scholarly journals Surface Modification of Cellulose Nanocrystals with Succinic Anhydride

Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 866 ◽  
Author(s):  
Agnieszka Leszczyńska ◽  
Paulina Radzik ◽  
Ewa Szefer ◽  
Matej Mičušík ◽  
Mária Omastová ◽  
...  

The surface modification of cellulose nanocrystals (CNC) is a key intermediate step in the development of new functionalities and the tailoring of nanomaterial properties for specific applications. In the area of polymeric nanocomposites, apart from good interfacial adhesion, the high thermal stability of cellulose nanomaterial is vitally required for the stable processing and improvement of material properties. In this respect, the heterogeneous esterification of CNC with succinic anhydride was investigated in this work in order to obtain CNC with optimised surface and thermal properties. The influence of reaction parameters, such as time, temperature, and molar ratio of reagents, on the structure, morphology and thermal properties, were systematically studied over a wide range of values by DLS, FTIR, XPS, WAXD, SEM and TGA methods. It was found that the degree of surface substitution of CNC increased with the molar ratio of succinic anhydride to cellulose hydroxyl groups (SA:OH), as well as the reaction time, whilst the temperature of reaction showed a moderate effect on the degree of esterification in the range of 70–110 °C. The studies on the thermal stability of modified nanoparticles indicated that there is a critical extent of surface esterification below which only a slight decrease of the initial temperature of degradation was observed in pyrolytic and oxidative atmospheres. A significant reduction of CNC thermal stability was observed only for the longest reaction time (240 min) and the highest molar ratio of SA:OH. This illustrates the possibility of manufacturing thermally stable, succinylated, CNC by controlling the reaction conditions and the degree of esterification.

2011 ◽  
Vol 415-417 ◽  
pp. 261-264
Author(s):  
Yuan Ren ◽  
Zheng Xi ◽  
Wen Jun Gan ◽  
Liang Zhang ◽  
Jing Zhang ◽  
...  

A siloxane-containing dianhydride, succinic anhydride terminated polydimethylsiloxane (DMS-Z21) was selected to cure diglycidyl ether of bisphenol-A based epoxy resin (DGEBA). The cure kinetics and thermal properties were investigated by nonisothermal and isothermal differential scanning calorimetry (DSC) and thermogravimetric analyses (TGA), respectively. The activation energy (Ea) of the curing reaction was obtained based on the methods of Kissinger and isothermal measurements. The results of the thermogravimetric analyses of the DGEBA/DMS-Z21 system showed that the thermal stability of the DGEBA/DMS-Z21 system was slightly higher than the DGEBA/MeTHPA system.


2019 ◽  
Vol 140 (1) ◽  
pp. 189-198 ◽  
Author(s):  
Marta Worzakowska

Abstract The thermal properties together with the identification of the emitted volatiles during heating of the starch-graft-poly(geranyl methacrylate) copolymers with the use of a TG/FTIR-coupled method and some of the physicochemical properties of the copolymers were determined. It was found that the use of the geranyl methacrylate monomer to the graft copolymerization with potato starch allowed to replace ca. 1.46 hydroxyl groups per glycosidic units of starch macromolecule by the poly(geranyl methacrylate) chains under the optimal reaction conditions. Generally, all tested starch graft copolymers exhibited a significant increase in polar solvent resistance, moisture resistance and chemical stability as compared to potato starch. However, the thermal stability of the obtained materials was substantially lower as compared to the thermal stability of potato starch. The beginning of the decomposition of the copolymers was observed below 150 °C. It was due to low thermal stability of the poly(geranyl methacrylate) chains. The decomposition of the prepared materials runs at least four, unseparated stages. The first stage was visible up to 220–240 °C. It was connected with the emission of some aldehyde, acid, alcohol, alkene, ester fragments, H2O and CO2 as a result of the depolymerization, destruction and partial decarboxylation of the poly(geranyl methacrylate) chains. The second stage was spread between ca. 220–240 and 358–375 °C. The emission of organic, saturated, unsaturated, aromatic, oxygen-rich fragments, CO, CO2 and H2O as a result of the decomposition and dehydration of starch was confirmed. Heating of the studied materials between 358–375 and 455–477 °C resulted in subsequent decomposition processes of the residues and the creation of some oxygen-rich saturated and unsaturated fragments, CO, CO2, H2O and CH4. Finally, above 455–477 °C, a minor mass loss as a result of the decomposition processes of the residues formed before was observed. The emission of CO, CO2, H2O, CH4 and some oxygen-rich saturated and unsaturated fragments was confirmed.


2021 ◽  
Author(s):  
Ahlem Bendaoued ◽  
Mouna Messaoud ◽  
Omar Harzallah ◽  
Sophie Bistac ◽  
Rached Salhi

Abstract Ceramics nanometric reinforced polymer composite is a significant material for catalysis, solar cells, production of hydrogen and energy applications, etc. In order to take benefit from the interesting mechanical properties and thermal stability of TiO2, these ceramic nanomaterials was synthesized by the Sol-Gel process in attempt to study the thermal stability, structure, and morphology of the resulting nanoparticles powders. The obtained results revealed that, the sphere is composed of 20-30 nm nanoparticles with excellent thermal stability of nano-TiO2. This work focused on the thermal characterization and the study of nanocomposite xWt. %TiO2/PP (x=0, 2.5, 5, 7.5 mol%). In this study, the obtained results revealed that the molar ratio of TiO2 influences the final thermal stability and degree of crystallinity of the composite. It was found that the use of TiO2 seems to be an effective and very promising way to increase the thermal properties of the resulting composite. The greatest degree of crystallinity (54.80%) and thermal degradation stability are obtained for composite reinforced by 7.5Wt. %TiO2.


2019 ◽  
Vol 10 (4) ◽  
pp. 63-76
Author(s):  
Wei Keat Ng ◽  
Wen Shyang Chow ◽  
Hanafi Ismail

Cellulose nanocrystals were extracted from agricultural waste corn cob using acid hydrolysis followed by freeze drying. Poly(lactic acid)/corn cob cellulose nanocrystals (PLA/CCNC) composites were prepared using solvent casting. The properties of CCNC were characterized using transmission electron microscope (TEM), zeta potential analyzer, and thermogravimetric analyzer (TGA). The effects of CCNC on the thermal properties of PLA were examined using differential scanning calorimetry (DSC) and TGA. From the SEM and TEM results, the irregular shaped and micron-sized corn cob powder was transformed to needle-like shaped nanocellulose (aspect ratio approximately 30.80) after the acid hydrolysis process. TGA results show that the thermal stability of CCNC is higher than that of corn cob powder. The zeta potential of CCNC is −24.6 mV, which indicates there is a repulsion force between the individual CCNC and making them disperse uniformly and stable in aqueous media. DSC and TGA results show that the crystallinity and thermal stability of PLA were increased by the incorporation of CCNC. This demonstrates that the CCNC is a potential bio-nanofiller with good thermal stability and nucleating-ability for PLA.


2018 ◽  
Vol 663 ◽  
pp. 145-156 ◽  
Author(s):  
Agnieszka Leszczyńska ◽  
Paulina Radzik ◽  
Katarzyna Haraźna ◽  
Krzysztof Pielichowski

Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2254
Author(s):  
Adeleke A. Oyekanmi ◽  
N. I. Saharudin ◽  
Che Mohamad Hazwan ◽  
Abdul Khalil H. P. S. ◽  
Niyi G. Olaiya ◽  
...  

Hydrophilic behaviour of carrageenan macroalgae biopolymer, due to hydroxyl groups, has limited its applications, especially for packaging. In this study, macroalgae were reinforced with cellulose nanofibrils (CNFs) isolated from kenaf bast fibres. The macroalgae CNF film was after that treated with silane for hydrophobicity enhancement. The wettability and functional properties of unmodified macroalgae CNF films were compared with silane-modified macroalgae CNF films. Characterisation of the unmodified and modified biopolymers films was investigated. The atomic force microscope (AFM), SEM morphology, tensile properties, water contact angle, and thermal behaviour of the biofilms showed that the incorporation of Kenaf bast CNF remarkably increased the strength, moisture resistance, and thermal stability of the macroalgae biopolymer films. Moreover, the films’ modification using a silane coupling agent further enhanced the strength and thermal stability of the films apart from improved water-resistance of the biopolymer films compared to unmodified films. The morphology and AFM showed good interfacial interaction of the components of the biopolymer films. The modified biopolymer films exhibited significantly improved hydrophobic properties compared to the unmodified films due to the enhanced dispersion resulting from the silane treatment. The improved biopolymer films can potentially be utilised as packaging materials.


2018 ◽  
Vol 9 (1) ◽  
pp. 39-49 ◽  
Author(s):  
Sharifah Nurul Ain Syed Hashim ◽  
Sarani Zakaria ◽  
Chin Hua Chia ◽  
Sharifah Nabihah Syed Jaafar

In this study, soda alkali lignin from oil palm empty fruit bunch (EFB-AL) and kenaf core (KC-AL) are esterified with maleic anhydride under two different conditions, namely i) pyridine at temperature of 120°C for 3h and ii) aqueous alkaline solution at room temperature for 4h. As a result, the weight percentage gain (WPG) of the esterified EFB-AL (EFB-EL) and esterified KC-AL (KC-EL) in pyridine demonstrated a higher compared to aqueous alkaline solution. The FT-IR results of EFB-EL and KC-EL in both solvents exhibited some changes at the carbonyl and hydroxyl groups. Furthermore, the esterification process induced the carboxylic peak to appear in both alkali lignin samples. The outcome is confirmed by conducting H-NMR analysis, which demonstrated ester and carboxylic acid peaks within the spectral analysis. Finally, the TGA results showed both EFB-EL and KC-EL that are exposed to aqueous alkaline actually possessed better thermal stability and higher activation energy (Ea) compared to the esterified samples in pyridine.


Author(s):  
Hongtao Zhang ◽  
Youjing Zhao ◽  
Jingli Li ◽  
Lijie Shi ◽  
Min Wang

AbstractThis paper focuses on thermal stability of molten salts, operating temperature range and latent heat of molten salts at a high temperature. In this experiment, multi-component molten salts (purified Solar Salt) composed of purified NaNO


Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1278
Author(s):  
Mariana E. Ghica ◽  
Cláudio M.R. Almeida ◽  
Mariana Fonseca ◽  
António Portugal ◽  
Luísa Durães

The present work describes for the first time the preparation of silica-based aerogel composites containing tetraethoxysilane (TEOS) and vinyltrimethoxysilane (VTMS) reinforced with Kevlar® pulp. The developed system was extensively investigated, regarding its physical, morphological, thermal and mechanical features. The obtained bulk density values were satisfactory, down to 208 kg·m−3, and very good thermal properties were achieved—namely a thermal conductivity as low as 26 mW·m−1·K−1 (Hot Disk®) and thermal stability up to 550 °C. The introduction of VTMS offers a better dispersion of the polyamide fibers, as well as a higher hydrophobicity and thermal stability of the composites. The aerogels were also able to withstand five compression-decompression cycles without significant change of their size or microstructure. A design of experiment (DOE) was performed to assess the influence of different synthesis parameters, including silica co-precursors ratio, pulp amount and the solvent/Si molar ratio on the nanocomposite properties. The data obtained from the DOE allowed us to understand the significance of each parameter, offering reliable guidelines for the adjustment of the experimental procedure in order to achieve the optimum properties of the studied aerogel composites.


Materials ◽  
2020 ◽  
Vol 13 (2) ◽  
pp. 309
Author(s):  
Yurong Wu ◽  
Longshan Xu ◽  
Yanying Jiang

A uniform, monodispersed superfine cuprous oxide (Cu2O) sphere with a mean diameter of 850 nm has been synthesized by solution reduction. The study reported the synthesis and thermal properties of Cu2O/PP composites for the first time. The surface modification of the superfine Cu2O sphere was carried out by using a silane coupling agent KH-570. Fourier-transform infrared (FTIR) spectroscopy and the thermogravimetric analysis (TGA) curve revealed that the Cu2O had been successfully modified by silane coupling agent KH570. The scanning electron microscope (SEM) shows that the modified Cu2O can be uniformly dispersed in the polypropylene (PP) matrix, because through surface modification, there are some active functional groups on its surface, such as the ester group, which improves its compatibility with the PP matrix. The thermal stability of Cu2O/PP composites was improved by adding a small amount of Cu2O (1 wt % of PP). Therefore, based on the potential bacteriostasis of cuprous oxide, the low cost of PP and the results of this study, it is predicted that Cu2O/PP composites can be used in infant preparation (such as milk bottles) with low cost and good thermal stability in the near future.


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