Fiber Optic Chemical Sensor Development

Author(s):  
John I. Peterson
Author(s):  
Budi Mulyanti ◽  
Yuski Maolid Rizki Faozan ◽  
Ajuni B. Pantjawati ◽  
Roer Eka Pawinanto ◽  
Lilik Hasanah ◽  
...  

1993 ◽  
Vol 47 (5) ◽  
pp. 590-597 ◽  
Author(s):  
Stephane Mottin ◽  
Canh Tran-Minh ◽  
Pierre Laporte ◽  
Raymond Cespuglio ◽  
Michel Jouvet

At pH 7 and with the excitation at wavelengths above 315 nm, previously unreported fluorescence of 5-HT (5-hydroxytryptamine) is observed. Two fluorescence bands were observed for 5-HT; the first emits at around 390 nm with an associated lifetime near 1 ns, and the other (well known) emits at 340 nm with an associated lifetime of 2.7 ns. With both static and time-resolved fluorescences, the spectral and temporal effects of the excitation wavelength were studied between 285 and 340 nm. With these basic spectroscopic properties as a starting point, a fiber-optic chemical sensor (FOCS) was developed in order to measure 5-HT with a single-fiber configuration, nitrogen laser excitation, and fast digitizing techniques. Temporal effects including fluorescence of the optical fiber were studied and compared with measurements both directly in cuvette and through the fiber-optic sensor. Less than thirty seconds are required for each measurement. A detection limit of 5-HT is reached in the range of 5 μM. Our system, with an improved sensitivity, could therefore be a possible and convenient “tool” for in vivo determination of 5-HT.


1991 ◽  
Vol 7 (Supple) ◽  
pp. 1465-1468 ◽  
Author(s):  
YUJI KAWABATA ◽  
KEN-ICHI YASUNAGA ◽  
TOTARO IMASAKA ◽  
NOBUHIKO ISHIBASHI

2016 ◽  
Vol 811 ◽  
pp. 74-80 ◽  
Author(s):  
Mohammed M. Rahman ◽  
Hadi M. Marwani ◽  
Abdelmohsen A. Alshehri ◽  
Hassan A. Albar ◽  
Juan Bisquert ◽  
...  

Author(s):  
Mohammed M. Rahman ◽  
M.M. Alam ◽  
Mohammad M. Hussain ◽  
Abdullah M. Asiri ◽  
Mohie E. Moustafa Zayed

Author(s):  
B Mulyanti ◽  
Y M R Faozan ◽  
W S Putro ◽  
R E Pawinanto ◽  
A H S Budi ◽  
...  

2019 ◽  
Vol 73 (10) ◽  
pp. 1218-1227
Author(s):  
Samantha Matthews ◽  
Frank V. Bright

Porous silicon (pSi) exhibits strong photoluminescence (PL) and its PL is often exploited for chemical sensor development. However, the sensor response is not uniform across a pSi specimen. We use co-localized confocal PL and Raman scattering mapping to establish a relationship between the analyte-induced PL response and the silicon nanocrystallite size, size distribution, and amorphous silicon (aSi) contribution across a pSi specimen. Using toluene as a model analyte, high analyte-induced PL response is associated with areas within the specimen that have (i) low aSi content, (ii) silicon nanocrystallites having diameters between 2 and 5 nm, and (iii) silicon nanocrystallites that exhibit a narrow size distributions (≤1% relative standard deviation).


Sign in / Sign up

Export Citation Format

Share Document