The Chemistry and Technology of Rubber-Bound and Related Novel Antioxidants

1972 ◽  
Vol 45 (1) ◽  
pp. 204-221 ◽  
Author(s):  
M. E. Cain ◽  
K. F. Gazeley ◽  
I. R. Gelling ◽  
P. M. Lewis

Abstract The discovery that C-nitrosoanilines react with olefins to give p-phenylenediamines has made possible the synthesis of powerful antioxidants from a wide range of naturally occurring and synthetic unsaturated compounds. Simple alkenes, vegetable oils, and factices may be converted to antidegradants whose behavior parallels that of commercially available materials. The reaction of 4-nitrosoanilines or 4-nitrosophenols with natural and synthetic rubber or latices gives rubber-bound antioxidants which are completely resistant to extraction by water or organic solvents. No major modification of technological processing or fabrication techniques is necessary, and the reaction takes place conveniently during vulcanization. Attachment of the protective group to the rubber molecule does not affect its antioxidant activity, but reduces its effectiveness when migration to the surface is required, e.g., in protection against ozone. Although faster at elevated temperatures, the nitroso-olefin reaction will occur at room temperature, and this allows the preparation of chemically modified raw rubbers by carrying out the reaction in latex before coagulation and drying.

Author(s):  
Ernest L. Hall ◽  
J. B. Vander Sande

The present paper describes research on the mechanical properties and related dislocation structure of CdTe, a II-VI semiconductor compound with a wide range of uses in electrical and optical devices. At room temperature CdTe exhibits little plasticity and at the same time relatively low strength and hardness. The mechanical behavior of CdTe was examined at elevated temperatures with the goal of understanding plastic flow in this material and eventually improving the room temperature properties. Several samples of single crystal CdTe of identical size and crystallographic orientation were deformed in compression at 300°C to various levels of total strain. A resolved shear stress vs. compressive glide strain curve (Figure la) was derived from the results of the tests and the knowledge of the sample orientation.


2020 ◽  
Author(s):  
Christopher Rudolf ◽  
Corey Love ◽  
Marriner Merrill

Abstract Electrolytes for lithium ion batteries which work over a wide range of temperatures are of interest in both research and applications. Unfortunately, most traditional electrolytes are unstable at high temperatures. As an alternative, solid state electrolytes are sometimes used. These are inherently safer because they have no flammable vapors, and solid state electrolytes can operate at high temperatures, but they typically suffer from very low conductivity at room temperatures. Therefore, they have had limited use. Another option which has been previously explored is the use of ionic liquids. Ionic liquids are liquid salts, with nominally zero vapor pressure. Many are liquid over the temperature of interest (20–200°C). And, there is a tremendous range of available chemistries that can be incorporated into ionic liquids. So, ionic liquids with chemistries that are compatible with lithium ion systems have been developed and demonstrated experimentally at room temperature. In this study, we examined a silicon-lithium battery cycling at room temperature and over 150°C. Using half-cell vial and split-cell structures, we examined a standard electrolyte (LiPF6) at room temperature, and an ionic liquid electrolyte (1-ethyl-3-methylimidazolium bis(trifluorosulfonyl)imide) at room temperature and up to ∼150°C. The ionic liquid used was a nominally high purity product purchased from Sigma Aldrich. It was selected based on results reported in the open literature. The anode used was a wafer of silicon, and the cathode used was an alumina-coated lithium chip. The cells were cycled either 1 or 5 times (charge/discharge) in an argon environment at constant current of 50 μA between 1.5 and 0.05 volts. The results for the study showed that at room temperature, we could successfully cycle with both the standard electrolyte and the lithium ion electrolyte. As expected, there was large-scale fracture of the silicon wafer with the extent of cracking having some correlation with first cycle time. We were unable to identify any electrolyte-specific change in the electrochemical behavior between the standard electrolyte and the ionic liquid at room temperature. Although the ionic liquid was successfully used at room temperature, when the temperature was increased, it behaved very differently and no cells were able to successfully cycle. Video observations during cycling (∼1 day) showed that flocs or debris were forming in the ionic liquid and collecting on the electrode surface. The ionic liquid also discolored during the test. Various mechanisms were considered for this behavior, and preliminary tests will be presented. All materials were stable at room temperature, and the degradation appeared to be linked to the electrochemical process. As a conclusion, our working hypothesis is that, particularly at elevated temperatures, ionic liquid cleanliness and purity can be far more important than at room temperature, and small impurities can cause significant hurdles. This creates an important barrier to research efforts, because the “same” ionic liquids could cause failure in one situation and not in another due to impurities.


1972 ◽  
Vol 26 (3) ◽  
pp. 372-378 ◽  
Author(s):  
P. Campani ◽  
C. S. Fang ◽  
H. W. Prengle

Quantitative analysis of gas mixtures by infrared spectroscopy requires a knowledge of the absorption coefficients,: kν−, as a function of optical path length and temperature. For the majority of pollutant gases, information is scarce or incomplete. The objective of this work was to determine absorption coefficients for CH4, C2H4, CO2, CO, SO2, NO2, NO, and H2S. Measurements were made at room temperature and elevated temperatures for certain wave lengths, and kν− was determined over a very wide range of optical path length, x. The validity of the Bouguer-Beer law was confirmed for a limiting range of x, and for larger values of x, kν− decreased and was correlated as a function of x and T.


1965 ◽  
Vol 180 (1) ◽  
pp. 1045-1058 ◽  
Author(s):  
G. P. Tilly

An alloy steel and a nickel-chromium alloy are shown to exhibit similar fatigue behaviour over a wide range of temperatures. Endurances tended to be time-dependent at elevated temperatures, and repeated-tension cycles were found to be more damaging than push-pull but less damaging than static-tension (creep). The behaviour was reversed at room temperature where failures tended to be cycle-dependent (number of cycles to failure independent of applied frequency) and creep loading was least damaging. Rupture data for repeated-tension tests at approximately 10 c/min were analysed by a creep technique. For a wide range of temperature, the expressions fitted the experimental points encouragingly closely and the technique appears to be a useful method of describing this type of data. Tests at room temperature having more than 104 cycles to failure were premature with respect to the analysed family of curves and this was attributed to failure occurring by a predominantly cycle-dependent mechanism. Fractures at higher stresses exhibited a ductile appearance attributed to a different fracture mechanism. Time-dependent behaviour was enhanced by increase in the peak tensile stress, tensile mean stress, and temperature, or by decrease in cyclic frequency.


1996 ◽  
Vol 318 (2) ◽  
pp. 539-545 ◽  
Author(s):  
Hanne GRØN ◽  
Ida B. THØGERSEN ◽  
Jan J. ENGHILD ◽  
Salvatore V PIZZO

The α-macroglobulins are proteinase inhibitors that form part of a superfamily along with components of the complement system. Internal β-cysteinyl–γ-glutamyl thiol ester bonds are an important structural feature of most α-macroglobulins and several complement components. We have studied the reversibility of thiol ester cleavage caused by NH3 or CH3NH2 in tetrameric human α2-macroglobulin (α2M) and monomeric rat α1-inhibitor-3 (α1 I3). When employing NH3 as the nucleophile, the thiol ester in α1I3 re-formed spontaneously at room temperature after gel filtration to remove excess nucleophile, and an active proteinase inhibitor was regained. When CH3NH2 was employed as the nucleophile, thiol ester reversibility was more energy-demanding. With either nucleophile, α2M once inactivated did not regain proteinase-inhibitory capacity at room temperature. At elevated temperatures, however, the reaction between α2M and NH3 or CH3NH2 was reversible and the inhibitory capacity could be recovered. Modification of the cysteinyl groups from the thiol ester prevented its re-formation but did not prevent the heat-induced retrieval of inhibitory capacity, suggesting that conformational features rather than the thiol ester are essential for α2M to function as an inhibitor. As demonstrated by non-denaturing PAGE, the conformation of native α2M is restored when the proteinase-inhibitory capacity is recovered.


Crystals ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 35
Author(s):  
Blanca Yamile Rosas ◽  
Alvaro A. Instan ◽  
Karuna Kara Mishra ◽  
S. Nagabhusan Achary ◽  
Ram S. Katiyar

The compound 0.9[KNbO3]-0.1[(BaNi1/2Nb1/2O3−δ] (KBNNO), a robust eco-friendly (lead-free) ferroelectric perovskite, has diverse applications in electronic and photonic devices. In this work, we report the dielectric, ferroelectric, and structural phase transitions behavior in the KBNNO compound using dielectric, X-ray diffraction, and Raman studies at ambient and as a function of temperature. Analyses of X-ray diffraction (XRD) data at room temperature (rtp) revealed the orthorhombic phase (sp. Gr. Amm2) of the compound with a minor secondary NiO cubic phase (sp. Gr. Fm3m). A direct optical band gap Eg of 1.66 eV was estimated at rtp from the UV–Vis reflectance spectrum analysis. Observation of non-saturated electric polarization loops were attributed to leakage current effects pertaining to oxygen vacancies in the compound. Magnetization studies showed ferromagnetism at room temperature (300 K) in this material. XRD studies on KBNNO at elevated temperatures revealed orthorhombic-to-tetragonal and tetragonal-to-cubic phase transitions at 523 and 713 K, respectively. Temperature-dependent dielectric response, being leaky, did not reveal any phase transition. Electrical conductivity data as a function of temperature obeyed Jonscher power law and satisfied the correlated barrier-hopping model, indicating dominance of the hopping conduction mechanism. Temperature-dependent Raman spectroscopic studies over a wide range of temperature (82–673 K) inferred the rhombohedral-to-orthorhombic and orthorhombic-to-tetragonal phase transitions at ~260, and 533 K, respectively. Several Raman bands were found to disappear, while a few Raman modes such as at 225, 270, 289, and 831 cm−1 exhibited discontinuity across the phase transitions at ~260 and 533 K.


2013 ◽  
Vol 740-742 ◽  
pp. 657-660 ◽  
Author(s):  
Oleg Jakovlev ◽  
Tino Fuchs ◽  
Franziska Rohlfing ◽  
Helmut Seidel

We introduce a novel high temperature PECVD process and use it for the deposition of silicon carbide thin films on oxidized silicon wafers at 900°C substrate temperature. A variation of the atomic composition over a wide range is achieved by altering the flow ratio of the precursors silane (SiH4) and acetylene (C2H2). XPS analysis is performed to verify the silicon to carbon ratio in the deposited layers. The resistivity of the obtained thin films shows a strong dependence on the Si/C-ratio. Four point measurements show the resistivity ranging between 5•10-3Ωcm for C-rich layers and >107Ωcm for near stoichiometric layers. We investigate the piezoresistivity of the SiC layers at room temperature under compressive and tensile strain using the four point bending method. The same method is used to analyze selected layers at elevated temperatures up to 600°C. Based on the results we evaluate the applicability of the obtained thin films for strain transducing in harsh environment MEMS sensors.


1950 ◽  
Vol 23 (2) ◽  
pp. 338-346 ◽  
Author(s):  
B. S. T. T. Boonstra

Abstract It is necessary to determine the physical properties of rubbers at relatively high temperatures when products made from them are to be used at such temperatures in actual service. The term heat aging is used when the vulcanizate is tested at room temperature, exposed to elevated temperatures for given periods of time, and then tested again at room temperature. The term high-temperature strength is proposed for values obtained when the vulcanizates are tested at the actual higher service temperatures. Effective comparison of natural and synthetic rubbers is best obtained by determining tensile product values, which are the result of the combining of tensile strength and elongation values. In the evaluating of vulcanizates of tire compounds of various rubbers, another factor must be taken into account. Synthetic-rubber tires develop more heat in service than do natural-rubber tires, and the former therefore generally operate at higher temperatures than do the latter. Synthetic-rubber tires therefore require a greater high temperature strength than do natural rubber tires, but, as has been shown, synthetic rubbers actually have a lower high-temperature strength. The part played by carbon black with respect to the tensile properties of some synthetic rubbers is considered that of a substitute for crystallization in natural and other synthetic rubbers, which substitute does not, however, possess the same favorable features. Carbon black even in noncrystallizing rubbers does not increase strength; it merely shifts the optimum strength value to a higher temperature so that this temperature is in the room temperature range. The temperature coefficient of strength for Butyl and Neoprene rubbers is so large at room temperature that a few degrees' difference in temperature causes large changes in strength. The tensile strength and elongation at break of these two rubbers decrease sharply between 20 and 40° C.


1984 ◽  
Vol 62 (6) ◽  
pp. 1134-1144 ◽  
Author(s):  
C. I. Ratcliffe ◽  
D. E. Irish

Raman spectra of perchloric acid in water have been measured for solutions spanning a wide concentration range and, for two specific concentrations, a wide range of temperatures. The acid is completely dissociated down to a water:acid mole ratio of about 1.8 at room temperature. At elevated temperatures it is still a very "strong" acid. As the concentration increases the apparent symmetry of the ClO4− ion decreases and a small amount of a new species assigned as associated ClO4−•(Haq)+ can be detected. The effects on the OH stretching bands of water, of temperature, ClO4−, and the excess acid protons are discussed.


: Isatin is a naturally occurring substance identified in humans, animals, plants and coal tar. Isatin derivatives are reported to possess a wide range of activites. This review is in continuation of “Part-1 (1877-2002)” review published by our team. This review encompasses the most signigicant reports published during 2002 to 2020 on the biological & pharmacological activites of isatin and its derivatives. The review includes the various synthetic reactions of isatin and activites reported. The pharmacological and biological activites reported were antimicrobial, antineoplastic & related activities; analgesic, anti-inflammatory, anticonvulsant, antioxidant, activity against veterinary pathogen, effects on cardiac & vascular smooth muscles; transthyretin fibrillogenesis inhibitor and antiglycation activity of isatin compounds.


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