Browse
Submit Data
Databases
API
Help

Dataset Information

26 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Strainer-Separable TiO₂ on Halloysite Nanocomposite-Embedded Alginate Capsules with Enhanced Photocatalytic Activity for Degradation of Organic Dyes.

ABSTRACT: Photocatalysis driven by natural sunlight is an attractive approach to removing pollutants from wastewater. Although TiO₂-based photocatalysts using various support nano-materials with high catalytic activity and reusability have been developed for purifying wastewater, the centrifugal separation methods used for the nanocatalysts limit their use for treating large amounts of water. Here, we prepared a TiO₂ nano-catalyst supported on a halloysite nanotube (HNT)-encapsulated alginate capsule (TiO₂@HNT/Alcap) to recapture the catalysts rapidly without centrifugation. The structure of TiO₂@HNT/Alcap was characterized by X-ray diffraction, SEM, and TGA. In our system, the combination of HNTs and alginate capsules (Alcaps) improved the efficiency of adsorption of organic pollutants to TiO₂, and their milli = meter scale structure allowed ultra-fast filtering using a strainer. The TiO₂@HNT/Alcaps showed ~1.7 times higher adsorption of rhodamine B compared to empty alginate capsules and also showed ~10 and ~6 times higher degradation rate compared to the HNT/Alcaps and TiO₂/Alcaps, respectively.

SUBMITTER: Lee J

PROVIDER: S-EPMC9320041 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Degradable and Photocatalytic Antibacterial Au-TiO₂/Sodium Alginate Nanocomposite Films for Active Food Packaging.

Project description:A degradable and antibacterial sodium alginate film containing functional Au-TiO₂ nanocomposites for food packaging was successfully developed. The Au-TiO₂ nanocomposites are synthesized hydrothermally and mixed with the alginate solution to form the film by a casting method. The Au-TiO₂ nanocomposites enable the film with excellent visible light absorption and transfer ability with the light absorption rang covering UV⁻visible wavelength (300⁻800 nm) and induce the increase of the film water contact angle from 40° to 74°, which contributes to the film shape stability. Furthermore, compared to the TiO₂ nanoparticle-incorporated film, the antibacterial ability of Au-TiO₂/sodium alginate composite film is improved approximately by 60% and 50% against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli), respectively, in light conditions. The antibacterial property of the film arises from the increased production of reactive oxygen species (ROS) induced by the surface plasmonic resonance of Au nanoparticles. The degradable and antibacterial properties render the composite film of great application potential in food packaging industry.

| S-EPMC6266112 | biostudies-literature

TiO2 decorated functionalized halloysite nanotubes (TiO2@HNTs) and photocatalytic PVC membranes synthesis, characterization and its application in water treatment.

Project description:In this study photocatalyst, TiO2@HNTs were prepared by synthesizing TiO2 nanoparticles in situ on the functionalized halloysite nanotubes (HNTs) surface. Photocatalytic PVC membrane TiO2@HNTs M2 (2 wt.%) and TiO2@HNTs M3 (3 wt.%) were also prepared. Photocatalyst TiO2@HNTs and photocatalytic PVC membranes were used to study the photocatalytic activity against the methylene blue (MB) and rhodamine B (RB) dyes in UV batch reactor. The structure and morphology of photocatalyst and photocatalytic PVC membrane were characterized by fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), transmission electron microscopy (TEM), UV-Vis spectrophotometer and photoluminescence (PL). The PL study showed that the oxygen vacancies and surface hydroxyl groups present on the surface of TiO2@HNTs act as excellent traps for charge carrier, reducing the electron-hole recombination rate.TiO2@HNTs 2 (2 wt.%) and TiO2@HNTs 3 (3 wt.%) degraded MB dye up to 83.21%, 87.47% and RB dye up to 96.84% and 96.87%, respectively. TiO2@HNT photocatalyst proved to be stable during the three consecutive cycle of photocatalytic degradation of the RB dye. TiO2@HNTs M2 and TiO2@HNTs M3 degraded MB dye up to 27.19%, 42.37% and RB dye up to 30.78%, 32.76%, respectively. Photocatalytic degradation of both the dyes followed the first-order kinetic model. Degradation product analysis was done using the liquid chromatography-mass spectrometry (LC-MS) and the results showed that the dye degradation was initiated by demethylation of the molecule. MB and RB dye degradation reaction were tested by TBA and IPA as OH* and H+ scavengers respectively. Mechanism of photocatalytic activity of TiO2@HNTs and photocatalytic PVC membrane were also explained.

| S-EPMC6416328 | biostudies-literature

Impact of atomic layer deposited TiO2 on the photocatalytic efficiency of TiO2/w-VA-CNT nanocomposite materials.

Project description:Titanium oxide (TiO2) has been widely investigated as a photocatalytic material, and the fact that its performance depends on its crystalline structure motivates further research on the relationship between preparation methods and material properties. In this work, TiO2 thin films were grown on non-functionalized wave-like patterned vertically aligned carbon nanotubes (w-VA-CNTs) via the atomic layer deposition (ALD) technique. Grazing incidence X-ray diffraction (GIXRD) analysis revealed that the structure of the TiO2/VA-CNT nanocomposites varied from amorphous to a crystalline phase with increasing deposition temperature, suggesting a "critical deposition temperature" for the anatase crystalline phase formation. On the other hand, scanning transmission electron microscopy (STEM) studies revealed that the non-functionalized carbon nanotubes were conformally and homogeneously coated with TiO2, forming a nanocomposite while preserving the morphology of the nanotubes. X-ray photoelectron spectroscopy (XPS) provided information about the surface chemistry and stoichiometry of TiO2. The photodegradation experiments under ultraviolet (UV) light on a model pollutant (Rhodamine B, RhB) revealed that the nanocomposite comprised of anatase crystalline TiO2 grown at 200 °C (11.2 nm thickness) presented the highest degradation efficiency viz 55% with an illumination time of 240 min. Furthermore, its recyclability was also demonstrated for multiple cycles, showing good recovery and potential for practical applications.

| S-EPMC9157531 | biostudies-literature

Natural Cotton Cellulose-Supported TiO2 Quantum Dots for the Highly Efficient Photocatalytic Degradation of Dyes.

Project description:The artificial photocatalytic degradation of organic pollutants has emerged as a promising approach to purifying the water environment. The core issue of this ongoing research is to construct efficient but easily recyclable photocatalysts without quadratic harm. Here, we report an eco-friendly photocatalyst with in situ generated TiO2 quantum dots (TQDs) on natural cotton cellulose (CC) by a simple one-step hydrothermal method. The porous fine structure and abundant hydroxyl groups control the shape growth and improve the stability of nanoparticles, making natural CC suitable for TQDs. The TQDs/CC photocatalyst was synthesized without the chemical modification of the TQDs. FE-SEM and TEM results showed that 5-6 nm TQDs are uniformly decorated on the CC surface. The long-term stability in photocatalytic activity and structure of more than ten cycles directly demonstrates the stability of CC on TQDs. With larger CC sizes, TQDs are easier to recycle. The TQDs/CC photocatalysts show impressive potential in the photocatalytic degradation of anionic methyl orange (MO) dyes and cationic rhodamine B (RhB) dyes.

| S-EPMC9504825 | biostudies-literature

Metal sensing-carbon dots loaded TiO2-nanocomposite for photocatalytic bacterial deactivation and application in aquaculture.

Project description:Nowadays, bioactive nanomaterials have been attracted the researcher's enthusiasm in various fields. Herein, Diplocyclos palmatus leaf extract-derived green-fluorescence carbon dots (DP-CDs) were prepared using the hydrothermal method. Due to the strong fluorescence stability, the prepared DP-CDs were coated on filter-paper to make a fluorometric sensor-strip for Fe3+ detection. After, a bandgap-narrowed DP-CDs/TiO2 nanocomposite (DCTN) was prepared using the methanolic extract of D. palmatus. The prepared DCTN exhibited improved photocatalytic bacterial deactivation under sunlight irradiation. The DCTN-photocatalysis slaughtered V. harveyi cells by the production of reactive oxygen species, which prompting oxidative stress, damaging the cell membrane and cellular constituents. These results suggest the plausible mode of bactericidal action of DCTN-photocatalysis under sunlight. Further, the DCTN has shown potent anti-biofilm activity against V. harveyi, and thereby, DCTN extended the survival of V. harveyi-infected shrimps during the in vivo trial with Litopenaeus vannamei. Notably, this is the first report for the disinfection of V. harveyi-mediated acute-hepatopancreatic necrosis disease (AHPND) using nanocomposite. The reduced internal-colonization of V. harveyi on the hepatopancreas as well as the rescue action of the pathognomonic effect in the experimental animals demonstrated the anti-infection potential of DCTN against V. harveyi-mediated AHPND in aquaculture.

| S-EPMC7393085 | biostudies-literature

Three-dimensional plasmonic Ag/TiO2 nanocomposite architectures on flexible substrates for visible-light photocatalytic activity.

Project description:In this study, a periodic three-dimensional (3D) Ag/TiO2 nanocomposite architecture of nanowires was fabricated on a flexible substrate to enhance the plasmonic photocatalytic activity of the composite. Layer-by-layer nanofabrication based on nanoimprint lithography, vertical e-beam evaporation, nanotransfer, and nanowelding was applied in a new method to create different 3D Ag/TiO2 nanocomposite architectures. The fabricated samples were characterized by scanning electron microscopy, transmission electron microscopy, focused ion-beam imaging, X-ray photoelectron spectrometry, and UV-visible spectroscopy. The experiment indicated that the 3D nanocomposite architectures could effectively enhance photocatalytic activity in the degradation of methylene blue solution under visible light irradiation. We believe that our method is efficient and stable, which could be applied to various fields, including photocatalysis, solar energy conversion, and biotechnology.

| S-EPMC5566718 | biostudies-literature

Synthesizing and Evaluating the Photocatalytic and Antibacterial Ability of TiO2/SiO2 Nanocomposite for Silicate Coating.

Project description:The TiO2/SiO2 nanocomposite has been synthesized by a sol-gel method and investigated the effect of the SiO2 content (0, 5, 10, 15, 20, and 50%) on the rutile-to-anatase phase transition of TiO2 NPs. In order to increase the photocatalytic efficiency of the nanocomposite and decrease the price of material, the TiO2/SiO2 Nc with content SiO2 of 15% sample is chosen for preparing silicate coating. The efficiency of photocatalytic MB and antibacterial ability in the air of W silicate coating (adding TiO2/SiO2 Nc (15%)) achieve almost 100% for 60 h and 94.35% for 3 h, respectively. While the efficiency of photocatalytic MB and antibacterial ability of WO silicate coating (adding commercial TiO2/SiO2) is about 25-30% for 60 h and 6.02% for 3 h, respectively. The presence of TiO2/SiO2 Nc (15%) with a larger surface area in W silicate coating can provide increased centers for absorption, photocatalytic reaction, and the contact between sample and bacteria lead to enhance the photocatalytic and antibacterial ability of W silicate coating.

| S-EPMC8485069 | biostudies-literature

Spent Coffee Grounds Derived Carbon Loading C, N Doped TiO2 for Photocatalytic Degradation of Organic Dyes.

Project description:Titanium dioxide (TiO2) is an ideal photocatalyst candidate due to its high activity, low toxicity and cost, and high chemical stability. However, its practical application in photocatalysis is seriously hindered by the wide band gap energy of TiO2 and the prone recombination of electron-hole pairs. In this study, C, N doped TiO2 were supported on spent coffee grounds-derived carbon (ACG) via in situ formation, which was denoted as C, N-TiO2@ACG. The obtained C, N-TiO2@ACG exhibits increased light absorption efficiency with the band gap energy decreasing from 3.31 eV of TiO2 to 2.34 eV, a higher specific surface area of 145.8 m2/g, and reduced recombination rates attributed to the synergistic effect of a spent coffee grounds-derived carbon substrate and C, N doping. Consequently, the optimal 1:1 C, N-TiO2@ACG delivers considerable photocatalytic activity with degradation efficiencies for methylene blue (MB) reaching 96.9% within 45 min, as well as a high reaction rate of 0.06348 min-1, approximately 4.66 times that of TiO2 (0.01361 min-1). Furthermore, it also demonstrated greatly enhanced photocatalytic efficiency towards methyl orange (MO) in the presence of MB compared with a single MO solution. This work provides a feasible and universal strategy of synchronous introducing nonmetal doping and biomass-derived carbon substrates to promote the photocatalytic performance of TiO2 for the degradation of organic dyes.

| S-EPMC10385829 | biostudies-literature

Ultrasmall Plasmonic Nanoparticles Decorated Hierarchical Mesoporous TiO2 as an Efficient Photocatalyst for Photocatalytic Degradation of Textile Dyes.

Project description:Hierarchical mesoporous TiO2 was synthesized via a solvothermal technique. The sonochemical method was adopted to decorate plasmonic nanoparticles (NPs) (Ag, Au) on the pores of mesoporous TiO2. The crystallinity, structure, and morphology were determined to understand the physicochemical nature of the nanocomposites. The catalytic efficiency of the plasmonic nanocatalysts was tested for the azo dyes (congo red, methyl orange, acid orange 10, and remazol red) under solar and visible light irradiations. The generation of hydroxyl radicals was also studied using terephthalic acid as a probe molecule. An attempt was made to understand the influence of size, work function and Fermi level of the metal NPs toward the efficiency of the photocatalyst. The efficiency of the nanocomposites was found to be in the order of P25 < mesoporous TiO2 < mesoporous Ag-TiO2 < mesoporous Au-TiO2 nanospheres under both direct solar light and visible light irradiation. The results indicated that the adsorption of dye, anatase phase, and surface plasmon resonance of NPs favored the effective degradation of dyes in aqueous solution. Further, the efficiency of the catalyst was also tested for xanthene (rose bengal), rhodamine (rhodamine B, rhodamine 6G), and thiazine (methylene blue) dyes. Both TiO2 and NPs (Ag & Au) possess a huge potential as an eco-friendly photocatalyst for wastewater treatment.

| S-EPMC6644734 | biostudies-literature

Enhanced removal of hexavalent chromium from aqueous media using a highly stable and magnetically separable rosin-biochar-coated TiO2@C nanocomposite.

Project description:Recently, nanosized metal-oxides have been extensively investigated for their ability to remove metal ions from aqueous media. However, the activity and capacity of these nanosized metal-oxides for removing metal ions decrease owing to their agglomeration in aqueous media. Herein, we synthesized a highly stable and magnetically separable rosin-biochar-coated (RBC) TiO2@C nanocomposite through a facile and environment-friendly wet chemical coating process, followed by a one-step heating route (pyrolysis) for efficient removal of Cr(vi) from aqueous solution. An array of techniques, namely, TEM, HRTEM, TEM-EDS, XRD, FTIR, VSM, BET and TGA, were used to characterize the prepared nanocomposite. The pyrolysis of rosin into biochar and the fabrication of Fe onto the RBC-TiO2@C nanocomposite were confirmed by FTIR and XRD examination, respectively. Moreover, TEM and HRTEM images and elemental mapping using TEM-EDS showed good dispersion of iron and carbon on the surface of the RBC-TiO2@C nanocomposite. Sorption of Cr(vi) ions on the surface of the RBC-TiO2@C nanocomposite was very fast and efficient, having a removal efficiency of ∼95% within the 1st minute of reaction. Furthermore, thermodynamic analysis showed negative values of Gibb's free energy at all five temperatures, indicating that the adsorption of Cr(vi) ions on the RBC-TiO2@C nanocomposite was favorable and spontaneous. Conclusively, our results indicate that the RBC-TiO2@C nanocomposite can be used for efficient removal of Cr(vi) from aqueous media due to its novel synthesis and extraordinary adsorption efficacy during a short time period.

| S-EPMC9082923 | biostudies-literature