Unveiling the unique potential of MXene with and without graphene nanoplatelet for thermal energy storage applications.

Solar thermal energy storage (TES) is an outstanding innovation that can help solar technology remain relevant during nighttime and cloudy days. TES using phase change material (PCM) is an avant-garde solution for a clean and renewable energy transition. The present study unveils the unique potential of MXene as a performance enhancer in lauric acid (LA), which functions as a base PCM. The addition of graphene nanoplatelet (GNP) into the LA-MXene composite is prepared to comprehend and evaluate the benefits and detriments of adding carbon-based nanomaterial into the PCM via a two-step homogenizing method. A similar weight percentage of MXene and GNP at 0.75 was used for composite synthesis. The study found that the enthalpy of LA-MXene is comparable to LA at 169.87 J/kg and greater than LA-MXene/GNP, which has 137.53 J/kg. Regarding thermal storage performance, LA-MXene exhibited outstanding performance compared to LA-MXene/GNP in terms of enthalpy efficiency (λ) and relative enthalpy efficiency (η), achieving 95.4% and 96.1%, respectively. This is supported by the XPS spectra, which show that the crosslinking structure acted as a barrier, reinforcing the material and preventing further thermal degradation. This has resulted in robust and denser shells that significantly improved light absorption, enhancing both the photothermal conversion and thermal energy storage efficiency of LA/MXene. The present study reveals that LA-MXene is a promising and optimal candidate for the feasibility and reliability of TES in solar renewable energy applications. It was observed that the incorporation of exclusive MXene may effectively address the limitations of LA as a conventional PCM and surpass the traditional role of GNP. This study offers valuable insights into the superior performance of MXene alone, eliminating the need for doping with various nanomaterials and thereby reducing the complexity in synthesizing the PCM.

Moisture Adsorption-Desorption Behaviour in Nanocomposite Copolymer Films.

Dehumidifying air via refrigerant cooling method consumes a tremendous amount of energy. Independent humidity control systems using desiccants have been introduced to improve energy efficiency. This research aimed to find an alternative to the commonly used solid desiccant, silica gel, which has weak physical adsorption properties. It also aimed to overcome the limitation of liquid desiccants that may affect indoor air quality and cause corrosion. This study reports on the synthesis of poly(vinyl alcohol-co-acrylic acid), P(VA-AA), through solution polymerisation by hydrolysing poly(vinyl acetate-co-acrylic acid), P(VAc-AA). This viable copolymer was then incorporated with graphene oxide (GO) at different concentrations (0 wt.%, 0.5 wt.%, 2 wt.% and 5 wt.%) to enhance the adsorption-desorption process. The samples were tested for their ability to adsorb moisture at different levels of relative humidity (RH) and their capability to maintain optimum sorption capacity over 10 repeated cycles. The nanocomposite film with 2% GO, P(VA-AA)/GO2, exhibited the highest moisture sorption capacity of 0.2449 g/g for 60-90% RH at 298.15 K, compared to its pristine copolymer, which could only adsorb 0.0150 g/g moisture. The nanocomposite desiccant demonstrated stable cycling stability and superior desorption in the temperature range of 318.15-338.15 K, with up to 88% moisture desorption.

Superhydrophobic nanocarbon-based membrane with antibacterial characteristics.

To overcome the biofouling challenge which faces membrane water treatment processed, the novel superhydrophobic carbon nanomaterials impregnated on/powder activated carbon (CNMs/PAC) was utilized to successfully design prepare an antimicrobial membrane. The research was conducted following a systematic statistical design of experiments technique considering various parameters of composite membrane fabrication. The impact of these parameters of composite membrane on Staphylococcus aureus growth was investigated. The bacteria growth was analyzed through spectrophotometer and SEM. The effect of CNMs' hydrophobicity on the bacterial colonies revealed a decrease in the abundance of bacterial colonies and an alteration in structure with increasing the hydrophobicity. The results revealed that the optimum preparative conditions for carbon loading CNMs/PAC was 363.04 mg with a polymer concentration of 22.64 g/100 g, and a casting knife thickness of 133.91 µm. These conditions have resulted in decreasing the number of bacteria colonies to about 7.56 CFU. Our results provided a strong evidence on the antibacterial effect and consequently on the antibiofouling potential of CNMs/PAC in membrane.

Investigation on the effect of sintering temperature on kaolin hollow fibre membrane for dye filtration.

Despite its extraordinary price, ceramic membrane can still be able to surpass polymeric membrane in the applications that require high temperature and pressure conditions, as well as harsh chemical environment. In order to alleviate the high cost of ceramic material that still becomes one of the major factors that contributes to the high production cost of ceramic membrane, various attempts have been made to use low cost ceramic materials as alternatives to well-known expensive ceramic materials such as alumina, silica, and zirconia in the fabrication of ceramic membrane. Thus, local Malaysian kaolin has been chosen as the ceramic material in this study for the preparation of kaolin hollow fibre membrane since it is inexpensive and naturally abundant in Malaysia. Due to the fact that the sintering process plays a prominent role in obtaining the desired morphology, properties, and performances of prepared ceramic membrane, the aim of this work was to study the effect of different sintering temperatures applied (ranging from 1200 to 1500 °C) in the preparation of kaolin hollow fibre membrane via dry/wet phase inversion-based spinning technique and sintering process. The morphology and properties of membrane were then characterised by SEM, AFM, FTIR, XRD, and three-point bending test, while the performances of membrane were investigated by conducting water permeation and Reactive Black 5 (RB5) dye rejection tests. From the experimental results obtained, the sintering temperature of 1400 °C could be selected as the optimum sintering temperature in preparing the kaolin hollow fibre membrane with the dense sponge-like structure of separation layer that resulted in the good mechanical strength of 70 MPa with the appreciable water permeation of 75 L/h m2 bar and RB5 rejection of 68%.

High Thermal Gradient in Thermo-electrochemical Cells by Insertion of a Poly(Vinylidene Fluoride) Membrane.

Thermo-Electrochemical cells (Thermocells/TECs) transform thermal energy into electricity by means of electrochemical potential disequilibrium between electrodes induced by a temperature gradient (ΔT). Heat conduction across the terminals of the cell is one of the primary reasons for device inefficiency. Herein, we embed Poly(Vinylidene Fluoride) (PVDF) membrane in thermocells to mitigate the heat transfer effects - we refer to these membrane-thermocells as MTECs. At a ΔT of 12 K, an improvement in the open circuit voltage (Voc) of the TEC from 1.3 mV to 2.8 mV is obtained by employment of the membrane. The PVDF membrane is employed at three different locations between the electrodes i.e. x = 2 mm, 5 mm, and 8 mm where 'x' defines the distance between the cathode and PVDF membrane. We found that the membrane position at x = 5 mm achieves the closest internal ∆T (i.e. 8.8 K) to the externally applied ΔT of 10 K and corresponding power density is 254 nWcm(-2); 78% higher than the conventional TEC. Finally, a thermal resistivity model based on infrared thermography explains mass and heat transfer within the thermocells.