Thermostable birefringent copolyimide films based on azobenzene-containing pyrimidine diamines

2017 ◽  
Vol 5 (39) ◽  
pp. 10375-10382 ◽  
Author(s):  
Faqin Tong ◽  
Zhao Chen ◽  
Xuemin Lu ◽  
Qinghua Lu

This work shows the key role played by the chemical structure of polyimides in the thermal stability of birefringence.

2021 ◽  
Author(s):  
Hongying Chu ◽  
Huabei Li ◽  
Xiaoyan Sun ◽  
Yaowang Zhang

Abstract In this paper, we synthesized a kind of bio-based plasticizer epoxidized linoleic acid cardanol ester(ELCE) from cardanol and linoleic acid. Its chemical structure was characterized with FT-IR and 1H NMR. Polyvinyl chloride(PVC) blends plasticized with ELCE were prepared via thermoplastic blending with torque rheometer. The performance including torque, mechanical property, thermal stability, plasticizing property and migration resistance of plasticized PVC blends were investigated and compared with plasticized PVC blends with commercial plasticizer dioctyl phthalate(DOP). The results showed that ELCE improved thermal stability of PVC blends. ELCE played more excellent plasticizing effect on PVC blends than DOP. The better solvent extraction resistance and volatile resistance of ELCE make it impossible to completely replace DOP in PVC products.


2012 ◽  
Vol 727-728 ◽  
pp. 1552-1556
Author(s):  
Renata Barbosa ◽  
Dayanne Diniz Souza ◽  
Edcleide Maria Araújo ◽  
Tomás Jefférson Alves de Mélo

Studies of degradation have verified that the decomposition of some quaternary ammonium salts can begin to be significant at the temperature of about 180 ° C and like most thermoplastics are processed at least around this temperature, the thermal stability of the salt in clay should always be considered. Some salts are more stable than others, being necessary to study the degradation mechanisms of each case. In this work, four quaternary ammonium salts were characterized by differential scanning calorimetry (DSC) and thermogravimetry (TG). The results of DSC and TG showed that the salts based chloride (Cl-) anion begin to degrade at similar temperatures, while the salt based bromide (Br-) anion degrades at higher temperature. Subsequently, a quaternary ammonium salt was chosen to be used in organoclays, depending on its chemical structure and its thermal behavior.


2015 ◽  
Vol 220-221 ◽  
pp. 218-223
Author(s):  
Tomasz Jan Kaldonski ◽  
Stanislaw Cudzilo

Some results of tests of the thermal stability (and volatility) of selected ionic liquids pondered as lubricating substances in comparison with typical lubricating, mineral and synthetic oils, are presented in the article. The research was carried out within the framework of PBR/15–249/2007/WAT–OR00002904 Research Project Financed by the Ministry of Science and Higher Education, during 2007–2011 [1]. The obtained results confirmed high thermal resistance of ionic liquids. It makes it possible to use the liquids as high temperature lubricating substances. At the same time, it has been stated that the thermal resistance of ionic liquids depends on the composition and chemical structure of anion and cation.


1981 ◽  
Vol 23 (5) ◽  
pp. 1204-1209 ◽  
Author(s):  
V.V Lisitskii ◽  
V.G Kalashnikov ◽  
V.P Biryukov ◽  
V.A Musikhin ◽  
K.S Minsker

Materials ◽  
2020 ◽  
Vol 13 (11) ◽  
pp. 2597
Author(s):  
Jakub Wręczycki ◽  
Dariusz M. Bieliński ◽  
Marcin Kozanecki ◽  
Paulina Maczugowska ◽  
Grzegorz Mlostoń

The superior ability of thiiranes (episulfides) to undergo ring-opening polymerization (ROP) in the presence of anionic initiators allows the preparation of chemically stable polysulfide homopolymers. Incorporation of elemental sulfur (S8) by copolymerization below the floor temperature of S8 permits the placement of a large quantity of sulfur atoms in the polysulfide mainchain. The utility of styrene sulfide (2-phenylthiirane; StS) for copolymerization with elemental sulfur is reported here. A few polysulfides differing depending on the initial ratio of S8 to StS and copolymerization time were synthesized. Various spectroscopic methods (1H NMR, 13C NMR, Raman spectroscopy and FTIR spectroscopy) were applied to characterize the chemical structure of the copolymers. Additionally, the phase structure and thermal stability of the synthesized polysulfides were investigated using DSC and TGA, respectively. The successful anionic copolymerization of styrene sulfide and elemental sulfur has been demonstrated.


2014 ◽  
Vol 9 (4) ◽  
pp. 155892501400900 ◽  
Author(s):  
Xuejia Li ◽  
Xin Wang ◽  
Qingqing Wang ◽  
Qufu Wei

A two-step process for preparing polyimide nanofiber was used in this work, and the nanofibers of precursor polyamic acid (PAA) were prepared by electrospinning. The polyimide nanofibers were obtained through thermal imidization at different thermal imidization temperatures. The influences of different imidization temperatures on morphology, chemical structure, thermal stability, and mechanical properties of the polyimide nanofibers were investigated by Fourier Transform Infrared Spectroscope (FT-IR), Scanning Electronic Microscopy (SEM), thermal gravimetric analysis (TGA) and Electromechanical Universal Testing Machine. The experimental results show that the imidization of PAA nanofibers was not complete under 290°C but complete under 350°C. With the rise of imidization temperature from 290 °C to 350°C, the polyimide nanofibers became thinner, and the thermal stability of polyimide nanofibers was also improved. The breaking strength and elongation at break of the nanofiber membranes increased at higher imidization temperature.


2019 ◽  
Vol 70 (2) ◽  
pp. 149-155
Author(s):  
Mohammad Ahmadi ◽  
Bita Moezzipour ◽  
Aida Moezzipour

In this study, thermal stability of fibers obtained from recycled MDF was investigated and compared with virgin fibers by using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). Two different methods, including electrical heating and hydrothermal treatment, were used for recycling the MDF wastes. Electrical heating method was performed at two different times (2 and 4 min) and hydrothermal method was done at three different temperatures (105, 125 and 150 °C). Chemical structure of wood fibers was also studied. TGA and DSC analysis showed higher weight loss of recycled fibers as compared to virgin fibers in a similar degradation region, which means that thermal stability of recycled fibers is lower than virgin fibers. In fact, thermal behavior of recycled fibers was medium between wood and UF resin. DSC analysis showed two exotherms at around 340 and 475 °C. The transition at around 340 °C in fibers thermogram was considered to be due to polysaccharides thermal deterioration and the exotherm at 475 °C was related to lignin carbohydrate complex deterioration. The results of chemical structure analysis showed that lignin and hemicellulose content of recycled fibers was significantly lower than that of virgin fibers, which resulted in decreased thermal stability.


1988 ◽  
Vol 134 ◽  
Author(s):  
Lisa R. Denny ◽  
Ivan J. Goldfarb ◽  
Edward J. Soloski

ABSTRACTOne of the primary factors influencing the research and development of rigid-rod polymers in the Materials Laboratory has been the excellent environmental resistance of this class of aromatic heterocyclic benzobisazole polymers. Thermal stability of these materials has been determined utilizing thermal analytical, Isothermal Aging and combined Thermal Gravimetric-Mass Spectrometry (TG-MS) techniques. Correlations between the thermal stability and chemical structure, varying substituent groups and processing conditions for these polymers have been observed. An overview of the thermal stability of these rigid-rod polymer systems is presented.


2009 ◽  
Vol 79-82 ◽  
pp. 1543-1546 ◽  
Author(s):  
Zhong Li Zhao ◽  
Zun Li Mo ◽  
Chao Feng ◽  
Jun Wang

A series of conductive composites polyaniline(PANI)-cellulose were heterogeneously synthesized by chemical oxidative polymerization of aniline with native cellulose pretreated by ultrasonic. The morphology and chemical structure of the composites were examined by SEM and FTIR. TGA was used to study their thermal properties. The electrical conductivity was measured at room temperature by the standard four-probe method. For the sake of illuminating the influence of ultrasonic pretreatment on the structure and properties of PANI-cellulose composites, the SEM microphotographs, FTIR spectrum and TG curve of the PANI-cellulose composites prepared with native cellulose without any treatment were also shown in this paper to serve as reference. The PANI content and electrical conductivity of these two composites were also compared. It was found that cellulose surface was severely eroded by ultrasonic wave, and PANI homogeneously dispersed on this eroded cellulose surface in the form of particles. In reverse, the PANI particles loaded on the surface of untreated cellulose with evident aggregation. The homogeneous dispersion of PANI particles would be favor for the improvement of the electrical conductivity of the composites. From the FTIR spectra, it was verified that there was no difference between these two composites. It indicated that ultrasonic force did not lead to the variation of the chemical structure of cellulose. TG curves revealed that the thermal stability of PANI-cellulose composites was obviously enhanced than pure cellulose due to the protection of PANI particles deposited on its surface. Nevertheless, ultrasonic has a negative effect on the thermal stability of the composites, which resulted in the long cellulose molecular chains change into shorter ones, so the decomposition of composite occurred at lower temperature. It was because that ultrasonic pretreatment contributed to the homogeneous dispersion of PANI and more PANI particle depositing on the cellulose surface. Therefore, the PANI-cellulose composites with ultrasonic pretreated cellulose have more PANI content and higher electrical conductivity than the composites with untreated cellulose. Moreover, the difference of these two factors between the two composites became more and more marked with increasing of the amount of aniline. When aniline used was up to 0.5 g, the PANI content in the former was 48.2% more than the latter. This work provided a facile method for the synthesis of PANI-cellulose conductive composites with excellent conductivity.


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