Green Catalytic Approach for the Synthesis of Platform Chemicals from Palm Tree Lignin

Article Preview

Abstract:

Lignin is the second most abundant naturally occurring macromolecule found in plant cell-wall, vascular components and woody stems. It is the largest renewable source of aromatic biopolymer. However, lignin is recalcitrant to be broken down by most chemicals. This is because of its complicated heterogeneous molecular structure. However, lignin depolymerization has huge potentials for the synthesis of a number of useful chemicals, perfumes and pharmaceuticals and toiletries. The oxidation products of lignin are important precursors for pulp/paper and food industries, synthetic thin films. Vanillin, veratryl aldehyde and para-benzoquinone are the oxidation products of lignin. These chemicals are the precursors of optically active alcohol, ketone, violuric acid and benzaldehyde. However, the oxidation of biolignin has been remaining a challenging task. Green catalytic approaches might be an interesting solution for the selective depolymerization of lignin into various platform chemicals. Metal oxide/silica supported nanoporous gold has received strong attention as green catalyst for the transformation of various natural polymers. Mesoporous metal oxide/silica provide enlarged surfaces for the breakdown of C-C, C-H and C-OH bonds. This paper has reviewed various green catalytic approaches for the control depolymerization of biolignin into platform chemicals.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

62-66

Citation:

Online since:

April 2014

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2014 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

[1] N. G Lewis, S. Sarkanen, editors, Lignin and Lignan Biosynthesis, ACS symposium series 697, Washington, DC: American Chemical Society, 697 (1998).

DOI: 10.1021/bk-1998-0697

Google Scholar

[2] Helsinki: Gummerus Kirjapaino Technical Association of the Pulp and paper Industry, EUCEPA, editor. Proceedings of the 8th international symposium on wood and pulping chemistry; European polymer journal 49 (2013)1151-1173.

Google Scholar

[3] E. Adler, Structural elements of lignin: early review, Ind Eng Chem 49(9) (1957)1377–83.

Google Scholar

[4] John Wiley & Sons, Lignin: Kirk-Othmer encyclopedia of chemical technology, European polymer journal, 49 (2013) 1151-117.

Google Scholar

[5] Haruta, M. Kobayashi, T. Sano, H. Yamada, N. Novel gold catalysts for the oxidation of carbon-monoxide at a temperature far below 0 °C, Chem. Lett, 16 (1987) 405–408.

DOI: 10.1246/cl.1987.405

Google Scholar

[6] Wu, P.P. Bai, P. Loh, K.P. Zhao, X.S. Au nanoparticles dispersed on functionalized mesoporous silica for selective oxidation of cyclohexane, Catal. Today, 158 (2010) 220–227.

DOI: 10.1016/j.cattod.2010.03.027

Google Scholar

[7] W. Adam, WA. Herrmann, CH. Saha-Moller, M. Shimadzu, Oxidation of methoxybenzenes to p-benzoquinones catalyzed by methyltrioxorhenium(VII), J Mol Catal A: Chem 97(1) (1995) 15–20.

DOI: 10.1016/1381-1169(94)00070-0

Google Scholar

[8] W. Adam, W.A. Herrmann, C.R. Saha-Moller, M. Shimadzu, J. Mol. Catal. A, 97 (1995) 15–20.

Google Scholar

[9] R. Amorati, G.F. Pedulli, L. Valmigli, O.A. Attanasi, P. Filippone, C. Fiorucci, et al., J. Chem. Soc., Perkin Trans, 2 (2001) 2142–2146.

DOI: 10.1039/b105079f

Google Scholar

[10] R. Saladino, E. Mincione, O.A. Attanasi, P. Filippone, Pure Appl. Chem, 75 (2003) 261–268.

Google Scholar

[11] D.C. Ayres, J.D. Loike, Lignans: Chemical, Biological and Clinical Properties, Cambridge University Press, (1990).

Google Scholar

[12] P.L. Nayak, Biodegradable polymers: opportunities and chanllenges, Macrom Chem Phys, 39(3) (1999) 481–505.

Google Scholar

[13] A. Haikarailen, J. Sipila, P. Pietikainen, A. Pajunen, I. Mutikainen. Synthesis and characterization of bulky salen-type complexes of Co, Cu, Fe, Mn and Ni with amphiphilic solubility properties, J ChemSoc, Dalton Trans, 7 (2001) 991–5.

DOI: 10.1039/b008167l

Google Scholar

[14] L. Zoia, C. Canevali, M. Orlandi, E.L. Tolppa, J. Sipila, F. Morazzoni, Radical foramtion on TMP fibers and related lignin chemicalchanges, BioRes, 3(1) (2008) 21–33.

DOI: 10.1021/bm050012i

Google Scholar

[15] E. Bolzacchini, L.B. Chiavetto, C. Canevali, F. Morazzoni, M. Orlandi, B Rindone, Oxidation of propenoidic phenols catalyzed by N, N'-ethylene bis(salicylideneiminato)cobalt(ll)[cosalen]: reactivity and spectroscopic studies, J Mol Catal 112(3) (1996).

DOI: 10.1016/1381-1169(96)00110-0

Google Scholar

[16] E. Bolzacchini, C. Canevali, F. Morazzoni, M. Orlandi, B. Rindone, R. Scotti, Spectromagnetic investigation of the active species in thoxidation of propenoidic phenols catalysed by [N, N'-bis(salicylidene)-ethane-1, 2-diaminato]cobalt(II), J Chem Soc, Dalton Trans, 24 (1997).

DOI: 10.1039/a705188c

Google Scholar

[17] C. Canevali, M. Orlandi, L. Pardi, B. Rindone, R. Scotti, J. Sipila, et al, Oxidative degradation of monomeric and dimeric phenylpropanoids: reactivity and mechanistic investigation, Chem Soc, Dalton Trans, 15 ( 2002) 3007–14.

DOI: 10.1039/b203386k

Google Scholar