X-Ray Diffraction Analysis of Various Calcium Silicate-Based Materials

Background: The purpose of this study was to evaluate the composition of the crystal phases of various calcium silicate-based materials (CSMs): ProRoot white MTAⓇ (mineral trioxide aggregate) (WMTA), Ortho MTAⓇ (OM), Endocem MTAⓇ (EM), Retro MTAⓇ (RM), Endocem ZrⓇ (EN-Z), BiodentineTM (BD), EZ-sealT...

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Main Authors: So-Youn An, Myung-Jin Lee, Youn-Soo Shim
Format: Article
Language:English
Published: The Korean Society of Dental Hygiene Science 2022-09-01
Series:치위생과학회지
Subjects:
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author So-Youn An
Myung-Jin Lee
Youn-Soo Shim
author_facet So-Youn An
Myung-Jin Lee
Youn-Soo Shim
author_sort So-Youn An
collection DOAJ
description Background: The purpose of this study was to evaluate the composition of the crystal phases of various calcium silicate-based materials (CSMs): ProRoot white MTAⓇ (mineral trioxide aggregate) (WMTA), Ortho MTAⓇ (OM), Endocem MTAⓇ (EM), Retro MTAⓇ (RM), Endocem ZrⓇ (EN-Z), BiodentineTM (BD), EZ-sealTM (EZ), and OrthoMTA III (OM3).Methods: In a sample holder, 5 g of the powder sample was placed and the top surface of the material was packed flat using a sterilized glass slide. The prepared slides were mounted on an X-ray diffraction (XRD) instrument (D8 Advance; Bruker AXS GmbH, Germany). The X-ray beam 2θ angle range was set at 10∼90o and scanned at 1.2o per minute. The Cu X-ray source set to operate at 40 kV and 40 mA in the continuous mode. The peaks in the diffraction pattern of each sample were analyzed using the software Diffrac (version 2.1). Then, the peaks were compared and matched with those of standard materials in the corresponding Powder Diffraction File (PDF-2, JCPDS International Center for Diffraction Data). A powder samples of the materials were analyzed using XRD and the peaks in diffraction pattern were compared to the Powder Diffraction File data.Results: Eight CSMs showed a similar diffraction pattern because their main component was calcium silicate. Eight CSMs showed similar diffraction peaks because calcium silicate was their main component. Two components were observed to have been added as radiopacifiers: bismuth oxide was detected in WMTA, OM, and EM while zirconium oxide was detected in RM, EN-Z, BD, EZ, and OM3. Unusual patterns were detected for the new material, OM3, which had strong peaks at low angles.Conclusion: It was caused by the presence of Brushite, which is believed to have resulted in crystal growth in a particular direction for a specific purpose.
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spelling doaj.art-1cad3579d9364693b48381275dfa81d22022-12-22T03:17:59ZengThe Korean Society of Dental Hygiene Science치위생과학회지2233-76792022-09-0122319119810.17135/jdhs.2022.22.3.191X-Ray Diffraction Analysis of Various Calcium Silicate-Based MaterialsSo-Youn An0https://orcid.org/0000-0002-8395-7881Myung-Jin Lee1https://orcid.org/0000-0002-9267-4947Youn-Soo Shim2https://orcid.org/0000-0002-2894-2441Department of Pediatric Dentristry & Wonkwang Bone Regeneration Research Institute, College of Dentistry, Wonkwang University, Daejeon 35233, KoreaDepartment of Dental Hygiene, Baekseok University, Cheonan 31065, KoreaDepartment of Dental Hygiene, Sunmoon University, Asan 31460, KoreaBackground: The purpose of this study was to evaluate the composition of the crystal phases of various calcium silicate-based materials (CSMs): ProRoot white MTAⓇ (mineral trioxide aggregate) (WMTA), Ortho MTAⓇ (OM), Endocem MTAⓇ (EM), Retro MTAⓇ (RM), Endocem ZrⓇ (EN-Z), BiodentineTM (BD), EZ-sealTM (EZ), and OrthoMTA III (OM3).Methods: In a sample holder, 5 g of the powder sample was placed and the top surface of the material was packed flat using a sterilized glass slide. The prepared slides were mounted on an X-ray diffraction (XRD) instrument (D8 Advance; Bruker AXS GmbH, Germany). The X-ray beam 2θ angle range was set at 10∼90o and scanned at 1.2o per minute. The Cu X-ray source set to operate at 40 kV and 40 mA in the continuous mode. The peaks in the diffraction pattern of each sample were analyzed using the software Diffrac (version 2.1). Then, the peaks were compared and matched with those of standard materials in the corresponding Powder Diffraction File (PDF-2, JCPDS International Center for Diffraction Data). A powder samples of the materials were analyzed using XRD and the peaks in diffraction pattern were compared to the Powder Diffraction File data.Results: Eight CSMs showed a similar diffraction pattern because their main component was calcium silicate. Eight CSMs showed similar diffraction peaks because calcium silicate was their main component. Two components were observed to have been added as radiopacifiers: bismuth oxide was detected in WMTA, OM, and EM while zirconium oxide was detected in RM, EN-Z, BD, EZ, and OM3. Unusual patterns were detected for the new material, OM3, which had strong peaks at low angles.Conclusion: It was caused by the presence of Brushite, which is believed to have resulted in crystal growth in a particular direction for a specific purpose.calcium silicatemineral trioxide aggregateroot canal filling materialsx-ray diffraction analysis
spellingShingle So-Youn An
Myung-Jin Lee
Youn-Soo Shim
X-Ray Diffraction Analysis of Various Calcium Silicate-Based Materials
치위생과학회지
calcium silicate
mineral trioxide aggregate
root canal filling materials
x-ray diffraction analysis
title X-Ray Diffraction Analysis of Various Calcium Silicate-Based Materials
title_full X-Ray Diffraction Analysis of Various Calcium Silicate-Based Materials
title_fullStr X-Ray Diffraction Analysis of Various Calcium Silicate-Based Materials
title_full_unstemmed X-Ray Diffraction Analysis of Various Calcium Silicate-Based Materials
title_short X-Ray Diffraction Analysis of Various Calcium Silicate-Based Materials
title_sort x ray diffraction analysis of various calcium silicate based materials
topic calcium silicate
mineral trioxide aggregate
root canal filling materials
x-ray diffraction analysis
work_keys_str_mv AT soyounan xraydiffractionanalysisofvariouscalciumsilicatebasedmaterials
AT myungjinlee xraydiffractionanalysisofvariouscalciumsilicatebasedmaterials
AT younsooshim xraydiffractionanalysisofvariouscalciumsilicatebasedmaterials