Hydrocarbon ions in fuel-rich, CH4–C2H2–O2 flames as a probe for the initiation of soot: an experimental approach

1981 ◽  
Vol 59 (12) ◽  
pp. 1760-1770 ◽  
Author(s):  
Scott D. Tanner ◽  
John M. Goodings ◽  
Diethard K. Bohme

The natural hydrocarbon ions CnHx± (n ≥ 2, x ≥ 0) present in premixed, fuel-rich, nearly sooting, CH4–C2H2–O2 flames at atmospheric pressure were studied as a probe of the early chemical stages of soot formation. Ion concentration profiles were measured mass-spectrometrically along the flame axis through the reaction zone into the burnt gas downstream. Total ionization profiles were examined for their dependence on both temperature and equivalence ratio, [Formula: see text] Families of individual CnHx− negative ion profiles exhibit concentration peaks in three distinct regions; predominantly oxygenated ions occur upstream, giving way to moderately unsaturated hydrocarbon ions near the end of the reaction zone, leading to highly unsaturated carbonaceous ions further downstream. The concentrations of the downstream ions alternate with the parity of n, the even-n species being larger. Series of CnHx+ positive ion profiles, for a given n, show profile peak positions which move steadily downstream with decreasing x, indicative of progressive dehydrogenation. The positive ion chemistry of these series is essentially independent of n. As [Formula: see text] is increased at constant temperature towards the sooting point, the concentrations of CnHx± ions increase while those of the oxygenated ions decrease; the positive ions show a relative enhancement of species having high values of n.

1982 ◽  
Vol 60 (22) ◽  
pp. 2766-2776 ◽  
Author(s):  
John M. Goodings ◽  
Scott D. Tanner ◽  
Diethard K. Bohme

The ion chemistry is discussed for fuel-rich, nearly sooting, methane–oxygen flames at atmospheric pressure with added acetylene. Different types of ion–molecule reactions, both positive and negative, which can contribute through chemical ionization (CI) processes are summarized including their dependence on temperature, pressure, and equivalence ratio [Formula: see text]. Extensive data were presented previously involving ion concentration profiles measured with a mass spectrometer as a function of distance along the axis of conical flames. An understanding of the dominant CI processes provides insight into the early chemical stage of soot formation associated with the flame reaction zone. The negative ion profiles show moderately unsaturated hydrocarbon ions upstream formed by proton transfer followed by progressive dehydrogenation; the highly unsaturated, carbonaceous ions observed downstream appear to arise by two- and three-body electron attachment, charge transfer, and H-atom stripping. The negative hydrocarbon ions can all be explained in terms of polyacetylene derivatives. The same build-up of carbonaceous species downstream is evident from the positive ion profiles. A major role is ascribed to proton transfer reactions with lesser contributions from charge transfer and ion–molecule condensation; three-body association is probably insignificant. Experiments with added acetylene indicate extensive fuel pyrolysis early in the reaction zone. There is no evidence that an ionic mechanism is dominant in forming soot precursors compared with neutral condensation reactions. Because of complexities in the positive ion chemistry, the negative ions appear to provide the more straightforward probe of the underlying neutral chemistry.


1983 ◽  
Vol 61 (8) ◽  
pp. 1703-1711 ◽  
Author(s):  
John M. Goodings ◽  
Kamal Elguindi ◽  
Diethard K. Bohme

Sulphurous negative ions S • SH • SO • SO2/S2• SO3• HSO3• SO4• and HSO4 were observed when 0.2% of carbonyl sulphide (OCS) was added to a conical, laminar, premixed. fuel-rich (equivalence ratio [Formula: see text]) CH4–O2 flame burning at atmospheric pressure. Profiles were obtained of ion concentration vs. distance along the flame axis by sampling the flame through a pinhole into a quadrupole mass spectrometer. Some of the ion signals observed in the flame reaction zone are very large, particularly that for HSO4. None of the sulphurous ions detected contain carbon. Of those listed above, only S−,•SH, • SO • and SO2 persist downstream through the burnt gas. The sulphurous ions are formed by chemical ionization processes of neutral sulphurous intermediates reacting with the naturally-occurring ions present in any hydrocarbon flame. The ion chemistry is discussed, as is the underlying neutral chemistry of sulphur relevant to the flame environment. The ion profiles show the rapidity with which OCS is oxidized through SH and SO to SO2 even within the reaction zone of this fuel-rich flame. No evidence was obtained for the presence of sulphuric or sulphurous acids, and the presence of S2: was not confirmed.


1936 ◽  
Vol 32 (3) ◽  
pp. 482-485 ◽  
Author(s):  
R. A. Smith

When an electron makes a transition from a continuous state to a bound state, for example in the case of neutralization of a positive ion or formation of a negative ion, its excess energy must be disposed of in some way. It is usually given off as radiation. In the case of neutralization of positive ions the radiation forms the well-known continuous spectrum. No such spectrum due to the direct formation of negative ions has, however, been observed. This process has been fully discussed in a recent paper by Massey and Smith. It is shown that in this case the spectrum would be difficult to observe.


1966 ◽  
Vol 45 (12) ◽  
pp. 4481-4492 ◽  
Author(s):  
Donald R. Davis ◽  
W. F. Libby ◽  
W. G. Meinschein

The ionized regions of the upper atmosphere include, not only neutral atoms and molecules, electrons and positive ions, but also negative ions. Of these, electrons are alone effective in producing reflexion of wireless waves; so that an electron attached to a neutral molecule to form a negative ion is as effectively removed from active participation in these phenomena as one recombined with a positive ion to form a neutral molecule. The decay of electron density at night has been attributed by some authors to recombination with positive.ions and by others to attachment by neutral molecules. The first process is in agreement with the observed law of decay and has the additional advantage of making it easily possible to understand the formation of layers of concentrated ionization; on the other hand, the chance of attachment to a molecule per impact would have to be extremely small for the attachment rate to be negligible, since the number of collisions per second with neutral atoms is very much greater than with positive ions.


The three previous papers of this series (Arnot and Milligan 1936 b ; Arnot 1937 a, b ) contain an account of experimental work which led the senior author to propose a new process of negative-ion formation. This process is the formation of negative ions at metal surfaces by bombardment of the surface with positive ions, the negative ion being formed by the positive ion capturing two electron from the surface. Further work carried out during the past year, which is described in this paper, has revealed a new variation of the above process. In this latter process the impinging positive ion causes an adsorbed atom on the surface to come off as a negative ion. It is believed that this newer process is essentially similar to the process previously reported, the difference being due merely to the transference of excitation energy from the incident positive ion, after its capture of an electron, to the atom adsorbed on the surface. The discovery of this second effect was made independently by Sloane and Press (1938), although they attribute it to a different process.


The quantal theory of negative ions has now been developed considerably (Massey and Smith 1936; Massey 1938), but on account of difficulties of computing it is usually necessary to assume rather than to prove that a given ion exists, and then to discuss the probability of its formation by different processes. The work described here is a contribution to the experimental side of this subject. It had its origin in a projected attempt to measure the capture cross-section of mercury atoms for electrons, as a verification of Massey and Smith's (1936) then unpublished theory of this process. In considering this it became clear that the experiment would be one of unusual difficulty. Before proceeding with it, therefore, it was decided to verify the existence of Hg - as a stable entity, which is assumed in the quantal theory. this was in doubt since Stille (1933), in some careful experiments, had recently failed to obtain it from the plasma of various forms of discharge through mercury vapour, although it is known that negative ions tend to accumulate in such regions (Emeleus and Sayers 1938). Whilst one of us was repeating his experiments, with modifications which led to essentially the same results and will be describes elsewhere, Arnot and Milligan (1936 b ) reported that they had obtained Hg - by bombardment of metal surfaces with Hg + . A comparison of their work with our own showed only one essential point of difference, namely that the construction of their apparatus did not permit of degassing in situ , a condition satisfied with our tubes. Both for this reason and because of the intrinsic importance of their discovery it was thought desirable to repeat part of their work, with apparatus geometrically similar in electrode construction, but capable of being degassed in a furnace under vacuum. We were again unable to obtain Hg - after the apparatus had been degassed and in operation for a short of that of Hg - was obtained. There were, however, always present several light negative ions, which had the excess energies found by Arnot and Milligan (1936 b ) with Hg - . The conditions under which these were formed led us to suppose that they were produced by bombardment of the metal surfaces by mercury positive ions (Press 1937; Sloane 1937) and not capture of electrons by positive ions of the same species, the process suggested by Arnot and Milligan (1936 b ). The existence of a process of this type, which may be conveniently termed "sputtering" (Sloane and Press 1938), is also implied by some earlier work by J. S. Thompson (1931) which has, so far as we know, never been published in detail. It is, however, impossible to decide definitely ion (e. g. CO - ) when it hits the surface, so long as one is producing the negative ions on a metal surface in a plasma or ionization chamber. One cannot overlook the possibility of the negative ion being formed from its own positive ion, since the latter may be present in the plasma or ionization chamber, and CO + , for example, was in fact shown in our work to be there from the positive-ion mass spectra, although in quantity only a fraction of 1% of Hg + . An unambiguous decision on this point can only be reached by first isolating a particular positive ion by a mass spectrograph, then bombarding a surface by this in a high vacuum , and finally making a mass spectrographic and energy distribution analysis of the resultant negative ions. We have built a double mass spectrograph for this purpose and find that negative ions of one kind possessing energies in excess of that imparted to them by the accelerating fields can be produced by bombardment with positive ions of another kind (Sloane and Press 1938). An account of the experiments with the single mass spectrograph is given in 1. the experiments with the double mass spectrograph are described in 2.


The velocity of ions in gases at reduced pressures was first investigated by Rutherford and by Langevin. Recently the author and others have carried out similar investigations. The results of these investigations show that for the negative ions in air the product of the mobility and the pressure is constant for pressures ranging from 760 mm. to 200 mm. of mercury, but with further reduction the product increases with the reduction of pressure, this increase becoming very great at low pressures. For the positive ions in air the product of the mobility and pressure is constant for pressures investigated between 760 mm. and 3 mm. of mercury. Similar results were obtained for the mobilities of the ions in other gases. The results show that if the ion is an aggregation of molecules, this aggregation becomes, at low pressures, less complex in the ease of the negative ion, while in the ease of the positive ion it persists down to 3 mm. of mercury. The purpose of the present research was the study of the mobilities of both kinds of ions in gases at high pressures. The method of investigation is based on the mathematical expression, developed by Prof. Rutherford, for the current between two plates, assuming that a very intense ionisation exists near the surface of one of the electrodes.


2013 ◽  
Vol 79 (5) ◽  
pp. 949-952 ◽  
Author(s):  
M. ROSENBERG ◽  
R. L. MERLINO

AbstractDrift wave instability in a magnetized plasma composed of positive ions and negative ions is considered using linear kinetic theory in the local approximation. We consider the case where the mass (temperature) of the negative ions is much larger (smaller) than that of the positive ions, and where the gyroradii of the two ion species are comparable. Weak collisional effects are taken into account. Application to possible laboratory parameters is discussed.


1. In a paper published in the ‘Proceedings of the Royal Society,’ vol. 80, p. 207, January, 1908, a method was given for comparing the charges on ions in liquids and gases. The first set of experiments gave results in accordance with the theory, and it was found that the charge on a positive ion in a gas was double that of a negative ion, the latter being equal to the charge on a monovalent ion in a liquid electrolyte. The ratio of the charges obtained was 2.4 / 1.23. The ions were produced by secondary Röntgen rays emitted by a brass surface, and further experiments have shown that positive ions with double or single atomic charges may be produced, the number of either kind depending on the nature of the secondary rays, which is determined by the state of the metallic surface from which they originate.


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