Ground tire rubber (GTR) surface modification using thiol-ene click reaction: Polystyrene grafting to modify a GTR/polystyrene (PS) blend

2019 ◽  
Vol 36 (2) ◽  
pp. 81-101
Author(s):  
Huan Liang ◽  
Jacob Dion Gagné ◽  
Adrien Faye ◽  
Denis Rodrigue ◽  
Josée Brisson

In this work, a thiol-ene click reaction was used to graft polystyrene (PS) chains onto the surface of ethylene propylene diene monomer-based ground tire rubber (GTR). A thiol-terminated PS (11 kg mol−1) was selected, due to its commercial availability, to modify a postconsumer GTR. The resulting PS-grafted GTR (GTR- g-PS) particles were analyzed via Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) to detect surface changes on treated samples. An increase in aliphatic and aromatic carbon atoms was observed by FTIR and XPS, while grafted material was observed by SEM on the GTR surface, confirming that grafting took place. Then, composites were prepared from these GTR- g-PS particles and from PS by solution evaporation, at 50 wt%. A significant increase in tensile (20%) and storage moduli (from 80% at 65°C to 510% at 95°C) was observed by dynamic mechanical thermal analysis when compared to composites prepared with untreated GTR. In addition, GTR samples showed improved thermal resistance, as attested by the shift in degradation temperature for 10% mass loss (from 400°C for GTR to 450°C for GTR- g-PS). This increases the possible range of processing temperature and service temperature (applications) for introduction of GTR in other polymer matrices.

BMC Chemistry ◽  
2020 ◽  
Vol 14 (1) ◽  
Author(s):  
Fereshteh Norouzi ◽  
Shahrzad Javanshir

AbstractA hybrid magnetic material γFe2O3@Sh@cu2O was easily prepared from Shilajit (Sh) decorated Fe3O4 and copper acetate. The prepared magnetic hybrid material was fully characterized using different analysis, including Fourier transform infrared (FT-IR), X-ray diffraction (XRD), inductively coupled plasma (ICP), scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM) thermal gravimetric analysis (TGA) and Brunauer–Emmett–Teller (BET). All these analysis revealed that during coating of Fe3O4@Sh using copper salt (II), synchronized redox sorption of CuII to CuI occurs at the same time as the oxidation of Fe3O4 to γFe2O3. This magnetic catalyst exhibited excellent catalytic activity for regioselective synthesis of 1,4-disubstituted-1,2,3-triazoles via one pot three-component click reaction of sodium azide, terminal alkynes and benzyl halides in the absence of any reducing agent. High yields, short reaction time, high turnover number and frequency (TON = 3.5 * 105 and TOF = 1.0 * 106 h−1 respectively), easy separation, and efficient recycling of the catalyst are the strengths of the present method.


2019 ◽  
Vol 75 (8) ◽  
pp. 1053-1059 ◽  
Author(s):  
Lin-Lu Qian ◽  
Zhi-Xiang Wang ◽  
Hai-Xin Tian ◽  
Min Li ◽  
Bao-Long Li ◽  
...  

Metal–organic frameworks (MOFs) have attracted much interest in the fields of gas separation and storage, catalysis synthesis, nonlinear optics, sensors, luminescence, magnetism, photocatalysis gradation and crystal engineering because of their diverse properties and intriguing topologies. A Cu–MOF, namely poly[[(μ2-succinato-κ2 O:O′){μ2-tris[4-(1,2,4-triazol-1-yl)phenyl]amine-κ2 N:N′}copper(II)] dihydrate], {[Cu(C4H4O4)(C24H18N10)]·2H2O} n or {[Cu(suc)(ttpa)]·2H2O} n , (I), was synthesized by the hydrothermal method using tris[4-(1,2,4-triazol-1-yl)phenyl]amine (ttpa) and succinate (suc2−), and characterized by IR, powder X-ray diffraction (PXRD), luminescence, optical band gap and valence band X-ray photoelectron spectroscopy (VB XPS). Cu–MOF (I) shows a twofold interpenetrating 4-coordinated three-dimensional CdSO4 topology with point symbol {65·8}. It presents good photocatalytic degradation of methylene blue (MB) and rhodamine B (RhB) under visible-light irradiation. A photocatalytic mechanism was proposed and confirmed.


Fuel ◽  
2004 ◽  
Vol 83 (14-15) ◽  
pp. 2041-2049 ◽  
Author(s):  
F.J. Navarro ◽  
P. Partal ◽  
F. Martı́nez-Boza ◽  
C. Gallegos

2017 ◽  
Vol 37 (2) ◽  
pp. 169-176 ◽  
Author(s):  
Jian Xiaoxia ◽  
Hu Yiwen ◽  
Zheng Qilong

Abstract This paper describes the influence of thermal processing temperature on the microphase separation, hydrogen bonding, phase transitions and mechanical properties of 3,3-bis(azidomethyl)oxetane (BAMO)/tetrahydrofuran (THF) polyurethane binder, which is used for propellant. Fourier transform infrared (FTIR) spectroscopy confirmed that the intended polyurethane was synthesized and was used to determine the state of the local hydrogen bonding in these polyurethanes. The results showed that the thermal processing clearly imparts significant changes to the H-bonded environment and this was confirmed in a quantitative fashion using small-angle X-ray scattering (SAXS). The dynamic mechanical analysis (DMA) revealed rather significant changes in dynamic segmental relaxations and storage moduli for this series of BAMO/THF polyurethanes, which are in keeping with the findings from other experiments.


2001 ◽  
Vol 688 ◽  
Author(s):  
Zhiqiang Wei ◽  
Minoru Noda ◽  
Masanori Okuyama

AbstractBaTiO3 (BTO) thin films with perovskite structure have been prepared on Pt/Ti/SiO2/Si substrates using a combined process of a conventional MOD (metal organic decomposition) process and a hydrothermal treatment. The BTO thin films with polycrystalline structure are grown on Pt/Ti/SiO2/Si substrates at a processing temperature of 140°C. The structural development, stoichiometry, spectroscopic, and dielectric properties of the BTO thin films have been systematically investigated. X-ray diffraction patterns show that well-developed crystallites with a pure perovskite phase have been formed. ICP (Inductively coupled plasma) and XPS (x-ray photoelectron spectroscopy) results show that stoichiometric BTO thin films were obtained.


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