Preparation of magnesium potassium phosphate cement using by-product MgO from Qarhan Salt Lake for low-carbon and sustainable cement production.

Herein, to reduce CO2 emissions and energy consumption and to promote the recycling of waste resources, two types of boron-containing MgO by-products, which were obtained by lithium extraction from Qarhan Salt Lake, China, were used as substitutes for dead-burned MgO to prepare magnesium phosphate potassium cement (MKPC) as a rapid repair material. First, the phase composition and particle-size distribution of the MgO by-product were investigated. The effects of different MgO sources, molar ratio of MgO to KH2PO4 (M/P), and curing age on the setting time and mechanical properties of MKPC were then studied. Based on the results, the mix proportion of MKPC was optimized. Finally, X-ray diffractometry, scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS), differential thermogravimetric (DTG) analysis, and mercury intrusion porosimetry were used to characterize the phase and microstructure evolution of MKPC prepared with different MgO contents. The results demonstrated that the by-product MgO prolonged the setting time of MKPC to more than 40 min. In addition, in the initial stage of hydration, the compressive strength of the MgO by-product was slightly lower than that of the dead-burned MgO; however, with increasing age, the mechanical properties of MKPC prepared by by-product MgO were excellent (up to 60 MPa). The phase and microstructure results revealed that the main hydration product of MKPC prepared using the three types of MgO was MgKPO4·6H2O. Combined with the physical and chemical properties of the raw materials, it was confirmed that the larger particle size and the coexisting impurities from the salt lake were the main reasons for the longer setting time of the MKPC prepared by the by-product MgO. We believe that this research will be of great significance for the preparation of low-carbon, low-cost, and high-performance MKPC materials.

Use of a Piezoelectric Bender Element for the Determination of Initial and Final Setting Times of Metakaolin Geopolymer Pastes, with Applications to Laterite Soils.

This study proposes the use of a non-destructive testing technique, based on piezoelectric bender element tests, to determine the initial and final setting times of metakaolin geopolymer pastes. (1) Background: Metakaolin geopolymer is a new eco-friendly building material that develops strength rapidly and is high in compressive strength. (2) Methods: The initial and the final setting times were investigated via bender element and Vicat needle tests. Metakaolin powder was prepared by treating kaolin at 0, 200, 800, 1000, and 1200 °C. All metakaolin powder samples were then mixed with geopolymer solution at different mixing ratios of 0.8:1.0, 1.0:1.0, 1.2:1.0, and 1.5:1.0. The geopolymer solution was prepared by adding 10 normal concentrations of sodium hydroxide (10 N NaOH) to sodium silicate (Na2SiO3) at various solution ratios of 1.0:1.0, 1.0:1.2, 1.0:1.5, 1.0:2.0, 1.2:1.0, 1.5:1.0 and 2.0:1.0. (3) Results: The optimum temperature for treating metakaolin is established at 1000 °C, with a mixing ratio between the metakaolin powder and the geopolymer solution of 1.0:1.0, as well as a solution ratio between NaOH and Na2SiO3 of 2.0:1.0. (4) Conclusions: The use of piezoelectric bender elements to determine the initial and final setting times of metakaolin geopolymer pastes is a useful method by which to detect geopolymerization by shear wave velocity in a real-time manner. Moreover, the penetration of the Vicat apparatus can confirm the setting times at specific intervals. The relationships between the shear wave velocity and the Vicat penetration appear to be linear, with an initial setting time of 168 m/s and a final setting time of 187 m/s. Finally, the optimum metakaolin geopolymer pastes are applied to improve laterite soils, as measured by CBR tests.

An ultrasonic-based experimental model to evaluate the setting time of endodontic sealers.

AIM: To evaluate an ultrasonic-based experimental model (US), to assess the setting time of AH Plus® , Bio-C Sealer® and MTA Fillapex® , and compare the results obtained with ANSI/ADA specifications (2012). METHODS: To determine the setting time according to the ANSI/ADA specification, moulds measuring 10 mm (diameter) × 2 mm (thickness) were used, and for the US tests a transducer (1 MHz) and an oscilloscope were used. Fourier-transform infrared spectroscopy (FTIR) was used to evaluate the changes on chemical structure at the different setting times found by the US and ANSI/ADA methods. After checking the normal distribution, setting time data were analysed using unilateral analysis of variance with Tukey-HSD post-test to compare the methods. RESULTS: AH Plus® and Bio-C Sealer® had longer mean setting time values for the US method than for the ANSI/ADA (p < .05), whilst for MTA Fillapex® no significant difference was found between the methods (p < .05). FTIR spectra demonstrated that at the setting time determined by the US method, AH Plus® and Bio-C Sealer® were in a more advanced stage of polymerization than at the ANSI/ADA, whilst there was no significant difference for MTA Fillapex® . CONCLUSIONS: The use of US was effective for setting time determination and measured longer values than ANSI/ADA specification for AH Plus® and Bio-C Sealer® , identifying the entire (and not only superficial) setting of the endodontic sealers.

Effect of heat application on the physical properties and chemical structure of calcium silicate-based sealers.

OBJECTIVE: To determine the effect of heat application on the setting and chemical properties of HiFlow BC Sealer and compare to other calcium silicate (CSBS) and epoxy resin-based root canal sealers. MATERIALS AND METHODS: AH Plus, BioRoot RCS (BioRoot), Endosequence BC (Endosequence), and HiFlow BC (HiFlow) sealers were placed at 37 °C or subjected to heat at 200 °C for 10 or 30 s, followed by incubation at 37 °C in a humidified incubator during experiments. Setting time, viscosity, and flow were assessed, and changes in chemical structure were evaluated using the Fourier-transform infrared spectroscopy (FTIR). Thermogravimetric analysis was also used to evaluate the weight change (%) of the sealers upon heating from room temperature to 37 °C or 200 °C at a rate of 20 °C/min. Data were analyzed using a two-way ANOVA with a Bonferroni post-hoc test (p = 0.05). RESULTS: Application of heat extended the setting time for Endosequence and HiFlow but resulted in a faster setting of AH Plus and BioRoot. The highest flow and lower viscosity were observed in HiFlow at high temperature (p < 0.05), whereas the lowest flow with the highest viscosity and greatest weight loss were observed in BioRoot after heat application (p < 0.05). FTIR spectra demonstrated no changes to functional groups after heat application, except for the strong H-O-H absorption peak corresponding to water in BioRoot. CONCLUSIONS: Endosequence and HiFlow showed similar chemical properties with a higher flow and lower viscosity in HiFlow after heat application. Heat application resulted in reduced flow, increased viscosity, and weight loss for BioRoot. The setting of AH Plus was fastened with heat, while its weight loss, viscosity, and flow characteristics were stable. CLINICAL RELEVANCE: HiFlow, Endosequence, and AH Plus can be all used with WVC obturation techniques. Heat application resulted in minor changes in their physical properties including setting time, flow, weight loss, and chemical properties, while BioRoot showed a significant amount of weight loss, increase in viscosity, and reduced flowability after heat application.

Determining the setting of root canal sealers using an in vivo animal experimental model.

OBJECTIVES: To present and explore the potential of an animal-based experimental model developed to determine the set of root canal sealers in vivo. The setting of AH Plus, BioC Sealer, TotalFill BC Sealer, and Sealapex was determined using either ISO 6876 or the novel in vivo method proposed in this study. MATERIAL AND METHODS: The in vitro setting time of the sealers tested was determined in accordance with ISO 6876:2012. In determining the in vivo set, 24 adult Wistar rats were followed up for two evaluation periods: 1 and 4 weeks. Their upper-right incisor was extracted, and its pulp tissue was removed. The root canal was then filled from retrograde with one of the 4 sealers, and the tooth was re-implanted and fixed with a layer of a flowable composite resin. After 1 or 4 weeks of the surgical procedures, the animals were euthanized, and their incisors were extracted. Two-mm-thick slices of the middle third of the tooth root were obtained and assessed with a Gillmore device, to determine whether or not the sealer had set. RESULTS: The following in vitro results were obtained by using ISO 6876 methodology: AH Plus set after a mean time of 423 ± 20 min and 476 ± 35 min, in metal and plaster molds, respectively. BioC Sealer set after 7 days (in dental plaster molds), whereas TotalFill BC Sealer and Sealapex did not set even after 25 days in both tested conditions (metal or dental plaster molds). Using the novel in vivo methodology, AH Plus, BioC Sealer, and TotalFill BC Sealer set after both 7 and 30 days. In contrast, Sealapex did not set at either time point. CONCLUSIONS: AH Plus and BioC Sealer set under both in vitro and in vivo test conditions. TotalFill BC Sealer did not set under in vitro conditions but did after 1 week under in vivo conditions. Sealapex did not set under either in vitro or in vivo conditions. CLINICAL RELEVANCE: The influence of the testing conditions on the setting results is a clear indication that new in vivo experimental models should be useful in future studies on Bioceramics root canal sealers.

Effect of exposure to etidronic acid on the bond strength of calcium silicate-based cements after 1 and 21 days: an in vitro study.

BACKGROUND: After reparation of root perforations with calcium silicate-based cements (CSBC), the surface of the material is expected to be exposed to root canal irrigants (RCI) while resuming the root canal treatment. METHODS: The aim of this study was to compare the effect of exposure to a mixture of sodium hypochlorite (NaOCl) and etidronic acid (HEBP) or other irrigants on the Push Out Bond Strength (POBS) of CSBC after two different setting times. 240 root slices 1 mm thick were obtained from single-rooted human teeth. A 1.4 mm diameter perforation was performed on each slice and filled with Biodentine (BD) or ProRoot MTA (PMTA). After 1 or 21 days they were exposed to 17% ethylenediaminetetraacetic acid, 5.25% NaOCl, a mixture of 5.25% NaOCl and 9% HEBP (NaOCl + HEBP) or saline (n = 15) and submitted to a push-out test. POBS results were analysed with ANOVA and Tukey tests. RESULTS: BD showed higher POBS than PMTA after 1 day (p < .05). After 21 days no differences were found between materials. After 1 day exposure to NaOCl + HEBP resulted in higher POBS, compared to the other irrigants (p < .05). CONCLUSION: POBS results are influenced by the cement, the setting time and the exposure to irrigants.

Thermal effect of light irradiation time on the setting time of mineral trioxide aggregate and calcium-enriched mixture cements.

This study aimed to assess the thermal effect of different light irradiation times on the setting time of mineral trioxide aggregate (MTA) and calcium-enriched mixture (CEM) cements. This in vitro experimental study evaluated 40 hydraulic cement specimens, including 20 MTA and 20 CEM specimens, according to the manufacturers'instructions. For each cement, the specimens were divided into 3 test groups light cured with a halogen light-curing unit (n = 5 per group) and 1 control group (n = 5) that was not exposed to irradiation. The specimens in the MTA test groups were light cured for 20, 40, or 60 seconds, and the specimens in the CEM test groups were light cured for 60, 90, or 120 seconds. All test and control groups had 60 seconds of rest time. Setting of the cements was assessed at different timepoints using a Gillmore needle weighing 113.4 g with a 12.2-mm diameter according to ASTM C266-03 standards. The data were analyzed with the Fisher exact test and the Mann-Whitney U test (α = 0.05). The setting of MTA specimens after different curing times was significantly different (P < 0.05). The setting time of MTA control specimens was significantly longer than that of test specimens (P = 0.008). The setting of CEM specimens after different curing times was not significantly different (P > 0.05). However, the setting time for CEM control specimens was significantly longer than that for test specimens (P = 0.008). Light curing with a halogen light-curing unit can significantly decrease the setting time for MTA and CEM cements.

Effects of fast- and slow-setting calcium silicate-based root-end filling materials on the outcome of endodontic microsurgery: a retrospective study up to 6 years.

OBJECTIVES: The purpose of this retrospective study was to evaluate and compare the effects of fast- and slow-setting calcium silicate-based materials (CSMs) used for root-end filling on the outcome of endodontic microsurgery. MATERIALS AND METHODS: We searched a clinical database for patients who had received endodontic microsurgery between 2001 and 2016. Included cases were divided into two groups according to the type of CSM used for root-end filling: slow-setting CSM (SCSM) and fast-setting CSM (FCSM). The cases in two groups were subjected to 1:1 nearest neighbor propensity score matching for the following variables: age, sex, tooth type, quality of canal filling, lesion type, and postoperative restoration. For each matched case, the outcome was determined as success or failure according to clinical and radiographic evaluations performed at least 1 year after surgery. Multivariate logistic regression analysis was performed to identify prognostic factors and estimate their effects. RESULTS: In total, 304 cases of endodontic microsurgery (179 SCSM and 125 FCSM) were identified, and 1:1 propensity score matching finally included 122 cases from each group. After matching, all covariates were associated with an absolute standardized difference of < 0.1. The overall success rates were 85.2% and 93.4% for the SCSM and FCSM groups, respectively (p = 0.062). Age, tooth type, lesion type, and CSM type were significantly associated with the outcome of endodontic microsurgery (p < 0.05). CONCLUSIONS: Within the limitations, the outcome of endodontic microsurgery using FCSMs was comparable with that of SCSMs. The findings suggest that the type of CSM used for root-end filling, particularly in terms of the initial setting time, could affect the outcome of endodontic microsurgery. CLINICAL RELEVANCE: FCSMs could be considered for use as root-end filling materials in endodontic microsurgery, particularly in complicated clinical situations which require rapid initial setting of the materials.

Bone tissue reaction, setting time, solubility, and pH of root repair materials.

OBJECTIVES: This study aims to compare the bone tissue reaction, setting time, solubility, and pH of NeoMTA Plus, Biodentine (BD), and MTA Angelus (MTA-A). MATERIALS AND METHODS: Initial and final setting times (n = 7) and solubility up to 7 days (n = 11) were evaluated in accordance with ASTM C266-15 and ANSI/ADA Specification No. 57, respectively. pH (n = 10) was measured up to 28 days. Bone tissue reactions in 48 rats' femur were histologically analyzed after 7, 30, and 90 days. ANOVA and Tukey's tests compared setting time, solubility, and pH data; bone reactions data were compared by Kruskal-Wallis and Dunn's tests. RESULTS: NeoMTA Plus had longer initial and final setting times than MTA-A and BD (P < 0.05). At 7 days, BD showed the highest solubility, similar to NeoMTA Plus (P > 0.05) and different from MTA-A (P < 0.05). NeoMTA Plus had a progressive mass loss over time; at 7 days, it was significantly different from the initial mass (P < 0.05). BD showed higher pH in the periods assessed when compared to the other materials (P < 0.05). Bone tissue repair had no differences between groups in each experimental period (P > 0.05). All groups presented no difference from 30 to 90 days (P > 0.05) and had better bone repair at 90 days than at 7 days (P < 0.05). CONCLUSIONS: NeoMTA Plus, BD, and MTA-A showed satisfactory setting time, high mass loss, alkaline pH, and allowed bone repair. CLINICAL RELEVANCE: Calcium silicate-based cements are indicated for multiple clinical situations. NeoMTA Plus and BD showed satisfactory physical-chemical and biological properties, being considered as alternatives to MTA-A, as root repair materials for clinical use.

Effect of different zinc concentrations on partially-stabilized cement for vital pulp therapy.

BACKGROUND/PURPOSE: We have developed and investigated the partially-stabilized cements (PSC) with Zn for vital pulp therapy due to their short setting time and high cell biocompatibility. However, the effect of PSC with different concentrations of Zn on setting time and biocompatibility remained unknown. Therefore, the purpose of this study was to determine the optimal concentration of Zn to be synthesized with PSC for vital pulp therapy. METHODS: PSC with different weight percentages of Zn (5%, 7%, 10%) were synthesized to attain 5%Zn-PSC, 7%Zn-PSC, and 10%Zn-PSC. The initial and final setting times were measured using the Gillmore needles method, and the compressive strength tests were conducted using a universal testing machine. The phases of Zn-PSC powders were observed using an X-ray diffractometer (XRD). Human dental pulp stem cells (hDPSCs) were used to evaluate the biocompatibility and cytotoxicity of the materials via Alamar blue and LDH assays. Mineral trioxide aggregate (MTA) was used to be compared with Zn-PSC samples. RESULTS: The initial and final setting times of PSC with different concentrations of Zn were reduced considerably compared to those of MTA. The results also indicated that the initial and final setting times decreased as the weight % of Zn increased. 5%Zn-PSC had the highest compressive strength among all tested materials. 5%Zn-PSC samples also displayed comparatively higher cell biocompatibility than 7% and 10% Zn-PSC samples. However, there was no significant difference between the 5%Zn-PSC and MTA in cell biocompatibility. In addition, the results of the LDH release assay indicated a low level of cytotoxicity among all the test samples. CONCLUSION: 5%Zn-PSC has a shorter setting time, better mechanical properties, and good biocompatibility and thus it has great potential for vital pulp therapy.

Comparison of Setting Time of White Mineral Trioxide Aggregate with and without Disodium Hydrogen Phosphate at Different Liquid-to-powder Ratios.

AIM: The present study was conducted with the objective of evaluating the effect of different liquid-to-powder ratios on setting time of white mineral trioxide aggregate (WMTA) and the effect of adding disodium hydrogen phosphate (Na2HPO4) to white MTA (NAMTA). MATERIALS AND METHODS: Sixty samples were prepared in plastic annular molds with a diameter of 10 mm and a height of 2 mm in order to record setting time where white MTA was placed in 30 samples and 2.5 wt% mixture of Na2HPO4 with white MTA was placed in other 30 samples. Setting times in different ratios of liquid to powder (50, 60, and 70%) and at different times including 5, 10, 15, 20, 25, 30, 40, and 50 minutes as well as 1, 1.5, 2.5, 3, 3.5, and 4 hours were measured with Vicat. Statistical Package for the Social Sciences version 16 software was used to examine the differences between groups. The values of p < 0.05 were considered to be statistically significant in this study. RESULTS: The average setting time of samples in two WMTA and NAMTA was 182.17 ± 57.86 and 67.00 ± 14.42 respectively, and this difference was statistically significant (p < 0.001). Also, the average setting time of samples in ratio groups of 50, 60, and 70% were 146.00 ± 75.90, 85.00 ± 31.71, and 142.5 ± 64.47 respectively, and results showed that there was no significant difference between groups. CONCLUSION: Adding 2.5 wt% of Na2HPO4 mixture to white MTA reduces the setting time, which is lower than the WMTA in 50, 60, and 70% liquid-to-powder ratios. CLINICAL SIGNIFICANCE: According to the findings of this study, it can be seen that adding Na2HPO4 to white MTA is a good way to reduce setting timing in clinical dentistry, especially in one-visit treatments.

The Influence of Nitrile Gloves on the Setting Behavior of Polyvinyl Siloxane Putty Impression Materials.

OBJECTIVE: The purpose of this study was to assess the gelation and polymerization time of three polyvinyl siloxane (PVS) putty materials and to determine if those times were affected by nitrile gloves under different conditions. MATERIALS AND METHODS: Ten specimens (n=10) were obtained for each PVS putty material (Express STD, 3M ESPE; Extrude Xtra, Kerr and Exafast, GC) and tested under different conditions (gloves washed, gloves unwashed and hands contaminated). The gelation and polymerization time were measured using an oscillating rheometer and recorded for 400 s at 37°C to simulate the oral environment. RESULTS: The mean gelation time of hand contaminated specimens was 157.50 minutes and was significantly slower than that by using nitrile washed gloves (mean=117.94, p=.004) and by using unwashed gloves (mean=99.46, p⟨0.001). Unwashed gloves had significantly quicker gelation times compared to washed gloves (p=.046). The gelation time was significantly delayed with Exafast compared to Extrude Xtra and Express STD across all the different types of glove conditions (p⟨0.043). No significant differences were observed between polymerization time with Exafast and Extrude Xtra Putty. CONCLUSIONS: Extrude Xtra putty material had significantly better performance than GC Exafast and Express. Hand contaminated specimens were affected by the gelation/polymerization time.

Physicochemical properties of calcium silicate cements associated with microparticulate and nanoparticulate radiopacifiers.

OBJECTIVES: The objective of this paper was to evaluate the physicochemical properties of calcium silicate cements with different chemical compositions, associated with radiopacifying agents. MATERIALS AND METHODS: Mineral trioxide aggregate (MTA) Angelus, calcium silicate cement with additives (CSC), and resinous calcium silicate cement (CSCR) were evaluated, with the addition of the following radiopacifiers: microparticles (micro) or nanoparticles (nano) of zirconium oxide (ZrO(2)), niobium oxide (Nb(2)O(5)), bismuth oxide (Bi(2)O(3)), or calcium tungstate (CaWO(4)). Setting time was evaluated using Gilmore needles. Solubility was determined after immersion in water. The pH and calcium ion release were analyzed after 3, 12, and 24 h and 7, 14, and 21 days. The data obtained were submitted to analysis of variance and Tukey's test, at a level of significance of 5 %. RESULTS: CSC + CaWO(4) and CSCR + ZrO(2) micro, Nb(2)O(5) and CaWO(4) presented results similar to MTA, with a shorter final setting time than the other associations. CSC and CSCR+ ZrO(2) micro presented a higher degree of flow. All the cements evaluated presented low solubility. The materials presented alkaline pH and released calcium ions. CONCLUSIONS: ZrO(2) micro radiopacifier may be considered a potential substitute for Bi(2)O(3) when associated with CSC or CSCR. CLINICAL RELEVANCE: The proposed materials, especially when associated with ZrO(2), are potential materials for use as alternatives to MTA.

Evaluation of selected properties of a new root repair cement containing surface pre-reacted glass ionomer fillers.

OBJECTIVE: This study evaluated selected properties of a prototype root repair cement containing surface pre-reacted glass ionomer fillers (S-PRG) in comparison to mineral trioxide aggregate (MTA) and intermediate restorative material (IRM). MATERIALS AND METHODS: The antibacterial effect of S-PRG, MTA, and IRM cements was tested against Porphyromonas gingivalis and Enterococcus faecalis after 1 and 3 days of aging of the cements. The set cements were immersed in distilled water for 4 h to 28 days, and ion-releasing ability was evaluated. Initial and final setting times of all cements were evaluated using Gilmore needles. The push-out bond strength between radicular dentin and all cements was tested at different levels of the roots. RESULTS: S-PRG and IRM cements, but not MTA cement, demonstrated significant antibacterial effect against P. gingivalis. All types of cements exhibited significant antibacterial effect against E. faecalis without being able to eliminate the bacterium. S-PRG cement provided continuous release of fluoride, strontium, boron, sodium, aluminum, and zinc throughout all tested time points. Both initial and final setting times were significantly shorter for S-PRG and IRM cements in comparison to MTA. The push-out bond strength was significantly lower for S-PRG cement in comparison to MTA and IRM at coronal and middle levels of the roots. CONCLUSIONS: S-PRG cement demonstrated significant antibacterial effects against endodontic pathogens, multiple ion-releasing ability, relatively short setting time, and low bonding strength. CLINICAL RELEVANCE: S-PRG cement can be used as a one-visit root repair material with promising antibacterial properties and ion-releasing capacity.

Influence of Thermal Treatment Conditions on the Properties of Dental Silicate Cements.

In this study the sol-gel process was used to synthesize a precursor mixture for the preparation of silicate cement, also called mineral trioxide aggregate (MTA) cement. This mixture was thermally treated under two different conditions (1400 °C/2 h and 1450 °C/3 h) followed by rapid cooling in air. The resulted material (clinker) was ground for one hour in a laboratory planetary mill (v = 150 rot/min), in order to obtain the MTA cements. The setting time and mechanical properties, in vitro induction of apatite formation by soaking in simulated body fluid (SBF) and cytocompatibility of the MTA cements were assessed in this study. The hardening processes, nature of the reaction products and the microstructural characteristics were also investigated. The anhydrous and hydrated cements were characterized by different techniques e.g., X-ray diffraction (XRD), scanning electron microscopy (SEM), infrared spectroscopy (FT-IR) and thermal analysis (DTA-DTG-TG). The setting time of the MTA cement obtained by thermal treatment at 1400 °C/2 h (MTA1) was 55 min and 15 min for the MTA cement obtained at 1450 °C/3 h (MTA2). The compressive strength values were 18.5 MPa (MTA1) and 22.9 MPa (MTA2). Both MTA cements showed good bioactivity (assessed by an in vitro test), good cytocompatibility and stimulatory effect on the proliferation of cells.

Viscosity of dysphagia-oriented cold-thickened beverages: effect of setting time at refrigeration temperature.

BACKGROUND: Although extensive literature is available on the viscosity of thickened beverages with food thickeners, no attempt has been made to study the effect of setting time on the viscosity of pudding-like cold-thickened beverages with xanthan gum (XG)-based thickeners by using a rheometer. In particular, it is of considerable practical importance to investigate the effect of setting time on their viscosity at 5°C because some cold-thickened beverages will be prepared in the kitchen in bulk and stored at 5°C before serving or consuming rather than serving immediately upon mixing with thickeners. AIMS: To examine the effect of different setting times (15-120 min) on the viscosity of cold-thickened beverages prepared with various XG-based food thickeners, and also to compare the viscosity differences among the various cold beverages and XG-based food thickeners in beverage-thickener mixture systems. METHODS & PROCEDURES: Four commercially available XG-based food thickeners (A-D) and three cold beverages (water, orange juice and milk) were used for the preparation of cold-thickened beverages. The thickened sample was portioned into six samples for the designated setting times and then stored at 5°C over setting time. Their apparent viscosity (η(a,50)) at 50 s(-1) was measured using a rheometer. OUTCOMES & RESULTS: The largest increases in η(a,50) values for thickened beverages, except for water, were observed at 15 min (p < 0.05), showing a pudding-like fluid, and at longer time periods their η(a,50) values gradually increased or were constant with an increase in setting time. The percentage increase in viscosity values at different setting times (15-120 min) as compared with the control (0 min) was less pronounced in the thickened orange juice and milk samples with thickener A over setting time, indicating that the thickened beverages with thickener A had more stable structure compared with those with other thickeners (B-D) over time. Statistical analysis showed that changes in the viscosity of cold-thickened beverages over setting time are greatly influenced by the type of beverages and thickeners. CONCLUSIONS & IMPLICATIONS: Cold-thickened beverages should be carefully prepared with instant commercial XG-based food thickeners because they produced different thickening patterns over setting time which clinicians must consider for a safe and easy swallowing. The information presented in this study will provide both clinicians and patients with additional knowledge to prepare cold-thickened beverages with the corrected viscosity for safe swallowing.

Addition of benzalkonium chloride to self-adhesive resin-cements: some clinically relevant properties.

OBJECTIVE: The clinical survival rates of the adhesive restorations are limited due to the deterioration of resin-dentin bonds over time, partly due to the endogenous enzymatic activity of dentin. Recently, benzalkonium chloride (BAC) has been shown to effectively inhibit endogenous protease activity of dentin. This study evaluated the effect of different concentrations of benzalkonium chloride (BAC) on the degree of conversion (DC), vickers hardness (VH), setting time (ST) and biaxial flexural strength (FS) of two self-adhesive resin luting cements (RC). METHODS: Two RC SpeedCEM (Ivoclar-Vivadent) and BisCem (Bisco) were modified by addition of 0.1, 0.5, 1, 1.5, 2 wt% BAC. The luting cements without the addition of BAC served as control. The DC (FT-IR/ATR from the bottom of the resin disc), vickers hardness (from top and bottom of the light-cured specimen), setting time (ISO 4049) and biaxial flexural strength (0.6 × 6 mm discs) of the specimens were tested. Data were analyzed using ANOVA and Tukeys HSD. RESULTS: DC results were in the range of 70-80%, with some significant changes in BisCem (p < 0.05). VH values of both materials increased significantly compared to control, with no significant change as the BAC percentage increases. BAC addition influenced the ST differently for both materials. For BisCem, a gradual decrease (p < 0.05) was observed whereas, for SpeedCEM, a gradual increase was observed until 1% BAC (p < 0.05). For FS values, a gradual decrease was observed for both materials with increased amounts of BAC (p < 0.05), compared to the control group. CONCLUSIONS: BAC addition of up to 1% seems to be acceptable considering the properties tested. Clinical significance. Incorporation of benzalkonium chloride to self-adhesive resin luting cements during the mixing procedure does not significantly affect the degree of conversion or flexural strength of the luting agent and may be a good option to improve the durability of adhesive interface.

Effects of various mixing techniques on physical properties of white mineral trioxide aggregate.

INTRODUCTION: The aim of this study was to evaluate the effects of three different mixing techniques on surface microhardness, initial setting time, and phase formation of white mineral trioxide aggregate. METHODS: Twenty-one cylindrical glass tubes were selected and divided into three groups of seven in each (n = 7). White mineral trioxide aggregate (WMTA) in groups A, B, and C were mixed by conventional, trituration, and ultrasonic techniques, respectively. Cements were mixed and packed into the glass tubes and incubated at 37°C for 3 days. After incubation, samples were subjected to microhardness evaluation, and four specimens from each group were prepared and observed under a scanning electron microscopy and X-ray diffraction. For setting time assessment, WMTA was mixed in three parts again, and Gilmore needle test was performed until the initial setting time of cement. Data were analyzed by one-way anova and post hoc Tukey's test. RESULTS: Samples mixed by trituration technique significantly showed the highest microhardness (P < 0.001) and the lowest setting time, while the ultrasonically mixed specimens significantly revealed the highest setting time in comparison with other groups (P < 0.001). Samples mixed by trituration technique showed the highest uniformity in the bulk and highest amount of hydrated calcium silicate (CS) phases, while the lowest value was observed in ultrasonically mixed cements, which also showed the highest amount of anhydrated CS phases. CONCLUSION: Trituration and conventional techniques were more suitable mixing methods for mineral trioxide aggregate in comparison with ultrasonic technique. Trituration resulted in better hydration and crystallization, which prevents clustering of powder and reduces voids and setting time of mixed cement.

Synthesis and Characterization of Sol-Gelled Barium Zirconate as Novel MTA Radiopacifiers.

Barium zirconate (BaZrO3, BZO), which exhibits superior mechanical, thermal, and chemical stability, has been widely used in many applications. In dentistry, BZO is used as a radiopacifier in mineral trioxide aggregates (MTAs) for endodontic filling applications. In the present study, BZO was prepared using the sol-gel process, followed by calcination at 700-1000 °C. The calcined BZO powders were investigated using X-ray diffraction and scanning electron microscopy. Thereafter, MTA-like cements with the addition of calcined BZO powder were evaluated to determine the optimal composition based on radiopacity, diametral tensile strength (DTS), and setting times. The experimental results showed that calcined BZO exhibited a majority BZO phase with minor zirconia crystals. The crystallinity, the percentage, and the average crystalline size of BZO increased with the increasing calcination temperature. The optimal MTA-like cement was obtained by adding 20% of the 700 °C-calcined BZO powder. The initial and final setting times were 25 and 32 min, respectively. They were significantly shorter than those (70 and 56 min, respectively) prepared with commercial BZO powder. It exhibited a radiopacity of 3.60 ± 0.22 mmAl and a DTS of 3.02 ± 0.18 MPa. After 28 days of simulated oral environment storage, the radiopacity and DTS decreased to 3.36 ± 0.53 mmAl and 2.84 ± 0.27 MPa, respectively. This suggests that 700 °C-calcined BZO powder has potential as a novel radiopacifier for MTAs.

The Impact of Nano- and Micro-Silica on the Setting Time and Microhardness of Conventional Glass-Ionomer Cements.

The objective of this study was to investigate the effect of the incorporation of 2, 4 or 6 wt% of amorphous nano- or micro-silica (Aerosil® OX 50 or Aeroperl® 300 Pharma (Evonik Operations GmbH, Essen, Germany), respectively) on the net setting time and microhardness of Ketac™ Molar (3M ESPE, St. Paul, MN, USA) and Fuji IX GP® (GC Corporation, Tokyo, Japan) glass-ionomer cements (GICs) (viz. KM and FIX, respectively). Both silica particles were found to cause a non-linear, dose-dependent reduction in setting time that was within the clinically acceptable limits specified in the relevant international standard (ISO 9917-1:2007). The microhardness of KM was statistically unaffected by blending with 2 or 4 wt% nano-silica at all times, whereas 6 wt% addition decreased and increased the surface hardness at 1 and 21 days, respectively. The incorporation of 4 or 6 wt% nano-silica significantly improved the microhardness of FIX at 1, 14 and 21 days, with no change in this property noted for 2 wt% addition. Micro-silica also tended to enhance the microhardness of FIX, at all concentrations and times, to an extent that became statistically significant for all dosages at 21 days. Conversely, 4 and 6 wt% additions of micro-silica markedly decreased the initial 1-day microhardness of KM, and the 21-day sample blended at 4 wt% was the only specimen that demonstrated a significant increase in this property. Scanning electron microscopy indicated that the nano- and micro-silica particles were well distributed throughout the composite structures of both GICs with no evidence of aggregation or zoning. The specific mechanisms of the interaction of inorganic nanoparticles with the constituents of GICs require further understanding, and a lack of international standardization of the determination of microhardness is problematic in this respect.