Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12323/8178| Title: | New Simple Method For The Determination Of Trace Level Copper (Ii) Using 1- [2- (Allylamino) -1-Methylethyl] Thiourea In Presence Of Hydrofob Amines By Molecular Absorption Spectral Method In The Uv And Visible Region |
| Authors: | Mammadov, P.R. Javadzade, T.A. Sucayev, A.R. Mammadova, R.E. Chiragov, F.M. |
| Keywords: | copper 1- [2- (allylamino) -1-methylethyl] thiocarbamide phenanthroline (Phen ) and α,α′ - dipyridine |
| Issue Date: | 2022 |
| Publisher: | Azerbaijan State Oil and Industry University |
| Series/Report no.: | Vol. 4;Azerbaijan Journal of Chemical News, № 2 |
| Abstract: | Cu(II) with 1- [2- (allylamino) -1-methylethyl] thiourea the rapid reacts to form orange complex and also it to form to form brownish complexes in presence of the phenanthroline (Phen) and α,α′ - dipyridine ( α,α′ -dip ). The absorption spectra of the Cu(II) - AMTIC system is a curve with the maximum absorbance at 415 nm and molar absorption coefficient of 1.95.104 l mol−1 cm−1. The absorption spectra of the Cu(II)- AMTIC- Phen and Cu(II) -AMTIC - α,α′-dip systems is a curve with the maximum absorbances at 437 nm and 443 nm and molar absorption coefficients of 2.94.104 l mol−1 cm−1 and 2.81.104 l mol−1 cm−1, respectively. The absorbance was linear for 0.25–2.07 mkg ml−1 of Cu(II) in the Cu(II)- AMTIC system and 0.12 –2.56 mkg ml−1 and 0.18–2.45 mkg ml−1 of Cu(II) in the Cu(II)-AMTIC- Phen and Cu(II)-AMTIC- α,α′-dipsystems, respectively. The proposed methods was successfully used in the determination of Cu(II) in several synthetic mixtures. The relative standard deviation (n = 5) was 0%–2.0%, for Cu(II), indicating that this methods are highly precise and reproducible. The results obtained agree well with synthetic mixture samples analyzed by inductively coupled plasma optical emission spectrometry (ICP-OES). |
| URI: | http://hdl.handle.net/20.500.12323/8178 |
| ISSN: | 2663-7006 |
| Appears in Collections: | Publications |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.