Simulated Dye Wastewater Research Articles

Efficient removal of cationic dyes by a bivanadyl capped, highly reduced Keggin polyoxometalate through flocculation

Flocculation is widely applied for dye wastewater treatment, due to its low cost, high efficiency and convenient operation. However, finding novel flocculant with high performance and low cost is still a challenge. Therefore, a fully characterized bivanadyl capped, highly reduced Keggin polyoxometalate (Et3NH)5[PMoV6MoVI6O40(VIVO)2] (PMoV2) was explored as flocculant for the treatment of simulated cationic dye wastewater. The effect of initial pH, PMoV2 dosage, and concentrations of dyes and inorganic salts on the flocculation rate of methylene blue (MB)/ crystal violet (CV)/rhodamine B (RhB) was investigated. Under the optimum conditions, the flocculation rates of MB, CV and RhB were 99.7%, 99.8% and 99.7% in 5min, respectively. In addition, PMoV2 and dyes could be easily recovered from flocs. PMoV2 exhibited high selectivity for CV in the binary systems of CV-MB and CV-MO. Even after five recycling tests, PMoV2 still kept high flocculation rate of MB/CV/RhB. The possible flocculation mechanisms for MB/CV/RhB single system, and MB-CV and MO-CV binary systems were charge neutralization, charge neutralization and π-π interaction, and charge neutralization and electrostatic interaction, respectively. PMoV2 was better than the reported flocculants in the respect of easy availability and operation conditions, reusability and high flocculation rate. The cost effectiveness, eco-friendly nature and excellent flocculation performance in individual and binary dye systems made PMoV2 competitive in the field of water environment remediation and material development. This is the first report about the flocculation activities of bivanadyl capped, highly reduced Keggin polyoxometalate.

Highly energy-efficient degradation of simulated dye wastewater by array type underwater bubble discharge plasma: Key factors identification and degradation pathways

The extensive use of dyes presents a significant safety concern for the reuse of water resources, highlighting the critical need for a rapid and efficient degradation method for dye mixtures in wastewater. This study introduces a degradation system based on an array type underwater bubble discharge plasma specifically designed to treat a dye mixture wastewater containing methylene blue (MB) and methyl violet 2B (MV2B). Analysis of the optical and electrical characteristics reveals that the device experiences minimal temperature increase, with the highest intensity of the band associated with N2 in the emission spectra, and discharges occurring predominantly during the rising and falling edges of a pulse cycle. Experimental results demonstrate that the most effective degradation efficiencies (MB = 94.83%, MV2B = 93.48%) are achieved at an initial dye concentration of 50 mg/L, a power supply frequency of 6 kHz, an air flow rate of 2.5 SLM and an initial electrical conductivity of 50 μS/cm. The degradation of dyes is primarily attributed to the demethylation process of O3(aq) and other species. Toxicity analysis indicates that the plasma degradation process significantly reduces the toxicity of the intermediate products of dyes. This study not only presents a novel approach for treating high concentration mixed dye wastewater, but also provides valuable insights for future research in this area.

Electrocoagulation treatment for Remazol Brilliant Blue R (Reactive Blue 19) removal of textile dye simulated wastewater using iron-aluminum electrodes

Abstract The presence of non-biodegradable dyes, such as Remazol Brilliant Blue R (Reactive Blue 19), in wastewater poses a significant environmental challenge. This study investigates the application of electrocoagulation using iron-aluminum (Fe-Al) electrodes to efficiently remove Reactive Blue 19 dye from simulated textile dye wastewater. It considers various parameters such as electrode material, current, stirring speed, as well as the influence of sodium chloride acting as a supporting electrolyte to enhance conductivity. Additionally, it evaluates the economic feasibility through electrode consumption analysis. The experimental setup involved a designed reactor with aluminum and iron electrodes arranged at bipolar parallel connection, along with a 30-minute electrocoagulation process conducted at ambient temperature and subsequent filtration of the treated wastewater for UV-VIS analysis. The optimal parameter combination obtained consists of Fe-Al electrode material, a 3 A current, and a 200-rpm stirring speed, achieving 96.87% dye removal. Furthermore, extending the operating time to 60 minutes improved the removal by 99.15%. Under these optimal conditions, the energy consumption measured was 36 kWh/m3. The high dye removal rate obtained shows the effectiveness of this electrocoagulation process in treating Reactive Blue 19 simulated wastewater. A t-test, employed as a hypothesis testing technique with a significance level of 0.05, confirmed the optimal levels of the factors and interactions within the treatment process. A remarkable coefficient of determination of 0.9794 in the dye removal sensitivity analysis signifies a strong goodness of fit, indicating that these three (3) parameters collectively explain how they affect the outcome while accounting for dye removal efficiency variation. These results showed that electrocoagulation is a promising technology for treatment of Reactive Blue 19 dye wastewater.

Removal of methylene blue and Congo red from the wastewater in a jet loop reactor using ozone and activated carbon

The textile industry consumes a large amount of fresh water, resulting in colored effluent due to the incomplete fixation of certain dyes. Traditional textile wastewater treatment such as coagulation-flocculation, membrane filtration, thermal separation and electrochemical processes are expensive and pose significant environmental challenges. To address these issues an alternative technique for decolorizing textile effluent using a modified sparged loop reactor was proposed in this study. The jet loop reactor basically a multiphase reactor was utilized to treat textile wastewater with ozone. In this study, the textile wastewater containing water-soluble basic dyes such as Methylene blue and Congo red was simulated at a concentration of 50 ppm and the color removal efficiency of the reactor was analyzed. The effect of process parameters such as effluent flow rate (0.2– 0.4 Liter/min), sparger openings (2−4), adsorbent weight (0.5 – 1.5 g) and ozone dosage time (10–30 min) on the decolorization efficiency of the reactor were examined and optimized using Response Surface Methodology. In this study, a maximum color removal of 93 % and 85 % for Congo red dye and Methylene blue dye simulated wastewater was achieved. A correlation was developed using Response Surface Methodology-Box Behnken Design and the developed model was successfully interpreted with experimental values. Based on our results, we believe that it is possible to replace the energy-intensive thermal separation process with jet loop sparged reactor to treat the textile effluent. As a sustainable process, loop reactor may result in a huge reduction of freshwater consumption.

Bioaugmented biological contact oxidation reactor for treating simulated textile dyeing wastewater

In this study, modified polyamide fibers were used as biocarriers to enrich dense biofilms in a multi-stage biological contact oxidation reactor (MBCOR) in which partitioned wastewater treatment zone (WTZ) and bioaugmentation zone (BAZ) were established to enhance the removal of methyl orange (MO) and its metabolites while minimizing sludge yields. WTZ exhibited high biomass loading capacity (5.75 ± 0.31 g/g filler), achieving MO removal rate ranging from 68 % to 86 % under different aeration condition within 8 h in which the most dominant genus Chlorobium played an important role. In the BAZ, Pseudoxanthomonas was the dominant genus while carbon starvation stimulated the enrichment of chemoheterotrophy and aerobic_chemoheterotrophy genes thereby enhanced the microbial utilization of cell-released substrates, MO as well as its metabolic intermediates. These results revealed the mechanism bioaugmentation on MBCOR in effectively eliminating both MO and its metabolites.

The self-boosting ultrafast removal of Cr(VI) and organic dye in textile wastewater through sulfite-induced redox processes

The treatment of textile wastewater containing harmful metal ions poses a significant challenge in industrial applications due to its environmental impact. In this study, the use of sulfite for treating simulated dye wastewater containing New Coccine (NC) and Cr(VI) was investigated. The removal of NC was influenced by the redox reaction between Cr(VI) and sulfite, demonstrating a strong self-boosting effect of Cr(VI) on NC removal. Remarkable NC decoloration (95%) and Cr(VI) reduction (90%) were achieved within 1 min, highlighting the effectiveness of the treatment. Quenching experiments and electron paramagnetic resonance (EPR) technology confirmed that singlet oxygen (1O2) was the main oxidative agent for organic dye removal and SO4•−, •OH and Cr(V) were also identified as key contributors to NC degradation. The Cr(VI)/sulfite system exhibited higher efficiency in degrading azo dyes, such as NC and Congo Red (CR), compared to non-azo dyes like Methylene Blue (MB). This superiority may be attributed to the action of Cr(V) on azo groups. Additionally, the COD removal experiments were conducted on the actual dye wastewater, showing the excellent performance of the Cr(VI)/Sulfite system in treating industrial textile wastewater. This approach presents a promising strategy for effective “waste control by waste”, offering great potential for addressing challenges related to dye wastewater treatment and environmental pollution control in practical industrial scenarios.

Recycling waste plastic to construct ultra-stable and multifunctional metal-organic framework for fast efficient dye adsorption and acetone vapor detection

Plastic pollution and water pollution are currently two major environmental problems. Exploring a strategy that can convert waste plastics into high value-added functional materials will be an effective solution to relieve above issues. Herein, we realized that the waste plastic of polyethylene terephthalate (PET) was converted into ultra-stable and multifunctional 3D pillared-layer Eu-based metal-organic framework (MOF) material (labelled as Eu-PET) through one-pot solvothermal method. The effects of reaction conditions on the waste plastic PET upcycling were explored in detail. The Eu-PET exhibits excellent Congo red (CR; Concentration: 1 g/L) adsorption capacity of 2312 mg/g in 2 h at nature pH (2988.11 mg/g at pH = 4). Moreover, the influence parameters containing dye concentration, adsorbent dosage, pH, temperature and simulated dye wastewater were studied. The adsorption mechanism was explained by pseudo-second order and Langmuir models, revealing the adsorption of CR on Eu-PET was mainly defined by electrostatic interaction, hydrogen bonding interaction and π-π interaction. Furthermore, Eu-PET as fluorescent sensor, a portable Eu-PET fluorescent film was developed. Experiments have shown that a noticeable fluorescent quenching response occurred within 10 s contact to acetone vapor, and the theoretically detectable limit (LOD) was as low as 0.048 % (v/v), and Eu-PET/acetone system was static quenching. Finally, Eu-PET has excellent water, acid-base and thermal stability, and recyclability over 7 cycles of CR adsorption and acetone detection. This work opens an avenue for the green recycling/utilization of plastic waste, providing meaningful insights into the effective processing of dyes wastewater and fluorescence sensing of volatile organic compounds.

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

In recent years, electrochemical synergistic activation of persulfate (PDS) degradation technology has demonstrated significant potential in wastewater treatment applications. Given the challenges posed by the complex water quality, high COD content, and recalcitrant degradation of dyeing wastewater, this study aimed to evaluate the efficacy of iron/aluminum dual-electrode electrochemical activation of PDS for degrading simulated dyeing wastewater. The results showed that under optimal conditions, utilizing both periodic reversal and direct current electrochemical activation of PDS achieved removal rates of 99.2% and 98.3% for Reactive Black 5 (RB5) and Reactive Red X-3B (RRX-3B), respectively, demonstrating promising removal efficiency. Notably, the removal efficiency of RB5 surpassed that of RRX-3B, suggesting a dependence on initial concentration influencing reaction kinetics. Furthermore, full-spectrum scanning and quenching experiments revealed that RB5 and RRX-3B were primarily degraded through the potent oxidation action of SO4−· and ·OH, with a small number of intermediates present in the solution. Periodic reversal proved effective in mitigating electrode passivation and enhancing electrode longevity. This study provides a highly effective removal method of binary dyes from dyeing wastewater by periodic reversal Fe-Al dual-electrode electrochemical activation of PDS technology, offering valuable insights for sustainable treatment of dyeing wastewater with binary components.

Enhanced interfacial evaporation of CF@NC fabric via coupled photo-thermal and Joule-heating effect

To address the challenges of global water pollution and scarcity, solar-driven interfacial water evaporation has emerged as a viable method for producing clean water. Nevertheless, the efficacy of most extant interfacial evaporation systems were contingent upon abundant sunlight, thereby constraining their utility. To surmount the limitation, this study introduced a coupled tunable photo-thermal and Joule-heating process for interfacial evaporation utilizing carbon fiber (CF) modified by N-doped carbon nanotubes (NC). The CF@NC had highly graphitized structure, excellent light-absorbing ability and hydrophilicity, which made it suitable for photo-thermal and Joule-heating conversion. Under the coupled effect of photo-thermal and Joule-heating, the evaporation rate reached 10.37 kg·m−2·h−1 with 1 sun and 2.5 V, while the rate was 1.81 kg·m−2·h−1 under only 1 sun and 7.63 kg·m−2·h−1 with 2.5 V. Meanwhile, the CF@NC fabric evaporator also showed promising potential in salt tolerance and dye wastewater treatment. Under continuous all-day operation, a superior purification performance was achieved, which realized long periods of no salt operation and effectively remove the Rhodamine B and methyl orange in the water. Considering the high evaporation rate and reliable water yields obtained from simulated seawater and dye wastewater, the CF@NC fabric evaporator hold great promise for highly efficient purification.

Sonophotocatalytic Degradation of Reactive Black 5 in Simulated Dye Wastewater Using ZnO and Activated Red Mud Sonophotocatalyst

Sonophotocatalytic Degradation of Reactive Black 5 in Simulated Dye Wastewater Using ZnO and Activated Red Mud Sonophotocatalyst

Flocculation of kaolin and anion dye by cationic cellulose-based flocculant: RSM-optimized synthesis and experimental study

An efficient cellulose-based flocculant, CMA, was synthesized using a free radical initiation method in a NaOH/Urea aqueous solution. The optimal synthesis conditions were determined through single-factor and RSM experiments: a molar ratio of MCC to AA of 1:3.6, MCC to CTA of 1:8.2, and a reaction temperature of 45.8 °C. CMA was characterized using FTIR, SEM, XRD, DLS, XPS, and TG and applied successfully to the flocculation treatments of kaolin, simulated dyes, and actual dye wastewater. It exhibited low pH sensitivity, achieving over 90% removal efficiency at pH 3–12, with a maximum of 98.3%. In simulated dye wastewater, the removal efficiency of various dyes was greater than 95%, with a maximum of 97%. After CMA flocculation and ozone aeration, 86.5% of COD and 93.6% of turbidity were removed from the actual dye wastewater. CMA carried out the flocculated dye removal process via charge neutralization, double layer compression, and bridging adsorption, as revealed by various instrument characterization and analysis. A polysaccharide-based flocculant, CMA exhibits environmentally friendly properties, low pH sensitivity, and high efficiency in removing wastewater pollutants, making it a promising flocculant for highly turbid wastewater and anionic dye wastewater.

Fabrication of Bi2MoO6/MIL-101 (Fe) Composites for Visible Light Photocatalytic Activity Enhancement

Bi2MoO6/MIL-101 (Fe) composite photocatalyst was prepared by a two-step solvothermal method, the photocatalytic decomposition reaction was carried out using visible light as light source and Congo red (CR) aqueous solution as the simulated dye wastewater. The results showed that the photocatalytic activity of Bi2MoO6/MIL-101 (Fe) composite photocatalyst was better than pure MIL-101(Fe) catalyst for the degradation of CR. Bi2MoO6/MIL-101(Fe) composite photocatalyst could compensate for the slower electron mobility and the easy compounding of photogenerated electron-hole pairs of MIL-101(Fe). The degradation efficiency of Bi2MoO6/MIL-101(Fe) photocatalyst for CR remained high after five cycles, indicating its good stability and reusability.

Photocatalytic treatment of landfill leachate using CaTiO3 nanoparticles

Perovskite Calcium titanate (CaTiO3)is a versatile material that can be used in several applications, such as biomedicine, electronic devices, photocatalysis, and wastewater treatment.In this study, CaTiO3nanoparticles were synthesized using the sol–gel method at 600 °C with the help of tetra butyl titanate, calcium nitrate, and citric acid as chelating agents. FESEM and TEM analysis shows the synthesized nanoparticle has particle sizes of less than 26.23 and 23.71 nm respectively with a bandgap of 3.57 eV. By using DTA, TGA, XRD, FESEM, TEM, EDX, and UV–Vis, the thermal, structural, and optical properties were examined. Several studies examined the photocatalytic capabilities of CaTiO3for the photocatalytic treatment of simulated dye solution and wastewater produced by the textile industry. In this study, the CaTiO3 nanoparticles are used in the photocatalytic treatment of landfill leachate. The results are promising, showing a 72 % reduction in chemical oxygen demand (COD),a 43.62 % decrease in colour,a 41.75 % improvement in turbidity, 59.01 % removal of total dissolved solids, and35.71 % removal of NH3-N from the landfill leachate under the optimum condition of 33 W UV irradiation for 8 h at a catalyst dose of 3.33 g/L and a pH of 6. After nano-photocatalytic treatment, the percentages of Cr, Ni, and Zn removed are 52.30 %, 63.46 %, and 87.50 %, respectively.

Integrating artificial neural networks and response surface methodology for predictive modeling and mechanistic insights into the detoxification of hazardous MB and CV dyes using Saccharum officinarum L. biomass

The presence of dye pollutants in industrial wastewater poses significant environmental and health risks, necessitating effective treatment methods. The optimal adsorption treatment of methylene blue (MB) and crystal violet (CV) dye-simulated wastewater utilising Saccharum officinarum L presents a key challenge in the selection of appropriate modelling approaches. While RSM and ANN models are frequently used, there is a noticeable knowledge gap when it comes to evaluating their relative strengths and weaknesses in this context. The study compared the predictive abilities of response surface methodology (RSM) and artificial neural network (ANN) for the adsorption treatment of MB and CV dye-simulated wastewater using Saccharum officinarum L. The process experimental variables were modelled and predicted using a three-layer artificial neural network trained using the Levenberg-Marquard backpropagation algorithm and 30 central composite designs (CCD). The adsorption study used a specific mechanism, which led to noteworthy maximum removals of 98.3% and 98.2% for dyes (MB and CV), respectively. The RSM model achieved an impressive R2 of 0.9417, while the ANN model achieved 0.9236 in MB. Adsorption is commonly used to remove colour from many different materials. Saccharum officinarum L., a byproduct of sugarcane processing, has shown potential as an efficient and ecological adsorbent in this environment. The purpose of this study is to evaluate sugarcane bagasse's potential as an adsorbent for the removal of dyes MB and CV from industrial wastewater, providing a long-term strategy for reducing dye pollution. Due to its beneficial economic and environmental characteristics, the Saccharum officinarum L. adsorbent has prompted research into sustainable resources with low pollutant indices.

Peroxymonosulfate-based catalytic degradation of reactive dyes in real wastewater by Fe/N-codoped carbocatalysts loaded on carbon cloth

This study simulated actual dyeing wastewater in dyeing factories with three types of dyeing wastewaters from laboratory cotton fabric dyeing to investigate the effects of catalyst and oxidant peroxymonosulfate (PMS) concentrations, pH level, and temperature on dye degradation in wastewater and determine the optimal conditions for dyeing wastewater treatment accordingly. The results demonstrated that the optimal conditions varied with the reactive dyes. Specifically, the optimal oxidant PMS concentration for degrading Reactive Yellow and Reactive Blue was 0.6 g/L, and that for degrading Reactive Red was 0.4 g/L. The optimal pH level for degrading Reactive Red and Reactive Blue was around 7.0, and that for degrading Reactive Yellow was about 5.0. The activation energy of the degradation and the mineralization degree of the three dyes were also discussed. Reactive Blue showed greater activation energy (47.0 kJ/mol) and a higher mineralization degree (81% chemical oxygen demand removal) than the other two dyes under optimal disposal conditions. The Fe/N-codoped carbocatalyst loaded on carbon cloth exhibited desirable reusability and good stability for the degradation of the three dyes. Mechanisms involved in their degradation were analyzed through X-ray photoelectron spectroscopy, focusing on N species, Fe-N binding, and C=C and C–N active components in the Fe/N-codoped carbocatalyst. Electron paramagnetic resonance experiments demonstrated that both the radical and non-radical pathways were accountable for the degradation of the three dyes, primarily the non-radical pathway. This study may contribute to the application of activated PMS for practical dyeing wastewater treatment.

A bifunctional graphene-based cathode for wastewater treatment in heterogeneous electro-fenton: Taking textile, old landfill leachate and simulated antibiotic wastewater as examples

Enhancing heterogeneous electro-Fenton (EF) efficiency to deal with water pollution cannot avoid the limitation of Fe(II) regeneration and low efficiency of H2O2 production. Herein, we demonstrate an efficient and robust strategy for the growth of reduced graphene oxide (rGO) and iron layered double hydroxide (FeIIFeIII-LDH) composites on graphite felt (rGO-FeIIFeIII-LDH/GF). rGO-FeIIFeIII-LDH/GF shows accelerated Fe(II) regeneration, and excellent 2e− oxygen reduction reaction (ORR) activity. It was revealed by electrochemical measurements and density functional theory (DFT) calculations that rGO acted as an electron mediator, which enables a feasible fast electron transfer pathway (rGOHOMO(−0.99 eV) → FeIIFeIII-LDHLUMO(0.53 eV)) for Fe(II) regeneration. The 2e− ORR activity can be attributed to the electron transfer number (1.77–1.94), N-doping and Fe occupied the defect site of rGO. The heterogeneous (total Fe leaching meet GB 5740–2006) EF process enabled immediate activation of H2O2 into OH and O2−. Various wastewaters including simulated dye and antibiotic wastewater, textile effluent, old landfill leachate can be efficiently treated in 120 min. Moreover, after avoiding the influence of Cl− in the actual water body, the pollution load and toxicity of the effluent were more acceptable. These results provide new insights into the heterogeneous EF system constructed with carbon fiber-based bifunctional electrode for the treatment of various actual wastewaters.

Effect of Enhanced Hydrolytic Acidification Process on the Treatment of Azo Dye Wastewater.

The hydrolysis acidification process is an economical and effective method, but its efficiency is still low in treating azo dye wastewater. It is therefore crucial to find more suitable and efficient means or techniques to further strengthen the process of treating azo dye wastewater by a hydrolytic acidification process. In this study, a hydrolytic acidification aerobic reactor was used to simulate the azo dye wastewater process. The change of wastewater quality during the reaction process was monitored, and the deep enhancement effect of single or composite biological intensification technology on the treatment of azo dye wastewater by the hydrolytic acidification process was also explored. Co-substrate strengthening and the addition of fructose co-substrate can significantly improve the efficiency of hydrolytic acidification. Compared with the experimental group without the addition of fructose, the decolorization ratio of wastewater was higher (93%) after adding fructose co-substrate. The immobilization technology was strengthened, and the immobilized functional bacteria DDMZ1 pellet was used to treat the simulated azo dye wastewater. The results showed that the composite technology experimental group with the additional fructose co-matrix had a better decolorization efficiency than the single immobilized bio-enhancement technology, with the highest decolorization ratio of 97%. As a composite biological intensification method, the fructose co-matrix composite with immobilized functional bacteria DDMZ1 technology can be applied to the treatment of azo dye wastewater.

Decolorization Performance of a Methyl Benzyl Diallyl Quaternary Ammonium Salt Copolymer in a Simulated Reactive Dyeing Wastewater

The source of dyeing wastewater and the composition of pollutants are very complex, direct discharge will bring great harm to living environment, and cause waste of water resources. For the treatment of reactive dyeing wastewater, this work developed and synthesized a novel cationic flocculant called Poly (DMDAAC-co-DAMBAC), which was made by copolymerizing dimethyl-diallyl-ammonium chloride (DMDAAC) and methyl-benzyl-diallyl-ammonium chloride (DAMBAC). To assess its flocculation effects, flocculation decolorization studies with 3RF reactive yellow, KN−R reactive blue, and 3BF reactive red were conducted. The copolymers′ lipophilicity considerably increased once atyl groups were added. The experimental results showed that Poly(DMDAAC-co-DAMBAC) had an optimal decolorization rate of over 94 % for three reactive dyes and a maximum decolorization rate of roughly 80 % for CODMn, both of which were significantly higher than those of PDMDAAC and nearly on par with those of PDAMBAC with a comparable viscosity. Instead, Theoretical calculations of the binding energy of the results demonstrated the accuracy of the findings. The study illustrated the flocculation mechanism and laid the foundation for further application of Poly(DMDAAC-co-DAMBAC).

DBD plasma reactor for the treatment of crystalline violet simulated dye wastewater

DBD plasma reactor for the treatment of crystalline violet simulated dye wastewater

Enhanced mechanism and experimental research of laser cavitation degradation of methylene blue by AuNPs

As a novel degradation method, laser cavitation degradation suffers from low degradation efficiency in the absence of medium gain. An enhancement method of laser cavitation using Au nanoparticles (AuNPs) is proposed for degrading organic dye wastewater. Methylene blue (MB) aqueous solution was employed as the simulated organic dye wastewater. The strong absorption characteristics of AuNPs and the mechanism underlying AuNPs-enhanced laser cavitation degradation were analyzed. The local field enhancement effect and shock wave signal were obtained. Therelationshipsamong the AuNPs, laser energy, the number of irradiations number and the degradation effect were investigated. The results show that the local field enhancement coefficient of AuNPs in Methylene blue (MB) aqueous solution reached 1.9, and the degradation degree increased by three times compared with that of pure solution because that thermal decomposition and oxidation of hydroxyl (OH) radicals were enhanced by AuNPs. With the laser energy levels increasing (70–110 mJ), the intensity of shock wave increased by 2–4 times and the degree of degradation increased by three times. The degradation rate reached 37.7 % within 3 min and the irradiation number reached 1600. Compared with other methods, the AuNPs-enhanced laser cavitation approach has exhibited remarkable controllability together with a higher degradation efficiency.