| 1. |
- Jogi, Ramakrishna, et al.
(författare)
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Understanding the formation of phenolic monomers during fractionation of birch wood under supercritical ethanol over iron based catalysts
- 2020
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Ingår i: Journal of the Energy Institute. - : Elsevier. - 1743-9671 .- 1746-0220. ; 93:5, s. 2055-2062
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Tidskriftsartikel (refereegranskat)abstract
- The liquefaction of biomass in ethanol, at the critical point, has high potential due to low temperature and pressure (243 °C, 63 bar) when compared with water (374 °C, 220 bar). The current study deals with the fractionation of birch wood powder which was liquefied under supercritical ethanol over acidic or non-acidic catalysts, 5 wt % Fe-Beta-H-150 and 5 wt % Fe–SiO2, respectively. Based on the results, the reaction mechanism for the formation of lignin degradation products was proposed. The main phenolic product was isoeugenol over 5 wt % Fe-Beta-H-150 while intermediate products, i.e. such as coniferyl, and sinapyl alcohol, 4-propenyl syringol, syringaresinol, as well as syringyldehyde reacted rapidly further. The thermodynamic analysis was performed by Joback approach and using Gibbs-Helmholtz equation supporting the obtained results.
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| 2. |
- Mukesh, Chandrakant, et al.
(författare)
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Production of C-14 Levulinate Ester from Glucose Fermentation Liquors Catalyzed by Acidic Ionic Liquids in a Solvent-Free Self-Biphasic System
- 2020
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Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 5:10, s. 4828-4835
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Tidskriftsartikel (refereegranskat)abstract
- Herein, we present the C-14 levulinate ester of 2,3-butanediol as the product of sugar fermentation liquors. The designed Brønsted acidic ionic liquid (BAIL) catalysts enable self-induced phase separation with ester products, and the role of anions has been investigated. Esterification reactions were carried out by 2,3-butanediol (2,3-BDO) and levulinic acid in solvent-free media and low temperatures (60–105 °C). For comparison, sulfuric acid, amberlite IR-120, and sulfonic acid-functionalized pyridinium ionic liquids with different anions were utilized as a catalyst upon esterification reaction. The diester product, namely, butane-2,3-diyl bis(4-oxopentanoate), was formed with a good yield (85%) and selectivity (85%) after complete conversion of 2,3-BDO in 24 h at 80 °C. The low yield (8%) of the monoester was observed. The monoester and diester were separated by a liquid–liquid extraction method. The ester products were characterized by various instrumental techniques such as 1H and 13C NMR, GC–FID, LC–MS, and FT-IR spectroscopy. The Hammett acidity functions of BAILs were determined from UV–vis spectroscopy. The catalyst was successfully recycled and reused in the processes. The spent BAILs were reused in six consecutive cycles with only a ∼7% diminished diester yield and selectivity. The produced levulinate ester will be useful as biofuel additives, solvents, plasticizers, and other applications.
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| 3. |
- Wang, Kai, et al.
(författare)
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A one-carbon chemicals conversion strategy to produce precursor of biofuels with Saccharomyces cerevisiae
- 2023
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Ingår i: Renewable Energy. - : Elsevier BV. - 0960-1481 .- 1879-0682. ; 208, s. 331-340
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Tidskriftsartikel (refereegranskat)abstract
- Utilization of one-carbon chemicals such as CO2, formate, and methanol by microorganisms can enable the sustainable production of fuels and chemicals. However, the low conversion efficiency of these chemicals by microorganisms is a major challenge. To address this, we designed a one-carbon strategy that can utilize CO2 and its derivative formate. Here, a platform yeast strain with improved formate utilization and NAD(P)H production was constructed and evaluated for its ability to produce free fatty acids (FFAs). Based on 13C-marked analysis, the one-carbon assimilation efficiency of the platform strain reached 11.24%. Through continuous optimization, under conditions of glucose feeding the formate utilization rate of the final strain reached 0.48 g/L/h, with the final titer of FFAs reached 10.1 g/L, which represented improvements of 21.8 times and 33.7 times, respectively. As such, the produced FFAs can be easily transformed into biodiesel by combining them with downstream technologies in future research.
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| 4. |
- Yahia, Mohamed, et al.
(författare)
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Effect of incorporating different ZIF-8 crystal sizes in the polymer of intrinsic microporosity, PIM-1, for CO2/CH4 separation
- 2021
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Ingår i: Microporous and Mesoporous Materials. - : Elsevier. - 1387-1811 .- 1873-3093. ; 312
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Tidskriftsartikel (refereegranskat)abstract
- Effective and economical carbon dioxide-methane separation (CO2/CH4) is highly desirable in several industries such as sweetening natural gases and renewable natural gas (RNG) from biogas and landfills. Among the different separation technologies, membrane separation has been shown to have lower cost of production and lower CH4 losses. In this study, Zeolitic Imidazole Frameworks (ZIF-8) crystals with sizes varying from 45 nm to 450 nm were synthesized and incorporated in the polymer of intrinsic microporosity, PIM-1, to form mixed matrix membranes (MMMs). The structure, morphology, and physicochemical properties of the MMMs were characterized by 1H NMR, FTIR, XRD, TGA, and SEM. ZIF-8 crystal size was controlled using the concentration of sodium formate. The influence of the ZIF-8 crystal size on MMMs was studied by sorption, gas permeability, and aging of the membranes. The MMMs with ZIF-8 crystals of 120 nm particle diameter yielded the greatest improvement in gas transport properties; the CO2/CH4 selectivity-CO2 permeability was 11.4 and 9700 Barrer compared to PIM-1 with 6.4 and 9300 Barrer respectively. The former is near the Robeson 2008 upper bound, while PIM-1 is on the 1991 upper bound. After 40 days of aging, selectivity increased and permeability decreased; the changes were parallel to the Robeson upper bounds indicating increased polymer packing and diffusivity selectivity.
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| 5. |
- Balachandran, Srija, et al.
(författare)
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Comparative study for selective lithium recovery via chemical transformations during incineration and dynamic pyrolysis of EV li-ion batteries
- 2021
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Ingår i: Metals. - : MDPI AG. - 2075-4701. ; 11:8
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Tidskriftsartikel (refereegranskat)abstract
- Selective leaching of Li from spent LIBs thermally pretreated by pyrolysis and incineration between 400 and 700 °C for 30, 60, and 90 min followed by water leaching at high temperature and high L/S ratio was examined. During the thermal pretreatment Li2CO3 and LiF were leached. Along with Li salts, AlF3 was also found to be leached with an efficiency not higher than 3.5%. The time of thermal pretreatment did not have a significant effect on Li leaching efficiency. The leaching efficiency of Li was higher with a higher L/S ratio. At a higher leaching temperature (80 °C), the leaching of Li was higher due to an increase in the solubility of present Li salts. The highest Li leaching efficiency of nearly 60% was observed from the sample pyrolyzed at 700 °C for 60 min under the leaching condition L/S ratio of 20:1 mL g−1 at 80 °C for 3 h. Furthermore, the use of an excess of 10% of carbon in a form of graphite during the thermal treatment did not improve the leaching efficiency of Li.
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| 6. |
- Ahlbom, Anders, 1993, et al.
(författare)
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Towards understanding kraft lignin depolymerisation under hydrothermal conditions
- 2021
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Ingår i: Holzforschung. - : Walter de Gruyter GmbH. - 1437-434X .- 0018-3830. ; 76:1, s. 37-48
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Tidskriftsartikel (refereegranskat)abstract
- Kraft lignin depolymerisation using hydrothermal liquefaction suffers from the formation of char, resulting in a decreased product yield as well as causing operational problems. While this may be mitigated by the addition of capping agents such as phenol and isopropanol, other reaction parameters, for example reaction time and temperature, are also important for the product yields. In this work, the effect of short reaction times on the hydrothermal liquefaction of kraft lignin in an alkaline water and isopropanol mixture was investigated at 1-12 min and 290 °C. The results show that there were swift initial reactions: the major ether bonds in the lignin were broken within the first minute of reaction, and the molecular weight of all product fractions was halved at the very least. Longer reaction times, however, do not cause as pronounced structural changes as the initial reaction, indicating that a recalcitrant carbon-carbon skeleton remained in the products. Nevertheless, the yields of both char and monomers increased slowly with increasing reaction time. The swift initial depolymerising reactions were therefore followed by slower repolymerisation as well as a slow formation of monomers and dimers, which calls for careful tuning of the reaction time.
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| 7. |
- Ghaffari, Roujin, 1994, et al.
(författare)
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Effect of alkalinity on the diffusion of solvent-fractionated lignin through cellulose membranes
- 2023
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Ingår i: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 30:6, s. 3685-3698
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Tidskriftsartikel (refereegranskat)abstract
- Mass transport of liberated lignin fragments from pits and fiber walls into black liquor is considered a determining step in the delignification process. However, our current understanding of the diffusion of lignin through cellulose and the influential parameter on this process is very limited. A comprehensive and detailed study of lignin mass transport through cellulosic materials is, therefore, of great importance. In this study, diffusion cell methodology is implemented to systematically investigate the transport of fractionated kraft lignin molecules through model cellulose membranes. Pulping is a complex process and lignin is very heterogenous material therefore to perform a more detailed study on lignin diffusion, we included an additional solvent fractionation step. One of the benefits of this method is that the setup can be adjusted to various experimental conditions allowing the complex chemical reactions occurring during pulping, which would affect the mass transfer of lignin, to be avoided. Here, the effects of the alkalinity of the aqueous solution and molecular weight of the kraft lignin molecules on their diffusion were investigated. Additionally, NMR spectroscopy, size exclusion chromatography, and UV/Vis spectroscopy were used to characterize the starting material and the molecules that passed through the membrane. Lignin molecules detected in the acceptor chamber of the diffusion cells had lower molecular weights, indicating a size fractionation between the donor and acceptor chamber. UV/Vis showed higher concentrations of ionized conjugated kraft lignin molecules in the acceptor chamber, which is a sign of chemical fractionation. This study suggests that the diffusion of lignin through small cellulose pores can be enhanced by decreasing the average molecular weight of the diffusing kraft lignin molecules and increasing alkalinity.
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| 8. |
- Ghavidel, Amir, et al.
(författare)
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Comparison of chemical compositions in wood and bark of Persian silk tree (Albizia julibrissin Durazz)
- 2022
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Ingår i: Wood Material Science & Engineering. - : Taylor & Francis. - 1748-0272 .- 1748-0280. ; 17:6, s. 759-770
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Tidskriftsartikel (refereegranskat)abstract
- This research was conducted to identify and compare the chemical compositions in Persian silk tree(Albizia julibrissin Durazz.) from different parts of wood and bark, using Fourier Transform Infrared(FTIR) Spectroscopy, gas and liquid chromatography coupled to mass spectrometry (GC-MS, LCMS),and elemental analysis. FTIR analysis showed significant differences in the chemical structureof bark and wood at peaks that belong to the cellulose and hemicelluloses. According to theresults, the C-O-C asymmetric stretch vibration in cellulose and hemicelluloses peak of Persian silktree was lower in the bark and ѵC=O in quinone or p-quinone peak was higher in the bark. Theresults of GC-MS showed 12 chemical constituents in the bark and 43 in the wood, respectively.Among these, hexadecanoic acid and inositol were in common. According to the LC-MS analyses,bark samples were rich in lignan compositions and triterpenoid saponins, whereas wood was poorin these compositions. Altogether 61 compositions have been tentatively identified and describedfrom bark and wood tissues; many of them were identified for the first time. Energy-dispersive Xray(EDX) spectrometry illustrated that the bark contained iron and aluminium, sodium,phosphorus, sulphur and chlorine, while these elements did not exist in wood.
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| 9. |
- Liu, Jun, et al.
(författare)
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FShrinkage behaviour, early hydration and hardened properties of sodium silicate activated slag incorporated with gypsum and cement
- 2020
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Ingår i: Construction and Building Materials. - : Elsevier BV. - 0950-0618. ; 248
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Tidskriftsartikel (refereegranskat)abstract
- As a novel low carbon cementitious material, alkali-activated slag (AAS) attracted many researchers’ interests, not only because of its environmental benefits, but also some superior properties than Portland cement (PC). Due to different chemical reactions of AAS, gypsum, a commonly used expansive agent in PC, exhibits a different behaviour in AAS. This paper reports the investigation on the shrinkage behaviour of sodium silicate activated slag (SSAS) incorporated with gypsum and PC. In addition, the early properties, including setting time and early hydration products, were determined by Vicat apparatus, XRD and TG. The hardened properties, namely flexural and compressive strength, were investigated as well. The results showed that, by incorporating gypsum and PC, the drying shrinkage of SSAS could be significantly reduced because of the formation of expansive sulfate-rich and calcium-rich hydration products in terms of ettringite and Portlandite. The initial setting was delayed by blending PC, although adding gypsum accelerated the hydration of SSAS. The addition of gypsum and blend with 20% PC slightly increased flexural and compressive strengths of SSAS at 7 days and 28 days. © 2020 Elsevier Ltd
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| 10. |
- Martinsson, Axel, 1992, et al.
(författare)
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The influence of transition metal ions on the oxidation of kraft pulp using hydrogen peroxide under mildly acidic conditions
- 2023
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Ingår i: Holzforschung. - : Walter de Gruyter GmbH. - 1437-434X .- 0018-3830. ; 77:5, s. 318-325
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Tidskriftsartikel (refereegranskat)abstract
- Oxidation of kraft pulp using hydrogen peroxide under mild acidic conditions can be applied in order to obtain new functionality of the fibres, in the form of carbonyl groups. The hydrogen peroxide concentration must, however, be higher than consumed by the oxidation reactions meaning that the liquid must be recirculated to fully utilize the hydrogen peroxide. This paper investigates the consequences of recirculation of the oxidation liquor. It was found that recirculation results in an accumulation of ions of transition metals (copper, iron and manganese) in the oxidation liquor. The transition metal ions are known for catalytic decomposition of hydrogen peroxide, producing radicals which may react with carbohydrates, forming carbonyl groups as well as causing carbohydrate degradation. This was confirmed through the recirculation of oxidation liquor as well as through controlled addition of transition metals. At high transition metal ion concentration the reactions were fast and a severe degradation of carbohydrates was observed, accompanied by a rapid hydrogen peroxide consumption. The consequence of this, in an industrial context, is that the concentration of metal ions must be carefully controlled in order to add functionality to the cellulose without causing excessive degradation of carbohydrates or consumption of hydrogen peroxide.
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