Dye Removal Research Articles

Removal of Dyes from Water Using Aluminum-Based Water Treatment Sludge as a Low-Cost Coagulant: Use of Response Surface Methodology

Removal of Dyes from Water Using Aluminum-Based Water Treatment Sludge as a Low-Cost Coagulant: Use of Response Surface Methodology

Sequestration of a food dye (sunset yellow) from wastewater using natural adsorbent: a kinetic, isotherm and interference study.

Cocos nucifera, commonly known as coconut is rich in coir dust (CCD) at its outer surface, which is a very significant agri waste used as biosorbent for wastewater treatment. The current work addresses use of CCD for removal of hazardous Sunset Yellow dye (SY) FCF widely used as coloring agent in food industry, from wastewater. The uptake capacity in batch and column mode is 82 mg/g and 160 mg/g respectively. Characterization study including SEM, FTIR and BET results also supported the adsorption process. The comparative analysis with other natural biosorbents showed best results of biosorption with CCD. The output was better at high pH (10) and lower concentration of dye (5 mg/L). The kinetic study suggested pseudo second order rate revealing both adsorbate-adsorbent interdependency. The presence of covalent bonding or valence forces between the interfaces, suggested chemisorption as the rate limiting mechanism with valence forces, hydrogen bonding and pi-pi stacking being the chief forces responsible in binding of the dye molecules to the surface. The isotherm supported Langmuir model with monolayer and uniform adsorption at the interfaces. The interference test confirmed slight decrease in percent adsorption with interference from chloride and sulfate as dominating ions. The techno-economic feasibility highly recommended in field application of the substitute (net profit value, 1.256 Rs/m3, input cost, 0.052 Rs/m3). The industrial sample analysis with lab to land approach justified sustainability and commercial viability of the present work.

A Novel Method for the Highly Effective Removal of Binary Dyes from Colored Dyeing Wastewater by Periodic Reversal/Direct Current-Activated Persulfate

A Novel Method for the Highly Effective Removal of Binary Dyes from Colored Dyeing Wastewater by Periodic Reversal/Direct Current-Activated Persulfate

Photocatalytic application of nickel oxide/zinc oxide nanoparticles decorated kaolinite nanocomposite for the degradation of crystal violet

The photocatalysis process, which is effective, economical, and environmentally friendly can overcome rapidly increasing environmental problems, has shown rapid development in recent years. Nontoxic, low-cost natural minerals are often used in photocatalysis processes that remove organic pollution from wastewater. In this study, a selective method for the removal of crystal violet (CV) from aqueous solutions using nanocomposite of nickel oxide/zinc oxide nanoparticles (NiO/ZnO) supported on kaolinite photocatalyst was investigated. The raw kaolinite, bare NiO, bare ZnO and nanocomposite samples were characterized by the XRD, TEM, SEM-EDX, XPS and FTIR techniques. The photocatalytic performances of kaolinite-NiOZnO (K-NiO/ZnO) nanocomposite and bare samples were also investigated and comparatively evaluated by the photodegradation of CV (cationic dye) dye under visible light irradiation. The effects of various parameters such as the dosage of photocatalysis, contact time, and initial dye concentration on the rate of removal of dye were investigated and optimized. The kinetics of decolorization by samples can be well described by the pseudo-first-order model. Finally, it can be used in advanced oxidative processes for the degradation of organic pollutants.

Research upon Cu-Doping Contents in TiO2 Nanoparticles Incorporated onto Cellulose Nanofibers for Dye Removal and Self-Cleaning Applications

Research upon Cu-Doping Contents in TiO₂ Nanoparticles Incorporated onto Cellulose Nanofibers for Dye Removal and Self-Cleaning Applications

Integration of hydrogen evolution and dye removal in flexocatalysis by centrosymmetric semiconductor nanorods

In this work, coupling of the hydrogen (H2) production and dye degradation was first realized in a single flexocatalytic process using cerium oxide nanorods (CeO2 NRs). The flexoelectric polarization in a bending nanorod created an internal electric field, which promoted the separation of the thermal-excited electrons and holes. As a consequence, the H2 evolution rate of the flexocatalysis in dark was twice higher than that of the photocatalysis by the same CeO2 NRs. Moreover, simultaneous dye degradation was realized without reducing the H2 evolution rate, with the degradation constant rate of 0.065 min−1, dye removal efficiency of 89.3%, and H2 generation at 486.4 μmol g−1 h−1. The dual-functional catalytic performance of the CeO2 NRs was benefited from the unique periodic flexoelectric field induced by the ultrasound vibration, which could not be achieved by photocatalysis. This work revealed the important role of flexoelectric effect in overcoming the limitation in photocatalysis, which could be extended to a wide range of semiconductor nanomaterials for designing novel kinds of advanced flexocatalysts.

Exploring the potential of Cu-LDHs composite for efficient Coomassie brilliant blue dye removal: evaluating adsorption isotherms and antibacterial activity

Exploring the potential of Cu-LDHs composite for efficient Coomassie brilliant blue dye removal: evaluating adsorption isotherms and antibacterial activity

Removal of Methylene blue dye from contaminated wastewater using lignocellulosic biomasses: A comparative study

In this study, lupine seed (Lu-SP) and pumpkin seed shells (PSSP) biomasses were used to create alternative and effective adsorbents. Methylene blue (MB) dye was removed from wastewater using the as-prepared adsorbents at variables solution pH 2.0 –11.0, contact period (0–180 min), and adsorbent mass (0.2–2.0 g/L). The solution pH had a synergistic effect on the improved removal of MB and the optimal adsorption removal for both adsorbents occurred at pH 8.0 and 120 min. The adsorption isotherm modelling results showed a good fit with the Langmuir model, with a maximum monolayer adsorption capacity of 48.98 and 77.48 mg/g for PSSP and Lu-SP, respectively. Similarly, the pseudo-first-order (PFO) model is regarded as the best-fit kinetic model for both adsorbents and suggests the predominance of physisorption via interfacial diffusion. Mechanistic investigation of the present system suggests that both intraparticle diffusion and surface sorption mechanisms control the adsorption rate. Notably, the Lu-SP with a lower surface area (54.013 m2/g) outperformed the PSSP (235.992 m2/g) in terms of adsorption capacity under varying pH. Therefore, in addition to electrostatic interaction, adsorption into the micropores via volume filling is considered one of the adsorption mechanisms. This study, therefore, revealed that the PSSP and Lu-SP may be very helpful for removing cationic MB dye from contaminated wastewater.

Adsorption potential of hydrochar derived from hydrothermal carbonization of waste biomass towards the removal of methylene blue dye from wastewater

Adsorption potential of hydrochar derived from hydrothermal carbonization of waste biomass towards the removal of methylene blue dye from wastewater

Evaluation of vat blue removal by Aspergillus niger using scanning electron microscopy and glucose oxidase enzyme activity

AbstractThe use of fungi to reduce dye removal in water from diverse industries can be an efficient option for solving environmental problems. However, the mycoremediation processes involved in color removal are unknown. In this article, Aspergillus niger CDBB‐H‐175 was applied for vat blue discoloration (DC). Hence, inactive biomass by two methods (metabolic inhibitor and heat) and active biomass were studied by scanning electron microscopy and enzyme activities to determine the vat blue DC. When using active biomass, 62% of DC, glucose oxidase (GOX) enzyme activity, 1.19 U/mL and 1.43 mg/L of H2O2 were obtained. It was observed that 68% of DC was due to the degradation process and 32% was due to biomass sorption. When the biomass was inactivated with sodium azide, DC increased by 90% (1.45‐fold), low GOX activity (0.138 U/mL), and H2O2 (0.25 mg/L) were detected. High DC might be due to a high dye sorption in hyphae, since an increase in the thickness and morphology of the hyphae were observed by SEM. Inactivated biomass through heating, showed a 69.5% of DC, where 0.01 U/mL GOX and 0.25 mg/L H2O2 were reached, demonstrating that inactivation of A. niger biomass by sodium azide can be considered as an alternative treatment for colored wastewater.

Fabrication of Magnetic Chitosan-Benzil Biopolymer with Organoclay for Remazol Brilliant Blue R Dye Removal: a Statistical Modeling and Adsorption Mechanism

Fabrication of Magnetic Chitosan-Benzil Biopolymer with Organoclay for Remazol Brilliant Blue R Dye Removal: a Statistical Modeling and Adsorption Mechanism

Sustainable Utilization of Food Biowaste (Papaya Peel) Extract for Gold Nanoparticle Biosynthesis and Investigation of Its Multi-Functional Potentials

Papaya contains high amounts of vitamins A, C, riboflavin, thiamine, niacin, ascorbic acid, potassium, and carotenoids. It is confirmed by several studies that all food waste parts such as the fruit peels, seeds, and leaves of papaya are potential sources of phenolic compounds, particularly in the peel. Considering the presence of numerous bioactive compounds in papaya fruit peels, the current study reports a rapid, cheap, and environmentally friendly method for the production of gold nanoparticles (AuNPs) employing food biowaste (vegetable papaya peel extract (VPPE)) and investigated its antioxidant, antidiabetic, tyrosinase inhibition, anti-inflammatory, antibacterial, and photocatalytic degradation potentials. The phytochemical analysis gave positive results for tannins, saponins, steroids, cardiac steroidal glycoside, protein, and carbohydrates. The manufactured VPPE-AuNPs were studied by UV–Vis scan (with surface plasmon resonance of 552 nm), X-ray diffraction analysis (XRD) (with average crystallite size of 44.41 nm as per the Scherrer equation), scanning electron microscopy–energy-dispersive X-ray (SEM-EDS), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FT-IR), particle size, zeta potential, etc. The mean dimension of the manufactured VPPE-AuNPs is 112.2 d.nm (PDI—0.149) with a −26.1 mV zeta potential. The VPPE-AuNPs displayed a significant antioxidant effect (93.24% DPPH scavenging and 74.23% SOD inhibition at 100 µg/mL); moderate tyrosinase effect (with 30.76%); and substantial α-glucosidase (95.63%) and α-amylase effect (50.66%) at 100 µg/mL. Additionally, it was found to be very proficient in the removal of harmful methyl orange and methylene blue dyes with degradation of 34.70% at 3 h and 24.39% at 5 h, respectively. Taken altogether, the VPPE-AuNPs have been proven to possess multiple biopotential activities, which can be explored by the food, cosmetics, and biomedical industries.

Comparative adsorption of cationic and anionic dye by using non-activated Black Plum seed biochar for aquatic phase: Isotherm, kinetic and thermodynamic studies

Industrial dye effluents play a major role in water pollution. Textile and leather industries are one of the important sectors that pollute the water by discharging many harmful cationic and anionic dyes during the dyeing process. This study aims to compare the dye removal efficiency of Black Plum seed biochar for the cationic and anionic dyes. The non-activated biochar was prepared through pyrolysis of Black Plum seed powder at 5700 C. The sample's surface chemistry was understood using various characterization techniques like Field Emission Scanning Electron Microscopy (FESEM), Energy-dispersive X-ray spectroscopy (EDS), Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), Raman-Spectroscopy and Zeta-potential. The experiments were successfully performed by conducting a batch adsorption study at different parameters such as pH, concentration, contact time and temperature. The coefficients of different isotherms and kinetics models were evaluated for non-linear study and the thermodynamic model was also applied. The maximum adsorption capacity was obtained as 42.39 mg/g for Crystal Violet (CV) dye and 6.22 mg/g for Eosin Blue (EB) dye by using the Langmuir isotherm model. Hence, the Black Plum seed biochar (BPSB) has superior adsorption capacity for the cationic dye CV ( removal - 98%) as compared to the anionic dye EB ( removal - 65%) at optimum parameters. Therefore, it is concluded that the BPSB is a natural toxin-free biosorbent and it can be used for the remediation of dyes from industrial wastewater.

Exploring the structural characteristics and dye removal capabilities of powder-, granule- and film- shaped magnetic activated carbon derived from Oleaster seed.

Dye pollution in water caused by excessive discharge of industrial effluent has become a major environmental problem in recent decades because of its irreversible effects on human health. In this study, low-cost carbon-based adsorbents synthesized from Oleaster seed (OS) were prepared in three forms of powder (PAC), film (FAC), and granule (GAC) and used for the removal of methylene blue dye. The properties of the synthesized adsorbents were characterized by SEM-EDX, BET, XPS and FTIR analyses. The maximum adsorption capacity (qmax) of PAC, FAC, and GAC adsorbents were obtained as 68.49, 32.25, and 15.10 mg/g, respectively at the optimum experimental conditions of pH = 10, adsorbent dosages of 0.5, 1, and 2 g/l, contact times of 60, 90, and 120 min, dye concentration of 10 mg/L, and temperature of 25°C. The Langmuir isotherm well described the equilibrium data for all three adsorbents. The pseudo-second-order kinetic model provided the best fit with the adsorption data obtained from all three adsorbents. Adsorption occurred spontaneously through a combination of chemical and physical mechanisms, with a thermodynamically exothermic process. The desorption experiments demonstrated that all the adsorbents have substantial potential for recovery. The novel activated carbon/alginate composite films are proposed as more promising biosorbents to remove MB dye from the aquatic environment compared to GAC adsorbents.

Furfuryl-pyridinium-functionalization of flaxseed gum for effective methylene blue removal from aqueous solution

This study describes the modification of flaxseed gum (FSG) via furfural to obtain a furfuryl-pyridinium modified adsorbent (Flax-Py) with improved adsorption characteristics towards methylene blue (MB) versus results obtained for unmodified FSG. Materials characterization was achieved via complementary spectral methods (NMR, XPS, FT-IR, Raman, and XRD) as well as thermogravimetric analysis (TGA) and ζ-potential measurements. Synthetic modification of FSG to yield Flax-Py that led to enriched N-content (2.75 atom-% versus 0.76 atom-% for FSG), and the conversion of furfuryl to pyridinium was incomplete (ca. 50 %), where both moieties were identified. The adsorption isotherms at pH 7 showed that FSG possessed favorably high MB adsorption capacity (ca. 540 mg/g); while Flax-Py was notably lower (167 mg/g). Flax-Py facilitated 100% MB removal at low dye concentrations (1-10 mg/L) versus 50 % MB removal for the FSG bioadsorbent. Further, Flax-Py showed moderate loss of adsorption with MB (ca. 12-16% dye removal) after five regeneration cycles. Flax-Py revealed improved settling characteristics (time, density, gelation, and solubility) that facilitate enhanced phase separation of FSG fractions by circumventing the need for centrifugation. The adsorption mechanism was attributed primarily to H-bonding effects with secondary contributions due to electrostatic interactions (negative ζ-potential above pH 4.2). This study successfully modified FSG to obtain an improved adsorbent (Flax-Py) attaining nearly quantitative MB dye removal at environmentally relevant concentrations (< 15 mg/L).

Heterojunction-Based Photocatalytic Degradation of Rose Bengal Dye via Gold-Decorated α-Fe2O3-CeO2 Nanocomposites under Visible-Light Irradiation

Developing photocatalytic nanomaterials with unique physical and chemical features using low-cost and eco-friendly synthetic methods is highly desirable in wastewater treatment. In this work, the magnetically separable α-Fe2O3-CeO2 nanocomposite (NC), with its respective metal oxides of α-Fe2O3 and CeO2 nanoparticles, was synthesized using a combination of hexadecyltrimethylammonium bromide (CATB) and ascorbic acid via the hydrothermal method. To tune the band gap, the heterojunction nanocomposite of α-Fe2O3-CeO2 was decorated with plasmonic Au nanoparticles (Au NPs). The various characterization methods, such as FTIR, UV-vis DRS, XRD, XPS, TEM, EDX, SEM, and PL, were used to determine the properties of the materials, including their morphology, elemental composition, optical properties, band gap energy, and crystalline phase. The nanocomposite of α-Fe2O3-CeO2@Au was utilized to remove Rose Bengal (RB) dye from wastewater using a photocatalytic technique when exposed to visible light. A comprehensive investigation of the impact of the catalyst concentration and initial dye concentration was conducted to establish the optimal photodegradation conditions. The maximum photocatalytic efficiency of α-Fe2O3-CeO2@Au (50 mg L−1) for RB (20 ppm) dye removal was found to be 88.9% in 120 min under visible-light irradiation at a neutral pH of 7 and 30 °C. Various scavengers, such as benzoquinone (BQ; 0.5 mM), tert-butyl alcohol (TBA; 0.5 mM), and ethylenediaminetetraacetic acid (EDTA; 0.5 mM), were used to investigate the effects of different free radicals on the photocatalytic process. Furthermore, the reusability of the α-Fe2O3-CeO2@Au photocatalyst has also been explored. Furthermore, the investigation of the potential mechanism demonstrated that the heterojunction formed between α-Fe2O3 and CeO2, in combination with the presence of deposited Au NPs, led to an enhanced photocatalytic efficiency by effectively separating the photogenerated electron (e−)–hole (h+) pairs.

Heat Treatment of Calcite to Enhance Its Removal of Color Dye Alizarin Red S

The use of color dyes in modern society presents a great challenge to the environment. Thus, extensive studies have been conducted in the last 30 years on the removal of color dyes from aqueous solutions such industrial wastewater. In this study, the removal of alizarin red S (ARS), an anionic dye, from solution by raw calcite (Cal) and heat-treated calcite (HCal) was conducted and compared under different physico-chemical conditions. Based on the isotherm study, the ARS removal capacities increased from 167 to 251 mmol/kg after the Cal was heated to 1000 °C for 3 h. The X-ray diffraction analyses showed no difference in the calcite phase between Cal and HCal after ARS sorption. Fourier-transform infrared results also showed no change in the calcite phase after ARS sorption, except a slightly increase in wavenumber from 713 to 727 cm−1 for the OCO bending of HCal at high ARS sorption levels. SEM observations showed about the same particle size and morphology before and after ARS sorption. The TGA data showed the formation of CaO after Cal was heated, and CaO converted back into calcite after being in contact with water or ARS solution for 24 h and then being air-dried. Thus, the high ARS removal could be due to CaO produced after Cal being heated. The findings from this research proved that there is great potential in the use of calcite, a low-cost and readily available Earth material, after heat treatment for the removal of contaminants from water.

Iron-Based Oxides Anchored on the Catechol/Silane-Coated Polypropylene Nonwoven Fabrics for Effective Removal of Anionic Dyes

Iron-Based Oxides Anchored on the Catechol/Silane-Coated Polypropylene Nonwoven Fabrics for Effective Removal of Anionic Dyes

One-step fabrication of millimeter-scale hollow vesicles with chitosan /DADMAC/ sodium alginate graft copolymer for enhanced anionic dye adsorption

Hollow vesicles are promising in water treatment due to their unique structure of the membrane and inner cavity. However, the adsorption capacity needs to be improved for targeted pollutants. Herein, millimeter-scale hollow vesicles were prepared with a one-step process of sequential stirring and grafting using chitosan, diallyldimethylammonium chloride, and sodium alginate as raw materials with the purpose of efficient removal of anionic dyes from wastewater. The composite vesicles were characterized using scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. The hollow vesicles showed the structure of the cationic membrane and the inner cavity, facilitating the dye adsorption. The adsorption capacity for the anionic dye Reactive Black 5 reached 698.1 mg/g, more than twice that of the binary composite vesicles without graft. The adsorption kinetics and isotherm data coincided with the pseudo-second-order and Langmuir models, respectively, and the adsorption mechanism was monolayer chemisorption. Moreover, the vesicles worked well in wide ranges of environment pH, temperature, and co-existing pollutants. They also possessed excellent cyclic regeneration performance, in which 93 % of the initial adsorption capacity was maintained after four cycles. These results indicate that the millimeter-scale hollow vesicles exhibit broad application prospects for wastewater purification.

Greenly synthesised novel microporous ZnO/GO for adsorption of methyl orange and malachite green

ABSTRACT This study presents a greenly synthesised novel nanocomposite composed of Zinc Oxide (ZnO) and Graphene Oxide (GO) for the adsorption of dyes from aqueous solutions. The nanocomposite was synthesised using algae thus representing a green and eco-friendly method, ensuring minimal environmental impact. The physical characterisation of zinc oxide and graphene oxide nanocomposite (ZnO/GO) was done using X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), Fourier transform infrared spectroscopy (FT-IR), Zeta Potential, and Particle Size Analyzer (PSA). The pore diameter of the ZnO/GO was 1.801 nm, and its total surface area was 54.062 m2/g. The nanocomposite’s adsorption performance was systematically investigated through batch adsorption experiments. With an adsorption efficiency of 296.73 mg/g and 259.74 mg/g for MO and MG, the Langmuir isotherm model outperforms the Freundlich isotherm model in terms of adsorption. The pseudo-second-order model having an R2 value of 0.99 for both MO and MG, offers a more convincing explanation of adsorption than the pseudo-first-order model. The results demonstrated rapid adsorption kinetics and high adsorption capacities for both cationic and anionic dyes. Additionally, the ZnO/GO has a high reusability without significant degradation. The sustainable nature of the nanocomposite was emphasised by its efficient dye removal, reusability, and minimal secondary waste generation.