Influence of functional group distribution on the thermal stability and catalytic activity of sulfonated styrene-DVB-copolymers

1984 ◽  
Vol 6 (S19841) ◽  
pp. 211-226 ◽  
Author(s):  
J. Klein ◽  
H. Widdecke ◽  
N. Bothe
Keyword(s):  
Thermal Stability ◽  
Catalytic Activity ◽  
Functional Group ◽  
Group Distribution

Catalytic activity of niobium oxynitride and carbide I. Preparation, characterization and thermal stability of finely divided niobium oxynitrides

1994 ◽  
Vol 119 (2) ◽  
pp. 223-240 ◽  
Author(s):  
Hak Soo Kim ◽  
Chae Ho Shin ◽  
Guy Bugli ◽  
Monique Bureau-Tardy ◽  
Gerald Djega-Mariadassou
Keyword(s):  
Thermal Stability ◽  
Catalytic Activity ◽  
Thermal Stability Of

scholarly journals Influence of Water Activity on Protease Adsorbed on Biochar in Organic Solvents

2017 ◽  
Vol 6 (4) ◽  
pp. 96 ◽  
Author(s):  
Hidetaka Noritomi ◽  
Jumpei Nishigami ◽  
Nobuyuki Endo ◽  
Satoru Kato ◽  
Katsumi Uchiyama
Keyword(s):  
Thermal Stability ◽  
Catalytic Activity ◽  
Organic Solvents ◽  
Water Activity ◽  
Initial Rate ◽  
Butyl Ester ◽  
Nitrogen Atmosphere ◽  
Bamboo Charcoal ◽  
Influence Of Water ◽  
Hydrolysis Of

We have found that the organic solvent-resistance of Alpha-chymotrypsin (Alpha-CT) is enhanced by adsorbing Alpha-CT onto bamboo charcoal powder (BCP), which is obtained by pyrolyzing bamboo waste under nitrogen atmosphere, and is markedly dependent on the thermodynamic water activity (aw) in organic solvents. When BCP-adsorbed　Alpha-CT was immersed in acetonitrile at an appropriate water activity, it effectively enhanced the transesterification of N-acetyl-L-tyrosine ethyl ester (N-Ac-Tyr-OEt) with n-butanol (BuOH) to produce N-acetyl-L-tyrosine butyl ester (N-Ac-Tyr-OBu), compared to the hydrolysis of N-Ac-Tyr-OEt with water to give N-acetyl-L-tyrosine (N-Ac-Tyr-OH). When the water activity was 0.28, the initial rate of transesterification catalyzed by BCP-adsorbed Alpha-CT was about sixty times greater than that catalyzed by free Alpha-CT. Regarding the reaction selectivity which is defined as a ratio of the initial rate of transesterification to that of hydrolysis, BCP-adsorbed α-CT was much superior to free Alpha-CT. The catalytic activity of BCP-adsorbed Alpha-CT was markedly dependent on the reaction temperature. Furthermore, concerning the thermal stability at 50 oC, the half-life of BCP-adsorbed Alpha-CT exhibited 3.8-fold, compared to that of free Alpha-CT.

scholarly journals ANALISIS KONDUKTIVITAS DAN TERMAL PADA POLIMER ELEKTROLIT DARI KITOSAN/PVA/GLISEROL/LiClO4 UNTUK APLIKASI BATERAI ION LITIUM

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Nurhadini . ◽  
Verry Andre Fabiani ◽  
Megawati Ayu Putri ◽  
Iin Lestari
Keyword(s):  
Thermal Stability ◽  
Polymer Electrolyte ◽  
Functional Group ◽  
Raw Materials ◽  
Lithium Ion ◽  
Electrolyte Composition ◽  
Wave Number ◽  
Natural Polymers ◽  
Casting Method ◽  
Absorption Intensity

Penggunaan polimer ramah lingkungan merupakan tantangan bagi industri baterai ion litium saat ini dikarenakan sifatnya yang mudah terbiodegradasi menjadi keunggulan polimer alam seperti kitosan dengan bahan baku dari alam yang melimpah. Komposisi polimer elektrolit dalam penelitian ini terdiri atas kitosan, PVA, gliserol yang didopan dengan LiClO4. Penelitian ini bertujuan untuk menganalisis sifat konduktivitas dan termal dari polimer elektrolit kitosan/PVA/gliserol/LiClO4. Pembuatan polimer elektrolit ini menggunakan metode casting. Peningkatan massa kitosan dalam komposisi polimer elektrolit menyebabkan adanya peningkatan intensitas pada bilangan gelombang 1718 cm-1 dan peningkatan intensitas serapan pada bilngangan gelombang 1271 cm-1 dengan masing-masing puncak serapan tersebut adalah gugus fungsi dari C=O dan gugus fungsi C-O.  Berdasarkan data konduktivitas menunjukkan bahwa komposisi 70/30/20/20 (kitosan /PVA/Gliserol/LiClO4) memiliki konduktivitas tertinggi sebesar 4,8 x 10-5S/cm. Hasil kurva TGA menunjukkan stabilitas termal komposisi polimer elektrolit hingga 210oC dan peningkatan jumlah kitosan dalam polimer elektrolit menurunkan kestabilan termal. Polimer elektrolit dari kitosan/PVA/Gliserol/LiClO4 dapat diaplikasikan untuk baterai ion litium berdasarkan analisis konduktivitas ionik dan kestabilan termal. ABSTRACT The use of environmentally friendly polymers is a challenge for the lithium-ion batteries industry today because its biodegradable nature is an advantage of natural polymers such as chitosan with abundant raw materials from nature. The polymer electrolyte composition in this study consisted of chitosan, PVA, glycerol doped with LiClO4. This study aims to analyze the conductivity and thermal properties of the polymer electrolyte chitosan/PVA/Glycerol/LiClO4. The polymer electrolyte was made using a casting method. The increasing of the chitosan mass in the polymer electrolyte composition led to an increase in intensity at the wave number 1718 cm-1 and an increase in absorption intensity at the wavenumber of 1271 cm-1 with absorption peaks being a functional group of C=O and C-O respectively. Based on the conductivity data, it showed that the composition of 70/30/20/20 (chitosan/PVA/Glycerol/LiClO4) had the highest conductivity of 4.8 x 10-5S/cm. The results of the TGA curve illustrated that polymer electrolyte had thermal stability until 210oC and the increasing amount of chitosan of polymer electrolyte decreased thermal stability. Polymer electrolyte chitosan

scholarly journals Preparation and Characteristics of an Environmentally Friendly Hyperbranched Flame-Retardant Polyurethane Hybrid Containing Nitrogen, Phosphorus, and Silicon

Polymers ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 720 ◽  
Author(s):  
Chen ◽  
Chiang
Keyword(s):  
Thermal Stability ◽  
Flame Retardant ◽  
Hybrid Material ◽  
Functional Group ◽  
Condensation Reaction ◽  
Sol Gel ◽  
Decomposition Temperature ◽  
Limiting Oxygen Index ◽  
Raman Analysis ◽  
Ring Opening Reaction

The NCO functional group of 3-isocyanatoproplytriethoxysilane (IPTS) and the OH functional group of 10-(2,5-dihydroxyphenyl)-10H-9-oxa-10-phospha-phenantbrene-10-oxide (DOPO-BQ) were used to conduct an addition reaction. Following completion of the reaction, triglycidyl isocyanurate (TGIC) was introduced to conduct a ring-opening reaction. Subsequently, a sol–gel method was used to initiate a hydrolysis–condensation reaction on TGIC–IPTS–DOPO-BQ to form a hyperbranched nitrogen–phosphorous–silicon (HBNPSi) flame retardant. This flame retardant was incorporated into a polyurethane (PU) matrix to prepare a hybrid material. Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), limiting oxygen index (LOI), UV-VIS spectrophotometry, and Raman analysis were conducted to characterize the structure and analyze the transparency, thermal stability, flame retardancy, and residual char to understand the flame retardant mechanism of the prepared hybrid material. After the flame retardant was added, the maximum degradation rate decreased from −36 to −17 wt.%/min, the integral procedural decomposition temperature (IPDT) increased from 348 to 488 °C, and the char yield increased from 0.7 to 8.1 wt.%. The aforementioned results verified that the thermal stability of PU can be improved after adding HBNPSi. The LOI analysis indicated that the pristine PU was flammable because the LOI of pristine PU was only 19. When the content of added HBNPSi was 40%, the LOI value was 26; thus the PU hybrid became nonflammable.

Enhanced catalytic activity with high thermal stability based on multiple Au cores in the interior of mesoporous Si–Al shells

RSC Advances ◽  
2015 ◽  
Vol 5 (60) ◽  
pp. 48187-48193 ◽  
Author(s):  
Yiwei Zhang ◽  
Sanming Xiang ◽  
Yuming Zhou ◽  
Yuanmei Xu ◽  
Zewu Zhang ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Catalytic Activity ◽  
High Activity ◽  
High Thermal Stability

Mesoporous Si–Al/Au nanocatalysts were synthesized by combining the advantage of good permeability from mesoporous Si–Al shells and the high activity upon multiple Au cores.

scholarly journals The Sintering of Au Nanoparticles on Flat {100}, {111} and Zigzagged {111}-Nanofacetted Structures of Ceria and Its Influence on Catalytic Activity in CO Oxidation and CO PROX

2020 ◽  
Author(s):  
O. S. Bezkrovnyi ◽  
P. Kraszkiewicz ◽  
W. Mista ◽  
L. Kepinski
Keyword(s):  
Electron Microscopy ◽  
Thermal Stability ◽  
Catalytic Activity ◽  
Beneficial Effect ◽  
Co Oxidation ◽  
Au Nanoparticles ◽  
Ceria Support ◽  
Ceria Catalysts ◽  
Thermal Stability Of

Abstract The thermal stability of Au nanoparticles on ceria support of various morphology (nanocubes, nanooctahedra, and {111}-nanofacetted nanocubes) in oxidizing and reducing atmospheres was investigated by electron microscopy. A beneficial effect of the reconstruction of edges of ceria nanocubes into zigzagged {111}-nanofacetted structures on the inhibition of sintering of Au nanoparticles was shown. The influence of different morphology of Au particles on various ceria supports on the reducibility and catalytic activity in CO oxidation, and CO PROX of Au/ceria catalysts was also investigated and discussed. It was shown, that ceria nanocubes with flat {110} terminated edges are more suitable as a support for Au nanoparticles, used to catalyze CO oxidation, than zigzagged {111}- nanofacetted structures. Graphic Abstract

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