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H lineshapes observed for the STE sequence recorded with bipolar gradient pulses.

H liquid-state NMR spectra of peat humic acid . Investigating the role of mineral-bound humic acid in phenanthrene sorption. Environ. Sci. Technol. 40,3260-3266, with permission from the American Chemical Society.

H llliisttjlitui ut lhe X-ray Mantling wave field formed h lhe inlcrtercnce between lhe iircuieni and reflected plane wave above a mirror. t. A ter ftedryk at IWOj Ctipynght IWO by ilw A A AS

H lone-pair electrons are also a factor in determining the specific angle a. Analogously, a for HS02OCH3 61,

H longitudinal relaxation time Ti

H magnetic resonance images in a sagittal plane through the knee of a rat with arthritis

H magnitude COSY spectra of Check it 3.3.2.1, both processed

H MAS . The double arrows indicate the chemical shift ranges of non-hydrogen-bonded silanols, physisorbed water and hydrogen bonded silanols. Reproduced by permission j. Phys. Chem. C 2009, 113, pp. 1865218660, American Chemical Society

H MAS NMR chemical shift ranges for H-forms of zeolites. This figure is drawn based on the data from references ,

H MAS NMR Hahn-echo spectrum of zeolite HBEA. .

H MAS NMR spectra for 2 supports. Sidebands are marked with an asterisk. Adapted from ref. reprinted with permission from Elsevier.

H MAS NMR spectra of activated SAPO-5

H MAS NMR spectra of calcined of sodium cations by ammonium ions , The spectra were recorded at a resonance frequency of 400.13 MHz and with a sample-spinning rate of v pl2 kHz. The components are plotted at the bottom

H MAS NMR spectra of dehydrated zeolite HZSM-5 recorded at

H MAS NMR spectra of dehydrated zeolite Y

H mas NMR spectra of diy silica after the adsorption of quinoline.

H MAS NMR spectra of glasses with different water contents. Upper and middle spectra are of orthoclase glass, lower spectum is of anorthite-silica-wollastonite glass. Note the change in the intensity of the sidebands which is used to determine the H2O OH ratio. From Eckert et al. , by permission of the American Chemical Society.

H MAS NMR spectra of H-ZSM-5 denotes a spinning sideband.

H MAS NMR spectra of hydrous silica glasses with different water contents. D is the simulation of spectrum C showing 4 separate proton resonances. Fitted peaks a and c are thought to be due to Si-OH groups in 2 different environments while peaks b and d are due to molecular water in 2 different environments. From Kohn et al. , by permission of the copyright owner.

H MAS NMR spectra of pretreated amorphous silica-aluminas of different composition

H MAS NMR spectra of proton-containing minerals, illustrating the difference between the spectral characteristics of OH groups as in tremolite, Ca2Mg5Si8022, by permission of the American Chemical Society.

H MAS NMR spectra of the hydrothermally dealuminated zeolite , activated under 670 SB conditions

H MAS NMR spectra of the nominally anhydrous minerals enstatite, forsterite and three synthetic clinopyroxenes. Note the sharp resonance at 4.8 ppm from fluid-like water inclusions. The peak at about 1.5 ppm is attributed to organic contamination. From Kohn , by permission of the Mineralogical Society of America.

H MAS NMR spectra of the reaction products of with ,

H MAS NMR spectra of the zeolite H-Y 92 loaded with C6D12. The temperature was switched at the start of the experiment from room temperature



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