 362 ◽  
pp. 202-206 ◽  
Author(s):  
M. Senthilkumar ◽  
M. Kalidasan ◽  
Sugan ◽  
R. Dhanasekaran

2013 ◽  
Vol 77 (1) ◽  
pp. 93-105 ◽  
Author(s):  
I. Kusachi ◽  
S. Kobayashi ◽  
Y. Takechi ◽  
Y. Nakamuta ◽  
T. Nagase ◽  
...  

AbstractShimazakiite occurs as greyish white aggregates up to 3 mm in diameter. Two polytypes, shimazakiite-4M and shimazakiite-4O, have been identified, the former in nanometre-sized twin lamellae and the latter in micrometre-sized lamellae. Shimazakiite was discovered in an irregular vein in crystalline limestone near gehlenite-spurrite skarns at Fuka mine, Okayama Prefecture, Japan. Associated minerals include takedaite, sibirskite, olshanskyite, parasibirskite, nifontovite, calcite and an uncharacterized hydrous calcium borate. The mineral is biaxial (–), with the following refractive indices (at 589 nm): α = 1.586(2), β = 1.650(2), γ = 1.667(2) and 2Vcalc = 53º [shimazakiite-4M]; and α = 1.584(2), β = 1.648(2), γ = 1.670(2) and 2Vcalc = 54.88º [shimazakiite-4O]. Quantitative electronmicroprobe analyses (means of 28 and 25 determinations) gave the empirical formulae Ca2B1.92O4.76(OH)0.24 and Ca2B1.92O4.76(OH)0.24 for shimazakiite-4M and shimazakiite-4O, respectively. The crystal structure refinements: P21/c, a = 3.5485(12), b = 6.352(2), c = 19.254(6) Å , β = 92.393(13)°, V = 433.6(3) Å3 [for shimazakiite-4M]; and P212121, a = 3.55645(8), b = 6.35194(15), c = 19.2534(5) Å , V = 434.941(18) Å3[for shimazakiite-4O], converged into R1 indices of 0.1273 and 0.0142, respectively. The crystal structure of shimazakiite consists of a layer containing B2O5 units (two near-coplanar triangular corner-sharing BO3 groups) and 6- and 7-coordinate Ca atoms. Different sequences in the c direction of four layers are observed in the polytypes. The five strongest lines in the powder-diffraction pattern [listed as d in Å (I)(hkl)] are: 3.02(84)(022); 2.92(100)(10) 2.81(56)(104); 2.76(32)(113); 1.880(32)(11,12,126,118) [for shimazakiite-4M]; and 3.84(33)(014); 3.02(42)(022); 2.86(100)(104); 2.79(29)(113); 1.903(44)(126,118) [for shimazakiite-4O].


Author(s):  
Mohamed Khairy ◽  
Haytham Ayouby ◽  
Farouk Rashwan ◽  
Hanan F. Abdel-Hafez

Developing of nanoagrochemicals has attracted much attention in the last decade to overcome the recent agricultural and environmental challenges associated with the intensive usage of insecticides. Herein, nanostructured calcium borate...


2020 ◽  
Vol 46 (17) ◽  
pp. 27099-27109
Author(s):  
Jaimson T. James ◽  
Jephin K. Jose ◽  
M. Manjunatha ◽  
Keenatampalle Suresh ◽  
A. Madhu

1999 ◽  
Vol 28 (2) ◽  
pp. 41-46 ◽  
Author(s):  
Isao KUSACHI ◽  
Shoichi KOBAYASHI ◽  
Chiyoko HENMI ◽  
Yasushi TAKECHI

2010 ◽  
Vol 434-435 ◽  
pp. 371-375
Author(s):  
Ming He ◽  
Shu Ren Zhang ◽  
Xiao Hua Zhou ◽  
Jian Geng Hu ◽  
Ting Zhang ◽  
...  

. A doping CaO-B2O3-SiO2 system low temperature co-fired ceramics (LTCC) was prepared with a mixture of high temperature melting glass and sol-gel glass for different ratio. The effects of sol-gel glass content on the microstructure, crystalline phases, sintering properties and dielectric properties of CaO-B2O3-SiO2 system were investigated at 850°C. The results show that the samples with sol-gel glass doping had little change in phase composition, but contained more calcium silicates, and less calcium borate. As the amount of sol-gel glass increased, the shrinkage improved, the sintered density slightly decreased, the dielectric constant (εr) reduced, and the dielectric loss (tgδ) decreased. When the amount of sol-gel glass was 14.5wt%, εr and tgδ of the doping sample were 5.80, 4.6×10-5 (at 1 MHz), respectively. Moreover, the doping system had a good matching ability with gold slurry and Au-Pt-Pd slurry.


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