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Journal articles on the topic 'SAPO-5'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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1

Felk, Angelika, Marianne Kretschmar, Antje Albrecht, et al. "Candida albicans Hyphal Formation and the Expression of the Efg1-Regulated Proteinases Sap4 to Sap6 Are Required for the Invasion of Parenchymal Organs." Infection and Immunity 70, no. 7 (2002): 3689–700. http://dx.doi.org/10.1128/iai.70.7.3689-3700.2002.

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ABSTRACT The ability to change between yeast and hyphal cells (dimorphism) is known to be a virulence property of the human pathogen Candida albicans. The pathogenesis of disseminated candidosis involves adhesion and penetration of hyphal cells from a colonized mucosal site to internal organs. Parenchymal organs, such as the liver and pancreas, are invaded by C. albicans wild-type hyphal cells between 4 and 24 h after intraperitoneal (i.p.) infection of mice. In contrast, a hypha-deficient mutant lacking the transcription factor Efg1 was not able to invade or damage these organs. To investigat
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2

Qiu, Lingfang, Zhiwei Zhou, Mengfan Ma, et al. "Enhanced Visible-Light Photocatalytic Performance of SAPO-5-Based g-C3N4 Composite for Rhodamine B (RhB) Degradation." Materials 12, no. 23 (2019): 3948. http://dx.doi.org/10.3390/ma12233948.

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Novel visible-light responded aluminosilicophosphate-5 (SAPO-5)/g-C3N4 composite has been easily constructed by thermal polymerization for the mixture of SAPO-5, NH4Cl, and dicyandiamide. The photocatalytic activity of SAPO-5/g-C3N4 is evaluated by degrading RhB (30 mg/L) under visible light illumination (λ > 420 nm). The effects of SAPO-5 incorporation proportion and initial RhB concentration on the photocatalytic performance have been discussed in detail. The optimized SAPO-5/g-C3N4 composite shows promising degradation efficiency which is 40.6% higher than that of pure g-C3N4. The degrad
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3

Michalik, Jacek, Naoto Azuma, Jaroslaw Sadlo, and Larry Kevan. "Silver Agglomeration in SAPO-5 and SAPO-11 Molecular Sieves." Journal of Physical Chemistry 99, no. 13 (1995): 4679–86. http://dx.doi.org/10.1021/j100013a045.

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4

Auwal, Ismail Alhassan, Ka-Lun Wong, Tau Chuan Ling, Boon Seng Ooi, and Eng-Poh Ng. "Metal Chlorides Grafted on SAPO-5 (MClx/SAPO-5) as Reusable and Superior Catalysts for Acylation of 2-Methylfuran Under Non-Microwave Instant Heating Condition." Processes 8, no. 5 (2020): 603. http://dx.doi.org/10.3390/pr8050603.

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Highly active metal chlorides grafted on silicoaluminophosphate number 5, MClx/SAPO-5 (M = Cu, Co, Sn, Fe and Zn) catalysts via simple grafting of respective metal chlorides (MClx) onto SAPO-5 are reported. The study shows that thermochemical treatment after grafting is essential to ensure the formation of chemical bondings between MClx and SAPO-5. In addition, the microscopy, XRD and nitrogen adsorption analyses reveal the homogeneous distribution of MClx species on the SAPO-5 surface. Furthermore, the elemental microanalysis confirms the formation of Si–O–M covalent bonds in ZnClx/SAPO-5, Sn
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5

Singh, Arvind Kumar, Rekha Yadav, Vasanthakumaran Sudarsan, Kondamudi Kishore, Sreedevi Upadhyayula, and Ayyamperumal Sakthivel. "Mesoporous SAPO-5 (MESO-SAPO-5): a potential catalyst for hydroisomerisation of 1-octene." RSC Advances 4, no. 17 (2014): 8727. http://dx.doi.org/10.1039/c3ra47298a.

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6

Elangovan, S. P., V. Krishnasamy, and V. Murugesan. "SAPO-5 and SAPO-11: Synthesis, characterization and camphene isomerization activity." Reaction Kinetics & Catalysis Letters 55, no. 1 (1995): 153–59. http://dx.doi.org/10.1007/bf02075846.

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7

Annen, Michael J., Mark E. Davis, and Brian E. Hanson. "129Xe NMR spectroscopy on molecular sieves SAPO-37, AIPO4-5, SAPO-5 and SSZ-24." Catalysis Letters 6, no. 3-6 (1990): 331–39. http://dx.doi.org/10.1007/bf00763999.

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8

Chen, Q. J., M. A. Springuel-Huet, and J. Fraissard. "129Xe NMR of xenon adsorbed on the molecular sieves AlPO4-5, SAPO-5, MAPO-5, and SAPO-37." Chemical Physics Letters 159, no. 1 (1989): 117–21. http://dx.doi.org/10.1016/s0009-2614(89)87465-2.

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9

Wang, Xingqiao, Xinsheng Liu, Tianyou Song, Jianzhi Hu, and Jianqing Qiu. "Substitution of Si in SAPO-5." Chemical Physics Letters 157, no. 1-2 (1989): 87–91. http://dx.doi.org/10.1016/0009-2614(89)87213-6.

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10

Murthy, K. V. V. S. B. S. R., S. J. Kulkarni, and S. Khaja Masthan. "Sorption properties of modified silicoaluminophosphate(SAPO)-5 and SAPO-11 molecular sieves." Microporous and Mesoporous Materials 43, no. 2 (2001): 201–9. http://dx.doi.org/10.1016/s1387-1811(00)00364-4.

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11

Sastre, German, Dewi W. Lewis, and C. Richard A. Catlow. "Modeling of Silicon Substitution in SAPO-5 and SAPO-34 Molecular Sieves." Journal of Physical Chemistry B 101, no. 27 (1997): 5249–62. http://dx.doi.org/10.1021/jp963736k.

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12

Briend, Marguerite, Afshine Shikholeslami, Marie-Jeanne Peltre, Denise Delafosse, and Denise Barthomeuf. "Thermal and hydrothermal stability of SAPO-5 and SAPO-37 molecular sieves." Journal of the Chemical Society, Dalton Transactions, no. 7 (1989): 1361. http://dx.doi.org/10.1039/dt9890001361.

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13

Dzwigaj, S., M. Briend, A. Shikholeslami, M. J. Peltre, and D. Barthomeuf. "The acidic properties of SAPO-37 compared to faujasites and SAPO-5." Zeolites 10, no. 3 (1990): 157–62. http://dx.doi.org/10.1016/0144-2449(90)90039-t.

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14

Sinha, A. K., S. Sainkar, and S. Sivasanker. "An improved method for the synthesis of the silicoaluminophosphate molecular sieves, SAPO-5, SAPO-11 and SAPO-31." Microporous and Mesoporous Materials 31, no. 3 (1999): 321–31. http://dx.doi.org/10.1016/s1387-1811(99)00081-5.

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15

Wang, Xiaoxiao, Zhenmin Liu, Xianxian Wei, Fang Guo, Peng Li, and Shaoqing Guo. "SYNTHESIS OF 2,6-DIMETHYLNAPHTHALENE OVER SAPO-11, SAPO-5 AND MORDENITE MOLECULAR SIEVES." Brazilian Journal of Chemical Engineering 34, no. 1 (2017): 295–306. http://dx.doi.org/10.1590/0104-6632.20170341s20160120.

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16

Valizadeh, Bardiya, Sima Askari, Rouein Halladj, and Amin Haghmoradi. "Effect of Synthesis Conditions on Selective Formation of SAPO-5 and SAPO-34." Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 44, no. 1 (2013): 79–83. http://dx.doi.org/10.1080/15533174.2013.768646.

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17

Campelo, J. M., F. Lafont, and J. M. Marinas. "Comparison ofn-decane hydroconversion with Pt/SAPO-5 and Pt/SAPO-11 catalysts." Reaction Kinetics and Catalysis Letters 62, no. 2 (1997): 371–76. http://dx.doi.org/10.1007/bf02475478.

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18

Chen, Zhou, Shaohong Zhu, Pengyun Li, et al. "Fabricating self-assembled SAPO-5 with tailored mesoporosity and acidity using a single template." CrystEngComm 19, no. 35 (2017): 5275–84. http://dx.doi.org/10.1039/c7ce01132f.

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SAPO-5 zeolite with a bimodal pore system was hydrothermally synthesized using di-n-butylamine as single template. The structural and catalytic properties of the hierarchical SAPO-5 were extensively characterized and compared to those of conventional SAPO-5 using triethylamine as template.
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19

Qiu, Ling Fang, Zhi Wei Zhou, Xiao Bin Qiu, and Shu Wang Duo. "Synthesis and Photocatalytic Degradation Performance of g-C3N4/ CQDs/SAPO-5 Ternary Composite." Key Engineering Materials 768 (April 2018): 201–5. http://dx.doi.org/10.4028/www.scientific.net/kem.768.201.

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Due to the fatal drawback of fast photoreduced electron-hole pair recombination rate of g-C3N4, g-C3N4/CQDs/SAPO-5 ternary composite were prepared. Both of carbon quantum dots and SAPO-5 can form heterojunction with g-C3N4to inhibit the recombination. Their properties were characterized by XRD, SEM, FT-IR, DRS and PL. Data of PL shows a much lower photoreduced electron-hole pair recombination rate of g-C3N4/CQDs/SAPO-5. The effect of CQDs amount loaded on ternary composite on the RhB photodegradation performance under visible light was discussed in detail. The observed RhB degradation performa
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20

Wang, Ya, Sheng-Li Chen, Yong-Jie Jiang, et al. "Influence of template content on selective synthesis of SAPO-18, SAPO-18/34 intergrowth and SAPO-34 molecular sieves used for methanol-to-olefins process." RSC Advances 6, no. 107 (2016): 104985–94. http://dx.doi.org/10.1039/c6ra23048b.

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21

Chen, Xueshuai, Rongli Jiang, Huilin Hou, Zihan Zhou, and Xingwen Wang. "Synthesis of ZSM-5/SAPO-34 zeolite composites from LAPONITE® and their catalytic properties in the MTO reaction." CrystEngComm 22, no. 37 (2020): 6182–88. http://dx.doi.org/10.1039/d0ce01002b.

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22

Bai, Ya Dong, Hai Rong Zhang, Pei Wan Bai, et al. "Phase-Selective Synthesis of a Silicoaluminophosphate Molecular Sieve with 3-Aminopropyltriethoxysilane as the Silica Source." Advanced Materials Research 1061-1062 (December 2014): 109–11. http://dx.doi.org/10.4028/www.scientific.net/amr.1061-1062.109.

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Silicoaluminophosphate (SAPO) molecular sieves with CHA and AFI structures have been synthesized under hydrothermal conditions from similar reaction mixtures using 3-Aminopropyl-triethoxysilane as silicon source. The XRD analysis indicated that the phase selectivity could follow the sequence of SAPO-34→SAPO-34+ SAPO-5→SAPO-5 →amorphous phase with increasing the amount of the silicon source. The phase selectivity can be explained by the increasing alkalinity of the medium with the 3-Aminopropyltriethoxysilane concentration.
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23

SAKAMOTO, Kou. "On the synthesis conditions of SAPO-5." NIPPON KAGAKU KAISHI, no. 3 (1989): 371–73. http://dx.doi.org/10.1246/nikkashi.1989.371.

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24

Bhattacharya, Anjana, Jagannath Das, Swapan Mitra, and Sisir K. Roy. "Studies on the synthesis of SAPO-5." Journal of Chemical Technology & Biotechnology 54, no. 4 (2007): 399–407. http://dx.doi.org/10.1002/jctb.280540415.

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25

Schueth, F., D. Demuth, B. Zibrowius, J. Kornatowski, and G. Finger. "FTIR microscopy with polarized IR radiation for the analysis of SAPO-5 and p-xylene-loaded SAPO-5." Journal of the American Chemical Society 116, no. 3 (1994): 1090–95. http://dx.doi.org/10.1021/ja00082a035.

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26

MARTENS, J. "Catalytic activity and Si, Al, P ordering in microporous silicoaluminophosphates of the SAPO-5, SAPO-11, and SAPO-37 type." Journal of Catalysis 126, no. 1 (1990): 299–305. http://dx.doi.org/10.1016/0021-9517(90)90068-u.

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27

Zibrowius, Bodo, Elke Löffler, and Michael Hunger. "Multinuclear MAS n.m.r. and i.r. spectroscopic study of silicon incorporation into SAPO-5, SAPO-31, and SAPO-34 molecular sieves." Zeolites 12, no. 2 (1992): 167–74. http://dx.doi.org/10.1016/0144-2449(92)90079-5.

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28

Kumar, Narendra, Jose Ignacio Villegas, Tapio Salmi, Dmitry Yu Murzin, and Teemu Heikkilä. "Isomerization of n-butane to isobutane over Pt-SAPO-5, SAPO-5, Pt-H-mordenite and H-mordenite catalysts." Catalysis Today 100, no. 3-4 (2005): 355–61. http://dx.doi.org/10.1016/j.cattod.2004.10.023.

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29

Zhang, Ling, Zhong-Xiang Jiang, Yue Yu, Chong-Shuai Sun, Yu-Jia Wang, and Hai-Yan Wang. "Synthesis of core–shell ZSM-5@meso-SAPO-34 composite and its application in methanol to aromatics." RSC Advances 5, no. 69 (2015): 55825–31. http://dx.doi.org/10.1039/c5ra10296k.

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30

Tian, Peng, Xiong Su, Yingxia Wang, et al. "Phase-Transformation Synthesis of SAPO-34 and a Novel SAPO Molecular Sieve with RHO Framework Type from a SAPO-5 Precursor." Chemistry of Materials 23, no. 6 (2011): 1406–13. http://dx.doi.org/10.1021/cm103512m.

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31

Xia, Wei, Qi Sun, Shang Wen Liu, Lin Ping Qiang, and Yuan Cun Cui. "SAPO-34/SiO2 Catalysts for the Transformation of Ethanol into Propylene." Advanced Materials Research 1004-1005 (August 2014): 707–10. http://dx.doi.org/10.4028/www.scientific.net/amr.1004-1005.707.

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Ethanol has great potential to be a candidate for the source of light olefins such as ethylene and propylene. However, ethanol to olefin (ETO) process has not been fully investigated. In this work, the conversion reactions of ethanol were carried out at 673 K under atmospheric pressure on SAPO-34 and SAPO-34/SiO2 catalysts. SAPO-34 and SAPO-34/SiO2 exhibit higher selectivity for propylene than H-ZSM-5 zeolite catalysts do. The SAPO-34 with silica binder showed better catalytic performance for the transformation of ethanol to propylene than the SAPO-34 catalyst.
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32

Kornatowski, Jan, Beate Kanz-Reuschel, Gerd Finger, Werner H. Baur, Martin Bülow, and Klaus K. Unger. "Kinetic Aspects of the Crystallization of SAPO-5 Molecular Sieves." Collection of Czechoslovak Chemical Communications 57, no. 4 (1992): 756–66. http://dx.doi.org/10.1135/cccc19920756.

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The kinetics of hydrothermal crystallization of microporous silicoaluminophosphate SAPO-5 have been studied as a function of water content using the templates tripropylamine (TPA) and triethylamine (TEA). The investigation included the formation of the SAPO-5 phase, its growth in large single crystals, and the size distribution of the crystals. An attempt to fit the experimental data to kinetic models of crystallization is presented. The systems studied have been found to be very similar except for the nucleation stage which is mainly responsible for both the dimensions of the resulting crysta
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33

Zhou, D., X. B. Luo, H. L. Zhang, et al. "Synthesis and characterization of organic-functionalized molecular sieves Ph-SAPO-5 and Ph-SAPO-11." Microporous and Mesoporous Materials 121, no. 1-3 (2009): 194–99. http://dx.doi.org/10.1016/j.micromeso.2009.01.033.

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34

Campelo, J. M., F. Lafont, and J. M. Marinas. "Hydroisomerization and Hydrocracking of n-Heptane on Pt/SAPO-5 and Pt/SAPO-11 Catalysts." Journal of Catalysis 156, no. 1 (1995): 11–18. http://dx.doi.org/10.1006/jcat.1995.1226.

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35

Campelo, J. M., F. Lafont, and J. M. Marinas. "Hydroisomerization and hydrocracking of n-hexane on Pt/SAPO-5 and Pt/SAPO-11 catalysts." Zeolites 15, no. 2 (1995): 97–103. http://dx.doi.org/10.1016/0144-2449(94)00003-b.

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36

Feng, Wang, Bai Ting, Duan Chao, Wen Ting Qu, Xi Ling Liu, and Zhang Xin. "Coke on HZSM-5/SAPO-34 Catalyst for Ethanol to Propylene." Advanced Materials Research 962-965 (June 2014): 751–54. http://dx.doi.org/10.4028/www.scientific.net/amr.962-965.751.

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The catalytic performance on HZSM-5/SAPO-34 catalyst in ethanol to propylene was tested in continuous-flow fixed-bed reactor. Coke on HZSM-5/SAPO-34 catalyst for ethanol to propylene was studied by O2-TPO, N2isothermal adsorption–desorption and NH3-TPD.The result showed that the strong and medium acid sites were the active centers of coke deposition; Coke mainly deposited in mesoporous and some coke blocked microporous orifice; In the initial stage of reaction, the high yield of propylene may be benefited from coke deposition, which adjusted the acidity and structure of HZSM-5/SAPO-34.
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37

Mohammadkhani, Bahman, Mohammad Haghighi, and Parisa Sadeghpour. "Altering C2H4/C3H6 yield in methanol to light olefins over HZSM-5, SAPO-34 and SAPO-34/HZSM-5 nanostructured catalysts: influence of Si/Al ratio and composite formation." RSC Advances 6, no. 30 (2016): 25460–71. http://dx.doi.org/10.1039/c6ra00432f.

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HZSM-5 zeolites with various Si/Al ratios were synthesized by hydrothermal method and the sample with optimum Si/Al ratio combined with SAPO-34. In MTO reaction, SAPO-34/HZSM-5 composite shows high activity and selectivity toward light olefins.
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38

Tsai, Tzeng-Guang, Han-Chang Shih, Sheng-Ju Liao, and Kuei-jung Chao. "Well-aligned SAPO-5 membrane: preparation and characterization." Microporous and Mesoporous Materials 22, no. 1-3 (1998): 333–41. http://dx.doi.org/10.1016/s1387-1811(98)00081-x.

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39

Minchev, Chr, V. Valtchev, and S. Mintova. "Thermal analysis of the crystallization of SAPO-5." Thermochimica Acta 264 (October 1995): 59–66. http://dx.doi.org/10.1016/0040-6031(95)02410-4.

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40

Hu, Enping, Zhiping Lai, and Kean Wang. "Adsorption Properties of the SAPO-5 Molecular Sieve." Journal of Chemical & Engineering Data 55, no. 9 (2010): 3286–89. http://dx.doi.org/10.1021/je100093u.

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41

Sano, T., Y. Kiyozumi, K. Maeda, et al. "Synthesis and characterization of polycrystalline SAPO-5 film." Journal of Molecular Catalysis 77, no. 2 (1992): L19—L26. http://dx.doi.org/10.1016/0304-5102(92)80192-j.

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42

Wang, R., C. F. Lin, Y. S. Ho, L. J. Leu, and K. J. Chao. "Silicon species in a SAPO-5 molecular sieve." Applied Catalysis 72, no. 1 (1991): 39–49. http://dx.doi.org/10.1016/0166-9834(91)85026-r.

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43

Segal, E., Irina Ivanova, and E. G. Derouane. "On the interaction between ammonia and SAPO-5." Thermochimica Acta 231 (January 1994): 277–85. http://dx.doi.org/10.1016/0040-6031(94)80030-8.

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44

Martin, C., N. Tosi-Pellenq, J. Patarin, and J. P. Coulomb. "Sorption Properties of AlPO4-5 and SAPO-5 Zeolite-like Materials." Langmuir 14, no. 7 (1998): 1774–78. http://dx.doi.org/10.1021/la960755c.

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45

Yaremov, P. S., and V. G. Il’in. "Crystallization kinetics of zeolite-like phosphates AIPO4-5 and SAPO-5." Theoretical and Experimental Chemistry 33, no. 3 (1997): 153–56. http://dx.doi.org/10.1007/bf02765915.

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46

Jhung, Sung Hwa, Jong-San Chang, Jin Soo Hwang, and Sang-Eon Park. "Selective formation of SAPO-5 and SAPO-34 molecular sieves with microwave irradiation and hydrothermal heating." Microporous and Mesoporous Materials 64, no. 1-3 (2003): 33–39. http://dx.doi.org/10.1016/s1387-1811(03)00501-8.

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47

Campelo, Juan M., Fernando Lafont, and Jose M. Marinas. "Catalytic properties of the silicoaluminophosphates SAPO-5 and SAPO-11 in n-octane and isooctane hydroconversion." Journal of the Chemical Society, Faraday Transactions 91, no. 22 (1995): 4171. http://dx.doi.org/10.1039/ft9959104171.

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48

Tang, B., X. H. Lu, D. Zhou, et al. "Co2+-exchanged SAPO-5 and SAPO-34 as efficient heterogeneous catalysts for aerobic epoxidation of alkenes." Catalysis Communications 31 (January 2013): 42–47. http://dx.doi.org/10.1016/j.catcom.2012.11.011.

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49

Jadav, Divya, Rajib Bandyopadhyay, Nao Tsunoji, Masahiro Sadakane, and Mahuya Bandyopadhyay. "Post-synthetic amine functionalized SAPO-5 & SAPO-34 molecular sieves for epoxide ring opening reactions." Materials Today: Proceedings 45 (2021): 3726–32. http://dx.doi.org/10.1016/j.matpr.2020.12.986.

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50

Auwal, Ismail Alhassan, Fitri Khoerunnisa, Florent Dubray, et al. "Effects of Synthesis Parameters on the Crystallization Profile and Morphological Properties of SAPO-5 Templated by 1-Benzyl-2,3-Dimethylimidazolium Hydroxide." Crystals 11, no. 3 (2021): 279. http://dx.doi.org/10.3390/cryst11030279.

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The formation of SAPO-5 molecular sieves is studied under hydrothermal conditions in the presence of a new templating agent, 1-benzyl-2,3-dimethylimidazolium hydroxide ([bzmIm]OH). The syntheses were carried out by varying the synthesis parameters, viz. crystallization temperature, heating time and reactants molar composition (SiO2, Al2O3, P2O5, [bzmIm]+, H2O) in order to investigate the role of each synthesis parameter on the formation of SAPO-5. The results showed that these synthesis parameters had significant influences on the entire crystallization process (induction, nucleation, crystal
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