Metal−organic frameworks (MOFs) have been of great interest for their outstanding properties, such as large surface area, low density, tunable pore size and functionality, excellent structural flexibility, and good chemical stability. A significant advancement in the preparation of MOF thin films according to the needs of a variety of applications has been achieved in the past decades. Yet there is still high demand in advancing the understanding of the processes to realize more scalable, controllable, and greener synthesis. This review provides a summary of the current progress on the manufacturing of MOF thin films, including the various thin-film deposition processes, the approaches to modify the MOF structure and pore functionality, and the means to prepare patterned MOF thin films. The suitability of different synthesis techniques under various processing environments is analyzed. Finally, we discuss opportunities for future development in the manufacturing of MOF thin films.

Pelleted biomass has a low, uniform moisture content and can be handled and stored cheaply and safely. Pellets can be made of industrial waste, food waste, agricultural residues, energy crops, and virgin lumber. Despite their many desirable attributes, they cannot compete with fossil fuel sources because the process of densifying the biomass and the price of the raw materials make pellet production costly. Leaves collected from street sweeping are generally discarded in landfills, but they can potentially be valorized as a biofuel if they are pelleted. However, the lignin content in leaves is not high enough to ensure the physical stability of the pellets, so they break easily during storage and transportation. In this study, the use of eucalyptus kraft lignin as an additive in tree-leaf pellet production was studied. Results showed that when 2% lignin is added the abrasion resistance can be increased to an acceptable value. Pellets with added lignin fulfilled all requirements of Europ... [more]

Carbon-silica composites with nanoporous structures were synthesized for the adsorption of volatile organic compounds (VOCs), taking tetraethyl orthosilicate (TEOS) as the silicon source and activated carbon powder as the carbon source. The preparation conditions were as follows: the pH of the reaction system was 5.5, the hydrophobic modification time was 50 h, and the dosage of activated carbon was 2 wt%. Infrared spectrum analysis showed that the activated carbon was dispersed in the pores of aerogel to form the carbon-silica composites material. The static adsorption experiments, dynamic adsorption-desorption experiments, and regeneration experiments show that the prepared carbon-silica composites have microporous and mesoporous structures, the adsorption capacity for n-hexane is better than that of conventional hydrophobic silica gel, and the desorption performance is better than that of activated carbon. It still has a high retention rate of adsorption capacity after multiple adso... [more]

Recently, the interest in converting waste cooking oils (WCOs) to raw materials has grown exponentially. The driving force of such a trend is mainly represented by the increasing number of WCO applications, combined with the definition, in many countries, of new regulations on waste management. From an industrial perspective, the simple chemical composition of WCOs make them suitable as valuable chemical building blocks, in fuel, materials, and lubricant productions. The sustainability of such applications is sprightly related to proper recycling procedures. In this context, the development of new recycling processes, as well as the optimization of the existing ones, represents a priority for applied chemistry, chemical engineering, and material science. With the aim of providing useful updates to the scientific community involved in vegetable oil processing, the current available technologies for WCO recycling are herein reported, described, and discussed. In detail, two main types of... [more]

Polymer flooding is a promising enhanced oil recovery (EOR) technique; sweeping a reservoir with a dilute polymer solution can significantly improve the overall oil recovery. In this overview, polymeric materials for enhanced oil recovery are described in general terms, with specific emphasis on desirable characteristics for the application. Application-specific properties should be considered when selecting or developing polymers for enhanced oil recovery and should be carefully evaluated. Characterization techniques should be informed by current best practices; several are described herein. Evaluation of fundamental polymer properties (including polymer composition, microstructure, and molecular weight averages); resistance to shear/thermal/chemical degradation; and salinity/hardness compatibility are discussed. Finally, evaluation techniques to establish the polymer flooding performance of candidate EOR materials are described.

Among a large number of current biomedical applications in the use of medical devices, carbon-based nanomaterials such as graphene (G), graphene oxides (GO), reduced graphene oxide (rGO), and carbon nanotube (CNT) are frontline materials that are suitable for developing medical devices. Carbon Based Nanomaterials (CBNs) are becoming promising materials due to the existence of both inorganic semiconducting properties and organic π-π stacking characteristics. Hence, it could effectively simultaneously interact with biomolecules and response to the light. By taking advantage of such aspects in a single entity, CBNs could be used for developing biomedical applications in the future. The recent studies in developing carbon-based nanomaterials and its applications in targeting drug delivery, cancer therapy, and biosensors. The development of conjugated and modified carbon-based nanomaterials contributes to positive outcomes in various therapies and achieved emerging challenges in preclinical... [more]

In this project, we present a comparative study of the electrochemical performance for tubular MCo2O4 (M = Cr, Mn, Ni) microstructures prepared using cotton fiber as a bio-template. Crystal structure, surface properties, morphology, and electrochemical properties of MCo2O4 are characterized using X-ray diffraction (XRD), gas adsorption, scanning electron microscopy (SEM), Fourier transforms infrared spectroscopy (FTIR), cyclic voltammetry (CV), and galvanostatic charge-discharge cycling (GCD). The electrochemical performance of the electrode made up of tubular MCo2O4 structures was evaluated in aqueous 3M KOH electrolytes. The as-obtained templated MCo2O4 microstructures inherit the tubular morphology. The large-surface-area of tubular microstructures leads to a noticeable pseudocapacitive property with the excellent electrochemical performance of NiCo2O4 with specific capacitance value exceeding 407.2 F/g at 2 mV/s scan rate. In addition, a Coulombic efficiency ~100%, and excellent cy... [more]

Recently, intensive efforts have been undertaken to find new, superior biomaterial solutions in the field of hybrid inorganic−organic materials. In our studies, biomicroconcretes containing hydroxyapatite (HAp)−chitosan (CTS) granules dispersed in an α tricalcium phospahate (αTCP) matrix were investigated. The influence of CTS content and the size of granules on the physicochemical properties of final bone implant materials (setting time, porosity, mechanical strength, and phase composition) were evaluated. The obtained materials were found to be promising bone substitutes for use in non-load bearing applications.

Composite films of polybutylene adipate terephthalate (PBAT) were prepared by adding thermoplastic starch (TPS) (TPS/PBAT) and nano-zinc oxide (nano-ZnO) (TPS/PBAT/nano-ZnO). The changes of surface morphology, thermal properties, crystal types and functional groups of starch during plasticization were analyzed by scanning electron microscopy, synchronous thermal analysis, X-ray diffraction, infrared spectrometry, mechanical property tests, and contact Angle and transmittance tests. The relationship between the addition of TPS and the tensile strength, transmittance, contact angle, water absorption, and water vapor barrier of the composite film, and the influence of nano-ZnO on the mechanical properties and contact angle of the 10% TPS/PBAT composite film. Experimental results show that, after plasticizing, the crystalline form of starch changed from A-type to V-type, the functional group changed and the lipophilicity increased; the increase of TPS content, the light transmittance and m... [more]

A new member of sodium metal diphosphate-diarsenate, Na2CuP1.5As0.5O7, was synthesized as polycrystalline powder by a solid-state route. X-ray diffraction followed by Rietveld refinement show that the studied material, isostructural with β-Na2CuP2O7, crystallizes in the monoclinic system of the C2/c space group with the unit cell parameters a = 14.798(2) Å; b = 5.729(3) Å; c = 8.075(2) Å; β = 115.00(3)°. The structure of the studied material is formed by Cu2P4O15 groups connected via oxygen atoms that results in infinite chains, wavy saw-toothed along the [001] direction, with Na+ ions located in the inter-chain space. Thermal study using DSC analysis shows that the studied material is stable up to the melting point at 688 °C. The electrical investigation, using impedance spectroscopy in the 260−380 °C temperature range, shows that the Na2CuP1.5As0.5O7 compound is a fast-ion conductor with σ350 °C = 2.28 10−5 Scm−1 and Ea = 0.6 eV. Na+ ions pathways simulation using bond-valence site e... [more]

This research investigates the simultaneous sintering and surface nitriding of 316L stainless steel alloy using powder metallurgy method. The influence of sintering temperature and dwell time are investigated for maximum nitrogen absorption, densification and increased microhardness using response surface methodology (RSM). In this study, 316L stainless steel powder was compacted at 800 MPa and sintered at two different temperatures of 1150 and 1200 °C with varying dwell times of 1, 3, 5 and 8 h in nitrogen atmosphere. The sintered compacts were then characterized for their microstructure, densification, microhardness and nitrogen absorption. The results revealed that increased dwell time assisted nitrogen to diffuse into stainless steel matrix along with the creation of nitride layer onto the sample surface. The microhardness and density also increased with increasing dwell time. A densification of 7.575 g/cm3 and microhardness of 235 HV were obtained for the samples sintered at 1200... [more]

Silver nanodecahedrons were successfully synthesized by a photochemical method under irradiation of blue light-emitting diodes (LEDs). The formation of silver nanodecahedrons at different LED irradiation times (0−72 h) was thoroughly investigated by employing different characterization methods such as ultraviolet−visible spectroscopy (UV−Vis), transmission electron microscopy (TEM), and Raman spectroscopy. The results showed that silver nanodecahedrons (AgNDs) were formed from silver nanoseeds after 6 h of LED irradiation. The surface-enhanced Raman scattering (SERS) effects of the synthesized AgNDs were also studied in comparison with those of spherical silver nanoparticles in the detection of 4-mercapto benzoic acid. Silver nanodecahedrons with a size of 48 nm formed after 48 h of LED irradiation displayed stronger SERS properties than spherical nanoparticles because of electromagnetic enhancement. The formation mechanism of silver nanodecahedrons is also reported in our study. The r... [more]

Natural gas (NG) production in Brazil has shown a significant increase in recent years. Oil and natural gas exploration and refining activities indicate circa 86% carbon dioxide content in NG, representing a serious problem for environmental issues related to greenhouse gas emissions and increases in global warming. New technologies using CO2 capture materials have been shown to be more efficient than conventional processes. In this work, a bimodal meso−macroporous silica adsorbent for CO2 adsorption in NG was synthesized and evaluated as a promising material for use in natural gas treatment systems, as silica has specific textural properties that facilitate the capture and storage of this gas. The adsorbent was obtained from silica via the hydrothermal method with n-dodecane emulsion and characterized by X-ray diffraction, scanning electron microscopy, infrared spectroscopy, and the BET specific surface area. Adsorption capacity tests were performed for CO2, methane, and their mixture... [more]

In this study, maleic anhydride (MA) grafted natural rubber (NR), known as maleated natural rubber (MNR), was melt-prepared with the MA content varied within 1−8 phr. MNR was used as the main matrix, with Halloysite Nanotubes (HNT) as a filler, in order to obtain composites with improved performance. The compounds were investigated for their filler−filler interactions by considering their Payne effect. On increasing the MA content, scorch and cure times increased along with maximum torque and torque difference. The MNR with 4 phr of MA exhibited the least filler−filler interactions, as indicated by the retention of the storage modulus after applying a large strain to the filled compound. This MNR compound also provided the highest tensile strength among the cases tested. It is interesting to highlight that MNR, with an appropriate MA content, reduces filler−filler interactions, and, thereby, enhances the HNT filler dispersion, as verified by SEM images, leading to improved mechanical a... [more]

Giving a “new life” to wastes should be the golden rule for all production processes in the forthcoming future, aiming at making them more sustainable and environmentally friendly. In the corrosion science field, the ambitious circular economy paradigm has recently led to the employment of extracts from plants (and, in less extent, from agri-food wastes) as green inhibitors against corrosion of metals. However, in spite of the number of scientific papers published in the field, a deep revision of the scientific approach is needed both in the execution of experiments and in the critical analysis of the results. Starting from some discrepancies in published data, the corrosion inhibition effect induced by a well-characterized methanolic extract from wastes of fermented Punica granatum and by its main component (ellagic acid, EA) was validated. The corrosion behaviour of Armco® pure iron in the presence of small concentrations of ellagic acid and extract (containing ca. 10 µM and 100 µM E... [more]

The research presented in this article concerns Zr−C coatings which were deposited on 304L steel by reactive magnetron sputtering from the Zr target in an Ar−C2H2 atmosphere at various acetylene flow rates, resulting in various atomic carbon concentrations in the coating. The article describes research covering the change in the antibacterial and anticorrosive properties of these coatings due to the change in their chemical and phase composition. The concentration of C in the coatings varied from 21 to 79 at.%. The coating morphology and the elemental distribution in individual coatings were characterized using field emission scanning electron microscopy with an energy-dispersive X-ray analytical system. X-ray diffraction and Raman spectroscopy were used to analyze their microstructure and phase composition. Parallel changes in the mechanical properties of the coatings were analyzed. Based on the obtained results, it was concluded that the wide possibility of shaping the mechanical pro... [more]

YVO4:Eu3+ nanoparticles were successfully synthesized by two methods, namely the sonochemical method and hydrothermal method. The X-ray diffraction (XRD) patterns showed the tetragonal phase of YVO4 (JCPDS 17-0341) was indexed in the diffraction peaks of all samples. The samples synthesized by the sonochemical method had a highly crystalline structure (X-ray diffraction results) and luminescence intensity (photoluminescence results) than those synthesized by the hydrothermal method. According to the results of field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM), the average size of YVO4:Eu3+ nanoparticles was around 25−30 nm for the sonochemical method and 15−20 nm for the hydrothermal method. YVO4:Eu3+ nanoparticles in the case of the sonochemical method had a better crystalline structure and stronger emissivity at 618 nm. The Eu3+ ions’ average lifetime in YVO4:Eu3+ at 618 nm emission under 275 nm excitation were at 0.955 ms for the sonoche... [more]

A new type of silica hybrid material functionalized with Schiff base-propyl-thiol and propyl-thiol groups (adsorbents 1 and 2, respectively) was synthesized using a co-condensation method. The synthesized materials and their starting materials were successfully characterized using a variety of techniques such as Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), nitrogen adsorption−desorption isotherms, the Brunauer−Emmett−Teller (BET) surface area calculation method, the Barrett, Joyner, and Halenda (BJH) pore size calculation method, thermogravimetry analysis (TGA), and 1H and 13C nuclear magnetic resonance (NMR) spectra. The results indicate that the new material (adsorbent 1) has a large surface and possesses different functional groups (-SH, -OH, -C=O and −N=C). The newly synthesized hybrid materials (1 and 2) were investigated as potential adsorbents for removal of toxic heavy metals, such as Pb(II) from aqueous solutions.... [more]

Among the several methods of producing graphene, the liquid-phase exfoliation of graphite is attractive because of a simple and easy procedure, being expected for mass production. The dispersibility of graphene can be improved by adding a dispersant molecule that interacts with graphene, but the appropriate molecular design has not been proposed. In this study, we focused on aromatic compounds with alkyl chains as dispersing agents. We synthesized a series of alkyl aromatic compounds and evaluated their performance as a dispersant for graphene. The results suggest that the alkyl chain length and solubility in the solvent play a vital role in graphene dispersion.

More recent attention has been focused on the utilization of Jatropha curcas in the field of water treatment. The potential of Jatropha oil in the synthesis of membrane for water filtration had been explored, its performance compared to the addition of graphene oxide (GO) in the polymer matrix. Jatropha oil was modified in a two-step method to produce Jatropha oil-based polyol (JOL) and was blended with hexamethylene diisocyanate (HDI) to produce Jatropha polyurethane membrane (JPU). JPU was synthesized in different conditions to obtain the optimized membrane and was blended with different GO loading to form Jatropha/graphene oxide composite membrane (JPU/GO) for performance improvement. The synthesized pristine JPU and JPU/GO were evaluated and the materials were analyzed using fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), contact angle, water flux, and field emission scanning electron microscopy (FESEM). Res... [more]

TiO2 membranes were prepared on porous Ti supports through the in situ oxidation method. The effects of oxygen concentration, oxidation temperature, and oxidation time on the thickness, pore size, and microstructure of the prepared TiO2 membrane were investigated. The results showed that with increasing oxygen concentration, oxidation temperature, and oxidation time, the thickness of the prepared TiO2 membrane gradually increased, and the pore diameter gradually decreased. The optimum preparation conditions were—oxygen concentration was N2:O2 = 2:1, oxidation temperature was 800 ℃, and oxidation time was 60 min. The prepared TiO2/Ti composite membranes had a flat and smooth surface, uniform thickness, and only a rutile TiO2 characteristic peak formed on the surface of the membrane. The prepared TiO2/Ti composite membrane had a narrow pore size distribution, and the average pore size was about 0.312 μm. In addition, the prepared TiO2/Ti composite membranes showed an excellent stability.

Magnesium silicate hydrate (M−S−H) cement, formed by reacting MgO, SiO2, and H2O, was used to encapsulate strontium (Sr) radionuclide. Samples were prepared using light-burned magnesium oxide and silica fume, with sodium hexametaphosphate added to the mix water as a dispersant. The performance of the materials formed was evaluated by leach testing and the microstructure of the samples was also characterized. The stabilizing/solidifying effect on Sr radionuclide in the MgO−SiO2−H2O system with low alkalinity is demonstrated in the study. The leaching rate in a standard 42-day test was 2.53 × 10−4 cm/d, and the cumulative 42-day leaching fraction was 0.06 cm. This meets the relevant national standard performance for leaching requirements. Sr2+ was effectively incorporated into the M−S−H hydration products and new phase formation resulted in low Sr leaching being observed.

Membranes, as the primary tool in membrane separation techniques, tend to suffer external deposition of pollutants and microorganisms depending on the nature of the treating solutions. Such issues are well recognized as biofouling and is identified as the major drawback of pressure-driven membrane processes due to the influence of the separation performance of such membrane-based technologies. Herein, the aim of this review paper is to elucidate and discuss new insights on the ongoing development works at facing the biofouling phenomenon in membranes. This paper also provides an overview of the main strategies proposed by “membranologists” to improve the fouling resistance in membranes. Special attention has been paid to the fundamentals on membrane fouling as well as the relevant results in the framework of mitigating the issue. By analyzing the literature data and state-of-the-art, the concluding remarks and future trends in the field are given as well.

The solid-layer growth kinetics and resulting crystal purity for a well-mixed p-xylene (PX) melt with impurity of o-xylene (OX) or ethylbenzene (EB) were studied in this work at various cooling temperatures. A correlation based on the energy balance was adopted to describe the dependence of growth rate on the temperature gradient between melt and cooling medium. An empirical equation based on the mass balance was proposed to relate the effective distribution coefficient with growth rate, mass transfer coefficient, and impurity mole fraction. By fitting the proposed empirical equation with the experimental effective distribution coefficients, the mass transfer coefficients for the PX/OX and PX/EB mixtures were retrieved respectively.

The sustainable development of materials is one of the key targets in the modern era of engineering. These materials are developed by different waste products, following the concept of the circular economy. This study focuses on investigating the properties of concrete using carbon black as a partial replacement of natural fine aggregate at different percentages. Experiments were designed according to the British Standard (BS1881-Part-119) and American Standard (ASTM C-78) by including carbon black in concrete beams to perform as filler material to develop sustainable concrete. In this study, mechanical properties of concrete were targeted by developing beams using different percentages (0%, 25%, 50%, 75%, and 100%) as a replacement of fine aggregates. These beams were tested for flexural strength and, later on, the same beams were cut in the form of cubes, following the equivalent cube test mechanism for the compressive strength test. The waste carbon black lightweight concrete develo... [more]