<p>The thesis deals partly with methodology including construction</p><p>of hardware and new pulse sequences in the field of electrophoretic</p><p>NMR, and partly with practical use of ENMR and</p><p>diffusion NMR in the investigation of charged colloidal systems.</p><p>Several sources of artefacts are investigated, including gas production</p><p>at the electrodes, electroosmosis and Joule heating</p><p>effects that can cause convection. The electrophoretic double</p><p>stimulated-echo pulse sequence is introduced to suppress these</p><p>artefacts and to increase the feasible measuring range to higher</p><p>electric fields and conductivities.</p><p>The interaction between the non-ionic polymer poly(ethylene</p><p>oxide) PEO and differently charged surfactants is investigated</p><p>using the above mentioned methods. The investigated surfactants</p><p>are the anionic sodium dodecyl sulphate (SDS) and</p><p>potassium laurate (KC12), the cationic dodecyltrimethylammonium</p><p>bromide (CTAB) and the non-ionic octyl β-D-glucoside.</p><p>ENMR is also used to investigate two different mixed micelle</p><p>systems, with SDS as the charged surfactant component and</p><p>dodecyl malono-bis-N-methylglucamide (C12BNMG) respectively</p><p>tetra(ethylene oxide) dodecyl ether (C12EO4) as the nonionic</p><p>surfactant component. A method to calculate the degree</p><p>of counter-ion dissociation, αdissociation, as a function of composition</p><p>is demonstrated.</p><p>Finally diffusion NMR is used to compare transport dynamics</p><p>in gel electrolyte systems based on two differently grafted polymers;</p><p>one amphiphilic system containing polymethacrylate</p><p>grafted partly with polyethylene oxide and partly with fluorocarbons</p><p>and the corresponding nonamphiphilic system grafted</p><p>with only polyethylene oxide. Both systems contain the electrolyte</p><p>lithium bis(trifluoromethylsulfonyl) imide salt dissolved in</p><p>γ-butyrolactone. The results show that the system based on the</p><p>amphiphilic polymer has better transport dynamics and therefore</p><p>is more suited as material for battery</p>

The thesis deals partly with methodology including construction of hardware and new pulse sequences in the field of electrophoretic NMR, and partly with practical use of ENMR and diffusion NMR in the investigation of charged colloidal systems. Several sources of artefacts are investigated, including gas production at the electrodes, electroosmosis and Joule heating effects that can cause convection. The electrophoretic double stimulated-echo pulse sequence is introduced to suppress these artefacts and to increase the feasible measuring range to higher electric fields and conductivities. The interaction between the non-ionic polymer poly(ethylene oxide) PEO and differently charged surfactants is investigated using the above mentioned methods. The investigated surfactants are the anionic sodium dodecyl sulphate (SDS) and potassium laurate (KC12), the cationic dodecyltrimethylammonium bromide (CTAB) and the non-ionic octyl β-D-glucoside. ENMR is also used to investigate two different mixed micelle systems, with SDS as the charged surfactant component and dodecyl malono-bis-N-methylglucamide (C12BNMG) respectively tetra(ethylene oxide) dodecyl ether (C12EO4) as the nonionic surfactant component. A method to calculate the degree of counter-ion dissociation, αdissociation, as a function of composition is demonstrated. Finally diffusion NMR is used to compare transport dynamics in gel electrolyte systems based on two differently grafted polymers; one amphiphilic system containing polymethacrylate grafted partly with polyethylene oxide and partly with fluorocarbons and the corresponding nonamphiphilic system grafted with only polyethylene oxide. Both systems contain the electrolyte lithium bis(trifluoromethylsulfonyl) imide salt dissolved in γ-butyrolactone. The results show that the system based on the amphiphilic polymer has better transport dynamics and therefore is more suited as material for battery