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Number of results: 3
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Abstract

The hydrolysis of lignocellulosic biomass results in the production of so-called fermentation inhibitors, which reduce the efficiency of biohydrogen production. To increase the efficiency of hydrogen production, inhibitors should be removed from aqueous hydrolysate solutions before the fermentation process. This paper presents a new approach to the detoxification of hydrolysates with the simultaneous formation of in-situ deep eutectic solvents (DES). In the first stage of the study, inhibitors were identified in the real hydrolysate samples using highperformance liquid chromatography (HPLC). Four monoterpenes were tested for their potential to extract furfural (FF) with simultaneous DES formation. An optimization process of the most important parameters affecting the extraction process and DES formation (Thymol:FF) was conducted using the Central Composite Design (CCD) model. A temperature of 40 °C, pH of 7, mHBD:mHYD ratio of 2:1, and time of 50 min were selected as the optimal conditions. These results indicate the high efficiency of FF removal from hydrolysates (92.1 - 94.6 %) in a onestep process. Meanwhile, the structural properties of the formed DES measured by Fouriertransform infrared spectroscopy (FT-IR) and Nuclear magnetic resonance spectroscopy (NMR) differed only slightly from those of the DES composed of pure substances (Furfural and Thymol).
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Authors and Affiliations

Patrycja Makoś-Chełstowska
1
ORCID: ORCID
Edyta Słupek
1
ORCID: ORCID
Karolina Kucharska
1
ORCID: ORCID
Jacek Gębicki
1
ORCID: ORCID

  1. Gdansk University of Technology, Faculty of Chemistry, Department of Process Engineeringand Chemical Technology, 80-233 Gdansk, Poland
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Abstract

The paper presents new non-ionic deep eutectic solvent (DES) composed of natural and non-toxic components i.e. guaiacol, camphor and levulinic acid in 1:1:3 molar ratio as a promising absorbent for removal of selected volatile organic compounds (VOCs) including dichloromethane, toluene, hexamethyldisiloxane and propionaldehyde from model biogas. The affi nity of DES for VOCs was determined as vapour-liquid coeffi cients and the results were compared with several well-known DESs based on quaternary ammonium salt as well as n-hexadecane and water. For new DES, the absorption process was carried out under dynamic conditions. The results indicate that non-ionic DES has high affi nity and capacity for VOCs being comparable to n-hexadecane. In addition, absorbed VOCs could be easily desorbed from DES using activated carbon and absorbent could be re-use minimum fi ve times without significant loss of absorption capacity.
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Authors and Affiliations

Edyta Słupek
1
ORCID: ORCID
Patrycja Makoś
1
Jacek Gębicki
1
ORCID: ORCID

  1. Gdansk University of Technology, Faculty of Chemistry, Department of Process Engineering and Chemical Technology, Gdańsk, Poland
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Abstract

A deep eutectic solvent, ethaline (as a typical representative of new-generation room temperature ionic liquids), was used to anodically treat the surface of copper-nickel alloy (55 wt.% Cu). Anodic treatment in ethaline allows flexibly affecting the patterns of surface morphology: formation of stellated crystallites and surface smoothing (i.e. electropolishing) are observed depending on the applied electrode potential. The measured values of roughness coefficient ( Ra ) well correlate with the changes in surface morphology. Anodic treatment of Cu-Ni alloy in ethaline contributes to a considerable increase in the electrocatalytic activity towards the hydrogen evolution reaction in an alkaline aqueous medium, which can be used to develop new high-efficient and inexpensive electrocatalysts within the framework of the concept of carbon-free hydrogen economy.
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Authors and Affiliations

V. Protsenko
1
ORCID: ORCID
T. Butyrina
1
ORCID: ORCID
D. Makhota
1
ORCID: ORCID
S. Korniy
1 2
ORCID: ORCID
F. Danilov
1
ORCID: ORCID

  1. Ukrainian State University of Chemical Technology, Department of Physical Chemistry, Gagarin Ave., 8, Dnipro, 49005, Ukraine
  2. Karpenko Physico-Mechanical Institute of the NAS of Ukraine, Naukova St. 5, Lviv, 79060, Ukraine

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