Sensors iodide

The imidazolium salt functionalized polymer 12 also functions as an iodide sensor, rapidly changing color in the presence of sodium iodide (Ho and Leclerc 2003). Iodide-mediated aggregation was highly sensitive to the length of the side chain coimecting the imidazolium salt to the polythiophene backbone. A variety of... 

The highly sensitive iodide sensor monitors the decrease in the iodide activity at the electrode surface. The assay of glucose was performed both in a stream and at a stationary electrode. Pretreatment of the blood sample was required to remove interfering reducing agents such as ascorbic acid, tyrosine, and uric acid. 

A PT-modified vitreous carbon electrode can be used as a universal response potentiometric sensor. This all-solid-state electrode is readily prepared, responds rapidly, and has good stability and reproducibility [798]. A potentiometric iodide sensor based on a PMT film electrode has been developed. This... 

Detection of Bromine Vapor. Bromine vapor in air can be monitored by using an oxidant monitor instmment that sounds an alarm when a certain level is reached. An oxidant monitor operates on an amperometric principle. The bromine oxidizes potassium iodide in solution, producing an electrical output by depolarizing one sensor electrode. Detector tubes, usefiil for determining the level of respiratory protection required, contain (9-toluidine that produces a yellow-orange stain when reacted with bromine. These tubes and sample pumps are available through safety supply companies (54). The usefiil concentration range is 0.2—30 ppm. 

Sensors based on the fluorescence quenching ofrhodamine 6G in resins by iodide ions(43) and in Nafion polymer by metal ions in solution 44,45) have been demonstrated. However, complex fluorescence decay mechanisms often hinder interpretation in lifetime-based sensing and much progress is still to be made in this area before the true potential of lifetime-based sensing becomes a reality. For example, rhodamine 6G in... 

W. A. Wyatt, F. V. Bright and G. M. Hieftje, Characterization and comparison of three fiber-optic sensors for iodide determination based on dynamic fluorescence quenching ofrhodamine 6G, Anal. Chem. 59, 2272-2276 (1987). 

In acetate buffer (pH 4), active chloride stoichiometrically oxidizes iodide to iodine, so that this sensor can be used to determine the concentration of active chlorine. This method is useful for the determination of active chlorine in the range, 3-100 ppb. 

Enzyme electrodes with amperometric indication have certain advantages over potentiometric sensors, chiefly because the product of the enzymic reaction is consumed at the electrode and thus the response time is decreased. For this reason, the potentiometric glucose enzyme electrode, based on reaction (8.1) followed by the reaction of HjO, with iodide ions sensed by an iodide ISE [39], has not found practical use. 

In addition to the sensors dealt with in Section 3.3.1.1, which could equally have been included in this Section as they use consumable immobilized reagents and regenerable fluorophores, Frei et al. developed a sensor for HPLC determinations based on the solid-state detection cell depicted in Fig. 3.38.B, where they immobilized 1-bromonaphthalene for measuring phosphorescence quenchers. Experiments demonstrated the sensor s usefulness for determining nitrate with a detection limit of ca. 10" M and an RSD of 4% for an analyte concentration of M. However, the scope of application of this sensor to chromatographically separated anions is rather narrow owing to the low sensitivity of the quenched phosphorescence detection for iodide and other halides [268]. 

In the method proposed by van Staden for the determination of three halides, these are separated in a short colunm packed with a strongly basic ion-exchange resin (Dowex i-X8) that is placed in an FI manifold. A laboratory-made tubular silver/silver halide ion-selective electrode is used as a potentiometric sensor. Van Staden compared the response capabilities of the halide-selective electrodes to a wide concentration range (20-5000 pg/mL) of individual and mixed halide solutions in the presence and absence of the ion-exchange column. By careful selection of appropriate concentrations of the potassixun nitrate carrier/eluent stream to satisfy the requirements of both the ion-exchange column and the halide-selective electrode, he succeeded in separating and determining chloride, bromide and iodide in mixed halide solutions with a detection limit of 5 /xg/mL [130]. 

Vetrichelvan M, Nagarajan R, Vahyaveettil S. Carbazole-containing conjugated copolymers as colorimetric/fluorimetric sensor for iodide anion. Mactomolecules 2006 39 8303-8310. 

The potentiometric determination of bromide anions with ion-selective electrodes is possible with commercial electrodes that are commonly based on solid Ag2S—AgBr ion conductor membranes [148-150]. Recently, a novel liquid film sensor has been proposed by Ganjali etal. [151] Determination of bromide was reliable without significant interference from common ions such as chloride and iodide, and was reported down to a micromolar level. The electroactive species in the liquid membrane... 

The oxidation of sulfite and thiosulfate becomes facile in the presence of iodide and novel disposable microband sensor electrodes have been developed by Williams and coworkers [187] to allow fast amperometric determination. A similar approach was proposed for the determination of sulfite in wine [188]. In this method, a coulometric titration is carried out in which S(IV) is indirectly oxidized to S(VI). Speciation of SO2 and sulfite was achieved down to micromolar levels. Sulfide and hydrogen sulfide can be determined elec-trochemically in the presence of an iodide mediator [189]. This process may be further enhanced at elevated temperatures. 

The determination of iodide with ion-selective electrodes is possible with commercial sensors often based on ion conducting Ag2S—Agl solid membranes [57]. A PVC membrane-based sensor employing a silver complex with thiourea derivatives has been reported by El Aamrani et al. [202]. Interference from thiocyanate and bromide was investigated and a limit of detection in the nanomolar range was determined. A study assessing the performance... 

Other early work in this field included the use of tetrakis(p-aminophenyl)-porphyrin (Fig. 7a), which was electrodeposited onto glassy carbon and showed a near-Nernstian response to iodide [76]. Electrodeposited methylthiophene-methylpyrrole copolymer was deposited and shown to give a near-Nernstian response to bromide [77]. Pyrrole-3-boronate (Fig. 7b) could be deposited to give films with a good response and marked selectivity to fluoride [78]. A cobalt aminophthalocyanine could also be electropolymerised to give a good sensor for nitrite [79] or sulphide ion [80]. 

Anion detection at microelectrodes has not been studied widely. Amongst the first was the work of de Beer et al. [ 111 ] who manufactured a nitrite sensor with a tip just a few microns in diameter, which could detect nitrite ions down to 1 pM. This proved to be suitable for profiling the concentrations of nitrite anion within biofilms less than 1-mm thick inside water treatment plants. Other workers have found that use of an interdigitated microelectrode array [ 112] allows measurement of iodide via monitoring of its redox peak down to sub-micromole levels, making it a suitable technique for analysing mineral water. Carbon nanotubes coated onto Pt microdiscs have been utilised to make a nitrite sensor [113,114] with detection levels of 0.1 pM. Sulphide has also been detected at nickel microdiscs (50 pm diameter) [115]. 

Cryptate 72, in which the aryl spacer of 71 is replaced with a furanyl unit, acts a colorimetric sensor for anions. UV-vis titrations in aqueous solution gave log K values for the 1 1 halide/receptor adducts of 3.98 for chloride, 3.01 for bromide and 2.39 for iodide. X-ray diffraction studies confirm that bromide is held between the two copper atoms. Under the same conditions 72 also interacts strongly with azide (log K=4.7) and thiocyanate (log X=4.28) anions. This receptor is interesting because of its lack of selectivity compared to 71. The complex appears to be able to expand and contract its bite length in order to accommodate anions of various sizes. 

More recently, a new class of covalent-linked calix[4]pyrrole-anthraquinone compounds (29-31) have been introduced by Sessler s group [48], These are considered to be powerful naked eye sensors for fluoride, chloride and dihydrogen phosphate ions in dichloromethane. The most pronounced colour change was observed upon the addition of the fluoride anion into a solution of the receptor 30 in dichloromethane. The addition of bromide, iodide or nitrate anions did not lead to significant colour changes. 

The high mass sensitivity of ETSM sensors renders them particularly suited for the analysis of monolayer and submonolayer films. In fact, the earliest applications of the ETSM involved studying the electrochemical deposition of monolayers, including the formation of metal oxides [207], electrosorption of halides [208], and the underpotential deposition of metal atoms [209-213]. In some cases, the electrovalency (i.e., the ratio of moles of electrons transferred at the electrode to moles of adsorbate deposited) was found to vary with adsorbing species the adsorption of iodide onto gold, for example, occurs with complete charge transfer from the halide to the electrode, whereas the adsorption of bro-... 

Indirect method based on reaction of sulfa drugs with bromine. Reduction of the resultant bromo-derivative with iodide forms I2. which is extracted and detected with TSM sensor. 

Many porous ion exchange membranes with high cation or anion selectivity have been described (B3, P13, S18). Sparingly soluble crystalline materials have been used as anion sensors, the membrane consisting of single crystals or pressed pellets often embedded in a vulcanized silicone rubber matrix. Examples include electrodes for fiuoride (LaF), sulfide (silver-silver sulfide), iodide, and sulfate. These probably function as... 

In this section, we discuss about the screen printed electrode (SPE) based AChE sensors for the selective determination of OP and CA pesticides. In the past decades, several attempts were made by the researchers to develop SPE based pesticide sensors, where the enzyme AChE was immobilized either directly onto the electrode or above other matrices incorporated SPE surfaces. Both approaches resulted in the good, rapid detection of OP and CA pesticides. Earlier, Hart et al. employed AChE/SPE to detect OP and CA pesticides [21], They measured the enzyme activity from the rate of hydrolysis of acetylthiocholine iodide. Three polymers such as hydroxyethyl cellulose, dimethylaminoethyl methacrylate, and polyethyleneimine were used as enzyme immobilization matrices. Initially, electrodes were exposed to drops of water or pesticide solution, dried and their activity was screened after 24 h. They found that, when the enzyme matrix was hydroxyethyl cellulose, electrode activity inhibited both by water as well as by pesticides. While with co-polymer matrix, a significant response towards pesticides alone was observed. Further, the long-term storage stability of electrodes was highest when the enzyme matrix consisted of the co-polymer. The electrodes retained their activity for nearly one year. In contrast, the electrodes made of hydroxyethyl cellulose or polyethyleneimine possess less stability. 

Wang, L.-G., Wang, X., Ottova, A.L., and Tien, H.T. (2005). Iodide sensitive sensor based on a supported bdayer hpid membrane containing a cluster form of carbon (fullerene C60). Electroanalysis, 8, 1020—2. 

The enzymes have been both physically entrapped in polyacrylamide on nylon netting and chemically bound to polyacrylic acid derivatives both preparations exhibited large measuring times. Improvement of the system in favour of the response time diminished the sensitivity of the sensor. The authors reported a response time between 77 and 235 s and a sensitivity of 40 mV per concentration decade. Besides the low selectivity of the iodide sensitive electrode (thiocyanate, sulfide, cyanide, and silver(I) ions interfere), disturbances by other HRP substrates, e.g. uric acid, ascorbic acid, and Fe(II) ions, restrict the applicability of the method. 

An analogous glucose sensor has been developed by Umana and Waller (1986). Glucose measurement was carried out by reduction of iodine formed from iodide in a molybdate-catalyzed reaction. The current did not reach a stationary value but increased linearly with time. Obviously the main part of glucose oxidation was catalyzed by GOD leached out into the measuring solution. Therefore the sensitivity dropped to 25% of the initial value after 5 measurements and after 10 days the enzyme was completely exhausted. 

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