New polyurethane materials from renewable resources: synthesis and characterization

e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Doina Macocinschi ◽  
Daniela Filip ◽  
Stelian Vlad
Keyword(s):  
Surface Properties ◽  
Renewable Resources ◽  
Tensile Tests ◽  
Cellulose Derivative ◽  
Alternative Methods ◽  
Synthesis And Characterization ◽  
Cellulose Derivatives ◽  
Domain Structures ◽  
Ft Ir ◽  
Mechanical Tensile

AbstractIn the present study new types of polyurethane-cellulose derivative biomaterials based on urethane prepolymers functionalized with hydroxypropylcellulose are presented. The aim of the present study is to obtain materials with better haemocompatibility, biocompatibility and amphiphilic microphase-separated domain structures. The outcome of remarkable chemical versatility characteristic to polyurethane materials combined with polymers derived from nature like cellulose derivatives resulting in bulk and surface properties is evidenced by means of different techniques like DSC, TGA, FT-IR, AFM and mechanical tensile tests. The influence of various factors on the developed morphologies and the microstructural changes is investigated. Both polyester and polyether macrodiols have been used to prepare these polyurethanes. The aim of this study is to find also alternative methods for improving biostability while maintaining the excellent biocompatibility and other properties.

scholarly journals Synthesis and Characterization of All Renewable Resources Based Branched Polyester: Poly(2,5-furandicarboxylic acid-co-glycerol)

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Ananda S. Amarasekara ◽  
Ashfaqur Razzaq ◽  
Paul Bonham
Keyword(s):  
Elemental Analysis ◽  
Renewable Resources ◽  
Polyester Resin ◽  
Synthesis And Characterization ◽  
Ft Ir ◽  
Furandicarboxylic Acid ◽  
C Nmr

Condensation of all renewable resources based monomers 2,5-furandicarboxylic acid and glycerol in the presence of 2 mol% Sb2O3 catalyst at 210°C gives a branched polyester resin in 70% yield. This resin was characterized by elemental analysis, 1H, 13C NMR, FT-IR, and TGA-DTG.

One Step Synthesis and Characterization of Zirconia-Graphene Composites

2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Composite ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Xrd Techniques

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.

Electrochemically Synthesis and Characterization of Copolymers Based on 1, 4-Diethoxybenzene and 3, 4-Ethylenedioxythiophene

2011 ◽  
Vol 335-336 ◽  
pp. 989-993
Author(s):  
Mi Ouyang ◽  
Zhen Wei Yu ◽  
Yi Xu ◽  
Yu Jian Zhang ◽  
Cheng Zhang
Keyword(s):  
Cyclic Voltammetry ◽  
Ir Spectroscopy ◽  
Feed Ratio ◽  
Synthesis And Characterization ◽  
Monomer Mixture ◽  
Long Wavelength ◽  
H Nmr ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

Copolymers based on 1, 4-diethoxybenzene (DEB) and 3, 4-ethylenedioxythiophene (EDOT) were electrochemically synthesized and characterized. The structures of the copolymers were established by 1H NMR and FT-IR spectroscopy. The results indicated the final product was a copolymer instead of a blend or a composite. The physical properties were systematically investigated by cyclic voltammetry, UV-vis absorption and fluorescence. The PL maximum of copolymers presented obviously red-shift to long wavelength as the feed ratio of EDOT in monomer mixture increased.

Synthesis and Characterization of a Trifunctional Aminoamide Cellulose Derivative

2006 ◽  
Vol 7 (1) ◽  
pp. 139-145 ◽  
Author(s):  
Changde Zhang ◽  
Loren M. Price ◽  
William H. Daly
Keyword(s):  
Cellulose Derivative ◽  
Synthesis And Characterization

scholarly journals Synthesis and Characterization of Some Novel Oxazine, Thiazine and Pyrazol Derivatives

2016 ◽  
Vol 13 (2) ◽  
pp. 244-252
Author(s):  
Baghdad Science Journal
Keyword(s):  
Acetic Acid ◽  
Ir Spectra ◽  
Glacial Acetic Acid ◽  
Basic Medium ◽  
Synthesis And Characterization ◽  
Pyrazole Derivatives ◽  
Phenyl Hydrazine ◽  
H Nmr ◽  
Ft Ir

In this paper, some chalcone derivatives (C1, C2) were synthesized based on the reaction of equal amount of substituted acetophenone and substituted banzaldehyde in basic medium. Oxazine and thiazine derivatives were prepared from the reaction of chalcones (C1-C2) with urea and thiourea respectively in a basic medium. Pyrazole derivatives were prepared based on the reaction of chalcones with hydrazine mono hydrate or phenyl hydrazine in the presence of glacial acetic acid as a catalyst. The new synthesized compounds were identified using various physical techniques like1 H-NMR and FT-IR spectra.

scholarly journals Synthesis and Characterization of some New 1,3,4-Oxadiazole derivatives based on 4-amino benzoic acid

2016 ◽  
Vol 13 (4) ◽  
pp. 762-769
Author(s):  
Baghdad Science Journal
Keyword(s):  
Schiff Base ◽  
Benzoic Acid ◽  
Spectral Data ◽  
1H Nmr ◽  
Synthesis And Characterization ◽  
Oxadiazole Derivatives ◽  
Ft Ir ◽  
Amino Benzoic Acid

Various of 2,5- disubstituted 1,3,4-oxadiazole (Schiff base, ?- lactam and azo) were synthesized from 2,5-di (4,4?-amino-1,3,4-oxadiazole which usequently synth-esized from mixture of 4- amino benzoic acid and hydrazine arch of polyphosphorus acid. The synthesized compounds were cherecterized by using some spectral data (UV, FT-IR , and 1H-NMR)

scholarly journals SYNTHESIS AND CHARACTERIZATION: COMPOSITE OF GRAPHENE OXIDE BASED PALM KERNEL SHELL WASTE WITH FE3O4

2021 ◽  
Vol 22 (2) ◽  
pp. 101
Author(s):  
Bernadeta Ayu Widyaningrum ◽  
Dita Apriani ◽  
Putri Amanda ◽  
Ismadi Ismadi ◽  
Sutanto Sutanto
Keyword(s):  
Raman Spectroscopy ◽  
Graphene Oxide ◽  
Palm Kernel ◽  
Energy Dispersive Spectrum ◽  
Energy Dispersive ◽  
Synthesis And Characterization ◽  
Palm Kernel Shell ◽  
Shell Waste ◽  
Ft Ir ◽  
Co Precipitation

SYNTHESIS AND CHARACTERIZATION: COMPOSITE OF GRAPHENE OXIDE BASED PALM KERNEL SHELL WASTE WITH Fe3O4. In this study, GO-Fe3O4 were fabricated by co-precipitation technique and the graphene oxide (GO) were synthesized from an agricultural biomass, palm kernel shell, via Hummer’s method. Field Emission Scanning Electron Microscopy and Energy Dispersive Spectrum (FESEM-EDS), Fourier Transform Infra-Red (FT-IR) spectroscopy, X-Ray Diffractometer (XRD), and Raman spectroscopy were used to analysis the successful attachment of Fe3O4 onto the surface of GO. Morphology observation showed that Fe3O4 were heterogeneously deposited on the surface of GO. FT-IR spectra shows peak that incorporated to oxygenated functional groups and sharp peak at 586 cm-1 confirmed to lattice absorption of Fe3O4. The percentage of composition of GO-Fe3O4 was characterized by energy dispersive spectroscopy and the results also confirmed in XRD exhibits similar properties with JCPDS 19-0629 for magnetite more dominant than GO. From Raman spectroscopy analysis shows that 1343.82 cm-1 (D-band) and 1584.62 cm-1 (G-band) and 2698 cm-1 (2D-band) indicates GO and GO-Fe3O4 were successfully synthesized.

scholarly journals Effect of 1,4-Napthaquinone (NQ) and benzophenone (BPH)on the photodegradation and biodegradation of methyl cellulose film

2010 ◽  
Vol 7 (1) ◽  
pp. 737-744
Author(s):  
Baghdad Science Journal
Keyword(s):  
Molecular Weight ◽  
Film Thickness ◽  
Carbonyl Compounds ◽  
Methyl Cellulose ◽  
Chain Scission ◽  
Cellulose Derivative ◽  
Accelerated Weathering ◽  
Cellulose Derivatives ◽  
Photodegradation Rate ◽  
Aromatic Carbonyl Compounds

The induced photodegradation of methyl cellulose (MC) films in air was investigated in the absence and presence of aromatic carbonyl compounds(photosenssitizers): 1,4-naphthaquinone (NQ) and benzophenone (BPH) by accelerated weathering tester. The addition of (0.01 wt %) of low molecular weight aromatic carbonyl compounds to cellulose derivatives films(25µm in thickness) enhanced the photodegradation of the polymer films.The photodegradation rate was measured by the increase in carbonyl absorbance. Decreases in solution viscosity and reduction of molecular weight were also observed in the irradiated samples. Changes in the number-average chain scission, the degree of deterioration and in the quantum yield of chain scission values are also observed, and it was concluded that branching or cross-linking has occurred for cellulose derivative with NQ and BPH. Findings from all analytical techniques indicated that the 1,4-naphthaquinone (NQ) photosensitizer enhance the photodegradation of methyl cellulose more than benzophenone (BPH). The effect of the photosensitizer concentration, (ranging from 0.01 to 0.1 %), on the rate of photodegradation was also monitored for MC films. The rates are increased with increasing the photosensitizer concentration. The effect of film thickness is also studied at fixed sensitizer concentration (0.05%), and results show that the rate of cellulose derivative photodegradation decreases with increasing film thickness. The rate constants of the photodegradation of the photosensitizers deduced in cellulose derivatives films, [at concentration of (0.1%)by weight and thickness (25µm)]. Biodegradation of irradiated cellulose derivatives films was conclusively established with bacteria type Pseudomonas aeuroginosa Rb-19 isolated from crude oil. The amount of bacteria growth on MC after 30 days was lower, while there was no growth observed in MC with BPH

Synthesis and Characterization of an Alendronate-Chitosan Conjugate

2011 ◽  
Vol 140 ◽  
pp. 53-57 ◽  
Author(s):  
Xiao Hong Shao ◽  
Ji Qing Xu ◽  
Yan Peng Jiao ◽  
Chang Ren Zhou
Keyword(s):  
Drug Delivery ◽  
Drug Delivery System ◽  
Synthesis And Characterization ◽  
Hydroxyl Groups ◽  
Amino Groups ◽  
H Nmr ◽  
Ft Ir ◽  
Novel Drug Delivery System ◽  
Novel Drug

The biomineral-binding alendronate-chitosan conjugate (Scheme 1) was developed as a novel drug delivery system. Alendronate was conjugated to the hydroxyl groups of chitosan, thereby maintaining the amino groups of chitosan intact. By means of FT-IR and 1H NMR, the characterization was conducted to confirm the successful synthesis of alendronate-chitosan conjugate.

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