Desorption and photodegradation of methylene blue from modified sugarcane bagasse surface by acid TiO2 hydrosol

2012 ◽  
Vol 258 (8) ◽  
pp. 4085-4090 ◽  
Author(s):  
Jun-Xia Yu ◽  
Ru-An Chi ◽  
Jia Guo ◽  
Yue-Fei Zhang ◽  
Zhi-Gao Xu ◽  
...  
Author(s):  
Ali H. Jawad ◽  
Ahmed Saud Abdulhameed ◽  
Noor Nazihah Bahrudin ◽  
Nurul Nadiah Mohd Firdaus Hum ◽  
S. N. Surip ◽  
...  

Abstract In this work, sugarcane bagasse waste (SBW) was used as a lignocellulosic precursor to develop a high surface area activated carbon (AC) by thermal treatment of the SBW impregnated with KOH. This sugarcane bagasse waste activated carbon (SBWAC) was characterized by means of crystallinity, porosity, surface morphology and functional groups availability. The SBWAC exhibited Type I isotherm which corresponds to microporosity with high specific surface area of 709.3 m2/g and 6.6 nm of mean pore diameter. Further application of SBWAC as an adsorbent for methylene blue (MB) dye removal demonstrated that the adsorption process closely followed the pseudo-second order kinetic and Freundlich isotherm models. On the other hand, thermodynamic study revealed the endothermic nature and spontaneity of MB dye adsorption on SBWAC with high acquired adsorption capacity (136.5 mg/g). The MB dye adsorption onto SBWAC possibly involved electrostatic interaction, H-bonding and π-π interaction. This work demonstrates SBW as a potential lignocellulosic precursor to produce high surface area AC that can potentially remove more cationic dyes from the aqueous environment.


Author(s):  
Thaisa Caroline Andrade Siqueira ◽  
Isabella Zanette da Silva ◽  
Andressa Jenifer Rubio ◽  
Rosângela Bergamasco ◽  
Francielli Gasparotto ◽  
...  

Adsorption in biomass has proven to be a cost-effective option for treatment of wastewater containing dyes and other pollutants, as it is a simple and low cost technique and does not require high initial investments. The present work aimed to study the adsorption of methylene blue dye (MB) using sugarcane bagasse (SCB). The biomass was characterized by scanning electron microscopy (SEM). Adsorption studies were conducted batchwise. Kinetics, adsorption isotherms, and thermodynamics were studied. The results showed that SCB presented a maximum adsorption capacity of 9.41 mg g−1 at 45 °C after 24 h of contact time. Adsorption kinetics data better fitted the pseudo-second order model, indicating a chemical process was involved. The Sips’s three-parameter isotherm model was better for adjusting the data obtained for the adsorption isotherms, indicating a heterogeneous adsorption process. The process showed to be endothermic, spontaneous, and feasible. Therefore, it was concluded that SCB presented as a potential biosorbent material for the treatment of MB-contaminated waters.


2017 ◽  
Vol 88 ◽  
pp. 122-127 ◽  
Author(s):  
Guoting Li ◽  
Xi Chen ◽  
Luyang Xu ◽  
Pengcheng Lei ◽  
Shan Zhang ◽  
...  

2015 ◽  
Vol 06 (04) ◽  
pp. 209-220 ◽  
Author(s):  
Handojo Djati Utomo ◽  
Ru Yi Natalie Phoon ◽  
Zhonghuan Shen ◽  
Li Hui Ng ◽  
Zheng Bang Lim

2017 ◽  
Vol 751 ◽  
pp. 671-676 ◽  
Author(s):  
Tawan Chaiwon ◽  
Panatda Jannoey ◽  
Duangdao Channei

This research aimed to study the preparation of activated carbon from sugarcane bagasse waste. The sugarcane bagasse adsorbent was prepared by calcination at 600°C for 2 hours with the use of sulfuric acid (H2SO4) as a chemical activation. The adsorption surface possessed high specific surface area (838 m2/g) with mesoporous diameter. Factors explaining adsorption including adsorption isotherm, adsorption kinetic and adsorption mechanism were constructed from methylene blue adsorption experiments. It was found that the equilibrium data was best represented by Freundlich isotherm, showing multilayer coverage of dye molecules at the outer surface of adsorbent with a cooperative adsorption (physisorption and chemisorption). The kinetic of methylene blue adsorption was found to follow pseudo-second-order rate kinetic model, with a good correlation coefficient. This indicated that the overall rate of the dye adsorption process was controlled by the chemisorption process.


2020 ◽  
Vol 3 (1) ◽  
pp. 59
Author(s):  
Maria Melania Golor ◽  
Dessy Rosma ◽  
Shella Permatasari Santoso ◽  
Felycia Soetaredjo ◽  
Maria Yuliana ◽  
...  

In this work, citric acid (CIT) is proposed as a harmless alternative to epichlorohydrin (ECH) for crosslinking in the synthesis of cellulose hydrogels. Sugarcane bagasse was utilized as a source of cellulose fibers. Cellulose fibers were disintegrated using the solvent-dissolution method before forming a gel-like solution. Subsequently, CIT was added to initiate crosslinking, and the behavior was evaluated by adding various amounts of citric acid (0, 20, 30, and 40 wt%). Cellulose hydrogel with a good mechanical strength (10 mm penetration depth) was obtained from crosslinking using 40 wt% of CIT (HCIT-4), which is comparable to ECH-cross-linked hydrogel (HECH) that has a penetration depth of 8 mm. A proper amount of CIT molecules allows the crosslinking of the cellulose fibers into the hydrogel. The FT-IR analysis reveals a C-O-C band blue-shifting for HCIT-4 compared to HECH, with a gap difference of 82 cm-1. The crystallinity from XRD patterns of HCIT-4 is comparable to that of HECH, which confirms that CIT can be used as a substitute for ECH. The adsorption ability was evaluated against methylene blue dye, the isotherm and kinetic adsorption models for the adsorption system were determined. Freundlich and pseudo-second-order models correlate well to isotherm and kinetics data, suggests that the adsorbent possesses heterogeneous surface sites which adsorption controlled by chemisorption. The prepared HCIT-4 was able to remove 24.88 mg methylene blue/g of the hydrogel at 70 °C, meanwhile HECH only able to remove 12.01 mg/g. The adsorption capacity was increased when adsorption temperature increased, suggesting endothermic behavior.


2017 ◽  
Vol 228 (7) ◽  
Author(s):  
Luana A. R. Giusto ◽  
Fábio L. Pissetti ◽  
Talita S. Castro ◽  
Fabiano Magalhães

Sign in / Sign up

Export Citation Format

Share Document