Carboxylic Elastomers

1955 ◽  
Vol 28 (4) ◽  
pp. 937-951 ◽  
Author(s):  
Harold P. Brown ◽  
Carlin F. Gibbs

Abstract Carboxyl groups can be introduced into elastomers by adding olefinic acids to suitable emulsion systems prior to polymerization. In general, such carboxyl groups elevate the elasticity temperature range, impart superior filming properties, increase resistance to swelling by hydrocarbon solvents, and render the polymers susceptible to cross-linkage, gelation, and vulcanization by polyvalent reagents. In vulcanization recipes based on sulfur but containing polyvalent metal salts, the presence of as little as 1 per cent of a carboxylic monomer is recognizable through its influence on vulcanizate properties. Carboxylic elastomers can be cross-linked by reactions of the carboxyl groups. Salt formation with zinc oxide, without pigmentation, gives stocks having stress-strain properties equaling or surpassing those of black-pigmented sulfur-cured vulcanizates of analogous noncarboxylic polymers. Several divalent metal oxides and other salts can be used as vulcanizing agents. The metal oxide vulcanizates possess excellent stress-strain properties, but poor compression sets. Certain vulcanizates are improved by the inclusion of small amounts of organic acids. An excess of organic acid causes devulcanization. Carbon blacks function principally as loading rather than reinforcing pigments.

2002 ◽  
Vol 739 ◽  
Author(s):  
Lionel Vayssieres ◽  
Arumugam Manthiram

ABSTRACTAdvanced nanoparticulate thin films of transition metal oxides consisting of nanorods with different orientations onto various substrates have been successfully grown by aqueous chemical growth without template, surfactant, or applied electric/magnetic field. The synthesis involves the aqueous condensation of metal ions from solutions of metal salts or metal complexes. Such low-cost fabrication of nanoengineered 3-D arrays consisting of 1-D nanorods of iron oxide (hematite), zinc oxide (zincite), and manganese oxyhydroxide (manganite) with parallel and perpendicular orientations onto various substrates are presented.


1963 ◽  
Vol 36 (4) ◽  
pp. 931-962 ◽  
Author(s):  
H. P. Brown

Abstract Carboxyl groups in elastomer molecules have been shown to contribute to the crosslinking or joining of these molecules through hydrogen bonding, salt formation, reaction with diepoxides or polyepoxides including epoxy resins, reaction with diamines or polyamines, esterification with di- or poly-hydric alcohols, reaction with carbodiimides, reaction with polyimines, and by reaction with polyisocyanates. Each of these reactions alone may produce useful crosslinkages. Or, they may be used in conjunction with crosslinking reactions operating in other parts of the molecule such as sulfur or peroxide vulcanization. This has been particularly true of salt formation, especially through the use of zinc oxide, with sulfur vulcanizarions. The carboxyl groups in some instances may be generated during the crosslinking reaction. Thus polyethylacrylate may be crosslinked with hexamethylene diamine, barium hydroxide and similar reagents. Many of the reactions of the carboxyl groups in elastomers are quite rapid. For some purposes such as surface toughening of elastomer films, this may be quite useful. For others such as the vulcanization of carboxylic elastomers with zinc oxide or with recipes containing zinc oxide, this may be objectionable because of the scorchiness of the stocks. The scorchiness of vulcanizates of carboxylic elastomers involving zinc oxide may be controlled with organic acid additives or by the use of zinc oxide coated with less reactive materials such as zinc sulfide or zinc phosphate. The speed of reaction of epoxides with carboxyl containing polymers is influenced by the structure of the epoxide. The ease with which carbodiimides induce crosslinkage is dependent upon the structure of the carbodiimide.


2021 ◽  
Vol 11 (2) ◽  
Author(s):  
E. Y. Shaba ◽  
J. O. Jacob ◽  
J. O. Tijani ◽  
M. A. T. Suleiman

AbstractIn this era, nanotechnology is gaining enormous popularity due to its ability to reduce metals, metalloids and metal oxides into their nanosize, which essentially alter their physical, chemical, and optical properties. Zinc oxide nanoparticle is one of the most important semiconductor metal oxides with diverse applications in the field of material science. However, several factors, such as pH of the reaction mixture, calcination temperature, reaction time, stirring speed, nature of capping agents, and concentration of metal precursors, greatly affect the properties of the zinc oxide nanoparticles and their applications. This review focuses on the influence of the synthesis parameters on the morphology, mineralogical phase, textural properties, microstructures, and size of the zinc oxide nanoparticles. In addition, the review also examined the application of zinc oxides as nanoadsorbent for the removal of heavy metals from wastewater.


2015 ◽  
Vol 1107 ◽  
pp. 326-332
Author(s):  
Abdul Rahim Yacob ◽  
Kamaluddeen Suleiman Kabo

The use of metal oxides in heterogeneous base catalysis has gained a large interest due to their application in many chemical and industrial processes and is environmental friendly. Basic metal oxides are commonly used and their structures, morphology and performance can be modified by method of preparation and thermal activation. In this study, surface modified amphoteric zinc oxide was prepared via hydration-dehydration method and characterised by TGA and FTIR. The basic strength at various temperatures is characterised by FTIR and back titration analyses. The results shows that surface modified zinc oxide has the highest basic strength of 1.453mmolg-1at 400°C making it a relatively good and suitable compound for use in heterogeneous basic catalysis. This result is also supported by FTIR spectra which show possible relationship between the Lewis O2-and increasing basic strength.


1977 ◽  
Vol 68 ◽  
pp. 436
Author(s):  
M.R Welton-Cook ◽  
M Prutton
Keyword(s):  

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