Synthesis and characterization of lignin–melamine–formaldehyde resin

2016 ◽  
Vol 30 (9) ◽  
pp. 1255-1266
Author(s):  
Amadou Diop ◽  
Kokou Adjallé ◽  
Benjamin Boëns ◽  
Daniel Montplaisir ◽  
Simon Barnabé

Lignin–melamine–formaldehyde (LMF) resin was prepared by three steps: (i) tosylation of lignin, (ii) synthesis of lignin-melamine (LM) copolymer, and (iii) formation of methylol LM. The synthesized resins were characterized by Fourier transform infrared (FTIR) spectroscopy and phosphorous 31 nuclear magnetic resonance analysis. The curing parameters of LMF resin were determined by differential scanning calorimetry (DSC) and thermal gravimetric analysis. The yield of tosylation is 80%. The FTIR spectrum of tosylated lignin shows the presence of two new bands at 1171 and 1370 cm−1. The formation of the LM was demonstrated by the disappearance of both bands and appearance of the absorbances at 3115, 3312, 3415, and 3470 cm−1 corresponding to the stretching vibrations of primary and secondary amine. The peaks observed at 147.0 and 148.5 ppm are attributed to the new aliphatic hydroxyl groups formed by the methylolation of LM. One exothermic peak was observed in the DSC analysis indicating a one cross-linking reaction.

2012 ◽  
Vol 519 ◽  
pp. 6-9 ◽  
Author(s):  
Wei Li ◽  
Xing Xiang Zhang ◽  
Xue Chen Wang

The phase change materials (PCMs) can absorb, store or release large latent heat over a defined temperature range while the materials change phase or state, so they can be potentially used in thermal energy storage. In this paper, a series of microencapsulated phase change materials (MicroPCMs) with n-octadecane and n-dodecanol as core were successfully fabricated respectively, where the styrene-based copolymer, acrylic based copolymer, melamine-formaldehyde resin and polyurea were selected as shell materials. The morphology of these MicroPCMs was observed by scanning electron microscopy (SEM), and the core-shell structure and the shell thickness of microcapsules were also characterized by SEM. In addition, the phase change properties of MicroPCMs were investigated using differential scanning calorimetry (DSC) analysis. Furthermore, thermal-regulated calcium alginate fiber was produced by adding MicroPCMs in wet-spinning process; and the effects of various types of MicroPCMs on fiber was discussed.


Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2575
Author(s):  
Smaher M. Elbayomi ◽  
Haili Wang ◽  
Tamer M. Tamer ◽  
Yezi You

The preparation of bioactive polymeric molecules requires the attention of scientists as it has a potential function in biomedical applications. In the current study, functional substitution of alginate with a benzoyl group was prepared via coupling its hydroxyl group with benzoyl chloride. Fourier transform infrared spectroscopy indicated the characteristic peaks of aromatic C=C in alginate derivative at 1431 cm−1. HNMR analysis demonstrated the aromatic protons at 7.5 ppm assigned to benzoyl groups attached to alginate hydroxyl groups. Wetting analysis showed a decrease in hydrophilicity in the new alginate derivative. Differential scanning calorimetry and thermal gravimetric analysis showed that the designed aromatic alginate derivative demonstrated higher thermo-stability than alginates. The aromatic alginate derivative displayed high anti-inflammatory properties compared to alginate. Finally, the in vitro antioxidant evaluation of the aromatic alginate derivative showed a significant increase in free radical scavenging activity compared to neat alginate against DPPH (2,2-diphenyll-picrylhydrazyl) and ABTS free radicals. The obtained results proposed that the new alginate derivative could be employed for gene and drug delivery applications.


2006 ◽  
Vol 11 (4) ◽  
pp. 332-336 ◽  
Author(s):  
Jun-Seok Hwang ◽  
Jin-Nam Kim ◽  
Young-Jung Wee ◽  
Jong-Sun Yun ◽  
Hong-Gi Jang ◽  
...  

Materials ◽  
2019 ◽  
Vol 12 (4) ◽  
pp. 664 ◽  
Author(s):  
Iwona Karbownik ◽  
Olga Rac-Rumijowska ◽  
Marta Fiedot-Toboła ◽  
Tomasz Rybicki ◽  
Helena Teterycz

The paper presents a method of modifying polyacrylonitrile (PAN) fibers using polyaniline (PANI). The PAN fibers were doped with polyaniline that was obtained in two different ways. The first consisted of doping a spinning solution with polyaniline that was synthesized in an aqueous solution (PAN/PANI blended), and the second involved the synthesis of polyaniline directly in the spinning solution (PAN/PANI in situ). The obtained fibers were characterized by the methods: X-ray powder diffraction (XRD), scanning electron microscope (SEM), fourier-transform infrared spectroscopy (FTIR), thermogravimetry (TG) and differential scanning calorimetry (DSC). Analysis of the results showed strong interactions between the nitrile groups of polyacrylonitrile and polyaniline in the PAN/PANI in situ fibers. The results of mechanical strength tests indicated that the performance of the PAN/PANI mixture significantly improved the mechanical parameters of polyaniline, although these fibers had a weaker strength than the unmodified PAN fibers. The fibers obtained as a result of the addition of PANI to PAN were dielectric, whereas the PANI-synthesized in situ were characterized by a mass-specific resistance of 5.47 kΩg/cm2.


e-Polymers ◽  
2006 ◽  
Vol 6 (1) ◽  
Author(s):  
J. L. Feng ◽  
C. Y. Yue ◽  
K. S. Chian

AbstractThis project aims to develop and characterize a series of bismaleimide (BMI) polymers based on maleic anhydride and aliphatic-ether diamines. The effects of varying the chain length of aliphatic-ether diamines on the resultant bismaleimide systems were evaluated so that their suitability for microelectronics applications could be evaluated. The synthetic reaction and properties of the bismaleimide materials were investigated using Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), Thermo- Gravimetric Analysis (TGA), Dielectric Thermal Analysis (DEA) and rheometry. Results showed that thermal, dielectric and rheological properties were all affected by the main chain length of BMI. The magnitude of the dielectric constant at 100 kHz increases with the increasing chain length. The curing peak temperature, curing heat and degradation temperature of BMI, all decrease with the increasing chain length.


Author(s):  
Guihong Han ◽  
Tao Jiang ◽  
Guanghui Li ◽  
Yanfang Huang ◽  
Yuanbo Zhang

Characterization of modified humic substances based binders for iron ore agglomeration was examined by chemical analysis, optical density, Fourier transform infrared spectrum (FTIR), and thermogravimetry and differential scanning calorimetry (TG–DSC). Chemical analysis displays the proportion of fulvic acid (FA) to humic acid (HA) in the binder is 1:10. Compared with the HA, the FA possesses more functional groups. Meantime, optical density ratio analysis shows that the molecular weight and aromatization degree of the FA are smaller than those of the HA. FTIR spectra further confirm aromatic and aliphatic fractions are associated with various types of oxygen-rich groups including carboxyl and hydroxyl groups. TG–DSC and chemical analysis indicate structural changes of the binder including thermal decomposition, dehydroxylation and/or decarboxylation are caused during heating. The structural characterization of the binder ensures its good performance in the field of iron ore agglomeration.


2008 ◽  
Vol 62 (4) ◽  
Author(s):  
Hamada Abdel-Razik

AbstractSynthesis, characterization and application of diaminomaleonitrile (DAMN)-functionalized polystyrene grafts were studied. Dibenzoyle peroxide (BP) was used as an initiator. Optimum conditions for grafting were found to be c(DAMN) = 0.5 M, c(BP) = 0.016 M, θ = 85 °C and t = 4 h. Water uptake of the polystyrene graft membranes was found to increase with the increase of the grafting yield. The chemical structure, thermal characteristics and thermal stability of the obtained membranes were investigated by means of FTIR spectroscopy, differential scanning calorimetry, and thermal gravimetric analysis. Polystyrene graft membrane with the degree of grafting of up to 96 % was found to be useful for the pervaporation separation of phenol/water mixtures.


2012 ◽  
Vol 488-489 ◽  
pp. 506-510 ◽  
Author(s):  
Sikander Rafiq ◽  
Zakaria Man ◽  
Abdulhalim Maulud ◽  
Nawshad Muhammad ◽  
Saikat Maitra

Composite membranes were prepared by incorporating inorganic silica nanoparticles into blends of polysulfone/polyimide (PSF/PI) membranes via sol-gel route. Morphological structures of the developed membranes were carried out by scanning electron microscopy (SEM). Spectroscopic analysis of the hybrid membranes were done by fourier transform infrared spectroscopy (FTIR) analysis. Differential scanning calorimetry (DSC) analysis shows that the glass transition temperature (Tg) increased from 209oC to 238oC in the hybrid membranes followed by thermogravimetric analysis (TGA) that showed significant improvement in thermal stability of the developed membranes.


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