Removal of antibiotic rifampicin from aqueous media by advanced electrochemical oxidation: Role of electrode materials, electrolytes and real water matrixes

2021 ◽  
pp. 139254
Author(s):  
Laysa R.D. Brito ◽  
Soliu O. Ganiyu ◽  
Elisama V. dos Santos ◽  
Mehmet A. Oturan ◽  
Carlos A. Martinez-Huitle
2000 ◽  
Vol 655 ◽  
Author(s):  
Cesar Guerrero ◽  
Florencio Sánchez ◽  
José Roldán ◽  
Frank Güell ◽  
María V. García-Cuenca

AbstractA comparison of pulsed laser deposited PbZr0.53Ti0.47O3 (PZT) thin film capacitors with SrRuO3 (SRO) and LaNiO3 (LNO) electrodes on (001) yttria-stabilized zirconia (YSZ) and lattice matched (001) LaAlO3 substrates is presented. Both electrode materials allow for the formation of ferroelectric capacitors with large remnant polarization (20-30 μC/cm2) and negligible fatigue, although slight differences arise regarding the promotion of either the rhombohedral or tetragonal phases of PZT. Far more crucial seems to be the tendency of SrRuO3 to develop a rougher surface at either small (<30 nm) or large thickness (>100 nm), and on YSZ substrates. In those cases a highly defective and possibly low dielectric interface forms between the electrode and the ferroelectric layer, resulting in greatly degraded ferroelectric performance. LaNiO3 is free from these limitations except for the cracks forming at very large thickness (>300 nm), and therefore appears as a more versatile electrode material.


2001 ◽  
Vol 688 ◽  
Author(s):  
St. Schneider ◽  
H. Kohlstedt ◽  
R. Waser

AbstractNoble metals like platinum or irdium are used as electrode materials in DRAM or FRAM devices. Their etch process is a challenge as conventional, sputter driven etch processes either result in redeposition problems (fences) or in a severe sloping (loss of dimension control) and are not acceptable for high density integration architectures. The high temperature etch regime offers a solution by increasing the chemical etch component and thus the volatility of the etch products.As previously reported, the platinum etch rate increases exponentially for a chlorine etch process with increasing wafer temperature. In this study we investigate the particular role of carbon monoxide in a Cl2/CO etch process. We find that carbon monoxide additions to a chlorine process boost the chemical component of the platinum etch rate very significantly, exceeding the effects in the chlorine only process regime by far. Additionally we compare these results with a Cl2/O2 and a Cl2/CO2 process chemistry, which are not found to be particularly beneficial.To better understand the etch process we use an energy dispersive quadrupole mass spectrometer for in situ monitoring, attached to the chamber at two different locations. We are able to position the probe orifice at the place of the wafer electrode, to record ion energy and ion mass spectra of species impinging on the wafer plane. A second off axis position allows for etch product monitoring.


2016 ◽  
Vol 121 (1) ◽  
pp. 656-665 ◽  
Author(s):  
Satu Lahtinen ◽  
Annika Lyytikäinen ◽  
Henna Päkkilä ◽  
Emmy Hömppi ◽  
Niina Perälä ◽  
...  

2016 ◽  
Vol 9 (3) ◽  
pp. 955-961 ◽  
Author(s):  
Jeongsik Yun ◽  
Jonas Pfisterer ◽  
Aliaksandr S. Bandarenka

This work reveals a three-stage mechanism of Na intercalation into one of the state-of-the-art battery electrode materials operating in aqueous electrolytes.


Metals ◽  
2018 ◽  
Vol 8 (7) ◽  
pp. 556 ◽  
Author(s):  
Nathalie Leclerc ◽  
Sophie Legeai ◽  
Maxime Balva ◽  
Claire Hazotte ◽  
Julien Comel ◽  
...  

This paper presents recent views on a hybrid process for beneficiation of secondary raw materials by combined electroleaching of targeted metals and electrodeposition. On the basis of several case studies with aqueous solutions or in ionic liquid media, the paper describes the potential and the limits of the novel, hybrid technique, together with the methodology employed, combining determination of speciation, physical chemistry, electrochemistry, and chemical engineering. On one hand, the case of electroleaching/electrodeposition (E/E) process in aqueous media, although often investigated at the bench scale, appears nevertheless relatively mature, because of the developed methodology, and the appreciable current density allowed, and so it can be used to successfully treat electrode materials of spent Zn/MnO2 batteries or Ni/Cd accumulators and Waelz oxide. On the other hand, the use of ionic liquids as promising media for the recovery of various metals can be considered for other types of wastes, as shown here for the case of electrodes of aged fuel cells. The combined (E/E) technique could be successfully used for the above waste, in particular by the tricky selection of ionic liquid media. Nevertheless, further investigations in physical chemistry and chemical engineering appear necessary for possible developments of larger-scale processes for the recovery of these strategic resources.


Supercapacitors are considered promising energy storage systems due to their high power density, fast charge-discharge, long service lifetime, wide operating temperature range and excellent capacitance retention. The electrochemical performance of the supercapacitors depends upon numerous factors such as nature of electrode materials, type of electrolyte and separator thickness, etc. Among these factors, electrolyte used in supercapacitor plays an important role in deciding final characteristics of supercapacitors. In recent decades, tremendous research work has been on the development of novel electrolytes and electrode/electrolyte configurations. In this chapter, we aimed to focus on the role of inorganic electrolytes used in supercapacitors.


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