B01J20/041

HIGH TEMPERATURE LAYERED MIXED-METAL OXIDE MATERIALS WITH ENHANCED STABILITY

Embodiments of the present disclosure are directed towards methods for preparing mixed-metal oxide particles by heating adamantane-intercalated layered double-hydroxide (LDH) particles at a reaction temperature of from 400° C. to 800° C. to form mixed-metal oxide particles. The adamantane-intercalated LDH particles have a general formula [M.sub.1-xAl.sub.x(OH).sub.2](A).sub.x.mH.sub.2O, where x is from 0.14 to 0.33, m is from 0.33 to 0.50, M is chosen from Mg, Ca, Co, Ni, Cu, or Zn, and A is adamantane carboxylate, and an aspect ratio greater than 100. The aspect ratio is defined by the width of an adamantane-intercalated LDH particle divided by the thickness of the adamantane-intercalated LDH particle. The mixed-metal oxide particles comprise a mixed-metal oxide phase containing M, Al or Fe, and carbon.

Catalytic adsorbents obtained from municipal sludges, industrial sludges, compost and tobacco waste and process for their production

Industrial waste derived adsorbents were obtained by pyrolysis of sewage sludge, metal sludge, waste oil sludge and tobacco waste in some combination. The materials were used as media to remove hydrogen sulfide at room temperature in the presence of moisture. The initial and exhausted adsorbents after the breakthrough tests were characterized using sorption of nitrogen, thermal analysis, XRD, ICP, and surface pH measurements. Mixing tobacco and sludges result in a strong synergy enhancing the catalytic properties of adsorbents. During pyrolysis new mineral phases are formed as a result of solid state reaction between the components of the sludges. High temperature of pyrolysis is beneficial for the adsorbents due to the enhanced activation of carbonaceous phase and chemical stabilization of inorganic phase. Samples obtained at low temperature are sensitive to water, which deactivates their catalytic centers.

Regenerable sorbent for carbon dioxide removal

A mixed salt composition adapted for use as a sorbent for carbon dioxide removal from a gaseous stream is provided, the composition being in solid form and including magnesium oxide, an alkali metal carbonate, and an alkali metal nitrate, wherein the composition has a molar excess of magnesium characterized by a Mg:X atomic ratio of at least about 3:1, wherein X is the alkali metal. A process for preparing the mixed salt is also provided, the process including mixing a magnesium salt with a solution comprising alkali metal ions, carbonate ions, and nitrate ions to form a slurry or colloid including a solid mixed salt including magnesium carbonate; separating the solid mixed salt from the slurry or colloid to form a wet cake; drying the wet cake to form a dry cake including the solid mixed salt; and calcining the dry cake to form a mixed salt sorbent.

Porous activated alumina based sorbent for lithium extraction

This invention relates to a method for preparing a lithium activated alumina intercalate solid by contacting a three-dimensional activated alumina with a lithium salt under conditions sufficient to infuse lithium salts into activated alumina for the selective extraction and recovery of lithium from lithium containing solutions, including brines.

Sorbents for the oxidation and removal of mercury

A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

LED SYSTEM
20170256688 · 2017-09-07 ·

A non-hermetically sealed LED system containing an active composition having an amount between 0.06 and 2.5 mg per cm.sup.2 of the system optical window area is described. The active composition contains an active material in powder form, wherein at least 75 wt % of the active material is chosen from one or more of active carbons, silver, copper, zinc, copper oxide, zinc oxide, calcium oxide, and silver oxide.

METAL SULFIDES ON ALKALI EARTH PARTICLE SUBSTRATES
20210402366 · 2021-12-30 ·

The present disclosure relates to methods for producing metal sulfide disposed on particle substrates. In at least one embodiment, a method for producing an alkali earth hydroxide particle having a metal sulfide disposed thereon includes introducing an alkali earth oxide particle with a metal sulfate to form a first composition. The method includes introducing an alkali sulfide or an alkali earth sulfide with the first composition to form a second composition. The present disclosure further relates to compositions of matter having metal sulfide disposed on a particle substrate. In at least one embodiment, a composition of matter includes an alkali earth hydroxide particle. The composition of matter includes a metal sulfide disposed on the alkali earth hydroxide particle.

Method of use for a solid form adsorbent

A method including adding to or positioning in a vehicle air conditioning system a solid form adsorbent. The solid form adsorbent includes a plurality of discrete adsorbent particles spatially bound in place by point bonding with a binder. At least about 25% of the external surface area of a majority of the particles is not sealed off by the binder and is available for adsorption.

ENHANCED HYDRATE PRODUCED FROM FLASH CALCINED LIME AND METHODS OF MAKING THE SAME
20210387908 · 2021-12-16 ·

A system and related methods for the production of lime sorbent compositions from a calcium carbonate feedstock formed using flash calcination to produce the intermediate calcium oxide material.

Mixed metal sorbents for CO.SUB.2./H.SUB.2.O displacement desorption

The disclosure generally relates to CCS sorbents, particularly for CO.sub.2/H.sub.2O displacement desorption process. The sorbents include an aluminum oxide support that includes two alkali metal salts impregnated on the support. The two alkali metals include a potassium metal salts and a second alkali metal salt which is not potassium. The second metal salt disrupts poisoning effects that degrade sorbent lifetime. The sorbents demonstrate improved CO.sub.2 loadings and better H.sub.2O/CO.sub.2 ratios, as well as improved stability. Compositions and methods of making are disclosed.