1970 ◽  
Vol 6 (6) ◽  
pp. 33-36 ◽  
Author(s):  
Raja Ram Pradhananga ◽  
Armila Rajbhandari Nyachhyon

Low cost all solid state pressed pellet Ag+, halides and sulphide sensitive electrodes based on silver sulphide were fabricated. The electrodes have been tested and results compare favorably with commercial electrodes. Pure Ag2S electrode with internal silver metal contact was found to follow Nernstian equation from 1 x 10-1 to 1 x 10-5 M of silver ion with slope equal to 59.8 mV per decade change in concentration of Ag+ - ion. Electrodes fabricated from equimolar mixture of Ag2S and Ag - halide was found to be sensitive to the respective halide and silver ions. Iodide ion selective electrode prepared from a equimolar mixture of Ag2S and AgI was found to be selective to iodide ion with negligible interference from bromide and chloride ions. The potentiometric selectivity coefficient Kpot I,Br, Kpot I,Cl were found to be 1.77x10-2 and 7.94x10-3 respectively. All these electrodes were found to be selective to Ag+ ion with negligible interference with Kpot Ag, Hg equal to 1 x 10-5 Hg++ ion with selectivity coefficient. Keywords: Ion selective electrodes; Potentiometric selectivity coefficient; Silver sulphide.   DOI: 10.3126/sw.v6i6.2631 Scientific World, Vol. 6, No. 6, July 2008 33-36


Sensors ◽  
2021 ◽  
Vol 21 (9) ◽  
pp. 3150
Author(s):  
Fatehy M. Abdel-Haleem ◽  
Sonia Mahmoud ◽  
Nour Eldin T. Abdel-Ghani ◽  
Rasha Mohamed El Nashar ◽  
Mikhael Bechelany ◽  
...  

Levofloxacin (LF) is a medically important antibiotic drug that is used to treat a variety of bacterial infections. In this study, three highly sensitive and selective carbon paste electrodes (CPEs) were fabricated for potentiometric determination of the LF drug: (i) CPEs filled with carbon paste (referred to as CPE); (ii) CPE coated (drop-casted) with ion-selective PVC membrane (referred to as C-CPE); (iii) CPE filled with carbon paste modified with a plasticizer (PVC/cyclohexanone) (referenced as P-CPE). The CPE was formulated from graphite (Gr, 44.0%) and reduced graphene oxide (rGO, 3.0%) as the carbon source, tricresyl phosphate (TCP, 47.0%) as the plasticizer; sodium tetrakis[3,5-bis(trifluoromethyl)phenyl] borate (St-TFPMB, 1.0%) as the ion exchanger; and levofloxacinium-tetraphenylborate (LF-TPB, 5.0%) as the lipophilic ion pair. It showed a sub-Nernstian slope of 49.3 mV decade−1 within the LF concentration range 1.0 × 10−2 M to 1.0 × 10−5 M, with a detection limit of 1.0 × 10−5 M. The PVC coated electrode (C-CPE) showed improved sensitivity (in terms of slope, equal to 50.2 mV decade−1) compared to CPEs. After the incorporation of PVC paste on the modified CPE (P-CPE), the sensitivity increased at 53.5 mV decade−1, indicating such improvement. The selectivity coefficient (log KLF2+,Fe+3pot.) against different interfering species (Na+, K+, NH4+, Ca2+, Al3+, Fe3+, Glycine, Glucose, Maltose, Lactose) were significantly improved by one to three orders of magnitudes in the case of C-CPE and P-CPE, compared to CPEs. The modification with the PVC membrane coating significantly improved the response time and solubility of the LF-TPB within the electrode matrix and increased the lifetime. The constructed sensors were successfully applied for LF determination in pharmaceutical preparation (Levoxin® 500 mg), spiked urine, and serum samples with high accuracy and precision.


2016 ◽  
Vol 2016 ◽  
pp. 1-7
Author(s):  
Geeta Rani ◽  
Sanjay Singh

Chemically modified mesoporous silica material (SBA-15) was used for the construction of Tl(I) selective carbon paste electrode. The best response was found with the electrode containing 10% modifier as electrode material. The electrode has a lower detection limit of 6.0 × 10−9 M in a working concentration range of 1.0 × 10−8–1.0 × 10−1 M. The selectivity coefficient calculated by match potential method (MPM) shows the high selectivity of electrode towards Tl(I) over other tested ions. The electrode was successfully applied as an indicator electrode for the titration of 0.01 M TlNO3solution with standards EDTA solution and for sequential titration of mixture of different anions.


2009 ◽  
Vol 73 (3) ◽  
pp. 928-942 ◽  
Author(s):  
Christophe Tournassat ◽  
Hélène Gailhanou ◽  
Catherine Crouzet ◽  
Gilles Braibant ◽  
Anne Gautier ◽  
...  

1994 ◽  
Vol 66 (5) ◽  
pp. 651-654 ◽  
Author(s):  
Akira. Ohki ◽  
Jian Ping. Lu ◽  
Richard A. Bartsch

Geoderma ◽  
1995 ◽  
Vol 68 (4) ◽  
pp. 301-308 ◽  
Author(s):  
Sébastien Sauvé ◽  
William H. Hendershot

Water SA ◽  
2018 ◽  
Vol 44 (3 July) ◽  
Author(s):  
Lawrence Mzukisi Madikizela ◽  
Silindile Senamile Zunngu ◽  
Nomchenge Yamkelani Mlunguza ◽  
Nikita Tawanda Tavengwa ◽  
Phumlane Selby Mdluli ◽  
...  

A molecularly imprinted polymer (MIP) that is selective to ketoprofen was synthesized and applied in the adsorption of the target compound from water. The MIP was synthesized using a bulk polymerization method at high temperatures (60–80°C), where ketoprofen, 2-vinylpyridine, ethylene glycol dimethacrylate, toluene and 1,1´-azobis(cyclohexanecarbonitrile) were used as template, functional monomer, cross-linker, porogen and initiator, respectively. Non-imprinted polymer (NIP) was synthesized similarly to the MIP but in the absence of ketoprofen. From molecular dynamics simulation, the nature of interactions that occurred between the template and the functional monomer were found to be based on hydrogen bonding. This was confirmed experimentally, where a high extraction efficiency of ≥ 90% was obtained at acidic conditions (pH 5) due to the protonation of ketoprofen. A contact time of 45 min was sufficient for the maximum adsorption of ketoprofen from 10 mL spiked water using 8 mg of the adsorbent. MIP showed greater selectivity than NIP by achieving a relative selectivity coefficient of 7.7 towards ketoprofen in the presence of structurally related pharmaceuticals. Furthermore, the order of sorption onto the MIPs from water was ketoprofen > fenoprofen > gemfibrozil. From a modelling perspective, the Langmuir adsorption isotherm and pseudo-second-order kinetic model gave the best fit, with maximum adsorption capacity of 8.24 mg·g−1 and sorption rate constant of 0.25 mg·g−1·min−1 for MIP. This was translated to chemisorption of ketoprofen onto the homogeneous MIP binding sites. This work demonstrated the great potential of MIP in selective recognition of ketoprofen from wastewater relative to closely related compounds.


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