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第 11 期 张 雄,等: 蔗糖酯表面活性剂化学合成工艺研究进展 ·2199·
phase transfer catalysis[J]. China Surfactant Detergent & Cosmetics Chimie, 1962, 40(12): 2376-2393.
(日用化学工业), 2004, 34(6): 358-393. [39] BRAGA C F, ABREU C A M, LIMA N M, et al. Kinetics of catalytic
[19] WANG L B (王利宾), LI W L (李文林), ZHANG Q (张强), et al. sucrose esterification in aqueous media[J]. Reaction Kinetics and
Synthesis of soybean sucrose polyester catalyzed by phase-transfer Catalysis Letters, 2002, 77(1): 91-102.
catalyse[J]. China Oils and Fats (中国油脂), 2010, 35(1): 32-36. [40] GUTIERREZ M F, SUAZA A, RIVERA J L, et al. Solid-liquid
[20] WANG L B (王利宾), LI W L (李文林), ZHANG Q (张强), et al. equilibria and characterization of the reaction mixture to produce
Synthesis of soybean sucrose polyester under microwave irradiation sucrose palmitate in solvent-free media[J]. Journal of Chemical and
and phase transfer catalyst[J]. Fine Chemicals (精细化工), 2010, Engineering Data, 2019, 64(5): 2052-2061.
27(2): 174-194. [41] POZZI G, FISH R H. Fluoroponytailed crown ethers and quaternary
[21] QIU S M (邱诗铭), TAN Y Q (谭义秋). Synthesis of sucrose ester of ammonium salts as solid-liquid phase transfer catalysts in organic
rosin acid catalyzed by K 2O/Al 2O 3 and Na 3PO 4/MgO solid base[J]. synthesis[J]. Topics in Current Chemistry, 2011, 308: 213-232.
Biomass Chemical Engineering (生物质化学工程), 2018, 52(5): [42] TOTTEN G E, CLINTON N A, MATLOCK P L. Poly(ethylene
41-45. glycol) and derivatives as phase transfer catalysts[J]. Journal of
[22] LIN X S, ZOU Y, ZHAO K H, et al. Tetraalkylammonium ionic Macromolecular Science-Reviews in Macromolecular Chemistry and
liquids as dual solvents-catalysts for direct synthesis of sugar fatty Physics, 1998, 38(1): 77-142.
acid esters[J]. Journal of Surfactants and Detergents, 2016, 19(3): [43] CHANGMAI B, SUDARSANAM P, ROKHUM L. Biodiesel
511-517. production using a renewable mesoporous solid catalyst[J]. Industrial
[23] CHEN J Z, LI Y, CHEN X T, et al. Efficient solvent-free synthesis of Crops and Products, 2020, 145: 111911.
sucrose esters via sand-milling pretreatment on solid-liquid [44] WANG K (王奎), JIANG J C (蒋剑春), SUN K (孙康), et al.
mixtures[J]. Journal of Surfactants and Detergents, 2019, 22(6): Synthesis of sucrose esters over solid base catalyst loaded on
1515-1520. activated carbon[J]. Chemical Reaction Engineering and Technology
[24] XU Y S (徐勇士), HANG F X (杭方学), LI D C (李大成), et al. (化学反应工程与工艺), 2011, 27(2): 139-143.
Synthesis of sucrose laurate via transesterification under ultrasonic [45] SASAYAMA T, KAMIKANDA Y, SHIBASAKI-KITAKAWA N.
irradiation[J]. Chemical Industry and Engineering Progress (化工进 Process design for green and selective production of bio-based
展), 2013, 32(7): 1656-1660. surfactant with heterogeneous resin catalyst[J]. Chemical
[25] WU H D (吴洪达), JIANG Y H (蒋业海), PENG H (彭辉), et al. Engineering Journal, 2018, 334: 2231-2237.
Synthesis of sucrose octanoic acid ester by heteropoly acid [46] WANG L, WANG H, LIU F J, et al. Selective catalytic production of
catalyst[J]. Food Science and Technology (食品科技), 2007, (6): 5-hydroxymethylfurfural from glucose by adjusting catalyst
165-168. wettability[J]. ChemSusChem, 2014, 7(2): 402-406.
[26] BOWER S, WICKRAMASINGHE R, NAGLE N J, et al. Modeling [47] ZHANG Y L, PAN J M, CHEN Y S, et al. Hipes template: Towards
sucrose hydrolysis in dilute sulfuric acid solutions at pretreatment the synthesis of polymeric catalysts with adjustable porous structure,
conditions for lignocellulosic biomass[J]. Bioresource Technology, acid-base strength and wettability for biomass energy conversation[J].
2008, 99(15): 7354-7362. Chemical Engineering Journal, 2016, 283: 956-970.
[27] SU Q Q, HUANG Y L, ZHOU L, et al. Study on direct synthesis of [48] LIU F J, WANG L, SUN Q, et al. Transesterification catalyzed by
sucrose rosinate with rosin and sugar[J]. Technology & Development ionic liquids on superhydrophobic mesoporous polymers:
of Chemical Industry, 2018, 47(4): 31-35. Heterogeneous catalysts that are faster than homogeneous catalysts[J].
[28] THEVENET S, WERNICKE A, BELNIAK S, et al. Esterification of Journal of the American Chemical Society, 2012, 134(41): 16948-
unprotected sucrose with acid chlorides in aqueous medium: Kinetic 16950.
reactivity versus acyl- or alkyloxycarbonyl-group migrations[J]. [49] CAO Y, LI H Q, ZHANG J. Homogeneous synthesis and
Carbohydrate Research, 1999, 318(1/2/3/4): 52-66. characterization of cellulose acetate butyrate (CAB) in 1-allyl-3-
[29] LI S J (李淑君), SONG Z J (宋子娟), CHEN X (陈曦), et al. methylimidazolium chloride (AmimCl) ionic liquid[J]. Industrial &
Synthesis of insecticidal sucrose esters[J]. Fine Chemicals (精细化 Engineering Chemistry Research, 2011, 50(13): 7808-7814.
工), 2005, 22(12): 56-66. [50] HUANG K L, WANG B, CAO Y, et al. Homogeneous preparation of
[30] PLAT T, LINHARDT R J. Syntheses and applications of sucrose- cellulose acetate propionate (CAP) and cellulose acetate butyrate
based esters[J]. Journal of Surfactants and Detergents, 2001, 4(4): (CAB) from sugarcane bagasse cellulose in ionic liquid[J]. Journal of
415-421. Agricultural and Food Chemistry, 2011, 59(10): 5376-5381.
[31] XIE D M (谢德明). Study on synthesis mechanism of sucrose [51] IBINGA S K K, FABRE J F, BIKANGA R, et al. Atypical reaction
polyester[J]. China Oils and Fats (中国油脂), 1999, 4: 58-60. media and organized systems for the synthesis of low-substitution
[32] LIU Q (刘强). Synthesis of sucrose stearate with improved solvent sugar esters[J]. Frontiers in Chemistry, 2019, 7: 587.
method[J]. Fine Chemicals (精细化工), 1987, 24(4): 64-69. [52] CHUN H (淳宏), XIE W L (谢文磊), WANG Y B (王迎宾), et al.
[33] HU P (胡鹏), HU J H (胡健华). The developments of research on Research on synthesis of sucrose esters in ionic liquids solvent[J].
sucrose esters[J]. Journal of Wuhan Food Industry College (武汉食 Cereals & Oils (粮油与油脂), 2008, 21(10): 22-24.
品工业学院学报), 1998, 10(2): 17-22. [53] MUCSI G. A review on mechanical activation and mechanical
[34] ZHOU L (周莉), LIU B (刘波), WANG W (王玮), et al. Preparation alloying in stirred media mill[J]. Chemical Engineering Research &
of sucrose esters by emulsion method[J]. Journal of Shenzhen Design, 2019, 148: 460-474.
University (Science & Engineering) (深圳大学学报:理工版), 1994, [54] ROGACHEV A S. Mechanical activation of heterogeneous
11: 87-91. exothermic reactions in powder mixtures[J]. Russian Chemical
[35] HU P (胡鹏). Synthesis on sucrose esters by solventless method Reviews, 2019, 88(9): 875-900.
(Ⅰ)—Synthesis of SE with solventless method[J]. China Oils and [55] MOSTAFAEI M, GHOBADIAN B, BARZEGAR M, et al.
Fats (中国油脂), 1999, 24(5): 61-64. Optimization of ultrasonic assisted continuous production of
[36] FITREMANN J, QUENEAU Y, MAITRE J P, et al. Co-melting of biodiesel using response surface methodology[J]. Ultrasonics
solid sucrose and multivalent cation soaps for solvent-free synthesis Sonochemistry, 2015, 27: 54-61.
of sucrose esters[J]. Tetrahedron Letters, 2007, 48(23): 4111-4114. [56] HUANG F X, SHI C R, XU Y S, et al. Green synthesis of sucrose
[37] GUTIERREZ M F, RIVERA J L, SUAZA A, et al. Kinetics of the laurate under different ultrasonic frequencies[J]. Sugar Tech, 2017,
transesterification of methyl palmitate and sucrose using 19(3): 241-247.
surfactants[J]. Chemical Engineering Journal, 2018, 347: 877-888. [57] HUANG D, JIANG X, ZHU H, et al. Improved synthesis of sucrose
[38] LEMIEUX R U, MCINNES A G. Preparation of sucrose fatty acid monoesters under ultrasonic irradiation[J]. Ultrasonics
monoesters[J]. Canadian Journal of Chemistry-Revue Canadienne De Sonochemistry, 2010, 17(2): 352-355.