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

Unsupported electrospun membrane for water desalination using direct contact membrane distillation

In this project, an unsupported electrospun poly(vinylidene fluoride)-co-hexafluoropropylene (PVDF-HFP) membrane was used for water desalination using direct contact membrane distillation (DCMD). The membrane was electrospun using a laboratory-scale machine with multiple nozzles that was developed in-house. Critical process parameters, including the applied voltage and polymer concentration, were optimized to obtain bead-free electrospun membranes with fiber diameters less than 300 nm. To improve the membrane thermal stability and performance, the selected electrospun membrane was heat-pressed at 160°C. The untreated and heat-pressed membranes were tested in a DCMD setup at different feed temperatures (60, 70, and 80°C) and feed flow rates (0.4, 0.6, and 0.8 L/min), while maintaining the permeate temperature and flow rate at 20°C and 0.2 L/min, respectively. The modified electrospun membrane exhibited a very high permeate flux (>37.5 kg/m2/h) and a salt rejection rate of 99.99% at a feed temperature of 70°C. The performance of the heat-pressed unsupported PVDF-HFP electrospun membrane was nearly identical to a commercially available polytetrafluoroethylene (PTFE) supported membrane. These promising results demonstrate that relatively low-cost electrospun membranes can be easily produced and successfully used in DCMD to minimize the capital cost and increase the energy efficiency of the process.Peer reviewe

New Synthesis Routes toward Improvement of Natural Filler/Synthetic Polymer Interfacial Crosslinking

Among the critical issues dictating bio-composite performance is the interfacial bonding between the natural fibers and polymer matrix. In this regard, this article presents new synthesis routes comprising the treatment and functionalization of both date palm powder (DPP) filler and a polypropylene (PP) matrix to enhance filler&ndash;polymer adhesion in the newly developed bio-composites. Specifically, four bio-composite forms are considered: untreated DPP filled PP (DPP-UT/PP), treated DPP filled PP (DPP-T/PP), treated DPP filled functionalized PP using 2-isocyanatoethyl methacrylate (DPP-T/PP-g-IEM), and treated and functionalized DPP using 4-toluenesulfonyl chloride filled functionalized PP using 2-acrylamide ((DPP-T)-g-TsCl/PP-g-AcAm). The functional groups created on the surface of synthesized PP-g-IEM react with activated hydroxyl groups attached to the filler, resulting in chemical crosslinking between both components. Similarly, the reaction of TsCl with NH2 chemical groups residing on the mating surfaces of the filler and polymer generates an amide bond in the interface region. Fourier transform infrared spectroscopy (FTIR) is used to confirm the successful coupling between the filler and polypropylene matrix after applying the treatment and functionalization schemes. Owing to the introduced crosslinking, the DPP-T/PP-g-IEM bio-composite exhibits the best mechanical properties as compared to the neat polymer, unfunctionalized polymer-based bio-composite, and (DPP-T)-g-TsCl/PP-g-AcAm counterpart. The applied compatibilizers assist in reducing the water uptake of the manufactured bio-composites, increasing their durability

Metal–Organic Framework-74 for Ultratrace Arsenic Removal from Water: Experimental and Density Functional Theory Studies

This study investigates and compares arsenic, As­(V), removal from aqueous media using the water-stable zinc metal–organic frameworks (Zn-MOF-74) prepared via room-temperature precipitation (RT-Zn-MOF-74) and a solvothermal procedure (HT-Zn-MOF-74). The Zn-MOF-74 crystals possess average particle sizes of 66 nm and 144 μm for RT-Zn-MOF-74 and HT-Zn-MOF-74, respectively. Moreover, nanosized RT-Zn-MOF-74 exhibited a superior performance to HT-Zn-MOF-74. While the Brunauer–Emmett–Teller surface area of RT-Zn-MOF-74 was smaller than that of HT-Zn-MOF-74, higher adsorption uptake took place on the room-temperature-synthesized ones because of their small particle size and better dispersion. Adsorption isotherm studies showed that the Langmuir isotherm was effective for the adsorption of As­(V) onto RT-Zn-MOF-74 and HT-Zn-MOF-74 with maximum adsorption uptake (<i>q</i>_max) values of 99.0 and 48.7 mg g^–1, respectively. These values exceed most reported maximum adsorption capacities at neutral pH. The thermodynamics of adsorption revealed a spontaneous endothermic process that is due to the substitution of adsorbed water molecules by arsenate in the pores of the MOF crystal. This was further investigated using plane-wave density functional theory calculations. This study constitutes direct evidence for the importance of tuning the size of the MOF crystals to enhance their properties

Competitive adsorption of Alizarin Red S and Bromocresol Green from aqueous solutions using brookite TiO2 nanoparticles: experimental and molecular dynamics simulation

In this work, the effective adsorption and the subsequent photodegradation activity, of TiO2 brookite nanoparticles, for the removal of anionic dyes, namely, Alizarin Red S (ARS) and Bromocresol Green (BCG) were studied. Batch adsorption experiments were conducted to investigate the effect of both dyes' concentration, contact time, and temperature. Photodegradation experiments for the adsorbed dyes were achieved using ultraviolet light illumination (6&nbsp;W, λ = 365&nbsp;nm). The single adsorption isotherms were fitted to the Sips model. The binary adsorption isotherms were fitted using the Extended-Sips model. The results of adsorption isotherms showed that the estimated maximum adsorption uptakes in the binary system were around 140&nbsp;mg&nbsp;g-1 and 45.5&nbsp;mg&nbsp;g-1 for ARS and BCG, respectively. In terms of adsorption kinetics, the uptake toward ARS was faster than BCG molecules in which the equilibrium was obtained in 7&nbsp;min for ARS, while it took 180&nbsp;min for BCG. Moreover, the thermodynamics results showed that the adsorption process was spontaneous for both anionic dyes. All these macroscopic competitive adsorption results indicate high selectivity toward ARS molecules in the presence of BCG molecules. Additionally, the TiO2 nanoparticles were successfully regenerated using UV irradiation. Moreover, molecular dynamics computational modeling was performed to understand the molecules' optimum coordination, TiO2 geometry, adsorption selectivity, and binary solution adsorption energies. The simulation energies distribution exhibits lower adsorption energies for ARS in the range from - 628 to - 1046 [Formula: see text] for both single and binary systems. In addition to that, the water adsorption energy was found to be between - 42 and - 209 [Formula: see text]