The objectives of the current study are to assess and compare the performance of a developed photocatalytic membrane reactor (PMR) in treating industrial waste (e.g., organic dye waste) against membrane distillation. The current PMR is composed of a feed tank, which is a continuous stirred photocatalytic reactor containing slurry Titanium dioxide (TiO₂) particles that are activated by using ultraviolet lamp irradiation at a wavelength of 365 nm, and a poly-vinylidene flouride (PVDF) membrane cell. The experimental setup was designed in a flexible way to enable both separate and integrated investigations of the photocatalytic reactor and the membrane, separately and simultaneously. The experimental work was divided into two phases. Firstly, the PVDF membrane was fabricated and characterized to examine its morphology, surface charge, and hydrophobicity by using a scanning electron microscope, surface zeta potential, and contact angle tests, respectively. Secondly, the effects of using different concentrations of the TiO₂ photocatalyst and feed (e.g., dye concentration) were examined. It is found that the PMR can achieve almost 100% dye removal and pure permeate is obtained at certain conditions. Additionally, a kinetic analysis was performed and revealed that the photocatalytic degradation of dye follows a pseudo-first-order reaction.

This study investigates how the inclusion of refuse-derived fuel (RDF) alters the surface chemistry and electrostatic behavior of oak-based biochar. Biochars were produced using downdraft gasification at 850 °C from 100% oak (HW) and a ternary blend comprising 50% oak, 30% pine, and 20% RDF (HW/SW/RDF). Characterization using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), zeta potential, pH, and electrophoretic mobility was conducted to assess surface functionality and colloidal behavior. The RDF-containing biochar exhibited a 43.3% increase in surface nitrogen content (from 0.24% to 0.90%) and a 6.6% rise in calcium content (from 2.07% to 2.27%) alongside the introduction of chlorine (0.20%) and elevated silicon levels (0.69%) compared to RDF-free counterparts. A concurrent reduction in oxygen-containing functional groups was observed, as O1s decreased from 15.75% in HW to 13.37% in HW/SW/RDF. Electrokinetic measurements revealed a notable decrease in zeta potential magnitude from −31.5 mV in HW to −24.2 mV in HW/SW/RDF, indicating diminished surface charge and colloidal stability. Moreover, the pH declined from 10.25 to 7.76, suggesting a loss of alkalinity and buffering capacity. These compositional and electrostatic shifts demonstrate that RDF inclusion significantly modifies the surface reactivity of biochar, influencing its performance in catalysis, ion exchange, and nutrient retention. The findings underscore the need for tailored post-treatment strategies to enhance the functionality of RDF-modified biochars in environmental applications.

Background: The textile industry represents a great portion of the global industry due to the increase in population and demand for sustainable products. Tons of textile wastewater contain predominantly synthetic complex organic dyes like direct dyes, processing dyes, reactive dyes, etc., making discharge of colored effluents challenging. Main body of the Textile wastewater treatment is essential to maintain the environmental balance and reduce public health threats. Conventional wastewater treatment methods cannot overcome and decompose these toxic wastes; therefore, numerous modern approaches have been studied and implemented for pollutant degradation to be suitable for environmental disposal. Membranes and photocatalysis have proven their significant effect on the photodegradation of different dyes and the production of pure water for further use in industrial purposes. Short conclusion: This review paper aims to represent a comprehensive review of textile dyeing wastewater treatment by integrating polyvinylidene fluoride (PVDF) and titanium dioxide (TiO₂) in a hybrid system named “photocatalytic membrane reactor, PMR”.

This study presents a comprehensive characterization of oak biochar produced via downdraft gasification at 850 °C. The research employs a wide range of advanced analytical techniques to examine the biochar’s physical, chemical, and structural properties. Scanning electron microscopy (SEM) revealed a mesoporous structure, while Brunauer–Emmett–Teller (BET) analysis showed a surface area of 88.97 m²/g. Thermogravimetric analysis (TGA) demonstrated high thermal stability and carbon content (78.7%). X-ray photoelectron spectroscopy (XPS) and ultimate analysis confirmed the high degree of carbonization, with low O/C (0.178) and H/C (0.368) ratios indicating high aromaticity. Fourier transform infrared spectroscopy (FTIR) identified functional groups suggesting potential for CO₂ adsorption. The biochar exhibited a negative zeta potential (−31.5 mV), indicating colloidal stability and potential for soil amendment applications. X-ray diffraction (XRD) and Raman spectroscopy provided insights into the biochar’s crystalline structure and graphitization degree. These findings highlight the oak biochar’s suitability for diverse applications, including soil improvement, carbon sequestration, and environmental remediation. By filling knowledge gaps in oak-specific biochar research, this study underscores the benefits of optimized downdraft gasification and sets a foundation for future advancements in sustainable biochar applications.

Membrane fabrication by the electrospinning can provide tunable structure membranes with interconnected pores, large surface area, and high porosity. This study focuses on studying the effect of different membrane compositions (i.e., polymer concentration and inorganic additives) and electrospinning conditions (i.e., internal needle diameter, tip to collector distance, and feed flow rate) on the quality of polyvinylidene fluoride (PVDF) flat sheet membrane. A homogeneous dope solution was prepared by dissolving the PVDF in a mixture of dimethylacetamide (DMAc) and acetone. By using a scanning electron microscope (SEM), the electrospinning conditions producing beadles fibers are as follows: 16 wt% polymer concentration, 0.004 wt% LiCl concentration, 0.51 mm internal needle diameter, 15 cm tip to collector distance, feed flow rate of 1 ml/hr. Further analysis was conducted by using Fourier Transform Infrared Spectrometer (FTIR) and X-Ray Diffraction (XRD) to assess the impact of electrospinning on fibers elemental composition. Additionally, static water contact angle, porosity, fiber diameter, and pore size measurements reveal the formation of submicron hydrophobic fibers with random alignment.