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Abstract

Despite its unique properties (biocompatibility and nontoxicity), chitin itself has limited application. Chitin is completely insoluble in most organic or inorganic solvents what can be beneficial when chitin is investigated as a support for chromatography or enzyme immobilization. These applications require the particles to have an extensive outer surface with a large number of reactive ligands. The increase in specific surface area of chitin particles can be performed by dissolution in ionic liquid and precipitation with water. To increase the number of reactive ligands (amine groups), deacetylation of the surface of chitin particles is necessary. The deacetylation process can be carried out by an enzymatic process with the enzyme, chitin deacetylase. In our investigation, 21 ionic liquids were used for chitin particle structure modification followed by enzymatic deacetylation. Results proved positive effect of modifications with ionic liquid on enzymatic deacetylation of the chitin surface with chitin deacetylase. For 12 samples the deacetylation gave an increase in number of active ligands in comparison to natural chitin. The best results were observed for [Bmim][Br], [Emim][Cl] and [MPpip][Ac]. That could be correlated with an increase in outer surface area by increasing porosity of particles or by structural changes in chitin particles.
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Authors and Affiliations

Małgorzata M. Jaworska
1
ORCID: ORCID
Dorota Biniaś
2
ORCID: ORCID
Katarzyna Dąbkowska-Susfał
1
ORCID: ORCID
Andrzej Górak
3
ORCID: ORCID

  1. Warsaw University of Technology, Faculty of Chemical and Process Engineering, Warynskiego 1, 00-645 Warsaw, Poland
  2. University of Bielsko-Biała, Faculty of Materials, Civil and Environmental Engineering, Department of Environmental Protection and Engineering, Willowa 2, 43-309 Bielsko-Biała, 9 Poland
  3. Faculty of Process Engineering and Environmental Protection, Lodz Technical University, ul. Wólczanska 213, 93-005 Lodz, Poland
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Abstract

The corrosion inhibition behaviour of 1-Ethyl-3-methylimidazolium-methanesulphonate (EMIM[MS]) and 1-Ethyl-3-methylimidazolium acetate (EMIM[Ac]) on API 5L X-52 carbon steel in 2 M HCl was investigated using weight loss, potentiodynamic polarization and electrochemical impedance methods. The corrosion rates of carbon steel decreased in the presence of these ionic liquids. The inhibition efficiencies of the compounds increased with concentration and showed a marginal decrease with a 10°C increase in temperature. Polarization studies showed the compounds to be mixed type inhibitors with stronger anodic character. The adsorption mechanism of both compounds on the metal surface was via physical adsorption and the process obeyed the El-Awardy kinetic-thermodynamic model. The associated activation energy of corrosion and other thermodynamic parameters were calculated to elaborate on the thermodynamics and mechanism of the corrosion inhibition process. EMIM[MS] was found to inhibit the corrosion of carbon steel better than EMIM[Ac] and is attributed to the presence of the highly electronegative sulphur atom in its structure and its larger molecular size.

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Authors and Affiliations

Magdalene Edet Ikpi
Okama Ebri Obono
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Abstract

The paper presents the results of investigation on a prototype sensor for measurement of benzaldehyde in air. Sensitivity and limit of quantification of the sensor were determined for different internal electrolytes using square wave voltammetry (SWV) as the detection technique. The working and counter electrodes were made of platinum. Ionic liquids 1-hexyl, 3-methylimidazolium chloride, 1-hexyl, 3-methylimidazolium bis (trifluoro-methanesulfonyl) imide and 1-butyl, 3-methylimidazolium tricyanomethan constituted the internal electrolyte. A polydimethylsiloxane (PDMS) membrane separated the gaseous medium from the electrolyte.

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Authors and Affiliations

Jacek Gębicki
Adam Kloskowski

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