The Nature of Silicon-oxygen Bonds in Silica Polymorphs

Author(s):  
B. Silvi ◽  
A. Savin ◽  
F. R. Wagner
Keyword(s):  
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.


2021 ◽  
Vol 25 (11) ◽  
pp. 36-41
Author(s):  
D.V. Bespolitov ◽  
N.A. Konovalova ◽  
O.N. Dabizha ◽  
P.P. Pankov ◽  
E.A. Rush

The possibility of utilization of inactive fly ash in road concrete compositions by bringing of ash into a non-equilibrium condition with increased reactivity by mechanical activation in a vibration eraser is investigated. It was revealed that the optimal content of binder and fly ash in samples of soil concrete was 8 and 10 wt. %, respectively. It is shown that, due to mechanical activation, the specific surface area of fly ash increases by 2 times, dehydration and carbonization occur and silicon is replaced by aluminum in silicon-oxygen tetrahedra. It has been established that an increase of the content of crystalline carbonate phases is the reason for an increase in the strength of ground concrete. It is determined that the introduction of mechanoactivated fly ash into the composition of soil concretes contributes to increasing their physical and mechanical characteristics to the maximum strength grade M100. This indicates the competitiveness of ground concrete and the possibility of direct use of inactive fly ash in road construction.


The chapter is devoted to structure and properties of composite adsorbents ‘salt inside porous matrix'. Characteristics of adsorbents ‘salt inside porous matrix', such as ‘zeolite – crystalline hydrate', ‘vermiculite – crystalline hydrate', ‘silica gel – crystalline hydrate' were analysed. Main advantages of composite adsorbents are shown to be higher adsorptive capacity and lower regeneration temperature as compared with host matrix. Adsorptive capacities of composite materials are shown to be significantly enhanced by introduction of salts in host matrix such as zeolite, vermiculite, or silica gel. Water uptake by composite adsorbent is shown to be increased by rising the salt content in it. The drawback of most of existing impregnation technologies is shown to be impossibility of obtaining composite with salt content more than 40 – 60% along with complexity. Sol gel method is shown to be an alternative for conventional impregnation methods. Properties of adsorbents ‘silica gel – sodium sulphate' synthesized according to sol gel method developed by authors were considered. The composite ‘silica gel – sodium sulphate' composition and structure were studied by IR-spectroscopy and wide-angle x-ray scattering. Adsorptive properties of crystalline Na2SO4 when allocated in silicon oxygen matrix are shown to result from dispersion up to nanoscale. Adsorptive capacities and heat of adsorption of composites ‘silica gel – sodium sulphate' and ‘silica gel – sodium acetate' surpass almost by 30% the value calculated from the linear superposition of the sorption capacities of the sorbent and massive salt. Their adsorption properties are shown to be not a linear combination of properties of silica gel and salt. The formation of a unique structure promoting an increase in the rate of reaction between crystalline hydrates and water vapor in the developed pores of the silicon-oxygen matrix is confirmed. It leads to increasing the heat of adsorption and the heat energy storage density. Strong difference of water sorption kinetic curves of composite ‘silica gel – sodium sulphate' and massive sodium sulphate is revealed. The correlation of their composition, structure, water adsorption kinetic, and operating characteristic as heat storage material is stated.


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