Near Infrared Spectroscopy of Aurichalcite (Zn,Cu2+)5(CO3)2(OH)6

2007 ◽  
Vol 15 (2) ◽  
pp. 115-121 ◽  
Author(s):  
B. Jagannadha Reddy ◽  
Ray L. Frost

In this endeavour, near infrared spectroscopy studies show evidence of variable composition in aurichalcite minerals of zinc copper carbonate hydroxides. The observation of a broad feature in the electronic part of the spectrum around 11,500 cm−1 (870 nm) is a strong indication of Cu2+ substitution for Zn2+ in the mineral. Overtones of OH vibrations in the spectra from 7250 to 5400 cm−1 (1380–1850 nm) show strong hydrogen bonding in these carbonates. A band common to spectra of all carbonates appears near 5400 cm−1 (1850 nm) due to the combination of both OH-stretching and HOH-bending vibrations, which may be attributed to adsorbed water. Aurichalcite minerals display a spectral sequence of five absorption bands with variation of both band positions and intensities and this is the chief spectral feature observed in the range 5200–5100 cm−1 (1920–2380 nm) due to vibrational processes of the carbonate ion. The frequency shift of carbonate bands suggests the effect of divalent cations and/or variations of the Zn/Cu ratio in aurichalcite minerals.

2002 ◽  
Vol 56 (11) ◽  
pp. 1413-1421 ◽  
Author(s):  
C. Billaud ◽  
M. Vandeuren ◽  
R. Legras ◽  
V. Carlier

Near-infrared spectroscopy was used to quantify the cure reaction of 4,4′-methylene- bis-(2,6-diethylaniline) (MDEA)–epoxy resins (E/A = 1.4) carried out at 72 and 160 °C. The absorption bands of the functional groups of interest in MDEA–epoxy resins are assigned according to the literature. A new assignment at 6580 cm−1 is also proposed for the secondary amine: it was supported by a synthesized model compound. Two different spectrum treatments were proposed. The first one is based only on a normalization at 4610–4620 cm−1, while the second one needs the subtraction of the normalized spectrum of a post-cure sample. To follow the curing process, amines and epoxy were studied at the same time in the combination and the overtone regions. The results are compared. In the combination region, quantitative results are obtained from absorbance measurements, while in the overtone region spectrum decompositions and area measurements are necessary. Complementary and reliable information are so obtained and allow us to calculate conversions of epoxide and amine I and concentrations in amine II, amine III, hydoxyl groups, and ether links. Kinetics are also established. The curing process mechanism is at last discussed for both curing temperatures.


2017 ◽  
Vol 735 ◽  
pp. 168-172
Author(s):  
Siraporn Soonthonhut ◽  
Alfred A. Christy

Water adsorption in proteins is the crucial process of protein folding and structure stabilizing. Adsorption of water on proteins can be evaluated by near-infrared spectroscopy, a useful technique for observing combination frequency of a water molecule. In this work, albumin, lysozyme, and silk, were used as models for α-helix and β-pleated sheet proteins. Their NIR spectra during water adsorption process were measured by using an NIR spectrometer equipped with a transflectance accessory. Moreover, the quantitative adsorption of water was determined by gravimetric technique. The results indicate that, there are five different NIR absorptions arise from the OH combination frequencies of water adsorbed by albumin in the 5300-5100 cm-1 region. But there are only four absorptions for lysozyme and silk. The OH combination frequencies arising from water molecules in albumin indicate that it acquires free water molecules (5280 cm-1) and adsorbed water molecules through carbonyl-water interactions (5248 and 5160 cm-1) and amino-water interactions (5200 and 5120 cm-1). Interestingly, there is no indication for the presence of free water molecules in lysozyme and silk. Furthermore, the gravimetric results indicate that the rate of water adsorbed follows the order RW.Alb<RW.Lys<RW.Sil and total mass of water adsorbed per gram solid follows the order WAlb<WLys=WSil.


2021 ◽  
Vol 20 (5) ◽  
pp. 255-260
Author(s):  
Kongphope Chaarmart ◽  
Sureeporn Narongwongwattana ◽  
Ronnarit Rittiron ◽  
Worawat Sa-Ngiamvibool

The chemical quality of juices and wine produced from Mamao fruit was evaluated by Fourier transform near-infrared (FT-NIR). The calibration equation was created by the cross-validation method to be si+mulated the accuracy. Statistical values composed of correlation coefficient (R), standard error of cross-validation (SECV) and bias were used. Brix values and acidity values of Mao juice and the Brix, acidity, and alcohol values of Mao wine products were evaluated through the standard and cross-validation relation. It was found that was observed with NIR spectrometer to be absorbed in the same IR wavelength (1450 nm) which indicated that the water is the main composition. Based on FT-NIR analysis, the spectrum latices of juices and wine were revealed in the same range of the absorption bands at 1450 nm and 1940 nm to be confirmed the water composition. Also, the FT-NIR spectra from region 2258-2312 nm in Mao wine product have been predicted to the Ethanol functions.


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