UV SPECTROSCOPY AND KINETIC RESEARCH OF PHOTODEGRADATION OF METHYL ORANGE IN THE PRESENCE OF TITANIUM DIOXIDE AND β-CYCLODEXTRIN OR ITS DERIVATIVES

2021 ◽  
Vol 43 (2) ◽  
pp. 103-112
Author(s):  
Yu.V. Bardadym ◽  
◽  
S.M. Kobylinskyi ◽  
L.V. Kobrina ◽  
S.V. Riabov ◽  
...  
Keyword(s):  
Titanium Dioxide ◽  
Methyl Orange ◽  
Natural Waters ◽  
Uv Spectroscopy ◽  
Significant Loss ◽  
Hydroxyl Groups ◽  
Sulfobutyl Ether ◽  
Kinetics Of ◽  
Irradiation Process ◽  
By Products

The research is devoted to the study of the effect of β-cyclodextrin (β-CD) and its derivatives on the photocatalytic degradation of methyl orange in aqueous solutions in the presence of titanium dioxide. It has been shown that the kinetics of photodegradation of methyl orange is more accurately described by the pseudo first order equation for all investigated pH values. In the presence of cyclodextrins β-CD and 2-hydroxypropyl-β-cyclodextrin, acceleration of photodegradation was observed only after 30 min of irradiation. As a result, the oxidation of hydroxyl groups of cyclodextrin occurred. A significant slowdown in photodestruction in the TiO2-β-CD sample during the first 45 min is explained by the formation of inclusion complexes of cyclodextrin with methyl orange, which prevented the destruction of dye. The use of the β-cyclodextrin, its derivatives and increasing the acidity of the medium accelerates the processes of photodestruction of methyl orange in distilled and natural waters. Methyl orange was decolorized for 20 – 25 min in solutions of all investigated cyclodextrin derivatives at pH 2.5. The destruction of methyl orange was most effective with the use of sulfobutyl ether β-CD. The bactericidal lamp (λ = 254 nm) allows to increase the rate of destruction during the irradiation process. Methyl orange discolored much faster under the action of a bactericidal lamp than using only ultraviolet lamps with λ = 365 nm. A slight slowdown in the decomposition process is observed after several irradiation cycles. This may be due to the influence of the formed products of destruction. However, under such conditions, the by-products of reactions decompose much faster. The use of cyclodextrins is possible without significant loss of efficiency up to 8 cycles.

scholarly journals Enhanced decolourization of methyl orange by immobilized TiO2/chitosan-montmorillonite

2020 ◽  
Author(s):  
Noor Nazihah Bahrudin ◽  
Mohd Asri Nawi ◽  
Zulkarnain Zainal ◽  
Raphaël Schneider ◽  
Sumiyyah Sabar
Keyword(s):  
Methyl Orange ◽  
Large Scale ◽  
Band Gap Energy ◽  
Significant Loss ◽  
Simultaneous Occurrence ◽  
Layer By Layer ◽  
Layer Arrangement ◽  
Immobilized Tio2 ◽  
By Products ◽  
Better Than

Abstract Many attempts have been made to improve the photocatalytic performance of immobilized photocatalysts for large-scale applications by modification of the photocatalyst properties. In this work, immobilized bilayer photocatalyst composed of titanium dioxide (TiO2) and chitosan–montmorillonite (CS–MT) were prepared in a layer-by-layer arrangement supported on glass substrate. This arrangement allows a simultaneous occurrence of adsorption and photocatalysis processes of pollutants, whereby each layer could be independently modified and controlled to acquire the desired degree of occurring processes. It was found that the addition of MT clay within the CS composite sub-layer improved the mechanical strength of CS, reduced its swelling and shifted its absorption threshold to higher wavelengths. In addition, the band gap energy of the photocatalyst was also reduced to 2.93 eV. The immobilized TiO2/CS–MT exhibited methyl orange (MO) decolourization rate of 0.071 min−1 under light irradiation, which is better than the single TiO2 due to the synergistic processes of adsorption by CS–MT and photocatalysis by TiO2 layer. The MO dye took 6 h to achieve complete mineralization and produced sulfate and nitrate ions as the by-products. Furthermore, the immobilized TiO2/CS–MT could be reused for at least ten cycles of application without significant loss of its activity.

Kinetic of oxidation of methyl orange by vanadium(V) under conditions VO2+ and decavanadates coexist: Catalysis by Triton X-100 micellar medium

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Methyl Orange ◽  
Solution Ph ◽  
Vanadium Concentration ◽  
Limiting Behavior ◽  
First Order ◽  
First Order Kinetics ◽  
Ph Range ◽  
Kinetic Pattern ◽  
Triton X ◽  
Kinetics Of

The kinetics of oxidation of methyl orange by vanadium(V) {V(V)} has been investigated in the pH range 2.3-3.79. In this pH range V(V) exists both in the form of decavanadates and VO2+. The kinetic results are distinctly different from the results obtained for the same reaction in highly acidic solution (pH < 1) where V(V) exists only in the form of VO2+. The reaction obeys first order kinetics with respect to methyl orange but the rate has very little dependence on total vanadium concentration. The reaction is accelerated by H+ ion but the dependence of rate on [H+] is less than that corresponding to first order dependence. The equilibrium between decavanadates and VO2+ explains the different kinetic pattern observed in this pH range. The reaction is markedly accelerated by Triton X-100 micelles. The rate-[surfactant] profile shows a limiting behavior indicative of a unimolecular pathway in the micellar pseudophase.

scholarly journals Osseointegrating and phase-oriented micro-arc-oxidized titanium dioxide bone implants

2021 ◽  
Vol 19 ◽  
pp. 228080002110068
Author(s):  
Hsien-Te Chen ◽  
Hsin-I Lin ◽  
Chi-Jen Chung ◽  
Chih-Hsin Tang ◽  
Ju-Liang He
Keyword(s):  
Titanium Dioxide ◽  
High Surface ◽  
Cell Activity ◽  
Active Surface ◽  
Rutile Phase ◽  
Hydroxyl Groups ◽  
Bone Implant ◽  
Implant System

Here, we present a bone implant system of phase-oriented titanium dioxide (TiO2) fabricated by the micro-arc oxidation method (MAO) on β-Ti to facilitate improved osseointegration. This (101) rutile-phase-dominant MAO TiO2 (R-TiO2) is biocompatible due to its high surface roughness, bone-mimetic structure, and preferential crystalline orientation. Furthermore, (101) R-TiO2 possesses active and abundant hydroxyl groups that play a significant role in enhancing hydroxyapatite formation and cell adhesion and promote cell activity leading to osseointegration. The implants had been elicited their favorable cellular behavior in vitro in the previous publications; in addition, they exhibit excellent shear strength and promote bone–implant contact, osteogenesis, and tissue formation in vivo. Hence, it can be concluded that this MAO R-TiO2 bone implant system provides a favorable active surface for efficient osseointegration and is suitable for clinical applications.

scholarly journals Effect of Na- and Organo-Modified Montmorillonite/Essential Oil Nanohybrids on the Kinetics of the In Situ Radical Polymerization of Styrene

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 474
Author(s):  
Ioannis S. Tsagkalias ◽  
Alexandra Loukidi ◽  
Stella Chatzimichailidou ◽  
Constantinos E. Salmas ◽  
Aris E. Giannakas ◽  
...  
Keyword(s):  
Essential Oil ◽  
Radical Polymerization ◽  
Food Packaging ◽  
In Situ Polymerization ◽  
Average Molecular Weight ◽  
Monomer Conversion ◽  
Hydroxyl Groups ◽  
Modified Montmorillonite ◽  
Kinetics Of

The great concern about the use of hazardous additives in food packaging materials has shown the way to new bio-based materials, such as nanoclays incorporating bioactive essential oils (EO). One of the still unresolved issues is the proper incorporation of these materials into a polymeric matrix. The in situ polymerization seems to be a promising technique, not requiring high temperatures or toxic solvents. Therefore, in this study, the bulk radical polymerization of styrene was investigated in the presence of sodium montmorillonite (NaMMT) and organo-modified montmorillonite (orgMMT) including thyme (TO), oregano (OO), and basil (BO) essential oil. It was found that the hydroxyl groups present in the main ingredients of TO and OO may participate in side retardation reactions leading to lower polymerization rates (measured gravimetrically by the variation of monomer conversion with time) accompanied by higher polymer average molecular weight (measured via GPC). The use of BO did not seem to affect significantly the polymerization kinetics and polymer MWD. These results were verified from independent experiments using model compounds, thymol, carvacrol and estragol instead of the clays. Partially intercalated structures were revealed from XRD scans. The glass transition temperature (from DSC) and the thermal stability (from TGA) of the nanocomposites formed were slightly increased from 95 to 98 °C and from 435 to 445 °C, respectively. Finally, better dispersion was observed when orgMMT was added instead of NaMMT.

Comparative investigation on the removal of methyl orange from aqueous solution using three different advanced oxidation processes

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Zahia Benredjem ◽  
Karima Barbari ◽  
Imene Chaabna ◽  
Samia Saaidia ◽  
Abdelhak Djemel ◽  
...  
Keyword(s):  
Methyl Orange ◽  
Current Density ◽  
Advanced Oxidation Processes ◽  
Degradation Rate ◽  
Supporting Electrolyte ◽  
Advanced Oxidation ◽  
Comparative Investigation ◽  
Oxidation Processes ◽  
The Comparative Study ◽  
Kinetics Of

Abstract The Advanced Oxidation Processes (AOPs) are promising environmentally friendly technologies for the treatment of wastewater containing organic pollutants in general and particularly dyes. The aim of this work is to determine which of the AOP processes based on the Fenton reaction is more effective in degrading the methyl orange (MO) dye. The comparative study of the Fenton, photo-Fenton (PF) and electro-Fenton (EF) processes has shown that electro-Fenton is the most efficient method for oxidizing Methyl Orange. The evolution of organic matter degradation was followed by absorbance (discoloration) and COD (mineralization) measurements. The kinetics of the MO degradation by the electro-Fenton process is very rapid and the OM degradation rate reached 90.87% after 5 min. The influence of some parameters such as the concentration of the catalyst (Fe (II)), the concentration of MO, the current density, the nature and the concentration of supporting electrolyte was investigated. The results showed that the degradation rate increases with the increase in the applied current density and the concentration of the supporting electrolyte. The study of the concentration effect on the rate degradation revealed optimal values for the concentrations 2.10−5 M and 75 mg L−1 of Fe (II) and MO respectively.

A poly(arylene ether sulfone) hybrid membrane using titanium dioxide nanoparticles as the filler

2016 ◽  
Vol 29 (1) ◽  
pp. 26-35 ◽  
Author(s):  
Yunwu Yu ◽  
Wenhao Pan ◽  
Xiaoman Guo ◽  
Lili Gao ◽  
Yaxin Gu ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Titanium Dioxide ◽  
Gas Separation ◽  
Proton Nuclear Magnetic Resonance ◽  
Separation Performance ◽  
Hydroxyl Groups ◽  
Hybrid Membranes ◽  
Permeability Coefficients ◽  
Arylene Ether ◽  
The Matrix

Poly(arylene ether sulfone) (PES)–titanium dioxide (TiO2) hybrid membranes were prepared via solution blending method using TiO2 nanoparticles as inorganic filler. The chemical structure and thermal stability of the matrix polymer were characterized by proton nuclear magnetic resonance, Fourier transform infrared, differential scanning calorimetry, and thermogravimetric analysis. The crystal structure, morphology, mechanical properties, and gas separation performance of hybrid membranes were characterized in detail. As shown in scanning electron microscopic images, TiO2 nanoparticles dispersed homogeneously in the matrix. Although the mechanical properties of hybrid membranes decreased certainly compared to the pure PES membranes, they are strong enough for gas separation in this study. All gas permeability coefficients of PES-TiO2 hybrid membranes were higher than pure PES membranes, attributed to the nanogap caused by TiO2 nanoparticles, for instance, oxygen and nitrogen permeability coefficients of Hybrid-3 (consists of PES with 4-amino-phenyl pendant group and hexafluoroisopropyl (Am-PES)-20 and TiO2 nanoparticles, 5 wt%) increased from 2.57 and 0.33 to 5.88 and 0.63, respectively. In addition, the separation factor increased at the same time attributed to the stimulative transfer effect caused by the interaction of hydroxyl groups on the TiO2 nanoparticle and polar carbon dioxide molecules.

Modeling of sorption kinetics of U(VI) micro-quantities nanostructured materials with anatase mesoporous structures

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Veniamin Zheleznov ◽  
Aleksey Golikov ◽  
Tatiana Sokolnitskaya ◽  
Sergey Ivannikov
Keyword(s):  
Nanostructured Materials ◽  
Sorption Kinetics ◽  
Uranyl Ion ◽  
Competitive Sorption ◽  
Hydroxyl Groups ◽  
Complex Ions ◽  
The Stability ◽  
Kinetics Of ◽  
Mesoporous Structures ◽  
Ionic Forms

Abstract The sorption kinetics of uranyl ions micro-quantities from fluoride solutions by nanostructured materials with anatase mesoporous structures has been studied. Using the model of competitive sorption of ions and positively charged complexes of uranyl ion on deprotonated hydroxyl groups of an anatase, kinetic curves of changes in the ratio of ionic forms of uranium in solution were calculated. Modeling was carried out under the assumption of a two-stage mechanism of uranium complex ions sorption. The modeling considered the influence of the uranyl ion carbonate complexes formation. The shift in equilibrium among ionic forms of uranyl correlates with the stability of the complexes in solution.

scholarly journals Titanium Dioxide Modified with Alcoholic Hydroxyl Groups

1994 ◽  
Vol 67 (8) ◽  
pp. 489-495 ◽  
Author(s):  
Tsuneo SUHARA ◽  
Hiroshi HUKUI ◽  
Michihiro YAMAGUCHI
Keyword(s):  
Titanium Dioxide ◽  
Hydroxyl Groups ◽  
Alcoholic Hydroxyl
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