Decolorization Rate Research Articles

Surface engineering-based S, N co-doped biochar for improved anaerobic digestion: Enhancing microbial-pollutant and inter-microbial electron transfer synergistic EPS protection

Enhancing extracellular electron transfer (EET) efficiency is crucial for improving the anaerobic digestion (AD) system's capability to treat recalcitrant wastewater. In this study, a novel S, N co-doped biochar (S-N-BC) was prepared through surface engineering to optimize EET within AD systems. The addition of S-N-BC significantly enhanced the performance of a mesophilic AD system treating Congo red wastewater, increasing the decolorization rate by 78%, COD degradation rate by 82%, and methane yield by 87% compared to the control. Additionally, the shock resistance of anaerobic granular sludge was improved, as evidenced by the formation of the protective extracellular polymeric substances (EPS) barrier and the enhanced activities of the electron transport system. Mechanistic analysis revealed that adding S-N-BC did not alter the Congo red decolorization pathway but significantly enriched various electrochemically active bacteria and established EET pathways between microbial-pollutant and inter-microbial. This significantly accelerated EET efficiency within the AD system, ensuring stable and efficient operation under challenging conditions. This study proposed a novel approach using S-N-BC to simultaneously enhance "dual-pathway EET" between microbial-pollutant and inter-microbial while constructing an EPS protective barrier, addressing the issues of low efficiency and fragile stability of AD systems for treating recalcitrant wastewater.

Preparation, morphology, antiradical and biological activity of quercetin-containing nanoparticles of zein and their submicron aggregates

Nanoparticles of corn prolamine protein zein (NPQ) containing 0.005–0.26 g/g quercetin (Q) were prepared by desolvation of a 25–30 mg/mL ethanol protein solution containing the encapsulated compound with an aqueous polystyrene sulfonate. The size of zein nanoparticles and their aggregates was characterized by dynamic light scattering and atomic force microscopy; the quercetin content – by the Folin-Ciocalteu assay. While the quercetin/zein ratio in solution is less than 0.08 g/g, the polyphenol is quantitatively included in the nanoparticles, and their hydrodynamic diameter is 60–75 nm. As the quercetin/zein ratio rises to 0.20 g/g, the average particle diameter increases to 150 nm. In concentrated dispersions, aggregates with a diameter of 500–600 nm are formed. The kinetics of quercetin release from NPQ with different mass fractions of Q in distilled water and solutions simulating the environment of the stomach and intestines at 37 °C were studied.Zein nanoparticles exhibit weak activity in the reaction with ABTS cation-radicals. Quercetin encapsulated in the zein matrix generally retains the antiradical activity characteristic of the free flavonoid, however, the rate of decolorization of ABTS cation-radicals decreases due to the prolonged release of quercetin from NPQ. The cytoprotective properties of quercetin in zein nanoparticles are significantly reduced and manifest themselves only in partial preservation of the integrity of cell membranes and a decrease in the release of lactate dehydrogenase from UV-C irradiated HaCaT cells. In contrast to free quercetin, the introduction of Q in zein nanoparticles or their submicron aggregates increases the number of metabolically dead UV-C-irradiated HaCaT cells, enhancing the cytotoxic effect of UV radiation. Empty zein aggregates of submicron size have a similar effect.

Decolorization of crystal violet by mixed culture under the influence of Bioelectrochemical stimulation

A significant variation in the relative representation of copies of bacterial genes of dye-decolorizing DyP peroxidases typical for the genus Shewanella and a number of other microorganisms was found in the bottom sediments of freshwater reservoirs. It was found that the specific rate of decolorization of crystal violet in a laboratory bioelectrochemical system by a mixed culture of bottom sediments, which showed the highest representation of DyP genes, depended on the method of electrical stimulation of the external circuit and the concentration of the dye. After an increase in the concentration of more than 20 microns, the maximum speed was achieved in the presence of an ionistor polarly connected to the external electrical circuit of the bioelectrochemical system and amounted to 3.23 ± 0.11 μM/h, while with the opposite polarity connection, a minimum value of 2.07 ± 0.08 μM/h was observed. In the case of an open circuit and a resistor, similar indicators occurred – 2.88 ± 0.09 and 2.67 ± 0.12 μM/h, respectively. When analyzing the decolorization products, a consistent decrease in the maxima of the absorption bands of the dye was noted, indicating its more complete degradation by mixed culture. The results may be of interest for the development of methods to improve the efficiency of bioelectrochemical methods of environmental biotechnology, by electrostimulation of the external circuit.

Biodecolorization of Reactive Red Using Bacillus cereus Isolated from Oil Contaminated Soil

Manufacturing and using organic dyes produce a variety of hazardous organic compounds which can be harmful to living organisms. Azol dyes, one of the most important synthetic organic components, are widely used in a variety of industries, particularly in the textile industry. As azo dyes breakdown, aromatic amines produce mutagenic products that can cause cancer in humans and aquatic life. In order to protect the environment, it was imperative to find a biological method for degrading these dyes. In recent years, microbial biodegradation has emerged as a promising method. Different bacterial isolates from oil-contaminated soil were investigated for their ability to decolorize reactive red. Under aerobic conditions at pH 7.0 and 35 °C with 0.1 mg/mL reactive red dye concentration, the isolated potential strain showed maximum decolorization of 84 % within 24 hr. Based on the 16S rRNA gene sequence analysis, the isolate was identified as Bacillus cereus strain BIOS MD2. A variety of agricultural wastes were supplemented along with medium to reduce the costs of the process, and extracts of apple and chikoo peels showed better decolorization rates. UV-visible spectroscopy was used to analyze the biodegradation property of reactive red, which confirmed that Bacillus cereus successfully degraded reactive red. The present study provides a valuable insight into practical applications for the removal of textile dye from the environment.

Green Combustion Synthesis of Copper Magnesium Vanadate (CuMgV) NPs Using Neem Extract: Its Photocatalytic and Supercapacitor Applications

ABSTRACTOrganic dyes are a substantial contribution to environmental pollution and are considered as hazardous. These compounds are widely used in various industries like textiles, food, paper, cosmetics, and printing. A cationic dye, such as Fast Blue (FB) and Congo Red (CR), is an example of organic compound with several commercial uses but dangerous for environment and human beings. Copper Magnesium Vanadate NPs (CuMgV NPs) were successfully prepared using the combustion method in which Neem extract was used as a fuel. The XRD, FTIR, and FESEM techniques were used to analyze the sample's structure and morphology. The XRD reveals monoclinic structure of the CuMgV NPs with average particle size around 30 nm. The presence of tiny particles that prefabricated to form a widely distributed, spherical shape, and size between 15 and 25 nm was observed by HRTEM microscopic investigations. The CuMgV NPs were assessed using several electrochemical techniques. In photocatalytic tests, 120 min of UV light irradiation was sufficient to achieve a 58% and 55.52% decolorization rate for the industrial pollutants CR and Fast FB dyes. CuMgV NPs were found to have a specific capacitance value of 560.5 Fg−1 at 1 Ag−1 and a retention rate of 89% after 4000 cycles. These features promote the production of NPs for energy and environmental applications and provide greater insight into the characteristics of the material.

Catalase-peroxidase StKatG2 from Salinicola tamaricis: a versatile Mn(II) oxidase that decolorizes malachite green.

Manganese (Mn) oxidation processes have garnered significant attention recently due to their potential for degrading organic pollutants. These processes are primarily catalyzed by Mn(II) oxidases. Salinicola tamaricis F01, an endophytic bacterium derived from wetland plants, has demonstrated Mn(II)-oxidizing capacity. In this study, a catalase-peroxidase, StKatG2, was cloned and overexpressed in Escherichia coli from the strain F01. The purified recombinant StKatG2 exhibited Mn(II)-oxidizing activity with K m and K cat values of 2.529 mmol/L and 2.82 min-1, respectively. Optimal catalytic conditions for StKatG2 were observed at pH 7.5 and 55°C, with 45.1% activity retention after an 8-h exposure to 80°C. The biogenic manganese oxides produced by StKatG2 exhibited mixed-valence states with Mn(II), including Mn(III), Mn(IV), and Mn(VII). Furthermore, StKatG2 demonstrated superior decolorization efficiency for malachite green (MG), achieving decolorization rates of 73.38% for 20 mg/L MG and 60.08% for 50 mg/L MG, while degrading MG into 4-(dimethylamino)benzophenone. Therefore, the catalase-peroxidase StKatG2 exhibits multifunctionality in Mn(II)-oxidizing activity and has the potential to serve as an environmentally friendly enzyme for MG removal.

Efficient treatment of coking wastewater by coal-based activated carbon prepared through coal blending method

In this study, the adsorption performance of coal-based activated carbon produced from Shandong gas-fertilized coal, Taixi anthracite coal, and Datong weakly viscous coal, was investigated for coking wastewater treatment. All prepared activated carbons demonstrated excellent adsorption performance, boasting an iodine number surpassing 1000 mg/g and achieving a chemical oxygen demand determined by the dichromate method (CODcr) removal rate of over 85 % under static coking wastewater adsorption. A positive correlation exists between the total pore volume of activated carbon and its iodine number, methylene blue value, and caramel decolorization rate. Furthermore, dynamic adsorption experiments were conducted and there was an evident increase in the CODcr removal rate as the flow rate decreased. However, increasing the bed height beyond 400 mm only marginally enhanced the CODcr removal rate. The burn-off rate of activated carbon and the ratio of raw materials significantly influenced the pore structure. Notably, with a high anthracite ratio (40 %), elevating the burn-off rate (up to 70 %) did not enhance the effective porosity of activated carbon. The mesopore volume, particularly within 1.2–2.8 nm range, exerted a substantial influence on the coking wastewater adsorption efficiency. Overall, coal-based activated carbon demonstrated significant promise as a cost-effective adsorbent for coking wastewater treatment.

Construction of two isomorphic multifunctional MOFs via a dual-ligand strategy for aromatic compounds detection and photocatalytic degradation performance

The development of multifunctional and structurally unique metal−organic frameworks (MOFs) presents a highly attractive yet challenging endeavor for chemists. In this study, we employ a dual-ligand strategy to synthesize two isomorphic Co/Zn MOFs, {[Co4(BMIP)3(MIP)4]·3DMF·H2O}n (SNUT-35-Co) and {[Zn4(BMIP)3(MIP)4]·2DMF·2H2O}n (SNUT-35-Zn). The photocatalytic performance of SNUT-35-Co and SNUT-35-Zn was evaluated using methylene blue (MB). Under UV/visible-light irradiation, the photocatalytic decolorization rates of MB for SNUT-35-Co and SNUT-35-Zn reached 95 % within 140 min and 120 min, respectively, indicating their superior degradation. Notably, SNUT-35-Zn demonstrated exceptional detection capabilities for aromatic compounds, such as aniline and nitrobenzene, at lower concentration range without interference from other components. The detection limits for these two small molecules were found to be 0.430 and 0.431 μM, respectively. Additionally, both MOFs exhibited large transient photocurrent and low impedance in electrochemical measurement. The results suggested that the photocatalytic activities of MOFs are influenced by their three-dimensional structures, which facilitate electrons passing due to the inherent semiconductor properties.

Biological decolorisation of the anionic Dye Acid Blue 9 by bacterial consortium: A sustainable and ecofriendly approach for the treatment of textile wastewater

Industrialization has led to the proliferation of dye waste, posing significant environmental challenges due to the structural complexity of dyes. Various industries discharge untreated toxic waste into water bodies, posing severe environmental hazards to humans as well as aquatic ecosystem. Synthetic dyes from textiles exacerbate this issue due to their toxicity, making the management of industrial wastewater a significant environmental challenge. This study offers a potential solution by investigating the degradation of hazardous Acid Blue-9 (AB9) dye using bacterial consortium containing Pseudomonas fluorescens and Bacillus subtilis. The experiments were conducted in minimal salt media with varying concentrations of different parameters (pH, temperature, initial dye concentration, size of inoculum, carbon and nitrogen sources) used for optimization process. Using the One-Factor-At-A-Time method, the consortium in the study was able to decolorize at a noteworthy rate of decolorisation about 85–87.2 %. This rate was notably increased to around 90.02 % with the implementation of Response Surface Methodology. Additionally, the decolorisation process was further confirmed by using UV-Visible Spectroscopy and Fourier Transform InfraRed Spectroscopy. Additionally, a phytotoxicity assessment test on crops of agricultural significance supports the potential of this bacterial consortium for the bioremediation of AB9 contaminated water. The dye samples treated with bacterial consortium showed significantly higher seed germination rates (∼82.9 %), along with increased shoot (∼9.13 cm) and root lengths(∼3.01 cm), compared to the untreated samples. This promising finding suggests the potential for reusing treated water in agriculture and industry, offering a sustainable solution to water pollution.

Preparation of grafted starch‐based cationic flocculants and its removal of reactive and disperse dyes

AbstractIn this paper, a starch‐based flocculant (ADSt) with medium and low temperature solubility and enhanced flocculation effect was synthesized using corn starch, acrylamide, and dimethyldiallyl ammonium chloride as main materials by the ethanol‐alkali method and grafting method. The main mechanism of ADSt's flocculation was electrical neutralization and bridging. The flocculation performance of ADSt was verified by using it along with polymeric aluminum chloride (PAC) as coagulant/flocculant, dispersible dye (dispersible yellow RGFL), and reactive dye (active trimeric blue KN‐G) to simulate dye wastewater. For the dispersed yellow water sample and active emerald blue water sample, the dosage of PAC was 40 and 35 mg/L respectively. When the dosage of ADSt was 10 mg/L with a dye content of 100 mg/L, the decolorization rates for both dyes reached up to 96.2% and 94.4% respectively. The properties of the flocs such as size and two‐dimensional fractal structure were described. The prepared ADSt maintained a good flocculation effect in the pH range of 5–9 due to its excellent water solubility achieved through the ethanol‐alkali preparation process, where its solubility reached 86.7% at 30°C. Overall, the preparation process for ADSt is simple, cost‐effective, while providing an effective solution for treating printing and dyeing wastewater.

Preparation of CIP@Fe3O4 particles and their impact on the fenton reaction processing performance of single-crystal SiC

This study proposes the preparation of CIP@Fe3O4 composite magnetic particles, which maintain excellent magnetic properties while exhibiting superior Fenton reaction performance for the magnetorheological chemical polishing of single-crystal SiC. The CIP@Fe3O4 particles were prepared by coating a nanoscale layer of Fe3O4 onto micron-sized carbonyl iron powder (CIP) using the co-precipitation method. Their Fenton reaction performance and magnetic properties were characterized, and CIP@Fe3O4 was used as a solid-phase catalyst in Fenton reaction-induced etching, frictional wear, and polishing experiments on single-crystal SiC. The prepared CIP@Fe3O4 particles have a saturation magnetization of 184.3 emu/g, representing only an 8.7 % reduction compared to CIP, yet achieved a decolorization rate of 76.2 % for the methyl orange indicator (compared to only 17.2 % with CIP alone). The Fenton reaction using CIP@Fe3O4 resulted in a prominent corrosion layer on the surface of single-crystal SiC, with the oxygen atomic fraction reaching 22.15 %. The study examined material removal from SiC under Fenton reactions with different solid-phase catalysts: CIP, CIP@Fe3O4, and CIP + Fe3O4. Frictional wear results indicated that the maximum scratch cross-sectional removal area on the SiC surface under the Fenton reaction with CIP@Fe3O4 was 474.38 μm2, representing a 207.3 % increase compared to without the Fenton reaction. Additionally, Si-O compounds were identified in the debris. Polishing experiments showed that the material removal rate (MRR) with the Fenton reaction was 3295 nm/h, an increase of 220.2 % compared to without the Fenton reaction, and the surface roughness was reduced to Ra 0.895 nm, a 73.4 % reduction compared to without the Fenton reaction. This study provides additional evidence for the application of magnetorheological technology and the Fenton reaction in the polishing field of single-crystal SiC.

Development of the novel advanced electrooxidation process for decolorization of recalcitrant dyes (Methylene Blue, Rhodamine B, Congo Red): Effect of operating factors

The research aims to develop an advanced electrooxidation process for decolorization of recalcitrant dye. To enhance the radical formation, a combination of UV irradiation and electrooxidation (UV/EO) is used. Methylene Blue (MB), Rhodamine B (RB) and Congo Red (CR) dyes were used as model compounds to represent recalcitrant dyes. The performance of UV/EO process was investigated under various operating factors (i.e., current density (CD), voltage, pH, NaCl, anodic material), and compared with chlorination, UV irradiation, and electrooxidation (EO) process. MB was the highest resistant dye to the UV/EO process. The UV/EO process exhibited a synergistic effect on decolorization, and it removed MB 1.35 time faster than the EO process. Based on indirect determination of •OH, the •OH formation in the EO process was 2.4 ×10−13 M, which lower than that in the UV/EO process by 4 times. The second-order rate constant for MB oxidation by HO• (kHO•,MB) was 3.31 × 109 M−1s−1. The pseudo 1st-order decolorization kinetic (k’) was independent with voltages, but directly depended on CD and NaCl concentrations. Lower pH enhanced the k’ value. The specific energy consumption was in a range of 0.408 – 5.303 kWh/m3, depending on the k’ value. The energy consumption decreased with higher the k’ value, except for increasing CD. The Boron Doped Diamond (BDD) was more effective in the decolorization rate than dimensional active anode (DSA) by 1.6 times. Treatment of industrial dye wastewater by the UV/EO process eliminated color intensity (ADMI), COD, and BOD5 by 80 %, 91 %, and 9 %, respectively.

Efficient biodecolorization of direct black 22 Azo Dye by Aspergillus tamarii Kita UCP1279 isolated from caatinga soil

The textile industry is a major consumer of water, generating large volumes of wastewater contaminated with harmful substances, particularly azo dyes, which contain aromatic rings, amines, and sulfonic groups that contribute to their environmental toxicity. The use of microbial agents for wastewater treatment offers a cost-effective and sustainable solution, minimizing sludge production. Fungi from the Caatinga biome have demonstrated potential for bioremediation, especially under extreme environmental conditions. This study explores the ability of Aspergillus tamarii Kita to decolorize the azo dye Direct Black 22 (DB22) under varying conditions, including the use of both active and inactive fungal biomass, in static and agitated systems (120 rpm), at a controlled temperature of 30°C. Dye concentrations of 50, 125, and 250 mg/L were evaluated over time intervals of 75, 180, and 180 minutes, respectively. The influence of dissolved oxygen concentration and redox potential on the decolorization process was also investigated to identify optimal treatment conditions. Decolorization efficiency was quantified via spectrophotometric analysis. Results revealed decolorization rates of 100%, 97%, and 63% for the respective dye concentrations, with active biomass in agitated conditions achieving the highest removal rates. The study further demonstrated that dissolved oxygen levels and redox potential are critical factors in enhancing dye decolorization. These findings underscore the bioremediation potential of Aspergillus tamarii Kita in treating textile dye effluents, offering a promising approach to sustainable industrial wastewater management.

Degradation of Azo-dye (Disperse Red) Using Rhizosphere Bacterial Consortium

This study investigates the degradation of the azo dye (Disperse Red) using a rhizosphere bacterial consortium. Standard microbiological and molecular techniques were employed to isolate and identify organisms from rhizosphere soil. Degradation of azodye was carried out in a fabricated anoxic and oxic chambers with hydraulic retention time of 40hrs. Initial identification of the bacterial isolates through Gram’s reaction and biochemical tests revealed the presence of organisms belonging to the genera Pseudomonas, Lysinibacillus, and Citrobacter. Molecular and phylogenetic analyses confirmed the isolates as Pseudomonas aeruginosa, Lysinibacillus sphaericus, Pseudomonas chengduensis, and Citrobacter freundii. During the preliminary testing, the degradation efficiency was assessed under varying glucose concentrations. Higher decolorization rate of 56.17% was observed in the medium with 10% glucose after 72 hours, while the medium with 5% glucose achieved a 44.17% colour reduction. Notably, lower degradation rates recorded were 11.96% and 12.85% for the 5% and 10% dye enhance glucose mineral salt media, respectively. However, During the actual degradation testing in a double-chamber system enhanced with biochar, the first anaerobic cycle achieved a maximum decolorization of 71.95% after 94 hours, with the first aerobic cycle further enhancing degradation to 90.51%. The second anaerobic cycle increased degradation to 94.78%, and the final aerobic cycle achieved a decolorization of 98.47%. These results show that the rate of Disperse Red degradation is highly dependent on glucose levels and alternating anaerobic-aerobic conditions. This study demonstrates the potential of using rhizosphere bacterial consortia to bioremediate wastewater contaminated with azo dyes, offering an efficient and sustainable method of environmental management. The results underline the need of optimizing ambient conditions to increase microbial degradation processes.

Enhanced removal of malachite green from wastewater using nonthermal plasma gliding arc discharge combined with ferrate oxidation

The rapid and complete removal of Malachite Green (MG) dye was effectively achieved by combining potassium ferrate (Fe(VI)) treatment with nonthermal plasma discharge in both deionized water (DIW) and tap water (TW). This study evaluated the decolorization and mineralization efficiencies under varying MG concentrations, Fe(VI) dosages, and pH levels, as well as the impact of radical scavengers on the process. Fe(VI) alone resulted in moderate decolorization (35.01 %) and low mineralization (21.46 %) at an MG concentration of 50 mg/L in DIW. Plasma discharge alone achieved mineralization rates of 20.6 % in TW and 24.16 % in DIW. While complete decolorization was observed for all initial MG concentrations, it required significantly longer treatment times (>30 min). However, the combination of Fe(VI) with plasma (Fe(VI)-Plasma) demonstrated significant synergistic effects, achieving total decolorization and high mineralization rates -up to 92.5 % in DIW and 88.7 % in TW for 20 mg/L MG- at much shorter treatment times. Radical scavenger tests revealed that hydroxyl radicals (OH) were the primary oxidants in MG degradation, followed by superoxide radicals and electrons. These findings suggest that the combined Fe(VI)-Plasma technology is a promising and efficient solution for dye removal, reducing both chemical usage and treatment time.

Utilization of laccase magnetic cross-link aggregates for decolorization of amido black 10B contained in water

Laccase has a wide range of substrates and the oxidation product is water, providing an ideal choice for the biological degradation and decolorization of dyeing wastewater. This study extracted laccase from the fruiting body of Agaricus bisporus, then used o-phthalaldehyde (OPA) as a cross-linking agent and added surface-aminated Fe3O4 nanoparticles (NH2-nanoFe3O4) to prepare magnetic cross-link enzyme aggregates (MCLEAs) of laccase, which was characterized by scanning electron microscope and vibrating sample magnetometer. The optimal temperature for the catalytic reaction of the MCLEAs was 35 °C, and the optimal pH was 3.0. The stability to temperature pH and storage stability were all enhanced. The immobilized laccase was utilized to treat amido black 10B solution, and the decolorization rate reached 92.48%. After five cycles of use, the MCLEAs of laccase could maintain 42.91% of the relative activity and 32.31% of the relative degradation ability to amido black 10B.

Fabrication of Silica–Titanium Composite Film on Wood Surface and Optimization of Its Structure and Properties

In this thesis, wood loaded with a silica–titanium (Si-Ti) composite film was prepared using the sol–gel method in order to achieve improved wood with high hydrophobicity and photocatalytic activity under visible light. The factors affecting the structure and properties of the composite film, as well as the optimization process, were discussed. Infrared analysis revealed that the vibrational intensity of Si-O-Si, Ti-O-Ti, and Ti-O-Si telescopic vibration peaks increased with an increase in vinyltriethoxysilane (VETS). Additionally, the number of Ti-O-Ti telescopic vibration peaks also increased with an increase in VETS. Furthermore, the intensity of -NO3, Si-O-Si, and Ti-O-Ti telescopic vibrational peaks was enhanced with a higher dosage of nitric acid. Conversely, the intensity of -OH telescopic vibrational peaks decreased with an increase in drying temperature. XRD analysis showed that nitric acid could promote the transformation of TiO2 from amorphous to anatase, while SiO2 would reduce the grain size of anatase TiO2 and promote the growth of rutile TiO2. Additionally, wood surfaces loaded with Si-Ti composite film changed from hydrophilic to hydrophobic, with significant differences observed between different levels of each factor. The photocatalytic activity of surface-loaded Si-Ti composite films on wood was most affected by the amount of nitric acid, which influenced crystallinity of TiO2 and thus impacted the photocatalytic activity. Furthermore, changes in VTES dosage not only affected the crystalline phase of TiO2 and the grain size of Si-Ti composite film but also influenced the crystallinity of TiO2 through generating SiO2. Finally, based on optimal preparation process (titanium–alcohol ratio of 1:5, titanium–silicon ratio of 1:0.2, titanium–acid ratio of 1:0.5, and drying temperature of 100 °C), wood surfaces loaded with Si-Ti composite film achieved a contact angle up to 125.9° and exhibited a decolorization rate for rhodamine B under UV light reaching 94% within 180 min.

Investigation of the mechanism and stability of highly efficient photocatalytic degradation of Methylene blue using Ni doped CdS photocatalyst

Methylene blue (MB) is commonly utilized in chemical indicators, dyes, biological colors, and pharmaceuticals. Its aqueous solution is poisonous and carcinogenic, posing a significant threat to the ecological environment. The wurtzite-phase NixCd1−xS was synthesized using the hydrothermal technique in this study. Ni doped CdS enhanced its photocatalytic efficiency and resistance to photocorrosion, enabling its application in the photocatalytic destruction of MB. The incorporation of Ni did not change the crystal structure and microstructure of CdS, but increased the visible light absorption range and decreased the band gap width slightly, which promoted the migration of photogenerated electrons and reduced their recombination with holes, resulting in higher photogenerated carrier separation efficiency of NixCd1−xS. The photocatalytic decolorization rate of Ni0.06Cd0.94S for 100 mL of 10 mg/L MB at 240 min is 91.3 %, and the reaction rate constant is 0.01102 min−1, which is 4.42 times that of wurtzite-phase CdS. The photocatalytic mechanism of NixCd1−xS and its composite was analyzed using trap experiments in conjunction with the band structure of the sample. Additionally, the stability of NixCd1−xS was evaluated. The results indicated that the stability was superior to that of CdS. The findings demonstrate that Ni0.06Cd0.94S exhibits good catalytic activity and stability, making it a viable catalyst for the photocatalytic degradation of organic pollutants in water.

Role of surfactants in the degradation and sustainable dyeing for reactive dyeing wastewater

To enhance the decolorization rate of thermally activated sodium persulfate in dye wastewater, C.I. Reactive Black 5 (RB5) was investigated in this study, which was evaluated by the decolorization of the dye solution. The effect of surfactant concentration (including anionic surfactant sodium dodecyl sulfate (SDS), nonionic surfactant Tween 80 (TW-80) and amphoteric surfactant (BS-12)), SPS concentration, and reaction temperature on the degradation of RB5 was studied. Furthermore, the relationship between free radicals and RB5 degradation was investigated. The results showed that the addition of SDS and TW-80 would inhibit the decolorization of RB5. Correspondingly, the effect would enlarge as the surfactant concentration increased. Nevertheless, the addition of BS-12 wouldn’t affect the final decolorization of RB5 dye solution, despite it could increase the decolorization rate in the initial stage. After 10 min of decolorization, compared to the dye liquor without BS-12, the decolorization could increase by 9.07 % and 0.69 %, respectively, after adding 0.5 and 1.0 CMC of BS-12. Besides, when reactive dyes were degraded by thermally activated sodium persulfate, the SO4-· and ·OH would work together, and SO4-· played a major role while ·OH played an auxiliary part. When the treated wastewater was used for dyeing, the addition of BS-12 could effectively regulate the dyeing rate. The fixation and K/S value were increased by 1.1 % and 0.20, respectively. Furthermore, the dyed fabrics also exhibited improved uniformity, with negligible differences in color fastness. The effects of adding SDS were similar to BS-12, while it decreased the exhaustion and fixation rate of RB5. In addition, non-ionic TW-80 was unfavorable to dyeing. This work provides a new way for efficient treatment of dyeing wastewater as well as reuse, opening an environmentally friendly treatment concept.

Electrochemical treatment of azo dye wastewater by dynamic flow diaphragm system: Response surface methodology optimization and energy consumption analysis

In this experiment, the degradation process of azo dye wastewater was studied based on the diaphragm double chamber electrochemical reactor, taking the mono azo dye amaranth as an example. Through the circulation flow of appropriate volume of wastewater in the cathode and anode chamber, the simultaneous action of cathode and anode was realized, and the degradation and decolorization efficiency of azo wastewater was improved while reducing energy waste. The optimal reaction conditions optimized by response surface methodology were as follows: the voltage was 20.74 V, the plate spacing was 4.89 cm, and the cycle speed was 60.66 rad / min. The optimal decolorization rate was 99.66 %. The energy consumption analysis of the dynamic flow diaphragm system electrochemical method and the static flow diaphragm system electrochemical method for the treatment of azo dye wastewater was compared and analyzed. In addition, the possible degradation process of azo dye wastewater by dynamic flow electrochemistry was inferred by ultraviolet spectroscopy and mechanism prediction analysis. The experimental results show the great potential of the dynamic flow membrane system process in the treatment of azo dyes.