15.08.2018 Views

Abstracts Book - IMRC 2018

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

• SB1-P072<br />

CHLOROPHYLL-SENSITIZED PHENOLIC RESINS FOR<br />

PHOTOCATALYTIC DECOLORIZATION OF METHYLENE BLUE<br />

UNDER VISIBLE LED IRRADIATION: SYNTHESIS,<br />

CHARACTERIZATION AND MECHANISMS<br />

Daniel Simon Olivo Alanis 1 , Elva Melisa Castellanos Escamilla 1 , Alcione Garcia Gonzalez 1 ,<br />

Refugio Bernardo Garcia Reyes 1 , Felipe de Jesús Cerino Córdova 1<br />

1 Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, Mexico.<br />

More efficient photocatalysts are required for water treatment, especially those<br />

materials that can be activated under visible irradiation. For instance, it is well<br />

known that plants make photosynthesis possible because chlorophyll absorb<br />

energy sunlight at visible range. Similarly, in the last five years, phenolic resins<br />

(PR) have shown promising results for dyes decolorization when they were<br />

applied as photocatalyst under visible light. In this research, solvent-extracted<br />

chlorophyll spinach was anchored on PR during the stage of curing with<br />

hexamethylenetetramine. FTIR spectra of phenolic resins with chlorophyll (PR-<br />

C) showed a strong band at 1700 cm -1 that is related to carbonyl groups present<br />

on chlorophyll, but this signal was not exhibited on PR. Energy gap of PR-C (2.18<br />

eV) was slightly lower than phenolic resins (2.23 eV), indicating that both<br />

semiconductors are active under visible light. Additionally, an absorption peak<br />

at 670 nm in DRUV-VIS spectrum was observed for PR-C, suggesting<br />

semiconductor activation at low energy due to chlorophyll and subsequent<br />

electron transfer across polymeric matrix until final electron acceptor is reached<br />

(Z-scheme mechanism). Photocatalytic decolorization of methylene blue (MB)<br />

under visible LED irradiation was studied on four different water matrices. PR-C<br />

showed a higher rate than PR for deionized, tap and acidify tap water matrices<br />

(2.64, 1.97 and 3.95-fold, respectively), achieving about 85-95% of decolorization<br />

in 6 h. In contrast, PR achieve a rate 1.39-fold (91% of decolorization) higher than<br />

PR-C for carbonate alkaline water matrix. This unexpected result could be<br />

associated with the release of magnesium that is originally coordinated with<br />

pyrrolic rings on chlorophyll or chlorophyll detachment polymer. Scattering<br />

property of PR-C revealed that recombination activity decreased at wavelength<br />

greater than 610 nm in comparison to PR. Finally, scavenger tests were<br />

conducted to elucidate the photocatalytic mechanisms of PR-C for MB<br />

decolorization under visible LED irradiation. Superoxide radical contributed in a<br />

higher extent in all tested water matrices (49-66%), followed by electron-hole<br />

pair redox processes (20-22% and 2-15%, respectively), and a low contribution

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!