| 1. |
- Hamngren Blomqvist, Charlotte, 1984, et al.
(författare)
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Pore size effects on convective flow and diffusion through nanoporous silica gels
- 2015
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Ingår i: Colloids and Surfaces A: Physicochemical and Engineering Aspects. - : Elsevier BV. - 0927-7757 .- 1873-4359. ; 484, s. 288-296
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Tidskriftsartikel (refereegranskat)abstract
- Material structure has great impact on mass transport properties, a relationship that needs to be understood on several length scales. Describing and controlling the properties of flow through soft materials are both challenges concerning the industrial use of gel structures. This paper reports on how the porous structure in nanoporous materials affects the water transport through them. We used three different silica gels with large differences in the pore sizes but of equal silica concentration. Particle morphology and gel structure were studied using high-resolution transmission electron microscopy and image analysis to estimate the pore size distribution and intrinsic surface area of each gel. The mass transport was studied using a flow measurement setup and nuclear magnetic resonance diffusometry. The average pore size ranged from approximately 500. nm down to approximately 40. nm. An acknowledged limit for convective flow to occur is in the pore size range between 100 and 200. nm. The results verified the existence of a non-linear relationship between pore size and liquid flow at length scales below 500. nm, experimentally. A factor of 4.3 in flow speed separated the coarser gel from the other two, which presented almost identical flow speed data despite a factor 3 in pore size difference. In the setup, the mass transport in the gel with the largest pores was flow dominated, while the mass transport in the finer gels was diffusion dominated. Besides providing new insights into mass transport as a function of pore sizes, we conclude that three-dimensional analysis of the structures is needed for a comprehensive understanding of the correlation between structure and mass transport properties.
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| 2. |
- MacGregor-Ramiasa, M., et al.
(författare)
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Magnetic alignment of nontronite dispersions
- 2015
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Ingår i: Applied Clay Science. - : Elsevier BV. - 0169-1317. ; 116-117, s. 167-174
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Tidskriftsartikel (refereegranskat)abstract
- The time dependent alignment of exfoliated nontronite dispersions subjected to moderate magnetic field strengths (B.
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| 3. |
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| 4. |
- Abrahamsson, Christoffer, 1984, et al.
(författare)
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Magnetic orientation of nontronite clay in aqueous dispersions and its effect on water diffusion
- 2015
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Ingår i: Journal of Colloid and Interface Science. - : Elsevier BV. - 0021-9797 .- 1095-7103. ; 437, s. 205-210
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Tidskriftsartikel (refereegranskat)abstract
- The diffusion rate of water in dilute clay dispersions depends on particle concentration, size, shape, aggregation and water-particle interactions. As nontronite clay particles magnetically align parallel to the magnetic field, directional self-diffusion anisotropy can be created within such dispersion. Here we study water diffusion in exfoliated nontronite clay dispersions by diffusion NMR and time-dependant 1H-NMR-imaging profiles. The dispersion clay concentration was varied between 0.3 and 0.7 vol%. After magnetic alignment of the clay particles in these dispersions a maximum difference of 20% was measured between the parallel and perpendicular self-diffusion coefficients in the dispersion with 0.7 vol% clay. A method was developed to measure water diffusion within the dispersion in the absence of a magnetic field (random clay orientation) as this is not possible with standard diffusion NMR. However, no significant difference in self-diffusion coefficient between random and aligned dispersions could be observed.
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| 5. |
- Abrahamsson, Christoffer, 1984
(författare)
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Microstructure and liquid mass transport control in nanocomposite materials
- 2015
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Some of the biggest problems currently facing the world are closely tied to unsolved technological challenges in the material sciences. Many materials have a porous microstructure that controls their overall properties. In the case of porous materials their properties often relate to how liquids and dissolved substances move (liquid mass transport) through the pores of the material and how these substances interact with the pore walls. Challenges related to such processes can be found in applications related to energy storage, oil well engineering, food, chromatography, and drug release. It is not a trivial matter to design a material synthesis method that reproducibly produces a robust material with the correct pore-structure and surface properties and in the end, the intended function. An added difficulty is that the material should maintain its function over the intended usage period. These generic difficulties summarizes why some technological problems related to porous materials still remains unsolved. The research community is therefore trying to acquire a better understanding of the mechanisms that governs how the synthesis process affects the microstructure and the resultant liquid mass transport properties.The focus of this work has been to investigate the nanoparticle organization in dispersions and in aggregated microporous materials, and how this organization affects the liquid diffusion and permeability through the material. To study these processes several model material synthesis methods, characterization techniques, and theoretical models were developed. Specifically the work investigated how the particle concentration, shape and aggregation conditions affected the formed microstructure. The role of microstructure anisotropy was investigated by aligning plate-shaped particles in magnetic fields during the material synthesis. In addition, the effect of several different additives on the magnetic alignment process was explored. Furthermore, a responsive nanocomposite material was synthesized in which temperature could be used to reversibly adjust the pore size of the material. The findings showed that particle concentration, aggregation conditions, magnetic fields and temperature responsive microgels can be used to control the liquid mass transport through colloidal dispersions and gels. In some cases the experimental results together with simulations were used to derive microstructure and mass transport correlations for different particle aggregation conditions. These correlations are of general application when predicting the pore size and liquid mass transport in aggregated nanoparticle materials.
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