scholarly journals Degradation of rhodamine B with manganese dioxide nanorods

2018 ◽  
Vol 16 (5) ◽  
pp. 846-856 ◽  
Author(s):  
V. Sabna ◽  
Santosh G. Thampi ◽  
S. Chandrakaran
Keyword(s):  
Manganese Dioxide ◽  
Rhodamine B ◽  
Initial Period ◽  
Oxidative Degradation ◽  
Cost Effective ◽  
Precipitation Method ◽  
Order Kinetic ◽  
Initial Concentration ◽  
Order Kinetic Model ◽  
Co Precipitation

Abstract This is an investigation on oxidative degradation of rhodamine B (RhB) by manganese dioxide (MnO2) nanorods synthesized by redox co-precipitation method. Field emission scanning electron microscopy of MnO2 nanorods at an electron voltage of 10 kV revealed a rod-like morphology for the synthesized nanoparticles. Fourier transform infrared spectra exhibited characteristic peaks of MnO2. Surface area of MnO2 nanorods was 277 m2/g. Effect of various parameters like initial concentration and pH of RhB solution, time of contact between MnO2 nanorods and RhB, dosage of MnO2, and stirring speed on decolouration of RhB was evaluated in batch experiments. Rapid decolouration in the initial period of the reaction was observed due to the adsorption of RhB molecules onto the surface of MnO2 nanorods followed by oxidative degradation. Percentage decolouration decreased with increase in initial concentration and increased with increase in dosage, speed of stirring the mixture and with increase in pH up to pH 7. Near complete decolouration was achieved at a dose of 0.5 g/L of MnO2 nanorods from 20 mg/L RhB solution within 3 min. Observations fitted best to the pseudo second order kinetic model. This study could pave the way for development of cost-effective, nontoxic nanostructures for treatment of wastewaters containing RhB.

scholarly journals Kinetic Studies on the Catalytic Degradation of Rhodamine B by Hydrogen Peroxide: Effect of Surfactant Coated and Non-Coated Iron (III) Oxide Nanoparticles

Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2246
Author(s):  
Mohd Shaban Ansari ◽  
Kashif Raees ◽  
Moonis Ali Khan ◽  
M.Z.A. Rafiquee ◽  
Marta Otero
Keyword(s):  
Electron Microscopy ◽  
Hydrogen Peroxide ◽  
Rhodamine B ◽  
Sodium Dodecyl ◽  
Kinetic Studies ◽  
Catalytic Degradation ◽  
Precipitation Method ◽  
Order Kinetic ◽  
Fe3o4 Nps ◽  
Co Precipitation

Iron (III) oxide (Fe3O4) and sodium dodecyl sulfate (SDS) coated iron (III) oxide (SDS@Fe3O4) nanoparticles (NPs) were synthesized by the co-precipitation method for application in the catalytic degradation of Rhodamine B (RB) dye. The synthesized NPs were characterized using X-ray diffractometer (XRD), vibrating sample magnetometer (VSM), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Fourier transform infra-red (FT-IR) spectroscopy techniques and tested in the removal of RB. A kinetic study on RB degradation by hydrogen peroxide (H2O2) was carried out and the influence of Fe3O4 and SDS@Fe3O4 magnetic NPs on the degradation rate was assessed. The activity of magnetic NPs, viz. Fe3O4 and SDS@Fe3O4, in the degradation of RB was spectrophotometrically studied and found effective in the removal of RB dye from water. The rate of RB degradation was found linearly dependent upon H2O2 concentration and within 5.0 × 10−2 to 4.0 × 10−1 M H2O2, the observed pseudo-first-order kinetic rates (kobs, s−1) for the degradation of RB (10 mg L−1) at pH 3 and temperature 25 ± 2 °C were between 0.4 and 1.7 × 104 s−1, while in presence of 0.1% w/v Fe3O4 or SDS@Fe3O4 NPs, kobs were between 1.3 and 2.8 × 104 s−1 and between 2.6 and 4.8 × 104 s−1, respectively. Furthermore, in presence of Fe3O4 or SDS@Fe3O4, kobs increased with NPs dosage and showed a peaked pH behavior with a maximum at pH 3. The magnitude of thermodynamic parameters Ea and ΔH for RB degradation in presence of SDS@Fe3O4 were 15.63 kJ mol−1 and 13.01 kJ mol−1, respectively, lowest among the used catalysts, confirming its effectiveness during degradation. Furthermore, SDS in the presence of Fe3O4 NPs and H2O2 remarkably enhanced the rate of RB degradation.

scholarly journals Degradation of dye wastewater by persulfate activated with Fe3O4/graphene nanocomposite

2016 ◽  
Vol 6 (4) ◽  
pp. 553-561 ◽  
Author(s):  
Xiao-Bao Gong
Keyword(s):  
Organic Contaminants ◽  
Precipitation Method ◽  
Order Kinetic ◽  
Dye Wastewater ◽  
X Ray Diffraction ◽  
First Order ◽  
Order Kinetic Model ◽  
Infrared Spectrometer ◽  
Graphene Nanocomposite ◽  
Co Precipitation

In this study, Fe3O4/graphene nanocomposite was synthesized through a liquid-phase co-precipitation method and characterized using X-ray diffraction and Fourier transform infrared spectrometer. The synthetic Fe3O4/graphene was used as a heterogeneous catalyst to activate persulfate to efficiently degrade methylene blue (MB). The target pollutant MB can be degraded by sulfate radicals depending on several parameters including persulfate and Fe3O4/graphene concentrations, pH and reaction temperature. Within 120 min of reaction time, almost 100% of 0.05 mM MB was removed by 1.5 mM persulfate in the presence of 150 mg/L of Fe3O4/graphene at pH = 6.0 and 25 °C. The degradation of MB was found to follow the pseudo-first-order kinetic model. The Fe3O4/graphene has much better stability and reusability than free Fe3O4 suggested by reuse tests. The results demonstrate that Fe3O4/graphene activated persulfate is a promising technology for remediation of water pollution caused by organic contaminants.

Removal of hexavalent chromium from aqueous solution by calcined Zn/Al-LDHs

2016 ◽  
Vol 74 (1) ◽  
pp. 229-235 ◽  
Author(s):  
Hui-Duo Yang ◽  
Yun-Peng Zhao ◽  
Shi-Feng Li ◽  
Xing Fan ◽  
Xian-Yong Wei ◽  
...  
Keyword(s):  
Hexavalent Chromium ◽  
Precipitation Method ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Effects Of Ph ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Co Precipitation ◽  
Double Hydroxides

In this study, Zn/Al-layered double hydroxides (Zn/Al-LDHs) were synthesized by a co-precipitation method and characterized with X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy. Then the hexavalent chromium Cr(VI) adsorption experiments on calcined Zn/Al-LDHs were carried out to analyze the effects of pH, temperature, adsorption time, initial Cr(VI) concentration and adsorbent dosage on the removal of Cr(VI) from aqueous solutions. The maximum adsorption capacity for Cr(VI) on calcined Zn/Al-LDHs under optimal conditions was found to be over 120 mg/g. The kinetic and isotherm of Cr(VI) adsorption on calcined Zn/Al-LDHs can be described with the pseudo-second-order kinetic model and Langmuir isotherm, respectively.

scholarly journals Optimal Synthesis and Mechanistic Performance of HCO-Doped-(Fe3O4)x Adsorbent for Sb(III)/Sb(V) Removal From Water

2020 ◽  
Author(s):  
Renjian Deng ◽  
Jun Zhang ◽  
Xiaoliang Hu ◽  
Chuanqu Zhu ◽  
Fubing Xie ◽  
...  
Keyword(s):  
Surface Area ◽  
Precipitation Method ◽  
Hydroxyl Groups ◽  
Complexation Reaction ◽  
Order Kinetic ◽  
Ionic Charge ◽  
Adsorption Performance ◽  
Potential Applications ◽  
Order Kinetic Model ◽  
Co Precipitation

Concern over potential antimony mediated toxicity from mining and smelting activities has instigated novel concepts toward removing aqueous antimony ions. The iron based adsorbent Fe3O4/HCO was found to be efficient for treating antimony-containing wastewater However, ineffective methodology for preparation limited its effective adsorption capacity and thus wider application. In this study, a new type of HCO-doped-(Fe3O4)x adsorbent was prepared by co-precipitation method for doping Fe3O4 into HCO sludge (HCO), thereby improving adsorption performance for Sb(III) and Sb(V) ions, with the maximum adsorbing capacity being 44.46 mg/g and 47.91 mg/g, respectively. According to the results of BET, SEM-EDS, XRD and XPS, it were confirmed that the FeOOH and X≡Fe-OH were formed during the preparation process, bring about the increased the surface area, thus resulting in further increase of surface area, hydroxyl groups and the net negative ionic charge. Moreover, the adsorption kinetics followed the pseudo-second-order kinetic model which indicated that adsorption process of Sb(III)/Sb(V) by HCO-doped-(Fe3O4)x adsorbent was controlled by chemical reaction. The main adsorption mechanism is that antimony ion and amorphous iron oxide X≡Fe-OH undergo coordination exchange reaction and complexation reaction with CeO2 or Ce2O3. Furthermore, HCO-doped-(Fe3O4)x could adapt to wide pH and had stable adsorption ability after regeneration. The good adsorption performance of HCO-doped-(Fe3O4)x makes it a potential applications of adsorbent for removal of antimony.

scholarly journals Enhanced Performance of Chitosan via a Novel Quaternary Magnetic Nanocomposite Chitosan/Grafted Halloysitenanotubes@ZngFe3O4 for Uptake of Cr (III), Fe (III), and Mn (II) from Wastewater

Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2714
Author(s):  
Mahmoud F. Mubarak ◽  
Ahmed H. Ragab ◽  
Rasha Hosny ◽  
Inas A. Ahmed ◽  
Hanan A. Ahmed ◽  
...  
Keyword(s):  
Metal Ions ◽  
High Efficiency ◽  
Precipitation Method ◽  
High Electron ◽  
Order Kinetic ◽  
Equilibrium System ◽  
Adsorption Removal ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Co Precipitation

A novel chitosan/grafted halloysitenanotubes@Zngmagnetite quaternary nanocomposite (Ch/g-HNTs@ZngM) was fabricated using the chemical co-precipitation method to remove the ions of Cr (III), Fe (III), and Mn (II) from wastewater. The characteristics of the synthesized Ch/g-HNTs@ZngM quaternary nanocomposite were investigated using FTIR, SEM, XRD, GPC, TGA, TEM, and surface zeta potential. The characterization analysis proved that the mentioned nanocomposite structure contains multiple functional groups with variable efficiencies. Additionally, they proved the existence of magnetic iron in the nanocomposite internal structure with the clarity of presentation of gaps and holes of high electron density on its surface. The results showed that the pH and time to reach an equilibrium system for all the studied metal ions were obtained at 9.0 and 60 min, respectively. The synthesized Ch/g-HNTs@ZngM nanocomposite exhibited maximum adsorption removal of 95.2%, 99.06%, and 87.1% for Cr (III), Fe (III), and Mn (II) ions, respectively. The pseudo-second-order kinetic model and, for isotherm, the Langmuir model were best fitted with the experimental data. The thermodynamic parameters indicated the exothermic and spontaneous nature of the adsorption reaction as proven by the ΔH° and ΔG° values. Additionally, chemical adsorption by the coordination bond is supposed as the main mechanism of adsorption of the mentioned metal ions on the nanocomposite. Finally, Ch/g-HNTs@ZngM displays prospected advantages, such as a low-expense adsorbent, high efficiency and availability, and an eco-friendly source, that will reduce the environmental load via an environmentally friendly method.

Studying adsorption of methylene blue onto chitosan – mangetite composite

2021 ◽  
Vol 11 (1) ◽  
pp. 60-66
Author(s):  
Quy Bui Minh ◽  
Oanh Do Thi ◽  
Vinh Nguyen Dinh ◽  
Linh Nguyen Thi Ngoc ◽  
Hoa Nguyen Thi Hong ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Diffraction Method ◽  
Precipitation Method ◽  
Isotherm Models ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Co Precipitation ◽  
Microscopy Techniques

The chitosan/mangetite composite in the mass ratio chitosan:mangetite of 9:1 (CM91) was synthesised by co-precipitation method. The characteristics of the chitosan/mangetite composite was estimated by X-ray diffraction method (XRD) and scanning electron microscopy techniques (SEM). The methylene blue adsorption ability onto CM91 composite was well at value pH 9, equilibrium contact time of 20 minutes. The experimental adsorption data fitted into pseudo–Langmuir adsorption isotherm models. The adsorption followed pseudo-second order kinetic model very well. The maximum adsorption capacity of that composite which caculated by Langmuir equation was 94,18 mg/g.

scholarly journals Development of Biochars Derived from Water Bamboo (Zizania latifolia) Shoot Husks Using Pyrolysis and Ultrasound-Assisted Pyrolysis for the Treatment of Reactive Black 5 (RB5) in Wastewater

Water ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 1615
Author(s):  
Thanh Tam Nguyen ◽  
Hung-Hsiang Chen ◽  
Thi Hien To ◽  
Yu-Chen Chang ◽  
Cheng-Kuo Tsai ◽  
...  
Keyword(s):  
Cost Effective ◽  
Reactive Black 5 ◽  
Order Kinetic ◽  
Sem Images ◽  
Zizania Latifolia ◽  
Surface Areas ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ultrasound Assisted ◽  
Green Technique

Adsorbent made by carbonization of biomass under oxygen-limited conditions has become a promising material for wastewater treatment owing to its cost-effective, simple, and eco-friendly processing method. Ultrasound is considered a green technique to modify carbon materials because it uses water as the solvent. In this study, a comparison of Reactive Black 5 (RB5) adsorption capacity between biochar (BC) generated by pyrolysis of water bamboo (Zizania latifolia) husks at 600 °C and ultrasound-assisted biochar (UBC) produced by pyrolysis at 600 °C assisted by ultrasonic irradiation was performed. UBC showed a greater reaction rate and reached about 80% removal efficiency after 4 h, while it took 24 h for BC to reach that level. Scanning electron microscope (SEM) images indicated that the UBC morphology surface was more porous, with the structure of the combination of denser mesopores enhancing physiochemical properties of UBC. By Brunauer, Emmett, and Teller (BET), the specific surface areas of adsorbent materials were analyzed, and the surface areas of BC and UBC were 56.296 m2/g and 141.213 m2/g, respectively. Moreover, the pore volume of UBC was 0.039 cm3/g, which was higher than that of BC at 0.013 cm3/g. The adsorption isotherms and kinetics revealed the better fits of reactions to Langmuir isotherm and pseudo-second-order kinetic model, indicating the inclination towards monolayer adsorption and chemisorption of RB5 on water bamboo husk-based UBC.

Immobilization of Nano-TiO2 on Expanded Perlite for Photocatalytic Degradation of Rhodamine B

2011 ◽  
Vol 110-116 ◽  
pp. 3795-3800 ◽  
Author(s):  
Xiao Zhi Wang ◽  
Wei Wei Yong ◽  
Wei Qin Yin ◽  
Ke Feng ◽  
Rong Guo
Keyword(s):  
Catalytic Activity ◽  
Photocatalytic Degradation ◽  
Rhodamine B ◽  
Degradation Kinetics ◽  
Irradiation Time ◽  
Sol Gel ◽  
Polluted Water ◽  
Order Kinetic ◽  
Expanded Perlite ◽  
Initial Concentration

Expanded perlite (EP) modified titanium dioxide (TiO2) with different loading times were prepared by Sol-Gel method. Photocatalytic degradation kinetics of Rhodamine B (RhB) in polluted water by the materials (EP-nanoTiO2), as well as the effects of different loading times and the initial concentration of RhB on photocatalysis rate were examined. The catalytic activity of the regenerated photocatalyst was also tested. The results showed that photocatalyst modified three times with TiO2had the highest catalytic activity. Degradation ratio of RhB by EP-nanoTiO2(modified three times) under irradiation for 6 h were 98.0%, 75.6% and 63.2% for 10 mg/L, 20 mg/L and 30 mg/L, respectively.The photocatalyst activity has little change after the five times recycling, and the degradation rate of RhB decreased less than 8%. The reaction of photocatalysis for RhB with irradiation time can be expressed as first-order kinetic mode within the initial concentration range of RhB between 10mg/L and 30 mg/L. EP-nanoTiO2photocatalyst has a higher activity and stability to degrade RhB in aqueous solution.

scholarly journals Fabrication of novel particle electrode γ-Al2O3@ZIF-8 and its application for degradation of Rhodamine B

2019 ◽  
Vol 80 (1) ◽  
pp. 109-116 ◽  
Author(s):  
Liguo Zhang ◽  
Caixia Ma ◽  
Lei Liu ◽  
Jingshi Pan ◽  
Qilin Wang
Keyword(s):  
Surface Area ◽  
Removal Efficiency ◽  
Rhodamine B ◽  
Three Dimensional ◽  
Cell Voltage ◽  
Bet Surface Area ◽  
Order Kinetic ◽  
Zeolitic Imidazolate Framework ◽  
Crystallization Method ◽  
Order Kinetic Model

Abstract Due to the high Brunauer–Emmett–Teller (BET) surface area of zeolitic imidazolate framework (ZIF)-8, a secondary crystallization method was used to prepare a particle electrode of γ-Al2O3@ZIF-8. According to the results from a field emission scanning electron microscope (SEM) and X-ray diffractometer (XRD), the particle electrode of γ-Al2O3 was successfully loaded with ZIF-8, and the BET surface area (1,433 m2/g) of ZIF-8 was over ten times that of γ-Al2O3. The key operation parameters of cell voltage, pH, initial RhB concentration and electrolyte concentration were all optimized. The observed rate constant (kobs) of the pseudo-first-order kinetic model for the electrocatalytic oxidation (ECO) system with the particle electrode of γ-Al2O3@ZIF-8 (15.2 × 10−2 min−1) was over five times higher than that of the system with the traditional particle electrode of γ-Al2O3 (2.6 × 10−2 min−1). The loading of ZIF-8 on the surface of γ-Al2O3 played an important role in improving electrocatalytic activity for the degradation of Rhodamine B (RhB), and the RhB removal efficiency of the three-dimensional (3D) electrocatalytic system with the particle electrode of γ-Al2O3@ZIF-8 was 93.5% in 15 min, compared with 27.5% in 15 min for the particle electrode of γ-Al2O3. The RhB removal efficiency was kept over 85% after five cycles of reuse for the 3D electrocatalytic system with the particle electrode of γ-Al2O3@ZIF-8.

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