Studies of the hydrogen held by solids XXI. The interaction between ethylene and hydroxyl groups of a Y-zeolite at elevated temperatures

1972 ◽  
Vol 25 (1) ◽  
pp. 161-172 ◽  
Author(s):  
N CANT
1969 ◽  
Vol 73 (6) ◽  
pp. 2086-2088 ◽  
Author(s):  
John William Ward
Keyword(s):  

2016 ◽  
Vol 4 (15) ◽  
pp. 5632-5638 ◽  
Author(s):  
Jian He ◽  
Xiaolei Li ◽  
Dong Su ◽  
Huiming Ji ◽  
Xing Zhang ◽  
...  

Hexamethyl-disilazane (HMDS) is introduced to replace the hydroxyl groups of ZrO2–SiO2 aerogels (ZSAs) to form inert methyl siloxy surface groups and produce SiO2 particles as the “pinning” particles in air at elevated temperatures. Thus, HMDS/ZSAs exhibit an excellent thermal stability and super-hydrophobic properties with a contact angle of 154°.


2020 ◽  
Vol 62 (4) ◽  
pp. 81-87
Author(s):  
Indira N. Bakirova ◽  

Thermal stability of polyurethane varnish coating prepared by using diphenylolpropane, polyetherpolyol and polyisocyanate with an equimolar ratio of isocyanate and hydroxyl groups was assessed in the air. The polyurethane weight loss thermogram shows three temperature regions: I – (217-275)°С, II – (275-380)°С, and III – above 380°С. For interpreting thermogram of the polyurethane under study the model substances simulating the urethane groups of a polymer were synthesized. The substance containing the urethane group formed by phenolic hydroxyl of diphenylolpropane was shown to demonstrate relatively low thermal stability and gets broken down into isocyanate and bisphenol. Decomposition of the substance containing the urethane group formed by alcoholic hydroxyl occurs at the higher temperature. The data obtained allow interpreting the occurrence of thermal decomposition step I in TGA curve by structural changes in the blocks formed by diphenylolpropane and polyisocyanate being the least stable when exposed to elevated temperatures. The next step can be attributed to decomposition of more thermostable urethane groups formed by functional groups of oligooxypropylenetriol and polyisocyanate. Transition to the step III accompanied by severe sample weight loss due to decomposition of urethane groups is explained by thermal oxidation of oligoether units of polymer. Based on the data obtained the conclusion was made that the presence of urethane groups formed by phenolic hydroxyl of diphenylolpropane in polymer structure results in the decreased thermooxidative decomposition onset temperature of polymer. At the same time, a deceleration of thermooxidative processes due to the stabilizing effect of diphenylolpropane released at the beginning of thermal decomposition of polyurethane is observed in a high-temperature region. The proposed polyurethane coating is inferior to commercial counterparts in thermal decomposition onset temperature but superior to them in the temperature corresponding to a 50% polymer weight loss.


1959 ◽  
Vol 32 (2) ◽  
pp. 337-345 ◽  
Author(s):  
J. H. Saunders

Abstract Qualitative and quantitative studies with model compounds have shown that a variety of reactions may occur at 100–300° in molecules containing isocyanate, urea and urethane groups. All or most of these reactions are subject to catalysis so that they may be induced to proceed at lower temperatures. These reactions are quite important as they may affect the production and practical use of polyurethanes and polyureas. By the proper selection of reaction components one may design a polyurethane or polyurea molecule which will give both a reasonable rate of cure to the final state and a degree of temperature stability suitable for many rigorous applications. The choice of reactive groups providing approximately the desired rates of reaction and of suitable catalysts may be used to achieve the necessary curing rate. The initial choice of a catalyst which will have a minimum effect on decomposition reactions, or the removal of the catalyst from the cured polymer will favor polymer stability. A selection of reactants which will minimize those decomposition reactions leading to chain rupture, and which will compensate for what rupture may occur, will promote polymer stability. Simple illustrations of such choices would include eliminating tertiary aliphatic hydroxyl groups from the hydroxyl-bearing component and including some degree of branching commensurate with the degree of elasticity or rigidity desired. Branching should be achieved through the more stable groups, e.g., urethane, urea or trimer, rather than through the less stable allophanate and biuret groups. Many thoroughly tested applications of polyurethanes and mixed polyureaurethanes show that it is readily possible to produce such polymers with excellent thermal stability.


Materials ◽  
2019 ◽  
Vol 12 (24) ◽  
pp. 4043 ◽  
Author(s):  
Harmaen Ahmad Saffian ◽  
Kim Hyun-Joong ◽  
Paridah Md Tahir ◽  
Nor Azowa Ibrahim ◽  
Seng Hua Lee ◽  
...  

In this study, the effects of lignin modification on the properties of kenaf core fiber reinforced poly(butylene succinate) biocomposites were examined. A weight percent gain (WPG) value of 30.21% was recorded after the lignin were modified with maleic anhydride. Lower mechanical properties were observed for lignin composites because of incompatible bonding between the hydrophobic matrix and the hydrophilic lignin. Modified lignin (ML) was found to have a better interfacial bonding, since maleic anhydrides remove most of the hydrophilic hydrogen bonding (this was proven by a Fourier-transform infrared (FTIR) spectrometer—a reduction of broadband near 3400 cm−1, corresponding to the –OH stretching vibration of hydroxyl groups for the ML samples). On the other hand, ML was found to have a slightly lower glass transition temperature, Tg, since reactions with maleic anhydride destroy most of the intra- and inter-molecular hydrogen bonds, resulting in a softer structure at elevated temperatures. The addition of kraft lignin was found to increase the thermal stability of the PBS polymer composites, while modified kraft lignin showed higher thermal stability than pure kraft lignin and possessed delayed onset thermal degradation temperature.


1960 ◽  
Vol 13 (4) ◽  
pp. 567 ◽  
Author(s):  
BM Lynch ◽  
RA Durie

A study was made of the products formed by treating brown coal or lignin with concentrated aqueous or ethanolic alkali at 200 �C. With brown coals a major redistribution of the oxygen-containing functional groups appeared to occur, because the products contained aliphatically linked carboxyl groups and aliphatic hydroxyl, as well as phenolic hydroxyl groups. The behaviour of lignin under the same conditions was less clear but sufficiently similar to that of brown coal to suggest that reactions of the same type were occurring in both cases. Reactions involving decarboxylation, ring scission of dihydric phenol structures, and subsequent hydrogenation are suggested tentatively as the main steps in the formation of the products. The results provide some additional evidence for the view that there is a simple chemical relation between Victorian brown coal and lignin.


1997 ◽  
Vol 8 (1-2) ◽  
pp. 29-37 ◽  
Author(s):  
Fumitaka Wakabayashi ◽  
Junko N. Kondo ◽  
Kazunari Domen ◽  
Chiaki Hirose

2020 ◽  
Vol 2020 ◽  
pp. 1-14
Author(s):  
Shuncheng Xiang ◽  
Yingli Gao ◽  
Caijun Shi

The prerequisite to synthesize PCE was to prepare new macromonomers with controlled molecular mass, adjustable hydrophilic-lipophilic groups, long-chain alkyl groups, and large terminal hydroxyl groups as well. Structural modifications in the molecular scale of polycarboxylate superplasticizer (PCE) would lead to changes in properties of dispersion and water retention as well as enhancement in the compatibility of Portland cement and so on. This paper reviewed recent developments from synthetic methods of macromonomers as the initial step of production of PCE, PCE at room and elevated temperatures, and relationships between structure and properties of PCE. Through the analysis of references, it was found that PCE synthesized at room temperature had the same performance with PCE synthesized at elevated temperature in terms of conversion rate and initial dispersion in cement but broader molecular weight distribution. Conclusively, the dispersion of PCE in cement might be explained by multiple theories rather than a single one based on development trends as discussed in this paper.


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