Homogeneous single C-S-H gels have been prepared for the investigation of alkali binding potential and crystallisation. A distribution coefficient, R_d, was introduced to express the partition of alkali between solid and aqueous phases at 25°C. R_d is independent of alkali hydroxide concentration and depends only on Ca:Si ratio over wide ranges of alkali concentration. The trend of numerical values of R_d indicates that alkali bonding into the solid improves as its Ca:Si ratio decreases. Reversibility is demonstrated, indicating a possibility of constant R_d value of the material. Al has been introduced to form C-A-S-H gels and their alkali sorption properties also determined. Al substituted into C-S-H markedly increases R_d, indicating enhancement of alkali binding. However, the dependence of R_d on alkali concentration is non-ideal with composition. A two-site model for bonding is presented. Crystallisation both under saturated steam and 1 bar vapour pressure has been investigated. It has been shown that heat treatment by saturated steam causes crystallisation of gels. The principal minerals obtained were (i) C-S-H gel and Ca(OH)₂ at ~55°C, (ii) 1.1 nm tobermorite, jennite and afwillite at 85-130°C, and (iii) xonotlite, foshagite and hillebrandite at 150-180°C. Properties of crystalline C-S-H were also reported for reversible phase transformation, pH conditioning ability, seeding effect and solubility. At 1 bar pressure, crystallisation is slower than in saturated steam due to lower water activity. Tobermorite-like nanodomains develop during reaction at low Ca/Si ratios. In some Ca-rich compositions, Ca(OH)₂ is exsolved and occurs as nano-sized crystallites.

No description available.

A new analytical technique to measure the chemical composition distribution (CCD) of polyolefins, crystallization elution fractionation (CEF), was introduced in 2006 during the First International Conference on Polyolefin Characterization. CEF is a faster and higher resolution alternative to the previous polyolefin CCD analytical techniques such as temperature rising elution fractionation (TREF) and crystallization elution fractionation (CRYSTAF) (Monrabal et al., 2007). Crystallization elution fractionation is a liquid chromatography technique used to determine the CCD of polyolefins by combining a new separation procedure, dynamic crystallization, and TREF. In a typical CEF experiment, a polymer solution is loaded in the CEF column at high temperature, the polymer is allowed to crystallize by lowering the solution temperature, and then the precipitated polymer is eluted by a solvent flowing through the column as the temperature is raised. CEF needs to be calibrated to provide quantitative CCD results. A CEF calibration curve consists of a mathematical relationship between elution temperature determined by CEF and comonomer fraction in the copolymer that could be estimated by Fourier transform infrared spectroscopy (FTIR) and carbon-13 nuclear magnetic resonance (13C NMR). Different comonomer types in ethylene/α-olefin copolymers will have distinct calibration curves. The main objective of this thesis is to obtain CEF calibration curves for several different ethylene/α-olefin copolymers and to investigate which factors influence these calibration curves. A series of homogeneous ethylene/α-olefin copolymers (1-hexene, 1-octene and 1-dodecene) with different comonomer fractions were synthesized under controlled conditions to create CEF calibration standards. Their average chemical compositions were determined by 13C NMR and FTIR and then used to establish CEF calibration curves relating elution temperature and comonomer molar fraction in the copolymer.

A comprehensive experimental study was conducted to determine the limitations in processing conditions for superdrawing. Experimental studies were carried out by uniaxial drawing tests at temperatures from 90 to 120°C and at strain rates ranging from 0.008/s to 0.425/s. Crystallinity and orientation of the drawn samples were evaluated using differential scanning calorimetry and birefringence measurements. This study revealed that increasing temperature from 110°C to 120°C leads to more crystallization at low strain rates (0.001/s), and less crystallization at high strain rates (0.1/s). Furthermore, it was shown for the first time that the mechanism of crystallinity development in PET undergoes a transition at draw temperature of 113°C and strain rate of 0.17/s. A new one-dimensional constitutive model was developed to predict the stress-strain behavior of PET fibers as they are drawn to very large draw ratios (up to 10) over a wide range of temperature (90-120°C) and strain rate (0.008-0.425/s). The model was based on the rubber elasticity theory and non-linear viscoelasticity.

Bibliography: leaves 228-237 / xii, 287 leaves : ill ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, Dept. of Chemical Engineering, 1990

Thesis (M.Eng.)(Metallurgical)--University of Pretoria, 2006. / Includes summary. Includes bibliographical references. Available on the Internet via the World Wide Web.

Thesis (Ph. D.)--Ohio State University, 2008. / Title from first page of PDF file. Includes bibliographical references (p. 144-152).

Mémoire (M.Sc.)-- Université du Québec à Chicoutimi, 1977. / "Mémoire présenté en vue de l'obtention de la maîtrise es sciences en géologie". CaQCU Document électronique également accessible en format PDF. CaQCU

Thesis (M.S.) -- Mississippi State University. Dave C. Swalm School of Chemical Engineering. / Title from title screen. Includes bibliographical references.

Diss. (sammanfattning) Uppsala : Sveriges lantbruksuniversitet, 2010. / Härtill 3 uppsatser.