Generation of Charge-control Ability of Pararosaniline Due to Protonation and its Protonation Mechanism
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- HITACHI Akio
- Sony Corporation, Media Format Department
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- IWATA Shohei
- Department of Applied Physics, Graduate School of Engineering Yokohama National University
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- MIZUGUCHI Jin
- Department of Applied Physics, Graduate School of Engineering Yokohama National University
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Description
Triphenyl-pararosaniline (TPPR)is a charge-control agent (CCA) of the positive type for toners in the electrophotographic process. Suganami et al. reported that the charge control ability of TPPR is greatly improved if TPPR forms a charge-transfer (CT) complex with CCAs of the negative type, as those of n-propyl gallate (TPPR/PG=1/2), 3,5-di-tert-butylsalicylate zinc complex (TPPR/SZC=1/3) and 3,5-di-tert-butylsalicylate (TPPR/TBS=1/6). On the contrary, we interpret here the enhanced charge-control ability as arising from protonation of TPPR due to phenolic hydroxides of TBS, SZC and PG. The ratio of TPPR to these acids can be explained in terms of their effective acidity weakened significantly by intra-and intermolecular hydrogen bonds in the solid state, as revealed from structure analysis of these acids.
Journal
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- NIHON GAZO GAKKAISHI (Journal of the Imaging Society of Japan)
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NIHON GAZO GAKKAISHI (Journal of the Imaging Society of Japan) 44 (5), 342-346, 2005
The Imaging Society of Japan
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Details 詳細情報について
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- CRID
- 1390282679074605312
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- NII Article ID
- 130004719699
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- NII Book ID
- AA1137305X
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- ISSN
- 18804675
- 13444425
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- NDL BIB ID
- 7692815
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- CiNii Articles
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- Abstract License Flag
- Disallowed