Polarization transfer methods for quantitative analysis of flowing mixtures with benchtop 13C NMR spectroscopy

被引:2
|
作者
Phuong, Johnnie [1 ,2 ]
Romero, Zeno [1 ,2 ]
Hasse, Hans [1 ,2 ]
Muennemann, Kerstin [1 ,2 ]
机构
[1] RPTU Kaiserslautern, Lab Engn Thermodynam LTD, Erwin Schrodinger Str 44, D-67663 Kaiserslautern, Germany
[2] RPTU Kaiserslautern, Lab Adv Spin Engn Magnet Resonance LASE MR, Kaiserslautern, Germany
关键词
H-1; C-13; benchtop NMR; flow NMR; polarization transfer; process monitoring; quantitative analysis; ULTRAFAST 2D NMR; QUANTIFICATION;
D O I
10.1002/mrc.5417
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Benchtop NMR spectroscopy is attractive for process monitoring; however, there are still drawbacks that often hamper its use, namely, the comparatively low spectral resolution in H-1 NMR, as well as the low signal intensities and problems with the premagnetization of flowing samples in C-13 NMR. We show here that all these problems can be overcome by using H-1-C-13 polarization transfer methods. Two ternary test mixtures (one with overlapping peaks in the H-1 NMR spectrum and one with well-separated peaks, which was used as a reference) were studied with a 1 T benchtop NMR spectrometer using the polarization transfer sequence PENDANT (polarization enhancement that is nurtured during attached nucleus testing). The mixtures were analyzed quantitatively in stationary as well as in flow experiments by PENDANT enhanced C-13 NMR experiments, and the results were compared with those from the gravimetric sample preparation and from standard H-1 and C-13 NMR spectroscopy. Furthermore, as a proxy for a process monitoring application, continuous dilution experiments were carried out, and the composition of the mixture was monitored in a flow setup by C-13 NMR benchtop spectroscopy with PENDANT. The results demonstrate the high potential of polarization transfer methods for applications in quantitative process analysis with benchtop NMR instruments, in particular with flowing samples.
引用
收藏
页码:398 / 411
页数:14
相关论文
共 50 条
  • [31] Development of quantitative 13C NMR characterization and simulation of C, H, and O content for pyrolysis oils based on 13C NMR analysis
    Wang, Rui
    Luo, Ying
    Jia, Hang
    Ferrell, Jack R., III
    Ben, Haoxi
    RSC ADVANCES, 2020, 10 (43) : 25918 - 25928
  • [32] Novel methods of automated structure elucidation based on 13C NMR spectroscopy
    Meiler, J
    Köck, M
    MAGNETIC RESONANCE IN CHEMISTRY, 2004, 42 (12) : 1042 - 1045
  • [33] Hyperpolarised 1H-13C Benchtop NMR Spectroscopy
    Robinson, Alastair D.
    Richardson, Peter M.
    Halse, Meghan E.
    APPLIED SCIENCES-BASEL, 2019, 9 (06):
  • [34] QUALITATIVE AND QUANTITATIVE-ANALYSIS OF MONOTERPENOID PRODUCT MIXTURES BY C-13 NMR-SPECTROSCOPY
    WEBER, L
    HAUFE, G
    JOURNAL FUR PRAKTISCHE CHEMIE, 1988, 330 (02): : 319 - 322
  • [35] Constitution of konjac glucomannan:: chemical analysis and 13C NMR spectroscopy
    Katsuraya, K
    Okuyama, K
    Hatanaka, K
    Oshima, R
    Sato, T
    Matsuzaki, K
    CARBOHYDRATE POLYMERS, 2003, 53 (02) : 183 - 189
  • [36] Analysis of conjugated linoleic acid isomers by 13C NMR spectroscopy
    Davis, AL
    McNeill, GP
    Caswell, DC
    CHEMISTRY AND PHYSICS OF LIPIDS, 1999, 97 (02) : 155 - 165
  • [37] Expanding capability of 13C NMR spectroscopy in comprehensive lignin analysis
    Balakshin, Mikhail
    Capanema, Ewellyn
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2018, 255
  • [38] Quantitative 13C NMR spectroscopy. Chemical structure of kraft and nitrosated lignins
    L. V. Kanitskaya
    A. F. Gogotov
    Dam Thi Thanh Khai
    A. V. Rokhin
    Russian Journal of Bioorganic Chemistry, 2012, 38 : 720 - 725
  • [39] 13C NMR Spectroscopy for the Quantitative Determination of Compound Ratios and Polymer End Groups
    Otte, Douglas A. L.
    Borchmann, Dorothee E.
    Lin, Chin
    Weck, Marcus
    Woerpel, K. A.
    ORGANIC LETTERS, 2014, 16 (06) : 1566 - 1569
  • [40] Quantitative 13C NMR spectroscopy. Chemical structure of kraft and nitrosated lignins
    Kanitskaya, L. V.
    Gogotov, A. F.
    Khai, Dam Thi Thanh
    Rokhin, A. V.
    RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY, 2012, 38 (07) : 720 - 725