1、Chapter 28 High-Performance Liquid Chromatography,Mobile Phase: Liquid Stationary Phase Separation Mechanism - Solid Adsorption- Liquid Layer Partition - Ion exchange resin Ion exchange- Microporous beads Size Exclusion- Chemically modified resin Affinity,HPLC Advantages vs GC,Not limited by sample
2、volatility or thermal stability Two interacting phases Room temperature analysis Ease of sample recovery,Instrumentation,Solvent Reservoirs Pump Sample Injector Column(s) Detector Data System,Mobile Phase Reservoirs,Inert container with inert lines leading to the pump are required. Reservoir filters
3、 (2-10 mm) at reservoir end of solvent delivery lines Degassed solvent - Vacuum filtration - Sparge with inert gas (N2 or He) - Ultrasonic under vacuum Elevate above pumps,Isocratic elution: A separation that employs a single solvent or solvent mixture of constant composition. Gradient elution: Here
4、 two or more solvent systems that differ significantly in polarity are employed. After elution is begun; the ratio of the solvents is varied in a programmed way, sometimes continuously and sometimes in a series of steps. Separation efficiency is greatly enhanced by gradient elution.,HPLC Pump Criter
5、ia,Constructed of materials inert toward solvents to be used Deliver high volumes (flow rates) of solvent (to 10 mL/min) Deliver precise and accurate flow (0.5% variation) Deliver high pressure (to 6000 psi) Deliver pulse free flow Have low pump-head volume Be reliable,HPLC Pumps: Types,Reciprocatin
6、g pumps Syringe pumps Constant pressure pumps,Reciprocating Pumps,One, two, or three pump heads - more heads, less pulse Small head volumes (50 to 250 mL) Short piston stroke Inert pistons (generally sapphire) Continuous use (no refill time) Pulse dampeners,Syringe Pumps,Constant flow rate pump Non-
7、pulsating flow Low flow rates (1 to 100 mL/min) Isocratic flow only Refill required when reservoir (50mL) expended,Constant Pressure Pump,Constant pressure pump, not constant flow Can deliver high pressures Stable flow during delivery stroke Stop flow on refill stroke Low cost,Sample Introduction,Va
8、lve-type injectors - Six port fixed volume Rheodyne reproducible injection volumes variable loop size easy to use, reliable - Six port variable volume Waters variable injection volumes without loop change increased maintenance, operator skill required more expensive,Auto Injectors,Continuous injecti
9、ons operator free Comparable precision and accuracy to manual Much more expensive initially Much more convenient Up 100 samples and standards with microprocessor control,Liquid-Chromatographic ColumnsLiquid-chromatographic columns are ordinarily constructed from smooth-bore stainless steel tubing, a
10、lthough heavy-walled glass tubing is occasionally encountered. The latter is restricted to pressures that are lower than about 600 psi.,Analytical ColumnsLiquid-chromatographic columns range in length from 10 to 30 cm. Normally, the columns are straight, with added length, where needed, being gained
11、 by coupling two or more columns together. The inside diameter of liquid columns is often 4 to 10 mm; the most common particle size of packings is 5 or 10 m. The most common column currently in use is one that is 25 cm in length, 4.6 mm inside diameter, and packed with 5 m particles. Columns of this
12、 type contain 40,000 to 60,000 plates/meter.,Guard ColumnsA guard column is introduced before the analytical column to increase the life of the analytical column by removing not only particulate matter and contaminants from the solvents but also sample components that bind irreversibly to the statio
13、nary phase. The guard column serves to saturate the mobile phase with the stationary phase so that losses of this solvent from the analytical column are minimized. The composition of the guard-column packing is similar to that of the analytical column; the particle size is usually larger. When the g
14、uard column has become contaminated, it is repacked or discarded and replaced with a new one.,Detectors: Unlike gas chromatography, liquid chromatography has no detectors that are as universally applicable and as reliable as the flame ionization and thermal conductivity detectors. A major challenge
15、in the development of liquid chromatography has been in detector improvement. Types of Detectors: Liquid chromatographic detectors are of two basic types. Bulk property detectors respond to a mobile-phase bulk property, such as refractive index, dielectric constant, or density. In contrast, solute p
16、roperty detectors respond to some property of solutes, such as UV absorbance, fluorescence, or diffusion current, that is not possessed by the mobile phase.,Absorbance Detectors: Is a Z-shaped, flow-through cell for absorbance measurements on eluents from a chromatographic column. Many absorbance de
17、tectors are double-beam devices in which one beam passes through the eluent cell and the other through a filter to reduce its intensity. Ultraviolet Absorbance Detectors with Filters: The simplest UV absorption detectors are filter photometers with a mercury lamp as the source. Most commonly the int
18、ense line at 254 nm is isolated by filters. Deuterium or tungsten filament sources with interference filters also provide a simple means of detecting absorbing species.,UV Absorbance Detector with Monochromator: There are detectors that consist of a scanning spectrophotometer with grating optics. So
19、me are limited to uv radiation; others encompass both uv and visible radiation. The most powerful uv spectrophotometric detectors are diode-array instruments. Infrared Absorbance Detectors: Two types of infrared detectors are offered commercially. The range of the first instrument is from 2.5 to 14.
20、5 m or 4000 to 690 cm-1. The second type of infrared detector is based upon Fourier transform instruments.,Fluorescence Detectors: Fluorescence is observed by a photoelectric detector located at 90 deg to the excitation beam. The simplest detectors employ a mercury excitation source and one or more
21、filters to isolate a band of emitted radiation. More sophisticated instruments are based upon a Xenon source and employ a grating monochromator to isolate the fluorescent radiation. An inherent advantage of fluorescence methods is their high sensitivity, which is typically greater by more than an or
22、der of magnitude than most absorbance procedures.,Refractive-Index Detectors: Refractive-index detectors have the significant advantage of responding to nearly all solutes. That is they are general detectors analogous to flame or thermal conductivity detectors in gas chromatography. In addition, the
23、y are reliable and unaffected by flow rate. They are, however, highly temperature sensitive and must be maintained at a constant temperature to a few thousandths of a degree centigrade. Furthermore, they are not as sensitive as most other types of detectors.,Electrochemical Detectors: These devices
24、are based upon amperometry, polarography, coulometry, and conductometry. They appear to offer advantages, in many instances, of high sensitivity, simplicity, convenience, and widespread applicability.,Mass Spectrometric Detectors: A problem in coupling liquid chromatography with mass spectrometry is
25、 the enormous mismatch between the relatively large solvent volumes and the vacuum requirements. Several interfaces have been developed for solving this problem. In a first type the eluent from the column is split, with only a tiny fraction being introduced directly into the mass spectrometer. In a
26、second type of interface the effluent is deposited on a continuous, moving-belt or moving-wire that transports the solvent and analyte to a heated chamber for removal of the former by volatilization.,PARTITION CHROMATOGRAPHY,Partition chromatography can be subdivided into (i) liquid-liquid chromatog
27、raphy and (ii) bonded-phase chromatography.With liquid-liquid, a liquid stationary phase is retained on the surface of the packing by physical adsorption. With bonded-phase, the stationary phase is bonded chemically to the support surfaces.,PARTITION CHROMATOGRAPHYEarly partition chromatography was
28、the liquid-liquid type; now the bonded-phase method has become predominate because of certain disadvantages of liquid-liquid systems. One of these disadvantages is the loss of stationary phase by dissolution in the mobile phase, which requires periodic recoating of the support particles. Furthermore
29、, stationary-phase solubility problems prohibit the use of liquid-phase packings for gradient elution.,Columns for Bonded-Phase ChromatographyThe supports for the majority of bonded-phase packings for partition chromatography are prepared from rigid silica, or silica-based, compositions. These solid
30、s are formed as uniform, porous, mechanically sturdy particles commonly having diameters of 3, 5, or 10m. The surface of fully hydrolyzed silica is made up of chemically reactive silanol groups. The most useful bonded-phase coatings are siloxanes formed by reaction of the hydrolyzed surface with an
31、organochlorosilane.,Reversed-Phase and Normal-Phase Packings Two types of partition chromatography are distinguishable based upon the relative polarities of the mobile and stationary phases.Liquid chromatography based upon highly polar stationary phases such as water or triethyleneglycol supported o
32、n silica or alumina particles; a relatively nonpolar solvent such as hexane or I-propylether then served as the mobile phase. This type of chromatography is referred to as normal-phase chromatography.,In reversed-phase chromatography, the stationary phase is nonpolar, often a hydrocarbon, and the mo
33、bile phase is relatively polar (such as water, methanol, or acetonitrile). In normal-phase chromatography, the least polar component is eluted first because it is the most soluble in the mobile phase; increasing the polarity of the mobile phase has the effect of decreasing the elution time. In contr
34、ast, in the reversed-phase method, the most polar component appears first, and increasing the mobile phase polarity increases the elution time.,HPLC Derivatization Methods,Why derivatize? Enhance detector response Improve analyte resolution Improve analyte peak shape Improve analyte sensitivity Esta
35、blish analyte identity Improve analyte stability during analysis Change analyte physical properties,Preparative Chromatography,Separation and isolation of relatively large quantities ( 0.1g) of solute Similar systems to analytical chromatography - higher flow rates (10 to 200 mL/min) - Large sample
36、loops - preparative columns - larger dimensions and packing size - detection not critical - not trace analysis - but non-destructive,Chromatographic Separations,Open column chromatography - Very slow analysis - Poor chromatographic efficiency - Inconvenient sample recovery HPLC - More rapid analysis
37、 - High efficiency packing materials - continuous flow-through detection,Gel Permeation LC,Also known as size exclusion or gel filtration Separation by effective size in solution - dependent on molecular size and shape - molecules large enough to be excluded from pores all co-elute at tm- smaller mo
38、lecules permeate the sp pores to differing degrees based on relative size and are proportionally retarded.,GPLC Stationary Phases,Stationary phase controls retention or selection Two types: rigid cross-linked polymer gels and other polymer gels Classification by pore size, or range of pore sizes Sma
39、ll molecules - pores 60 to 100 Mixed bed columns for wide size ranges,GPLC Mobile Phases,Mobile phase not generally used to control retention or selection Selection primarily based on solubility - low viscosity solvent - detector compatible - column compatible polstryrene - less polar solvents silic
40、a gel - water, wide range of solvents, limited pH,Ion Exchange Chromatography,Reversible exchange of ionic species between the stationary phase and mobile phase Ionic species chemically bound to insoluble matrix serves as exchange site (adsorption),IEC Separations,Insoluble matrix (M+) and counter i
41、on (E-) as stationary phase Analyte ion (A-) in mobile phase M+E- + A- M+A- + E-,IEC Stationary Phases,Silica based materials - Pellicular particles Organic materials - porous beads - styrene/divinylbenzene crosslinked co- polymers - methacrylic acid/divinylbenzene crosslinked co-polymers Inorganic
42、materials,IEC Stationary Phases,Functional group addition through surface reactions with appropriate reagents to produce the desired cation or anion exchange resin Cation exchangers (strong & weak) - Acid functional groups Anion exchangers (strong & weak) - Basic functional groups,Resin Cross-linkag
43、e,Pore size a degree of crosslinkage High degrees of Crosslinkage: - increase mechanical strength of the resin - decrease the degree of swelling - decrease the permeability of the resin,IEC Mobile Phases,Aqueous solutions of salt or salts with a small % of organic modifier and perhaps a buffer,Reten
44、tion & Selectivity Factors,Size and shape of the solvated molecule Mobile phase pH Concentration & type of competing ion Addition of organic solvent to mobile phase Column temperature,Cation M-A+ Bond Strengths,Ce3+ Al3+ Ba2+ Pb2+ Ca2+ Ni2+ Cu2+ Mg2+ UO22+ Tl+ Ag+ K+ NH4+ H+,Anion M+A- Bond Strength
45、s,Citrate SCN- CrO42- SO42- NO3- Br- CN- Cl- HCO3- HCOO- OH- Anion selectivities are not as rigidly defined as those of cations,Prediction of MxAy Bond Strengths,Factors: - charge on the solute ion - size of the solvated ion - degree of resin crosslinkage - polarizability of the solute molecule- ion
46、-exchange capacity of the resin- functional group on the resin - degree of interaction between the solute and the resin,Ion Chromatography,Separation of inorganic cations and anions and low molecular weight water-soluble organic acids and bases Non-suppressed IC methods Suppressed IC methods,Ion Exc
47、lusion Chromatography,Separation of ionic solutes from weakly ionized of neutral solutes using strong cation and anion exchange resins,Factors Affecting Retention in IC,Degree of ionization of the solute - solute pKa - eluent pH - organic modifier content hydrophobic interactions between solute and
48、sp molecular size of the solute degree of X-linkage of the sp system temperature,Affinity Chromatography,Separation of proteins and biomolecules through the use of a biologically specific immobilized ligand (sp). Biologically specific ligand is chemically attached to a gel matrix pH of the system is
49、 controlled to control the strength of the interaction between the ligand and the solute molecule,Complexation Chromatography,Separation based on the rapid reversible formation of a complex between metal ions and ligands Suitable ligands are immobilized on sp,Chiral Chromatography,Separation based on the use of chiral stationary phases which interact to varing degrees with optical isomers of the soluteSystems differ little from conventional HPLC systems Limited applications for a given sp,
