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http://nopr.niscpr.res.in/handle/123456789/23659| Title: | Characterization of modified polypropylene powder (Accurel) and its use for adsorption of phenolics from aqueous solution |
| Authors: | Singh, Kaman Singh, Vimalesh Kumar Verma, Sudhir Kumar Bharose, Ram Suman, Anita |
| Keywords: | Accurel MP 1002 powder;Antioxidant;Hydrophobic adsorption;L2 adsorption;Phenolics |
| Issue Date: | Nov-2013 |
| Publisher: | NISCAIR-CSIR, India |
| Abstract: | The polypropylene based Accurel has been modified
using surfactant and then characterized for selective adsorption of phenolics.
The pore distribution falls between macroporous and mesoporous domains. The SEM
images of Accurel reveal that it has porous structure of typically 73% void
volume with cells of 5-10 μm connected by pores of 0.0028 μm diameter. The BET
surface area of the Accurel is typically found as 27 m2/g. The
titled adsorbate-sorbent system follows
L2 type of adsorption. The adsorption of studied phenolic acids depends on
several factors, such as pKa, ionic strength, and steric effect
(molecular size). The adsorption coefficients for the studied phenolics follow
the sequence: chlorogenic acid > p-cumaric acid > syringic acid >
p-hydroxy benzoic acid. The adsorption capacity of phenolics grows with
increase in –OH groups in the structure of the acids. The amount of adsorbed
phenolics increases with increasing ionic strength and obeys the sequence: Cl < SO < PO .
Similarly, the cations are added in the same concentration range as anions and
the effectiveness is found to obey the sequences: Na+ < Ca2+
< fe3+. The adsorbed amount decreases at both high and low pH values. Adsorption is found to
increase significantly with increase in ionic strength, suggesting a role for
the hydrophobic force in this adsorption process. Urea, a hydrogen bond
breaker, reduces the adsorption, suggesting that the hydrogen bonding may also
play a role in the adsorption of phenolics on modified Accurel. The modified
Accurel shows significant sorption capacity for phenolics under suitable
experimental condition and hence, will serve as a useful sorbent which can be
extended to other chemical systems for the isolation of anti-oxidant phenolics.
Furthermore, Accurel is available commercially and hence, scalable for
industrial purpose.
|
| Page(s): | 385-391 |
| ISSN: | 0975-0991 (Online); 0971-457X (Print) |
| Appears in Collections: | IJCT Vol.20(6) [November 2013] |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCT 20(6) 385-391.pdf | 785.24 kB | Adobe PDF | View/Open |
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< SO
< PO
.
Similarly, the cations are added in the same concentration range as anions and
the effectiveness is found to obey the sequences: Na+ < Ca2+
< fe3+. The adsorbed amount decreases at both high and low pH values. Adsorption is found to
increase significantly with increase in ionic strength, suggesting a role for
the hydrophobic force in this adsorption process. Urea, a hydrogen bond
breaker, reduces the adsorption, suggesting that the hydrogen bonding may also
play a role in the adsorption of phenolics on modified Accurel. The modified
Accurel shows significant sorption capacity for phenolics under suitable
experimental condition and hence, will serve as a useful sorbent which can be
extended to other chemical systems for the isolation of anti-oxidant phenolics.
Furthermore, Accurel is available commercially and hence, scalable for
industrial purpose.