This item was digitized as part of the Million Books Project led by Carnegie Mellon University and supported by grants from the National Science Foundation (NSF). Cornell University coordinated the participation of land-grant and agricultural libraries in providing historical agricultural information for the digitization project; the University of Arizona Libraries, the College of Agriculture and Life Sciences, and the Office of Arid Lands Studies collaborated in the selection and provision of material for the digitization project.

This item was digitized as part of the Million Books Project led by Carnegie Mellon University and supported by grants from the National Science Foundation (NSF). Cornell University coordinated the participation of land-grant and agricultural libraries in providing historical agricultural information for the digitization project; the University of Arizona Libraries, the College of Agriculture and Life Sciences, and the Office of Arid Lands Studies collaborated in the selection and provision of material for the digitization project.

Fouling, slagging, corrosion, and emission of submicron particulate from pulverized coal combustors have been linked to vapor alkali. Size segregated fly ash samples extracted from a 17 kW down-fired pulverized coal combustor showed strong evidence of alkali vaporization. The fraction of sodium in sizes smaller than 0.65 μm (f(8A)) showed a correlation with acid soluble sodium divided by total silicates in the parent coal. Addition of silicates to coal reduced f(8A) for sodium. Potassium existing primarily in the mineral matter, did not show a similar correlation, but f(8A) for potassium did correlate with f(8A) for sodium. Bench scale experiments indicated potassium does not vaporize in the presence of Na or Cl alone, but requires both, and was only released when sodium was captured. Additional of sodium acetate to coal increased f(8A) for potassium. Equilibrium calculations, experiment, and modelling of sodium capture by silicates during pulverized coal combustion identified several important mechanisms governing alkali behavior. The mode of occurrence of alkali in the parent coal dictates its ability to vaporize, its release kinetics, and its sate as it diffuses to the char surface. Other species such as chlorine, sulfur, moisture, and other metals influence alkali stability in the vapor, its reactivity, and its condensation characteristics. Char oxidation can influence alkali vaporization, and capture by affecting included silicate surface area. Sodium reaction with silicates captures from 70 to over 95% of total sodium for typical coals. Silicate additive appears to be a viable technique for reducing the fraction of alkali in the vapor during combustion.

This item was digitized as part of the Million Books Project led by Carnegie Mellon University and supported by grants from the National Science Foundation (NSF). Cornell University coordinated the participation of land-grant and agricultural libraries in providing historical agricultural information for the digitization project; the University of Arizona Libraries, the College of Agriculture and Life Sciences, and the Office of Arid Lands Studies collaborated in the selection and provision of material for the digitization project.

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Call number: LD2668 .T4 1958 C43 / Master of Science

The undesirable expansion of concrete because of a reaction between alkalis and certain type of reactive siliceous aggregates, known as alkali-silica reactivity (ASR), continues to be a major problem across the entire world. The renewed interest to minimize distress resulting from ASR has emphasized the need to develop predictable modeling of concrete ASR behavior under field conditions. Current test methods are either incapable or need long testing periods in which to only offer rather limited predictive estimates of ASR behavior in a narrow and impractical band of field conditions. Therefore, an attempt has been made to formulate a robust performance approach based upon basic properties of aggregate and concrete ASR materials derived from dilatometry and a kinetic-based mathematical expressions for ASR behavior. Because ASR is largely an alkali as well as a thermally activated process, the use of rate theory (an Arrhenius relationship between temperature and the alkali solution concentration) on the dilatometer time-expansion relationship, provides a fundamental aggregate ASR material property known as “activation energy.” Activation energy is an indicator of aggregate reactivity which is a function of alkalinity, particle size, crystallinity, calcium concentration, and others. The studied concrete ASR material properties represent a combined effects of mixture related properties (e.g., water-cementitious ratio, porosity, presence of supplementary cementitious materials, etc.) and maturity. Therefore, the proposed performance-based approach provides a direct accountability for a variety of factors that affect ASR, such as aggregate reactivity (activation energy), temperature, moisture, calcium concentration, solution alkalinity, and water-cementitious material ratio. Based on the experimental results, the following conclusion can be drawn concerning the performance-based approach to evaluate ASR potential of aggregate and concrete using dilatometer method; (i) the concept of activation energy can be used to represent the reactivity of aggregate subjected to ASR, (ii) the activation energy depends on the reactivity of aggregate and phenomenological alkalinity of test solution, and (iii) The proposed performance-based model provides a means to predict ASR expansion development in concrete.