Clinoptilolite is one of the most common, widespread and abundant zeolites in nature. Its availability, low cost, and outstanding ion exchange properties make clinoptilolite an excellent candidate for both direct use and various modifications to create new low-cost functional materials for sustainable development. Specific applications in which clinoptilolite is already being used include water treatment and heavy metal ion removal, agricultural purposes, storage and conversion of unwanted gaseous emissions into the atmosphere, production of catalysts and photocatalysts, bioactive materials, and a number of others. Unlike some other zeolites, clinoptilolite is difficult to synthesize, which is why most publications refer to this zeolite in its natural form, either directly from the deposit or after applying various processes to this mineral to improve its properties. Among the modification methods used, ion exchange stands out. This review is devoted to the study of ion exchange processes in natural clinoptilolite with two goals: first, as its strategic property for use in processes in which cation exchange is fundamentally necessary; second, as a way to modify it to create composite materials with predetermined desired properties.

This review deals with the destabilization methods for improvement of storage properties of metal hydrides. Both theoretical and experimental approaches were used to point out the influence of various types of defects on structure and stability of hydrides. As a case study, Mg, and Ni based hydrides has been investigated. Theoretical studies, mainly carried out within various implementations of DFT, are a powerful tool to study mostly MgH₂based materials. By providing an insight on metal‐hydrogen bonding that governs both thermodynamics and hydrogen kinetics, they allow us to describe phenomena to which experimental methods have a limited access or do not have it at all: to follow the hydrogen sorption reaction on a specific metal surface and hydrogen induced phase transformations, to describe structure of phase boundaries or to explain the impact of defects or various additives on MgH₂stability and hydrogen sorption kinetics. In several cases theoretical calculations reveal themselves as being able to predict new properties of materials, including the ways to modify Mg or MgH₂that would lead to better characteristics in terms of hydrogen storage. The influence of ion irradiation and mechanical milling with and without additives has been discussed. Ion irradiation is the way to introduce a well‐defined concentration of defects (Frankel pairs) at the surface and sub‐surface layers of a material. Defects at the surface play the main role in sorption reaction since they enhance the dissociation of hydrogen. On the other hand, ball‐milling introduce defects through the entire sample volume, refine the structure and thus decrease the path for hydrogen diffusion. Two Severe Plastic Deformation techniques were used to better understand the hydrogenation/dehydrogenation kinetics of Mg‐ and Mg₂Ni‐based alloys: Equal‐Angular‐Channel‐Pressing and Fast‐Forging. Successive ECAP passes leads to refinement of the microstructure of AZ31 ingots and to instalment therein of high densities of defects. Depending on mode, number and temperature of ECAP passes, the H‐sorption kinetics have been improved satisfactorily without any additive for mass H‐storage applications considering the relative speed of the shaping procedure. A qualitative understanding of the kinetic advanced principles has been built. Fast‐Forging was used for a “quasi‐instantaneous” synthesis of Mg/Mg₂Ni‐based composites. Hydrogenation of the as‐received almost bi‐phased materials remains rather slow as generally observed elsewhere, whatever are multiple and different techniques used to deliver the composite alloys. However, our preliminary results suggest that a synergic hydrogenation / dehydrogenation process should assist hydrogen transfers from Mg/Mg₂Ni on one side to MgH₂/Mg₂NiH₄on the other side via the rather stable a‐Mg₂NiH_0.3, acting as in‐situ catalyser.