Home » Dysprosium Metal Organic Framework (Dy-MOF, Purity: 99%, APS:30-40µm)
|Product||Dysprosium Metal Organic Framework|
|Molecular Formula||Dy(pyda)3Ca1.5(H2O)6} ⋅ 5.5H2O (1)||Confirm|
|Molecular Weight||158.925 g/mol||Confirm|
|Density||0.35 g/ cm3||Confirm|
|SSA||~1300 m2/g (BET)||Confirm|
|Linker||H3B Dy (1,3,5-tris(4-carboxyphenyl)benzene)|
|Application||adsorbing dyes and fluorescence detecting aromatic pollutants|
|Quality Control||Each lot of Dysprosium Metal Organic Framework was tested successfully.|
|Main Inspect Verifier||Manager QC|
|Total Metal Impurities||8500ppm|
Dysprosium Metal Organic Framework: Metal Organic Frameworks (MOFs) are a class of crystalline materials that consists of coordination bonds between transition metal cations and multidentate organic linkers. MOFs are well ordered, lattice like crystals. The nodes of lattices are metals- such as copper, zinc, nickel and cobalt.
Dysprosium Metal Organic Framework: The most impressive features of MOFs are their high surface area (up to 10000 m2g-1), high porosity (up to 90%) and tunable pore sizes, which are remarkable advantages over other porous materials (e.g Zeolites and carbons).
Dysprosium Metal Organic Framework: With their special structure and large surface area, MOFs open up new opportunities for alternative systems for gas and energy storage (e.g. carbon dioxide and hydrogen storage), chemical sensing, as nano reactors, in drug delivery, and separation in catalysis.
Dysprosium Metal Organic Framework:The inherent properties of MOFs make them great candidates for drug delivery systems. Firstly, there are multiple pathways to incorporate guest molecules within the MOFs and Secondly, the tailorable interactions between the guest molecules and MOF linkers or metal nodes allow for high drug loading capacity.
Dysprosium Metal Organic Framework: Additionaly, the tunable sizes of MOF crystals enhance optimization for cellular uptake, the potential for chemical-environment-dependent dissociation of MOF species for stimuli-responsive and triggered guest release, as well as the biocompatibility of certain classes of MOFs at uptake concentrations.
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