Infrared Spectra of Reaction Products of Natural Rubber with Alkylphenol Formaldehyde Resins

1968 ◽  
Vol 41 (3) ◽  
pp. 621-625
Author(s):  
Yu N. Nikitin ◽  
V. G. Epshtein ◽  
M. A. Polyak

Abstract Infrared spectroscopic studies were carried out with reaction products of natural rubber with 101K tertiary butylphenol-formaldehyde resin without activators and in the presence of stannous chloride dihydrate and zinc oxide. No reduction was observed in unsaturated rubber content during reaction with resin. Reaction of resin with rubber probably takes place at the α-carbon atom and not at the double bonds. A reduction in the proportion of resin phenol hydroxyl is basically due to its participation in recombination reactions of radicals formed during breakdown of ether bridges of resin. At 150° C activators accelerate decomposition of resin ether bridges, but increase the stability of phenol hydroxyl. In the case of zinc oxide, phenol hydroxyl is sufficiently resistant even at 180° C.


1960 ◽  
Vol 33 (2) ◽  
pp. 490-501
Author(s):  
Z. T. Ossefort

Abstract It has been shown that the age resistance of elastomeric vulcanizates is influenced to a very marked degree by residues formed in situ in the vulcanizate during the curing process. By a dual process of removal of these residues and incorporation of selected ingredients subsequent to vulcanization, it has been shown that age resistance (as measured by accelerated oven-aging tests at 212° F) in rubbers cured by sulfur and/or sulfur bearing accelerators, is a prime function of these residues and nearly independent of the stability of the network structure. An extremely active inhibitor is formed in situ during vulcanization of SBR and natural rubber using thiuram accelerators. This inhibitor can be used to “reinhibit” acetone-extracted accelerator-cured rubber. When added to sulfur/accelerator, peroxide, or radiation-cured vulcanizates, it improves their age resistance, but only in the case of the sulfur/accelerator cured rubber is this improvement better than with conventional inhibitors. This leads to the conclusion that the efficiency with which an inhibitor protects a vulcanizate varies widely, and conversely it appears that certain types of network structures are more readily protected or that certain inhibitors can function more efficiently in the protection of certain structures than others. In the case of natural rubber cured with TMTD (zinc oxide present), the bulk of the accelerator residue is ZnDMDC, and this residue has been shown to function as a very efficient antioxidant when incorporated into acetone-extracted, accelerator-cured vulcanizate. It is no more effective than conventional inhibitors, however, when incorporated into an acetone-extracted, sulfur/accelerator-cured vulcanizate. Finally, it has been shown that acetone extraction of the various vulcanizates may lead to improvement or worsening of their age resistance, depending upon the nature of the residues resulting from the curing process.



1952 ◽  
Vol 25 (3) ◽  
pp. 641-650 ◽  
Author(s):  
G. E. van Gils

Abstract A review of the factors which determine the zinc oxide stability of latex has been given. The work of Lepetit and our own experiments lead to the conclusion that the zinc oxide stability of latex is determined in the first place by substances which promote the solubilization of zinc oxide (minus factors); in the second place by substances which stabilize the colloid against the activity of the complex zinc cations or reduce the activity of these ions (plus factors). It has been generally accepted that the higher the KOH number of a latex, the lower is the zinc oxide stability. Since the KOH number is based primarily on neutralization of the acidic components of the serum only, a general correlation with zinc oxide stability could not be found when latexes of different origin were examined. Intrinsic factors or factors depending on the properties of the latex itself that influence zinc oxide stability are: (1) the dry rubber content of the latex, where high values are accompanied by low zinc oxide stability values and vice versa; (2) the yellow content fraction of latex, which in increasing amounts adds to the stability of the latex; (3) the protein content of the latex which, when degraded either artificially or naturally, reduces the zinc oxide stability. The effect of materials added to latex on zinc oxide stability includes: (1) fatty acid and sulfonic acid soaps, which have only slight influence; (2) Emulphor-O, sequestering agents, and sodium phosphates and silicates, which have a stabilizing effect; (3) ammonium salts and amines, which have a marked destabilizing effect, although triethanolamine hydrochloride is not active. Quebrachitol has a slight destabilizing effect.



2021 ◽  
Vol 87 (10) ◽  
pp. 90-102
Author(s):  
Elena Trunova ◽  
Michailo Artamonov ◽  
Tamara Makotryk

Complexation in M (II) – Rut systems (M(II) = Co, Cu) was studied by electron absorption spectroscopy and pH-metric titration in water-ethanol solutions depending on the metal: ligand ratio (1: 1; 2: 1) and the pH of the medium. It was shown that the structure and stoichiometric composition of the complexation reaction products are influenced by such basic parameters as L:M and the pH value of the medium. Depending on the pH value,  chelation involves certain binding sites, which primarily is associated with the redistribution of the electron density in the flavonoid molecule. In a weakly acidic or neutral medium, regardless of the M(II): Rut ratio, the formation of monoligand complexes of rutin with 3-d metals occurs with the participation of 5-OH and 4-C=O fragments of the A and C rings, and in an alkaline medium, chelation proceeds on the catecholic fragment of  ring B rutin. Biligand complexes are formed with the participation of the gydroxo groups of the catechol fragment of each rutin molecule, and the formation of compounds with a ratio of 2:1 occurs both due to 5-OH and 4C=O and due to 3 ', 4'-OH groups. The calculated values of the stability constants of the complexes showed that the stability of the Co (II) complexes is several orders of magnitude lower than the stability of the corresponding Cu (II) complexes.



Author(s):  
P. Sadhukhan ◽  
J. B. Zimmerman

Rubber stocks, specially tires, are composed of natural rubber and synthetic polymers and also of several compounding ingredients, such as carbon black, silica, zinc oxide etc. These are generally mixed and vulcanized with additional curing agents, mainly organic in nature, to achieve certain “designing properties” including wear, traction, rolling resistance and handling of tires. Considerable importance is, therefore, attached both by the manufacturers and their competitors to be able to extract, identify and characterize various types of fillers and pigments. Several analytical procedures have been in use to extract, preferentially, these fillers and pigments and subsequently identify and characterize them under a transmission electron microscope.Rubber stocks and tire sections are subjected to heat under nitrogen atmosphere to 550°C for one hour and then cooled under nitrogen to remove polymers, leaving behind carbon black, silica and zinc oxide and 650°C to eliminate carbon blacks, leaving only silica and zinc oxide.



Author(s):  
Ю.И. Цой

Задача получения однородного состава ЛКМ сводится к правильному выбору пленкообразователей и соответствующих растворителей и, в случае необходимости, разбавителей и добавок. На основе положений теории растворимости была проведена оценка совместимости компонентов и стабильности таких систем. Критериями оценки были приняты параметры растворимости и термодинамического взаимодействия. Исследовали совместимость алкидных лаков с аминоформальдегидными смолами в бутаноле, и результаты этих исследований представлены в треугольной фазовой диаграмме. Для оценки совместимости смол по результатам расчета параметров термодинамического взаимодействия были построены спинодали для тройных систем. Как показывает анализ результатов проведенных исследований, даже при большой разности ?? = |?12 – ?13| = 0,2 наблюдается небольшая область несовместимости. С уменьшением разности ?? область несовместимости сужается. При ?23 > ?с область несовместимости расширяется как для ? = 0,2, так и для ?? = 0,1 и ?? = 0. Таким образом, для таких систем на совместимость компонентов, в первую очередь, влияет их взаимодействие между собой – чем оно больше, тем лучше они совместимы. Проведенные исследования показали, что парциальные параметры растворимости, учитывающие природу когезионных сил, более объективно характеризуют растворимость пленкообразующих смол в органических растворителях, чем их общий параметр растворимости. Растворимость пленкообразующих алкидных и этерифицированных аминоформальдегидных смол в органических растворителях обусловлена термодинамическим взаимодействием молекулярных сил различной природы. Стабильность смеси алкидной и этерифицированной аминоформальдегидной смолы в бутаноле обусловлена в большей степени термодинамическим взаимодействием молекулярных сил; при этом степень бутанолизации меламиноформальдегидной смолы оказывает наибольшее влияние на стабильность cистемы. Проведенные исследования по стабильности лакокрасочных смесей из различных пленкообразующих смол на основе рассмотренных критериев оценки могут быть использованы для совершенствования технологии защитно-декоративной отделки древесины. The problem of obtaining a homogeneous composition of the coatings is reduced to the proper selection of film-forming agents, and diluent and, if appropriate, diluents and additives. On the basis of the theory of solubility, we have carried out the assessment of the compatibility of the components and stability of such systems. The evaluation criteria were adopted the parameters of the solubility and thermodynamic interaction. Researched the compatibility with alkyd varnishes aminoformaldehyde resin in butanol, and the results of these studies are presented in the triangular phase diagram. To evaluate the compatibility of the resins according to the results of calculation of thermodynamic parameters of interaction were built spinodal for ternary systems. As the analysis of the results of the studies, even when the difference ??|?12 – ?13| = 0,2 there is a small area of incompatibility. With the decrease of the difference ? ? region incompatibility narrows. When ?23> ?с region incompatibility extends to ?? = 0,2, and for ?? = 0.1 and ?? = 0. Thus, for such systems, compatibility of components, primarily, affects their interaction with each other – the further away it is, the better they are compatible. Studies have shown that the partial solubility parameters, which take into account the nature of cohesive forces, more objectively characterize the solubility of film-forming resins in organic solvents than their total solubility parameter. The solubility and film-forming aminoformaldehyde esterified alkyd resins in organic solvents due to thermodynamic interaction of molecular forces of different nature. Тhe stability of the mixture and aminoformaldehyde esterified alkyd resin in butanol is generated largely by thermodynamic forces of molecular interaction; the degree of butanolate melamine-formaldehyde resin has the greatest effect on the stability of the system. Conducted research on the stability of the paint mixtures of various film-forming resins on the basis of the evaluation criteria can be used to improve the technology of protective and decorative wood finish.



2021 ◽  
Vol 2 (7) ◽  
pp. 2408-2418
Author(s):  
Le Wan ◽  
Cong Deng ◽  
Ze-Yong Zhao ◽  
Hai-Bo Zhao ◽  
Yu-Zhong Wang

Titanium oxide-carbon nanotube hybrids may efficiently promote the stability of nature rubber under extreme frictional conditions.



Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 443
Author(s):  
Kunakorn Chumnum ◽  
Ekwipoo Kalkornsurapranee ◽  
Jobish Johns ◽  
Karnda Sengloyluan ◽  
Yeampon Nakaramontri

The self-healing composites were prepared from the combination of bromobutyl rubber (BIIR) and natural rubber (NR) blends filled with carbon nanotubes (CNT) and carbon black (CB). To reach the optimized self-healing propagation, the BIIR was modified with ionic liquid (IL) and butylimidazole (IM), and blended with NR using the ratios of 70:30 and 80:20 BIIR:NR. Physical and chemical modifications were confirmed from the mixing torque and attenuated total reflection-fourier transform infrared spectroscopy (ATR-FTIR). It was found that the BIIR/NR-CNTCB with IL and IM effectively improved the cure properties with enhanced tensile properties relative to pure BIIR/NR blends. For the healed composites, BIIR/NR-CNTCB-IM exhibited superior mechanical and electrical properties due to the existing ionic linkages in rubber matrix. For the abrasion resistances, puncture stress and electrical recyclability were examined to know the possibility of inner liner applications and Taber abrasion with dynamic mechanical properties were elucidated for tire tread applications. Based on the obtained Tg and Tan δ values, the composites are proposed for tire applications in the future with a simplified preparation procedure.



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