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Common Detectors for GPC/SEC Applications

A brief overview of the detectors used in GPC/SEC Chromatography with the purpose of showing detection principles and differences of the instruments now commercially available.

Detector Classes

Concentration Detectors (RI, UV, IR)

Molar Mass Sensitive Detectors (Viscometer, SLS, DLS)

Unspecific Detectors (ELSD, Corona)


Concentration Detectors

Refractive Index Detector (RI)

Refractometer Scheme
For Polychromatic light source: Polychromatic RI Equation
For Monochromatic light source: Monochromatic RI Equation

Classic UV Detector

UV Scheme
Signal Response: UV Equation


Photodiode Array detector (PDA)

PDA UV Scheme
Signal Response: UV Equation


Comparison of Concentration Detectors

Polychromatic RI
Wide dynamic range, high linearity, good sensitivity
No dn/dc information

Monochromatic RI
Wide dynamic range, high linearity, good sensitivity and dn/dc values.

Classic UV
Highest sensitivity and selectivity.
Limited dynamic range
PDA
High sensitivity, delivers full absorbance Spectra
Limited dynamic range, selectivity not fully defined


Viscometers

Single Capillary (Ouano)

Single Capillary Viscometer
Signal: Dual-Detector Signals
Where: K = Capillary Constant, Q = Flow Rate, eta = Viscosity

Differential Viscometer (Haney)

Differential Viscometer (Haney)
Signal: Differential Viscometer Signals

Differential Viscometer (Bures)

Differential Viscometer (Bures)

Combined Viscometer / RI (Bures)

Dual Detector (Bures)

External vs. Internal combination Viscometer / RI

External vs. Internal Detector Combination

Comparison of Viscometers

Single Capillary
Huge dynamic range, intrinsically linear, simple combination.
Poor sensitivity, highly sensitive to temperature and pump pulses.
Haney Bridge
High sensitivity, little influence of temperature or pump pulses.
Shows "Breakthrough" after sample peak, complex combination.
Bures Bridge
High sensitivity, little influence of temperature or pump pulses, no "Breakthrough" after sample peak, low band broadening.
Complex combination.
Combined Bures Viscometer/RI
Highest sensitivity, simple combination with other detectors


Static Light Scattering Detectors

Single Angle SLS Detectors

Single Angle Light Scattering

Multi Angle Light Scattering (Wyatt)

Multi Angle Light Scattering (Wyatt)

Multi Angle Light Scattering (Reed)

Multi Angle Light Scattering (Reed)

Comparison of SLS Detectors

Small Angle
Limited sensitivity, no extrapolation possible thus no Rg information, obsolete.
Right Angle SLS (RALLS)
Needs Viscometer and RI to obtain MW, no Rg information, questionable method.
MALLS (Wyatt)
Excellent sensitivity and linearity. Non optimal Flowpath.
MALLS (Reed)
Excellent sensitivity. Optimal Flowpath.


Unspecific Detectors

Evaporative Light Scattering detector (ELSD)
Solvent is separated from solute via evaporation, scattering of solute is then detected. Response (Signal) is substance dependent, individual calibration necessary. Limited dynamic range. Good sensitivity.

Corona
Uses the "Corona" effect. Solvent is separated from solute via evaporation. The solute is then "wrapped" in a layer of ionized nitrogen and detected.

Common Detector Combinations

UV-polyRI
Co-Polymer composition analysis

RI-Viscometer
MW via universal calibration, MHS-coefficients, Rh, Branching

RI-MALS
"Absolute" MW, Rg

RI-Viscometer-Single Angle SLS
MW via "Triple detection"

RI-Viscometer-MALS
Absolute MW, Structure analysis, Branching


Practical Aspects of Combinations

Practical Aspects of Detector Combination