Academic literature on the topic 'Acid blue 113'

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Journal articles on the topic "Acid blue 113"

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Priya, V., S. K. Krishna, V. Sivakumar, and P. Sivakumar. "Adsorption of Acid Blue 113 using Nanocarbon Spheres and its Kinetic and Isotherm Studies." Asian Journal of Chemistry 31, no. 8 (2019): 1653–60. http://dx.doi.org/10.14233/ajchem.2019.21944.

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Nanocarbon spheres were prepared from the stems of Alternanthera sessilis. Their characterization studies were performed and the application of nanocarbon spheres for the adsorption of acid blue 113 from the aqueous solution was studied. Effect of pH of effluent, effect of initial acid blue 113 concentration and the effect of solution temperature were analyzed. Pseudo-first order model, pseudo-second order model, Elovich model, Intra-particle diffusion model, Langmuir model, Freundlich model and thermodynamic parameters were used to evaluate the percentage and the amount of acid blue 113 dye r
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Marin, Nicoleta Mirela. "Natural and Synthetic Polymers Modified with Acid Blue 113 for Removal of Cr3+, Zn2+ and Mn2+." Polymers 14, no. 11 (2022): 2139. http://dx.doi.org/10.3390/polym14112139.

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This research had two stages of development: during the first stage, the purpose of the research was to evaluate the adsorption properties of the natural polymer represented by shredded maize stalk (MS) and by Amberlite XAD7HP (XAD7HP) acrylic resin for removal of toxic diazo Acid Blue 113 (AB 113) dye from aqueous solutions. The AB 113 concentration was evaluated spectrometrically at 565 nm. In the second stage, the stability of MS loaded with AB 113 (MS-AB 113) and of XAD7HP loaded with AB 113 (XAD7HP-AB 113) in acidic medium suggests that impregnated materials can be used for selective remo
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Sugha, Aditi, and Manpreet Singh Bhatti. "Optimization of electrocoagulation removal of a mixture of three azo dyes: spectrophotometric colour characteristics for best operating conditions." RSC Advances 15, no. 9 (2025): 6492–505. https://doi.org/10.1039/d4ra08485c.

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Singh, Pradeep Kumar, Pankaj Singh, Rajat Pratap Singh, and Ram Lakhan Singh. "Biodecolorization of Azo Dye Acid Blue 113 by Soil Bacterium Klebsiella variicola RMLP1." Journal of Ecophysiology and Occupational Health 21, no. 2 (2021): 64. http://dx.doi.org/10.18311/jeoh/0/27108.

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The present study was aimed to isolate a new bacterial strain for the degradation/decolorization of azo dye Acid Blue 113 (AB 113). The physico-chemical method is inadequate for degradation of azo dyes; therefore, an environmental friendly and competent method such as use of the biological organism was studied for decolorization of AB 113. Bushnell and Hass (BHM) medium containing AB 113 dye were used to perform the decolorization study. 16S rRNA gene sequencing approach was used for identification of bacterial isolate as a <em>Klebsiella variicola</em>. The optimum process paramet
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Karimi, Afzal, Fatemeh Mahdizadeh, and Mohammadreza Eskandarian. "Enzymatic in-situ generation of H2O2 for decolorization of Acid Blue 113 by fenton process." Chemical Industry and Chemical Engineering Quarterly 18, no. 1 (2012): 89–94. http://dx.doi.org/10.2298/ciceq110722050k.

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Decolorization of Acid Blue 113 in an aqueous medium by bio-Fenton process has been investigated in this research. Enzymatic oxidation of glucose was performed to in-situ generation of H2O2 which was employed to react with Fe2+ for producing hydroxyl radicals. The effect of various parameters include concentrations of 113, glucose, and FeSO4, activity of glucose oxidase (GOx) and the effect of pH were assessed. The highest decolorization of AB 113 were achieved at Fe2+ concentration of 0.2 mmol/L, pH =4.0, glucose concentration of 0.018 mol/L, and glucose oxidase activity of 2500 U/L in the co
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Kazikundi Kingudi, Grace, and Şifa Doğan. "Acid Blue 113 Degradation and Mineralization by UV/Persulfate Process." Afyon Kocatepe Üniversitesi Uluslararası Mühendislik Teknolojileri ve Uygulamalı Bilimler Dergisi 7, no. 2 (2024): 78–82. https://doi.org/10.53448/akuumubd.1509834.

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In this work, decolorization of reactive Alcain Blue 8GX dye solution were investigated by persulfate oxidation activated by ferrous ion and heat. Three different temperature (40 °C, 60 °C and 80 °C) were tested during heat activated persulfate and ferrous ion activated persulfate were tested under various molar ratios of dye:Fe2+:persulfate ratio (1:1:1, 1:2:1, 1:1:0.5, 1:4:1). In addition, pH effect has been tested at ambient conditions (5.23) and pH of 3. The results showed that increasing the temperature and persulfate concentration was favorable to the degradation of the dye with decolori
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Sekar, Sudharshan, Surianarayanan Mahadevan, Bhuvanesh Kumar Shanmugam, and Asit Baran Mandal. "Bioenergetics and pathway of acid blue 113 degradation byStaphylococcus lentus." Biotechnology Progress 28, no. 6 (2012): 1400–1408. http://dx.doi.org/10.1002/btpr.1626.

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Saravanan, Mohan, Nurani Pabmanavhan Sambhamurthy, and Meenatchisundaram Sivarajan. "Treatment of Acid Blue 113 Dye Solution Using Iron Electrocoagulation." CLEAN - Soil, Air, Water 38, no. 5-6 (2010): 565–71. http://dx.doi.org/10.1002/clen.200900278.

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Biala, Sunil, Priyanka Chauhan, Bhupinder Singh Chadha, Bikram Singh, and Harvinder Singh Saini. "Biotransformation of CI Acid Blue 113 and other dyes byShewanellasp. P6." Coloration Technology 129, no. 5 (2013): 330–37. http://dx.doi.org/10.1111/cote.12045.

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Mahadevan, D. S., S. Sekar, and S. S. Dhilipkumar. "Biocalorimetric investigation of degradation of Acid Blue 113 by halotolerant strains." New Biotechnology 25 (September 2009): S49. http://dx.doi.org/10.1016/j.nbt.2009.06.257.

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Dissertations / Theses on the topic "Acid blue 113"

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TSENG, CHANG-HSUAN, and 曾昶瑄. "Study on the Degradation of Dye Acid Blue 113 by Diamond-Like Carbon Film Electrode." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/84170010896723009818.

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碩士<br>逢甲大學<br>環境工程與科學學系<br>104<br>In this study, an arc ion plating (AIP) technique was used to deposit diamond-like carbon (DLC) film on a Nomex substrate (Poly(m-phenyleneisophthalamide)), which develop a high specific surface area of the anode electrode film and test the feasibility of dye wastewater treatment. Two differences of carbon sources film electrode are prepared by using the C2H2 flow rate 150 and 250 sccm respectively. By scanning electron microscopy (SEM), four-point probe and laser Raman microscope (UniRAM-Raman) analysis, the electrochemical characteristics of the film electro
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Huang, Shi-Wei, and 黃士瑋. "Treatment of Acid Blue 113 azodye in wastewater by UV photocatalytic oxidation process using persulfate oxidants." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/9w267t.

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碩士<br>弘光科技大學<br>環境工程研究所<br>103<br>Abstact Wastewater from textile dyeing industry contents various chemicals such as dyestuffs and dyeing add agent which is hard to be proper treated and sometime toxic or carcinogenic. The target pollutant in this work is Acid Blue 113 (AB113) azodye. In this study, two different oxidants, i.e. sodium persulfate and Oxone, were used under UV irradiation to produce sulfate radicals to decolorize and mineralize AB113 dye wastewater. In control experiments, Oxone itself with 6.3mM concentration can decolorize AB113 effectively. Integrating persulfate or Oxone wit
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張吉辰. "The study of decoloration of azo dye Acid Blue 113 wastewater using nanoscale zero-valent iron and Fe/Ni and Fe/Zn." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/85602084392761210663.

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碩士<br>弘光科技大學<br>環境工程研究所<br>97<br>In general, effluents discharged from dye manufacturing and industries with strong color and high level of chemical oxygen demand (COD) which can not meet the stricter Taiwan’s Nation Effluent Standard by convention wasterwater treatment system. Thus, it demands urgently to develop an economic and effective technique for increase of color removal of wastewater treatment efficiency and time-saving operation. This study proposed decoloration of azo dye Acid Blue 113 wastewater using nanoscale zero-valent iron (NZVI) and bimetal Fe/Ni, Fe/Zn by considering the ope
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Book chapters on the topic "Acid blue 113"

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"gluten quality involves the addition of low levels of gluten, ied typically are compared to results obtained by some about 2%, to a standard test flour, which often is of a type of baking test. McDermott [85] compared baking "weak" type, and observing the effects on bread quality. (Chorleywood bake test) and other properties of 30 com-Water absorption is adjusted as appropriate for the gluten mercial glutens, mostly of European origin (Table 8), and levels added [23]. A stressed gluten-enriched baking test found that under his test conditions six samples were of was identified [31], which assumes that gluten is added to relatively poor quality; correlation between baking perfor-enable production of specialty breads using substantial mance and other measured properties was not high. levels of non-gluten-containing ingredients such as rye Weegels and Hamer [130] studied a group of 32 European flour, dietary fiber, bran and germ, or raisins [49]. Czucha-commercial glutens. These workers devised a test involv-j owska and Pomeranz [31] described a simple, repro-ing protein content, denaturation index (based on a series ducible method for baking undiluted gluten, highly corre-of sodium dodecyl sulfate sedimentation measurements), lated with the gluten-enrichment baking test. and extensigraph resistance; a model utilizing these tests A prime reason for performing end-use tests of func-was able to predict 59% of the baking quality variation of tionality, of course, is to monitor variations in the quality the glutens. Bushuk and Wadhawan [20] examined 27 of commercial wheat glutens that can occur. Differences commercial gluten samples, although only 8 were subject-among commercial gluten are usually attributable to varia-ed to extensive end-use testing; the highest correlation co-tions in the starting material, wheat or flour, and/or efficients were between loaf volume and acetic acid-solu-changes caused by production processing conditions. Dur-ble protein (r = 0.88) and between loaf volume and ing processing, the drying of gluten is critical, as noted fluorescence of acetic acid extract (r = 0.98). above, and investigators have shown that less than opti-mum heat treatment can lower the baking quality of gluten (b) Nonbaking Tests. Considerable efforts have been [14,49,98,111,130]. However, McDermott [85] reported expended in developing nonbaking tests to evaluate the no definite relationship between manufacturing variables quality or vitality of wheat gluten for baking purposes. The and gluten quality in a group of 30 commercial glutens. baking test is often cited as being labor intensive, relative-Dreese et al. [38] studied commercial and hand-washed ly expensive, requiring skilled workers, and not effectively lyophilized gluten and found that differences were more differentiating gluten quality [86]. The farinograph has attributable to washing procedures than to drying proce-been used to evaluate gluten for many years. The usual ap-dures. proach has been to test the gluten as a gluten-flour mixture Results obtained by other methods that have been stud-(e.g., Refs. 5, 18, 36, and 49), while an alternative method TABLE 8 Properties of 30 Commercial Glutens Baking performance Property Average Range Poor Average Good Increase in loaf volume, %a 10 7.7-12.2 8.3 10.2 11.8 Protein, %b 77.4 66.4-84.3 76.2 77.4 81.1 Moisture, % 7.55.3-10.2 8.877.7 Particle size, % <160 p.m 88.8 55.8-98 80.5 91 90.3 Color 68.3 56.5-75 65.2 68.9 69.5 Lipid, % 5.84.2-7.65.86.15.1 Ash, % 0.69 0.44-0.94 0.71 0.74 0.6 Chloride, %` 0.08 0.01-0.28 0.10.08 0.08 Water absorption, mug protein 2.37 1.84-2.93 2.26 2.45 2.29 SDS sedimentation volume, ml/g protein 99 55-159 70 107 127 Lactic acid sedimentation, % reduction in turbidity 18 2-68 49 11 7 Hydration time, min 0.90.2-10 2.72.40.6 Extensibility, units/min 3.80.7-9.33.23.93.9 Viscosity, cP 117 73-222 159 109 101 '2% gluten protein. Dry matter basis. `As NaCl. Source: Ref. 85." In Handbook of Cereal Science and Technology, Revised and Expanded. CRC Press, 2000. http://dx.doi.org/10.1201/9781420027228-83.

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Conference papers on the topic "Acid blue 113"

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Salla, Sunitha, and A. Nageswara Rao. "Visible light assisted photocatalytic degradation of acid blue 113 using nano ZnO particles." In 2013 International Conference on Advanced Nanomaterials and Emerging Engineering Technologies (ICANMEET). IEEE, 2013. http://dx.doi.org/10.1109/icanmeet.2013.6609254.

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Sunitha, S., A. Nageswara Rao, J. Karthikeyan, and T. Krithiga. "ZnO/carbon nano composite: Effective catalyst for the photo degradation of Acid Blue 113." In CARBON MATERIALS 2012 (CCM12): Carbon Materials for Energy Harvesting, Environment, Nanoscience and Technology. AIP, 2013. http://dx.doi.org/10.1063/1.4810047.

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Caebron, J. Y., M. Joseph, H. Vorng, J. Pincemail, M. Lagaede, and A. Capron. "OXYGEN FREE RADICAL-DEPENDENT STEP IN THE CYTOTOXICITY OF DEC-TREATED PLATELETS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642819.

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Over the past 35 years, diethylcarbamazine (DEC) has been the most widely used agent for the treatment of filarial diseases. However, in spite of millions of individuals treated, the mode of action of this drug remained unexplained until recently when we reported that the microfilaricidal activity of DEC was mediated by blood platelets with the additional triggering of a filarial excretory antigen (FEA) (Nature, 1987).To set up the mechanism of the larvicidal action of platelets activatedby both DEC and FEA, various inhibitors of the arachidonic acid metabolism were added in the cytotoxic assa
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Reports on the topic "Acid blue 113"

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Christopher, David A., and Avihai Danon. Plant Adaptation to Light Stress: Genetic Regulatory Mechanisms. United States Department of Agriculture, 2004. http://dx.doi.org/10.32747/2004.7586534.bard.

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Original Objectives: 1. Purify and biochemically characterize RB60 orthologs in higher plant chloroplasts; 2. Clone the gene(s) encoding plant RB60 orthologs and determine their structure and expression; 3. Manipulate the expression of RB60; 4. Assay the effects of altered RB60 expression on thylakoid biogenesis and photosynthetic function in plants exposed to different light conditions. In addition, we also examined the gene structure and expression of RB60 orthologs in the non-vascular plant, Physcomitrella patens and cloned the poly(A)-binding protein orthologue (43 kDa RB47-like protein).
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