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  • 201.
    Bellais, Michel
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology.
    Sjöström, Krister
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology.
    Svenson, J.
    Pettersson, J. B. C.
    Omrane, Alaa
    KTH.
    Ossler, F.
    Aldén, M.
    Fast drying of large wood particles under pyrolysing conditions: experimental study and modellingIn: Fuel, ISSN 0016-2361, E-ISSN 1873-7153Article in journal (Other academic)
  • 202.
    Bellander, Hampus
    KTH, School of Chemical Science and Engineering (CHE).
    Evaluation of a hygroscopic condenser2011Independent thesis Advanced level (degree of Master (Two Years)), 20 credits / 30 HE creditsStudent thesis
    Abstract [en]

    In Sweden the industries releases about 50 TWh / year of low temperature waste heat[1], often in the form of humid air flows. Today, conventional flue gas condensation is only exploiting a minor part of the energy from these flows. It is a well-established and profit­able way of improving the efficiency of district heating plants and other boilers for wet fuels. How­ever, the condensation is only applicable when the dew point of the flue gas is above the temperature demand for the heating net. The paper industry gives a good illustration of the limitations for conventional condensation: several MW of wet air streams with dew points of 60-65 ̊ C are released but cannot be recovered since the tempe­ra­ture demand is 70-80 ̊ C for the heating net. Different technologies for more advanced waste heat recovery are developing and this report is evaluating a demonstration plant for “hygro­scopic condenser”, which uses a hygroscopic solution that allows condensation above the dew point. The hygro­scopic solution is potassium formate, which enables condensation to start about 20 ̊ C above the dew point and is sufficiently non-toxic and non-corrosive.

    The objective of this work is to evaluate both the equipment and the process during some initial tests at the paper mill at Holmen, Braviken. The aim is also to suggest improvements of the process, the components and the additional equipment for future continuous operation. 

    The equipment consists of two main parts:  a hygroscopic absorption stage and a regene­ration stage. The major part of the humid air is led into an absorption column where vapor is absorbed by the formate solution and rises its temperature. This recovered waste heat is transferred to the heating net by a plate heat exchanger. The regeneration unit is used to maintain the hygroscopic concentrations by evaporation of vapor from the formate solution (amount of absorbed vapor = amount of evaporated vapor). The regene­rator is driven by process steam from the existing 3.5 bar net. The evaporated vapor is led to a conventional condenser where the regeneration energy can be recovered and the condensate is bled off.  The recovered heat from the process (hygroscopic absorber + regeneration condenser) is used in the heating net at Holmen, Braviken (VVG-net).   

    The initial tests have been made during 15 hours of initial operation, when the equipment has delivered about 3 MWh in total. The tests show a good temperature performance since the dew point of the humid air has been lowered from about 60oC to 47oC. The reco­vered heat was used for heating from 65oC to about 80oC. During the initial tests the capacity has not yet reached the design values. As an example the delivered heat was measured to 280 kW where­of 46kW from absorbed vapor, 129 kW from the sensible heat in the incoming humid air and 105 kW from the regeneration. The bottle-neck parts of the equipment have been localized and will be overseen during the summer of 2011 and the process is planned to be in use during the autumn with an output capacity of 500kW. The coefficient of performance (COP) is calculated to just below 2 during normal operation but was about 2.7 in the test runs due to the high portion of sensible heat.

    [1]Förekomst av industriellt spillvärme vid låga temperaturer,  Ingrid Nyström, Per-Åke Franck, Industriell Energianalys AB, 2002-04-15

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  • 203.
    Belonoshko, Anatoly B.
    et al.
    KTH, Superseded Departments, Physics.
    Rosengren, Anders
    KTH, Superseded Departments, Physics.
    Dong, Qian
    KTH, Superseded Departments, Materials Science and Engineering.
    Hultquist, Gunnar
    KTH, Superseded Departments, Materials Science and Engineering.
    Leygraf, Christofer
    KTH, Superseded Departments, Materials Science and Engineering.
    First-principles study of hydrogen diffusion in α-Al 2O3 and liquid alumina2004In: Physical Review B Condensed Matter, ISSN 0163-1829, E-ISSN 1095-3795, Vol. 69, no 2, p. 243021-243026Article in journal (Refereed)
    Abstract [en]

    We have studied the energetics and mobility of neutral hydrogen in alumina Al2O3 using ab initio density-functional calculations. The mobility of hydrogen was studied in corundum (α-Al2O 3) as well as in liquid alumina. Using both static as well as molecular-dynamics calculations, and applying classical transition state theory, we derive the temperature-dependent diffusivity of hydrogen in α-Al 2O3 as D(T)=(21.7 × 10-8 m 2/s)exp(-1.24 eV/kT). The corresponding diffusivity of hydrogen in liquid/amorphous alumina, derived directly from ab initio molecular dynamics calculations, is D(T)=(8.71 × 10-7 m2/s)exp(-0.91 eV/kT). The computed diffusivity compares very well to experimental data. We conclude that diffusion of neutral hydrogen through the bulk of alumina is a good approximation of the mechanism for hydrogen mobility in corrosion scales. The representation of grain-boundary structures by amorphous alumina is, probably, realistic at higher temperatures.

  • 204.
    Benamira, M.
    et al.
    ENSCP, Paris.
    Albin, V.
    ENSCP, Paris.
    Ringuedé, A.
    ENSCP, Paris.
    Vannier, R-N.
    UMR 8181 CNRS.
    Bodén, Andreas
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Applied Electrochemistry.
    Lagergren, Carina
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Applied Electrochemistry.
    Cassir, M.
    ENSCP, Paris.
    Structural and Electrical Properties of Gadolinia-doped Ceria Mixed with Alkali Earth Carbonates for SOFC Applications2007In: SOLID OXIDE FUEL CELLS 10 (SOFC-X), PTS 1 AND 2 / [ed] Eguchi, K; Singhai, SC; Yokokawa, H; Mizusaki, H, 2007, p. 2261-2268Conference paper (Refereed)
    Abstract [en]

    The properties of composite materials based on mixtures of gadolinium-doped ceria (GDC) and Li(2)CO(3)-K(2)CO(3) are analyzed as potential SOFC electrolytes. In a temperature range higher than 500 degrees C, their ionic conductivity is significantly higher than for single GDC. Discontinuities were found in the conductivity Arrhenius diagram (sigma vs. 1/T) around the melting point of the carbonate mixture (490 degrees C), showing, at least partially, the contribution of molten carbonates. At this stage, precise mechanisms are still under analysis.

  • 205.
    Benamira, M.
    et al.
    Chimie ParisTech.
    Ringuede, A.
    Chimie ParisTech.
    Hildebrandt, Lars
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Applied Electrochemistry.
    Lagergren, Carina
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Applied Electrochemistry.
    Vannier, R-N
    UMR 8181 CNRS.
    Cassir, M.
    Chimie ParisTech.
    Gadolinia-doped ceria mixed with alkali carbonates for SOFC applications: II - An electrochemical insight2012In: International journal of hydrogen energy, ISSN 0360-3199, E-ISSN 1879-3487, Vol. 37, no 24, p. 19371-19379Article in journal (Refereed)
    Abstract [en]

    Composite materials based on gadolinia-doped ceria (GDC) and alkali carbonates (Li2CO3-K2CO3 or Li2CO3-Na2CO3) are potential electrolytes for low temperature solid oxide fuel cell applications (LTSOFC). This paper completes a first one dedicated to the thermal, structural and morphological study of such compounds; it is fully focussed on their electrical/electrochemical properties in different conditions, temperature, composition and gaseous atmosphere (oxidative or reductive). The influence of the gaseous composition on the Arrhenius conductivity plots is evidenced, in particular under hydrogen atmosphere. Finally, electrical conductivity determined by impedance spectroscopy is presented as a function of time to highlight the stability of such composites over 6000 h. First results on single cells showed performance at 600 degrees C of 60 mW cm(-2).

  • 206.
    Benavente Araoz, Fabian Andres
    et al.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Applied Electrochemistry. UMSA Univ Mayor San Andres, Inst Invest Quim, La Paz, Bolivia..
    Varini, Maria
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Applied Electrochemistry.
    Lundblad, Anders
    Res Inst Sweden, Div Safety & Transport Elect, RISE, SE-50462 Boras, Sweden..
    Cabrera, Saul
    UMSA Univ Mayor San Andres, Inst Invest Quim, La Paz, Bolivia..
    Lindbergh, Göran
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Applied Electrochemistry.
    Effect of Partial Cycling of NCA/Graphite Cylindrical Cells in Different SOC Intervals2020In: Journal of the Electrochemical Society, ISSN 0013-4651, E-ISSN 1945-7111, Vol. 167, no 4, article id 040529Article in journal (Refereed)
    Abstract [en]

    A quasi-realistic aging test of NCA/graphite lithium-ion 18650 cylindrical cells is performed during a long-term low c-rate cycling and using a new protocol for testing and studying the aging. This to emulate a characteristic charge/discharge profile of off-grid PV-battery systems. The cells were partially cycled at four different cut-off voltages and two state of charge ranges (Delta SOC) for 1000 and 700 cycles over 24 months. Differential voltage analysis shows that a combination of loss of active material (LAM) and loss of lithium inventory (LLI) are the causes of capacity loss. Cells cycled with high cut-off voltages and wide Delta SOC (20% to 95%) were severely affected by material degradation and electrode shift. High cut-off voltage and narrow Delta SOC (65% to 95%) caused greater electrode degradation but negligible cell unbalance. Cell impedance is observed to increase in both cells. Cells cycled with middle to low cut-off voltages and narrow Delta SOC (35%-65% and 20% to 50%) had comparable degradation rates to calendar-aged cells. Cycling NCA/graphite cells with low c-rate and high cut-off voltages will degrade the electrode in the same way high c-rate would do. However, low c-rate at low and middle cut-off voltages greatly decrease cell degradation compared to similar conditions at middle to high c-rate, therefore increasing battery lifetime.

  • 207.
    Benavente, Martha
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Adsorption of Metallic Ions onto Chitosan: Equilibrium and Kinetic Studies2008Licentiate thesis, comprehensive summary (Other academic)
    Abstract [en]

    Equilibrium isotherms and the adsorption kinetics of heavy metals onto chitosan were studied experimentally. Chitosan, a biopolymer produced from crustacean shells, has applications in various areas, particularly in drinking water and wastewater treatment due to its ability to remove metallic ions from solutions. The adsorption capacity of chitosan depends on a number of parameters: deacetylation degree, molecular weight, particle size and crystallinity. The purpose of this work was to study the adsorption of copper, zinc, mercury, and arsenic on chitosan produced from shrimp shells at a laboratory level.

    The experimental work involved the determination of the adsorption isotherms for each metallic ion in a batch system. The resulting isotherms were fitted using the Langmuir model and the parameters of the equation were determined. Kinetic studies of adsorption for different metallic ions at different concentrations and with different particle sizes were performed in batch and column systems. Simplified models such as pseudo-first-order, pseudo-second-order, and intra-particle diffusion equations were used to determine the rate-controlling step. Some preliminary studies were carried out to address the application of chitosan as an adsorbent in the removal of heavy metals or other metallic ions from natural water and wastewater. The regeneration of chitosan was also studied.

    The results showed that the adsorption capacity depends strongly on pH and on the species of metallic ions in the solution. The optimum pH value for the metallic cation adsorption was between 4 and 6, whereas for arsenic adsorption it was about 3. When the pH is not controlled, the adsorption capacity is independent of the initial pH with the solution reaching a final pH of about 7. It was also found that the Langmuir equation described very well the experimental adsorption data for each metallic ion. The adsorption capacity for the metals on chitosan follows the sequence Hg>Cu>Zn>As.

    The study of the adsorption kinetics of these metallic ions shows that the particle size has a significant influence on the metal uptake rate for copper; but that it has only a slight influence on the adsorption rate of zinc and mercury in the range studied. Arsenic adsorption exhibited an interesting behaviour which depends strongly on the pH of the solution; the uptake increased at short adsorption times and then decreased at long times. The analysis of kinetic models showed that the pseudo-second-order adsorption mechanism is predominant, and the overall rate of the metallic ion adsorption process is therefore controlled by adsorption reactions and not by mass transfer for the range of particle sizes examined in this study.

    With regard to the regeneration of chitosan, it was found that sodium hydroxide is a good agent for zinc and arsenic desorption, whereas ammonium sulphate and sodium chloride were the most suitable for copper and mercury desorption, respectively. The ability of chitosan to remove arsenic from natural water, and copper and zinc from mining waste water was verified. The use of these results for designing purposes is a subject for future work.

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  • 208.
    Benavente, Martha
    et al.
    Department of Chemical Engineering, National University of Engineering, Managua, Nicaragua.
    Arévalo, Marcos
    Department of Chemical Engineering, National University of Engineering, Managua, Nicaragua.
    Martinez, Joaquin
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Speciation and Removal of Arsenic in column packed with chitosan2006In: Water Practice & Technology, ISSN 1751-231X, Vol. 1, no 4, p. 2006-89Article in journal (Refereed)
    Abstract [en]

    The arsenic speciation and arsenic removal in chitosan packed column were studied. Arsenic removal experiments were carried out with an arsenic standard solution (1.0 mg/l) and drilled well water samples from Limon Mine Community at different pH, water flowrate, and volume of adsorbent material. The simulation of arsenic speciation was carried out at a pH range from 0 to 12, a temperature of 25ºC, a pE equal to 4, and a total arsenic concentration of 1.34 x 10-5 mol kg-1. According to speciation calculations arsenic is found mainly in oxidized form in the conditions of Limon Mine’s drilled well waters, dihydrogen arsenate ion (H2AsO4-), and hydrogen arsenate ion (HAsO42-) being the major species. The experiments showed that arsenic adsorption depends mainly on the pH as well as the activity of functional groups that compose the chitosan structure. At pH 3 and volume of adsorbent material of 337.8 cm3 an adsorption of 94% was obtained from arsenic standard solution, and the arsenic present in the Limon Community’s water was almost totally removed at pH 3 and 7. The use of the results for designing purposes demands the breakthrough curves for chitosan to be determined.

  • 209.
    Benavente, Martha
    et al.
    Faculty of Chemical Engineering, National University of Engineering (UNI), Managua, Nicaragua.
    Martínez, Joaquín
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Especiación Acuosa de Cianuro y Componentes Derivados en Lavados de Colas de Minerales de Oro2006In: Nexo, ISSN 1818-6742, Vol. 19, no 1, p. 1-9Article in journal (Refereed)
    Abstract [es]

    En este trabajo se simuló la especiación del cianuro y componentes relacionados en soluciones de lavado de colas cianuradas de minerales de oro de la Mina El Limón, utilizando el programa geoquímico PHREEQC. Se consideró un modelo de especiación iónica formado por un conjunto de reacciones químicas y de especies principales en fase acuosa (hierro, cobre, cinc, calcio y aluminio, cloruro y cianuro), en distintas condiciones de pH, Eh y concentraciones de cianuro. Las simulaciones muestran que las concentraciones de las especies iónicas y complejas dependen principalmente del pH de la solución y de la concentración de cianuro disponible en el sistema, reproduciéndose en forma satisfactoria los valores de pH y solubilidad de metales medidos en el sistema. El cianuro forma complejos de alta estabilidad química con los metales disueltos, observándose que las especies de Fe-CN son altamente estables incluso a pH ácido donde prácticamente no existe el ión cianuro libre (CN-) producto de la formación del componente gaseoso HCN.

  • 210.
    Benavente, Martha
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena. National University of Engineering (UNI), Nicaragua.
    Moreno, Luis
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Chemical Engineering.
    Martinez, Joaquin
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Sorption of heavy metals from gold mining wastewater using chitosan2011In: Journal of the Taiwan Institute of Chemical Engineers / Elsevier, ISSN 1876-1070, E-ISSN 1876-1089, Vol. 42, no 6, p. 976-988Article in journal (Refereed)
    Abstract [en]

    This study is concerned with the use of chitosan produced from shrimp shell waste for the removal of Cu(II), Hg(II), Pb(II) and Zn(II) from gold ore tailing solutions containing cyanide. This work involved the study of equilibrium and kinetic adsorption, the physicochemical characterization of mining effluents and desorption using different regenerating solutions. The experimental results showed that the adsorption capacity of chitosan is a function of the solution pH and that the optimum pH for these metallic ions is 6, except for Hg (pH 4). The equilibrium data were described using the Langmuir, Freundlich, Redlich-Peterson and SIPS isotherm models. The Langmuir equation was used to find the maximum adsorption capacity for Cu (79.94 mg/g), Hg (109.55 mg/g), Pb (58.71 mg)g) and Zn (47.15 mg/g). To determine the rate-controlling mechanism for metallic ion adsorption, pseudo-first-order, pseudo-second-order and the Elovich equation kinetic models were tested with experimental adsorption kinetic data. Tests conducted with gold ore tailing solutions indicated that chitosan is effective to remove these metallic ions above 70%. Desorption studies revealed that the regeneration of chitosan saturated with these metallic ions depends on the type and concentration of the regenerating solution ((NH(4))(2)SO(4), H(2)SO(4), HCl, NaOH and NaCl).

  • 211.
    Benavente, Martha
    et al.
    Faculty of Chemical Engineering, National University of Engineering (UNI), Managua, Nicaragua.
    Moreno, Luis
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Chemical Engineering.
    Martínez, Joaquín
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Adsorption Kinetic of Copper and Zinc from Binary Solutions using Chitosan2010In: Hydro Process 2010: Proceedings of the 3rd International Workshop on Process Hydrometallurgy / [ed] Marcelo Jo, Juan Patricio Ibáñez, Jesús Casas, Santiago, Chile: GECAMIN, 2010, p. 22-23Conference paper (Refereed)
  • 212.
    Benavente, Martha
    et al.
    Faculty of Chemical Engineering, National University of Engineering (UNI), Managua, Nicaragua.
    Moreno, Luis
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Chemical Engineering.
    Martínez, Joaquín
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Biosorption of Lead using Chitosan2009In: Advances in Chitin Science, Volumen XI: EUCHIS 2009 / [ed] Franco Rustichelli, Carla Caramella, Sevda Senel, Kjell M. Vaarum, Venice, Italy, 2009, p. 487-492Conference paper (Refereed)
  • 213.
    Benavente, Martha
    et al.
    Faculty of Chemical Engineering, National University of Engineering (UNI), Managua, Nicaragua.
    Moreno, Luis
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Chemical Engineering.
    Martínez, Joaquín
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Production of Glucosamine Hydrochloride from Crustacean Shell2011In: Advances in Chitin Science, Volume XIII: EUCHIS 2011 / [ed] Valery Varlamov, Svetlana Bratskaya, Irina Yakovleva, Sevda Senel, SAINT-PETERSBURG, RUSSIA, 2011, p. 29-35Conference paper (Refereed)
  • 214.
    Benavente, Martha
    et al.
    Faculty of Chemical Engineering, National University of Engineering (UNI), Managua, Nicaragua.
    Sjörén, Anna
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology.
    Martínez, Joaquín
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Remoción de Mercurio de Efluentes Mineros por Biosorción2007In: Nexo, ISSN 1818-6742, Vol. 20, no 2, p. 47-55Article in journal (Refereed)
    Abstract [es]

        La minería y la extracción de oro en operaciones a pequeña escala han contribuido a la contaminación de los recursos acuáticos de Nicaragua durante décadas. En este trabajo se investigó un proceso de biosorción a bajo costo para la remoción de iones mercurio (II) de soluciones estándar y de aguas naturales usando quitosano como adsorbente. La regeneración del adsorbente también fue estudiada. Los resultados mostraron que la adsorción de iones mercurio fue independiente del pH en el rango de pH 4-10 y que la capacidad se reduce considerablemente a pH 2. Los estudios de la cinética mostraron una fase inicial rápida de adsorción seguida por una fase más lenta. Por otro lado, se comprobó que los datos experimentales se ajustan al modelo de Langmuir, y se determinó, mediante el uso de este modelo, una capacidad de adsorción de 106 mg Hg/g quitosano. Una solución acuosa de NaCl demostró ser una opción barata y eficiente para la regeneración del adsorbente; además, el adsorbente mostró una capacidad de adsorción alta después de la regeneración. Se encontró que la concentración de mercurio en 4 de las 8 muestras recolectadas cerca de la ciudad de la Libertad, excedían ligeramente los niveles permisibles (1.09-2.25 μg Hg L-1) para agua de consumo humano según las normas CAPRE. Además, se determinó que la capacidad de adsorción de mercurio es menor en aguas naturales que en las soluciones estándares.

  • 215.
    Benavente, Martha
    et al.
    National University of Engineering, Nicaragua.
    Sjörén, Anna
    KTH, School of Chemical Science and Engineering (CHE).
    Westergren, Robin
    KTH, School of Chemical Science and Engineering (CHE).
    Moreno, Luis
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Chemical Engineering.
    Martinez, Joaquin
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Biosorption of Heavy Metals on Chitosan2007In: Hydro Copper 2007 / [ed] Jorge M. Menacho and Jesús M. Casas de Prada, Santiago, Chile: GECAMIN Ltda. , 2007, p. 283-290Conference paper (Refereed)
  • 216.
    Benavente, Martha
    et al.
    National University of Engineering, Nicaragua.
    Álvarez, Erick
    National University of Engineering, Nicaragua.
    Moreno, Luis
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Chemical Engineering.
    Martinez, Joaquin
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Transport Phenomena.
    Removal of Copper and Zinc from Gold Ore Tailings Solutions using Chitosan2008In: Hydro Process 2008 / [ed] Jorge M. Menacho and Jesús M. Casas de Prada, Santiago, Chile: GECAMIN Ltda. , 2008, p. 139-152Conference paper (Refereed)
  • 217. Bengtsson, M.
    et al.
    Wallström, Stina
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Karlsson, Sigbritt
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Svanberg, S.
    Fluorescence lidar imaging of fungal growth on high-voltage outdoor composite insulators2005In: Optics and lasers in engineering, ISSN 0143-8166, E-ISSN 1873-0302, Vol. 43, no 6, p. 624-632Article in journal (Refereed)
    Abstract [en]

    Remote fluorescence imaging of fungal growth on polymeric high-voltage insulators was performed using a mobile lidar system with a laser wavelength of 355 nm. Insulator areas contaminated by fungal growth could be distinguished from clean surfaces and readily be imaged. The experiments were supported by detailed spectral studies performed in laboratory using a fibre-optic fluorosensor incorporating an optical multi-channel analyser system (OMA) and a nitrogen laser emitting radiation at 33 7 nm.

  • 218. Bengtsson, M.
    et al.
    Wallström, Stina
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Sjöholm, M.
    Grönlund, R.
    Anderson, B.
    Larsson, A.
    Karlsson, Sigbritt
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Kröll, Stefan
    Svanberg, S.
    Fungus covered insulator materials studied with laser-induced fluorescence and principal component analysis2005In: Applied Spectroscopy, ISSN 0003-7028, E-ISSN 1943-3530, Vol. 59, no 8, p. 1037-1041Article in journal (Refereed)
    Abstract [en]

    A method combining laser-induced fluorescence and principal component analysis to detect and discriminate between algal and fungal growth on insulator materials has been studied. Eight fungal cultures and four insulator materials have been analyzed. Multivariate classifications were utilized to characterize the insulator material, and fungal growth could readily be distinguished from a clean surface. The results of the principal component analyses make it possible to distinguish between algae infected, fungi infected, and clean silicone rubber materials. The experiments were performed in the laboratory using a fiber-optic fluorosensor that consisted of a nitrogen laser and an optical multi-channel analyzer system.

  • 219.
    Benselfelt, Tobias
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology, Fibre Technology. KTH, School of Chemical Science and Engineering (CHE), Centres, Wallenberg Wood Science Center.
    Cranston, Emily D.
    Department of Chemical Engineering, McMaster University.
    Ondaral, Sedat
    Department of Pulp and Paper Technology, Karadeniz Technical University.
    Johansson, Erik
    Cellutech AB.
    Brumer, Harry
    The Michael Smith Laboratories and the Department of Chemistry, The University of British Columbia.
    Rutland, Mark W.
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Wågberg, Lars
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology, Fibre Technology. KTH, School of Chemical Science and Engineering (CHE), Centres, Wallenberg Wood Science Center.
    Adsorption of Xyloglucan onto Cellulose Surfaces of Different Morphologies: An Entropy-Driven Process2016In: Biomacromolecules, ISSN 1525-7797, E-ISSN 1526-4602, Vol. 17, no 9, p. 2801-2811Article in journal (Refereed)
    Abstract [en]

    The temperature-dependence of xyloglucan (XG) adsorption onto smooth cellulose model films regenerated from N-methylmorpholine N-oxide (NMMO) was investigated using surface plasmon resonance spectroscopy, and it was found that the adsorbed amount increased with increasing temperature. This implies that the adsorption of XG to NMMO-regenerated cellulose is endothermic and supports the hypothesis that the adsorption of XG onto cellulose is an entropy-driven process. We suggest that XG adsorption is mainly driven by the release of water molecules from the highly hydrated cellulose surfaces and from the XG molecules, rather than through hydrogen bonding and van der Waals forces as previously suggested. To test this hypothesis, the adsorption of XG onto cellulose was studied using cellulose films with different morphologies prepared from cellulose nanocrystals (CNC), semicrystalline NMMO-regenerated cellulose, and amorphous cellulose regenerated from lithium chloride/dimethylacetamide. The total amount of high molecular weight xyloglucan (XGHMW) adsorbed was studied by quartz crystal microbalance and reflectometry measurements, and it was found that the adsorption was greatest on the amorphous cellulose followed by the CNC and NMMO-regenerated cellulose films. There was a significant correlation between the cellulose dry film thickness and the adsorbed XG amount, indicating that XG penetrated into the films. There was also a correlation between the swelling of the films and the adsorbed amounts and conformation of XG, which further strengthened the conclusion that the water content and the subsequent release of the water upon adsorption are important components of the adsorption process.

  • 220.
    Benyahia Erdal, Nejla
    et al.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology, Polymer Technology.
    Adolfsson, Karin H.
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Pettersson, Torbjörn
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Hakkarainen, Minna
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Green Strategy to Reduced Nanographene Oxide through Microwave Assisted Transformation of Cellulose2018In: ACS Sustainable Chemistry and Engineering, ISSN 2168-0485, Vol. 6, no 1, p. 1245-1255Article in journal (Refereed)
    Abstract [en]

    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.

  • 221.
    Berendson, Jaak
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Applied Electrochemistry.
    Electrochemical methods2007In: Surface Characterization: A User's Sourcebook, Wiley-Blackwell, 2007, p. 590-606Chapter in book (Other academic)
  • 222.
    Beretta, A.
    et al.
    Dipartiemento Energia- Politecnico di Milano.
    Groppi, G.
    Dipartiemento Energia- Politecnico di Milano.
    Lualdi, Matteo
    Dipartiemento Energia- Politecnico di Milano.
    Tavazzi, I.
    Dipartiemento Energia- Politecnico di Milano.
    Forzatti, P.
    Dipartiemento Energia- Politecnico di Milano.
    Experimental and modeling analysis of methane partial oxidation: transient and steady-state behavior of rh-coated honeycomb monoliths2009In: Industrial & Engineering Chemistry Research, ISSN 0888-5885, E-ISSN 1520-5045, Vol. 48, no 8, p. 3825-3836Article in journal (Refereed)
    Abstract [en]

    The present study consists of an experimental and theoretical study of the performance of Rh-coated honeycomb monoliths for methane partial oxidation. The thermal behavior of Rh-coated honeycomb monoliths was studied under representative operating conditions, at steady state and during light-off. Model analysis (based on a dynamic heterogeneous reactor model that incorporates a kinetic scheme of the process independently developed, and well-assessed correlations for heat and mass transfer) provided a key for interpreting the observed effects. The comprehension of how transport phenomena and surface kinetics affect the reactor behavior leads to the conclusion that the feasibility of small-scale production of syngas via CH(4) catalytic partial oxidation relies on thermal management of the short contact time reactor and not the obtainment of high syngas yields (which is not a challenging task). Severe operating conditions (and high surface temperatures) can deplete the catalyst activity and cause unstable reactor operation. Guidelines for optimal reactor design are proposed.

  • 223.
    Bergenstrahle-Wohlert, Malin
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    d'Ortoli, Thibault Angles
    Sjoberg, Nils A.
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    Widmalm, Goran
    Wohlert, Jakob
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology.
    On the anomalous temperature dependence of cellulose aqueous solubility2016In: Cellulose (London), ISSN 0969-0239, E-ISSN 1572-882X, Vol. 23, no 4, p. 2375-2387Article in journal (Refereed)
  • 224.
    Berggren, Frida
    KTH, School of Chemical Science and Engineering (CHE).
    Development of an Expancel Product through Optimisation of Polymer Composition and the Suspension Stabilising System2014Independent thesis Advanced level (degree of Master (Two Years)), 20 credits / 30 HE creditsStudent thesis
    Abstract [en]

    Thermally expandable microspheres are spherical particles around 5-­‐40 µm in size, consisting of a polymeric shell in which a blowing agent has been encapsulated. The microspheres are expanded upon heating, resulting in a particularly low density. Microspheres are therefore suitable to use as light weight filler or as foaming agent.

    AkzoNobel is world leading in the production of expandable microspheres, which are commercialised under the name Expancel. Sustainability is a great focus at AkzoNobel and two issues that AkzoNobel works with today is to develop products free from chlorine and Me1. The aim with this thesis has been to investigate whether it is possible to produce microspheres free from these chemicals and to see if they can be a more sustainable alternative to one of the existing Expancel grades.

    In this study, the microspheres have been produced through free radical suspension polymerisation and analysed by measuring mainly the particle size and expansion properties. The polymeric shell was composed of the monomers acrylonitrile, methacrylonitrile, and methyl acrylate. The main focus has been to evaluate the silica-­‐based stabilisation system, which stabilise the monomer droplets during the suspension polymerisation. The stabilisation is possible due to the formation of silica flocs that is adsorbed on the surface of the droplets. It has been investigating how different parameters, e.g. amount of stabiliser or mixing procedure, affects the formation of silica flocs and the stabilisation of monomer droplets.

    For the silica-­‐based system, it was found that the mixing order, stirring rate, and amount of stabilisers affect the formation of flocs. It was also seen that the amount of stabiliser affect the stabilisation of droplets, and that some stabilisers is more significant than others.

    Microspheres without chlorine and Me1 have successfully been produced in laboratory scale (50 mL and 1 L). The expansion and size of the microspheres produced in this study was relatively similar to one of the existing Expancel grades. However, the reproducibility of polymerisations in 1 litre reactors has been poor.

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  • 225.
    Bergkvist, Kristofer
    KTH, School of Chemical Science and Engineering (CHE).
    Utvärdering av hur aktiv akustisk mätning kan skapa en intelligentare process2015Independent thesis Basic level (professional degree), 10 credits / 15 HE creditsStudent thesis
    Abstract [en]

    In many process industries, it is important to be able to measure the properties of process fluids in a good way. This can be done in different ways. The company Acosense AB produces and sells an instrument that is able to analyze the properties of process fluids. This method is an online analysis based on active acoustic spectroscopy. The online analysis functions by sending an audio signal with different frequencies through a pipe where the process fluid flows through. At the other side of the pipe a sensor is located that registers the audio signal. Depending on the properties of the process fluids the audio signal is affected to a certain degree and in different ways. What is measured is how the audio signal changes.

    Stora Enso Skutskär where paper and fluff pulp is produced is one of the industries that use the technology. By measuring certain characteristics of the process fluid in real time the production of pulp can get more effective.

    The purpose of the thesis is to find out how well the technology is working to analyze the variables TOC (total organic carbon), unwashed pulp concentration, washed pulp concentration and kappa number. An evaluation of what benefits Stora Enso Skutskär may get from using the online analysis is also made. To investigate the technology pulp samples are taken at boiler 2 at Stora Enso Skutskär. The samples are analyzed with regard to the mentioned variables. The test results are then linked together to the acoustic spectrum that the acoustic measurement equipment generates. The idea is that it should possible to predict the variables TOC, unwashed pulp concentration, washed pulp concentration and kappa number by using only the acoustic spectrum and statistical modeling methods. This connection is made with multivariate analysis by creating PCA and PLS models in the software SIMCA. Samples and acoustic spectrum that are considered to stand out to much or are non-representative of the pulping process or of the acoustic measurement equipment are excluded so they don’t affect the models in a negative way.

    The PLS models are developed for TOC, unwashed pulp concentration and washed pulp concentration has, according to SIMCA poor ability to predict. When testing with the observations that do not affect the models, the results are still poor. The reason for the poor ability to predict is believed to be the low number of observations which the models are based on.

    When creating the PLS model for the kappa number a significantly higher number of observations are used. This models ability to predict is better.I

    In order to make better models it is suggested that more samples are taken so that the models can be based on more observations.

    By using a functional acoustic online analysis the production can probably get more efficient in more than one location at Stora Enso Skutskär.

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  • 226.
    Berglund, Jennie
    et al.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Centres, Wallenberg Wood Science Center.
    Azhar, Shoaib
    Lawoko, Martin
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Centres, Wallenberg Wood Science Center.
    Lindström, Mikael
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Centres, Wallenberg Wood Science Center.
    Vilaplana, Francisco
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Glycoscience. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Centres, Wallenberg Wood Science Center. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology.
    Wohlert, Jakob
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Centres, Wallenberg Wood Science Center.
    Henriksson, Gunnar
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Fibre- and Polymer Technology. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Centres, Wallenberg Wood Science Center.
    The structure of galactoglucomannan impacts the degradation under alkaline conditions2018In: Cellulose (London), ISSN 0969-0239, E-ISSN 1572-882XArticle in journal (Refereed)
    Abstract [en]

    Galactoglucomannan (GGM) from sprucewas studied with respect to the degradation behavior inalkaline solution. Three reference systems includinggalactomannan from locust bean gum, glucomannanfrom konjac and the linear water-soluble carboxymethylcellulose were studied with focus onmolecular weight, sugar composition, degradationproducts, as well as formed oligomers, to identifyrelative structural changes in GGM. Initially allmannan polysaccharides showed a fast decrease inthe molecular weight, which became stable in the laterstage. The degradation of the mannan polysaccharidescould be described by a function corresponding to thesum of two first order reactions; one slow that wasascribed to peeling, and one fast that was connectedwith hydrolysis. The galactose side group wasstable under conditions used in this study (150 min,90 C, 0.5 M NaOH). This could suggest that, apartfrom the covalent connection to C6 in mannose, thegalactose substitutions also interact non-covalentlywith the backbone to stabilize the structure againstdegradation. Additionally, the combination of differentbackbone sugars seems to affect the stability of thepolysaccharides. For carboxymethyl cellulose thedegradation was linear over time which furthersuggests that the structure and sugar composition playan important role for the alkaline degradation. Moleculardynamics simulations gave details about theconformational behavior of GGM oligomers in watersolution, as well as interaction between the oligomersand hydroxide ions.

  • 227.
    Bergman, Bill
    et al.
    KTH, School of Industrial Engineering and Management (ITM), Materials Science and Engineering.
    Lagergren, Carina
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology.
    Lindbergh, Göran
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology.
    Schwartz, Stephan
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology.
    Zhu, Baohua
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology.
    Contact Corrosion Resistance Between the Cathode and the Current Collector Plate in the MCFC1999In: Carbonate Fuel Cell Technology V / [ed] I. Uchida, K.Hemmes, G. Lindbergh, D.A. Shores and J.R. Selman, 1999, p. 150-Conference paper (Refereed)
  • 228. Bergman, Susanna
    et al.
    Dahlin, Sandra
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Process Technology.
    Mesilov, Vitaly
    Xiao, Yang
    Englund, Johanna
    Xi, Shibo
    Tang, Chunhua
    Skoglundh, Magnus
    Pettersson, Lars
    Bernasek, Steven
    In-situ studies of oxidation/reduction of copper in Cu-CHA SCR catalysts:comparison of fresh and SO2-poisoned catalystsIn: Article in journal (Other academic)
    Abstract [en]

    SO2-poisoning results in deactivation of Cu-CHA SCR under standard SCR conditions; however regeneration at 700 ◦C completely restores the SCR performance. To understand the nature of these effects, Cu-species in the fresh and poisoned catalystswere characterized by in-situ temperature-dependent time-resolved Cu K-edge X-ray absorption spectroscopy using the multivariate curve resolution alternating least squares (MCR-ALS) approach and continuous Cauchy wavelet transforms. The extracted chemically-meaningful reference spectra of Cu-species were analyzed by DFT-assisted XANES calculations. Cu-bisulfates werefound as the most energetically favorable poisoned Cu-species. The response of Cu-species to a reducing environment differs inthe fresh and SO2-poisoned catalysts. Differences in reducibility are related to the formation of quasi-linear Cu-complexes in the SO2-poisoned catalyst formed during heating in H2/He. Heating in H2/He leads to partial desulfurization of the poisoned catalyst. Cooling in H2/He after heating results in more facile formation of Cu-metal clusters in fresh catalyst than in SO2-poisoned.

  • 229.
    Bergman, Susanna L
    et al.
    Princeton University, Science Division, Yale-NUS College, Singapore.
    Granestrand, Jonas
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering.
    Tang, Yu
    University of Kansas.
    Suárez Paris, Rodrigo
    Scania CV.
    Nilsson, Marita
    Scania CV.
    Feng Tao, Franklin
    University of Kansas.
    Tang, Chunhua
    National University of Singapore.
    Pennycook, Stephen J
    National University of Singapore.
    Pettersson, Lars J
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering.
    Bernasek, Steven L
    Princeton University, Science Division, Yale-NUS College, Singapore.
    In-situ characterization by Near-Ambient Pressure XPS of the catalytically active phase of Pt/Al2O3 during NO and CO oxidation2018In: Applied Catalysis B: Environmental, ISSN 0926-3373, E-ISSN 1873-3883, Vol. 220, p. 506-511Article in journal (Refereed)
    Abstract [en]

    This study concerns near ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) studies of a Pt/Al2O3 diesel oxidation catalyst used in exhaust aftertreatment. We apply the technique to an industrial-grade porous catalyst, thus bridging both the pressure and materials gap, and probe the shift in binding energy of Pt 4d under different atmospheres. We observe that oxidizing atmospheres induce a shift in binding energy, corresponding to changes in Pt oxidation state, especially pronounced under an atmosphere of NO and O2. Such changes in Pt oxidation state have previously been linked to dynamic changes in NO oxidation activity.

  • 230. Bergnor, Elisabeth
    et al.
    Ek, Monica
    KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology, Wood Chemistry and Pulp Technology.
    Johansson, E
    The role of metal ions in TCF-bleaching.1994In: Proceedings 3rd European Workshop on Lignocellulosics and Pulp, 1994, p. 284-289Conference paper (Refereed)
  • 231.
    Bergström, Johan
    KTH, School of Chemical Science and Engineering (CHE).
    Utveckling av en experimentell uppställning för studie av massöverföring genom membran2015Independent thesis Basic level (professional degree), 10 credits / 15 HE creditsStudent thesis
    Abstract [en]

    The primary goal of this project is to develop an experimental setup for testing membrane materials. The membranes tested are all porous, hydrophilic and non- selective. The secondary goal is that the module finds use as an educational tool for learning about diffusion on a university level. The final setup consisted of two modified 250 ml polyethylene bottles with a wide neck joined together with a flange pinning the test object in between. In the experiments one side is loaded with a sodium chloride solution, while the other is loaded with pure deionized water. The conductivity change is then monitored in the chamber loaded with deionized water using a conductivity probe. Two test subjects are tested, an alpha Cellulose filter and a polycarbonate membrane. The mass transfer coefficient are determined to be 8.99*10-6 ± 3.90*10-6 [cm/min] and 3.62*10-5 ± 1.49*10-6 [cm/min] respectively. The large inconsistencies in the alpha cellulose filters results in large standard deviations, whereas the polycarbonate is very consistent and therefore have very small error bars. Meaning that the largest error in this design originates from inconsistencies between samples of the test subject. The setup is suitable as an educational tool due to short run times of one hour, the generated data only requires simple linear regression to extract mass transfer coefficients from the slope. The experiment can be varied further by adjusting temperature and stirring.

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  • 232.
    Bergström, L. Magnus
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Aratono, Makoto
    Synergistic effects in mixtures of two identically charged ionic surfactants with different critical micelle concentrations2011In: Soft Matter, ISSN 1744-683X, E-ISSN 1744-6848, Vol. 7, no 19, p. 8870-8879Article in journal (Refereed)
    Abstract [en]

    Expressions for the critical micelle concentration (cmc) and activity coefficients as functions of surfactant composition in mixtures of two identically charged monovalent ionic surfactants are derived from the nonlinear Poisson-Boltzmann (PB) theory. For the special case of no added salt, the simple expression cmc(alpha) = xcmc(1)(alpha) + (1 - x)cmc(2)(alpha) is deduced, where the exponential parameter alpha > 1 depends on the number of ionic species in a surfactant molecule as well as the curvature of the self-assembled interface. Theoretical predictions are compared with cmc values obtained with some different experimental techniques for mixtures of the two cationic surfactants didodecyldimethylammonium bromide (DDAB) and dodecyltrimethylammonium bromide (DTAB) in water and in the absence of added salt. It is demonstrated that the PB theory generates significantly better agreement with experimental data than predicted by ideal behaviour or the regular mixture theory. We find that maximum synergistic effects occur at a DDAB mole fraction in solution y = 0.005. According to the PB theory, this very low value of y corresponds to a mole fraction of DDAB in the self-assembled interfacial aggregates equal to x = 0.995. Moreover, our calculations of the surfactant composition in the self-assembled interfacial aggregates above cmc demonstrate that the transition from small micelles to large bilayer aggregates is found to consistently occur at a mole fraction of DDAB equal to about x = 0.41-0.42, irrespective of the surfactant molar ratio in solution. Experimental observations strongly support the fact that concentrations of free surfactant, as well as the surfactant composition in the self-assembled interfacial aggregates, may be accurately calculated from the non-linear Poison-Boltzmann theory. On the other hand, a micelle-to-bilayer transition induced by changes in surfactant mole fraction in the self-assembled interfacial aggregates is consistent with neither ideal surfactant behaviour nor synergistic behaviour according to the regular mixture theory.

  • 233.
    Bergström, L. Magnus
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Garamus, Vasil M.
    Geometrical Shape of Micelles Formed by Cationic Dimeric Surfactants Determined with Small-Angle Neutron Scattering2012In: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 28, no 25, p. 9311-9321Article in journal (Refereed)
    Abstract [en]

    The influence of spacer group on the geometrical shape of micelles formed by quaternary-bis dimeric (Gemini) surfactants C12H25N(CH3)(2)(CH2)(5)N(CH3)(2)C12H25 (12-s-12) has been investigated with small-angle neutron scattering (SANS). Dimeric surfactants with a short spacer unit (12-3-12 and 124-12) are observed to form elongated general ellipsoidal micelles with half axes a < b < c, whereas SANS data demonstrate that 12-s-12 surfactants with 6 <= s <= 12 form rather small spheroidal micelles rather than strictly spherical micelles. By means of comparing our present SANS results with previously determined growth rates using time-resolved fluorescence quenching, we are able to conclude that micelles formed by 12-6-12, 12-8-12, 12-10-12, and 12-12-12 are shaped as oblate rather than prolate spheroids. As a result, our present investigation suggests a never before reported structural behavior of Gemini surfactant micelles, according to which micelles transform from elongated ellipsoids to nonelongated oblate spheroids as the length of the spacer group is increased. The aggregation number of oblate micelles is observed to monotonously decrease with an increasing length of the surfactant spacer group, mainly as a result of a decreasing minor half axis (a), whereas the major half axis (b) is rather constant with respect to s. We argue that geometrically heterogeneous elongated micelles are formed by dimeric surfactants with a short spacer group mainly as a result of the surface charges becoming less uniformly distributed over the micelle interface. As the length of the spacer group increases, the distance between intramolecular charges become approximately equal to the average distance between charges on the micelle interface, and as a result, rather small oblate spheroidal micelles with a more uniform distribution of surface charges are formed by dimeric 12-s-12 surfactants with 6 <= s <= 12.

  • 234.
    Bergström, Lars Magnus
    et al.
    KTH, Superseded Departments, Chemistry. YKI, Institute for Surface Chemistry, Sweden .
    Eriksson, Jan Christer
    KTH, Superseded Departments, Chemistry. YKI, Institute for Surface Chemistry, Sweden .
    Synergistic effects in binary surfactant mixtures2004In: Progress in Colloid and Polymer Science, ISSN 0340-255X, E-ISSN 1437-8027, Vol. 123, p. 16-22Article in journal (Refereed)
    Abstract [en]

    By considering the main contributions to the micellar free energy we have analysed the synergistic effect often seen on the CMC of a binary surfactant mixture. The synergistic effects are due mainly to the entropic free energy contributions related with the surfactant head groups. Several cases have been treated: (i) For a mixture of a monovalent ionic and a non-ionic surfactant in the absence of added salt we obtain, entirely because of electrostatic reasons, a negative deviation from the ideal behaviour corresponding to an interaction parameter β≈-1. Upon adding an inert salt we found that the magnitude of the synergistic effect first increases, reaches a maximum and eventually decreases. (ii) For mixtures of two ionic surfactants with the same charge number but with different hydrocarbon moieties β-values as low as -10 may arise. (iii) For mixtures of an anionic and a cationic surfactant enormous effects are anticipated yielding β≤-20 depending on the CMCs of respective pure surfactant. (iv) Synergistic effects due to different cross-section areas of the head groups are found to be rather small, with 0 > β > -1, provided the difference in head group size is modest but can become more significant when the size difference is larger.

  • 235.
    Bergström, Lennart Magnus
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Grillo, I.
    Correlation between the geometrical shape and growth behaviour of surfactant micelles investigated with small-angle neutron scattering2014In: Soft Matter, ISSN 1744-683X, E-ISSN 1744-6848, Vol. 10, no 46, p. 9362-9372Article in journal (Refereed)
    Abstract [en]

    The correlation between the growth behaviour and geometrical shape for CTAB-rich mixed micelles formed by the cationic surfactant hexadecyl trimethyl ammonium bromide (CTAB) and the anionic surfactant sodium octyl sulphate (SOS) has been investigated with small-angle neutron scattering (SANS). Small tablet-shaped micelles formed by CTAB are found to grow only weakly in size with increasing surfactant concentration. The extent of growth becomes increasingly stronger as the fraction of SOS is increased. At higher fractions of SOS, a rather weak growth at low surfactant concentrations is followed by a sharp increase in aggregation numbers beyond a certain surfactant concentration. Such an abrupt transition from weakly to strongly growing micelles has been observed in the past for several micellar systems and is usually referred to as the second critical micelle concentration. The growth behaviour has been rationalized from a theoretical point of view by means of employing the recently developed general micelle model. The theory excellently predicts micellar growth behaviours as well as the observed correlation between the geometrical shape and micellar growth. In accordance, both width and length are found to slightly increase for weakly growing tablet-shaped micelles. On the other hand, strongly growing micelles that are observed above the second cmc display a completely different behaviour, according to which the length increases considerably while the width of the micelles decreases. Most interestingly, by means of optimizing the agreement between the general micelle model and experimentally determined aggregation numbers, we are able to determine the three bending elasticity constants: spontaneous curvature, bending rigidity and saddle-splay constant.

  • 236.
    Bergström, Magnus
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Garamus, V. M.
    Structural behaviour of mixed cationic surfactant micelles: A small-angle neutron scattering study2012In: Journal of Colloid and Interface Science, ISSN 0021-9797, E-ISSN 1095-7103, Vol. 381, no 1, p. 89-99Article in journal (Refereed)
    Abstract [en]

    Self-assembly in mixtures of two single-chain cationic surfactants, with different tail lengths (CTAB and DTAB) as well as of a single-chain (DTAB) and a double-chain (DDAB) cationic surfactant, with identical tail lengths, have been investigated with small-angle neutron scattering (SANS) and rationalised in terms of bending elasticity properties. The growth behaviour of micelles with respect to surfactant composition appears completely different in the two surfactant mixtures. DTAB form small oblate spheroidal micelles in presence of [NaBr]. =. 0.1. M that transform into prolate spheroidal mixed CTAB/DTAB micelles upon adding moderate amounts of CTAB, so as to give a mole fraction . y=. 0.20 in solution. Most unexpectedly, upon further addition of CTAB the mixed CTAB/DTAB micelles grow with an almost equal rate in both length and width directions to form tablets. In contrast to this behaviour, mixed DDAB/DTAB micelles grow virtually exclusively in the length direction, in presence of [NaBr]. =. 0.1. M, to form elongated ellipsoidal (tablet-shaped) and subsequently long wormlike micelles as the fraction of DDAB in the micelles increases. Mixed DDAB/DTAB micelles grow to become as long as 2000. å before an abrupt transition to large bilayer structures occurs. This means that the micelles are much longer at the micelle-to-bilayer transition as compared to the same mixture in absence of added salt. It is found that the point of transition from micelles to bilayers is significantly shifted towards higher fractions of aggregated DTAB as an appreciable amount of salt is added to DDAB/DTAB mixtures, indicating a considerable reduction of the spontaneous curvature with an increasing [NaBr]. By means of deducing the various bending elasticity constants from our experimental results, according to a novel approach by ours, we are able to conclude that the different growth behaviours appear as a consequence of a considerably lower bending rigidity, as well as higher saddle-splay constant, for DDAB/DTAB surfactant mixtures in presence of [NaBr]. =. 0.1. M, as compared to mixtures of CTAB/DTAB in [NaBr]. =. 0.1. M and DDAB/DTAB in absence of added salt.

  • 237. Bernardini, A.
    et al.
    Gemo, N.
    Biasi, P.
    Canu, P.
    Mikkola, J. P.
    Salmi, T.
    Lanza, Roberto
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology.
    Direct synthesis of H2O2 over Pd supported on rare earths promoted zirconia2015In: Catalysis Today, ISSN 0920-5861, E-ISSN 1873-4308, Vol. 256, p. 294-301Article in journal (Refereed)
    Abstract [en]

    In this work Pd (0.3 or 0.6 wt.%) was supported on both ZrxM1-xO2 (M = La, Y, Ce) and on mechanical mixtures of CeO2 and ZrO2. The synthesized catalysts were characterized by XRD, TPR, AAS and CO chemisorption and tested for the direct synthesis of hydrogen peroxide in a high pressure semibatch apparatus. The reactants conversion was limited in order to avoid mass-transfer limitations. No selectivity enhancers of any kind were used and the all the materials were halide free. Small metal particles were obtained (1-2.6 nm). Supports with smaller pore diameters leaded to larger Pd particles, which in turn were found to preferentially support the formation of the peroxide. Moreover, supports with higher reducibility favored the production of H2O2, probably due to an easier reduction of the active metal, essential to achieve high selectivity. Notwithstanding the absence of enhancers, the specific activity and selectivity recorded were very high.

  • 238.
    Bertini, Lorenzo
    KTH, School of Chemical Science and Engineering (CHE).
    Modeling and Optimization of a Fuel Cell Hybrid System2011Independent thesis Advanced level (degree of Master (Two Years)), 20 credits / 30 HE creditsStudent thesis
    Abstract [en]

    The purpose of this project was the modeling, optimization and prediction of a hybrid system composed of a fuel cell, a dc-dc converter and a supercapacitor in series. Lab tests were performed for each device to understand their behavior, and then each one was modeled using software (Simulink). The validation of the model was done by comparing its results with measured data; finally the model was used for the optimization and the prediction of the hybrid system

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  • 239. Bertram, F.
    et al.
    Zhang, Fan
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Evertsson, J.
    Carla, F.
    Pan, Jinshan
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Messing, M. E.
    Mikkelsen, A.
    Nilsson, J-O
    Lundgren, E.
    In situ anodization of aluminum surfaces studied by x-ray reflectivity and electrochemical impedance spectroscopy2014In: Journal of Applied Physics, ISSN 0021-8979, E-ISSN 1089-7550, Vol. 116, no 3, p. 034902-Article in journal (Refereed)
    Abstract [en]

    We present results from the anodization of an aluminum single crystal [Al(111)] and an aluminum alloy [Al 6060] studied by in situ x-ray reflectivity, in situ electrochemical impedance spectroscopy and ex situ scanning electron microscopy. For both samples, a linear increase of oxide film thickness with increasing anodization voltage was found. However, the slope is much higher in the single crystal case, and the break-up of the oxide film grown on the alloy occurs at a lower anodization potential than on the single crystal. The reasons for these observations are discussed as are the measured differences observed for x-ray reflectivity and electrochemical impedance spectroscopy.

  • 240.
    Bessman, Alexander
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Applied Electrochemistry.
    Interactions between battery and power electronics in an electric vehicle drivetrain2018Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    The electric machine and power electronics in electric and hybrid electric vehicles inevitably cause AC harmonics on the vehicle's DC-link. These harmonics can be partially filtered out by large capacitors, which today are overdimensioned in order to protect the vehicle's battery pack. This is done as a precaution, since it is not known whether ripple-current has any harmful effect on Li-ion  cells.

    We have measured and analyzed the ripple-current present in a hybrid electric bus, and found that a majority of the power was carried by frequencies in the range 100~Hz to 1~kHz. The single most energetic harmonic in this particular vehicle is believed to have been caused  by a misaligned resolver in the motor.

    We have also designed and built an advanced experimental set-up in order to study the effect of ripple-current on Li-ion cells in the lab. The set-up can cycle up to 16 cells simultaneously, with currents of up to 50~A including a superimposed AC signal with a frequency of up to 2~kHz. The cells' temperatures are controlled by means of a climate chamber. The set-up also includes a sophisticated safety system which automatically acts to prevent dangerous situations before they arise.

    Using this set-up we tested whether superimposing AC with a specific frequency improves the charging performance of Li-ion cells. Statistical analysis found no improvement over regular DC cycling, and a physics-based model explains the experimental findings.

    We have also investigated whether ripple-current accelerates the aging of Li-ion cells. Twelve cells were either calendar or cycle  aged for one year, with some cells being exposed to superimposed AC with a frequency of 1~Hz, 100~Hz, or 1~kHz. No effect was observed on any of capacity fade, power fade, or aging mechanism.

    Finally we also tested whether it is possible to heat Li-ion cells from low temperatures using only AC. We propose a method for AC heating of Li-ion cells, and open the discussion for generalizing the technique to larger battery packs.

    In conclusion, ripple-current has negligible effect on Li-ion cells, except for heating them slightly.

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  • 241.
    Bessman, Alexander
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Applied Electrochemistry.
    Soares, Rúdi
    KTH, School of Electrical Engineering (EES), Electric Power and Energy Systems.
    Vadivelu, Sunilkumar
    KTH, School of Electrical Engineering (EES), Electric Power and Energy Systems.
    Wallmark, Oskar
    KTH, School of Electrical Engineering (EES), Electric Power and Energy Systems.
    Svens, Pontus
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Applied Electrochemistry.
    Ekström, Henrik
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Applied Electrochemistry.
    Lindbergh, Göran
    KTH, School of Chemical Science and Engineering (CHE), Chemical Engineering and Technology, Applied Electrochemistry.
    Challenging Sinusoidal Ripple-Current Charging of Lithium-Ion Batteries2018In: IEEE transactions on industrial electronics (1982. Print), ISSN 0278-0046, E-ISSN 1557-9948, Vol. 65, no 6, p. 4750-4757Article in journal (Refereed)
    Abstract [en]

    Sinusoidal ripple-current charging has previously been reported to increase both charging efficiency and energy efficiency and decrease charging time when used to charge lithium-ion battery cells. In this paper, we show that no such effect exists in lithium-ion battery cells, based on an experimental study of large-size prismatic cells. Additionally, we use a physics-based model to show that no such effect should exist, based on the underlying electrochemical principles.

  • 242.
    Bessman, Alexander
    et al.
    KTH.
    Soares, Rúdi
    KTH.
    Wallmark, Oskar
    KTH, School of Engineering Sciences (SCI), Aeronautical and Vehicle Engineering.
    Svens, Pontus
    KTH.
    Lindbergh, Göran
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering.
    Aging effects of AC harmonics on lithium-ion cellsManuscript (preprint) (Other academic)
  • 243.
    Bessman, Alexander
    et al.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Applied Electrochemistry.
    Soares, Rúdi
    KTH, School of Electrical Engineering and Computer Science (EECS), Electric Power and Energy Systems.
    Wallmark, Oskar
    KTH, School of Electrical Engineering and Computer Science (EECS), Electric Power and Energy Systems.
    Svens, Pontus
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Applied Electrochemistry.
    Lindbergh, Göran
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Applied Electrochemistry.
    Aging effects of AC harmonics on lithium-ion cells2019In: Journal of Energy Storage, E-ISSN 2352-152X, Vol. 21, p. 741-749Article in journal (Refereed)
    Abstract [en]

    With the vehicle industry poised to take the step into the era of electric vehicles, concerns have been raised that AC harmonics arising from switching of power electronics and harmonics in electric machinery may damage the battery. In light of this, we have studied the effect of several different frequencies on the aging of 28 Ah commercial NMC/graphite prismatic lithium-ion battery cells. The tested frequencies are 1 Hz, 100 Hz, and 1 kHz, all with a peak amplitude of 21 A. Both the effect on cycled cells and calendar aged cells is tested. The cycled cells are cycled at a rate of 1C:1C, i.e., 28 A during both charging and discharging, with the exception of a period of constant voltage at the end of every charge. After running for one year, the cycled cells have completed approximately 2000 cycles. The cells are characterized periodically to follow how their capacities and power capabilities evolve. After completion of the test about 80% of the initial capacity remained and no increase in resistance was observed. No negative effect on either capacity fade or power fade is observed in this study, and no difference in aging mechanism is detected when using non-invasive electrochemical methods of post mortem investigation.

  • 244.
    Bettini, Eleonora
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Influence of carbides and nitrides on corrosion initiation of advanced alloys: A local probing study2013Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    Advanced alloys often present precipitated carbides and nitrides in their microstructure following exposure to elevated temperatures. These secondary phases are usually undesirable, because potentially deleterious for the corrosion and mechanical performances of the material. Carbides and nitrides are enriched in key alloying elements that are subtracted from their surrounding matrix areas, creating alloying element depleted zones, which might become initial sites for corrosion initiation. In this study, the influence of micro- and nano-sized precipitated carbides and nitrides on the corrosion initiation of biomedical CoCrMo alloys and duplex stainless steels has been investigated at microscopic scale, by using a combination of local probing techniques. The microstructures of the alloys were first characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and magnetic force microscopy (MFM). The Volta potential mapping of carbides and nitrides revealed their higher nobility compared to the matrix, and particularly compared to their surrounding areas, suggesting the occurrence of some alloying element depletion in the latter locations, which may lead to a higher susceptibility for corrosion initiation. In-situ electrochemical AFM studies performed at room temperature showed passive behavior for large potential ranges for both alloy families, despite the presence of the precipitated carbides or nitrides. At high anodic applied potential, at which transpassive dissolution occurs, preferential dissolution started from the areas adjacent to the precipitated carbides and nitrides, in accordance with the Volta potential results. Thus, the presence of carbides and nitrides doesn’t largely affect the corrosion resistance of the tested advanced alloys, which maintain passive behavior when exposed to highly concentrated chloride solutions at room temperature with no applied potential. The effect of nitrides on the corrosion initiation of duplex stainless steels was investigated also at temperatures above the critical pitting temperature (CPT). Depending on the type, distribution and size range of the precipitated nitrides different corrosion behaviors were observed. Intragranular (quenched-in) nano-sized nitrides (ca. 50-100 nm) finely dispersed in the ferrite grains have a minor influence on the corrosion resistance of the material at temperatures above the CPT, while larger intergranular (isothermal) nitrides (ca. 80-250 nm) precipitated along the phase boundaries cause a detrimental reduction of the corrosion resistance of the material, in particular of the austenite phase

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    Thesis
  • 245.
    Bettini, Eleonora
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Kivisäkk, Ulf
    Sandvik Materials Technology.
    Leygraf, Christofer
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Pan, Jinshan
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Study of corrosion behavior of a 22% Cr duplex stainless steel: influence of nano-sized chromium nitrides and exposure temperature2013In: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 113, p. 280-289Article in journal (Refereed)
    Abstract [en]

    Chromium nitrides may precipitate in duplex stainless steels during processing and their influence on the corrosion behavior is of great importance for the steel performance. In this study, the influence of nano-sized quenched-in chromium nitrides on the corrosion behavior of a heat treated 2205 duplex stainless steel was investigated at room temperature and 50 °C (just above critical pitting temperature). The microstructure was characterized by SEM/EDS and AFM analyses, and quenched-in nitrides precipitated in the ferrite phase were identified by TEM analysis. Volta potential mapping at room temperature suggests lower relative nobility of the ferrite matrix. Electrochemical polarization and in-situ AFM measurements in 1 M NaCl solution at room temperature show a passive behavior of the steel despite the presence of the quenched-in nitrides in the ferrite phase, and preferential dissolution of ferrite phase occurred only at transpassive conditions. At 50 °C, selective dissolution of the austenite phase was observed, while the ferrite phase with the quenched-in nitrides remained to be stable. It can be concluded that the finely dispersed quenched-in nitrides do not cause localized corrosion, whereas the exposure temperature has a strong influence on the corrosion behavior of the duplex stainless steel.

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    Paper 4
  • 246.
    Bettini, Eleonora
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Kivisäkk, Ulf
    Leygraf, Christofer
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Pan, Jinshan
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Study of Corrosion Behavior of a 2507 Super Duplex Stainless Steel: Influence of Quenched-in and Isothermal Nitrides2014In: International Journal of Electrochemical Science, ISSN 1452-3981, E-ISSN 1452-3981, Vol. 9, no 1, p. 61-80Article in journal (Refereed)
    Abstract [en]

    Precipitation of different types of chromium nitrides may occur during processing of super duplex stainless steels, affecting the properties of the material. In this study the influence of quenched-in (size range ca. 50-100 nm) and isothermal (size range ca. 80-250 nm) types of nitrides on the corrosion behavior of a 2507 super duplex stainless steel has been investigated at room temperature and at 90 degrees C (above the critical pitting temperature) in 1 M NaCl solution. The microstructure has been characterized by scanning electron microscopy and magnetic force microscopy. The isothermal nitrides exhibit a higher Volta potential compared to the matrix, but such difference could not be observed for the quenched-in nitrides. In-situ electrochemical AFM measurements at room temperature show stable surfaces for a wide range of applied potentials despite the presence of either type of nitrides. In the transpassive region isothermal nitrides appear to be slightly more deleterious than quenched-in nitrides. At 90 degrees C isothermal nitrides largely reduce the corrosion resistance of the austenite phase, while the quenched-in nitrides reduce the corrosion resistance of the material to a much lesser extent. The size difference between isothermal and quenched-in chromium nitrides may be crucial, in particular above the critical pitting temperature.

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    Paper 5
  • 247.
    Bettini, Eleonora
    et al.
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Leygraf, Christofer
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Pan, Jinshan
    KTH, School of Chemical Science and Engineering (CHE), Chemistry, Surface and Corrosion Science.
    Nature of current increase for a CoCrMo alloy: "transpassive" dissolution vs. water oxidation2013In: International Journal of Electrochemical Science, ISSN 1452-3981, E-ISSN 1452-3981, Vol. 8, no 10, p. 11791-11804Article in journal (Refereed)
    Abstract [en]

    The “transpassive” behavior of a CoCrMo alloy has been investigated to clarify the nature of the current increase at high anodic potential (0.5-0.7 VAg/AgCl). The total amount of released metal ions was determined after the potentiostatic measurements. According to the calculation through Faradays’ law, the metal dissolution only contributes to part of the total current recorded. Electrochemical AFM mapping did not show pronounced topography changes at 0.65 VAg/AgCl, while light optical microscopy observation revealed fast evolution of oxygen bubbles. Evidently water oxidation is another important process largely contributing to the current increase at the high potential.

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    Paper 3
  • 248. Bełdowski, P.
    et al.
    Weber, P.
    Dédinaité, Andra
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Surface and Corrosion Science. RISE Research Institutes of Sweden, Box 5607, SE-114 86 Stockholm, Sweden.
    Claesson, Per M.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Surface and Corrosion Science. RISE Research Institutes of Sweden, Box 5607, SE-114 86 Stockholm, Sweden.
    Gadomski, A.
    Correction: Physical crosslinking of hyaluronic acid in the presence of phospholipids in an aqueous nano-environment (Soft Matter (2018) DOI: 10.1039/c8sm01388h)2018In: Soft Matter, Vol. 14, no 47Article in journal (Refereed)
    Abstract [en]

    Correction for 'Physical crosslinking of hyaluronic acid in the presence of phospholipids in an aqueous nano-environment' by Piotr Bełdowski et al., Soft Matter, 2018, DOI: 10.1039/c8sm01388h. 

  • 249.
    BHANDARI, SHASHANK
    KTH, School of Chemical Science and Engineering (CHE).
    Design of a solvent recovery system in a pharmaceutical manufacturing plant2016Independent thesis Advanced level (degree of Master (Two Years)), 20 credits / 30 HE creditsStudent thesis
    Abstract [en]

    Solvents play a crucial role in the Active Pharmaceutical Ingredient (API) manufacturing and are used in large quantities. Most of the industries incinerate the waste solvents or send it to waste management companies for destruction to avoid waste handling and cross-contamination. It is not a cost effective method and also hazardous to the environment. This study has been performed at AstraZeneca’s API manufacturing plant at Sodertalje, Sweden. In order to find a solution, a solvent recovery system is modeled and simulated using ASPEN plus and ASPEN batch modeler. The waste streams were selected based on the quantity and cost of the solvents present in them. The solvent mixture in the first waste stream was toluene-methanol in which toluene was the key-solvent whereas in the second waste stream, isooctane-ethyl acetate was the solvent mixture in which isooctane was the key-solvent. The solvents in the waste stream were making an azeotrope and hence it was difficult to separate them using conventional distillation techniques. Liquid-Liquid Extraction with water as a solvent followed by batch distillation was used for the first waste stream and Pressure Swing Distillation was used for the second waste stream. The design was optimized based on cost analysis and was successful to deliver 96.1% toluene recovery with 99.5% purity and 83.6% isooctane recovery with 99% purity. The purity of the solvents was decided based on the quality conventions used at AstraZeneca so that it can be recovered and recycled in the same system. The results were favorable with a benefit of €335,000 per year and preventing nearly one ton per year carbon dioxide emissions to the environment. A theoretical study for the recovery system of toluene-methanol mixture was performed. The proposed design was an integration of pervaporation to the batch distillation. A blend of polyurethane / poly(dimethylsiloxane) (PU / PDMS) membrane was selected for the separation of methanol and toluene mixture. The results of preliminary calculations show 91.4% toluene recovery and 72% methanol recovery with desired purity.

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  • 250.
    Bhasin, Aditi
    KTH, School of Chemical Science and Engineering (CHE).
    Recovery of Phosphorus from Incineration of Sewage Sludge2017Independent thesis Advanced level (degree of Master (Two Years)), 20 credits / 30 HE creditsStudent thesis
    Abstract [en]

    The primary source of phosphorus, phosphate rock, is a non-renewable resource which is expected to get exhausted in the next 50 – 100 years. Sewage sludge in Sweden constitutes 25% of the annual phosphorus in the country, making it a potentially significant source for phosphorus recovery. The aim of this project was to identify the potential for phosphorus recovery from incineration of dewatered and digested sewage sludge in Fortum Värme’s power plants in Stockholm. The study was limited to two boilers located at Bristaverket, Stockholm - boiler B1, a bio-fired fluidized bed boiler and boiler B2, a waste-fired grate incinerator. A theoretical analysis for boiler B1 showed that it is possible to reach a concentration of 4.6% phosphorus in fly ash if sludge and recycled wood fuel are mixed in the ratio 48:52. A test program was executed in boiler B2 to burn up to 12.5% sludge with a mixture of household waste and industrial waste. A total of 755 tons of sludge was used over a period of three weeks during the test in boiler B2. The test was successful in terms of combustion and emissions. There was no increase in the emissions of nitrogen oxides, sulphur dioxide and hydrochloric acid in the flue gas. Mercury emissions in the chimney increased with an increase in the share of sludge, nevertheless, the emission level was below the limit set by the Swedish Environmental Protection Agency. Decrease in the amount of unburnt materials in bottom ash and in the emission of carbon monoxide showed that the burning of fuel was more efficient with input of sludge. The maximum phosphorus concentration was 0.7% in both bottom ash and fly ash from boiler B2 and occurred at an input of 12.5% sludge. This concentration is close to the expected theoretical value, however it is not expected to be feasible to recover phosphorus at such a low concentration. The ashes were sent to Fortum Waste Solutions and Ragn-Sells for recovery of phosphorus, however the results are not included in this report due to time constraints for thesis study. In order to increase the concentration of phosphorus in the ashes, a system approach is recommended, for instance, recirculation of bottom ash into the incinerator.

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