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Ứ Ƣ Ứ -KETO-L-GULONIC TRONG -2015 -2015 Ứ Ƣ Ứ -KETO-L-GULONIC TRONG uy t uy t v s ƣ 01.19 ƣ u GS.TSKH Mai Tuyên -2015 T ố , ố ố ố N , T L I CAM ƠN ủ Lyon é ĩ ỗ , Tôi xin ỗ quí KÝ Ữ Ắ (*) AAS Atomic Absorption Spectrophotometric - P ổ BET Brunauer Emmett Teller - Ph ơ DTA Differential Thermal Analysis - P EDX Energy Dispersive X-ray spectroscopy- P ổ HPA Acid 12- phosphotungstic (H3PW12O40) HPLC High Performance Liquid Chromatography - P ỏ IR Infrared Spectroscopy- P ổ KPW M ố Me-2KLG Methyl 2-keto-L-gulonat MeOH Me Methanol Methyl SBET D SEM Scanning Electron Microscopy - K SNDH Enzym Sorbosone Dehydrogenase TEM Transmission Electron Microscopy - K TGA Thermal Gravimetric Analysis - P TPD-NH3 Temperature Programmed Desorption NH3 XRD X-Ray Diffraction - P ổ XT/NL Xúc tác/ N ZS Zirconi sulfat hóa (SO42-/ZnO2) 13 Proton Nuclear Magnetic Resonance - P ổ 13 C C-NMR 2-KLGA - ắ X ắ ặ ễ ể ể ơng pháp ọ N X Acid 2-keto-L-gulonic “ ủ lu ” ý – phosphotungstic (KxH3-xPW12O40) (*) t ẳ & v t u t theo T ý Giá ị ằ 3.1 T T -KLGA ố o ú acid ắ ố ị eton ố T- ố 33 ú K Dữ ố ỷ T-C- sulf carbon sulf ú ú KxH3-xPW12O40 PA K2,25H0,75 ổ ion 50 K 3.8 D 39 Vị ú ố 68 ố ặ ú MxH3-xPW12O40 ú ổ ể K N ằ 92 B ng 3.11 Đ chuyển dịch hóa học c a nguyên t C K ị 92 + ổ 71 74 ọ 63 66 + 47 T-C- sulf 48 ú acid TPD-NH3 26 ặ ố 3.6 23 ể D 96 ể Anh 97 Hình 1.1 Hình 1.2 Hình 1.3 Sơ Sơ Dạ Hình 1.5 Hình 1.6 Hình 1.7 Hình 2.1 Hình 2.2 Dị Sơ Đ ọ acid ascorbic ố hai ổ vitamin C ổ -KL A L-sorbose zirconi hydroxide ú K ( ) ú D w ( ) ú K ú H3PW12O40.6H2O ạ ể ù ễ Đ Hình 2.4 Các ẳ Sơ ị ố , , N, S, O P ổ DX ú T-C-sulf ể S M ú T-C-sulf P ổ IR TT-C-sulf Đ ể -KL A ú A BT-C-sulf T A DTA Z O(O )2 T M Z O(O )2 XRD ú ZS- ặ P ổ ú ZS- ặ S M ú ZS- ặ Gi TPD-NH3 c a xúc tác ZS- ặ ỷ XT NL ú ZS- ặ ể -KLGA Đ ể 2-KLGA xúc tác ZS, ZS- ặ Amberlyst-15 Đ ể -KL A ú ZS- ặ P ổ IR ZS- ặ tái Hình 3.2 3.3 3 3.7 3.8 Hình 3.9 Hình 3.10 Hình 3.11 3 Hình 3.14 3 ị ễ ở 3 ể P theo P/P0 W (P0 P) Hình 2.3 ổ ion ố ỏ ú tác Đ S M ẳ ú ọ ị ú 3PW12O40 N2-BET ú K2,25H0,75 K2,21H0,79, K2,25H0,75 K2,45H0,55 7 17 20 21 21 33 34 38 39 41 48 49 49 51 52 53 53 54 55 55 57 58 59 60 61 62 64 65 Hình 3.19 ú K2,25H0,75 Hình 3.20 TPD-NH3 úc tác HPA Hình 3.21 TPD-NH3 ú K2,25H0,75 Đ ể -KL A ú KPW PA 3 P ổ XRD ú PA, K2,25H0,75, Rb2,24H0,76 2,26H0,74 P ổ IR ú PA, K2,25H0,75, Rb2,24H0,76 Cs2,26H0,74 Hình 3.25 M ú K Hình 3.26 S M ú K2,25H0,75, Rb2,24H0,76 Cs2,26H0,74 Đ ể -KLGA ú K2,25H0,75; Rb2,24H0,76 2,26H0,74 Hình 3.28 ỷ ú ể 2-KLGA Hình 3.29 ỷ 2-KLGA /methanol ể 2-KLGA Hình 3.30 ể 2-KLGA Hình 3.31 ố ể 2-KLGA Hình 3.32 Đ ể -KL A ú , ú , ọ ỏ ú 33 ú K2,25H0,75 ba t ú 33 P ổ ú K2,25H0,75 ester -KLGA Hình 3.35 Sắ ý PL ẩ =7 Hình 3.36 Sắ ý PL n ố 3,3 ú Hình 3.37 Sắ ý PL M - KL 3, ú Hình 3.38 Sắ ý PL ẩ =9 Hình 3.39 Sắ ý PL ẩ = o Hình 3.40 Sắ ý PL ẩ C o Hình 3.41 Sắ ý PL ẩ 50 C o Hình 3.42 Sắ ý PL ẩ C Hình 3.43 ễ X ẩ Hình 3.44 P ổ ẩ 13 Hình 3.45 P ổ C-NMR ẩ natri ascorbat Hình 3.46 ễ X Hình 3.47 P ổ 13 Hình 3.48 Phổ C-NMR c a ascorbic 65 67 67 70 72 73 73 75 76 77 78 79 80 81 83 83 84 85 86 86 87 88 88 89 90 91 91 94 94 95 ……………… … … …………………………… C ƣơ ……………… ………………… … Sơ …………………………………………… 1.2 -keto -L…………………….… 1.2.1 M ố -keto-L……………… Q ổ acid 2-keto-L…………… P ester hóa ……………………………………………… Đặ ể ester…………………………… ester hóa…………………………… 33 ố ester ………… P ester ú ị ể… ……… …… Xú ị ể…………………………………………… Xú ………………………………… 1.4.2 Xú z (SO42-/ZrO2)… ……… … … Xú ị PA … … ……………… ƣơ Ự …………………………….… ……… Tổ ú ……………………………………… ……… Tổ ú ………… … …… Tổ ú zirconi ……… ……… … 2.2.3 Tổ ú ị ……………………… … …………………… ặ ú …………………… P (T A – DTA)……………… 2.2.2 Ph ễ X (XRD)… ………… …… 2.2.3 P ổ (IR)… ………… …… P ể (S M)… ……… …… P ể (T M)…………… P ổ ắ X ( DX)…… 2.2.7 Ph ẳ ( T) … P ổ (AAS)……… …… P ố , ,N,S,O…………… 2.2.9 P g N (TPD- NH3)……………………………………………………… 4 6 9 10 11 12 12 17 19 29 29 29 29 31 32 32 33 35 36 37 37 37 40 41 41 P NH3 2.3 uá trình ẩ ………… ………… 2.3.1 Q …………………………………… … Q …………………………… ……… 2.3.3 T ……………………………………… ẩ ………………………… P ắ ý ỏ ( PL )…… …… 13 P ổ C (13C-NMR) ƣơ K ………………………… 3.1 Xúc tác carbon …………………………………… 3.1.1 Đặ ý ú carbon … 3.1.2 H ú T- ester 2-KL A………………………………… 3.2 Xúc tác zirconi ……………………………… ……… 3.2.1 Đặ ý Z O(O )2…………… 3.2.2 Đặ ý ú zirconi sulfat hóa …… 3 ú SO42-/ZnO2…… …… … 3 Xú ị PA…………………………… … 3 Tổ ặ ú …………… 3.3.2 Nghiê ester -KL A methanol ú K2,25H0,75………………………………………………… N -keto-L-gulonat 3.4.1 …………… ……………… …………… 3 P ú ẩ T ẩ …… A ố T …………………… 3 Đ ẩ ……………… K ………………………………………………………… Ữ Ƣ Ứ ………… Ủ ………… K Ã Ố… K …………………… …………………… 10 43 44 44 44 45 45 45 46 47 47 47 50 51 51 53 56 60 60 77 84 84 88 90 92 92 93 93 98 100 101 102 104 K Đ ổ ú ặ , ), - , ẩ ẩ ( KL A ù 93,3%) ú , %) K A -15 ( ú ( ú -KL A Đ ổ ặ ú z V z N , , ặ ơ -KLGA ẩ 99,9%) K ol ( ú ẵ , ẹ N ố ể ổ ú ị ị ữ ù - -KL A ú K2,25H0,75PW12O40, ỏ ọ , ú, ố ò Đ ú K , ố ú ý AAS, BET, XRD, IR, TEM, SEM-EDX, TPD-NH3, T A-DTA, N ể ặ ổ ọ ữ ỷ o ổ -KL A XT NL = , o , ỷ ú K2,25H0,75PW12O40 -KLGA/methanol = 1/24 (mol/mol), , ố ò 98 ú Đ ị - - ể -Lo -L- , , + ổ ể ể ; , ẩ 99 = 9; o Ữ Ƣ Ứ N carbon sulfonat tác acid ị z ú r hóa nói ú ể 100 ú Ủ L ố ể ổ ú ị ú - acid K2,25H0,75PW12O40, ổ -L- Đ hóa acid 2-keto-L-gulonic ú ị ể, ặ ố ú K2,25H0,75PW12O40 ố , ố ữ S I ữ Đ V ằ N ổ ẩ ị Đ ố , , ẩ 101 ẩ K Vũ T ị T D ,P Q M T ,N ễ T ịT T ắ , ,( ú hóa acid 2-keto-L- Ã ị Ố M ,T Tọ , ) N ể SO42-/ZrO2 , 49(5AB), 276-279 Tâm, N ( ễ T ịT ) N “ gulonic P M ,P M T , Vũ T ị T ” -keto-L- , 50(5A), 297-300 M T , Vũ T ị T ,N , Vũ T ị T ễ T ịT ,( ụ ổ ò , Vũ T ị T Tọ ,( ,N ễ T ịT M ,P ị ụ ,N M ,N ễ T ịT ú T , , Đ Mạ ể ể ú T , – II ẩ Vũ T ị T M ) N Đ M ,P Tọ , , 3(13), 1-3 T M ,T ) N sorbitol – I Q ú , ọ , 4(14), 15-18 ,N ù ,( ễ T ịT ) V ò –I ắ , 7, 41-45 Thu Ha Vu Thi, Hang Thi Au, Tuyet Mai Thi Nguyen, Minh Tu Pham, Tam Thi Bach and Hong Nhan Nong, (2013) Esterification of 2-keto-Lgulonic acid catalyzed by a solid heteropoly acid Catalysis Science & Technology, 3, 699-705 ằ ữ - Vũ T ị T ,N Q ố T P ú -L- ễ T ịT ị Số M ,T 33 QĐ-S TT, 102 ị Tọ T ,P M T , Vũ T ị T ( , ) N 2-keto-L-gulonic ù N ọ Q ổ , N ú , ị – ụ 3, 20-25 103 , K Food Standards Agency (UK), Retrieved 2007-02-19 Giovanno J.J (2007) A new plant gene in the pathway to vitamin C Proceedings of the National Academy of Sciences, 104, 9109–9110 U.S Patent, 6573400 (2003) Milton K (2003) Micronutrient intakes of wild primates: are humans different Comp Biochem Physiol a Mol Integr Physiol, 136(1), 47-59 Linus Pauling (1970) Evolution and the need for ascorbic acid Proceedings of the National Academy of Sciences, 67(4), 1643–8 PMID5275366 Linus Pauling (2004) Researchers Claim RDA For Vitamin C is Flawed PR Newswire July 2004 Retrieved on 2007-02-20 Sebastian J P., Arie K., Yaohui W et al (2003) Vitamin C as an Antioxidant: Evaluation of Its Role in Disease Prevention Journal of the American College of Nutrition, 22(1), 18-35 Cavani F (1998) Heteropolycompound-based catalysts: A blend of acid andoxidizing properties Catalysis Today, 41, 73-86 U.S Patent, 5744634, (1998) 10 U.S Patent, 4877735, (1989) 11 Lana Amine Nassif (1997) The production 0f 2-keto-L-gulonic Acid by Different Gluconobacter Strains, Master of science Faculty of Virginia Polytechnic Institute and State University 12 U.S Patent, 4935359, (1990) 13 Zhang Yang, Ma Li, Yang Jichu (2004) Kenitics of esterification of lactic acid with ethanol catalyzed by cation-exchange resins Reactive & Functional Polymers, 61(1), 101-114 14 Ma Li, Zhang Yang, Yang Jichu (2005) Purificatin of lactic acid by heterogeneous catalytic distillation using ion-exchange resins Chinese Journal of Chemical Engineering, 13(1), 24-31 15 Harmer M.A., Sun Q (2000) Solid acid catalysis using ion-exchange resins Applied Catalysis A- General, 221(1/2), 45-62 16 Alime (2007) Liquid-phase esterification of acetic acid with isobutanol 104 catalyzed by ion-exchange resin Reactive & Functonal Polymers, 67 (12),1458-1464 17 Joachim Veiets (1998) Process for Producing 2-keto-L-gulonic Acid Ester [P] US, 5744634, 04-28 18 Andeas Böttcher, Wolfram Burst (2003) Preparation of 2-keto-Lgulonic Esters [P] US, 6573400, 01-03 19 Wang Q.G (2002) Study on the methylgulonate by ion exchange resin catalyst Hebei Chemical Engineering and Industry, (2), 16-19 (in Chinese) 20 Bhaskar K.A., Steven T.P (2002) Process for the Prearation of Ascorbic Acid [P] US, 6476239,01-05 21 Oklobdzija M (1999) Method for Producing Ascorbate [P] WO, 9903853, 01-28 22 Tang Qinghai (2003) Studies on Esterification and Conversion Technology of Gulonic Acid [D] School of Chemical Engineering and Technology, Tianjin University, Tianjin, (in Chinese) 23 Xiao Yan Liu, Miao Huang, Hai Long Ma et al (2010) Preparation of a Carbon Based Solid Acid Catalyst by Sulfonating Activated Carbon in a Chemical Reduction Process, Molecules, 15, 7188-7196 24 Masaaki Kitano, Keisuke Arai, Atsushi Kodama et al (2009) P S P w S fi Surface Area, Catal Lett, 131, 242–249 25 Feng Peng, Lei Zhang, Hongiuan Wang et al (2005) Sulfonated carbon nanotubes as a strong protomic acid catalyst, Letters to the Editor/ Carbon, 43, 2397-2429 26 Xunhua Mo, Edgar Lotero, Changqing Lu et al (2008) A Novel Sulfonated Carbon Composite Solid Acid Catalyst for Biodiesel Synthesis, Catal Lett, 123, 1–6 27 Titantian Li, Zhilong Li, Wei Li et al (2013) Preparation and characterization of biomass carbon-based solid acid catalyst for the esterification of oleic acid with methanol, Bioresource Technology, 133, 618-621 28 Win Win Mar and Somsook E (2012) Sulfonic functionalized Carbon catalyst for esterification of high free fatty acid, Procedia Engineering, 32, 212-218 105 29 Atsushi Takagaki, Masakazu Toda, Mai Okamura et al (2006) fi , Catalysis Today, 116, 157- 161 30 Coma A., Fornes V., Juan-Rajadell M.I et al (1994) Influence of preparation conditions on the structure and catalytic properties of ZrO2/SO42- superacid catalysts Appl.Catal., A: General, 116, 151-156 31 Teterycz H., Klimkiewicz R., Laniecki M (2003) The role of Lewis acidic centers in stabilizied zirconium dioxide Appl.Catal., A: General 249, 313 - 326 32 Tichit D., Hami D.E., Figuegas F (1996) Preparation and anion exchange properties of zirconia Appl Catal., A: General, 145, 195-210 33 Ertl G., Knozinger H., Weikamp J (1997) Handbook of Heterogeneous Catalysis, Wiley – VCH, Weinheim, 5, 2184 34 Yori J.C., Pareta J.M (1996) n - butane isomerization on metal promoted sufated zirconia Appl Catal., A: General, 147, 145-157 35 Kazushi Arata (1996) Preparation of superacids by metal oxides for reaction of butanes and pentanes Appl.Catal., A: General, 146, 332 36 Jing Qui Li, Farcasu D (1995) Prepararation of sulfated zirconia catalysts with improved control of sulfur content, Appl Catal., A General, 128, 97-105 37 Dalip Kumar, Braja Gopal Mishra (2006) Sulfated zirconia and phosphotungstic acid catalyzed synthesis of some biologically potent heterocyclic compounds Bullentin of Catalysis Society of India,5, 121127 38 Teterycz H., Klimkiewicz R., Laniecki M (2003) The role of Lewis acidic centers in stabilizied zirconium dioxide Appl.Catal., A: General, 249, 313-326 39 Bhorodwaj S.K., Dutta D.K (2011) Activated Clay Supported Heteropoly Acid Catalysts for Esterification of Acetic Acid with Butanol Applied Clay Science, 53(2), 347-352 40 Pizzio L.R., Blanco M.N (2003) Isoamyl Acetate Production Catalyzed by H3PW12O40 on Their Partially Substituted Cs or K Salts Applied Catalysis A: General, 255(2), 265-277 41 Izumi Y., Hasebe R and Urabe K (1983) Catalysis by Hetero Geneous Supported Heteropoly Acid Journal of Catalysis, 84(2), 402 106 42 Haber J , Pamin K., Matachowski L et al (2002) Potassium and Silver Salts of Tungstophosphoric Acid as Catalysts in Dehydration of Ethanol and Hydration of Ethylene Journal of Catalysis, 207(2), 296-306 43 Alhanash A., Kozhevnikova E.F and Kozhevnikov I.V (2010) GasPhase Dehydration of Glycerol to Acrolein Catalysed by Caesium Heteropoly Salt Applied Catalysis A, 378(1), 11-18 44 Misono M (2009) Recent Progress in the Practical Applications of Heteropoly Acid and Perovskite Catalysts: Catalytic Technology for the Sustainable Society Catalysis Today, 144(3,4), 2009, 285-291 45 Yang W., Billy J., Taarit Y.B et al (2002) H3PW12O40 Supported on Cs Modified Mesoporous Silica: Catalytic Activity in n-Butane Isomerisation and in Situ FTIR Study: Comparison with Microporous CsxH3− PW12O40 Catalysis Today, 73(1,2), 153-165 46 Sepúlveda J.H., Yori J.C., Vera C.R (2005) Repeated Use of Supported H3PW12O40 Catalysts in the Liquid Phase Esterification of Acetic Acid with Butanol Applied Catalysis A: General, 288(1), 18-24 47 Misono M (2005) A View on the Future of Mixed Oxide Catalysts: The Case of Heteropolyacids (Polyoxometalates) and Perovskites Catalysis Today, 100(1,2), 95-100 48 Rao K.N., Reddy K.M., Lingaiah N et al (2006) Structure and Reactivity of Zirconium Oxide Supported Ammonium Salt of 12Molybdophosphoric Acid Catalysts Applied Catalysis A: General, 300(2), 139-146 49 Kuang W., Rives A., Fournier M et al (2003) Structure and Reactivity of Silica Supported 12-Tungstophosphoric Acid Applied Catalysis A: General, 250(2), 221-229 50 Okuhara T., Mizuno N and Misono M (1996) Catalytic Chemistry of Heteropoly Compounds Advances in Catalysis, 41, 113 51 Kozhevinkov V., Matveev K.I (1983) Homogeneous Catalysts Based on Heteropoly Acids Applied Catalysis A: General, 5(2), 135 52 Kharat N., Pendleton Ph., Badalyan A et al (2006) Oxidation of Aldehydes Using Silica Supported Co(II) Substituted Heteropolyacid Journal of Molecular Catalysis A: Chemical, 175(2), 139-146 53 Bachiller-Baeza, Anderson J.A (2004) FTIR and Reaction Studies of the Acylation of Anisole with Acetic Anhydride over Supported HPA Catalysts Journal of Catalysis, 228(1), 225-233 107 54 López Salinas E., Hernández Cortéz J.G., Schifter I et al (2000) Thermal Stability of 12-Tungstophosphoric Acid Supported on Zirconia Applied Catalysis A: General, 193(1), 215-225 55 Choi S., Wang Y., Nie Z et al (2000) Cs Substituted Tungstophosphoric Acid Salt Supported on Mesoporous Silica Catalysis Today, 55(1), 117124 56 Kim J.H., Shul Y.G., Han H (2006) Synthesis of Heteropolyacid (H3PW12O40)/SiO2 Nanoparticles and Their Catalytic Properties Applied Catalysis A: General, 299(1), 46-51 57 Haber J., Pamin K., Matachowski L., Mucha D (2003) Catalytic Performance of the Dodecatungstophosphoric Acid on Different Supports Applied Catalysis A: General, 256(1), 141-152 58 Soled S., Miseo S., McVicker G et al (1997) Preparation of Bulk and Supported Heteropolyacid Salts Catalysis Today, 36(4), 441-450 59 Alsalme A., Kozhevnikova E.F., Kozhevnikov I.V (2010) α-Pinene Isomerisation over Heteropoly Acid Catalysts in the Gas Phase Applied Catalysis A, 390(1,2), 219-224 60 Cavani F (1998) Heteropolycompound based catalysts: A blend of acid andoxidizing properties Catalysis Today, 41, 73-86 61 Misono M (1987) Heterogeneous Catalysis by Heteropoly Compounds of Molybdenum and Tungsten Cat Rev Sci Eng, 29(2,3), 269-321 62 Kozhevnikov I.V (1987) Advances in Catalysis by Heteropolyacids Russ Chem Rev, 56(9), 811-825 63 Wu H (1920) Contribution to the chemistry of phosphomolybdic acids, phosphotungstic acids and allied substances The Journal of Biological Chemistry, 43(1), 189 64 Kozhevnikov I.V (1995) Heteropoly acids and related compounds as catalysts for fine Chemical Synthesis Catal Rev Sci Eng, 37(2), 311-352 65 Kozhevnikov I.V., Matveev K.I (1983) Homogeneous Catalysts Based on Heteropoly Acids (Review) Applied Catalysis, 5, 135-150 66 Mizuno M., Misono M (1998) Heterogeneous Catalysis Chem Rev, 98, 199-217 67 Pierre Yves Gayraud (2000) Alkylation isobutene butenes en presence z f ’ , 108 T , ’I ,F 68 Marignac M.C (1864) Researches on silicotungstic acids Ann Chim Phys, 4(3) , 5-76 69 Okuhara T., Mizuno N., Misono M (1996) Catalytic Chemistry of Heteropoly Compounds Advance in Catalysis, 41, 113 70 Hayashi H., Moffat J.B (1982) The properties of heteropoly acids and the conversion of methanol to hydrocarbons Journal of Catalysis, 77(2), 473 71 Okuhara T., Kasai A., Hayakawa N et al (1983) Catalysis by Heteropoly Compounds VI The Role of the Bulk Acid Sites in Catalytic Reactions over NaxH3-xPW12040 Journal of Catalysis, 83, 121-130 72 Kozhevnikov I.V (1995) Heteropoly acids and related compounds as catalysts for fine chemical synthesis Catalysis Reviews-Science and Engineering, 37, 311 73 Heravi M., Sadjadi S (2009) Recent Developments in Use of Heteropolyacids, Their Salts and Polyoxometalates in Organic Synthesis J Iran Chem Soc, 6(1), 1-54 74 Majid M., Heravi M.M., Mahdiyeh V.F et al (2013) Heteropoly acidcatalyzed organic reactions in water: doubly green reactions Green Chemistry Letters and Reviews, 6(4), 282-300 75 Bamoharram F.F., Heravi M.M , Roshani M et al (2006) Efficient and reusable catalyst for esterification of salicylic acid with aliphatic and benzylic alcohols J Appl Catal A: Gen.l, 302, 42-47 76 Xu L., Yang X., Yu X et al (2008) Preparation of mesoporous polyoxometalate–tantalum pentoxide composite catalyst for efficient esterification of fatty acid Catal Commun, 9, 1607-1611 77 Terrones M.G.H (2011) Heterogeneous Catalysts Based on H3PW12O40 Heteropolyacid for Free Fatty Acids Esterification Alternative Fuel, Brazil, 17, 359-378 78 Weihong Zhang, Yan Leng, Pingping Zhao et al (2011) Heteropolyacid salts of N-methyl-2-pyrrolidonium as highly efficient and reusable catalysts for Prins reactions of styrenes with formalin Green Chem 13, 832-834 79 Deqing Chu, Li Liu (2011) Photodegradation of crystal violet using zinc salts of Heteropoly (Zn3.5PMO8V4O40 as the photocatalysis) Electric Technology and Civil Engineering (ICETCE), China International 109 Conference, 6750 - 6752 80 Tian J., Fang C., Cheng M., Wang X (2011) Hydrolysis of Cellulose over CsxH3–xPW12O40 (x=1–3) Heteropoly Acid Catalysts Chemical Engineering & Technology, 34(3), 482–486 81 Jean M.R Gallo, José M.C et al (2014) Catalytic Transformations of Ethanol for Biorefineries J Braz Chemical Society, 25(12) , 2229-2243 82 Thu Ha Vu Thi, Hang Thi Au, Thuy Ha Thi Nguyen et al (2013) Esterification of lactic acid by catalytic extractive reaction: An efficient way to produce a biosolvent composition Catalysis Letters, 143(9), 950956 uyễ 83 ( ) , NX Đạ ọ Q ố N 84 Anderson J.R., Pratt K.C (1985) Introduction to characterrization and testing of catalysts Academic Press, Australia ă 85 86 87 ( ) NX ổ ọ & ỹ uyễ r u( NX Đạ ọ Q ố ) N uyễ r u( NX Đạ ọ Q ố ) ụ N 88 Heinrichs B , John W., Lambert S et al (2006) A TEM study on the localization of metal particles in cogelled xerogel catalyst Journal of catalysis , 241, 229-231 89 David R Williams (1996) Transmission Electron Microscopy, A Textbook for Materials Science, Kluwer academic plennum publishers ă 90 91 92 93 rầ ứ (2007) NX K rầ uyễ PL gulonic ƣ ( ) NX K u uyễ ă ọ & ỹ uyễ u ru ụ ọ & ỹ ( ) Hóa phân tích, T uy t u , NX Y ọ v ẩ 49 (2ABC), 925-929 ( ) Ứ -keto-L- 94 Essayem N., Coudurier G., Fournier M et al (1995) Acidic and 110 catalytic properties of CsxH3-xPW12O40 heteropolyacid compounds Catalysis Letters, 34, 223 95 Haber J., Matchowski L , Mucha D et al (2005) New Evidence on the Structure of Potassium Salts of 12-Tungstophosphoric Acid, KxH3xPW12O40 Inorg Chem., 44 (19), 6695 -6703 96 tu v č U.B., Todorovic M et al (2010) Characterization of potassium salts of 12-tungstophosphoric acid Materials Research Bulletin, 45(11), 1679-1684 97 Deltcheff C.R., Thouvenot R (1972) Raman spectra of heteropolyanions with Keggin-type structure Spectrochim Acta Part, A 32, 143 98 Deltcheff C.R., Fournier, Franck M et al (1983) Vibrational investigations of polyoxometalates Inorg Chem., 22, 207 99 Corma, Martinez A and Martinez C (1996) Acidic Cs+, NH4+ and K+ salts of 12-Tungstophosphoric acid as solid catalysts for Isobutane/2butene alkylation Journal of Catalysis,164, 422-432 100 Luis R Pizzio, Mirta N Blanco (2003) Isoamyl acetate production catalyzed by H3PW12O40 on their partially substituted Cs or K salts Applied Catalysis, 255, 265-277 101 Shaimaa M I (2013) Catalytic activity and selectivity of Unsupported Dodecatungstophosphoric acid, and Its Cesium and potassium salts supported on silica Modern Research in Catalysis, 2, 110-118 111 K t qu K t qu p K t qu K t qu K t qu t -DTA [...]... ỏ -KL A ằ ester acid acid A x c t c l nh ạ acid ũ ằ ú acid ắ Tang [22 ] ổ trên x c t c Mặ ù ớ -KL A ớ methanol ester D ị , ú ố ị ổ ( ị ú ớ ể o ớ ị ạ ơ Xú ớ ) ạ siêu acid ị ú ể ạ , ổ ú ú 1.4 SIÊU ACID tá r su Trong ố t ú acid ị ể, ú ơ ở carbon sulfonat ố ữ acid acetic ớ ethanol, acid ữ ester ữ acid acetic ớ (acid palmitic, acid caprylic hay acid acid ) - (triaceti , ) ớ methanol X c t c trên ơ ở carbon... ơ ằ , M-O-M ú ơ ớ ị ú ạ D ò acid ằ ù Đ acid K ị N ú , ữ ị ò ị ất ủ acid [64] d đ acid acid ị acid- base ổ ữ ớ ù ) ẽ ữ ú 1.4.3.3 í bên ạ ị acid , ố ớ , ú ạ T acid, ể ị ễ ị ễ ằ ọ ị c tính acid ố ơ ú ữ acid acid ắ c c acid ị ố ạ acid ể acid ơ [60] ạ ơ ớ S O2-Al2O3, H3PO4/SiO2, zeolit HX và HY và 2SO4, HCl, acid p- ạ … ị ể ớ ớ , ặ ơ c c proton và anion 22 acid này ữ L ể acid acid Hammett Ho: Ho = pKBH+... ncol, ankyl hóa, M ester hóa, ạ acid ố ạ ơ ớ HCl, acid p-sulfonic toluen… Tuy nhiên HPA (< 15 m2 ) ặ ễ ị ò , Dị ớ ể ữ ý ặ ể ị ể ặ ú ị ể ù , ể cho ester ú ,z , ặ ạ -KLGA ớ , ị ơ D ú , ữ ú ố ặ ú ơ ú ạ -KL A ẽ ù ú ặ ạ acid ổ ơ ở ú - Tổ ổ n ẽ , - ố ạ ổ Để ị ể ữ , 2- keto- L- gulonic ị acid ắ S O2-Al2O3, H3PO4/SiO2, zeolit HX và HY và c c acid vô 2SO4, V c -phosphotungstic, H3PW12O40 ( PA) , acid l ể ú acid. .. tv t 1.1 ơ ủ -KLGA OH OH O ạ OH OH OH O K ố 194,14 Đặ ý M ắ ắ M Mùi Không mùi Để 159 C -1 62 C uá tr t p acid 2- keto- L- gulonic T ể ổ L- -KL A ạ HO OH men OH HO CH2OH L- sorbose L- sorbosone Q ếs tổ men t p -K H H OH HO H CH2OH ơ HO H H H 1 .2. 2.1 C O O H HO COOH CHO O H ơ Đ CH2OH HO ắ H CH2OH acid acid 2- keto- L- glulonic 2- keto- L- gulonic t -sorbose ợ 2- KLGA từ L- sorbose ổ -KL A L- ò Q ổ -KL A enzym sorbosone... ổ ị acid acid Ho= -11,94 D , ị 2SO4 o , ể acid ố 100% acid c giá ị %) ổ % ớ ị B + H+ ẩ 2SO4 C c siêu acid ằ acid ơ ơ T ạ + ằ [ ạ, ể ]/[B] ị ;[ ; KBH+ Tỷ + ơ - o SO3F - SbF5 ạ acid [65] 8 ( ạ ị ố ớ acid H2SO4 ị ố acid ắ 1 .2 1 .2 o t t p STT ủ ts tx acid rắ ự acid Ho acid 1 H2SO4 -11,94 2 Nafion - 12, 0 3 H3PW12O40 -13 ,2 4 AlCl3 – CuCl2 -13,7 5 SbF5/SiO2 – Al2O3 -13,7 6 SO 42- /TiO2 -14,5 7 SO 42- /ZrO2 -16,1... ạ ơ ủ p ứ ơ c a ph n ng ester hóa dùng x c t c acid x y ra theo c c ester hóa ớ 9 : Acid carboxylic ẽ ú ẽ acid, ặ S ẽ ơ Đ acid carboxylic ơ carbon ị ở ặ ancol 3 T ớ 4: Proton ị ( á y ut L ạ ƣ ạ ẽ ú ) p ở ứ ester ằ ancol T , ancol - 0,67 mol ester ancol - 0,60 mol ester ancol - 0,05 mol ester ancol N , ố ạ ễ 3 ở ẩ N , ể ị ơ ố ẩ , ể , T ổ ester ạ ạ ằ ở ổ ạ ũ ổ, ằ ằ ổ T ể , ẩ ( ớ ester ớ ester ơ ể ằ ơ... (genetically modified organisms - GMOs) H % S ơ ổ , ữ Reichstein ơ, ố ễ ơ ơ ạ ễ , ố ạ , ạ ơ ơ , ặ ạ ởT Q ố ,N ạ L- 5 , Q ố ,Đ , ớ ( P ơ ): L D- L- sorbose thành 2- KLGA, ester hoá 2- KLGA ằ ặ ổ vòng (lacton hoá) và tr , ú , ể ố ù acid L- ascorbic ACID 2- KETO- L- GULONIC ts t P ơ ớ – OO , 2- KLGA –OH ( acid t ủ acid 2- keto- L- gulonic ) D ố , 2- KLGA ổ ạ h ạ =O ị , ỏ ị 6 base và ố, , ớ ạ ớ (x c t c H+),… ester và. .. ạ acid acetic (ở 3 3K), acid N z l ơ carbon ố ester ớ ở carbon Xú ố ú ẩ ớ ể ú ạ carbon, cho ở acid, trong khi ạ [25 ] carbon ớ acid sulfo 13 ằ ữ acid sulfuric ặ ớ carbon ẩ ú acid , ẹ tro ester ũ ố ú ớ ố acid ỏ ễ NT ) ạ ở3 ớ 2SO4 ú K % ( ơ 9 ằ ặ 3 ằ ớ ú NT ú 2SO4 ằ acid ắ H , ú M ù ú ạ [26 ] Xú carbon ẩ h sulfonat , D- ạ ú N ổ ú ớ carbon SA -13 hay H2SO4, ạ ơ ú acid ester hóa c c ( ) hay acid ( -ester... sulfonat hóa ể ạ ơ ớ ú ester hóa Xiao-Yan Liu [23 ] ố ố ọ ổ acid ị ổ ú z ữ ạ ú ester hóa acid ớ ặ N , ũ ớ c c x c t c acid ắ Nafion NR50 và Amberlyst- -benzene- acid H3PO2 l m t c nhân -SO3 2 ể ằ ạ Xú ớ A -SO3 ơ , ớ carbon ặ ể carbon sulfonat z ặ K ơ ạ ằ ,S ữ acid acetic ớ ancol ethylic, A -SO3 ( %) 12 ơ ớ ể ặ Amberlyst-15 ( %), ể ơ AC-SO3 ớ A ể nhiên, AC-SO3 ơ ớ ú ể ú ơ ớ , ể ạ ơ ơ ặ ạ ester hóa carbon... acid ( -ester hóa , ớ ) ớ methanol ỏ -ester ớ methanol, x c t c carbon hó ú , ơ (65 ò ớ T 3 Tố A -H2SO4 (20 mmol.min-1.g-1) ú ọ , ổ, X ớ ũ hay HNO3-CNTs (18 mmol.min-1.g-1) Mặ ạ ắ ữ methanol và acid acetic trong 1 mmol.min-1.g-1) ớ ể ớ hóm -SO3H c trong cetat ớ Đố ” ằ ị x c t c ạ ú ù acid ) S , carbon 3, ằ ạ K acid -SO3 ester , ẽ ạ N o ( ạ ể carbon ở ơ ể ơ ớ acid sulfuric trong chu trình 1 ạ ị TOF ... phộp carbon c c x c t c carbon acid , ỳ ỳ 3K acid acetic ( 3K), acid N z l carbon ester carbon Xỳ ỳ ỳ carbon, cho acid, [25 ] carbon acid sulfo 13 acid sulfuric carbon ỳ acid. .. sulfonat acid acetic ethanol, acid ester acid acetic (acid palmitic, acid caprylic hay acid acid ) - (triaceti , ) methanol X c t c trờn carbon sulfonat húa ỳ ester húa Xiao-Yan Liu... ũ acid ự acid K N ỳ , ũ t acid [64] d acid acid acid- base ự ) ỳ 1.4.3.3 bờn acid , , ỳ T acid, c tớnh acid ỳ acid acid c c acid acid acid [60] S O2-Al2O3,