90 research outputs found

    5-Hydroxymethylfurfural (HMF) formation during subcritical water extraction

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    The aim of this study was to investigate the effect of material type (artichoke leave, lemon peel, flaxseed meal), extraction temperature (50, 100, 120, 140, 160, 180, 200 C) and static extraction time (5, 15, 30, 45 min) on 5-hydroxymethylfurfural (5-HMF) formation during subcritical water extraction. 5-HMF content of artichoke leave and lemon peel extracts increased 7.2 and 26.1 times with the rise of extraction temperature from 160 to 180 C for 5 min during subcritical water extraction, respectively. Besides, 5-HMF content of artichoke leave, lemon peel and flaxseed meal extracts increased 1.4, 2.0 and 4.5 times as static extraction time increased from 15 to 45 min at 180 C during subcritical water extraction, respectively. The highest 5-HMF content of artichoke leave and lemon peel extracts were obtained as 58.83 and 231.21 mg/L at 180 C and 45 min, respectively. However, for flaxseed meal, the highest 5-HMF content (222.94 mg/L) was obtained at 200 C and 15 min during subcritical water extraction.Project Nos. 2014.M80.02.03, 2014.M80.02.04 by Artvin Coruh University Scientific Research Project Uni

    Green Pathways for the Enzymatic Synthesis of Furan-Based Polyesters and Polyamides

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    The attention towards the utilization of sustainable feedstocks for polymer synthesis has grown exponentially in recent years. One of the spotlighted monomers derived from renewable resources is 2,5-furandicarboxylic acid (FDCA), one of the most promising bio-based monomers, due to its resemblance to petroleum-based terephthalic acid. Very interesting synthetic routes using this monomer have been reported in the last two decades. Combining the use of bio-based monomers and non-toxic chemicals via enzymatic polymerizations can lead to a robust and favorable approach towards a greener technology of bio-based polymer production. In this chapter, a brief introduction to FDCA-based monomers and enzymatic polymerizations is given, particularly focusing on furan-based polymers and their polymerization. In addition, an outline of the recent developments in the field of enzymatic polymerizations is discussed. </p

    Transformation of Biomass into Commodity Chemicals Using Enzymes or Cells

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    Valorisation of Biowastes for the Production of Green Materials Using Chemical Methods

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    With crude oil reserves dwindling, the hunt for a sustainable alternative feedstock for fuels and materials for our society continues to expand. The biorefinery concept has enjoyed both a surge in popularity and also vocal opposition to the idea of diverting food-grade land and crops for this purpose. The idea of using the inevitable wastes arising from biomass processing, particularly farming and food production, is, therefore, gaining more attention as the feedstock for the biorefinery. For the three main components of biomass—carbohydrates, lipids, and proteins—there are long-established processes for using some of these by-products. However, the recent advances in chemical technologies are expanding both the feedstocks available for processing and the products that be obtained. Herein, this review presents some of the more recent developments in processing these molecules for green materials, as well as case studies that bring these technologies and materials together into final products for applied usage

    Stereoselective Synthesis and Isolation of (&plusmn;)-trans,trans-Cyclohexane-1,2,4,5-tetraol

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    Cyclohexanetetrols belong to the family of cyclitols, a class of natural products known for their diverse bioactivity. Their synthesis has been reported using hydrogen peroxide as a green oxidant and water or tert-butanol as a solvent. Due to the high polarity of those compounds, a green approach for their isolation from aqueous solutions can be challenging. Here, we report the stereoselective synthesis of (&plusmn;)-trans,trans-cyclohexane-1,2,4,5-tetraol combined with a novel isolation method, where is possible the isolation of the product in excellent yield without the need for derivatization, column chromatography or organic solvent extraction

    Synthesis of 2,4,6-Tri-substituted-1,3,5-Triazines

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    Abstract: Several specific synthetic protocols were developed for the preparation from cyanuric chloride of a range of symmetric and non-symmetric di- and tri-substituted 1,3,5-triazines containing alkyl, aromatic, hindered, chiral and achiral hydroxyalkyl, ester and imidazole groups via sequential nucleophilic substitution of the C-Cl bond by C-O, C-N and C-S bonds

    Toxicity assessment of various ionic liquid families towards Vibrio fischeri marine bacteria

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    The increasing interest on the application of ionic liquids (ILs) to a wide range of processes and products has been hampered by a lack of toxicological data, mainly in what concerns novel cations, such as guanidinium, phosphonium, and functionalized and non-functionalized imidazolium-based ILs. The present study reports the toxicity of five guanidinium-, six phosphonium, and six imidazolium-based ILs, towards the luminescent marine bacteria Vibrio fischeri. These new results clearly show that guanidinium-, unlike the imidazolium- and phosphonium-based ILs, do not follow the trend of increasing toxicity with the increase in the alkyl chain length. Moreover, the introduction of oxygenated groups on the alkyl chains, such as ether and ester, leads to a decrease of the toxicity of guanidinium and also imidazolium compounds. In what respects the effect of the different cations, it is possible to recognize that the phosphonium-based ILs seem to be more toxic when compared to the analog imidazolium-based ILs (with the same anion and alkyl chains).publishe

    Chitin-glucan complex – Based biopolymeric structures using biocompatible ionic liquids

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    This work explores the novelty of dissolving chitin-glucan complex (CGC), from two fungal strains, Komagataella pastoris (CGCP) and Aspergillus niger (CGCKZ) (KiOnutrime-CG™), using biocompatible ionic liquids (ILs). Three cholinium-based ILs were tested, choline acetate, choline propionate and choline hexanoate. Although all tested ILs resulted in the dissolution of the co-polymer at a concentration of 5 % (w/w), distinct polymeric structures, films or gels, were obtained from CGCP and CGCKZ, respectively. CGCP films were dense, flexible and elastic, with high swelling capacity (> 200 %). The IL anion alkyl chain length influenced the polymeric structures’ properties, namely, the CGCP films elongation at break and swelling degree. CGCKZ resulted in weak gels. For both polymeric structures, exposure to the ILs under the dissolution conditions caused significant changes in the co-polymers’ chemical structure, namely, reduction of their glucan moiety and reduction of the degree of acetylation, thus yielding chitosan-glucan complexes (ChGC) enriched in glucosamine (53.4 ± 0.3–60.8 ± 0.3 %)info:eu-repo/semantics/publishedVersio

    Solubility of carbon dioxide in ammonium based CO2-induced ionic liquids

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    The solubility of carbon dioxide in ionic liquids was measured in a new apparatus. The ionic liquids chosen have ammonium-based cations and show melting temperature decreases under CO2 pressure that range from low (25 K) to extremely high (120 K). The main purpose of this study was to check whether the solubility of the gas in each liquid could explain the previously reported wide differences in melting point depression (MPD). The results show there is no correlation between solubility and MPD
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