preconcentration procedure
Recently Published Documents


TOTAL DOCUMENTS

49
(FIVE YEARS 1)

H-INDEX

19
(FIVE YEARS 0)

2018 ◽  
Vol 135 ◽  
pp. 57-60 ◽  
Author(s):  
T.D. Rathod ◽  
M. Tiwari ◽  
S. Maity ◽  
S.K. Sahu ◽  
G.G. Pandit

2018 ◽  
Vol 42 (18) ◽  
pp. 15444-15452 ◽  
Author(s):  
Magdalena Krawczyk-Coda

A preconcentration procedure for gallium, indium, and thallium using HNTs was developed prior to their sequential determination by HR-CS GFAAS.


2017 ◽  
Vol 48 (4) ◽  
pp. 761-771 ◽  
Author(s):  
Ivo Safarik ◽  
Eva Baldikova ◽  
Mirka Safarikova ◽  
Kristyna Pospiskova

A new preconcentration procedure named “Magnetic textile solid phase extraction” was developed. A piece of nonwoven textile (fabric) was used for the immobilization of copper phthalocyanine dye and employed for the adsorption of crystal violet and safranin O from large volumes of sample. The bound dye was eluted into small volume of methanol. The limit of detection and limit of quantification values for safranin O were 2.66 µg/L and 8.87 µg/L, while for crystal violet these values were 2.17 µg/L and 7.23 µg/L, respectively. Linearity in the range 5–100 µg/L was observed. In order to prepare magnetically responsive adsorbent, an iron-based standard staple was inserted in the textile material using an office stapler. The developed procedure can be easily adapted for the detection of large variety of analytes in biochemistry, biotechnology, environmental technology, and forensic analysis.


2016 ◽  
Vol 31 (7) ◽  
pp. 1505-1514 ◽  
Author(s):  
Magdalena Krawczyk ◽  
Somaye Akbari ◽  
Magdalena Jeszka-Skowron ◽  
Elmira Pajootan ◽  
Farnaz Shahamati Fard

A preconcentration procedure for cadmium and lead using dendrimer modified HNTs was developed prior to its sequential determination by HR-CS GFAAS.


2015 ◽  
Vol 7 (12) ◽  
pp. 5081-5091 ◽  
Author(s):  
Ramazan Gürkan ◽  
Nail Altunay ◽  
Sema Korkmaz

The developed method was simple, fast, inexpensive and eco-friendly with a low detection limit of 1.45 μg L−1 in the linear range of 5–360 μg L−1. The method is an alternative to expensive methods such as ET-AAS, ICP-OES, and HR-CS-MAS.


Sign in / Sign up

Export Citation Format

Share Document