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Review articles on the study of combustion. Combustion Theory and Modelling. Volumes Part 2 1-13 PDF

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Preview Review articles on the study of combustion. Combustion Theory and Modelling. Volumes Part 2 1-13

This article was downloaded by: On: 24 January 2010 Access details: Access Details: Free Access Publisher Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37- 41 Mortimer Street, London W1T 3JH, UK Combustion Theory and Modelling Publication details, including instructions for authors and subscription information: http://www.informaworld.com/smpp/title~content=t713665226 Oscillations in a combustible gas bubble V. Gol'dshtein a; I. Goldfarb a; I. Shreiber b; A. Zinoviev a a Department of Mathematics and Computer Sciences, Ben Gurion University of the Negev, POB 653, 84105, Beer Sheva, Israel. b Institute of Industrial Mathematics, 22 Ha-histadrut str., 84213, Beer Sheva, Israel. To cite this Article Gol'dshtein, V., Goldfarb, I., Shreiber, I. and Zinoviev, A.(1998) 'Oscillations in a combustible gas bubble', Combustion Theory and Modelling, 2: 1, 1 — 17 To link to this Article: DOI: 10.1080/713665366 URL: http://dx.doi.org/10.1080/713665366 PLEASE SCROLL DOWN FOR ARTICLE Full terms and conditions of use: http://www.informaworld.com/terms-and-conditions-of-access.pdf This article may be used for research, teaching and private study purposes. Any substantial or systematic reproduction, re-distribution, re-selling, loan or sub-licensing, systematic supply or distribution in any form to anyone is expressly forbidden. The publisher does not give any warranty express or implied or make any representation that the contents will be complete or accurate or up to date. The accuracy of any instructions, formulae and drug doses should be independently verified with primary sources. The publisher shall not be liable for any loss, actions, claims, proceedings, demand or costs or damages whatsoever or howsoever caused arising directly or indirectly in connection with or arising out of the use of this material. Combust. TheoryModelling2(1998)1–17. PrintedintheUK PII:S1364-7830(98)83244-0 Oscillations in a combustible gas bubble V Gol’dshteiny, I Goldfarby, I Shreiberz and A Zinovievy y Department of Mathematics and Computer Sciences, Ben Gurion University of the Negev, POB653,84105,BeerSheva,Israel zInstituteofIndustrialMathematics,22Ha-histadrutstr.,84213,BeerSheva,Israel Received9April1997,infinalform24November1997 Abstract. The dynamical behaviour of an isolated combustible gas bubble surrounded by unlimited inviscid liquid is analysed in the case of large activation energy and using spatially uniform assumptions. The pressure effect is crucial in this problem because of the limited gasvolume. Themathematicalmodelusedisasystemofthreenonlinearordinarydifferential equationsincludingtheenergyequation,theconcentrationequationandtheRayleighequation. Thethermalbehaviourisclassifiedintoslowandexplosiveregimes,andthethermalexplosion criterionisobtainedanalytically,alongthelinesoftheclassicalSemenovtheory. Thesystemis showntorevealtemperatureandvolumetricoscillations,theamplitudeandfrequencyofwhich dependstronglyontheintensityofthethermalprocess. Inparticular,theamplitudeofslowand 10 explosiveregimesdiffersbyatleastanorderofmagnitude. 0 2 y r a u n a J 1. Introduction 4 2 0 0 9: This paper is motivated by a number of industrial and scientific problems concerning 0 : flame propagation in multiphase media of complex structures. In particular, a series of t A experimentsonpressurewavepropagationinliquidcontainingcombustiblegasbubbleshas d e ad been conducted (Meier and Thompson 1989). There is also the unsolved problem of the o nl structure and velocity of combustion wave propagation in a gas–liquid foam containing w o D a combustible gas mixture within foam bubbles (Zamashchikov and Kakutkina 1994). The phenomenon of spontaneous insulation fires represents another example of problems which are connected with the self-ignition event taking place in a combustible gas bubble surrounded by liquid media (McIntosh etal 1994). One of the hypothetical mechanisms of combustion wave propagation in such media is the following. At the early stages of the process, the self-ignition occurs in an arbitrary single bubble. The heat produced by the exothermic chemical reaction leads to pressure changes in the bubble which, in turn, cause changes of the bubble volume (radius). This generates a spherical pressure wave propagating from the bubble to the surrounding liquid. The pressure disturbance reaches another bubble (containing the same gas mixture) and causes compression of this bubble and, consequently, an increase of the gas temperature. This may produce an intensive self-heating and, as a result, a self-ignition event in this secondary bubble, since the rate of the exothermic chemical reaction is extremely sensitive to temperature changes. This secondary bubble repeats the dynamical behaviour of the originalbubbleandbecomesthesourceofasecondarypressurewavewhichalsopropagates in all directions. Thus the original bubble generates a chain of self-ignition events in the neighbouring bubbles, and this mechanism can represent one of the factors determining 1364-7830/98/010001+17$19.50 (cid:13)c 1998IOPPublishingLtd 1 2 VGol’dshteinetal the structure and velocity of combustion wave propagation in such media. The case of spontaneous insulation fires is more complicated because of a solid skeleton (which may conduct heat much better than the liquid) and the evaporation effect from the gas bubble surface (the porous insulation material is impregnated with a flammable fluid). The purpose of this work is to investigate qualitatively the dynamics of an isolated combustiblegasbubblesurroundedbyunlimitedinviscidliquid. Weareprimarilyseekingto studytheinteractionbetweenthethermalprocessestakingplacewithinthebubble(including theself-ignitionphenomenon)andthehydrodynamicsoftheunlimitedliquidsurroundingthe bubble. Thesimplifiedphysicalmodelusedheretakesaspatiallyuniformapproachtoboth the energy and concentration equations. The gas temperature is controlled by the following main processes: heat release associated with the exothermic oxidation reaction, heat losses due to the cooling and the pressure changes. The chemical reaction is considered as a single-step reaction obeying an Arrhenius temperature dependence, and the hydrodynamics of the liquid surrounding the gas bubble is governed by the Rayleigh equation. Themathematicalmodelisdevelopedasasystemofthreenonlinearordinarydifferential equations: theenergyequation, theconcentrationequation, andtheRayleighequation. The systemcanbeconsideredasamulti-scalesystembecauseofthehighlyexothermicchemical reaction. The energy equation is fast (with a small parameter before the derivative) and the other equations are slow. This system hierarchy allows us to apply the geometrical asymptotic methods developed in earlier works on self-ignition (Babushok and Gol’dshtein 1988, Babushok etal 1990, 1992, Gol’dshtein and Sobolev 1992, Gol’dshtein etal 1996). Conceptual qualitative information about the system behaviour is obtained analytically and 0 1 detailed quantitative characteristics are the object of consequent numerical simulations. 0 2 y Theprincipaldifferenceoftheproposedmodelfromtheconventionalapproachestoself- r ua ignition theory is that it takes into account the pressure effects on the process development. n a J The system is shown to reveal temperature and volumetric oscillations, for any initial 4 2 conditions(withintheframeworkofourmodel). Thedistinctcharacterofthenonlinearities 0 :0 for the chemical and the hydrodynamical processes leads to the fact that the oscillations 9 0 start after the exothermic reaction is almost completed. The amplitude and frequency of : t A these oscillations depends strongly on the thermal process intensity. The thermal behaviour d de isnaturallyclassifiedintoslowandexplosive,andtheself-ignitioncriterionwhichseparates a o l these two types of regimes is obtained analytically. The oscillation amplitude for slow and n w Do explosive regimes differs by at least an order of magnitude. 2. Problem statement A single gas bubble is considered which is surrounded by unlimited liquid, and contains someinitialamountofacombustiblegasmixture(combustiblegas, oxidizerandinertgas). Themaininterestistheinvestigationofthebubbledynamicsduringtheself-ignitionevent. The main physical assumptions of the suggested model are the following. We restrict ourselves to a spatially homogeneous approximation. The liquid flow is assumed to be inviscid and the liquid to be incompressible. Normally in the open air the velocity of the pressure wave propagation is much larger than the rate of the thermal effects. Therefore pressuredisturbancesrunawayfromthereactionzone. Thiscanexplainwhythetraditional approach to the thermal explosion theory ignores the effect of pressure changes on the process. Inthepresentproblemthepressurevariationswithinthebubblearecrucialbecause of the limited gas volume. We assume that the gas is ideal, and that its equation of state is the Mendeleev–Clapeiron equation and the total amount of the gas within the bubble (number of moles) is constant, i.e. the stoichiometry of the chemical reaction conserves the Oscillationsinacombustiblegasbubble 3 number of moles. We also assume that the molecular masses of all the gas components are equal. The energy equation describes the temperature changes of the gaseous phase within the bubble. To simplify the mathematical description of the real complex problem we make someadditionalassumptions. Weassumethattheliquidandtheinterphaseboundaryremain at a constant temperature during the process, and that this temperature is low enough for evaporation effects to be neglected. The heat flux from the gas phase to the liquid phase is considered to be proportional to the temperature difference between the phases. It is also assumed that the thermal conductivity of the liquid is much higher than that of the gas for the heat transfer coefficient to be defined by the thermal properties of the gas phase. The energy equation used here is similar to that in the work of Gol’dshtein et al (1994) in which the phenomenon of creeping detonation in filtration combustion was analysed for the adiabatic and spatially distributed assumptions. The present energy equation has a heat release term associated with the chemical oxidation reaction, a heat loss term controlled by the heat transfer from the gas to the liquid, and also a term associated with the pressure changes within the bubble: (cid:0) (cid:1) dT (cid:11) 4(cid:25)R2 dP C (cid:26) g Dc Q (cid:22) W − (cid:0) b(cid:1).T −T/C g (2.1) pg g dt f f f 4(cid:25)R3 g l dt 3 b0 where C is the specific heat capacity (Jkg−1 K−1), P the pressure (Pa), Q the combustion energy (Jkg−1), R the radius (m), T the temperature (K), W the reaction rate (s−1), c the combustible gas concentration (kmolm−3), (cid:11) the heat transfer coefficient (Wm−2 K−1), 0 01 (cid:22) the molecular weight (kgkmol−1), (cid:26) the density (kgm−3); subscripts are related to: b, 2 ry bubble; g, gas; f, combustible gas component of the mixture; l, liquid; p, under constant a nu pressure; 0, undisturbed state. a J The reaction rate W is given in the Arrhenius form: 4 2 (cid:18) (cid:19) 00 E 9: W DAexp − (2.2) : 0 BTg t d A where A is the pre-exponential factor .s−1/, E the activation energy .Jmol−1/ and B the e ad universal gas constant. o l n The combustible gas content (per unit volume) in the bubble is controlled by the w o D oxidationchemicalreactionandbythebubblevolumetricvariations. Toderivetherelevant governing equation we first write the continuity equation for the gas in the bubble, using the spherical coordinates and taking into account the gas consumption due to the chemical reaction: (cid:0) (cid:1) @c 1 @ f C r2u c D−c W (2.3) @t r2@r g f f where u is the velocity (m s−1) and r the current coordinate from the centre of the bubble (m). Multiplying by r2 and then integrating the obtained equality with respect to r from 0 to R we obtain the relation between the concentration, temperature and velocity of the b gas on the bubble boundary r D R (we remind the reader that the concentration and b temperature are spatially uniform in our assumptions). In the absence of phase transitions on the interphase boundary we may put u D dR =dt (Nakoryakov et al 1993). The g b concentration equation thus becomes dc 3 dR f D−c W −c b: (2.4) f f dt R dt b 4 VGol’dshteinetal The chemical reaction within the bubble causes the gas temperature to increase, which, in turn, leads to the bubble radius variations. Those are controlled by the unlimited liquid surrounding the gas bubble. To take this hydrodynamical mechanism into account, we suggest using the Rayleigh equation (Nakoryakov et al 1993) which relates pressure variationsinaliquidtoabubbleradius. RecallhowtheRayleighequationcanbeobtained. Let us write the equations of hydrodynamics in a spherically symmetrical case: (i) the Euler equation: @u @u 1 @P l Cu l D− l (2.5) l @t @r (cid:26) @r l (ii) the continuity equation: (cid:0) (cid:1) @ r2u D0: (2.6) l @r Integratingequation(2.6)givesr2u DF.t/,whereF.t/isanarbitrarytimefunction. Using l the boundary conditions, we obtain F.t/ D R2.dR =dt/: Hence we get the distribution of b b u with respect to r: l (cid:18) (cid:19) R2 dR u D b b: (2.7) l r2 dt Under the assumption that the liquid is incompressible and the pressure changes are small enough (of the same order as the bubble radius), equation (2.5) can be integrated with respecttor fromthevaryingvalueR toinfinity. Theboundaryconditionsare: Pl DPl1 at 2010 r D1, Pl DPl.Rb/ and ul.r DRb/DdRb=dt at r DRb. Initially, the system is supposed ry to be at an equilibrium state and therefore the following equality is true: Pg0 D Pl1. ua Integrating equation (2.5), taking account of the expression for u (2.7), we get the well n l a J known Rayleigh equation: 24 (cid:18) (cid:19) (cid:18) (cid:19) :00 R d2R C 3 dR 2 D Pl.Rb/−Pl1: 09 dt2 2 dt (cid:26) l : t A TodefineP.R /weneglectbothviscouseffectsontheboundaryandsurfacetensioneffects l b d de (the heat transfer effect has already been taken into account in the simplest approximation). a nlo Thus Pl.Rb/ D Pg where Pg is the gas pressure in the bubble determined by the equation w o of state for an ideal gas: D (cid:26) m BT P D gBT (cid:17) g g : (2.8) g (cid:22) g (cid:22) 4(cid:25)R3 g g3 b From the above it follows that the system of governing equations is given by: (i) the energy equation for the reacting gas: dT 3(cid:11)R2 dP C (cid:26) g Dc Q (cid:22) W − b.T −T/C g (2.9) pg g dt f f f R3 g l dt b0 (ii) the concentration equation for the reacting gas: dc 3 dR f D−c W −c b (2.10) f f dt R dt b (iii) the Rayleigh equation: (cid:18) (cid:19) (cid:18) (cid:19) d2R 3 dR 2 .P −P / R b C b D g g0 : (2.11) b dt2 2 dt (cid:26) l Here W and P are defined by (2.2) and (2.8), respectively. g Oscillationsinacombustiblegasbubble 5 The initial conditions for equations (2.9)–(2.11) are given by t D0 T DT (cid:17)T c Dc R DR P DP : (2.12) g g0 l f f0 b b0 g g0 We will rewrite the system (2.9)–(2.11) in the dimensionless form using the conventional dimensionlesstemperature(cid:18) andconcentration(cid:17)ofthecombustiblegas(Frank-Kamenetskii 1969), and the natural dimensionless radius of the bubble r: T −T E c R (cid:18) D g g0 (cid:17)D f r D b : (2.13) T BT c R g0 g0 f0 b0 As in the previous works (e.g. Babushok et al 1990, Gol’dshtein and Sobolev 1992, Gol’dshtein et al 1996), we choose the characteristic reaction time as the basis for the time scale, i.e. (cid:18) (cid:19) (cid:14) t E (cid:28) D t Dexp A: (2.14) r t BT r g0 The reaction time t is the time required for the reactant concentration to fall e-times from r its initial value under the isothermal condition T D T . In the dimensionless form, the g g0 system of governing equations reads (cid:18) (cid:19) γ(cid:18)P Dγ (cid:17)r3exp (cid:18) −(cid:15) r2(cid:18) −(cid:15) dr 1C(cid:12)(cid:18) (2.15) c 1C(cid:12)(cid:18) 1 2d(cid:28) r (cid:18) (cid:19) (cid:17) dr (cid:18) (cid:17)P D−3 −(cid:17)exp (2.16) r d(cid:28) 1C(cid:12)(cid:18) 0 (cid:18) (cid:19) 1 20 3 1C(cid:12)(cid:18) ary rrRC 2rP2 D(cid:15)3 r3 −1 : (2.17) u n Ja The initial conditions are (cid:28) D 0; (cid:18) D 0; (cid:17) D r D 1; rP D 0, where a dot denotes a 0 24 derivative with respect to the dimensionless time (cid:28). The parameter γc Dcp=cv is the ratio :0 of the specific heat capacities. The system dynamics is defined by the five dimensionless 9 0 parameters(cid:15) ;(cid:15) ;(cid:15) ;(cid:12) andγ. Theparameters(cid:12) andγ arecommonlyusedinthecontextof : 1 2 3 t A thermalexplosionproblems: (cid:12) isthereducedinitialgastemperatureandγ isthereciprocal d de of the adiabatic temperature rise: a o ownl (cid:12) D BTg0 γ D Cpg(cid:26)g0Tg0(cid:12): (2.18) D E c Q (cid:22) f0 f f Theparameters(cid:15) ;(cid:15) and(cid:15) arenewintheconsideredresearchfield. Theparameters(cid:15) ;(cid:15) 1 2 3 1 2 describetherelationsbetweenthethermophysicalpropertiesofthegasandtheliquidphases 3(cid:11)γ (cid:12)T 3γ (cid:26) BT (cid:15) D c g0 exp.1=(cid:12)/ (cid:15) D c g0 g0: (2.19) 1 Ac Q (cid:22) R 2 Q (cid:22)2c f0 f f b0 f f f0 The parameter (cid:15) correlates the two characteristic times: the characteristic reaction time t 3 r and the characteristic time of harmonic bubble oscillations t : osc (cid:18) (cid:19) t 24 (cid:15) D r (cid:25)2=γ (2.20) 3 c t 3 osc where the characteristic time of harmonic bubble oscillations t is proportional to the osc reciprocal of the Minnaert frequency of the bubble under initial values of the size and the gas pressure (Nakoryakov etal 1993): (cid:18) (cid:19) (cid:26)R2 1=2 t D2(cid:25)=! D2(cid:25) l b0 : osc m 3γ P c 0 6 VGol’dshteinetal Let us analyse the physical meaning of parameters (cid:15) and (cid:15) in more detail. Parameter (cid:15) 1 2 1 can be presented as (cid:15) Dγ .t =t /. Here the characteristic time t is given by 1 c ad N ad C (cid:26) (cid:12)T t D pg g g0 exp.1=(cid:12)/ ad Ac Q (cid:22) f0 f f andrepresentsthetimeafterwhichthetemperaturewouldbecomeinfiniteintheabsenceof heatlosses(byheattransferfromthegastothecoolliquidphase)andintheapproximation (cid:12) D0 (Frank-Kamenetskii 1969). The thermal relaxation time (Newtonian cooling time) C (cid:26) R t D pg g b0 N 3(cid:11) is the characteristic time of gas cooling caused by the heat transfer only. To calculate t N we solve the energy equation under the assumptions: (i) an absence of chemical heat sources .c D0/; f (ii) bubble radius R remains at the initial value R during the thermal relaxation b b0 (such an approach is acceptable during the initial stages of the process). A solution of the energy equation (2.9) under the above-mentioned conditions involves the connection .T −T/(cid:24)exp.−t=t /, and thereby t is the time required for the temperature difference g l N N .T −T/ to fall e-times from its arbitrary value. Thus the parameter (cid:15) is proportional to g l 1 theratioofthecharacteristictimesofthecombustionandheattransferprocesses,andhence it is defined by the competition between the intensities of the combustion and heat transfer processes. Parameter (cid:15) can be rewritten as 0 2 1 20 N BT uary (cid:15)2 D3γcNfgQf(cid:22)g0f n 4 Ja where Ng D mg=(cid:22)g is the total number of gas moles in the bubble and Nf D cf0Vb0 is 2 the total number of combustible gas moles in the bubble at the initial conditions. We can 0 :0 see that physically (cid:15) represents the ratio between the potential energy of the combustible 9 2 0 gas in the bubble at the initial moment (i.e. the energy to be released after total burning of : t A the flammable gas) and the energy corresponding to a single degree of freedom of the gas d de within the bubble. a o l n w o D 3. Dimensionless model and its phenomenology The system of governing equations (2.15)–(2.17) can be rewritten as a system of four ordinary differential equations of the first order, by introducing the new formal variable v dDefrP: (cid:18) (cid:19) γ(cid:18)P Dγ (cid:17)r3exp (cid:18) −(cid:15) r2(cid:18) −(cid:15) v1C(cid:12)(cid:18) dDefF.(cid:18);(cid:17);v;r/ (3.1) c 1C(cid:12)(cid:18) 1 2 r (cid:18) (cid:19) (cid:17)v (cid:18) (cid:17)P D−3 −(cid:17)exp (3.2) r 1C(cid:12)(cid:18) (cid:18) (cid:19) 1C(cid:12)(cid:18) 1 3v2 vP D(cid:15) − − : (3.3) 3 r4 r 2 r rP Dv: (3.4) The subsystem (3.1), (3.2) describes thermo-chemical processes and the subsystem (3.3), (3.4) describes hydrodynamic processes. The parameters γ and (cid:12) are small, due to the assumption of a highly exothermic chemical reaction. This defines the scaling of the Oscillationsinacombustiblegasbubble 7 system: (cid:18) is a rapidly varying variable, and (cid:17);v and r are slowly varying variables. Note that the big parameter (cid:15) ((cid:15) is large because of the small pulsation time) in the right-hand 3 3 s(cid:0)ide of equation (3.3(cid:1)) does not affect the system hierarchy. This is because of the term .1C(cid:12)(cid:18)/=r4 −1=r which is small for two reasons: first, the term (cid:12)(cid:18) is small because of the small parameter (cid:12), and secondly variable r changes slowly from the initial value r D 1, and hence 1=r4 is comparable with 1=r. The same conclusion evidently holds in 0 any case when the radius is close to unity that is always true for the considered system, as will be shown below. The system behaviour can be either slow or explosive, due to the highly exothermic chemical reaction. These two main types of system behaviour are studied in sections 5 and 6bytheuseofthedifferentasymptotics. Slowregimesareanalysedintheapproximationof rapidlyandslowlyvaryingvariables(.1(cid:2)3/-approximation: (cid:18) isarapidlyvaryingvariable and (cid:17);v and r are slowly varying variables). The explosive regimes are investigated by a combination of the two relevant asymptotics. Namely, the fast explosive temperature increaseismodelledinanadiabaticapproachsinceheatlossesduringthethermalexplosion canbeignored,andthefurthertemperaturedecreaseisanalysedinthe.1(cid:2)3/-approximation, similar to the case of the slow regimes. Thecriteriawhichseparatetheslowsystembehaviourfromtheexplosiveonearestudied in the next section. Remark. The system reveals oscillation behaviour whichever regimes (slow or explosive) occur. Thecharacteroftheseoscillationsisanalysedqualitativelybyusinga.1(cid:2)3/-system 0 01 hierarchy. 2 y r a u an 4. The thermal explosion criterion J 4 2 0 The thermal explosion problem studies the critical parameter conditions which separate the 0 : 9 slow system behaviour from the explosive one. Remember that the character of the system 0 t: hierarchy is .1(cid:2)3/, i.e. (cid:18) is a rapidly varying variable and (cid:17);v and r are slowly varying A d variables. In the zeroth-order approximation of the small parameter γ (γ D0), the slowly e ad varying variables are fixed and equal to their initial values (cid:17) D 1; v D 0; r D 1 and the o l own problem is reduced to an anal(cid:18)ysis of th(cid:19)e following equation: D d(cid:18) (cid:18) γ Dγ exp −(cid:15) (cid:18): (4.1) d(cid:28) c 1C(cid:12)(cid:18) 1 Thefirsttermintheright-handsideofthisequationcorrespondstotheheatproduction,and the second term corresponds to the heat losses. In this situation we can use the classical theory of Semenov (1928), according to which the critical parameter condition which separates slow and explosive regimes is defined as a contact point of the heat production curve and the heat losses lines (see the Semenov diagram, figure 1). The contact point condition is given by (cid:18) (cid:19) (cid:18) (cid:19) (cid:18) (cid:18) 1 γ exp −(cid:15) (cid:18) D0 γ exp −(cid:15) D0: c 1C(cid:12)(cid:18) 1 c 1C(cid:12)(cid:18) .1C(cid:12)(cid:18)/2 1 This determines the critical parameter value (cid:15) , and also the maximum subcritical 1cr temperature (cid:18) (which is the temperature corresponding to the critical parameter value): m (cid:15) Dγ e.1−(cid:12)/ (cid:18) D1C2(cid:12): (4.2) 1cr c m For (cid:15) > (cid:15) the system behaviour is slow with maximum temperatures less than (cid:18) and 1 1cr m for (cid:15) < (cid:15) the system behaviour is explosive. Figure 2 gives the regions of the slow 1 1cr 8 VGol’dshteinetal heat heat release I II III heat losses 0 q Figure1. TheSemenovdiagram. SituationI,slowregimes;II,criticality;III,ignitionevent. 0 1 0 2 y r a u n a J 4 2 0 0 : 9 0 : t A d e d a o l n w o D Figure2. Parametricdescriptionoftheslowandexplosiveregimes,intheplane.(cid:12);(cid:15)N1/(where (cid:15)N1isobtainedfrom(cid:15)1givenby(2.19)as(cid:15)N1D3(cid:11)E=ABecf0Qf(cid:22)fRb0). Thetypicalphaseplots andtimehistoriesaregiveninfigures3–6. and explosive regimes in the plane .(cid:12);(cid:15)N /, where the parameter (cid:15)N is obtained from the 1 1 parameter (cid:15) (see equation (2.19)) by excluding (cid:12): (cid:15)N D .3(cid:11)E/=.ABec Q (cid:22) R /. This 1 1 f0 f f b0 figure illustrates the effect of the reduced initial temperature (cid:12) (see equation (2.18)) on the system behaviour. We study the cases of the slow and explosive behaviour using relevant asymptotics. 5. Slow regimes ((cid:15) >(cid:15) ) 1 1cr Remember that the system (3.1)–(3.4) has one rapidly varying variable (cid:18) and three slowly varying variables (cid:17);v and r. The equation (cid:18) (cid:19) (cid:18) 1C(cid:12)(cid:18) γ (cid:17)r3exp −(cid:15) r2(cid:18) −(cid:15) v dDefF.(cid:18);(cid:17);v;r/D0 c 1C(cid:12)(cid:18) 1 2 r Oscillationsinacombustiblegasbubble 9 defines a three-dimensional surface in the phase space which is termed the slow surface of the system. On this surface the rapidly varying variable (cid:18) and the slowly varying variables (cid:17);v and r are comparable, and beyond this surface the slowly varying variables (cid:17);v;r are assumed to be constant, in the zeroth-order approximation (γ D 0). A trajectory with the starting point at r D (cid:17) D 1; (cid:18) D v D 0 (this is the initial condition of the process) is attracted by the stable leaf of the slow surface (where F0.(cid:18);(cid:17);v;r/ < 0). The point at (cid:18) which the trajectory hits the slow surface is given by r D(cid:17) D1; v D0 and (cid:18) D(cid:18)(cid:3) where (cid:18)(cid:3) is a root of the equation (cid:18) (cid:19) (cid:18)(cid:3) F.(cid:18)(cid:3);1;0;1/(cid:17)γ exp −(cid:15) (cid:18)(cid:3) D0 (5.1) c 1C(cid:12)(cid:18)(cid:3) 1 which satisfies the condition 0<(cid:18)(cid:3) <(cid:18) (cid:25)1 C2(cid:12). The trajectory reaches the maximum m temperature(cid:18)(cid:3) andthenpassesalongtheslowsurfacedowntothefinalsteadystate. Letus analyse the system dynamics on the slow surface. For a fixed value of (cid:18) the system (3.3), (3.4) can be rewritten as (cid:18) (cid:19) 1C(cid:11) 1 3 vP D(cid:15) − − v2=r (5.2) 3 r4 r 2 rP Dv (5.3) where(cid:11) D(cid:12)(cid:18) issmallbecauseofthesmallparameter(cid:12). Thissystemhasauniquesingular point v D0 r D.1C(cid:11)/1=3: (5.4) 0 201 The Jacobi mat(cid:18)rix of the system (5.2) a(cid:19)nd (5.3) at this singular point is given by ary 0 −3(cid:15)3=.1C(cid:11)/2=3 u n 1 0 a J 4 and has the purely imaginary eigenvalues 2 0 : 09:0 (cid:21)1;2 D(cid:6).1.3C(cid:15)3(cid:11)/1/=12=3I: t A Hence for the linear system the singular point is a centre, for any set of the parameters. In d e ad this case the character of the singular point of equations (5.2) and (5.3) is not determined o nl by the linearized equations, according to the Liapunov theory on the stability of the steady w o D states(see,forexample,Andronovetal 1966). Thispointcancorrespondtoeitheracentre or a multiple focus, and the character of the singular point can be established by means of the Liapunov coefficients. More precisely, if at least one Liapunov coefficient is non-zero, then the steady state is a multiple focus. Otherwise when all the Liapunov coefficients are zero, the steady state is a centre. We have shown that the two first Liapunov coefficients are zero, using the formulae presented in the book by Bautin (1984). For the sake of brevity we do not give these tedious calculations here (see, for example, Bautin 1984, pp 28, 36). Since the analytical investigations of the model are approximate, it is reasonable to assume that the steady state is a centre. Under this assumption the system reveals harmonic radius oscillations with the amplitude defined as the difference between the radius values at the initial moment and the steady state: (cid:0) (cid:1) amD .1C(cid:11)/1=3−1 and the frequency .3(cid:15) /1=2 !D 3 : .1C(cid:11)/1=3

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