Green synthesis of a carbon-rich layer on the surface of SiC at room temperature by anodic etching in dilute hydrofluoric acid/ethylene glycol solution

2016 ◽  
Vol 5 (5) ◽  
Author(s):  
Tuan Anh Cao ◽  
Truc Quynh Ngan Luong ◽  
Tran Cao Dao

AbstractCarbide-derived carbons (CDCs) are a growing class of nanostructured carbon materials with properties that are desirable for many applications, ranging from electrical energy to gas storage. However, the synthesis of CDCs often requires high temperatures and/or pressures, as well as toxic chemicals. In this report, we demonstrate environmentally friendly synthesis of a carbon-rich layer on the surface of SiC by anodic etching at room temperature in a highly diluted solution of hydrofluoric acid in ethylene glycol. In our opinion, the carbon-rich layer was formed thanks to the fact that we have used the etching conditions in which the rate of removal of carbon from SiC has become significantly lower compared with the silicon removal rate. More specifically, we have created an environment for SiC anodic etching where there is little water. In such conditions, silicon is still being removed from SiC, thanks to the direct dissolution, whereas the carbon removal rate is significantly reduced, due to the fact that carbon can be lost only by oxidation, but there is not enough water to oxidize carbon as in solutions with plenty of water. Thus, a carbon-rich layer is created on the etched SiC surface.

1963 ◽  
Vol 41 (1) ◽  
pp. 889-895 ◽  
Author(s):  
Phyllis S. Roberts

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.


2005 ◽  
Vol 486-487 ◽  
pp. 436-439 ◽  
Author(s):  
Dong Sik Bae ◽  
Eun Jung Kim ◽  
Sang Whan Park ◽  
Kyong Sop Han

Nanosized ZnxMn1-xFe2O4 powders were prepared in ethylene glycol solution under mild temperature and pressure conditions by precipitation from metal nitrates. The average size and distribution of the synthesized ZnxMn1-xFe2O4 powders were 10- 20 ㎚ and narrow, respectively. The magnetic property of the synthesized ZnxMn1- xFe2O4 powder was of superparamagnetic character at room temperature.


1996 ◽  
Vol 449 ◽  
Author(s):  
Hongqiang Lu ◽  
Ziming Wu ◽  
Ishwara Bhat

ABSTRACTIn this paper, the first study of photo-assisted anodic etching of unintentionally doped n-GaN at room temperature is reported. The electrolyte used is a mixture of buffered aqueous solution of tartaric acid and ethylene glycol. The etching rate varies from ∼20 Å/min to as high as 1600 Å/min. A systematic study shows that i) the etch rate, as well as the surface roughness, increases with the current density; ii) the etching rate is the highest when the pH of the electrolyte is around 7; iii) the etching is faster when there is more ethylene glycol in the electrolyte solution.


1963 ◽  
Vol 41 (4) ◽  
pp. 889-895 ◽  
Author(s):  
Phyllis S. Roberts

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.


2021 ◽  
Vol 132 ◽  
pp. 107155
Author(s):  
Hang Yusen ◽  
Yang Tao ◽  
Xu Zhengyang ◽  
Zeng Yongbin

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2047
Author(s):  
Naofumi Naga ◽  
Mitsusuke Sato ◽  
Kensuke Mori ◽  
Hassan Nageh ◽  
Tamaki Nakano

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.


2015 ◽  
Vol 1117 ◽  
pp. 52-55
Author(s):  
Artis Linarts ◽  
Maris Knite

Polymer conductive filler composites are believed to be promising materials for flexible force sensor manufacture. Polyisoprene various carbon allotrope hybrid composites were made and their piezoresistive properties depending on the two type’s filler concentration and their ratio have been determined. Electrical resistance relaxations of hybrid composites at constant pressure in room temperature were determined as well. Experimental data of resistance relaxation was analyzed and fitted similarly to stress relaxation of polymers at constant pressure.


1977 ◽  
Vol 23 (9) ◽  
pp. 1170-1177 ◽  
Author(s):  
David A. Cotter

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.


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