Th. 3e cycle--océanologie biologique--Paris VI, 1986. / Bibliogr. p. 86-105 et p. 9.

Th. univ.--Chimie--Paris 6, 1993. / Bibliogr. p. 192-206. 1993 d'après la déclaration de dépôt légal.

No description available.

No description available.

Stable passive mode-locked fiber lasers(MLFLs) employing graphene saturable absorber (SA) are demonstrated. The graphene were dispersed in de-ionized water by two different dispersants including fluorinated mica clay (Mica) and poly(oxyethylene)-segmented imide (POEM). Using the SA made by graphene dispersed in Mica with thickness and concentration product (TCP) of 36 (£gm*wt%), the MLFLs exhibited pulsewidth, 3-dB spectral bandwidth, and modulation depth (MD) of 382 fs, 6.80 nm, and 2.57%, respectively. The graphene dispersed in POEM provides a TCP of 38 (£gm*wt%) to make the MLFLs deliver pulsewidth, 3-dB spectral bandwidth, and MD of 422 fs, 6.35 nm, and 1.70%, respectively. In comparison, the graphene SA dispersed by Mica performs a better MLFL pulse quality than that dispersed by POEM. Lastly, for investigating the dispersed uniformity between Mica and POEM, we randomly chose 9 pieces and measured the MLFL performance. The result showed that using the SA made by graphene dispersed in Mica with TCP of 36 (£gm*wt%), the MLFLs exhibited pulsewidth of 393¡Ó14 fs, By contrast, the graphene dispersed in POEM provided a TCP of 38 (£gm*wt%) to make the MLFLs delivered pulsewidth of 442¡Ó32 fs. This result reveals that graphene SA film dispersed by Mica exhibited better uniformity than POEM. The MLFL of 21-layes CVD process graphene SA showed a pulsewidth of 432.47 fs, a bandwidth of 6.16nm, and a time-bandwidth product (TBP) of 0.323. This result showed that the solution blending process graphene SA exhibited better MLFL performance than CVD.

Th. univ.--Chim. et physicochim. des polymères--Paris 6, 1998. / Bibliogr. f. 154-160. Résumé en français et en anglais. 1999 d'après la déclaration de dépôt légal.

Novel electrocchemical and chemical strategies have been developed for the fabrication of functional nanocomposites. New scientific and engineering contribution of this work to colloidal nanotechnology included the development of advanced chelating dispersing agents, such as various small organic molecules and chelating polymers. The unique feature of such dispersion agents is their strong adsorption on the surface of different materials, which allows superior dispersion. The chelating monomers of chelating polymers, such as PAZO and PMSS provided multiple adsorption sites for bonding to metal atoms on the particles surface. We analyzed and developed new fundamental adsorption and dispersion mechanisms. An important finding was the possibility of co-dispersion and co-deposition of advanced materials such as oxides, nitrides, complex oxides and minerals using universal dispersing agents and formation of composites by EPD method. It was found that Caffeic acid (CA) can be used as an efficient dispersing agent for the synthesis of ZnO nanorods of reduced size and a dispersing agent for the EPD of ZnO films. Another important achievement of this work was the application of tannic acid as an efficient capping and dispersing agent for synthesis and EPD of inorganic materials and composites. An important discovery was the use of lauryl gallate dispersant as a reducing agent for the synthesis of AgNp and a vehicle for particle dispersion and extraction in the liquid-liquid extraction method. Further advancements in our new technologies allowed us to develop composite films using anodic EPD using weak polyelectrolytes, such as alginate. The composite coatings exhibited protective and flame retardant properties. We analyzed the deposition mechanisms and kinetics as well as microstructure of the coatings. In another strategy, we developed electrochemical strategies for the deposition of composites, based on strong polyelectrolytes. The approach is based on the EPD of the polyelectrolyte molecules and electrosynthesis of EPD of ceramic particles. The electrostatic heterocoagulation mechanism was proposed for the deposit formation. We investigated the deposition kinetics, composition and microstructure of the composites prepared by the new strategies. The new electrochemical strategies can be used for the deposition of other composites, based on functional polymers with pH independent charge. New methods have been developed for the chemical synthesis of PPy based composites, using PMSS, PMSS–SR11 and PMSS–SR31 as anionic dopants for chemical polymerization and dispersants for MWCNT. The composites showed promising performance for application in electrodes of electrochemical supercapacitors. Good electrochemical performance was achieved at high active mass loadings. The electrodes showed high capacitance, large voltage window and low impedance. The analysis of electrochemical testing results and chemical structure of PMSS, PMSS–SR11 and PMSS–SR31 provided an insight into the influence of the anionic functional groups on the capacitance and capacitance retention a high charge-discharge rates. / Thesis / Master of Applied Science (MASc)

Modeling the transport and fate of spilled crude oil is important for estimating short and long-term toxicity effects in coastal ecosystems. This research project investigates the partitioning of hydrocarbons from a surface crude oil slick, the resurfacing of chemically dispersed crude oil droplets, the suitability of in-situ field instruments for oil and sediment characterization, and the aggregation and settling of dispersed oil and suspended sediments. An initial laboratory study was conducted to investigate apparent hydrocarbon solubility in petroleum/water systems. Mixing shear and initial crude oil layer thickness were related empirically to oil entrainment rate. A model describing hydrocarbons partitioned in colloidal and soluble phases was consistent with experimental data. A second laboratory study was conducted to investigate the influence of coalescence kinetics on mean droplet size and resurfacing rate of chemically dispersed crude oil droplets. Increased mean shear rates resulted in mean droplet diameters and oil resurfacing rates. A third laboratory study was conducted to compare particle size and fractal dimension measurements obtained using a submersible flow cytometer, an electrozone particle counter, and a light scattering particle sizer. Measured particles included latex beads, crude oil, clay, crude oil-clay aggregates, and crude oil-silica aggregates. Tested instruments gave consistent size measurements for all particle systems, suggesting their suitability for sizing marine particles. To describe the aggregation kinetics of oil-sediment systems, a modified Smoluchowski model based on coalesced sphere (CS) assumptions was developed. Observed collision efficiency values (αOBS) were related to collision efficiency values for single particle type systems (αHOMO) and those for two particle type systems (αHET) using a probabilistic approach. For clay and crude oil, αHOMO values were higher than the αHOMO value for silica. Clay-oil and silica-oil have similar αHET values. Thus, crude oil can significantly increase the aggregation rates of noncohesive sediments such as silica. The CS model above was modified to incorporate sediment fractal geometry. The ability of this modified coalesced fractal sphere (mCFS) model to fit experimental data sets was better than that of a coalesced sphere (CS) model. Because of their reduced settling rates, sediments with lower fractal dimension form more aggregate with dispersed oil.

This thesis provides a detailed evaluation of different environmentally friendly dispersants in invert-emulsion drilling fluids that can be used to drill wells under difficult conditions such as HPHT. The drilling fluid is weighted by manganese tetraoxide (Mn3O4) particles, which have a specific gravity of 4.8 and a mean particle diameter of ca1 micrometers. Manganese tetraoxide has different wetting properties and surface chemistry than other weighting agents. Hence, there is a need to find dispersants for manganese tetraoxide that give reduced sag, reduced rheology, and low fluid-loss at HPHT conditions. This is particularly important for deep wells with narrow operating windows between pore-pressure and fracture pressure gradients. The stricter global environmental regulations mandated the dispersants to be environmentally friendly, e.g. within OCNS group D or E. First, oil compatibility tests and particle settling time experiments were conducted on 31 dispersants. From the experiments, we identified 3 oil-compatible dispersants that gave the longest settling time in base oil and belonged to OCNS group D. We investigated the effectiveness of selected chemicals in dispersing manganese tetraoxide at HPHT conditions. 1.95 and 2.4 S.G. drilling fluid samples were first prepared and tested without any contaminant and then in the presence of rev dust and cement as contaminants. Drilling fluid samples were statically aged at 400 degrees F and 500 psi for 16 hours. Sag and rheological measurements were taken before and after aging to determine the effect of HPHT conditions on fluid properties. Then, HPHT dynamic filtration tests were done at 500 psi differential pressure and 300 degrees F to determine HPHT dynamic fluid-loss. We have found that one of the dispersants (nonionic) gives low rheology and reduced sag before and after static aging. It also gives the lowest fluid-loss of the selected dispersants. For 2.4 S.G. fluid without contaminants, 10-minute gel strength was reduced from 50 to 32 lb/100 ft^2, plastic viscosity from 37 to 25 cp, sag from 0.249 to 0.135 lbm/gal, and fluid-loss was reduced from 44.4 to 39.6 cm^3 with the addition of dispersant. This dispersant prevents agglomeration of particles, thereby reducing fluid rheology, sag, and fluid-loss.

For decades, global regulations and government mandates have driven technological developments to improve vehicle fuel economy. Tribological components found in all automotive engines contain metal-on-metal contact zones that may result in increased friction and wear, reducing overall engine efficiency. Lubricant additives such as antiwear and friction modifying components are added to motor oils to prevent some of the damages that may occur at contact zones and improve friction. The effects of other additive components, such as dispersants, that are prevalent in a lubricant additive package on the anti-wear layer remain relatively unknown. Polyisobutenyl Succinimide (PIBSI) dispersants were evaluated for their interactions with the ZDDP antiwear component. The physical and chemical properties and friction of the tribofilms formed in presence of dispersants were defined revealing a previously unknown structure-activity relationship. Further analysis of ZDDP and dispersants revealed surface and bulk fluid interactions.