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相关概念视频

Urea Cycle01:23

Urea Cycle

51.2K
The urea cycle describes how liver cells convert ammonia to urea. Ammonia is a toxic waste product of protein catabolism. Land animals must convert ammonia into the less toxic urea which can be safely eliminated by the kidneys through urine. Marine animals excrete ammonia directly, and the surrounding water dilutes the ammonia to safe levels.
51.2K
Metabolism of Chemolithotrophs01:15

Metabolism of Chemolithotrophs

1.0K
Chemolithotrophs are microorganisms that obtain energy by oxidizing inorganic molecules such as hydrogen gas (H₂), ammonia (NH₃), reduced sulfur compounds (H₂S, S²⁻), and ferrous iron (Fe²⁺). Unlike heterotrophic organisms that rely on organic carbon, chemolithotrophs transfer electrons from these inorganic donors to the electron transport chain (ETC), generating a proton motive force (PMF) that drives ATP synthesis through oxidative phosphorylation.
1.0K
Protein Modifications in the RER01:26

Protein Modifications in the RER

7.3K
Modification of secretory and transmembrane proteins entering the rough ER begins in the ER lumen. These modifications aid in protein folding and stabilize the acquired tertiary structure. Protein modifications in the rough ER co-occur at different stages of protein folding.
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal...
7.3K
EDTA: Auxiliary Complexing Reagents01:26

EDTA: Auxiliary Complexing Reagents

1.4K
EDTA titrations are usually carried out in highly basic conditions, where the fully deprotonated form of EDTA, Y4−, actively complexes with the free metal ions in the solution. Several metal ions precipitate as hydrous oxide (hydroxides, oxides, or oxyhydroxides) under these conditions, lowering the concentration of free metal ions in the solution. For this reason, auxiliary complexing agents or ligands such as ammonia, tartrate, citrate, or triethanolamine are used in EDTA titrations to...
1.4K

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相关实验视频

Updated: Mar 3, 2026

Laboratory Simulation of an IronII-rich Precambrian Marine Upwelling System to Explore the Growth of Photosynthetic Bacteria
09:45

Laboratory Simulation of an IronII-rich Precambrian Marine Upwelling System to Explore the Growth of Photosynthetic Bacteria

Published on: July 24, 2016

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通过铁加速重建调节尿素氧化,并调整阳离子微环境.

Zhanhong Zhao1, Yi Zhou1, Tingting Kang1

  • 1School of Minerals Processing and Bioengineering, Central South University, Changsha 410083, China.

Inorganic chemistry
|March 2, 2026
PubMed
概括

用铁添加的硫化物纳米片通过增强电极重建和抑制中毒,促进尿素氧化 (UOR). 这一策略提高了生产和化学合成效率.

科学领域:

  • 电化学 电化学 电化学
  • 材料科学 材料科学 材料科学
  • 催化剂是一种催化剂.

背景情况:

  • 阳极小分子电氧化是生产和化学合成的关键.
  • 用于尿素氧化 (UOR) 的基阳极面临着缓慢的重建,中毒和大规模运输限制等挑战.

研究的目的:

  • 为高效的UOR设计Fe-doped Ni3S2纳米板阵列.
  • 制定一个策略来调节活性站点和阳离子微环境.

主要方法:

  • 自助式合铁的Ni3S2纳米板阵列的制造. 自助式合铁的Ni3S2纳米板阵列.
  • 操作光谱学和电化学分析.
  • 调查铁剂和界面硫酸盐层的作用.

主要成果:

  • 铁剂加快了Ni(Fe) OOH的形成和离子衍生的重建.
  • 一个界面SO4(2-) 层介导电子转移并抑制碳酸盐吸附.
  • 优化的电极在UOR的1.355V下达到200mA cm-2和演变的59mV超电位.

结论:

  • 用Fe合的Ni3S2电极显示出增强的UOR活性和双功能进化.

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Electrochemical Detection of Deuterium Kinetic Isotope Effect on Extracellular Electron Transport in Shewanella oneidensis MR-1
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Electrochemical Detection of Deuterium Kinetic Isotope Effect on Extracellular Electron Transport in Shewanella oneidensis MR-1

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Experimental Column Setup for Studying Anaerobic Biogeochemical Interactions Between Iron OxyHydroxides, Trace Elements, and Bacteria
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Experimental Column Setup for Studying Anaerobic Biogeochemical Interactions Between Iron OxyHydroxides, Trace Elements, and Bacteria

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Electrochemical Detection of Deuterium Kinetic Isotope Effect on Extracellular Electron Transport in Shewanella oneidensis MR-1
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Electrochemical Detection of Deuterium Kinetic Isotope Effect on Extracellular Electron Transport in Shewanella oneidensis MR-1

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  • 接口门和核心结构的机制驱动策略为电氧化反应提供了可转移的蓝图.