scholarly journals A SILICON PHOTODIODE ARRAY DETECTOR COVERING A LARGE SOLID ANGLE FOR FLUORESCENCE EXAFS MEASUREMENTS FROM 2 TO 25 keV

1986 ◽  
Vol 47 (C8) ◽  
pp. C8-143-C8-147 ◽  
Author(s):  
A. RETOURNARD ◽  
M. LOOS ◽  
I. ASCONE ◽  
J. GOULON ◽  
M. LEMONNIER ◽  
...  
1973 ◽  
Vol 27 (5) ◽  
pp. 366-370 ◽  
Author(s):  
Edward G. Codding ◽  
Gary Horlick

Direct current arc emission spectra have been measured for 35 elements over a 140 Å range in the 3240 to 3380 Å region employing a monochromator self-scanned linear silicon photodiode array detector system. Each spectrum was reduced to a binary representation by compressing the spectral intensity information such that a logic 1 and a logic 0 represented the presence and absence of spectral features. It is shown that with the application of the logic operations AND and exclusive-or (XOR) it is possible to identify uniquely each of the 35 elemental emission spectra. The feasibility of extending the procedure to multicomponent spectra is illustrated and discussed.


2009 ◽  
Vol 38 (3) ◽  
pp. 359-363
Author(s):  
Jee-Eun Hong ◽  
Mi-Ran Kim ◽  
Sang-Hee Cheon ◽  
Jung-Young Chai ◽  
Eun-Ryong Park ◽  
...  

2013 ◽  
Vol 96 (3) ◽  
pp. 670-675 ◽  
Author(s):  
Balwinder Singh ◽  
Kousik Mandal ◽  
Sanjay K Sahoo ◽  
Urvashi Bhardwaj ◽  
Raminderjit Singh Battu

Abstract An easy and simple analytical method was standardized and validated for the estimation of residues of spirotetramat and its metabolite spirotetramat cis enol in various substrates: okra fruits, brinjal leaves and fruits, green chili, red chili, and soil. The samples were extracted with acetonitrile, diluted with brine solution, partitioned into dichloromethane, dried over anhydrous sodium sulfate, and cleaned up by treatment with activated charcoal powder. Final clear extracts were concentrated under vacuum and reconstituted with HPLC grade acetonitrile. Residues were estimated using HPLC with a photodiode array detector and a C18 column, and confirmed by HPTLC. Acetonitrile was used as the mobile phase at 0.4 mL/min. Both spirotetramat and spirotetramat cis enol presented distinct peak at retention times of 8.518 and 7.598 min, respectively. Consistent recoveries ranging from 82 to 97% for spirotetramat and spirotetramat cis enol were observed when samples were spiked at 1.00 to 0.03 mg/kg levels. The LOQ of the method was found to be 0.03 mg/kg. The analytical method was validated in terms of parameters, including selectivity, linearity, precision, and accuracy.


1992 ◽  
Vol 258 (2) ◽  
pp. 269-273 ◽  
Author(s):  
M.E. León-González ◽  
L.V. Pérez-Arribas ◽  
M.J. Santos-Delgado ◽  
L.M. Polo-Díez

The Analyst ◽  
1987 ◽  
Vol 112 (5) ◽  
pp. 619-622 ◽  
Author(s):  
Marcelo Blanco ◽  
Jordi Gené ◽  
Hortensia Iturriaga ◽  
Santiago Maspoch

2016 ◽  
Vol 8 (30) ◽  
pp. 5949-5956 ◽  
Author(s):  
Soumia Boulahlib ◽  
Ali Boudina ◽  
Kahina Si-Ahmed ◽  
Yassine Bessekhouad ◽  
Mohamed Trari

In this study, a rapid and simple method based on reversed-phase high performance liquid chromatography (RP-HPLC) using a photodiode array detector (PDA) for the simultaneous analysis of five pollutants including aniline and its degradation products, para-aminophenol, meta-aminophenol, ortho-aminophenol and phenol, was developed.


Sign in / Sign up

Export Citation Format

Share Document