| 11. |
- Maric, Jelena, 1983, et al.
(författare)
-
Valorization of Automobile Shredder Residue Using Indirect Gasification
- 2018
-
Ingår i: Energy & Fuels. - : American Chemical Society (ACS). - 1520-5029 .- 0887-0624. ; 32:12, s. 12795-12804
-
Tidskriftsartikel (refereegranskat)abstract
- Dual fluidized bed (DFB) gasification offers the possibility to convert solid fuels into a valuable gas, comprised of syngas, and hydrocarbons that can be readily handled in petrochemical units. DFB gasifiers are especially suitable for nonhomogeneous fuels, such as waste fractions. In this work, the possibility to use DFB gasification as a recycling/valorization method of automobile shredder residue is investigated. The gasification tests were carried out in the Chalmers 2–4 MWth gasifier over 4 days. The effects of ash on the gas and tar compositions, as well as on the activity of the bed inventory, were evaluated. The results show that 60% of the total carbon in the fuel can be recovered in the form of a permanent gas, whereby the produced gas contains 12%mol of C2–3 hydrocarbons. The tar levels measured in the produced gas were high, although it was clear that decomposition into monomer-like compounds occurred in the reactor, which resulted in the production of valuable petrochemical compounds, corresponding to 8–9% of the carbon in the feed. Using a higher operating temperature was found to be beneficial in terms of obtaining a higher gas yield, regardless of the level of ash enrichment in the system. The high ash levels in the fuel feed did not negatively affect the technical operation of the fluidized bed. Possible routes of carbon recovery are discussed.
|
|
| 12. |
- Mukesh, Chandrakant, et al.
(författare)
-
Production of C-14 Levulinate Ester from Glucose Fermentation Liquors Catalyzed by Acidic Ionic Liquids in a Solvent-Free Self-Biphasic System
- 2020
-
Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 5:10, s. 4828-4835
-
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.
|
|
| 13. |
- Wang, Kai, et al.
(författare)
-
A one-carbon chemicals conversion strategy to produce precursor of biofuels with Saccharomyces cerevisiae
- 2023
-
Ingår i: Renewable Energy. - : Elsevier BV. - 0960-1481 .- 1879-0682. ; 208, s. 331-340
-
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.
|
|
| 14. |
- Yahia, Mohamed, et al.
(författare)
-
Effect of incorporating different ZIF-8 crystal sizes in the polymer of intrinsic microporosity, PIM-1, for CO2/CH4 separation
- 2021
-
Ingår i: Microporous and Mesoporous Materials. - : Elsevier. - 1387-1811 .- 1873-3093. ; 312
-
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.
|
|
| 15. |
- Balachandran, Srija, et al.
(författare)
-
Comparative study for selective lithium recovery via chemical transformations during incineration and dynamic pyrolysis of EV li-ion batteries
- 2021
-
Ingår i: Metals. - : MDPI AG. - 2075-4701. ; 11:8
-
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.
|
|
| 16. |
- Bylin, Susanne, 1982
(författare)
-
Mechanisms of Biopolymer Solvation: Development of a two-component ionic liquid solvent system
- 2014
-
Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Ionic liquids are of potential interest in the processing of lignocellulosic biomass, and/or its components, for the purpose of producing renewable and value-added biomaterials. An understanding of how solvation can be achieved and the way in which the feedstock biopolymers are affected, however, needs to be gained prior to a viable implementation. In this thesis, the solvation of the wood biopolymers cellulose, xylan and lignin in the ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate (EMIMAc) in a novel combination with the second system component 1-methylimidazole (MIM) have been investigated:The solvation of dissolving pulp, beech xylan and LignoBoost lignin model materials, was studied using FBRM (focused beam reflectance measurements) particle characterization in combination with microscopic analysis (cellulose and xylan), determination of molecular weights (xylan and lignin) and 13C- and 31P-NMR (nuclear magnetic resonance spectroscopy) of lignin.It was concluded that the most efficient solvation of cellulose and xylan occurred using 3-4% and 9% IL (n/n anhydroglucose units and n/n anhydroxylose Units), respectively, while polymer integrity was maintained. Cellulose solvation was found to be greatly dependent on the IL to AGU ratio whereas xylan solvation varied greatly with temperature. Moreover, a theoretical model was developed for the solvation of cellulose in the present system. The solvation of lignin was achieved at ~20% lignin loading (w/w), in any combination of MIM/EMIMAc. Regeneration of lignin resulted in two sets of fractions; one exhibiting a general and higher apparent molecular weight (Mw) along with an enrichment of condensed/aliphatic ether linkages and aliphatic hydroxyls, and the other exhibiting a lower apparent Mw and an enrichment of carboxylic and phenolic groups. The knowledge of biopolymer solvation gained in the present solvent system provides future opportunities of tuning extraction and/or fractionation processes to suite the specifications of a particular biomass-derived product.
|
|
| 17. |
- Palme, Anna, 1986, et al.
(författare)
-
Development of an efficient route for combined recycling of PET and cotton from mixed fabrics
- 2017
-
Ingår i: Textiles and Clothing Sustainability. - : Springer Science and Business Media LLC. - 2197-9936. ; 3:4
-
Tidskriftsartikel (refereegranskat)abstract
- Most textile waste is either incinerated or landfilled today, yet, the material could instead be recycled through chemical recycling to new high-quality textiles. A first important step is separation since chemical recycling of textiles requires pure streams. The focus of this paper is on the separation of cotton and PET (poly(ethylene terephthalate), polyester) from mixed textiles, so called polycotton. Polycotton is one of the most common materials in service textiles used in sheets and towels at hospitals and hotels. A straightforward process using 5–15 wt% NaOH in water and temperature in the range between 70 and 90 °C for the hydrolysis of PET was evaluated on the lab-scale. In the process, the PET was degraded to terephthalic acid (TPA) and ethylene glycol (EG). Three product streams were generated from the process. First is the cotton; second, the TPA; and, third, the filtrate containing EG and the process chemicals. The end products and the extent of PET degradation were characterized using light microscopy, UV-spectroscopy, and ATR FT-IR spectroscopy, as well as solution and solid-state NMR spectroscopy. Furthermore, the cotton cellulose degradation was evaluated by analyzing the intrinsic viscosity of the cotton cellulose. The findings show that with the addition of a phase transfer catalyst (benzyltributylammonium chloride (BTBAC)), PET hydrolysis in 10% NaOH solution at 90 °C can be completed within 40 min. Analysis of the degraded PET with NMR spectroscopy showed that no contaminants remained in the recovered TPA, and that the filtrate mainly contained EG and BTBAC (when added). The yield of the cotton cellulose was high, up to 97%, depending on how long the samples were treated. The findings also showed that the separation can be performed without the phase transfer catalyst; however, this requires longer treatment times, which results in more cellulose degradation.
|
|
| 18. |
|
|
| 19. |
- Becker, Elin, 1981
(författare)
-
Interactions of methane and carbon monoxide with platinum - Supported catalysts and chemical sensors
- 2010
-
Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- This thesis aims at increasing the understanding of the interactions of methane and carbon monoxide with platinum in connection to catalysis and sensor technology for emission control. Specifically, the low-temperature oxidation of methane and carbon monoxide over supported platinum catalysts and the sensor response mechanism towards CO of platinum-based chemical field effect sensors were studied. Flow-reactor experiments and in situ spectroscopic methods (mainly FTIR and energy dispersive XAS) in combination with mass spectrometry were employed at both steady-state and transient reaction conditions. The results show that the support material for platinum has a considerable impact on the low-temperature activity for oxidation of both CO and methane in oxygen excess. Under such conditions methane oxidation over platinum is generally low due to oxygen-poisoning, hindering the dissociative adsorption of methane. However, by employing transient operation of the feed-gas composition, the activity for methane oxidation can be substantially increased. A new method was developed and applied for analysis of in situ XAS spectra. It was found that transient operation of the feed-gas affects the surface composition of reactants and the state of the catalyst surface. At low temperatures, the CO oxidation reaction often suffers from self-poisoning by carbon monoxide. By supplying oxygen to the reaction through alternative routes, e.g. via additional compounds or via the support material, the low-temperature activity for CO oxidation can be significantly increased. Further, the CO coverage and the reduction of oxygen from the surface of platinum-based field effect sensors were found to be important factors in the sensing mechanism towards carbon monoxide of such devices.
|
|
| 20. |
- Bordes, Romain, 1981, et al.
(författare)
-
Role of an amide bond for self-assembly of surfactants
- 2010
-
Ingår i: Langmuir. - : American Chemical Society (ACS). - 1520-5827 .- 0743-7463. ; 26:5, s. 3077-3083
-
Tidskriftsartikel (refereegranskat)abstract
- Self-assembly in Solution and adsorption at the air-water interface and at Solid Surfaces were investigated for two amino-acid-based surfactants with conductimetry, NMR, tensiometry, quartz crystal microbalance with monitoring or the dissipation (QCM-D), and surface plasmon resonance (SPR). The surfactants studied were sodium N-lauroylglycinate and sodium N-lauroylsarcosinate, differing only in a methyl group on the amide nitrogen for the sarcosinate. Thus, the glycinate but not the surfactant is capable of forming intermolecular hydrogen bonds via the amide group. It was found that the amide bond, N-methylated or not, gave a substantial contribution to the hydrophilicity of the amphiphile. The ability to form intermolecular hydrogen bonds led to tighter packing at the air-water interface and ill a hydrophobic surface. It also increased the tendency for precipitation as all acid-soap pair oil addition of acid. Adsorption of the surfactants at a gold surface Was also investigated and gave unexpected results. The sarcosine-based surfactant seemed to give bilayer adsorption, while the glycine derivative adsorbed as a monolayer.
|
|
