scholarly journals Paper trapping research after adding Mulberry tree branches bark cellulose pulp

2021 ◽  
Vol 25 ◽  
pp. 97-105
Author(s):  
Kh.A. Babakhanova ◽  
◽  
Z.K. Galimova ◽  
M.M. Аbdunazarov ◽  
I.I. Ismailov ◽  
...  
Keyword(s):  
Microscopic Analysis ◽  
Paint Layer ◽  
Paper Surface ◽  
Low Viscosity ◽  
Cellulose Pulp ◽  
Study Results ◽  
Inkjet Printers ◽  
Density Values ◽  
Probe Microscope ◽  
Mulberry Tree

The paper presents the study results of paper trapping during inkjet printing which contains cellulose pulp from the inner bark layer of mulberry branches. The connection between the print density and the paper surface structure, in particular, water absorption and raggedness, is established. The study of the stepwise gradation transition and color rendition, the graphic accuracy of reproduction of the slur element of the image is carried out. Densitometric and microscopic analysis of the impressions printed on an inkjet printer was performed. It was revealed that the pigments of water ink, depending on the microgeometry of the paper surface, penetrated deeper in different ways. It was found that the maximum thickness of the paint layer, expressed using the optical density values for the primary colors of the subtractive synthesis, and the best color reproduction were provided by the surface of the paper sample with 100 % addition of cellulose pulp from the inner layer of the bark of mulberry tree branches, which has the least roughness, according to the scanning probe microscope Solver HV. Recommendations are given for testing paper data on inkjet printers that use pigment inks and are less demanding on the surface properties of paper, or by printing methods that do not use low-viscosity printing inks.

scholarly journals Histo-morphology of cutaneous papillomatosis in indigenous cattle

2019 ◽  
Vol 1 (17) ◽  
Author(s):  
U. Ayman ◽  
S. K. Das
Keyword(s):  
Morphological Changes ◽  
Microscopic Analysis ◽  
Viral Disease ◽  
Skin Lesions ◽  
Eosin Y ◽  
Body Parts ◽  
Indigenous Cattle ◽  
Study Results ◽  
Internal Core ◽  
Perineal Region

Background: Papillomatosis is a viral disease manifested with benign cutaneous growths (skin epithelium hyperplasia) in different body parts which is encountered in cattle, goat, dog, rabbit, horse, rodent and also in human. The purpose of the present study is to detect the histo-morphological changes of cutaneous papillomatosis in indigenous cattle. Methods: Ten (10) random samples from skin lesions of warts were collected from adult indigenous cattle (10 cattle) that were diagnosed as cutaneous papillomatosis by clinical examination at Veterinary Teaching Hospital, Bangladesh Agricultural University, Mymensingh-2202, Bangladesh. For gross observations, location of appearance of warts, color and size was taken into consideration. Immediately after collection of sample, they were preserved in Bouin’s fluid followed by dehydration, clearing and infiltration and finally embedded by paraffin wax. Then samples were sectioned using rotatory microtome and stained with Harris’s Haematoxylin and Eosin Y to facilitate microscopic study. Results: The results of present study revealed that cutaneous papillomas were mostly located on the head and neck, around eyes, under the chin and perineal region in indigenous cattle. Grossly, warts in cattle are bumpy or cauliflower-like masses of various sizes and numbers that projected from the skin having grey, rough, scaly, and dry surface. When incised, its cut surface has an external layer- keratinized epithelium and an internal core- moist white connective tissue. Histopathological changes indicate hyperplastic features of the affected skin layers of epidermis. Further, the microscopic analysis also revealed orthokeratotic hyperkeratosis, acanthosis and down word hyperplasia, fibrovascular area, keratohyalin granules and koilocytes at different layers of the affected skin. Conclusion: The results of this present study might be useful for the classification and treatment of this common malady based on its histological changes.

Ballast Flying DEM Microscopic Analysis and Counteracting Measures

2011 ◽  
Vol 97-98 ◽  
pp. 266-270 ◽  
Author(s):  
Guo Qing Jing ◽  
Liang Gao ◽  
Xiao Lin Sun
Keyword(s):  
Friction Coefficient ◽  
Microscopic Study ◽  
High Speed ◽  
Microscopic Analysis ◽  
Dynamic Force ◽  
High Speed Railway ◽  
Model Method ◽  
Study Results

Ballast flying problems obsess the high speed railway developments, causing damages to the train and deteriorations to the rail. In the paper, DEM is used to conduct ballast flying mechanism microscopic study, results show ballast flying increases with train dynamic force, and decreases with ballast size and friction coefficient, ballast flying counteracting measures are presented, such as ballast bed parameter and ballast glue. In the end, future possible microscopic ballast flying model method is presented by DEM coupled with CFD.

Alpha-Mangostin Phase Inversion Induced In Situ Forming Gel

2019 ◽  
Vol 819 ◽  
pp. 202-208
Author(s):  
Setthapong Senarat ◽  
Takorn Chantadee ◽  
Wichai Santimaleeworagun ◽  
Yaowaruk Phorom ◽  
Thawatchai Phaechamud
Keyword(s):  
Phase Inversion ◽  
Extended Release ◽  
Initial Time ◽  
Low Viscosity ◽  
Microbial Inhibition ◽  
Formation Behavior ◽  
Density Values ◽  
Methyl Pyrrolidone ◽  
Rapid Transformation

Alpha-mangostin (aMG) phase inversion induced in situ forming gel (ISG) was prepared by dissolving matrix formers including palmitic acid (P) and lauric acid (L) in dimethyl sulfoxide (DMSO) and N-methyl pyrrolidone (NMP). The pH and density values were in range of 4.42-6.22 and 0.9731-1.0943 g.cm-3, respectively. The prepared formulas have low viscosity and high injectability which were suitable for injection. The gel formation behavior was affected by type of fatty acid and solvent. P dissolved in DMSO showed a rapid transformation into matrix at initial time. The extended release of aMG was attained in P-based ISG. aMG phase inversion induced ISG improved microbial inhibition.

Comparison of ultraviolet inkjet printing on different synthetic fibrous papers

TAPPI Journal ◽  
2010 ◽  
Vol 9 (5) ◽  
pp. 17-25
Author(s):  
MIRICA DEBELJAK ◽  
SABINA BRAČKO ◽  
ALEŠ HLADNIK ◽  
DIANA GREGOR-SVETEC
Keyword(s):  
Inkjet Printing ◽  
Microscopic Analysis ◽  
Inkjet Printers ◽  
Inkjet Printer

We investigated the printability of fibrous synthetic papers with ultraviolet (UV) inkjet technology. Cyan, magenta, yellow, and black (CMYK) color fields were printed on two types of fibrous synthetic papers using two different wide-format UV inkjet printers. Spectrophotometric and densitometric measurements were performed on CMYK color fields with different ink coverages, along with a microscopic analysis of unprinted paper, black prints with 100% ink coverage, and a print mottle of magenta and black prints. Colorimetry and optical densities of the CMYK prints were qualitatively and quantitatively compared. Color deviations in CMYK prints were affected by paper type and were dependent on the UV inkjet printer used.

scholarly journals THE INVESTIGATION OF THE DEVELOPMENT OF A CREAM COMPOSITION WITH THE SAPROPEL EXTRACT

2018 ◽  
Vol 11 (7) ◽  
pp. 147 ◽  
Author(s):  
Oksana Strus ◽  
Natalya Polovko ◽  
Yuliya Plaskonis
Keyword(s):  
Corn Oil ◽  
Ph Value ◽  
Microscopic Analysis ◽  
Colloid Stability ◽  
Organoleptic Properties ◽  
Ph Values ◽  
Low Viscosity ◽  
Organoleptic Characteristics ◽  
The Stability ◽  
Physical Instability

Objective: The objective of this research was the development of cream with sapropel extract on the emulsifying base and the investigation of the possibility for cream samples to be in future applied in medicine, cosmetics, and veterinary.Methods: To carry out the research a set of methods (centrifugal, thermal, and potentiometric) to analyze colloidal and thermal stability and determine pH values of the tested samples were used. Organoleptic characteristics of the tested samples and possible signs of physical instability were studied. Rheological properties of the samples were determined on the rotating viscometer. The method of microscopic analysis was carried out to analyze the stability of the emulsion system.Results: The research outcomes revealed that all the prototype samples have thermal and colloid stability, neutral pH value, and consistency that depends on the content of the oil phase and the emulsifying mixture. The samples, containing 15% of Vaseline oil and 4% and 6% of emulsifier no. 1, have low viscosity indexes, and the sample with 10% of emulsifier has a rather dense consistency. The samples containing 20% of oil phase possess unsatisfactory organoleptic properties. Since the sample with 4% of emulsifier possessed low rates of viscosity and phase separation occurred during its storage.Microscopic studies have shown that the sample containing 6% of emulsifier no. 1 exhibits monodisperse and a uniform roundness of drops that indicates the stability of the system.Conclusion: The outcome of the research is the development of the composition of the cream with sapropel extract with the emulsifying base containing 15% of corn oil, 6% of emulsifier no. 1, and 1% of Cetostearyl alcohol and purified water.

Preparatory Procedures for Electron Microscopic Analysis at the Molecular Level of Resolution

1978 ◽  
Vol 36 (3) ◽  
pp. 516-520
Author(s):  
F.J. Sjostrand
Keyword(s):  
Electron Microscope ◽  
Molecular Level ◽  
Microscopic Analysis ◽  
Resolving Power ◽  
Cellular Structures ◽  
Electron Microscopic ◽  
Systematic Analysis ◽  
Technical Developments ◽  
Thin Sectioning ◽  
Obvious Reason

In the 1940's and 1950's electron microscopy conferences were attended with everybody interested in learning about the latest technical developments for one very obvious reason. There was the electron microscope with its outstanding performance but nobody could make very much use of it because we were lacking proper techniques to prepare biological specimens. The development of the thin sectioning technique with its perfectioning in 1952 changed the situation and systematic analysis of the structure of cells could now be pursued. Since then electron microscopists have in general become satisfied with the level of resolution at which cellular structures can be analyzed when applying this technique. There has been little interest in trying to push the limit of resolution closer to that determined by the resolving power of the electron microscope.

The Use of Styrenes as Embedding Media for Electron Microscopy

1971 ◽  
Vol 29 ◽  
pp. 488-489
Author(s):  
Edward D. De-Lamater ◽  
Eric Johnson ◽  
Thad Schoen ◽  
Cecil Whitaker
Keyword(s):  
Electron Microscopy ◽  
Surface Tension ◽  
Ultraviolet Light ◽  
Methyl Ethyl Ketone Peroxide ◽  
Methyl Ethyl ◽  
Styrene Polymerization ◽  
Radical Initiation ◽  
Tertiary Butyl ◽  
Low Viscosity ◽  
Free Radical Initiation

Monomeric styrenes are demonstrated as excellent embedding media for electron microscopy. Monomeric styrene has extremely low viscosity and low surface tension (less than 1) affording extremely rapid penetration into the specimen. Spurr's Medium based on ERL-4206 (J.Ultra. Research 26, 31-43, 1969) is viscous, requiring gradual infiltration with increasing concentrations. Styrenes are soluble in alcohol and acetone thus fitting well into the usual dehydration procedures. Infiltration with styrene may be done directly following complete dehydration without dilution.Monomeric styrenes are usually inhibited from polymerization by a catechol, in this case, tertiary butyl catechol. Styrene polymerization is activated by Methyl Ethyl Ketone peroxide, a liquid, and probably acts by overcoming the inhibition of the catechol, acting as a source of free radical initiation.Polymerization is carried out either by a temperature of 60°C. or under ultraviolet light with wave lengths of 3400-4000 Engstroms; polymerization stops on removal from the ultraviolet light or heat and is therefore controlled by the length of exposure.

Electron Microscopic Analysis of Myonecrosis Induced by a Pure Component Isolated From Rattlesnake Venom

1976 ◽  
Vol 34 ◽  
pp. 292-293
Author(s):  
Charlotte L. Ownby ◽  
David Cameron ◽  
Anthony T. Tu
Keyword(s):  
Gel Filtration ◽  
Microscopic Analysis ◽  
The United States ◽  
Exchange Chromatography ◽  
Pure Component ◽  
Electron Microscopic Level ◽  
Electron Microscopic ◽  
Mouse Muscle ◽  
Major Health Problem ◽  
Rattlesnake Venom

In the United States the major health problem resulting from snakebite poisoning is local tissue damage, i.e. hemorrhage and myonecrosis. Since commercial antivenin does not usually prevent such damage to tissue, a more effective treatment of snakebite-induced myonecrosis is needed. To aid in the development of such a treatment the pathogenesis of myonecrosis induced by a pure component of rattlesnake venom was studied at the electron microscopic level.The pure component, a small (4,300 mol. wt.), basic (isoelectric point of 9.6) protein, was isolated from crude prairie rattlesnake (Crotalus viridis viridis) venom by gel filtration (Sephadex G-50) followed by cation exchange chromatography (Sephadex C-25), and shown to be pure by electrophoresis. Selection of the myotoxic component was based on light microscopic observations of injected mouse muscle.

Some quantitative applications of vascular corrosion casting

1992 ◽  
Vol 50 (1) ◽  
pp. 738-739
Author(s):  
Fred E. Hossler
Keyword(s):  
Blood Vessels ◽  
Nuclear Orientation ◽  
Three Dimensional ◽  
Surrounding Tissue ◽  
Confocal Laser ◽  
Corrosion Casting ◽  
Venous Valve ◽  
Casting Technique ◽  
Low Viscosity ◽  
Quantitative Measurements

Preparation of replicas of the complex arrangement of blood vessels in various organs and tissues has been accomplished by infusing low viscosity resins into the vasculature. Subsequent removal of the surrounding tissue by maceration leaves a model of the intricate three-dimensional anatomy of the blood vessels of the tissue not obtainable by any other procedure. When applied with care, the vascular corrosion casting technique can reveal fine details of the microvasculature including endothelial nuclear orientation and distribution (Fig. 1), locations of arteriolar sphincters (Fig. 2), venous valve anatomy (Fig. 3), and vessel size, density, and branching patterns. Because casts faithfully replicate tissue vasculature, they can be used for quantitative measurements of that vasculature. The purpose of this report is to summarize and highlight some quantitative applications of vascular corrosion casting. In each example, casts were prepared by infusing Mercox, a methyl-methacrylate resin, and macerating the tissue with 20% KOH. Casts were either mounted for conventional scanning electron microscopy, or sliced for viewing with a confocal laser microscope.

Investigation of thin sections of biological standards by EDX, EELS, and Auger electron spectroscopy

1990 ◽  
Vol 48 (2) ◽  
pp. 184-185
Author(s):  
S. Lehner ◽  
H.E. Bauer ◽  
R. Wurster ◽  
H. Seiler
Keyword(s):  
Processing System ◽  
Beam Current ◽  
Beam Diameter ◽  
Thin Sections ◽  
Biologically Relevant ◽  
Energy Filtering ◽  
Low Viscosity ◽  
Carbon Foils ◽  
Electron Microscopical ◽  
Exchange Membrane

In order to compare different microanalytical techniques commercially available cation exchange membrane SC-1 (Stantech Inc, Palo Alto), was loaded with biologically relevant elements as Na, Mg, K, and Ca, respectively, each to its highest possible concentration, given by the number concentration of exchangeable binding sites (4 % wt. for Ca). Washing in distilled water, dehydration through a graded series of ethanol, infiltration and embedding in Spurr’s low viscosity epoxy resin was followed by thin sectioning. The thin sections (thickness of about 50 nm) were prepared on carbon foils and mounted on electron microscopical finder grids.The samples were analyzed with electron microprobe JXA 50A with transmitted electron device, EDX system TN 5400, and on line operating image processing system SEM-IPS, energy filtering electron microscope CEM 902 with EELS/ESI and Auger spectrometer 545 Perkin Elmer.With EDX, a beam current of some 10-10 A and a beam diameter of about 10 nm, a minimum-detectable mass of 10-20 g Ca seems within reach.

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