| Project/Area Number |
11440218
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
分離・精製・検出法
|
|---|
| Research Institution | Tokyo University of Science |
|---|
Principal Investigator |
KEN Sakai Faculty of Science, Department of Applied Chemistry, Tokyo University of Science Assistant Professor, 理学部, 講師 (30235105)
|
|---|
| Project Period (FY) |
1999 – 2001
|
| Project Status |
Completed (Fiscal Year 2001)
|
| Budget Amount *help |
¥7,900,000 (Direct Cost: ¥7,900,000)
Fiscal Year 2001: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2000: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1999: ¥5,700,000 (Direct Cost: ¥5,700,000)
|
|---|
| Keywords | Kinetics / Spectrophotometry / Flash Dissolution / Equilibria in Solution / Spectral Analysis / Reactions in Solution / SPECFIT / 反応速度解析 / 個体瞬間溶解装置 / 磁気天秤 |
|---|
| Research Abstract |
In this project, efforts have been made to develop a new instrument that enables the detection of an extremely rapid reaction that takes right after dissolution of a solid sample. The fundamental concept is very simple and is to develop a 'flash-solid-dissolution equipment' facilitating not only a prompt dissolution of a solid but also a prompt filtration for the removal of undissolved solid at the same time. To this end, experiments were carried out to find out an appropriate method offiltration. As a result, we found that a Teflon wool is a good candidate. We further endeavored to design to construct the main part of the above mentioned dissolution equipment. In our equipment, a solution is rapidly transferred into a solid-dissolution room equipped with a filtration facility. Injection is carried out by use of air pressure of about 3 atm. A freshly prepared filtrate is simultaneously transferred into an optical measurement cell. Finally, a rapid chemical reaction that takes place immediately after the dissolution event can be monitored by use of a multi-channel photodiode array spectrophotometer to analyze the kinetics of the reaction. In our new equipment, it is possible to minimize the dead time corresponding to the unobservable time domain into ca. 0.5 sec or so. With this methodology, we have succeeded in observing a very rapid reaction that takes place after dissolution of a mixed-valence tetranuclear platinum complex. We have been for a long time unaware of this reaction. Thus we have demonstrated that such an approach is indeed valid to better understand the chemical phenomena that are occurring right after dissolution of a certain chemical into a solution.
|
