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Journal articles on the topic 'Orthovanadates'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 September 2023

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1

Nabar, M. A., and B. G. Mhatre. "Studies on triple orthovanadates." Journal of Alloys and Compounds 323-324 (July 2001): 83–85. http://dx.doi.org/10.1016/s0925-8388(01)00991-4.

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2

Kurina, L. N., and L. M. Potalitsyna. "Adsorption of methanol on orthovanadates." Journal of Applied Spectroscopy 49, no. 1 (1988): 736–40. http://dx.doi.org/10.1007/bf00662916.

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3

Nguyen, Hoan C., and John B. Goodenough. "Magnetic studies of some orthovanadates." Physical Review B 52, no. 1 (1995): 324–34. http://dx.doi.org/10.1103/physrevb.52.324.

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4

Santos, C. C., E. N. Silva, A. P. Ayala, et al. "Raman investigations of rare earth orthovanadates." Journal of Applied Physics 101, no. 5 (2007): 053511. http://dx.doi.org/10.1063/1.2437676.

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5

PATEL, D. "Oxidative dehydrogenation of butane over orthovanadates." Journal of Catalysis 125, no. 1 (1990): 132–42. http://dx.doi.org/10.1016/0021-9517(90)90084-w.

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6

Tamilmani, Vairapperumal, Kalarical Janardhanan Sreeram, and Balachandran Unni Nair. "Catechin assisted phase and shape selection for luminescent LaVO4 zircon." RSC Advances 5, no. 100 (2015): 82513–23. http://dx.doi.org/10.1039/c5ra17800b.

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7

Vasylechko, Leonid, Andrii Tupys, Vasyl Hreb, Volodymyr Tsiumra, Iryna Lutsiuk, and Yaroslav Zhydachevskyy. "New Mixed Y0.5R0.5VO4 and RVO4:Bi Materials: Synthesis, Crystal Structure and Some Luminescence Properties." Inorganics 6, no. 3 (2018): 94. http://dx.doi.org/10.3390/inorganics6030094.

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The results are reported on a precise crystal structure and microstructure determination of new mixed YVO4-based orthovanadates of Y0.5R0.5VO4 (R = Sm, Tb, Dy, Ho, Tm, Yb, Lu) as well as some Bi3+-doped RVO4 (R = La, Gd, Y, Lu) nano- (submicro-) materials. The formation of continuous solid solutions in the YVO4–RVO4 pseudo-binary systems (R = Sm, Tb, Dy, Ho, Tm, Yb, Lu) has been proved. The lattice constants and unit cell volumes of the new mixed orthovanadates were analyzed as a function of R3+ cation radius. The impact of crystal structure parameters on the energy band gap of the materials w

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8

Denisova, Liubov T., and Liubov G. Chumilina. "Heat Capacity of the Cerium and Ytterbium Orthovanadates." Journal of Siberian Federal University. Chemistry 8, no. 2 (2015): 306–11. http://dx.doi.org/10.17516/1998-2836-2015-8-2-306-311.

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9

Denisova, L. T., L. G. Chumilina, and V. M. Denisov. "Heat capacity of RVO4 (R = La-Gd) orthovanadates." Physics of the Solid State 57, no. 5 (2015): 1051–54. http://dx.doi.org/10.1134/s1063783415050091.

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10

Dorogova, M., A. Navrotsky, and L. A. Boatner. "Enthalpies of formation of rare earth orthovanadates, REVO4." Journal of Solid State Chemistry 180, no. 3 (2007): 847–51. http://dx.doi.org/10.1016/j.jssc.2006.12.001.

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11

Nord, Anders G., and Per-Erik Werner. "Cation distribution studies of three (Ni, Mg) orthovanadates." Zeitschrift für Kristallographie 194, no. 1-2 (1991): 49–55. http://dx.doi.org/10.1524/zkri.1991.194.1-2.49.

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12

Au, Chak-Tong, and Wei-De Zhang. "Oxidative dehydrogenation of propane over rare-earth orthovanadates." Journal of the Chemical Society, Faraday Transactions 93, no. 6 (1997): 1195–204. http://dx.doi.org/10.1039/a607565g.

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13

Gallert, Thomas, Marzia Casanova, Francesco Puzzo, Paolo Strazzolini, and Alessandro Trovarelli. "SO2 resistant soot oxidation catalysts based on orthovanadates." Catalysis Communications 97 (July 2017): 120–24. http://dx.doi.org/10.1016/j.catcom.2017.04.037.

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14

Kumari, Puja, and J. Manam. "Structural, optical and special spectral changes of Dy3+ emissions in orthovanadates." RSC Advances 5, no. 130 (2015): 107575–84. http://dx.doi.org/10.1039/c5ra18982a.

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This paper reports on the structural, optical and photometric characterization of yttrium gadolinium orthovanadates (Y<sub>1−x</sub>Gd<sub>x</sub>VO<sub>4</sub>) doped with Dy<sup>3+</sup> for white emission in solid state lighting.

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15

Deshpande, Parag A., and Giridhar Madras. "Photocatalytic degradation of phenol by base metal-substituted orthovanadates." Chemical Engineering Journal 161, no. 1-2 (2010): 136–45. http://dx.doi.org/10.1016/j.cej.2010.04.046.

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16

Errandonea, Daniel. "High pressure crystal structures of orthovanadates and their properties." Journal of Applied Physics 128, no. 4 (2020): 040903. http://dx.doi.org/10.1063/5.0016323.

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17

Voloshyna, O. V. "Peculiarities of the solid-state synthesis of yttrium and gadolinium orthovanadates raw material." Functional materials 22, no. 3 (2015): 299–303. http://dx.doi.org/10.15407/fm22.03.299.

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18

A. N., Goltsev. "APPLICATION OF NANOPARTICLES BASED ON RARE EARTH ORTHOVANADATES TO INACTIVATE EHRLICH CARCINOMA GROWTH." Biotechnologia Acta 8, no. 4 (2015): 113–21. http://dx.doi.org/10.15407/biotech8.04.113.

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19

Varma, Salil, B. N. Wani, and N. M. Gupta. "Synthesis, characterization, and redox behavior of mixed orthovanadates La1−xCexVO4." Materials Research Bulletin 37, no. 13 (2002): 2117–27. http://dx.doi.org/10.1016/s0025-5408(02)00888-7.

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20

Garg, Alka B. "Phase Stability Behaviour of Rare Earth Orthovanadates under High Pressure." Journal of Physics: Conference Series 950 (October 2017): 032001. http://dx.doi.org/10.1088/1742-6596/950/3/032001.

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21

Krasnikov, A., V. Tsiumra, L. Vasylechko, S. Zazubovich, and Ya Zhydachevskyy. "Photoluminescence origin in Bi3+ - doped YVO4, LuVO4, and GdVO4 orthovanadates." Journal of Luminescence 212 (August 2019): 52–60. http://dx.doi.org/10.1016/j.jlumin.2019.04.019.

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22

Tamilmani, Vairapperumal, Kalarical Janardhanan Sreeram, and Balachandran Unni Nair. "Tuned synthesis of doped rare-earth orthovanadates for enhanced luminescence." RSC Adv. 4, no. 9 (2014): 4260–68. http://dx.doi.org/10.1039/c3ra44979c.

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23

Elfakir, A., J. P. Souron, and M. Quarton. "X-Ray Powder Diffraction Data for AITh2(VO4)3Compounds with AI= Li, Na, Ag." Powder Diffraction 5, no. 4 (1990): 219–20. http://dx.doi.org/10.1017/s0885715600015840.

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AbstractThree orthovanadates ATh2(VO4)3with A = Li, Na, Ag have been synthesized by solid state reaction. Single crystals of AgTh2(VO4)3were obtained. This compound is isotypic with sheelite whose space group is I41/a(88). The two other compounds (A = Li, Na) have a zircon type structure: I41/ amd(141). Unit-cell parameters and powder diffraction data for the three compounds are reported.

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24

Elfakir, A., J. P. Souron, and M. Quartern. "Crystal and X-Ray Powder Data for Three Orthovanadates M Th2 (VO4)3 (M = K, Rb, Cs)." Powder Diffraction 4, no. 3 (1989): 165–67. http://dx.doi.org/10.1017/s0885715600016663.

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AbstractThree isotopic orthovanadates MTh2 (VO4)3 with M = K, Rb, Cs have been syndiesized by solid state reaction. Single crystals of K Th2 (VO4)3 and Rb Th2 (VO4)3 were obtained. These compounds are isotypic with the corresponding orthophosphates: monoclinic, space group C2/c, Z = 4. Unit-cell parameters for die diree compounds were determined. Powder diffraction data for each phase are reported.

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25

Denisova, L. T., L. G. Chumilina, N. V. Belousova, and V. M. Denisov. "High-temperature heat capacity of orthovanadates Ce1–x Bi x VO4." Physics of the Solid State 58, no. 9 (2016): 1933–37. http://dx.doi.org/10.1134/s1063783416090122.

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26

Salagre, Pilar, and Jes�s E. Sueiras. "Hexagonal orthovanadates as catalysts in the oxidation of methanol to formaldehyde." Journal of the Chemical Society, Chemical Communications, no. 16 (1988): 1084. http://dx.doi.org/10.1039/c39880001084.

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27

Denisova, L. T., Yu F. Kargin, L. G. Chumilina, and V. M. Denisov. "Heat capacity of the MVO4 (M = Al, Ga, In, Tl) orthovanadates." Inorganic Materials 52, no. 6 (2016): 573–77. http://dx.doi.org/10.1134/s0020168516060030.

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28

Ter-Gabrielyan, Nikolay, and Viktor Fromzel. "Wavelength tuning in cryogenically cooled lasers based on Er-doped orthovanadates." Applied Optics 56, no. 3 (2016): B70. http://dx.doi.org/10.1364/ao.56.000b70.

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29

Tao, Zhengxu, Taiju Tsuboi, Yanlin Huang, Wei Huang, Peiqing Cai, and Hyo Jin Seo. "Photoluminescence Properties of Eu3+-Doped Glaserite-Type Orthovanadates CsK2Gd[VO4]2." Inorganic Chemistry 53, no. 8 (2014): 4161–68. http://dx.doi.org/10.1021/ic500208h.

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30

G., Shwetha, Kanchana V., and Vaitheeswaran G. "Optical properties of orthovanadates, and periodates studied from first principles theory." Materials Chemistry and Physics 163 (August 2015): 376–86. http://dx.doi.org/10.1016/j.matchemphys.2015.07.053.

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31

Au, C. T., W. D. Zhang, and H. L. Wan. "Preparation and characterization of rare earth orthovanadates for propane oxidative dehydrogenation." Catalysis Letters 37, no. 3-4 (1996): 241–46. http://dx.doi.org/10.1007/bf00807761.

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32

Owen, Ozie S., and Harold H. Kung. "Effect of cation reducibility on oxidative dehydrogenation of butane on orthovanadates." Journal of Molecular Catalysis 79, no. 1-3 (1993): 265–84. http://dx.doi.org/10.1016/0304-5102(93)85107-5.

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33

Gayathri, T. H., A. A. Yaremchenko, J. Macías, P. Abhilash, and S. Ananthakumar. "Magnesium-doped zircon-type rare-earth orthovanadates: Structural and electrical characterization." Ceramics International 44, no. 1 (2018): 96–103. http://dx.doi.org/10.1016/j.ceramint.2017.09.130.

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34

Rghioui, Lotfi, Lahcen El Ammari, Abderrazzak Assani, and Mohamed Saadi. "Two new glaserite-type orthovanadates: Rb2KDy(VO4)2 and Cs1.52K1.48Gd(VO4)2." Acta Crystallographica Section E Crystallographic Communications 75, no. 7 (2019): 1041–45. http://dx.doi.org/10.1107/s2056989019008685.

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The crystal structures of dirubidium potassium dysprosium bis(vanadate), Rb2KDy(VO4)2, and caesium potassium gadolinium bis(vanadate), Cs1.52K1.48Gd(VO4)2, were solved from single-crystal X-ray diffraction data. Both compounds, synthesized by the reactive flux method, crystallize in the space group P\overline{3}m1 with the glaserite structure type. VO4 tetrahedra are linked to DyO6 or GdO6 octahedra by common vertices to form sheets stacking along the c axis. The large twelve-coordinate Cs+ or Rb+ cations are sandwiched between these layers in tunnels along the a and b axes, while the K+ catio

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35

Elfakir, A., P. Mahe, and M. Quarton. "Crystal morphology and crystal data for six double orthovanadates AITh2(VO4)3." Zeitschrift für Kristallographie 181, no. 1-4 (1987): 235–39. http://dx.doi.org/10.1524/zkri.1987.181.1-4.235.

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36

Mahapatra, Sudarshan, Giridhar Madras, and T. N. Guru Row. "Synthesis, Characterization and Photocatalytic Activity of Lanthanide (Ce, Pr and Nd) Orthovanadates." Industrial & Engineering Chemistry Research 46, no. 4 (2007): 1013–17. http://dx.doi.org/10.1021/ie060823i.

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37

Li, Kuo-Tseng, and Zen-Hai Chi. "Selective oxidation of hydrogen sulfide on rare earth orthovanadates and magnesium vanadates." Applied Catalysis A: General 206, no. 2 (2001): 197–203. http://dx.doi.org/10.1016/s0926-860x(00)00603-7.

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38

Demesh, M. P., А. S. Yasukevich, А. N. Shekhovtsov, M. B. Kosmyna, W. Paszkowicz, and N. V. Kuleshov. "Compositional dependence of spectroscopic properties of Nd3+ ions in binary calcium orthovanadates." Journal of Luminescence 224 (August 2020): 117270. http://dx.doi.org/10.1016/j.jlumin.2020.117270.

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39

Kumar, Ashok, Anurag Sharma, Madhav Sharma, Vinod Singh, Anita Dhaka, and Rajendra S. Dhaka. "Structural, vibrational and electronic properties of Nb substituted orthovanadates LaV1−Nb O4." Journal of Alloys and Compounds 966 (December 2023): 171506. http://dx.doi.org/10.1016/j.jallcom.2023.171506.

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40

Petit, Christophe T. G., Rong Lan, Peter I. Cowin, and Shanwen Tao. "Structure and conductivity of strontium-doped cerium orthovanadates Ce1−xSrxVO4 (0≤x≤0.175)." Journal of Solid State Chemistry 183, no. 6 (2010): 1231–38. http://dx.doi.org/10.1016/j.jssc.2010.03.032.

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41

Errandonea, Daniel, and Alka B. Garg. "Recent progress on the characterization of the high-pressure behaviour of AVO4 orthovanadates." Progress in Materials Science 97 (August 2018): 123–69. http://dx.doi.org/10.1016/j.pmatsci.2018.04.004.

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42

Mahapatra, Sudarshan, Susanta K. Nayak, Giridhar Madras, and T. N. Guru Row. "Microwave Synthesis and Photocatalytic Activity of Nano Lanthanide (Ce, Pr, and Nd) Orthovanadates." Industrial & Engineering Chemistry Research 47, no. 17 (2008): 6509–16. http://dx.doi.org/10.1021/ie8003094.

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43

López-Solano, J., P. Rodríguez-Hernández, and A. Muñoz. "Ab initiostudy of high-pressure structural properties of the LuVO4and ScVO4zircon-type orthovanadates." High Pressure Research 29, no. 4 (2009): 582–86. http://dx.doi.org/10.1080/08957950903417444.

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44

Díaz-Anichtchenko, Daniel, and Daniel Errandonea. "Comparative Study of the Compressibility of M3V2O8 (M = Cd, Zn, Mg, Ni) Orthovanadates." Crystals 12, no. 11 (2022): 1544. http://dx.doi.org/10.3390/cryst12111544.

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We report herein a theoretical study of the high-pressure compressibility of Cd3V2O8, Zn3V2O8, Mg3V2O8, and Ni3V2O8. For Cd3V2O8, we also present a study of its structural stability. Computer simulations were performed by means of first-principles methods using the CRYSTAL program. In Cd3V2O8, we found a previously unreported polymorph which is thermodynamically more stable than the already known polymorph. We also determined the compressibility of all compounds and evaluated the different contributions of polyhedral units to compressibility. We found that the studied vanadates have an anisotr

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45

Nabar, M. A., and S. S. Mangaonkar. "Studies on triple orthovanadates VII*: spectro-structural studies on dimorphic CdBiTh(AsO4)3." Journal of Materials Science Letters 13, no. 3 (1994): 225–26. http://dx.doi.org/10.1007/bf00278170.

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46

Djemal, Amal, Bassem Louati, and Kamel Guidara. "Synthesis and characterization of orthovanadates compounds Li(1−x) NaxCdVO4 (x = 0, 0.25)." Journal of Alloys and Compounds 683 (October 2016): 610–18. http://dx.doi.org/10.1016/j.jallcom.2016.05.107.

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47

Schnabel, Simone, and Caroline Röhr. "Gemischte Thio/Oxo-Orthovanadate Na3[VSxO4 –x] (x = 2, 3): Darstellung – Strukturen – Eigenschaften / Mixed Thio/Oxo Orthovanadates Na3[VSxO4−x] (x = 2, 3): Synthesis – Crystal Structures – Properties." Zeitschrift für Naturforschung B 60, no. 5 (2005): 479–90. http://dx.doi.org/10.1515/znb-2005-0501.

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Mixed sodium thio/oxo orthovanadates(V), dark red Na3[VS3O] and orange red Na3[VS2O2], were synthesized via reactions in the melt starting from V, Na, Na2S, Na2O and sulfur. The structure of the low temperature phase of Na3[VS3O] (space group Pnma, a = 589.5(3), b = 962.8(5), c = 1186.6(6) pm, Z = 4, R1 = 0.0494) contains anions [VS3O]3− almost identical to those known from the high temperature form, β -Na3[VS3O] (space group Cmc21, a = 968.4(4), b = 1194.6(4), c = 590.5(2) pm, Z = 4, R1 = 0.0291). The second order phase transition between these two forms at 536 °C was studied by temperature d

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48

Panchal, V., D. Errandonea, A. Segura, et al. "The electronic structure of zircon-type orthovanadates: Effects of high-pressure and cation substitution." Journal of Applied Physics 110, no. 4 (2011): 043723. http://dx.doi.org/10.1063/1.3626060.

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49

Ryzhkov, M. V., M. Ya Khodos, V. A. Gubanov, L. P. Benderskaya, and N. M. Korablev. "Electronic structure of bismuth and terbium centers in solid solutions of orthovanadates and orthophosphates." Journal of Structural Chemistry 26, no. 3 (1985): 336–41. http://dx.doi.org/10.1007/bf00749366.

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50

David, A. Duke John, G. Shakil Muhammad, and V. Sivakumar. "Synthesis and optical properties of Eu3 + -substituted glaserite-type orthovanadates CsK2 Y[VO4 ]2." Luminescence 32, no. 5 (2017): 735–44. http://dx.doi.org/10.1002/bio.3244.

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