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Master's Dissertation
DOI
https://doi.org/10.11606/D.85.2010.tde-29082011-102142
Document
Author
Full name
Terezinha Elizabeth Mendes de Carvalho
E-mail
Institute/School/College
Knowledge Area
Date of Defense
Published
São Paulo, 2010
Supervisor
Committee
Fungaro, Denise Alves (President)
Mierzwa, José Carlos
Yamaura, Mitiko
Title in Portuguese
Adsorção de corantes aniônicos de solução aquosa em cinza leve de carvão e zeólita de cinza leve de carvão
Keywords in Portuguese
adsorção
cinza leve de carvão
corante índigo carmina
corante reativo laranja 16
zeólita sintética
Abstract in Portuguese
Cinza leve de carvão, resíduo gerado em usina termelétrica, foi usada para sintetizar zeólita por meio de tratamento hidrotérmico com solução de NaOH. A cinza leve (CL-2) e a zeólita sintética (ZM-2) que foi predominantemente identificada como hidroxi-sodalita foram utilizadas como adsorventes dos corantes aniônicos índigo carmina (IC) e reativo laranja 16 (RL16) de soluções aquosas. Nos processos de adsorção, os efeitos de tempo de contato, concentração inicial de corantes, pH, massa de adsorventes e temperatura foram avaliados. O estudo cinético de adsorção demonstrou que os resultados apresentaram melhor ajuste ao modelo de pseudo-segunda ordem e que adsorção de superfície e difusão intrapartícula participaram no mecanismo de adsorção. Os parâmetros termodinâmicos demonstraram que a adsorção foi espontânea em todos os processos de adsorção. Os processos de adsorção foram de natureza endotérmica para todos os sistemas, com exceção do sistema IC/ZM-2, em que foi exotérmico. Os dados de entropia mostraram a ocorrência do aumento da desordem na interface sólido/solução durante a adsorção em todos os sistemas, exceto novamente no IC/ZM-2, no qual se verificou a diminuição da desordem na interface. As isotermas de adsorção ajustaram-se à equação linear de Langmuir. As capacidades máximas de adsorção foram 1,48 mg/g para o sistema IC/CL-2; 1,13 mg/g para IC/ZM-2; 0,96 mg/g para RL16/CL-2 e 1,14 mg/g para RL16/ZM-2 à temperatura ambiente. O estudo de dessorção realizado com água, com soluções aquosas ácidas e com solução aquosa básica demonstrou ser ineficiente tanto para a recuperação dos corantes quanto para a regeneração dos adsorventes.
Title in English
Adsorption of anionic dyes from aqueous solutions onto coal fly ash and zeolite synthesized from coal fly ash
Keywords in English
adsorption
coal fly ash
dye indigo carmine
dye reactive orange 16
zeolite synthesized
Abstract in English
Coal fly ash, a waste generated in coal-fired electric power plant, was used to synthesize zeolite by hydrothermal treatment with NaOH solution. The fly ash (CL-2) and this synthesized zeolite (ZM-2) that was characterized as hydroxy-sodalite were used as adsorbents for anionic dyes indigo carmine (IC), and reactive orange 16 (RO16) from aqueous solutions. Effects of contact time, initial dye concentration, pH, adsorbent mass, and temperature were evaluated in the adsorption processes. The kinetics studies indicated that the adsorption followed the pseudo-second order kinetics and that surface adsorption and intraparticle diffusion were involved in the adsorption mechanism. The thermodynamics parameters demonstrated that the adsorption was spontaneous for all adsorption processes. The enthalpy data confirmed the endothermic nature for all adsorption processes except for IC/ZM-2 system which was exothermic. The entropy data showed an increased disorder at the solid/solution interface during the adsorption for all systems except for IC/ZM-2 whose negative entropy value indicated a decreased disorder at the interface. The adsorption isotherms were closely fitted to the Langmuir linear equation. The maximum adsorption capacities were 1.48 mg/g for the IC/CL-2 system; 1.13 mg/g for IC/ZM-2; 0.96 mg/g for RO16/CL-2, and 1.14 mg/g for RO16/ZM-2 at room temperature. The desorption study carried out with water, with acid aqueous solutions, and with an alkali aqueous solution showed to be inefficient both for recovering the dyes and regenerating the adsorbents.
 
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Publishing Date
2011-08-31
 
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