Page 53 - 《精细化工》2020年第11期
P. 53

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.
   48   49   50   51   52   53   54   55   56   57   58