scholarly journals Fabrication of an All-Solid-State Ammonium Paper Electrode Using a Graphite-Polyvinyl Butyral Transducer Layer

Chemosensors ◽  
2021 ◽  
Vol 9 (12) ◽  
pp. 333
Author(s):  
Irena Ivanišević ◽  
Stjepan Milardović ◽  
Antonia Ressler ◽  
Petar Kassal
Keyword(s):  
Solid State ◽  
Graphite Powder ◽  
Polyvinyl Butyral ◽  
Environmental Water ◽  
Fast Response ◽  
Flow Mode ◽  
Batch Mode ◽  
Ph Response ◽  
Potentiometric Response ◽  
Ph Range

A planar solid-state ammonium-selective electrode, employing a composite mediator layer of graphite particles embedded in a polyvinyl butyral matrix on top of an inkjet-printed silver electrode, is presented in this paper. The effect of graphite powder mass fraction on the magnitude of the potentiometric response of the sensor was systematically verified using a batch-mode and a flow injection measurement setup. Under steady-state conditions, the paper electrode provided a Nernstian response of 57.30 mV/pNH4 over the concentration range of 10−5 M to 10−1 M with a detection limit of 4.8 × 10−6 M, while the analytical performance of the array in flow mode showed a narrower linear range (10−4 M to 10−1 M; 60.91 mV/pNH4 slope) with a LOD value of 5.6 × 10−5 M. The experimental results indicate that the prepared electrode exhibited high stability and fast response to different molar concentrations of ammonium chloride solutions. The pH-response of the paper NH4-ISE was also investigated, and the sensor remained stable in the pH range of 2.5–8.5. The potentiometric sensor presented here is simple, lightweight and inexpensive, with a potential application for in-situ analysis of environmental water samples.

scholarly journals Potentiometric Response Characteristics of Membrane-BasedCs+-Selective Electrodes Containing Ionophore-Functionalized Polymeric Microspheres

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Shane Peper ◽  
Chad Gonczy
Keyword(s):  
Ethylene Glycol ◽  
Response Characteristic ◽  
Polymeric Membrane ◽  
Ion Selective Electrodes ◽  
Polymeric Microspheres ◽  
Response Characteristics ◽  
Ph Response ◽  
Potentiometric Response ◽  
Response Slope ◽  
Ph Range

Cs+-selective solvent polymeric membrane-based ion-selective electrodes (ISEs) were developed by doping ethylene glycol-functionalized cross-linked polystyrene microspheres (P-EG) into a plasticized poly(vinyl chloride) (PVC) matrix containing sodium tetrakis-(3,5-bis(trifluoromethyl)phenyl) borate (TFPB) as the ion exchanger. A systematic study examining the effects of the membrane plasticizers bis(2-ethylhexyl) sebacate (DOS), 2-nitrophenyl octyl ether (NPOE), and 2-fluorophenyl nitrophenyl ether (FPNPE) on the potentiometric response and selectivity of the corresponding electrodes was performed. Under certain conditions, P-EG-based ion-selective electrodes (ISEs) containing TFPB and plasticized with NPOE exhibited a super-Nernstian response between1×10−3and1×10−4 M Cs+, a response characteristic not observed in analogous membranes plasticized with either DOS or FPNPE. Additionally, the performance of P-EG-based ISEs was compared to electrodes based on two mobile ionophores, a neutral lipophilic ethylene glycol derivative (ethylene glycol monooctadecyl ether (U-EG)) and a charged metallacarborane ionophore, sodium bis(dicarbollyl)cobaltate(III) (CC). In general, P-EG-based electrodes plasticized with FPNPE yielded the best performance, with a linear range from 10-1–10-5 M Cs+, a conventional lower detection limit of8.1×10−6 M Cs+, and a response slope of 57.7 mV/decade. The pH response of P-EG ISEs containing TFPB was evaluated for membranes plasticized with either NPOE or FPNPE. In both cases, the electrodes remained stable throughout the pH range 3–12, with only slight proton interference observed below pH 3.

A novel copper selective sensor based on ion imprinted 2-vinylpyridine polymer

2018 ◽  
Vol 96 (12) ◽  
pp. 1027-1036
Author(s):  
Murat Yolcu ◽  
Nurşen Dere
Keyword(s):  
Environmental Water ◽  
Pvc Membrane ◽  
Indicator Electrode ◽  
Potentiometric Response ◽  
Ion Imprinted ◽  
Aas Method ◽  
Ph Range ◽  
Determination Of Copper ◽  
Selective Sensor

A novel potentiometric Cu2+-selective microsensor has been developed that is based upon ion imprinted 2-vinylpyridine polymer. The polymer was synthesized using Cu(II) ions, 2-vinylpyridine, methacrylic acid, and ethylene glycol dimethacrylate as a template, functional monomer, and cross-linker, respectively. The resultant polymer was used as ionophore to obtain a selective potentiometric response towards Cu(II) ions in the structure of the PVC membrane. The detection limit of the microsensor was determined to be 8.4 × 10−7 mol/L, and its response time was considerably short (less than 15 s). The prepared microsensor exhibited a near-Nernstian response for Cu(II) ions over the concentration range of 10−1 to 10−6 mol/L, with a slope of 28.5 mV per decade over 2 months, and without any considerable divergence in potentials. The microsensor was effectively performed in a pH range between 4.0 and 7.0 and used as an indicator electrode in the potentiometric titration of Cu(II) ions with EDTA. The proposed microsensor has been successfully demonstrated for the determination of copper in a number of environmental water samples. The obtained potentiometric results were in good harmony with the results obtained by the AAS method.

Reduction of COD from Micro-Polluted Water through Adsorption of Activated Carbon-Attapulgite Composite Adsorbent

2010 ◽  
Vol 450 ◽  
pp. 445-448
Author(s):  
Zheng Wang ◽  
Zhao Qian Jing ◽  
Yu Kong ◽  
Wei Shen
Keyword(s):  
Activated Carbon ◽  
Oxygen Demand ◽  
Polluted Water ◽  
Adsorption Model ◽  
Batch Mode ◽  
Composite Adsorbent ◽  
Adsorption Data ◽  
Complete Study ◽  
Ph Range ◽  
Optimum Ph Range

The aim of this study was the assessment of reduction of chemical oxygen demand (COD) from micro-polluted water using activated carbon-attapulgite composite adsorbent prepared using activated carbon and natural attapulgite through compounding, granulation and calcination. The complete study was done in batch mode to investigate the effect of operating parameters. Adsorption of COD was found to be dependent on contact time, pH, temperature and initial COD concentration. Adsorption equilibrium attained within 80 minutes time. The optimum pH range for adsorption of organics was found to be 8. The sorption of organics decreased with rise of temperature because adsorption process was exothermic. The studied adsorption data fitted well to Langmuir adsorption model with the correlation coefficient 0.9947. The activated carbon-attapulgite composite adsorbent in this study shows very good promise for practical applicability on removal of COD from micro-polluted water.

Different Types of Microbial Fuel Cell (MFC) Systems for Simultaneous Electricity Generation and Pollutant Removal

2015 ◽  
Vol 74 (3) ◽  
Author(s):  
S. M. Zain ◽  
N. L. Ching ◽  
S. Jusoh ◽  
S. Y. Yunus
Keyword(s):  
Nitrogen Removal ◽  
Continuous Flow ◽  
Electricity Generation ◽  
Pollutant Removal ◽  
Flow Mode ◽  
Oxidizing Agent ◽  
Batch Mode ◽  
Carbon And Nitrogen ◽  
Different Types ◽  
The Relationship

The aim of this study is to identify the relationship between the rate of electricity generation and the rate of carbon and nitrogen removal from wastewater using different MFC processes.  Determining whether the generation of electricity using MFC process could be related to the rate of pollutant removal from wastewater is noteworthy. Three types of MFC process configurations include the batch mode (SS), a continuous flow of influent with ferricyanide (PF) as the oxidizing agent and a continuous flow of influent with oxygen (PU) as the oxidizing agent. The highest quantity of electricity generation was achieved using the continuous flow mode with ferricyanide (0.833 V), followed by the continuous flow mode with oxygen (0.589 V) and the batch mode (0.352 V). The highest efficiency of carbon removal is also achieved by the continuous flow mode with ferricyanide (87%), followed by the continuous flow mode with oxygen (51%) and the batch mode (46%). Moreover, the continuous flow mode with ferricyanide produced the highest efficiency for nitrogen removal (63%), followed by the continuous flow mode with oxygen (54%) and the batch mode (27%).

scholarly journals A SOLID Fe2O3-GRAPHITE COMPOSITE ELECTRODE FOR pH MEASUREMENT

2015 ◽  
Vol 12 (12) ◽  
pp. 44-47
Author(s):  
Suchi Srivastava ◽  
Raja Ram Pradhananga
Keyword(s):  
Electrode Potential ◽  
Composite Electrode ◽  
Low Cost ◽  
Ph Sensor ◽  
Potential Gradient ◽  
Graphite Composite ◽  
Ph Response ◽  
Potentiometric Response ◽  
Unit Change ◽  
Oxidized Graphite

A solid Fe2O3-graphite composite electrode was prepared and investigated for use as a potentiometric pH sensor. The electrode was constructed by mixing iron (III) oxide, oxidized graphite and wax that was put over silver disc onto a polypropylene rod. The response of the electrode was investigated by measuring electrode potential as a function of pH.The effect of composition of the electrode material (Fe2O3 and oxidized graphite ration) on the electrode response was investigated. The electrode with 40% Fe2O3, 30% graphite and 30% wax by mass was found to give the best potentiometric response. This electrode behaves in Nernstian manner with a potentiometric gradient of 56.6±0.4 mV per unit change in pH at 25?C within the working range of pH 2-9.The electrode was also used for the end-point detection in potentiometric acid-base titrations and found to be an excellent electrode for pH-metric titration. The effect of oxidation of electrode on pH response was investigated by dipping electrode in 0.1N KMnO4, 1:1HNO3 and 0.1N Ce4+ solutions for different interval of time. This treatment of the electrode with oxidizing agents increased the standard electrode potential of the electrode however potential gradient per unit change in pH remains unaltered. Low cost, quick response and easy to prepare are the advantages of the iron oxide - graphite composite electrode as a pH sensor. However some metal ions and oxidising agents interfered in the determination of pH using this electrode which is the limitation of using these electrodes.Scientific World, Vol. 12, No. 12, September 2014, page 44-47

Development of A Novel Solid-State pH Sensor Based on Tin Oxide Thin Film

2004 ◽  
Vol 59 (8) ◽  
pp. 877-880 ◽  
Author(s):  
Taher M. El-Agez ◽  
Manal R. Al-Saraj ◽  
Monzir S. Abdel-Latif
Keyword(s):  
Solid State ◽  
Tin Oxide ◽  
Glass Substrate ◽  
Ph Sensor ◽  
Chemical Vapor ◽  
Calibration Graph ◽  
Oxide Thin Film ◽  
Solution Temperature ◽  
Graphite Film ◽  
Ph Range

AbstractA solid-state pH sensor was fabricated using a transparent conductive tin oxide film on a glass substrate. The coating of the glass substrate was achieved by a novel simple chemical vapor deposition (CVD) procedure. The response time of the pH sensor was substantially reduced when a thin graphite film was deposited onto the tin oxide conductive film. The sensor slope was found to increase as the temperature of the solution was increased. The performance of the sensor was investigated in the pH range from 0.3 to 11.0. A straight-line calibration graph was achieved throughout the whole range tested, especially when the solution temperature was 80 ℃. The working pH range was found to decrease on the expense of the lower range as the temperature was decreased. Results obtained by the suggested sensor compares very well with conventional pH electrodes where the square of the correlation coefficient was 0.999.

A Schiff base-based fluorescent probe for the quick detection of ClO− ions

2020 ◽  
Vol 98 (8) ◽  
pp. 403-407
Author(s):  
Min Zhang ◽  
Tao Hu ◽  
Changyan Sun ◽  
Wenjun Li ◽  
Zhidong Chang
Keyword(s):  
Schiff Base ◽  
Fast Response ◽  
Ionization Mass ◽  
X Ray Diffraction ◽  
Detection Mechanism ◽  
Esi Ms ◽  
Wide Ph Range ◽  
Nuclear Magnetic Resonance Spectrometry ◽  
Magnetic Resonance Spectrometry ◽  
Ph Range

A new Schiff base 2-hydroxy-5-[(2,7-dihydroxy-1-naphthyl)methylideneamino]benzoic acid (HNMB) has been designed and synthesized. HNMB was characterized by Fourier-transform infrared spectroscopy (FTIR), electrospray ionization mass spectrometry (ESI–MS), nuclear magnetic resonance spectrometry (NMR), and single crystal X-ray diffraction. Fluorescence spectra show that HNMB could be used as a “turn-on” probe to detect ClO− ions from other anions in DMSO/H2O (v/v = 1:1) with a fast response time of 10 s and a low detection limit of 3.6 × 10−7 mol/L. Moreover, the probe could work in a wide pH range of 4–10. The detection mechanism was studied by ESI–MS.

scholarly journals Control of pH-Responsiveness in Graphene Oxide Grafted with Poly-DEAEMA via Tailored Functionalization

Nanomaterials ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 614 ◽  
Author(s):  
Roxana Noriega-Navarro ◽  
Jésica Castro-Medina ◽  
Martha V. Escárcega-Bobadilla ◽  
Gustavo A. Zelada-Guillén
Keyword(s):  
Graphene Oxide ◽  
Polymer Chains ◽  
The Novel ◽  
Potentiometric Response ◽  
Solid State Sensor ◽  
Material History ◽  
Multiple Variables ◽  
Ph Sensitive Polymer ◽  
Ph Range ◽  
Range Interval

Polymer-grafted nanomaterials based on carbon allotropes and their derivatives (graphene oxide (GO), etc.) are typically prepared by successive reaction stages that depend upon the initial functionalities in the nanostructure and the polymerization type needed for grafting. However, due to the multiple variables involved in the functionalization steps, it is commonly difficult to predict the properties in the final product and to correlate the material history with its final performance. In this work, we explored the steps needed to graft the carboxylic acid moieties in GO (COOH@GO) with a pH-sensitive polymer, poly[2-(diethylamino)ethyl methacrylate] (poly[DEAEMA]), varying the reactant ratios at each stage prior to polymerization. We studied the combinatorial relationship between these variables and the behavior of the novel grafted material GO-g-poly[DEAEMA], in terms of swelling ratio vs. pH (%Q) in solid specimens and potentiometric response vs. Log[H+] in a solid-state sensor format. We first introduced N-hydroxysuccinimide (NHS)-ester moieties at the –COOH groups (GO-g-NHS) by a classical activation with N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide (EDC). Then, we substituted the NHS-ester groups by polymerizable amide-linked acrylic moieties using 2-aminoethyl methacrylate (AEMA) at different ratios to finally introduce the polymer chains via radical polymerization in an excess of DEAEMA monomer. We found correlated trends in swelling pH range, interval of maximum and minimum swelling values, response in potentiometry and potentiometric linear range vs. Log[H+] and could establish their relationship with the combinatorial stoichiometries in synthetic stages.

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