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This work presents a new oscillating reaction based on chlorate and observed in a CSTR at room temperature. This can be the first member of a new family of oscillating reactions. In addition, it is also the first oscillating reaction to use nitrous acid as a reactant. Four different behaviors were observed: simple oscillations, mixed mode oscillations, bursts, and quasiperiodicity. The period of oscillations is very short, which is around 1 s. Together with the fact that it also shows fast bursts, it opens the possibility that it can be used to simulate fast biological events, like the neuron’s communications signals.

The present work proposes the development of an analytical procedure for paracetamol determination in pharmaceutical formulations using a system of continuous flow analysis associated with potentiometric detection allowing the study of the Belousov–Zhabotinskii (BZ) oscillating reaction. This method is based on paracetamol determination using the disturbance in the oscillation pattern of the BZ reaction promoted by this substance. The analytical curve showed the detection and quantification limits of 4 × 10–6 and 1.2 × 10–5 M, respectively. The relative standard deviation (n = 6) of the standard solution with paracetamol concentration of 6 mM was 2.3%. The analysis of real samples by the proposed and official methods (spectrophotometry/UV) showed similar results.

Briggs-Rauscher oscillating reaction has been investigated in hydrochloric acid media and in the presence of added chloride ions in phosphoric acid media in a batch reactor using ethylacetoacetate as the organic substrate. The changes in key oscillation parameters, namely, induction period, oscillation period, amplitude, and so forth, have been explained in terms of the steps of the skeleton mechanism proposed by Furrow and Noyes and by de Kepper and Epstein. In spite of several shortcomings as outlined in section 2 in the text, the same mechanistic steps are good enough to explain qualitatively most of the changes in oscillation parameters under different stirring rates and temperatures in phosphoric acid and hydrochloric acid media, particularly stirring effects explained well by the theory of imperfect mixing. Potential data indicate that 0.018 M HCl medium has the ability to exhibit near-zero/zero amplitudes before cessation of oscillations. Inhibition reactions from a low Cl- concentration in the 0.018 M HCl media appear to be responsible for this interesting dynamical transformation, as toward the end of oscillations, the difference between [I-] and [I-]crit [see eq J in the text] becomes very small because of depleted component chemicals due to chemical reactions.

The peroxidase-oxidase oscillating reaction was the first (bio)chemical reaction to show chaotic behaviour. The reaction is rich in bifurcation scenarios, from period-doubling to peak-adding mixed mode oscillations. Here, we study a state-of-the-art model of the peroxidase-oxidase reaction. Using the model, we report systematic numerical experiments exploring the impact of changing the enzyme concentration on the dynamics of the reaction. Specifically, we report high-resolution phase diagrams predicting and describing how the reaction unfolds over a quite extended range of enzyme concentrations. Surprisingly, such diagrams reveal that the enzyme concentration has a huge impact on the reaction evolution. The highly intricate dynamical behaviours predicted here are difficult to establish theoretically due to the total absence of an adequate framework to solve nonlinearly coupled differential equations. But such behaviours may be validated experimentally.

The calcium phosphate tungsten bronze (Ca-PWB) has been synthesized and characterized (TGA, DSC, XRPD, FTIR, SEM). The influence of solid insoluble materials Ca-PWB, as well as lithium doped (Li-PWB) and cation free phosphate tungsten (PWB) bronzes on the oscillatory Briggs-Rauscher (BR) reaction dynamics, is compared. The results show that doping with Li and Ca reduces sensitivity of the BR reaction towards bronzes addition. These findings suggest the usage of the BR reaction as an innovative method for testing of different properties of bronze material. The behavior of PWB in the BR reaction is significantly changed with divalent cation (Ca2+) doping. The reasons for the different bronzes behavior were found in their calculated unit cell volumes. Namely, the compressed Ca-PWB unit cell volume indicates the difficult availability of the active site for heterogeneous catalysis. Hence, the linear correlation (slope) of the BR oscillogram’s length (τosc) vs. mass of bronze in BR reaction might be considered as a new parameter for the evaluation of the bronzes catalytic activity. У овом раду синтетисана је и окарактерисана (TGA, DSC, XRPD, FTIR, SEM) нова калцијумом допирана фосфат волфрамова бронза (Ca-PWB). Испитан је и упоређен утицај фосфат волфрамове бронзе (PWB), литијумом допиране фосфат волфрамове бронзе (Li-PWB) и калцијумом допиране фосфат волфрамове бронзе (Ca-PWB) на осцилаторну динамику Briggs-Rauscher (БР) реакције. Резултати показују да допирање катјонима Li+ и Ca2+ смањује осетљивост БР реакције на додатак нерастворних бронзи, што се огледа у смањивању нагиба праве осцилаторног времена (τosc) БР реакције у функцији масе додате допиране бронзе. Добијени резултати сугеришу употребу БР реакције као иновативне методе за испитивање различитих својстава допираних и недопиране фосфат волфрамове бронзе. Разлози за различито понашање бронзи у осцилаторној реакцији пронађени су у различитим величинама јединичних ћелија PWB, Li-PWB и Ca-PWB. Наиме, најмања вредност, тј. сабијање јединичне ћелије допирањем калицијумом указује на тежу доступност активних места за хетерогену катализу. Каталитичка активност бронзи усмерена је ка реакцијама оксидације које укључују водоник-пероксид (један од реактаната БР реакције). Стога би се линеарна корелација (нагиб) τosc у функцији масе бронзе у БР реакцији могла сматрати новим параметром за процену каталитичке активности бронзе, али и других материјала.

Periodical transformation of ferroin to ferriin is accompanied by changes in magnetic properties of liquids during Belousov&ndash, Zhabotinsky (BZ) reaction malonic acid, sodium bromide, sodium bromate, ferroin, and sulfuric acid. Instead of the earlier studied oscillation of microwave conductivity accompanying an oscillating reaction, we propose a flash technique to interrupt the BZ reaction by rapid freezing. Rapid cooling of a solution during chemical oscillations results in a frozen system with a fixed concentration of paramagnetic centers Fe3+. EPR spectrum recorded at different stages of the interrupted reaction corresponds to the exact concentration of the ferroin and ferriin components. Following unfreezing unblocks the BZ reaction, and oscillations are still observed. A simulated spectrum allows one to distinguish two groups of Fe3+ ions of different symmetries. The obtained results are important to explain the earlier observed effect of inhomogeneous magnetic field on BZ reaction front velocity.

Self-regulation of the dynamic actuation of a chemical oscillating reaction-based gel was realized by altering the network structure of the gradient double network gel. We demonstrated that the propagation mode of the chemical wave was influenced by the network structure, and consequently determined the dynamic feature of the gel actuator.

Phosphate tungsten bronzes, obtained by thermal treatment, are insufficiently investigated bronzes and there is scarce literature data on their chemical behavior and structure. Due to high-sensitivity of the Briggs-Rauscher (BR) reaction to addition of different analytes, this oscillatory reaction presents a potentially important chemical system for investigation and characterization of phosphate-tungsten bronzes, doped and undoped. The reaction mixture for the oscillatory BR reaction typically consists of H2O2, HClO4, KIO3, Mn(II) (catalyst), and CH2(COOH)2 (malonic acid, as an organic substrate). This paper deals with phosphate tungsten bronzes (PWB) and lithium doped phosphate tungsten bronzes (LiPWB) and their effects on the Briggs-Rauscher reaction dynamics. It is shown that the addition of phosphate tungsten bronzes decreases the oscillatory period length in this reaction. Furthermore, the obtained results show that PWB has a stronger influence on the BR reaction dynamics then LiPWB. In both cases, the oscillatory period is a linear function of the added bronze mass. The obtained linear functions can be successfully used for determination of the unknown bronze mass. Furthermore, due to different slopes of these functions, the Briggs-Rauscher reaction can be used as a system-detector for lithium doped and undoped phosphate tungsten bronzes. In order to elucidate the mechanism of bronze action, the inductively coupled plasma optical emission spectrometry (ICP-OES) was used to measure the total contents of K, Mn, W, Li. The aliquots of the above solution (i.e. CH2(COOH)2, MnSO4, HClO4, KIO3 but without H2O2) with the identical masses of PWB and LiPWB were examined. For the sake of comparison, contents of the metals in the solution without the bronze addition were measured, as well. Results obtained by the ICP-OES analysis show that the bronze structure is disturbed in the strong oxidizing environment (iodate in acidic solution) so that both, tungsten and lithium, leach into the BR solution. Accordingly, the proposed mechanism of the bronze action is probably by the reaction of tungsten ion with hydrogen-peroxide resulting in formation of a tungsten-peroxo complex. This complex is a stronger oxidizing agent then hydrogen peroxide itself. Thus, formation of the tungsten-peroxo complex potentially affects the kinetics of the Briggs-Rauscher reaction. [Project of the Serbian Ministry of Education, Science and Technological Development, Grant no. 172015, Grant no. III45001 and Grant no. III45014]

The simultaneous influence of temperature and flow rate (k0) in the oscillatory regime of the bromate-oxalic acid-acetone-Ce(III) oscillating reaction was investigated. The influence of temperature was evaluated in terms of the oscillatory activation energy (Eω), which was determined at different flow rates. Increasing k0, the oscillatory activation energy is decreased, tending to a limit value, Eω∞. The sensitivity of Eω with k0 is described by the parameter η = dEω/d(1/k0). Eω∞ and η are global properties of any particular oscillating reaction and describes a correlation between the dynamical behavior and temperature, and should be used when comparing different oscillating reactions.

An alternative approach for carbaryl determination based on the change in the oscillation period of the Belousov-Zhabotinsky (BZ) reaction under the addition of carbaryl is demonstrated. The oscillations were observed by spectrophotometric measurement at 320 nm, corresponding to the maximum absorption wavelength of cerium(IV) catalyst. The oscillation periods increase with the carbaryl concentrations, which can be discussed based on the Field-Körös-Noyes (FKN) mechanism. The increase of oscillation periods is proportional to the concentration of carbaryl in the range of 0.1-200 mg L-1 with the regression coefficient of 0.9938. The limits of detection and quantification were 0.044 and 0.147 mg L-1, respectively. The precisions in terms of intra-day and inter-day measurements were efficient with relative standard deviation (RSD) lower than 2.1%. Accuracy of carbaryl in different water samples was obtained with high recoveries in the range of 94-106% and also comparable to the results of high performance liquid chromatography (HPLC) analysis. The proposed method is precise, cost-effective and can be alternatively employed for the screening and determination of carbaryl residues in water samples.

Current efforts to design functional molecular systems have overlooked the importance of coupling out-of-equilibrium behaviour with changes in the environment. Here, the authors use an oscillating reaction network and demonstrate that the application of environmental forcing, in the form of periodic changes in temperature and in the inflow of the concentration of one of the network components, removes the dependency of the periodicity of this network on temperature or flow rates and enforces a stable periodicity across a wide range of conditions. Coupling a system to a dynamic environment can thus be used as a simple tool to regulate the output of a network. In addition, the authors show that coupling can also induce an increase in behavioural complexity to include quasi-periodic oscillations.

Oscillating reactions are reactions in which it is possible to observe oscillations in the concentrations of some reaction intermediates. The reaction studied here is composed of acetone, sulfuric acid, bromate, oxalic acid, and Ce(IV). Chemical oscillators may have different behaviors in batch, for example, the presence of an induction period and change of oscillations' pattern. A much rarer event is the presence of a break, or pause, between two groups of oscillations, which is shown by this system. To better determine the conditions under which this behavior occurs, we built several phase diagrams for the initial concentrations of reactants. These phase diagrams show that there is a well-defined range of concentrations that produce a pause in the oscillations. The initial bromate concentration is special because increasing this concentration eliminates the pause in the oscillations, but a further increase can make a pause appear again. These results can be interpreted considering that the reaction mechanism is controlled by at least two intermediates. In addition, this work presents a representative set of data that must be acknowledged by any detailed proposal of mechanism for this oscillating reaction.

Localized oscillations can develop thanks to the interplay of reaction and diffusion processes when two reactants A and B of an oscillating reaction are placed in contact, meet by diffusion, and react. We study numerically the properties of such an A + B → oscillator configuration using the Brusselator model. The influence of a hydrodynamic viscous fingering instability on localized concentration oscillations is next analyzed when the oscillating chemical reaction changes the viscosity of the solutions involved. Nonlinear simulations of the related reaction-diffusion-convection equations with the fluid viscosity varying with the concentration of an intermediate oscillatory species show an active coupling between the oscillatory kinetics and the viscously driven instability. The periodic oscillations in the concentration of the intermediate species induce localized changes in the viscosity, which in turn can affect the fingering instability. We show that the oscillating kinetics can also trigger viscous fingering in an initially viscously stable displacement, while localized changes in the viscosity profile can induce oscillations in an initially nonoscillating reactive system., SCOPUS: ar.j, info:eu-repo/semantics/published

The Briggs-Rauscher (BR) reaction is free radical based where the kinetics of formation of different iodide species leads to potentiometric and color oscillations. These oscillations were monitored in this study using a UV/Vis attenuated total reflection probe to develop an assay to measure the antioxidant content in complex matrices. The periodicity of the BR reaction was found to be very consistent (range 24–25 seconds, n = 16). Adding various amounts of ascorbic acid, a well-known antioxidant, led to an inhibition of the reaction with a linear calibration curve of antioxidant periodicity time (APT, r 2 > 0.99). The validity of this test in complex matrices was studied by determining the APT of nine fruits, and the resulting antioxidant capacity in ascorbic acid equivalency was calculated. The results generated by this assay were found be accurate through comparison with the well-established FRAP assay. These results show that visual or spectrometric monitoring of BR reaction can be used as a reliable, quick, and inexpensive alternative to more established assays with the added advantage that values generated from this assay is at pH 2 which is similar to that in the human stomach.

Pt is a common redox electrode used to follow oscillations qualitatively in the Briggs–Rauscher (BR) and the Bray–Liebhafsky (BL) reactions from the time of their discovery. Although the potential oscillations of the electrode reflect the temporal pattern of the reaction properly, there is no general agreement as to how that potential is determined by the components of the reaction mixture. In this article, first we investigate how iodine species in different oxidation states affect the potential of a Pt electrode. It was found that I(+3) and I(+5) species do not affect the potential; only I–, I2, and HOI may have an influence. Although the latter three species are always present simultaneously as participants of the rapid iodine hydrolysis equilibrium, it was found that below and above the so-called hydrolysis limit potential (HLP, where the iodide and HOI concentrations are equal) the actual potential determining redox couple is different. Below the HLP, it is the traditional I2/I– redox couple, but abo...

The Briggs-Rauscher (BR) oscillatory reaction is the oxidation of malonic acid in the presence of hydrogen peroxide and iodate in the acidic environment, which is catalyzed by ions of manganese. This reaction is very sensitive to the presence of additives. In this paper, the BR reaction has been used to investigate the phosphate tungsten bronze as well as calcium doped tungsten bronze, obtained by thermal treatment. The addition (0.01-0.08 g) of phosphate tungsten bronze and calcium doped phosphate tungsten bronze has a different effect on the dynamics of the Briggs-Rauscher reaction. In the case of the addition of phosphate tungsten bronze in the Briggs-Rauscher reaction, the linear dependence of the length of the oscillatory period on the mass of the added bronze was obtained, while in the case of addition of calcium doped phosphate tungsten bronze, the oscillatory period does not significantly change with an increase of added mass. The mechanism of calcium doped and undoped phosphate tungsten bronze action in BR reaction is probably adsorptive, and it will be the subject of future work. Keywords: oscillatory reactions, Briggs-Rauscher reaction, phosphate tungsten bronze, calcium doped phosphate tungsten bronze, thermal treatment.

Anisotropic chemical wave propagation of self-oscillating Belousov–Zhabotinsky (BZ) reaction was demonstrated in the poly(N-isopropylacrylamide) gel films embedded with macroscopically aligned liquid crystalline inorganic nanosheets. Although the average propagation rate of chemical wave v was 3.56 mm min–1 in the gels without nanosheets, the propagation was retarded in the gels with 1 wt % of nanosheets: v∥ = 1.89 mm min–1 and v⊥ = 1.33 mm min–1 along the direction parallel and perpendicular to the nanosheet planes, respectively. Thus, the wave propagation is anisotropic with the anisotropy ratio v∥/v⊥ = 1.42 in these gels and the periodic patterns formed by the BZ reaction were concentric ellipses, different from circles seen in isotropic gels. Furthermore, the propagation rate and degree of anisotropy were controllable by nanosheet concentration. These phenomena can be explained that the diffusion of molecules inside the gel is effectively hindered along the direction perpendicular to the nanosheet...

In nature, an important example of chemical communication and synchronicity can be found in cell populations where long-range chemical communication takes place over micrometer distance. In vitro laboratory systems can be useful to understand and control such complex biological mechanisms and, in a biomimetic approach, we present in this paper a model based on three basic features, namely (i) the compartmentalization of chemical information (using microfluidics), (ii) a stable emitter of periodic chemical signals inside compartments (Belousov-Zhabotinsky oscillating reaction) and (iii) a suitable spatio-temporal monitoring of the emitted chemical signal. In particular, starting from our recent work on the communication among oscillators via chemical intermediates in networks of lipid-stabilised droplets, we discuss here the role of compartments and of the geometry of the system. We present 3 different experimental configurations, namely liposomes (water-in-water dispersions), double emulsions (water-in-oil-in-water dispersions) and simple emulsions (water-in-oil dispersions) and we show that the global behaviour of networks can be influenced and controlled by several experimental parameters, like the nature of the collecting solvent, the presence of dopants and the network geometry. Numerical models supporting and explaining the experimental findings are also discussed.

We consider the case of the Belousov–Zhabotinsky (BZ) oscillating reaction where the metal catalyst is confined in a discrete phase of cation-exchange resin particles. We show that modelling of the sudden transitions from the steady state to fully synchronized oscillations, which were previously described only in terms of quorum sensing, does not necessarily require fine-graining of the models into individual particles. As a minimal representation of the system, we propose a generalized version of the Oregonator with only one additional parameter φ that corresponds to the total volume fraction of the catalytic phase in the system. We show that the kinetic consequences of catalyst confinement can be interpreted through φ acting as the second variable stoichiometric factor in the Oregonator mechanism that decreases the order of autocatalysis and simultaneously weakens the negative feedback. Based on the proposed model, an analysis of the so-called quorum sensing is provided in terms of the standard concepts of Hopf bifurcation. The model reproduces correctly that (1) oscillations are only exhibited above a certain critical threshold of φ; (2) as φ decreases, so do the amplitudes of oscillations; whereas (3) the periods of oscillations are almost independent of φ. The model thus appears to be a reasonable minimal representation of uniform states in the BZ reaction with catalyst confinement, and therefore might be a convenient starting point for further refinements representing more complicated transitions in this system.

The Briggs-Rauscher reaction containing malonic acid may undergo a sudden transition from low (state I) to high iodide and iodine (state II) concentration states after a well-defined and strongly reproducible oscillatory period. This study clearly shows that even though the time-dependent behavior of the oscillatory state is reproducible, the time lag necessary for the appearance of the state I to state II transition after the system leaves the oscillatory state becomes irreproducible for an individual kinetic run. This crazy clock behavior of the state I to state II transition is identified by repeated experiments in which stirring rate is taken as a control parameter and all other parameters such as initial conditions, temperature, vessel surface, and the age of solution were kept constant. Surprisingly, a better stirring condition does not make the transition reproducible; it simply does not allow the transition to happen at all. The proposed mechanism, additional explanations, and proposals for this irreproducibility of state I to state II transition have been presented. Considering the fact that the number of crazy clock reactions is only a few, this study may contribute to a better understanding of fundaments of this phenomenon.

It is well documented that different surface structures of catalytically active metals may exhibit different catalytic properties. This is typically examined by comparing the catalytic activities and/or selectivities of various well-defined smooth and stepped/kinked single crystal surfaces. Here we report the direct observation of the heterogeneity of active polycrystalline surfaces under reaction conditions, which is manifested by multifrequential oscillations during hydrogen oxidation over rhodium, imaged in situ by photoemission electron microscopy. Each specific surface structure, i.e. the crystallographically different µm-sized domains of rhodium, exhibits an individual spiral pattern and oscillation frequency, despite the global diffusional coupling of the surface reaction. This reaction behavior is attributed to the ability of stepped surfaces of high-Miller-index domains to facilitate the formation of subsurface oxygen, serving as feedback mechanism of the observed oscillations. The current experimental findings, backed by microkinetic modeling, may open an alternative approach towards addressing the structure-sensitivity of heterogeneous surfaces., The structurally different domains of a polycrystalline material may exhibit differing catalytic properties. Here, the authors directly visualize this phenomenon by observing the catalytic hydrogen oxidation that oscillates, simultaneously exhibiting different frequencies for structurally different rhodium domains.

Based on a ten-step chemical model involving the concentrations of I2(aq), O2(aq), and the intermediates of I- and HIO2, four independent variables and seven irreversible steps, the nonlinear behavior of Bray-Liebhafsky (BL) oscillating reaction was investigated. The results showed that with different values of initial concentrations of reactants in the process of simulation, both periodic oscillation and chaotic behavior could be observed. In addition, at the same initial concentrations and rate constants, the system becomes more and more regular after being chaos. That is to say, the translation from chaos to periodic oscillation at the same initial conditions appeared in the BL system. The nonlinear behavior of system was also investigated briefly

Oscilatorna dinamička stanja su veoma česta u prirodim procesima i stoga važna za postojanje živog sveta. Složeni prirodni sistemi poseduju veliki broj vrsta koje međusobno interaguju na različite načine i kao takvi su veoma komplikovani, ili gotovo nemogući, za detaljna eksperimentalna istraživanja, pa je potrebno da se osnovni fenomeni ispitaju u jednostavnijim hemijskim oscilatorima. U ove jednostavnije hemijske oscilatore spadaju oksihalogenidni oscilatori, od kojih su najpoznatiji Bray-Liebhafsky i Briggs-Rauscher predmet ove teze. U uzanom delu oscilatorne oblasti mogu se zapaziti i aperiodična dinamička stanja odnosno haos. Poseban oblik haosa predstavljaju intermitentne oscilacije odnosno intermitentan haos. Intermitentan haos je ono haotično stanje gde se dva kvalitativno različita dinamička stanja naizmenicno i haotično smenjuju, pri konstantnim vrednostima kontrolnih parametara. Kao takav uočen je u mnogim složenim nelinearnim sistemima mada su saznanja o intermitentnim stanjima u oksihalogenidnim sistemima veoma skromna. Intermitentan haos, koji je u okviru ove teze eksperimentalno generisan, predstavlja haotičnu i naizmeničnu smenu intervala oscilacija velikih amplituda i intervala oscilacija malih amplituda. Za eksperimentalno praćenje intermitentnog haosa u ovoj tezi je korišćena potenciometrijska metoda, koja se inače široko primenjuje za praćenje dinamike hemijskih oscilatora. U oba oksihalogenidna sistema, obuhvaćena tezom, intermitentne oscilacije su uočene u zatvorenom i otvorenom reaktoru, i to u uzanom intervalu kontrolnih parametara u Bray-Liebhafsky sistemu i u uzanom opsegu koncentracija hemijskog perturbatora u Briggs-Rauscher sistemu. Kako bi se omogućila kvantitativna analiza dobijenih rezultata u okviru teze su razvijene i nove metode analize eksperimentalno dobijenog intermitentnog haosa. Pored toga pojedini rezultati su analizirani i primenom numeričkih metoda, poput onih koja se često koriste u analizi haosa, i to Poincaré-ove mape, Lyapunov-ljevi eksponenti i autokorelaciona metoda. Oscillatory dynamic states are very common in natural processes and therefore very important for existence of the living world. Complex natural processes have numerous species that interact between one another in different manners, and so they are very complicated, or almost impossible, for detailed experimental investigations, so principal phenomena sould be examined in simpler chemical oscillators. Such systems are oxi-halide oscillators. The most famous oxi-halide oscillators are Bray-Liebhafsky and Briggs-Rauscher and they are the object of study in this thesis. In the narrow part of the oscillatory region, aperiodic dynamic states or chaos can be found. Intermittent oscillations or intermittent chaos represents a specific form of the chaotic state. Intermittent chaos is considered a chaotic state where transition between two qualitatively different dynamic states occurs randomly and wherein control parameters are constant. As such it was found in many complex nonlinear systems, however knowledge about intermittent states in oxi-halide systems are very modest. Experimentally generated intermittent chaos, within this thesis, represents dynamic state where intervals of high-amplitude oscillations chaotically alternate with intervals of low-amplitude oscillations. For experimental recording of the intermittent chaos, within this thesis, a potentiometric method was used. This method is widely used to follow the dynamics of the chemical oscillators. In this thesis, in both oxi-halide systems, intermittent oscilations were found in open and in closed reactor. Namely, intermitent oscillations were found in narrow interval of control parameters in Bray-Liebhafsky and in narrow range of concentrations of the chemical perturbator in Briggs-Rauscher reaction system. In order to allow quantitative analysis of obtained results, in this thesis new methods of the analysis of the experimentaly obtained intermittent states are developed. Besides, some results were analysed by numerical methods like Poincaré maps, Lyapunov exponents and autocorrelation function since those methods are often used in the analysis of chaos.