A sustainable and eco-friendly technique for dye adsorption from aqueous media using waste from Jatropha curcas (isotherm and kinetic model)

2020 ◽  
Vol 182 ◽  
pp. 365-374
Author(s):  
Musa Yahaya Pudza ◽  
Zurina Z. Abidin
Author(s):  
Musa Yahaya pudza ◽  
Zurina Z. Abidin

The Batch process of Adsorption were conducted using Congo red (CR) as the adsorbate and Jatropha curcas seed (chaff) as the adsorbent material. Adsorption kinetics and isotherms analysis were conducted and results obtained confirmed the adsorption process as highly dependent on effects such as; contact time, adsorbent dosage, initial dye concentration and the particle sizes of adsorbate. However, the sorption equilibrium for Congo red dye unto jatropha curcas seed (chaff) was reached within 180 minutes, more so, the Adsorption efficiency was recorded at 82.05%. The process of the experimental sorption kinetics followed a pseudo-second-order kinetic model while Freundlich isotherm model was best applicable for obtaining the equilibrium of the parameters. These is an effective confirmation and validation of jatropha curcas seed (chaff) application as environmentally friendly and low-cost biomaterial for dye removal from aqueous solutions and industrial effluents.


2020 ◽  
Vol 4 (3) ◽  
pp. 95
Author(s):  
Dexu Kong ◽  
Lee D. Wilson

To address the need to develop improved hybrid biopolymer composites, we report on the preparation of composites that contain chitosan and pectin biopolymers with tunable adsorption properties. Binary biopolymer composites were prepared at variable pectin–chitosan composition in a solvent directed synthesis, dimethyl sulfoxide (DMSO) versus water. The materials were characterized using complementary methods (infrared spectroscopy, thermal gravimetric analysis, pH at the point-of-zero charge, and dye-based adsorption isotherms). Pectin and chitosan composites prepared in DMSO yielded a covalent biopolymer framework (CBF), whereas a polyelectrolyte complex (PEC) was formed in water. The materials characterization provided support that cross-linking occurs between amine groups of chitosan and the –COOH groups of pectin. CBF-based composites had a greater uptake of methylene blue (MB) dye over the PEC-based composites. Composites prepared in DMSO were inferred to have secondary adsorption sites for enhanced MB uptake, as evidenced by a monolayer uptake capacity that exceeded the pectin–chitosan PECs by 1.5-fold. This work provides insight on the role of solvent-dependent cross-linking of pectin and chitosan biopolymers. Sonication-assisted reactions in DMSO favor CBFs, while cross-linking in water yields PECs. Herein, composites with tunable structures and variable physicochemical properties are demonstrated by their unique dye adsorption properties in aqueous media.


2020 ◽  
Vol 4 (1) ◽  
pp. 15 ◽  
Author(s):  
Mohamed H. Mohamed ◽  
Inimfon A. Udoetok ◽  
Lee D. Wilson

Pelletized biomaterial composites that contain chitosan (C) and torrefied wheat straw (S) at variable weight composition (C:S) were prepared using a facile blending process. The fractional content of the wheat straw was studied to elucidate the role of biomass on the pelletized product and effects of S-content on the physicochemical properties relevant to adsorption phenomena. Chitosan pellets (with and without S) were characterized by spectroscopic (FT-IR and 13C NMR) and thermal (TGA and DSC) techniques to provide support for their respective C:S composition. Confocal microscopy using fluorescein (FL) as a dye probe revealed the presence and an increase in the accessibility of the active sites for the composite pellets according to the S-content (wt %). Equilibrium and kinetic sorption studies using FL and reactive black (RB) dyes revealed an incremental adsorption affinity of the pellets with anionic dyes in variable charge states (FL and RB). The trend for dye adsorption parallels the incremental S-content (wt %) in the composite pellets. This study reports a first-example of a low-cost, facile, and sustainable approach for the valorization of straw and chitosan suitable for sorption-based applications in aqueous media.


2014 ◽  
Vol 2 (35) ◽  
pp. 14334-14338 ◽  
Author(s):  
O. Mashtalir ◽  
K. M. Cook ◽  
V. N. Mochalin ◽  
M. Crowe ◽  
M. W. Barsoum ◽  
...  

Herein we report on the adsorption and photocatalytic decomposition of organic molecules in aqueous environments containing two-dimensional Ti3C2Tx, a representative of the MXene family.


Nanomaterials ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 1164 ◽  
Author(s):  
Sang Yeob Lee ◽  
Ha Eun Shim ◽  
Jung Eun Yang ◽  
Yong Jun Choi ◽  
Jongho Jeon

This paper describes a novel chromatographic method for efficient removal of anionic dyes from aqueous solutions. Chitosan-coated Fe3O4 nanoparticles can easily be immobilized on a dextran gel column. Single elution of Evans Blue (EB) solution to the nanoadsorbent-incorporated columns provides high removal efficiency with a maximum adsorption capacity of 243.9 mg/g. We also investigated the influence of initial concentration and solution pH on the removal efficiency of EB. The electrostatic interaction between the adsorbent surface and negatively charged sulfate groups on EB molecules promotes the efficient adsorption of dyes. The equilibrium data matched well with the Langmuir isotherm model, which indicated monolayer dye adsorption onto the adsorbent surface. To extend the application of the current method, we performed further adsorption experiments using other anionic dyes of different colors (Cy5.5, Acid Yellow 25, Acid Green 25, and Acid Red 1). All of these molecules can efficiently be captured under continuous flow conditions, with higher removal efficiency obtained with more negatively charged dyes. These findings clearly demonstrate that the present approach is a useful method for the removal of anionic dye contaminants in aqueous media by adsorption.


2020 ◽  
Vol 41 (8) ◽  
pp. 843-850 ◽  
Author(s):  
Sungjune Kim ◽  
Jihyun Lee ◽  
Younghu Son ◽  
Minyoung Yoon

2009 ◽  
Vol 146 (3) ◽  
pp. 486-497 ◽  
Author(s):  
María Eugenia Lovato ◽  
Carlos A. Martín ◽  
Alberto E. Cassano

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