Journal articles on the topic 'Thermogravimetric analysis'

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1

Donato, D. I., G. Lazzara, and S. Milioto. "Thermogravimetric analysis." Journal of Thermal Analysis and Calorimetry 101, no. 3 (March 19, 2010): 1085–91. http://dx.doi.org/10.1007/s10973-010-0717-9.

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2

Rosa, M. Em�lia, and M. A. Fortes. "Thermogravimetric analysis of cork." Journal of Materials Science Letters 7, no. 10 (October 1988): 1064–65. http://dx.doi.org/10.1007/bf00720828.

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3

Hong, Peng-Zhi, Si-Dong Li, Chun-Yan Ou, Cheng-Peng Li, Lei Yang, and Chao-Hua Zhang. "Thermogravimetric analysis of chitosan." Journal of Applied Polymer Science 105, no. 2 (2007): 547–51. http://dx.doi.org/10.1002/app.25920.

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4

Гурський, Петро Васильович, Ірина Олексіївна Крапивницька, and Федір Всеволодович Перцевой. "Thermogravimetric analysis of pectin gels." ScienceRise 7, no. 2 (12) (July 26, 2015): 23. http://dx.doi.org/10.15587/2313-8416.2015.45905.

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5

SAKAKIBARA, Mikio, Fumio OKADA, Michiyo HORIUCHI, and Kirnihiro Suzuki. "Kinetic analysis of thermogravimetric data." NIPPON KAGAKU KAISHI, no. 10 (1989): 1729–32. http://dx.doi.org/10.1246/nikkashi.1989.1729.

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6

SHARMA, R. N., I. SHAH, S. GUPTA, P. SHARMA, and A. A. BEIGH. "Thermogravimetric Analysis of Urinary Stones." British Journal of Urology 64, no. 6 (December 1989): 564–66. http://dx.doi.org/10.1111/j.1464-410x.1989.tb05308.x.

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7

He, Rong, Jun'Ichi Sato, Qun Chen, and Changhe Chen. "Thermogravimetric analysis of char combustion." Combustion Science and Technology 174, no. 4 (April 2002): 1–18. http://dx.doi.org/10.1080/713713015.

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8

Abou-Zeid, Mohamed Nagib, and Stephen A. Cross. "Thermogravimetric Analysis of Carbonate Aggregates." Journal of Materials in Civil Engineering 11, no. 2 (May 1999): 98–104. http://dx.doi.org/10.1061/(asce)0899-1561(1999)11:2(98).

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9

Mather, Bryant. "Thermogravimetric Analysis of Carbonate Aggregates." Journal of Materials in Civil Engineering 13, no. 3 (June 2001): 239. http://dx.doi.org/10.1061/(asce)0899-1561(2001)13:3(239).

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10

Liu, Ji-da, and Chang Bian. "Thermogravimetric Analysis of Arson Evidence." Procedia Engineering 211 (2018): 456–62. http://dx.doi.org/10.1016/j.proeng.2017.12.036.

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11

Morgan, Paul A., Struan D. Robertson, and John F. Unsworth. "Combustion studies by thermogravimetric analysis." Fuel 66, no. 2 (February 1987): 210–15. http://dx.doi.org/10.1016/0016-2361(87)90243-2.

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12

Sharma, H. S. S., and K. Kernaghan. "Thermogravimetric analysis of flax fibres." Thermochimica Acta 132 (September 1988): 101–9. http://dx.doi.org/10.1016/0040-6031(88)87099-0.

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13

Morgan, Paul A., Struan D. Robertson, and John F. Unsworth. "Combustion studies by thermogravimetric analysis." Fuel 65, no. 11 (November 1986): 1546–51. http://dx.doi.org/10.1016/0016-2361(86)90331-5.

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14

Zsakó, J., G. Liptay, Cs Várhelyi, Cs Novák, and I. Ganescu. "Kinetic analysis of thermogravimetric data." Journal of Thermal Analysis 37, no. 11-12 (November 1991): 2681–91. http://dx.doi.org/10.1007/bf01912812.

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15

Zsakó, J., I. Ganescu, Cs Várhelyi, and L. Chirigiu. "Kinetic analysis of thermogravimetric data." Journal of Thermal Analysis 48, no. 2 (February 1997): 367–71. http://dx.doi.org/10.1007/bf01979281.

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16

Zsakó, J. "Kinetic analysis of thermogravimetric data." Journal of Thermal Analysis 46, no. 6 (June 1996): 1845–64. http://dx.doi.org/10.1007/bf01980788.

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17

Galo Cárdenas, T., and L. H. D. Tagle. "Thermogravimetric analysis of organometallic films." Thermochimica Acta 184, no. 1 (July 1991): 131–39. http://dx.doi.org/10.1016/0040-6031(91)80144-8.

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18

Liptay, G., J. Zsakó, Cs Várhelyi, and Cs Novák. "Kinetic analysis of thermogravimetric data." Journal of Thermal Analysis 38, no. 10 (October 1992): 2301–10. http://dx.doi.org/10.1007/bf02123983.

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19

Niu, Shengli, Mengqi Liu, Chunmei Lu, Hui Li, and Mengjia Huo. "Thermogravimetric analysis of carbide slag." Journal of Thermal Analysis and Calorimetry 115, no. 1 (June 11, 2013): 73–79. http://dx.doi.org/10.1007/s10973-013-3268-z.

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20

Mulani, Khudbudin, Vijay Chandegaokar, and Hemantini Deshpande. "Thermogravimetric Analysis of Rubber for Forensic Purposes: A Case Report." Arab Journal of Forensic Sciences & Forensic Medicine 1, no. 8 (December 30, 2018): 1067–71. http://dx.doi.org/10.26735/16586794.2018.026.

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21

Liu, Ying, Liutao Yang, Chunping Ma, and Yingzhe Zhang. "Thermal Behavior of Sweet Potato Starch by Non-Isothermal Thermogravimetric Analysis." Materials 12, no. 5 (February 27, 2019): 699. http://dx.doi.org/10.3390/ma12050699.

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In this study, X-ray diffraction (XRD), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC) methods were used to study the structure, the thermal degradation kinetics, and the thermogram of sweet potato starch, respectively. The thermal decomposition kinetics of sweet potato starch was examined within different heating rates in a nitrogen atmosphere. Different models of kinetic analysis were used to calculate the activation energies using the thermogravimetric data of the thermal degradation process. The activation energies got from Kissinger, Flynn–Wall–Ozawa, and Šatava–Šesták models were 173.85, 174.87, and 174.34 kJ·mol−1, respectively. Thermogravimetry–Fourier transform infrared spectroscopy (TG-FTIR) analysis showed that the main pyrolysis products included water, carbon dioxide, and methane.
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22

Fodor, Csaba, János Bozi, Marianne Blazsó, and Béla Iván. "Unexpected thermal decomposition behavior of poly(N-vinylimidazole)-l-poly(tetrahydrofuran) amphiphilic conetworks, a class of chemically forced blends." RSC Advances 5, no. 23 (2015): 17413–23. http://dx.doi.org/10.1039/c4ra16881j.

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The underlying chemical processes of the unexpected thermal decomposition behavior of poly(N-vinylimidazole)-l-poly(tetrahydrofuran) amphiphilic conetworks were investigated by thermogravimetric analysis and thermogravimetry-mass spectrometry.
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23

Janković, B., B. Adnadjević, J. Jovanović, D. Minić, and Lj Kolar-Anić. "Thermogravimetric Analysis of Superabsorbing Polyacrylic Hydrogel." Materials Science Forum 494 (September 2005): 193–98. http://dx.doi.org/10.4028/www.scientific.net/msf.494.193.

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The thermogravimetric analysis of superabsorbing polyacrylic hydrogel dehydration, performed under non-isothermal conditions at different heating rates was discussed. Particularly, the influence of the heating rate on the obtained results is given in detail. For this purpose the Weibull distribution function was applied. The thermogravimetric curve when the heating rate tends to zero was evaluated. The activation energy E = 63 kJ/mol, pre-exponential factor A = 2.97 × 108 min−1, and rate constant k = 2.76 × 10−3 min−1 were determined on the basis of this curve.
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24

Konai, Noel, Danwe Raidandi, Antonio Pizzi, Pierre Girods, Marie-Christine Lagel, and Melhyas Kple. "Thermogravimetric analysis of anningre tannin resin." Maderas. Ciencia y tecnología, ahead (2016): 0. http://dx.doi.org/10.4067/s0718-221x2016005000022.

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25

Chala, Girma T., Ying P. Lim, Shaharin A. Sulaiman, and Chin L. Liew. "Thermogravimetric analysis of empty fruit bunch." MATEC Web of Conferences 225 (2018): 02002. http://dx.doi.org/10.1051/matecconf/201822502002.

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This paper presents the characteristics of empty fruit bunch (EFB) using thermogravimetric analysis (TGA) and shows its potential as a renewable energy sources. A set of data were collected from the thermal reaction and plotted in mass or percentage of the initial mass against either temperature or time, respectively. In the thermogravimetric analysis, mass, temperature and time were considered as base measurements and important data for derivative thermogravimetric (DTG) curve were analysed while many additional measures could be derived from these three base measurements. It was observed that heating rate of 8.5°C/min and air flow rate of 85mL/min provided a maximum weight loss rate of 0.209%/°C at the temperature of 313.5°C and the derivative weight peak of -0.1895mg/°C at 292°C. The time taken to reach the maximum temperature of 899.9°C was 46.74 minutes, and ΔT endo-up reflected minimum point of -0.2°C at 15.82 minutes and maximum ΔT endo-up of 888°C at 42 minutes. Heat flow endo-up also showed that the minimum heat flow was 15.39mW at 15.85 minutes and reaching the peak heat flow endo-up of 47.73mW at 43.27 minutes.
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26

Tagle, L. H., and F. R. Diaz. "Polycarbonate Resins: Synthesis and Thermogravimetric Analysis." Journal of Macromolecular Science: Part A - Chemistry 28, no. 3-4 (March 1991): 397–411. http://dx.doi.org/10.1080/00222339108052150.

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27

Khare, P., and B. P. Baruah. "Thermogravimetric Analysis of Perhydrous Indian Coals." Energy Sources, Part A: Recovery, Utilization, and Environmental Effects 36, no. 7 (February 21, 2014): 774–82. http://dx.doi.org/10.1080/15567036.2010.547919.

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28

HATCHER, WILLIAM J., and THOMAS H. BURTON. "CATALYST REGENERATION KINETICS VIA THERMOGRAVIMETRIC ANALYSIS." Chemical Engineering Communications 61, no. 1-6 (November 1987): 1–12. http://dx.doi.org/10.1080/00986448708912027.

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29

Lapuerta, M., R. Ballesteros, and J. Rodríguez-Fernández. "Thermogravimetric analysis of diesel particulate matter." Measurement Science and Technology 18, no. 3 (January 24, 2007): 650–58. http://dx.doi.org/10.1088/0957-0233/18/3/015.

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30

Abidi, Noureddine, Luis Cabrales, and Eric Hequet. "Thermogravimetric analysis of developing cotton fibers." Thermochimica Acta 498, no. 1-2 (January 2010): 27–32. http://dx.doi.org/10.1016/j.tca.2009.09.007.

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31

Elder, Thomas, John S. Kush, and Sharon M. Hermann. "Thermogravimetric analysis of forest understory grasses." Thermochimica Acta 512, no. 1-2 (January 2011): 170–77. http://dx.doi.org/10.1016/j.tca.2010.10.001.

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32

Ceylan, K., H. Karaca, and Y. Önal. "Thermogravimetric analysis of pretreated Turkish lignites." Fuel 78, no. 9 (July 1999): 1109–16. http://dx.doi.org/10.1016/s0016-2361(99)00009-5.

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33

Çulcuoğlu, Elif Ünay, Filiz Karaosm, Esin. "Thermogravimetric Analysis of the Rapeseed Cake." Energy Sources 23, no. 10 (December 2001): 889–95. http://dx.doi.org/10.1080/009083101317071333.

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34

Radhakrishnan Nair, M. N., George V. Thomas, and M. R. Gopinathan Nair. "Thermogravimetric analysis of PVC/ELNR blends." Polymer Degradation and Stability 92, no. 2 (February 2007): 189–96. http://dx.doi.org/10.1016/j.polymdegradstab.2006.11.014.

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35

Dimitrakopoulos, A. P. "Thermogravimetric analysis of Mediterranean plant species." Journal of Analytical and Applied Pyrolysis 60, no. 2 (August 2001): 123–30. http://dx.doi.org/10.1016/s0165-2370(00)00164-9.

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36

Otero, M., M. E. Sanchez, X. Gómez, and A. Morán. "Thermogravimetric analysis of biowastes during combustion." Waste Management 30, no. 7 (July 2010): 1183–87. http://dx.doi.org/10.1016/j.wasman.2009.12.010.

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37

Jovanovic, Jelena D., Milutin N. Govedarica, Petar R. Dvornic, and Ivanka G. Popovic. "The thermogravimetric analysis of some polysiloxanes." Polymer Degradation and Stability 61, no. 1 (January 1998): 87–93. http://dx.doi.org/10.1016/s0141-3910(97)00135-3.

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38

Gargallo, L., N. Hamidi, L. H. Tagle, and D. Radic. "Thermogravimetric analysis of poly(dialkylphenyl methacrylates)." Thermochimica Acta 143 (May 1989): 75–84. http://dx.doi.org/10.1016/0040-6031(89)85043-9.

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39

Caldeira, Vinícius P. S., Anne G. D. Santos, Daniele S. Oliveira, Rafael B. Lima, Luiz D. Souza, and Sibele B. C. Pergher. "Polyethylene catalytic cracking by thermogravimetric analysis." Journal of Thermal Analysis and Calorimetry 130, no. 3 (July 3, 2017): 1939–51. http://dx.doi.org/10.1007/s10973-017-6551-6.

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40

Alfredsen, Gry, Thomas K. Bader, Janka Dibdiakova, Tore Filbakk, Susanne Bollmus, and Karin Hofstetter. "Thermogravimetric analysis for wood decay characterisation." European Journal of Wood and Wood Products 70, no. 4 (July 29, 2011): 527–30. http://dx.doi.org/10.1007/s00107-011-0566-7.

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41

Li, Baozhen, and C. B. Alcock. "A thermogravimetric analysis of Sr14−xCaxCu24Oy." Materials Letters 10, no. 1-2 (September 1990): 84–85. http://dx.doi.org/10.1016/0167-577x(90)90020-m.

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42

van der Merwe, E. M., and C. A. Strydom. "Quantitative thermogravimetric analysis of binary mixtures." Journal of Thermal Analysis and Calorimetry 76, no. 1 (2004): 149–56. http://dx.doi.org/10.1023/b:jtan.0000027814.93703.0c.

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43

Zsakó, J., J. Sztatisz, Á. Czégeni, G. Liptay, and Cs Várhelyi. "Kinetic analysis of thermogravimetric data. XXVI." Journal of Thermal Analysis 32, no. 2 (March 1987): 463–70. http://dx.doi.org/10.1007/bf01912698.

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44

Hu, Zongjie, Liguang Li, and Shui Yu. "Thermogravimetric analysis of fuel film evaporation." Chinese Science Bulletin 51, no. 17 (September 2006): 2150–57. http://dx.doi.org/10.1007/s11434-006-2091-3.

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45

Zeman, Svatopluk, and Ljubov A. Tokárová. "Thermogravimetric analysis of urea-formaldehyde polycondensates." Thermochimica Acta 202 (June 1992): 181–89. http://dx.doi.org/10.1016/0040-6031(92)85162-o.

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46

Piga, L., F. Villieras, and J. Yvon. "Thermogravimetric analysis of a talc mixture." Thermochimica Acta 211 (December 1992): 155–62. http://dx.doi.org/10.1016/0040-6031(92)87015-3.

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47

Toft Sørensen, O. "Computer controlled thermogravimetric stepwise isothermal analysis." Thermochimica Acta 85 (April 1985): 291–94. http://dx.doi.org/10.1016/0040-6031(85)85584-2.

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48

Netravali, A. N., R. E. Fornes, R. D. Gilbert, and J. D. Memory. "Thermogravimetric analysis of water-epoxy interaction." Journal of Applied Polymer Science 31, no. 5 (April 1986): 1531–35. http://dx.doi.org/10.1002/app.1986.070310535.

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49

Filip, Daniela, and Doina Macocinschi. "Thermogravimetric analysis of polyurethane-polysulfone blends." Polymer International 51, no. 8 (2002): 699–706. http://dx.doi.org/10.1002/pi.972.

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50

Guo, Yalou, Hui Zhang, and Yingshu Liu. "Desorption characteristics and kinetic parameters determination of molecular sieve by thermogravimetric analysis/differential thermogravimetric analysis technique." Adsorption Science & Technology 36, no. 7-8 (May 3, 2018): 1389–404. http://dx.doi.org/10.1177/0263617418772665.

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The kinetics of the thermal desorption of CO2 adsorbed on zeolite 13X were obtained using a differential thermogravimetric analyser under two different carrier gas conditions. The varying heating rates were set as 8, 12, 16, and 20 K min−1, respectively. The desorption activation energy of the physisorption sites for this experiment evaluated by an integral method without prediction of the reaction order ranged from 12.15 to 14.12 kJ mol−1 (CO2 as the carrier gas) and 43.32 to 50.42 kJ mol−1 (Ar as the carrier gas), respectively. The desorption activation energy of the chemisorption sites ranged from 57.95 to 58.53 kJ mol−1 (CO2 as the carrier gas) and 74.02 to 79.92 kJ mol−1 (Ar as the carrier gas), respectively.
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