| 51. |
- Andersson, Viktor, 1983, et al.
(författare)
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Alkali-wall interactions in a laboratory-scale reactor for chemical looping combustion studies
- 2021
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Ingår i: Fuel Processing Technology. - : Elsevier BV. - 0378-3820 .- 1873-7188. ; 217
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Tidskriftsartikel (refereegranskat)abstract
- Alkali metal-containing compounds are readily released during thermal conversion of solid fuels, and may have both detrimental and beneficial effects on chemical looping combustion. Here, we characterize alkali interactions with the inner walls of a laboratory-scale reactor under oxidizing, reducing and inert conditions at temperatures up to 900 °C. KCl aerosol particles are continuously introduced to the stainless steel reactor and the alkali concentration is measured on-line with a surface ionization detector. Aerosol particles evaporate at temperatures above 500 °C and KCl molecules rapidly diffuse to the reactor wall. Up to 92% of the alkali reaching the wall below 700 °C remains adsorbed, while re-evaporation is important at higher temperatures, where up to 74% remains adsorbed. Transient changes in alkali concentration are observed during repeated redox cycles, which are associated with changes in chemical composition of the wall material. Metal oxides on the reactor wall are partially depleted under reducing conditions, which allow for the formation of a new potassium-rich phase that is stable in a reducing atmosphere, but not under inert conditions. The observed wall effects are concluded to be extensive and include major transient effects depending on gas composition, and the implications for laboratory studies and improved experimental methodology are discussed.
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| 52. |
- B. Erdal, Nejla, et al.
(författare)
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Green Strategy to Reduced Nanographene Oxide through Microwave Assisted Transformation of Cellulose
- 2018
-
Ingår i: ACS Sustainable Chemistry and Engineering. - : American Chemical Society (ACS). - 2168-0485. ; 6:1, s. 1245-1255
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Tidskriftsartikel (refereegranskat)abstract
- A green strategy for fabrication of biobased reduced nanographene oxide (r-nGO) was developed. Cellulose derived nanographene oxide (nGO) type carbon nanodots were reduced by microwave assisted hydrothermal treatment with superheated water alone or in the presence of caffeic acid (CA), a green reducing agent. The carbon nanodots, r-nGO and r-nGO-CA, obtained through the two different reaction routes without or with the added reducing agent, were characterized by multiple analytical techniques including FTIR, XPS, Raman, XRD, TGA, TEM, AFM, UV-vis, and DLS to confirm and evaluate the efficiency of the reduction reactions. A significant decrease in oxygen content accompanied by increased number of sp2 hybridized functional groups was confirmed in both cases. The synergistic effect of superheated water and reducing agent resulted in the highest C/O ratio and thermal stability, which also supported a more efficient reduction. Interesting optical properties were detected by fluorescence spectroscopy where nGO, r-nGO, and r-nGO-CA all displayed excitation dependent fluorescence behavior. r-nGO-CA and its precursor nGO were evaluated toward osteoblastic cells MG-63 and exhibited nontoxic behavior up to 200 μg mL-1, which gives promise for utilization in biomedical applications.
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| 53. |
- Chyrkin, Anton, 1984, et al.
(författare)
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Effect of Hydrogen on the Internal Oxidation of a Pd–Cr Alloy in Dual-Atmosphere Conditions
- 2022
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Ingår i: Oxidation of Metals. - : Springer Science and Business Media LLC. - 1573-4889 .- 0030-770X. ; 97:5-6, s. 527-538
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Tidskriftsartikel (refereegranskat)abstract
- The effect of hydrogen on oxygen permeability has been studied in a diluted Pd–Cr alloy in dual- and single- atmosphere conditions between 600 and 950 °C. The 0.3 mm thick Pd–1.5Cr foil was exposed in dry and humid air as well as in dual-atmosphere conditions, with one sample surface being exposed to air and one to hydrogen, as encountered in solid oxide fuel cells. At all temperatures, Cr oxidized internally forming internal oxidation zones which were measured in metallographic cross sections. Below 800 °C, an external layer of PdO formed on the surface decreasing the internal oxidation kinetics. No measurable effect of hydrogen on the internal oxidation of Cr in Pd has been detected.
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| 54. |
- Gagliani, Luca, 1991, et al.
(författare)
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The Influence of Humidity Content on Ferritic Stainless Steels Used in Solid Oxide Fuel Cell under Dual Atmosphere Conditions at 600 C
- 2021
-
Ingår i: ECS Transactions. - : The Electrochemical Society. - 1938-5862 .- 1938-6737. ; 103:1, s. 1809-1815
-
Konferensbidrag (refereegranskat)abstract
- In Solid Oxide Fuel Cells (SOFC), interconnects are simultaneously exposed to dual atmosphere conditions in a range of temperature between 600 and 900 C. The presence of dissolved hydrogen in the steel can cause accelerated corrosion on the side exposed to air compared to exposures in air only. Moreover, the interconnect is subject to different humidity levels on the fuel side depending on fuel utilization. It has been already observed that a protective layer of chromia (Cr2O3) at the fuel side can mitigate the dual effect at the airside acting as a barrier for hydrogen permeation into the material. In this work, AISI 441 and Crofer 22 APU samples were exposed to dual atmosphere at 600 C under controlled humidity levels at the fuel side (20% vs. dry). Analysis performed showed how the humidity content on the fuel side largely affects the breakaway corrosion of the samples at the airside.
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| 55. |
- 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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| 56. |
- Ghavidel, Amir, et al.
(författare)
-
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
-
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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| 57. |
- Goebel, Claudia, 1988
(författare)
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Corrosion of Ferritic Stainless Steels Used in Solid Oxide Fuel Cells
- 2018
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Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Solid oxide fuel cells (SOFC) are energy conversion systems with clean emissions (depending on the fuel used) and high electrical efficiencies, which could potentially replace conventional conversion systems such as combustion engines. However, other issues, such as high costs and limited lifetime, must be resolved before widespread commercialization of SOFCs can be achieved. One of the major cost factors and the component that reduces the lifetime of SOFCs immensely, is the interconnect, which electrically connects multiple fuel cells to form a stack. Interconnects are typically made of ferritic stainless steels, and, due to high temperatures (600 °C – 900 °C) and the aggressive environments prevalent in fuel cells, the interconnects corrode over time. The protective Cr2O3 that forms on ferritic stainless steels at high temperatures mitigates the corrosion process to a certain extent. However, this oxide layer leads to two other issues: (i) vaporization of hexavalent Cr species, which leads to cathode poisoning and (ii) an increase in the electrical resistance of the interconnect caused by a continuously growing oxide layer. Both these problems can be reduced to a certain extent with coatings. Especially spinel coatings have been proven highly effective at decreasing Cr-evaporation. The first part of this work examines the influence of the Co3O4 spinel coating on area specific resistance (ASR). It was found that the Co3O4 thickness of Crofer 22 APU, which was exposed in air for 500 h at 600 °C, did not significantly impact the ASR, and, instead, the main contributor to overall resistance was the thermally grown Cr2O3. The second part of this work focuses on the long-term stability of Ce/Co-coated (10 nm Ce/640 nm Co) AISI 441. Coated AISI 441 was exposed by AB Sandvik Materials Technology for up to 37 000 hours at 800 °C in laboratory air. Subsequent analysis showed very low Cr-evaporation rates compared to uncoated AISI 441, and ASR values below 40 mΩcm2, suggesting that, under these conditions, the coating is effective in reducing Cr-evaporation rates and Cr2O3-growth rates even after long exposure times. The last part of the work analyzes the influence of pre-oxidation on the dual atmosphere effect at 600 °C with regard to two parameters: the pre-oxidation time and the pre-oxidation location. It was demonstrated that longer pre-oxidation times for AISI 441 result in extended resistance against dual atmosphere corrosion on the air-facing side. It was also found that the pre-oxidation layer on the hydrogen-facing side is more important for corrosion resistance in dual atmosphere than the pre-oxidation layer on the air-facing side.
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| 58. |
- Lehmusto, Juho, et al.
(författare)
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Should the oxygen source be considered in the initiation of KCl-induced high-temperature corrosion?
- 2021
-
Ingår i: Corrosion Science. - : Elsevier BV. - 0010-938X. ; 183
-
Tidskriftsartikel (refereegranskat)abstract
- The role of two oxygen sources, oxygen and water vapor, in the initiation of KCl-induced high-temperature corrosion was addressed by studying two high-alloyed commercial materials at 550 °C. The differentiation between the two oxygen sources was implemented with 18O-enriched water and 16O2. Based on the results, the solid-solid reaction between KCl(s) and the protective oxide on the alloy surface appeared to be more responsible for corrosion than the gas-solid reaction between KCl(g) and the protective oxide. Water was more involved in the abovementioned reactions than O2: 18O was the main oxygen isotope found in the formed surface oxides and intermediates.
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| 59. |
- 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
-
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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| 60. |
- 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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