Handbook of Size Exclusion Chromatography and Related ...

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Table 6 SEC Conditions for Characterization of CTC Using THF as Mobile Phase Except for Where LiCl/DMAc Was Used Packing material Exclusion limits of each column (A ˚ ) a Temperature (8C) Detector(s) and wavelength (nm) Flow rate (mL/min) Reference TSK-Gel HXL — UV (245) — 128 G7000 4 10 8 G6000 4 10 7 G5000 4 10 6 Shodex — UV (235) 1.0 119 KF-806 20 10 6 KF-805 4 10 6 KF-804 4 10 5 Shodex — UV (235) 1.0 130,131 KF805 4 10 6 KF803 7 10 4 mStyragel 100 Shodex — UV (236) 1.0 120 KF-806 20 10 6 KF-805 4 10 6 KF-804 or 4 10 5 PL gel 10 6 ,10 6 ,10 3 Ultrastyragel 10 6 , linear, 10 5 , 10 35 UV (278) 1.0 136 4 PL gel 10 6 ,10 5 25 UV (225) 1.0 137 Phenogel PHOOH Ambient DRI 1.0 125 0447KO 10 6 0446KO 10 5 0445KO 10 4 Waters Ambient DRI and UV (236) — 129,138 Ultrastyragel 10 6 ,10 5 ,10 4 ,10 3 Shodex — — — 139 KF807 2 10 8 KF805 4 10 6 KF803 7 10 4 Waters mStyragel 100 A˚ LiChrogel 25 LALLS (633)/ 0.5 121 b PS40000 PS4 — DRI Waters 20 UV (235) 1.0 132 Ultrastyragel 10 4 ,10 3 Shodex Ambient UV (254)/ 0.6 117 KF-serie 10 6 ,10 5 ,10 5 MALLS (690) © 2004 by Marcel Dekker, Inc.
Table 6 (Continued) Packing material Exclusion limits of each column (A ˚ ) a Temperature (8C) Detector(s) and wavelength (nm) Flow rate (mL/min) Reference Waters — RI/ 0.735 122 HT6 2 10 5 to 10 6 MALLS (488) HT5 5 10 3 to 6 10 5 HT4 5 10 2 to 3 10 4 PL gel 80 UV (295)/DRI 1.0 134 c 4 mixed A 40 10 6 a A ˚ ¼ 10 2 10 m, generally defined as the exclusion limit of polystyrene dissolved in THF. b CTCs having different DS of substituents on the phenyl group. c Phenyl, ethyl, and propyl carbanilate, LiCl/DMAc as mobile phase. Unbleached wood pulp samples need to be (chlorite) delignified prior to derivatization (115,116), but for cellulose fibers having a lignin content below approximately 2.5%, delignification is not necessary (117). The general procedure for derivatization of cellulose includes several steps: (a) activation, (b) reaction of cellulose with phenyl isocyanate (OCNC 6H 5), (c) addition of methanol to react with the excess reagent, (d) precipitation in a nonsolvent, (e) repeated washing of the precipitated derivative, (f) freeze-drying, and (g) dissolution in THF. The long preparation time and the risk of losing low molecular mass constituents of the sample in the precipitation step are some disadvantages of this procedure. Activation to open up the structure of the sample prior to derivatization has been pointed out as necessary for some sample types such as regenerated cellulose samples and high molecular mass cellulose samples. The activation has been carried out in water (116,118), liquid ammonia:pyridine (119,120), ammonia (121), pyridine (122), ammonia:DMSO (119), DMSO (123), DMSO:pyridine (124), and LiCl/DMAc (125). The heterogeneous carbanilation reaction is commonly performed in dimethylsulfoxide (DMSO) or pyridine. Since the reaction proceeds faster in DMSO (120), the reaction temperature is kept lower than when pyridine is used, typically 708C for DMSO and 808C for pyridine. It has however been reported that DMSO degrades high molecular mass samples when the reaction time is longer than 32 hours, although a CTC prepared from the same source, that is, bleached cotton linters, did not suffer appreciable loss of the molecular mass (M) after treatment in phenylisocyanate in DMSO at 708C for 72 hours (120). Using an online MALLS detector during the chromatography, LaPierre and Bouchard (117,126) found that the DP of CTCs prepared from softwood kraft pulps was © 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-
Page 289 and 290: Figure 2 TDS chromatograms for full
Page 291 and 292: Figure 5 Comparison of molecular we
Page 293 and 294: Table 3 Summary of TDS Molecular We
Page 295 and 296: thepartiallyhydrolyzedPVAwiththecol
Page 297 and 298: Table 5 Summary of Conformation and
Page 299 and 300: a¼0.627andlog(K) ¼23.249.Theseare
Page 301 and 302: The limits of detection of the PVA
Page 303 and 304: Figure 12 PVAc broad molecular weig
Page 305 and 306: 4 SUMMARY Advances in SEC character
Page 307 and 308: 11 Size Exclusion Chromatography of
Page 309 and 310: 2.1 Molecular Weight Grades of PVP
Page 311 and 312: exclusion chromatography with low-a
Page 313 and 314: weightandmolecularweightdistributio
Page 315 and 316: © 2004 by Marcel Dekker, Inc. Figu
Page 317 and 318: Figure 4 PEOcalibrationofUltrahydro
Page 319 and 320: Figure 6 Overlay of GPC chromatogra
Page 321 and 322: plus Ultrahydrogel 120 A ˚ ,Shodex
Page 323 and 324: Figure 10 SEC traces of PVP/AA copo
Page 325 and 326: Figure 11 Molecular weight distribu
Page 327 and 328: 12 Size Exclusion Chromatography of
Page 329 and 330: 2 CHEMICAL, MACROMOLECULAR AND MORP
Page 331 and 332: Table 2 The Relative Composition of
Page 333 and 334: considered to be 3. After the DS ha
Page 335 and 336: een extensively studied by methods
Page 337 and 338: The silylation was performed in LiC
Page 339: observed using column materials hav
Page 343 and 344: 4.5 Other Cellulose Derivatives Bes
Page 345 and 346: Table 8 SEC Conditions for Characte
Page 347 and 348: dextrans swell too much in cadoxen
Page 349 and 350: stirring at room temperature for an
Page 351 and 352: Figure 2 MMDofunbleached(HP)andblea
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
Page 383 and 384: compoundsandwasexplainedbyadsorptio
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
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liquor is highest throughout the co
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topological anisotropy in the polym
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29. M Ristolainen, R Alen, J Knuuti
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eds. Proc Int Symp 1998. Canton, Pe
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92. L Jurasek. Towards a three dime
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Table 1 Selected Industries Connect
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into C3-metabolites, which then may
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Table 4 Key Enzymes in the Biosynth
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Table 5 Cloned Mutants of Starch En
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Figure 3 Modeled x-ray diffraction
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In the native environment (plant ce
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Figure 6 (a) Large starch granules
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number of branching points); crossl
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Both absolute approaches are extrao
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Table 7 (Continued) Approach Experi
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structures, excluded volumes, and t
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Figure 10 (a) SEC elution profile o
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Figure 12 Wheat glucans: DRI elutio
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Figure 13 Wheat glucans. Normalized
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Figure 16 Wheat glucan. Normalized
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Figure 18 Wheat glucan.Elution prof
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Figure 20 Wheat glucans. Absolute m
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Figure 22 Wheat glucan. (a) Intrins
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Figure 24 Wheat PA-glucan. Elution
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an Ubbelohde-viscometer for concent
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Rheological investigations of stabi
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shifts to applied laser light, whic
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Table 8 Characteristic Parameters f
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Table 8 (Continued) and H2O. A part
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10. SG Ball, MHBJ van de Wal, RGF V
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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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Page 479 and 480:
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
Page 543 and 544:
where Cand Dare constants for apart
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ThisisimportantwhenLCCCisappliedtoc
Page 547 and 548:
Page 549 and 550:
Page 551 and 552:
However, strong adsorption of macro
Page 553 and 554:
elution step may be sufficient for
Page 555 and 556:
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
Page 565 and 566:
(Sec. 7) and therefore they can be
Page 567 and 568:
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
Page 577 and 578:
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
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Table 3 Summary of Column Performan
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Figure 11 Dependence of column perf
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. Two-dimensional chromatography ru
Page 591 and 592:
The standard deviations for the mol
Page 593 and 594:
Figure 15 Comparison of time requir
Page 595 and 596:
Figure 17 Accuracy and precision of
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polymer analysis. Samples are “ru
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just ignoring the fractionation of
Page 601 and 602:
20 Automatic Continuous Mixing Tech
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out at low enough concentration tha
Page 605 and 606:
educed viscosity, h r, to be comput
Page 607 and 608:
© 2004 by Marcel Dekker, Inc. Figu
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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
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Finally, the use of a light-scatter
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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
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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
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5 THE IMPORTANCE OF SOFTWARE Like a
Page 645 and 646:
standard deviations of the measured
Page 647 and 648:
These include the differential weig
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Figure 8 Data of Fig. 7corrected fo
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Figure 11 Data of Fig. 10 with spik
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Figure 13 Fitstodatacollectedatasli
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Table 1 Errors (in %) Characteristi
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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
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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
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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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