Disclosed are a core-shell structure type wave absorbing material and a preparation method therefor. The wave absorbing material has a core-shell structure with two-dimensional transition metal-chalcogen compound nanosheets as cores and hollow carbon spheres as shells. The preparation method includes: dissolving the hollow carbon spheres in a solvent, sequentially adding a transition metal source and a chalcogen source, taking a solvothermal reaction after dissolution through stirring, and then performing posttreatment to obtain the wave absorbing material. The present invention further discloses an application of the wave absorbing material in fields of military and civilian high-frequency electromagnetic compatibility and protection. The core-shell structure type wave absorbing material of the present invention has a density of 0.3 to 1.5 g/cm.sup.3, a maximum reflection loss value and an effective bandwidth of the material can be effectively improved in a frequency range of 2 to 40 GHz, and the core-shell structure type wave absorbing material is an electromagnetic compatibility and protection material capable of meeting requirements of civilian high-frequency electronic devices and military weapons and equipment such as airships and artillery shells.

Disclosed are a core-shell structure type wave absorbing material and a preparation method therefor. The wave absorbing material has a core-shell structure with two-dimensional transition metal-chalcogen compound nanosheets as cores and hollow carbon spheres as shells. The preparation method includes: dissolving the hollow carbon spheres in a solvent, sequentially adding a transition metal source and a chalcogen source, taking a solvothermal reaction after dissolution through stirring, and then performing posttreatment to obtain the wave absorbing material. The present invention further discloses an application of the wave absorbing material in fields of military and civilian high-frequency electromagnetic compatibility and protection. The core-shell structure type wave absorbing material of the present invention has a density of 0.3 to 1.5 g/cm.sup.3, a maximum reflection loss value and an effective bandwidth of the material can be effectively improved in a frequency range of 2 to 40 GHz, and the core-shell structure type wave absorbing material is an electromagnetic compatibility and protection material capable of meeting requirements of civilian high-frequency electronic devices and military weapons and equipment such as airships and artillery shells.

Methods of sulfurizing metal containing particles in the absence of hydrogen are described. One method includes contacting a bed of metal containing particles with a gaseous stream comprising hydrogen sulfide and inert gas under reaction conditions sufficient to produce sulfided metal containing particles. The gaseous stream is introduced into a vertical reactor at an inlet positioned at the bottom portion of the reactor and any unreacted hydrogen sulfide and inert gas is removed at an outlet positioned above the inlet. The sulfided metal containing particles can be removed from the reactor and stored.

Methods of sulfurizing metal containing particles in the absence of hydrogen are described. One method includes contacting a bed of metal containing particles with a gaseous stream comprising hydrogen sulfide and inert gas under reaction conditions sufficient to produce sulfided metal containing particles. The gaseous stream is introduced into a vertical reactor at an inlet positioned at the bottom portion of the reactor and any unreacted hydrogen sulfide and inert gas is removed at an outlet positioned above the inlet. The sulfided metal containing particles can be removed from the reactor and stored.

Systems for improving metal leach kinetics and metal recovery during atmospheric or substantially atmospheric leaching of a metal sulfide are disclosed. In some embodiments, an oxidative leach circuit 200 may employ Mechano-Chemcial/Physico-Chemical processing means for improving leach kinetics and/or metal recovery. In preferred embodiments, the Mechano-Chemcial/Physico-Chemical means comprises various combinations of stirred-tank reactors 202 and shear-tank reactors 212. As will be described herein, the stirred-tank reactors 202 and shear-tank reactors 212 may be arranged in series and/or in parallel with each other, without limitation. In some non-limiting embodiments, a shear-tank reactor 212 may also be disposed, in-situ, within a stirred-tank reactor 202.

An array of transition metal tubular architectures, where the transition metal tubular architectures are comprised of a transition metal oxide, sulfide, or selenide, and wherein transition metal tubular architectures are less than 100 nm in length. The transition metal tubular architectures can be at least partially crystalline. Within the array of transition metal tubular architectures, at least 80% of the transition metal tubular architectures can be less than 100 nm in length.

The present disclosure relates to sulfur-containing zerovalent iron nanoparticles and the use of same for transforming chlorinated solvent pollutants and which may therefore be useful as water treatment technology for restoration of groundwater resources contaminated with toxic, chlorinated solvent pollutants.

The present disclosure relates to sulfur-containing zerovalent iron nanoparticles and the use of same for transforming chlorinated solvent pollutants and which may therefore be useful as water treatment technology for restoration of groundwater resources contaminated with toxic, chlorinated solvent pollutants.

The present invention relates to a compound represented by the general formula Li.sub.2+2xM.sub.1-xZS.sub.4, wherein 0.3≤x≤0.9; wherein M is one or more elements selected from the group consisting of Pb, Mg, Ca, Ge and Sn; and wherein Z is one or more elements selected from the group consisting of Ge, Si, Sn and Al.

The present invention also relates to a method for preparing the material of the present invention, comprising the steps of: (a) providing a mixture of lithium sulfide Li.sub.2S, sulfides MS and ZS.sub.2, in a stoichiometric ratio ensuring Li.sub.2+2xM.sub.1-xZS.sub.4 to be obtained, wherein M, Z and x are as defined above; (b) pelletizing the mixture prepared in step (a); (c) heating at a maximum plateau temperature.

In still another aspect, the present invention relates to a use of the compound of the present invention as a solid electrolyte, in particular in an all solid-state lithium battery.

The present invention relates to a compound represented by the general formula Li.sub.2+2xM.sub.1-xZS.sub.4, wherein 0.3≤x≤0.9; wherein M is one or more elements selected from the group consisting of Pb, Mg, Ca, Ge and Sn; and wherein Z is one or more elements selected from the group consisting of Ge, Si, Sn and Al.

The present invention also relates to a method for preparing the material of the present invention, comprising the steps of: (a) providing a mixture of lithium sulfide Li.sub.2S, sulfides MS and ZS.sub.2, in a stoichiometric ratio ensuring Li.sub.2+2xM.sub.1-xZS.sub.4 to be obtained, wherein M, Z and x are as defined above; (b) pelletizing the mixture prepared in step (a); (c) heating at a maximum plateau temperature.

In still another aspect, the present invention relates to a use of the compound of the present invention as a solid electrolyte, in particular in an all solid-state lithium battery.