An adsorbent is provided which can improve the fluorine adsorption capacity and the breakthrough time compared with conventional adsorbents, particularly an adsorbent which can be suitably used as a fluorine adsorbent. The adsorbent comprises rare earth compound particles comprising a rare earth oxycarbonate or a hydrate thereof.

A fluorescent nanocomposite which includes a thallium doped gadolinium chalcogenide having formula Tl.sub.xGd.sub.1-xY, wherein x is 0.01 to 0.1, and Y is selected from the group consisting of S, Se, or Te, and a benzothiazolium salt bound to a surface of the thallium doped gadolinium chalcogenide. A method of detecting antimony ions in a fluid sample whereby the fluid sample is contacted with the fluorescent nanocomposite to form a mixture, and a fluorescence emission profile of the mixture is measured to determine a presence or absence of antimony ions in the fluid sample, wherein a reduction in intensity of a fluorescence emissions peak associated with the fluorescent nanocomposite indicates the presence of antimony ions in the fluid sample.

A NO.sub.x adsorber catalyst and its use in an emission treatment system for internal combustion engines, is disclosed. The NO.sub.x adsorber catalyst comprises a first layer consisting essentially of a support material, one or more platinum group metals disposed on the support material, and a NO.sub.x storage material.

The present disclosure provides a hydrocarbon adsorbent including a core-shell particle including a core and a shell surrounding the core, wherein the core includes ion-exchanged zeolite that is ion-exchanged with a metal other than silicon (Si) and aluminum (Al) and the shell includes a mesoporous metal oxide.

The present disclosure provides a purification material for a rare earth metal or rare earth alloy and a preparation method thereof and a purification method for a rare earth metal or rare earth alloy. The purification material includes the following raw materials in mass percentage: 30% to 45% of a tungsten powder, 30% to 50% of a rare earth oxide, 5% to 10% of zirconia, 10% to 15% of a binder, and 1% to 5% of a rare earth hydride.

A fluorescent nanocomposite which includes a thallium doped gadolinium chalcogenide having formula Tl.sub.xGd.sub.1-xY, wherein x is 0.01 to 0.1, and Y is selected from the group consisting of S, Se, or Te, and a benzothiazolium salt bound to a surface of the thallium doped gadolinium chalcogenide. A method of detecting antimony ions in a fluid sample whereby the fluid sample is contacted with the fluorescent nanocomposite to form a mixture, and a fluorescence emission profile of the mixture is measured to determine a presence or absence of antimony ions in the fluid sample, wherein a reduction in intensity of a fluorescence emissions peak associated with the fluorescent nanocomposite indicates the presence of antimony ions in the fluid sample.

A fluorescent nanocomposite which includes a thallium doped gadolinium chalcogenide having formula Tl.sub.xGd.sub.1-xY, wherein x is 0.01 to 0.1, and Y is selected from the group consisting of S, Se, or Te, and a benzothiazolium salt bound to a surface of the thallium doped gadolinium chalcogenide. A method of detecting antimony ions in a fluid sample whereby the fluid sample is contacted with the fluorescent nanocomposite to form a mixture, and a fluorescence emission profile of the mixture is measured to determine a presence or absence of antimony ions in the fluid sample, wherein a reduction in intensity of a fluorescence emissions peak associated with the fluorescent nanocomposite indicates the presence of antimony ions in the fluid sample.

Disclosed is a method of decontamination by exposing a zirconium oxy(hydroxide) aerogel to a liquid, vapor, or gaseous sample suspected of containing a phosphonate compound. The aerogel may be doped with Fe.sup.3+ ions, Ce.sup.3+ ions, or SO.sub.4.sup.2− ions. The aerogel may be made by: providing a solution of ZrCl.sub.4; FeCl.sub.3, CeCl.sub.3, or Zr(SO.sub.4).sub.2; and a solvent; adding a cyclic ether to the solution to form a gel; infiltrating the gel with liquid carbon dioxide; applying a temperature and pressure to form supercritical fluid carbon dioxide; and removing the carbon dioxide for form an aerogel.

Nanosheets of Ca.sup.2+ and Y.sup.3+, with CO.sub.3.sup.2− in the interlayer with a uniform diameter and lengths of several tens of microns have been successfully synthesized in a hydrotalcite layer structure (a layered double hydroxide), using a hydrothermal method. The formation mechanism of lamellar CaY—CO.sub.3.sup.2− layered double hydroxides (LDHs) depends on the molar ratio of Ca and Y and the reaction time and temperature. The resulting LDH materials exhibit excellent affinity and selectivity for heavy transition metal and metalloid ions.

A method of removing hydrogen interstitially dissolved within an object can include: positioning a sorption pad having a contact surface and comprising a sorptive material; urging the contact surface into metallurgical contact with the first target surface while at a treatment temperature that is greater than about 200 degrees Celsius; c) maintaining the metallurgical contact for a treatment period during which the hydrogen migrates from the target object to the sorptive material; and at the conclusion of the treatment period, separating the contact surface from the first target surface and moving the sorption pad and any hydrogen sequestered therein away from the object.