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I fluorometri e gli spettrofluorimetri sono due tipi di strumenti che vengono usati per misurare la fluorescenza molecolare. Questi strumenti si diffe…
I fluorimetri e gli spettrofluorimetri sono due strumenti utilizzati per misurare la fluorescenza molecolare, ciascuno dotato di una sorgente luminosa, filtri o monocromatori, cella campione, trasduttore e processore di segnale.
I fluorimetri utilizzano lampade a vapori di mercurio a bassa pressione come sorgente di eccitazione, impiegando filtri di assorbimento o interferenza per selezionare le lunghezze d'onda di eccitazione ed emissione.
Al contrario, gli spettrofluorimetri utilizzano una lampada ad arco allo xeno ad alta pressione e un monocromatore per selezionare le lunghezze d'onda di eccitazione ed emissione.
Entrambi i dispositivi rilevano la fluorescenza attraverso un trasduttore, come un tubo fotomoltiplicatore o un dispositivo ad accoppiamento di carica, convertendo il segnale in una misura elettrica.
La fosforescenza molecolare viene misurata utilizzando un fosforimetro, che tiene conto del ritardo tra l'eccitazione e l'emissione di fosforescenza impiegando chopper rotanti fuori fase.
Questi elicotteri bloccano alternativamente l'emissione fluorescente durante l'eccitazione e la sorgente di eccitazione durante la misurazione dell'emissione fosforescente.
Qui, il campione viene disciolto in una miscela di solventi organici e congelato a temperature di azoto liquido o immobilizzato su un substrato solido per evitare la disattivazione dello stato eccitato mediante conversione esterna.
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Q1: What is the main difference between a fluorometer and a spectrofluorometer?
Fluorometers use low-pressure mercury vapor lamps and absorption or interference filters to select excitation and emission wavelengths, making them suitable for quantitative measurements but unable to record spectra. Spectrofluorometers employ high-pressure xenon arc lamps and monochromators to select wavelengths, allowing them to record excitation or emission spectra for more detailed fluorescence analysis.
Q2: How do transducers in fluorometers and spectrofluorometers convert light signals?
Both instruments use transducers such as photomultiplier tubes or charge-coupled devices to detect fluorescence emission and convert the light signal into an electrical measurement. The signal processor then analyzes this electrical output, enabling quantitative determination of fluorescence intensity from the sample.
Q3: Why is a phosphorimeter different from a fluorometer?
A phosphorimeter measures phosphorescence, which has a longer lifetime than fluorescence. It uses out-of-phase rotating choppers to discriminate between the two: one blocks fluorescent emission during excitation, while the other blocks the excitation source during phosphorescent emission measurement, allowing accurate phosphorescence detection.
Q4: What sample preparation methods are used for phosphorescence measurements?
Samples for phosphorescence are typically dissolved in an organic solvent mixture and frozen at liquid nitrogen temperatures to form an optically clear solid matrix that minimizes external conversion, a radiationless relaxation process. Alternatively, samples can be immobilized on a solid substrate, enabling phosphorescence measurement at room temperature.
Q5: What type of light source does a spectrofluorometer use and why?
Spectrofluorometers use high-pressure xenon arc lamps that produce a continuum emission spectrum across a wide range of wavelengths. This continuous spectrum allows the monochromator to select any desired excitation or emission wavelength, enabling detailed spectral analysis and flexibility in fluorescence measurements.
Q6: How do choppers in a phosphorimeter prevent fluorescence interference?
Phosphorimeters employ two out-of-phase rotating choppers that work sequentially: one blocks fluorescent emission when the excitation source illuminates the sample, and the other blocks the excitation source when measuring phosphorescent emission. This temporal separation allows accurate phosphorescence detection without fluorescence interference.
Q7: What is external conversion and how does it affect phosphorescence measurements?
External conversion is a radiationless relaxation process where energy transfers to the solvent or sample matrix instead of being emitted as light, causing loss of the excited state. To prevent this deactivation, phosphorescence samples are frozen at liquid nitrogen temperatures or immobilized on solid substrates, preserving the excited state long enough for phosphorescence emission.