Transcript Document
Evaluation of Dextran in Sugar Factories Presented WIRAT VANICHSRIRATANA Department of Biotechnology, Faculty of Agro-Industries, Kasetsart University, Thailand Research Parties Amano Enzyme Inc. Cinnamon Company Limited Kasetsart University Outline Project Objectives Where is dextran Factory trial Dextran measurement Dextranase application Process improvement Cost analysis Conclusion Objectives To evaluate the amount of dextran in cane mixed juice and in product (raw syrup). To reduce dextran in the process. To publicize the obtained results and methodologies to the Thai sugar factories. Sugarcane in Thailand: where dextran comes from Sugarcane Labors Transports Processing Sugarcane in Thailand Sugarcane cultivation in Thailand for the year 2011/2012 was around 98 million tonnes. Sugar cane harvesting Sugarcane Labors Transports Processing Products Sugar cane burning The shortage of labour for harvesting the sugarcane was the main reason why the cane was burnt before harvesting. In Thailand over 50% of the cane is burnt. Sugar cane harvesting Leuconostoc mesenteroides n Sucrose Leuconostoc mesenteroides Dextran + Fructose the lactic acid bacterium which mainly attacks the sucrose in the cane and produces dextran. Leuconostoc mesenteroides Dextran The straight chain consists of α-1,6 glycosidic linkages between glucose molecules, while branches begin from α-1,3 linkages. The name dextran refers to a large family of glucose polymers whose structures and subsequent properties can vary widely. This variation in structure poses a huge challenge for any analyst trying to detect the molecules especially against a substantial background of saccharides with similar structures and properties Sucrose Crystals Sucrose Crystals (dextran contamination) (without dextran contamination) Source: http://www.dextran.co.uk Economic loss “1 ppm of dextran in sugar juice” results in “a loss of 0.0011 kg of raw sugar / 1 ton of sugarcane” At 2011/2012; sugarcane production in Thailand around 98 Million tons, (1 ppm of dextran), results in “Raw sugar lost of 98,000 kg” How to reduce dextran: Sugarcane Labors Transports Processing Products Dextranase Dextranase is the enzyme that hydrolyses the α -1,6 linkages mainly present in the dextran structure and is frequently used in the sugar factory to remove dextran from juice where contamination exists. Dextranase (α-D-1,6 glucan-6-glucano hydrolase) (EC 3.2.1.11) Dextran Glucose Chain (α-1,6) + Dextranase + Fructose Dextranase Factory Trial 1. Factory A (yield 110 kg sugar/TC) Milling Period: November-May 2.9 MT (Fresh 1.05 + Burnt 1.9) 2. Factory B (yield 101 kg sugar/TC) Milling Period: November-May 1.9 MT (Fresh 0.3 + Burnt 1.7) Factory Trial Determination of dextran contamination Factory A Factory B daily composite samples I. Mixed juice II. Clarified juice III. Raw syrup IV. Final molasses (For the period of 14 days) Dextran Contamination “Dextran ELISA Kit” Determination of dextran contamination 1. Haze method 2. Eliza test kit Determination of dextran contamination Determination of dextran contamination Dextran concentration at factories A and B before the application of dextranase 4000 Dextran concentration (ppm) Factory A Factory B 3000 2000 1000 0 mixed juice clarified juice raw syrup final molasses The application of dextranase Clarified Juice Raw syrup Evaporator Set (60-70 ˚C, pH 6-7) Dextranase Without dextranase 2 ppm of dextranase* 5 ppm of dextranase* *mg/kg cane Dextran Determination Raw syrup Final molasses The application of dextranase Temperature: 60-70 OC CLARIFICATION CLARIFIED JUICE EVAPORATOR RAW SYRUP TANK The application of dextranase Dextran content in raw syrup and final molasses from factory A, before and after adding dextranase enzyme Date (D/M/Y) 18.04.12 19.04.12 20.04.12 21.04.12 22.04.12 23.04.12 25.04.12 26.04.12 27.04.12 29.04.12 01.05.12 03.05.12 05.05.12 07.05.12 09.05.12 11.05.12 Dextranase concentration (mg/kg cane) 0 ppm 0 ppm 0 ppm 0 ppm 0 ppm 0 ppm 2 ppm 2 ppm 2 ppm 2 ppm 2 ppm 5 ppm 5 ppm 5 ppm 5 ppm 5 ppm Dextran content (ppm)* Raw syrup Final molasses 520 1671 496 4765 3825 4392 331 5629 3919 3629 815 613 393 395 440 467 251 187 138 152 251 235 320 497 600 497 1478 1199 1644 Process improvement Dextran quantity depending on cane quality. Dextran causes sugar loss. High dextran also causes molasses purity to increased Parameters for Process improvement Yield of sugar per ton cane Purity of molasses Purity and sugar yield in factory A, before and after adding dextranase enzyme 120 Purity and sugar weight % cane 100 80 purity final molasses 60 sugar weight %cane 10 ccs Linear (purity final molasses) Linear (sugar weight %cane 10 ccs) 40 20 0 0 5 10 15 enzyme 27 April - 12 May 20 25 Purity and sugar yield in factory B, before and after adding dextranase enzyme 140 120 Purity and Sugar wiegh % cane 100 80 purity final molasses sugar weight %cane 10 ccs 60 Linear (purity final molasses) Linear (sugar weight %cane 10 ccs) 40 20 0 0 5 10 15 enzyme 25 April - 11 May 20 25 Cost Analysis Process Enzyme Production Improvement Sugarcane “High Income” The application of dextranase enzyme to reduce dextran content in sugar mill process streams and to demonstrate the effective level of enzyme. Sugar yield in factory A, before and after adding dextranase enzyme Factory A 120 Yield sugar/ton cane 100 80 82 88 60 40 20 0 0 5 10 15 Day 20 25 Cost Analysis (Factory A) (Approximation based on estimating yield) 1. Cane crushing during the application of enzyme: 159,900 tons 2. Amount of enzyme dextranase: 500 litres ($35,000) (@$70 /litre) 3. Yield sugar before application of enzyme: 82 kg/TC (13,110 TS) 4. Yield sugar after application of enzyme: 88 kg/TC (14,070 TS) 5. Increase in sugar: 960 TS ($528,000) (@550 $/TS) 6. Profit gain: $493,000 ($3.1 /TC) Sugar yield in factory B, before and after adding dextranase enzyme Factory B Yield 96Pol, 10CCS 100.00 84.8 82.37 80.00 60.00 40.00 20.00 1/4/2555 6/4/2555 11/4/2555 16/4/2555 21/4/2555 29/4/2555 4/5/2555 9/5/2555 Cost Analysis (Factory B) (Approximation based on estimating yield) 1. Cane crushing during the application of enzyme: 112,000 tons 2. Amount of enzyme dextranase: 300 litres ($21,000) (@70 $/litre) 3. Yield sugar before application of enzyme: 82.5 kg/TC (9,240 TS) 4. Yield sugar after application of enzyme: 84 kg/TC (9,408 TS) 5. Increase in sugar: 168 TS ($92,400) (@550 $/TS) 6. Profit gain: $71,400 ($0.64 /TC) Conclusion Dextran formation associated with the processing of a high portion of burnt sugarcane and long delay times before milling. Dextranase is an effective and practical way to reduce the dextran contamination in the milling processes. Dextranase L “Amano” was used to reduce dextran in the process. The suitable dosing point was at the 4th -5th effect of the evaporator. Temperature was at 60-70OC, pH was around 5.9 to 6.1 and Retention time was around 30 minutes. Conclusion The suggested enzyme dosage was in the range of 2-5 ppm. Based on sugar yield calculation, profit gain of $0.6 - $3 per ton cane can be obtained due to higher sugar recovery. Further test and analysis may be needed to confirmed the enzyme benefit and determine the return of investment to the sugar factories. Research publication THAILAND SUGAR SEMINAR 2012 “Technology for improving sugar process efficiency ” October, 5 2012 Royal Hill Golf Resort and Spa Nakhon Nayok Acknowledgment The authors are grateful to the Amano Enzyme for the financial funding of this research. Department of Biotechnology, Faculty of agro-industry Kasetsart University, Thailand