scholarly journals The Effect of Simulated Field Storage Conditions on Dental Restorative Materials for Military Field Use

2019 ◽  
Vol 185 (5-6) ◽  
pp. e831-e838
Author(s):  
David J Lemon ◽  
Wen Chen ◽  
Trevor Smith ◽  
April A Ford ◽  
Steven X Moffett ◽  
...  

Abstract Introduction Dental readiness, one critical component of medical readiness, is adversely impacted by dental emergencies. Many dental emergencies require restorative materials such as glass ionomers, resins, and zinc oxide eugenols to remedy them. The Authorized Dental Allowance List (ADAL) and Authorized Medical Allowance List (AMAL) contain the equipment and materials used by Navy dentists to treat Sailors and Marines. These supplies are subjected to harsh storage conditions on deployments. Much is known about how materials behave when stored at room temperature, but less is known about how their properties are affected after exposure to high temperatures and humidity. We subjected five dental restorative materials to storage in aggravated conditions, and then tested them to determine which products are more robust. Materials and Methods Unopened packages of Fuji Triage, Fuji IX GP (both GC America Inc., Alsip, Illinois), TPH Spectra ST Low Viscosity, Intermediate Restorative Material (both Dentsply Sirona, York, Pennsylvania), and Herculite XRV (Kerr Corporation, Orange, California) were exposed to 0, 5, or 10 days’ storage at 30–60°C with 95% relative humidity. After storage in these aggravated conditions, we tested the compressive strength, hardness, elastic modulus, flexural strength, flexural modulus, sorption, and solubility of each material. Results The physical properties of all materials were affected by storage in aggravated conditions, though the properties of some materials degraded more than others. Both glass ionomers, Fuji Triage (P = 0.0012) and Fuji IX GP (P = 0.0031), and the composite Herculite XRV (P = 0.0253) lost compressive strength after 5 or 10 days in aggravated conditions. The hardness values for all materials were affected (P < 0.05) by the aggravated conditions, though the elastic modulus of TPH Spectra was not affected (P > 0.05). None of the materials lost flexural strength (P > 0.05) or had changes in their flexural modulus (P > 0.05). The water sorption behavior of Fuji Triage (P = 0.0426) and Fuji IX GP (P = 0.0201) changed after 10 days of aggravated storage, and the solubility of all materials was altered by the harsh conditions. Conclusion Some materials degrade more than others in aggravated conditions. Both resin composite materials were more resistant to high temperatures and humidity levels than the glass ionomers tested. These changes in physical characteristics should be considered when reviewing or optimizing the ADAL/AMAL for different projected operational environments.

2008 ◽  
Vol 47-50 ◽  
pp. 1339-1342 ◽  
Author(s):  
Zhong Zi Xu ◽  
Qing Lin ◽  
Yan Bao Li ◽  
Xiang Hui Lan ◽  
Chun Hua Lu

The aim of this study was to evaluate the suitability of CaF2 doping tricalcium silicate (Ca3SiO5, C3S) as dental restorative materials. The solid state reaction method was used to prepare CaF2 doping C3S (F-C3S) using CaCO3, SiO2 and CaF2 as the starting materials. The in vitro bioactivity, the rate of heat evolution and the compressive strength were investigated. The in vitro bioactivity was examined by soaking the pastes in simulated body fluid (SBF). The FTIR and SEM results indicated the hydroxycarbonate apatite (HCA) layers of F-C3S pastes and pure C3S pastes occurred after soaking for 1 day and 3 days, respectively. The difference in bioactivity was attributed to the formation of F-substituted apatite, which has a Ksp lower than HCA. As compared with the pure C3S, the rate of heat evolution during the hydration of F-C3S was slower. This was avail to the dimensional stability of dental restorative materials. The pastes of F-C3S had a lower early compressive strength in the early stage, but a higher compressive strength in the later stage. Our results indicated that F-C3S would be bonded better to the teeth because of the earlier formation of HCA and the higher later compressive strength. F-C3S may be a progressive candidate for dental restorative materials.


2022 ◽  
Vol 6 (1) ◽  
pp. 17
Author(s):  
Hiroshi Ikeda ◽  
Yohei Kawajiri ◽  
Minako Kibune Sodeyama ◽  
Haruka Takesue Yano ◽  
Yuki Nagamatsu ◽  
...  

SiO2-poly(2-hydroxyethyl methacrylate) (pHEMA)-based composites have been widely used as biomaterials owing to their biocompatibility. However, they have not yet been applied as tooth restorative materials because of their poor mechanical properties. In the present paper, we develop a novel SiO2/pHEMA-based composite with a polymer-infiltrated network (PICN) structure for use in dental restorative materials. A mixture of SiO2 nanoparticles and a poly(vinyl alcohol) binder was sintered at 950 °C to fabricate a porous SiO2 block. A monomer mixture containing 70 wt%-HEMA/30 wt%-ethylene glycol dimethacrylate and a benzoyl peroxide initiator was infiltrated into the porous SiO2 block and heat-polymerized to fabricate the SiO2/pHEMA-based composite with a PICN structure. The composite was characterized according to its mechanical properties, surface free energy, and bonding properties with a dental adhesive. The flexural strength was 112.5 ± 18.7 MPa, the flexural modulus was 13.6 ± 3.4 GPa, and the Vickers hardness was 168.2 ± 16.1, which are similar values to human teeth. The surface free energy of the polar component of the composite was 19.6 ± 2.5 mN/m, suggesting that this composite has an active surface for bonding with the adhesive. The composite bonded well to the adhesive, in the presence of a silane coupling agent. The SiO2/pHEMA-based composite was demonstrated to be a potential candidate for dental restorative materials.


Author(s):  
Leif Hermansson ◽  
Lars Kraft ◽  
Karin Lindqvist ◽  
Nils Otto Ahnfelt ◽  
Håkan Engqvist

2021 ◽  
Vol 11 (7) ◽  
pp. 3032
Author(s):  
Tuan Anh Le ◽  
Sinh Hoang Le ◽  
Thuy Ninh Nguyen ◽  
Khoa Tan Nguyen

The use of fluid catalytic cracking (FCC) by-products as aluminosilicate precursors in geopolymer binders has attracted significant interest from researchers in recent years owing to their high alumina and silica contents. Introduced in this study is the use of geopolymer concrete comprising FCC residue combined with fly ash as the requisite source of aluminosilicate. Fly ash was replaced with various FCC residue contents ranging from 0–100% by mass of binder. Results from standard testing methods showed that geopolymer concrete rheological properties such as yield stress and plastic viscosity as well as mechanical properties including compressive strength, flexural strength, and elastic modulus were affected significantly by the FCC residue content. With alkali liquid to geopolymer solid ratios (AL:GS) of 0.4 and 0.5, a reduction in compressive and flexural strength was observed in the case of geopolymer concrete with increasing FCC residue content. On the contrary, geopolymer concrete with increasing FCC residue content exhibited improved strength with an AL:GS ratio of 0.65. Relationships enabling estimation of geopolymer elastic modulus based on compressive strength were investigated. Scanning electron microscope (SEM) images and X-ray diffraction (XRD) patterns revealed that the final product from the geopolymerization process consisting of FCC residue was similar to fly ash-based geopolymer concrete. These observations highlight the potential of FCC residue as an aluminosilicate source for geopolymer products.


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