scholarly journals Enhanced Performance of Hydrogen Peroxide Modified Pozzolan-based Geopolymer for Abatement of Methylene blue from Aqueous Medium

2021 ◽  
Author(s):  
Dzoujo Tamaguelon Hermann ◽  
Tome Sylvain ◽  
Victor O Shikuku ◽  
Jean T Tchuigwa ◽  
Alex Spieß ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Methylene Blue ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Textural Properties ◽  
Blue Dye ◽  
Order Kinetic ◽  
X Ray ◽  
Freundlich Isotherms ◽  
Adsorption Rates

Abstract Pozzolan-based eco-adsorbents were synthesized by geopolymerization with addition of hydrogen peroxide (H2O2) with mass ratios 0% (GP0) and 1% (GP1) and the products used to sorb cationic methylene blue (MB) dye from water. The chemical composition, textural properties, mineral composition, surface functions, as well as morphology and internal structure of these samples were determined by the X-ray fluorescence, adsorption of nitrogen by the B.E.T (Bruamer Emmet Teller) method, X-ray diffraction, Fourier Transformed Infrared Spectroscopy (FTIR) and scanning electron microscopy (SEM), respectively. The effects of contact time, dye initial concentration, adsorbent dosage, pH and temperature were examined and are herein reported. Incorporation of 1% H2O2 increased the specific surface area from 4.344 to 5.610 m2/g representing ~ 29% increase in surface area. This translated an increase in the MB adsorption capacity by 15 orders of magnitude from 24.4 to 366.2 mg/g for GP0 and GP1, respectively. The adsorption rates of methylene blue on the two geopolymers were best described by the pseudo-second order kinetic model. The adsorption equilibrium data were best described by the Sips and Freundlich isotherms models for GP0 and GP1, respectively. Thermodynamically, it was determined that the adsorption of methylene blue onto GP0 and GP1 is a physical and endothermic process. The results show that incorporation of low amount of hydrogen peroxide into pozzolan-based geopolymers increases their adsorption capacity for methylene blue dye stupendously while preserving the surface chemistry.

Physicochemical Properties of Oxalic Acid-Modified Chitosan/Neem Leave Composites from Pessu River Crab Shell

2019 ◽  
Vol 17 (9) ◽  
Author(s):  
Oluwadayo Francis Asokogene ◽  
Muhammad Abbas Ahmad Zaini ◽  
Misau Muhammad Idris ◽  
Surajudeen Abdulsalam ◽  
Aliyu El-Nafaty Usman
Keyword(s):  
Methylene Blue ◽  
Oxalic Acid ◽  
Surface Area ◽  
Dye Adsorption ◽  
Textural Properties ◽  
Bet Surface Area ◽  
Blue Dye ◽  
Crab Shell ◽  
Sem Images ◽  
X Ray

Abstract This study was aimed to evaluate the characteristics of chitosan from Pessu river crab shell and its derivatives as prospective adsorbent. The synthesized chitosan (CH) was modified with 10 % (w/v) oxalic acid (CHOx), while the composites (CHOx-ANL1, CHOx-ANL2 and CHOx-ANL3) were designated according to the amount of activated neem leave (ANL). The materials were characterized by Fourier transform infrared (FTIR), energy-dispersive X-ray (EDAX), X-ray diffraction (XRD), scanning electron microscope (SEM), Brunauer-Emmett-Teller (BET), thermal gravimetric (TGA) and methylene blue dye adsorption. The FTIR spectra of chitosan samples show the characteristics of primary and secondary amine/amide groups. The SEM images exhibit a tight, porous and fractured surface, which is covered with activated neem leave for the composites. The BET surface area of chitosan materials is in the increasing order of, CH < CHOx-ANL1 < CHOx-ANL2 < CHOx < CHOx-ANL3. CHOx-ANL3 displays a higher surface area of 389 m2/g, and 70.9 % mesoporosity. Despite its lower surface area of 258 m2/g (65.4 % mesoporosity), CHOx-ANL1 exhibits a greater methylene blue adsorption of 90.8 mg/g at dye concentration of 300 mg/L. The possible removal mechanisms include ionic interaction between dye molecules and functional groups, and surface adsorption due to the textural properties of chitosan samples. Chitosan from Pessu river crab shell and its derivatives are promising adsorbent candidate for dyes and heavy metals removal from water.

scholarly journals Heterogeneous Fenton-Like Oxidation of Methylene Blue Using Alternative Catalysts

2021 ◽  
Vol 29 (48) ◽  
pp. 91-97
Author(s):  
Juraj Michálek ◽  
Kseniya Domnina ◽  
Veronika Kvorková ◽  
Kristína Šefčovičová ◽  
Klaudia Mončeková ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Methylene Blue ◽  
Low Cost ◽  
Hydrogen Peroxide Solution ◽  
Blue Dye ◽  
Order Kinetic ◽  
Heterogeneous Fenton ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Black Nickel

Abstract The usage of the low-cost catalysts for methylene blue removal from wastewater was investigated. Heterogeneous Fenton-like process consists of the use of a hydrogen peroxide solution, and an iron-rich catalyst, red mud and black nickel mud were used for that purpose. The factors such as the catalyst dose and the hydrogen peroxide solution volume were monitored. The results of experiments showed that the degradation of methylene blue dye in Fenton-like oxidation process using selected catalysts can be described by a pseudo-second-order kinetic model. The highest dye removal efficiency (87.15 %) was achieved using the black nickel mud catalyst after 30 minutes of reaction.

scholarly journals Sheet-like Skeleton Carbon Derived from Shaddock Peels with Hierarchically Porous Structures for Ultra-Fast Removal of Methylene Blue

Water ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 2554
Author(s):  
Panlong Dong ◽  
Hailin Liu ◽  
Shengrui Xu ◽  
Changpo Chen ◽  
Suling Feng ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Adsorption Process ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Initial Concentration ◽  
Hierarchically Porous ◽  
Column Adsorption

To remove the pollutant methylene blue (MB) from water, a sheet-like skeleton carbon derived from shaddock peels (SPACs) was prepared by NaOH activation followed by a calcination procedure under nitrogen protection in this study. Characterization results demonstrated that the as-prepared SPACs displayed a hierarchically porous structure assembled with a thin sheet-like carbon layer, and the surface area of SPAC-8 (activated by 8 g NaOH) was up to 782.2 m2/g. The as-prepared carbon material presented an ultra-fast and efficient adsorption capacity towards MB due to its macro-mesoporous structure, high surface area, and abundant functional groups. SPAC-8 showed ultrafast and efficient removal capacity for MB dye. Adsorption equilibrium was reached within 1 min with a removal efficiency of 99.6% at an initial concentration of 100 mg/g under batch adsorption model conditions. The maximum adsorption capacity for MB was up to 432.5 mg/g. A pseudo-second-order kinetic model and a Langmuir isotherm model described the adsorption process well, which suggested that adsorption rate depended on chemisorption and the adsorption process was controlled by a monolayer adsorption, respectively. Furthermore, column adsorption experiments showed that 96.58% of MB was removed after passing through a SPAC-8 packed column with a flow rate of 20 mL/min, initial concentration of 50 mg/L, and adsorbent dosage of 5 mg. The as-prepared adsorbent displays potential value in practical applications for dye removal due to its ultrafast and efficient adsorption capacity.

scholarly journals Methylene Blue Dye Adsorption from Wastewater Using Hydroxyapatite/Gold Nanocomposite: Kinetic and Thermodynamics Studies

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1403
Author(s):  
Kashma Sharma ◽  
Shreya Sharma ◽  
Vipasha Sharma ◽  
Pawan Kumar Mishra ◽  
Adam Ekielski ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Dye Adsorption ◽  
Precipitation Method ◽  
Diffusion Method ◽  
Blue Dye ◽  
Order Kinetic ◽  
Economic Point ◽  
X Ray ◽  
First Order ◽  
Pseudo First Order

The present work demonstrates the development of hydroxyapatite (HA)/gold (Au) nanocomposites to increase the adsorption of methylene blue (MB) dye from the wastewater. HA nanopowder was prepared via a wet chemical precipitation method by means of Ca(OH)2 and H3PO4 as starting materials. The biosynthesis of gold nanoparticles (AuNPs) has been reported for the first time by using the plant extract of Acrocarpus fraxinifolius. Finally, the as-prepared HA nanopowder was mixed with an optimized AuNPs solution to produce HA/Au nanocomposite. The prepared HA/Au nanocomposite was studied by using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and Scanning Electron Microscopy (SEM) with Energy Dispersive X-Ray Analysis (EDX) analysis. Adsorption studies were executed by batch experiments on the synthesized composite. The effect of the amount of adsorbent, pH, dye concentration and temperature was studied. Pseudo-first-order and pseudo-second-order models were used to fit the kinetic data and the kinetic modeling results reflected that the experimental data is perfectly matched with the pseudo-first-order kinetic model. The dye adsorbed waste materials have also been investigated against Pseudomonas aeruginosa, Micrococcus luteus, and Staphylococcus aureus bacteria by the agar well diffusion method. The inhibition zones of dye adsorbed samples are more or less the same as compared to as-prepared samples. The results so obtained indicates the suitability of the synthesized sample to be exploited as an adsorbent for effective treatment of MB dye from wastewater and dye adsorbed waste as an effective antibacterial agent from an economic point of view.

Adsorption Mechanism of Rectorite Modified by Lithium

2014 ◽  
Vol 919-921 ◽  
pp. 2017-2021
Author(s):  
Yin An Ming ◽  
Ying Ru Wang ◽  
Zheng Liu ◽  
Fu Rong Zhou
Keyword(s):  
Methylene Blue ◽  
Adsorption Capacity ◽  
Adsorption Mechanism ◽  
Interlayer Spacing ◽  
Blue Dye ◽  
Adsorption Efficiency ◽  
X Ray Diffraction ◽  
X Ray ◽  
Index Measurement ◽  
Infrared Spectrophotometer

In this paper, the mechanism that lithium-modified rectorite (Rec-Li) and raw rectorite adsorbed methylene blue dye in wastewater was investigated, and the adsorption properties of the two adsorbents were also compared. The results showed that the static saturated adsorption capacity of raw rectorite was 77.75mg/g, however, the capacity of lithium-modified rectorite was up to 189.62mg/g, the adsorption efficiency was increased by 144%. Therefore, the adsorption capacity of Rec-Li to methylene blue was much higher than raw rectorite. The Rec-Li and raw rectorite were characterized respectively by means of fourier transform infrared spectrophotometer (FTIR), X-ray diffraction (XRD), scanning electron microscope (SEM) and colloid index measurement. The analysis indicated that, after modification by lithium, the colloid index was changed from 12mL/3g to 198mL/3g and the interlayer spacing was changed from 0.01~0.1μm to 1~1.5μm. With the increasing of the colloid index, the dispersion effect of adsorbent in wastewater and the contact area between adsorbent and pollutants were improved. And the increase of interlayer spacing was conducive to pollutants entering the hole and so that the adsorption capacity of Rec-Li was increased significantly.

scholarly journals Photocatalytic Performance of a Novel Sr-Ce-TiO2/HAp for Degradation of Methylene Blue Dye in the Presence of Visible Light

2021 ◽  
Author(s):  
Alireza Esmaeilzadeh ◽  
Felora Heshmatpour
Keyword(s):  
Methylene Blue ◽  
Surface Area ◽  
Energy Gap ◽  
Blue Dye ◽  
X Ray Diffraction ◽  
Pseudo First Order Reaction ◽  
Visible Radiation ◽  
X Ray ◽  
Bet Method

Abstract In this study, Sr-Ce-TiO2/HAp as a novel and efficient nanocomposite was synthesized and characterized by Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), scanning electron microscopy (SEM), and surface area determination of porous using the Brunauer–Emmett–Teller (BET) method and degradation of methylene blue under visible radiation was investigated. Evaluations showed that doped with metal cations and the presence of hydroxyapatite reduced energy gap, increased surface area, increased adsorption and decreased electron-hole recombination. The results also showed that more than 92% of methylene blue was removed within 100 min. The pseudo-first order reaction synthetic was obtained.

Using of modified-bentonite as low-cost sorbent for removal of methylene blue dye from aqueous solution

2020 ◽  
Vol 27 (2) ◽  
pp. 45-54
Author(s):  
Saraa Muwafaq Ibrahim ◽  
Ziad T. Abd Ali
Keyword(s):  
Aqueous Solution ◽  
Methylene Blue ◽  
Silanol Group ◽  
Infrared Spectrometry ◽  
Blue Dye ◽  
Ammonium Bromide ◽  
Vibration Band ◽  
Order Kinetic ◽  
Methylene Blue Dye ◽  
Modified Bentonite

Batch experiments have been studied to remove methylene blue dye (MB) from aqueous solution using modified bentonite. The modified bentonite was synthesized by replacing exchangeable calcium cations in natural bentonite with cationic surfactant cetyl trimethyl ammonium bromide (CTAB). The characteristics of modified bentonite were studied using different analysis such as Scanning electronic microscopy (SEM), Fourier transform infrared spectrometry (FTIR) and surface area. Where SEM shows the natural bentonite has a porous structure, a rough and uneven appearance with scattered and different block structure sizes, while the modified bentonite surface morphology was smooth and supplemented by a limited number of holes. On other hand, (FTIR) analysis that proved NH group aliphatic and aromatic group of MB and silanol group are responsible for the sorption of contaminate. The organic matter peaks at 2848 and 2930 cm-1 in the spectra of modified bentonite which are sharper than those of the natural bentonite were assigned to the CH2 scissor vibration band and the symmetrical CH3 stretching absorption band, respectively, also the 2930 cm-1 peak is assigned to CH stretching band. The batch study was provided the maximum removal efficiency (99.99 % MB) with a sorption capacity of 129.87 mg/g at specified conditions (100 mg/L, 25℃, pH 11 and 250rpm). The sorption isotherm data fitted well with the Freundlich isotherm model. The kinetic studies were revealed that the sorption follows a pseudo-second-order kinetic model which indicates chemisorption between sorbent and sorbate molecules.

scholarly journals Pristine and Magnetic Kenaf Fiber Biochar for Cd2+ Adsorption from Aqueous Solution

2021 ◽  
Vol 18 (15) ◽  
pp. 7949
Author(s):  
Anwar Ameen Hezam Saeed ◽  
Noorfidza Yub Harun ◽  
Suriati Sufian ◽  
Muhammad Roil Bilad ◽  
Zaki Yamani Zakaria ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Textural Properties ◽  
Ion Concentration ◽  
Solution Temperature ◽  
Maximum Adsorption Capacity ◽  
Magnetic Biochar ◽  
X Ray ◽  
Study Results ◽  
Capacity Surface

Development of strategies for removing heavy metals from aquatic environments is in high demand. Cadmium is one of the most dangerous metals in the environment, even under extremely low quantities. In this study, kenaf and magnetic biochar composite were prepared for the adsorption of Cd2+. The synthesized biochar was characterized using (a vibrating-sample magnetometer VSM), Scanning electron microscopy (SEM), X-ray powder diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The adsorption batch study was carried out to investigate the influence of pH, kinetics, isotherm, and thermodynamics on Cd2+ adsorption. The characterization results demonstrated that the biochar contained iron particles that help in improving the textural properties (i.e., surface area and pore volume), increasing the number of oxygen-containing groups, and forming inner-sphere complexes with oxygen-containing groups. The adsorption study results show that optimum adsorption was achieved under pH 5–6. An increase in initial ion concentration and solution temperature resulted in increased adsorption capacity. Surface modification of biochar using iron oxide for imposing magnetic property allowed for easy separation by external magnet and regeneration. The magnetic biochar composite also showed a higher affinity to Cd2+ than the pristine biochar. The adsorption data fit well with the pseudo-second-order and the Langmuir isotherm, with the maximum adsorption capacity of 47.90 mg/g.

scholarly journals Magnetically Recyclable Wool Keratin Modified Magnetite Powders for Efficient Removal of Cu2+ Ions from Aqueous Solutions

Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1068
Author(s):  
Xinyue Zhang ◽  
Yani Guo ◽  
Wenjun Li ◽  
Jinyuan Zhang ◽  
Hailiang Wu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Ion Concentration ◽  
Bet Surface Area ◽  
Chemical Compositions ◽  
Ion Adsorption ◽  
X Ray ◽  
Wool Keratin

The treatment of wastewater containing heavy metals and the utilization of wool waste are very important for the sustainable development of textile mills. In this study, the wool keratin modified magnetite (Fe3O4) powders were fabricated by using wool waste via a co-precipitation technique for removal of Cu2+ ions from aqueous solutions. The morphology, chemical compositions, crystal structure, microstructure, magnetism properties, organic content, and specific surface area of as-fabricated powders were systematically characterized by various techniques including field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM), thermogravimetric (TG) analysis, and Brunauer–Emmett–Teller (BET) surface area analyzer. The effects of experimental parameters such as the volume of wool keratin hydrolysate, the dosage of powder, the initial Cu2+ ion concentration, and the pH value of solution on the adsorption capacity of Cu2+ ions by the powders were examined. The experimental results indicated that the Cu2+ ion adsorption performance of the wool keratin modified Fe3O4 powders exhibited much better than that of the chitosan modified ones with a maximum Cu2+ adsorption capacity of 27.4 mg/g under favorable conditions (0.05 g powders; 50 mL of 40 mg/L CuSO4; pH 5; temperature 293 K). The high adsorption capacity towards Cu2+ ions on the wool keratin modified Fe3O4 powders was primarily because of the strong surface complexation of –COOH and –NH2 functional groups of wool keratins with Cu2+ ions. The Cu2+ ion adsorption process on the wool keratin modified Fe3O4 powders followed the Temkin adsorption isotherm model and the intraparticle diffusion and pseudo-second-order adsorption kinetic models. After Cu2+ ion removal, the wool keratin modified Fe3O4 powders were easily separated using a magnet from aqueous solution and efficiently regenerated using 0.5 M ethylene diamine tetraacetic acid (EDTA)-H2SO4 eluting. The wool keratin modified Fe3O4 powders possessed good regenerative performance after five cycles. This study provided a feasible way to utilize waste wool textiles for preparing magnetic biomass-based adsorbents for the removal of heavy metal ions from aqueous solutions.

Morphology dependent adsorption of methylene blue on trititanate nanoplates and nanotubes prepared by the hydrothermal treatment of TiO2

2016 ◽  
Vol 75 (2) ◽  
pp. 350-357
Author(s):  
Graham Dawson ◽  
Wei Chen ◽  
Luhua Lu ◽  
Kai Dai
Keyword(s):  
Methylene Blue ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Pore Volume ◽  
Hydrothermal Reaction ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
High Capacity ◽  
Adsorption Properties

The adsorption properties of two nanomorphologies of trititanate, nanotubes (TiNT) and plates (TiNP), prepared by the hydrothermal reaction of concentrated NaOH with different phases of TiO2, were examined. It was found that the capacity for both morphologies towards methylene blue (MB), an ideal pollutant, was extremely high, with the TiNP having a capacity of 130 mg/g, higher than the TiNT, whose capacity was 120 mg/g at 10 mg/L MB concentration. At capacity, the well-dispersed powders deposit on the floor of the reaction vessel. The two morphologies had very different structural and adsorption properties. TiNT with high surface area and pore volume exhibited exothermic monolayer adsorption of MB. TiNP with low surface area and pore volume yielded a higher adsorption capacity through endothermic multilayer adsorption governed by pore diffusion. TiNP exhibited a higher negative surface charge of −23 mV, compared to −12 mV for TiNT. The adsorption process appears to be an electrostatic interaction, with the cationic dye attracted more strongly to the nanoplates, resulting in a higher adsorption capacity and different adsorption modes. We believe this simple, low cost production of high capacity nanostructured adsorbent material has potential uses in wastewater treatment.

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