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Journal articles on the topic 'Organic matrix'

To see the other types of publications on this topic, follow the link: Organic matrix.

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Veis, A. "Mineralization in Organic Matrix Frameworks." Reviews in Mineralogy and Geochemistry 54, no. 1 (January 1, 2003): 249–89. http://dx.doi.org/10.2113/0540249.

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2

Matsushita, Yohsuke, Hiroyuki Shimada, Takuya Miyashita, Miki Shibata, Shigeki Naka, Hiroyuki Okada, and Hiroyoshi Onnagawa. "Organic Bi-function Matrix Array." Japanese Journal of Applied Physics 44, no. 4B (April 21, 2005): 2826–29. http://dx.doi.org/10.1143/jjap.44.2826.

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3

Nausieda, I., Ryu Kyungbum, I. Kymissis, A. I. Akinwande, V. Bulovic, and C. G. Sodini. "An Organic Active-Matrix Imager." IEEE Transactions on Electron Devices 55, no. 2 (February 2008): 527–32. http://dx.doi.org/10.1109/ted.2007.913081.

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4

Sakaguchi, Yoshikazu, Hiroshi Tada, Kenji Mori, Yuichi Iketsu, and Joji Suzuki. "Color Passive-matrix Organic Electroluminescent Displays." Journal of Photopolymer Science and Technology 15, no. 2 (2002): 247–52. http://dx.doi.org/10.2494/photopolymer.15.247.

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5

Kim, Eunjin, Jisu Kim, Inseong Choi, Jeongwook Lee, and Woon-Seok Yeo. "Organic matrix-free imaging mass spectrometry." BMB Reports 53, no. 7 (July 31, 2020): 349–56. http://dx.doi.org/10.5483/bmbrep.2020.53.7.078.

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6

Kobayashi, Iwao, and Tetsuro Samata. "Bivalve shell structure and organic matrix." Materials Science and Engineering: C 26, no. 4 (May 2006): 692–98. http://dx.doi.org/10.1016/j.msec.2005.09.101.

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7

ZURER, PAMELA. "Nanowires isolated in organic polymer matrix." Chemical & Engineering News 74, no. 34 (August 19, 1996): 38. http://dx.doi.org/10.1021/cen-v074n034.p038.

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8

Pribat, D., and F. Plais. "Matrix addressing for organic electroluminescent displays." Thin Solid Films 383, no. 1-2 (February 2001): 25–30. http://dx.doi.org/10.1016/s0040-6090(00)01645-x.

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9

Arai, Michio, Kenji Nakaya, Osamu Onitsuka, Tetsushi Inoue, Mitsufumi Codama, Masaru Tanaka, and Hiroshi Tanabe. "Passive matrix display of organic LEDs." Synthetic Metals 91, no. 1-3 (December 1997): 21–25. http://dx.doi.org/10.1016/s0379-6779(97)03968-4.

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10

Zhu, Bizhong, Yuhong Wu, Herschel H. Reese, Dimitris E. Katsoulis, and Frederick J. McGarry. "Silicone-Organic Resin Hybrid Matrix Composites." Macromolecular Materials and Engineering 291, no. 9 (September 15, 2006): 1052–60. http://dx.doi.org/10.1002/mame.200600042.

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11

Zhou, Lisong, Alfred Wanga, Sheng-Chu Wu, Jie Sun, Sungkyu Park, and Thomas N. Jackson. "All-organic active matrix flexible display." Applied Physics Letters 88, no. 8 (February 20, 2006): 083502. http://dx.doi.org/10.1063/1.2178213.

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12

Morantz, Daniel J., and John W. Wigley. "Matrix interactions with organic triplet states." Journal of the Chemical Society, Faraday Transactions 2 82, no. 12 (1986): 2117. http://dx.doi.org/10.1039/f29868202117.

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13

Molodtsova, O. V., I. M. Aristova, D. V. Potorochin, S. V. Babenkov, I. I. Khodos, S. L. Molodtsov, M. Vorokhta, T. Skála, and V. Yu Aristov. "Noble metal nanoparticles in organic matrix." Applied Surface Science 506 (March 2020): 144980. http://dx.doi.org/10.1016/j.apsusc.2019.144980.

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14

Gao, Chloe Y., Susanne E. Bauer, and Kostas Tsigaridis. "Can semi-volatile organic aerosols lead to fewer cloud particles?" Atmospheric Chemistry and Physics 18, no. 19 (October 8, 2018): 14243–51. http://dx.doi.org/10.5194/acp-18-14243-2018.

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Abstract. The impact of condensing organic aerosols on activated cloud number concentration is examined in a new aerosol microphysics box model, MATRIX-VBS. The model includes the volatility basis set (VBS) framework coupled with the aerosol microphysical scheme MATRIX (Multiconfiguration Aerosol TRacker of mIXing state) that resolves aerosol mass and number concentrations and aerosol mixing state. By including the condensation of organic aerosols, the new model produces fewer activated particles compared to the original model, which treats organic aerosols as nonvolatile. Parameters such as aerosol chemical composition, mass and number concentrations, and particle sizes that affect activated cloud number concentration are thoroughly tested via a suite of Monte Carlo simulations. Results show that by considering semi-volatile organics in MATRIX-VBS, there is a lower activated particle number concentration, except in cases with low cloud updrafts, in clean environments at above-freezing temperatures, and in polluted environments at high temperatures (310 K) and extremely low-humidity conditions.

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15

Mori, K., Y. Sakaguchi, Y. Iketsu, and J. Suzuki. "Full-color passive-matrix organic EL displays." Displays 22, no. 2 (May 2001): 43–47. http://dx.doi.org/10.1016/s0141-9382(00)00060-3.

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16

Kubota, Hirofumi, Satoshi Miyaguchi, Shinichi Ishizuka, Takeo Wakimoto, Jun Funaki, Yoshinori Fukuda, Teruichi Watanabe, et al. "Organic LED full color passive-matrix display." Journal of Luminescence 87-89 (May 2000): 56–60. http://dx.doi.org/10.1016/s0022-2313(99)00229-x.

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17

George, Lisa, K. Sankaran, K. S. Viswanathan, and C. K. Mathews. "Matrix-Isolation Infrared Spectroscopy of Organic Phosphates." Applied Spectroscopy 48, no. 1 (January 1994): 7–12. http://dx.doi.org/10.1366/0003702944027705.

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Matrix-isolation infrared spectra of trimethyl phosphate (TMP), triethyl phosphate (TEP), and tri- n-butyl phosphate (TBP), in argon and nitrogen matrices, are reported for the first time. The peak widths of the sharpest features in our matrix-isolated spectra are typically 2 cm−1, compared with peak widths of 40 cm−1 seen in liquids for these compounds. Comparison with the vapor-phase spectrum of TMP reported earlier indicates that TMP is trapped in two different conformations in these matrices. Similar spectra were also obtained for TEP. Our matrix-isolated spectra indicate that the intramolecular hydrogen bonding (which is believed to be responsible for the lowering of the P=O frequency in the C3, conformer relative to the C3 conformer in these compounds) is stronger in TEP than in TMP. In the case of TBP, the peak widths were larger (8–10 cm−1) than those obtained for TMP and TEP. This observation is probably due to a distribution of conformers that may be trapped in the matrix, as a result of the increased alkyl chain length in TBP.

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18

Dusevich, V. M., J. McGuire, J. P. Gorski, Y. Wang, and M. P. Walker. "Morphology of Organic Matrix of Human Enamel." Microscopy and Microanalysis 21, S3 (August 2015): 189–90. http://dx.doi.org/10.1017/s1431927615001749.

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19

Liu, Hongyu, and Runguang Sun. "Laminated active matrix organic light-emitting devices." Applied Physics Letters 92, no. 6 (February 11, 2008): 063304. http://dx.doi.org/10.1063/1.2844854.

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20

Siddique, H., E. Rundquist, Y. Bhole, L. G. Peeva, and A. G. Livingston. "Mixed matrix membranes for organic solvent nanofiltration." Journal of Membrane Science 452 (February 2014): 354–66. http://dx.doi.org/10.1016/j.memsci.2013.10.012.

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21

Kijima, Y., N. Asai, N. Kishii, and S. I. Tamura. "RGB luminescence from passive-matrix organic LED'S." IEEE Transactions on Electron Devices 44, no. 8 (1997): 1222–28. http://dx.doi.org/10.1109/16.605458.

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22

Andersson, P., R. Forchheimer, P. Tehrani, and M. Berggren. "Printable All-Organic Electrochromic Active-Matrix Displays." Advanced Functional Materials 17, no. 16 (August 31, 2007): 3074–82. http://dx.doi.org/10.1002/adfm.200601241.

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23

Fukuda, Yoshinori, Satoshi Miyaguchi, Shinichi Ishizuka, Takeo Wakimoto, Jun Funaki, Hirofumi Kubota, Teruichi Watanabe, et al. "Organic LED Full Color Passive-Matrix Display." SID Symposium Digest of Technical Papers 30, no. 1 (1999): 430. http://dx.doi.org/10.1889/1.1834049.

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24

Miyaguchi, Satoshi, Shinichi Ishizuka, Takeo Wakimoto, Jun Funaki, Yoshinori Fukuda, Hirofumi Kubota, Kenji Yoshida, et al. "Organic LED full-color passive-matrix display." Journal of the Society for Information Display 7, no. 3 (1999): 221. http://dx.doi.org/10.1889/1.1984479.

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25

Zhang, Bu-xin, Zhi-lin Zhang, Wen-qing Zhu, Xue-yin Jiang, and Shao-hong Xu. "Organic thin film electroluminescent passive matrix display." Journal of Shanghai University (English Edition) 5, no. 2 (June 2001): 151–55. http://dx.doi.org/10.1007/s11741-001-0013-9.

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26

Jodaikin, A., S. Weiner, Y. Talmon, E. Grossman, and W. Traub. "Mineral-organic-matrix relations in tooth enamel." International Journal of Biological Macromolecules 10, no. 6 (December 1988): 349–52. http://dx.doi.org/10.1016/0141-8130(88)90027-x.

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27

Tan, Li-Wei, Chan-Choy Chum, Kian-Soo Ong, Xiaotao Hao, Eric C. W. Ou, and Furong Zhu. "Semitransparent passive matrix organic light-emitting displays." Journal of Materials Science: Materials in Electronics 18, no. 9 (December 21, 2006): 913–18. http://dx.doi.org/10.1007/s10854-006-9061-z.

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28

Natali Sora, I., R. Pelosato, L. Zampori, D. Botta, G. Dotelli, and M. Vitelli. "Matrix optimisation for hazardous organic waste sorption." Applied Clay Science 28, no. 1-4 (January 2005): 43–54. http://dx.doi.org/10.1016/j.clay.2004.01.015.

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29

Stanculescu, A., L. Tugulea, H. V. Alexandru, F. Stanculescu, and M. Socol. "Molecular organic crystalline matrix for hybrid organic–inorganic (nano) composite materials." Journal of Crystal Growth 275, no. 1-2 (February 2005): e1779-e1786. http://dx.doi.org/10.1016/j.jcrysgro.2004.11.210.

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30

Jagannathan, S., J. R. Cooper, and C. L. Wilkins. "Matrix Effects in Matrix Isolation Infrared Spectroscopy." Applied Spectroscopy 43, no. 5 (July 1989): 781–86. http://dx.doi.org/10.1366/0003702894202274.

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A major factor limiting extensive use of matrix isolation gas chromatography-Fourier transform infrared spectrometry is the incompatibility of matrix-isolated spectra with available vapor- or condensed-phase spectral data bases. Here, matrix and surface effects on matrix isolation infrared spectra of organic molecules are investigated. Use of xenon at −215°C (58 K) to obtain matrix isolation spectra that are similar to condensed-phase spectra is demonstrated. Finally, the effect of temperature on reflection-absorption infrared spectra of matrix-isolated molecules is discussed, and guidelines for obtaining and interpreting matrix isolation infrared spectra of gas chromatographic eluants using the existing condensed phase data bases are provided.

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31

Lee, Sangyun, Bon‐Won Koo, Eun‐Jeong Jeong, Eunkyung Lee, Sangyeol Kim, Jungwoo Kim, Ho‐Nyeon Lee, et al. "Integration of 4.5” active matrix organic light‐emitting display with organic transistors." Journal of Information Display 7, no. 4 (January 2006): 21–23. http://dx.doi.org/10.1080/15980316.2006.9652016.

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32

Clark II, George R. "Organic matrix taphonomy in some molluscan shell microstructures." Palaeogeography, Palaeoclimatology, Palaeoecology 149, no. 1-4 (June 1999): 305–12. http://dx.doi.org/10.1016/s0031-0182(98)00208-9.

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33

Jeszka, J. K., A. Tracz, D. Wostek, G. Boiteux, and M. Kryszewski. "Preparation of organic metal nanocrystals in polymer matrix." Synthetic Metals 109, no. 1-3 (March 2000): 165–68. http://dx.doi.org/10.1016/s0379-6779(99)00221-0.

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34

Bruce, Robert A., and Dominic D. Dziewiatkowski. "Differentiation of the organic matrix in bone repair." Journal of Oral and Maxillofacial Surgery 45, no. 11 (November 1987): 939–44. http://dx.doi.org/10.1016/0278-2391(87)90445-9.

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35

Guenet, Jean-Michel, and Daniel López. "Bicopper Organic Complexes in a Thermoreversible Gel Matrix." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 324, no. 1 (December 1998): 197–203. http://dx.doi.org/10.1080/10587259808047155.

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36

Iwata, Hidenobu, Osamu Kamei, Yukichi Abe, Shunji Nishio, Akira Wakatsuki, Kenji Ochi, and Masafumi Takeuchi. "The Organic Matrix of Urinary Uric Acid Crystals." Journal of Urology 139, no. 3 (March 1988): 607–10. http://dx.doi.org/10.1016/s0022-5347(17)42542-0.

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37

Duverger, Olivier, Elia Beniash, and Maria I. Morasso. "Keratins as components of the enamel organic matrix." Matrix Biology 52-54 (May 2016): 260–65. http://dx.doi.org/10.1016/j.matbio.2015.12.007.

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38

Peebles, L. H. "An Assessment of Carbon Fiber/Organic Matrix Interactions." Journal of Adhesion 54, no. 1-4 (November 1995): 1–22. http://dx.doi.org/10.1080/00218469508014377.

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39

Tej Mallajosyula, Arun, Naveen Srivastava, S. Sundar Kumar Iyer, and Baquer Mazhari. "Characterization of matrix and isolated organic solar cells." Solar Energy Materials and Solar Cells 94, no. 8 (August 2010): 1319–23. http://dx.doi.org/10.1016/j.solmat.2008.09.027.

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40

Lignell, H., M. L. Hinks, and S. A. Nizkorodov. "Exploring matrix effects on photochemistry of organic aerosols." Proceedings of the National Academy of Sciences 111, no. 38 (September 8, 2014): 13780–85. http://dx.doi.org/10.1073/pnas.1322106111.

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41

Kinsel, Gary R., Josef Lindner, and Jürgen Grotemeyer. "Matrix-assisted laser desorption of neutral organic molecules." Organic Mass Spectrometry 26, no. 12 (December 1991): 1052–56. http://dx.doi.org/10.1002/oms.1210261204.

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42

von Borczyskowski, C. "Optically detected NQR on matrix-isolated organic molecules." Berichte der Bunsengesellschaft für physikalische Chemie 91, no. 11 (November 1987): 1137–41. http://dx.doi.org/10.1002/bbpc.19870911112.

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43

Wakimoto, T., H. Ochi, S. Kawami, H. Ohata, K. Nagayama, R. Murayama, Y. Okuda, et al. "Dot-matrix display using organic light-emitting diodes." Journal of the Society for Information Display 5, no. 3 (1997): 235. http://dx.doi.org/10.1889/1.1985157.

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44

Swift, Debbie M., and A. P. Wheeler. "EVIDENCE OF AN ORGANIC MATRIX FROM DIATOM BIOSILICA1." Journal of Phycology 28, no. 2 (April 1992): 202–9. http://dx.doi.org/10.1111/j.0022-3646.1992.00202.x.

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45

do Espirito Santo, Alexandre R., Pedro D. Novaes, and Sergio R. P. Line. "Anisotropic properties of the enamel organic extracellular matrix." European Journal of Oral Sciences 114, s1 (May 2006): 333–37. http://dx.doi.org/10.1111/j.1600-0722.2006.00326.x.

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46

Ambroż, Hanna B., Grażyna K. Przybytniak, and Teresa Wrońska. "Matrix effects in gamma-radiolysis of organic sulphides." International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry 37, no. 3 (January 1991): 479–81. http://dx.doi.org/10.1016/1359-0197(91)90022-t.

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47

Martinez, Gregory M. "Fast cures for thick laminated organic matrix composites." Chemical Engineering Science 46, no. 2 (1991): 439–50. http://dx.doi.org/10.1016/0009-2509(91)80005-j.

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48

Williams, J. G., M. R. James, and W. L. Morris. "Formation of the interphase in organic-matrix composites." Composites 25, no. 7 (January 1994): 757–62. http://dx.doi.org/10.1016/0010-4361(94)90212-7.

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49

Sriarj, Wantida, Kazuhiro Aoki, Keiichi Ohya, Yuzo Takagi, and Hitoyata Shimokawa. "Bovine dentine organic matrix down-regulates osteoclast activity." Journal of Bone and Mineral Metabolism 27, no. 3 (March 20, 2009): 315–23. http://dx.doi.org/10.1007/s00774-009-0063-9.

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50

Williams, J. G., M. E. Donnellan, M. R. James, and W. L. Morris. "Properties of the interphase in organic matrix composites." Materials Science and Engineering: A 126, no. 1-2 (June 1990): 305–12. http://dx.doi.org/10.1016/0921-5093(90)90137-r.

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