Fluorescence Lifetime Studies of Crude Oils

1994 ◽  
Vol 48 (8) ◽  
pp. 977-984 ◽  
Author(s):  
Xin Wang ◽  
Oliver C. Mullins

The fluorescence lifetimes of a series of crude oils at various concentrations have been measured for UV-visible excitation and emission wavelengths. The lifetime results are compared with fluorescence spectra and quantum yields for these solutions. The concentration effects of energy transfer and quenching are large and result in a significant decrease in fluorescence lifetimes for high concentrations and for heavy crude oils. Thus, radiationless processes dominate in energy transfer. At high concentrations, energy transfer produces large red shifts in fluorescence emission spectra, while quenching produces a large reduction in quantum yields. Stern-Volmer analyses of lifetime and quenching data show a linear dependence of energy transfer and quenching rates on concentration. The rate constants are consistent with collisions which are very efficient at energy transfer and quenching, and the rates of these two processes are comparable.

1995 ◽  
Vol 49 (6) ◽  
pp. 754-764 ◽  
Author(s):  
Taggart D. Downare ◽  
Oliver C. Mullins

Fluorescence emission spectra and absolute quantum yields have been measured for ten diverse crude oils at various concentrations over a broad range of excitation and emission wavelengths in the visible and the near-infrared. Energy transfer produces large red shifts and large widths in the fluorescence emission spectra for shorter wavelength excitation particularly for heavier crude oils. However, the effects of energy transfer are nearly absent for near-infrared excitation; all crude oils exhibit nearly the same emission spectra for long wavelength excitation. In addition, the fraction of emission resulting from collisional energy transfer relative to nascent emission is almost independent of oil type; it is governed by quantum yield characteristics. Absolute fluorescence quantum yields of ten crude oils (and three rhodamine dyes for validation) were measured with respect to scattering of latex microspheres in distilled water. Fluorescence quantum yields vary systematically with crude oil type as well as excitation wavelength; quantum yields are lower for high fluorophore concentrations (heavy crude oils) and for longer wavelength excitation. Stern-Volmer analyses of the quantum yields indicate that simple models apply and show the relative quenching rates for different excitation wavelengths.


2018 ◽  
Vol 22 (09n10) ◽  
pp. 847-852 ◽  
Author(s):  
Xian-Fu Zhang ◽  
Xiaojie Sun

The synthesis, fluorescence properties and singlet oxygen generation capability of germanium tetrabenzotriazacorrole (LGeTBC), germanium phthalocyanine (Cl[Formula: see text]GePc) and their derivatives are described. Measurements include UV-vis absorption spectra, fluorescence emission spectra, fluorescence quantum yields fluorescence lifetimes, and singlet delta oxygen quantum yields. LGeTBC and its derivatives exhibit quite different spectral and fluorescence properties from their phthalocyanine precursor. Both LGeTBC and Cl[Formula: see text]GePc show high singlet delta oxygen quantum yields and suitable fluorescence quantum yields, indicating that they can act as good singlet oxygen photosensitizers for photodynamic therapy.


Author(s):  
Yuichi Niibori ◽  
Masayuki Narita ◽  
Akira Kirishima ◽  
Taiji Chida ◽  
Hitoshi Mimura

Calcium silicate hydrate (CSH) is a main component of cement-based material required for constructing the geological repository. As in many countries, since the repository in Japan is constructed below water table, we must consider the interaction of radionuclide with cement materials altered around the repository after the backfill. Using fluorescence emission spectra, so far, the authors have investigated the interaction of Eu(III) (as a chemical analog of Am(III)) with CSH gels formed with no dried process, considering a condition saturated with groundwater. However, in such fluorescence emission behaviors, a deexcitation process of OH vibrators of light water and a quenching effect caused by Eu-Eu energy transfer between Eu atoms incorporated in the CSH gel must be considered. This study examined the fluorescence emission behavior of Eu(III) sorbed on CSH gels formed with no dried process, by using La(III) (non-fluorescent ions) as a diluent of Eu(III). Furthermore, the CSH samples were synthesized with CaO, SiO2, and heavy water (D2O) as a solvent in order to avoid the obvious deexcitation process of OH vibrators of light water. This study prepared CSH samples with the Ca/Si ratio set to 1.6, 1.0, and 0.5. A 1 mM solution of a given combination of Eu(III) and La(III) (Eu(III) content: 100%, 67%, 50% or 33%) was added into CSH gel sample. The contact time-period of the CSH gel with the Eu(III)/La(III) solution was set to 60 days. In the results, the peak around 618 nm was split into two peaks of 613 nm and 622 nm in the cases of Ca/Si = 1.0 and 1.6. Then, the peak of 613 nm decreased with increment of Eu(III)/La(III) ratio. This means that the relative intensity of 613 nm is useful to quantify the amount of Eu(III) incorporated in CSH gel. Besides, the intensity peak of 584 nm decayed with increment of Eu/La ratio, suggesting a quenching effect due to Eu-Eu energy transfer. However, the decay behavior of the fluorescence emission did not depend on the Eu/La concentration ratio. That is, such a quenching effect is neglectable. Additionally, the low Ca/Si ratio samples underwent slow attenuation of fluorescence and showed profiles similar to those of high Ca/Si ratio samples. Therefore, low Ca/Si ratio samples also include the reaction forming a complex on the surface of CSH gel with Eu(III). In other words, even if Ca/Si ratio is lower than 1.0, CSH gels would retard the migration of radionuclides released from the repository.


2014 ◽  
Vol 68 (8) ◽  
Author(s):  
Daniel Mártire ◽  
Walter Massad ◽  
Hernán Montejano ◽  
Mónica Gonzalez ◽  
Paula Caregnato ◽  
...  

AbstractThe fluorescence emission spectra and fluorescence quantum yields of hemicyanine dyes LDS 698, LDS 722, and LDS 730 were measured in different media. No transient species was detected in the laser flash-photolysis experiments performed with Ar-saturated solutions of the dyes in methanol. However, in the presence of 0.08 M potassium iodide, the absorption of the triplet states was clearly observed. Oxygen consumption measurements in the absence and presence of a chemical trap (furfuryl alcohol) in MeOH: H2O (φ r = 1: 1) solutions of the dyes containing KI confirmed the generation of singlet molecular oxygen.


1995 ◽  
Vol 312 (1) ◽  
pp. 267-271 ◽  
Author(s):  
L Polgár

Prolyl oligopeptidase is the prototype of a new serine protease family, unrelated to trypsin and subtilisin. In contrast with these proteases, prolyl oligopeptidase is remarkably sensitive to ionic strength, being more active in the presence of high concentrations of salt. The enzyme has two catalytic forms, which interconvert with changing pH. To reveal the structural bases of these phenomena, the effects of 0.5 M NaCl on the stability of the enzyme were investigated by studying its denaturation as a function of pH, temperature, and urea concentration. The three independent methods have unequivocally demonstrated that denaturation of the enzyme is promoted in the presence of NaCl. Furthermore, destabilization of the low-pH form by urea is more significant than that of the high-pH form. Examination of the fluorescence emission spectra of various denatured forms indicates that the enzyme is not fully unfolded in 8 M urea, nor at acidic pH. The tryptophan residues in the acid-denatured state are mainly buried. The results are interpreted in terms of the decay of the protective water shell at the higher ionic strength. The higher enthalpy and entropy of activation for heat denaturation provide further evidence that a more ordered water structure stabilizes the protein in the absence of salt. The biphasic kinetics obtained with denaturation by heat and urea suggest that the enzyme has two domains of different stabilities.


2015 ◽  
Vol 465 (1) ◽  
pp. 401-405 ◽  
Author(s):  
V. I. Stadnichuk ◽  
E. P. Lukashev ◽  
M. F. Yanyushin ◽  
D. V. Zlenko ◽  
E. M. Muronez ◽  
...  

2019 ◽  
Vol 29 (4) ◽  
pp. 134
Author(s):  
Mahasin F. Hadi Al-Kadhemy ◽  
Asrar Abdulmunem ◽  
Husam Sabeeh Al-Arab

For different amount of masses of TiO2 nanoparticles in dye solution, absorption and Fluorescence profiles of the suspension for TiO2 nanoparticles with Fluorescein (F) in distilled water solution, has been explored. An absorption spectra enhancement were detected for changed amount of masses, which specifies that the doping with TiO2 nanoparticles has a major effect on the dye absorption spectra. Contrarily, all fluorescence emission spectra for the dye, were quenched as TiO2 nanoparticles amount of masses increases because of Förster resonance energy transfer (FRET).


1983 ◽  
Vol 209 (2) ◽  
pp. 299-307 ◽  
Author(s):  
S P Leytus ◽  
L L Melhado ◽  
W F Mangel

A new fluorogenic substrate for serine proteinases, bis(N-benzyloxycarbonyl-L-argininamido)Rhodamine [(Cbz-Arg-NH)2-Rhodamine], was synthesized, purified and chemically and enzymically characterized. This compound, which employs Rhodamine as a fluorophoric leaving group, is the first in a series of substrates designed to measure the amidase activity of proteinases. Cleavage of one of the amide bonds of (Cbz-Arg-NH)2-Rhodamine by a trypsin-like serine proteinase converts the non-fluorescent bisamide substrate into a highly fluorescent monoamide product. Significant differences in the electronic absorption and fluorescence emission spectra and quantum yields of bis-, mono- and un-substituted Rhodamine are reported. Macroscopic kinetic constants for the interaction of (Cbz-Arg-NH)2-Rhodamine with bovine trypsin, human and dog plasmin and human thrombin were determined. Compared with the corresponding 7-amino-4-methylcoumarin-based analogue, (Cbz-Arg-NH)2-Rhodamine exhibits an increase in sensitivity with these enzymes of 50-300-fold. The physical basis for this increase in sensitivity is discussed.


Sign in / Sign up

Export Citation Format

Share Document