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Cu CMP Slurry and Colloidal Chemistry Cu CMP浆料和胶体化学
Pub Date : 2008-01-01 DOI: 10.4011/SHIKIZAI.81.341
T. Itakura
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引用次数: 0
Determination of Particle Size Distribution (PSD) of Highly Concentrated Inorganic Fine Particle Suspensions Using Ultrasonic Attenuation Spectroscopy, Examination of Measurement Reproducibility and Accuracy 用超声衰减光谱法测定高浓度无机细颗粒悬浮液的粒径分布,测量的再现性和准确性检验
Pub Date : 2008-01-01 DOI: 10.4011/SHIKIZAI.81.280
Kinue Yada, Kazuyuki Hosoi, S. Takeda
近年開発された超音波減衰法を用いて高濃度系無機粉体スラリーの粒度分布を測定し, 従来から用いられているレーザー回折法, 光子相関法による希薄系粒度分布測定との再現性および精度の比較を行った。その結果, 測定の再現性については, 超音波減衰法を用いた場合は従来法と同等以上の良好な再現性を得た。また測定精度については, 従来法と同等の粒子径の値を得た。これらの結果から, 超音波減衰法を用いた粒度分布測定によって, 高濃度系無機粉体スラリーを希釈することなく粒子径を評価することが可能であり, この手法が工程管理に有用であることが見いだせた。
利用近年来开发的超声波衰减法测定了高浓度类无机粉体浆的粒度分布,并与此前使用的激光衍射法和光子相关法测定稀薄类粒度分布进行了再现性和精度的比较。结果,在测定的再现性方面,采用超声波衰减法时获得了与传统方法相同以上的良好再现性。另外,在测量精度方面,得到了与传统方法相同的粒子直径值。从这些结果来看,通过使用超声波衰减法测定粒度分布,可以在不稀释高浓度类无机粉体浆的情况下对粒径进行评价,表明该方法对工程管理非常有用。
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引用次数: 0
The Color Sift of Cerium Molybdenum Sheelite by Substituting Bi3 + or W6 + Ion 用Bi3 +或W6 +离子取代铈钼板的颜色筛选
Pub Date : 2008-01-01 DOI: 10.4011/SHIKIZAI.81.73
T. Odaki, K. Hashimoto, Y. Toda
We prepared chemical compounds whose Ce 3+ ions are replaced with Bi 3 + ions at a certain rate in LiCeMo 2 O 8 , NaCeMo 2 O 8 , Ca 0.5 CeMo 2 O 8 , and Sr 0.5 CeMo 2 O 8 that have the sheelite crystal structure, and the change of the hue of these materials was investigated. In addition, the cause of Ce 3+ ion color development in the sheelite structure was studied based on the result of substituting Bi 3+ ions for Ce 3+ ions and change of the hue of the compounds whose Mo 6+ ions are replaced with W 6+ ions. The result revealed that the absorption edge shifted to the longer wavelength side as the amount of the replaced Bi 3 + ions increased, and the hue of the product changed from yellow to reddish yellow. The changes in the chemical bonding nature of the crystal were found to give a great impact on the color development of the Ce 3+ ion. Although the Ce 3+ ion takes on the yellow hue in the sheelite crystal structure, its absorption edge can be shifted freely by generating the substitutional solid solution of metal ions with different electronegativity.
我们在licemo2o8、nacemo2o8、ca0.5 cemo2o8和sr0.5 cemo2o8中制备了具有层状晶体结构的ce3 +离子以一定速率被bi3 +离子取代的化合物,并研究了这些材料的色相变化。此外,通过用bi3 +离子取代ce3 +离子的结果,以及用w6 +离子取代mo6 +离子后化合物的色相变化,研究了ce3 +离子在板层结构中显色的原因。结果表明,随着bi3 +取代量的增加,吸收边向较长波边偏移,产物的颜色由黄色变为红黄色。发现晶体化学键性质的变化对ce3 +离子的显色有很大的影响。虽然ce3 +离子在膜层晶体结构中呈现黄色色调,但通过产生不同电负性金属离子的取代固溶体,其吸收边可以自由移动。
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引用次数: 3
Addition Effect of Fatty Alcohol with Long Alkyl Chains on the Size of Oleic Acid Droplets in Aqueous Solutions without Surfactant 无表面活性剂水溶液中长烷基链脂肪醇加成对油酸液滴大小的影响
Pub Date : 2008-01-01 DOI: 10.4011/SHIKIZAI.81.111
H. Akatsuka, Tadahito Seto, Mariko Hayashi, T. Sakai, H. Sakai, M. Abe
オレイン酸 (OA) を油相とする界面活性剤無添加O/W型エマルション (SFE) 溶液中の油滴の粒子径に及ぼす長鎖脂肪族アルコール (FA) の添加効果を検討した。その結果, OA濃度が10mM以上のSFE滴の成長速度には, 主として合一が関与していることが示唆された。一方, OAに対して種々のFAを重量比9 : 1で混合したところ, 1-オクタデカノール (OD) および1-ドコサノールの場合, OA単独系に比べてSFEの分散安定性が飛躍的に向上した。次に, 種々の重量比で混合したOA/OD混合油のDSC測定, レオロジー測定, 小角X線散乱測定を行ったところ, OAとODを重量比6 : 4で混合した場合のみ, ラメラ構造をもつ剛直なα-ゲルを形成した。さらに, 表面圧―面積等温曲線測定から, 重量比6 : 4で混合したOA/OD二成分系はOA単独に比べて気―液界面へ密に配向し, かつ膜の崩壊圧は高かった。これらの結果から, 水溶液中のOAにODを混合すると, その油滴界面で自発的に (自然発生的に) α-ゲルを形成して強固な界面膜となるために油滴の合一を抑制することがわかった。
研究了添加长链脂肪族醇(FA)对以油酸(OA)为油相的无添加界面活性剂的O/W型乳胶(SFE)溶液中的油滴粒子直径产生的影响。结果表明,OA浓度在10mm以上的SFE滴的增长速度主要与合一有关。另一方面,以9:1的重量比对OA混合各种FA后,在使用1-屋大癸醇(OD)和1- docossano时,与OA单独系统相比,SFE的分散稳定性得到了飞跃性的提高。接着,对以各种重量比混合的OA/OD混合油进行了DSC测量、流变测量、小角X射线散射测量,结果将OA和OD的重量比为6:仅在4中混合时,形成了具有拉梅拉结构的刚直α-凝胶。另外,通过表面压—面积等温曲线测量发现,以重量比6∶4混合的OA/OD双组分系统与OA单独相比,向气—液界面定向更紧密,而且膜的崩溃压也更高。从这些结果可知,在水溶液中OA中混合OD后,在油滴界面会自发地(自然地)形成α-凝胶,成为坚固的界面膜,从而抑制油滴合一。
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引用次数: 3
Viscoelastic Behavior of Organo-gels 有机凝胶的粘弹性行为
Pub Date : 2008-01-01 DOI: 10.4011/SHIKIZAI.81.87
T. Shikata
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引用次数: 0
Solidification of Perfluoropolyether Using Nonaqueous Emulsification Surfactant 用非水乳化表面活性剂固化全氟聚醚
Pub Date : 2008-01-01 DOI: 10.4011/SHIKIZAI.81.150
K. Yoda, M. Shibata
撥油性と薬品安定性に優れた液状物質であるパーフルオロポリエーテル (PFPE) を固形化する目的で, 炭化水素系オイル中にPFPEの液滴を分散させた非水乳化系の検討を行った。パーフルオロアルキルメタクリレート・アルキルメタクリレート共重合体を乳化剤として用いることで炭化水素系オイルとPFPEの乳化が可能であった。炭化水素系オイルの固形化剤として汎用されているパラフィンワックスを添加することで固形の乳化物が得られた。また, ワックスに分岐パラフィンを添加することで連続相であるオイル相の固形化能は飛躍的に高まり, それによりPFPEの含有量を最大95%まで高めることが可能であった。
为了将具有良好疏油性和药品稳定性的液态物质全氟聚醚(PFPE)固化,研究了在碳氢类油中分散PFPE液滴的非水乳化体系。使用全氟烷基甲基丙烯酸甲酯共聚物作为乳化剂可以实现碳氢类油和PFPE的乳化。通过添加作为碳氢类油固体化剂而通用的石蜡,得到了固体的乳化物。另外,通过在蜡中添加分支石蜡,作为连续相的油相的固化能力得到了飞跃性的提高,因此PFPE的含量最高可提高到95%。
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引用次数: 1
Antioxidant activity of noble metal (gold, platinum)-biopolymer nanocomposites 贵金属(金、铂)-生物聚合物纳米复合材料的抗氧化活性
Pub Date : 2005-01-01 DOI: 10.4011/SHIKIZAI1937.78.112
Shintaro Akiyama, Tomokazu Yoshimura, K. Esumi
Three different platinum-biopolymer nanocomposites have been prepared independently in the presence of hexachloroplatinic acid and biopolymers like fucoidan, alginic acid and sodium hyaluronate (NaHA) via sodium borohydride reduction. The average particle diameter of platinum nanoparticles using fucoidan becomes slightly smaller, with a decrease of the concentration of fucoidan, ranging from 3.1 to 2.6nm. On the other hand, the average particle diameter of platinum nanoparticles using NaHA becomes slightly larger, with a decrease of the concentration of NaHA, ranging from 3.4nm to 3.8nm. The average particle diameter of platinum nanoparticles using alginic acid is 3.2-3.4nm which is independent of the biopolymer concentrations. The antioxidant activities of the platinum-biopolymer nanoconiposites upon elimination of hydroxyl radicals formed in an H 2 O 2 /FeSO 4 system have been studied using a spin-trapping method; All the nanocomposites exhibit high catalytic activities that are affected by the concentration and the kind of the biopolymer. In addition, the activities of the platinum-biopolymer nanocomposites are higher than those of the gold biopolymer nanocomposites. The highest antioxidant activity for the platinum-alginic acid nanocomposites was 110 times higher than that of ascorbic acid.
在六氯铂酸和岩藻糖聚糖、海藻酸和透明质酸钠(NaHA)等生物聚合物存在下,通过硼氢化钠还原制备了三种不同的铂-生物聚合物纳米复合材料。随着褐藻糖胶浓度的降低,使用褐藻糖胶制备的铂纳米颗粒的平均粒径逐渐变小,在3.1 ~ 2.6nm之间。另一方面,随着NaHA浓度的降低,使用NaHA制备的铂纳米颗粒的平均粒径略有增大,在3.4nm ~ 3.8nm之间。褐藻酸制备的铂纳米粒子的平均粒径为3.2 ~ 3.4nm,与生物聚合物的浓度无关。采用自旋俘获法研究了铂-生物聚合物纳米复合材料在消除h2o2 / feso4体系中形成的羟基自由基后的抗氧化活性;所有的纳米复合材料都表现出较高的催化活性,这些活性受生物聚合物的浓度和种类的影响。此外,铂-生物聚合物纳米复合材料的活性高于金-生物聚合物纳米复合材料。铂-褐藻酸纳米复合材料的抗氧化活性最高,是抗坏血酸的110倍。
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引用次数: 10
Water/Supercritical CO2 Microemulsions with a Fluorinated Double-tail Surfactant for Syntheses of Semiconductor Ultrafine Particles 含氟双尾表面活性剂的水/超临界CO2微乳用于半导体超细颗粒的合成
Pub Date : 1900-01-01 DOI: 10.4011/SHIKIZAI.81.331
Masanobu Sagisaka, M. Hino, H. Sakai, M. Abe, A. Yoshizawa
A water/supercritical CO 2 microemulsion (W/scCO 2 μE) with a fluorinated double-tail surfactant bis (1H,1H,2Η,2H-heptadecanuorodecyl)-2-sulfosuccinate (8FS(EO) 2 ) was evaluated in terms of its nanoreactor performance for synthesizing semiconductor ultrafine particles of TiΟ 2 , ZnS, and CdS. By the addition of tetraisopropylorthotitanate (TIP) in W/scCO 2 μE, TiO 2 ultrafine particles were successfully synthesized with a spherical shape and sizes of several tens of nanometers, which were similar to those synthesized in W/cyclohexane μE with a typical hydrocarbon double-tail surfactant AOT. Interestingly, in contrast to the μE system, TiO 2 particle syntheses in liquid-crystal-like (LC-like) surfactant precipitant phase yielded a dendritical morphology of TiO 2 . For metal sulfide synthesis, the addition of metal nitrates as precursors in W/scCO 2 μE was found to lower the maximum W 0 value at which W/scCΟ 2 μE can form, which would result from the promoted aggregation and fusion between reverse micelles, i.e., LC formation. After mixing both the W/scCΟ 2 μEs containing metal nitrate and Na 2 S, metal sulfide ultrafine particles were yielded with spherical shape and sizes of several tens of nanometers. These results suggested that W/scCΟ 2 μE with 8FS (EO) 2 may become a valuable nanoreactor when further investigations reveal size-control techniques for the products.
采用氟化双尾表面活性剂bis (1H,1H,2Η, 2h -庚十四烷基)-2-磺基琥珀酸盐(8FS(EO) 2)制备了水/超临界co2微乳液(W/ scco2 μE),并对其纳米反应器性能进行了评价,以制备TiΟ 2、ZnS和CdS半导体超细颗粒。通过在W/scCO 2 μE中加入四异丙基氯钛酸酯(TIP),成功合成了粒径为几十纳米的球形二氧化钛超细颗粒,与在W/环己烷μE中使用典型碳氢化合物双尾表面活性剂AOT合成的二氧化钛超细颗粒相似。有趣的是,与μE体系相比,在类液晶(LC-like)表面活性剂沉淀相中合成的tio2颗粒产生了树枝状的tio2形貌。对于金属硫化物的合成,在W/scCO 2 μE中加入金属硝酸盐作为前驱体可以降低W/scCΟ 2 μE形成的最大W 0值,这是由于促进了反胶束之间的聚集和融合,即LC的形成。将含有硝酸金属的W/scCΟ 2 μEs与Na 2s混合后,可以得到球形、几十纳米大小的金属硫化物超细颗粒。这些结果表明,当进一步研究产品的尺寸控制技术时,W/scCΟ 2 μE与8FS (EO) 2可能成为一种有价值的纳米反应器。
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引用次数: 10
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Shikizai Kyokaishi
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