1957
DOI: 10.1021/ac60126a021
|View full text |Cite
|
Sign up to set email alerts
|

Anodic Stripping Polarography

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

1
16
0

Year Published

1960
1960
2021
2021

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 64 publications
(17 citation statements)
references
References 9 publications
1
16
0
Order By: Relevance
“…Subsequently, the oxidizing response of M n+ is promoted (Equation ( 6)) by the previous amalgamation, which enhances the enrichment of HMIs on the surface of electrodes. [40] However, the formation of intermetallic compounds still represents a challenge for multi-HMIs detections. Intermetallic compounds were reported to influence the HMIs detection.…”
Section: Advantages Of Post-transition Metals For Sensing Hmismentioning
confidence: 99%
“…Subsequently, the oxidizing response of M n+ is promoted (Equation ( 6)) by the previous amalgamation, which enhances the enrichment of HMIs on the surface of electrodes. [40] However, the formation of intermetallic compounds still represents a challenge for multi-HMIs detections. Intermetallic compounds were reported to influence the HMIs detection.…”
Section: Advantages Of Post-transition Metals For Sensing Hmismentioning
confidence: 99%
“…5,6 Various electrode materials have been employed for ASV measurements. In the past, a mercury electrode [7][8][9][10] was preferred for ASV because it forms an amalgam with various metals and has a low noise current in the cathodic potential range. However, it is now recommended that mercury not be used in the construction of commercial analysis systems because of its high toxicity.…”
Section: ¹3mentioning
confidence: 99%
“…(1) (deposition step) ascribes the electrolytic accumulation of the analyte in the working electrode under controlled conditions [9]. The deposition potential to be applied varies with several factors including type of analyte, solvent and pH, among others; however, in ASV, the common rule is the application of a potential around 300 mV more negative than the peak potential of the least easily reduced analyte to be analyzed.…”
Section: Introductionmentioning
confidence: 99%