silicon-oxygen tetrahedron

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1529
Author(s):  
Haihong Fan ◽  
Mengqi Lv ◽  
Xiaosha Wang ◽  
Jianmin Xiao ◽  
Xiaofan Mi ◽  
...  

In order to reveal the solidification behavior of Cr in the cement clinker mineral phase, 29Si magic-angle spinning nuclear magnetic resonance, X-ray diffraction, and scanning electron microscopy with energy-dispersive X-ray spectroscopy techniques were used to analyze the morphology and composition of the cement clinker mineral phase doped with Cr. The results showed that the addition of Cr did not change the chemical environment of 29Si in the clinker mineral phase, and it was still an isolated silicon–oxygen tetrahedron. Cr affected the orientation of the silicon–oxygen tetrahedron and the coordination number of calcium, leading to the formation of defects in the crystal structure of the clinker mineral phase, by replacing Ca2+ into the mineral phase lattice to form a new mineral phase Ca3Cr2(SiO4)3. Cr acted as a stabilizer for the formation of β-C2S in the clinker calcination. As the amount of Cr increased, the relative content of C3S decreased and the relative content of C2S increased. Further, Cr easily dissolved in C2S, while it was not found in C3S. This study is conducive to further research on the mechanism of heavy metal solidification in cement clinker. Furthermore, it is important to evaluate the environmental risk of heavy metals in the process of sludge disposal through cement kiln and promote the utilization of sludge resources and the sustainable development of the cement industry.


2011 ◽  
Vol 233-235 ◽  
pp. 2589-2594 ◽  
Author(s):  
Qing Jun Ding ◽  
Yu Wang ◽  
Xiu Lin Huang

By using XRD, isothermal microcalorimetry, ESEM, EDS, NMR, the effects silica fume and polycarboxylate superplasticizer (PC) on the hydration behavior of tricalcium silicate (C3S) paste were researched. The results show that: PC suppresses the hydration of C3S while silica fume promotes the hydration of C3S by consumption of generated Ca(OH)2. Both PC and silica fume change the morphology of hydration products C-S-H gel from needle-bar-like to reunion-like, along with the polymerization state of silicon-oxygen tetrahedron varied greatly. Especially silica fume significantly affects Q1, Q2 percentage of silicon-oxygen tetrahedron.


2018 ◽  
Vol 57 (9) ◽  
pp. 4799-4802 ◽  
Author(s):  
Qing-fang Lin ◽  
Jing Li ◽  
Xi-ming Luo ◽  
Chen-hui Cui ◽  
You Song ◽  
...  

2004 ◽  
Vol 85 (7) ◽  
pp. 1876-1878 ◽  
Author(s):  
Hans-Joerg Woelk ◽  
Bettina Hoffmann ◽  
Gerhard Mestl ◽  
Robert Schloegl

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1080
Author(s):  
Karol Zalewski ◽  
Zbigniew Chyłek ◽  
Waldemar A. Trzciński

Polysiloxanes are reviewed for their properties depending on the functionalization of a silicon–oxygen backbone chain. Next, the properties were referred to the requirements that polymers used in plastic/polymer-bonded explosive (PBX)-type explosives must meet. Finally, the current state and prospects for the implementation of polysiloxanes in plastic/polymer-bonded explosive (PBX) formulations are presented.


1991 ◽  
Vol 6 (12) ◽  
pp. 2723-2734 ◽  
Author(s):  
Gary M. Renlund ◽  
Svante Prochazka ◽  
Robert H. Doremus

Silicon oxycarbide glass is formed by the pyrolysis of silicone resins and contains only silicon, oxygen, and carbon. The glass remains amorphous in x-ray diffraction to 1400 °C and shows no features in transmission electron micrographs (TEM) after heating to this temperature. After heating at higher temperature (1500–1650 °C) silicon carbide lines develop in x-ray diffraction, and fine crystalline regions of silicon carbide and graphite are found in TEM and electron diffraction. XPS shows that silicon-oxygen bonds in the glass are similar to those in amorphous and crystalline silicates; some silicons are bonded to both oxygen and carbon. Carbon is bonded to either silicon or carbon; there are no carbon-oxygen bonds in the glass. Infrared spectra are consistent with these conclusions and show silicon-oxygen and silicon-carbon vibrations, but none from carbon-oxygen bonds. 29Si-NMR shows evidence for four different bonding groups around silicon. The silicon oxycarbide structure deduced from these results is a random network of silicon-oxygen tetrahedra, with some silicons bonded to one or two carbons substituted for oxygen; these carbons are in turn tetrahedrally bonded to other silicon atoms. There are very small regions of carbon-carbon bonds only, which are not bonded in the network. This “free” carbon colors the glass black. When the glass is heated above 1400 °C this network composite rearranges in tiny regions to graphite and silicon carbide crystals. The density, coefficient of thermal expansion, hardness, elastic modulus, index of refraction, and viscosity of the silicon oxycarbide glasses are all somewhat higher than these properties in vitreous silica, probably because the silicon-carbide bonds in the network of the oxycarbide lead to a tighter, more closely packed structure. The oxycarbide glass is highly stable to temperatures up to 1600 °C and higher, because oxygen and water diffuse slowly in it.


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