Micronized cellulose from citrus processing waste using water and electricity only

Along with a water-soluble fraction rich in pectin, the hydrodynamic cavitation of citrus processing waste carried out in water demonstrated directly on semi-industrial scale affords an insoluble fraction consisting of micronized cellulose of low crystallinity ("CytroCell"). Lemon and grapefruit CytroCell respectively consist of 100-500 nm wide cellulose nanorods, and of 500-1000 nm wide ramified microfibrils extending for several ?m. These findings establish a technically viable route to low crystallinity micronized cellulose laying in between nano- and microcellulose, using water and electricity only

Synthesis and Surface Modification of TiO2-Based Photocatalysts for the Conversion of CO2

Among all greenhouse gases, CO2 is considered the most potent and the largest contributor to global warming. In this review, photocatalysis is presented as a promising technology to address the current global concern of industrial CO2 emissions. Photocatalysis utilizes a semiconductor material under renewable solar energy to reduce CO2 into an array of high-value fuels including methane, methanol, formaldehyde and formic acid. Herein, the kinetic and thermodynamic principles of CO2 photoreduction are thoroughly discussed and the CO2 reduction mechanism and pathways are described. Methods to enhance the adsorption of CO2 on the surface of semiconductors are also presented. Due to its efficient photoactivity, high stability, low cost, and safety, the semiconductor TiO2 is currently being widely investigated for its photocatalytic ability in reducing CO2 when suitably modified. The recent TiO2 synthesis and modification strategies that may be employed to enhance the efficiency of the CO2 photoreduction process are described. These modification techniques, including metal deposition, metal/non-metal doping, carbon-based material loading, semiconductor heterostructures, and dispersion on high surface area supports, aim to improve the light absorption, charge separation, and active surface of TiO2 in addition to increasing product yield and selectivity

Recent progress of MXene as a cocatalyst in photocatalytic carbon dioxide reduction

Due to the excessive consumption of fossil fuel resources and the emission of a substantial quantity of CO2 into the environment, it is urgent to develop clean energy solutions. In order to reduce carbon emissions from the source, it is effective approach to convert CO2 into various renewable energy fuels. Inspired by the photosynthesis of green plant, CO2 is converted into clean fuel with the aid of catalysts. Regarding the separation and transfer of photogenerated charge carriers, and inadequate adsorption and activation of CO2 on the surface of catalysts, the current semiconductors utilized in photocatalysis have low efficiency. As a result, the current efficiency of photocatalysts is far from meeting the need for practical industrial demands. MXene materials, for example Ti3C2Tx (9980 S cm−1), have emerged as a promising candidate for CO2 reduction due to the significant number of active sites for functional groups, high conductivity and low defects, large surface areas, and outstanding visible light photoelectronic properties. This review provides a critical overview of the recent progress regarding MXene as a co-catalyst in photocatalytic CO2 reduction systems. We systemically explore the fundamental principles and reaction mechanisms associated with separating and transferring photogenerated charge carriers. Additionally, we investigate the basic properties of MXene as a co-catalyst in the context of CO2 reduction. Furthermore, this review also elucidates the impacts of the microstructure of photocatalysts on enhancing photocatalytic performance. Finally, the challenges and opportunities in using MXene as a co-catalyst for CO2 reduction have been presented to inspire further research in this field

3D printed photocatalytic feed spacers functionalized with β-FeOOH nanorods inducing pollutant degradation and membrane cleaning capabilities in water treatment

[Display omitted] •Novel photocatalytic 3D printed feed spacers developed for (waste)water treatment.•β-FeOOH nanorods were mineralized on PDA/PEI-coated polyamide spacer.•The spacers degraded methylene blue and 4-nitrophenol in the feed during filtration.•Photocatalytic spacer also cleaned the organic foulants deposited on the membrane.•New approach enables a shift to spacer-centered photocatalytic membrane systems. A novel 3D printed photocatalytic feed spacer was developed for use in membrane-based water and wastewater filtration systems. The spacer fulfilled two new functions; degradation of membrane-permeating pollutants in the feed and membrane cleaning, in addition to its basic role as membrane support. The spacer, designed based on a triply periodic minimal surface architecture, was coated with polydopamine-polyethyleneimine, on which a photocatalytic layer of β-FeOOH nanorods was mineralized. The photocatalytic performance of the spacer was demonstrated through the degradation of methylene blue and 4-nitrophenol, both in batch and crossflow ultrafiltration (UF) modes. The spacer also exhibited the ability to clean the membrane surface of three organic foulants (humic acid (HA), sodium alginate (SA) and bovine serum albumin (BSA)), with a flux recovery ratio of 92 %, 60 %, and 54 % achieved for SA, HA, and BSA, respectively. This enables a shift to spacer-centered photocatalytic membrane system approach in water and wastewater treatment

Improved photocatalytic activity of SnO2_2-TiO2_2 nanocomposite thin films prepared by low-temperature sol-gel method

The objective of this research was to investigate how the photocatalytic activity of pure TiO$_2$ can be improved by SnO$_2$ modification. Different molar ratios of tin to titanium were prepared. The correlation between tin concentration and structural properties was investigated to explain the mechanism of photocatalytic efficiency and to optimize the synthesis conditions to obtain enhanced activity of the SnO$_2$-modified TiO$_2$ photocatalysts under UV-irradiation. The SnO$_2$-modified TiO$_2$ photocatalysts were prepared by a low-temperature sol-gel method based on organic tin and titanium precursors. The precursors underwent sol-gel reactions separately to form SnO$_2$-TiO$_2$ sol. The sol-gels were deposited on a glass substrate by a dip-coating technique and dried at 150 °C to obtain the photocatalysts in the form of a thin film. To test the thermal stability of the material, an additional set of photocatalysts was prepared by calcining the dried samples in air at 500 °C. The photocatalytic activity of the samples was determined by measuring the degradation rate of an azo dye. An increase of up to 30% in the photocatalytic activity of the air-dried samples was obtained when the TiO$_2$ was modified with the SnO$_2$ in a concentration range of 0.1–1 mol.%. At higher SnO$_2$ loadings, the photocatalytic activity of the photocatalyst was reduced compared to the unmodified TiO$_2$. The calcined samples showed an overall reduced photocatalytic activity compared to the air-dried samples. Various characterization techniques (UV-Vis, XRD, N$_2$-physisorption, TEM, EDX, SEM, XAS and photoelectrochemical characterization) were used to explain the mechanism for the enhanced and hindered photocatalytic performances of the SnO$_2$-modified TiO$_2$ photocatalysts. The results showed that the nanocrystalline cassiterite SnO$_2$ is attached to the TiO$_2$ nanocrystallites through the Sn-O-Ti bonds. In this way, the coupling of two semiconductors, SnO$_2$ and TiO$_2$, was demonstrated. Compared to single-phase photocatalysts, the coupling of semiconductors has a beneficial effect on the separation of charge carriers, which prolongs their lifetime for accessibility to participate in the redox reactions. The maximum increase in activity of the thin films was achieved in the low concentration range (0.1–1 mol.%), which means that an optimal ratio and contact of the two phases is achieved for the given physical parameters such as particle size, shape and specific surface area of the catalyst

Improved photocatalytic activity of SnO2−TiO2SnO_{2}-TiO_{2} nanocomposite thin films prepared by low-temperature sol-gel method

The objective of this research was to investigate how the photocatalytic activity of pure TiO$_2$ can be improved bySnO$_2$ modification. Different molar ratios of tin to titanium were prepared. The correlation between tin concentration and structural properties was investigated to explain the mechanism of photocatalytic efficiency and to optimize the synthesis conditions to obtain enhanced activity of the SnO$_2$-modified TiO$_2$ photocatalysts under UV-irradiation. The SnO$_2$-modified TiO$_2$ photocatalysts were prepared by a low-temperature sol-gel method based on organic tin and titanium precursors. The precursors underwent sol-gel reactions separately to form SnO$_2$-TiO$_2$ sol. The sol-gels were deposited on a glass substrate by a dip-coating technique and dried at 150 °C to obtain the photocatalysts in the form of a thin film. To test the thermal stability of the material, an additional set of photocatalysts was prepared by calcining the dried samples in air at 500 °C. The photocatalytic activity of the samples was determined by measuring the degradation rate of an azo dye. An increase of up to 30% in thephotocatalytic activity of the air-dried samples was obtained when the TiO$_2$ was modified with the SnO$_2$ in a concentration range of 0.1–1 mol.%. At higher SnO$_2$ loadings, the photocatalytic activity of the photocatalystwas reduced compared to the unmodified TiO$_2$. The calcined samples showed an overall reduced photocatalyticactivity compared to the air-dried samples. Various characterization techniques (UV-Vis, XRD, N2-physisorption,TEM, EDX, SEM, XAS and photoelectrochemical characterization) were used to explain the mechanism for the enhanced and hindered photocatalytic performances of the SnO$_2$-modified TiO$_2$ photocatalysts. The results showed that the nanocrystalline cassiterite SnO$_2$ is attached to the TiO$_2$ nanocrystallites through the Sn-O-Ti bonds. In this way, the coupling of two semiconductors, SnO$_2$ and TiO$_2$, was demonstrated. Compared to single-phase photocatalysts, the coupling of semiconductors has a beneficial effect on the separation of charge carriers, which prolongs their lifetime for accessibility to participate in the redox reactions. The maximum increase in activity of the thin films was achieved in the low concentration range (0.1–1 mol.%), which means that an optimal ratio and contact of the two phases is achieved for the given physical parameters such as particle size, shape and specific surface area of the catalyst