Hydrogen Peroxide Formation by Electric Discharge with Fine Bubbles

Pulsed discharge plasma is typical oxidation technology for disposing organic compounds in aqueous solutions. When this electrical discharge plasma was applied in water, it may produce hydrogen peroxide (H₂O₂) without any catalyst or chemical agent. In order to increase H₂O₂ production by electrical discharge plasma in water, fine bubbles were introduced into the electrical discharge plasma in this experiment. Bipolar pulsed voltages were applied to cylindrical electrodes in the water while Ar or O₂ bubbles were introduced, generating a pulsed discharge plasma. The introduction of the bubbles seemed to enhance the dissociation of water molecules and increased H₂O₂ formation, especially with O₂ bubbling. Dissolved oxygen in the water contributed to H₂O₂ formation by pulsed discharge plasma with the bubbles, while dissociation of water molecules was the cause of H₂O₂ formation by pulsed discharge plasma without bubbles. More H₂O₂ was formed by pulsed discharge plasma with O₂ bubbles, because the amount of dissolved oxygen in the water increased upon bubbling with O₂.     

Kinetic study for liquefaction of tar in sub- and supercritical water

Liquefaction of tar from oil distillation was studied under sub- and supercritical water conditions using a batch reactor at 623 and 673 K and 25-40 MPa. The reaction scheme for tar liquefaction was determined as follows: the liquefaction process of tar occurs first and then intermediate chemical compounds are transformed into lighter molecular weight species. The effects of pressure and treatment time were combined into a single severity parameter that was used to monitor the conversion of tar. The main products from the liquefaction of tar were phenol (3.44 wt%), biphenyl (2.23 wt%), diphenylether (13.70 wt%) and diphenylmethane (1.30 wt%), respectively. Liquefaction of tar clearly increased with increasing water density at the same temperature reaction. It indicates that hydrolysis was important in the cleavage of the macromolecular structure of tar under sub- and supercritical conditions. Based on the results, this method could become an efficient method for tar liquefaction, producing high yields of valuable chemical intermediates.     

Bitumen upgrading under solvothermal/hydrothermal conditions

Bitumen is known as a mixture of organic liquids which has great importance to the chemical industry because of its great variety of special properties, which has favored the development of a wide field of applications. Bitumen has been mainly obtained as a residue of the petroleum refining process. Recently, the development of a process has been proposed to recover chemical resources from bitumen that can accomplish the destruction of the bitumen to produce harmless but useful compounds. Water at hydrothermal conditions is considered a promising and an environmentally acceptable solvent for a wide variety of chemical reactions such as organic syntheses and decomposition of hazardous waste into harmless compounds. In these works, water at supercritical conditions was applied as a solvent for upgrading of bitumen. The experiments were conducted at a temperature of 673 K and at various reaction pressures. The effect of pressure and reaction time on the decomposition process is presented. The chemical species in the aqueous products were analyzed by gas chromatography?Cmass spectrometry and matrix-assisted laser desorption ionization time-of-flight mass spectroscopy. Ultimate analysis of solid residue was also conducted using a CHN analyzer. The results showed that the amounts of bitumen-derived compounds formed increased with increasing reaction time. In addition, the study of bitumen model compounds by using a batch reactor was also conducted. Furthermore, this method could become an efficient method for upgrading bitumen into harmless compounds with a high yield of valuable chemical intermediates on the basis of the experimental results.     

Silver nanoparticles generated by pulsed laser ablation in supercritical CO2 medium

Pulsed laser ablation (PLA) has been widely employed in industrial and biological applications and in other fields. The environmental conditions in which PLA is conducted are important parameters that affect both the solid particle cloud and the deposition produced by the plume. In this work, the generation of nanoparticles (NPs) has been developed by performing PLA of silver (Ag) plates in a supercritical CO₂ medium. Ag NPs were successfully generated by allowing the selective generation of clusters. Laser ablation was performed with an excitation wavelength of 532 nm under various pressures and temperatures of CO₂ medium. On the basis of the experimental result, both surface of the irradiated Ag plate and structure of Ag NPs were significantly affected by the changes in supercritical CO₂ pressure and temperature. With increasing irradiation pressure, plume deposited in the surrounding crater created by the ablation was clearly observed. In Field Emission Scanning Electron Microscopy (FE-SEM) the image of the generated Ag NPs on the silicon wafer and the morphology of Ag particles were basically a sphere-like structure. Ag particles contain NPs with large-varied diameter ranging from 5 nm to 1.2 μm. The bigger Ag NPs melted during the ablation process and then ejected smaller spherical Ag NPs, which formed nanoclusters attached on the molten Ag NPs. The smaller Ag NPs were also formed around the bigger Ag NPs. Based on the results, this new method can also be used to obtain advanced nano-structured materials.     

One-step synthesis of water–dispersible carbon nanocapsules by pulsed arc discharge over aqueous solution under pressurized argon

Research on Chemical Intermediates - Water–dispersible carbon nanocapsules were synthesized in a one-step process by a pulsed arc discharge over glycine solution under pressurized argon....     

Macroporous zirconia particles prepared by subcritical water in batch and flow processes

Porous zirconia particles were synthesized through a low-temperature hydrothermal synthesis process. Under hydrothermal conditions, water can control the direction of crystal growth, morphology, particle size, and size distribution because thermodynamics and transport properties can be controlled by pressure and temperature. In a batch process, the hydrothermal synthesis was conducted at 200–300 °C and 30 MPa with an SUS-304 tube as the reactor. At the same reaction pressure, experiments were also performed for a flow process with temperatures of 180–200 °C. The synthesized products were calcined and characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). The results showed that the macroporous zirconia particles that were formed had pore diameters around 419 nm. The XRD pattern indicated that the products were composed of zirconium oxide particles with monoclinic, tetragonal, and cubic structures.     

Production of nanofibers by electrospinning under pressurized CO2

Electrospinning is one of the simple technical methods for the production of polymer nanoparticles and nanofibers. Various polymers have been successfully electrospun into ultrafine particles and fibers in recent years mostly in solvent solution and some in melt form. In this work, near- and supercritical CO₂ were used as media for this process. At these conditions, the solubility can be tuned by controlling the temperature and pressure. Therefore, it is possible to form particles and fibers within a thermodynamic window where the biopolymer has been softened, but not dissolved. The experiments were conducted by using electrospinning under pressurized CO₂ system at pressures of ～ 8.0 MPa and temperature of 313 K to produce several polymers fibers. Polyvinylpyrrolidone was used as the starting material. During the electrospinning process, the applied voltage was 10–17 kV and the distance of nozzle and collector was 8 cm. The concentration of polymer solution was 4 wt%. The morphology- and structure-produced fibers were observed by scanning electron microscopy. The results showed that temperature and pressure affected the morphology of fibers produced by electrospinning in pressurized CO₂. This suggests that the thermal behavior of the polymer can be optimized by adjusting the polymer through the adjustment of pressure and temperature by using CO₂ as a solvent.     

Gold nanoparticles fabricated by pulsed laser ablation in supercritical CO2

Nanosecond pulsed laser ablation (PLA) of gold plate with an excitation wavelength of 532?nm was carried out in supercritical CO₂ (scCO₂) to fabricate gold nanoparticles. Surface morphology of the gold plate after irradiation and the crater depth after PLA were observed by scanning electron microscopy and laser scanning microscopy, while extinction spectra of gold nanoparticles collected in the glass slide was measured by UV?CVis spectrophotometer. The gold plate was ablated at various scCO₂ densities and irradiation times at constant temperature of 40??C. The ablation was also conducted at atmospheric condition with air to evaluate the environmental dependence of ablation. Both surface morphology of the irradiated gold plate and crater depth formation were significantly affected by the changes in scCO₂ density, the surrounding environment, and irradiation time. As expected, the increasing scCO₂ density resulted in a deeper ablation crater, however, the deepest crater was obtained at a density of 0.63?g/cm³ or pressure of 10?MPa. Gold nanoparticles generated by PLA in scCO₂ have been confirmed at the spectra band near 530?nm.     

Nickel nanoparticles generated by pulsed laser ablation in liquid CO2

Research on Chemical Intermediates - Nickel nanoparticles with various structures were synthesized by a pulsed laser ablation process in liquid CO2 at 17 °C and 5.2 MPa. A...