An anionic sorption agent, method for forming the anionic sorption agent and a barrier system are disclosed. The anionic sorption agent including a modified pseudo or glycol-boehmite base comprising a structure having cationic metal ion sites. The method for forming the anionic sorption agent includes providing a pseudo or glycol-boehmite base and contacting the pseudo or glycol-boehmite base a modifying composition comprising a metallic ion to form the modified pseudo or glycol-boehmite base comprising a structure having cationic metal ion sites. The barrier system includes the anionic sorption agent comprising a first barrier component comprising a modified pseudo or glycol-boehmite base comprising a structure having cationic metal ion sites and a second barrier component comprising a cationic sorption agent.

A process of removing at least one metal contaminant, such as copper, from a fluid hydrocarbon, for example, crude oil or a liquid hydrocarbon fuel, such as an aviation fuel. The process involves contacting the metal-contaminated fluid hydrocarbon with a sorbent selected from graphene oxide or a functionalized graphene oxide, particularly, a graphene oxide treated with a polycarboxylic acid, such as a saccharide polycarboxylic acid or a salt thereof, examples of which include alginic acid and Group IA and IIA salts thereof. The process removes greater than 99 percent of the metal contaminant without reducing concentrations of advantageous fuel additives, such as, antioxidants, icing inhibitors and corrosion inhibitors. Also described are a purified fluid hydrocarbon composition and a metal contaminant filter system.

Disclosed in certain embodiments are catalyst-adsorbent compositions that include a metal oxide catalyst adapted for converting gaseous pollutants into chemically-benign species, and an adsorbent adapted for adsorbing the chemically-benign species together with other gaseous species and volatile organic compounds.

The present invention is related to highly oxygenated nanoribbons and highly microporous carbon (mPC) produced by the oxidation of a series of carbon blacks in nitric acid followed by fast and slow pyrolysis, respectively. New porous carbons according to the invention does not need to be activated by strong alkaline activators, for example, KOH and NaOH. The best prepared mPC showed a high capacity for carbon dioxide capture of 1 to 3.9 mmol/g at pressures between 0.15 and 1 bar and 25° C.

An adsorbent includes a porous substrate and a carboxylic acid dimer loaded onto the porous substrate. The carboxylic acid dimer is loaded on the surface or in the plurality of holes of the porous substrate. The average pore size of the porous substrate is not smaller than 2 nm. The carboxylic acid dimer is loaded onto the porous substrate by at least one of the following manners: a) the carboxylic acid dimer is loaded onto the porous substrate through a Si—OH bond; b) the carboxylic acid dimer is loaded onto the porous substrate through the exchange between a carboxyl group and chlorine; c) the carboxylic acid dimer is loaded onto the porous substrate through the exchange between a carboxyl group and a hydroxyl group; and d) the carboxylic acid dimer is loaded onto the porous substrate through the coordination of a carboxyl group and aluminum or silicon.

Embodiments of the present disclosure pertain to methods of sorption of H.sub.2O from an environment by associating the environment with a porous material such that the association results in the sorption of H.sub.2O to the porous material. The porous material includes a (M)-2,4-pyridinedicarboxylic acid coordination polymer, where M is a divalent metal ion selected from the group consisting of Mn, Fe, Co, Ni, Mg, and combinations thereof. The coordination polymer has a one-dimensional pore structure and shows reversible soft-crystal behavior. The porous material may be a Mg(II) 2,4-pyridinedicarboxylic acid coordination polymer (i.e., Mg-CUK-1). The methods of the present disclosure may also include one or more steps of releasing the sorbed H.sub.2O from the porous material and reusing the porous material after the releasing step for sorption of additional H.sub.2O from the environment.

The present disclosure provides for alkyl-aryl amine-rich small molecules that are prepared by nucleophilic substitution from tri- and hexa-bromine-substituted aromatic cores with various aliphatic diamines. The resulting products can be subsequently subjected by solution impregnation into solid mesoporous supports. Various types of alkyl-aryl amine-rich small molecules can fill the support's pores up to ˜90% and displayed good thermal stability

Activated carbon, e.g., from waste tires, modified by bimetallic Fe and Ce nanoparticles can provide high surface area and active sites for enhanced dye adsorption. Such nanocomposites can offer magnetic removal from aqueous solutions containing, e.g., Methylene Blue or Rhodamine B. Adsorption equilibrium data fit well to the Langmuir isotherm model, with an adsorption capacity was 324.6 mg/g. Rhodamine B adsorption by such activated carbon-Fe—Ce magnetic adsorbents has an endothermic character and pseudo-second-order kinetics. In ethanol solution, rhodamine B was desorbed at high efficiency and such materials, which could be recycled up to 5 cycles. Such magnetic nanocomposites are adsorbents for treating dyes such as rhodamine B in wastewater, even in large scale adsorption systems. Polyamides can be grafted to such nanocomposites.

A filtering and adsorbent sampling and enrichment system comprising a stationary phase consisting of a felt of activated carbon fibres with a micro-meso porous conformation and specific surface area of about 1500 m2/g and sampling and/or enrichment standards, confined within a closed casing, is described, as well as the method for obtaining it and the relative process for the analysis of organic and inorganic analytes that uses said system.

Disclosed herein are nanostructured hierarchical zeolitic materials comprising: a plurality of zeolite nanotubes, each zeolite nanotube comprising a zeolitic wall perforated by a plurality of pores, the zeolitic wall defining a single longitudinal lumen. Also disclosed herein are bolaform structure directing agents comprising: a first hydrophilic end and a second hydrophilic end with a hydrophobic core therebetween; the hydrophobic core comprising one or more aromatic rings and one or more hydrophobic alkyl groups; the one or more aromatic rings comprising a biphenyl group; the one or more hydrophobic alkyl groups each independently comprising a C.sub.10 alkyl group; and the first hydrophilic end and the second hydrophilic end each independently comprising a quinuclidinium group. Also disclosed herein are methods of making and use of the plurality of zeolite nanotubes and the bolaform structure directing agents.