Abstract:
One embodiment of the invention comprises an ion exchange composition formed by reacting unsaturated carbon to carbon moieties pendant from derivatized ion binding cryptands with a support substrate under free radical activation conditions to form a covalent bond therebetween. In another embodiment, a cryptand ion exchange composition is made by covalently bonding unsaturated carbon to carbon moieties pendant from a derivatized ion binding cryptands with unsaturated carbon to carbon moieties pendant from a support substrate under free radical activation conditions to form covalent bond.
Abstract:
An object of the present invention is to provide a heavy metal ion scavenger having more excellent scavenging performance than previously. In order to attain this object, organic polymer materials of the present invention are characterized in that they have a polymer side chain derived from a haloalkyl-substituted styrene on the backbone of an organic polymer base and a functional group capable of forming a complex with a heavy metal ion has been introduced onto said polymer side chain. These organic polymer materials have excellent heavy metal ion scavenging performance so that they can be suitably used as heavy metal ion scavengers.
Abstract:
Apparatus, materials, and methods for removing ammonia from fluid using metal hydroxides (e.g. zinc hydroxide) and metal cation loaded media (e.g. zinc loaded ion exchange resins); the metal hydroxides and metal cation loaded media may be regenerated with a weak acid (pKa between 3 and 7). Alternatively, ammonia is removed from fluids by using H2SO4 and ZnSO4 and metal cation loaded media; the metal cation loaded media may be regenerated with H2SO4 and ZnSO4; the ammonia containing H2SO4 and H2SO4 may be concentrated as necessary to form (NH4)2SO4.ZnSO4.6H2O (ammonium zinc sulfate hexahydrate) crystals. These crystals are removed from the mother liquor and heated to temperatures exceeding 200° C. releasing NH3 and H2O vapor upon the decomposition of the crystals.
Abstract translation:使用金属氢氧化物(例如氢氧化锌)和金属负载介质(例如负载锌的离子交换树脂)从流体中除去氨的设备,材料和方法; 金属氢氧化物和金属负载介质可以用弱酸(pKa在3和7之间)再生。 或者,通过使用H 2 SO 4和ZnSO 4和金属负载介质从流体中除去氨; 金属负载介质可以用H 2 SO 4和ZnSO 4再生; 可以根据需要浓缩含有H 2 SO 4和ZnSO 4的氨以形成(NH 4)2 SO 4·ZnSO 4·6H 2 O(六水合硫酸锌)晶体。 将这些晶体从母液中除去并加热到超过200℃的温度,在晶体分解时释放出NH 3和H 2 O的蒸气。
Abstract:
In accordance with the present invention, an improved bifunctional cation-exchange composition has been formed which comprises synthetic resin support particles and both crown ether and non-crown ether functional groups attached thereto. The compositions of the present invention provide for novel, enhanced cation separation capabilities and, depending upon the type of functional groups employed, permit effective separation of cations which elute at approximately the same time off standard and commonly used cation-exchange columns. The presently described bifunctional cation-exchange compositions also permit the effective separation of one cation from a mixture comprising another cation that is present at a significantly greater concentration. Formed articles and methods employing the bifunctional cation-exchange composition are also provided.
Abstract:
A process of selectively separating a target metal contained in an aqueous solution by contacting the aqueous solution containing a target metal with an aqueous solution including a water-soluble polymer capable of binding with the target metal for sufficient time whereby a water-soluble polymer-target metal complex is formed, and, separating the solution including the water-soluble polymer-target metal complex from the solution is disclosed.
Abstract:
A process for removing ions of dissolved heavy metals and complex heavy metals comprises provides a treatment zone in which is contained an extraction material having an activated surface that has an affinity for heavy metal ions and complex heavy metal ions. The activated surface is the reaction product of a polyamine with a covalently anchored trifunctional hydrocarbyl silyl that yields non-crosslinked amino groups to which functional chelator groups can be covalently attached. The activated surface of the extraction material is formed by first hydrating the extraction material surface and then silanizing the hydrated surface with a short chain trifunctional silane having a hydrocarbon substituent containing 1-6 carbon atoms and a terminal leaving group, and then reacting a polyamine with the hydrocarbylsilyl from the silanization of the hydrated surface so as to form an aminohydrocarbyl polymer covalently bound to the extraction material surface. The extraction material surface yields amino groups that are available for bonding to chelator groups. As thus formed, the polymer may be alkylated with a carboxyl or sulfur containing alkylating reagent on at least some of the amino groups to enhance and specialize the chelating ability of the extraction material's activated surface.
Abstract:
A composite material useful for removing heavy metal ions from solutions such as aqueous waste streams comprises a ceramic inorganic support such as silica gel which is covalently bonded, through a silane coupling agent, to a hydroxyquinoline ligand or such a support which has been reacted with a silylating agent and then on which is deposited a hydroxyquinoline ligand.
Abstract:
A process for removing complexed or chelated ions from an aqueous solution using a cationic chelating resin in the sodium form. The process is particularly useful for removing metal ions chelated during a metal plating process with specific utility for recovering cadmium from a cadmium cyanide complex.
Abstract:
The present invention relates to bis-imidazolyl compounds of the formula: ##STR1## and polymers having the above-identified bis-imidazolyl compounds as a polymerizable unit. The present invention further relates to a method for scavenging trace quantities of metal ions from various effluents sources using the polymers of the instant invention. The instant invention also is directed to the use of the above-identified polymers as corrosion inhibiting agents and as a film for use in gel electrophoresis.