Academic literature on the topic 'Decolorization'

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Journal articles on the topic "Decolorization"

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Kaur, Baljinder, Balvir Kumar, Neena Garg, and Navneet Kaur. "Statistical Optimization of Conditions for Decolorization of Synthetic Dyes byCordyceps militarisMTCC 3936 Using RSM." BioMed Research International 2015 (2015): 1–17. http://dx.doi.org/10.1155/2015/536745.

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In the present study, the biobleaching potential of white rot fungusCordyceps militarisMTCC3936 was investigated. For preliminary screening, decolorization properties ofC. militariswere comparatively studied using whole cells in agar-based and liquid culture systems. Preliminary investigation in liquid culture systems revealed 100% decolorization achieved within 3 days of incubation for reactive yellow 18, 6 days for reactive red 31, 7 days for reactive black 8, and 11 days for reactive green 19 and reactive red 74. RSM was further used to study the effect of three independent variables such as pH, incubation time, and concentration of dye on decolorization properties of cell free supernatant ofC. militaris. RSM based statistical analysis revealed that dye decolorization by cell free supernatants ofC. militarisis more efficient than whole cell based system. The optimized conditions for decolorization of synthetic dyes were identified as dye concentration of 300 ppm, incubation time of 48 h, and optimal pH value as 5.5, except for reactive red 31 (for which the model was nonsignificant). The maximum dye decolorizations achieved under optimized conditions for reactive yellow 18, reactive green 19, reactive red 74, and reactive black 8 were 73.07, 65.36, 55.37, and 68.59%, respectively.
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dos Santos, A. B., J. Traverse, F. J. Cervantes, and J. B. van Lier. "Thermophilic treatment by anaerobic granular sludge as an effective approach to accelerate the electron transfer and improve the reductive decolorization of azo dyes in bioreactors." Water Science and Technology 52, no. 1-2 (July 1, 2005): 363–69. http://dx.doi.org/10.2166/wst.2005.0540.

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The effects of temperature, hydraulic retention time (HRT), and the redox mediator, anthraquinone-2,6-disulfonate (AQDS), on electron transfer and subsequent reductive decolorization of dyes from textile wastewater was assessed in mesophilic and thermophilic anaerobic bioreactors. The results clearly show that compared to mesophilic anaerobic treatment, thermophilic treatment at 55 °C is an effective approach for increasing the electron transfer capacity in bioreactors, and thus improving the decolorization rates. At an HRT of 2.5 h and in the absence of AQDS, the color removal was 5.3-fold higher at 55 °C compared to 30 °C. Furthermore, similar decolorizations were found at 55 °C between the AQDS-free and AQDS-supplemented reactors, whereas a significant difference (up to 3.6-fold) on dye reduction occurred at 30 °C.
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Afiya, Hamisu, Erkurt Emrah Ahmet, and M. Manjur Shah. "Enzymatic Decolorization of Remazol Brilliant Blue Royal (RB 19) textile dye by White Rot Fungi." Journal of Applied and Advanced Research 4, no. 1 (January 27, 2019): 11. http://dx.doi.org/10.21839/jaar.2019.v4i1.260.

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Synthetic dyes are widely used by different industries with over 7 ×105 metric tons produce globally each year. Dyes pose adverse effects including chemical oxygen demand, visual pollution, cytotoxicity, genotoxicity, mutagenicity and carcinogenicity on various types of living organisms. The versatile white rot fungi (basidiomycetes fungi) have developed specialized ligninolytic enzymes for reductive cleavage of dyes and xenobiotics. The present study optimized the decolorization of Remazol brilliant blue royal (RBBR) dye by enzymatic extracts of Coriolus versicolor and Pleurotusostreatus. Experiments were carried out by varying one parameter i.e. pH (2.5-6.5), temperature (30oC-60oC), enzyme activity (3.3U-20U), dye concentration (10mg/L-125mg/L) and time (0-480mins), while others constant to study its effects on decolorization of RBBR. From the results obtained, the optimum conditions for decolorization of RBBR by extracts of C. versicolor and P. ostreatus were pH 4.0, temperature of 300C, enzyme activity 20U, dye concentrations of 100mg/L and 50mg/L for C. versicolor and P. ostreatus respectively at the end of 480 minutes. At the optimized conditions, decolorizations for C. versicolor and P. ostreatus were 80.42% and 70.42% respectively. Highest laccase activity (19.50U) was recorded in C. versicolor compare to P. ostreatus (1.41U).
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Zeng, Jian Zhong, Jun Yue Lin, Song Zhou, Xiu Guang Yi, and Shi Sheng Zeng. "Decolorization Effect of Mycelium Pellet on Saline Azo Dye Wastewater." Applied Mechanics and Materials 130-134 (October 2011): 3784–87. http://dx.doi.org/10.4028/www.scientific.net/amm.130-134.3784.

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A fungus with efficient dye decolorization and that generates a microbial flocculation agent was isolated from a wastewater environment and screened. This bacterial strain imposed a significant decolorization effect on azo dyes. On the basis of morphological and microscopic features, the fungus was identified and named A-6. The results show that the decolorization process of the fungus exhibited two types of actions: adsorption decolorization of mycelium and flocculated decolorization of extracellular products in the dyes. The decolorization ratio reached 99.20%
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Pang, Xiu-Yan. "Decolorization Kinetics and Thermodynamics of Auramine Lake Yellow O on Expanded Graphite Loaded with Titania." E-Journal of Chemistry 8, no. 4 (2011): 1644–53. http://dx.doi.org/10.1155/2011/208909.

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In order to investigate the decolorization characteristics of expanded graphite (EG) loaded with titania for auramine lake yellow O adsorbate, the adsorbent is prepared with 50 mesh natural graphite as raw materials, potassium permanganate as oxidant and vitriol, tetranbutyl titanate as intercalation compound. The expanded volume of EG loaded with titania is 320 mL/g. We detect the equilibration time, influence of ionic strength and initial concentration of the adsorbate on decolorization rate. Based on pseudo first-order and second-order kinetic model, the decolorization model is discussed. Decolorization rate and activation energy were calculated. Studies show that decolorization rate of EG loaded with titania for auramine lake yellow O decrease with the increase of the adsorbate initial concentration and increase with the increase of ionic strength; the decolorization process can be well described by the pseudo second-order kinetic model; decolorization equilibrium time and half decolorization time decrease with the increase of temperature.
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Chmelová, Daniela, and Miroslav Ondrejovič. "Effect Of Metal Ions On Triphenylmethane Dye Decolorization By Laccase From Trametes Versicolor." Nova Biotechnologica et Chimica 14, no. 2 (December 1, 2015): 191–200. http://dx.doi.org/10.1515/nbec-2015-0026.

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Abstract The aim of this study was investigate the influence of different metal ions on laccase activity and triphenylmethane dye decolorization by laccase from white-rot fungus Trametes versicolor. Laccase activity was inhibited by monovalent ions (Li+, Na+, K+ and Ag+) but the presence of divalent ions increased laccase activity at the concentration of 10 mmol/l. The effect of metal ions on decolorization of triphenylmethane dyes with different structures namely Bromochlorophenol Blue, Bromophenol Blue, Bromocresol Blue and Phenol Red was tested. The presence of metal ions (Na+, K+, Mg2+, Ca2+, Ba2+, Mn2+, Zn2+) slightly decreased triphenylmethane dye decolorization by laccase from T. versicolor except Na+ and Mg2+, which caused the increase of decolorization for all tested dyes. Decolorization of selected dyes showed that the presence of low-molecular-weight compounds is necessary for effective decolorization. Hydroxybenzotriazole (HBT) is the most frequently used. Although HBT belongs to most frequently used redox mediator and generally increase decolorization efficiency, so its presence decreased decolorization percentage of Bromophenol Blue and Bromochlorophenol Blue, the influence of metal ions to dye decolorization by laccase has the similar course with or without presence of redox mediator HBT.
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Wang, Jie, and Xueyan Wang. "GPCC catalyzed hydrogen peroxide for decolorization of C.I. Reactive Red 24 from simulated dyeing wastewater." Water Science and Technology 82, no. 11 (October 23, 2020): 2381–88. http://dx.doi.org/10.2166/wst.2020.508.

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Abstract A kind of gelatin protein copper complex (GPCC for short) was synthesized by us. GPCC acting as catalyst was applied to catalyzed hydrogen peroxide for decolorization of C.I. Reactive Red 24 from simulated dyeing wastewater. The influence of catalyzed hydrogen peroxide by GPCC on the decolorization of C.I. Reactive Red 24 from simulated dyeing wastewater was discussed. The optimum decolorization technology condition was optimized. And the effect of salt on decolorization of C.I. Reactive Red 24 in this catalytic system was also investigated. The results showed that hydrogen peroxide can be catalyzed by GPCC. In the catalytic system, the structure of C.I. Reactive Red 24 can be degraded and a high decolorization rate can be obtained in a wide pH range. In addition, the decolorization percentage and decolorization rate will be further improved when salt is present in the catalytic system.
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Liu, Bo, Wan Qian Guo, and Nan Qi Ren. "Decontamination of Wastewaters Containing Synthetic Organic Dyes by Electrochemical Methods: A Review." Advanced Materials Research 788 (September 2013): 405–8. http://dx.doi.org/10.4028/www.scientific.net/amr.788.405.

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Bioelectrochemical systems or electrochemical reduction reactors have great potential for treating wastewater that contains dyes for decolorization. They are reported to enhance decolorization rate and degree with external energy supply and to help microorganisms or noble metal as catalysts. Till now literatures regarding dye decolorization with electron reduction using BESs or electrochemical reactors is deficient. This paper reviews the performance limitations, future prospects, and improvements of the common used dyes decolorization and decolorization with external voltage or current supply in Bioelectrochemical systems.
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Beyhill, M. I., R. D. Matthews, and S. G. Pavlostathis. "Decolorization of a reactive copper-phthalocyanine dye under methanogenic conditions." Water Science and Technology 43, no. 2 (January 1, 2001): 333–40. http://dx.doi.org/10.2166/wst.2001.0108.

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The objective of this research was to assess the biological decolorization of the copper-phthalocyanine dye Reactive Blue 7 (RB7) under methanogenic conditions using a mixed, methanogenic culture in a repetitive dye addition batch assay. The initial rate of decolorization was 13.2 mg/L-d and 5.7 mg/L-d for the first and second dye addition, respectively. For an initial RB7 concentration of ca. 300 mg/L, the extent of decolorization remained constant (about 62%) for each repetitive RB7 addition and resulted in a residual color build up. Declining absorbance ratio values (A664/A620) with increasing incubation time confirmed that the observed color removal was due to transformation as opposed to adsorption on the biomass. Chemical decolorization assays using sodium dithionite as the reducing agent resulted in similar absorbance spectra to that obtained after biological decolorization. In addition, in both the chemical and biological decolorization assays, partial oxidation of the reduced dye solution upon exposure to air resulted in higher residual color, indicating that the reduction and decolorization of RB7 are partially reversible. These results also suggest that RB7 reduction and decolorization both chemically and biologically most likely followed a similar reduction mechanism.
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He, Fang, Aya Obara, Shi Long Wang, and Li Guo Wang. "Degradation Characteristics of a Microbial Consortium on Direct Fast Scarlet 4BS." Advanced Materials Research 518-523 (May 2012): 2464–68. http://dx.doi.org/10.4028/www.scientific.net/amr.518-523.2464.

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High-effective decolorization microbial consortium was isolated and selected by enrichment and optimizing combination decolorization experiments. The optimal microbial consortium consisting of a fungus P6 and a bacterium H5 could use Direct Fast Scarlet 4BS as sole source of carbon and energy. The microbial consortium showed a significant improvement on dye decolorization rate under shaking culture that might be attributed to the synergetic reaction of single strains. This study also examined the kinetics of 4BS decolorization by immobilized microbial consortium. The results demonstrated that the activity of microorganisms inside the immobilized beads can be increased remarkably and the dependence of specific decolorization rate on 4BS concentration could be described as a typical first-order reaction kinetic model. The changes of proliferation and distribution of microbial consortium in gel beads were microscopically observed, which could be used for analysis of decolorization mechanism of 4BS.
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Dissertations / Theses on the topic "Decolorization"

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Kamat, Rohit Babli. "Phytoremediation for dye decolorization." Diss., Kansas State University, 2014. http://hdl.handle.net/2097/17548.

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Doctor of Philosophy
Department of Biochemistry and Molecular Biophysics
Lawrence C. Davis
Synthetic dyes are capable of producing the whole color spectrum on account of their structural diversity but this diversity poses challenges in the degradation of dyeing wastes. Laccases and peroxidases from bacterial or fungal sources and parts of plants in the presence of hydrogen peroxide (H₂O₂) plus a mediator have been exploited in the bioremediation of synthetic dyes. However, intact plants have not found much favor despite their phytoremediation potential. The goal of this research was to further clarify ways by which whole plants bring about decolorization of different types of synthetic dyes. Hydroponically cultivated plants from two dicot families namely Arabidopsis thaliana and sunflowers (Helianthus annuus) were exposed to representative dyes from several classes: monoazo (Methyl Red and Methyl Orange), disazo (Trypan Blue, Evans Blue and Chicago Blue 6B), and arylmethane (Brilliant Blue G, Bromocresol Green, Malachite Green and Phenol Red). Tests were done in presence or absence of externally added H₂O₂, with or without a free radical mediator, 1-hydroxybenzotriazole, using UV-Visible spectrophotometry. The initial rate of decolorization and the overall percentage decolorization was calculated for each dye in the different treatments. Decolorization of the dyes from different classes varied between plant species and depending on the treatment. Except for Methyl Red, all dyes required added H₂O₂ as well as mediator to achieve rapid decolorization. Added H₂O₂ was found to be the limiting factor since it was degraded by plants within a few hours. Both species were able to slowly decolorize dyes upon daily addition of fresh dye even in the absence of added H₂O₂ and mediator, provided that nutrients were supplied to the plants with the dye. A. thaliana was found to be more effective in dye decolorization per gram tissue than sunflower when treated under similar conditions. Analysis of the residual dye solution by ESI/MS did not reveal any potential by-products following the decolorization treatment with plants, suggesting that the plant roots might be trapping the by-products of dye decolorization and preventing their release into the solution. All these findings support the potential application of whole plants for larger scale remediation.
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Matthews, Rosalyn D. "Transformation and decolorization of reactive phthalocyanine." Diss., Available online, Georgia Institute of Technology, 2004:, 2003. http://etd.gatech.edu/theses/available/etd-04062004-164728/unrestricted/matthews%5Frosalyn%5Fd%5F200312%5Fphd.pdf.

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Thesis (Ph. D.)--School of Civil and Environmental Engineering, Georgia Institute of Technology, 2004. Directed by Spyros G. Pavlostathis.
Vita. Includes bibliographical references (leaves 381-393).
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Yang, Hanbae. "Zero-Valent Iron Decolorization of the Anthraquinone Dye Reactive Blue 4 and Biodegradation Assessment of its Decolorization Products." Thesis, Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/6920.

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Anthraquinone dyes constitute the second largest class of textile dyes, and are used extensively in the textile industry. A high fraction of the initial reactive dye mass used in the dyeing process remains in the spent dyebath. Reactive dyes are not readily removed by typical wastewater treatment processes and the high salt concentration typical of reactive dyeing further complicates the management of spent reactive dyebaths. Investigation of the reductive transformation of reactive anthraquinone dyes and their decolorization products has been very limited. Additionally, very limited research has been conducted on the decolorization of spent reactive dyebaths. Research was conducted to investigate the key operational parameters of batch and continuous-flow ZVI decolorization of a reactive anthraquinone dye, Reactive Blue 4 (RB4), under anoxic conditions, as well as the potential for the biodegradation of its decolorization products in a halophilic culture under aerobic conditions. The effect of two operational parameters, such as mixing intensity and initial dye concentration, on the ZVI batch decolorization kinetics indicates that ZVI decolorization of RB4 is a surface-catalyzed, mass transfer-limited process. The high salt and base concentrations enhanced the rate of RB4 decolorization. Based on parameters such as porosity, hydraulic conductivity, pore water velocity, and dispersion coefficient, non-ideal transport characteristics were observed in a continuous-flow ZVI column. The results of a long-term continuous-flow ZVI decolorization kinetics demonstrated that continuous-flow ZVI decolorization is feasible. However, column porosity losses and a shift of reaction kinetics occur in long-term column operation. ZVI decolorization of RB4 was successfully described with a pseudo first-order or a site saturation model. Lastly, the RB4 decolorization products generated by ZVI treatment had no inhibitory effect on the halophilic culture. However, biodegradation and/or mineralization of RB4 decolorization products was not observed after a long-term incubation of the culture. This research demonstrated the feasibility of ZVI decolorization of reactive anthraquinone dyes, which will help in the development of a continuous-flow, dyebath decolorization process and the possible reuse of the renovated dyebath in the dyeing operation. Such a system could lead to substantial reduction of water usage, as well as a decrease of salt and dye discharges.
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Beydilli, Mumtaz Inan. "Reductive biotransformation and decolorization of reactive azo dyes." Diss., Georgia Institute of Technology, 2001. http://hdl.handle.net/1853/21451.

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Lee, Young H. "Reductive biotransformation and decolorization of reactive anthraquinone dyes." Diss., Available online, Georgia Institute of Technology, 2004:, 2003. http://etd.gatech.edu/theses/available/etd-04062004-164708/unrestricted/lee%5Fyoung%5Fh%5F200312%5Fphd.pdf.

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Thesis (Ph. D.)--School of Electrical and Computer Engineering, Georgia Institute of Technology, 2004. Directed by Spyros G. Pavlostathis.
Vita. Includes bibliographical references (leaves 332-345).
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Fontenot, Eric John. "Decolorization of selective reactive blue dyes under methanogenic conditions." Thesis, Georgia Institute of Technology, 1998. http://hdl.handle.net/1853/21697.

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Perng, Yuan-Shing, and Ha-Manh Bui. "Decolorization of reactive dyeing wastewater by Poly Aluminium Chloride." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-176575.

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Color removal of some reactive dyes (Blue 19, Black 5 and Red 195) using a local Poly Aluminium Chloride (PAC) was investigated with Jar-test experiment. The dyes were removed (above 94%) at optimal pH 7 (Red 195) and pH 10 (Blue 19 and Black 5). The PAC dosage of 220 mg/L (Blue 19 and Black 5) and 160 mg/L (Red 195) were found to be best for decreasing dye up to 50 mg/L (Black 5, Red 195) and 100 mg/L (Blue 19). Reaction time and agit ation speed also affected the decolorization process. That result indicates that Vietnamese PAC can be a robust and economical coagulant for discolorization of reactive dyeing process
Chất keo tụ Poly Aluminium Chloride (PAC) sản xuất tại Việt nam được ứng dụng khử màu của một số màu nhuộm hoạt tính phổ biến (Blue 19, Black 5 and Red 195) trên thí nghiệm Jar-test. Kết quả cho thấy màu bị loại gần như hoàn toàn (trên 94 %) tại pH 7 (Red 195) hoặc 10 (Blue 19 và Black 5). Nồng độ PAC đạt hiệu quả tốt nhất tại 220 mg/L (Blue 19 và Black 5) và 160 mg/L (Red 195) ứng với nồng độ màu 50 mg/L (Black 5, Red 195) hay 100 mg/L (Blue 19). Thời gian phản ứng, tốc độ khuấy cũng có tác động đến hiệu suất khử màu. Kết quả nghiên cứu cho thấy PAC sản xuất tại Việt nam không những là một chất keo tụ tốt mà còn rất kinh tế cho việc khử màu hoàn toàn trong nước thải nhuộm hoạt tính
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Perng, Yuan-Shing, and Ha-Manh Bui. "Decolorization of Reactive Red 195 solution by electrocoagulation process." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-176597.

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In this study, the application of bipolar electrocoagulation (EC) with iron electrode has been assessed for color removal of simulated wastewater containing Reactive Red 195. The influence of initial pH, sodium sulfate concentration, initial dye concentration, electrolysis time, and electric current were examined. The optimum operational parameters were found to be pH =11, concentration of dye = 50 mg L-1, sodium sulfate concentration = 1200 mg L-1, electrolysis time = 5 min and electric current = 4 A. In such condition, color removal efficiency achieved over 99%. This result indicates that EC can be used as an efficient and “green” method for color removal from reactive dye solution
Trong nghiên cứu này, quá trình khử màu nhuộm hoạt tính (Reactive Red 195) được khảo sát bằng hệ thống keo tụ điện hóa điện cực kép, với vật liệu sắt. Các yếu tố ảnh hưởng đến quá trình khử màu như pH, nồng độ màu nhuộm, nồng độ muối Na2SO4, thời gian phản ứng và cường độ dòng được lựa chọn nghiên cứu. Kết quả cho thấy hệ thống điện hóa trên loại gần như hoàn toàn màu nhuộm với hiệu suất đạt trên 99 % tại pH 11, nồng độ màu 50 mgL-1 và nống độ muối Na2SO4 1200 mgL-1 trong khoảng thời gian 5phút. Kết quả trên cho thấy keo tụ điện hóa có thể xem là một phương pháp xử lý hiệu quả và “xanh” trong việc loại bỏ hoàn toàn màu từ nước thải nhuộm hoạt tính
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Yoo, Eui Sun. "Biological and chemical mechanisms of reductive decolorization of azo dyes." [S.l.] : [s.n.], 2000. http://edocs.tu-berlin.de/diss/2000/yoo_eui.pdf.

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Perng, Yuan-Shing, and Ha-Manh Bui. "Decolorization of reactive dyeing wastewater by ferrous ammonium sulfate hexahydrate." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-176606.

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This paper presents the result of dyeing solution coagulation with the use of ferrous ammonium sulfate hexah ydrate (FAS). The examined solution contains two reactive dyes: Black 5 and Blue 19. It has been shown that the efficiency of the dye removal depends on the type of dye, coagulation dosage and the initial pH. Our result showed that the increase of initial pH up to 12 enhanced the color removal efficiency; the FAS dose was 280 ml (Black 5) and 180 mg/l (Blue 19) at slow mixing time (15 min), agitation speed 60 rpm, and the initial dye concentration should be 50 and 100 mg/L for Black 5 and Blue 19, respectively
Chất keo tụ sắt (II) amoni sulfate (FAS) được sử dụng khử màu của hai màu nhuộm hoạt tính phổbiến (Blue 19 và Black 5). Kết quả cho thấy, quá trình keo tụ bịảnh hưởng nhiều bởi loại màu nhuộm, nồng độ chất keo tụ và pH của dung dịch đầu vào. Với nồng độ FAS 280 mg/l (Black 5) và 180 mg/l (Blue 19), pH đầu vào dung dịch khoảng 12, thời gian phản ứng 15 phút, tốc độ khuấy 60 vòng/phút ứng với nồng độ màu Black 50 mg/L và blue 100 mg/L dung dịch gần như mất màu hoàn toàn
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Books on the topic "Decolorization"

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Jarvis, Timothy Stephen. Electrochemical decolorization of bleached kraft effluents. 1993.

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Singh, Ram Lakhan, Rajat Pratap Singh, and Pradeep Kumar Singh. Recent Advances in Decolorization and Degradation of Dyes in Textile Effluent by Biological Approaches. Taylor & Francis Group, 2019.

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Singh, Ram Lakhan, Pradeep Kumar Singh, and Rajat Pratap Singh. Recent Advances in Decolorization and Degradation of Dyes in Textile Effluent by Biological Approaches. CRC Press, 2019. http://dx.doi.org/10.1201/9780429244322.

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Singh, Ram Lakhan, Rajat Pratap Singh, and Pradeep Kumar Singh. Recent Advances in Decolorization and Degradation of Dyes in Textile Effluent by Biological Approaches. Taylor & Francis Group, 2019.

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Singh, Ram Lakhan, Rajat Pratap Singh, and Pradeep Kumar Singh. Recent Advances in Decolorization and Degradation of Dyes in Textile Effluent by Biological Approaches. Taylor & Francis Group, 2019.

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Recent Advances in Decolorization and Degradation of Dyes in Textile Effluent by Biological Approaches. Taylor & Francis Group, 2019.

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Singh, Ram Lakhan, Rajat Pratap Singh, and Pradeep Kumar Singh. Recent Advances in Decolorization and Degradation of Dyes in Textile Effluent by Biological Approaches. Taylor & Francis Group, 2019.

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Jamal, Farrukh. Functional Suitability of Soluble Peroxidases from Easily Available Plant Sources in Decolorization of Synthetic Dyes. INTECH Open Access Publisher, 2011.

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Book chapters on the topic "Decolorization"

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Zhao, Ye, and Zakiya Tamimi. "Spectral Image Decolorization." In Advances in Visual Computing, 747–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-17274-8_73.

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Zemko, Michal, and Elena Sikudova. "Saliency Enhanced Decolorization." In Computer Vision and Graphics, 184–93. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-46418-3_17.

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Rapp, Douglas B., Melissa A. Dorsey, Melissann M. Ashton-Patton, and James E. Shelby. "Decolorization of Amber Glass." In Ceramic Transactions Series, 323–30. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118405949.ch31.

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Jasińska, Anna, Katarzyna Paraszkiewicz, Mirosława Słaba, and Jerzy Długoński. "Microbial Decolorization of Triphenylmethane Dyes." In Microbial Degradation of Synthetic Dyes in Wastewaters, 169–86. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-10942-8_8.

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Kuhad, Ramesh Chander, Rishi Gupta, and Yogender Pal Khasa. "Microbial Decolorization of Colored Industrial Effluents." In Microorganisms in Environmental Management, 787–813. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-2229-3_35.

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Tochhawng, Lalrokimi, Vineet Kumar Mishra, Ajit Kumar Passari, and Bhim Pratap Singh. "Endophytic Fungi: Role in Dye Decolorization." In Advances in Endophytic Fungal Research, 1–15. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-03589-1_1.

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Dias, Albino A., Marco S. Lucas, Ana Sampaio, José A. Peres, and Rui M. F. Bezerra. "Decolorization of Azo Dyes by Yeasts." In The Handbook of Environmental Chemistry, 183–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/698_2009_49.

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Pokharia, Anamika, and Sarabjeet Singh Ahluwalia. "Bioremediation Technologies for Decolorization of Effluent." In Advances in Environmental Biotechnology, 93–123. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-4041-2_6.

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Sasidharan Pillai, Indu M., and K. L. Priya. "TiO2-Based Composites for Water Decolorization." In Sustainable Textiles: Production, Processing, Manufacturing & Chemistry, 103–42. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-2892-4_5.

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Ancuti, Codruta O., Cosmin Ancuti, Chris Hermans, and Philippe Bekaert. "Image and Video Decolorization by Fusion." In Computer Vision – ACCV 2010, 79–92. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-19315-6_7.

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Conference papers on the topic "Decolorization"

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Song, Yibing, Linchao Bao, Xiaobin Xu, and Qingxiong Yang. "Decolorization." In SIGGRAPH Asia 2013 Technical Briefs. New York, New York, USA: ACM Press, 2013. http://dx.doi.org/10.1145/2542355.2542374.

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Zhou, Mingqi, Bing Sheng, and Lizhuang Ma. "Saliency preserving decolorization." In 2014 IEEE International Conference on Multimedia and Expo (ICME). IEEE, 2014. http://dx.doi.org/10.1109/icme.2014.6890153.

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Cewu Lu, Li Xu, and Jiaya Jia. "Contrast preserving decolorization." In 2012 IEEE International Conference on Computational Photography (ICCP). IEEE, 2012. http://dx.doi.org/10.1109/iccphot.2012.6215215.

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Cai, Bolun, Xiangmin Xu, and Xiaofen Xing. "Perception Preserving Decolorization." In 2018 25th IEEE International Conference on Image Processing (ICIP). IEEE, 2018. http://dx.doi.org/10.1109/icip.2018.8451303.

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Ancuti, Cosmin, and Codruta O. Ancuti. "Laplacian-guided image decolorization." In 2016 IEEE International Conference on Image Processing (ICIP). IEEE, 2016. http://dx.doi.org/10.1109/icip.2016.7533132.

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Lu, Cewu, Li Xu, and Jiaya Jia. "Real-time contrast preserving decolorization." In SIGGRAPH Asia 2012 Posters. New York, New York, USA: ACM Press, 2012. http://dx.doi.org/10.1145/2407156.2407174.

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Lu, Cewu, Li Xu, and Jiaya Jia. "Real-time contrast preserving decolorization." In SIGGRAPH Asia 2012 Technical Briefs. New York, New York, USA: ACM Press, 2012. http://dx.doi.org/10.1145/2407746.2407780.

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Ancuti, Codruta Orniana, Cosmin Ancuti, and Phillipe Bekaert. "Enhancing by saliency-guided decolorization." In 2011 IEEE Conference on Computer Vision and Pattern Recognition (CVPR). IEEE, 2011. http://dx.doi.org/10.1109/cvpr.2011.5995414.

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Chen, Jie, Xin Li, Xiuchang Zhu, and Jin Wang. "Global Color Saliency Preserving Decolorization." In Computer, Information and Application 2016. Science & Engineering Research Support soCiety, 2016. http://dx.doi.org/10.14257/astl.2016.134.23.

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Liang, Huixing, Aihui Chen, Xin Chen, Zhaoxia Li, and Cheng Ding. "Isolation of Dye Decolorization Bacteria and the Study on the Conditions of Dyes Decolorization." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5518259.

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