Lima Rose Miranda
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Lima Rose Miranda has a total of 66 co-authors. Here are the top co-authors by number of shared publications:
M. Helen Kalavathy
7 shared publicationsM. Velan
4 shared publications- Iyyaswami Regupathi
Department of Chemical Engineering, National Institute of Technology Karnataka, Surathkal, Mangalore, India
3 shared publications N. Premalatha
Department of Chemical Engineering, A. C. College of Technology, Anna University, Chennai, India
3 shared publicationsB.G. Prakash Kumar
2 shared publicationsE. Padmini
2 shared publications
Latest Publications
- 31 January 2022
- Published by Springer Nature in Reaction Kinetics, Mechanisms and Catalysis
- Vol. 135 (2) , 1031-1046
Photocatalytic degradation of Rhodamine B over TiO2/g-C3N4 and immobilized TiO2/g-C3N4 on stainless steel wire gauze under UV and visible light: A detailed kinetic analysis and mechanism of degradation
- 31 January 2022
- Published by Springer Nature in Reaction Kinetics, Mechanisms and Catalysis
- Vol. 135 (2) , 1031-1046
Photocatalytic degradation of Rhodamine B over TiO2/g-C3N4 and immobilized TiO2/g-C3N4 on stainless steel wire gauze under UV and visible light: A detailed kinetic analysis and mechanism of degradation
- Open Access
- 1 January 2022
- Published by SAGE Publications in Adsorption Science & Technology
- Vol. 2022
Surface-Modified Adsorbent from Artocarpus heterophyllus Lam Biomass to Confine Reactive Red 194 in Real and Synthetic Effluents: Kinetics and Equilibrium Study
Chemical activation of Artocarpus heterophyllus Lam (jackfruit peel) via phosphoric acid was focused on this study for the preparation of activated carbon. Carbonization was done at a temperature of 400°C based on the nature of biomass after the impregnation ratio of 1 : 1 (weight of phosphoric acid/weight of raw material). Titanium dioxide was doped on the prepared activated carbon through the sol-gel method. Titanium dioxide doped activated carbon was synthesized to perceive the nature of adsorbents under ambient conditions. Both JPAC and JPAC/TiO2 adsorbents were characterized by the point of zero charges, Fourier transform of infrared spectroscopy, X-ray diffraction spectroscopy, Brunauer-Emmett-Teller analysis, and scanning electron microscopy with energy-dispersive X-ray analysis. The adsorption capacity of Reactive Red 194 (Red 2BN) dye on jackfruit peel activated carbon (JPAC) is 32.271 mg/g, and JPAC/TiO2 is 34.900 mg/g was observed under optimum conditions. Desorption efficiency of JPAC/TiO2 (≥93.4%) is slightly higher compared to JPAC (≥89.2%). Tannery effluents of various parameters were analyzed, and their chemical oxygen demand (COD) values trim down within the permissible limits of JPAC (97%) and JPAC/TiO2 (98%). Experimental data were studied using both two-parameter and three-parameter models of adsorption isotherm, namely, the Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, Redlich-Peterson, Sips, Toth, and Khan. In which the Langmuir isotherm ([ ]) best described the experimental data with an optimum monolayer capacity for adsorption capacity of 49.7 mg/g at 323 K on Red 2BN molecules. A proposed scheme of Red 2BN molecules on the active sites of adsorbents was illustrated. Regeneration of spent carbons was studied through different cycles of the run.
- 1 January 2022
- Published by SAGE Publications in Adsorption Science & Technology
- Vol. 2022
Open AccessSurface-Modified Adsorbent from Artocarpus heterophyllus Lam Biomass to Confine Reactive Red 194 in Real and Synthetic Effluents: Kinetics and Equilibrium Study
Chemical activation of Artocarpus heterophyllus Lam (jackfruit peel) via phosphoric acid was focused on this study for the preparation of activated carbon. Carbonization was done at a temperature of 400°C based on the nature of biomass after the impregnation ratio of 1 : 1 (weight of phosphoric acid/weight of raw material). Titanium dioxide was doped on the prepared activated carbon through the sol-gel method. Titanium dioxide doped activated carbon was synthesized to perceive the nature of adsorbents under ambient conditions. Both JPAC and JPAC/TiO2 adsorbents were characterized by the point of zero charges, Fourier transform of infrared spectroscopy, X-ray diffraction spectroscopy, Brunauer-Emmett-Teller analysis, and scanning electron microscopy with energy-dispersive X-ray analysis. The adsorption capacity of Reactive Red 194 (Red 2BN) dye on jackfruit peel activated carbon (JPAC) is 32.271 mg/g, and JPAC/TiO2 is 34.900 mg/g was observed under optimum conditions. Desorption efficiency of JPAC/TiO2 (≥93.4%) is slightly higher compared to JPAC (≥89.2%). Tannery effluents of various parameters were analyzed, and their chemical oxygen demand (COD) values trim down within the permissible limits of JPAC (97%) and JPAC/TiO2 (98%). Experimental data were studied using both two-parameter and three-parameter models of adsorption isotherm, namely, the Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, Redlich-Peterson, Sips, Toth, and Khan. In which the Langmuir isotherm ([ ]) best described the experimental data with an optimum monolayer capacity for adsorption capacity of 49.7 mg/g at 323 K on Red 2BN molecules. A proposed scheme of Red 2BN molecules on the active sites of adsorbents was illustrated. Regeneration of spent carbons was studied through different cycles of the run.
- 20 February 2021
- Published by Springer Nature in Journal of Material Cycles and Waste Management
- Vol. 23 (3) , 1002-1014
Pyrolysis of polypropylene waste using sulfonated carbon catalyst synthesized from sugarcane bagasse
- 20 February 2021
- Published by Springer Nature in Journal of Material Cycles and Waste Management
- Vol. 23 (3) , 1002-1014
Pyrolysis of polypropylene waste using sulfonated carbon catalyst synthesized from sugarcane bagasse
- 3 December 2019
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 27 (1) , 438-455
Catalytic activity of acid-treated biomass for the degradation of expanded polystyrene waste
Pyrolysis processes were investigated using expanded polystyrene waste (EPW) with a catalyst synthesized from rice husk (RH). Biomass was treated with different acids, i.e., sulfuric acid, oxalic acid, and hydrochloric acid. The effect of normality on the oxalic acid-treated catalyst and the effects of polymer to catalyst ratio on (i) oil, gas, and residues yields; (ii) temperature; and (iii) time for the complete reaction were investigated for the effective use of oil for fuel production. The catalyst treated with 0.25 N (RHOA0.25) resulted in a high oil yield of 96 wt% and a residue yield of 3.47 wt%. The oil produced contained mainly aromatic compounds, which contributed 67.86% in an area-based GC-MS analysis. The synthesized catalyst showed a stable capacity for three regeneration runs. The significant factor is that the synthesized catalyst decreased the activation energy during the pyrolysis of EPW.
- 3 December 2019
- Published by Springer Nature in Environmental Science and Pollution Research
- Vol. 27 (1) , 438-455
Catalytic activity of acid-treated biomass for the degradation of expanded polystyrene waste
Pyrolysis processes were investigated using expanded polystyrene waste (EPW) with a catalyst synthesized from rice husk (RH). Biomass was treated with different acids, i.e., sulfuric acid, oxalic acid, and hydrochloric acid. The effect of normality on the oxalic acid-treated catalyst and the effects of polymer to catalyst ratio on (i) oil, gas, and residues yields; (ii) temperature; and (iii) time for the complete reaction were investigated for the effective use of oil for fuel production. The catalyst treated with 0.25 N (RHOA0.25) resulted in a high oil yield of 96 wt% and a residue yield of 3.47 wt%. The oil produced contained mainly aromatic compounds, which contributed 67.86% in an area-based GC-MS analysis. The synthesized catalyst showed a stable capacity for three regeneration runs. The significant factor is that the synthesized catalyst decreased the activation energy during the pyrolysis of EPW.
- 1 September 2019
- Published by Elsevier in Journal of Environmental Management
- Vol. 246, 259-266
Surfactant modified ZnO–Bi2O3 nanocomposite for degradation of lambda- cyhalothrin pesticide in visible light: A study of reaction kinetics and intermediates
- 1 September 2019
- Published by Elsevier in Journal of Environmental Management
- Vol. 246, 259-266
Surfactant modified ZnO–Bi2O3 nanocomposite for degradation of lambda- cyhalothrin pesticide in visible light: A study of reaction kinetics and intermediates
- 1 June 2018
- Published by Elsevier in Waste Management
- Vol. 76, 528-536
Pyrolysis of polystyrene waste in the presence of activated carbon in conventional and microwave heating using modified thermocouple
- 1 June 2018
- Published by Elsevier in Waste Management
- Vol. 76, 528-536
Pyrolysis of polystyrene waste in the presence of activated carbon in conventional and microwave heating using modified thermocouple
- 10 April 2018
- Published by Taylor & Francis in Preparative Biochemistry & Biotechnology
- Vol. 48 (4) , 343-351
Improved stability and catalytic activity of graphene oxide/chitosan hybrid beads loaded with porcine liver esterase
Graphene oxide/chitosan and reduced graphene oxide/chitosan (GO/CS and RGO/CS) beads were prepared by precipitation with NaOH. Porcine liver esterase was immobilized on these beads to give GO/CS/E and RGO/CS/E beads. The optimum conditions for the maximum activity of RGO/CS/E beads were pH 8 and 50°C. The stability of the enzyme immobilized on GO/CS/E and RGO/CS/E was high in the pH range of 5–8. The GO/CS/E beads showed superior stability compared to that of the free enzyme and CS/E beads between 20 and 50°C. Kinetic analysis showed that GO/CS/E was a better catalyst than the RGO/CS/E beads with a lower Km value of 0.9 mM. The hybrid beads also retained more than 95% activity after 10 consecutive cycles. The GO/CS/E and RGO/CS/E beads retained 84% and 87% activity after 40 days at 4°C. The GO/CS/E beads were used for the successful hydrolysis of methyl 4-hydroxy benzoate.
- 10 April 2018
- Published by Taylor & Francis in Preparative Biochemistry & Biotechnology
- Vol. 48 (4) , 343-351
Improved stability and catalytic activity of graphene oxide/chitosan hybrid beads loaded with porcine liver esterase
Graphene oxide/chitosan and reduced graphene oxide/chitosan (GO/CS and RGO/CS) beads were prepared by precipitation with NaOH. Porcine liver esterase was immobilized on these beads to give GO/CS/E and RGO/CS/E beads. The optimum conditions for the maximum activity of RGO/CS/E beads were pH 8 and 50°C. The stability of the enzyme immobilized on GO/CS/E and RGO/CS/E was high in the pH range of 5–8. The GO/CS/E beads showed superior stability compared to that of the free enzyme and CS/E beads between 20 and 50°C. Kinetic analysis showed that GO/CS/E was a better catalyst than the RGO/CS/E beads with a lower Km value of 0.9 mM. The hybrid beads also retained more than 95% activity after 10 consecutive cycles. The GO/CS/E and RGO/CS/E beads retained 84% and 87% activity after 40 days at 4°C. The GO/CS/E beads were used for the successful hydrolysis of methyl 4-hydroxy benzoate.
- 28 November 2016
- Published by Taylor & Francis in Chemical Engineering Communications
- Vol. 204 (2) , 238-248
Optimization of Activated Carbon Preparation from Pomegranate Peel (Punica granatumPeel) Using RSM
This research involves the optimization of different variables of the operating conditions to prepare activated carbon from pomegranate peels (Punica granatum peel). For this purpose, a statistical method called Response Surface Methodology (RSM) has been adopted to economize the number of experiments and their meaningful interpretation. Activated carbon was produced by chemical activation (H3PO4). RSM was used to evaluate the variables considered in the preparation of activated carbon such as impregnation ratio (2–4 g H3PO4/g pomegranate peel), temperature (400–600°C), and activation time (30–90 min), experimented using a three-variable Box–Behnken Design (BBD) based on a quadratic model and an RSM tool provided by Design Expert 8.0.4 (STAT-EASE Inc., Minneapolis, USA). The responses analyzed for optimization were the methylene blue number and the iodine number. The factors that are significant influencing the activated carbon preparation have been identified by an analysis of variance (ANOVA). The optimum conditions established were impregnation ratio of 2.78, activation temperature of 575°C, and activation time of 73 min.
- 28 November 2016
- Published by Taylor & Francis in Chemical Engineering Communications
- Vol. 204 (2) , 238-248
Optimization of Activated Carbon Preparation from Pomegranate Peel (Punica granatumPeel) Using RSM
This research involves the optimization of different variables of the operating conditions to prepare activated carbon from pomegranate peels (Punica granatum peel). For this purpose, a statistical method called Response Surface Methodology (RSM) has been adopted to economize the number of experiments and their meaningful interpretation. Activated carbon was produced by chemical activation (H3PO4). RSM was used to evaluate the variables considered in the preparation of activated carbon such as impregnation ratio (2–4 g H3PO4/g pomegranate peel), temperature (400–600°C), and activation time (30–90 min), experimented using a three-variable Box–Behnken Design (BBD) based on a quadratic model and an RSM tool provided by Design Expert 8.0.4 (STAT-EASE Inc., Minneapolis, USA). The responses analyzed for optimization were the methylene blue number and the iodine number. The factors that are significant influencing the activated carbon preparation have been identified by an analysis of variance (ANOVA). The optimum conditions established were impregnation ratio of 2.78, activation temperature of 575°C, and activation time of 73 min.
- 1 March 2016
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 4 (1) , 534-541
Photodegradation of methylene blue using magnetically reduced graphene oxide bismuth oxybromide composite
- 1 March 2016
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 4 (1) , 534-541
Photodegradation of methylene blue using magnetically reduced graphene oxide bismuth oxybromide composite