scholarly journals Positively Charged Water as a Plant Germination Stimulator

2021 ◽  
Vol 9 (1) ◽  
pp. 1
Author(s):  
Yuri Pivovarenko
2004 ◽  
Vol 82 (10) ◽  
pp. 1462-1467 ◽  
Author(s):  
George E Walrafen ◽  
Hugh R Carlon

A new method is presented by which energy–mass, volume–mass, and enthalpy–mass dispersion curves may be determined for charged water vapor clusters. This method involves two closely spaced partial pressures at a fixed temperature. The method is exemplified by using mass spectral data from positively charged water vapor clusters (H+(H2O)M) where 6 ≤ M ≤ 45. A ΔG–mass dispersion was also determined using the ΔH–mass dispersion for comparison. ΔG displays an enormous minimum, which is of signal importance because it indicates that a size of maximum stability (SMS) exists. The SMS corresponds to M = 13 for pressures between 0.056 and 0.151 bar (1 bar = 100 kPa) at 373.15 K, and to M = 32±1 for pressures between 0.473 and 0.556 bar at 372.15 K. The free energy corresponding to M = 45 occurs far above that corresponding to the SMS. The resultant instability leads to condensation for pressures above 0.556 bar at 372.15 K.Key words: clusters, mass spectrometry, thermodynamics, water vapour.


2004 ◽  
Vol 689 (25) ◽  
pp. 4729-4738 ◽  
Author(s):  
Edward Rosenberg ◽  
Fabrizio Spada ◽  
Kent Sugden ◽  
Brooke Martin ◽  
Roberto Gobetto ◽  
...  

2021 ◽  
Vol 3 (1) ◽  
Author(s):  
Yuri Pivovarenko

It was previously found that the electric charge of water determines its ability to interact with other substances, including biologically significant ones. It is shown here that the electric charge of water can also determine its ability to penetrate and accumulate in living cells. In particular, it has been shown that the high penetrating ability of positively charged water determines both its active penetration into cells and accumulation in them, which creates favourable conditions for cell proliferation. At the same time, it has been shown that the low penetrating ability of negatively charged water determines its ability to slow down cell proliferation. It also discusses how medics can obtain and use water at different charges.


1919 ◽  
Vol 2 (1) ◽  
pp. 87-106 ◽  
Author(s):  
Jacques Loeb

1. Amphoteric electrolytes form salts with both acids and alkalies. It is shown for two amphoteric electrolytes, Al(OH)3 and gelatin, that in the presence of an acid salt water diffuses through a collodion membrane into a solution of these substances as if its particles were negatively charged, while water diffuses into solutions of these electrolytes, when they exist as monovalent or bivalent metal salts, as if the particles of water were positively charged. The turning point for the sign of the electrification of water seems to be near or to coincide with the isoelectric point of these two ampholytes which is a hydrogen ion concentration of about 2 x 10–5 N for gelatin and about 10–7 for Al(OH)3. 2. In conformity with the rules given in a preceding paper the apparently positively charged water diffuses with less rapidity through a collodion membrane into a solution of Ca and Ba gelatinate than into a solution of Li, Na, K, or NH4 gelatinate of the same concentration of gelatin and of hydrogen ions. Apparently negatively charged water diffuses also with less rapidity through a collodion membrane into a solution of gelatin sulfate than into a solution of gelatin chloride or nitrate of the same concentration of gelatin and of hydrogen ions. 3. If we define osmotic pressure as that additional pressure upon the solution required to cause as many molecules of water to diffuse from solution to the pure water as diffuse simultaneously in the opposite direction through the membrane, it follows that the osmotic pressure cannot depend only on the concentration of the solute but must depend also on the electrostatic effects of the ions present and that the influence of ions on the osmotic pressure must be the same as that on the initial velocity of diffusion. This assumption was put to a test in experiments with gelatin salts for which a collodion membrane is strictly semipermeable and the tests confirmed the expectation.


1997 ◽  
Vol 410-411 ◽  
pp. 77-79 ◽  
Author(s):  
Marek Procházka ◽  
Jana Hanzliková ◽  
Josef Štěpánek ◽  
Vladimir Baumruk

Author(s):  
D.P. Bazett-Jones ◽  
F.P. Ottensmeyer

Dark field electron microscopy has been used for the study of the structure of individual macromolecules with a resolution to at least the 5Å level. The use of this technique has been extended to the investigation of structure of interacting molecules, particularly the interaction between DNA and fish protamine, a class of basic nuclear proteins of molecular weight 4,000 daltons.Protamine, which is synthesized during spermatogenesis, binds to chromatin, displaces the somatic histones and wraps up the DNA to fit into the small volume of the sperm head. It has been proposed that protamine, existing as an extended polypeptide, winds around the minor groove of the DNA double helix, with protamine's positively-charged arginines lining up with the negatively-charged phosphates of DNA. However, viewing protamine as an extended protein is inconsistent with the results obtained in our laboratory.


Author(s):  
D.P. Bazett-Jones ◽  
F.P. Ottensmeyer

It has been shown for some time that it is possible to obtain images of small unstained proteins, with a resolution of approximately 5Å using dark field electron microscopy (1,2). Applying this technique, we have observed a uniformity in size and shape of the 2-dimensional images of pure specimens of fish protamines (salmon, herring (clupeine, Y-l) and rainbow trout (Salmo irideus)). On the basis of these images, a model for the 3-dimensional structure of the fish protamines has been proposed (2).The known amino acid sequences of fish protamines show stretches of positively charged arginines, separated by regions of neutral amino acids (3). The proposed model for protamine structure (2) consists of an irregular, right-handed helix with the segments of adjacent arginines forming the loops of the coil.


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