A Novel Class of Rubber to Steel Tire Cord Adhesion Promoters

1984 ◽  
Vol 57 (4) ◽  
pp. 686-702 ◽  
Author(s):  
W. J. van Ooij ◽  
M. E. F. Biemond

Abstract A series of eight novel rubber-brass adhesion promoter systems are introduced and discussed. They can be divided in four categories, viz., homogeneous inorganic polyborosilicates of cobalt or nickel; inorganic cobalt or nickel ions adsorbed on an inert substrate, e.g., silica or alumina; metal-organic cobalt or nickel salts deposited on a similar substrate; and inorganic ion exchangers loaded with cobalt or nickel. The organic systems have the major advantage that they are much more active than if they were used without support. Because of this effect, they can replace the currently used metal-organic cobalt salts but at reduced levels. The inorganic systems all show an improvement of initial and of aged adhesion which is comparable to that of currently used commercial systems. However, they can be used at much higher levels than metal-organic salts since for the first time, promoters are offered which show virtually no negative effect on physical compound properties. Such promoters are insoluble in rubber and act solely as corrosion inhibitors. At high levels, therefore, the performance of the inorganic promoters is far superior to that of the metal-organic systems. A consequence of such promoters being corrosion inhibitors is that nickel salts generally perform as well as the cobalt-containing materials. Another advantage is that such promoters can also reduce the rate of iron corrosion. This was demonstrated for the polyborosilicates. It is expected that the rate of rust formation in the tire will be reduced because of this propensity and also because the inorganic systems have a long-range action due to a slow-release effect. In the development of these unusual promoter systems, extensive use has been made of liquid low molecular weight model systems. A good correlation is reported between crosslinking of NR and of squalene if the levels of sulfur, DCBS accelerator, or ZnO are varied. If levels of cobalt or antioxidant are varied, squalene does not react as NR. For such studies, dodecene-1 is shown to be a better model molecule. This system further has the advantage that it is amenable to gas chromatography analysis which allows the crosslink distribution to be determined quantitatively.

Proceedings ◽  
2019 ◽  
Vol 41 (1) ◽  
pp. 60
Author(s):  
Zahra Rezaee ◽  
Faranak Manteghi

In this study, a terephthalate and pyrazine-based metal–organic framework (MOF) was prepared using the oxygen and nitrogen donor ligands through the hydrothermal method. In the MOF, cobalt and nickel ions were selected as metal nodes which are connected by terephthalate and pyrazine linkers. The as-prepared MOF was utilized as Cr adsorbent in water by an ultrasonic method. The MOF capacity towards chromium ion adsorption was obtained about 96% in 50 ppm initial concentration. In order to characterize and determine the morphology of the title MOF, the FT-IR and XRD methods were applied, while the chromium concentration before and after adsorption was determined by the ICP method.


2014 ◽  
Vol 612 ◽  
pp. 295-301 ◽  
Author(s):  
Takuya Sugimoto ◽  
Tatsuroh Mizushima ◽  
Akisumi Okamoto ◽  
Noriyuki Kurita

2004 ◽  
Vol 19 (7) ◽  
pp. 2028-2039 ◽  
Author(s):  
M. Eremtchenko ◽  
D. Bauer ◽  
J.A. Schaefer ◽  
F.S. Tautz

Organic semiconductors on single-crystalline metal surfaces are model systems for injection contacts in organic field-effect transistors (OFET) and light-emitting diodes. They allow us to classify possible metal–organic interaction scenarios and to elucidate general tendencies, which most likely will also be found at metal–organic interfaces in real devices. In this contribution, we report a comprehensive investigation of the interface of perylene, a promising material for OFETs, with the close-packed noble metal surface Ag(111), using high-resolution electron energy loss spectroscopy, low-energy electron diffraction, and scanning tunneling microscopy as surface analytical techniques. The most important findings are: In the monolayer, molecules are oriented flat and form an incommensurate, most probably fluid overlayer. The molecules interact electronically with the substrate and become weakly metallic. Scanning tunneling microscopy reveals a propensity of perylene molecules toward a specific adsorption site on Ag(111), if the influence of intermolecular interactions is inhibited. Film growth at room temperature is similar to Stranski–Krastanov type. Finally, co-planar adsorption of perylene on Ag(111) is metastable, and annealing the monolayer at 420 K leads to a structural transformation of the film. The perylene–Ag(111) interface can therefore be classified as weakly interacting.


2014 ◽  
Vol 70 (a1) ◽  
pp. C1007-C1007
Author(s):  
Charlotte Jones ◽  
Chick Wilson ◽  
Lynne Thomas

The key aim of multi-component crystallisation is modification of the physicochemical properties for a specific task.[1] Tuning colour using molecular components is a relatively unexplored area, which is surprising given the possible advantages in pigment development. In crystalline materials, the optical characteristics are not solely dependent on the molecules but also on the crystal packing;[2] it follows that the optical properties could be modified using crystal engineering techniques. We have systematically investigated co-crystallising haloanilines with dinitrobenzoic acids to build an understanding of the intermolecular interactions. Molecular disorder of one or more of the components tends to lead to layered crystal structures that include stacking interactions and therefore strong colour, indicating that molecular disorder is desirable. Defects in inorganic systems are routinely exploited as a route to enhancing or introducing physical properties but similar effects in organic systems are yet to be properly exploited. We will discuss the methods by which disorder can be designed into molecular complexes, and the local ordering effects which give rise to strong diffuse scattering. Additionally we have identified a pair of thermochromic molecular complexes, 2-iodoaniline/2-bromoaniline 3,4-dinitrobenzoic acid, where disorder appears to be crucial in lending the materials their properties. Both complexes undergo a temperature-induced colour change from red to yellow corresponding to a significant molecular rearrangement. The thermochromic transition is a single-crystal to single-crystal effect; the role of molecular disorder as a facilitator for the molecular rearrangement, maintaining the crystal integrity, will be discussed. Despite the complexes being isostructural, only the bromoaniline complex shows reversible thermochromic behaviour; subtleties in the manifestation of this disorder can explain the differences in the reversibility of the transition.


2004 ◽  
Vol 126 (41) ◽  
pp. 13170-13171 ◽  
Author(s):  
Jerry L. Atwood ◽  
Leonard J. Barbour ◽  
Scott J. Dalgarno ◽  
Michaele J. Hardie ◽  
Colin L. Raston ◽  
...  

2009 ◽  
Vol 65 (6) ◽  
pp. 707-714
Author(s):  
Anna Collins ◽  
Chick C. Wilson ◽  
Christopher J. Gilmore

The dSNAP computer program has been used to classify searches of the Cambridge Structural Database for two ligands: —O—CH2—CH2—O— and N(CH2CH2O—)3 commonly found in metal-organic systems. The clustering method used is based on total geometries (i.e. all the lengths and angles involving all the atoms in the search fragment, whether bonded or not) and proved capable of distinguishing in a wholly automatic, objective way between different types of metal complex purely on the basis of the geometry of the ligand and the relative positions of the O atoms to the metals.


CrystEngComm ◽  
2009 ◽  
Vol 11 (11) ◽  
pp. 2516 ◽  
Author(s):  
Fangna Dai ◽  
Haiyan He ◽  
Dongliang Gao ◽  
Fei Ye ◽  
Xiaoliang Qiu ◽  
...  

Due to a growing awareness of environmental protection, an interest in replacing toxic corrosion inhibitors with more environmentally acceptable alternatives is also growing. Chromates, as one of the best inhibitors, have been eliminated as technically viable inhibitors because of their high toxicity, and the use of polyphosphates has diminished as they disrupt the balance in the Plantae kingdom. The emphasis is on exploration and testing of organic compounds that can be obtained from plant material. Rosemary extracts (leaf and flower) have been shown to have inhibitory activity on iron corrosion in 3% NaCl and seawater. Corrosion rate values ​​show that rosemary flower extracts are better inhibitors of corrosion than the leaf extracts and that the maximum inhibitory protection has not been achieved in the range of tested concentrations.


2019 ◽  
Author(s):  
Parvej Alam ◽  
Nelson Leung ◽  
Junkai Liu ◽  
Xuepeng Zhang ◽  
Zikai He ◽  
...  

Because of their innate ability to store and then release energy, long persistent luminescence (LPL) materials have garnered strong research interest in a wide range of multidisciplinary fields, such as biomedical sciences, theranostics, and photonic devices. Although many inorganic LPL systems with afterglow durations of up to hours and days have been reported, organic systems have had difficulties reaching similar timescales. We propose in this work a design principle based on the successes of inorganic systems to produce an organic LPL (OLPL) system through the use of a strong organic electron trap. The resulting system generated detectable afterglow for up to 7 hours, significantly longer than any other reported OLPL system. The design strategy demonstrates an easy methodology to develop organic long persistent phosphors, opening the door to new OLPL materials.


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