Effects of the KMnO4/Salt Shrinkproofing Treatment on the Frictional Properties of Wool Fibers

1969 ◽  
Vol 39 (8) ◽  
pp. 710-721 ◽  
Author(s):  
K. Rachel Makinson

Following on the observation that the KMnO4/salt shrinkproofing process attacks the scales on the intrados of the crimp of wool fibers preferentially, the “static” friction of wool fibers over polished horn in aqueous media has been measured by the standard capstan method under conditions chosen to ensure that some contact is made with the intrados of the crimp. It has been found that the treatment causes a large increase in the with-scale friction and in some circumstances a decrease in the frictional difference. When the proportion of contact with the intrados of the crimp is reduced, these effects become much smaller. Both types of frictional change are the result of degradation of the material inside the scale-cells, which makes the scales, when wet, softer and less elastic than the scales of untreated fibers. Experimental conditions determine whether this softening is expressed as an increase in with-scale friction or as a decrease in the frictional difference.

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Abbas Khan ◽  
Naila ◽  
Muhammad Humayun ◽  
Muhammad Sufaid Khan ◽  
Luqman Ali Shah ◽  
...  

Abstract To understand the expected mode of action, the physicochemical study on the solution properties of medicinal compounds and their interaction with deoxyribonucleic acid (DNA), under varying experimental conditions, is of prime importance. The present research work illustrates the physicochemical study and interaction of certain medicinal compounds such as; Levofloxacin, Ciprofloxacin, and Ibuprofen with DNA. Density, viscosity and surface tension measurements have been performed in order to determine, in a systematic manner, the physicochemical, volumetric and thermodynamic properties of these compounds; and most of these parameters have shown different behavior with varying concentration of solution, temperature of the medium and chemical nature/structure of the compound. In addition, these drugs showed a spontaneous surface-active and association behavior in aqueous solutions. The flow behavior, surface properties, volumetric behavior and solute–solvent interaction of these drugs were prominently influenced by experimental variables and addition of DNA to their solutions. UV–Visible spectroscopy was also used to examine the interaction of these drugs with DNA in aqueous media in detail. Calculated values of binding constants (Kb) for all complexes of drug-DNA are positive, indicating a fruitful binding process. It is seen that a smaller Kb value reflects weaker binding of the drug with DNA and vise versa. Due to the difference in the chemical structure of drugs the values of binding constant are different for various drug-DNA complexes and follow the order Kb(Levofloxacin-DNA) > Kb(Ciprofloxacin-DNA) > Kb(Ibuprofen-DNA). On the basis of spectral changes and Kb it can be said that the binding of all these drugs with DNA may be of physicochemical nature and the dominating binding force be of hydrogen bonding between oxygen of drugs and hydrogen of DNA units and the drug having more oxygen atoms showed stronger binding ability. The data further suggest a limited possibility of chemical type attachment of these drugs with DNA.


2007 ◽  
Vol 11 (04) ◽  
pp. 269-276 ◽  
Author(s):  
Jing Shen ◽  
Zhongping Ou ◽  
Jianguo Shao ◽  
Michał Gałęzowski ◽  
Daniel T. Gryko ◽  
...  

A series of free-base corroles with different electron-donating or electron-withdrawing substituents were reacted with piperidine, 4-aminopyridine, 2-methylimidazole, 2-aminopyridine or pyridine in PhCN and the UV-visible spectral changes monitored during conversion of ( Cor ) H 3 to [( Cor ) H 2]- as a function of the concentration and strength of the added organic base. Analysis of the UV-visible spectral changes as a function of the added base concentration enabled calculation of equilibrium constants ( logK ) for deprotonation of each corrole under the given experimental conditions. Relationships are examined between the experimentally measured logK values and previously published spectroscopic and structural properties of the compounds.


1969 ◽  
Vol 115 (1) ◽  
pp. 11-18 ◽  
Author(s):  
A. Massaglia ◽  
U. Rosa ◽  
G. Rialdi ◽  
C. A. Rossi

1. The iodination of insulin was studied under various experimental conditions in aqueous media and in some organic solvents, by measuring separately the uptake of iodine by the four tyrosyl groups and the relative amounts of monoiodotyrosine and di-iodotyrosine that are formed. In aqueous media from pH1 to pH9 the iodination occurs predominantly on the tyrosyl groups of the A chain. Some organic solvents increase the iodine uptake of the B-chain tyrosyl groups. Their efficacy in promoting iodination of Tyr-B-16 and Tyr-B-26 is in the order: ethylene glycol and propylene glycol≃methanol and ethanol>dioxan>8m-urea. 2. It is suggested that each of the four tyrosyl groups in insulin has a different environment: Tyr-A-14 is fully exposed to the solvent; Tyr-A-19 is sterically influenced by the environmental structure, possibly by the vicinity of a disulphide interchain bond; Tyr-B-16 is embedded into a non-polar area whose stability is virtually independent of the molecular conformation; Tyr-B-26 is probably in a situation similar to Tyr-B-16 with the difference that its non-polar environment depends on the preservation of the native structure.


1948 ◽  
Vol 18 (8) ◽  
pp. 475-480 ◽  
Author(s):  
Daniel Frishman ◽  
Arthur L. Smith ◽  
Milton Harris

2020 ◽  
Author(s):  
Matt Ikari ◽  
Andre Hüpers

<p>On major plate-boundary fault zones, it is generally observed that large-magnitude earthquakes tend to nucleate within a discrete depth range in the crust known as the seismogenic zone.  This is generally explained by the contrast between frictionally stable, velocity strengthening sediments at shallow depths and lithified, velocity-weakening rocks at seismogenic (10’s of km) depth. Thus, it is hypothesized that diagenetic and low-grade metamorphic processes are responsible for the development of velocity-weakening frictional behavior in sediments that make up fault gouges.  Previous laboratory studies comparing the frictional properties of intact rocks and powdered versions of the same rocks generally support this hypothesis, however controlling lithification in the laboratory and systematically quantifying frictional behavior as a function of lithification and remains a challenge.</p><p>Here, we simulate the lithification process in the laboratory by using mixtures of halite and shale powders with halite-saturated brine, which we consolidate under 10 MPa normal stress and subsequently desiccate.  The desiccation allows precipitation of halite as cement, creating synthetic rocks.  We vary the proportion of salt to shale in our samples, which we use as a proxy for degree of lithification.  We measure the frictional properties of our lithified samples, and equivalent powdered versions of these samples, with velocity-step tests in the range 10<sup>-7</sup> – 3x10<sup>-5</sup> m/s.  We quantify lithification by two methods: (1) direct measurement of cohesion, and (2) measuring the porosity reduction of lithified samples compared to powders.  Using these measurements, we systematically investigate the relationship between lithification and frictional slip behavior.</p><p>We observe that powdered samples of every halite-shale proportion exhibits predominantly velocity-strengthening friction, whereas lithified samples exhibit a combination of velocity strengthening and significant velocity weakening when halite constitutes at least 30 wt% of the sample.  Larger velocity weakening generally coincides with friction coefficients of > 0.62, cohesion of > ~1 MPa, and porosity reduction of > ~50 vol%.  Although none of our lithified samples exhibit strictly velocity-weakening friction, this is consistent with the frictional behavior of pure halite under our experimental conditions.  Scanning electron microscopy images do not show any clear characteristics attributable to velocity-weakening, but did reveal that the shear surfaces for powders tends to exhibit small cracks not seen in the lithified sample shear surfaces.  These results suggest that lithification via cementation and porosity loss may facilitate slip instability, but that microstructural indicators are subtle.</p>


2007 ◽  
Vol 61 (9) ◽  
pp. 1021-1024 ◽  
Author(s):  
Xiao Fang ◽  
S. Rafi Ahmad

Various sample presentation configurations for elemental analysis in aqueous media by laser-induced breakdown spectroscopy (LIBS) have been tested and analyzed. Direct and quantitative comparison between the two different sample presentation methods, plasma excitation within water bulk and on the surface in a water jet, has been carried out using the same LIBS system under the same experimental conditions. Temporal characteristics of light emitted from the plasma induced in both the water bulk and the jet surface containing calcium (Ca) were recorded and presented. Spectral data recorded under optimum detection gating conditions showed that the signal-to-noise ratio (S/N) for excitation in the water jet configuration is approximately 10 times higher than that in the bulk excitation, the actual values of enhancement being dependent on the element type. The typical spectra of aqueous samples containing sodium (Na), calcium (Ca), zinc (Zn), cadmium (Cd), and mercury (Hg) were detected and the signal-to-noise ratios were evaluated and compared for the sample presentation configurations under considerations. The results suggest that for better sensitivity of detection, a simple water jet sample presentation configuration could be designed and implemented for cost-effective commercial use of this technique for elemental analysis in a water environment.


1995 ◽  
Vol 73 (8) ◽  
pp. 1298-1304 ◽  
Author(s):  
Paul-Louis Fabre ◽  
Paule Castan ◽  
Diane Deguenon ◽  
Nicole Paillous

Croconic acid, H2C5O5, is readily oxidized. This may be attested by decolorization of the solutions and by observation of oxalic acid complexes. The oxidation products are identified by 13C NMR spectroscopy as oxalic and mesoxalic acids, and experimental conditions are specified. The oxidation process requires dioxygen and photons. In parallel, the electrochemical oxidation of croconic acid is studied in aqueous media and in acetonitrile. A potential–pH diagram is drawn. Keywords: croconic acid, oxalic acid, oxidation, electrochemistry, photochemistry.


2020 ◽  
Vol 17 (1) ◽  
pp. 47
Author(s):  
Haiyam Alayan ◽  
Mustafa Mohammed Aljumaily ◽  
Mohammed Abdulhakim Alsaadi ◽  
Mohd Ali Hashim

              The present work investigates the effect of the type of carbon precursor on the adsorptive proficiency of as-prepared carbon nanomaterials (CNMs) for the removal of methylene blue dye (MB) from aqueous media. A comparison study was applied to assess the growth of CNMs from the decomposition of methane (CNMY1) and acetylene (CNMY2) using response surface methodology with central composite design (RSM/CCD). The produced nanomaterials were characterized using FESEM, EDX, TEM, BET surface area, Raman, TGA, FTIR, and zeta potential. The as-prepared adsorbent displayed different morphologies and under the experimental conditions, 10 mg of CNMY1 and CNMY2 was responsible for 97.7 % and 96.80% removal of dye. The maximum adsorptive uptake predicted by Langmuir isotherm was about 250 and 174 mg/g for CNMY1 and CNMY2, respectively. The as-synthesized carbon nanomaterial in this study could be explored as a great potential candidate for dye-bearing wastewater treatment.


2004 ◽  
Vol 69 (8-9) ◽  
pp. 683-688 ◽  
Author(s):  
Jurij Vucina ◽  
Dagoljub Lukic ◽  
Milovan Stoiljkovic

The conditions for the efficient separation of tungsten(VI) and rhenium (VII) on alumina were established. The distribution coefficients K d for tungstate and perrhenate anions, as well as the separation factors ?(? = KdWO42-/Kd ReO4-) were determined using hydrochloric or nitric acid as the aqueous media. Asolution of sodium chloride in the pH range 2?6 was also examined. Under all the tested experimental conditions, alumina is a much better adsorbent for tungsten than for rhenium. The obtained results indicated that the best separation of these two elements is achieved when 0.01? 0.1 mol dm-3HCl or 1.0mol dm-3 HNO3 are used as the aqueous media. If NaCl is used as the aqueous phase, the best separation is achieved with 0.20 mol dm-3 NaCl pH 4?6. Under these experimental conditions, the breakthrough and saturation capacities of alumina for tungsten at pH4 are 17 and 26 mg W/g Al2O3 respectively. With increasing pH, these values decrease. Thus, at pH 6 they are only 4 and 13 mg W/g Al2O3, respectively.


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