Electrochemical reactions and charge transport in undiluted room-temperature melts of oligo(ethylene glycol)-based electron carriers

1993 ◽  
Vol 115 (17) ◽  
pp. 7896-7897 ◽  
Author(s):  
Christopher S. Velazquez ◽  
James E. Hutchison ◽  
Royce W. Murray
Keyword(s):  
Ethylene Glycol ◽  
Charge Transport ◽  
Room Temperature ◽  
Electrochemical Reactions ◽  
Electron Carriers

scholarly journals Synthesis of Network Polymers by Means of Addition Reactions of Multifunctional-Amine and Poly(ethylene glycol) Diglycidyl Ether or Diacrylate Compounds

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2047
Author(s):  
Naofumi Naga ◽  
Mitsusuke Sato ◽  
Kensuke Mori ◽  
Hassan Nageh ◽  
Tamaki Nakano
Keyword(s):  
Ethylene Glycol ◽  
Room Temperature ◽  
Addition Reaction ◽  
Monomer Concentration ◽  
Diglycidyl Ether ◽  
Porous Polymers ◽  
Addition Reactions ◽  
Poly Ethylene Glycol ◽  
Network Polymers ◽  
Poly Ethylene

Addition reactions of multi-functional amine, polyethylene imine (PEI) or diethylenetriamine (DETA), and poly(ethylene glycol) diglycidyl ether (PEGDE) or poly(ethylene glycol) diacrylate (PEGDA), have been investigated to obtain network polymers in H2O, dimethyl sulfoxide (DMSO), and ethanol (EtOH). Ring opening addition reaction of the multi-functional amine and PEGDE in H2O at room temperature or in DMSO at 90 °C using triphenylphosphine as a catalyst yielded gels. Aza-Michael addition reaction of the multi-functional amine and PEGDA in DMSO or EtOH at room temperature also yielded corresponding gels. Compression test of the gels obtained with PEI showed higher Young’s modulus than those with DETA. The reactions of the multi-functional amine and low molecular weight PEGDA in EtOH under the specific conditions yielded porous polymers induced by phase separation during the network formation. The morphology of the porous polymers could be controlled by the reaction conditions, especially monomer concentration and feed ratio of the multi-functional amine to PEGDA of the reaction system. The porous structure was formed by connected spheres or a co-continuous monolithic structure. The porous polymers were unbreakable by compression, and their Young’s modulus increased with the increase in the monomer concentration of the reaction systems. The porous polymers absorbed various solvents derived from high affinity between the polyethylene glycol units in the network structure and the solvents.

scholarly journals Nonreciprocal charge transport up to room temperature in bulk Rashba semiconductor α-GeTe

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yan Li ◽  
Yang Li ◽  
Peng Li ◽  
Bin Fang ◽  
Xu Yang ◽  
...  
Keyword(s):  
Charge Transport ◽  
Room Temperature ◽  
Theoretical Calculations ◽  
Ferromagnetic Layer ◽  
Spin Splitting ◽  
New Paradigm ◽  
Rashba Spin ◽  
Rashba Spin Splitting ◽  
Fundamental Insight ◽  
Insight Into

AbstractNonmagnetic Rashba systems with broken inversion symmetry are expected to exhibit nonreciprocal charge transport, a new paradigm of unidirectional magnetoresistance in the absence of ferromagnetic layer. So far, most work on nonreciprocal transport has been solely limited to cryogenic temperatures, which is a major obstacle for exploiting the room-temperature two-terminal devices based on such a nonreciprocal response. Here, we report a nonreciprocal charge transport behavior up to room temperature in semiconductor α-GeTe with coexisting the surface and bulk Rashba states. The combination of the band structure measurements and theoretical calculations strongly suggest that the nonreciprocal response is ascribed to the giant bulk Rashba spin splitting rather than the surface Rashba states. Remarkably, we find that the magnitude of the nonreciprocal response shows an unexpected non-monotonical dependence on temperature. The extended theoretical model based on the second-order spin–orbit coupled magnetotransport enables us to establish the correlation between the nonlinear magnetoresistance and the spin textures in the Rashba system. Our findings offer significant fundamental insight into the physics underlying the nonreciprocity and may pave a route for future rectification devices.

The effects of osmotic pressure changes on the germination of Dictyostelium discoideum spores

1977 ◽  
Vol 23 (9) ◽  
pp. 1170-1177 ◽  
Author(s):  
David A. Cotter
Keyword(s):  
Ethylene Glycol ◽  
Dictyostelium Discoideum ◽  
Room Temperature ◽  
Thermal Inactivation ◽  
Sucrose Concentration ◽  
Lag Phase ◽  
Activation Process ◽  
Sucrose Solutions ◽  
Spore Population ◽  
Pressure Changes

Polyalcohols such as ethylene glycol and glycerol at 3 M penetrate and activate spores of Dictyostelium discoideum incubated at room temperature. Higher concentrations of ethylene glycol result in lysis upon suspension of spores in dilute phosphate buffer. Erythritol and arabitol at 3 M do not penetrate or activate D. discoideum spores.Air-dried spores or those incubated in 2 M sucrose solutions are not activated with the usual heat treatment of 45 °C for 30 min. The plasmolyzed spores are activated at temperatures above 45 °C when heated in the presence of 2 M sucrose for 30 min. The temperature for maximum activation and the temperature for thermal inactivation of spores are raised 7–10 °C in high sucrose concentrations. Long-term incubation of heat-activated spores in 2 M sucrose solutions does not result in a return to dormancy.Moderate sucrose concentrations near 0.2 M do not block the heat-induced activation process but must be removed from the spore population to prevent a return to dormancy within 6 h. Other polyhydric compounds at 0.25 M concentration also cause spore deactivation within 6 h of room temperature incubation. Oxygen uptake of spores undergoing deactivation in 0.18 M sucrose is inhibited as compared to control levels. Moderate concentrations of sucrose do not block the early events of postactivation lag and the spores accumulate at the end of the lag phase. The longer the spores remain unswollen at the end of the postactivation lag phase, the greater the percentage of spores which return to dormancy. The effects of moderate sucrose concentration (lowered water activity) are not duplicated by the same quantity of Ficoll, indicating that the colligative properties of the sucrose solutions are responsible for deactivation.

scholarly journals Semiconducting polymer blends that exhibit stable charge transport at high temperatures

Science ◽  
2018 ◽  
Vol 362 (6419) ◽  
pp. 1131-1134 ◽  
Author(s):  
Aristide Gumyusenge ◽  
Dung T. Tran ◽  
Xuyi Luo ◽  
Gregory M. Pitch ◽  
Yan Zhao ◽  
...  
Keyword(s):  
High Temperature ◽  
Polymer Blends ◽  
Charge Transport ◽  
Organic Semiconductors ◽  
Room Temperature ◽  
Elevated Temperatures ◽  
Hole Mobility ◽  
General Strategy ◽  
Semiconducting Polymer ◽  
High Temperature Operation

Although high-temperature operation (i.e., beyond 150°C) is of great interest for many electronics applications, achieving stable carrier mobilities for organic semiconductors at elevated temperatures is fundamentally challenging. We report a general strategy to make thermally stable high-temperature semiconducting polymer blends, composed of interpenetrating semicrystalline conjugated polymers and high glass-transition temperature insulating matrices. When properly engineered, such polymer blends display a temperature-insensitive charge transport behavior with hole mobility exceeding 2.0 cm2/V·s across a wide temperature range from room temperature up to 220°C in thin-film transistors.

THE ACTIVATION OF PURIFIED HUMAN PLASMINOGEN IN SOLUTIONS OF ETHYLENE GLYCOLS

1963 ◽  
Vol 41 (1) ◽  
pp. 889-895 ◽  
Author(s):  
Phyllis S. Roberts
Keyword(s):  
Methyl Ester ◽  
Ethylene Glycol ◽  
Diethylene Glycol ◽  
Room Temperature ◽  
Fast Rate ◽  
Triethylene Glycol ◽  
Ethylene Glycols ◽  
Human Plasminogen ◽  
Glycol Solution ◽  
Rate Of Accumulation

Ethylene glycols have been found to allow activation of purified preparations of human plasminogen. The activity of the enzyme formed, plasmin, was measured using TAMe (p-toluene-sulphonyl-L-arginine methyl ester) as a substrate. In 50% (v/v) solutions of these compounds at pH 7.6 and 30 °C, plasmin accumulated faster in diethylene and triethylene glycols than in glycerol, but in ethylene glycol no plasmin was found. When lower concentrations of ethylene glycol (from zero to 50%) and shorter times of incubation were used, plasmin was found. With equimolar solutions (4.3 M) of glycerol and the three glycols, only diethylene glycol showed a fast rate of accumulation of plasmin. A 50% triethylene glycol solution partially inhibited the rate of spontaneous activation but stabilized the plasmin formed and therefore enzyme accumulated. At room temperature more plasmin accumulated than at higher temperatures when plasminogen was incubated in 50% triethylene glycol solution, and no plasmin was found when plasminogen was incubated at pH 7.6, 30 °C, in 50% solutions of propylene glycols, several ethers of the ethylene glycols, several polymers of various glycols, and dioxane.

The Effect of Ultrasonic Treatment on the Morphology and Microstructure of TiO2 Nanotubes Prepared by DC Anodization

2016 ◽  
Vol 860 ◽  
pp. 17-20
Author(s):  
Buagun Samran ◽  
Emmanuel Nyambod Timah ◽  
Udom Tipparach
Keyword(s):  
Surface Morphology ◽  
Ethylene Glycol ◽  
Ultrasonic Treatment ◽  
Room Temperature ◽  
Ammonium Fluoride ◽  
Deionized Water ◽  
Dc Voltage ◽  
Anodization Method

This paper presents the effect of ultrasonic treatment on the morphology and microstructure of TiO2 nanotubes prepared by DC anodization method. The TiO2 nanotubes were grown by one-face anodization at room temperature on titanium sheets of 0.25 mm thickness and 99.7% purity. The electrolyte was composed of ethylene glycol (EG), ammonium fluoride (0.3% wt NH4F) and deionized water (2% V H2O). A constant DC voltage of 50 V was applied during anodization for 2 hours. The samples were ultrasonically cleansed in ethanol for different extended periods of time: 0, 10, 30 and 50 minutes respectively. The samples were annealed at 450 °C for 2 hours. The surface morphology and microstructure of the TiO2 nanotubes formed were studied by XRD and SEM. The best result was obtained when the sampleswere ultrasonicated for 30 minutes.

AuPd/polyaniline as the anode in an ethylene glycol microfluidic fuel cell operated at room temperature

2014 ◽  
Vol 50 (60) ◽  
pp. 8151-8153 ◽  
Author(s):  
N. Arjona ◽  
A. Palacios ◽  
A. Moreno-Zuria ◽  
M. Guerra-Balcázar ◽  
J. Ledesma-García ◽  
...  
Keyword(s):  
Fuel Cell ◽  
Ethylene Glycol ◽  
Room Temperature ◽  
Microfluidic Fuel Cell ◽  
First Time

AuPd/polyaniline was used for the first time, for ethylene glycol electrooxidation in a microfluidic fuel cell operated at room temperature.

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