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Immobilization of divalent transition metals from aqueous solutions using crystalline hydrated titania fibers 用结晶水合二氧化钛纤维从水溶液中固定化二价过渡金属
Pub Date : 1985-01-01 DOI: 10.2109/JCERSJ1950.93.1077_225
Y. Fujiki, T. Sasaki, Y. Komatsu
From a viewpoint of the treatment of high level radioactive liquid waste , the immobilization of divalent transition metal ions from aqueous solutions was studied by the use of the crystalline hydrated titania (H2Ti2O5• nH2O) fibers as an ion-adsorbent . The each metal ion was saturately adsorbed on the fibrous adsorbent from the aqueous solution of the divalent transition metal acetate. The adsorbed metal ions were immobilized in crystal lattices as main components of various titanate minerals after the sintering treatment. The copper ions were immobilized into the mineral assemblage of rutile, and Cu2TiO3 and Cu3TiO4 phases having a complex crystal structure . Zinc ions were fixed into the mineral assemblage of rutile and a Zn2TiO4 phase of the inverse spinel structure. Each metal ion of manganese, cobalt and nickel was immobilized into the same mineral assemblage of rutile and a MTiO3 (M=Mn, Co, and Ni) phase of the ilmenite structure . Rutile in these immobilizers occurs as a matrix mineral in the largest amount. The leachability of each metal ion in the immobilizers was measured under normal atmospheric and hydrothermal conditions . The results of the former indicated to be very stable with high leach resistance of maximal 3.210-9 gcmd-1 of mangnese ion, and the results of the latter also indicated to be very stable with maximal 9.1109g• cm2d-1 of nickel ion. [Received September 13, 1984]
从高放废液处理的角度出发,研究了水合二氧化钛(H2Ti2O5•nH2O)结晶纤维作为离子吸附剂对水溶液中二价过渡金属离子的固定化。从二价过渡金属醋酸酯水溶液中提取的金属离子在纤维吸附剂上被饱和吸附。经烧结处理后,吸附的金属离子作为钛酸盐矿物的主要成分固定在晶格中。铜离子被固定在金红石、Cu2TiO3和Cu3TiO4相的矿物组合中,具有复杂的晶体结构。锌离子被固定在金红石和逆尖晶石结构的Zn2TiO4相矿物组合中。锰、钴和镍的每一种金属离子被固定在相同的矿物组合金红石和钛铁矿结构的MTiO3 (M=Mn、Co和Ni)相中。金红石在这些固定化剂中以基质矿物的形式出现的量最大。测定了固定剂中各金属离子在常压和水热条件下的浸出率。前者的结果非常稳定,锰离子的最大抗浸出能力为3.210-9 gcmd-1;后者的结果也非常稳定,镍离子的最大抗浸出能力为9.1109g•cm2d-1。[1984年9月13日收到]
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引用次数: 5
ラマン分光法によるCaO-Al2O3-B2O3系ガラスの研究 拉曼光谱法对ao - al2o3 - b2o3系玻璃的研究
Pub Date : 1984-12-01 DOI: 10.2109/JCERSJ1950.92.1072_680
幸平 福味, 二郎 福永, 吉田 直次郎, 将昌 井原
CaO-Al2O3-B2O3系ガラスの低ホウ素含有領域における構造をラマンスペクトル法を用い調べた. この領域に存在する特徴的な構造群はアルミネート網目, オルソボーレート群, 2CaO・Al2O3・B2O3結晶類似の構造である. ラマンスペクトルではアルミネート網目によるピークは540cm-1と770cm-1に, オルソボーレート群によるピークは930cm-1に, 2CaO・Al2O3・B2O3結晶に特徴的な構造群のピークは980cm-1に観測される. B2O3を5mol%又は10mol%含むガラスでは, アルミネート網目とオルソボーレート群が主要な構造群であり, 2CaO・Al2O3・B2O3結晶類似の構造も多少共存する. B2O3を20mol%含むガラスでは, アルミネート網目, オルソボーレート群, 2CaO・Al2O3・B2O3結晶類似の構造が主体を占め, B2O325mol%含むガラスでは, オルソボーレート群と2CaO・Al2O3・B2O3結晶類似構造が主体をなす. すなわち, ホウ素含有量が増加するにつれて, アルミネート網目は減少し, 2CaO・Al2O3・B2O3結晶類似の構造が増加する. またAl2O3をCaOで置換するとオルソボーレート群の量は増加する.
采用拉曼谱法调查了在CaO-Al2O3-B2O3系玻璃的低硼含量区域的结构。该区域存在的特特性结构群有:铝层压网目;2cao、Al2O3、B2O3结晶类似的构造。在拉曼光谱中,由alm压板组成的峰值为540cm-1和770cm-1,由orsoborate组组成的峰值为930cm-1,2cao、Al2O3、B2O3结晶的特征结构群的峰值在980cm-1被观测到。在含有5mol%或10mol% B2O3的玻璃中,铝制层压网状和烯烃硼酸盐是主要的结构群,2cao、Al2O3、B2O3结晶类似的结构也多少共存。在含有20mol% B2O3的玻璃中,铝制层压网状;olsoborate组,2cao、Al2O3、B2O3晶体类似的结构占主体,在含有B2O325mol%的玻璃中,olsoborate组和2cao、Al2O3、B2O3结晶类似结构构成主体。也就是说,随着硼含量的增加,层压网格减少,2cao、Al2O3、B2O3结晶类似的结构增加。另外,用CaO置换Al2O3时,olsoborate组的量增加。
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引用次数: 5
Z=1の組成をもつβ-サイアロン熱間加圧焼結体の強度 组成Z=1的β-重离子热加压烧结体的强度
Pub Date : 1984-01-01 DOI: 10.2109/JCERSJ1950.92.45
正気 梅林, 和司 岸, 英治 谷, 和夫 小林
α-Si3N4, α-Al2O3及びAlNを出発原料にして, 熱間加圧焼結法により製造したβ-サイアロン焼結体の室温及び1400℃における曲げ強度を測定した. β-サイアロン焼結体の製造に用いた混合粉末の組成は, Z=1 (1.8), Z=1 (2.8), Z=1 (4) 及びZ=1 (5.5) である. ここで, 括弧内の数字は, Z=1の組成をもつβ-サイアロンからの酸素の過剰の当量%を示す.(1) Z=1 (5.5) 及びZ=1 (4) は, 十分ち密化したが, Z=1 (2.8) 及びZ=1 (1.8) は, ち密な焼結体とならなかった.(2) 焼結体の組成は, いずれもβ-サイアロンからなるが, Z=1 (4) 及びZ=1 (5.5) から得た焼結体には, 走査型電子顕微鏡観察から, ガラス質粒界相が認められた.(3) Z=1 (4) の室温における曲げ強度は, 55.5kg/mm2と最も高く, 混合粉末の組成がZ=1 (4) より酸素側へ又は窒素側へ移行しても, 焼結体の曲げ強度は, 低下した. Z=1 (5.5), Z=1 (4), Z=1 (2.8) 及びZ=1 (1.8) 焼結体の1400℃曲げ試験で, 各焼結体とも強度の低下は認められなかった.(4) 各焼結体の室温及び1400℃破断は, いずれも各焼結体内部の欠陥 (空孔, 未焼結部分及び粗大粒子の集合部) から始まっていた. 破断のモードは, 室温及び1400℃とも, 粒内破断であった.
以α-Si3N4、α-Al2O3及AlN为起始原料,通过热加压烧结法测定了制造β-赛龙烧结体在室温和1400℃下的弯曲强度。用于制造β-赛龙烧结体的混合粉末的组成:Z=1 (1.8), Z=1 (2.8)Z=1(4)和Z=1(5.5)。其中,括号内的数字表示来自组成Z=1的β-重离子的氧的过剩当量%。(1)Z=1(5.5)和Z=1(4)表示:经过充分致密化,Z=1(2.8)和Z=1(1.8)没有成为致密的烧结体。根据扫描电子显微镜观察,Z=1(4)和Z=1(5.5)得到的烧结体具有玻璃质粒界相。(3)Z=1(4)室温下的弯曲强度为:最高达到55.5kg/mm2,即使混合粉末的组成从Z=1(4)向氧侧或氮侧转移,烧结体的弯曲强度也降低了。Z=1(2.8)和Z=1(1.8)烧结体的1400℃弯曲试验中,各烧结体均未发现强度下降。都是从各烧结体内的缺陷(空穴、未烧结部分以及大件粒子的集合体)开始的。断裂模式在室温及1400℃下均为颗粒内断裂。
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引用次数: 5
β-サイアロン (Z=3) の窒素ガス圧焼結 β-赛龙(Z=3)氮气压烧结
Pub Date : 1983-11-01 DOI: 10.2109/JCERSJ1950.92.1072_675
英治 谷, 弘道 一ノ瀬, 和司 岸, 正気 梅林, 和夫 小林
Si3N4, Al2O3, AlNの混合粉末を用いてz=3組成のβ-サイアロン (Si6-zAlzOzN8-z; z=0-4.2) を温度1800°-2000℃, 窒素圧力0.1-4MPaの条件下で雰囲気加圧焼結を行った. 焼結には, 詰め粉としてβ-サイアロンのz=3(+4) (4当量%酸素過剰) 組成に相当するSi3N4, Al2O3, AlNの混合粉末を用いた.z=3(+4) 組成のβ-サイアロンを1800℃, 0.1MPaで焼成した場合, 最高密度3.05g/cm3 (理論密度の99%) の焼結体を得た. また2000℃においてもz=3(+2) 組成のβ-サイアロンは2MPaで2.96g/cm3 (理論密度の96%) の高密度焼結体を得ることができた.β-サイアロン単相の熱分解は, 1800℃では1MPa, 1900℃では2MPa, 2000℃では4MPa以上の窒素圧により抑えることができた. 一方, β-サイアロンとX相からなる2相サイアロンの熱分解は2000℃以上で生じ, 2000℃では4MPa以上の窒素圧により抑えることができた.β-サイアロンの雰囲気加圧焼結には, 詰め粉, 試料中の過剰酸素成分量及び窒素圧の効果が大きいことが明らかになった.
采用Si3N4、Al2O3、AlN的混合粉末制成z=3组成的β- cyon (si - zalzozn8 -z;z=0-4.2)在温度1800°-2000℃、氮气压力0.1- 4mpa的条件下进行气氛加压烧结。烧结时,作为填料粉,采用了相当于β-重离子z=3(+4)(4当量%氧过剩)组成的Si3N4、Al2O3、AlN的混合粉末。将z=3(+4)组成的β-重离子加热至1800℃,在0.1MPa烧结时,得到了最高密度为3.05g/cm3(理论密度的99%)的烧结体。另外,即使在2000℃下,z=3(+2)组成的β-重离子在2mpa下为2.96g/cm3(理论密度的96%)的高密度烧结体。1800℃时1mpa、1900℃时2mpa、2000℃时4mpa以上的氮压可以抑制β-重离子单相的热分解。另一方面,β-重叠层和X相构成的两相重叠层的热分解在2000℃以上发生,在2000℃时通过4mpa以上的氮压就能抑制。研究表明,样品中过量氧成分和氮压的效果显著。
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引用次数: 2
加水分解によるSi(OC2H5)4-H2O-C2H5OH溶液の粘度変化と曳糸性 水解引起的Si(OC2H5)4-H2O-C2H5OH溶液的粘度变化和曳丝性
Pub Date : 1982-09-01 DOI: 10.2109/JCERSJ1950.90.1045_555
済夫 作花, 寛一 神谷, 武史 加藤
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引用次数: 12
Hydration and Derivatives of Potassium Dititanate Fibers 二钛酸钾纤维的水化及其衍生物
Pub Date : 1982-01-01 DOI: 10.2109/JCERSJ1950.90.27
Y. Fujiki, T. Ohsaka
ニチタン酸 カリウム (K2Ti2O5) 繊維 をメル ト法 によ り育成 した. K2CO3とTiO2の 化学量論比 組成 の混合物 を1100°C で30分 間溶融 し, 底 を水冷 してい る他 の金属容器の 中へ流 し出 して繊維 状集 合体 としてすみや かに結 晶化 させた. 繊維分離 は結晶化体 を水 中に浸漬 して行 った. この水和 反 応は カ リウムイオンの溶 出を伴 って水和相KHTi2O5・nH2Oを 形成 した. 水和相 は900°C 付近 で熱処理 すれ ば四チタン酸 カリウム繊維 に移行す る. また, ニ チタン酸 カ リウム繊維 を温水及び沸 騰 水で処理後900°C 付近 で熱処理 すれ ば六 チタン酸 カ リウム繊維, 酸水溶液で処理すれ ば結晶質 チ タン酸 (TiO2・nH2O) 繊維な どの誘導体 を合成 するこ とができる. (昭和56年4月13日 受付)
二钛酸钾(K2Ti2O5)纤维采用熔融法培育而成。将K2CO3和TiO2化学成份的混合物在1100°C下熔融30分钟,流到水冷底部的其他金属容器中,作为纤维状集合体迅速结晶化。纤维分离是将结晶体浸泡在水中进行的,这种水合反应伴随着锂离子的溶出,形成水合相KHTi2O5·nH2O。水合相只要在900°C附近进行热处理,就会转变为四钛酸钾纤维。用温水和沸水处理钛酸化镓纤维,然后在900°C附近热处理,就可以得到六钛酸化镓纤维,如果用酸水溶液处理,可以合成结晶质钛酸(TiO2·nH2O)纤维等衍生物。(昭和56年4月13日受理)
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引用次数: 4
Direct Observation of the Formation Process of TiN Particles by CVD Method 用CVD法直接观察TiN颗粒的形成过程
Pub Date : 1981-05-01 DOI: 10.2109/JCERSJ1950.89.1029_277
J. Hojo, A. Kato
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引用次数: 14
Effects of water vapor on the electrical conductivity of the interface of semiconductor ceramic-ceramic contacts. 水蒸气对半导体陶瓷-陶瓷触点界面电导率的影响。
Pub Date : 1979-01-01 DOI: 10.2109/JCERSJ1950.87.1002_112
K. Kawakami, H. Yanagida
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引用次数: 21
Microstructure of hot-pressed SiC with AlB2 additive. AlB2添加剂对热压SiC显微组织的影响。
Pub Date : 1979-01-01 DOI: 10.2109/JCERSJ1950.87.1010_541
Hidehiko Tanaka, Y. Inomata
Pure SiC powder cannot be densified by normal pressure sinteiring or by hot-pressi and some additives are needed to densify it The studies reported previously showed tha B or B compounds1),2), and Al or Al com pounds3) were the most effective additives. I is well known that B and C additives can sinter SiC powder under normal pressure and that B4C, BP and BN are also effectiv The author have been studying the sinte ing behaviors of SiC by an addition of Al compounds, such as AlB2, AlN and Al4C They have found that a small amount of AlB addition could sinter SiC powder by hot-pres ing. Recently, J. A. Coppola et al.4) reporte a sintering of SiC with AlB2 additive in their
纯SiC粉不能用常压烧结或热压致密化,需要添加一些添加剂来致密化。以前的研究表明,B或B化合物1),2)和Al或Al化合物3)是最有效的添加剂。众所周知,B和C添加剂能在常压下烧结SiC粉末,B4C、BP和BN也能有效烧结SiC粉末。作者研究了添加AlB2、AlN和Al4C等Al化合物对SiC的烧结行为,发现添加少量AlB可以通过热压烧结SiC粉末。最近,J. a . Coppola等人(4)报道了一种用AlB2添加剂烧结SiC的方法
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引用次数: 0
Si-Al-O-Nセラミックス単相の合成 si-al-o-n陶瓷单相的合成
Pub Date : 1978-11-01 DOI: 10.2109/JCERSJ1950.86.999_526
護 三友, 信行 倉元, 正幸 堤, 弘茂 鈴木
(1) “Balanced” powder mixture of Si3N4, AlN and Al2O3 for sialon (Si6-zAlzOzN8-z with z=1, 2, 3 or 4) was hot pressed at 1750°C for 1h under 200kg/cm2. The densification was incomplete in a sialon with z=1. Other sialons were pore free.(2) The reactions included in the process of β-sialon formation were inferred to be, (a) the formation of 15 R-sialon, x-phase and β-sialon with z=2.3-2.5 at low temperature (equations (2) and (3)), (b) steep densification at higher temperature than 1600°C by “transient liquid phase sintering” with x-phase as a liquid, (c) the final step to approach z value of β-sialon into predicted one (equations (5) and (6)).(3) Density measurement and chemical etching with diluted HF+HNO3 of fracture surface of sialon revealed that there was unreacted materials in sialons with z=3 and 4. A single phase and fully dense sialon was obtained in the composition z=2 with very small amount of grain boundary phase, if any.(4) Small amount of excess oxide (about 3 wt%) in a sialon with z=2, which existed as grain boundary phase, was detected by chemical etching.
(1) Si3N4、AlN和Al2O3的“平衡”粉末混合物用于sialon (Si6-zAlzOzN8-z, z= 1,2,3或4),温度为1750℃,温度为200kg/cm2,热压1h。z=1时,莎龙致密化不完全。(2) β-sialon形成过程中包含的反应可以推断为:(a)在低温下形成15 R-sialon, x相和z=2.3-2.5的β-sialon(式(2)和(3)),(b)在高于1600℃的温度下以x相为液体的“瞬态液相烧结”急剧致密化。(c)将β-sialon的z值逼近到预测值的最后一步(式(5)和(6))。(3)密度测量和稀释HF+HNO3对sialon断裂面的化学蚀刻表明,z=3和4的sialon中存在未反应物质。(4)化学腐蚀法检测到z=2组分中存在少量过量氧化物(约3 wt%),以晶界相形式存在。
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引用次数: 23
期刊
Journal of the Ceramic Association, Japan
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