Disclosed herein are modified zeolites and methods for making modified zeolites. In one or more embodiments disclosed herein, a modified zeolite may include a microporous framework including a plurality of micropores having diameters of less than or equal to 2 nm. The microporous framework may include at least silicon atoms and oxygen atoms. The modified zeolite may further include organometallic moieties each bonded to bridging oxygen atoms. The organometallic moieties may include a platinum atom. The platinum atom may be bonded to a bridging oxygen atom, and the bridging oxygen atom may bridge the platinum atom of the organometallic moiety and a silicon atom of the microporous framework.

Disclosed herein are modified zeolites and methods for making modified zeolites. In one or more embodiments disclosed herein, a modified zeolite may include a microporous framework comprising a plurality of micropores having diameters of less than or equal to 2 nm. The microporous framework may include at least silicon atoms and oxygen atoms. The modified zeolite may further include organometallic moieties each bonded to bridging oxygen atoms. The organometallic moieties may include a titanium atom. The titanium atom may be bonded to a bridging oxygen atom, and the bridging oxygen atom may bridge the titanium atom of the organometallic moiety and a silicon atom of the microporous framework.

Disclosed herein are modified zeolites and methods for making modified zeolites. In one or more embodiments disclosed herein, a modified zeolite may include a microporous framework including a plurality of micropores having diameters of less than or equal to 2 nm. The microporous framework may include at least silicon atoms and oxygen atoms. The modified zeolite may further include organometallic moieties each bonded to a nitrogen atom of a secondary amine functional group comprising a nitrogen atom and a hydrogen atom. The organometallic moieties may comprise a hafnium atom that is bonded to the nitrogen atom of the secondary amine functional group. The nitrogen atom of the secondary amine function group may bridge the hafnium atom of the organometallic moiety and a silicon atom of the microporous framework.

The present document describes an oral care composition comprising a cuttlefish bone powder, comprising particles having more than 95% (w/w) calcium carbonate content, a specific surface area of at least 5 m.sup.2/g, a mechanical hardness about 4.75 to 6.87 GPa, and at least 20% of said particles of the powder have a particle size of from about 50 microns to about 70 microns and a mean of about 60 microns, and a suitable carrier, and uses of the composition for oral hygiene.

Provided are a zirconia sol having a transmittance of 45% or more at a wavelength of 400 nm, having a transmittance of 75% or more at a wavelength of 550 nm, and containing zirconia particles in an amount of 20 wt % or more, and a method for manufacturing the zirconia sol.

A negative electrode material for a lithium-ion secondary battery includes composite particles, each of the composite particles having a structure in which plural flat graphite particles are stacked, wherein the composite particles have a particle size distribution D90/D10 of from 2.0 to 5.0, or wherein the plural flat graphite particles have a particle size distribution D90/D10 of from 2.0 to 4.4.

The present invention provides a method for producing a nitrogen-doped highly graphitic porous carbon body, and a nitrogen-doped highly graphitic porous carbon body produced according to the same. Also, the present invention provides a method for producing a sulfur and nitrogen double-doped highly graphitic porous carbon body, a sulfur and nitrogen double-doped highly graphitic porous carbon body produced according to the same, and an electrode catalyst for a fuel cell and/or a water electrolysis reaction comprising the carbon body.

The invention is related to a layered double hydroxide electride which can be produced without high-temperature treatment, and a production method of which cost can be reduced. The layered double hydroxide electride contains electrons between layers and has an electron density of 2.0×10.sup.18 cm.sup.−3 or more. The method of producing the layered double hydroxide electride includes a step of mixing a starting layered double hydroxide with an electron exchanger for exchanging anions existing between layers of the starting layered double hydroxide for electrons to produce the layered double hydroxide electride.

A method for producing an ion conductor containing LiCB.sub.9H.sub.10 and LiCB.sub.11H.sub.12 includes: preparing a homogeneous solution by mixing LiCB.sub.9H.sub.10 and LiCB.sub.11H.sup.12 in a solvent at a LiCB.sub.9H.sub.10/LiCB.sub.11H.sub.12 molar ratio of from 1.1 to 20; obtaining a precursor by removing the solvent from the homogeneous solution; and obtaining an ion conductor by subjecting the precursor to a heat treatment.

The present disclosure is directed to providing a carbon film having an excellent shield performance against electromagnetic waves. The carbon film of the present disclosure is a carbon film made of a carbon nanotube assembly, wherein a pore distribution curve of the carbon film indicating the relationship between the pore size and the Log differential pore capacity obtained from an adsorption isotherm at 77 K of liquid nitrogen based on the Barrett-Joyner-Halenda method has a peak in which the Log differential pore capacity is maximized within a pore size range of 10 nm or more and 100 nm or less, and the value of the Log differential pore capacity at the peak is 1.2 cm.sup.3/g or more.