Graphene Oxide Membrane Reactor for Electrochemical Deuteration Reactions.

The deuteration of organic molecules is considerably important in organic and medicinal chemistry. An electrochemical membrane reactor using proton-conducting graphene oxide (GO) nanosheets was developed to synthesize valuable deuterium-labeled products via an efficient hydrogen-to-deuterium (H/D) exchange under mild conditions at ambient temperature and atmospheric pressure. Deuterons (D+) formed by the anodic oxidation of heavy water (D2O) at the Pt/C anode permeate through the GO membrane to the Pt/C cathode, where organic molecules with functional groups (C≡C and C═O) are deuterated with adsorbed atomic D species. Deuteration occurs in outstanding yields with high levels of D incorporation. We also achieved the electrodeuteration of a drug molecule, ibuprofen, demonstrating the promising feasibility of the GO membrane reactor in the pharmaceutical industry.

Energy Application of Graphene Based Membrane: Hydrogen Separation.

Hydrogen gas (H2 ) is a viable energy carrier that has the potential to replace the traditional fossil fuels and contribute to achieving zero net emissions, making it an attractive option for a hydrogen-based society. However, current H2 purification technologies are often limited by high energy consumption, and as a result, there is a growing demand for alternative techniques that offer higher H2 purity and energy efficiency. Membrane separation has emerged as a promising approach for obtaining high-purity H2 gas with low energy consumption. Nevertheless, despite years of development, commercial polymeric membranes have limited performance, prompting researchers to explore alternative materials. In this context, carbon-based membranes, specifically graphene-based nanomaterials, have gained significant attention as potential membrane materials due to their unique properties. In this review, we provide a comprehensive overview of carbon-based membranes for H2 gas separation, fabrication of the membrane, and its characterization, including their advantages and limitations. We also explore the current technological challenges and suggest insights into future research directions, highlighting potential ways to improve graphene-based membranes performance for H2 separations.

Selective Detection of CO Using Proton-Conducting Graphene Oxide Membranes with Pt-Doped SnO2 Electrocatalysts: Mechanistic Study by Operando DRIFTS.

To reduce the risk of carbon monoxide (CO) poisoning, there is a strong need for small, compact gas sensors to detect and monitor CO at ppm concentrations. In this study, we focused on detecting CO with electrochemical sensors based on proton-conducting graphene oxide (GO) nanosheets at room temperature. We found that a Ce-doped GO nanosheet membrane fitted with the sensing electrode composed of Pt (10 wt %)-doped SnO2 nanocrystals exhibits an excellent sensor response to CO at 25 °C. Pt doping of SnO2 nanocrystals has made it possible to detect CO more selectively than H2 and ethanol. The CO detection mechanism is analyzed by operando diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), Fourier transform infrared gas cell measurements, and comprehensive density functional theory-based calculations. The results revealed that adsorption of CO occurs predominantly on Pt sites, and the adsorbed CO is anodically oxidized at the interface between the sensing electrode and proton-conducting membrane, generating the selective sensor response. The strong adsorption of CO was realized with Pt (10 wt %)-doped SnO2 nanocrystals, as revealed by the DRIFTS analysis and temperature-programed desorption technique.

Bandgap Engineering of Melon using Highly Reduced Graphene Oxide for Enhanced Photoelectrochemical Hydrogen Evolution.

The uncondensed form of polymeric carbon nitrides (PCN), generally known as melon, is a stacked 2D structure of poly(aminoimino)heptazine. Melon is used as a photocatalyst in solar energy conversion applications, but suffers from poor photoconversion efficiency due to weak optical absorption in the visible spectrum, high activation energy, and inefficient separation of photoexcited charge carriers. Experimental and theoretical studies are reported to engineer the bandgap of melon with highly reduced graphene oxide (HRG). Three HRG@melon nanocomposites with different HRG:melon ratios (0.5%, 1%, and 2%) are prepared. The 1% HRG@melon nanocomposite shows higher photocurrent density (71 µA cm-2 ) than melon (24 µA cm-2 ) in alkaline conditions. The addition of a hole scavenger further increases the photocurrent density to 630 µA cm-2 relative to the reversible hydrogen electrode (RHE). These experimental results are validated by calculations using density functional theory (DFT), which revealed that HRG results in a significant charge redistribution and an improved photocatalytic hydrogen evolution reaction (HER).

Single Crystallization of Cs4PbBr6 Perovskite from Supersaturated Organic Solutions Optimized Through Solubility Studies.

We demonstrate the fabrication of millimeter-sized single crystals of 0D-Cs4PbBr6 grown in a supersaturated solution consisting of organic solvents without HBr (aq). One of the precursors, CsBr, was dissolved in ethylene glycol (EG) mixed with dimethyl sulfoxide, which is a good solvent for the other precursor, PbBr2. At a solvent ratio of 20 vol % EG, the solubility of cesium bromide decreased and the title compound, Cs4PbBr6, was selectively formed, whereas, with an EG ratio of 80 vol %, 3D-CsPbBr3 was formed. A phase diagram (solubility curve) of Cs4PbBr6 in the mixed solvent containing 20 vol % EG was obtained by visually observing dissolution and crystal precipitation while changing the temperature. Because the solubility was proportional to the temperature, the solubility curve demonstrated an upper critical solution phenomenon. The solubility near the boiling point of the solution (150 °C) was approximately 0.14 M. A single crystal of Cs4PbBr6 was formed by growing a seed crystal in a supersaturated solution on the low-temperature side of the solubility curve. X-ray analysis established the crystal structure; a fluorescence emission at 520 nm with a full width at half maximum of 20 nm confirms the composition of the single crystal to be Cs4PbBr6.

Fast and selective production of quercetin and saccharides from rutin using microwave-assisted hydrothermal treatment in the presence of graphene oxide.

Rutin is a flavonoid glycoside, well-known for its antioxidant, anticarcinogenic, and cardioprotective properties. However, it exhibits lower bio absorptivity and bioactivity than its aglycon form, quercetin. Although liquid acid catalysts are conventionally utilized to obtain quercetin via rutin hydrolysis, the neutralization procedure is a major disadvantage owing to the added cost. In this study, graphene oxide (GO) was used as an alternative catalyst under microwave (MW) irradiation, owing to its easy separation from the reaction solution and high MW absorptivity, resulting in improved thermal efficiency. Two types of GOs were prepared (GO-HU using Hummer's method and GO-TO using Tour's method), and their catalytic performance for rutin hydrolysis was evaluated and compared. The highest rutin conversion (98.8 %) and quercetin yield (81.9 %) were obtained at 180 °C when the reaction was conducted for 15 min using 3 mg of GO-TO and 2400 ppm of initial rutin concentration in 50 mL of water.

Light-Stimulated Luminescence Control of Lead Halide-Based Perovskite Nanocrystals Coupled with Photochromic Molecules via Electron and Energy Transfer.

Photoswitchable nanomaterials are key materials in the development of advanced imaging techniques, such as super-resolution fluorescence microscopy. The combination of perovskite CsPbBr3 nanocrystals (NCs) with bright photoluminescence (PL) emission and diarylethenes (DAEs) with structural changes in response to ultraviolet (UV) and visible light is a promising candidate system. Herein, CsPbBr3 NCs are coupled with photochromic DAE molecules to control the PL emission from the NCs by light stimulation. The PL emission is successfully switched ON and OFF by alternating UV and visible light irradiation. Time-resolved PL emission studies suggest that Förster resonance energy transfer from CsPbBr3 NCs to the closed-ring form of DAE occurs after UV irradiation, and the PL emission is quenched. Upon visible-light irradiation, DAE is converted to the open-ring isomer, and the PL emission is restored. Femtosecond pump-probe spectroscopy reveals that light stimulation induces not only energy transfer but also photoinduced electron transfer in the NC-DAE pair on the picosecond timescale to form DAE radicals. Thus, it is suggested that the holes residing in the NCs react with the NCs, degrading the PL emission. Stable PL switching is realized using 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) as a hole scavenger to avoid the reaction between the holes and NCs.

Study on Sensing Mechanism of Volatile Organic Compounds Using Pt-Loaded ZnO Nanocrystals.

Understanding the surface chemistry of target gases on sensing materials is essential for designing high-performance gas sensors. Here, we report the effect of Pt-loading on the sensing of volatile organic compounds (VOCs) with ZnO gas sensors, demonstrated by diffuse reflection infrared Fourier transform (DRIFT) spectroscopy. Pt-loaded ZnO nanocrystals (NCs) of 13~22 nm are synthesized using the hot soap method. The synthesized powder is deposited on an alumina substrate by screen-printing to form a particulate gas sensing film. The 0.1 wt% Pt-loaded ZnO NC sensor shows the highest sensor response to acetone and ethanol at 350 °C, while the responses to CO and H2 are small and exhibit good selectivity to VOCs. The gas sensing mechanism of ethanol with Pt-ZnO NCs was studied by in situ DRIFT spectroscopy combined with online FT-IR gas analysis. The results show that ethanol reacts with small Pt-loaded ZnO to produce intermediate species such as acetaldehyde, acetate, and carbonate, which generates a high sensor response to ethanol in air.

Nano-pulsed discharge plasma-induced abiotic oligopeptide formation from diketopiperazine.

Conventional oligopeptide synthesis techniques involve environmentally harmful procedures and materials. In addition, the efficient accumulation of oligopeptides under Hadean Earth environments regarding the origin of life remains still unclear. In these processes, the formation of diketopiperazine is a big issue due to the strong inhibition for further elongation beyond dipeptides. Hydrothermal media enables environmentally friendly oligopeptide synthesis. However, hydrothermal oligopeptide synthesis produces large amounts of diketopiperazine (DKP), due to its thermodynamic stability. DKP inhibits dipeptide elongation and also constitutes an inhibitory pathway in conventional oligopeptide synthesis. Here, we show an efficient pathway for oligopeptide formation using a specially designed experimental setup to run both thermal and non-thermal discharge plasma, generated by nano-pulsed electric discharge with 16-23 kV voltage and 300-430 A current within ca. 500 ns. DKP (14%) was converted to dipeptides and higher oligopeptides in an aqueous solution containing alanine-DKP at pH 4.5, after 20 min of 50 pps thermal plasma irradiation. This is the first study to report efficient oligopeptide synthesis in aqueous medium using nano-pulsed plasma (with thermal plasma being more efficient than non-thermal plasma) via DKP ring-opening. This unexpected finding is implicative to evaluate the pathway how the oligopeptides could have accumulated in the primitive Earth with high-energy plasma sources such as thunder as well as to facilitate the green synthesis of oligopeptides.

Electrochemical Detection of Ethanol in Air Using Graphene Oxide Nanosheets Combined with Au-WO3.

Detection, monitoring, and analysis of ethanol are important in various fields such as health care, food industries, and safety control. In this study, we report that a solid electrolyte gas sensor based on a proton-conducting membrane is promising for detecting ethanol in air. We focused on graphene oxide (GO) as a new solid electrolyte because it shows a high proton conductivity at room temperature. GO nanosheets are synthesized by oxidation and exfoliation of expanded graphite via the Tour's method. GO membranes are fabricated by stacking GO nanosheets by vacuum filtration. To detect ethanol, Au-loaded WO3 is used as the sensing electrode due to the excellent activity of gold nanoparticles for the catalysis of organic molecules. Au-WO3 is coupled with rGO (reduced graphene oxide) to facilitate the electron transport in the electrode. Ce ions are intercalated into the GO membrane to facilitate proton transport. The sensor based on the Ce doped-GO membrane combined with Au-WO3/rGO as a sensing electrode shows good electric potential difference (ΔV) responses to ethanol in the air at room temperature. The sensor signal reaches more than 600 mV in response to ethanol at 40 ppm in air, making it possible to detect ethanol at a few ppb (parts per billion) level. The ethanol sensing mechanism was discussed in terms of the mixed-potential theory and catalysis of ethanol on Au-WO3.

Facile and Green Fabrication of Microwave-Assisted Reduced Graphene Oxide/Titanium Dioxide Nanocomposites as Photocatalysts for Rhodamine 6G Degradation.

Organic pollutants, such as synthetic dyes, are treated to prevent them from contaminating natural water sources. One of the treatment methods is advanced oxidation process using a photocatalyst material as the active agent. However, many photocatalysts are hindered by their production cost and efficiency. In this study, nanocomposites consisting of reduced graphene oxide and titanium dioxide (rGO/TiO2) were prepared by a simple and green approach using the microwave-assisted method, and we utilized a graphene oxide (GO) precursor that was fabricated through the Tour method. The ratios of rGO/TiO2 in nanocomposites were varied (2:1, 1:1, and 1:2) to know the influence of rGO on the photocatalytic performance of the nanocomposites for rhodamine 6G degradation. Transmission electron microscopy (TEM) observation revealed that a transparent particle with a sheetlike morphology was detected in the rGO sample, suggesting that a very thin film of a few layers of GO or rGO was successfully formed. Based on scanning electron microscopy (SEM) observation, the rGO/TiO2 nanocomposites had a wrinkled and layered rGO structure decorated by TiO2 nanoparticles with average diameters of 125.9 ± 40.6 nm, implying that rGO layers are able to prevent TiO2 from agglomeration. The synthesized product contained only rGO and TiO2 in the anatase form without impurities that were proven by Raman spectra and X-ray diffraction (XRD). The nanocomposite with rGO/TiO2 ratio 1:2 (composite C) was found to be the best composition in this study, and it was able to degrade 82.9 ± 2.4% of the rhodamine 6G after UV irradiation for 4 h. Based on a time-resolved photoluminescence study at wavelength emission 500 nm, the average decay lifetime of R6G-rGO/TiO2 composites (2.91 ns) was found to be longer than that of the R6G-TiO2 sample (2.05 ns), implying that the presence of rGO in rGO/TiO2 composites successfully suppressed the electron-hole recombination process in TiO2 and significantly improved their photocatalytic performance. This study showed that the rGO/TiO2 nanocomposites synthesized through relatively simple and eco-friendly processes display promising prospects for photocatalytic degradation of dyes and other recalcitrant pollutants in a water stream.

Synergizing Sulfonated Hydrothermal Carbon and Microwave Irradiation for Intensified Esterification Reaction.

The synergy of sulfonated hydrothermal carbon and microwave (MW) irradiation was applied for the esterification of oleic acid with methanol (MeOH) to produce biodiesel. The effects of temperature, reaction time, ratio of oleic acid to methanol, and catalyst loading were investigated at a fixed MW power of 400 W. The addition of hexane, serving as a co-solvent and separator, was also investigated. The optimum conditions for the proposed process were oleic acid-to-methanol molar ratio of 1:5 and hexane-to-methanol ratio of 0.5 (v/v) in the presence of a 5 wt % catalyst, at 100 °C for 60 min, obtaining a 97% yield of oleic acid methyl ester. The addition of slight amounts of hexane resulted into an eightfold reduction in the amount of MeOH needed to obtain a yield above 90%, which normally required a MeOH-to-oil ratio of 40:1. This proposed novel approach could provide a more cost-effective method for the esterification of oil to produce biodiesel, that is, reactive separation utilizing carbon-based catalysts under MW irradiation.

Biogasoline production from linoleic acid via catalytic cracking over nickel and copper-doped ZSM-5 catalysts.

Catalytic cracking of vegetable oil mainly processed over zeolites, and among all the zeolites particularly HZMS-5 has been investigated on wide range for renewable and clean gasoline production from various plant oils. Despite the fact that HZSM-5 offers a higher conversion degree and boost aromatics yield, the isomerate yield reduces due to high cracking activity and shape selectivity of HZSM-5. Hence, to overcome these problems, in this study the transition metals, such as nickel and copper doped over HZSM-5 were tested for its efficiencies to improve the isoparaffin compounds. The catalysts were screened with linoleic acid in a catalytic cracking reaction conducted at 450 ᵒC for 90 min in an atmospheric condition in batch reactor. Then, the gasoline composition of the organic liquid product (OLP) was analysed in terms of paraffin, isoparaffin, olefin, naphthenes and aromatics (PIONA). The results showed that Cu/ZSM-5 produced the highest liquid yield of 79.1%, at the same time reduced the production of gas and coke to 18.8% and 0.7%. Furthermore, the desired isoparaffin composition in biogasoline increased from 1.6% to 6.8% and at the same time reduced the oxygenated and aromatic compounds to 15.4% and 59.7%, respectively. The linoleic acid as model compound of rubber seed oil, in the catalytic cracking reaction provides a clearer understanding of the process. Besides, the water gas shift (WGS) reaction in catalytic cracking reaction provides insitu hydrogen production to saturate the branched olefin into the desired isoparaffin and the aromatics into naphthenes.

WO3-Based Gas Sensors: Identifying Inherent Qualities and Understanding the Sensing Mechanism.

Semiconducting metal oxide-based gas sensors are an attractive option for a wide array of applications. In particular, sensors based on WO3 are promising for applications varying from indoor air quality to breath analysis. There is a great breadth of literature which examines how the sensing characteristics of WO3 can be tuned via changes in, for example, morphology or surface additives. Because of variations in measurement conditions, however, it is difficult to identify inherent qualities of WO3 from these reports. Here, the sensing behavior of five different WO3 samples is examined. The samples show good complementarity to SnO2 (the most commonly used material)-based sensors. A surprising homogeneity, despite variation in morphology and preparation method, is found. Using operando diffuse reflectance infrared Fourier transform spectroscopy, it is found that the oxygen vacancies are the dominant reaction partner of WO3 with the analyte gas. This surface chemistry is offered as an explanation for the homogeneity of WO3-based sensors.

Role of alkan-1-ol solvents in the synthesis of yellow luminescent carbon quantum dots (CQDs): van der Waals force-caused aggregation and agglomeration.

Carbon quantum dots (CQDs; luminescent carbon nanoparticles, size < 10 nm) have attracted much attention with respect to their eco-friendliness and multi-functionality. The solvent-dependent photoluminescence of CQDs has been well investigated to optimize the synthesis process and homogeneous dispersion. Although some alkan-1-ol solvents, such as ethanol, have been well utilized empirically as good solvents when synthesizing highly photoluminescent CQDs, the role of alkan-1-ol solvents, particularly long-chain alkan-1-ols (e.g., 1-nonanol, 1-decanol), has not yet been clarified. Herein, we demonstrate a method for the synthesis of strongly yellow emitting CQDs using solvothermal treatment and elucidate the role of alkan-1-ol solvents in the photoluminescence of CQDs. These CQDs have been characterized using theoretical calculations, ex situ morphological observations using transmission electron microscopy (TEM) and dynamic light scattering (DLS), and 500 MHz 1H nuclear magnetic resonance (NMR) and 13C NMR spectroscopy. A comparative study of alkan-1-ol solvents suggests a mechanism for the agglomeration and aggregation of carbon precursors, intermediates, and CQDs, which is expected to lead to further synthesis studies on highly luminescent CQDs.

Reversible ON/OFF switching of photoluminescence from CsPbX3 quantum dots coated with silica using photochromic diarylethene.

Highly luminescent silica-coated CsPbX3 quantum dots (QDs) with good photostability were synthesized and coupled with photochromic diarylethene to modulate the QDs' photoluminescence (PL). Upon successive UV and visible light irradiation, the PL emission from the silica-coated CsPbX3 QDs was repeatedly quenched and restored, demonstrating the promising feasibility of the QD/diarylethene-based photoswitches.

Synthesis of Cu2O/CuO Nanocrystals and Their Application to H2S Sensing.

Semiconducting metal oxide nanocrystals are an important class of materials that have versatile applications because of their useful properties and high stability. Here, we developed a simple route to synthesize nanocrystals (NCs) of copper oxides such as Cu2O and CuO using a hot-soap method, and applied them to H2S sensing. Cu2O NCs were synthesized by simply heating a copper precursor in oleylamine in the presence of diol at 160 °C under an Ar flow. X-ray diffractometry (XRD), dynamic light scattering (DLS), and transmission electron microscopy (TEM) results indicated the formation of monodispersed Cu2O NCs having approximately 5 nm in crystallite size and 12 nm in colloidal size. The conversion of the Cu2O NCs to CuO NCs was undertaken by straightforward air oxidation at room temperature, as confirmed by XRD and UV-vis analyses. A thin film Cu2O NC sensor fabricated by spin coating showed responses to H2S in dilute concentrations (1⁻8 ppm) at 50⁻150 °C, but the stability was poor because of the formation of metallic Cu2S in a H2S atmosphere. We found that Pd loading improved the stability of the sensor response. The Pd-loaded Cu2O NC sensor exhibited reproducible responses to H2S at 200 °C. Based on the gas sensing mechanism, it is suggested that Pd loading facilitates the reaction of adsorbed oxygen with H2S and suppresses the irreversible formation of Cu2S.

Utilization of rice husk to enhance calcium oxide-based sorbent prepared from waste cockle shells for cyclic CO2 capture in high-temperature condition.

The CO2 capture capacity and cyclic stability of calcium oxide (CaO) prepared from cockle shells (CS) were enhanced by incorporating rice husk (RH) and binder through wet-mixing method. The cyclic reaction of calcination and carbonation was demonstrated using thermal gravimetric analyzer (TGA) which the calcination was performed in a pure N2 environment at 850 °C for 20 min and carbonation at 650 °C for 30 min in 20 vol% of CO2 in N2. The analysis using x-ray fluorescence (XRF) identified silica (Si) as the major elements in the sorbents. The RH-added sorbents also contained several types of metal elements such as which was a key factor to minimize the sintering of the sorbent during the cyclic reaction and contributed to higher CO2 capture capacity. The presence of various morphologies also associated with the improvement of the synthesized sorbents performance. The highest initial CO2 capture capacity was exhibited by CS+10%RH sorbent, which was 12% higher than the RH-free sorbent (CS). However, sorbents with the higher RH loading amount such as 40 and 50 wt% were preferred to maintain high capture capacity when the sorbents were regenerated and extended to the cyclic reaction. The sorbents also demonstrated the lowest average sorption decay, which suggested the most stable sorbent for cyclic-reaction. Once regenerated, the capture capacity of the RH-added sorbent was further increased by 12% when clay was added into the sorbent. Overall, the metal elements in RH and clay were possibly the key factor that enhances the performance of CaO prepared from CS, particularly for cyclic CO2 capture. Graphical abstract Cyclic calcination and carbonation reaction.

Production of gasoline range hydrocarbons from catalytic cracking of linoleic acid over various acidic zeolite catalysts.

Employment of edible oils as alternative green fuel for vehicles had raised debates on the sustainability of food supply especially in the third-world countries. The non-edible oil obtained from the abundantly available rubber seeds could mitigate this issue and at the same time reduce the environmental impact. Therefore, this paper investigates the catalytic cracking reaction of a model compound named linoleic acid that is enormously present in the rubber seed oil. Batch-scale experiments were conducted using 8.8 mL Inconel batch reactor having a cyclic horizontal swing span of 2 cm with a frequency of 60 cycles per minute at 450 °C under atmospheric condition for 90 min. The performance of HZSM-5, HBeta, HFerrierite, HMordenite and HY catalysts was tested for their efficiency in favouring gasoline range hydrocarbons. The compounds present in the organic liquid product were then analysed using GC-MS and classified based on PIONA which stands for paraffin, isoparaffin, olefin, naphthenes and aromatics respectively. The results obtained show that HZSM-5 catalyst favoured gasoline range hydrocarbons that were rich in aromatics compounds and promoted the production of desired isoparaffin. It also gave a higher cracking activity; however, large gaseous as by-products were produced at the same time.

Carbocatalysed hydrolytic cleaving of the glycosidic bond in fucoidan under microwave irradiation.

Biomass valorization involves breaking down naturally occurring long chain polysaccharides into their constituent monomers. The polysaccharide chain consists of monomers adjoined via C (carbon)-O (oxygen) glycosidic linkages that are typically cleaved via hydrolytic scission. In this study, we aimed to recover fucose from the polysaccharide fucoidan, which can be extracted from seaweed biomass. We investigated the depolymerisation behavior of fucoidan sourced from two different species of seaweeds, namely Undaria pinnatifida (F-UP) and Fucus vesiculosus (F-FV). Catalytic depolymerisation experiments were performed using four different carbon-based catalysts - graphene, multiwalled carbon nanotubes (MWCNT), graphene oxide (GO), and reduced graphene oxide (rGO) - under microwave (MW) irradiation. Our results showed that the depolymerisation of fucoidan was best achieved using GO, which was attributed to the abundance of oxygen functionalities on its surface. Furthermore, based on gel permeation chromatography analyses, the depolymerisation of fucoidan was found to follow a two-step process: (1) random scission leading to the production of short-chain oligosaccharides and (2) acid-catalysed hydrolysis of the oligosaccharides to fucose. Because of the longer chain length of F-UP (61 kDa), the highest fucose yield of 17.4% using this species was obtained at a higher temperature of 120 °C in a closed vessel. Meanwhile, in the case of F-FV (1.1 kDa), the highest yield of 54.0% was obtained under reflux conditions at a lower temperature of 104 °C. Our mechanistic study based on semi-empirical quantum calculations also revealed that the recovery of fucose from F-FV is more energetically favoured than from F-UP as a result of their structural differences.