Biomass: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Milton Beychok
m (→‎Uses of biomass: More wiki links)
imported>Milton Beychok
(Extensively re-formating and re-writing to improve the technical content of the article.)
Line 1: Line 1:
{{subpages}}
{{subpages}}
{{TOC|right}}
{{TOC|right}}
'''Biomass''', a source of [[renewable energy]], is [[biology|biological]] material such as wood, wood waste, straw, sugar cane, algae, and many other byproducts derived from agricultural and forestry production as well as other sources. Since biomass derives from plants generated by [[solar energy]] in the [[photosynthesis]] process, it can also be defined as the biological material on [[Earth]] that has stored solar energy in the chemical bonds of the organic material.
'''Biomass''', a source of [[renewable energy]], is [[biology|biological]] material such as wood, wood waste, municipal solid waste, straw, sugar cane, algae, and many other byproducts derived from agricultural and forestry production as well as other sources. Since biomass derives from plants generated by [[solar energy]] in the [[photosynthesis]] process, it can also be defined as the biological material on [[Earth]] that has stored solar energy in the chemical bonds of the organic material.


==Uses of biomass==
The [[fossil fuels]] ([[coal]], [[Petroleum crude oil|petroleum]] and [[natural gas]]) are currently thought to have been formed from prehistoric, ancient biomass buried deeply underground over millions of years of [[geological time]]. Therefore, they  are not considered to be renewable sources of energy


The [[Energy (science)|chemical energy]] contained in biomass can be processed to create useable fuels.  Several processes have been developed to convert biomass into various forms of fuel such as [[biodiesel]], and [[ethanol]].  The resulting fuels can provide a cleaner alternative to fossil fuels because they emit lower levels of by-products such as [[carbon monoxide]] (CO) and [[carbon dioxide]] (CO2).  While there are many methods for processing biomass currently in use, the most important three are [[gasification]], [[syngas]] cleaning/processing, and [[Fischer-Tropsch synthesis]].<ref name=Damartzis>{{cite journal| author=T. Damartzis and A. Zabaniotou|title=Thermochemical conversion of biomass to second generation biofuels through integrated process design-A review|journal=Renewable & Sustainable Energy Reviews|volume=15|issue=1|pages=366-378|date=Jan. 2011|id=|url=}}</ref>
==Production of fuels and other products from biomass==


== Biomass gasification ==
===Biomass fuel for electric power production===


Gasification is a process of burning the biomass source at a relatively high temperature to release carbon monoxide and [[hydrogen]].  This process can occur through the use of [[oxygen]], [[air]], [[steam]], or mixtures similar to these.<ref>{{cite journal| author=S. Albertazzi et al|title=The technical feasibility of biomass gasification for hydrogen production|journal=Catalysis Today|volume=106|issue=1-4|pages=297-300|date=Oct. 15, 2005|id=|url=}}</ref> When air is used to carry out the gasification process the required amount of [[heat]] is a relatively low to medium heating value.  This process requires less thermal energy to complete but creates higher levels of unwanted by-products such as [[methanol]] and less of the useable hydrogen product.  The use of steam requires a higher amount of thermal energy to carry out the process but will yield higher amounts of actual hydrogen and lower amounts of by-products.  Gasification involves four main steps, drying, [[pyrolysis]], [[reduction]] and [[combustion]]. The drying process consists of taking the biomass source and removing all the moisture. After the moisture is removed the resulting substance enters the pyrolysis zone. This is where [[Volatility (chemistry)|volatiles]] are removed in the form of carbon monoxide and carbon dioxide and also where tar is produced. After this process occurs the resulting substance goes over to the reduction zone where the raw materials are completely gasified in order to create a syngas product. Finally in the combustion zone the left-over char material is burned which produces more gaseous product and also produces the necessary heat for the reactions in the previously mentioned reduction zone. The end product is known as syngas.  Syngas can be used as a fuel or it can be further processed to create [[synthetic natural gas]] (SNG) or synthetic [[Petroleum crude oil|petroleum]]
The direct combustion of biomass for producing [[heat]] and [[Electrical power plant|electric power]] provides a ready disposal mechanism for municipal, agricultural, and industrial organic wastes. In 2009, about 11,350 [[Watt (unit)|megawatts]] (MW) of electric power, amounting to 1.1% of the summertime electrical supply in the [[United States]] was generated by burning biomass that included: wood, wood waste, [[municipal solid waste]] (MSW), [[landfill gas]], and agricultural byproducts and waste.<ref>[http://www.eia.doe.gov/cneaf/alternate/page/renew_energy_consump/table4.html U.S. Electric Net Summer Capacity] [[U.S. Energy Information Administration]] (EIA), part of the [[U.S. Department of Energy]] (DOE)</ref>


== Syngas purification ==
The New Hope Power Partnership in [[Florida]] is the largest [[biomass power plant]] in [[North America]]. It generates 140 MW of power using uses sugar cane fiber ([[bagasse]]) and recycled wood as fuel.<ref>[http://www.psc.state.fl.us/utilities/electricgas/RenewableEnergy/Cepero-OCFC.pdf Agriculture & Renewable Energy: The Partnership for a New Frontier] Florida Power Service Commission (FPSC) Workshop, July 26, 2007.</ref> It has been in operation for more than 10 years. 


When syngas is used for further processing it undergoes a cleaning and purification stage.  The gas cleaning stage is the first stage of syngas purification.  This process involves the use of mechanical filters which remove [[particulate matter]], and [[Adsorption|adsorbents]] that remove the [[alkali]] and [[sulfur]] compounds in the gas.  The remaining tar in the gas is then broken down through the use of [[catalysis]] and steam.<ref name=Damartzis/> Syngas cleaning is a crucial step in preventing the fouling of machinery or contamination of catalysts when further processing the gas. 
===Production of liquid transportation fuels===


== Fischer-Tropsch synthesis ==
There are several processes  available for converting the [[Energy (science)|chemical energy]] contained in biomass into liquid automotive transport fuels such as [[biodiesel]] and [[ethanol]].<ref>[http://www1.eere.energy.gov/biomass/abcs_biofuels.html ABC's of Biofuels] From the website of the [[Office of Energy Efficiency and Renewable Energy]] (EERE) in the U.S. Department of Energy (DOE).</ref>


The last commonly used stage of processing biomass is known as Fischer-Tropsch synthesis.  Purified syngas will be processede through a series of catalytic steps which will eventually transform the gas into a liquid fuel.<Ref name=Damartzis/> This fuel can be used in standard piston engines and can substitute for the use of fossil fuels.  This process requires substantial thermal energy to carry out and is a relatively costly process.  Efforts have been made to reduce the costs of this process to make it a reasonable competitor to the processing of oil for the creation of petroleum based fuels. 
'''''Ethanol fuel''''':


==Risks of biomass processing==
Ethanol fuel is [[Ethanol|ethyl alcohol]] (C<sub>2</sub>H<sub>5</sub>OH) and it is most often used as an automotive [[motor fuel]], mainly as an additive for [[gasoline]]. Ethanol can be produced by [[fermentation]] of [[sugar cane]], [[bagasse]], [[sugar beet]]s, [[barley]], [[potato]]es, [[corn]] and many other grains as well as many agricultural byproducts and wastes.


The risk level of biomass processing depends largely on the inspection and maintenance standards of the processing facility. From 2006 to 2010 there have been approximately 100 incidents in the United States regarding the processing of biomass to produce biofuels. From 2006 to 2009 there have been 8 fires and 6 explosions on the basis of about 200 biodiesel facilities.  Some of these explosions were responsible for the complete destruction of their respective plants.  However, 50% of the incidental cases in the last 5 years have not involved the process under normal conditions and 22 % of the incidents have been related to tank storage (overfilling, leaks, etc.).<ref>{{cite journal| author=E. Salzano, M. Di Serio and E. Santacesaria|title=Emerging Risks in the Biodiesel Production by Transesterification of Virgin and Renewable Oils|journal=Energy & Fuels|volume=24|issue=| pages=6103-6109|date=Nov. 2010|id=|url=}}</ref> Given that maintenance is properly carried out, incidents such as these will rarely occur.  The unstable nature of the materials in addition to the poor plant regulation is the reason why incidents are so frequent.  As a result, improvement efforts on regulation, inspection, and maintenance of the processing plants have been carried out with the goal of drastically reducing the number of incidents.
The worldwide production of ethanol for automotive fuel in 2007 was 52,000,000,000 [[litre]]s (13,700,000,000 [[gallon]]s). From 2007 to 2008, the share of ethanol in global gasoline use increased from 3.7% to 5.4%.<ref name=UNEP>[http://www.unep.fr/scp/rpanel/pdf/Assessing_Biofuels_Full_Report.pdf Assessing Biofuels (2009)] From the website of the [[United Nations Environment Programme]] (UNEP)</ref> In 2009, worldwide ethanol fuel production reached 73,900,000,000 litres (19,500,000,000 gallons) and was expected to reach 85,900,000,000 litres (22,700,000,000 gallons) in 2010.<ref name=RFA-News>[http://www.ethanolrfa.org/news/entry/global-ethanol-production-to-reach-85.9-billion-litres-22.7-billion-ga/ Global ethanol production to reach 85.9 billion litres (22.7 billion gallons) in 2010] March 22, 2010. From the website of the Renewable Fuels Association (RFA).</ref>


==Setbacks and the future of biomass==
Ethanol fuel is widely used in [[Brazil]] and in the United States, and together both countries were responsible for about 86 percent of the world's ethanol fuel production in 2009.<ref>[http://www.ethanolrfa.org/pages/statistics Ethanol Industry Statistics] ''2009 World Fuel Ethanol Production'' from the website of the Renewable Fuels Association.</ref>


The cost of collecting and processing biomass is the current main concern for the energy and transportation industriesEfforts are being made to expand the production and distribution of these fuels in order to lower costs to the consumer. However, costs of biofuels are still far higher than the costs of petroleum based fuels. The environmental availability of biomass is not an issue because sources such as food waste and other forms of waste are constantly being renewedAs prices for petroleum based fuels continue to rise and more efficient technologies for processing biomass are developed, demand for these alternative fuels will begin to increase considerably. As a result, biomass may very well be the alternative fuel source of choice for the immediate future.
'''''Biodiesel fuel''''':
 
[[Biodiesel]] refers to a [[Diesel oil|diesel fuel]] produced by chemically [[Chemical reaction|reacting]] [[lipids]] such as  vegetable oils or animal fats with an [[alcohol]] such as [[methyl alcohol]] (CH<sub>3</sub>OH). The resulting biodiesel consists of [[esters]] of long-chain [[fatty acid]]s. The process is known as "transesterification" and it may be carried out by several methods: the common batch process, supercritical processes and ultrasonic methods.
 
In 2009, the worldwide production of biodiesel was 17,900,000,000 litres (4,730,000,000 gallons). The three countries with the largest annual biodiesel production were [[Germany]] (16%), [[France]] (12%) and the United States (11%).<ref>[http://www.plateforme-biocarburants.ch/en/infos/production.php?id=biodiesel Production of biofuels in the world in 2009] August 30, 2010. From the website of the Biofuels Platform published in Switzerland.</ref>
 
{| border="0" width="240" align="right"
|
{| class = "wikitable" border="1" align="right" width="220"
|+ Worldwide Gasification Plants<br/>as of 2010<ref>[http://www.netl.doe.gov/technologies/coalpower/gasification/worlddatabase/2010_Worldwide_Gasification_Database.pdf Worldwide Gasification Database] [[National Energy Technology Laboratory]] (NETL), U.S. Department of Energy (DOE)</ref>
!Feedstock!!Plants!!Gasifiers
|- align=center
|Coal||53||201
|- align=center
|Petroleum||59||143
|- align=center
|Natural gas||23||&nbsp;59
|- align=center
|Biomass||&nbsp;9||&nbsp; 9
|- align=center
|Totals||144||412
|}
|}
 
===Biomass gasification to produce syngas===
 
[[Gasification]] is a process that reacts [[Carbon|carbon-containing]] materials (such as coal or biomass) at high [[temperature]]s with reagent gases (namely, [[steam]], pure [[oxygen]] and/or [[air]]) to produce a mixture of [[carbon monoxide]] (CO) and [[hydrogen]] (H<sub>2</sub>) commonly called ''syngas'' (a contraction of ''synthesis gas''). It has been in use since the early 1800s when coal and [[peat]] were gasified to produce what was then called ''town gas'' for lighting and cooking ... later to be replace by [[electricity]] and natural gas. As of 2010, 412 modern industrial-scale gasifiers were in operation in 29 countries worldwide (see adjacent table).<ref name=DOE-Overview>[http://www.netl.doe.gov/technologies/coalpower/gasification/pubs/pdf/DOE%20Gasification%20Program%20Overview.pdf DOE Gasification Program Overview] Jenny B. Tennant (December 2010, National Energy Technology Laboratory (NETL), U.S. Department of Energy. An excellent overview of the worldwide gasification technology.</ref>
 
The syngas may be directly burned as a fuel, converted into methyl alcohol or hydrogen, subjected to [[methanation]] to produce [[synthetic natural gas]] (SNG),<ref>M.R. Beychok (May 1975), "Process and environmental technology for producing SNG and liquid fuels", ''[[U.S. EPA]] report EPA-660/2-75-011''.</ref> or converted into synthetic liquid [[hydrocarbon]]s via the [[Fischer-Tropsch]] process.
 
The vessel in which the gasification process takes place is called a ''gasifier''. There are various types of gasifiers in current use,<ref name=DOE-Overview/><ref name=NETL>[http://www.netl.doe.gov/technologies/coalpower/gasification/gasifipedia/4-gasifiers/4-1_types.html Gasifiers in detail: Types of gasifiers] National Energy Technology Laboratory ((NETL), U.S. Department of Energy (DOE)</ref> including:
 
*'''''Counter-current fixed bed gasifier:''''' This gasifier is a vertical, cylindrical vessel containing a bed of carbon-containing material (e.g., coal or biomass) through which steam, oxygen and/or air flow upward. Although commonly  referred to as a fixed bed gasifier, the crushed coal or biomass is fed into the gasifier through a lock hopper mounted on top of the gasifier and the carbonaceous material slowly moves downward as it is converted into syngas, which is removed from the upper portion of the gasifier,  and ash or slag removed from the bottom of the gasifier.<ref name=Visagie>[http://upetd.up.ac.za/thesis/available/etd-07022009-133535/unrestricted/dissertation.pdf Generic gasifier modelling: Evaluating model by gasifier type] J.P. Visagie (October 2008), Master's dissertation, [[University of Pretoria]], [[South Africa]]</ref><ref>{{cite journal|author=M.R. Beychok|title=Coal gasification for clean energy|journal=Energy Pipelines and Systems|volume=|issue=| pages=|date=March 1974|id=|url=}}</ref><ref>M.R. Beychok (September 1974), "Coal gasification and the Phenosolvan process", ''American Chemical Society 168th National Meeting'', [[Atlantic City, New Jersey]]</ref>
 
{{Image|SiemensEntrainedGasifier.png|right|210px|Fig.1: A top-fired, oxygen-blown, dry feed, entrained flow gasifier}}
 
*'''''Co-current fixed bed gasifier:''''' This gasifier is also a vertical cylindrical vessel, which is quite similar to the counter-current gasifier type except that the steam, oxygen and/or air enter at the top of the bed, flow downward co-current with the slowly moving bed of carbonaceous material, and the product syngas is removed below the bed. <ref name=Visagie/><ref>M.J. Groeneveld and W.P.M. Van Swaaij, "The Design of Co-Current Moving-Bed Gasifiers Fueled by Biomass" published in this book: {{cite book|author=Jerry Latham Jones and Shirley B. Radding (Editors)| title=Thermal conversion of solid wastes and biomass: based on a symposium|edition=Volume 130 of ACS symposium series|publisher=American Chemical Society|date= 1980|id=ISBN 0-8412-0565-5}}</ref><ref name=Groeneveld>[http://doc.utwente.nl/68447/1/Groeneveld79gas.pdf Gasification and solid waste -- Potential and application of co-current moving bed gasifiers] M.J. Groeneveld and W.P.M. Van Swaaij, [[Twente University of Technology]], [[The Netherlands]].</ref>
 
*'''''Fluidized bed gasifier:''''' This gasifier is again a vertical, cylindrical vessel. It differs from the fixed bed reactors in that the feedstock biomass is very finely crushed before it enters the gasifier and the reaction bed of ground biomass is fluidized by the reagent gases (steam, oxygen and/or air) flowing upward through the bed. The fluidization of the reaction bed increases the height of the bed (as compared to the fixed bed gasifiers) and the finely crushed biomass results in much more biomass surface area being exposed to the reagent gases. The product syngas contains fine particles of crushed biomass which are removed by routing the syngas through a [[cyclone]] to recover the fines and recycle them back into the reaction bed.<ref name=Visagie/><ref name=Kreutz>[http://web.mit.edu/mitei/docs/reports/kreutz-fischer-tropsch.pdf Fischer-Tropsch Fuels from Coal and Biomass] Thomas G. Kreutz et al (October 2008), [[Princeton University]], presented at 25th Annual International Pittsburgh Coal Conference, [[Pittsburgh, Pennsylvania]], September 29 to October 2, 2008.</ref>
 
*'''''Entrained flow gasifier:''''' This gasifier, like the other three discussed above, is also a vertical, cylindrical vessel. The feedstock biomass is finely crushed and flows downward co-currently with pure oxygen. Air is seldom used as a reagent gas in an entrained gasifier. The gasification [[Chemical reaction|reactions]] take place in a dense cloud of fine biomass particles. The syngas exits from the bottom section of the gasifier and is routed through a cyclone (and perhaps a water scrubber) for removal of the fines. Entrained gasifiers operate at temperatures of about 1000 to 1800 °[[Celsius (unit)|C]] and at pressures of 30 to 70 [[Bar (unit)|bar]] which is a much higher pressure than is the case for the other types of gasifiers. The adjacent Fig. 1 depicts an entrained flow gasifier of the type discussed here.<ref name=DOE-Overview/><ref name=Visagie/><ref name=Kreutz/><ref>[http://www.ecn.nl/docs/library/report/2004/c04039.pdf Entrained Flow Gasification of Biomass] A. van der Drift et al (April 2004), [[Energy research Centre of the Netherlands]] (ECN), Report ECN-C--04-039.</ref>
 
====Gasification chemistry====
 
It is difficult to state exactly what chemical reactions occur during gasification. However, most researchers have reached agreement on the primary reactions and the syngas composition ranges shown just below:<ref name=DOE-Overview/><ref name=Visagie/>
 
{{Image|GasifierReax.png|center|476px|}}
 
=== Fischer-Tropsch synthesis of liquid hydrocarbons===
{{Image|BTL.png|right|225px|Fig.2: Biomass-To-Liquids (BTL) process}}
 
Fischer-Tropsch synthesis is a catalytic chemical process developed in the 1920s to convert a mixture of carbon monoxide and hydrogen (i.e., syngas), into hydrocarbon [[Molecule|molecular]] chains of varying lengths.
 
The process was invented by [[Franz Fischer]] and [[Hans Tropsch]] working in [[Germany]]'s [[Kaiser Wilhelm Institute]] (today the [[Max Planck Institute]]) in the 1920's. It was first commercialized in Germany in 1936 and it was used extensively by Germany during [[World War II]] to produce synthetic fuels. Later, facing isolation and embargoes during the [[apartheid]] era (1948 - 1990), [[South Africa]] turned to coal gasification and the Fischer-Tropsch process to supply significant quantities of its hydrocarbon fuel needs. Since that time, the process has been extensively improved and refined.<ref name=NETL-FT>[http://www.netl.doe.gov/technologies/coalpower/gasification/gasifipedia/5-support/5-11_ftsynthesis.html Fischer-Tropsch (FT) Synthesis]] From the website of the National Energy Technology Laboratory (NETL) in the U.S. Department of Energy.</ref><ref>{{cite journal|author=Hans Schulz|title=Short history and present trends of Fischer–Tropsch synthesis|journal=Applied Catalysis A: General|volume=186|issue=1 - 2| pages = pp. 3 - 12|date=October 4, 1999|id=|url=}}</ref>
 
The process is relatively simple: syngas is fed at high temperatures through [[Catalysis|catalysts]] (usually the transition metals [[cobalt]] or [[iron]]) which facilitate the hydrocarbon formation. When paired with syngas from the gasification of fossil fuels or biomass, the Fischer-Tropsch process is a method of converting any available carbon source into hydrocarbon liquids consisting of [[molecule]]s having from 5 to 20 carbon [[atoms]] in accordance with the following equation for the formation of [[alkane]]s (C<sub>n</sub>H<sub>2n+2</sub>), which are the primary hydrocarbons formed:<ref name=NETL-FT/><ref name=knowl>[http://knol.google.com/k/the-fischer-tropsch-ft-process# The Fischer-Tropsch (FT) Process] From the [[Knowl]] website</ref>
 
:<math>\mathrm{(2n+1)\,H_2} + \mathrm{n\,CO} \rightarrow \mathrm{C_nH_{2n+2}} + \mathrm{n\,H_2O}</math>
 
where n is an integer. For example, if n = 5, the equation represents the formation of [[pentane]] (C<sub>5</sub>H<sub>12</sub>) which is a liquid hydrocarbon that is a component of [[gasoline]] (petrol). As another example, if n = 12, the equation represents the formation of [[decagon]] (C<sub>12</sub>H<sub>26</sub>) which is a liquid hydrocarbon  component of diesel fuel.
 
Lesser amounts of [[alkene]]s (C<sub>n</sub>H<sub>2n</sub>) and [[alcohol]]s (C<sub>n</sub>H<sub>2n+1</sub>OH) are formed in accordance with these equations:<ref name=knowl/>
 
:<math>\mathrm{n\,CO} + \mathrm{2n\,H_2} \rightarrow \mathrm{C_nH_{2n}} + \mathrm{n\,H_2O}</math>
:<math>\mathrm{n\,CO} + \mathrm{2n\,H_2} \rightarrow \mathrm{C_nH_{2n+1}OH} + \mathrm{(n\!-\!1)\,H_2O}</math>
 
 
There are a good many different reactor designs for the Fischer-Tropsch process as well as different operating conditions. There are two general process temperature ranges:<ref name=knowl/><ref name=Davis>[http://accessscience.com/content/Fischer-Tropsch-synthesis/YB109990 Fischer-Tropsch Synthesis] Burtron H. Davis (2010) in AccessScience, McGraw-Hill Companies.</ref>
*Low temperature (200 to 260 °C): Designs using this temperature are referred to LTFT (a contraction of "low temperature Fischer-Tropsch") and generally use a cobalt catalyst.
*High temperature (300 to 350 °C): Designs using this temperature are referred to HTFT (a contraction of "high  temperature Fischer-Tropsch")and generally use an iron catalyst.
 
The LTFT designs produce predominantly hydrocarbons in the [[Boiling point|boiling range]] of diesel fuel and [[Wax|waxes]]. Fixed-bed reactors are considered to be the "conventional" technology for LTFT designs and slurry phase reactors are considered to be "advanced" technology.
 
The HTFT designs produce predominantly gaseous alkene hydrocarbons having 2 to 4 carbon atoms and liquid hydrocarbons in the boiling range of gasoline. Circulating fluidized bed reactors are considered to be the "conventional" technology for HTFT designs and fixed fluidized bed reactors are considered to be "advanced" technology.


==References==
==References==
{{reflist}}
{{reflist}}

Revision as of 10:20, 5 April 2011

This article is developing and not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article is under development and subject to a disclaimer.

Biomass, a source of renewable energy, is biological material such as wood, wood waste, municipal solid waste, straw, sugar cane, algae, and many other byproducts derived from agricultural and forestry production as well as other sources. Since biomass derives from plants generated by solar energy in the photosynthesis process, it can also be defined as the biological material on Earth that has stored solar energy in the chemical bonds of the organic material.

The fossil fuels (coal, petroleum and natural gas) are currently thought to have been formed from prehistoric, ancient biomass buried deeply underground over millions of years of geological time. Therefore, they are not considered to be renewable sources of energy

Production of fuels and other products from biomass

Biomass fuel for electric power production

The direct combustion of biomass for producing heat and electric power provides a ready disposal mechanism for municipal, agricultural, and industrial organic wastes. In 2009, about 11,350 megawatts (MW) of electric power, amounting to 1.1% of the summertime electrical supply in the United States was generated by burning biomass that included: wood, wood waste, municipal solid waste (MSW), landfill gas, and agricultural byproducts and waste.[1]

The New Hope Power Partnership in Florida is the largest biomass power plant in North America. It generates 140 MW of power using uses sugar cane fiber (bagasse) and recycled wood as fuel.[2] It has been in operation for more than 10 years.

Production of liquid transportation fuels

There are several processes available for converting the chemical energy contained in biomass into liquid automotive transport fuels such as biodiesel and ethanol.[3]

Ethanol fuel:

Ethanol fuel is ethyl alcohol (C2H5OH) and it is most often used as an automotive motor fuel, mainly as an additive for gasoline. Ethanol can be produced by fermentation of sugar cane, bagasse, sugar beets, barley, potatoes, corn and many other grains as well as many agricultural byproducts and wastes.

The worldwide production of ethanol for automotive fuel in 2007 was 52,000,000,000 litres (13,700,000,000 gallons). From 2007 to 2008, the share of ethanol in global gasoline use increased from 3.7% to 5.4%.[4] In 2009, worldwide ethanol fuel production reached 73,900,000,000 litres (19,500,000,000 gallons) and was expected to reach 85,900,000,000 litres (22,700,000,000 gallons) in 2010.[5]

Ethanol fuel is widely used in Brazil and in the United States, and together both countries were responsible for about 86 percent of the world's ethanol fuel production in 2009.[6]

Biodiesel fuel:

Biodiesel refers to a diesel fuel produced by chemically reacting lipids such as vegetable oils or animal fats with an alcohol such as methyl alcohol (CH3OH). The resulting biodiesel consists of esters of long-chain fatty acids. The process is known as "transesterification" and it may be carried out by several methods: the common batch process, supercritical processes and ultrasonic methods.

In 2009, the worldwide production of biodiesel was 17,900,000,000 litres (4,730,000,000 gallons). The three countries with the largest annual biodiesel production were Germany (16%), France (12%) and the United States (11%).[7]

Worldwide Gasification Plants
as of 2010[8]
Feedstock Plants Gasifiers
Coal 53 201
Petroleum 59 143
Natural gas 23  59
Biomass  9   9
Totals 144 412

Biomass gasification to produce syngas

Gasification is a process that reacts carbon-containing materials (such as coal or biomass) at high temperatures with reagent gases (namely, steam, pure oxygen and/or air) to produce a mixture of carbon monoxide (CO) and hydrogen (H2) commonly called syngas (a contraction of synthesis gas). It has been in use since the early 1800s when coal and peat were gasified to produce what was then called town gas for lighting and cooking ... later to be replace by electricity and natural gas. As of 2010, 412 modern industrial-scale gasifiers were in operation in 29 countries worldwide (see adjacent table).[9]

The syngas may be directly burned as a fuel, converted into methyl alcohol or hydrogen, subjected to methanation to produce synthetic natural gas (SNG),[10] or converted into synthetic liquid hydrocarbons via the Fischer-Tropsch process.

The vessel in which the gasification process takes place is called a gasifier. There are various types of gasifiers in current use,[9][11] including:

  • Counter-current fixed bed gasifier: This gasifier is a vertical, cylindrical vessel containing a bed of carbon-containing material (e.g., coal or biomass) through which steam, oxygen and/or air flow upward. Although commonly referred to as a fixed bed gasifier, the crushed coal or biomass is fed into the gasifier through a lock hopper mounted on top of the gasifier and the carbonaceous material slowly moves downward as it is converted into syngas, which is removed from the upper portion of the gasifier, and ash or slag removed from the bottom of the gasifier.[12][13][14]
(PD) Drawing: U.S. Dept. of Energy
Fig.1: A top-fired, oxygen-blown, dry feed, entrained flow gasifier
  • Co-current fixed bed gasifier: This gasifier is also a vertical cylindrical vessel, which is quite similar to the counter-current gasifier type except that the steam, oxygen and/or air enter at the top of the bed, flow downward co-current with the slowly moving bed of carbonaceous material, and the product syngas is removed below the bed. [12][15][16]
  • Fluidized bed gasifier: This gasifier is again a vertical, cylindrical vessel. It differs from the fixed bed reactors in that the feedstock biomass is very finely crushed before it enters the gasifier and the reaction bed of ground biomass is fluidized by the reagent gases (steam, oxygen and/or air) flowing upward through the bed. The fluidization of the reaction bed increases the height of the bed (as compared to the fixed bed gasifiers) and the finely crushed biomass results in much more biomass surface area being exposed to the reagent gases. The product syngas contains fine particles of crushed biomass which are removed by routing the syngas through a cyclone to recover the fines and recycle them back into the reaction bed.[12][17]
  • Entrained flow gasifier: This gasifier, like the other three discussed above, is also a vertical, cylindrical vessel. The feedstock biomass is finely crushed and flows downward co-currently with pure oxygen. Air is seldom used as a reagent gas in an entrained gasifier. The gasification reactions take place in a dense cloud of fine biomass particles. The syngas exits from the bottom section of the gasifier and is routed through a cyclone (and perhaps a water scrubber) for removal of the fines. Entrained gasifiers operate at temperatures of about 1000 to 1800 °C and at pressures of 30 to 70 bar which is a much higher pressure than is the case for the other types of gasifiers. The adjacent Fig. 1 depicts an entrained flow gasifier of the type discussed here.[9][12][17][18]

Gasification chemistry

It is difficult to state exactly what chemical reactions occur during gasification. However, most researchers have reached agreement on the primary reactions and the syngas composition ranges shown just below:[9][12]

(CC) Diagram: Milton Beychok

Fischer-Tropsch synthesis of liquid hydrocarbons

(CC) Diagram: Milton Beychok
Fig.2: Biomass-To-Liquids (BTL) process

Fischer-Tropsch synthesis is a catalytic chemical process developed in the 1920s to convert a mixture of carbon monoxide and hydrogen (i.e., syngas), into hydrocarbon molecular chains of varying lengths.

The process was invented by Franz Fischer and Hans Tropsch working in Germany's Kaiser Wilhelm Institute (today the Max Planck Institute) in the 1920's. It was first commercialized in Germany in 1936 and it was used extensively by Germany during World War II to produce synthetic fuels. Later, facing isolation and embargoes during the apartheid era (1948 - 1990), South Africa turned to coal gasification and the Fischer-Tropsch process to supply significant quantities of its hydrocarbon fuel needs. Since that time, the process has been extensively improved and refined.[19][20]

The process is relatively simple: syngas is fed at high temperatures through catalysts (usually the transition metals cobalt or iron) which facilitate the hydrocarbon formation. When paired with syngas from the gasification of fossil fuels or biomass, the Fischer-Tropsch process is a method of converting any available carbon source into hydrocarbon liquids consisting of molecules having from 5 to 20 carbon atoms in accordance with the following equation for the formation of alkanes (CnH2n+2), which are the primary hydrocarbons formed:[19][21]

where n is an integer. For example, if n = 5, the equation represents the formation of pentane (C5H12) which is a liquid hydrocarbon that is a component of gasoline (petrol). As another example, if n = 12, the equation represents the formation of decagon (C12H26) which is a liquid hydrocarbon component of diesel fuel.

Lesser amounts of alkenes (CnH2n) and alcohols (CnH2n+1OH) are formed in accordance with these equations:[21]


There are a good many different reactor designs for the Fischer-Tropsch process as well as different operating conditions. There are two general process temperature ranges:[21][22]

  • Low temperature (200 to 260 °C): Designs using this temperature are referred to LTFT (a contraction of "low temperature Fischer-Tropsch") and generally use a cobalt catalyst.
  • High temperature (300 to 350 °C): Designs using this temperature are referred to HTFT (a contraction of "high temperature Fischer-Tropsch")and generally use an iron catalyst.

The LTFT designs produce predominantly hydrocarbons in the boiling range of diesel fuel and waxes. Fixed-bed reactors are considered to be the "conventional" technology for LTFT designs and slurry phase reactors are considered to be "advanced" technology.

The HTFT designs produce predominantly gaseous alkene hydrocarbons having 2 to 4 carbon atoms and liquid hydrocarbons in the boiling range of gasoline. Circulating fluidized bed reactors are considered to be the "conventional" technology for HTFT designs and fixed fluidized bed reactors are considered to be "advanced" technology.

References

  1. U.S. Electric Net Summer Capacity U.S. Energy Information Administration (EIA), part of the U.S. Department of Energy (DOE)
  2. Agriculture & Renewable Energy: The Partnership for a New Frontier Florida Power Service Commission (FPSC) Workshop, July 26, 2007.
  3. ABC's of Biofuels From the website of the Office of Energy Efficiency and Renewable Energy (EERE) in the U.S. Department of Energy (DOE).
  4. Assessing Biofuels (2009) From the website of the United Nations Environment Programme (UNEP)
  5. Global ethanol production to reach 85.9 billion litres (22.7 billion gallons) in 2010 March 22, 2010. From the website of the Renewable Fuels Association (RFA).
  6. Ethanol Industry Statistics 2009 World Fuel Ethanol Production from the website of the Renewable Fuels Association.
  7. Production of biofuels in the world in 2009 August 30, 2010. From the website of the Biofuels Platform published in Switzerland.
  8. Worldwide Gasification Database National Energy Technology Laboratory (NETL), U.S. Department of Energy (DOE)
  9. 9.0 9.1 9.2 9.3 DOE Gasification Program Overview Jenny B. Tennant (December 2010, National Energy Technology Laboratory (NETL), U.S. Department of Energy. An excellent overview of the worldwide gasification technology.
  10. M.R. Beychok (May 1975), "Process and environmental technology for producing SNG and liquid fuels", U.S. EPA report EPA-660/2-75-011.
  11. Gasifiers in detail: Types of gasifiers National Energy Technology Laboratory ((NETL), U.S. Department of Energy (DOE)
  12. 12.0 12.1 12.2 12.3 12.4 Generic gasifier modelling: Evaluating model by gasifier type J.P. Visagie (October 2008), Master's dissertation, University of Pretoria, South Africa
  13. M.R. Beychok (March 1974). "Coal gasification for clean energy". Energy Pipelines and Systems.
  14. M.R. Beychok (September 1974), "Coal gasification and the Phenosolvan process", American Chemical Society 168th National Meeting, Atlantic City, New Jersey
  15. M.J. Groeneveld and W.P.M. Van Swaaij, "The Design of Co-Current Moving-Bed Gasifiers Fueled by Biomass" published in this book: Jerry Latham Jones and Shirley B. Radding (Editors) (1980). Thermal conversion of solid wastes and biomass: based on a symposium, Volume 130 of ACS symposium series. American Chemical Society. ISBN 0-8412-0565-5. 
  16. Gasification and solid waste -- Potential and application of co-current moving bed gasifiers M.J. Groeneveld and W.P.M. Van Swaaij, Twente University of Technology, The Netherlands.
  17. 17.0 17.1 Fischer-Tropsch Fuels from Coal and Biomass Thomas G. Kreutz et al (October 2008), Princeton University, presented at 25th Annual International Pittsburgh Coal Conference, Pittsburgh, Pennsylvania, September 29 to October 2, 2008.
  18. Entrained Flow Gasification of Biomass A. van der Drift et al (April 2004), Energy research Centre of the Netherlands (ECN), Report ECN-C--04-039.
  19. 19.0 19.1 Fischer-Tropsch (FT) Synthesis] From the website of the National Energy Technology Laboratory (NETL) in the U.S. Department of Energy.
  20. Hans Schulz (October 4, 1999). "Short history and present trends of Fischer–Tropsch synthesis". Applied Catalysis A: General 186 (1 - 2): pp. 3 - 12.
  21. 21.0 21.1 21.2 The Fischer-Tropsch (FT) Process From the Knowl website
  22. Fischer-Tropsch Synthesis Burtron H. Davis (2010) in AccessScience, McGraw-Hill Companies.