Free-Flowing Polymer-Bonded Powder Composition of Hexahydro-1,3,5-trinitro-1,3,5-triazine Using Solvent-Slurry Coating.

A number of coating techniques have been used to improve the processability of high explosives. These techniques are typically used for developing compositions, such as boosters and fillers. The most typically used technique is the "solvent-slurry coating". Several compositions of polymer-bonded explosives have been industrialized using this technique. The NUPC-6 polymer-bonded powder composition of hexahydro-1,3,5-trinitro-1,3,5-triazine is optimized using the solvent-slurry coating. It involved multiple processes, i.e., preparing a slurry of high explosives in an aqueous phase, dissolving the modified polymer binder in an organic solvent, maintaining both the solvent and slurry at controlled temperatures, introducing polymer binder solution and ingredients in the slurry, distilling the solvent, mixing contents homogeneously, filtering the polymer-coated hexahydro-1,3,5-trinitro-1,3,5-triazine composition, and drying in a vacuum oven. The phlegmatizing and hydrophobic agents enhance flowability and hydrophobicity. The mass flow rate, bulk density, tapped density, compressibility index, and Hausner ratio are determined to evaluate its flowability during filling operations. The results show that the composition is flowable using a filling funnel, with a 150 mm upper diameter, 25 mm flow diameter, and 136 mm total funnel height. The raw polymer binder was modified using diisooctylsebacate and SAE-10 oil. The additives in the composition enhance its flowability, and it might be used in underwater applications.

Investigation of the effect of Ni and Cu variant MOF-74 in the Polydimethylsiloxane (PDMS)-based Mixed Matrix Membranes (MMMs) for efficient gas separation applications.

Mixed matrix membranes (MMMs) containing metal-organic frameworks (MOFs) have been an emerging and promising membrane technology to contribute to different gas separation applications including carbon dioxide (CO2) and oxygen (O2) separation, because of their large surface areas and distinctive gas adsorption features. In this work, the fabrication process of Polydimethylsiloxane (PDMS)-based MMMs was reported, in which 0.5 to 2 wt.% of each type of (Cu, Ni)-based MOF-74 variants were incorporated into a PDMS matrix in order to achieve high CO2/N2, O2/N2, and CO2/O2 separation efficiency. These MMMs and their nanofillers (MOF-74) were extensively characterized using scanning electron microscopy (SEM) along with Energy Dispersive X-Ray (EDX) mapping, X-ray Diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), a single gas permeation testing system, and an ultimate tensile strength testing (UTS) unit in order to gain insight into their properties in relation to their gas separation performance. The 1 wt.% of both (Cu and Ni)-MOF-74@PDMS were selected as the most optimum MMMs due to their uniform morphology and enhanced tensile strength, which exhibited high CO2 permeabilities of 4432 Barrer (37.9% increase) and 4288 Barrer (33.5% increase), respectively. Furthermore, in the case of 1 wt.% Ni-MOF-74@PDMS, the CO2/N2, O2/N2, and CO2/O2 selectivities were also enhanced to 36.2 (141.6% increase), 3.2 (21.9% increase), and 11.25 (98.1% increase), respectively. While, in the case of 1 wt.% Cu-MOF-74@PDMS the CO2/N2 and O2/N2 selectivities showed an increment up-to 94.7 (531.5% increase) and 6.47 (145% increase), respectively, Whereas, at 0.5 wt.%, Cu-MOF-74@PDMS showed the best CO2/O2 selectivity of 25.26 (344.7% increase).

Investigation on the Redox Properties of a Novel Cu-Based Pr-Modified Oxygen Carrier for Chemical Looping Combustion.

CO2 levels in the atmosphere are growing as a result of the burning of fossil fuels to meet energy demands. The introduction of chemical looping combustion (CLC) as an alternative to traditional combustion by transporting oxygen emphasizes the need to develop greener and more economical energy systems. Metal oxide, also defined as an oxygen carrier (OC), transports oxygen from the air to the fuel. Several attempts are being made to develop an OC with a reasonable material cost for superior fuel conversion and high oxygen transport capacity (OTC). This study aims to synthesize a potential OC using the wet impregnation method for the CLC process. Thermogravimetric analysis (TGA) was used to determine the cyclic redox properties using 5% CH4/N2 and air as reducing and oxidizing gases, respectively. The 10CuPA-based OC retained a high OTC of about 0.0267 mg O2/mg of OC for 10 cycles that was higher than 10CuA-based OC. Furthermore, the oxygen transfer rate for 10CuPA-based OC was relatively higher compared to 10CuA-based OC over 10 cycles. In comparison to 10CuA-based OC, the 10CuPA-based OC presented a steady X-ray diffraction (XRD) pattern after 10 redox cycles, implying that the phase was stably restored due to praseodymium-modified γ alumina support.

Challenges and issues with the performance of boron nitride rooted membrane for gas separation.

Various fillers such as zeolites, metal-organic framework, carbon, metal framework, graphene, and covalent organic framework have been incorporated into the polymers. However, these materials are facing issues such as incompatibility with the polymer matrix, which leads to the formation of non-selective voids and thus, reduces the gas separation properties. Recent studies show that hexagonal boron nitride (h-BN) possesses attractive characteristics such as high aspect ratio, good compatibility with polymer materials, enhanced gas barrier performance, and improved mechanical properties, which could make h-BN the potential candidate to replace conventional fillers. The synthesis of materials and membranes is the subject of this review, which focuses on recent developments and ongoing problems. Additionally, a summary of the mathematical models that were utilised to forecast how well polymer composites would perform in gas separation is provided. It was found in the previous studies that tortuosity is the governing factor for the determination of the effectiveness of a nanofiller as a gas barrier enhancer in polymer matrices. The shape of the nanofiller particles and sheets, disorientation and distribution of the nanofillers within the polymer matrix, state of aggregation and rate of reaggregation of the nanofiller particles, as well as the compatibility of the nanofiller with the polymer matrix all played a significant role in determining how well a particular nanofiller will perform in enhancing the gas barrier properties of the nanocomposites. For this purpose, this review has been focused not only on the experimentation work but also on the effect of tortuosity, exfoliation quality, compatibility, disorientation, and reaggregation of nanofillers.

Model analysis on effect of temperature on the solubility of recycling of Polyethylene Terephthalate (PET) plastic.

The massive increase in the use of PET plastic bottles has raised the challenge of accumulated waste plastics disposal and its related environmental concerns. Reusing this plastic waste through a solvent-based recycling process seems to be an eco-friendly solution for eliminating waste plastic and converting them into high quality products. The selection of solvent with its temperature requirement for the dissolution of polymeric materials is crucial in the solvent-based recycling process. Therefore, an innovative MATLAB program named HSPs-TPT was designed and constructed in this work to evaluate the dissolving power of solvents. Through this program, the solubility of the waste PET polymer was examined in thirteen (13) different solvents at different temperatures. As a results, the degree of waste PET polymer dissolution in the solvents was presented as the polymer-solvent solubility diagram, which provided the information about the relative energy difference (RED) change with the temperature rise. The program also provided the temperature range effective for the dissolution of PET by indicating the minimum and maximum solubility point for each solvent, which was further validated by the experimental data found in the literature. The proposed MATLAB program can numerically analyse the solubility of a polymer in different solvents in a short time for the recycling process and fabrication of different value-added plastic products such as polymer monoliths and membrane filters.

Environmental treatment and remediation using h-BN based smart and hybrid membrane.

Corrosion is a major problem resulting from acid gases found in natural gas being transported in pipelines. To solve this problem, high aspect ratio h-BN nanosheets have been incorporated and are properly assimilated in the CA matrix, this led to an increase in tortuous path of flow for the gas resulting in smooth, dense membrane samples causing exceptional permeability reduction. Hexagonal Boron Nitride (h-BN) nanosheets have been synthesized and incorporated into cellulose acetate (CA) matrix using solution casting method. Nanosheets of various sizes, separated by varying centrifugation speeds (i.e. 500 rpm, 700 rpm, 1500 rpm, 2000 rpm and 2500 rpm), have been prepared and used for our work. The resulting nanocomposites, having thickness ranging between 40 and 60 µm, were then tested for CO2 gas permeability reduction using both short-term (8 h) tests as well as long-term (72-h tests). As a result of these tests, a maximum CO2 permeability reduction of 99.84% is found with a minimum CO2 permeability of 3.25 barrer. For dimensional analysis of both nanosheets and nanocomposites, scanning electron microscopy (SEM) analysis is used. For verifying the presence of the required functional groups in our synthesized samples, FT-IR spectroscopy is used. Moreover, to confirm the presence of crystalline phases, X-ray Diffraction (XRD) analysis is used. Also, tensile testing is used to analyze the mechanical robustness and it was found that nanocomposite samples exhibited higher tensile strength as compared to pristine samples. Furthermore, tribological property analysis was also carried out for adhesion testing of polymeric material with steel.

Future advances and challenges of nanomaterial-based technologies for electromagnetic interference-based technologies: A review.

The emerging growth of the electronic devices applications has arisen the serious problems of electromagnetic (EM) wave pollution which resulting in equipment malfunction. Therefore, polymer-based composites have been considered good candidates for better EMI shielding due to their significant characteristics including, higher flexibility, ultrathin, lightweight, superior conductivity, easy fabrication processing, environmentally friendly, corrosion resistive, better adhesion with physical, chemical and thermal stability. This review article focused on the concept of the EMI shielding mechanism and challenges with the fabrication of polymer-based composites. Subsequently, recent advancements in the polymer composites applications have been critically reviewed. In addition, the impact of polymers and polymer nanocomposites with different fillers such as organic, inorganic, 2D, 3D, mixture and hybrid nano-fillers on EMI shielding effectiveness has been explored. Lastly, future research directions have been proposed to overcome the limitations of current technologies for further advancement in EMI shielding materials for industrial applications. Based on reported literature, it has been found that the low thickness based lightweight polymer is considered as a best material for excellent material for next-generation electronic devices. Optimization of polymer composites during the fabrication is required for better EMI shielding. New nano-fillers such as functionalization and composite polymers are best to enhance the EMI shielding and conductive properties.

Green synthesized nano-cellulose polyethylene imine-based biological membrane.

In hemodialysis process, membrane serves as a barrier between blood and the dialysate. The barrier when contacted by blood accompanied activation of coagulation, immunity, and cellular passageways. In the recent years, hemodialysis membrane's biocompatibility has become a issue which leads to reduce the performance during the separation process. In previous work, we developed and evaluated a cellulose-based membrane blended with polyaziridine or polyetyleneimine in formic acid for hydrophilicity, pure water flux, surface morphology, and permeation efficiency. Biocompatibility was accessed, by conducting cellular viability and cellular attachments tests. In this study, the membrane compared to a non-treated control, and cell viability revealed active and growing cell cultures after 14 days. During the cellular attachment experiment, cell cultures attached to the fabricated membrane simulated the formation of cell junctions, proving that the membrane is non-toxic and biocompatible. CA + PEI + FA membrane tested with a blood mimic fluid having density identical to renal patient's blood. The BSA concentration in the feed solution was the same as that in the blood of the renal patient. The results revealed that the CA + PEI + FA membrane was able to reject 99% bovine serum albumin (BSA) and 69.6% urea. Therefore, from biocompatibility and blood mimic fluid testing, it is confirmed that the CA + PEI + FA membrane is the finest implant for dialysis applications.

Design and Development of a Computational Tool for a Dialyzer by Using Computational Fluid Dynamic (CFD) Model.

In order to reduce the hemodialysis cost and duration, an investigation of the effect of dialyzer design and process variables on the solute clearance rate is required. It is not easy to translate the in vivo transfer process with in vitro experiments, as it involves a high cost to produce various designs and membranes for the dialyzer. The primary objective of this study was the design and development of a computational tool for a dialyzer by using a computational fluid dynamic (CFD) model. Due to their complexity, only researchers with expertise in computational analysis can use dialyzer models. Therefore, COMSOL Inc. (Stockholm, Sweden) has made an application on membrane dialysis to study the impact of different design and process parameters on dialyzed liquid concentration. Still, membrane mathematical modeling is not considered in this application. This void hinders an investigation of the impact of membrane characteristics on the solute clearance rate. This study has developed a stand-alone computational tool in COMSOL Multiphysics 5.4 to fill this void. A review of the literature conducted shows that there are no suitable stand-alone computational tools for kidney dialysis. Very little work has been undertaken to validate the stand-alone computational tool. Medical staff in the hospitals require a computational tool that can be installed quickly and provide results with limited knowledge of dialysis. This work aims to construct a user-friendly computational tool to solve this problem. The development of a user-friendly stand-alone computational tool for the dialyzer is described thoroughly. This application simulates a mathematical model with the Finite Element Method using the COMSOL Multiphysics solver. The software tool is converted to a stand-alone version with the COMSOL compiler. The stand-alone computational tool provides the clearance rate of six different toxins and module packing density. Compared with the previous application, the stand-alone computational tool of membrane dialysis enables the user to investigate the impact of membrane characteristics and process parameters on the clearance rate of different solutes. The results are also inconsistent with the literature data, and the differences ranges are 0.09-6.35% and 0.22-2.63% for urea clearance rate and glucose clearance rate, respectively. Statistical analysis of the results is presented as mean with 95% confidence intervals (CIs) and p values 0.9472 and 0.833 of the urea and glucose clearance rates, respectively.

Novel Cellulose Triacetate (CTA)/Cellulose Diacetate (CDA) Blend Membranes Enhanced by Amine Functionalized ZIF-8 for CO2 Separation.

Currently, cellulose acetate (CA) membranes dominate membrane-based CO2 separation for natural gas purification due to their economical and green nature. However, their lower CO2 permeability and ease of plasticization are the drawbacks. To overcome these weaknesses, we have developed high-performance mixed matrix membranes (MMMs) consisting of cellulose triacetate (CTA), cellulose diacetate (CDA), and amine functionalized zeolitic imidazolate frameworks (NH2-ZIF-8) for CO2 separation. The NH2-ZIF-8 was chosen as a filler because (1) its pore size is between the kinetic diameters of CO2 and CH4 and (2) the NH2 groups attached on the surface of NH2-ZIF-8 have good affinity with CO2 molecules. The incorporation of NH2-ZIF-8 in the CTA/CDA blend matrix improved both the gas separation performance and plasticization resistance. The optimized membrane containing 15 wt.% of NH2-ZIF-8 had a CO2 permeability of 11.33 Barrer at 35 °C under the trans-membrane pressure of 5 bar. This is 2-fold higher than the pristine membrane, while showing a superior CO2/CH4 selectivity of 33. In addition, the former had 106% higher CO2 plasticization resistance of up to about 21 bar and an impressive mixed gas CO2/CH4 selectivity of about 40. Therefore, the newly fabricated MMMs based on the CTA/CDA blend may have great potential for CO2 separation in the natural gas industry.

Performance Analysis of Blended Membranes of Cellulose Acetate with Variable Degree of Acetylation for CO2/CH4 Separation.

The separation and capture of CO2 have become an urgent and important agenda because of the CO2-induced global warming and the requirement of industrial products. Membrane-based technologies have proven to be a promising alternative for CO2 separations. To make the gas-separation membrane process more competitive, productive membrane with high gas permeability and high selectivity is crucial. Herein, we developed new cellulose triacetate (CTA) and cellulose diacetate (CDA) blended membranes for CO2 separations. The CTA and CDA blends were chosen because they have similar chemical structures, good separation performance, and its economical and green nature. The best position in Robeson's upper bound curve at 5 bar was obtained with the membrane containing 80 wt.% CTA and 20 wt.% CDA, which shows the CO2 permeability of 17.32 barrer and CO2/CH4 selectivity of 18.55. The membrane exhibits 98% enhancement in CO2/CH4 selectivity compared to neat membrane with only a slight reduction in CO2 permeability. The optimal membrane displays a plasticization pressure of 10.48 bar. The newly developed blended membranes show great potential for CO2 separations in the natural gas industry.

Sonochemical synthesis of Co3O4 nanoparticles deposited on GO sheets and their potential application as a nanofiller in MMMs for O2/N2 separation.

In this study we report an environmentally friendly, facile and straightforward sonochemical synthetic strategy for a Co3O4/GO nanocomposite using N,N'-bis(salicylidene)ethylenediaminocobalt(ii) as a precursor and graphene oxide sheets as an immobilization support for Co3O4 nanoparticles. The synthesis was facilitated by physical and chemical effects of cavitation bubbles. The synthesized nanocomposite was thoroughly characterized for its composition and morphology using Fourier transform infrared spectroscopy (FTIR), Energy dispersive X-ray spectroscopy (EDS), Scanning electron microscopy (SEM), UV-visible, Raman and X-ray diffraction spectroscopy (XRD), etc. The results show Co3O4 nanoparticles of 10 nm (SD 3 nm) were prepared on well exfoliated sheets of GO. The applicability of the synthesized Co3O4/GO nanocomposite was optimized as a nanofiller for mixed matrix membranes (MMMs) comprised of poly(2-acrylamido-2-methyl-1-propanesulfonic acid) and polyvinyl chloride. The affinity of the prepared MMMs was evaluated for the separation of O2/N2 gases by varying the concentration of nanofiller, i.e. 0.03%, 0.04%, 0.05% and 0.075% (w/v). The results display high separation performance for O2/N2 gases with excellent permeance (N2 167 GPU and O2 432 GPU at 1 bar) and O2/N2 selectivity of 2.58, when the MMMs were loaded with 0.05% (w/v) of Co3O4/GO nanocomposite.

Enhancement in the selectivity of O2/N2 via ZIF-8/CA mixed-matrix membranes and the development of a thermodynamic model to predict the permeability of gases.

Zeolitic imidazolate framework-8 (ZIF-8) has a sodalite topology. ZIF-8 is composed of zinc ion coordinated by four imidazolate rings. The pore aperture of ZIF-8 is 3.4 Å, which readily retains large gas molecules like N2. In this work, mixed-matrix membranes (MMMs) have been fabricated by utilizing ZIF-8 and pristine cellulose acetate (CA) for O2/N2 separation. Membranes of pristine CA and MMMs of ZIF-8/CA at various ZIF-8 concentrations were prepared in tetrahydrofuran (THF). Permeation results of the fabricated membranes revealed increasing selectivity for O2/N2 with increasing pressure as well as ZIF-8/CA concentration up to 5% (w/w). The selectivity of O2/N2 increased 4 times for MMMs containing 5% (w/w) of ZIF-8/CA as compared with the pristine CA membrane. A thermodynamic model has also been developed to predict the permeability of gases through polymeric membranes. The results were compared with literature data as well as the pristine CA membrane produced in this work for model validation.

Adsorption of CO2 on amine-functionalized green metal-organic framework: an interaction between amine and CO2 molecules.

The efficient capture of CO2 is a critical problem for porous adsorbents. The inadequacy of conventional adsorbents has low adsorption capacity towards CO2 removal. Metal organic frame work has been considered as very effective for CO2 adsorption as it shows higher rate of CO2 adsorption at room temperature. In conventional amine processes, a comparatively high energy penalty is required, whereas a novel class of metal-organic framework by the combination of amine solvent have improve the potential of adsorption process and also the efficiency of separation. Amine-functionalized MOFs become more fascinated due to strong interaction between carbon dioxide and amine-functionalized MOF. A renewable green γCD-MOF was synthesized by using vapor diffusion method. Post-synthetic modification of γCD-MOF was done with piperazine and analyzed to expose its crystalline structure, morphology, and porous structure. The main aim of this paper is to enhance the CO2 adsorption by functionalization of inexpensive, green, nanoporous γCD-MOF and also to highlight the effects of amine-based functionalization towards potential application. Gravimetric CO2 adsorption isotherms for γCD-MOF, pip-γCD-MOF are reported up to 60 °C and found to follow a pseudo-second-order reaction. The pip-γCD-MOF confirms comparatively increased rapid adsorption rate of CO2 than that of γCD-MOF and desorption of CO2, and need less energy for regeneration. These results are the complete evidence of piperazine as an efficient amine group for increasing the CO2 adsorption uptake capacity.

Highly integrated nanocomposites of RGO/TiO2 nanotubes for enhanced removal of microbes from water.

Highly integrated nanocomposite of Graphene oxide (GO) and its derivatives with metal oxides is essential for enhanced performance for various applications. Tuning the morphology is an important aspect during nanomaterials synthesis; this has an amplifying influence upon physicochemical properties of advanced functional materials. In this research work, GO/TiO2 nanotube composites have been successfully synthesized via alkaline hydrothermal treatment method by augmenting GO layers with two different phases of TiO2 (anatase and rutile) nanoparticles, followed by the hydrothermal treatment that also have caused reduction of GO to reduced GO (RGO). The morphology of the as-prepared samples appeared to be nanotubes with a large aspect ratio (length to diameter). The synthesized materials have been characterized using various techniques to determine their morphological and functional properties. Large surface area (158 m2/g) nanotube composites found accountable as effective disinfectant for water containing microorganisms. The antimicrobial activity of the synthesized composites was examined by disk diffusion method and optical density for bacterial growth using two different bacterial species; Escherichia Coli (E.coli, Gram-negative) and Staphylococcus Aureus (Methicillin-resistant Staphylococcus aureus, Gram-positive). The antibacterial study revealed that, the anatase phase RGO/TiO2 nanotube composites manifested appreciable effect on both bacteria as compared to rutile phase RGO/TiO2 nanotubecomposite.

Carbon capture from natural gas using multi-walled CNTs based mixed matrix membranes.

Most of the polymers and their blends, utilized in carbon capture membranes, are costly, but cellulose acetate (CA) being inexpensive is a lucrative choice. In this research, pure and mixed matrix membranes (MMMs) have been fabricated to capture carbon from natural gas. Polyethylene glycol (PEG) has been utilized in the fabrication of membranes to modify the chain flexibility of polymers. Multi-walled carbon nanotubes (MWCNTs) provide mechanical strength, thermal stability, an extra free path for CO2 molecules and augment CO2/CH4 selectivity. Membranes of pure CA, CA/PEG blend of different PEG concentrations (5%, 10%, 15%) and CA/PEG/MWCNTs blend of 10% PEG with different MWCNTs concentrations (5%, 10%, 15%) were prepared in acetone using solution casting techniques. Fabricated membranes were characterized using SEM, TGA and tensile testing. Permeation results revealed remarkable improvement in CO2/CH4 selectivity. In single gas experiments, CO2/CH4 selectivity is enhanced 8 times for pure membranes containing 10% PEG and 14 times for MMMs containing 10% MWCNTs. In mix gas experiments, the CO2/CH4 selectivity is increased 13 times for 10% PEG and 18 times for MMMs with 10% MWCNTs. Fabricated MMMs have a tensile strength of 13 MPa and are more thermally stable than CA membranes.