Pyrolysis, slow temperature

The volatilization of arsenic during the thermal destruction of CCA-treated wood may be reduced by utilizing low-temperature pyrolysis. Low-temperature pyrolysis uses temperatures of approximately 300-400 °C with a limited air supply (Helsen and Van den Bulck, 2004, 286, 290 Helsen and Van den Bulck, 2003). Pyrolysis includes slow and flash methods (Helsen and Van den Bulck, 2004). Flash pyrolysis, which produces an oil byproduct, is not effective with CCA-treated wood because only 5-18% of the arsenic... 

Pyrolysis of biomass is divided into slow pyrolysis, which is well known to produce charcoal, for example, fast pyrolysis, which produces a high yield of liquid biofuels and other chemicals (Bridgwater, 2000) and flash pyrolysis. Slow pyrolysis (or carbonisation) requires low temperatures and very long residence time. In the carbonisation process the amount of char is maximised. 

There are several procedures to perform pyrolysis flash pyrolysis (pulse mode), slow gradient heating pyrolysis (continuous mode), step pyrolysis, etc. Commonly, the pyrolysis for analytical purposes is done in pulse mode. This consists of a very rapid heating of the sample from ambient temperature, targeting isothermal conditions at a temperature where the sample is completely pyrolysed. Controlled slow temperature gradients are also possible in pyrolysis, but their use in analytical pyrolysis is limited. Step pyrolysis heats the sample rapidly but in steps, each step following a plateau of constant temperature kept for a limited time period. 

PhenoHc and furfuryl alcohol resins have a high char strength and penetrate into the fibrous core of the fiber stmcture. The phenoHc resins are low viscosity resoles some have been neutralized and have the salt removed. An autoclave is used to apply the vacuum and pressure required for good impregnation and sufficient heat for a resin cure, eg, at 180°C. The slow pyrolysis of the part foUows temperatures of 730—1000°C are recommended for the best properties. On occasion, temperatures up to 1260°C are used and constant weight is possible even up to 2760°C (93). 

Other large-scale coal pyrolysis process developments were carried out by the Tosco Corp., with its TOSCO AT, process (36). Essentially a direct copy of Tosco s rotating kiln technology that was developed for pyrolysis of oil shale, this slow heating scheme achieved tar yields at maximum temperatures of 482—521°C that were essentially identical to those obtained by a Eischer assay. 

Biochar from dairy manure also has pofenfial for environmenfal remediation or for creating slow release phosphorus fertilizers (Cau and Harris, 2010). Dairy manure was converted by heating at temperatures below pyrolysis temperatures (< 500 °C) and in the presence of air. The potential benefit for lowering GHGs was nof defermined but the products have the potential of creating new markets for manure. 

The question of the stability of the biomolecules is a vital one. Could they really have survived the tremendous energies which would have been set free (in the form of shock waves and/or heat) on the impact of a meteorite Blank et al. (2000) developed a special technique to try and answer this question. They used an 80-mm cannon to produce the shock waves the shocked solution contained the two amino acids lysine and norvaline, which had been found in the Murchison meteorite. Small amounts of the amino acids survived the bombardment , lysine seeming to be a little more robust. In other experiments, the amino acids aminobutyric acid, proline and phenylalanine were subjected to shock waves the first of the three was most stable, the last the most reactive. The products included amino acid dimers as well as cyclic diketopiperazine. The kinetic behaviour of the amino acids differs pressure seems to have a greater effect on the reaction pathway than temperature. As had been recognized earlier, the effect of pressure would have slowed down certain decomposition reactions, such as pyrolysis and decarboxylation (Blank et al., 2001). 

This follows by a steady state energy balance of the surface heated by qe, outside the flame-heated region S. It appears that a critical temperature exists for flame spread in both wind-aided and opposed flow modes for thin and thick materials. Tstmn has not been shown to be a unique material property, but it appears to be constant for a given spread mode at least. Transient and chemical effects appear to be the cause of this flame spread limit exhibited by 7 smln. For example, at a slow enough speed, vp, the time for the pyrolysis may be slower than the effective burning time ... 

Pyrolysis is a type of gasification that breaks down the biomass in oxygen deficient environments, at temperatures of up to 400°F. This process is used to produce charcoal. Since the temperature is lower than other gasification methods, the end products are different. The slow heating produces almost equal proportions of gas, liquid and charcoal, but the output mix can be adjusted by changing the input, the temperature, and the time in the reactor. The main gases produced are hydrogen and carbon... 

As stated earlier, the benzene molecule is stabilized by strong resonance consequently, removal of a H from the ring by pyrolysis or 02 abstraction is difficult and hence slow. It is not surprising, then, that the induction period for benzene oxidation is longer than that for alkylated aromatics. The high-temperature initiation step is similar to that of all the cases described before, that is,... 

Poly(a-phenylethyl isocyanide), however, yields complex products distinguishable from monomer upon thermal degradation at 20 mm Hg (13). At 300° C a viscous condensate is produced which is free of isocyanide absorption in its infrared spectrum and appears very similar to the recently synthesized oligo-isocyanides, a,co-dihydrotri(a-phenylethyl isocyanide) and a,co-dihydrohexa(a-phenylethyl isocyanide) (15). Pyrolysis at 500° C produces an intense broad infrared absorption band in the range about 3300 cm-1, which is the range of associated N il bonds. Pyrolysates obtained at 700° C reveal nitrile absorption at 2270 cm"1, that becomes more intense in pyrolysates produced at temperatures up to 1300° C. A slow pyrolysis at 200-300° C is indicated for the study of primary structural changes in poly(a-phenylethyl isocyanide). Pyrolysates of poly(<7-... 

Considering the volatiles that evolve from hot pressing and heat-treating operations, it is concluded that the major chemical changes occurring in this stage are pyrolytic. Methanol, acetic acid, furfural, and ligneous tars are the common volatiles produced by the slow pyrolysis of wood practiced in destructive-distillation processes. The temperatures used in the board conversion operations approach pyrolysis temperatures of wood and the evidence indicates that pyrolysis is indeed active in board conversion. 

---