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氢化钆 | 7440-54-2

中文名称
氢化钆
中文别名
钆锭;钆棒;镓;钆;金属钆
英文名称
gadolinium
英文别名
Gd
氢化钆化学式
CAS
7440-54-2;13572-97-9
化学式
Gd
mdl
——
分子量
157.25
InChiKey
UIWYJDYFSGRHKR-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    1313 °C (lit.)
  • 沸点:
    3273 °C (lit.)
  • 密度:
    7.886 g/mL at 25 °C (lit.)
  • 闪点:
    3266°C
  • 溶解度:
    溶于稀酸溶液
  • 暴露限值:
    ACGIH: TWA 2 ppm; STEL 4 ppmOSHA: TWA 2 ppm(5 mg/m3)NIOSH: IDLH 25 ppm; TWA 2 ppm(5 mg/m3); STEL 4 ppm(10 mg/m3)
  • 物理描述:
    Silvery white, malleable metal that tarnishes in moist air; [Reference #2]
  • 颜色/状态:
    Silvery metal; hexagonal
  • 蒸汽压力:
    VP: 1 Pa at 1563 °C; 10 Pa at 1755 °C; 100 Pa at 1994 °C; 1 kPa at 2300 °C; 10 kPa at 2703 °C; 100 kPa at 3262 °C (calculated from ideal gas hermodynamic functions)

计算性质

  • 辛醇/水分配系数(LogP):
    0.0
  • 重原子数:
    1
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

ADMET

毒理性
  • 毒性总结
鉴定和使用:钆是一种银白色的稀土金属。它被用作核控制棒材料以捕获热中子,制造钆钇石榴石,并提高铁、铬及其相关合金的高温和抗氧化性能。人类暴露和毒性:没有找到相关信息。动物研究:没有找到相关信息。
IDENTIFICATION AND USE: Gadolinium is a silvery rare-earth metal. It is used as nuclear control rod material to capture thermal neutrons, to make gadolinium yttrium garnets, and to improve the workability and resistance of iron, chromium, and related alloys to high temperature and oxidation. HUMAN EXPOSURE AND TOXICITY: No information has been found. ANIMAL STUDIES: No information has been found.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 副作用
Nephrotoxin - The chemical is potentially toxic to the kidneys in the occupational setting. 肾毒素 - 该化学品在职业环境中可能对肾脏有毒。
Nephrotoxin - The chemical is potentially toxic to the kidneys in the occupational setting.
来源:Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
毒理性
  • 解毒与急救
/SRP:/ 立即急救:确保已经进行了充分的中和。如果患者停止呼吸,请开始人工呼吸,最好使用需求阀复苏器、球囊阀面罩设备或口袋面罩,按训练操作。如有必要,执行心肺复苏。立即用缓慢流动的水冲洗受污染的眼睛。不要催吐。如果患者呕吐,让患者向前倾或将其置于左侧(如果可能的话,头部向下),以保持呼吸道畅通,防止吸入。保持患者安静,维持正常体温。寻求医疗救助。 /毒物A和B/
/SRP:/ Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR if necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on the left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. /Poisons A and B/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
/SRP:/ 基本治疗:建立专利气道(如有需要,使用口咽或鼻咽气道)。如有必要,进行吸痰。观察呼吸不足的迹象,如有需要,辅助通气。通过非循环呼吸面罩以10至15升/分钟的速度给予氧气。监测肺水肿,如有必要,进行治疗……。监测休克,如有必要,进行治疗……。预防癫痫发作,如有必要,进行治疗……。对于眼睛污染,立即用水冲洗眼睛。在运输过程中,用0.9%的生理盐水(NS)持续冲洗每只眼睛……。不要使用催吐剂。对于摄入,如果患者能吞咽、有强烈的干呕反射且不流口水,则用温水冲洗口腔,并给予5毫升/千克,最多200毫升的水进行稀释……。在去污后,用干燥的无菌敷料覆盖皮肤烧伤……。/毒药A和B/
/SRP:/ Basic treatment: Establish a patent airway (oropharyngeal or nasopharyngeal airway, if needed). Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if needed. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with 0.9% saline (NS) during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 mL/kg up to 200 mL of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool ... . Cover skin burns with dry sterile dressings after decontamination ... . /Poisons A and B/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
/SRP:/ 高级治疗:对于昏迷、严重肺水肿或严重呼吸困难的病人,考虑进行口咽或鼻咽气管插管以控制气道。使用气囊面罩装置的正压通气技术可能有益。考虑使用药物治疗肺水肿……。对于严重的支气管痉挛,考虑给予β激动剂,如沙丁胺醇……。监测心率和必要时治疗心律失常……。开始静脉输注D5W TKO /SRP: "保持开放",最低流量/。如果出现低血容量的迹象,使用0.9%生理盐水(NS)或乳酸钠林格氏液(LR)。对于伴有低血容量迹象的低血压,谨慎给予液体。注意液体过载的迹象……。用地西泮或劳拉西泮治疗癫痫……。使用丙美卡因氢氯化物协助眼部冲洗……。/毒素A和B/
/SRP:/ Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in severe respiratory distress. Positive-pressure ventilation techniques with a bag valve mask device may be beneficial. Consider drug therapy for pulmonary edema ... . Consider administering a beta agonist such as albuterol for severe bronchospasm ... . Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start IV administration of D5W TKO /SRP: "To keep open", minimal flow rate/. Use 0.9% saline (NS) or lactated Ringer's (LR) if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Treat seizures with diazepam or lorazepam ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Poisons A and B/
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
镓-153(153Gd)标记的钆喷酸葡胺(马根维斯特)、钆特醇(普罗翰斯)、钆特酸(多特雷姆)和钆二酰胺(奥姆尼扫描)通过静脉给药给小鼠(0.48 mmol/kg)和大鼠(0.1 mmol/kg)。在治疗后长达14天内的不同时间点,测量选定组织中的残留153Gd。所得到的组织分布用于进行螯合物内部分布和间分布评估及比较,关于组织清除和可能的钆螯合物体内解离。在研究螯合物中,相对于在已知螯合自由钆的组织中存在的残留153Gd的量存在差异,特别是在小鼠和大鼠给药后7天和14天的肝脏和股骨中。153Gd的分布模式表明,线性螯合物,钆喷酸葡胺和钆二酰胺,在体内解离,导致在较长的停留时间内在骨骼和肝脏中存在的153Gd比注射了大环螯合物,钆特醇和钆特酸的受试者更多。唯一发现影响分布特征的辅料是钙(DTPA-BMA);这种辅料在配方钆二酰胺中减少了与单独注射钆二酰胺相比,在小鼠全身、骨骼和肝脏中测得的残留钆的量。
... Gadolinium-153 ((153)Gd)-labeled gadopentetate (Magnevist), gadoteridol (ProHance), gadoterate (Dotarem), and gadodiamide (Omniscan) were administered iv to mice (0.48 mmol/kg) and rats (0.1 mmol/kg). At various times up to 14 days posttreatment, the residual 153Gd was measured in selected tissues. The tissue distributions obtained were used to make intra- and interchelate distribution evaluations and comparisons regarding tissue clearance and any possible in vivo dissociation of the Gd chelates. .... Differences were found among the chelates studied relative to the amounts of residual 153Gd present in tissues known to sequester free Gd, particularly in liver and femur at 7 and 14 days after administration, in both mice and rats. The pattern of the 153Gd distribution suggested that the linear chelates, gadopentetate and gadodiamide, dissociated in vivo resulting in more 153Gd present in bone and liver at the longer residence times than in the subjects injected with the macrocyclic chelates, gadoteridol and gadoterate. The only excipient found to affect the distribution profile was calcium(DTPA-BMA); this excipient in formulated gadodiamide decreased the amounts of residual Gd measured in whole body, bone, and liver in mice compared with levels obtained when gadodiamide was injected alone. ...
来源:Hazardous Substances Data Bank (HSDB)

安全信息

  • TSCA:
    Yes
  • 危险等级:
    8
  • 危险品标志:
    Xi
  • 安全说明:
    S26,S43,S7/8
  • 危险类别码:
    R15
  • WGK Germany:
    3
  • 危险品运输编号:
    UN 3208 4.3/PG 3
  • 危险类别:
    8
  • RTECS号:
    LW3850000
  • 包装等级:
    III
  • 危险标志:
    GHS02
  • 危险性描述:
    H261
  • 危险性防范说明:
    P231 + P232,P422

SDS

SDS:cc3048c7681c28f4fde110376eb8056e
查看

制备方法与用途

简介 钆是一种银白色的金属,具有延展性,熔点为1313°C,沸点为3266°C,相对密度7.9004。它的化学符号是Gd(英语:Gadolinium),在元素周期表中位于原子序号64的位置,属于镧系元素和稀土元素。钆具有铁磁性,其居里点约为室温(19℃或66℉)。将一块钆放入冰水中冷却时,它可以吸附磁铁;但当温度回升后,钆会脱离磁铁掉落。

化学性质 钆能够与大多数元素直接化合,形成Gd(III)化合物。加热或在高温条件下,它可以与氮气、硫、磷、硒、碳、硅或砷反应,生成二元化合物。与其他稀土元素不同的是,金属钆在干燥空气中相对稳定;但在潮湿的空气下会迅速失去光泽,并形成一层易脱落的氧化钆薄膜。这一过程遵循化学方程式:4 Gd + 3 O2 → 2 Gd2O3。

应用 由于其具有最高的热中子俘获截面,钆被用于反应堆控制材料和核辐射防护结构。此外,它还作为钇铁石榴石和钇铝石榴石的添加剂,用于制造新型磁性材料。利用钆盐进行磁场冷却的方法,可以实现接近绝对零度(0.002K)的超低温状态。钆化合物还可作为荧光粉的基础材料,用于制造X射线增感屏及投影电视装置。

用途 主要用于原子能工业中,是制备磁性材料和有色合金添加剂的重要成分。

生产方法 采用氟化物的钙热还原法。这种方法的优势在于:反应过程平缓;金属钙容易提纯且供应稳定;还原温度一般在金属和渣熔点以上50~100℃之间,在真空感应炉中进行,该设备需能调节控制炉温至1800℃并保持控温精度±10℃。氟化钙的蒸发压低,便于金属凝聚和分离。

还原剂钙需经过799.93Pa氦分压下的蒸馏提纯,并储存在充氦密封干燥箱内以避免氧化及吸入空气中的水分。还原过程中,过量10%~15%的钙屑或钙粒与氟化钆混合后装入钽坩埚中并压实盖好,随后在真空感应炉中抽至10-2Pa,缓慢加热至400~600℃脱气,然后充入净化氩气至6×10^4Pa,继续升温至800~1000℃使材料开始发生还原反应。将温度升至1800℃并保持10~15min,让金属与渣熔化充分分层分离,最终获得致密的金属锭。

通常情况下,采用此法生产的稀土金属纯度可达95%~98%,为了进一步提高产品纯度,需使用更纯净的氟化物。还原剂钙在使用前要经过提纯并保存在充氦密封干燥箱内。

反应信息

  • 作为反应物:
    描述:
    氢化钆air 作用下, 生成 gadolinium(III) oxide
    参考文献:
    名称:
    Greene, N. D.; Hodge, F. G., Corrosion, 1966, vol. 22, p. 206 - 213
    摘要:
    DOI:
  • 作为产物:
    描述:
    氯化钆 以 melt 为溶剂, 生成 氢化钆
    参考文献:
    名称:
    Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Sc: MVol.B2, 2.2.1, page 218 - 222
    摘要:
    DOI:
  • 作为试剂:
    描述:
    三氢化钐铁粉氢化钆 作用下, 以 melt 为溶剂, 生成
    参考文献:
    名称:
    Temperature-compensated Sm1−Gd (Co0.74Fe0.10Cu0.12Zr0.04)7.50 permanent magnets (x = 0, 0.2, 0.4, 0.6, 0.8)
    摘要:
    The high-temperature magnetic properties of the Sm1-xGdx(Co0.74Fe0.10Cu0.12Zr0.04)(7.50) (x = 0, 0.2, 0.4, 0.6, 0.8) series of magnets are investigated in the range between 50 and 650degreesC. The pertinent properties are the saturation magnetization, the coercivity H-c and their temperature coefficients, a and, respectively. Gd substitution is made in order to improve the temperature coefficient of magnetization. The values of the coefficient alpha are in the range (-0.3, 0.3%/degreesC) while the values of the coefficient beta are in the range (-0.2, 0.2%/degreesC). The best results were obtained for the x = 0.4 sample, for which the saturation magnetization was almost independent of temperature in the range between 150 and 500degreesC. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jallcom.2003.08.049
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文献信息

  • U(IV)/LN(III) unexpected mixed site in polymetallic oxalato complexes. Part II. Substitution of U(IV) for Ln(III) in the new oxalates (N2H5)Ln(C2O4)2·nH2O (Ln=Nd, Gd)
    作者:B. Chapelet-Arab、G. Nowogrocki、F. Abraham、S. Grandjean
    DOI:10.1016/j.jssc.2005.06.032
    日期:2005.10
    lanthanide and oxalate ions. The lanthanide atom is coordinated by eight oxygen atoms from four tetradentate oxalate ions and one aqua oxygen. Alternating lanthanide and oxalate ions form six-membered rings that delimit tunnels running down three directions and occupied by hydrazinium and water molecules. Starting from these lanthanide(III) compounds two isotypic mixed Ln(III)/U(IV) oxalates, (N2H5)0.75[Nd0
    两种新的草酸镧系元素镧(III)草酸盐(N 2 H 5)[Nd(C 2 O 4)2(H 2 O)]·4H 2 O(1)和(N 2 H 5)[Gd(C 2 O制备了4)2(H 2 O)]·4.5H 2 O(2),并通过单晶X射线衍射确定了它们的晶体结构。晶体结构通过直接法和傅立叶差分技术求解,并在F 2的基础上通过最小二乘法进行细化。对于所有独特的思考。晶体学数据:1,三斜晶系,空间群P1 ,a = 8.507(3)Å ,b = 9.762(4)b = 9.762(4),c = 10.249(4)Å ,α= 62.378(5)α= 62.378 (5),对于172个参数的3430次反射,β= 76.681(5)β= 76.681(5),γ= 73.858(5)γ= 73.858(5),Z = 2Z = 2 ,R 1 = 0.0335R1 = 0.0335 I⩾2σ(I)I⩾2σ(I); 2,三斜空间群P1′
  • Primary aminomethyl derivatives of kaempferol: hydrogen bond-assisted synthesis, anticancer activity and spectral properties
    作者:Shuanglian Cai、Yangyang Kong、Dan Xiao、Yun Chen、Qiuan Wang
    DOI:10.1039/c7ob02927f
    日期:——
    products of kaempferol. The formation of appropriate hydrogen bonds between strong nucleophilic amino acids and phenol is essential for the smooth reaction of the SN2 nucleophilic substitution. The SN2 mechanism hypothesis involving a hydrogen bond-assisted process was also supported by the density functional theory (DFT) analysis. An antiproliferative test of synthetic compounds shows the moderate to potent
    通过涉及曼尼希反应和S N 2亲核取代两个步骤的组合策略合成了山emp酚的一系列伯氨甲基伯衍生物。产物的结构表明,优先的氨基甲基化在山emp酚的A环的C-6或C-8位置,尤其是后者。有趣的是,实验数据表明分子间氢键在山ka酚的主要氨基甲基产物的形成中起关键作用。在强亲核氨基酸和苯酚之间形成适当的氢键对于S N 2亲核取代的平稳反应是必不可少的。在S Ñ密度泛函理论(DFT)分析也支持涉及氢键辅助过程的2种机理假说。合成化合物的抗增殖测试显示,通过CCK-8分析,它对三种人类癌细胞系(HeLa,HCC1954和SK-OV-3)具有中等至有效的细胞毒活性。化合物4e对HeLa细胞显示出选择性的抗增殖活性,且IC50值较低(4.27μm),值得进一步开发。另一个有趣的结果是,大多数金属络合物的最大发射带位于约480 nm处,而Tm和Yb络合物的最大发射带出现在约533 nm处。
  • Synthesis, Potentiometric, Kinetic, and NMR Studies of 1,4,7,10-Tetraazacyclododecane-1,7-bis(acetic acid)-4,10-bis(methylenephosphonic acid) (DO2A2P) and its Complexes with Ca(II), Cu(II), Zn(II) and Lanthanide(III) Ions
    作者:Ferenc K. Kálmán、Zsolt Baranyai、Imre Tóth、István Bányai、Róbert Király、Ernö Brücher、Silvio Aime、Xiankai Sun、A. Dean Sherry、Zoltán Kovács
    DOI:10.1021/ic7024704
    日期:2008.5.1
    Gd(DO2A2P) (at pH = 3.45 and 8.5) between 274 and 350 K are practically the same, characteristic of a q = 0 complex. Detailed kinetic studies of the Ce (3+) and Gd (3+) complexes with DO2A2P showed that complex formation is slow and involves a high stability diprotonated intermediate Ln(H 2DO2A2P)*. Rearrangement of the diprotonated intermediate into the final complex is an OH (-) assisted process but, unlike
    合成了一个基于环素的配体,该配体包含反乙酸酯和反甲基膦酸酯侧基H 6DO2A2P,并通过pH电位法和(1)H测定其质子化常数(12.6、11.43、5.95、6.15、2.88和2.77) NMR光谱。已显示前两个质子化发生在两个大环N-CH 2-PO 3(2-)氮原子上,而第三和第四质子化发生在两个膦酸酯基团上。与两个-PO 3(2-)基团的质子化同时,来自NH(+)-CH 2-PO 3(2-)的质子转移到N-CH 2-COO(-)氮中。Ca(2 +),Cu(2+)和Zn(2+)(ML,MHL,MH 2L和M 2L)配合物的稳定常数是通过直接pH电位法测定的。镧系元素离子(Ln(3+))形成相似的物种,但络合物的形成缓慢。因此,“单元外” pH电位法(La(3 +),Eu(3 +),Gd(3 +),Y(3+))和竞争性分光光度法与Cu(II)离子(Lu(3+))用于确定稳定性常数。通过将log
  • Magnetic properties of a new series of rare-earth iron nitrides: R<sub>2</sub>Fe<sub>17</sub>N<sub>y</sub>(y approximately 2.6)
    作者:Hong Sun、J M D Coey、Y Otani、D P F Hurley
    DOI:10.1088/0953-8984/2/30/013
    日期:1990.7.30
    A series of interstitial ternary nitrides R2Fe17Ny with 2.3
    一系列间隙三元氮化物 R2Fe17Ny 与 2.3
  • Magnetic properties of R2Fe14M3 compounds with M = Ga and SI; R = Y, Nd, Sm, Gd, Tb, Dy, Ho, Er and Tm
    作者:Bao-gen Shen、Bing Liang、Zhao-hua Cheng、Hua-yang Gong、Wen-shan Zhan、Hong Tang、F.R. de Boer、K.H.J. Buschow
    DOI:10.1016/s0038-1098(97)00152-x
    日期:1997.7
    and Si; R = Y, Nd, Sm, Gd, Tb, Dy, Ho, Er and Tm) have been prepared by are-melting. Crystal-structure studies have shown that the prepared samples are single phase with the rhombohedral Th2Zn17 and/or the hexagonal Th2Ni17 structure. Substitution of Ga for Fe in R2Fe17 leads to an increase of the unit-cell volume, whereas Si substitution reduces the unit-cell volume. The Curie temperatures of the R2Fe14Ga3
    已经通过熔化制备了组成为 R2Fe14M3(M = Ga 和 Si;R = Y、Nd、Sm、Gd、Tb、Dy、Ho、Er 和 Tm)的样品。晶体结构研究表明,制备的样品是具有菱形 Th2Zn17 和/或六角形 Th2Ni17 结构的单相。在 R2Fe17 中用 Ga 替代 Fe 导致晶胞体积增加,而 Si 替代降低了晶胞体积。R2Fe14Ga3 和 R2Fe14Si3 化合物的居里温度远大于相应的 R2Fe17 化合物的居里温度。Fe 矩在 Ga 或 Si 取代时降低。R2Fe14Ga3 和 R2Fe14Si3(R = Er 和 Tm)化合物在低温下表现出自旋-重定向转变。(C) 1997 Elsevier Science Ltd.
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