Pyrolysis is a
thermochemical decomposition of organic material at elevated temperatures in
the absence of oxygen. Pyrolysis typically occurs under pressure and at
operating temperatures above 430 °C (800 °F). In practice it is not possible to
achieve a completely oxygen-free atmosphere. Because some oxygen is present in
any pyrolysis system, a small amount of oxidation occurs. The word is coined
from the Greek-derived elements pyr"fire"
and lysis "loosening".
Pyrolysis is a special case of thermolysis, and is most commonly used for organic
materials, being then one of the processes involved in charring. The pyrolysis
of wood, which starts at 200–300 °C (390–570 °F), occurs for example in fires
or when vegetation comes into contact with lava in volcanic eruptions. In general,
pyrolysis of organic substances produces gas and liquid products and leaves a
solid residue richer in carbon content. Extreme pyrolysis, which leaves mostly
carbon as the residue, is called carbonization.
This
chemical process is heavily used in the chemical industry, for example, to
produce charcoal, activated carbon, methanol and other chemicals from wood, to
convert ethylene dichloride into vinyl chloride to make PVC, to produce coke
from coal, to convert biomass into syngas, to turn waste into safely disposable
substances, and for transforming medium-weight hydrocarbons from oil into
lighter ones like gasoline. These specialized uses of pyrolysis may be called
various names, such as dry distillation, destructive distillation, or cracking.
Pyrolysis
also plays an important role in several cooking procedures, such as baking,
frying, grilling, and caramelizing. And it is a tool of chemical analysis, for
example in mass spectrometry and in carbon-14 dating. Indeed, many important
chemical substances, such as phosphorus and sulphuric acid, were first obtained
by this process. Pyrolysis has been assumed to take place during catagenesis, the conversion of buried organic matter to
fossil fuels. It is also the basis of pyrography. In their embalming process,
the ancient Egyptians used a mixture of substances, including methanol, which
they obtained from the pyrolysis of wood.
Pyrolysis
differs from other high-temperature processes like combustion and hydrolysis in
that it does not involve reactions with oxygen, water, or any other reagents.
However, the term has also been applied to the decomposition of organic
material in the presence of superheated water or steam (hydrous pyrolysis), for
example in the steam cracking of oil.
Pyrolysis
is usually the first chemical reaction that occurs in the burning of many solid
organic fuels, like wood, cloth, and paper, and also of some kinds of plastic.
In a wood fire, the visible flames are not due to combustion of the wood
itself, but rather of the gases released by its pyrolysis; whereas the
flame-less burning of embers is the combustion of the solid residue (charcoal)
left behind by it. Thus, the pyrolysis of common materials like wood, plastic,
and clothing is extremely important for fire safety and fire-fighting.
Pyrolysis
occurs whenever food is exposed to high enough temperatures in a dry
environment, such as roasting, baking, toasting, grilling, etc.. It is the chemical process responsible for the
formation of the golden-brown crust in foods prepared by those methods.
In
normal cooking, the main food components that suffer pyrolysis are
carbohydrates (including sugars, starch, and fibre) and proteins. Pyrolysis of
fats requires a much higher temperature, and since it produces toxic and
flammable products (such asacrolein), it is generally
avoided in normal cooking. It may occur, however, when barbecuing fatty meats
over hot coals.
Even
though cooking is normally carried out in air, the temperatures and
environmental conditions are such that there is little or no combustion of the
original substances or their decomposition products. In particular, the
pyrolysis of proteins and carbohydrates begins at temperatures much lower than
the ignition temperature of the solid residue, and the volatilesubproducts are too diluted in air to ignite. (In
flambé dishes, the flame is due mostly to combustion of the alcohol, while the
crust is formed by pyrolysis as in baking.)
Pyrolysis
of carbohydrates and proteins require temperatures substantially higher than
100 °C (212 °F), so pyrolysis does not occur as long as free water is present,
e.g. in boiling food — not even in a pressure cooker. When heated in the
presence of water, carbohydrates and proteins suffer gradual hydrolysis rather
than pyrolysis. Indeed, for most foods, pyrolysis is usually confined to the
outer layers of food, and only begins after those layers have dried out.
Food
pyrolysis temperatures are however lower than the boiling point of lipids, so
pyrolysis occurs when frying in vegetable oil or suet, or basting meat in its
own fat.
Pyrolysis
also plays an essential role in the production of barley tea, coffee, and
roasted nuts such as peanuts and almonds. As these consist mostly of dry
materials, the process of pyrolysis is not limited to the outermost layers but
extends throughout the materials. In all these cases, pyrolysis creates or
releases many of the substances that contribute to the flavor, color, and biological properties of the final product. It
may also destroy some substances that are toxic, unpleasant in taste, or those
that may contribute to spoilage.
Controlled
pyrolysis of sugars starting at 170 °C (338 °F) produces caramel, a beige to
brown water-soluble product which is widely used in confectionery and (in the
form of caramelcoloring) as a coloring agent for soft drinks and other
industrialized food products.
Solid
residue from the pyrolysis of spilled and splattered food creates the
brown-black encrustation often seen on cooking vessels, stove tops, and the
interior surfaces of ovens.
Pyrolysis
has been used since ancient times for turning wood into charcoal in an
industrial scale. Besides wood, the process can also use sawdust and other wood
waste products.
Charcoal
is obtained by heating wood until its complete pyrolysis (carbonization)
occurs, leaving only carbon and inorganic ash. In many parts of the world,
charcoal is still produced semi-industrially, by burning a pile of wood that
has been mostly covered with mud or bricks. The heat generated by burning part
of the wood and the volatile byproducts pyrolyzes the rest of the pile. The limited supply of
oxygen prevents the charcoal from burning too. A more modern alternative is to
heat the wood in an airtight metal vessel, which is much less polluting and
allows the volatile products to be condensed.
The
original vascular structure of the wood and the pores created by escaping gases
combine to produce a light and porous material. By starting with dense wood-like
material, such as nutshells or peach stones, one obtains a form of charcoal
with particularly fine pores (and hence a much larger pore surface area),
called activated carbon, which is used as an adsorbent for a wide range of
chemical substances.
Residues
of incomplete organic pyrolysis, e.g. from cooking fires, are thought to be the
key component of the terra preta soils
associated with ancient indigenous communities of the Amazon basin. Terra preta is much sought by local farmers for its superior
fertility compared to the natural red soil of the region. Efforts are underway
to recreate these soils through biochar, the solid residue of pyrolysis of
various materials, mostly organic waste.
Biochar
improves the soil texture and ecology, increasing its ability to retain
fertilizers and release them slowly. It naturally contains many of the
micronutrients needed by plants, such as selenium. It is also safer than other
"natural" fertilizers such as manure or sewage since it has been
disinfected at high temperature, and since it releases its nutrients at a slow
rate, it greatly reduces the risk of water table contamination.
Biochar
is also being considered for carbon sequestration, with the aim of mitigation
of global warming.
Pyrolysis
is used on a massive scale to turn coal into coke for metallurgy, especially
steelmaking. Coke can also be produced from the solid residue left from
petroleum refining.
Those
starting materials typically contain hydrogen, nitrogen or oxygen atoms
combined with carbon into molecules of medium to high molecular weight. The
coke-making or "coking" process consists in heating the material in
closed vessels to very high temperatures (up to 2,000 °C or 3,600 °F), so that
those molecules are broken down into lighter volatile substances, which leave
the vessel, and a porous but hard residue that is mostly carbon and inorganic
ash. The amount of volatiles varies with the source material, but is typically
25-30% of it by weight.
Carbon fibers are filaments of carbon that can be used to
make very strong yarns and textiles. Carbon fiber items
are often produced by spinning and weaving the desired item from fibers of a suitable polymer, and then pyrolyzing the material at a high temperature (from
1,500–3,000 °C or 2,730–5,430 °F).
The
first carbon fibers were made from rayon,
but polyacrylonitrilehas become the most common
starting material.
For
their first workable electric lamps, Joseph Wilson Swan and Thomas Edison used
carbon filaments made by pyrolysis of cotton yarns and bamboo splinters,
respectively.
Pyrolysis
is the basis of several methods that are being developed for producing fuel
from biomass, which may include either crops grown for the purpose or
biological waste products from other industries.
Although
synthetic diesel fuel cannot yet be produced directly by pyrolysis of organic
materials, there is a way to produce similar liquid ("bio-oil") that
can be used as a fuel, after the removal of valuable bio-chemicals that can be
used as food additives or pharmaceuticals.[8] Higher efficiency is achieved by the so-called
flash pyrolysis where finely divided feedstock is quickly heated to between 350
and 500 °C (660 and 930 °F) for less than 2 seconds.
Fuel
bio-oil resembling light crude oil can also be produced by hydrous pyrolysis
from many kinds of feedstock, including waste from pig and turkey farming, by a
process called thermaldepolymerization (which
may however include other reactions besides pyrolysis).
Anhydrous
pyrolysis can also be used to produce liquid fuel similar to diesel from
plastic waste.
In
many industrial applications, the process is done under pressure and at
operating temperatures above 430 °C (806 °F). For agricultural waste, for
example, typical temperatures are 450 to 550 °C (840 to 1,000 °F).
In vacuum
pyrolysis, organic material is heated in a vacuum in order to decrease
boiling point and avoid adverse chemical reactions. It is used in organic
chemistry as a synthetic tool. Inflash vacuum thermolysis or FVT,
the residence time of the substrate at the working temperature is limited as
much as possible, again in order to minimize secondary reactions.
Since
pyrolysis is endothermic, various methods have been proposed to provide heat to
the reacting biomass particles:
● Partial combustion of the biomass products through air
injection. This results in poor-quality products.
● Direct heat transfer with a hot gas, ideally product
gas that is reheated and recycled. The problem is to provide enough heat with
reasonable gas flow-rates.
● Indirect heat transfer with exchange surfaces (wall,
tubes). It is difficult to achieve good heat transfer on both sides of the heat
exchange surface.
● Direct heat transfer with circulating solids: Solids
transfer heat between a burner and a pyrolysis reactor. This is an effective
but complex technology.
For
flash pyrolysis the biomass must be ground into fine particles and the
insulating char layer that forms at the surface of the reacting particles must
be continuously removed. The following technologies have been proposed for
biomass pyrolysis:
● Fixed beds were used for the traditional production of
charcoal. Poor, slow heat transfer resulted in very low liquid yields.
● Augers: This technology is adapted from a Lurgi process for coal gasification. Hot sand and
biomass particles are fed at one end of a screw. The screw mixes the sand and
biomass and conveys them along. It provides a good control of the biomass
residence time. It does not dilute the pyrolysis products with a carrier or
fluidizing gas. However, sand must be reheated in a separate vessel, and
mechanical reliability is a concern. There is no large-scale commercial
implementation.
● Ablative processes: Biomass particles are moved at
high speed against a hot metal surface. Ablation of any char forming at the
particles surface maintains a high rate of heat transfer. This can be achieved
by using a metal surface spinning at high speed within a bed of biomass
particles, which may present mechanical reliability problems but prevents any
dilution of the products. As an alternative, the particles may be suspended in
a carrier gas and introduced at high speed through a cyclone whose wall is
heated; the products are diluted with the carrier gas. A problem shared with
all ablative processes is that scale-up is made difficult since the ratio of
the wall surface to the reactor volume decreases as the reactor size is
increased. There is no large-scale commercial implementation.
● Rotating cone: Pre-heated hot sand and biomass
particles are introduced into a rotating cone. Due to the rotation of the cone,
the mixture of sand and biomass is transported across the cone surface by
centrifugal force. Like other shallow transported-bed reactors relatively fine
particles are required to obtain a good liquid yield. There is no large scale commercial
implementation.
● Fluidized beds: Biomass particles are introduced into
a bed of hot sand fluidized by a gas, which is usually a recirculated product
gas. High heat transfer rates from fluidized sand result in rapid heating of
biomass particles. There is some ablation by attrition with the sand particles,
but it is not as effective as in the ablative processes. Heat is usually
provided by heat exchanger tubes through which hot combustion gas flows. There
is some dilution of the products, which makes it more difficult to condense and
then remove the bio-oil mist from the gas exiting the condensers. This process
has been scaled up by companies such as Dynamotive and Agri-Therm. The main challenges are in improving the
quality and consistency of the bio-oil.
● Circulating fluidized beds: Biomass particles are
introduced into a circulating fluidized bed of hot sand. Gas, sand and biomass
particles move together, with the transport gas usually being a recirculated
product gas, although it may also be a combustion gas. High heat transfer rates
from sand ensure rapid heating of biomass particles and ablation is stronger
than with regular fluidized beds. A fast separator separates the product gases
and vapors from the sand and char
particles. The sand particles are reheated in fluidized burner vessel and
recycled to the reactor. Although this process can be easily scaled up, it is
rather complex and the products are much diluted, which greatly complicates the
recovery of the liquid products.
Many
sources of organic matter can be used as feedstock forpyrolosis.
Suitable plant material includes: greenwaste,
sawdust, waste wood, woody weeds; and agricultural sources including: nut
shells, straw, cotton trash, rice hulls, switch grass; and poultry litter,
dairy manure and potentially other manures. Pyrolysis is used as a form of
thermal treatment to reduce waste volumes of domestic refuse. Some
industrial byproducts are also suitable
feedstock including paper sludge and distillers grain.
There
is also the possibility of integrating with other processes such as mechanical
biological treatment and anaerobic digestion.
● syngas (flammable mixture of carbon monoxide and
hydrogen): can be produced in sufficient quantities to both provide the energy
needed for pyrolysis and some excess production
● solid char that can either be burned for energy or
recycled as a fertilizer (biochar).
Destructive
fires in buildings will often burn with limited oxygen supply, resulting in
pyrolysis reactions. Thus, pyrolysis reaction mechanisms and the pyrolysis
properties of materials are important in fire protection engineering for
passive fire protection. Pyrolytic carbon is also important to fire
investigators as a tool for discovering origin and cause of fires.