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ZINC;carbonate;hydroxide;hydrate

中文名称
——
中文别名
——
英文名称
ZINC;carbonate;hydroxide;hydrate
英文别名
——
ZINC;carbonate;hydroxide;hydrate化学式
CAS
——
化学式
CO3*6HO*H2O*4Zn
mdl
——
分子量
441.629
InChiKey
QBRFEBMQJCEDHP-UHFFFAOYSA-K
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

计算性质

  • 辛醇/水分配系数(LogP):
    -3.45
  • 重原子数:
    7
  • 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:
    65.2
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    ZINC;carbonate;hydroxide;hydrate 在 air 作用下, 反应 0.25h, 生成 zinc(II) oxide
    参考文献:
    名称:
    Preparation and sensing properties of hierarchical 3D assembled porous ZnO from zinc hydroxide carbonate
    摘要:
    通过水热反应合成了前驱体氢锌矿,并通过在 400 °C 煅烧 15 分钟制备了分层组装的三维多孔氧化锌。三维多孔氧化锌由纳米片组装而成的微米球体组成。与二维多孔氧化锌纳米板相比,基于三维多孔氧化锌的传感器显示出更好的乙醇响应。在工作温度为 420 ℃、420 ℃ 和 340 ℃ 时,基于三维多孔 ZnO-2 的传感器对 100 ppm 丙酮、苯和乙醇的灵敏度最高,分别为 77.5、9.8 和 49.7。在工作温度为 420 ℃ 时,传感器对丙酮也有选择性。基于 ZnO-3 的传感器对 100 ppm 乙醇的灵敏度最高,达到 59.9,在 10-1000 ppm 范围内,响应随乙醇浓度的增加而线性增加。三维多孔氧化锌传感器良好的传感性能表明,分层组装的三维多孔氧化锌有望成为高灵敏度气体传感器的候选材料。
    DOI:
    10.1039/c3ra45254a
  • 作为产物:
    描述:
    zinc(II) acetate dihydrate 在 溶剂黄146尿素 作用下, 以 为溶剂, 反应 12.0h, 生成 ZINC;carbonate;hydroxide;hydrate
    参考文献:
    名称:
    Nanosized inorganic metal oxides as heterogeneous catalysts for the degradation of chemical warfare agents
    摘要:
    Nanosized inorganic metal oxides, such as TiO2, ZnO, gamma-Al2O3, are proposed as heterogeneous catalysts for the oxidative degradation of chemical warfare agents (CWA), particularly of organosulfur toxic agents, into oxidised products with reduced toxicity. The morphology, structural and textural properties of the catalysts were investigated. Furthermore, their catalytic properties were evaluated in the oxidative abatement of (2-chloroethyl)ethylsulfide, CEES, a simulant of sulfur mustard (blistering CWA). Their performance was also compared to a conventional decontamination powder and a commercial Nb2O5 sample. The metal oxides powders were then employed in the active oxidative decontamination of CEES from a cotton textile substrate, mimicking a real contamination occurrence. Remarkable results in terms of abatement and degradation into desired products were recorded, achieving good conversions and decontamination efficiency with Nb2O5, TiO2 and gamma-Al2O3, under very mild conditions, with hydrogen peroxide (as aqueous solution or as urea-hydrogen peroxide adduct), at room temperature and ambient pressure. In the aim of a real on-field use, the potential environmental impact of these solids was also evaluated by bioluminescence toxicity tests on reference bacteria (Photobacterium leiognathi Sh1), showing a negligible negative impact for TiO2, gamma-Al2O3, and Nb2O5. A major biotoxic effect was only found for ZnO. (C) 2016 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.cattod.2015.12.023
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文献信息

  • Preparation method for zeolitic imidazolate frameworks
    申请人:China University of Petroleum-Beijing
    公开号:US10815253B2
    公开(公告)日:2020-10-27
    The present invention provides a preparation method for zeolitic imidazolate frameworks. The preparation method comprises: adding a metal carbonate or oxide, an organic ligand to a hydrophilic liquid to obtain a mixture; introducing an acidic gas to reach a reaction pressure of 0.1 MPa to 2.0 MPa, and reacting for a predetermined time; heating to 30° C.-60° C. and vacuuming to obtain the zeolitic imidazolate framework. The present invention also provides a zeolitic imidazolate framework obtained by the above preparation method. The preparation method according to the present invention is environmentally friendly and has a high yield.
    本发明提供了一种沸石咪唑酸盐框架的制备方法。所述制备方法包括:将金属碳酸盐或氧化物、有机配体加入到亲水性液体中以获得混合物;引入酸性气体以达到0.1 MPa至2.0 MPa的反应压力,并进行预定时间的反应;加热至30°C至60°C并进行真空处理以获得沸石咪唑酸盐框架。本发明还提供了通过上述制备方法获得的沸石咪唑酸盐框架。本发明的制备方法环保且产率高。
  • Enhanced separation of photogenerated charge carriers and catalytic properties of ZnO-MnO2 composites by microwave and photothermal effect
    作者:Ruiting Wang、Qiang Hao、Jianrui Feng、Gui-Chang Wang、Hao Ding、Daimei Chen、Bingjie Ni
    DOI:10.1016/j.jallcom.2019.02.009
    日期:2019.5
    composite are much higher than that of ZnO or α-MnO2. The main active species in the reaction progress were confirmed by electron paramagnetic resonance spectra and trapping experiments. According to the DFT calculation result and photothermal images, the enhanced catalytic activity is attributed to the photothermal and microwave-assisted effect. The addition of α-MnO2 improves the absorption of light and microwave
    摘要 为提高ZnO和α-MnO2的太阳能利用率和光降解​​效率,采用简便的方法制备了ZnO/MnO2复合材料。通过XRD、拉曼光谱、X射线光电子能谱、扫描电子显微镜、透射电子显微镜和紫外-可见漫反射光谱对材料进行表征。复合材料的光催化活性和微波辅助光催化活性远高于ZnO或α-MnO2。反应过程中的主要活性物种通过电子顺磁共振光谱和捕获实验得到证实。根据 DFT 计算结果和光热图像,催化活性的增强归因于光热和微波辅助作用。α-MnO2 的加入提高了复合材料对光和微波的吸收,这可以进一步加热催化剂。结果,加速了光生载流子的分离。最后,提出了提高复合材料催化性能的机制。
  • Controlled Photoinduced Generation of “Visual” Partially and Fully Charge Separated States in Viologen Analogues
    作者:Lu Liu、Qing Liu、Rong Li、Ming-Sheng Wang、Guo-Cong Guo
    DOI:10.1021/jacs.0c10183
    日期:2021.2.10
    state for viologen analogues. One pale yellow 4,4′-bipyridine-based metalloviologen compound, with an interannular dihedral angle of 1.84° in 4,4′-bipyridine, directly decays to the purple FCS state after photoexcitation. The other pale yellow compound, with a similar coordination framework but a larger interannular dihedral angle (33.74°), changes first to a yellow PCS state and then relaxes slowly (in
    生命周期数秒或更长时间的电荷分离状态,不仅有利于使用各种稳态分析技术进行研究,而且对于光能转换和其他应用也很重要。通过空间位阻诱导的方法,在激发态衰减为通常观察到的完全电荷分离(FCS)的“视觉”模式下,已经检测到了空前的,寿命为数天的部分电荷分离(PCS)状态的空前光诱导生成。 )的状态。一种浅黄色的4,4'-联吡啶基金属lovolologen化合物,在4,4'-联吡啶中的环间二面角为1.84°,在光激发后会直接衰减为紫色FCS状态。另一种淡黄色化合物,具有相似的配位骨架,但环形二面角较大(33.74°),先变为黄色PCS状态,然后缓慢放松(在Ar中处于黑暗中,约2天;在Ar中70°C,约1小时),变为紫色FCS状态。对于紫精化合物及其类似物而言,两步着色现象是前所未有的,而对于其他光致变色物质,这种现象也很少见。EPR和拉曼数据表明,光诱导的电荷分离首先产生一价的锌和自由基,然后在Zn(I)中接收的电子缓慢地进一步分布到4
  • Sheet-tube-rod transformation for ZnO nanorods prepared by a simple reflux route
    作者:Han Han、Enhong Sheng、Yonghong Ni、Yue Ma、Nannan Xiang、Xiang Ma
    DOI:10.1016/j.materresbull.2015.10.012
    日期:2016.2
    Abstract As an important semiconductor material, ZnO nanocrystals with various morphologies have been extensively investigated in the literature. In this paper, we designed a simple reflux route to prepare ZnO nanorods, employing Zn(NO3)2·6H2O and urea as the original reactants. Our interest mainly focused on the formation process of ZnO nanorods. The reaction was carried out at 120 °C. XRD analyses
    摘要 作为一种重要的半导体材料,各种形貌的 ZnO 纳米晶在文献中得到了广泛的研究。在本文中,我们设计了一种简单的回流路线来制备 ZnO 纳米棒,采用 Zn(NO3)2·6H2O 和尿素作为原始反应物。我们的兴趣主要集中在 ZnO 纳米棒的形成过程。反应在120°C下进行。XRD 分析表明,随着反应时间从 10 分钟延长到 120 分钟,最终产物经历了从 Zn4(OH)6CO3·H2O 到 ZnO 的转化。SEM 观察发现,在上述转化过程中,最终产品分别由纳米片、纳米管和纳米棒组成。同时,发现纳米片、纳米管或/和纳米棒在某些时期共存。
  • Preparation and sensing properties of hierarchical 3D assembled porous ZnO from zinc hydroxide carbonate
    作者:Zhidong Lin、Fei Guo、Chen Wang、Xuehua Wang、Ke Wang、Yang Qu
    DOI:10.1039/c3ra45254a
    日期:——
    The precursor hydrozincite was synthesized through hydrothermal reaction and hierarchically assembled 3D porous ZnO was prepared by calcination of the precursor at 400 °C for 15 min. The 3D porous ZnO was composed of micrometer spheres which were assembled from nanoflakes. The sensor based on 3D porous ZnO showed improved ethanol response compared to 2D porous ZnO nanoplates. The highest sensitivity of 77.5, 9.8 and 49.7, respectively, for the sensor based on 3D porous ZnO-2 were obtained for 100 ppm acetone, benzene and ethanol at the operation temperature of 420 °C, 420 °C and 340 °C, respectively. The sensor also show selectivity to acetone at the operation temperature of 420 °C. The highest sensitivity of the sensor based on ZnO-3 was of 59.9 to 100 ppm ethanol, the response increased linearly with the concentration of ethanol in the range of 10–1000 ppm. All the response and recovery times of the sensors were less than 20 s. The good sensing performance of the 3D porous ZnO sensor indicated that the hierarchically assembled 3D porous ZnO could be a promising candidate for highly sensitive gas sensors.
    通过水热反应合成了前驱体氢锌矿,并通过在 400 °C 煅烧 15 分钟制备了分层组装的三维多孔氧化锌。三维多孔氧化锌由纳米片组装而成的微米球体组成。与二维多孔氧化锌纳米板相比,基于三维多孔氧化锌的传感器显示出更好的乙醇响应。在工作温度为 420 ℃、420 ℃ 和 340 ℃ 时,基于三维多孔 ZnO-2 的传感器对 100 ppm 丙酮、苯和乙醇的灵敏度最高,分别为 77.5、9.8 和 49.7。在工作温度为 420 ℃ 时,传感器对丙酮也有选择性。基于 ZnO-3 的传感器对 100 ppm 乙醇的灵敏度最高,达到 59.9,在 10-1000 ppm 范围内,响应随乙醇浓度的增加而线性增加。三维多孔氧化锌传感器良好的传感性能表明,分层组装的三维多孔氧化锌有望成为高灵敏度气体传感器的候选材料。
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