scholarly journals Iodoform-Blended Portland Cement for Dentistry

Prosthesis ◽  
2020 ◽  
Vol 2 (4) ◽  
pp. 277-296
Author(s):  
Qiu Li ◽  
Andrew D. Deacon ◽  
Nichola J. Coleman
Keyword(s):  
Portland Cement ◽  
Antimicrobial Properties ◽  
Antimicrobial Effect ◽  
Magic Angle Spinning ◽  
Cement Matrix ◽  
Resonance Spectroscopy ◽  
Magic Angle ◽  
Filling Materials ◽  
Human Osteosarcoma Cells ◽  
Angle Spinning

Portland cement-based formulations blended with radiopacifying agents are popular endodontic materials for various root filling and pulp capping applications. Iodoform (CHI3) is an alternative candidate radiopacifier whose impact on the setting, bioactivity, antimicrobial properties and cytotoxicity of white Portland cement were evaluated in this study. Isothermal conduction calorimetry and 29Si magic angle spinning nuclear magnetic resonance spectroscopy (MAS NMR) showed that 20 wt% iodoform had no significant impact on the kinetics of cement hydration with respect to the formation of the major calcium silicate hydrate (C-S-H) gel product (throughout the 28-day observation). Conversely, transmission electron microscopy demonstrated that iodine was incorporated into the ettringite (Ca₆Al₂(SO₄)₃(OH)₁₂·26H₂O) product phase. Both iodoform-blended and pure Portland cements exhibited comparable biocompatibility with MG63 human osteosarcoma cells and similar bioactivity with respect to the formation of a hydroxyapatite layer upon immersion in simulated body fluid. By virtue of their high alkalinity, both cements inhibited the growth of Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli. However, in all cases, iodoform enhanced the antimicrobial effect and significantly reduced the minimum bactericidal concentration of the cement. In conclusion, iodoform offers antimicrobial advantages in Portland cement-based formulations where oral biofilm formation threatens the success of root filling materials and dentine substitutes. The reactivity with the calcium aluminosulfate components of the hydrating cement matrix warrants further research to understand the long-term stability of the cement matrix in the presence of iodoform.

scholarly journals Impact of Bi2O3 and ZrO2 Radiopacifiers on the Early Hydration and C–S–H Gel Structure of White Portland Cement

2019 ◽  
Vol 10 (4) ◽  
pp. 46 ◽  
Author(s):  
Qiu Li ◽  
Nichola J. Coleman
Keyword(s):  
Portland Cement ◽  
Magic Angle Spinning ◽  
Cement Matrix ◽  
Resonance Spectroscopy ◽  
Magic Angle ◽  
Gel Structure ◽  
Early Hydration ◽  
Setting Times ◽  
The Impact ◽  
White Portland Cement

Bismuth oxide (monoclinic α-Bi2O3) and zirconium oxide (monoclinic ZrO2) are the most popular radiopacifiers in commercial Portland cement-based endodontic restoratives, yet their effects on the setting and hydration reactions are not fully understood. This study compares the impact of 20 wt.% of Bi2O3 or ZrO2 on the early hydration reactions and C–S–H gel structure of white Portland cement (WPC). Cement paste samples were hydrated at 37.5 °C prior to analysis by 29Si and 27Al magic angle spinning nuclear magnetic resonance spectroscopy at 3 h and 24 h, and transmission electron microscopy at 3 h. Initial and final setting times were determined using a Vicat apparatus and reaction kinetics were monitored by isothermal conduction calorimetry. Bi2O3 was found to prolong initial and final setting times and retard the degree of hydration by 32% at 24 h. Heat evolution during the acceleration and deceleration phases of the hydration process was reduced and the exotherm arising from renewed ettringite formation was delayed and diminished in the presence of Bi2O3. Conversely, ZrO2 had no significant impact on either setting time; although, it accelerated hydration by 23% within 24 h. Increases in the mean silicate chain length and the extent of aluminum substitution in the C–S–H gel were observed in the presence of both radiopacifying agents after 24 h relative to those of the unblended WPC. The Bi2O3 and ZrO2 particles remained intact within the cement matrix and neither bismuth nor zirconium was chemically incorporated in the hydration products.

scholarly journals Hydration of Ordinary Portland Cement in Presence of Lead Sorbed on Ceramic Sorbent

Materials ◽  
2018 ◽  
Vol 12 (1) ◽  
pp. 19 ◽  
Author(s):  
Martin Keppert ◽  
Lenka Scheinherrová ◽  
Miloš Jerman ◽  
Barbora Doušová ◽  
Libor Kobera ◽  
...  
Keyword(s):  
Portland Cement ◽  
Ordinary Portland Cement ◽  
Low Cost ◽  
Waste Product ◽  
Industrial Effluents ◽  
Magic Angle Spinning ◽  
Resonance Spectroscopy ◽  
Magic Angle ◽  
High Sorption ◽  
Angle Spinning

Lead, a highly toxic element, is frequently present in various solid wastes as well as in industrial effluents. Sorption with a low cost sorbent is a simple way of Pb removal from liquid streams, but stabilization of spent sorbent has to be ensured in order to prevent Pb leaching out and possible environmental contamination. In previous research, ceramic sorbent, generated as waste product in brick industry, was tested as sorbent and proved high sorption capacity for lead. Lead was sorbed partially as hydrocerussite and partially as adsorbed surface layer. The Pb leaching from sorbent was very high and thus further immobilization of sorbent was necessary. Lead, as well as other heavy metals, is known as retarder of the hydration process of Ordinary Portland Cement (OPC), used for the immobilization. In this paper, influence of sorbed Pb and PbO, as reference compound, on cement hydration was studied by calorimetry, thermogravimetry and Magic Angle Spinning Nuclear Magnetic Resonance Spectroscopy (MAS NMR). The sorbed lead was found to be less detrimental to hydration retardation due to the lower solubility of precipitated hydrocerussite in basic environment compared to PbO, which forms plumbate anion.

scholarly journals Preparation of Li3PS4–Li3PO4 Solid Electrolytes by Liquid-Phase Shaking for All-Solid-State Batteries

2021 ◽  
Vol 2 (1) ◽  
pp. 39-48
Author(s):  
Nguyen H. H. Phuc ◽  
Takaki Maeda ◽  
Tokoharu Yamamoto ◽  
Hiroyuki Muto ◽  
Atsunori Matsuda
Keyword(s):  
Solid Solution ◽  
Solid State ◽  
Liquid Phase ◽  
Room Temperature ◽  
Reaction Medium ◽  
Magic Angle Spinning ◽  
Resonance Spectroscopy ◽  
Synthesis Methods ◽  
Magic Angle ◽  
Angle Spinning

A solid solution of a 100Li3PS4·xLi3PO4 solid electrolyte was easily prepared by liquid-phase synthesis. Instead of the conventional solid-state synthesis methods, ethyl propionate was used as the reaction medium. The initial stage of the reaction among Li2S, P2S5 and Li3PO4 was proved by ultraviolet-visible spectroscopy. The powder X-ray diffraction (XRD) results showed that the solid solution was formed up to x = 6. At x = 20, XRD peaks of Li3PO4 were detected in the prepared sample after heat treatment at 170 °C. However, the samples obtained at room temperature showed no evidence of Li3PO4 remaining for x = 20. Solid phosphorus-31 magic angle spinning nuclear magnetic resonance spectroscopy results proved the formation of a POS33− unit in the sample with x = 6. Improvements of ionic conductivity at room temperature and activation energy were obtained with the formation of the solid solution. The sample with x = 6 exhibited a better stability against Li metal than that with x = 0. The all-solid-state half-cell employing the sample with x = 6 at the positive electrode exhibited a better charge–discharge capacity than that employing the sample with x = 0.

Leucite-pollucite structure-type variability and the structure of a synthetic end-member calcium wairakite (CaAl2Si4O12·2H2O)

1998 ◽  
Vol 62 (2) ◽  
pp. 165-178 ◽  
Author(s):  
C. M. B. Henderson ◽  
A. M. T. Bell ◽  
S. C. Kohn ◽  
C. S. Page
Keyword(s):  
Rietveld Analysis ◽  
Structure Type ◽  
Magic Angle Spinning ◽  
Resonance Spectroscopy ◽  
Magic Angle ◽  
Synthetic Sample ◽  
Cation Site ◽  
Wide Range ◽  
Angle Spinning ◽  
Cation Sites

AbstractThe structure of a synthetic end-member wairakite (CaAl2Si4O12·2H2O) has been determined using Rietveld analysis of high-resolution, synchrotron X-ray powder diffraction data, and 29Si and 27Al magic angle spinning nuclear magnetic resonance spectroscopy. The framework in the synthetic sample is more disordered than that in natural wairakite. Ca is distributed over the cavity cation sites M2, M12A, M12B in the approximate proportions 0.8:0.1:0.1, respectively, with M11 being vacant. 29Si MAS NMR data are consistent with about 80% of the Si occupying tetrahedral T11 and T12 sites linked to two Al atoms [Q4(2Al) silicons]. Tetrahedral and cavity cation site disorder are coupled so that Al mainly occupies T2 sites, with Ca in M12A and M12B being balanced by Al in T12A and T12B; T11A and T11B sites appear to only contain Si, in agreement with the M11 site being vacant. The crystal chemistries of the wide range of stoichiometries which crystallize with the leucite/pollucite structure-type are also reviewed, with particular attention being paid to the tetrahedral ordering configurations present in these phases, and the implications to crystallographic phase transitions.

Sign in / Sign up

Export Citation Format

Share Document