نمایش مختصر رکورد

dc.contributor.authorLoulidi, Ilyasseen_US
dc.contributor.authorBoukhlifi, Fatimaen_US
dc.contributor.authorOuchabi, Mbarkaen_US
dc.contributor.authorAmar, Abdelouaheden_US
dc.contributor.authorJabri, Mariaen_US
dc.contributor.authorKali, Abderahimen_US
dc.contributor.authorAziz, Faissalen_US
dc.date.accessioned1399-07-08T19:04:24Zfa_IR
dc.date.accessioned2020-09-29T19:04:24Z
dc.date.available1399-07-08T19:04:24Zfa_IR
dc.date.available2020-09-29T19:04:24Z
dc.date.issued2020-09-01en_US
dc.date.issued1399-06-11fa_IR
dc.date.submitted2020-04-01en_US
dc.date.submitted1399-01-13fa_IR
dc.identifier.citationLoulidi, Ilyasse, Boukhlifi, Fatima, Ouchabi, Mbarka, Amar, Abdelouahed, Jabri, Maria, Kali, Abderahim, Aziz, Faissal. (2020). Kinetic, Isotherm and Mechanism Investigations of the Removal of Basic Violet 3 from Water by Raw Spent Coffee Grounds. Physical Chemistry Research, 8(3), 569-584. doi: 10.22036/pcr.2020.225170.1751en_US
dc.identifier.issn2322-5521
dc.identifier.issn2345-2625
dc.identifier.urihttps://dx.doi.org/10.22036/pcr.2020.225170.1751
dc.identifier.urihttp://www.physchemres.org/article_108343.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/58461
dc.description.abstractThis work examines the possibility of removing the crystal violet (a cationic dye), used in the dyeing of cotton, wood, and silk, onto untreated coffee waste. The influence of various experimental parameters on the adsorption of crystal violet has been analysed: pH, adsorbent dose and initial dye concentration. Optimum adsorption of crystal violet took place at pH 6 and at lower temperatures. Further, the adsorbent was characterised by Fourier Transform Infrared Spectroscopy (FTIR). FTIR analysis revealed the presence of several functional groups that are responsible for the adsorption process. Adsorption equilibrium follows Langmuir's model with maximum retention of 63.3 mg/g. The kinetics of the crystal violet adsorption were studied using the pseudo-first order and pseudo-second order equations. Adsorption of the dye can be described by pseudo-second order kinetics, reaching the equilibrium at 40 min. The value of the activation energy shows that adsorption is physisorption. Weber-Morris model indicates that this adsorption occurs in two steps. Thermodynamic parameters suggest that the adsorption is spontaneous and exothermic.en_US
dc.format.extent3442
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherIranian Chemical Societyen_US
dc.relation.ispartofPhysical Chemistry Researchen_US
dc.relation.isversionofhttps://dx.doi.org/10.22036/pcr.2020.225170.1751
dc.subjectAdsorptionen_US
dc.subjectCationic dyeen_US
dc.subjectSpent coffee groundsen_US
dc.titleKinetic, Isotherm and Mechanism Investigations of the Removal of Basic Violet 3 from Water by Raw Spent Coffee Groundsen_US
dc.typeTexten_US
dc.typeRegular Articleen_US
dc.contributor.departmentLaboratory of Chemistry and Biology Applied to the Environment, Faculty of Sciences, Moulay Ismail University, BP 11201-Zitoune, Meknes, Moroccoen_US
dc.contributor.departmentLaboratory of Chemistry and Biology Applied to the Environment, Faculty of Sciences, Moulay Ismail University, BP 11201-Zitoune, Meknes, Moroccoen_US
dc.contributor.departmentLaboratory of Catalysis and Corrosion of Materials, Chouaïb Doukkali University, Faculty of Sciences El Jadida, BP. 20, El Jadida, Moroccoen_US
dc.contributor.departmentLaboratory of Chemistry and Biology Applied to the Environment, Faculty of Sciences, Moulay Ismail University, BP 11201-Zitoune, Meknes, Moroccoen_US
dc.contributor.departmentLaboratory of Chemistry and Biology Applied to the Environment, Faculty of Sciences, Moulay Ismail University, BP 11201-Zitoune, Meknes, Moroccoen_US
dc.contributor.departmentLaboratory of Chemistry and Biology Applied to the Environment, Faculty of Sciences, Moulay Ismail University, BP 11201-Zitoune, Meknes, Moroccoen_US
dc.contributor.departmentLaboratory of Water,Biodiversity & Climate Changes, Semlalia, Faculty of Sciences, Cadi Ayyad University, Marrakech, Moroccoen_US
dc.citation.volume8
dc.citation.issue3
dc.citation.spage569
dc.citation.epage584


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