The present invention relates to a carbon sorbent the can selectively remove platinum-group metals and other heavy metals such as tin without co-removing organic synthesis products including pharmaceutical intermediates and finished Active Pharmaceutical Ingredients (APIs). The carbon sorbents of the present invention are made from low-cost, high purity starting materials and the resulting carbon sorbents are also very pure. The carbon sorbents possess a combination of certain nitrogen and phosphorous groups combined with mesoporosity (2 to 50 nm diameter pores) that proves the high metal adsorption.

A coated substrate (2a, 2b) adapted for hydrocarbon adsorption having at least one surface, and a coating on the at least one surface, the coating comprising particulate carbon and a binder, wherein the particulate carbon has a BET surface area of at least about 1300 m.sup.2/g; and at least one of: (i) a butane affinity of greater than 60% at 5% butane; (ii) a butane affinity of greater than 35% at 0.5% butane; (iii) a micropore volume greater than about 0.2 ml/g and a mesopore volume greater than about 0.5 ml/g. A bleed emission scrubber (1) and an evaporative emission control canister system (30) comprising the coated substrate (2a,2b) are provided. They can control evaporative hydrocarbon emissions and may provide low diurnal breathing loss (DBL) emissions even under a low purge condition.

Compositions are provided for binding mercury based in porous organic polymers having (i) a plurality of repeat units having heavy metal chelator moieties covalently attached thereto and (ii) a plurality of pores having a hierarchical pore size distribution over a range of pore sizes. In some aspects, the range of pore sizes is about 5 nm to 10 nm. The compositions can have a maximum mercury uptake capacity of 1,000 mg g.sup.−1 to 2,000 mg g.sup.−1 at 1 atm and 296 K and has a mercury uptake capacity that is stable and recyclable. Methods of making the compositions and methods of using the compositions for uptake of mercury are also provided.

A water harvesting device includes at least a first adsorption column including a first inlet, a first outlet, and a first interior region. A sorbent material is located within the first interior region of the first adsorption column. The sorbent material includes a metal organic framework (MOF) material including a plurality of metal ions or clusters of metal ions coordinated to one or more organic linkers, a plurality of nanofabrics comprising a hydrogel material, or a combination thereof.

A method for selective removal of polycyclic aromatic hydrocarbons from oils obtained as a result of petroleum processing, including two separate processes: filtration through a porous carbon-containing bed comprising and filtration through microfiltration membranes. The method is particularly useful for purifying oils selected from unconverted oils obtained in hydrocracking processes, products of further processing of these oils, engine oil and used engine oil.

A carbon-based porous material microscopically exhibiting a three-dimension 1 cross-linked net-like hierarchical pore structure, a specific surface area of 500˜2,500 m.sup.2/g and a water contact angle greater than 90°. The surface of the carbon-based porous material has a through hierarchical pore structure with mesopores nested in macropores and micropores nested in mesopores, the content of mesopores is high, and there are more adsorption activity sites exposed on the surface of the material, so that the diffusion path for organic gas molecules in the adsorption process is shortened. At the same time, the absorption and desorption rates may also be accelerated and the desorption temperature may be lowered. Furthermore, benefits result for solving the desorption and recovery problems of organic gas molecules. Moreover, the defects of ordinary porous carbon materials being easily hygroscopic, having a weakened capacity to adsorb target gas molecules in a humid environment, etc. are further effectively solved.

The invention relates to a method to produce a particulate activated carbon material for capturing CO.sub.2 from air,

wherein the particulate activated carbon is impregnated with alkali carbonate salt such as K.sub.2CO.sub.3; and wherein the impregnated particulate activated carbon either has, determined using nitrogen adsorption methods, a pore volume of at least 0.10 cm.sup.3/g for pore sizes of at least 5 nm and a pore volume of at most 0.30 cm.sup.3/g for pore sizes of less than 2 nm or is based on a mixture of different alkali carbonate salts, or has a particular pore surface for pore sizes in the range of 2 nm-50 nm.

An object of the present invention is to provide a new form of adsorbent suitable for a motor vehicle canister. An activated carbon fiber sheet satisfies one or two or more of conditions for indices, such as a specific surface area, a pore volume of pores having a given pore diameter, and a sheet density. An embodiment, for example, may have: a specific surface area ranging from 1400 to 2200 m.sup.2/g; a pore volume ranging from 0.20 to 1.20 cm.sup.3/g for pores having pore diameters of more than 0.7 nm and 2.0 nm or less; and a sheet density ranging from 0.030 to 0.200 g/cm.sup.3.

A metal organic framework and a method for preparing the same, and an adsorption device employing the metal organic framework are provided. The metal organic framework includes a 3,5-pyridinedicarboxylic acid and a metal ion, which is an aluminum ion, a chromium ion, or a zirconium ion, wherein the 3,5-pyridinedicarboxylic acid is coordinated to the metal ion.

A carbon adsorbent storage and dispensing system is provided with a structurally modified particulate carbon adsorbent designed with optimal volumetric surface area for a certain range of particle sizes. Bulk density and specific surface area are carefully balanced to ensure the volumetric surface area remains within an optimal range to create high performance, as measured by dispensing capacity of the dopant fluid that is reversibly adsorbed onto the structurally modified particulate carbon adsorbent.