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[in Japanese], [in Japanese], [in Japanese]
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1
Published: 2002
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[in Japanese], [in Japanese], [in Japanese], Thi Lai Le
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[in Japanese]
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[in Japanese], [in Japanese], [in Japanese]
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[in Japanese]
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[in Japanese], [in Japanese]
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[in Japanese], [in Japanese], [in Japanese]
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7
Published: 2002
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[in Japanese], [in Japanese]
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8
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Zaenal Abidin, Naoto Matue, Teruo Henmi
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9
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The previous experiments result showed that during dissolution process structure of KyP is more vulnerable to attack as compared to the structure of KnP. This features show that the type of dissolution of allophane is significantly affected by Si/Al ratio. The present experiment examines the dissolution rate of allophane at temperatures of 20 30 and 35C. The activation energy Ea will be determined to know stability of structure of allophane during dissolution process occurred.
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[in Japanese], [in Japanese], [in Japanese]
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10
Published: 2002
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Erni Johan, Naoto Matsue, Teruo Henmi
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11
Published: 2002
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Our previous experiment showed that surface acidity of allophane was increased by P adsorption The increase of acidity is may be originated from Bronsted acidity or Lewis acidity. In this presentation calculation by molecular orbital method was carried out to clarify the mechanism of increasing the surface acidity.
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Gay Necita Padilla, Naoto Matsue, Teruo Henmi
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12
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Results from previous experiment showed that sulfate were strongly adsorbed on allophane. The adsorption was proposed to be anion and ligand exchange reactions. Adsorption of anions on clay minerals through ligand exchange reaction is likely to cause a change in the surface charge and since the amounts of sulfate adsorbed were greater than the AEC values these leads to the assumption that the new formed compound have different chemical properties than the original allophane.
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[in Japanese], [in Japanese]
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13
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[in Japanese], [in Japanese], [in Japanese]
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14
Published: 2002
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[in Japanese], [in Japanese], [in Japanese]
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15
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
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16
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[in Japanese], [in Japanese], [in Japanese], Juraj Bujdak, [in Japanes ...
Pages
17
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[in Japanese], [in Japanese], [in Japanese]
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18
Published: 2002
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[in Japanese], [in Japanese], [in Japanese]
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19
Published: 2002
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[in Japanese], [in Japanese], [in Japanese]
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20
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[in Japanese]
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21
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
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22
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
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23
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
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24
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[in Japanese], [in Japanese], [in Japanese]
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25
Published: 2002
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
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26
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
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27
Published: 2002
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
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28
Published: 2002
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
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29
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
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30
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[in Japanese], [in Japanese]
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31
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
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32
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[in Japanese], Temuujin Jadambaa, [in Japanese], [in Japanese]
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33
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[in Japanese], [in Japanese]
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34
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
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35
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[in Japanese], [in Japanese], [in Japanese]
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36
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S. Khodijah Chaerun, [in Japanese], [in Japanese]
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37
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The preliminary laboratory test to assess the ability of various clays sand and other mineral types (i.e. kaolinite bentonite 50% sand-50%bentonite river sand and CaCO3) as adsorbent of heavy oil was conducted. The result showed that bentonite alone was the best adsorbent of heavy oil than others. According to the findings we undertook the further laboratory assay to investigate their role on degradation rate of heavy oil. It was expected that these clays will be able to play a multiuse role not only as adsorbent but also as microorganism growth supporting media in accelerating degradation of heavy oil. In the present study we employed two types of clays that is smectite (bentonite) and kaolinite. In addition to the clays we also employed sand and organic-rich soil as comparison. The laboratory experiment was designed in batch culture. A pack of heavy oil sample collected from a heavy oil contaminated coastal area at Wajima Seashore (Ishikawa Prefecture) in! > Japan was used as the initial inoculum. Approximately 1% (v/v) of heavy oil was used to inoculate 250-ml flasks containing 200 ml of seawater medium supplied in the culture as the sole carbon and energy source. Cultures were inoculated with 300 mg/l of sand organic-rich soil mixture of bentonite and kaolinite (ratio 1:1) bentonite and kaolinite respectively and incubated at the room temperature for 60 days. Clay-uninoculated flask was also incubated as control. Thereafter microorganism growth was monitored by measuring the optical density at 600nm and deletion of heavy oil was detected using FTIR at wavenumber 2500-3500 cm-1. Organic compound removal was detected as COD (mg/l) and observation of microorganism morphology was conducted with using optical and epi-fluorescence microscope with DAPI staining and scanning electron microscope. Additionally measurement of pH dissolved-oxygen (DO) temperature electrode potential versus the standard hydrogen electrode (Eh) and electrical conductivity (EC) was undertaken to investigate the biodegradation process. The composition of minerals was estimated by using XRD analyzer. The results pointed out that the smectite type of clay was the best one to adsorb heavy oil than others and play an important role as microorganism growth supporting media in accelerating degradation of heavy oil. It can be concluded that degradation of heavy oil undergone was combination of two processes that is physical process by clay or other minerals and biological process by hydrocarbon-degrading microorganism.
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[in Japanese]
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38
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[in Japanese]
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39
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[in Japanese]
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40
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[in Japanese], [in Japanese]
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41
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
Pages
42
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
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43
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
Pages
44
Published: 2002
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[in Japanese], [in Japanese], [in Japanese]
Pages
45
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
Pages
46
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[in Japanese], [in Japanese]
Pages
47
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
Pages
48
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[in Japanese]
Pages
49
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[in Japanese], [in Japanese], [in Japanese]
Pages
50
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