The Influence of Solution Composition on the Effectiveness of Degradation of Ibuprofen Sodium Salt in a Hybrid Photocatalysis – Membrane Distillation System

2012 ◽  
Vol 15 (1) ◽  
Author(s):  
Sylwia Mozia ◽  
Antoni W. Morawski ◽  
Masahiro Toyoda

AbstractThe results of the investigations on the photodegradation of a non-steroidal anti-inflammatory drug ibuprofen sodium salt (IBU) in a photocatalytic membrane reactor (PMR) coupling photocatalysis using suspended TiO

Author(s):  
Sylwia Mozia ◽  
Tomoki Tsumura ◽  
Masahiro Toyoda ◽  
Antoni W. Morawski

AbstractThe present paper describes photodegradation of non-steroidal anti-inflammatory drug ibuprofen sodium salt (C


Membranes ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 276
Author(s):  
Zeyad Zeitoun ◽  
Ahmed H. El-Shazly ◽  
Shaaban Nosier ◽  
Mohamed R. Elmarghany ◽  
Mohamed S. Salem ◽  
...  

The objectives of the current study are to assess and compare the performance of a developed photocatalytic membrane reactor (PMR) in treating industrial waste (e.g., organic dye waste) against membrane distillation. The current PMR is composed of a feed tank, which is a continuous stirred photocatalytic reactor containing slurry Titanium dioxide (TiO2) particles that are activated by using ultraviolet lamp irradiation at a wavelength of 365 nm, and a poly-vinylidene flouride (PVDF) membrane cell. The experimental setup was designed in a flexible way to enable both separate and integrated investigations of the photocatalytic reactor and the membrane, separately and simultaneously. The experimental work was divided into two phases. Firstly, the PVDF membrane was fabricated and characterized to examine its morphology, surface charge, and hydrophobicity by using a scanning electron microscope, surface zeta potential, and contact angle tests, respectively. Secondly, the effects of using different concentrations of the TiO2 photocatalyst and feed (e.g., dye concentration) were examined. It is found that the PMR can achieve almost 100% dye removal and pure permeate is obtained at certain conditions. Additionally, a kinetic analysis was performed and revealed that the photocatalytic degradation of dye follows a pseudo-first-order reaction.


Materials ◽  
2021 ◽  
Vol 14 (8) ◽  
pp. 1880
Author(s):  
Lubos Zauska ◽  
Stefan Bova ◽  
Eva Benova ◽  
Jozef Bednarcik ◽  
Matej Balaz ◽  
...  

Mesoporous SBA-15 silica material was prepared by the sol–gel method and functionalized with thermosensitive polyethylenimine polymers with different molecular weight (g·mol−1): 800 (SBA-15(C)-800), 1300 (SBA-15(C)-1300) and 2000 (SBA-15(C)-2000). The nonsteroidal anti-inflammatory drug (NSAID) diclofenac sodium was selected as a model drug and encapsulated into the pores of prepared supports. Materials were characterized by the combination of infrared spectroscopy (IR), atomic force microscopy (AFM), transmission electron microscopy (TEM), photon cross-correlation spectroscopy (PCCS), nitrogen adsorption/desorption analysis, thermogravimetry (TG), differential scanning calorimetry (DSC) and small-angle X-ray diffraction (SA-XRD) experiments. The drug release from prepared matrixes was realized in two model media differing in pH, namely small intestine environment/simulated body fluid (pH = 7.4) and simulated gastric fluid (pH = 2), and at different temperatures, namely normal body temperature (T = 37 °C) and inflammatory temperature (T = 42 °C). The process of drug loading into the pores of prepared materials from the diclofenac sodium salt solutions with different concentrations and subsequent quantitative determination of released drugs was analyzed by UV-VIS spectroscopy. Analysis of prepared SBA-15 materials modified with polyethylenimines in solution showed a high ability to store large amounts of the drug, up to 230 wt.%. Experimental results showed their high drug release into the solution at pH = 7.4 for both temperatures, which is related to the high solubility of diclofenac sodium in a slightly alkaline environment. At pH = 2, a difference in drug release rate was observed between both temperatures. Indeed, at a higher temperature, the release rates and the amount of released drug were 2–3 times higher than those observed at a lower temperature. Different kinetic models were used to fit the obtained drug release data to determine the drug release rate and its release mechanism. Moreover, the drug release properties of prepared compounds were compared to a commercially available medicament under the same experimental conditions.


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