scholarly journals XVII. Note on the development of voltaic electricity by atmospheric oxidation of combustible gases and other substances

1890 ◽  
Vol 46 (280-285) ◽  
pp. 372-376 ◽  

About fourteen months ago we had the honour of communicating to the Society (‘Roy. Soc. Proc.,’ vol. 44, p. 182) the results of a large number of experiments made with electromotor cells, of which a special feature was that one of the plates of the combination consisted of an “aeration plate,” or layer of conducting material exposed to the atmosphere, and consequently superficially charged with a film of condensed air, which served as a means of indirectly effecting the oxidation of the other plate (when made of oxidisable metal), or of the fluid surrounding it (when the plate is of non-oxidisable material immersed in an oxidisable fluid). We showed that the E. M. F. of a given combination varies very considerably with the nature of the material of which the aeration plate is made, surfaces of platinum sponge, and especially platinum black, yielding the highest results when the electrolyte is dilute sulphuric acid; a convenient way of constructing the plates being to apply the spongy metal to the surface of unglazed earthenware, or other similar porous non-conducting material, so as to form a conducting film, the electrolytic fluid being absorbed in the porous material and so making contact.

1913 ◽  
Vol 32 ◽  
pp. 12-16
Author(s):  
Alexander Charles Cumming ◽  
E. W. Hamilton Smith

So many papers have appeared on this subject that some apology seems desirable before making an additional contribution. The amount of published work on reduction with sulphurous acid is in itself an indication that many workers have found difficulties. It has been shown that the reduction does not take place in presence of large excess of hydrochloric or sulphuric acid, but the reduction will still occur while the reaction of the solution is strongly acid. On the other hand, Hillebrand (“Analysis of Silicate and Carbonate Rocks,” U.S. Bulletin, 442, p. 113) states if the solution after addition of sulphite is red in colour, it is too alkaline and acid must be added.


1940 ◽  
Vol 18b (12) ◽  
pp. 405-409 ◽  
Author(s):  
W. E. Parker ◽  
W. D. McFarlane

By treating a petrol ether solution of wheat-germ oil with 85% sulphuric acid, centrifuging, and washing the supernatant petrol ether with dilute alkali, carotenoids and other substances that interfere with the iron-dipyridyl method for determining tocopherol are removed. Tocopherol is not affected by the treatment. The tocopherol content of the solution is finally determined by a modification of Emmerie's method.


1947 ◽  
Vol s3-88 (4) ◽  
pp. 467-478
Author(s):  
A. J. CAIN

1. Baker's acid haematein test for phospholipines is specific provided that only a definite positively result is considered. Very pale blues and greys may be caused by other lipoids, which if present in very large masses may possibly show medium to dark blue granules but will not be coloured all through. 2. The mechanism of the test appears to be as follows: (a) Phospholipine is not fixed by formal-calcium but is restrained from passing into solution by the calcium ions, which play no other part. (b) Phospholipine combines readily with chromium from the mordanting fluid, and is then rendered insoluble and mordanted. Other substances, acidic and usually containing phosphorus, are mordanted as well. (c) On staining, blue and brown colorations are formed; in both cases the dye attaches itself to the chromium in the various substrates. (d) On differentiation, some browns and most blues, particularly those with phosphoric substrates, remain nearly fast, but most browns and the weak blues of certain lipoids (not phospholipines) are greatly reduced or removed entirely. The period of differentiation must not be shortened. (e) Blue-staining lipoids (phospholipines) are distinguished from other blue-staining substances by an extraction with the lipoid solvent pyridine, after special fixation. The other substances, and any bound lipoid not removable with pyridine, remain. 3. Since the specificity of the test depends on the relatively greater affinity of phospholipines among lipoids for the mordant, the period of chroming must not be lengthened. 4. One reason why some substances are coloured after pyridine extraction but not after acid haematein is that in the former case they are precipitated and so concentrated; in the latter they are not. This is not a general explanation for the whole class of such substances.


1993 ◽  
Vol 2 (5) ◽  
pp. 429-436 ◽  
Author(s):  
Jean-Pierre Hallé ◽  
Danielle Landry ◽  
Alain Fournier ◽  
Michèle Beaudry ◽  
Francois A. Leblond

Alginate is a key reagent in the preparation of microcapsules for cell transplantation. To address the question of the intracapsular alginate concentration, a sensitive assay has been developed to quantify the alginate content of microcapsules. The method is based on the metachromatic change induced by alginate binding to the dye, 1,9-dimethyl methylene blue (DMMB). The assay has a high sensitivity and precision. It covers a wide concentration range enabling the measurement of alginate in dilute supernatants as well as in microcapsules. For the latter, the membrane is initially dissolved by incubating the microcapsules in an alkaline medium. The effect of potentially interfering substances (poly-l-lysine (PLL), citrate, chloride, sodium) and of pH has been studied. Poly-l-lysine interfered with the assay at pH 6.5 but not at pH 13. Interference by sodium augmented with increasing sodium concentration and reached a plateau at 200 mM. This problem was overcome by routinely adjusting all samples to 500 mM sodium. The other substances tested had a negligible effect on the assay. The reliable measurement of alginate with this new assay will allow the optimization of the intracapsular alginate concentration.


2019 ◽  
Vol 10 (3) ◽  
pp. 1961-1969
Author(s):  
Talal Aburjai ◽  
Rudaina Othman Yousif ◽  
Mahmood Jasim AlSamydai ◽  
Ali Al-Samydai ◽  
Farah Al-Mamoori ◽  
...  

The consumption of dietary supplements has nowadays become popular, especially in Jordanian sports clubs and gyms. In fact, there is a widespread idea, among consumers, that these proteins contain hormones in order to increase their efficiency. The objective of this study is to develop a better understanding of customer opinion in an era that increased growth in Jordan and improves a chromatographic method to detect the testosterone in protein supplements. The method of this study, six popular types of proteins in the Jordan market have been chosen after conducting a primary study of the proteins' users by questionnaires to identify their opinions about these proteins. These proteins have been analyzed by reverse-phase high-performance liquid chromatography by developing an easy and fast method to detect testosterone signal between 8-9 minutes of the chromatogram. The results of the study showed that 61% of the users believe that sport proteins contain hormones and other substances that are not mentioned in the list of ingredients. While 39% believe otherwise. On the other side, HPLC results of six proteins showed no signs for testosterone hormone. The main reason that drives them to take sport proteins is for building muscles in spite of they believe it could be harmful due to containing hormones and other substances. So in future investigations, it might be possible to use different brands and investigate them by using the same method.


2015 ◽  
Vol 724 ◽  
pp. 53-56
Author(s):  
Qin Zhang ◽  
Lin Li ◽  
You Mo

The housing construction grouting technique is to select a specific pressure feed approach to pour the slurry in gel into the loose soil or the rock cracks with water. The slurry, through condensation and the particles consolidation in this category, will be filled into the rock cracks in the section so as to improve the inherent nature of the soil and the mechanical properties of the other substances. During the construction period, the slurry can be fed into the injected holes within this segment through the unique role of the pressure. The small opening surrounding the grouting holes, the preset requirements will be met. Therefore, it is necessary to clarify the specific applications of grouting techniques.


1833 ◽  
Vol 123 ◽  
pp. 95-142 ◽  

Mr. Faraday's highly interesting papers, entitled “Experimental Researches in Electricity,” having been referred to me, to report on, by the President and Council of this Society, I necessarily entered minutely into all the experiments and conclusions of the author, and the more so that I had had the advantage of witnessing many of the most important of these experiments. It is foreign to my present purpose to descant upon the value of Mr. Faraday’s discovery, or the merits of his communication ; the President and Council have marked their opinion of these by the award of the Copley Medal: but I may be permitted to state, that no one can concur more cordially than I do in the propriety of that award. Agreeing as I did generally with the author, both in the views which he took of the subject, and in the conclusions which he drew from his experiments, there was one, however, which I felt great difficulty in adopting, viz. “That when metals of different kinds are equally subject, in every circumstance, to magneto-electric induction, they exhibit exactly equal powers with respect to the currents which either are formed, or tend to form, in them :" and that “the same is probably the case in all other substances.” Although the experiments might appear to indicate that this was possibly the case, I did not consider them to be conclusive. The most conclusive experiment, that of two spirals, one of copper and the other of iron, transmitting opposite currents, was quite consistent with the absolute equality of the currents excited in copper and iron; but, at the same time, the apparent equality of the currents might be due to their inequality being counteracted by a corresponding inequality in the facility of transmission.


1874 ◽  
Vol 22 (148-155) ◽  
pp. 366-368

Since the time of Réaumur it has been stated, with very various degrees of evidence, that certain metals expand in volume at or near their points of consolidation from fusion. Bismuth, cast iron, antimony, silver, copper, and gold are amongst the number, and to these have recently been added certain iron furnace-slags. Considerable physical interest attaches to this subject from the analogy of the alleged facts to the well-known one that water expands between 39°F. and 32°, at which it becomes ice; and a more extended interest has been given to it quite recently by Messrs. Nasmyth and Carpenter having made the supposed facts, more especially those relative to cast iron and to slags, the foundation of their peculiar theory of lunar volcanic action as developed in their work, ‘The Moon as a Planet, as a World, and a Satellite’ (4 to, London, 1874). There is considerable ground for believing that bismuth does expand in volume at or near consolidation; but with respect to all the other substances supposed to do likewise, it is the object of this paper to show that the evidence is insufficient, and that with respect to cast iron and to the basic silicates constituting iron slags, the allegation of their expansion in volume, and therefore that their density when molten is greater than when solid, is wholly erroneous. The determination of the specific gravity, in the liquid state, of a body having so high a fusing temperature as cast iron is attended with many difficulties. By an indirect method, however, and operating upon a sufficiently large scale, the author has been enabled to make the determination with considerable accuracy. A conical vessel of wrought iron of about 2 feet in depth and 1·5 foot diameter of base, and with an open neck of 6 inches in diameter, being formed, was accurately weighed empty, and also when filled with water level to the. brim; the weight of its contents in water, reduced to the specific gravity of distilled water at 60°F., was thus obtained. The vessel being dried was now filled to the brim with molten grey cast iron, additions of molten metal being made to maintain the vessel full until it had attained its maximum temperature (yellow heat in daylight) and maximum capacity. The vessel and its content of cast iron when cold were weighed again, and thus the weight of the cast iron obtained. The capacity of the vessel when at a maximum was calculated by applying to its dimensions at 60° the expansion calculated from the coefficient of linear dilatation, as given by Laplace, Riemann, and others, and from its range of increased temperature; and the weight of distilled water held by the vessel thus expanded was calculated from the weight of its contents when the vessel and water were at 60°F. We have now, after applying some small corrections, the elements necessary for determining the specific gravity of the cast iron which filled the vessel when in the molten state, having the absolute weights of equal volumes of distilled water at 60° and of molten iron. The mean specific gravity of the cast iron which filled the vessel was then determined by the usual methods. The final result is that, whereas the specific gravity of the cast iron at 60°F. was 7·170, it was only 6·650 when in the molten condition; cast iron, therefore, is less dense in the molten than in the solid state. Nor does it expand in volume at the instant of consolidation, as was conclusively proved by another experiment. Two similar 10-inch spherical shells, 1·5 inch in thickness, were heated to nearly the same high temperature in an oven, one being permitted to cool empty as a measure of any permanent dilatation which both might sustain by mere heating and cooling again, a fact well known to occur. The other shell, when at a bright red heat, was filled with molten cast iron and permitted to cool, its dimensions being taken by accurate instruments at intervals of 30 minutes, until it had returned to the temperature of the atmosphere (53°F.), when, after applying various corrections, rendered necessary by the somewhat complicated conditions of a spherical mass of cast iron losing heat from its exterior, it was found that the dimensions of the shell, whose interior surface was in perfect contact with that of the solid ball which filled it, were, within the limit of experimental error, those of the empty shell when that also was cold (53°F.), the proof being conclusive that no expansion in volume of the contents of the shell had taken place. The central portion was much less dense than the exterior, the opposite of what must have occurred had expansion in volume on cooling taken place.


1815 ◽  
Vol 105 ◽  
pp. 203-213 ◽  

In the two papers containing researches on iodine which the Royal Society has done me the honour of publishing in the Transactions, I have described a class of bodies consisting of iodine, oxygene, and different bases analogous to the hyper-oxymuriates. In the last of these papers, I mentioned, that I had not been able to procure any binary combination of iodine and oxygene from these compounds, neither by the method proposed by M. Gay Lussac, namely, the action of sulphuric acid on the oxyiode of barium, nor by other methods of my own institution; and that in experiments on the effects of the acids on the oxyiodes, new combinations only were formed. I have lately resumed this enquiry, and by pursuing a new and entirely different plan of operation, I have at last succeeded in combining oxygene and iodine. In the following pages I shall describe the circumstances which led me to ascertain the existence of this compound, and I shall detail some experiments on its analysis and its chemical agencies. In the course of my researches, I observed, that when a solution of the compound of iodine and chlorine was poured into alkaline solutions, or even into certain muriatic solutions, the precipitate was an oxyiode; and this fact seemed to indicate, that iodine had a stronger attraction for oxygene than chlorine; iodine, likewise, has an attraction for chlorine; it appeared, therefore, extremely probable, that euchlorine, or the gaseous combination of oxygene and chlorine, would be decomposed by heat, and two compounds formed, one of oxygene and iodine, and the other of iodine and chlorine, or that a triple compound would be produced from which chlorine could be easily separated, and on submitting the idea to the test of experiment, I found that I had not been deceived.


2006 ◽  
Vol 20 (25n27) ◽  
pp. 3611-3616 ◽  
Author(s):  
B. WITHY ◽  
M. HYLAND ◽  
B. JAMES

Chemical pretreatments are often used to improve the adhesion of coatings to aluminium. XPS and AFM were used to study the effect of these pretreatments on the surface chemistry and morphology of Al 5005. Four pretreatments were investigated, an acetone degrease, boiling water immersion, and two sulphuric acid etches, FPL and P2. Degreasing had no affect on surface morphology and simply added to the adventitious carbon on the surface. Boiling water immersion produced a chemically stable pseudo-boehmitic surface that was quite porous. The acid etches produced porous pitted surfaces similar to each other but significantly different to the other surfaces. The surface chemistry of the acid etched surfaces was variable and dependant on atmospheric conditions on removal from etch due to the very active surface that the etch produced.


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