Solution plasma exfoliation of graphene flakes from graphite electrodes

RSC Advances ◽  
2014 ◽  
Vol 4 (93) ◽  
pp. 51758-51765 ◽  
Author(s):  
Hoonseung Lee ◽  
Maria Antoaneta Bratescu ◽  
Tomonaga Ueno ◽  
Nagahiro Saito
Keyword(s):  
Bubble Formation ◽  
Distilled Water ◽  
Graphite Electrodes ◽  
Graphene Flakes

Proposed mechanisms for the bubble formation on the graphite electrodes discharged in distilled water.

Influence of Enveloping Water Layer on the Rise of Air Bubbles in Newtonian Fluids

1974 ◽  
Vol 41 (1) ◽  
pp. 29-34 ◽  
Author(s):  
J. L. Mercier ◽  
F. M. da Cunha ◽  
J. C. Teixeira ◽  
M. P. Scofield
Keyword(s):  
Mass Transfer ◽  
Water Mass ◽  
Bubble Formation ◽  
Water Layer ◽  
Terminal Velocity ◽  
Newtonian Fluids ◽  
Distilled Water ◽  
Air Bubbles ◽  
Low Viscosity ◽  
Water Layers

The rise of air bubbles in five Newtonian fluids is compared for two different cases of bubble formation and release: (a) directly into the five homogeneous fluids and (b) directly into a layer of distilled water underlying each one of the five liquids. It was found in Case (b) that medium-sized bubbles rise steadily through the upper liquid with an enveloping water layer of variable thickness. The influence of this water layer on the trajectory, shape, and terminal velocity of bubbles is particularly significant in low viscosity upper phases. The resulting water mass transfer per bubble through the lower density upper phase depends on viscosity and was markedly greater for the higher viscosity fluids. The behavior and the nature of the detachment of the water layers from the larger size bubbles are also presented and discussed.

A STUDY ON ANTIWEAR PROPERTIES OF GRAPHENE WATER-BASED LUBRICANT AND ITS CONTACT WITH METALLIC MATERIALS

Tribologia ◽  
2018 ◽  
Vol 281 (5) ◽  
pp. 71-81
Author(s):  
Anna PIĄTKOWSKA ◽  
Magdalena ROMANIEC ◽  
Danuta GRZYBEK ◽  
Małgorzata MOŻDŻONEK ◽  
Anna ROJEK ◽  
...  
Keyword(s):  
316L Stainless Steel ◽  
Armco Iron ◽  
Protective Layer ◽  
Bearing Steel ◽  
Distilled Water ◽  
Metallic Materials ◽  
Iron Metal ◽  
Graphene Flakes ◽  
Water Based ◽  
Antiwear Properties

Due to their ecological and financial aspects, water-based lubricants may be competitive in use for production and sustainable technology. The paper presents tribological measurements results in the ball-flat friction node with reciprocal movement. The friction element manufactured of 316L stainless steel and 100Cr6 bearing steel cooperated under mixed friction with the use of water-based lubricants. Firstly, graphene flakes and graphite were applied as lubricant additives, both used as a similar reference material. Secondly, graphene lubricant reduced the friction coefficient and wear of friction elements. Interaction between water and graphene lubricants with 0.1 wt % and 1 wt % of graphene flakes and metal was also investigated. After 30 days of oxidation test in water and graphene lubricants, the Fe sample (Armco iron) surface was covered in graphene flakes with iron oxide structures. A compact coverage of the surface creates a protective layer against intensive oxidation in the distilled water-based graphene lubricant. The tests results have proven that the greater density of graphene flakes in the lubricant, the smaller is the amount of detected oxides. Graphene flakes agglomeration was observed in contact with the iron metal.

Graphite/Metal Electrodes for Electrochemical Exfoliation: Few Layers Graphene with Low Defects

2017 ◽  
Vol 371 ◽  
pp. 131-134
Author(s):  
F.C. Rodrigues ◽  
G.A. Nobre ◽  
E.E. da Silva ◽  
Mauro Cesar Terence ◽  
Juan Alfredo Guevara Carrió
Keyword(s):  
Electrochemical Process ◽  
Rapid Expansion ◽  
Structural Defects ◽  
X Rays ◽  
Electrochemical Exfoliation ◽  
Graphite Electrodes ◽  
Low Degree ◽  
Electrical Conductivities ◽  
Graphene Flakes

Graphene was obtained by electrochemical exfoliation of graphite and metal/graphite electrodes of different compositions and electrical conductivities. Metal/graphite electrodes were prepared using high purity copper and nickel precursor and commercial graphite. Processes of rapid expansion and direct exfoliation of graphite in a H2SO4 solution were observed using voltages from 2V to 15V and currents of 0.03 mA to 0.08 mA. The total time for each process was one hour and the maximal concentration of few layers graphene flakes was 0.002 mg/mL. X rays powder diffraction of the expanded electrodes showed the effect of the electrochemical process in the crystallinity and the increasing of interlayer distance. A characterization of a large amount of graphene flakes was performed by Raman spectroscopy and optical microscopy. Typical size of the flakes are between 1 μm and 10 μm and the Raman spectra indicate number of layers from single or bilayers to approximately ten layers. The greatest variations in thickness of flakes are observed when the intercalation process concludes before the expansion of the layers. A low degree of oxidation and of structural defects was characteristic of the experiments with lower acid concentration.

Biophysical Measurement of Molecular Weight of Foot-and-Mouth Disease RNA Fragments

1974 ◽  
Vol 32 ◽  
pp. 262-263
Author(s):  
Sydney S. Breese ◽  
Howard L. Bachrach
Keyword(s):  
Chemical Properties ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Distilled Water ◽  
Bovine Plasma ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Carbon Coated ◽  
Rna Fragments ◽  
Physical And Chemical

Continuing studies on the physical and chemical properties of foot-and-mouth disease virus (FMDV) have included electron microscopy of RNA strands released when highly purified virus (1) was dialyzed against demlneralized distilled water. The RNA strands were dried on formvar-carbon coated electron microscope screens pretreated with 0.1% bovine plasma albumin in distilled water. At this low salt concentration the RNA strands were extended and were stained with 1% phosphotungstic acid. Random dispersions of strands were recorded on electron micrographs, enlarged to 30,000 or 40,000 X and the lengths measured with a map-measuring wheel. Figure 1 is a typical micrograph and Fig. 2 shows the distributions of strand lengths for the three major types of FMDV (A119 of 6/9/72; C3-Rezende of 1/5/73; and O1-Brugge of 8/24/73.

Freeze-fracture, freeze-etch complementary pairs of virus-infected cells reveal value of etching even when relatively high concentrations of cryoprotectants are used

1978 ◽  
Vol 36 (2) ◽  
pp. 136-137
Author(s):  
Russell L. Steere ◽  
Eric F. Erbe
Keyword(s):  
Plant Tissue ◽  
Phosphate Buffer ◽  
Infected Plant ◽  
Freeze Fracture ◽  
Distilled Water ◽  
Virus Infected Plant ◽  
Infected Cells ◽  
High Concentrations

It has been assumed by many involved in freeze-etch or freeze-fracture studies that it would be useless to etch specimens which were cryoprotected by more than 15% glycerol. We presumed that the amount of cryoprotective material exposed at the surface would serve as a contaminating layer and prevent the visualization of fine details. Recent unexpected freeze-etch results indicated that it would be useful to compare complementary replicas in which one-half of the frozen-fractured specimen would be shadowed and replicated immediately after fracturing whereas the complement would be etched at -98°C for 1 to 10 minutes before being shadowed and replicated.Standard complementary replica holders (Steere, 1973) with hinges removed were used for this study. Specimens consisting of unfixed virus-infected plant tissue infiltrated with 0.05 M phosphate buffer or distilled water were used without cryoprotectant. Some were permitted to settle through gradients to the desired concentrations of different cryoprotectants.

Direct observations of radiation-enhanced transformations in glass

1983 ◽  
Vol 41 ◽  
pp. 354-355
Author(s):  
J. F. DeNatale ◽  
D. G. Howitt
Keyword(s):  
Glass Matrix ◽  
Diffusion Mechanism ◽  
Bubble Formation ◽  
Silicate Glasses ◽  
Phase Decomposition ◽  
Direct Observations ◽  
Thin Foils ◽  
Oxygen Bubble ◽  
Electron Energy Loss ◽  
Kinetics Of

The electron irradiation of silicate glasses containing metal cations produces various types of phase separation and decomposition which includes oxygen bubble formation at intermediate temperatures figure I. The kinetics of bubble formation are too rapid to be accounted for by oxygen diffusion but the behavior is consistent with a cation diffusion mechanism if the amount of oxygen in the bubble is not significantly different from that in the same volume of silicate glass. The formation of oxygen bubbles is often accompanied by precipitation of crystalline phases and/or amorphous phase decomposition in the regions between the bubbles and the detection of differences in oxygen concentration between the bubble and matrix by electron energy loss spectroscopy cannot be discerned (figure 2) even when the bubble occupies the majority of the foil depth.The oxygen bubbles are stable, even in the thin foils, months after irradiation and if van der Waals behavior of the interior gas is assumed an oxygen pressure of about 4000 atmospheres must be sustained for a 100 bubble if the surface tension with the glass matrix is to balance against it at intermediate temperatures.

Comparison of Acrylamide and Agar Gels by Freeze-Etching

1977 ◽  
Vol 35 ◽  
pp. 606-607
Author(s):  
Russell L. Steere ◽  
Eric F. Erbe
Keyword(s):  
Electron Microscope ◽  
Sodium Hydroxide ◽  
Sodium Hypochlorite ◽  
Chromic Acid ◽  
Distilled Water ◽  
Thin Sheets ◽  
Acid Cleaning ◽  
Agar Gels ◽  
Freeze Etching ◽  
Water Cut

Thin sheets of acrylamide and agar gels of different concentrations were prepared and washed in distilled water, cut into pieces of appropriate size to fit into complementary freeze-etch specimen holders (1) and rapidly frozen. Freeze-etching was accomplished in a modified Denton DFE-2 freeze-etch unit on a DV-503 vacuum evaporator.* All samples were etched for 10 min. at -98°C then re-cooled to -150°C for deposition of Pt-C shadow- and C replica-films. Acrylamide gels were dissolved in Chlorox (5.251 sodium hypochlorite) containing 101 sodium hydroxide, whereas agar gels dissolved rapidly in the commonly used chromic acid cleaning solutions. Replicas were picked up on grids with thin Foimvar support films and stereo electron micrographs were obtained with a JEM-100 B electron microscope equipped with a 60° goniometer stage.Characteristic differences between gels of different concentrations (Figs. 1 and 2) were sufficiently pronounced to convince us that the structures observed are real and not the result of freezing artifacts.

Heterogeneity of Size and Distribution of Intramembrane Particles in the Plasma Membrane of Yeast

1977 ◽  
Vol 35 ◽  
pp. 596-597
Author(s):  
E. Keyhani
Keyword(s):  
Plasma Membrane ◽  
Candida Utilis ◽  
Synthetic Medium ◽  
Freeze Fracture ◽  
Translational Diffusion ◽  
Yeast Cells ◽  
Distilled Water ◽  
Intramembrane Particles ◽  
The Matrix ◽  
Water Cell

The matrix of biological membranes consists of a lipid bilayer into which proteins or protein aggregates are intercalated. Freeze-fracture techni- ques permit these proteins, perhaps in association with lipids, to be visualized in the hydrophobic regions of the membrane. Thus, numerous intramembrane particles (IMP) have been found on the fracture faces of membranes from a wide variety of cells (1-3). A recognized property of IMP is their tendency to form aggregates in response to changes in experi- mental conditions (4,5), perhaps as a result of translational diffusion through the viscous plane of the membrane. The purpose of this communica- tion is to describe the distribution and size of IMP in the plasma membrane of yeast (Candida utilis).Yeast cells (ATCC 8205) were grown in synthetic medium (6), and then harvested after 16 hours of culture, and washed twice in distilled water. Cell pellets were suspended in growth medium supplemented with 30% glycerol and incubated for 30 minutes at 0°C, centrifuged, and prepared for freeze-fracture, as described earlier (2,3).

Variations in Surface Textures of Quartz Sand using Electron Microscopy

1970 ◽  
Vol 28 ◽  
pp. 494-495
Author(s):  
Eugene J. Amaral
Keyword(s):  
Electron Microscopy ◽  
Glass Industry ◽  
Glass Slide ◽  
Distilled Water ◽  
Early Paleozoic ◽  
Secondary Effects ◽  
Surface Textures ◽  
High Silica ◽  
Sand Deposit ◽  
The U.S

Examination of sand grain surfaces from early Paleozoic sandstones by electron microscopy reveals a variety of secondary effects caused by rock-forming processes after final deposition of the sand. Detailed studies were conducted on both coarse (≥0.71mm) and fine (=0.25mm) fractions of St. Peter Sandstone, a widespread sand deposit underlying much of the U.S. Central Interior and used in the glass industry because of its remarkably high silica purity.The very friable sandstone was disaggregated and sieved to obtain the two size fractions, and then cleaned by boiling in HCl to remove any iron impurities and rinsed in distilled water. The sand grains were then partially embedded by sprinkling them onto a glass slide coated with a thin tacky layer of latex. Direct platinum shadowed carbon replicas were made of the exposed sand grain surfaces, and were separated by dissolution of the silica in HF acid.

Scanning Electron Microscopy-cuticular Lesions on the Roundworm Ascaris Suum

1970 ◽  
Vol 28 ◽  
pp. 114-115
Author(s):  
P. A. Madden ◽  
W. R. Anderson
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Freeze Drying ◽  
Room Temperature ◽  
Secondary Electron ◽  
Distilled Water ◽  
Freeze Dried ◽  
Silver Paint ◽  
To Come ◽  
Scanning Electron

The intestinal roundworm of swine is pinkish in color and about the diameter of a lead pencil. Adult worms, taken from parasitized swine, frequently were observed with macroscopic lesions on their cuticule. Those possessing such lesions were rinsed in distilled water, and cylindrical segments of the affected areas were removed. Some of the segments were fixed in buffered formalin before freeze-drying; others were freeze-dried immediately. Initially, specimens were quenched in liquid freon followed by immersion in liquid nitrogen. They were then placed in ampuoles in a freezer at −45C and sublimated by vacuum until dry. After the specimens appeared dry, the freezer was allowed to come to room temperature slowly while the vacuum was maintained. The dried specimens were attached to metal pegs with conductive silver paint and placed in a vacuum evaporator on a rotating tilting stage. They were then coated by evaporating an alloy of 20% palladium and 80% gold to a thickness of approximately 300 A°. The specimens were examined by secondary electron emmission in a scanning electron microscope.

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