The infrared spectrum of the ultra quality maize hybrid preferable for human consumption: the identification of organic molecules and excited state of functional groups in spectral bands of the kernel, endosperm, pericarp and the germ

2021 ◽  
Vol 53 (4) ◽  
pp. 279-291
Author(s):  
C.N. Radenovic ◽  
◽  
G.V. Maksimov ◽  
D. Bajuk Bogdanovic ◽  
J. Hao ◽  
...  
2018 ◽  
Author(s):  
Maximiliano Riquelme ◽  
Alejandro Lara ◽  
David L. Mobley ◽  
Toon Vestraelen ◽  
Adelio R Matamala ◽  
...  

<div>Computer simulations of bio-molecular systems often use force fields, which are combinations of simple empirical atom-based functions to describe the molecular interactions. Even though polarizable force fields give a more detailed description of intermolecular interactions, nonpolarizable force fields, developed several decades ago, are often still preferred because of their reduced computation cost. Electrostatic interactions play a major role in bio-molecular systems and are therein described by atomic point charges.</div><div>In this work, we address the performance of different atomic charges to reproduce experimental hydration free energies in the FreeSolv database in combination with the GAFF force field. Atomic charges were calculated by two atoms-in-molecules approaches, Hirshfeld-I and Minimal Basis Iterative Stockholder (MBIS). To account for polarization effects, the charges were derived from the solute's electron density computed with an implicit solvent model and the energy required to polarize the solute was added to the free energy cycle. The calculated hydration free energies were analyzed with an error model, revealing systematic errors associated with specific functional groups or chemical elements. The best agreement with the experimental data is observed for the MBIS atomic charge method, including the solvent polarization, with a root mean square error of 2.0 kcal mol<sup>-1</sup> for the 613 organic molecules studied. The largest deviation was observed for phosphor-containing molecules and the molecules with amide, ester and amine functional groups.</div>


2014 ◽  
Vol 513-517 ◽  
pp. 161-164
Author(s):  
Xing Kai Chen

In the present investigation, carbon nanofibers (CNF) were dispersed in epoxy matrix to form CNF/glass fiber/epoxy composites. Before blending, CNF was oxidated to get more functional groups on CNF and improve the interface combination between resin and CNF, the infrared spectrum was used to test the efficiency. After that, tensile modulus tests were carried on for CNF/glass fiber/epoxy composites with different CNF fractions, the results indicated that there were slight improvements of tensile modulus when adding CNF. At 3.0 wt% of CNF, composites have the high improvement of tensile modulus, but the reinforcement of CNF decreased at 5.0 wt% of CNF. And the CNF reinforcement efficiency was analyzed using modified Coxs model and rule of mixture.


2019 ◽  
Vol 2019 ◽  
pp. 1-18 ◽  
Author(s):  
Dun Wu ◽  
Wenyong Zhang

Owing to the complexity and heterogeneity of coal during pyrolysis, the ex situ analytical techniques cannot accurately reflect the real coal pyrolysis process. In this study, according to the joint investigation of Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD), the structural evolution characteristics of lignite-subbituminous coal-bituminous coal-anthracite series under heat treatment were discussed in depth. The results of the infrared spectrum of coal show that the different functional groups of coal show different changes with the increase of coal rank before pyrolysis experiment. Based on in situ infrared spectroscopy experiments, it was found that the infrared spectrum curves of the same coal sample have obvious changes at different pyrolysis temperatures. As a whole, when the pyrolysis temperature is between 400 and 500°C, the coal structure can be greatly changed. By fitting the infrared spectrum curve, the infrared spectrum parameters of coal were obtained. With the change of temperature, these parameters show regular changes in coal with different ranks. In the XRD study of coal, the absorption intensity of the diffraction peak (002) of coal increases with increasing coal rank. The XRD patterns of coal have different characteristics at different pyrolysis temperatures. Overall, the area of (002) diffraction peak of the same coal sample increases obviously with the increase of temperature. The XRD structural parameter of coal was obtained by using the curve fitting method. The changing process of two parameters (interlayer spacing (d002) and stacking height (Lc)) can be divided into two main stages, but the average lateral size (La) does not change significantly and remains at the 2.98 ± 0.09 nm. In summary, the above two technologies complement each other in the study of coal structure. The temperature range of both experiments is different, but the XRD parameters of coal with different ranks are reduced within the temperature range of less than 500°C, which reflects that the size of coal-heated aromatic ring lamellae is reduced and the distance between lamellae is also reduced, indicating that the degree of condensation of coal aromatic nuclei may be increased. Correspondingly, the FTIR parameters of coal also reflect that, with increasing temperature, the side chains of coal are constantly cracked, the oxygen-containing functional groups are reduced, and the degree of aromatization of coal may be increased.


2012 ◽  
Vol 9 (1) ◽  
pp. 253-259 ◽  
Author(s):  
Hamid Najib ◽  
Siham Hmimou ◽  
Hicham Msahal

The high-resolution Fourier transform infrared spectrum of nitrogen trifluoride NF3has been studied in the v1+ v4perpendicular band region around 1523 cm−1. All experimental data have been refined applying various reduction forms of the effective rovibrational Hamiltonian developed for an isolated degenerate state of a symmetric top molecule. The v1= v4= 1 excited state of the14NF3oblate molecule was treated with models taking into account ℓ- andk-type intravibrational resonances. Parameters up to sixth order have been accurately determined and the unitary equivalence of the derived parameter sets in different reductions was demonstrated.


2000 ◽  
Vol 658 ◽  
Author(s):  
Slavi C. Sevov

ABSTRACTHybrid inorganic/organic materials with open-framework or layered structures are known for many transition metals linked by functionalized organic molecules such as organic diphosphonates, polycarboxylates, polynitriles, etc., species with more than one equivalent functional groups. We have studied the effect of pH on such a system of cobaltmethylenediphosphonate and report three new compounds, Na3Co[(O3PCH2PO3)(OH)],Na2Co(O3PCH2PO3)•H2O, and Co2[(O3PCH2PO3)(H2O)], that form at very basic, moderately basic, and acidic conditions, respectively. More interestingstructural chemistry should be expected from linkers with two or more different functionalities. Both the carboxylic and phosphonic groups in carboxyethylphosphonic acid are used to coordinate to cobalt or calcium atoms in the new compounds Co3(O3PCH2CH2COO)2•6H2O and Ca(O3PCH2CH2COOH)•H2O. Taking one more step further in complexity we have also studied linkers with three different functional groups, phosphonated amino acids. The structures of two new compounds, Zn(O3PCH2CH(NH3)COO) and Zn(O3PCH2CH2CH(NH3)COO), are threedimensional frameworks made of zinccoordinated by both the carboxylic and phosphonic ends of the organic molecules. The amino groups are protonated and terminal in the voids of the frameworks.


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