Handbook of Size Exclusion Chromatography and Related ...

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Table 3 Annually Assimilated Biomass with Details on Carbohydrate/Polysaccharide Fraction Biomass Starch or starch-equivalent glucans are produced by green plants, sea organisms, microbes, insects, and all kinds of mammals. The annually assimilated mass of biomaterials is in the range 100–400 10 9 tonnes (Gt) of dry matter (Table 3). Approximately three-quarters of this biomass is formed of polysaccharides, the major fraction of which consists of glucans, polymers made of glucose as basic building blocks. Cellulose and starch represent the most prominent glucan materials. The mass of annually assimilated starch is in the same range as that of annually produced petroleum. However, the amount of industrially utilized/ manufactured starch is approximately one-fifth of the share of petroleum used to produce synthetic polymers only. 2 BIOLOGICAL BACKGROUND: (BIO-)SYNTHESIS AND COMPOSITION OF STARCH Dry matter annually, 10 9 tonnes (Gt) Lignin 20–80 20% Lipids 2–8 2% Proteins 2–8 2% Others 2–8 1% Carbohydrates/polysaccharides 75–300 75% Nonbranched b(1!4) linked glucan cellulose 50–200 45% of 75% Hemicellulose 20–100 20–25% of 75% Others: mannan, xylan, glactan, fructan, etc. a(1!4) linked þ a(1!6) branched glucan starch 1–5 2–5% of 75% Industrial utilized starch glucan 0.02 Annual yield of petroleum 2 Synthetic polymers based on petroleum 0.1–0.2 5–10% Most starch is produced by aboveground organs of green plants, in particular by their leaves, which transform CO 2,H 2O, and electromagnetic radiation (680 nm) © 2004 by Marcel Dekker, Inc.
into C3-metabolites, which then may be merged to form transient carbohydrates. The synthesis of starch from such metabolites involves interconversion of sugars, sugar-phosphates, and nucleotide-sugars (3–9). The substrate for one of the key metabolites of starch synthesis, adenosinediphosphate-glucose (ADP-glucose, Fig. 1a), glucose-1-phosphate is formed either by hydrolysis from UDP-glucose (E.2.7.7.9) or by isomerization from glucose-6-phosphate (E.5.4.2.2). ADP-glucose pyrophosphorylase (E.2.7.7.27) is the major controlling enzyme for the rate of starch synthesis and the amount of amylose-type glucans in starch granules (10). Nonbranched (nb)/long-chain branched (lcb) starch glucans (amylose) and short-chain branched (scb) starch glucans (amylopectin) are synthesized in the amyloplast from ADP-glucose, primarily by the catalytic action of starch synthases [E.2.4.1.21; granular bound starch synthase (GBSSx) or soluble forms of starch synthase (SSx) and branching enzymes (BEx)]. Additionally,enzymes such as debranching enzymes and disproportionating enzymes are involved (Table 4). Elongation of glucans by subsequential coupling of ADP-glucose to a Glc n-chain, probably starting with a maltodextrosyl-protein as primer, via a(1 !4)-glycosidic linkages, results in nonbranched (nb) glucans with high symmetry(helix)andcomplexingpotentialforhydrophobicandanionicmaterials within the helix. Catalytic action of branching enzymes (BE) introduces a(1 !6)-glycosidic linkages and results in long-chain branched (lcb) and more or less short-chain branched (scb) starch glucans (Fig. 2b). Branches act as symmetry breakers when compared to nonbranched compounds: hydrophilic and hydrophobic domains become less pronounced with increasing scb-characteristics. In general, branches increase molecular packing density(masswithinoccupiedvolume)andenforceintramolecularstabilization(11). Intheinitialstateamixofnb-,lcb-,andscb-glucansformlooseamorphous clusters, which are soluble in aqueous media. By subsequent action of disproportionating enzyme, these clusters are rearranged by increasing packing densityandorder(amorphous !crystallinity)andareprecipitatedingranulesfor temporary storage. Simultaneously, debranching enzymes provide nb-glucans, which are elongated by granular bound starch synthase (GBSS), yielding amylose-type starch glucans.The amountofnb-starch glucansof course depends ontheGBSSconcentration located in the amyloplast-matrix and local temperature (12–14). Although the formation of nb-glucans (amylose) by debranching of lcb- and scbglucansisgenerallyaccepted,itshouldbenotedthatthesenb-glucansarefoundin storage starch granules only and not in the transient cluster structures of leaves (15,16). Manyof thekeyenzymes of starch biosynthesis havebeen cloned (Table5) from plant species, in particular from maize endosperm, rice endosperm, barley © 2004 by Marcel Dekker, Inc.
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MARCEL DEKKER Handbook of Size Excl
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CHROMATOGRAPHIC SCIENCE SERIES A Se
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60. Modern Chromatographic Analysis
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Preface to the Second Edition Gel p
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Preface to the First Edition Molecu
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Contents Preface to the Second Edit
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17. Size Exclusion Chromatography o
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James F. Curry Analytical Departmen
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Iwao Teraoka, Ph.D. Othmer Departme
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The graphical data display typicall
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polymer molecule can elute. The tot
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individual states) allowed to them.
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unsaturation while the IR detector
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Sampleconcentrationshouldbeminimize
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averagesdefinedintermsofthemolecula
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information regarding appropriate M
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Analytical. Two models, the KMX-6 a
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Figure 6 Overlay of time-sliced pea
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accurately for very large and very
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4 GENERAL REFERENCES The interested
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46. TA Chamberlin, HE Tuinstra. US
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materials are commercially availabl
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Table 1 Commercial Column Packing M
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necessarily comparable. For this re
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adjusted such that the pore size di
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narrowmolecular weight range, indiv
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Figure 8 Effect of particle size on
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Figure 9 SEC calibration using poly
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Table 4 Typical Eluent Systems for
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Figure 12 Analysis of poly-2-vinyl
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24. E Meehan, S O’Donohue. The ro
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into accepted laboratory techniques
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Table 1 Trace Metal Impurities in C
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mass and biological activity, for m
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Experimental efficiency vs. velocit
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Table 3 Properties of SEC Silica Ge
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operate at aflow rate that can easi
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Figure 3 Efficiency of amide-bonded
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mechanically stable packing materia
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Figure 5 Pore size distributions of
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Figure 6 Separation of polystyrenes
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60-120 A ˚ are large enough to be
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Table 6 Selected Silica-Based Colum
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Table 7 Separation Ranges for Polym
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the decline in permeability is perm
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sample components can be varied by
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Figure 10 Diol bonding reactions. I
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ecause of the higher relative molec
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valuesfork1,k2,anda,theunknownmolec
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water-soluble and detergent-soluble
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the importance of secondary retenti
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discussed in Table 8(33). Based on
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individual dispersion processes ins
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The detector time constant can dist
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5.3 Mobile Phase A mobile phase is
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less steep and still linear at high
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35. P Bristow, J Knox. Chromatograp
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112. K Gooding, K Lu, G Vanecek, F
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for branched polymers or copolymers
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Figure 1 “Bridge design” flow-r
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Figure 3 A light-scattering photome
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Figure 5 SEC universal calibration
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where hn is the hydrodynamic volume
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It should be noted that dn=dc also
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sensitivity for many samples compar
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that is, log[h] vs. logM,generated
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Figure 8 Effect of band broadening
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Table 1 Measurement of Molecular We
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Figure 10 Differential refractomete
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Figure 11 (A) Mark-Houwink plot of
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Table 3 Measurement of Molecular We
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size information is derived from un
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Table 5 Molecular Weight Distributi
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By measuring the scattered intensit
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8 APPENDIX: INSTRUMENT COMPANIES 8.
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53. G Marot, J Lesec. J Liq Chromat
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125. D Slootmaekers, JAPP Van Dijk,
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200. JG Bindels, GJJ Bessems, BM De
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possibly with hydrodynamic volume (
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An insurmountable limitation of SEC
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to sDR(V) when either nPS ¼nPB ¼c
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1,4-trans;and8%1,2-vynil.TheglobalC
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The goal is to find the MWD and CCD
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As expected, pS is closer to the no
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Figure 3 Example 3: MWD and BD of a
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9. BH Zimm, WH Stockmayer. The dime
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45. RO Bielsa, GR Meira. Linear cop
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solubility properties. They are use
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determination of the absolute molec
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Figure 4 Result of the PBT analysis
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Figure 8 Result of natural spider s
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7 Size Exclusion Chromatography of
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As pointed out earlier, rubber must
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Table 2 Various Solvents and Operat
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Figure 2 Typical GPC calibrations w
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© 2004 by Marcel Dekker, Inc. Figu
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Natural and Synthetic Rubbe177 vari
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Another example, shown in Fig. 5 (3
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APPENDIX: SEC CONDITIONS FOR RUBBER
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Appendix (Continued) Polymer Column
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5. J West, E Rodriguez. Rubber Chem
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associate. Girdler (67) and Speight
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Table 1 Fractions Obtained Using Co
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Figure 1 SEC analyses of an aged as
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Apparently more polar compounds are
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40% was fractionated into four frac
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Figure 7 SEC analyses of an unaged
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Figure 9 Comparison of percentage L
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Figure 11 Comparison of SEC chromat
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Figure 12 Comparisons of SEC chroma
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percentage LMS at the other locatio
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the total area into up to 12 sectio
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attempted to develop an SEC method
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parameterisbasedontheinternalpressu
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5 MODIFIED ASPHALTS The addition of
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Oxidation of the rubber and asphalt
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Figure 20 SEC chromatogram for an a
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Figure 21 Comparisons of apparent m
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© 2004 by Marcel Dekker, Inc. S/
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PS/10 4 þ 10 3 þ 500 þ 100 THF/1
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Nevertheless, SEC of asphalts is es
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56. NW Garrick, RR Biskur. Trans Re
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Asphalts 235 122. M-S Lin, JM Chaff
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Table 1 Applications of Acrylamide
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(AM/AA), and acrylamide/dimethyldia
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polymer, a large size filter of 5,
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Figure 1 Size exclusion chromatogra
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Table3 MWandMWDofaBroad-MWDPAMStand
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Another commercially available MW d
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Table 5 Weight-Average Molecular We
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Figure 6 (a) Size exclusion chromat
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compared to anormal product. By com
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StudyingtheKineticsofaChemicalReact
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this information, the higher MW pea
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46. CJ Kim, A Hamielec, A Bendek. J
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A relatively new technique utilizin
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where ais the exponent of the Mark-
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Figure 2 TDS chromatograms for full
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Figure 5 Comparison of molecular we
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Table 3 Summary of TDS Molecular We
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thepartiallyhydrolyzedPVAwiththecol
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Table 5 Summary of Conformation and
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a¼0.627andlog(K) ¼23.249.Theseare
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The limits of detection of the PVA
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Figure 12 PVAc broad molecular weig
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4 SUMMARY Advances in SEC character
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2.1 Molecular Weight Grades of PVP
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exclusion chromatography with low-a
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weightandmolecularweightdistributio
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Figure 4 PEOcalibrationofUltrahydro
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Figure 6 Overlay of GPC chromatogra
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plus Ultrahydrogel 120 A ˚ ,Shodex
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Figure 10 SEC traces of PVP/AA copo
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Figure 11 Molecular weight distribu
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2 CHEMICAL, MACROMOLECULAR AND MORP
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Table 2 The Relative Composition of
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considered to be 3. After the DS ha
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een extensively studied by methods
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The silylation was performed in LiC
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observed using column materials hav
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Table 6 (Continued) Packing materia
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4.5 Other Cellulose Derivatives Bes
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Table 8 SEC Conditions for Characte
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dextrans swell too much in cadoxen
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stirring at room temperature for an
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Page 353 and 354: Figure 4 MMDofbirchkraftpulpdegrade
Page 355 and 356: adequate when evaluating the influe
Page 357 and 358: differential refractive index (DRI)
Page 359 and 360: 30. HA Krässig. Effects of structu
Page 361 and 362: 67. E Sjöholm, K Gustafsson, A Col
Page 363 and 364: 104. B Fleury, J Dubois, C Léonard
Page 365 and 366: 136. D Miller, D Senior, R Sutcliff
Page 367 and 368: 166. SS Cutié, CG Smith. Determina
Page 369 and 370: 200. R Berggren, F Berthold, E Sjö
Page 371 and 372: 13 Molar Mass and Size Distribution
Page 373 and 374: measurements, and vapor pressure os
Page 375 and 376: The calibration of SEC columns by c
Page 377 and 378: The division according to eluent ty
Page 379 and 380: Apolymer produced by UV irradiation
Page 381 and 382: Because DMAC/LiCl is also agood sol
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Page 385 and 386: isolated lignins because they are e
Page 387 and 388: The Separon HEMA and Separon HEMA B
Page 389 and 390: Figure 4 GPC elution curves of the
Page 391 and 392: liquor is highest throughout the co
Page 393 and 394: topological anisotropy in the polym
Page 395 and 396: 29. M Ristolainen, R Alen, J Knuuti
Page 397 and 398: eds. Proc Int Symp 1998. Canton, Pe
Page 399 and 400: 92. L Jurasek. Towards a three dime
Page 401: Table 1 Selected Industries Connect
Page 405 and 406: Table 4 Key Enzymes in the Biosynth
Page 407 and 408: Table 5 Cloned Mutants of Starch En
Page 409 and 410: Figure 3 Modeled x-ray diffraction
Page 411 and 412: In the native environment (plant ce
Page 413 and 414: Figure 6 (a) Large starch granules
Page 415 and 416: number of branching points); crossl
Page 417 and 418: Both absolute approaches are extrao
Page 419 and 420: Table 7 (Continued) Approach Experi
Page 421 and 422: structures, excluded volumes, and t
Page 423 and 424: Figure 10 (a) SEC elution profile o
Page 425 and 426: Figure 12 Wheat glucans: DRI elutio
Page 427 and 428: Figure 13 Wheat glucans. Normalized
Page 429 and 430: Figure 16 Wheat glucan. Normalized
Page 431 and 432: Figure 18 Wheat glucan.Elution prof
Page 433 and 434: Figure 20 Wheat glucans. Absolute m
Page 435 and 436: Figure 22 Wheat glucan. (a) Intrins
Page 437 and 438: Figure 24 Wheat PA-glucan. Elution
Page 439 and 440: an Ubbelohde-viscometer for concent
Page 441 and 442: Rheological investigations of stabi
Page 443 and 444: shifts to applied laser light, whic
Page 445 and 446: Table 8 Characteristic Parameters f
Page 447 and 448: Table 8 (Continued) and H2O. A part
Page 449 and 450: 10. SG Ball, MHBJ van de Wal, RGF V
Page 451 and 452: 52. W Praznik, R Beck. J Chromatogr
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3 PROTEIN PARTITIONING IN SEC 3.1 G
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Figure 1 Plot of Kav vs. log M for
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yconsideringtheproteinsolutestobesp
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globular proteins and selected flex
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silanol groups (52-54); even capped
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most proteins to be maximally stabl
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Figure 4 Chromatograms of BSA and P
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concentrated) steps of protein puri
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Table 3 Characteristics of Dextran-
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preparative SEC. The capabilities o
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37. GR Noll, N Nagle, JO Baker, DJ
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Figure 2 Separation of total E. col
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Figure 3 Separation of HaeIII-cleav
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The recovery of DNA fragments has b
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Endotoxin should also be removed fr
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Table 3 Best Columns for the Separa
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Figure 10 Dependence of HETP on flo
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Appendix (Continued ) Polymer Colum
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REFERENCES 1. CT Wehr, SR Abbott. J
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MALDI-MS has been applied to determ
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Figure 1 Calibration curvesof SEC c
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Figure 3 Chromatograms of epoxy res
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wherenandn0 aretheRIsofthesample an
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Figure 5 SEC chromatogram of n-alka
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Figure 7 Refractive indexes of comm
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Another detector recently applied i
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Figure 11 Absolute MW calibration p
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Figure 12 Chromatogram of Acrawax C
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18 Two-Dimensional Liquid Chromatog
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largerispressuredropandresultingexp
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elations between molar masses and s
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Figure 2 (Continued) chapter, one o
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where Nis the column efficiency exp
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composition/architecture/molar mass
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solvent. Here again, solvent-solven
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or repulsive interactions between m
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macromolecules may strongly differ
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temperature. The efficacy of an ads
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however, aliphatic bonded groups ma
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Figure 10 Schematic representation
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packing materials for SEC of synthe
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Quantitative relations between sila
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Both strength and thermodynamic qua
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where Cand Dare constants for apart
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ThisisimportantwhenLCCCisappliedtoc
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Page 549 and 550:
Page 551 and 552:
However, strong adsorption of macro
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elution step may be sufficient for
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Figure 16 Block scheme of a full ad
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processing of 2D-HPLC data. Knowled
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Figure 20 Set of full retention-elu
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distributions of complex polymers a
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constituents were not discriminated
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(Sec. 7) and therefore they can be
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2. Identify sample solvents. First
Page 569 and 570:
1 Segmental interaction energy para
Page 571 and 572:
58. BG Belenkii. Pure Appl Chem 51:
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19 Methods and Columns for High-Spe
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Table 1 Summary of Methods for Incr
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not savealot of time and solvent, d
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Figure 3 Conventional SEC chromatog
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chromatogram at 4mL/min, which is f
Page 583 and 584:
Sincethereductionoftheinternaldiame
Page 585 and 586:
Table 3 Summary of Column Performan
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Figure 11 Dependence of column perf
Page 589 and 590:
. Two-dimensional chromatography ru
Page 591 and 592:
The standard deviations for the mol
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Figure 15 Comparison of time requir
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Figure 17 Accuracy and precision of
Page 597 and 598:
polymer analysis. Samples are “ru
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just ignoring the fractionation of
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20 Automatic Continuous Mixing Tech
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out at low enough concentration tha
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educed viscosity, h r, to be comput
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Page 609 and 610:
Figure 2 Raw ACOMP signals from mul
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Figure 4 Mw vs. monomer conversion,
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decreases smoothly and monotonicall
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Figure 7 Effects of fluctuating rea
Page 617 and 618:
Finally, the use of a light-scatter
Page 619 and 620:
Figure 8 Linear and cubic increases
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where r(t) is now given by 2 6 r(t)
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Figure 11 Light scattering from sol
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3.1 ASimple System: Equilibrium Cha
Page 627 and 628:
Figure 13 (a) ACM applied to the ch
Page 629 and 630:
Also of note in Fig. 13b is how hig
Page 631 and 632:
15. JM Starita, CL Rohn. Rheologica
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52. M Hulden. Hydrophobically modif
Page 635 and 636:
21 Light Scattering and the Solutio
Page 637 and 638:
therefore, is to remove any lingeri
Page 639 and 640:
is often found in the literature wh
Page 641 and 642:
Figure 2 Configuration of an SEC se
Page 643 and 644:
5 THE IMPORTANCE OF SOFTWARE Like a
Page 645 and 646:
standard deviations of the measured
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These include the differential weig
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Figure 8 Data of Fig. 7corrected fo
Page 651 and 652:
Figure 11 Data of Fig. 10 with spik
Page 653 and 654:
Figure 13 Fitstodatacollectedatasli
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Table 1 Errors (in %) Characteristi
Page 657 and 658:
homogeneous copolymer, that is, tak
Page 659 and 660:
process may be used to identify the
Page 661 and 662:
fractionated sample. They represent
Page 663 and 664:
Figure 16 An example of poor SEC ch
Page 665 and 666:
on) methods, whereby the average di
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23. WH Stockmayer, LD Moore Jr, M F
Page 669 and 670:
condition, as is explained in this
Page 671 and 672:
Figure 2 Partition coefficients KL
Page 673 and 674:
4 COLUMNS FOR HOPC Detailsaregiveni
Page 675 and 676:
and concomitant clogging of columns
Page 677 and 678:
Figure 5 Concentration dependence o
Page 679 and 680:
Table 1 Solution Volume, Polymer Ma
Page 681 and 682:
in Fig. 4a. The middle fractions (8
Page 683 and 684:
Figure 10 SEC chromatograms for som
Page 685 and 686:
appropriate for the early fractions
Page 687 and 688:
23 Size Exclusion/ Hydrodynamic Chr
Page 689 and 690:
Figure 2 Calibration curve for the
Page 691 and 692:
Figure 5 Elutionbehaviorofpolystyre
Page 693 and 694:
Table 1 Comparison Between SEC and
Page 695 and 696:
egular SEC column in which the pore
Page 697:
Such an ideal separation can be obt
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