Managing the Heat Release of Calcium Sulfoaluminate Cement by Modifying the Ye'elimite Content.

Nowadays, calcium sulfoaluminate cement (CSA) is garnering a large amount of attention worldwide and is being promoted as a sustainable alternative to Portland cement for specific applications. This study aimed to control the heat release of CSA cement paste by choosing the appropriate composition. For this purpose, different calcium sulfoaluminate clinkers with up to 75 wt. % of ye'elimite were synthetized. Then, a reactivity study on the synthesized clinkers was conducted while varying the amount of gypsum added. The heat of hydration was measured by isothermal calorimetry. The influence of the ye'elimite content on the heat release and on the compressive strength was investigated. According to the findings, the amount of ye'elimite in the cement has a direct relationship with the heat release. The heat release as well as the mechanical performance increase with the increase in the ye'elimite content in the CSA cement. An equation allowing the prediction of the total heat release after 24 h is provided. Such data can be of particular interest to consultants aiming at the reduction of thermal cracking in massive concrete.

Design and Manufacturing of Si-Based Non-Oxide Cellular Ceramic Structures through Indirect 3D Printing.

Additive manufacturing of Polymer-Derived Ceramics (PDCs) is regarded as a disruptive fabrication process that includes several technologies such as light curing and ink writing. However, 3D printing based on material extrusion is still not fully explored. Here, an indirect 3D printing approach combining Fused Deposition Modeling (FDM) and replica process is demonstrated as a simple and low-cost approach to deliver complex near-net-shaped cellular Si-based non-oxide ceramic architectures while preserving the structure. 3D-Printed honeycomb polylactic acid (PLA) lattices were dip-coated with two preceramic polymers (polyvinylsilazane and allylhydridopolycarbosilane) and then converted by pyrolysis respectively into SiCN and SiC ceramics. All the steps of the process (printing resolution and surface finishing, cross-linking, dip-coating, drying and pyrolysis) were optimized and controlled. Despite some internal and surface defects observed by topography, 3D-printed materials exhibited a retention of the highly porous honeycomb shape after pyrolysis. Weight loss, volume shrinkage, roughness and microstructural evolution with high annealing temperatures are discussed. Our results show that the sacrificial mold-assisted 3D printing is a suitable rapid approach for producing customizable lightweight highly stable Si-based 3D non-oxide ceramics.

Investigation of the structure and compressive strength of a bioceramic root canal sealer reinforced with nanomaterials.

OBJECTIVES: A root canal sealer that can increase the resistance of endodontically treated teeth to compressive strength would be of great advantage. The purpose of this study is to use three different nanoparticles: multi-walled carbon nanotubes (MWCNTs), Titanium carbides (TC), and Boron nitrides (BN) into a bioceramic adhesive root canal sealer; BioRoot™ RCS, in an attempt to improve its structural and compressive strength properties. METHODS: Three composites of two weight fractions (1- and 2-wt.%) were produced by mixing each nanomaterial separately with a pre-weighed mass of Bioroot powder. The microstructural properties and compressive strength of the different hardened composites obtained were investigated. The composites have been characterized by X-ray Diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy. Compression testing was performed. RESULTS: The 1-wt.% composites, Bioroot/MWCNTs, and Bioroot/TC, except for the one reinforced with BN, displayed a significant improvement in the compressive strength compared to pristine BioRoot™ RCS. The 2-wt.% composites showed no significant improvement in the compressive strength. CONCLUSION: The addition of 1-wt.% MWCNTs and TC nanomaterials can be considered in the future for enhancing the microstructure and compressive strength properties of pristine BioRoot™ RCS.

Effect of sintering temperature on the physiochemical properties, microstructure, and compressive strength of a bioceramic root canal sealer reinforced with multi-walled carbon nanotubes and titanium carbide.

AIM: Bioceramic root canal sealers like BioRoot RCS have received significant attention for use in endodontics. The addition of a nanophase material like multi-walled carbon nanotubes (MWCNTs) and titanium carbide (TC) to its matrix combined with pressureless sintering might have the potential for improved physiochemical, microstructure, and compressive strength properties. METHOD: ology: MWCNTs and TC nanomaterials were added at a percentage of 1 wt% to a definite weight of pristine BioRoot RCS. Two composites were prepared by ball milling followed by pressureless sintering in static nitrogen at temperatures 600 °C and 800 °C. The setting time, solubility, pH, compressive strength, and density were determined and compared to pristine BioRoot RCS. The microstructural properties of the composites were investigated by XRD, FTIR, Raman spectroscopy, and SEM. RESULTS: The final setting time before and after sintering at 600 °C of the composites was accelerated compared to Bioroot RCS (p = 0.016). The solubility of Bioroot/TC sintered at 600 °C was the lowest (p = 0.07) and its compressive strength was the highest among the sintered samples (p = 0.01). The incorporation of MWCNTs and TC had a significant increase in the compressive strength of Bioroot RCS (p < 0.05). CONCLUSION: The obtained results support the addition of nanomaterials to Bioroot RCS and the use of pressureless sintering.

Physiochemical properties of a bioceramic-based root canal sealer reinforced with multi-walled carbon nanotubes, titanium carbide and boron nitride biomaterials.

AIM: Bioceramic-containing root canal sealers are the most recently introduced sealers in endodontics. The present work reported experiments on a bioceramic-based root canal sealer with the objective of improving its physiochemical properties via reinforcement with each one of the three different nanomaterials: multi-walled carbon nanotubes (MWCNTS), titanium carbide (TC) or boron nitride (BN) in two weight percentages (1 wt% and 2 wt%). METHODOLOGY: Each nanomaterial was added to a definite weight of BioRoot root canal sealer (BioRoot™ RCS, Septodont, Saint-Maur-des-Fossés, France). Three composite groups of each weight percentage were prepared for evaluation: BioRoot/MWCNTS, BioRoot/TC and BioRoot/BN. The initial and final setting times, solubility, elution and pH values of the freshly-mixed and set samples were evaluated and compared to pristine BioRoot™ RCS. Setting times were evaluated using Gilmore needles. Solubility and elution were determined after immersion in water for 24 h. Scanning electron microscopy was used to examine the microstructure of the composite materials. RESULTS: The 1-wt. % composites possessed significantly shorter initial and final setting times compared with the pristine BioRoot™ RCS (p < 0.05). The 2-wt.% composites exhibited longer initial setting times but significantly shorter final setting times than BioRoot RCS (p < 0.05). Most of the composites had relatively lower solubility and elution profiles, with BioRoot/1-wt.% TC and BioRoot/1-wt.% BN being the lowest (p < 0.05). BioRoot™ RCS and all composites exhibited an alkaline pH profile over a period of 4 weeks and a significantly higher alkaline pH (p < 0.05) was recorded for BioRoot/1-wt.% and Bioroot/2-wt.% TC. CONCLUSIONS: A bioceramic-containing root canal sealer (BioRootTM RCS) with a shorter setting time, an alkaline pH profile, and a relatively lower solubility may be developed by incorporation of nanomaterials.

The Mg-Rich Phase NdNiMg15: Structural and Magnetic Properties.

The intermetallic NdNiMg15 is the Mg-richest phase (more than 88 atom % of Mg) discovered in the Mg-Nd-Ni system. Its structure was determined by X-ray diffraction on single crystal with the following crystal data: tetragonal system, P4/ nmm, Z = 2, a = 10.0602(1) Å, c = 7.7612(2) Å, dcalc = 2.40 g·cm-3. Its structure is made of a three-dimensional framework of magnesium atoms showing channels filled by one-dimensional chain consisting of alternating Nd and Ni atoms along the c-axis. Anti-ferromagnetic ordering was observed with TN = 9 K, which is remarkably high considering the long distances between magnetic atoms, that is, Nd atoms. The effective magnetic moment µeff is equal to 3.58 µB, which is consistent with magnetic Nd3+ ions and weakly or nonmagnetic Ni atoms. Below TN, the M( H) curves show field-induced metamagnetic transitions at critical fields increasing with decreasing temperatures. The magnetic structure of NdNiMg15 was determined from neutron powder diffraction data by considering the propagation vector k = (1/2 1/2 0). This magnetic structure consists in ferromagnetic chains along the c-axis of Nd atoms carrying moments, only separated by Ni atoms. The chains are ferromagnetically coupled within planes perpendicular to the [110] direction, and these planes are anti-ferromagnetically coupled to neighboring planes forming a checkerboard-like magnetic structure.