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Wyświetlanie 1-7 z 7
Tytuł:
Characteristics of physicochemical and rheological properties of chitosan hydrogels based on selected hydroxy acids
Autorzy:
Zavyalova, Olga
Gajewska, Sandra
Dąbrowska-Wisłocka, Dominika
Sionkowska, Alina
Powiązania:
https://bibliotekanauki.pl/articles/2058389.pdf
Data publikacji:
2021
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
chitosan
lactobionic acid
mandelic acid
rheology
FTIR spectra
chitozan
reologia
hydrożele
Opis:
Chitosan is a natural cationic polymer that dissolves in an acidic environment and forms gels. Its properties depend on the degree of deacetylation and molecular weight. It is a bioactive compound with antibacterial and film-forming properties that allow to increase the regenerative capacity of the skin. Moreover, it is biodegradable, biocompatible, non-toxic, and stable. In this research, chitosan was combined with mandelic and lactobionic acids which are characterized by biological activity and low toxicity. This combination not only has a positive effect on the chitosan solubility, but it also allows to obtain new biomaterials whose positive features of the base ingredients are enhanced by their synergistic effect. The obtained hydrogels were assessed regarding the interaction of chitosan and hydroxy acid molecules, and the stability of the resulting structures was examined. The research was performed by using rheological methods and IR spectroscopy. Chitosan hydrogels made with mandelic acid are characterized by higher viscosity values, as compared to hydrogels containing lactobionic acid. The samples of the obtained hydrogels stored for 7 days showed no signs of degradation and their viscosity values were constantly increasing, which proves the ongoing process of creating new bonds between hydroxy acid molecules and chitosan chains. After this time, the hydrogels with mandelic acid revealed higher viscosity values in comparison to hydrogels made with lactobionic acid. Based on the obtained IR spectra, the shifts of the characteristic chitosan bands as a result of interaction with the tested hydroxy acids were analyzed.
Źródło:
Engineering of Biomaterials; 2021, 24, 161; 2--7
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Infrared spectral analysis of waste pet samples
Autorzy:
Vijayakumar, S.
Rajakumar, P. R.
Powiązania:
https://bibliotekanauki.pl/articles/411833.pdf
Data publikacji:
2012
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
butelki PET
ABS
FTIR
mieszanki kompozytowe
PET bottles
FT-IR spectra
blended composites
Opis:
There are fifteen waste pet bottles and a commercial grade ABS was collected from local supplier of Chidambaram town. The ABS was used to study the mechanical properties of PET blend composites. This study was performed by FT-IR spectroscopy. From the characteristics infra-red stretching bands the mechanical properties of samples were discussed.
Źródło:
International Letters of Chemistry, Physics and Astronomy; 2012, 4; 58-65
2299-3843
Pojawia się w:
International Letters of Chemistry, Physics and Astronomy
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Równowagi asocjacyjne alkilopochodnych mocznika i tiomocznika
Association equilibria of alkyl derivatives of urea and thiourea
Autorzy:
Rospenk, M.
Koll, A.
Obrzud, M.
Powiązania:
https://bibliotekanauki.pl/articles/172815.pdf
Data publikacji:
2017
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
model samoasocjacji
momenty dipolowe
średnia masa cząsteczkowa
obliczenia DFT
pochodne mocznika i tiomocznika
model of self-association
dipole moments
average molecular weight
FTIR spectra
DFT calculation
derivatives of urea and thiourea
Opis:
The studies and comparison of a series of molecular mono- and di-substituted derivatives of urea and thiourea in solvents of increasing polarity are presented [1–4]. These substances are characterized by a high tendency to self-associate through the formation of intermolecular hydrogen bonds due to the presence in their structure both groups as donors (NH) as well as proton acceptors (C=O) or (C=S). Studies were performed by using IR spectroscopy, method of measuring the average molecular weight and the dipole moments. The experimental data were verified by DFT quantum chemical calculations with B3PW91 correlation functional. Simultaneous use of these techniques alowed establishing not only the efficiency of aggregation, but also the structure and polarity of formed aggregates. It was shown, that in solvents with weak acidic C-H groups the aggregation was strongly limited because of molecular interactions between solute and solvent. The theoretical DFT calculations which included the impact of the environment on the nature of interactions in the complex were carried out [e.g. Scheme 4.1.4]. A combination of geometry optimization in polarizable continuum model (PCM) with the connection of chloroform molecules (1,2-dichloroethane) with urea dimers enabled to obtain the expected theoretical simulation compliance with the experiment. The equilibrium constants were calculated on the basis of data obtained in two independent methods of measurement: IR spectroscopy and measurements of average molecular weights. Good agreement of experimental data of both research techniques were found up to concentration of 0.03 mol/dm3 [Fig. 2.5]. The type of associates have been assessed following the dipole moments measured as a function of concentration, and on the results of density-functional theory (DFT) calculations on the structure and energy of particular species. All of the urea derivatives demonstrated an increase in dipole moment with increased concentration, suggesting linear-type aggregation [Fig. 4.1.3]. Contrastingly, the dipole moments of the N,N-dimethylthiourea and mono-N-alkyl-substituted thioureas decreased with concentration and suggest that cyclic dimers or trimers are formed by C=S…(HR)2N-C=S interactions [Fig. 4.2.2]. The efficiency of self-aggregation was described by use of two equilibrium constants. The first constant, K1, was describing dimer formation and the second constant, K2, the subsequent multimer formation. In N,N’-thioureas aggregation was lower than for the related urea compounds [Table 4.1.1 and Table 4.2.1]. Differences between urea and thiourea derivatives result from the fact that the ureas are stronger bases and, therefore, more active in aggregation.
Źródło:
Wiadomości Chemiczne; 2017, 71, 7-8; 559-608
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Przemiany struktury smarów plastycznych po testach tribologicznych
Conversion of the structure of greases after tribological tests
Autorzy:
Pawelec, E.
Siwiec, E.
Powiązania:
https://bibliotekanauki.pl/articles/188552.pdf
Data publikacji:
2013
Wydawca:
Stowarzyszenie Inżynierów i Techników Mechaników Polskich
Tematy:
smar plastyczny
właściwości przeciwzużyciowe
widmo IR
spektrofotometria w podczerwieni
dodatki smarne
grease
antiwear properties
IR spectra
FTIR spectrophotometry
lubricating additives
Opis:
W artykule przedstawiono wyniki badania składu smarów plastycznych po testach tribologicznych prowadzonych w warunkach stałego obciążenia węzła tarcia. W tym celu wykonano widma IR smaru wyjściowego i porównano je z widmami uzyskanymi dla smarów po testach tribologicznych. Zidentyfikowano pasma charakterystyczne dla badanych smarów i oceniono zmiany w tych zakresach. Uzyskane wyniki wykazały, że właściwości przeciwzużyciowe badanych smarów nie są jedynie funkcją ilościowego udziału dodatków, ale także produktów oksydacji, jakim ulegają składniki smaru.
This paper presents the results of grease composition analysis when tribological tests are performed under constant load. The analysis was conducted by comparing the IR spectra of grease before and after tribological tests. The changes in the identified spectra characteristic of the greases were used to evaluate changes in the grease structures. The results showed that the anti-wear properties of lubricants tested are both a function of the quantitative contribution of additives and the oxidation products that are components of the grease.
Źródło:
Tribologia; 2013, 2; 141-150
0208-7774
Pojawia się w:
Tribologia
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Electromagnetic field of extremely low frequency has an impact on selected chemical components of the honeybee
Autorzy:
Koziorowska, A.
Depciuch, J.
Białek, J.
Woś, I.
Kozioł, K.
Sadło, S.
Piechowicz, B.
Powiązania:
https://bibliotekanauki.pl/articles/2087262.pdf
Data publikacji:
2020
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
Apis mellifera
ELF-EMF
FTIR
spectra analysis
body chemical composition
Źródło:
Polish Journal of Veterinary Sciences; 2020, 23, 4; 537-544
1505-1773
Pojawia się w:
Polish Journal of Veterinary Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The impact of heat treatment on the components of plant biomass as exemplified by Junniperus sabina and Picea abies
Autorzy:
Drygaś, B.
Depciuch, J.
Puchalski, Cz.
Zaguła, G.
Powiązania:
https://bibliotekanauki.pl/articles/411289.pdf
Data publikacji:
2016
Wydawca:
Polska Akademia Nauk. Oddział w Lublinie PAN
Tematy:
torrefaction
biomass
FTIR spectra
changes
biochars
Opis:
Torrefaction is the process of drying biomass at high temperatures in order to transform it into biofuels with properties and composition resembling carbon. The impact of high temperature breaks the chains of hemicellulose, lignin and cellulose and degrades the biomass to simpler organic compounds. The aim of this publication was to specify the impact of the duration of the heat treatment on the stability of biomass structures such as lignocellulose illustrated with examples of selected species of conifers. The research material consisted of shoot tips of Junniperus sabina and Picea abies. The material used in the process was air-dried, dried at 150oC and torrefied at temperatures of 200, 250 and 300oC in a LECO camera – TGA 701 apparatus for 30 minutes. Fresh needles and their torrefied products were measured spectroscopically using FTIR Vertex 70v made by Bruker. Microscopic photographs of samples were taken in the scales 10 μm, 20 μm, and 50 μm using the TESCAN VEGA3 scanning electron microscope. The unprocessed plant material did not differ significantly from one another – the FTIR spectra of both plants exhibited the same functional groups. The biomass heat treatment led to significant changes in its chemical composition and topographic changes in the obtained biochars.
Źródło:
ECONTECHMOD : An International Quarterly Journal on Economics of Technology and Modelling Processes; 2016, 5, 3; 41-50
2084-5715
Pojawia się w:
ECONTECHMOD : An International Quarterly Journal on Economics of Technology and Modelling Processes
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Optical Properties of Soda-Lime-Silica Glasses Doped with Eggshell Powder
Autorzy:
Aktas, B.
Albaskara, M.
Yalcin, S.
Dogru, K.
Powiązania:
https://bibliotekanauki.pl/articles/1030117.pdf
Data publikacji:
2017-09
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
soda-lime-silica glass
eggshell powder
optical properties
FTIR spectra
Opis:
The optical properties of soda-lime-silica glasses doped with eggshell powder were investigated using UV-visible and the Fourier transform infrared spectroscopies. Pure soda-lime-silica glass, which is colorless and transparent, turned dark green after the addition of the eggshell powder. When the eggshell powder content was ≥ 3 wt%, the glass became translucent. The maximum wavelengths in the UV spectra of the soda-lime-silica glasses doped with 0.5, 1, 3, and 5 wt% eggshell powder were observed at 300.20, 277.40, 284.40, and 312.40 nm, respectively. The Fourier transform infrared spectra of the eggshell-doped soda-lime-silica glass samples were very similar to that of the base undoped glass. The bands at approximately 770-820 cm¯¹ could be attributed to the Si-O-Si symmetric stretching of the bridging oxygen between the tetrahedra, while the bands at approximately 970 cm¯¹ were related to the Si-O-Si antisymmetric stretching of the bridging oxygen within the tetrahedra.
Źródło:
Acta Physica Polonica A; 2017, 132, 3; 442-444
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-7 z 7

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