Can metal based lewis acid catalysis be used for plastic recycling?4 answersMetal-based Lewis acid catalysis can indeed be utilized for plastic recycling. Various studies have highlighted the potential of metal-free acidic carbocatalysts for efficient plastic waste fragmentation, offering a promising solution for environmental applications. Additionally, the development of water-tolerant Lewis acid catalysts, such as LASC, combining Lewis metals with surfactants, has shown significant performance in polylactic acid (PLA) production, enhancing the yield while tolerating water presence. Furthermore, bioinspired supramolecular architectures have been employed to compartmentalize aqua scandium ions into chiral hydrophobic scaffolds, enabling Lewis acid-catalyzed asymmetric reactions with effective recycling capabilities even in highly basic environments, showcasing the robustness of the chiral Lewis acid catalyst. These findings collectively demonstrate the potential of metal-based Lewis acid catalysis in contributing to the chemical recycling of plastic waste.
Does glycerol helps inhibition by substrate?4 answersGlycerol can have varying effects on inhibition by substrate depending on the specific microorganism and process. Research indicates that glycerol supplementation can reduce inhibition effects caused by high lipid content in anaerobic digestion of grease trap waste, leading to enhanced methane production. However, in the case of the environmental strain Aeromonas salmonicida subsp. pectinolytica, glycerol completely abolishes melanin production, indicating an inhibitory effect on melanin synthesis. On the other hand, in the industrial production of dihydroxyacetone (DHA) via glycerol oxidation by Gluconobacter oxydans, glycerol concentrations did not inhibit cellular divisions, but DHA was shown to inhibit bacterial growth at certain concentrations. Additionally, in thraustochytrids, higher glycerol concentrations inhibited glycerol utilization, leading to lower biomass and lipid production, which was alleviated by supplementing with calcium and magnesium ions.
How can glycerol be oxidized without catalyst?5 answersGlycerol can be oxidized without a catalyst by using a base-free method at ambient temperature in the presence of gaseous H2 and O2. This method involves the in situ formation of highly reactive surface-bound oxygenated species, which promote the dehydrogenation of glycerol. The presence of a PdFe bimetallic catalyst has been found to significantly enhance the catalytic performance in this oxidative transformation. Fe leaching occurs during the reaction, but the reaction is predominantly heterogeneous in nature. The use of stabilizing agents such as polyvinyl alcohol (PVA) is not necessary for the preparation of active catalysts for glycerol oxidation. Catalysts prepared without PVA have shown similar catalytic performances and can be tailored to achieve desired oxidation products. These findings suggest that the presence of stabilizing polymers can affect the reaction pathways and control selectivity.
Polyol ester from glycerol?3 answersPolyol esters can be synthesized from glycerol through various methods. One approach involves the base-catalyzed reaction of glycerol with aliphatic dicarboxylic acid esters, resulting in the formation of mono- and di-esterified glycerols. Another method involves subjecting a mixture of a hydroxylated triglyceride and a polyether polyol to transesterification conditions, followed by the removal of glycerin to drive the formation of polyol esters. Additionally, polyol esters can be prepared by reacting polyols with linear or branched aliphatic monocarboxylic acids, with the possibility of partial recycling of the removed acid into the esterification reaction or subsequent batches. The invention also provides polyglycerol alkoxylate esters, which can be prepared and utilized. These methods offer a range of applications for polyol esters, including elastomers, coatings, adhesives, lubricants, surfactants, and more.
What are catalytic applications of frustrated lewis pairs?5 answersFrustrated Lewis pairs (FLPs) have found catalytic applications in various areas. They have been successfully used as catalysts for the activation of small molecules, such as H2, NO, CO, CO2, SO2, N2O, alkenes, and alkynes. FLPs have also been employed in the hydrogenation of unsaturated species, including imine, nitrile, enamine, aziridine, aldehyde, ketone, alkene, and alkyne. In addition, FLPs have shown potential in copolymerization reactions, such as the copolymerization of CO2 and epoxides. The catalytic activity of FLPs is influenced by the electronic and steric properties of the Lewis bases and acids involved. Furthermore, FLPs have been explored for their potential in electrochemical reduction reactions, particularly for the selective activation of carbon dioxide. Overall, FLPs have emerged as versatile catalysts with applications in hydrogenation, copolymerization, and electrochemical reduction reactions.
How does acetic acid reactivity as a catalyst in the bromination of valine contribute to electrophilic substitution chemical reactions?1 answersAcetic acid, as a catalyst in the bromination of valine, contributes to electrophilic substitution chemical reactions by providing a Lewis acid catalysis effect. The use of acetic acid as a catalyst allows for alternative procedures in electrophilic aromatic substitution reactions, such as bromination, without the need for traditional Lewis acid catalysts like aluminium chloride. Acetic acid can act as a Lewis acid by accepting electron pairs from the valine molecule, facilitating the formation of a bromonium ion intermediate. This intermediate can then undergo nucleophilic attack by bromide ions, leading to the substitution of a hydrogen atom with a bromine atom on the valine molecule. The reactivity of acetic acid as a catalyst in bromination reactions can be further enhanced by the presence of ortho-chloro-substituents, which promote direct p-orbital overlap between the chlorine atom and the incipient carbocation.