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Hou et al. Microstructures 2023;3:2023039  https://dx.doi.org/10.20517/microstructures.2023.37  Page 11 of 17






























                                          Figure 5. MOF derivatives treatment as flame retardants.

               re-coordination with other ligands or functional groups, leading to a new MOF with altered properties .
                                                                                                        [73]
               The acid-base theory of ligand removal in MOFs has found diverse applications, ranging from the synthesis
               of novel MOFs to the functionalization of existing ones with guest molecules and the recovery of metals
               from them [74-76] . The judicious selection of acids and solvents can significantly impact both the extent and
               selectivity of ligand removal, rendering this approach highly versatile and tunable.

               Previously, Pan s group have done a series of work to derive LDH by etching ZIF [Figure 6] [77-82] .
                             '
               We incorporated mesoporous zinc hydroxystannate (ZHS) nanoparticles into NiCo-LDH nanocages that
               were derived  from  ZIF-67.  The  resulting  composite  material  was  then  tested  for  its  flame  retardancy
               properties, and it was found that the LOI value of an epoxy composite containing 6 wt.% of these fillers
               increased  to 27.2%. This improvement was significant enough to meet the UL-94 V-0 level, which is a
               widely recognized standard for flame retardancy. Subsequently, polyphosphazenes (PZS) is often used
               in  modification  and compounding  of  flame  retardants  because  of  its  rich  phosphorus  and  nitrogen,
               ZIF@LDH@PZS core-shell structures and LDH@PZS@NH trishell structures were synthesized through
               surface  polycondensation  on ZIF-67  using  PZS,  followed  by  ligand  etching  via  nickel  brine
               acidification.  The  interface  of  LDH  was analyzed  by  adjusting  the  reaction  time  to  enhance
               compatibility  with  the  resin  matrix.  Recently,  we  have synthesized  several  hollow  LDH  nanocages
               with  high  thermal  stability,  featuring  single-yolk  shell nanostructures  (s-CBC@LDH)  and  multi-
               yolk  shell  nanostructures  (m-CBC@LDH).  By  incorporating phosphorus-based  flame  retardants,  we
               have further enhanced their flame-retardant properties.


               In the context of flame retardancy, LDHs are often used as additives to reduce the flammability of polymers.
               When LDHs are added to a polymer, they act as a physical barrier that prevents the diffusion of oxygen and
               other flammable gases to the surface of the material, thereby reducing the rate of combustion. One issue
               with the physical barrier effect of LDHs is that the thickness and width of the barrier layer are limited by the
               amount of the LDH that can be added to the polymer matrix without affecting its properties. Thicker
               barriers may be required to achieve adequate flame retardancy in some applications, but a small length-
               diameter ratio of LDH may not meet the flame-retardant demand. One of the main challenges in using
               LDHs as pure inorganic flame retardants is achieving proper dispersion in the polymer matrix. Inadequate
               dispersion can lead to the formation of voids or weak points in the barrier layer, which can compromise its
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