The Kinetics of the Coagulation of Latex of Hevea Brasiliensis and the Separation of the Hydratant Acid

1938 ◽  
Vol 11 (1) ◽  
pp. 60-74 ◽  
Author(s):  
N. H. van Harpen

Abstract In the present work, an attempt is made to study the process of coagulation of Hevea brasiliensis latex, so familiar to every rubber expert, from a general colloid-chemical point of view, and to ascertain the physical conditions under which the kenetic phenomena take place. Hevea Brasiliensis Latex as a Physical System In “The Electrometric Determination of the Hydrogen Ion Concentration in the Latex of Hevea brasiliensis and Its Applicability to Technical Problems” the true character of Hevea brasiliensis latex as a physical system and the phenomena which take place during coagulation of this system are discussed in the light of investigations and observations of various rubber experts. Latex is a dispersion composed of polydispersed rubber hydrocarbon, serum components, and water. The rubber component consists of microscopically visible solid or semi-solid particles, in Brownian movement, and judged by the degree of affinity of rubber for water these particles are unquestionably lyophobic. Since the serum components are in a colloidal state, they are present as sols or emulsions, and they impart to the latex its lyophilic properties. It is possible, however, to choose the conditions of coagulation so that, for a given concentration of dispersed substances and at a given temperature, the dispersion will be predominantly lyophobic or lyophilic. This dual standard leads to the conclusion that Hevea brasiliensis latex is a pseudo-lyophilic dispersion. In saying this, it should be noted that, although the dispersion has several lyophilic properties, it is nevertheless essentially a lyophobic system, the properties of which become manifest under the right conditions.

1923 ◽  
Vol 5 (3) ◽  
pp. 311-325 ◽  
Author(s):  
Wallace O. Fenn

1. Leucocytes ingest quartz particles more readily than carbon in acid solutions, and carbon more readily than quartz in alkaline solutions. 2. In the presence of acacia carbon is always preferred to quartz even in acid solutions. 3. Manganese dioxide particles are ingested by leucocytes with extraordinary rapidity as compared with manganese silicate or quartz. 4. Leucocytes are not attracted toward carbon or quartz particles but manganese dioxide exerts a distinct attraction for them. 5. Spores of Penicillium are ingested more readily than quartz. 6. Very small quartz particles, 1 micron in diameter, are not ingested as readily as larger particles of the same material. This result being contrary to the predictions of surface tension indicates that some other factor is involved in the ingestion of these small particles. 7. Measurements of the carbon electrode potentials and the cataphoretic charges on the particles have failed to supply an explanation for the varying relative rates of ingestion of carbon and quartz with varying hydrogen ion concentration.


1992 ◽  
Vol 12 (3) ◽  
pp. 529-532 ◽  
Author(s):  
G. L. Ludbrook ◽  
S. C. Helps ◽  
D. F. Gorman

The stability of cerebral function and blood flow (CBF), and the CBF response to changes in arterial carbon dioxide tension (CBF reactivity) during alfentanil anesthesia were examined in rabbits. This model was first shown to provide stable anesthesia, cortical function, and CBF for 4 h. CBF increased significantly to 159% [of baseline] in the left hemisphere and to 167% in the right within 5 min of an exposure to 5% CO2 ( p = 0.009 on the left and p = 0.003 on the right), but then decreased to 123% on the left and to 137% on the right (not significantly different from baseline, p = 0.11 on the left and p = 0.07 on the right) while PaCO2 was still rising. Steady state reactivity levels (0.8 ml 100 g−1/min−1/mm Hg−1 CO2 on the left and 0.65 ml 100 g−1/min−1/mm Hg−1 CO2 on the right) were consistent with previous work and were reached at 20 min. These results suggest that mechanisms other than perivascular hydrogen ion concentration mediate the CBF response to changes in arterial CO2 tension during alfentanil anesthesia.


1941 ◽  
Vol 14 (1) ◽  
pp. 133-136
Author(s):  
Paul Stamberger

Abstract In a study made on plantations in Malaya, it was found that the cause of instability is not the same for both fresh and preserved latex. The autocoagulation of fresh latex, as it will be shown, is not caused by the acid formed by bacterial action on the serum components (autoacidification). Coagulation takes place, in fact, when decomposition of the serum components is prevented by the addition of strong antiseptics. These experiments, carried out in 1938 and 1939 in Malaya, support Whitby's view that autocoagulation is not due to autoacidification, but is probably caused by enzyme action on the protein or other serum components of the latex. The behavior of preserved latex is entirely different. Coagulation on storage was found to be due to acid formation and neutralization of the preserving agent applied. Decomposition of serum components was found in cases when coagulation did not take place, which would naturally influence the further behavior of latex. The action of the preserving agents is not a simple one. Inhibiting bacterial growth and preventing decomposition are not enough to keep the latex in the liquid, colloidal state. In addition to antiseptics, chemical compounds which act specifically as coagulation preventatives must be present. Rhodes recommends 0.1 per cent ammonia in addition to sodium pentachlorophenate. This small quantity of ammonia, as it was found, is the specific substance, probably an enzyme poison, which prevents coagulation. A number of additional substances in combination with sodium pentachlorophenate were tried, and it was found that adjusting the hydrogen ion concentration on the alkali side was not sufficient to prevent coagulation, although bacterial decomposition was inhibited. Observing the changes in the specific conductivity of latex during storage was the most satisfactory method found to measure the value of preserving agents or combinations of preserving agents. An increase in the specific conductivity of latex was found after a few days' storage, provided that the preserving agent did not inhibit decomposition of the serum components. From this increase in conductivity on storage, it could be predicted whether or not the preserving agent tested would give satisfactory results, or whether or not the concentration of the preserving agent was sufficiently high.


2021 ◽  
Vol 2071 (1) ◽  
pp. 012020
Author(s):  
A H A Bakar ◽  
W N W Q W Hilmi ◽  
M N A Uda ◽  
N A Parmin ◽  
A M Noor ◽  
...  

Abstract This paper focuses on the ongoing development of real-time monitoring system with implementing the Internet of Things (IoT) element for arsenic heavy metal concentration in paddy field using pH sensor for data collection. The pH sensor will detect the hydrogen ion concentration from the prepared soil put in pot contained with various arsenic concentration. The developed system is then compared with the pH sensor in the market to verify its accuracy and sensitivity. The collected data will be transferred wirelessly into data cloud so that it can store the previous and current reading data. Besides, the system’s function is also to ensure the safeness of paddy plant to be planted with knowing the right amount of arsenic concentration can be passed.


1923 ◽  
Vol 6 (2) ◽  
pp. 215-237 ◽  
Author(s):  
Jacques Loeb

1. The effect of eight salts, NaCl, Na2SO4, Na4Fe(CN)6, CaCl2, LaCl3, ThCl4, and basic and acid fuchsin on the cataphoretic P.D. between solid particles and aqueous solutions was measured near the point of neutrality of water (pH 5.8). It was found that without the addition of electrolyte the cataphoretic P.D. between particles and water is very minute near the point of neutrality (pH 5.8), often less than 10 millivolts, if care is taken that the solutions are free from impurities. Particles which in the absence of salts have a positive charge in water near the point of neutrality (pH 5.8) are termed positive colloids and particles which have a negative charge under these conditions are termed negative colloids. 2. If care is taken that the addition of the salt does not change the hydrogen ion concentration of the solution (which in these experiments was generally pH 5.8) it can be said in general, that as long as the concentration of salts is not too high, the anions of the salt have the tendency to make the particles more negative (or less positive) and that cations have the opposite effect; and that both effects increase with the increasing valency of the ions. As soon as a maximal P.D. is reached, which varies for each salt and for each type of particles, a further addition of salt depresses the P.D. again. Aside from this general tendency the effects of salts on the P.D. are typically different for positive and negative colloids. 3. Negative colloids (collodion, mastic, Acheson's graphite, gold, and metal proteinates) are rendered more negative by low concentrations of salts with monovalent cation (e.g. Na) the higher the valency of the anion, though the difference in the maximal P.D. is slight for the monovalent Cl and the tetravalent Fe(CN)6 ions. Low concentrations of CaCl2 also make negative colloids more negative but the maximal P.D. is less than for NaCl; even LaCl3 increases the P.D. of negative particles slightly in low concentrations. ThCl4 and basic fuchsin, however, seem to make the negative particles positive even in very low concentrations. 4. Positive colloids (ferric hydroxide, calcium oxalate, casein chloride—the latter at pH 4.0) are practically not affected by NaCl, are rendered slightly negative by high concentrations of Na2SO4, and are rendered more negative by Na4Fe(CN)6 and acid dyes. Low concentrations of CaCl2 and LaCl3 increase the positive charge of the particles until a maximum is reached after which the addition of more salt depresses the P.D. again. 5. It is shown that alkalies (NaOH) act on the cataphoretic P.D. of both negative and positive particles as Na4Fe(CN)6 does at the point of neutrality. 6. Low concentrations of HCl raise the cataphoretic P.D. of particles of collodion, mastic, graphite, and gold until a maximum is reached, after which the P.D. is depressed by a further increase in the concentration of the acid. No reversal in the sign of charge of the particle occurs in the case of collodion, while if a reversal occurs in the case of mastic, gold, and graphite, the P.D. is never more than a few millivolts. When HCl changes the chemical nature of the colloid, e.g. when HCl is added to particles of amphoteric electrolytes like sodium gelatinate, a marked reversal will occur, on account of the transformation of the metal proteinate into a protein-acid salt. 7. A real reversal in the sign of charge of positive particles occurs, however, at neutrality if Na4Fe(CN)6 or an acid dye is added; and in the case of negative colloids when low concentrations of basic dyes or minute traces of ThCl4 are added. 8. Flocculation of the suspensions by salts occurs when the cataphoretic P.D. reaches a critical value which is about 14 millivolts for particles of graphite, gold, or mastic or denatured egg albumin; while for collodion particles it was about 16 millivolts. A critical P.D. of about 15 millivolts was also observed by Northrop and De Kruif for the flocculation of certain bacteria.


The utility of fuller’s earth as a decolourising agent in the industrial prepara­tion of oils has long been recognised. More recently also fuller’s earth, in common with other powerful adsorbents has proved of the greatest use in the isolation of rare substances in the laboratory. Despite, however, the impor­tance of fuller’s earth both from the industrial and from the theoretical point of view, the ideas expressed in chemical literature as to its origin and nature, and the mechanism by which it acts as an adsorbent are diverse in the extreme. It was the object of the investigations here described to throw some light on the mechanism by which fuller’s earth adsorbs organic acids and bases from aqueous solutions. In particular the influence of hydrogen-ion concentration upon the adsorption of these bodies was studied. The results indicate that two types of adsorption take place; that of unionised molecules and that of cations which displace calcium ions from the surface. Geologists seem to be agreed that fuller’s earth consists essentially of alu­minium silicate associated with a little free silica and smaller quantities of iron, calcium and alkalis. It differs from ordinary clays in having a higher percentage of combined water. The exact nature of the silicates actually present in fuller’s earth is necessarily uncertain as a rational analysis of so complex a mixture is obviously extremely difficult to obtain.


2014 ◽  
Vol 21 (1) ◽  
pp. 16-22 ◽  
Author(s):  
Ilze Barene ◽  
Irena Daberte ◽  
Sanita Siksna

The aim of the study. The objective of this study was to investigate microscopic, physical and chemical properties of bee bread collected in three regions of Latvia in order to compare the quality and to investigate the possibility of producing granules containing bee bread. Material and methods. Microscopic analysis of bee bread samples was performed. Plant herbaria, special literature and internet sources were used for identification of pollen. Thin layer chromatography was used for identification of carotenoids and flavonoids. Granules were prepared by wet granulation method. Lactose, calcium lactate, calcium carbonate, potato starch and purified water were used as excipients. Appearance, loss on drying, pH of aqueous solution and content of carotenes were estimated. Results. Microscopic analysis showed mostly native pollen identified as willow pollen. Beta-carotene identified and 2 carotenoids found by thin layer chromatography. Two zones of flavonoids found on chromatograms at day light and 6 zones at ultra violet light. The comparison of bee bread samples of 3 regions of Latvia showed insignificant differences in appearance and consistency, hydrogen ion concentration 3.93–4.23, loss on drying 7.72–11.07 %; content of carotenes calculated to bcarotene 6.77–9.35 mg%. Stability study of bee bread samples showed greater changes after storage at 40ºC temperature. All compositions of granules showed appropriate appearance and flowability. Quality of granules: loss on drying 5.48–13.5%, content of carotenes calculated to b-carotene 5.77–6.75 mg%. Conclusions. Pollen of willow can be considered as an indicator of the origin of bee bread in Latvia. Bee bread samples of three regions of Latvia have insignificant differences in physical, chemical parameters.


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