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- FTIR spectroscopy (4)
- Numerical simulations (3)
- Azodicarboxylates (2)
- Biomass (2)
- Car fire (2)
- Differential scanning calorimetry (DSC) (2)
- Explosive properties (2)
- Hot storage tests (2)
- Kinetics (2)
- Pyrolysis (2)
Organisationseinheit der BAM
Eingeladener Vortrag
- nein (1)
Data and prediction for the mass burning rate of a tert-butyl-peroxy-benzoat (TBPB) pool fire (pool diameter = 3 m) is presented. The mass burning rates of TBPB fires are up to six times higher and less dependent on pool diameter compared to hydrocarbon pool fires caused by an additional heat release rate due to exothermic decomposition reaction in the liquid phase. This heat release rate is calculated using a 1st order reaction kinetic obtained from micro calorimetric measurements. A new model is derived considering the heat release rate due to the decomposition reaction which is shown to be 100 % of the heat release rate radiated to the pool surface. With the presented model, including also physical quantities, especially the limiting fuel concentration for upward flame propagation, it is possible to predict the mass burning rates of large TBPB pool fires. The predicted values are in very good agreement with the experiments.
A kinetic model of smouldering of pine wood is determined by thermo-gravimetric analysis (TGA), describing the reactions of wood pyrolysis, wood oxidation and char oxidation. Thermo-gravimetric experiments were conducted with constant heating rates ranging from 2.5 to 10 K/min in atmospheres of pure nitrogen and mixtures of nitrogen and oxygen (with 20.5%, 8.2% and 4.3% O2). At first wood pyrolysis and char oxidation experiments are carried out in an independent way. Then smouldering experiments are conducted, which combine the two previous reactions with wood oxidation. Finally, the heats of the reactions are determined by differential scanning calorimetry (DSC). The results are discussed, compared with the literature and the derived kinetic model is presented, which includes five components: three pseudo-components of wood – representing roughly cellulose, hemi-cellulose and lignin – as well as char and ashes.
Self-ignition of deposited combustibles is a possible reason for excessive fires occurring on deposits for recycling materials or on waste dumps. Two series of experiments were performed to assess the hazard of self-ignition: hot storage tests with different homogeneous mixtures of combustible material and inert material and tests with pockets of combustible material embedded in inert matter. In the first test series considerable exothermicity (ΔT>60K) was observed for mass fractions of combustible material as low as 2.5%. In the second series it could be shown that the heat transfer from a pocket of burning material through the inert matter can ignite a second pocket of combustible matter.
Based on the experimental data, numerical simulations were performed to predict self-ignition on real-scale waste deposits. For a deposit of specific size and shape, the influence of the ambient temperature on the occurrence of self-ignition has been investigated.
Chemical-analytical investigation of fire products in intermediate storages of recycling materials
(2012)
Organic materials like paper, cardboard, textiles or plastics are mostly flammable. In intermediate storages for recycling products, these materials are stored in large amounts. If fire occurs in these stores, large emissions of smoke and other potentially harmful products are likely. In the present study, the gaseous products released from fires of such materials—for example, because of self-ignition—were investigated. Different fractions (paper/cardboard, textiles and plastics) were crushed at low temperatures (about 80 K) and subsequently allowed to smoulder at different temperatures using the German standard Deutsches Institut für Normung 53436. The gases produced were sampled and analysed using Fourier transform infrared spectroscopy. The chemical composition of these gases differed considerably depending on fuel type. For flammable materials without heteroatom, the gases consisted predominantly of toxic compounds like carbon monoxide and carbon dioxide. Smouldering of materials containing heteroatoms showed, in addition to carbon monoxide, carbon dioxide and water vapour, further toxic components containing the heteroatom. Materials containing chlorine produced hydrogen chloride, and materials containing nitrogen produced ammonia and hydrogen cyanide.
Präsentation zum geplanten BAM-Forschungsvorhaben ("Safe transport of stabilized polymerizing substances: Investigation on the degradation of selected stabilizers"), bezogen auf den sicheren Transport (Straße, See) von polymerisierenden Substanzen. Der Schwerpunkt liegt dabei auf den systematischen Untersuchungen - mittels Thermal Activity Monitor (TAM IV) - zum zeitlichen Abbau des Stabilisators bei der Polymerisation sowie auf der Bestimmung der entsprechenden volumenabhängigen selbstbeschleunigenden Polymerisation (SAPT).
The hazards for passengers during vehicle fires result from the increasing temperature and the emitted smoke gases. A fire was set on a car to investigate the development of temperature and of gaseous fire products in the passenger compartment. The study was based on a full-scale test with a reconstructed scene of a serious car fire. The aim of this work was to identify the conditions for self-rescuing of passengers during a car fire.
A dummy, equipped with several thermocouples, was placed on the driver’s seat. Also, the smoke gases were continuously collected through a removable probe sensor corresponding to the nose of the dummy in the passenger compartment and analyzed using Fourier transform infrared spectroscopy. Additionally, several car components were investigated in the smoke density chamber (smoke emission and smoke gas composition). It was found that the toxic gases already reached hazardous levels by 5 min, while the temperatures at the dummy were at that time less than 80 °C. The toxicity of smoke gases was assessed using the
fractional effective dose concept. The various experimentally parameters (temperature and smoke gas composition) were implemented into numerical simulations with fire dynamics simulator. Both the experimental data and the numerical simulations are presented and discussed.
This paper discusses a method for determining the kinetics of biomass pyrolysis based on comparing isoconversional methods, such as the Kissinger and KAS methods, and least squares fitting in a parallel reaction scheme with three pseudo-components roughly representing cellulose, hemicellulose and lignin. The activation energies of the different pseudo-components reported in the literature vary widely. This variation could be reduced if care were taken to determine the kinetics of biomass pyrolysis: First, the reference experiments with pure cellulose are reproduced to validate the thermogravimetric analysis. Then, experiments are performed and analyzed with different heating rates and isoconversional methods are employed to verify the reliability of the experiments and to avoid selecting inappropriate reaction models in a fitting routine.
A large number of azodicarboxylates and their derivatives are produced and used in the chemical industries. The versatile applications of these azodicarboxylates in research institutes and in the chemical industries for chemical synthesis arouse additional hazards. The intent of this paper is to obtain first knowledge about the structure–response relationship regarding the explosive properties and the thermal hazards of different versatile used azodicarboxylates. The substances are examined with the differential scanning calorimetry (DSC). Furthermore, different laboratory test methods, based on the UN Recommendations on the Transport of Dangerous Goods, are applied to determine the explosive properties of the mentioned substances. On the basis of the obtained results, the known influence of the nitrogen content within the molecule regarding their thermal behaviour could be confirmed. The measured heat of decomposition appeared to be proportional to the nitrogen content within the group of the aliphatic and the aromatic azodicarboxylates. To emphasize this dependency, further investigations should be done. The long term objective of this research is to develop structure–response relationships of the explosive properties and the thermal hazards originating from azodicarboxylates.
Fires on waste dumps, surface landfills, Underground stowing or storage facilities of Recycling factories may have multiple harmful effects on individuals on site and on environment.
Possibly several tens of thousands of tons flare up plunging vast areas in smoke and releasing large amounts of flue gases. Experience shows that fire fighting takes days or even weeks and moreover, as long as hidden glowing nests exist fires may break out repeatedly weeks or months later. In the light of this, fire prevention is much easier to manage than extinction. It is of internst to identify the geometrical and physical conditions under which the mid-term or long-term storage of recycling materials can be performed avoiding self-ignition. Our Guideline presents a novel method developed at BAM which combines experimental tests on lab-scale with numerical simulations in Order to obtain permissible geometries of deposits and storage times at which self-ignition can be certainly avoided (Berger 2010).