Ultrasound-enhanced photodegradation of Diclofenac Na

Diclofenac sodium, a non-steroidal anti-inflammatory drug, is an emerging water pollutant that cannot be removed by conventional wastewater treatment plants. Combined processes based on hydrodynamic cavitation (sonolysis) and heterogeneous photocatalysis are highly promising for the degradation and mineralization of refractory drugs [1,2]. Nevertheless, the use of nanoparticles as photocatalyst is not suitable in real applications for environmental and health hazard [3] as well as for the complex photocatalyst retrieval at the end of the process. For this reasons, we studied the photocatalyzed degradation of Diclofenac Na using micrometric titanium dioxide photocatalyst (Kronos 1077, 0.1 g/L), both bare and decorated with silver. Moreover, the synergic effect of pulsed ultrasound was tested. Initial concentrations of diclofenac sodium in the 25-50 ppm range were tested. Tests were performed in a batch jacketed reactor. A UVA lamp set sideway irradiated the solution with a power of 30 W/m2 and an ultrasonic horn (20 kHz) sonicated the solution. HPLC-UV and HPLC-MS determined Diclofenac degradation and the main byproducts. A total organic carbon analyzer (TOC, Shimadzu) calculated the fraction of Diclofenac mineralized. An example of photodegradation run is reported in figure. A positive synergy coupling ultrasounds with photocatalysis is confirmed, mainly with the use of Ag nanoparticles-TiO2. We observed both a faster molecule degradation and its complete mineralization

Ultrasound-assisted impregnation for high temperature Fischer-Tropsch catalysts

A fraction of the petroleum extracted from oil reservoirs contains associated natural gas. Rather than building infrastructure to recover low volumes of this natural gas, the industry flares or vents it to the atmosphere, which contributes to atmospheric greenhouse gas emissions but also reduces the air quality locally because it contains gaseous sulphur and nitrogen compounds. Converting the natural gas (NG) to hydrocarbons with a small-scale two-step gas-to-liquids process, is an alternative to flaring and venting. In the first step, NG reacts with oxygen to form syngas (Catalytic Partial Oxidation) and in the second step the syngas reacts over metallic catalysts to form higher paraffins at 210 degrees C to 300 degrees C-Fischer Tropsch synthesis (FT). For the first time, we synthesize bimetallic FeCo FT catalysts with ultrasound. An ultrasonic horn agitates the solution during the entire impregnation process. The active phase dispersion of the sonicated catalysts was superior to the catalyst synthesized without ultrasound, while reducing the impregnation time by a factor of three. We tested our catalysts in a lab-scale, fixed-bed reactor at 270 degrees C and 300 degrees C, and achieved 80% conversion over 3-days on stream and a 40% yield of C2+

In Vitro Models of Bacterial Biofilms: Innovative Tools to Improve Understanding and Treatment of Infections

Bacterial infections are a growing concern to the health care systems. Bacteria in the human body are often found embedded in a dense 3D structure, the biofilm, which makes their eradication even more challenging. Indeed, bacteria in biofilm are protected from external hazards and are more prone to develop antibiotic resistance. Moreover, biofilms are highly heterogeneous, with properties dependent on the bacteria species, the anatomic localization, and the nutrient/flow conditions. Therefore, antibiotic screening and testing would strongly benefit from reliable in vitro models of bacterial biofilms. This review article summarizes the main features of biofilms, with particular focus on parameters affecting biofilm composition and mechanical properties. Moreover, a thorough overview of the in vitro biofilm models recently developed is presented, focusing on both traditional and advanced approaches. Static, dynamic, and microcosm models are described, and their main features, advantages, and disadvantages are compared and discussed

Hybrid injectable platforms for the in situ delivery of therapeutic ions from mesoporous glasses

Copper-containing bioactive glasses (Cu-MBGs) are attracting increasing interest as multifunctional agents for hard and soft tissue healing due to the ability of released copper ions to stimulate osteogenesis as well as angiogenesis and to impart anti-bacterial properties. The conjugation of these nanomaterials with a vehicle phase based on thermosensitive hydrogels represents an effective strategy to design non-invasive injectable devices for the in situ delivery of therapeutic ions from MBGs. In this contribution, Cu-containing MBGs were prepared by an aerosol-assisted spray-drying method (MBG_Cu 2%_SD) in the form of microspheres (surface area of ca 220m2 g−1) and through a sol-gel synthesis (MBG_Cu 2% _SG) in the form of spheroidal nanoparticles (surface area above 700m2 g−1). Both Cu-containing samples were able to release copper ions, although with different rates and percentage release. MBG_Cu 2%_SG released the total incorporated amount of Cu ions with a faster kinetics compared to MBG_Cu 2%_SD, that released approximately the 60% of copper. Cu-MBGs were incorporated with a final concentration of 20 mg/mL into a thermosensitive sol-gel system consisting of a novel amphiphilic poly(ether urethane) based on a commercialy available Poloxamer 407 (P407), with improved gelation ability, mechanical strength and stability in aqueous solution with respect to native P407. Cu-MBG-loaded hydrogels were characterised in terms of sol-to-gel transition temperature and time, injectability and stability in aqueous environment at 37 °C. The hybrid formulations showed fast gelation in physiological conditions (1 mL underwent complete sol-to-gel transition within 3–5 min at 37 °C) and injectability in a wide range of temperatures (5–37 °C) through different needles (inner diameter in the range 0.6–1.6 mm)

Sonophotocatalytic degradation of sodium diclofenac using low power ultrasound and micro sized TiO2

The nonsteroidal anti-inflammatory drug sodium diclofenac (DC) is an emerging water pollutant which resists conventional wastewater treatments. Here the sonophotocatalytic degradation of DC was carried out using micrometric TiO2 (both pristine and Ag-decorated), UV-A irradiation and 20 kHz pulsed ultrasound. Sonophotocatalytic tests were compared with photolysis, sonolysis, sonophotolysis, sonocatalysis and photocatalysis data performed in the same conditions. A synergy index of over 2 was determined for tests with pristine TiO2, while values close to 1.3 were observed for Ag-TiO2. Reaction intermediates were studied by HPLC-MS, showing degradation mechanisms activated by hydroxyl radicals. Similar pathways were identified for photocatalytic and sonophotocatalytic tests, although the latter led to more oxidized compounds. Different reactor configurations (static and dynamic set ups) were studied. Sequential and simultaneous application of UV light and ultrasound led to similar performance. The role of water matrix was investigated using ultrapure and drinking water, showing marked detrimental effects of electrolytes on the DC degradation. Overall, the combined treatment proved more efficient than photocatalysis alone especially in demanding working conditions, like in drinking water matrices