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Biofuel co-products as livestock feed - Opportunities and challenges

Biofuel co-products as livestock feed - Opportunities and challenges

Biofuel co-products as livestock feed - Opportunities and challenges

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Co-<strong>products</strong> of the United States biofuels industry <strong>as</strong> alternative <strong>feed</strong> ingredients for aquaculture 415minimal in the Midwest United States, where most ethanolproduction plants are located. In addition, more ethanolplants have implemented stricter st<strong>and</strong>ards for grainselection. Again, knowing the source of DDGS <strong>and</strong> testresults, especially during growth se<strong>as</strong>ons with most risk ofmy<strong>co</strong>toxin development, are important for safe utilizationof DDGS. Recently, <strong>co</strong>ncerns about antimicrobial residuesin DDGS have surfaced. Antimicrobials, such <strong>as</strong> penicillin,virginiamycin, erythromycin <strong>and</strong> others, are <strong>co</strong>mmonlyadded to the fermentors to <strong>co</strong>ntrol bacterial infections withthe goal to optimize ethanol production by ye<strong>as</strong>ts. Theseantibiotics can end up in the DDGS; however, it is believedthat they will be <strong>co</strong>mpletely deactivated under the extremetemperatures <strong>and</strong> pH <strong>co</strong>nditions applied during ethanolproduction. In addition, heat treatments <strong>as</strong>sociated withextrusion <strong>co</strong>oking <strong>co</strong>uld further inhibit such substances.Thus, the issue of antimicrobials in DDGS, althoughserious, is more speculation rather than a reality in animal<strong>feed</strong>s. Pigmentation of tissues is also of <strong>co</strong>ncern when<strong>feed</strong>ing DDGS, especially to salmonids. Feeding DDGS tosalmonids is believed to alter flesh pigmentation from thetypical pink <strong>co</strong>lour to a less desirable yellowish <strong>co</strong>lour, butto date there are no published studies evaluating the effectof DDGS on the pigmentation of fish tissues.Finally, <strong>as</strong> the ethanol industry incre<strong>as</strong>es the efficiencyof producing ethanol, different distillers <strong>co</strong>-<strong>products</strong>will be<strong>co</strong>me available, creating more <strong>challenges</strong> <strong>and</strong>opportunities for the aqua<strong>feed</strong>s industry. These <strong>products</strong>are expected to be more nutrient dense, <strong>as</strong> the fibrefraction can be further fermented <strong>and</strong> the fat extracted,leading to <strong>products</strong> <strong>co</strong>mposed mainly of protein <strong>and</strong><strong>as</strong>h. Such <strong>products</strong> may be more <strong>co</strong>mpatible with fishrequirements, but will need research to characterize them<strong>and</strong> <strong>as</strong>sess their nutritional value <strong>and</strong> efficacy for differentfish species.PROPERTIES OF CRUDE GLYCERINEThe principal <strong>co</strong>-product of biodiesel production is crudeglycerin. Common <strong>feed</strong>stocks used in the biodiesel industryinclude pure or w<strong>as</strong>te vegetable oils, or a mixture, <strong>and</strong> renderedanimal fats. Refining of crude glycerin is often limitedto large scale biodiesel producers, which make high purityglycerol for applications in the food, pharmaceutical <strong>and</strong><strong>co</strong>smetic industries. Small-scale producers generally limitthe purification process to the removal of excess al<strong>co</strong>hol toyield a low value <strong>co</strong>-product with limited uses (Thompson<strong>and</strong> He, 2006).Physical <strong>and</strong> chemical propertiesCrude glycerine <strong>co</strong>ntains impurities, including spentcatalysts, residual methanol, methyl esters, oils <strong>and</strong> fats,soaps, free fatty acids <strong>and</strong> various minerals such <strong>as</strong> Ca,Na, Cl, K, Mg, P <strong>and</strong> S (Thompson <strong>and</strong> He, 2006; D<strong>as</strong>ari,2007). Some of the physio chemical properties of crudeglycerine are presented in Table 7. Considerable variationexists among crude glycerine sources, largely becauseof differences in the biodiesel production processes <strong>and</strong>the parent <strong>feed</strong>stock used. Mader (2011) showed thatcrude glycerine derived from animal fats <strong>co</strong>ntained lessglycerol <strong>and</strong> more impurities than that derived fromvegetable oil <strong>feed</strong>stocks. Common glycerol <strong>co</strong>ntent isbetween 75 <strong>and</strong> 85 percent; however, glycerol <strong>co</strong>ntent<strong>as</strong> low <strong>as</strong> 38.4 <strong>and</strong> <strong>as</strong> high <strong>as</strong> 96.5 percent of the totalcrude glycerine can be found on the market (Hansen etal., 2009). Other major <strong>co</strong>nstituents are moisture, fat <strong>and</strong>a variety of minerals. Residual methanol is usually foundat low <strong>co</strong>ncentration (15 percent) can befound, creating some health <strong>co</strong>ncerns when crude glycerineis fed to <strong>livestock</strong> (Hansen et al., 2009). The USDA Food<strong>and</strong> Drug Administration (FDA) limits methanol <strong>co</strong>ntentTABLE 7Physiochemical properties of crude glycerineItem n Average Min. Max. ReferencePure glycerol (%) 39 78.58 38.4 96.5 1, 2, 3, 4, 5, 6, 7, 8, 9Moisture (%) 27 8.20 0 24.37 4, 5, 6, 7, 8, 9, 10Protein (%) 10 0.26 0.05 0.82 1, 3, 4, 5, 9Fat (%) 11 5.54 0.12 15 1, 3, 4, 5, 10Ash (%) 31 4.15 0 29.4 1, 3, 4, 5, 6, 7, 9Na (%) 2 1.23 1.2 1.26 5, 9Cl (%) 2 1.78 1.7 1.86 5, 9GE (KJ/kg) 9 18340 15119 20510 1, 5, 10pH 25 6.20 2 10.8 4, 5, 6, 7, 10Methanol (%) 31 1.72 0.0009 14.99 2, 3, 4, 5, 6, 7, 8, 10Density (g/cm 3 ) 11 1.20 1.07 1.26 6Vis<strong>co</strong>sity (4.45 °C, cSt) 6 60.00 82 38 10Vis<strong>co</strong>sity (40 °C, cSt) 2 8.60 8.8 8.46 1Colour (c.u.) 2 7.25 3.5 11 10Key to references: 1. Thompson <strong>and</strong> He, 2006; 2. D<strong>as</strong>ari, 2007; 3. Groesbeck et al., 2008; 4. Lammers et al., 2008a; 5. Lammers et al., 2008b; 6. Hansen etal., 2009; 7. Kerr et al., 2009; 8. Mach, Bach <strong>and</strong> Devant, 2009; 9. Gunn et al., 2010; 10. Mader, 2011.

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