由玉米浸渍水制取肌醇的方法研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
湿法生产玉米淀粉时产生大量的玉米浸渍水,利用在玉米生产淀粉过程中产生的玉米浸渍水为原料,以离子交换树脂吸附法制取肌醇,提高肌醇产品收率、缩短生产工艺流程、减少能量消耗,提高农副产品的利用价值,为玉米深加工开辟新的途径,为我国农业经济的可持续发展做出贡献。
    文中研究了由玉米浸渍水制取肌醇的工艺过程。通过统计分析法对三维图形的曲面进行非线性参数估算,优选了离子交换树脂,对植酸吸附等温线进行了测定,在统计分析的基础上确定了植酸吸附与解吸过程和植酸钠溶液水解过程的最佳工艺条件,对试验结果进行了预测,并研究了肌醇分析的新方法;建立了植酸钠水解动力学模型,并通过三维曲面拟合法对植酸吸附动力学和植酸钠水解动力学进行了研究,此研究成果可以为生产实践提供理论依据。通过本文由玉米浸渍水制取肌醇的新方法与其它方法进行对比分析可知本文研究方法将有更好应用前景。
Inositol is a kind of saturation ring polyols, and its molecular formula is C6H12O6. It exists in all kinds of natural tissue of animal, plant and microorganism. Inositol is one of B-group vitamin, which is used extensively in medicine, food, forage industry and high-grade cosmetics. The main materials of inositol production in China are the by-products produced in the processing of farm products, such as maceration water of corn and rice bran. Accompanying with the improving of living standard, the demand for inositol is increasing continuously and the market price has trended stable. In the national markets, the global demands for inositol are about 6000 ton per year, while the domestic producing capacity is only about 2500 ton per year. China is the main exporter of inositol, about 90% of inositol produced in domestic is exported, but the productive technology is backward, and the productivity is low. Moreover, the research and development of deep processing for inositol are not enough, new productive technology which has high productivity and low cost needs to been developed. Now, in order to improve economic benefit, how to reduce the productive cost and improve technology level and market competitiveness has been a critical task.
    On the basis of investigation and research for productive technology of inositol, the technological process of inositol from maceration water of corn is studied in detail in this paper. At the meantime, technical parameters were optimized. The technological process of inositol production is as follows: adsorption of phytic acid through ion exchange resin, desorption of phytic base to form sodium phytate, concentration of sodium phytate, hydrolysis of concentrated liquid, crystallization and filter to remove disodium hydrogen phosphate, refinement of hydrolyzate, concentration of hydrolyzate, drying, crystallization, and the product inositol is obtained. This new method has lots of advantages, such as wider raw materials, lower cost, higher pure of the product. The main and the innovations in this
    dissertation are as following: (1) In the process of adsorption of phytic acid through ion exchange resin, choose a suitable ion exchange resin is vital for the adsorption. Through experiments the effects of adsorption quantity to the total adsorptive capacity of different ion exchange resins and the diameters of ion exchange resins are determined. Based on the experimental data, suitable anion exchange resins are chosen to adsorb phytic acid. For the adsorptive experiments of phytic acid, the main factors affecting the results are the adsorption space velocity of raw material liquid, the desorptive space velocity of desorbent, the temperature of desorption and the concentration of desorbent. Through orthogonal experiments, the optimum technical conditions are determined as follows. The adsorption space velocity of raw material liquid is 3h-1, the desorption space velocity of desorbent is 2h-1, the temperature of desorption is 35℃, and the concentration of desorbent is 6.5%. With the optimal conditions, the recovery rate of sodium phytate reaches over 98.59%. Before the process of desorption, the temperature of preheating washing water is 40℃~50℃, and after desorption the Ph value of sodium phytate should be adjusted to 7~8 by using ion exchange resin. In the process of concentration of desorbent, vacuum distillation is used to keep the vacuity above 0.08Mpa. The changing curves of space velocity of adsorption to time, lost quantity of resin to the pressure and lost quantity of resin to space velocity of liquid are measured, all these data can be used to guide practical production. (2) In the process of hydrolysis of sodium phytate, orthogonal experiments are used again to determine the optimal technological conditions: the reaction time is 10h, the reaction pressure is 10atm, and the concentration of desorbent is 20%. Though the repeating experiments, the recovery rate of inositol is obtained for above 80%. The operation method for purifying disodium hydrogen phosphate is determined. (3) New calculating method for the recovery rate of inositol is presented, which can reflect accurately the recovery rate of inositol. The method is: 100%the inositol quality in theorythe recovery rate of inositol= the inositol quality actually ×(4) Meanwhile the product inositol produced from maceration water of corn with ion exchange resin method is analyzed through infrared spectrum, and the error-trial dioptric high-performance liquid chromatography is adopted to analyze the product. Through the
引文
[1] 孙灵霞,陈锦屏.肌醇生产、应用研究及前景展望[J].粮食与油脂,2004(11):6~8
    [2] 李亚文.20t/a 肌醇工程可行性研究报告[J].精细化工,1991(8):10~17
    [3] 李亚文.肌醇项目的可行性研究[J].化工商品科技情报,1997(2):13~17
    [4] 杨东辉.开发肌醇产品可行性研究[J].精细化工,1989(6):18~20
    [5] 李亚文.开发肌醇的可行性研究与探讨[J].精细化工,1991(4):5~9
    [6] 刘小勇,钱和,刘建利.肌醇研究近况与展望[J].江苏食品与发酵,2003(4):7~10
    [7] 汪家铭.肌醇生产应用与市场趋势[J].化工技术经济,1995(6):57~58
    [8] 任鸿均.植酸、植酸钙和肌醇[J].化工科技市场,2003(4):25~30
    [9] Laura G. Barrientos, Pushpalatha P.N. Murthy. Conformational studies of myo-inositol phosphates [J]. Carbohydrate Research, 1996, 296: 39-54
    [10]Andrew M. Riley, David J. Jenkins, Barry V.L. Potter. A concise synthesis of neo-inositol [J]. Carbohydrate Research, 1998, 314: 277–281
    [11]中华人民共和国卫生部药典委员会.中华人民共和国药典(二部)[M].北京:人民卫生出版社,1977.160-161.
    [12]Graf E.Application of phytic acid[J].JAOCS,1993(11):1861~1867
    [13]York John D,Guo Shuling,Odom Audrey,et al.An expanded view of inositol signaling [J].Advances in Enzyme Regulation,2001(1):57~71
    [14]Sebastián Cerdán, Roberto Parrilla, Jorge Santoro and Manuel Rico, lH NMR detection of cerebral myo-inositol [J]. FEBS LETTERS, 1985,18(1): 167-172
    [15] De Witte, B.; Patarin, J.; Le Nouen, D.; Delmotte, L.; Guth, J.L.; Cholley, T.Cyclic polyols: A new class of structure-directing agents. Study of inositol in the synthesis of FAU-and LTA-type zeolites [J].Microporous and Mesoporous Materials,1998(1-2):11-22
    [16] G. March, B. M. Simonet and F. Grases. Phytic acid level in infant flours. Journal of Chromatography.B [J].Bimedical Sciences and Applications. 2001,757(2).-247-255
    [17]C.I. Febles, A. Arias, A. Hardisson, C. Rodríguez-álvarez and A. Sierra . Phytic acid in wheat bran affects colon morphology, cell differentiation and apoptosis [J]. Food Chemistry.2001,74(4).-437-44
    [18]Vucenik I,Zhang Z.S,Shamsuddin A.M.IP6 in treatment of liver cancer Ⅱ[J].Anticancer Res.,1998(18):4091~4096
    [19]Steiner S,Lester R.L.Studies on the diversity of inositolcontaining yeast phospholipids:incorporation of 2-deoxyglucose into lipid [J].J Bacteriol, 1972(1):81~88
    [20]Levine J,Chengappa K.N,Reddy R.Acute myo-inositol enhances swimming activity in goldfish [J]. J.Neural Transm,1999(5-6):41
    [21] 五洲咨询中心.肌醇市场调研报告[M].2005:11~21
    [22]庄海燕.植酸肌醇联产工艺的可行性研究[J].食品工业科技,2004,3:114~116
    [23]David Chapon, Christian Husson.Solution properties of trivalent lanthanide trinuclear complexes with ligand 1,3,5-triamino-1,3,5-trideoxy-cis-inositol [J].Journal of alloys and compounds,2001(323-324):128-132
    [24]李好管,朱凌皓.肌醇的技术与市场[J].化工生产与技术,2001(2):7~9
    [25]Mattias Fredrikson, Marie Larsson Alminger, Nils-Gunnar Carlsson. Phytate content and phytate degradation by endogenous phytase in pea (Pisum sativum) [J]. JOURNAL OF THE SCIENCE OF FOOD & AGRICULTURE.-2001.81(12):1139-1144
    [26]C. I. Febles, A. Arias, A. Hardisson, C. Rodríguez-Alvarez and A. Sierra. Phytic Acid Level in Wheat Flours [J]. Journal of Cereal Science. 2002, 36(1):19-23
    [27]J. G. March, B. M. Simonet and F. Grases. R. P. SARTINI and C. C. OLIVEIRA. Journal of Chromatography.B [J]. Bimedical Sciences and Applications.2001, 757(2):247-255
    [28]Lori Oatway ; Thava Vasanthan ; James H. Helm. PHYTIC ACID [J]. Food Reviews International.2001,17(4):419 –431
    [29]Rosa M García-Estepa, Eduardo Guerra-Hernández. Phytic acid content in milled cereal products and breads [J]. Food Research International.1999,
    32(3):217-221
    [30]Ermanno Vasca, Stefano Materazzi. Biochemical and Molecular Characterization of a Mutation That Confers a Decreased Raffinosaccharide and Phytic Acid Phenotype on Soybean Seeds[J]. Fresenius’Journal of Analytical Chemistry. 2002,374(1).173-178
    [31] Ramakrishnan S,Sulochana K N,Punitha m R. Two newfunctions of inositol in the eye lens:antioxidation andantiglycation and possible mechanisms[J]. Indian J.Bioche m.Biophys.,1999,36(2) :129~133
    [32]Philippy B Q,Johnston M R. Determination of phytic acid infoods byion 一chromatography with post 一column derivatization[J].J .Food Sci.,1985, 50:541~542
    [33]余以刚.浅谈肌醇生产关键技术[J].粮食与饲料工业,2003,7:38~39
    [34]邵建华.从米糠中提取菲汀并制取肌醇[J].化学世界,1990,11:518~521
    [35]小川洋.肌醇的制造方法.日本,日本特许公报.COTC35/16 昭64-96439.1987-05-02
    [36] 王树清,李健秀,景丽洁,邢永恒.由玉米浸渍水制取肌醇新工艺研究[J].吉林化工学院学报,1996,3:8~11
    [37] 张书文,杨桂珠.用离子交换树脂制取高纯度肌醇的新工艺[J].精细化工,1994,4:25~28
    [38]雷得漾,伍先云.化工小商品生产法(第十一集)[M].长沙:湖南科学技术出版社,1991.159~163
    [39]刘志炯.制取高纯度肌醇的离子膜法及其设备.CN:1159441,1997.09.17
    [40]王克军.常压分解法生产肌醇的工艺.CN:1076425A,1993.6.23
    [41]喻圣梅.生产肌醇的低压催化水解法.CN:1207382A,1999.2.10
    [42]Sung-Kee Chung, Yong-Uk Kwon. Practical synthesis of all inositol stereoisomers from myo-inositol [J]. Bioorganic & Medicinal Chemistry Letters, 1999(9): 2135-2140
    [43]Adilson David da Silva, Aloisio Antonio A. Benicio and Sttphane D. Gero. Enantioselective synthesis of some 6-deoxy-halodeoxy inositol derivatives [J]. Tetrabedron Letters, 1999, 40:6531-6534
    [44]Rajindra Aneja, Sarla G. Aneja. Practical unequivocal synthesis of phosphatidyl-myo-inositols [J]. Tetrahedron Letters, 2000, 41: 847–850
    [45]Tomas Hudlicky, Nora Restrepo-Sánchez , Pierre D. Kary, Luz M. Jaramillo-Gómez. A short, stereoselective synthesis of neo-inositol [J]. Carbohydrate Research, 2000,324: 200–203
    [46]Venerando Pistarà, Pier Luigi Barili, Giorgio Catelani, Antonino Corsaro, Felicia D’Andrea and Salvatore Fisichella. A new highly diastereoselective synthesis of epi-inositol from D-galactose1 [J] . Tetrahedron Letters. 2000, 41: 3253–3256
    [47]Manash P. Sarmah, Mysore S. Shashidhar. Sulfonate protecting groups. Improved synthesis of scyllo-inositol and its orthoformate from myo-inositol[J]. Carbohydrate Research, 2003, 338: 999–1001
    [48]Watanabe, Yutaka .Synthetic strategy and total synthesis of inositol phospholipids in signal transduction [J].Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry,1997(8):705-713
    [49]A.M.P. van Steijn, H.A.M. Willems, Th. de Boer, J.L.T. Geurts and C.A.A. van Boeckel. Synthesis of myo-inositol-1-phosphatase Inhibitors in Which the Phosphate Group is Replaced by Less Polar Groups[J]. Bioorganic & Medicinal Chemistry Letters, 1995, 5(5): 469-474
    [50]Greiner R , Carlsson N. G , Alminger M . L . Stereospecificity of myo-inositol hexakiphosphate dephosphorylation by a phyate-degrading enzyme of Escherichia coli [J]. Journal of Biotechology , 2000(1):53~62
    [51]Justin Anne-Marrie , et al . Synthetic capacity of arabidopsis phosphatidylinositol synthase lexpressed in Escherichia coli [J]. Molecular and cell Biology of Lipids , 2003 (1-2):52~60
    [52]Youn W . Har , Antenia G , W . Ilferd . Phydrolysis in soybean and cottonseed meals by a sperillus ficuuym phystase [J]. Journal of Agricultural and Food Chemistry,1988(2):259~262
    [53]White M . J ,Hirsch J . P ,Henry S . A . The OPII gene of saccharomyces cerevisiae , a negative regulator of phospholipid biosynthisis , encodes a
    protein containing polyglutamine tracts and a leucine zipper [J] .J . Biol .
    Chem. ,1991(2):72
    [54]Eisenberg F ,Bolden A. H , Loewus F . A . Inositol formation by cyclization of glucose chain in rat testis [J]. Biochem . Iophys . Res . Commun. , 1964(14):24
    [55]Cecilia Vitelio, Ana Bellomo, Margarita Brovetto, Gustavo Seoane and David Gonzalez. Concise chemoenzymatic synthesis of epi-inositol[J]. Carbohydrate Research, 2004,339: 1773–1778
    [56]Anil K. Tyagi and Ram A. Vishwakarma. Recombinant Bacillus Subtilis Whole Cell System as a Catalyst for Enzymatic Synthesis of Cyclic Inositol Phosphate[J]. Tetrahedron Letters, 1998, 39: 6069-6072
    [57]罗晓明,蒋雪薇. 离子交换树脂法制取高纯度肌醇新工艺[J]. 河南化工,2003(5):13~15
    [58]Ralf Greiner, Marie Larsson Alminger. Purification and characterization of a phytate-degrading enzyme from germinated oat (Avena sativa) [J]. JOURNAL OF THE SCIENCE OF FOOD & AGRICULTURE.-1999.79(11):1453-1460
    [59]刘家祺.分离过程[M].北京.化学工业出版社,2002:293~330
    [60]李健秀,王树清,景丽杰,邢永恒.吸附法制取植酸钠的工艺研究[J].化学世界,1998,10:518~519
    [61]李健秀,王树清,景丽杰,邢永恒.植酸钠水解制取肌醇新工艺研究[J].化学世界,1998(11):283~285
    [62]朱炳辰.化学反应工程(第三版)[M].北京.化学工业出版社,2001:23~33
    [63]R.柯宁.离子交换树脂[M].北京.科学技术出版社,1960:5~32
    [64]钱庭宝,刘维琳.离子交换树脂应用手册[M].天津.南开大学出版社,1989:44~54
    [65] 王树清,高崇.由脱脂米糠浸泡液制备植酸钠工艺[J].化工时刊,2003,3:43~45
    [66]任露泉.试验优化设计与分析[M].吉林科学技术出版社,2001
    [67] 张旭东.植酸的应用[J].化学世界,1989(6):274
    [68] R. P. SARTINI and C. C. OLIVEIRA. A New Strategy for Exploiting Ion Exchange in Sequential Injection Analysis: In-Line Phytic Acid Separation/Determination in Foods as
    an Example [J]. Analytical Sciences.2002,18(6):675-680
    [69] Stephen P.J. Brooks, Donald Oberleas. Proposed Phytic Acid Standard Including a Method for Its Analysis [J]. Journal of AOAC international.2001,84(4):1125-1129
    [70] J. G. March, B. M. Simonet and F. Grases. Kineticˉturbidimetric determination of phytic acid by sequential injection analysis [J]. Analytica chimica acta.2000,409(1-2):9-16
    [71] Phil S. Kerr, and Scott A. Sebastian . Determination of phytic acid by gas chromatographyˉmass spectroscopy: application to biological samples [J]. Plant Physiology.2002,128(2).-650-660
    [72] J. G. March, B. M. Simonet. Conformational Inversion Processes in Phytic Acid: NMR Spectroscopic and Molecular Modeling Studi. The Analyst.1999,124(6).-897 –900
    [73] 唐启令,张岩,宫钦红.正交实验法优选肺炎颗粒水提取工艺[J].中国药师,2004,8:603~604
    [74]薛明强,吴康,张振江.离子交换树脂最适再生条件探索[J].苏州大学学报(自然科学版),1994(4):77~80
    [75]周衡.离子交换树脂再生方法的研究[J].黄金,1994(12):12~14
    [76]王本富,赵志民,苗爱东,冯冰,张伟,商晓英.离子交换树脂再生条件的优化[J].中国医院药学杂志,1997(6):257~260
    [77]叶华进,吴小彤.离子交换树脂再生的工艺探讨[J].浙江化工,1997(2):44~45
    [78]刘丽箐,张成敏,薛新望.离子交换树脂再生方法的改进[J].海峡预防医学杂志,2000(5):44~45
    [79]C. I. Febles, A. Arias, A. Hardisson, C. Rodríguez-Alvarez and A. Sierra. Phytic Acid Level in Wheat Flours [J]. Journal of Cereal Science.2002, 36(1):19-23
    [80]Tadao NAKANO, Toshio Jon. Purification and Characterization of Phytase from Bran of Triticum aestivum L. cv. Nourin #61 [J]. FOOD SCIENCE AND TECHNOLOGY RESEARCH.-1999.5(1):18-23
    [81]Rosa M García-Estepa, Eduardo Guerra-Hernández. Phytic acid content in milled cereal products and breads [J]. Food Research International.1999, 32(3):217-221
    [82] 罗晓明,蒋雪薇. 离子交换树脂法制取高纯度肌醇新工艺[J]. 河南化工,2003(5):13~15
    [83]余以刚.浅谈肌醇生产关键技术[J].粮食与饲料工业,2003,7:38~39
    [84]孟祥考.提高肌醇收率的工艺技术研究[J].河北化工,2003,3:27~28
    [85]肇立春.关于肌醇生产工艺中提高产率与质量的几点思考[J].粮食与饲料工业,1999,11:50
    [86]白姝,李玉龙,孙彦,胡宗定.乳酸的离子交换动力学模型[J].天津大学学报,1995(5):565~568
    [87]赵肖为,郑重鸣,杨深,岑沛霖.柠檬酸在D354 树脂上的离子交换研究[J].离子交换与吸附,1996,12(2):97-104
    [88]周定,王建龙,侯文华,刘建斌.离子交换树脂提取柠檬酸的研究[J].1994(5):99~102
    [89]董文明,王卫,陶祖贻.富里酸在强碱性阴离子交换树脂201x7 上的吸附研究[J].离子交换与吸附1994, 10 (4):311~315
    [90]董彦杰,盖轲.W—305C树脂吸附铌的性能及动力学研究[J].湿法冶金,2004(1):43~46
    [91]李希明,张建兵,柯家骏.F-950 哌啶树脂吸附金的动力学研究[J].黄金,1996(3):34~37
    [92]李希明,张建兵,柯家骏.P-950 哌啶树脂吸附把的动力学研究[J].化工冶金,1996(4):300~303
    [93]刘峙嵘,郭锦勇,周祥友.P951 树脂吸附铂的动力学性质[J].山东冶金,1997(2):25~27
    [94]董彦杰. D 296 大孔径阴离子交换树脂吸附钽的性能及动力学研究[J].1997(4):305~307
    [95]董彦杰,刘建宁.D290 大孔阴离子交换树脂吸附钽的性能及动力学研究[J].1998(3):200~204
    [96]董彦杰.707 阴离子交换树脂吸附钽的性能及动力学研究[J]. 湿法冶金,1997(1):31~33
NGLC 2004-2010.National Geological Library of China All Rights Reserved.
Add:29 Xueyuan Rd,Haidian District,Beijing,PRC. Mail Add: 8324 mailbox 100083
For exchange or info please contact us via email.