Gel permeation chromatography

Last updated

Gel permeation chromatography (GPC) [1] is a type of size-exclusion chromatography (SEC), that separates high molecular weight or colloidal analytes on the basis of size or diameter, typically in organic solvents. The technique is often used for the analysis of polymers. As a technique, SEC was first developed in 1955 by Lathe and Ruthven. [2] The term gel permeation chromatography can be traced back to J.C. Moore of the Dow Chemical Company who investigated the technique in 1964. [3] The proprietary column technology was licensed to Waters Corporation, who subsequently commercialized this technology in 1964. [4] GPC systems and consumables are now also available from a number of manufacturers. It is often necessary to separate polymers, both to analyze them as well as to purify the desired product.

Contents

When characterizing polymers, it is important to consider their size distribution and dispersity (Đ) as well their molecular weight. Polymers can be characterized by a variety of definitions for molecular weight including the number average molecular weight (Mn), the weight average molecular weight (Mw) (see molar mass distribution), the size average molecular weight (Mz), or the viscosity molecular weight (Mv). GPC allows for the determination of Đ as well as Mv and, based on other data, the Mn, Mw, and Mz can be determined.

How it works

GPC is a type of chromatography in which analytes are separated, based on their size or hydrodynamic volume (radius of gyration). This differs from other chromatographic techniques, which depend upon chemical or physical interactions between the mobile and stationary phases to separate analytes. [5] Separation occurs via the use of porous gel beads packed inside a column (see stationary phase (chemistry)). The principle of separation relies on the differential exclusion or inclusion of the macromolecules by the porous gel stationary phase. Larger molecules are excluded from entering the pores and elute earlier, while smaller molecules can enter the pores, thus staying longer inside the column. The entire process takes place without any interaction of the analytes with the surface of the stationary phase.

Schematic of pore vs analyte size Pore size schematic.jpg
Schematic of pore vs analyte size

The smaller analytes relative to the pore sizes can permeate these pores and spend more time inside the gel particles, increasing their retention time. Conversely, larger analytes relative to the pores sizes spend little if any time inside the column, hence they elute sooner. Each type of column has a range of molecular weights that can be separated, according to their pores sizes.

Range of molecular weights that can be separated for each packing material Size Limits for GPC.jpg
Range of molecular weights that can be separated for each packing material

If an analyte is too large relative to the column's pores, it will not be retained at all and will be totally excluded; conversely, if the analyte is small relative to the pores sizes, it will be totally permeating. Analytes that are totally excluded, elute with the free volume outside around the particles (Vo), the total exclusion limit, while analytes that are completely delayed, elute with the solvent, marking the total permeation volume of the column, including also the solvent held inside the pores (Vi). The total volume can be considered by the following equation, where Vg is the volume of the polymer gel and Vt is the total volume: [5]

As can be inferred, there is a limited range of molecular weights that can be separated by each column, therefore the size of the pores for the packing should be chosen according to the range of molecular weight of analytes to be separated. For polymer separations the pore sizes should be on the order of the polymers being analyzed. If a sample has a broad molecular weight range it may be necessary to use several GPC columns with varying pores volumes in tandem to resolve the sample fully.

Application

GPC is often used to determine the relative molecular weight of polymer samples as well as the distribution of molecular weights. What GPC truly measures is the molecular volume and shape function as defined by the intrinsic viscosity. If comparable standards are used, this relative data can be used to determine molecular weights within ± 5% accuracy. Polystyrene standards with dispersities of less than 1.2 are typically used to calibrate the GPC. [6] Unfortunately, polystyrene tends to be a very linear polymer and therefore as a standard it is only useful to compare it to other polymers that are known to be linear and of relatively the same size.

Material and methods

Instrumentation

A typical GPC instrument including: A. Autosampler, B. Column, C. Pump, D. RI detector, E. UV-vis detector GPC instrument.jpg
A typical GPC instrument including: A. Autosampler, B. Column, C. Pump, D. RI detector, E. UV-vis detector
Inside of an autosampler for running several samples without user interaction, e.g. overnight Sample holder.jpg
Inside of an autosampler for running several samples without user interaction, e.g. overnight

Gel permeation chromatography is conducted almost exclusively in chromatography systems. The experimental design is not much different from other techniques of High Performance liquid chromatography. Samples are dissolved in an appropriate solvent, in the case of GPC these tend to be organic solvents and after filtering the solution it is injected onto a column. The separation of multi-component mixture takes place in the column. The constant supply of fresh eluent to the column is accomplished by the use of a pump. Since most analytes are not visible to the naked eye a detector is needed. Often multiple detectors are used to gain additional information about the polymer sample. The availability of a detector makes the fractionation convenient and accurate.

Gel

Gels are used as stationary phase for GPC. The pore size of a gel must be carefully controlled in order to be able to apply the gel to a given separation. Other desirable properties of the gel forming agent are the absence of ionizing groups and, in a given solvent, low affinity for the substances to be separated. Commercial gels like PLgel & Styragel (cross-linked polystyrene-divinylbenzene), [7] [8] LH-20 (hydroxypropylated Sephadex), [9] Bio-Gel (cross-linked polyacrylamide), HW-20 & HW-40 (hydroxylated methacrylic polymer), [10] and agarose gel are often used based on different separation requirements. [11]

Column

The column used for GPC is filled with a microporous packing material. The column is filled with the gel. Since the total penetration volume is the maximum volume permeated by the analytes, and there is no retention on the surface of the stationary phase, the total column volume is usually large, relatively to the sample volume.

Eluent

The eluent (mobile phase) should be the appropriate solvent to dissolve the polymer, should not interfere with the response of the polymer analyzed, and should wet the packing surface and make it inert to interactions with the polymers. The most common eluents for polymers that dissolve at room temperature GPC are tetrahydrofuran (THF), o-dichlorobenzene and trichlorobenzene at 130–150 °C for crystalline polyalkynes and hexafluoroisopropanol (HFIP) for crystalline condensation polymers such as polyamides and polyesters. [12]

Pump

There are two types of pumps available for uniform delivery of relatively small liquid volumes for GPC: piston or peristaltic pumps. The delivery of a constant flow free of fluctuations is especially important to the precision of the GPC analysis, as the flow-rate is used for the calibration of the molecular weight, or diameter. [13]

Detector

In GPC, the concentration by weight of polymer in the eluting solvent may be monitored continuously with a detector. There are many detector types available and they can be divided into two main categories. The first is concentration sensitive detectors which includes UV-VIS absorption, differential refractometer (DRI) or refractive index (RI) detectors, infrared (IR) absorption and density detectors. The second category is molecular weight sensitive detectors, which include low angle light scattering detectors (LALLS) and multi angle light scattering (MALS). [14] The resulting chromatogram is therefore a weight distribution of the polymer as a function of retention volume.

GPC chromatogram; Vo= no retention, Vt= complete retention, A and B = partial retention GPC Chromatogram.jpg
GPC chromatogram; Vo= no retention, Vt= complete retention, A and B = partial retention

The most sensitive detector is the differential UV photometer and the most common detector is the differential refractometer (DRI). When characterizing copolymer, it is necessary to have two detectors in series. [6] For accurate determinations of copolymer composition at least two of those detectors should be concentration detectors. [14] The determination of most copolymer compositions is done using UV and RI detectors, although other combinations can be used. [15]

Data analysis

Gel permeation chromatography (GPC) has become the most widely used technique for analyzing polymer samples in order to determine their molecular weights and weight distributions. Examples of GPC chromatograms of polystyrene samples with their molecular weights and dispersities are shown on the left.

GPC Separation of Anionically Synthesized Polystyrene; Mn=3,000 g/mol, D=1.32 Anionic Polystyrene GPC Spectrum.jpg
GPC Separation of Anionically Synthesized Polystyrene; Mn=3,000 g/mol, Đ=1.32
GPC Separation of Free-Radical Synthesized Polystyrene; Mn=24,000 g/mol, D=4.96 Free Radical Polystyrene GPC.jpg
GPC Separation of Free-Radical Synthesized Polystyrene; Mn=24,000 g/mol, Đ=4.96
Standardization (calibration) of a size-exclusion column Size exclusion standardisation.png
Standardization (calibration) of a size-exclusion column

Benoit and co-workers [16] proposed that the hydrodynamic volume, Vη, which is proportional to the product of [η] and M, where [η] is the intrinsic viscosity of the polymer in the SEC eluent, may be used as the universal calibration parameter. If the Mark–Houwink–Sakurada constants K and α are known (see Mark–Houwink equation), a plot of log [η]M versus elution volume (or elution time) for a particular solvent, column and instrument provides a universal calibration curve which can be used for any polymer in that solvent. By determining the retention volumes (or times) of monodisperse polymer standards (e.g. solutions of monodispersed polystyrene in THF), a calibration curve can be obtained by plotting the logarithm of the molecular weight versus the retention time or volume. Once the calibration curve is obtained, the gel permeation chromatogram of any other polymer can be obtained in the same solvent and the molecular weights (usually Mn and Mw) and the complete molecular weight distribution for the polymer can be determined. A typical calibration curve is shown to the right and the molecular weight from an unknown sample can be obtained from the calibration curve.

Advantages

As a separation technique, GPC has many advantages. First of all, it has a well-defined separation time due to the fact that there is a final elution volume for all unretained analytes. Additionally, GPC can provide narrow bands, although this aspect of GPC is more difficult for polymer samples that have broad ranges of molecular weights present. Finally, since the analytes do not interact chemically or physically with the column, there is a lower chance for analyte loss to occur. [5] For investigating the properties of polymer samples in particular, GPC can be very advantageous. GPC provides a more convenient method of determining the molecular weights of polymers. In fact most samples can be thoroughly analyzed in an hour or less. [17] Other methods used in the past were fractional extraction and fractional precipitation. As these processes were quite labor-intensive molecular weights and mass distributions typically were not analyzed. [18] Therefore, GPC has allowed for the quick and relatively easy estimation of molecular weights and distribution for polymer samples

Disadvantages

There are disadvantages to GPC, however. First, there is a limited number of peaks that can be resolved within the short time scale of the GPC run. Also, as a technique GPC requires around at least a 10% difference in molecular weight for a reasonable resolution of peaks to occur. [5] In regards to polymers, the molecular masses of most of the chains will be too close for the GPC separation to show anything more than broad peaks. Another disadvantage of GPC for polymers is that filtrations must be performed before using the instrument to prevent dust and other particulates from ruining the columns and interfering with the detectors. Although useful for protecting the instrument, there is the possibility of the pre-filtration of the sample removing higher molecular weight sample before it can be loaded on the column. Another possibility to overcome these issues is the separation by field-flow fractionation (FFF).

Orthogonal methods

Field-flow fractionation (FFF) can be considered as an alternative to GPC, especially when particles or high molar mass polymers cause clogging of the column, shear degradation is an issue or agglomeration takes place but cannot be made visible. FFF is separation in an open flow channel without having a static phase involved so no interactions occur. With one field-flow fractionation version, thermal field-flow fractionation, separation of polymers having the same size but different chemical compositions is possible. [19]

Related Research Articles

In chemical analysis, chromatography is a laboratory technique for the separation of a mixture into its components. The mixture is dissolved in a fluid solvent called the mobile phase, which carries it through a system on which a material called the stationary phase is fixed. Because the different constituents of the mixture tend to have different affinities for the stationary phase and are retained for different lengths of time depending on their interactions with its surface sites, the constituents travel at different apparent velocities in the mobile fluid, causing them to separate. The separation is based on the differential partitioning between the mobile and the stationary phases. Subtle differences in a compound's partition coefficient result in differential retention on the stationary phase and thus affect the separation.

<span class="mw-page-title-main">Size-exclusion chromatography</span> Chromatographic method in which dissolved molecules are separated by their size & molecular weight

Size-exclusion chromatography, also known as molecular sieve chromatography, is a chromatographic method in which molecules in solution are separated by their shape, and in some cases size. It is usually applied to large molecules or macromolecular complexes such as proteins and industrial polymers. Typically, when an aqueous solution is used to transport the sample through the column, the technique is known as gel-filtration chromatography, versus the name gel permeation chromatography, which is used when an organic solvent is used as a mobile phase. The chromatography column is packed with fine, porous beads which are commonly composed of dextran, agarose, or polyacrylamide polymers. The pore sizes of these beads are used to estimate the dimensions of macromolecules. SEC is a widely used polymer characterization method because of its ability to provide good molar mass distribution (Mw) results for polymers.

<span class="mw-page-title-main">High-performance liquid chromatography</span> Technique in analytical chemistry

High-performance liquid chromatography (HPLC), formerly referred to as high-pressure liquid chromatography, is a technique in analytical chemistry used to separate, identify, and quantify specific components in mixtures. The mixtures can originate from food, chemicals, pharmaceuticals, biological, environmental and agriculture, etc., which have been dissolved into liquid solutions.

<span class="mw-page-title-main">Gas chromatography</span> Type of chromatography

Gas chromatography (GC) is a common type of chromatography used in analytical chemistry for separating and analyzing compounds that can be vaporized without decomposition. Typical uses of GC include testing the purity of a particular substance, or separating the different components of a mixture. In preparative chromatography, GC can be used to prepare pure compounds from a mixture.

<span class="mw-page-title-main">Column chromatography</span> Method to isolate a compound in a mixture

Column chromatography in chemistry is a chromatography method used to isolate a single chemical compound from a mixture. Chromatography is able to separate substances based on differential absorption of compounds to the adsorbent; compounds move through the column at different rates, allowing them to be separated into fractions. The technique is widely applicable, as many different adsorbents can be used with a wide range of solvents. The technique can be used on scales from micrograms up to kilograms. The main advantage of column chromatography is the relatively low cost and disposability of the stationary phase used in the process. The latter prevents cross-contamination and stationary phase degradation due to recycling. Column chromatography can be done using gravity to move the solvent, or using compressed gas to push the solvent through the column.

<span class="mw-page-title-main">Ion chromatography</span> Separates ions and polar molecules

Ion chromatography is a form of chromatography that separates ions and ionizable polar molecules based on their affinity to the ion exchanger. It works on almost any kind of charged molecule—including small inorganic anions, large proteins, small nucleotides, and amino acids. However, ion chromatography must be done in conditions that are one pH unit away from the isoelectric point of a protein.

In polymer chemistry, the molar mass distribution describes the relationship between the number of moles of each polymer species and the molar mass of that species. In linear polymers, the individual polymer chains rarely have exactly the same degree of polymerization and molar mass, and there is always a distribution around an average value. The molar mass distribution of a polymer may be modified by polymer fractionation.

<span class="mw-page-title-main">Solid-phase extraction</span> Process to separate compounds by properties

Solid-phase extraction (SPE) is a solid-liquid extractive technique, by which compounds that are dissolved or suspended in a liquid mixture are separated, isolated or purified, from other compounds in this mixture, according to their physical and chemical properties. Analytical laboratories use solid phase extraction to concentrate and purify samples for analysis. Solid phase extraction can be used to isolate analytes of interest from a wide variety of matrices, including urine, blood, water, beverages, soil, and animal tissue.

Reversed-phase liquid chromatography (RP-LC) is a mode of liquid chromatography in which non-polar stationary phase and polar mobile phases are used for the separation of organic compounds. The vast majority of separations and analyses using high-performance liquid chromatography (HPLC) in recent years are done using the reversed phase mode. In the reversed phase mode, the sample components are retained in the system the more hydrophobic they are.

<span class="mw-page-title-main">Hydrophilic interaction chromatography</span> Type of chromatography

Hydrophilic interaction chromatography is a variant of normal phase liquid chromatography that partly overlaps with other chromatographic applications such as ion chromatography and reversed phase liquid chromatography. HILIC uses hydrophilic stationary phases with reversed-phase type eluents. The name was suggested by Andrew Alpert in his 1990 paper on the subject. He described the chromatographic mechanism for it as liquid-liquid partition chromatography where analytes elute in order of increasing polarity, a conclusion supported by a review and re-evaluation of published data.

<span class="mw-page-title-main">Elution</span> Extraction of a material by washing with a solvent

In analytical and organic chemistry, elution is the process of extracting one material from another by washing with a solvent: washing of loaded ion-exchange resins to remove captured ions, or eluting proteins or other biopolymers from a gel electrophoresis or chromatography column.

<span class="mw-page-title-main">Mark–Houwink equation</span>

The Mark–Houwink equation, also known as the Mark–Houwink–Sakurada equation or the Kuhn–Mark–Houwink–Sakurada equation or the Landau–Kuhn–Mark–Houwink–Sakurada equation or the Mark-Chrystian equation gives a relation between intrinsic viscosity and molecular weight :

Absolute molar mass is a process used to determine the characteristics of molecules.

<span class="mw-page-title-main">Field flow fractionation</span> Separation technique to characterize the size of colloidal particles

Field-flow fractionation, abbreviated FFF, is a separation technique invented by J. Calvin Giddings. The technique is based on separation of colloidal or high molecular weight substances in liquid solutions, flowing through the separation platform, which does not have a stationary phase. It is similar to liquid chromatography, as it works on dilute solutions or suspensions of the solute, carried by a flowing eluent. Separation is achieved by applying a field or cross-flow, perpendicular to the direction of transport of the sample, which is pumped through a long and narrow laminar channel. The field exerts a force on the sample components, concentrating them towards one of the channel walls, which is called accumulation wall. The force interacts with a property of the sample, thereby the separation occurs, in other words, the components show differing "mobilities" under the force exerted by the crossing field. As an example, for the hydraulic, or cross-flow FFF method, the property driving separation is the translational diffusion coefficient or the hydrodynamic size. For a thermal field, it is the ratio of the thermal and the translational diffusion coefficient.

<span class="mw-page-title-main">Two-dimensional chromatography</span>

Two-dimensional chromatography is a type of chromatographic technique in which the injected sample is separated by passing through two different separation stages. Two different chromatographic columns are connected in sequence, and the effluent from the first system is transferred onto the second column. Typically the second column has a different separation mechanism, so that bands that are poorly resolved from the first column may be completely separated in the second column. Alternately, the two columns might run at different temperatures. During the second stage of separation the rate at which the separation occurs must be faster than the first stage, since there is still only a single detector. The plane surface is amenable to sequential development in two directions using two different solvents.

<span class="mw-page-title-main">Polymer characterization</span>

Polymer characterization is the analytical branch of polymer science.

Multi-Angle light scattering describes a technique for measuring the light scattered by a sample into a plurality of angles. It is used for determining both the absolute molar mass and the average size of molecules in solution, by detecting how they scatter light. A collimated beam from a laser source is most often used, in which case the technique can be referred to as multiangle laser light scattering (MALLS). The insertion of the word laser was intended to reassure those used to making light scattering measurements with conventional light sources, such as Hg-arc lamps that low-angle measurements could now be made.

<span class="mw-page-title-main">Polymer Char</span>

Polymer Char is a company which designs and manufactures instrumentation for polymer analysis.

<span class="mw-page-title-main">Asymmetric flow field flow fractionation</span>

Asymmetrical flow field-flow fractionation (AF4) is most versatile and most widely used sub-technique within the family of field flow fractionation (FFF) methods. AF4 can be used in aqueous and organic solvents and is able to characterize nanoparticles, polymers and proteins. The theory for AF4 was conceived in 1986 and was established in 1987 and first published by Wahlund and Giddings. AF4 is distinct from symmetrical Flow FFF because it contains only one permeable wall so the cross-flow is caused only by the carrier liquid. The cross-flow is induced by the carrier liquid constantly exiting by way of the semi-permeable wall on the bottom of the channel.

Thermoresponsive polymers can be used as stationary phase in liquid chromatography. Here, the polarity of the stationary phase can be varied by temperature changes, altering the power of separation without changing the column or solvent composition. Thermally related benefits of gas chromatography can now be applied to classes of compounds that are restricted to liquid chromatography due to their thermolability. In place of solvent gradient elution, thermoresponsive polymers allow the use of temperature gradients under purely aqueous isocratic conditions. The versatility of the system is controlled not only through changing temperature, but through the addition of modifying moieties that allow for a choice of enhanced hydrophobic interaction, or by introducing the prospect of electrostatic interaction. These developments have already introduced major improvements to the fields of hydrophobic interaction chromatography, size exclusion chromatography, ion exchange chromatography, and affinity chromatography separations as well as pseudo-solid phase extractions.

References

  1. ↑ Striegel, André M., ed. (2009). Modern size-exclusion liquid chromatography: practice of gel permeation and gel filtration chromatography (2nd ed.). Hoboken, N.J: Wiley. ISBN   978-0-471-20172-4.
  2. ↑ Lathe, G.H.; Ruthven, C.R.J. The Separation of Substance and '1956', 62, 665–674. PMID   13249976
  3. ↑ Moore, J. C. (1964). "Gel permeation chromatography. I. A new method for molecular weight distribution of high polymers". Journal of Polymer Science Part A: General Papers. 2 (2): 835–843. doi:10.1002/pol.1964.100020220.
  4. ↑ Ettre, Leslie S. (2005). "Jim Waters: The Development of GPC and the First Commercial HPLC Instruments" (PDF). LCGC North America. 23 (8): 752–761.
  5. 1 2 3 4 Skoog, D.A. Principles of Instrumental Analysis, 6th ed.; Thompson Brooks/Cole: Belmont, California, 2006, Chapter 28.
  6. 1 2 Sandler, S.R.; Karo, W.; Bonesteel, J.; Pearce, E.M. Polymer Synthesis and Characterization: A Laboratory Manual; Academic Press: San Diego, 1998.
  7. ↑ Agilent Technologies. "AGILENT ORGANIC GPC/SEC COLUMNS" (PDF). Retrieved 2019-12-06.
  8. ↑ Waters Corporation. "STYRAGEL COLUMN CARE AND USE MANUAL" (PDF). Retrieved 2019-12-06.
  9. ↑ GE Healthcare. "Sephadex LH-20" . Retrieved 2019-12-06.
  10. ↑ TOSOH BIOSCIENCE. "TOYOPEARL HW-40" . Retrieved 2019-12-06.
  11. ↑ Helmut, D. Gel Chromatography, Gel Filtration, Gel Permeation, Molecular Sieves: A Laboratory Handbook; Springer-Verlag, 1969.
  12. ↑ Rudin, Alfred; Wagner, R. A. (1976). "Solvent and concentration dependence of hydrodynamic volumes and GPC elution volumes". Journal of Applied Polymer Science. 20 (6): 1483–1490. doi:10.1002/app.1976.070200607.
  13. ↑ Bly, D. D.; Stoklosa, H. J.; Kirkland, J. J.; Yau, W. W. (1975-09-01). "Errors caused by flowrate variation in high performance size exclusion chromatography (GPC) [gel permeation chromatography]". Analytical Chemistry. 47 (11): 1810–1813. doi:10.1021/ac60361a009. ISSN   0003-2700.
  14. 1 2 Trathnigg, B. Determination of MWD and Chemical Composition of Polymers by Chromatographic Techniques. Prog. Polym. Sci.1995, 20, 615-650. doi : 10.1016/0079-6700(95)00005-Z
  15. ↑ Pasch, H. Hyphenated Techniques in Liquid Chromatography of Polymers. Adv. Polym. Sci.2000, 150, 1-66. doi : 10.1007/3-540-48764-6
  16. ↑ Grubisic, Z.; Rempp, P.; Benoit, H. (1967). "A universal calibration for gel permeation chromatography". Journal of Polymer Science Part B: Polymer Letters. 5 (9): 753–759. Bibcode:1967JPoSL...5..753G. doi:10.1002/pol.1967.110050903.
  17. ↑ Cowie, J.M.G.; Arrighi, V. Polymers: Chemistry and Physics of Modern Materials, 3rd ed. CRC Press, 2008.
  18. ↑ Odian G. Principles of Polymerization, 3rd ed.; Wiley Interscience Publication, 1991.
  19. ↑ Thermal Field-Flow Fractionation: Ultra-Broad Polymer Separation | http://www.chemeurope.com/en/products/77045/thermal-field-flow-fractionation-ultra-broad-polymer-separation.html Archived 2013-10-19 at the Wayback Machine
This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.