Application of nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy, UV–Visible spectroscopy and kinetic modeling for elucidation of adsorption chemistry in uptake of tetracycline by zeolite beta

2011 ◽  
Vol 354 (1) ◽  
pp. 261-267 ◽  
Author(s):  
Jin Kang ◽  
Huijuan Liu ◽  
Yu-Ming Zheng ◽  
Jiuhui Qu ◽  
J. Paul Chen
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Magnetic Resonance ◽  
Magnetic Resonance Spectroscopy ◽  
Kinetic Modeling ◽  
Zeolite Beta ◽  
Resonance Spectroscopy ◽  
Visible Spectroscopy ◽  
Uv Visible

Synthesis and biocidal activity of novel N-halamine hydantoin-containing polystyrenes

e-Polymers ◽  
2014 ◽  
Vol 14 (1) ◽  
pp. 15-25 ◽  
Author(s):  
Marta Chylińska ◽  
Marta Ziegler-Borowska ◽  
Halina Kaczmarek ◽  
Aleksandra Burkowska ◽  
Maciej Walczak ◽  
...  
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Magnetic Resonance ◽  
Magnetic Resonance Spectroscopy ◽  
Chemical Modification ◽  
Chemical Structure ◽  
Resonance Spectroscopy ◽  
Biocidal Activity ◽  
Biocidal Properties

AbstractThree homopolymers containing hydantoin substituents were obtained by chemical modification of reactive p-chloromethylated polystyrene. The prepared polymers were chlorinated to yield N-halamine materials with biocidal properties. The chemical structure of polymers was characterized by Fourier transform infrared spectroscopy and nuclear magnetic resonance spectroscopy. All of the hydantoin polymers are insoluble in water and common organic solvents. Microbiological investigations prove the high biocidal activity of the obtained chlorinated polystyrene derivatives containing spirohydantoin moieties. The obtained polymers will be useful in designing and constructing medical and pharmaceutical equipment. The ability to crosslink allows to expect easy grafting of these biocidal macrochains, for example, on textiles.

Study of Configurational Sequence Structures of Poly(Butadiene)s by Carbon-13 Proton Decoupled Fourier Transform Nuclear Magnetic Resonance Spectroscopy

1973 ◽  
Vol 46 (2) ◽  
pp. 350-358 ◽  
Author(s):  
Yasuhide Alaki ◽  
Toshio Yoshimoto ◽  
Mamoru Imanari ◽  
Makoto Takeuchi
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Fourier Transform ◽  
Magnetic Resonance ◽  
Magnetic Resonance Spectroscopy ◽  
Polymer Chains ◽  
Proton Nuclear Magnetic Resonance ◽  
Resonance Spectroscopy ◽  
Sequence Structure ◽  
Nmr Method ◽  
Nuclear Magnetic

Abstract Carbon-13 proton nuclear magnetic resonance (NMR) of poly(butadiene) s consisting of various ratios of cis-1,4-, trans-1,4- and 1,2-structures were measured by the pulsed Fourier transform NMR method. The spectra of poly(butadiene)s with two or three kinds of butadiene configurations show several new signals which were not observed for homopolymers comprising merely one kind of butadiene configuration. All of these peaks are ascribed to the carbons linked by different kinds of configurations. From these results, the configurational sequence structure of butadiene units in polymer chains has been revealed.

scholarly journals Identification of Ambergris from the New Bedford Whaling Museum by Nuclear Magnetic Resonance Spectroscopy

1996 ◽  
Vol 79 (2) ◽  
pp. 423-425 ◽  
Author(s):  
George A Moniz ◽  
Gerald B Hammond
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Fourier Transform ◽  
Magnetic Resonance ◽  
Magnetic Resonance Spectroscopy ◽  
Nuclear Magnetic Resonance Spectroscopy ◽  
Adsorption Chromatography ◽  
New Method ◽  
Major Constituent ◽  
Resonance Spectroscopy ◽  
Nuclear Magnetic

Abstract A new method for the separation and identification of ambrein in ambergris using adsorption chromatography and 1H and 13C Fourier transform nuclear magnetic resonance spectroscopy (FT-NMR) is presented. We demonstrated the effectiveness of this method by analyzing an approximately 85-year-old sample of suspected ambergris from the New Bedford Whaling Museum (New Bedford, MA). Results prove that ambrein remains a major constituent of ambergris even after 85 years of storage under ordinary conditions.

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