2014
DOI: 10.1002/elan.201300468
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Electrochemical Detection of Nitrite in Meat and Water Samples Using a Mesoporous Carbon Ceramic SiO2/C Electrode Modified with In Situ Generated Manganese(II) Phthalocyanine

Abstract: Mesoporous carbon ceramic SiO2/50 wt % C (SBET=170 m2 g−1), where C is graphite, were prepared by the sol‐gel method. The materials were characterized using N2 sorption isotherms, scanning electron microscopy, and conductivity measurements. The matrix was used as support for the in situ immobilization of Mn(II) phthalocyanine (MnPc) on their surface. XPS was used to determine the Mn/Si atomic ratios of the MnPc‐modified materials. Pressed disk electrodes were prepared with the MnPc‐modified matrix, and tested … Show more

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Cited by 36 publications
(17 citation statements)
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“…However, it must be note that, these methods involved in time consuming, expensive and tedious protocol. In contrary, the electrochemical methods used for the detection of nitrite due to the simple procedure, rapid response and high sensitive methods than that of the other aforementioned analytical methods2728.…”
mentioning
confidence: 99%
“…However, it must be note that, these methods involved in time consuming, expensive and tedious protocol. In contrary, the electrochemical methods used for the detection of nitrite due to the simple procedure, rapid response and high sensitive methods than that of the other aforementioned analytical methods2728.…”
mentioning
confidence: 99%
“…As for the electrochemical performance of SiC NWs based nitrite sensor, the comparison with the reported result in the literature, such as metal, organics, oxide, carbon modified composites and SiC modified GC, is listed in Table 1 . It can be seen that SiC NWs based electrode exhibits larger linear response range while with comparable higher sensitivity 21 34 36 37 50 51 52 53 54 55 56 57 , demonstrating the promising application of modified SiC electrode for nitrite determination. At the same time, it should be pointed out that the sensor preparation in this work is also relatively simpler than that reported in the literature.…”
Section: Resultsmentioning
confidence: 94%
“…The samples were grinded adequately in a juicer; a portion of 10 g of puree was mixed with 50 mL of water, followed by sonication for 30 min in a beaker. Then 2.5 mL of 30% ZnSO 4 solution was added to precipitate the proteins [51] and the resulting mixture was centrifuged for 10 min at 4000 rpm. Finally, the supernatant was diluted to 100 mL using the supporting electrolyte for electrochemical determination according to the established procedure.…”
Section: Analytical Applicationsmentioning
confidence: 99%