Kenneth J.D. MacKenzie

ORCID: 0000-0003-3460-6708
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Research Areas
  • Clay minerals and soil interactions
  • Concrete and Cement Materials Research
  • Advanced ceramic materials synthesis
  • Glass properties and applications
  • Nuclear materials and radiation effects
  • Zeolite Catalysis and Synthesis
  • Chemical Synthesis and Characterization
  • Mesoporous Materials and Catalysis
  • Magnesium Oxide Properties and Applications
  • Recycling and utilization of industrial and municipal waste in materials production
  • Advanced NMR Techniques and Applications
  • Iron oxide chemistry and applications
  • Thermal and Kinetic Analysis
  • Fluorine in Organic Chemistry
  • Layered Double Hydroxides Synthesis and Applications
  • X-ray Diffraction in Crystallography
  • Organic Chemistry Cycloaddition Reactions
  • Asymmetric Synthesis and Catalysis
  • Innovative concrete reinforcement materials
  • Microwave Dielectric Ceramics Synthesis
  • Solid-state spectroscopy and crystallography
  • Chemical Reactions and Mechanisms
  • Luminescence Properties of Advanced Materials
  • Building materials and conservation
  • Ferroelectric and Piezoelectric Materials

Victoria University of Wellington
2016-2025

MacDiarmid Institute for Advanced Materials and Nanotechnology
2016-2025

Keio University
2024

Arizona State University
2024

University of Calgary
2023

American University of the Middle East
2019

Plasma Processes (United States)
2017

Marymount University
2000-2015

University of Aberdeen
1999-2014

Mrag Americas (United States)
2014

The effect of SiO 2 addition on the anatase‐to‐rutile phase transition was investigated by DTA, XRD, FTIR, and XPS. TiO xerogels containing up to 20 mol% were prepared mixing hydrolyzing titanium tetraisopropoxide (TTIP) tetraethylorthosilicate (TEOS) with HNO 3 as a catalyst. With increased amounts in xerogels, following results obtained: (1) crystallization temperature anatase from 415°C pure 609°C 20‐mol%‐SiO ‐containing xerogel DTA curves; (2) formation rutile, according quantitative XRD...

10.1111/j.1151-2916.2001.tb00882.x article EN Journal of the American Ceramic Society 2001-07-01

Structural models previously proposed for metakaolinite are examined in light of the most recent published experimental data and new information obtained by solid‐state high resolution 29 Si 27 AI NMR. A model is proposed, consisting anhydrous regions distorted AI‐0 tetrahedra containing randomly distributed isolated residual hydroxyls associated with A1‐0 configurations regular octahedral tetrahedpal symmetry. Such a structure, which can readily be formed from kaolinite removal certain...

10.1111/j.1151-2916.1985.tb15228.x article EN Journal of the American Ceramic Society 1985-06-01

Solid‐state 29 Si and 27 Al NMR spectra of kaolinite fired at 800° to 1450°C, interpreted in light a newly proposed metakaolinite structure complementary X‐ray diffraction results, lead the following conclusions about hightemperature reactions: (1) Removal final residual hydroxyl radicals ∼9707deg;C triggers separation considerable amount amorphous free silica formation poorly crystalline mullite spinel phase. (2) Mullite form tandem, former originating vicinity AI‐0 units regular octahedral...

10.1111/j.1151-2916.1985.tb15229.x article EN Journal of the American Ceramic Society 1985-06-01

Solid-state 27Al and 25Mg MAS NMR X-ray powder diffraction in combination with thermal analysis indicates that synthetic hydrotalcite decomposes thermally at least three weight-loss steps. The first step, 250–280 °C, principally involves the loss of interlayer water, but appearance some tetrahedral Al spectra suggests this is accompanied by onset dehydroxylation. second 300–400 a rapid increase proportion to maximum 400 indicating full dehydroxylation regions. third above represents...

10.1039/jm9930301263 article EN Journal of Materials Chemistry 1993-01-01

A simple ion-exchange method is reported for replacing the charge-balancing cations in aluminosilicate inorganic polymers with a range of other cations. Complete exchange Na+ conventional Na-inorganic polymer by K+, Ag+, NH4+ and Pb2+ was achieved this method, lower degree Li+ (82%), Cd2+ (78%) Mg2+ (57%). The NH4+-compound can be completely exchanged but less efficient compound than when using Na-compound as starting material. X-ray-amorphous nature Al Si environment original Na are...

10.1039/c0jm01254h article EN Journal of Materials Chemistry 2010-01-01

N. H. Brett, K. J. D. MacKenzie and Sharp, Q. Rev. Chem. Soc., 1970, 24, 185 DOI: 10.1039/QR9702400185

10.1039/qr9702400185 article EN Quarterly Reviews Chemical Society 1970-01-01
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