TL;DR: In this article, a molecular spray is directed against a substrate to deposit a solid thin film thereon, or discharged into a collection chamber to collect a fine powder, and any clusters of solvent are broken up and vaporized and pumped away.
Abstract: Solid films are deposited, or fine powders formed, by dissolving a solid material into a supercritical fluid solution at an elevated pressure and then rapidly expanding the solution through a short orifice into a region of relatively low pressure. This produces a molecular spray which is directed against a substrate to deposit a solid thin film thereon, or discharged into a collection chamber to collect a fine powder. Upon expansion and supersonic interaction with background gases in the low pressure region, any clusters of solvent are broken up and the solvent is vaporized and pumped away. Solute concentration in the solution is varied primarily by varying solution pressure to determine, together with flow rate, the rate of deposition and to control in part whether a film or podwer is produced and the granularity of each. Solvent clustering and solute nucleation are controlled by manipulating the rate of expansion of the solution and the pressure of the lower pressure region. Solution and low pressure region temperatures are also controlled.
TL;DR: In this paper, a molecular spray is directed against a substrate to deposit a solid thin film thereon, or discharged into a collection chamber to collect a fine powder, which is discharged in the form of long, thin fibers.
Abstract: Solid films are deposited, or fine powders formed, by dissolving a solid material into a supercritical fluid solution at an elevated pressure and then rapidly expanding the solution through a heated nozzle having a short orifice into a region of relatively low pressure. This produces a molecular spray which is directed against a substrate to deposit a solid thin film thereon, or discharged into a collection chamber to collect a fine powder. In another embodiment, the temperature of the solution and nozzle is elevated above the melting point of the solute, which is preferably a polymer, and the solution is maintained at a pressure such that, during expansion, the solute precipitates out of solution within the nozzle in a liquid state. Alternatively, a secondary solvent mutually soluble with the solute and primary solvent and having a higher critical temperature than that of primary solvent is used in a low concentration (<20%) to maintain the solute in a transient liquid state. The solute is discharged in the form of long, thin fibers. The fibers are collected at sufficient distance from the orifice to allow them to solidify in the low pressure/temperature region.
TL;DR: A molecular spray which is directed against a substrate to deposit a solid thin film thereon, or discharged into a collection chamber to collect a fine powder is vaporized and pumped away as mentioned in this paper.
Abstract: Solid films are deposited, or fine powders formed, by dissolving a solid material into a supercritical fluid solution at an elevated pressure and then rapidly expanding the solution through a short orifice into a region of relatively low pressure. This produces a molecular spray which is directed against a substrate to deposit a solid thin film thereon, or discharged into a collection chamber to collect a fine powder. The solvent is vaporized and pumped away. Solution pressure is varied to determine, together with flow rate, the rate of deposition and to control in part whether a film or powder is produced and the granularity of each. Solution temperature is varied in relation to formation of a two-phase system during expansion to control porosity of the film or powder. A wide variety of film textures and powder shapes are produced of both organic and inorganic compounds. Films are produced with regular textural feature dimensions of 1.0-2.0 μm down to a range of 0.01 to 0.1 μm. Powders are formed in very narrow size distributions, with average sizes in the range of 0.02 to 5 μm.
TL;DR: In this article, the authors considered the factors which determine the electron resonance line widths of transition metal complexes in solution and showed that the dominant relaxation mechanism arises from coupling of zero-field splitting of the spin multiplet with the random tumbling of the molecules in fluid solution.
Abstract: The factors which determine the electron resonance line widths of transition metal complexes in solution are considered. For complex ions possessing two or more unpaired electrons the dominant relaxation mechanism arises from coupling of the zero-field splitting of the spin multiplet with the random tumbling of the molecules in fluid solution. The theory of this effect is re-examined using the time-dependent density matrix methods of Redfield.