Thomas Pielhop
ETH Zurich
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Publication
Featured researches published by Thomas Pielhop.
Green Chemistry | 2015
Thomas Pielhop; Gastón O. Larrazábal; Michael H. Studer; Simone Brethauer; Christoph-M. Seidel; Philipp Rudolf von Rohr
This study presents a modified autohydrolysis pretreatment which helps to overcome the recalcitrance of softwood for enzymatic hydrolysis of its cellulose. Autohydrolysis pretreatments of spruce wood were performed with 2-naphthol, which prevents lignin repolymerisation reactions, thereby increasing the enzymatic digestibility of cellulose by up to 64%. The negative influence of repolymerised lignin structures on enzymatic hydrolysis was confirmed by the addition of resorcinol in autohydrolysis, which is known to promote repolymerisation reactions and decreased the biomass digestibility. Several analyses were performed to study the underlying mechanism of this effect on hydrolysis, indicating that cellulolytic enzymes are adsorbed and deactivated especially by repolymerised lignin structures, which accounts for the high differences in biomass digestibility. It was shown that lignin repolymerisation significantly increases its specific surface area through modification of the lignin nanostructure, which is supposed to increase the unproductive binding of enzymes.
Green Chemistry | 2016
Thomas Pielhop; Gastón O. Larrazábal; Philipp Rudolf von Rohr
The effects of different additives on lignin repolymerisation in the autohydrolysis pretreatment of softwood and the consequences for enzymatic cellulose digestibility have been studied. The study comprised 35 substances including alcohols, amines, heterocyclic and other compounds. It has been shown that lignin repolymerisation does not only hinder hydrolysis by the deactivation of cellulases, but can also obstruct their access to cellulose. A new class of phenolic additives has been discovered that can block lignin repolymerisation and thus increase glucose yields in hydrolysis by more than 40%. Dimethylphloroglucinol was found to be even more effective than 2-naphthol, the most effective lignin repolymerisation blocker reported to date. The study reveals that effective additives have to be highly nucleophilic and must not act as a crossing agent for lignin fragments, which can dramatically worsen glucose yields. Phenolic compounds activated by several hydroxy groups with only a single reactive aromatic site are however very beneficial in enhancing pretreatment. The order of effectiveness of the tested compounds is consistent with the hypothesis that they compete with the aromatic rings present in lignin for lignin carbocations. These ions have been proposed earlier to be intermediates in the formation of repolymerised lignin structures. While compounds activated towards electrophilic substitution generally had a high impact, compounds that can stop radical repolymerisation had no effect. The gained insights open up the possibility to identify numerous further additives that can enhance autohydrolysis, steam and acidic pretreatments of lignocellulose.
Biotechnology for Biofuels | 2016
Thomas Pielhop; Janick Amgarten; Philipp Rudolf von Rohr; Michael H. Studer
Faraday Discussions | 2017
Christoph-Maximilian Seidel; Thomas Pielhop; Michael H. Studer; Philipp Rudolf von Rohr
Biofuels, Bioproducts and Biorefining | 2017
Merten Morales; Thomas Pielhop; Philippe Saliba; Konrad Hungerbühler; Philipp Rudolf von Rohr; Stavros Papadokonstantakis
Biotechnology for Biofuels | 2017
Thomas Pielhop; Janick Amgarten; Michael H. Studer; Philipp Rudolf von Rohr
Biomass & Bioenergy | 2017
Thomas Pielhop; Claudio Reinhard; Christian Hecht; Luca Del Bene; Michael H. Studer; Philipp Rudolf von Rohr
Archive | 2012
Thomas Pielhop; Michael H. Studer; Von Rohr Philipp Rudolft
International Symposium on Green Chemistry 2017 | 2017
Christoph-Maximilian Seidel; Thomas Pielhop; Michael H. Studer; Philipp Rudolf von Rohr
Proceedings of the 4th Symposium on Biotechnology Applied to Lignocelluloses (Lignobiotech IV) | 2016
Thomas Pielhop; Christoph-Maximilian Seidel; Michael H. Studer; Philipp Rudolf von Rohr