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COLORATION TECHNOLOGY · 2023 ·Vol. 140 ·期 2 ·300-312 · IF 1.8

Rapid decolorisation of dyeing wastewater by FeIII(2,2′:6′,2″-terpyridine)activated peroxymonosulphate

Jianing Fan,Shouying Wu,Zixian Wang,Minglong Zheng,Miaomiao Zhang,Linping Zhang,Yi Zhong,Xiaofeng Sui,Hong Xu,Zhiping Mao

The discharge of coloured textile printing and dyeing wastewater causes environmental pollution. Disposing of wastewater efficiently, simply and with low consumption, is a problem that must be addressed. Herein, a catalytic method for rapid decolorisation of organic dyes was devised employing a terpyridine iron complex to activate oxidised permonosulphate. CI Acid Red 1 was used as the simulated pollutant, the influences of operating parameters on the fading effects of wastewater were explored. According to the results, the produced catalytic system exhibits a universal catalytic effect. Even when the dye concentration reaches 76.4 mg/L, the dyeing wastewater may be effectively decolorised. In addition, when anions (HCO 3 − , SO 4 2− , Cl − ) were present in the solution, the degradation effect of CI Acid Red 1 was still effective. Interestingly, active species such as sulphate radicals and singlet oxygen were detected in the catalytic degradation system by radical capture experiments. The removal rate of total organic carbon can achieve a percentage of 26.22% in 2 hours. This research provides a unique, enzyme-like catalytic system for the rapid breakdown of dye contaminants.

研究领域: 环境科学 · 化学工程
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Surfaces and Interfaces · 2023 · IF 6.2

Superior photocatalytic performance of ancillary-oxidant-free novel starch supported nano MFe2O4 (M = Zn, Ni, and Fe) ferrites for degradation of organic dye pollutants

A.V. Ravindra,M. Chandrika,Andem Sandeep

This work presents the effectual degradation of MB and MO dyes in an aqueous solution under UV light irradiation on nano ZnFe 2 O 4 , NiFe 2 O 4 , and Fe 3 O 4 without using any supplementary oxidants has been reported. Nano ZnFe 2 O 4 , NiFe 2 O 4 , and Fe 3 O 4 are successfully prepared via a co-precipitation technique utilizing biodegradable starch as a surfactant . XRD patterns reveal a pure spinel phase for all the samples. FTIR spectra confirm the successful embedding of the starch surfactant. SEM micrographs exhibit tiny spherical particles of size 5–8 and 4–6 nm for ZnFe 2 O 4 and NiFe 2 O 4 but spherical particles of 8–10 nm and flake-like particles of ∼14 nm thick for Fe 3 O 4 . N 2 sorption studies show type-IV isotherms typical of mesoporous structures. The direct bandgap of these ferrite nanoparticles is 2.03–2.15 eV, related to the metal D-d onsite transfers, which are permitted by spin but prohibited by parity. MB decolorization of 99% is achieved in less than 2 h for all the samples; in contrast, MO decolorization takes relatively longer irradiation. The decolorization kinetics suggests that the pseudo-second-order model is more appropriate to explain the decolorization process of MB and MO by the catalysts. The order of photocatalytic activity evaluated from rate constant (k 1 ) per SSA values is Fe 3 O 4 < ZnFe 2 O 4 < NiFe 2 O 4 for both MB and MO decolorization. NiFe 2 O 4 photocatalyst shows the best effect on the decolorization of both dyes due to its low bandgap and high surface area. All the ferrite catalysts demonstrate high stability with no substantial deterioration of photocatalytic activity even after three cycles. The results of this study endorse that the nano ferrites prepared in this work are potential candidates for the photocatalytic degradation of aqueous solutions of MB and MO.

研究领域: 环境科学 · 材料科学 · 化学
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Desalination and Water Treatment · 2024 · IF 1

Application of CuO/AC in DBD plasma for dye wastewater treatmnent: synthesis, optimization, and coupling mechanism

Yongjun Shen,Yunli Wang,Kaixia Fan

ABSTRACT Acid turquoise blue A (ATBA) is treated by the combined dielectric barrier discharge (DBD) plasma and AC supported CuO (CuO/AC). CuO/AC is prepared by incipient wetness impregnation method. X-ray diffraction, N 2 adsorption/desorption isotherm, and scanning electron microscope are used to characterize the CuO/AC. Interactive effects of initial pH, conductivity value, input power, and CuO/AC dosage on the decolorization rate of ATBA are investigated. The predicted decolorization rate of ATBA reaches to 97.12% under the optimal condition, only have 1.95% error compared with the experimental value (95.87%). The possible coupling mechanisms of combined DBD plasma and CuO/AC are proposed.

研究领域: 环境科学 · 材料科学
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CHEMOSPHERE · 2016 · IF 3.698

Evaluation of anaerobic sludge volume for improving azo dye decolorization in a hybrid anaerobic reactor with built-in bioelectrochemical system

Min-Hua Cui,Dan Cui,Lei Gao,Ai-Jie Wang,Hao-Yi Cheng

A hybrid anaerobic reactor with built-in bioelectrochemical system (BES) has been verified for efficiently treating mixed azo dye wastewater, yet still facing many challenges, such as uncertain reactor construction and insufficient electron donors. In this study, an up-flow hybrid anaerobic reactor with built-in BES was developed for acid orange 7 (AO7) containing wastewater treatment . Cathode and real domestic wastewater both served as electron donor for driving azo dye decolorization. The decolorization efficiency (DE) of AO7 (200 mg/L) in the hybrid reactor was 80.34 ± 2.11% with volume ratio between anaerobic sludge and cathode (VR slu:cat ) of 0.5:1 and hydraulic retention time (HRT) of 6 h, which was 15.79% higher than that in BES without sludge zone. DE was improved to 86.02 ± 1.49% with VR slu:cat increased to 1:1. Further increase in the VR slu:cat to 1.5:1 and 2:1, chemical oxygen demand (COD) removal efficiency was continuously improved to 28.78 ± 1.96 and 32.19 ± 0.62%, but there was no obvious DE elevation (slightly increased to 87.62 ± 2.50 and 90.13 ± 3.10%). BES presented efficient electron utilization, the electron usage ratios (EURs) in which fluctuated between 11.02 and 13.06 mol e − /mol AO7. It was less than half of that in sludge zone of 24.73–32.06 mol e − /mol AO7. The present work optimized the volume ratio between anaerobic sludge and cathode that would be meaningful for the practical application of this hybrid system.

研究领域: 环境工程 · 废水处理
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Journal of Chemistry · 2015 ·Vol. 2015 ·期 1 ·670194 · IF 0.772

ABTS-Modified Silica Nanoparticles as Laccase Mediators for Decolorization of Indigo Carmine Dye

Youxun Liu,Mingyang Yan,Yuanyuan Geng,Juan Huang

Efficient reuse and regeneration of spent mediators are highly desired for many of the laccases’ biotechnology applications. This investigation demonstrates that a redox mediator 2,2′-azino-bis-(3-ethylbenzothiazoline)-6-sulfonic acid (ABTS) covalently attached to silica nanoparticles (SNPs) effectively mediated dye decolorization catalyzed by laccase. Characteristics of ABTS-modified silica nanoparticles (ABTS-SNPs) were researched by scanning electron microscopy and Fourier-transformed infrared spectroscopy. When ABTS and ABTS-SNPs were used as laccase mediators, the decolorization yields of 96 and 95% were, respectively, obtained for indigo carmine dye. The results suggest that ABTS immobilized on SNPs can be used as laccase mediators as they retain almost the same efficiency as the free ABTS. The oxidized ABTS-SNPs were regenerated by their reduction reaction with ascorbic acid. Decolorization efficiency of regenerated ABTS-SNPs and their initial forms were found to be almost equivalent. Six reuse cycles for spent ABTS-SNPs were run for the treatment of indigo carmine, providing decolorization yields of 96–77%. Compared with free mediator, the immobilized mediators have the advantage of being easily recovered, regenerated, and reused making the whole process environmentally friendly.

研究领域: 环境生物技术 · 纳米生物技术 · 酶工程 · 污染物降解 · 绿色化学
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Journal of Cleaner Production · 2021 · IF 9.297

Use of posnjakite containing sludge as catalyst for decoloring dye via photo-Fenton-like process

Tong Wen,Yunliang Zhao,Xiangke Jiao,Guang Yang,Zixuan Zhang,Wei Wang,Tingting Zhang,Qiwu Zhang,Shaoxian Song

The use of sediment wastes after water treatment , from traditional wastewater management to secondary resource recycling, has attracted increasing attention. In this work, the feasibility, catalytic effect and mechanism of using artificial copper-based precipitation as photo-Fenton-like catalysts were investaged. According to the XRD , SEM-EDS, XPS and various photoelectric characterizations, the copper-based precipitation showed the potential acting as a photo-Fenton-like catalyst due to its abundant copper ions and photoresponse characteristics. The 0.06 g L −1 copper-based precipitation decolors 97% of methylene blue with initial concentration of 20 mg L −1 within 20 min assisted by H 2 O 2 and light, which is superior to the commonly used catalysts in terms of decolorization rate and catalysts dosage. Excellent catalytic performance is by virtue of the enhanced reduction reaction from Cu(II) to Cu(I), resulting in an increasing utilization rate of hydrogen peroxide, and increasing ·OH for decoloration. In addition, the catalyst activity can be replicated in successive experiments without a significant decline, further suggesting the feasibility from wastes to materials. The research progress shows the potential value of secondary resources containing posnjakite based on its unique character.

研究领域: 环境科学 · 材料科学
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WATER SCIENCE AND TECHNOLOGY · 2019 ·Vol. 80 ·期 9 ·1673-1682 · IF 1.624

Photoelectrocatalytic decolorization of methylene blue using reduced graphene oxide modified TiO2 on filter paper

Li Xiaoqiang,Zhang Jialin,Pang Zengyuan,Zhu Yanan,Chen Xin,Sun Qian,Li Yonggui

In this work, titanium dioxide (TiO 2 ) was modified with reduced graphene oxide (rGO), and then coated on filter paper to prepare the rGT/FP photoelectrode for the photoelectrocatalytic (PEC) decolorization of methylene blue (MB). The physicochemical properties of the rGT/FP photoelectrode were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD) analysis and UV-Vis diffuse reflectance spectroscopy (DRS). The decolorization results demonstrated that the photocatalytic (PC) and electrocatalytic (EC) efficiency of the photoelectrode could be significantly improved by the modification of rGO. The improvement of PC and EC efficiency might attribute to the existence of rGO, which could extend the light-harvesting efficiency, promote the photocurrent response value and suppress the charge recombination. Furthermore, the PEC decolorization of MB using the rGT/FP photoelectrode presented higher efficiency than the sum of PC and EC decolorization, indicating the synergistic effect between the photo and electrical energy.

研究领域: 环境化学 · 材料科学 · 催化化学 · 光催化 · 电化学 · 水处理技术
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Materials · 2018 ·Vol. 11 ·期 1 ·86 · IF 2.467

Carbon/Attapulgite Composites as Recycled Palm Oil-Decoloring and Dye Adsorbents

Guangyan Tian,Wenbo Wang,Yongfeng Zhu,Li Zong,Yuru Kang,Aiqin Wang

Activated clay minerals have been widely used in the edible oil refining industry for decolorization of crude oil by adsorption, and so far many methods have been used to improve their decolorization efficiency. Herein, we successfully prepared a series of carbon/attapulgite (C/APT) composite adsorbents by a one-step in-situ carbonization process with natural starch (St) as the carbon source. It has been revealed that the adsorbent had better decolorization efficiency for crude palm oil than acid-activated APT. However, more than a million tons of decolorized waste is produced every year in the oil-refining industry, which was often treated as solid waste and has not yet been reutilized effectively. In order to explore a viable method to recycle and reuse the decolorant, the waste decolorant was further prepared into new C/APT adsorbents for the removal of dyes from wastewater, and then the dyes adsorbed on the adsorbent were used as the carbon sources to produce new C/APT adsorbents by a cyclic carbonization process. The results showed that the adsorbents prepared from the decolorized waste could remove more than 99.5% of the methylene blue (MB), methyl violet (MV), and malachite green (MG) dyes from the simulated wastewater with the dye concentration of 200 mg/L, and the C/APT–Re adsorbent consecutively regenerated five times using the adsorbed dyes as a carbon source still exhibit good adsorption efficiency for dyes. As a whole, this process opens a new avenue to develop efficient decolorants of palm oil and achieves recyclable utilization of decolored waste.

研究领域: 材料科学 · 环境工程 · 化学工程
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RSC Advances · 2022 ·Vol. 12 ·期 5 ·3147-3156 · IF 4.036

An effective and recyclable decolorization method for polysaccharides from Isaria cicadae Miquel by magnetic chitosan microspheres

Bingbing Yu,Yao Chen,Lijun Zhu,Mengmeng Ban,Li Yang,Yeda Zeng,Shijie Li,Chunzhi Tang,Danyan Zhang,Xiaoqing Chen

The purpose of this research was to develop an efficient and non-destructive method for decolorizing of polysaccharides extracted from Isaria cicadae Miquel by magnetic chitosan microspheres (MCM). The optimum decolorization parameters were achieved by response surface methodology as follows: the MCM amount was 8.0%, the adsorption temperature was 48 °C, the adsorption time was 82 min and the pH was 7. Under these optimal conditions, the Dr%, Rr%, and Kc were 90.31 ± 0.12%, 95.40 ± 0.11% and 19.66 ± 0.49, respectively. MCM adsorption of pigment molecules was a spontaneous and endothermic process that could be fitted with the pseudo-second-order equation and the Freundlich equation. Besides, the adsorption mechanism could be controlled by multiple-diffusion steps, including film diffusion and intra-particle diffusion. Furthermore, MCM is a recyclable material. Adsorption with MCM is a promising method to remove pigment molecules of polysaccharide, it may replace the traditional decolorization method.

CAS / MDL: 9012-76-4 1317-61-9
研究领域: 生物化学 · 食品科学 · 环境工程
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ACS Omega · 2018 · IF 0

Decolorization and Mineralization of Rhodamine B in Aqueous Solution with a Triple System of Cerium(IV)/H2O2/Hydroxylamine

Shengli Wang,Yanping Jia,Lianfa Song,Haifeng Zhang

Hydroxylamine (HA) can react with hydrogen peroxide (H2O2) to generate hydroxyl radical (HO•), but the reaction rate between them is very slow (2.2 × 10–4 M–1 s–1). We propose a new system to accelerate the formation of aminoxyl radical (NH2O•) by the addition of cerium [Ce(IV)] to induce the continuous production of HO• through reaction with H2O2. We also investigate the decolorization and mineralization of rhodamine B (RhB) and mechanism in the Ce(IV)/H2O2/HA system. The initial pH plays a significant role in decolorization of RhB. In this work, observation of the rapid decolorization process after 60 min revealed that approximately 80% of RhB was degraded at the initial pH of 4.0. The HO• radicals were considered as the primary reactive oxidant in the system, during its investigation through coumarin capturing, benzoic acid capturing, and radical quenching experiments. The results of the present study suggest that the addition of Ce(IV) can greatly enhance the production of HO•, and the rapid decolorization and mineralization of RhB can occur through the Ce(IV)/H2O2/HA system at acidic pH conditions.

研究领域: 环境化学 · 水处理 · 高级氧化过程
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Journal of Cleaner Production · 2022 · IF 11.072

Probing the performance and mechanisms of Congo red wastewater decolorization with nanoscale zero-valent iron in the continuing flow reactor

Jing Liu,Airong Liu,Ji Li,Shiting Liu,Wei-xian Zhang

Rapid and efficient decolorization is great challenging for wastewater treatment , and nanoscale zero-valent iron (nZVI) was recognized as an environmental-friendly and economical-cost agent for effective decolorization of textile wastewater . Herein, the performance and mechanisms of Congo Red (CR) wastewater treatment with nZVI were probed in a continuous flow nano-iron reactor (NIR), which included the “reaction, separation and reuse” process. CR wastewater (initial concentration up to 500 mg·L −1 ) was successfully decolorized by nZVI in the NIR during the 125 d continuous running period. The color removal efficiency achieved 98.59%, accompanied with a large removal capacity of 6.64 mg-CR/g-nZVI at an average low nZVI dose (0.075 g-nZVI/L-CR). The decolorization mechanism of CR wastewater was ascribed to the chromophore groups (–N=N–) breaking, the final productive products were 4-Amino-1-naphthalene sulfonic acid and 4,4′-diaminodiphenyl, which were proved by liquid chromatography coupled to mass spectrometry, X-ray photoelectron spectroscopy, UV–Vis spectrophotometer, infrared spectroscopy . Decolorization efficiencies were up to 77.82% and 87.95% on average for two actual textile wastewater in the NIR, during the 83.5 h and 445 h continuous running period. This work provides proof that the nZVI technology can offer tremendous potential for the decolorization of recalcitrant organic dye wastewater.

研究领域: 环境科学 · 废水处理技术
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ENVIRONMENTAL MICROBIOLOGY · 2020 ·Vol. 23 ·期 1 ·160-173 · IF 4.933

Links among extracellular enzymes, lignin degradation and cell growth establish the models to identify marine lignin-utilizing bacteria

Xiaopeng Wang,Lu Lin,Jizhong Zhou

Summary A major conundrum in the isolation of prokaryotes from open environments is stochasticity. It is especially difficult to study low abundance groups where very little biological information exists, although single-cell genomics and metagenomics have alleviated some of this bottleneck. Here, we report an approach to capture lignin-utilizing bacteria by linking a physical model to actual organisms. Extracellular enzymes, lignin degradation and cell growth are crucial phenotypes of lignin-utilizing bacteria, but their interrelationships remain poorly understood. In this study, the phenotypes of bacteria isolated from in situ lignocellulose enrichment samples in coastal waters were traced and statistically analysed. It suggested cell growth, dye-decolorizing peroxidase (DyP) and reactive oxygen species (ROS) were significantly correlated with lignin degradation, exhibiting a genus-specific property. The established models enabled us to efficiently capture lignin-utilizing bacteria and rapidly evaluate lignin degradation for Bacillus and Vibrio strains. Through the model, we identified several previously unrecognized marine bacterial lignin degraders. Moreover, it demonstrated that the isolated marine lignin-utilizing bacteria employ a DyP-based system and ROS for lignin depolymerization, providing insights into the mechanism of marine bacterial lignin degradation. Our findings should have implications beyond the capture of lignin-utilizing bacteria, in the isolation of other microorganisms with as-yet-unknown molecular biomarkers.

研究领域: 微生物学 · 环境科学
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