Page 148 - Illustrated Pocket Dictionary of Chromatography
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148     PHOTODIODE-ARRAY DETECTOR (PDA)

                                   H 3 PO 4
                                Phosphoric acid

        The three pK a values are: pK 1: 2.1, pK 2: 7.2, pK 3: 12.3. Phosphoric acid
        and its alkali salts (e.g., sodium and potassium) are frequently used
        in LC separations as solution buffers. Note, however, that the solu-
        bility of phosphate salts in acetonitrile is limited.

        photodiode-array detector (PDA)    A PDA detector uses a deu-
        terium lamp for the UV spectrum and a tungsten lamp for the visible
        spectrum. The PDA detector differs from the single-wavelength detec-
        tor in that all the source light passes through the sample. Discrete
        wavelengths are then generated by a dispersive element (e.g., prism)
        that is placed between the sample cell and a series of detector diodes.
        Each diode subtends a fixed wavelength range depending on its dis-
        tance from the element, the angular position from the element, and
        the dispersive power of the element.

        o-phthalaldehyde (OPA) A derivatizing reagent used to react
        with 1° amines: OPA is commonly used for the derivatization and
        analysis of amino acids and other primary amine compounds. Fluo-
        rescence detection is done with excitation at 240nm and emission at
        455nm.

            H
                 O                                             SR'
                   O            H
                                            R'SH
                         +  H 2 N  C  COOH                      N   R
                  OH            R
                             General amino
           OPA                      acid


        pinkerton column See ISRP (internal surface reversed phase).
        Pirkle column Named for its inventor, the original Pirkle column
        was a monomeric bonded phase that had the following structure: This
        bonded phase and many others having similar construction are chiral
        in nature (*denotes the chiral center) and are used in the separation
        of enantiomers.
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