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辛烯基琥珀酸淀粉酯的制备、性质及应用研究
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摘要
以非晶颗粒态玉米淀粉和蜡质玉米淀粉为原料,采用热解、酶解方法,以及羟丙基改性的方法制备不同种类的低粘度辛烯基琥珀酸淀粉酯,并对其吸附和包埋性质及机理做了研究。具体可分为以下几个部分:
     制备非晶颗粒态辛烯基琥珀酸淀粉酯的过程包括:以普通玉米淀粉原料,在醇-水相中制备非晶颗粒态玉米淀粉,采用酶解的方法低粘度制备非晶颗粒态辛烯基琥珀酸淀粉酯,其吸附性能比较强,吸油率原淀粉辛烯基琥珀酸淀粉酯的3倍多,最大吸油率可达到161%。最佳制备条件为:反应温度为35℃,反应的pH值为8.5,反应时间为2h,淀粉乳的浓度为0.25g/ml,得到产品的取代度为0.0166。
     热解法制备蜡质玉米淀粉辛烯基琥珀酸淀粉酯的过程包括:以蜡质玉米淀粉为原料制备辛烯基琥珀酸淀粉酯,然后对其进行热解和微胶囊化处理。该产品的包埋能力比较强,最高的包埋率超过了98%,与国内产品相比,表面油降低最高可以达到71%。制备条件为:反应温度为165℃,反应时间5h,酸酐的加入量为淀粉(干基的)的5.2%,反应的pH为3.5。微胶囊化工艺的最佳工艺是:壁材和心材的比例是2:1,均质压力是30~40Mpa,均质次数为2~3次,进风温度为210℃,出风温度为80℃,通针为10次/min。
     酶解法制备辛烯基琥珀酸淀粉酯的过程包括:以蜡质玉米淀粉为原料,采用高温α-淀粉酶制备低粘度辛烯基琥珀酸淀粉酯,产品的透明度比较高,包埋率偏低为90.3%。最佳制备条件为:酯化淀粉乳的浓度为20%(w/w),反应时间为10min,反应温度为95℃,反应pH为6.0,α-淀粉酶添加量的范围为10mL/g,此时的粘度为120maps左右。
     热解制备羟丙基改性辛烯基琥珀酸淀粉酯的过程包括:以辛烯基琥珀酸淀粉酯为原料,采用羟丙基改性的方法制备低粘度的辛烯基琥珀酸淀粉酯,与改性前相比,产品的包埋能力更强,最高可以达到99.2%,表面油最高可以下降33.6%。工艺条件为:羟丙基酯化淀粉:淀粉酯的浓度是35%,环氧丙烷加入量为淀粉酯的10%(干基),常温维持30min,反应温度为50℃,时间为10h。
     非晶颗粒态淀粉是吸水性比较强,以非晶颗粒态玉米为原料,经过辛烯基琥珀酸淀粉酯改性质后,可以大大改善吸附油脂的性能,拓宽了非晶颗粒态淀粉的应用范围。蜡质玉米淀粉制备的辛烯基琥珀酸淀粉酯的适合制备微胶囊,可以用来包埋易氧化的油脂如DHA,AA油和一些对身体有危害的食品添加剂,可以延长食品的货架保质期和降低食品添加剂的危害。
Octenyl succinic anhydride modified starch (SSOS) was prepared from non-crystal granular corn starch and waxy corn starch in this paper, then respectively dealed them withα-amylase or hot temperatuter, moreover using the products to prepare for different kinds of microcapsule.finally the embedding mechanism and reaction mechanisms were preliminarily studied.Including following several sections.
     The process of preparing Non-crystal corn SSOS was:Non-crystal granular starch was prepared in ethanol-water system, low viscosity non-crystal granular SSOS was produced through enzymolysis and the properties of adsorption was very well, the maximal oil adsoption exceeded 161%,which was treble the adsorption of native SSOS,the optimum processcondition was: reactive temperature 35℃,pH8.5, reactive time 2h, the concentration of starch 0.25g/ml, the DS 0.0166..
     The process of preparing waxy corn SSOS was: SSOS was prepared from waxy corn starch, then dealing it with pyrolysis and microcapsule, the embedding property of the product was very well, the rate of embedding oil exceeding 98%. Compared with home products, the surface oil was reduced 71%.The optimize condition was: the last temperature 165℃, reactive time 5h. The optimum technology of microcapsule was: the rate of the modified starch and oil 2:1, homogeneous pressure 30-40Mpa, homogeneous times 2-3, entering air temp 210℃, leaving air temp 80℃,nozzle cleaner 10 times/min.
     The process of preparing SSOS including: SSOS was dealed with thermostable alphaα-amylase, taking apparent viscosity as index to decide the degree. The embedding property of product was not very well, the rate of embedding oil was 90.3%. The optimum condition was : the concentration of starch 20% (w/w), reactive temperature 95℃, pH 6.0, amylase added 10ml.
     Hydroxypropyl modified SSOS was prepared from waxy corn starch, then dealing it with pyrolysis and microcapsule, the embedding property of the product is very well, themaximun rate of embedding oil 99.2%, the rudction of the surface oil was 33.6%. The preparing technics: the concentration of starch 35%, epoxy chloropropane addition 10%( dry basis of esterification), at 18℃reactive time half an hour, at 50℃reactive time 10h.
     Non-crystal granular SSOS was hydrophilic, after modification, the abilty of oil obsorption was improved largely. Waxy corn starch is suit to prepare microcapsule, which could reduce the harm of food additive and prolong the shelf life of functional components of health product, such as DHA and AA oil.
引文
[1]梁治齐.微胶囊技术及其应用.北京:中国轻工业出版社,1999.
    [2]吴克刚,柴向华.食品微胶囊技术.北京:中国轻工业出版社, 2006.
    [3]宋健,陈磊,李效军.微胶囊化技术及应用.北京:化学工业出版社,2001.
    [4] Beristain C I, Azuara E, Vernon E J. Effect of water activity on the stability to oxidation of spray-dried encapsulated orange peel oil using mesquite gum ( Prosopis Juliflora ) as wall material.Journal of Food Science, 2002,67 (1):206~211.
    [5] Augustin M A,Sanguansri L,Margetts C.Microencapsulation of food ingredients [J].Food Australia,2001,53:220~223.
    [6]张峻,齐葳,韩志慧等.食品微胶囊、超微粉碎加工技术.北京:化学工业出版社,2005.
    [7]张本山.交联非糊化淀粉物态性质与机理研究[D].广州:华南理工大学,1999:1~6.
    [8]梁勇.非晶颗粒态淀粉及其生物与化学反应活性研究[D].广州:华南理工大学, 2002:44~68.
    [9]张向阳.溶剂法制备非晶颗粒态羧甲基玉米淀粉及性质研究[D].广州:华南理工大学, 2009:20~45
    [10]王斌.非晶颗粒态淀粉的制备及性质研究[D].广州:华南理工大学, 2007:9~50.
    [11]赵永青.非晶淀粉吸附材料的制备与吸附机理研究[D].广州:华南理工大学, 2009:3~60.
    [12]刘莲芳.中国食品添加剂的新品种,新进展[J].食品工业科技,1999,20(3):1~3.
    [13] CALDWELL C G, HILLS F,WURZBURG O B.Polysaccharides derivative of substituted dicarboxylic acids:US,Patent,2661349[P].1953.
    [14]郑茂强,张燕萍,鲁云霞.辛烯基琥珀酸淀粉酯的制备工艺研究[J].食品科技, 2002 (8) : 28~29.
    [15]凌关庭.食品添加剂手册[M].北京:化学工业出版社,2000:883~884.
    [16] CALDWELL C G, HILLS F,WURZBURG O B.Polysaccharides derivative of substituted dicarboxylic acids: US, Patent,2661349[P].1953.
    [17] JEON Y S,VVIWANATHAN A,GROSS R A.Studies of starch esterification: reaction swithalkenyl-succinate sinaqueous slurrysy stems[J]. Starch, 1999, 51(2): 90~93.
    [18] Shogren R.L.,Viswanathan A., Felker F., etal. Distribution of octenyl succinate groups in octenyl succinic anhydride modified waxy maize starch [J].Starch, 2000, 52 (4) : 196~204.
    [19] Tesch S,Gerhards Ch.,Schubert H. Stabilization of emulsions by OSA starches [J].Journal of Food Eng,2002,54(3):167~174.
    [20] Song X Y,He G Q, Ruan H,et al. Preparation and properties of octenyl succinic anhydride modified early indicarice starch[J]. Starch/Starke,2006(58):109~117.
    [21]罗发兴,黄强,扶雄.辛烯基琥珀酸淀粉钠的制备及其结构表征[J].精细化工, 2004,21(6) 42~45.
    [22]王骏涛,刘亚伟.基于响应面法辛烯基琥珀酸淀粉酯制备的优化研究[J].粮油食品与科技,2006,(28):83~89.
    [23] Rajesh B, Rekha S. Process optimization for the synthesis of octenyl succinyl derivative of waxy corn and amaranth starches[J].Carbohydrate Polymers,2006,66:521~527.
    [24]许琼,何国庆,宋晓燕.马铃薯辛烯基琥珀酸淀粉酯的制备研究[J].中国食品学报,2006,6(6):19~24.
    [25]宋晓燕.糯玉米辛烯基琥珀酸淀粉酯的制备及其RVA谱特性分析[J].中国粮油学报,2006,21(1): 55~59.
    [26] Arvind V. Effect of Degree of Substitution of Octenyl Succinate Starch on the Emulsification Activity on Different Oil Phases [J]. Journal of Environmental Polymer Degradation,1999,4 (7): 191~196.
    [27] Shogren R L,Viswanathan A, Felker F,et al. Distribution of octenyl succinate groups in octenyl succinic anhydride modified waxy maize starch[J]. Starch, 2000, 52, 196~204.
    [28] J S Bao, J Xing, D L Phillips,et al. Physical properties of octenyl succinic anhydride modified rice,wheat,and potato starches[J].Food Chem,2003,51,2283~2287.
    [29]胡飞.辛烯基琥珀酸淀粉酯的表面性质[J].食品与生物技术学报,2005,24(2):27~29.
    [30]陈均志,银鹏.微波有机相法制备辛烯基琥珀酸淀粉的研究[J].粮油食品科技, 2004, 12(1):16~18.
    [31] Doungjai T,Sanguansri C.Thermal and pasting properties of native and acid-treated starches derivatized by 1-octenyl succinic anhydride[J]. Carbohydrate Polymers, 2006(66): 258~265.
    [32]柳志强,平立风,李胤,等.辛烯基琥珀酸淀粉酯的制备及其酶法降解的研究[J].食品科学,2007,28(1):110~114.
    [33] Kuentz M,Egloff.P. A technical feasibility study of surfactant-free drug suspensions using octenyl succinate-modified starches [J].European Journal of Pharmaceutics and Biopharmaceutics, 2006(63): 37~43.
    [34]张燕萍,郑茂强.辛烯基琥珀酸木薯淀粉酯在乳化桔子香精中的应用[J].无锡轻工大学学报,2004,23(5):74~77.
    [35] Heacock P M,Hertzler S R,Wolf B. The glycemic, insulinemic, and breath hydrogen responses in humans to a food starch esterified by 1-octenyl succinic anhydride [J]. Nutr. Res, 2004(24), 581~592.
    [36]吴克刚,郑东方,柴向华.辛烯基琥珀酸淀粉微胶囊化浓缩鱼油的研究[J].食品研究与开发,2006.26(3):4~6.
    [37]李艳,郝艳宾,王克建等.利用辛烯基琥珀酸酯化淀粉进行核桃油微胶囊化的研究[J].食品工业科技,2006,27(4):120~122.
    [38]王春杰,徐仲伟,宁正祥.喷雾干燥法制备微胶囊化甜橙油的研究[J].食品工业与发酵,2006,32(9):56~60.
    [39]刘兆丽,曹亚峰,谭凤芝.辛烯基琥珀酸淀粉酯对月见草油的微胶囊化[J].大连轻工业学院学报,2007,26(4):337~341
    [40]林红辉,郑为完,赵伟学等.辛烯基琥珀酸淀粉酯的合成及应用研究[J],食品科学,2008, 29(8):314~317.
    [41]陶宁萍,王锡昌,康吟.微胶囊化宝石鱼油配方的优化及对脂肪酸组成的影响[J].食品科学,2009,30(6):48~51.
    [42]王斌,张本山,刘培玲.乙醇溶剂保护法制备松散化玉米淀粉[J].食品与发酵工业,2007,25~32.
    [43] G.E.P.Box,N.R.Draper.Empirical Model Building and Response Surface, John Wiley & Sons, New York,1987:508~515.
    [44]叶兴乾,张贵平,苏平,等.栗粉的理化与功能特性研究[J].中国粮油学报,2001,(4):43~46.
    [45] Radley J A..The microscopy of starch. In examination and analysis of starch and starch products[M].London:Applied science publishers ltd,1976:1~31.
    [46] Whistler R L,Smith R J, BEmiller J N,et al.Microscopie technique for determing starch granule properties.In Methods in Carbohydrate chemistry[M].NewYork: Academic Press, 1964:233~240.
    [47]铃木繁男,中村道德.淀粉科学实验法[M].东京:1979,121~130.
    [48] Wakelin J H, Virgin H S. Crystal E Development and comparison of two X~ray methods for determining the crystallinity of cotton cellulose[J]. Journal of applied physics.1959, 30:1654~1662.
    [49]裴光文,钟维烈,岳书彬.单晶,多晶和非晶物质的X射线衍射[M].济南:山东大学出版社.1985,447~481.
    [50] Nara S,Mori A,Kamihama T K.Study on relative crystallinity of moist potato starch. Starch[J].1978,30(4):111~114.
    [51] Statton W O.An X-ray crystallinity index methods with application to poly(ethylenetereph)[J].Journal of applied polymer science. 1963,7:803~815.
    [52]沈德言.红外光谱法在高分子研究中的应用[M].北京:科学出版社,1982.
    [53] Manual Book of Brabender Measurement&Control Systems.Brabender OHG Duisbur.
    [54]高嘉安.淀粉与淀粉制品工艺学[M].中国农业出版社,2001.
    [55] Chang C P,Kinura Miho,YamamotoT,Nobe M,Dobashi T,Effect of dispersing medium on permeability of microcapsule membrane.Colloids and Surfaces B:Biointerfaces,2003,30:108~120.
    [56] Hubner H,Buchholz.Microencapsulation.In:Flickinger M C,Drew S W.ed. Encyclopedia of biopro-cess technology:fermentation,biocatalysis, and bioseparation. New York:John Wiley and Sons,Inc,1999.
    [57] Al-Zahrani S M.Controlled-release of fertilizers:modeling and simulation. International Journal of Engineering Science,1999,37:1299~1307.
    [58]张力田,变性淀粉,广州,华南理工大学出版社.31~55.
    [59]罗发兴,黄强,阳元娥,等.辛烯基琥珀酸淀粉酯的制备与应用[J].华南理工大学学报,2003,31(7),82~85.
    [60] Slade Levine H1 Beyond water activity:recent advances based on an alternative approach to the assessment of food quality and safety[J].Crit Rev Food Sci Nutr , 1991 ,30:424~426
    [61] Zanoni Bschivaldi A ,Simonetta R1 A native model of starch gelatinization Kinetics[J ] . J Food Eng,1995,24:25~33
    [62]陆冬梅.微波处理及双酶协同微孔木薯淀粉的制备与机理研究[D].广州:华南理工大学博士学位论文,2004,5
    [64]王航.交联木薯淀粉酶解特性研究[D].广州:华南理工大学硕士学位论文, 2003,6.
    [65]张燕萍.多糖与糖化学分析实验讲义[M].江南大学出版社,2002.
    [66]大连轻工业学院等合编.食品分析[M].北京:中国轻工业出版社,1994.
    [67] Blue EK,Chiu CW.Use of an enzymatic ally converted starch derivative as an encapsulating agent. EP:0,922,449:1998
    [68] PaulettiMS,Amestoy P.Butter microencap sule as affected by composition ofwallmaterial and fat.Journal of Food Science,1999,64:279~282. [ 69] J J Warthesen,Analysis of saccharides in low-dextrose equivalent starch hydrolysates using high-performance liquid chromatography[J].Cereal Chemstry,1984, 61(2):194~195.
    [70]黄立新,不同品种淀粉的分子量分布研究[J].华南理工大学学报,1997(7): 30~34.
    [71]刘晓欣,顾正彪,洪雁.麦芽糊精糖分组成和分子量分布的研究及其对性质的影响[J].食品工业科技,2006,27(2):97~100.
    [72]李明,高红艳,陈卫栋等.HI_CAP100为壁材微胶囊化共轭亚油酸研究[J],粮食与油脂,2006,12,3~6.
    [73] Hogan S A ,Mcnamee B F.Microencapsulating properties of whey protein concentrate 75 [J].Journal of Food Science,2001,66(5):675~680.
    [74]朱丽云,李素芬,邵慧娟.复凝聚喷雾干燥法制备香精香料微胶囊的研究[J].食品科技,2006,4:25~27.
    [75]张春红,黄晓杰.酶改性大豆分离蛋白作为壁材微胶囊化海豹油研究孙焕[J].粮食与油脂,2006~5,3~5.
    [76] JIMENEZ M,GARCIA H S,BERISTAIN C I.Spray-drying microencapsulation and oxidative stability of conjugated linoleicacid[J].European Food Research Technology, 2004,219:588~592.
    [77] YOUNG S L,SARADA X,ROSENBERG M.Microencapsulating properties of whey protein-1:Microencapsulating of anhydrous milk fat[J].Journal of Dairy Science,1993,76(10): 2868~2877.
    [78] YOUNG S L,SARADA X,ROSENBERG M.Microencapsulating properties of whey protein-2: Combination of whey protein with carbohydrates[J].Journal of Dairy Science,1993,76(10):2878~2885.
    [79] Ahn J H, Kim Y P, Lee Y M, et al. Optimization of microencapsulation of seed oil by response surface methodology[J]. Food Chemistry,2008,107(1):98~105.
    [80]储茂全,刘国杰.喷雾干燥法制备载药微球时的形貌与粒度控制[J].化工学报,2004 ,55(11):1903~1907.

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