2008
DOI: 10.1016/j.cemconres.2008.02.012
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The influence of water removal techniques on the composition and microstructure of hardened cement pastes

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Cited by 174 publications
(90 citation statements)
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“…Oven drying causes a lot of damage and leads to high pore entry sizes. Solvent exchange followed by vacuum drying seems to be the best method to stop the hydration [9,[11][12][13] although isopropanol might affect the very small gel porosity of the C-S-H [14]. Comparison with past results shows the critical or threshold pore entry sizes to be more than one order of magnitude larger for oven dried samples than for samples dried by solvent exchange.…”
Section: Introductionmentioning
confidence: 73%
“…Oven drying causes a lot of damage and leads to high pore entry sizes. Solvent exchange followed by vacuum drying seems to be the best method to stop the hydration [9,[11][12][13] although isopropanol might affect the very small gel porosity of the C-S-H [14]. Comparison with past results shows the critical or threshold pore entry sizes to be more than one order of magnitude larger for oven dried samples than for samples dried by solvent exchange.…”
Section: Introductionmentioning
confidence: 73%
“…For quantitative XRD analysis, hydrated paste samples were crushed to a fine powder by manual 74 grinding in a pestle and mortar without any prior hydration stopping, so as to minimise any damage 75 to phases present 15,16 . The powders were backloaded into 16 mm diameter sample holders and 76 diffraction patterns P P X P MPD 77 C K X-ray source, an X C ator detector and operated at 40kV and 40mA.…”
Section: Methodsmentioning
confidence: 99%
“…The early-age hardened grout composition was investigated by casting samples of the control grout and grouts containing either 2% (by weight of cement) sodium phosphate or sodium borate, and hydrothermally curing them at 120°C for 7, 14 and 28 d. After each time interval, hydration was arrested using acetone as a solvent replacement technique (Collier et al, 2008) and the composition was determined by means of X-ray diffraction (XRD) and thermogravimetric analysis/derivative thermogravimetric analysis (TGA/DTG). A Bruker D2 Phaser X-ray diffractometer was operated between 5 and 90°2θ at 2°/min and a Perkin Elmer Pyris 1 thermogravimetric analyser was operated using a heating profile of 30-1000°C at 10°C/min in flowing nitrogen.…”
Section: Sample Analysismentioning
confidence: 99%