Carbonation Effects in Hardened Fly Ash Cements

1985 ◽  
Vol 65 ◽  
Author(s):  
Inger Meland

ABSTRACTCarbonation in hardened pastes of fly ash cements, stored in a CO2 atmosphere and exposed to different relative humidities, has been investigated in order to study its effects upon different properties of cement pastes. Thermogravimetry (TG), x-ray diffractometry, SEM, and mercury porosimetry (MIP) have been used to characterize the carbonation phenomenon. The results indicate that different relative humidities in the storage chambers lead to carbonation of different solid phases in the hydrated pastes. This effect is discussed in terms of TG- and x-ray analysis. Changes in pore size distribution due to carbonation have been analyzed by MIP and SEM.

1986 ◽  
Vol 85 ◽  
Author(s):  
Th.A. Bier

ABSTRACTDifferent series of cement paste specimens were prepared with ordinary portland cement, with portland, blast furnace slag cements having slag contents of 30, 50 and 75% by mass, with commercial fly ash cement and with portland cement containing fly ash additions of 10, 20, 30 and 50% by mass. Moist curing of the specimens varied between 3 and 28 days before the pore size distribution and characteristics of the phase composition were analyzed. Subsequent to curing, the specimens were subjected to drying in air of 65% RH with a controlled CO2 content of 0, 0.03 and 2% CO2 by volume. Depth of carbonation, pore size distribution of the carbonated paste, and the phase composition were investigated after 28 days and 6 months of drying, respectively. The results show that carbonation alters the prevailing pore structure of the hydrated paste. Important parameters are the type of cement used and the duration of curing.


2010 ◽  
Vol 97-101 ◽  
pp. 453-456 ◽  
Author(s):  
Xi Lai Chen ◽  
Ya Wei Li ◽  
Yuan Bing Li ◽  
Shao Bai Sang ◽  
Lei Zhao

The effect of reactive-Al2O3 addition on the pore size distribution and thermal conductivity of carbon blocks for blast furnace was investigated by using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray, mercury porosimetry, and a laser thermal conductivity meter. The results showed that the pore size distribution and the thermal conductivity of carbon block were mainly influenced by SiC whiskers and reactive-Al2O3. With increasing addition of reactive-Al2O3, the mean pore diameter reduced and < 1μm pore volume increased of open pores owing to the more efficient filling of pores by SiC and reactive-Al2O3, and the thermal conductivities of samples increased due to the facts that the higher thermal conductivity of reactive-Al2O3 than that of brown corundum and the more formation amount of high thermal conductivity of SiC.


Membranes ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 78
Author(s):  
Marius Gheorghe Miricioiu ◽  
Violeta-Carolina Niculescu ◽  
Constantin Filote ◽  
Maria Simona Raboaca ◽  
Gheorghe Nechifor

In order to obtained high selective membrane for industrial applications (such as natural gas purification), mixed matrix membranes (MMMs) were developed based on polysulfone as matrix and MCM-41-type silica material (obtained from coal fly ash) as filler. As a consequence, various quantities of filler were used to determine the membranes efficiency on CO2/CH4 separation. The coal fly ash derived silica nanomaterial and the membranes were characterized in terms of thermal stability, homogeneity, and pore size distribution. There were observed similar properties of the obtained nanomaterial with a typical MCM-41 (obtained from commercial silicates), such as high surface area and pore size distribution. The permeability tests highlighted that the synthesized membranes can be applicable for CO2 removal from CH4, due to unnoticeable differences between real and ideal selectivity. Additionally, the membranes showed high resistance to CO2 plasticization, due to permeability decrease even at high feed pressure, up to 16 bar.


1991 ◽  
Vol 74 (10) ◽  
pp. 2538-2546 ◽  
Author(s):  
Susan Krueger ◽  
Gabrielle G. Long ◽  
David R. Black ◽  
Dennis Minor ◽  
Pete R. Jemian ◽  
...  

Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2247
Author(s):  
Claire Delaroa ◽  
René Fulchiron ◽  
Eric Lintingre ◽  
Zoé Buniazet ◽  
Philippe Cassagnau

The impact of polypropylene and high-density polyethylene backbone binders on the structure of organic matrix, feedstock, and ceramic parts is investigated in terms of morphology in this paper. The miscibility of wax with polyethylene and polypropylene is investigated in the molten state via a rheological study, revealing wax full miscibility with high-density polyethylene and restricted miscibility with polypropylene. Mercury porosimetry measurements realized after wax extraction allow the characterization of wax dispersion in both neat organic blends and zirconia filled feedstocks. Miscibility differences in the molten state highly impact wax dispersion in backbone polymers after cooling: wax is preferentially located in polyethylene phase, while it is easily segregated from polypropylene phase, leading to the creation of large cracks during solvent debinding. The use of a polyethylene/polypropylene ratio higher than 70/30 hinders wax segregation and favors its homogeneous dispersion in organic binder. As zirconia is added to organic blends containing polyethylene, polypropylene, and wax, the pore size distribution created by wax extraction is shifted towards smaller pores. Above zirconia percolation at 40 vol%, the pore size distribution becomes sharp attesting of wax homogeneous dispersion. As the PP content in the organic binder decreases from 100% to 0%, the pore size distribution is reduced of 30%, leading to higher densification ability. In order to ensure a maximal densification of the final ceramic, polyethylene/polypropylene ratios with a minimum content of 70% of high-density polyethylene should be employed.


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