• Journal of the Korean Chemical Society
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• v.18 no.3
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• pp.180-188
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• 1974

Adsorption mechanism of alkyl aldehydes, acetaldehyde, acrolein, and crotonaldehyde on cations supported by layer silicates was studied by means of IR spectroscopy and X-ray. An analysis of four characteristic split bands in the region of $1720∼1580㎝^{-1}$ was made. The carbonyl stretching band which shifted about $130㎝^{-1}$ to lower frequencies was observed only for $Ni^{2+}$ and Al^{3+}$ but slightly with $Ca^{2+}$ at high sample temperature and was attributed to >C=O…M complex formation. A sharp band which appeared as a shoulder at 1722 for acetaldehyde and 1690 for acrolein and crotonaldehyde was responsible for the interaction of carbonyl with surface hydroxyl. The second broad band which appeared at about 1710~1660 was responsible for hydrogen bonding between carbonyl oxygen and cationic hydroxyl group. The third band which appeared at about 1640~1660 was attributed to induced >C=C< double bond due to the strong carbonyl interaction. This was supported by the interlamellar spacings obtained by X-ray diffractometry.

• Journal of the Korean Chemical Society
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• v.21 no.4
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• pp.246-255
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• 1977

The adsorption of methylmethacylate on layer silicates containing various interlayer cations has been studied by means of infrared spectroscopy and X-Ray. Several characteristic carbonyl bands of adsorbed methylmethacrylate appeared differently at the region of 1723∼1547$cm^{-1}$depending on the species of cation and the dehydration temperature. The carbonyl stretching band shifted about 190$cm^{-1}$ to lower frequencies has been observed only for polyvalent cations, which has been attributed to $>C=O{\cdot}{\cdot}{\cdot}M^{n+}$ complex formation. The band appeared at 1703∼1640$cm^{-1}$ is responsible for hydrogen bonding between carbonyl oxygen and cationic water or cationic hydroxyl group, and the degree of shift indicates good correlation with the polarizing power of the interlayer cations. However, the band appeared at 1723$cm^{-1}$ has not been correlated with the species of cation but assigned to the carbonyl stretching which reacted with the surface hydroxyl group. On the basis of interlamellar spacing, it is suggested that the molecular plane of MMA molecule is parallel to silicate layers.

• Nuclear Engineering and Technology
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• v.54 no.1
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• pp.255-261
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• 2022

A reliable and well-characterized dosimetry system which is traceable to the international measurement system, is the key element to quality assurance in radiation processing with cobalt-60 gamma rays, X-rays, and electron beam. This is specifically the case for health-regulated processes, such as the radiation sterilization of single use medical devices and food irradiation for preservation and disinfestation. Polyethylene is considered to possess a lot of interesting dosimetric characteristics. In this work, a detailed study has been performed to determine the dosimetric characteristics of a commercialized high-density polyethylene (HDPE) film using Fourier transformed infrared spectrometry (FTIR). Correlations have been established between the absorbed dose and radiation induced infrared absorption in polyethylene having a maximum at 965 cm^-1 (transvinylene band) and 1716 cm^-1 (ketone-carbonyl band). We have found that polyethylene dose-response is linear with dose for both bands up to1000 kGy. For transvinylene band, the dose-response is more sensitive if irradiations are made in helium. While, for ketone-carbonyl band, the dose-response is more sensitive when irradiations are carried out in air. The dose-rate effect has been found to be negligible when polyethylene samples are irradiated with electron beam high dose rates. The irradiated polyethylene is relatively stable for several weeks after irradiation.

• Journal of the Korean Chemical Society
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• v.14 no.2
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• pp.147-153
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• 1970

Band assignments in the infrared absorption spectra of the four substituted Urea compounds, Fenuron (3-phenyl-1,1-dimethyl urea), OMU (3-cyclooctyl-1,1-dimethyl urea), Herban (3-(hexahydro-4,7-methanoidan-5-yl)-l,1-dimethyl urea), and Monuron (3-(p-chlorophenyl)-1,1-dimethyl urea), are made by analyzing the spectra obtained with various solvents. The results suggest that Fenuron and Monuron, each of which contain an unsaturated benzene ring, have a strong tendency to bond through both the amino group and the carbonyl oxygen. Herban and OMU, however, exhibit a much greater change in strength of the carbonyl bond than of the amino bond. It means that a strong hydrogen bonding occurs only at the carbonyl oxygen in the compounds.

• Textile Coloration and Finishing
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• v.15 no.4
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• pp.17-23
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• 2003

Fourier transform infrared spectroscopy(FT-IR) was used to characterize the intermolecular ester crosslinkages in cotton cellulose. The FT-IR data show that the band of the ester carbonyl group can be separated from overlapping carboxyl/carbonyl band by converting carboxyl group to carboxylate. When esterification occurs between a polycarboxylic acid and cotton cellulose, the carbonyl groups retained in the cotton exist in three forms; ester, carboxyl, and carboxylate anion. The FT-IR data were also correlated to the durable press rating result obtained. The appearance of BTCA-finished durable press silk/cotton fabrics were improved.

• Journal of the Korean Chemical Society
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• v.27 no.6
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• pp.399-404
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• 1983

Raman spectra for the carbonyl stretching mode of the amides, and amide-solvent systems have been recorded to investigate the effect of alkyl substitutions at the carbonyl carbon and at the nitrogen on the amide hydrogen-bonding. The data have shown that the interaction affinities are in the order of amide-amide > amide-water > amide-alcohol in formamide system, and amide-water > amide-amide > amide-alcohol in acetamide and propionamide systems. The strength of the proton acceptor of the carbonyl oxygen is increased by the presence of alkyl group to the carbonyl carbon and the proton donorcity of the amide is decreased by the alkyl substitution at the nitrogen. The above results are in good agreement with the ab initio SCF MO calculation.

• Applied Chemistry for Engineering
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• v.24 no.2
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• pp.138-143
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• 2013

This paper studied the possibility to predict a mechanical property variation from changes in created carbonyl bands by irradiating the surface of high-density polyethylene with short-wavelength ultraviolet radiation of 254 nm to induce a fast chemical degradation. The meaning of this study lies in checking whether a mechanical property change with the same chemical property as the induced optical deterioration is caused by using a UVC lamp with high photon energy instead of optical deterioration via xenon arc light source and outdoor exposure test via natural sunlight requiring a long time. The mechanical strength of high-density polyethylene checked by a tensile test and a creep destruction test showed a similar tendency with CI changes. In particular, the yield strength and elongation had a close relationship with the exposure time to ultraviolet radiation. Accordingly, this paper presented a method to grasp the mechanical property change outdoors requiring a long time more fast through the relationship between the mechanical property change and the carbonyl index using a UVC lamp causing the fast surface degradation.

• Journal of the Korean Chemical Society
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• v.19 no.6
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• pp.454-462
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• 1975

The photodegradation of polystyrene and polyethylene was studied utilizing several additives to promote photooxidation. Polymer films with small amount of additives were irradiated with ultraviolet lamps in Rayonet Photochemical Reactor. The progress of photodegradation was followed by measuring the intensities of carbonyl and hydroxyl stretching bands in infrared spectra as well as the viscosity changes. It was found that the increase of carbonyl or hydroxyl peaks was proportional to the decrease of the molecular weight of polymers under study. Iron(II, III) complexes of dithiocarbamate and their analogs showed good results.

• Journal of the Korean Wood Science and Technology
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• v.11 no.3
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• pp.58-69
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• 1983

This research is performed to compare lignin compounds isolated in Pinus koraiensis Sieb et Zucco, with those compounds which have been already isolated. and to elucidate IR spectra of functional groups and aromatic nucleus for chemical structure of lignin. In vanillin and dehydrodivanillin having carbonyl group ill ${\alpha}$-position. characteristic absorption band of carbonyl group was confirmed in 1665 $cm^{-1}$. Absorption band of vanillic and syringic acid with carboxyl group were indicated in 1675 and 1690 $cm^{-1}$ respectively. Syringic acid showed low wave number because this was affected by methoxyl group. Characteristic absorption bands of guaiacyl, syringly and guaiacyl-syringyl co-polymer nucleus were clearly disclosed in diarylpropane compounds. It were reconfirmed that absorption band of guaiacyl showed longer wave number than of syringly nucleus.

• Textile Coloration and Finishing
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• v.15 no.4
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• pp.24-31
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• 2003

In this research, we applied FT-IR spectroscopy to study the hydrolysis of the ester-crosslinking formed by various polycarboxylic acids on the cotton fabric. We observed the following; (1) the ester-crosslinking is less durable to hydrolysis than ether-crosslinking under all conditions; (2) the ester-crosslinking formed by polycarboxylic acids having more than three carboxyl groups, such as butanetetracarboxylic acid (BTCA), are substantially more durable to hydrolysis than the acids having two or three carboxyl groups, such as maleic and citric acid; (3) alkaline conditions drastically accelerate the hydrolysis of both urea- and ester-crosslinking; and (4) the ester-crosslinking formed by poly(maleic acid) is more resistant to hydrolysis at alkaline conditions than BTCA. (5) polycarboxylic acid molecules were removed from the fabric at same rate as the hydrolysis of the ester linkage. FT-IR spectroscopy has proved to be a useful analytical technique for evaluating the hydrolysis of the crosslinked cotton fabric.