15
7/26/2019 Digman Brett Food Processing Wastes http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 1/15 See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/229441294 Review: Alternative energy from food processing wastes  ARTICLE in ENVIRONMENTAL PROGRESS · DECEMBER 2008 Impact Factor: 1.31 · DOI: 10.1002/ep.10312 CITATIONS 28 READS 212 2 AUTHORS, INCLUDING: Dong-Shik Kim University of Toledo 54 PUBLICATIONS 587 CITATIONS SEE PROFILE Available from: Dong-Shik Kim Retrieved on: 04 April 2016

Digman Brett Food Processing Wastes

Embed Size (px)

Citation preview

Page 1: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 1/15

See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/229441294

Review: Alternative energy from food processingwastes

 ARTICLE  in  ENVIRONMENTAL PROGRESS · DECEMBER 2008

Impact Factor: 1.31 · DOI: 10.1002/ep.10312

CITATIONS

28

READS

212

2 AUTHORS, INCLUDING:

Dong-Shik Kim

University of Toledo

54 PUBLICATIONS  587 CITATIONS 

SEE PROFILE

Available from: Dong-Shik Kim

Retrieved on: 04 April 2016

Page 2: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 2/15

Review: Alternative Energy from

Food Processing WastesBrett Digman and Dong-Shik KimDepartment of Chemical and Environmental Engineering, University of Toledo, Toledo, OH 43606; [email protected] (forcorrespondence)

Published online 14 October 2008 in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/ep.10312

 Food processes generate large amounts of various waste types. The environmental impact of these wastes is generally high if disposed untreated due to their high BOD and COD contents. By utilizing the high

 potential energy available in food processing wastes, sustainable energy can be obtained while reducing the waste disposal costs and impact on the environ-ment. According to the unique compositions of vari-ous food processing wastes, proper conversion meth-ods must be selected to optimize the economic and environmental benefits. In this review, food process-ing wastes are categorized in six groups, and various energy conversion technologies are addressed in asso-

ciation with them. Future direction for better utiliz-ing food process wastes in alternative energy genera-tion is also suggested.     2008 American Institute of Chemical Engineers Environ Prog, 27: 524–537, 2008

 Keywords: food processes, food process wastes, al-ternative energy, incineration, gasifiction, pyrolysis,anaerobic digestion, fermenttion

INTRODUCTION

Food processing wastes play a very unique posi-tion in the production of renewable energy and envi-ronmental sustainability. Because of the high contentof organic components, proteins, oils and fats, and

polysaccharides, the potential energy available infood processing wastes is high and various energy generation techniques may be used. Compared toraw biomass, e.g., corn stalk, wood chips, switchgrass, etc., food processing wastes can be more read-ily converted to various forms of energy with lesspretreatment steps in conversion processes. Also,food processing wastes may have an adverse impacton the environment when they are discarded withoutproper treatments. Therefore, utilizing food process-ing wastes for generating energy not only produces

revenue gains by recovering the energy and reducingthe cost for waste treatment, but also helps enhanceenvironmental sustainability.

There are many types of food processing wastesand it is difficult to categorize them into a fewgroups. Each category would have a wide variety of chemical components and physical characteristicsmaking it hard to generalize how to process the

 wastes to generate alternative energy. In this review,as rough as it may be, food processing wastes arecategorized according to the final processed products:dairy products (such as milk, cheese, and butter), seafoods, meat and poultry products, edible oils, brew-

ery products, and confectionary products (such aspotato chips and fries). Table 1 shows the compari-son of chemical compositions between the food proc-essing wastes.

 As the food supply has increased over the years,the amount of food processing waste has alsoincreased. For example, according to the 2007 Dairy Market News [3], milk production increased 2.2% in2007 from 2006, reaching 185.7 billion pounds in theUnited States. As 80–90% of milk is collected as whey separated from all the dairy products, it means thatmore than 148 billion pounds of whey were pro-duced in the United States in 2007. Although 0.7%

 whey protein is recovered for human consumption,and some of the whey wastes are used for fertilizerand animal feed, the rest of it is discarded to waste-

 water treatment facilities or landfills [4]. Recently,dairy wastes were used for producing value addedchemicals, such as propionic acid [5] and lactic acid[6, 7]. As oil prices increase, and the supply remainsunstable, it may be advantageous to utilize the highenergy available in food processing wastes, such ascheese whey waste, by converting it to alternativeenergy. Furthermore, there have been many new

 waste treatment technologies developed recently, which may well be applied directly to food processing  2008 American Institute of Chemical Engineers

524 December 2008 Environmental Progress (Vol.27, No.4) DOI 10.1002/ep

Page 3: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 3/15

Table 1.  Comparison of chemical compositions of food processing wastewater [1].

Food processing WastesCharacteristics and selected

elements of the waste

Dairy processing Cheese/whey plant wastewater BOD5: 377–2214 mg/LCOD: 189–6219 mg/LFOG (mg/L)NH4-N: 0.7–28.5 mg/L

Cheese processing waste BOD5: (mg/L)COD: 63,300 mg/LFOG: 2.6 g/L

 Whey wastewater BOD5: 35,000 mg/LCOD: (mg/L)FOG: 0.8 g/LNH4-N: (mg/L)

Raw cheese whey waste BOD5:(mg/L)COD: 68,814 mg/LFOG:(g/L)NH4-N: 64.3 mg/L

Sea food processing (cannedand preserved)

Farm-raised catfish processing wastewater

BOD5: 340 mg/LCOD: 700 mg/LFOG: 200 mg/L

Breaded shrimp processing wastewater

BOD5: 720 mg/LCOD: 1200 mg/LFOG:(mg/L)

Tuna processing BOD5: 700 mg/LCOD: 1600 mg/LFOG: 250 mg/L

Herring BOD5: 1200–1600 mg/LCOD: 3,000–10,000mg/LFOG: 600–5000 mg/L

Scallops BOD5: 300–1100mg/LCOD: 27–4000 mg/LFOG: 15–25 mg/L

Meat processing Cattle BOD5: 448–7237 mg/LFOG: 250 mg/L

Hog BOD5: 1000–2200 mg/LCOD: 3000 mg/L

Mixed BOD5: 400–11,000 mg/LCOD: 583–18,768 mg/L

Edible oil processing Palm oil wastewater BOD5: 25,000 mg/LCOD: 50,000 mg/LOG: 6000 mg/LNH4: 35 mg/L

Olive oil BOD5: 4000–100,000 mg/LCOD: 15,000–225,000 mg/L

Confectionary food processing Potato peeling (steam) BOD5: 62 60 mg/LCOD: 10,000 mg/L

French fry plant (plantcomposite)

BOD5: 1150 mg/LCOD: 1790 mg/L

Soft drink processing wastewater BOD5: 600–4500 mg/LCOD: 1200–8000 mg/L

Bakery process wastewater(Bread plant)

BOD5: 155–620 mg/LCOD: 1500 mg/LG: 60–80 mg/L

Brewery processing [2] Wastewater from spent grain BOD5: 1000 mg/LCOD: 33,000 mg/LTSS: 4800 mg/L

BOD5: five day biological oxygen demand, COD: chemical oxygen demand, FOG: fats, oil, and grease, OG: oiland grease, G: grease, TSS: total suspended solid, NH4: ammonia, NH4-N: ammonia/nitrogen.

Environmental Progress (Vol.27, No.4) DOI 10.1002/ep December 2008 525

Page 4: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 4/15

 wastes. Some old technologies have even been modi-fied and revived, and become available for effectiveprocessing of the wastes.

In this review, we focus on the recent progress inalternative energy generation techniques for foodprocessing wastes, and the various energy forms thatcan possibly be extracted from them. Based on thisreview, we suggest the future direction for more

effective ways of utilizing food processing wastes foralternative energy generation.

THERMAL ENERGY PROCESSES

Incineration Thermal processing is probably the most popular

 way of generating heat from wastes in general. Incin-eration of municipal wastes has been used in many parts of the world [8–10]. For hazardous industrialand medical wastes, incineration is currently the mostcommon process used [8, 9]. The heat generated by burning the wastes can be used to operate steam tur-bines for energy production or for heat exchangers

used to heat up process streams in industry [11, 12].Utilization of thermal energy from waste incineratorsis reported for many cases [13–15].

There are four incinerator types commonly used inindustry: fixed-hearth, rotary-kiln, liquid injection,and fluidized bed [16, 17]. Fixed-hearth incineratorsare used extensively for medical and municipal wasteincineration. The rotary-kiln incinerators are used by municipalities and by large industrial plants [15]. Co-combustion of wastes, in particular in coal-firedpower plants, is the single largest growing conversionroute for biomass wastes in many EU countries (e.g.,in Spain, Germany, and the Netherlands) [18–20].Food processing wastes can be readily used in the

co-combustion process only after the moisture con-tent is reduced enough.

However, very few reports on incineration of foodprocessing wastes are found in the literature [21, 22].Unlike general municipal wastes and raw biomasssuch as wood and grass, most food processing wastesare not proper for burning because of the high mois-ture content and non-combustible components [23– 25]. An increasing concern of adverse environmentalimpact from emissions is another reason for the lowuse of incineration. Many problems have beenreported recently concerning problems with hazard-ous pollutants such as TSP and dioxins [26–28].

Pyrolysis and Gasification Considering the environmental concerns and low

energy utilization efficiency of incineration (typically about 15% [29]), pyrolysis, gasification, or both com-bined appear to be a better option for thermal proc-essing of food processing wastes. In pyrolysis andgasification processes, high temperatures are used tobreak down the wastes containing mostly hydrocar-bons with no (pyrolysis) or less oxygen than inciner-ation (gasification) [30–32]. The pyrolysis processdegrades the wastes to produce char, or ash, pyroly-sis oil, and synthetic gas (i.e., syngas) at 500–10008C

 without oxygen. The gasification process decomposesthe hydrocarbons left into a syngas using a controlledamount of oxygen at above 10008C.

 As both processes rely on carbon-based wastes,they are regarded as appropriate for food processing

 wastes and food scraps. Both produce a syngas madeup mainly of carbon monoxide and hydrogen (85%),

 with small amounts of carbon dioxide and methane.

Fast pyrolysis produces 75% bio-oil, of which theheating value is around 17 MJ/kg [33]. The syngascan be used to generate steam or electricity througha fuel cell. Moreover, these processes can mitigate airemissions by using no or low oxygen. It is also easierto control emissions because they are scrubbed toremove contaminants [32].

Despite many advantages over traditional incinera-tion [34–36], pyrolysis and gasification of food proc-essing wastes still seems to have a long way to go tosatisfy the energy profitability. Currently, there aremore than 100 pyrolysis facilities operating or or-dered around the world capable of processing over 4million tons of waste per year. Some plants—particu-

larly in Europe and Japan—have been operatingcommercially for more than 5 yr. However, many of the proprietary systems currently being promotedhave only operated so far as small scale pilots. Therehave also been some noteworthy problems in partic-ular projects over the last 5 yr, which raise concernsabout operational reliability. Compared with the heat-ing values of gasoline, 43.5 MJ/kg (Low Heating

 Value) and ethanol, 26.7 MJ/kg [37], the heating valueof pyrolysis-oil and the amount of syngas from pyrol-

 ysis is considered too low to be economically feasi-ble, as it cannot make up for the energy spent in theprocess, and as a result, the total cost of pyrolysis-oilis 10–100% more than fossil fuel.

 A pyrolysis process, Siemens Westinghouse’s‘‘Schwel-Brenn/Thermal waste recycling’’ process [38]operates at 4508C for about an h, which is followedby high temperature combustion (13008C) and steamgeneration at 4008C, 40 bar. The plant in Furth, Ger-many, processed 100–150 kilotons/yr, but shut downon August 1998 after an accident with pyrolysis gas[39]. A small pyrolysis process, R21 process, devel-oped by Mitsui Engineering and Shipbuilding, canprocess 150 tons of municipal solid waste per yearand demonstrates good dioxin removal [40].

 Although mass-burn incineration is a proven tech-nology, the effectiveness of full-size commercial py-rolysis and gasification has not yet been fully demon-

strated. Although several gasification systems havebeen designed and constructed in the past two deca-des, most have been demonstration and laboratory-scale systems. Large scale demonstration plants usingcoal and wood chips in the United States experiencedtechnological problems and are no longer operatingbecause of operating and financial problems [41].There are currently no commercial-scale solid wastegasification systems operating in the United States,except for a few proof-of-concept facilities. Some gas-ification/pyrolysis plants were built and operated inEurope in the early 1980s. The DOE Clean Coal Dem-onstration Project helped to construct three integrated

526 December 2008 Environmental Progress (Vol.27, No.4) DOI 10.1002/ep

Page 5: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 5/15

gasification process with combined cycle (IGCC) plantsin the 1990s: Wabash River Power Station in West TerreHaute, Indiana, Polk Power Station in Tampa, Florida,and Pinon Pine in Reno, Nevada. In the Reno demon-stration project, researchers found that IGCC technol-ogy at the time would not work more than 300 feet(100 m) above sea level [42]. The plant failed.

The first generation of IGCC plants polluted air

less than contemporary coal-based technology, butthey polluted water: For example, the Wabash RiverPlant ‘‘routinely’’ violated its water permit, because itemitted arsenic, selenium, and cyanide. The WabashRiver Generating Station, however, is now wholly owned and operated by the Wabash River Power

 Association, and currently operates as one of thecleanest solid fuel power plants in the world.

Currently, gasification seems to be the closest tofull-size commercialization among the other alterna-tive energy conversion options. IGCC utilizes the syn-gas directly for steam turbines. With the optimizedprocess design of integrating a gasification unit withthe electrical power generating plant’s combined

cycle, IGCC provides competitive operational costsfor generating electricity with efficiencies up to 59%.In the case of combined heat and power generation,the efficiency can increase to 85%. There are cur-rently only two IGCC plants generating power in theUnited States. However, several new IGCC plants areexpected to come online in the United States in the2012–2020 time frame.

The main problem for IGCC is its extremely highcapital cost, upwards of $3,593/kW [43]. Official USgovernment figures give more optimistic estimates[44] of $1,491/kW installed capacity (2005 dollars)

 versus $1290 for a conventional clean coal facility.This is about 20% greater cost than a conventional

pulverized coal plant. The U.S. Department of Energy and many states offer subsidies for clean coal tech-nology projects that could help to bridge the costgap. However, the per megawatt-hour cost of anIGCC plant versus a pulverized coal plant comingonline in 2010 would be $56 versus $52. IGCCbecomes even more attractive when you include thecosts of carbon capture and sequestration, IGCCbecomes $79 per megawatt h versus $95 per mega-

 watt h for pulverized coal [45]. When the environmental concern on toxic pollu-

tants and environmental hormones is great, pyrolysisand gasification can be a good choice for hazardous

 wastes disposal. In addition, with the advent of 

$1001/barrel crude oil and $81/MM Btu natural gas,the economics of gasification once again make sense. A modest investment in capital equipment can be off-set by a 1–2 yr savings—especially when making useof fuels that simply cannot be directly combusted in aclean manner. As demonstrated in De Filippis  et al . [46],the energy content of syngas produced from wastefeedstock (except in the case of MSW from low-incomecountries) shows potential for generating electric powerfrom gasification. It is possible to achieve the actualenergy gain depending on the type of feedstock.

There seems to be no gasification/pyrolysis proc-esses that have been solely developed for food proc-

essing wastes. However, we can gain insight from thereports on these processes designed for other wastes,not to mention for biomass. With profits from theenergy gain and less environmental burdens in theequation, the processes may well be more economi-cally attractive than the existing incineration or sludgeprocesses for food processing wastes. As the energy efficiency of both processes are getting better [47],

the energy profitability may increase, especially whenthe syngas is used with a fuel cell to produce electric-ity. The use of pyrolysis and gasification may resultin a net energy gain, especially when the cost for

 waste disposal or treatment is high. Therefore, it isnecessary to carefully examine the chemical composi-tions of the waste, including moisture content inorder to optimize the benefit from the process. Forexample, hydrogen-rich syngas was successfully pro-duced in steam gasification of food wastes [48]. Anup-to-date and in-depth discussion as well as casestudies on gasification are well presented in Faaij [49].

CHEMICAL ENERGY PROCESSES

Methanol Partly due to the oil crises, biomass-derived syngas

has become an important part of alternative energy since the 1980s, and pressurized gasification formethanol production from biomass was tested anddeveloped in France and Sweden [49]. After a fewunsuccessful operations in industries in Finland andformer East Germany [50], renewed attention in pro-ducing methanol and hydrogen as transport fuelsusing gasification technology has arisen, in particularthe Fischer-Tropsch process has been recently revived. Despite its techno-economic potential, thereare technological challenges such as more effective

gas cleaning to protect the downstream catalyticprocess. Once clean syngas is available, the knownprocess technology can be used to produce metha-nol, Fischer-Tropsch diesel oil, and hydrogen. How-ever, strict gas cleaning is the main challenge, andscale-up and integration of processes have not beensufficiently investigated. Be that as it may, liquid meth-anol production and the well-established Fischer-Tropsch process combined with electricity generationhave been demonstrated efficient and economically profitable [51–53]. Therefore, these processes should beconsidered as a possible option for effective energy production from food process wastes.

Biodiesel Biodiesel production using waste oil and grease

have recently become more attractive. For the foodprocessing wastes that have high contents of oil andgrease, the production of biodiesel from them is anattractive option. The food processes that generatehigh oil and grease wastes are vegetable refinery, ani-mal rendering, fish and meat processes, and all theprocesses that include frying steps [54].

Chemically, biodiesel is known as monoalkylesters of fatty acids. The production of biodiesel by transesterification process to form fatty acid alkyl

Environmental Progress (Vol.27, No.4) DOI 10.1002/ep December 2008 527

Page 6: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 6/15

esters using acid and base catalysts has been industri-ally accepted for its high conversion and reactionrates [55]. Downstream processing costs and environ-mental problems associated with biodiesel productionand byproducts recovery have led to the search foralternative production methods and alternative sub-

strates [56, 57]. One of the highly regarded processesis the enzymatic method. Enzymatic reactions involv-ing lipases can be an excellent alternative to producebiodiesel through a process commonly referred to asalcoholysis, a form of transesterification reaction, orthrough an interesterification (ester interchange) reac-tion [58, 59].

 Although the high enzyme price is a major barrierfor commercialization of enzymatic biodiesel production[60], enzymatic processing is a promising option for theoil and fat waste producing industries as higher effi-ciency, low cost enzymes are being developed throughprotein engineering and the use of recombinant DNA technology to produce large quantities of enzymes at

cheaper prices [61]. The use of immobilized enzymesand immobilized cells may lower the overall cost, whilepresenting less downstream processing problemsto biodiesel production. In addition, the enzymaticapproach is environmentally friendly (considered a‘‘green reaction’’), and needs to be explored for indus-trial production of biodiesel.

BIOLOGICAL ENERGY PROCESSES

Methane Anaerobic digestion has been used for decades to

produce methane from organic wastes. As shown in

Table 1, food processing wastes consist mostly of or-ganic components making anaerobic digestion agood choice for alternative energy generation. Thereare many anaerobic digesters being used throughoutthe world for livestock wastes, such as feces fromcows, pigs, and chickens [62–64], and food process-

ing wastes [65, 66]. To achieve effective energy recov-ery, various processes have been developed: up-flowanaerobic sludge blanket (UASB) [67, 68], anaerobicfluidized bed reactor (AFBR) [69, 70], anaerobicattached film expanded bed reactor (AAFEB) [71, 72],all designed to improve cell retention and the two-phase digestion process [73] optimizing acidogenesisand methanogenesis.

 Anaerobic digesters are widely used for methaneproduction from food processing wastes [66, 74–76].For example, wastewaters from food processing fac-tories, which produce beer, sugar, fruit jams, andpotatoes, are processed for methane fermentation [74,77, 78]. As is well known, anaerobic digestion pro-

ceeds through three different microbial mechanisms(Figure 1 [79]): 1. acidogenesis, 2. acetogenesis, and3. methanogenesis [80, 81]. In acidogenesis, acido-genic bacteria produce extracellular enzymes for hy-drolysis of all organic solids and dissolve colloids.Carbohydrates are hydrolyzed to mono- and disac-charides, proteins to amino acids, and lipids to fatty acids. These compounds are transformed to acetateand longer chain fatty acids as well as CO2   and H2.In acetogenesis, low molecular weight fatty acidssuch as butyrate and propionate are transformed toacetate, CO2, and H2  by acetogenic bacteria. The pro-duced hydrogen should be oxidized by other anaero-

Figure 1.  Anaerobic metabolism.

528 December 2008 Environmental Progress (Vol.27, No.4) DOI 10.1002/ep

Page 7: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 7/15

bic bacteria; otherwise the propionate concentration would continually increase. Then, hydrogen and ace-tate are utilized by methanogenic bacteria producingmethane and CO2.

There are several major issues to be addressed formore efficient methane production from food proc-essing wastes: protein content, the presence of salt,solid materials, dry organic wastes containing less

than 80% moisture, and lipids characterized as eitherfats or oils and grease. Protein inhibits methane pro-duction after being converted to ammonia [82] fromnitrogen-rich feedstock, such as fish processing resi-dues [83], dairy wastewater [84], or high-solid anaero-bic digester liquor [85, 86]. High levels of ammonia

 were noted to form, which could inhibit anaerobicdigestion operation [87, 88]. Ammonia toxicity hasbeen extensively discussed on both acetogenesis andmethanogenesis phases [89–92] or solely on theacidogenesis phase [93–97]. The volatile fatty acids(VFA) and pH significantly suppress hydrolysis of or-ganic substrates [98–100]. However, few works inves-tigate the inhibitory effects of ammonium at different

pHs on protein or lipid hydrolysis [84, 101].One way to resolve the ammonia problem wasproposed by Michaelsen   et al . [102] They suggestedpassing the biogas through an acid scrubber beforerecycling it into the digester. The return gas will serveto mix the digester content and allow the process tobe suitable for both single- and dual-stage digestion.In a study of the removal of protein in excess sludgefrom wastewater treatment plants, it was found thatnot only the quality of the biogas was improved butso was the rate of generation [103].

High salt concentration in many food processing wastes also inhibits anaerobic digestion because of the presence of cations [104–109]. The treatment of 

saline and hypersaline wastewater could represent asmuch as 5% of worldwide effluent treatment require-ments. It has already been reported that a sodiumconcentration exceeding 10 g/L strongly inhibitsmethanogenesis [109–111].

Despite obstacles created by high salinity, a certainnumber of processes have been used successfully forthe anaerobic treatment of saline wastewater. Someof them used a halophilic inoculum [112–115],

 whereas others required the adaptation of a non-hal-ophilic inoculum to increase salt concentrations [107,108, 116–120].

Lipid-rich wastes from meat and fish processingindustries, edible oil, and dairy industries pose a chal-

lenge to methanogenic processes. Despite a high the-oretical methane yield from lipids as compared withother organic compounds, methanogenic processes

 with lipid-rich wastes are less stable and not able toaccommodate lower substrate-loading rates [121, 122].This is reported to be partly because of the toxicity of long-chain fatty acids (LCFA) to anaerobicmicrobes [123], and partly because of its absorptiononto the biomass and flowing out of the reactor. Inaddition, because the methanogenic   b-oxidation of LCFA is carried out by syntrophic LCFA-degrading,hydrogen- (and/or formate-) producing fermentativebacteria and hydrogenotrophic methanogens, LCFA-

degrading anaerobes can gain only a small amount of energy through syntrophic reactions, and thus, theirgrowth is generally slow. The oxidation of LCFA isthermodynamically unfavorable in such environmentsunless the consumption of reducing equivalents(hydrogen and/or formate) is coupled with oxidation,because of the syntrophic metabolism and toxicity of LCFA isolation of LCFA-degrading bacteria has

been difficult and not many species/subspecies arereported [124]. Therefore, efficient degradation of these LCFA is essential for the successful treatment of lipid-rich wastes in methanogenic processes.

Recent approaches include the separation of lipidsand fatty acids from wastes by UASB reactors [121]and the use of anaerobic thermophilic strains [125].

 When designing or selecting a process for lipid-rich wastes, it seems reasonable to carefully examine thecost and efficiency between the production processesof biodiesel and methane.

Ethanol Ethanol has gained huge interest in both industry and research as a plausible renewable energy sourcein the future. Food processing wastes, as shown inTable 1, have a great potential for ethanol produc-tion. Wastes that have high contents of hydrocarbon,such as brewery wastes and potato chip process

 wastes, can be good sources of ethanol. Unlike thegeneral biomass wastes such as corn stalk, woodchip, switch grass, etc., food processing wastes haveless pretreatment problems, which is one of the majorchallenges to overcome in lowering the price of thefuel ethanol [126]. For food processing wastes, pre-treatment is not needed as much.

The greatest concern in ethanol production fromfood processing wastes (or biomass wastes in gen-eral) is probably the production cost. The final mar-ket price of fuel ethanol must be lower than that of gasoline. There are many ways to lower the produc-tion cost of ethanol. One of them is to use genetically modified microorganisms. Common wild-type bacte-ria such as yeast and   zymomonas   only convert su-crose and hexose sugars. Many pentose sugars suchas xylose, ribose, and arabinose, which are as abun-dant as hexose sugars in biomass, are not properly used. By utilizing all the available sugars, ethanolproduction yield can increase. A great number of studies have been performed to mutate the cells with

some of the mutant cells being used in industry. E. coli  KO11,  E. coli  SL40,   E .   coli  FBR3,   E. coli  LY01, Zymomonas   CP4 (pZB5), and   Saccharomyces   1400(pLNH32) are some of them to name a few.   E. coli KO11 was reported to be successfully used in abrewery company and in some research applications[127–129]. These mutant cells are not only capable of converting various sugars, but also have stronger re-sistance to ethanol and acidity [130–132]. Some havehigher temperature tolerance [131], which makes itpossible to control the fermentation kinetics and tooperate at a higher temperature for better simultane-ous enzymatic hydrolysis and fermentation.

Environmental Progress (Vol.27, No.4) DOI 10.1002/ep December 2008 529

Page 8: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 8/15

Hydrogen Hydrogen can be directly or indirectly produced

from biological processes of food processing wastes.Interest in biohydrogen has resurfaced over the lastdecade as hydrogen has taken as a future energy alternative and the fuel-cell capacity has recently accelerated. Although there are a great number of articles on biohydrogen from biomass in general,

there are only a few articles published on biohydro-gen production from food processing wastes as of 2007. One of them is about successful hydrogen pro-duction from brewery wastewater, which achieves62% hydrogen content [133]. Hydrogen fermentationof dairy wastes [134, 135] and olive or palm oil proc-essing wastes [136, 137] are also available.

There is a wide range of approaches to producehydrogen depending on the microbiologic metabo-lism. These include direct and indirect biophotolysis,photo-fermentation, and dark-fermentation [138]. A previous study showed that photosynthesis-based sys-tems do not produce H2   at rates that are sufficientenough to meet the goal of providing enough H2   to

power a 1 kW proton exchange membrane fuel cell(PEMFC) on a continuous basis [139]. However, itdoes not mean that these processes should be aban-doned. Photosynthetic bacteria such as  Rhodospirilla-ceae gelatinosus   can grow in the dark using CO asthe sole carbon source to generate ATP with the con-comitant release of H2  and CO2  [140, 141]. The oxida-tion of CO to CO2  with the release of H2  occurs via a water–gas shift reaction. This process provides very promising results [139].

Dark fermentation is regarded as having greatpotential in the development of practical biohydro-gen systems. As carbohydrates are the preferred sub-

strate for hydrogen-producing bacteria, food process-ing wastes with high contents of carbohydrates canbe a good feedstock for dark fermentation. One of the several major problems of dark fermentation isthe product gas composition. Although direct andindirect photolysis systems produce pure H2, darkfermentation produces a mixed biogas consisting of primarily H2   and carbon dioxide and lesser amountsof methane, CO, and H2S. The gas composition may be a technical challenge when using the biogas infuel cells. Another problem is the low hydrogen pro-duction yields, typically 10–20% stoichiometrically.

The advantages of biohydrogen from food proc-essing wastes are so great that it cannot be marginal-

ized in renewable energy research. Many technolo-gies are under investigation. As mentioned above, theuse of mixed cultures of photosynthetic and anaero-bic fermentation bacteria would be an option toenhance the yield [142]. Another plausible approachis to produce a mixture of hydrogen and methane ina two-state process [143]. The first step would pro-duce hydrogen and organic acids, which would beconverted to methane in a second fermentation stage.The hydrogen–methane mixture may be at an advant-age over pure methane as a fuel because it signifi-cantly reduces air pollutants in internal combustionengines. Effective process designs are reported to

evolve hydrogen more rapidly. For example, theimmobilization of bacteria on fibers was reported toprovide long-term stable hydrogen evolution at a rea-sonable rate [144].

 Although there is no commercial biohydrogenprocess in association with food processing wastes, itis exciting to see the recent technological progress inbiohydrogen production accompanying fuel cell tech-

nology. The economics of hydrogen fermentationseems to be favorable at even less than stoichiometric yields. Compared to methane fermentation of whicha cost range of approximately $3–$8 per MMBTU,hydrogen produced by the same type of fermentationequipment could be sold for as much as $15 perMMBTU-depending on location, scale, and other fac-tors [145]. The ultimate goal for hydrogen fermenta-tion research is to achieve the production yield of 60–80%, which can sustain economic feasibility.

OTHER PROCESSES

There are many other energy conversion processesthat can be used for food processing wastes. Thermal

plasma waste treatment systems use plasma arctorches that produce ionized gases with arc centerlinetemperatures as high as 20,000 F. The thermal energy is transferred to the material to be treated throughradiation, convection, and conduction. Thus, theplasma arc torch provides the energy necessary tomelt inorganic material and breakdown organic mate-rial so that it will react to form harmless byproducts[146]. Plasma waste treatment systems are being usedin many industries all over the world, primarily fortoxic wastes. The advantages of plasma technology are the complete destruction of the wastes into harm-less materials and syngas production. The generatedsyngas from the waste can be possibly converted into

electric energy, supplying the torches and the plantand also generate additional revenues for the projectfrom the sale of the net electric production to thelocal utilities [147].

Microbial fuel cells (MFC) directly produce electric-ity through the catalytic reaction of microorganismsgrowing on organic matters [148, 149]. Although theinterest in microbial fuel cells was relatively highin the 1960s, the study of microbial fuel cells wanedas the cost of other energy sources remained low andthe available microbial fuel cells lacked efficiency and long-term stability. However, in the past 4–5 yr,there has been a resurgence in microbial fuel cellresearch. Recent advances in system design, materials

for electrodes, and microbial species, have made itpossible for MFC to compete with conventionalpower sources [150]. Many food processing wastes

 with high contents of carbohydrates and sugar can bedirectly processed with MFC’s.

CONCLUSIONS

Food processing wastes have great potential forproducing alternative energy. High contents of carbo-hydrates, proteins, and lipids can be used for varioustypes of energy. However, careful analysis of themain components of the waste and economic analysis

530 December 2008 Environmental Progress (Vol.27, No.4) DOI 10.1002/ep

Page 9: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 9/15

of the possible conversion process must be per-formed to effectively use the food processing wastes.For example, the wastewaters from dairy processescan be used for either production of value addedchemicals such as lactic acid and propionic acid [5,151], or they can be also used to produce ethanol,methane, or hydrogen [84, 135]. Potato chip processand brewery wastes can be used for animal feed orfertilizer, and for ethanol or methane production [152,153].

 When designing the conversion process for food

processing wastes, all the possible problems andaccompanying extra costs must be considered too.For example, anaerobic systems are usually wellsuited to the treatment of the high organic substrate

 waste contents, because they can achieve a highdegree of BOD removal at a significantly lower costthan other processes as well as the advantage of methane production. However, as stated before, foroil- and fat-rich wastes, they need special equipmentand additional treatment processes with extra costs.

 Also, anaerobic treatment suffers from the disadvant-age of odor generation and large amounts of sus-pended matters in the influent require more sophisti-

cated reactor design. Therefore, to select a processthat brings in economic and environmental benefits,the process design must include economic analysesthat include capital costs, operating cost, and returnon investigation (ROI) of the final products.

Once the energy conversion method is deter-mined, it must be well analyzed between differentforms of energy to optimize the potential of the

 wastes. Wastes with high contents of protein and/orfatty acids may better opt hydrogen fermentation orgasification than methane or ethanol production.Process modeling and optimization must also be per-formed [154].

Energy conversion processes are suggested forfood processing wastes and research articles relatedto the process are listed in Table 2.

FUTURE DIRECTION

It appears that many investigations have been per-formed on the integration of different processes tomaximize the production yield and minimize thepotential problems: Fermentation process is com-bined with catalytic reforming [158], gasification with

fuel cell [155, 157], and anaerobic digestion with gasi-fication [159]. Integrated energy conversion systemsmust also be considered for conversion of food proc-essing wastes into energy.

Mixed cultures of different bacterial species formulti-energy production have been studied recently,for example, simultaneous production of biogas andhydrogen from solid food processing [160] and mixedculture anaerobic digestion for simultaneous produc-tion of methane and hydrogen [161].

Processes of mixed feedstock are also thought tobe useful approaches for food processing wastes and

 will be used more in the future. Dairy manure, bio-solids (sludge), and food wastes are co-digested to

produce methane or hydrogen [162], and mixed wastes of liquids and solids are used to producerenewable energy and fertilizers [163]. Co-firing of biomass and coal in a coal gasification or in a pyroly-sis/gasification system is thought to be a promisingapproach [156, 164].

Novel approaches such as solid-state fermentations(SSF) [165] may be a better option for solid foodprocessing wastes. Compared with submerged fer-mentation, SSF can provide high productivities,extended stability of products and low productioncosts [166]. Although there are challenges in scalingup with increasing progress and application of 

Table 2.  Selected conversion processes for food processing wastes.

Food processing  Waste

characteristics Energy conversion process

Dairy processing High lactose and salts Ethanol fermentation [129]Hydrogen by anaerobic digestion [134, 135]

High lipids Methane by anaerobic digestion [68]Sea food processing

(canned andpreserved)

High lipids Methane by anaerobic digestion [82, 107, 114, 122]

High protein Biodiesel process [54, 55]

Meat processing Syngas and oil by pyrolysis/gasification [48]Edible oil processing High oil Biodiesel [54, 59]

High carbohydrates(grain wastes)

Methane by anaerobic digestion [121, 122]Biohydrogen by anaerobic digestion [137, 143]Syngas by gasificaiton [46, 155]Hydrogen by pyrolysis/gasification [32]

Confectionary foodprocessing

High carbohydrates Syngas and oil by pyrolysis [30, 31]Syngas by pyrolysis/gasification [156]Methane by anaerobic digestion [68, 69, 70, 72]

Brewery processing Ethanol fermentation [126]Biohydrogen by anaerobic digestion [133]Hydrogen by anaerobic digestion and gasification [157]

Environmental Progress (Vol.27, No.4) DOI 10.1002/ep December 2008 531

Page 10: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 10/15

rational methods in engineering, SSF will achievehigher levels in standardization and reproducibility inenergy production from food processing wastes inthe future.

LITERATURE CITED

1. Wang, L.K., Hung, Y.-T., Lo, H.H., & Yapijakis,

C. (Eds.) (2006). Waste treatment in the foodprocessing industry, New York: CRC Press.2. Ochieng, A., Odiyo, J.O., & Mutsago, M. (2003).

Biological treatment of mixed industrial waste- waters in a fluidised bed reactor. Journal of Haz-ardous Materials, 96, 79–90.

3. United States Department of Agriculture, Dairy Market Statistics 2007 Annual Summary,   http://

 www.ams.usda.gov/dairy/mncs/weekly.html (accessed, September 2008).

4. Hamilton, R.B. (2006). Processing waste materialproduced from dairy industry for recovering fatuseful as biodiesel and protein useful as feedsupplement. (Fonterra Co-Operative Group Lim-

ited, N.Z.) PCT International Application, 21.5. Morales, J., Choi, J.-S., & Kim, D.-S. (2006). Opti-mization of propionic acid production by Propio-nibacterium acidipropionici through enzyme inhi-bition. Environmental Progress, 25, 228–234.

6. Vasala, A., Panula, J., & Neubauer, P. (2005). Effi-cient lactic acid production from high salt contain-ing dairy by-products by Lactobacillus salivariusssp. Salicinius with pre-treatment by proteolyticmicroorganisms. Journal of Biochemistry, 117,421–431.

7. Reddy, D., & Satyanarayana, V.S. (2004). Lacticacid production from dairy waste by fermenta-tion using Lactobacillus delbrueckii. Asian Jour-

nal of Microbiology, Biotechnology and Envi-ronmental Sciences, 6, 139–140.8. Li, J., Bai, Q., & Nie, Y. (2002). Future solutions

for the treatment and disposal of hazardous wastes in China. Environmental Management,29, 591–597.

9. Ibanez, R., Andres, A., Viquri, J.R., Ortiz, I., &Irabien, J.A. (2000). Characterisation and man-agement of incinerator wastes. Journal of Haz-ardous Wastes, 79, 215–227.

10. Zhang, F., Yamasaki, S., & Nanzyo, M. (2001). Application of waste ashes to agricultural land-effect of incineration temperature on chemicalcharacteristics. The Science of the Total Environ-

ment, 264, 205–214.11. Stillman, G.I. (1983). Municipal solid waste (Gar-bage): Problems and Benefitsa. Annals of theNew York Academy of Sciences, 403, 1–26.

12. Autret, E., Berthier, F., Luszezanec, A., & Nico-las, F. (2007). Incineration of municipal andassimilated wastes in France: Assessment of lat-est energy and material recovery performances.

 Journal of Hazard Materials, 139, 569–574.13. Chang, N.B., & Davila, E. (2008). Municipal solid

 waste characterizations and management strat-egies for the Lower Rio Grande Valley. Texas

 Waste Management, 28, 776–794.

14. Koukouzas, N., Katsiadakis, A., Karlopoulos, E.,& Kakaras, E. (2008). Co-gasification of solid

 waste and lignite—A case study for WesternMacedonia. Waste Management, 28, 1263– 1275.

15. Cheng, H., Zhang, Y., Meng, A., & Li, Q. (2007).Municipal solid waste fueled power generationin China: A case study of waste-to-energy in

Changchun City. Environmental Science andTechnology, 41, 7509–7515.16. Santoleri, J.J. (2007). Incineration,  http://www.

pollutionissues.com/Ho-Li/Incineration.html (accessed, September 2008).

17.   http://en.wikipedia.org/wiki/Incinerator .18. Meij, R., & te Winkel, H. (2007). The emissions

of heavy metals and persistent organic pollu-tants from modern coal-fired power stations.

 Atmospheric Environment, 41, 9262–9272.19. vom Berg, W., & Feuerborn, H.J. (2007). Coal

combustion products in Europe trends anddevelopments. World of Coal Ash, Covington,Kentucky, USA, May 7–10.

20. Adanez, J., de Diego, L.F., Gayan, P., Garcia-Labiano, F., Cabanillas, A., & Bahillo, A. (2003).Co-Combustion of biomass and coal in circulat-ing fluidized bed. Modeling and validation. 46thInternational Energy Agency- Fluidized BedConversion (IEA-FBC), Jacksonville, Florida, USA,May 18th.

21. Hang, Y.D. (2004). Management and utilizationof food processing wastes. Journal of Food Sci-ence, 69, 104–107.

22. Nakajima, K., & Wakabayashi, N. (2006). Wasteheat recovery system and thermoelectric conver-sion system. US Patent Application 0,157,102.

23. Mardikar, S.H., & Niranjan, K. (1995). Food

processing and the environment. EnvironmentalManagement and Health, 6, 23–26.24. Jones, A. (1994). Dairy: 8–9 February 1995, 4th

 Annual Conf. on Incineration: Towards a wastemanagement strategy-the Government’s res-ponse. Surface Engineering, 10, 164–165.

25. Humphreys, G.B., & Escobar, B.C. (1980). Utiliz-ing urban and dairy wastes to provide energy for industry. National Conference on MunicipalIndustry Sludge Utility Disposal, 196–206.

26. Kulkarni, P.S., Crespo, J.G., & Afonso, C.A.(2008). Dioxins sources and current remediationtechnologies—a review. Environment Interna-tional, 34, 139–153.

27. Kobylecki, R.P., Ohira, K., Ito, I., Fujiwara, N., &Horio, M. (2001). Dioxin and fly ash free incin-eration by ash pelletization and reburning. Envi-ronmental Science and Technology, 35, 4313– 4319.

28. Hallenbeck, W.H. (1995). Health impact of aproposed waste-to-energy facility in Illinois. Bul-letin of Environmental Contamination and Toxi-cology, 54, 342–348.

29. Malkow, T. (2004). Novel and innovative pyroly-sis and gasification technologies for energy effi-cient and environmentally sound MSW disposal.

 Waste Management, 24, 53–79.

532 December 2008 Environmental Progress (Vol.27, No.4) DOI 10.1002/ep

Page 11: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 11/15

30. Yaman, S. (2004). Pyrolysis of biomass to pro-duce fuels and chemical feedstocks. Energy Conversion and Management, 45, 651–671.

31. Demirbas, A. (2007). Effect of temperature onpyrolysis products from biomass. Energy Sour-ces, Part A; Recovery, Utilization, and Environ-mental Effect, 29, 329–336.

32. Demirbas, A. (2002). Gaseous products from

biomass by pyrolysis and gasification. Energy Conversion and Management, 43, 897–909.33. Czernik, S. (2002). Review of fast pyrolysis of 

biomass,  http://www.nh.gov/oep/programs/energy/documents/biooil-nrel.pdf   (accessed,September 2008).

34. Azapagic, A. (2007). Energy from municipalsolid waste: Large-scale incineration or small-scale pyrolysis? Environmental Engineering andManagement Journal, 6, 337–346.

35. Bell, P.R., & Varjavandi, J.J. (1974). Pyrolysis-resource recovery from solid waste. Australian

 Waste Management and Control Conference,207–210.

36. Aberley, R.C., Sieger, R.B., & Bracken, B.D.(1978). Pyrolysis gas from solid waste will pro- vide total power demand for a major wastewaterreclamation plant. Alternative Energy Source, 9,4221–4243.

37. Oak Ridge National Laboratory, http://bioenergy.ornl.gov/papers/misc/energy_conv.html (accessed, September 2008).

38. Juniper Consultancy Services Ltd. (1997). Themarket for pyrolysis and gasification of waste inEurope, Uley, Glouchestershire, UK: JuniperConsultancy Services Ltd.

39. Dirks, E. (2000). Praxishandbuch Abfallverbren-nung. Herrentor Fachbuchverlag, Germany:

Emden.40. Bryce, W.B. (2002). Bringing the R21 process toEurope. Modern Power Systems, 22, 29–31.

41. Europe. Modern Power Systems, 22, 29–31,http://www.osti.gov/bridge/servlets/purl/805670-S8pCpG/native/805670.pdf .

42. DOE/NETL-2003/1183 (2002). Pinon Pine IGCCPower Project A DOE Assessment,  http://www.osti.gov/bridge/servlets/purl/805670-S8pCpG/native/805670.pdf  (accessed, September 2008).

43.   http://www.eh.doe.gov/nepa/docs/deis/eis0382d/v2%20appendix%20files/Appx_f.pdf .

44.   http://www.eia.doe.gov/oiaf/aeo/assumption/

pdf/electricity.pdf .45. Goodell, J. (2006). Big coal, New York:Houghton Mifflin.

46. De Filippis, P., Borgianni, C., Paolucci, M., &Pochetti, F. (2004). Prediction of syngas quality for two-stage gasification of selected waste feed-stocks. Waste Management, 24, 633–639.

47. Saft, R.J. (2007). Life cycle assessment of pyroly-sis/gasification plant for hazardous paint waste.International Journal of Life Cycle Assessment,12, 230–238.

48. Masaaki, T., Hitoshi, O., & Hiroshi, M. (2007).Basic study on steam gasification of food

 wastes. Journal of the Japan Society of WasteManagement Experts, 18, 49–57.

49. Faaij, A. (2006). Assessment of the energy pro-duction industry. In Dewulf, J., & van Lan-genhove, H., (Eds.), Renewables-based technol-ogy: Sustainability assessment (pp. 214–220),New York: Wiley.

50. Kaltschmitt, M., Rosch, C., & Dinkelbach, L.

(1998). Biomass gasification in Europe, Instituteof Energy Economics and the Rational Use of Energy (IER), Report prepared for the EuropeanCommissions, DG XII, EUR 18224, University of Stuttgart.

51. Wu, M., Wu, Y., & Wang, M. (2006). Energy andemission benefits of alternative transportationliquid fuels derived from switchgrass: A fuel lifecycle assessment. Biotechnology Progress, 22,1012–1024.

52. Hamelinck, C., van Hooijdonk, G., & Faaij, A.(2005). Ethanol from lignocellulosic biomass:Techno-economic performance in short-, middle-and long-term. Biomass and Bioenergy, 28, 384– 

410.53. Williams, R.H., & Larson, E.D. (1996). Biomassgasifier gas turbine power generating technol-ogy. Biomass and Bioenergy, 10, 149–166.

54. Saydut, A., Duz, M.Z., Kaya, C., Kafadar, A.B., &Hamamci, C. Transesterified sesame ( Sesamumindicum L.) seed oil as a biodiesel fuel. Biore-source Technology, in press.

55. Zafiropoulos, N.A., Ngo, H.L., Foglia, T.A.,Samulski, E.T., & Lin, W. (2007). Catalytic syn-thesis of biodiesel from high free fatty acid-con-taining feedstocks. Chemical Communications,21, 3670–3672.

56. Behzadi, S., & Farid, M.M. (2007). Review:

Examining the use of different feedstock of theproduction of biodiesel. Asia-Pacific Journal of Chemical Engineering, 2, 480–486.

57. Haas, M., & Foglia, T.A. (2005). Alternate feed-stocks and technologies for biodiesel produc-tion. In Krahl, J., (Ed.), Biodiesel handbook,Urbana: Amer Oil Chemists Society.

58. Akoh, C.C., Chang, S.W., Lee, G.C., & Shaw, J.F.(2007). Enzymatic approach to biodiesel produc-tion. Journal of Agriculture and Food Chemistry,55, 8995–9005.

59. Sanchez, F., & Vasudevan, P.T. (2006). Enzymecatalyzed production of biodiesel from olive oil.

 Applied Biochemistry and Biotechnology, 135,

1–14.60. Ranganathana, S.V., Narasimhana, S.L., &Muthukumar, K. An overview of enzymaticproduction of biodiesel. Bioresource Technol-ogy, in press.

61. Cherry, J.R., & Fidantsef, A.L. (2003). Directedevolution of industrial enzymes: An update. Cur-rent Opinion in Biotechnology, 14, 438–443.

62. Campos, E., Almirall, M., Mtnez-Almela, J., Pal-atsi, J., & Flotats, X. (2008). Feasibility study of the anaerobic digestion of dewatered pig slurry by means of polyacrylamide. Biosource Tech-nology, 99, 387–395.

Environmental Progress (Vol.27, No.4) DOI 10.1002/ep December 2008 533

Page 12: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 12/15

63. Taiganides, E.P. (1963). Anaerobic digestion of poultry manure. World’s Poultry Science Journal,19, 256–261.

64. Peng, W., Hu, W., Li, X., Zeng, B., Lin, Q., & Si,H. (1995). Anaerobic digestion project of cow

 wastes from large dairy. Gongye Weishengwu,25, 5–12.

65. Van den Berg, L., & Lentz, C.P. (1978). Food

processing waste treatment by anaerobic diges-tion. Proceedings of the Industrial Waste Confer-ence, 32, 252–258.

66. Stafford, D.A. (1984). The anaerobic digestion of food processing wastes. Institution of ChemicalEngineers Symposium Series, 84, 89–108.

67. Nishio, N., & Nakashimada, Y. (2004). High rateproduction of hydrogen/methane from varioussubstrates and wastes. Advances in BiochemicalEngineering/ Biotechnology, 90, 63–87.

68. Cui, Q., Zhao, D., Ni, S., Zhu, Y., & Yu, L.(2007). A two-step anaerobic reactor used in thetreatment of confectionery industry wastewater.Shandong Daxue Xuebao, Lixueban, 42, 55–58.

69. Hickey, R., & Owens, R. (1982) Treatment of cheese-whey and soft-drink-bottling wastes inan anaerobic biological fluidized-bed reactor.Technical Report OSTI ID: 5761571, Ecolotrol,Inc., Bethpage, NY.

70. Ozturk, I., Anderson, G.K., & Saw, C.B. (1989). Anaerobic fluidized-bed treatment of brewery  wastes and bioenergy recovery. Water and Sci-ence Technology, 21, 1681–1684.

71. Switzenbaum, M.S., & Danskin, S.C. (1982). An-aerobic expanded bed treatment of whey. Agri-culatural waste, 4, 411–426.

72. Zheng, P., Yu, X., Fang, S., & Feng, X. (1990).Treatment of brewery saccharification wastewater

 with an anaerobic attached microbial film ex-panded bed reactor. Water Treatment, 5, 339–347.73. Saddoud, A., Hassairi, I., & Sayadi, S. (2007).

 Anerobic membrane reactor with phase separa-tion for the treatment of cheese whey. Biore-source Technology, 98, 2102–2108.

74. Van den Berg, L., & Lentz, C.P. (1977). Methaneproduction during treatment of food plant

 wastes by anaerobic digestion. Food, Fertilizerand Agricultural Residues: Proceedings of the1977 Cornell Agriculture Waste ManagementConference, 9th, 381–393.

75. Van Drooge, B. Anaerobic digestion of foodindustry waste. Effluent Treatment. Process Bio-

chemistry International Conference, 3rd (1980),Meeting Date 1979, Paper No. 10, p 4.76. Kirsop, B.H. (1986). Food wastes. Progress in

Industrial Microbiology, 23, 285–306.77. Henry, M.M. (1985). Industrial performance of a

fixed-film anaerobic digestion process for meth-ane production and stabilization of sugar distill-ery and piggery wastes. Energy from Biomassand Wastes, 9, 829–855.

78. Nishio, N., & Nakashimada, Y. (2007). Recentdevelopment of anaerobic digestion processesfor energy recovery from wastes. Journal of Bio-science and Bioengineering, 103, 105–112.

79. Wiesmann, U., Choi, I.S., & Dombrowski, E.-M.(2007). Fundamentals of biological wastewatertreatment. Weinheim: Wiley.

80. Gavala, H.N., Angelidaki, I., & Ahring, B.K.(2003). Kinetics and modeling of anaerobicdigestion process. Advances in Biochemical En-gineering/Biotechnology. 81, 57–93.

81. Haartrick, A., Hampel, D.C., Ostermann, K.,

 Ahrens, H., & Dinkler, D. (2001). Modeling of the biodegradation of organic matter in munici-pal landfills. Waste Management and Research,19, 320–331.

82. Lu, F., He, P.-J., Shao, L.-M., & Lee, D.-J. (2007).Effects of ammonia on hydrolysis of proteinsand lipids from fish residues. Applied Microbiol-ogy and Biotechnology, 75, 1201–1208.

83. Guerrero, L., Omil, F., Mendez, R., & Lema, J.M.(1999). Anaerobic hydrolysis and acidogenesisof wastewaters from food industries with highcontent of organic solids and protein. WaterResearch, 33, 3281–3290.

84. Demirel, B., Yenigun, O., & Onay, T.T. (2005).

 Anaerobic treatment of dairy wastewaters: A review. Process Biochemistry, 40, 2583–2595.85. Calli, B., Mertoglu, B., Inanc, B., & Yenigun, O.

(2005). Methanogenic diversity in anaerobic bio-reactors under extremely high ammonia levels.Enzyme and Microbial Technology, 37, 448–455.

86. Hafner, S.D., Bisogni, Jr., J.J., & Jewell, W.J.(2006). Measurement of Un-ionized Ammonia inComplex Mixtures. Environmental Science andTechnology, 40, 1597–1602.

87. Wang, Z.J., & Banks, C.J. (2003). Evaluation of atwo stage anaerobic digester for the treatmentof mixed abattoir wastes. Process Biochemistry,38, 1267–1273.

88. Yu, H.Q., & Fang, H.H.P. (2003). Acidogenesisof gelatin-rich wastewater in an upflow anaero-bic reactor: Influence of pH and temperature.

 Water Research, 37, 55–66.89. Angelidaki, I., Ellegaard, L., & Ahring, B. (1999).

 A comprehensive model of anaerobic biocon- version of complex substrates to biogas. Bio-technology and Bioengineering, 63, 363–372.

90. Koster, I.W., & Lettinga, G. (1988). Anaerobicdigestion at extreme ammonia concentrations.Biological Wastes, 25, 51–59.

91. Lokshina, L.Y., Vavilin, V.A., Salminen, E., & Rin-tala, J. (2003). Modeling of anaerobic degrada-tion of solid slaughterhouse waste-inhibition

effects of long-chain fatty acids or ammonia. Applied Biochemistry and Biotechnology, 109,15–32.

92. Poggi-Varaldo, H.M., Rodrıguez-Vazquez, R.,Fernandez-Villagomez, G., & Esparza-Garcıa, F.(1997). Inhibition of mesophilic solid-substratedigestion by ammonia nitrogen. Applied Micro-biology and Biotechnology, 47, 284–291.

93. Breure, A.M., & van Andel, J.G. (1984). Hydroly-sis and acidogenic fermentation of a protein,gelatin, in an anaerobic continuous culture.

 Applied Microbiology and Biotechnology, 20,40–45.

534 December 2008 Environmental Progress (Vol.27, No.4) DOI 10.1002/ep

Page 13: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 13/15

94. Gallert, C., & Winter, J. (1997). Mesophilic andthermophilic anaerobic digestion of source-stored organic wastes: Effect of ammonia onglucose degradations and methane production.

 Applied Microbiology and Biotechnology, 48,405–410.

95. Gallert, C., Bauer, S., & Winter, J. (1998). Effectof ammonia on the anaerobic degradation of 

protein by a mesophilic and thermophilic bio- waste population. Applied Microbiology andBiotechnology, 50, 495–501.

96. Salerno, M.B., Park, W., Zuo, Y., & Logan, B.E.(2006). Inhibition of biohydrogen production by ammonia. Water Research, 40, 1167–1172.

97. Sterling, Jr., M.C., Lacey, R.E., Engler, C.R., &Ricke, S.C. (2001). Effects of ammonia nitrogenon H2 and CH4 production during anaerobicdigestion of dairy cattle manure. BioresourceTechnology, 77, 9–18.

98. He, P.J., Lu, F., Shao, L.M., Pan, X.J., & Lee, D.J.(2006). Enzymatic hydrolysis of polysaccharide-rich particulate organic waste. Biotechnology 

and Bioengineering, 93, 1145–1151.99. Vavilin, V.A., Jonsson, S., Ejlertson, J., & Svens-son, B.H. (2006). Modeling MSW decompositionunder landfill conditions considering hydrolyticand methanogenic inhibition. Biodegradation,17, 389–402.

100. Veeken, A., Kalyuzhnyi, S., Scharff, H., & Ham-elers, B. (2000). Effect of pH and VFA on hydro-lysis of organic solid waste. Journal of Environ-mental Engineering-ASCE, 126, 1076–1081.

101. Ramsay, I.R., & Pullammanappallil, P.C. (2001).Protein degradation during anaerobic waste-

 water treatment: Derivation of stoichiometry.Biodegradation, 12, 247–257.

102. Michaelsen, T., & Kloss, R. (1987). Removal of ammonia by gas scrubbing in anaerobic diges-tion of high strength organic loaded residualand waste matter. GWF-Wasser/Abwasser, 128,247–250.

103. Rong, C., & Deokjin, J. (2006). Enhanced meth-ane production from anaerobic digestion of dis-integrated and deproteinized excess sludge. Bio-technology Letters, 28, 531–538.

104. Lefebvre, O., Quentin, S., Torrijos, M., Godon, J.J., Delgenes, J.P., & Moletta, R. (2007). Impactof increasing NaCl concentrations on the per-formance and community composition of twoanaerobic reactors. Applied Microbiology and

Biotechnology, 75, 61–69.105. Nagai, H., Kobayashi, M., Tsuji, Y., Nakashi-mada, Y., Kakizono, T., & Nishio, N. (2002). Bio-logical and chemical treatment of solid wastefrom soy sauce manufacture. Water Science andTechnology, 45, 335–338.

106. Feijoo, G., Soto, M., Mendez, R., & Lema, J.M.(1995). Sodium inhibition in the anaerobicdigestion process: Antagonism and adaptationphenomena. Enzyme and Microbial Technology,17, 180–188.

107. Gebauer, R. (2004). Mesophilic anaerobic treat-ment of sludge from saline fish farm effluents

 with biogas production. Bioresource Technol-ogy, 93, 155–167.

108. Guerrero, L., Omil, F., Mendez, R., & Lema, J.M.(1997). Treatment of saline wastewaters fromfish meal factories in an anaerobic filter underextreme ammonia concentrations. BioresourceTechnology, 61, 69–78.

109. Rinzema, A., Lier, V.V., & Lettinga, G. (1998). So-

dium inhibition of acetoclastic methanogens ingranular sludge from a UASB reactor. Enzymeand Microbial Technology, 10, 24–32.

110. Gourdon, R., Comel, C., Vermande, P., & Veron, J. (1989). Kinetics of acetate, propionate and bu-tyrate removal in the treatment of a semisyn-thetic landfill leachate on anaerobic filter. Bio-technology and Bioengineering, 33, 1167–1181.

111. Kugelman, I.J., & McCarty, P.L. (1965). Cationtoxicity and stimulation in anaerobic waste treat-ment. I. Slug feed studies Journal-Water Pollu-tion Control Federation, 37, 97–116.

112. Aspe, E., Martı, M.C., Jara, A., & Roeckel, M.(2001). Ammonia inhibition in the anaerobic

treatment of fishery effluents. Water Environ-ment Research, 73, 154–164.113. Lefebvre, O., Vasudevan, N., Torrijos, M., Thana-

sekaran, K., & Moletta, R. (2006). Anaerobicdigestion of tannery soak liquor with an aerobicpost-treatment. Water Research, 40, 1492–1500.

114. Mosquera-Corral, A., Sanchez, M., Campos, J.L.,Mendez, R., & Lema, J.M. (2001). Simultaneousmethanogenesis and denitrification of pretreatedeffluents from a fish canning industry. WaterResearch, 35, 411–418.

115. Vidal, G., Aspe, E., Martı, M.C., & Roeckel, M.(1997). Treatment of recycled wastewaters fromfishmeal factory by an anaerobic filter. Biotech-

nology Letters, 19, 117–121.116. Boardman, G.D., Tisinger, J.L., & Gallagher, D.L.(1995). Treatment of clam processing waste-

 waters by means of upflow anaerobic sludgeblanket technology. Water Research, 29, 1483– 1490.

117. Gangagni Rao, A., Venkata Naidu, G., KrishnaPrasad, K., Chandrasekhar Rao, N., VenkataMohan, S., Jetty, A., & Sarma, P.N. (2005). An-aerobic treatment of wastewater with high sus-pended solids from a bulk drug industry usingfixed film reactor (AFFR). Bioresource Technol-ogy, 96, 87–93.

118. Habets, L.H.A., Engelaar, A.J.H.H., & Groene-

 veld, N. (1997). Anaerobic treatment of inulineeffluent in an internal circulation reactor. WaterScience and Technology, 35, 189–197.

119. Omil, F., Mendez, R., & Lema, J.M. (1995). An-aerobic treatment of saline wastewaters underhigh sulphide and ammonia content. Biore-source Technology, 54, 269–278.

120. Rovirosa, N., Sanchez, E., Cruz, M., Veiga, M.C.,& Borja, R. (2004). Coliform concentrationreduction and related performance evaluation of a down-flow anaerobic fixed bed reactor treat-ing low-strength saline wastewater. BioresourceTechnology, 94, 119–127.

Environmental Progress (Vol.27, No.4) DOI 10.1002/ep December 2008 535

Page 14: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 14/15

121. Saatci, Y., Arslan, E.I., & Konar, V. (2003). Re-moval of total lipids and fatty acids from sun-flower oil factory effluent by UASB reactor. Bio-resource Technology, 87, 269–272.

122. Tagawa, T., Takahashi, H., Sekiguchi, Y., Oha-shi, A., & Harada, H. (2002). Pilot-plant study on anaerobic treatment of a lipid- and protein-rich food industrial wastewater by a thermo-

philic multi-staged UASB reactor. Water Scienceand Technology, 45, 225–230.123. Lalman, J.A., & Bagley, D.M. (2001). Anaerobic

degradation and methanogenic inhibitory effectsof oleic and stearic acids. Water Research, 35,2975–2983.

124. Hatamoto, M., Imachi, H., Ohashi, A., & Har-ada1, H. (2007). Identification and cultivation of anaerobic, syntrophic long-chain fatty acid-degrading microbes from mesophilic and ther-mophilic methanogenic sludges. Applied andEnvironmental Microbiology, 73, 1332–1340.

125. Angelidaki, I., & Birgitte, K.A. (1995). Establish-ment and characterization of an anaerobic ther-

mophilic (558C) enrichment culture degradinglong-chain fatty acids. Applied and Environmen-tal Microbiology, 61, 2442–2445.

126. Rao, K., Chaudhari, V., Varanasi, S., & Kim, D.S.(2007). Enhanced ethanol fermentation of brew-ery wastewater using genetically modified strain,E. coli KO11. Applied Microbiology and Bio-technology, 74, 50–60.

127. Lin, Y., & Tanaka, S. (2006). Ethanol fermenta-tion from biomass resources: Current state andprospects. Applied Microbiology and Biotech-nology, 69, 627–642.

128. Bothast, R.J., Nichols, N.N., & Dien, B.S. (1999).Fermentations with new recombinant organisms.

Biotechnology Progress, 15, 867–875.129. Dumsday, G.J., Zhou, B., Buhmann, S., Stanley,G.A., & Pamment, N.B. (1997). Continuous etha-nol production by Escherichia coli KO11 in con-tinuous stirred tank and fluidized bed fermentors.

 Australasian Biotechnology, 7, 300–303.130. Gonzalez, R., Tao, H., Purvis, J.E., York, S.W.,

Shanmugam, K.T., & Ingram, L.O. (2003). Genearray-based identification of changes that con-tribute to ethanol tolerance in ethanologenicEscherichia coli: Comparison of KO11(parent) toLY01 (resistant mutant). Biotechnology Progress,19, 612–623.

131. Zaldivar, J., & Ingram, L.O. (1999). Effect of or-

ganic acids on the growth and fermentation of ethanologenic Escherichia coli LY01. Biotech-nology and Engineering, 66, 203–210.

132. Lawford, H.G., Rousseau, J.D., & Tolan, J.S.(2001). Comparative ethanol productivities of different Zymomonas recombinants fermentingoat hull hydrolysate. Applied Biochemistry andBiotechnology, 91–93, 133–146.

133. Vijayaraghavan, K., Ahmad, D., & Samson, M.(2007). Biohydrogen generation from beerbrewery wastewater using an anaerobic contactfilter. Journal of the American Society of Brew-ing Chemists, 65, 110–115.

134. Yang, P., Zhang, R., McGarvey, J.A., & Bene-mann, J.R. (2007). Biohydrogen production fromcheese processing wastewater by anaerobic fer-mentation using mixed microbial communities.International Journal of Hydrogen Energy, 32,4761–4771.

135. Mohan, S.V., Babu, V.L., & Sarma, P.N. (2007). Anaerobic biohydrogen production from dairy 

 wastewater treatment in sequencing batch.Enzyme and Microbial Technology, 41, 506– 515.

136. Eroglu, E., Eroglu, I., Gunduz, U., Lemi, T., & Yucel, M. (2006). Biotransformation of olive mill wastewater into valuable products through bio-hydrogen processes. AIChE Annual Meeting,Conference Proceedings, San Francisco, CA,USA, Nov. 12–17, 2006.

137. O-Thong, S., Prasertsan, P., Intrasungkha, N.,Dhamwichukorn, S., & Birkeland, N.-K. (2007).Improvement of biohydrogen production andtreatment efficiency on palm oil mill effluent

 with nutrient supplementation at thermophilic

condition using an anaerobic sequencing batchreactor. Enzyme and Microbial Technology, 41,583–590.

138. Nandi, R., & Sengupta, S. (1998). Microbial pro-duction of hydrogen: An overview. CriticalReviews in Microbiology, 24, 61–84.

139. Levin, D.B., Pitt, L., & Love, M. (2004). Biohy-drogen production: Prospects and limitations topractical application. International Journal of Hydrogen Energy, 29, 173–185.

140. Kerby, R.L., Ludden, P.W., & Robert, G.P. (1995).Carbon monoxide-dependent growth of Rhodo-spirillum rubrum. Journal of Bacteriology, 177,2241–2244.

141. tUffen, R.L. (1983). Metabolism of carbon mon-oxide by Rhodopseudomonas gelatinosa: Cellgrowth and properties of the oxidation system.

 Journal of Bacteriology, 155, 956–965.142. Franchi, E., Tosi, C., Scolla, G., Penna, G.D.,

Rodriguez, F., & Pedroni, P.M. (2004). Metabol-ically engineered Rhodobacter sphaeroides RV strains for improved biohydrogen photoproduc-tion combined with disposal of food wastes.Marine Biotechnology, 6, 552–565.

143. Ueno, Y., Fukui, H., & Goto, M. (2007). Opera-tion of a two-stage fermentation process pro-ducing hydrogen and methane from organic

 waste. Environmental Science and Technology,

41, 1413–1419.144. Oh, Y.-K., Kim, S.-H., Kim, M.-S., & Park, S.(2004). Thermophilic biohydrogen productionfrom glucose with trickling biofilter. Biotech-nology and Bioengineering, 88, 690–698.

145. Benemann, J. (1996). Hydrogen biotechnology:Progress and prospects. Nature Biotechnology,14, 1101–1103.

146. Cyranoski, D. (2006). Waste management: Oneman’s trash. Nature, 444, 262–263.

147. Allen, R.M., & Bennetto, H.P. (1993). Microbial.http://www.solenagroup.com/html/tech/

 white.asp.

536 December 2008 Environmental Progress (Vol.27, No.4) DOI 10.1002/ep

Page 15: Digman Brett Food Processing Wastes

7/26/2019 Digman Brett Food Processing Wastes

http://slidepdf.com/reader/full/digman-brett-food-processing-wastes 15/15

148. Allen, R.M., & Bennetto, H.P. (1993). Microbialfuel cells-Electricity production from carbohy-drates. Applied Biochemistry and Biotechnol-ogy, 39–40, 27–40.

149. Logan, B.E., Hamelers, B., Rozendal, R.,Schroder, U., Keller, J., Freguia, S., Aelterman,P., Verstraete, W., & Rabaey, K. (2006). Microbialfuel cells: Methodology and technology. Environ-

mental Science and Technology, 40, 5181–5192.150. Lovley, D.R. (2006). Microbial fuel cells: Novelmicrobial physiologies and engineering ap-proaches. Current Opinion in Biotechnology,17, 327–332.

151. Jin, B., Yin, P., Ma, Y., & Zhao, L. (2005). Pro-duction of lactic acid and fungal biomass by Rhizopus fungi from food processing wastestreams. Journal of Industrial Microbiology andBiotechnology, 32, 678–686.

152. Van Bellegem, T.M. (1980). Methane productionfrom the effluent of the potato starch industry.Biotechnology Letters, 2, 219–224.

153. Yu, H., Zhu, Z., Hu, W., & Zhang, H. (2002).

Hydrogen production from rice winery waste- water in an upflow anaerobic reactor by usingmixed anaerobic cultures. International Journalof Hydrogen Energy, 27, 1359–1365.

154. Hawkes, F.R., Dinsdale, R., Hawkes, D.L., &Hussy, I. (2002). Sustainable fermentative hydro-gen production: Challenges for process optimi-zation. International Journal of HydrogenEnergy, 27, 1339–1347.

155. Lunghi, P., & Burzacca, R. (2004). Energy recovery from industrial waste of a confectionery plant by means of BIGFC plant. Energy, 29, 2601–2617.

156. Lu, P.M., Xiong, Z.H., Chang, J., Wu, C.Z., Chen, Y., & Zhu, J.X. (2004). An experimental study 

on biomass air-steam gasification in a fluidizedbed. Bioresource Technology, 95, 95–101.157. Lobachyov, K.V., & Richter, H.J. (1998). An

advanced integrated biomass gasification andmolten fuel cell power system. Energy Conver-sion and Management, 39, 1931–1943.

158. Swami, S., Chaudhari, V., Sim, S.J., Kim, D.S., & Abraham, M. (2008). Production of hydrogenfrom biomass: Integrated biological and thermo-chemical approach. Industrial and EngineeringChemistry Research, 47, 3645–3651.

159. Tarman, P.B., & Chynoweth, D.P. (1981). Hybridbio-thermal gasification. US Patent, US4,289,625, US4,334,026.

160. Hansen, C.L., & Cheong, D.Y. (2007). Fermenta-tion, biogas, and biohydrogen production fromsolid food processing. In K. Waldron, (Ed.),Handbook of waste management and co-prod-uct recovery in food processing (pp. 611–648),Cambridge: Woodhead Publishing Limited.

161. Kleerebezem, R., & van Loosdrecht, M.C.M.(2007). Mixed culture biotechnology for bioen-ergy production. Current Opinion in Biotechnol-ogy, 18, 207–212.

162. Shang, Y., Soroushian, F., Lindgren, G., & Whit-man, E.J. Co-digestion-potential increase of renewable energy production from waste forCalifornia. Conference Proceedings, Annual

Technical Exhibition & Conference, 78th, Wash-ington, DC, Oct. 29–Nov. 2, 2005.163. Winkelkoetter, P. (2000). Process and installation

for complete pollution-free conversion of wastesinto energy and fertilizers. German Patent, DE1,985,7870.

164. Chen, G., Andries, J., Luo, Z., & Splietho, H.(2003). Biomass pyrolysis/gasification for prod-uct gas production: The overall investigation of parametric effects. Energy Conversion and Man-agement, 44, 1875–1884.

165. Amin, G., & Allah, A.M.K. (1992). Byproductsformed during direct conversion of sugar beetsto ethanol by Zymomonas mobilis in conven-

tional submerged and solid-state fermentations.Biotechnology Letters, 14, 1187–1192.166. Holker, U., & Lenz, J. (2005). Solid-state fermen-

tation - are there any biotechnological advan-tages? Current Opinion in Microbiology, 8, 301– 306.

Environmental Progress (Vol.27, No.4) DOI 10.1002/ep December 2008 537