This invention is directed to amorphous and crystalline titanosilicate materials that have an unexpected selectivity for cesium and strontium, especially in the presence of high levels of competing ions. The titanosilicates of this invention show very high, unexpected selectivity in the presence of such competing cations such as sodium, calcium, magnesium and potassium, such as present in seawater.

This invention is directed to amorphous and crystalline titanosilicate materials that have an unexpected selectivity for cesium and strontium, especially in the presence of high levels of competing ions. The titanosilicates of this invention show very high, unexpected selectivity in the presence of such competing cations such as sodium, calcium, magnesium and potassium, such as present in seawater.

The present invention relates to a process, methods and materials for generating fertilizers from seawater resources, especially in conjunction with seawater desalination plants. Here, we demonstrate that varying compositions of fertilizers such as nitrogen/potassium, nitrogen/phosphorus/potassium, nitrogen/potassium/sulfur, and nitrogen/phosphorus/potassium/sulfur, potassium/sulfur, potassium along with micro and secondary nutrients can directly be generated as part of the extraction process to meet the requirements of both starter and sustained phases of plant growth.

The present invention relates to a process, methods and materials for generating fertilizers from seawater resources, especially in conjunction with seawater desalination plants. Here, we demonstrate that varying compositions of fertilizers such as nitrogen/potassium, nitrogen/phosphorus/potassium, nitrogen/potassium/sulfur, and nitrogen/phosphorus/potassium/sulfur, potassium/sulfur, potassium along with micro and secondary nutrients can directly be generated as part of the extraction process to meet the requirements of both starter and sustained phases of plant growth.

The present application relates to a method for synthesizing nanozeolite Y crystals, nanozeolite Y crystals obtainable by said method, and the use of the synthesized nanozeolite Y crystals in cracking hydrocarbons, as molecular sieves or as ion-exchangers.

A heavy metal capture composition, devices including the composition, and a method of reducing heavy metal contamination in the environment is described.

The present invention relates to zirconium silicate compositions having a lead content that is below 0.6 ppm and methods of manufacturing zirconium silicate at reactor volumes exceeding 200-L with a lead content below 1.1 ppm. The lead content of the zirconium silicate of this invention are within the levels that are considered acceptable for extended use given the dose requirements for zirconium silicate.

The present invention relates to zirconium silicate compositions having a lead content that is below 0.6 ppm and methods of manufacturing zirconium silicate at reactor volumes exceeding 200-L with a lead content below 1.1 ppm. The lead content of the zirconium silicate of this invention are within the levels that are considered acceptable for extended use given the dose requirements for zirconium silicate.

A lithium ion sorbent includes an organosilane-grafted lithium ion sieve. The organosilane-grafted lithium ion sieve is a reaction product of a lithium ion sieve and an organosilane. The lithium ion sieve is either a delithiated orthosilicate or a delithiated metal oxide. The organosilane reagent is of the general formula: R.sup.1—(CH.sub.2).sub.n—Si—R.sup.4.sub.3 where R.sup.1 is an organic moiety containing a functional group selected from an acrylate, methacrylate or vinyl group or their derivatives, R.sup.4 is either a hydrolysable alkoxy group or a methyl group, where at least one of the three R.sup.4 groups is a hydrolysable alkoxy group and n is 1-3. This lithium ion sorbent is durable and useful for adsorbing lithium from aqueous resources. The lithium ion sorbent can also be used in the manufacture of a composite material where the organosilane-grafted lithium ion sieve is covalently incorporated into a porous crosslinked polymeric support scaffold.

Disclosed is an ion exchange resin comprising a polymer having strong acid and strong base groups on the same polymer. In some forms the resin comprises a high density of polymers having strong acid and strong base groups on the same polymer. In some forms the strong acid and strong base groups are in close proximity to one another on the polymer. The disclosure further relates to a mixed bead resin for high salt level desalination.

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