Chelation compositions
Biodegradable chelating agents comprising a substituted iminodisuccinic acid having six coordination sites and a simplified method for making same are disclosed. The method calls for mixing together an acid anhydride or lactone with a polyfunctional amine to obtain an amide which is further reacted with an amine. The chelating agents are particularly useful for agricultural applications such as fertilizers.
1. A chelating composition comprising a modified iminodisuccinic acid, or a salt thereof, having the ability to donate at least five nonbonded pairs of electrons without hindrance or bond strain, and having one or more of the following formulas:
where X is H, alkali, alkaline earth, ammonium-substituted radical, ammonium or transition metal;
where n is 1 to 10; and
where R is a Lewis base capable of donating a nonbonded pair of electrons, and wherein said composition is synthesized in a single vessel, at ambient pressure, without the addition of heat, whereunder a primary or secondary amide reaction occurs first followed by a radical reaction.
2. A method for making a modified iminodisuccinic acid having the ability to donate at least five nonbonded pairs of electrons without hindrance or bond strain, said method comprising:
mixing together an acid anhydride or lactone with monoethanolamine and allowing said mixture to react to form an amide;
adding to said amide a second polyfunctional amine, maleic anhydride or acid salt, and water and allowing said mixture to react in said water to form said modified iminodisuccinic acid; and
wherein said synthesis occurs in a single vessel, at ambient pressure, and without the addition of heat.
3. The method of claim 2 wherein said modified iminodisuccinic acid has one of the following formulas:
where X is H, alkali, alkaline earth, ammonium-substituted radical, ammonium or transition metal;
where n is 1 to 10; and
where R is a Lewis base capable of donating a nonbonded pair of electrons.
4. A method for making a modified iminodisuccinic acid comprised of 2,2-amino N,N-diethanolsuccinic amide having the ability to donate at least five nonbonded pairs of electrons without hindrance or bond strain, said method comprising:
mixing together maleic anhydride with ethanol amine;
and allowing said mixture to react to form an amide;
adding to said amide NH 3 , and water and allowing said mixture to react in said water to form said modified iminodisuccinic acid, and wherein said synthesis occurs in a single vessel, at ambient pressure, and without the addition of heat.
5. A method for making a modified iminodisuccinic acid having the ability to donate at least five nonbonded pairs of electrons without hindrance or bond strain, said method comprising:
mixing together an acid anhydride or lactone with monoethanolamine and allowing said mixture to react to form an amide;
adding to said amide an acid anhydride and alkali metal hydroxide and R—NH 2 where R is hydroxyl, and water and allowing said mixture to react in said water to form an amino acid alkali metal salt of the amide, which in said water will become a modified iminodisuccinic acid; and
wherein said synthesis occurs in a single vessel, at ambient pressure, and without the addition of heat.
6. The method of claim 2 wherein said anhydride or lactone is selected from the group consisting of: maleic anhydride; and said polyfunctional amines is selected from the group of difunctional amines consisting of organic diamines, hydroxylamines, polyamines, poly hydroxylamines, acid amines, and mixtures thereof.
7. The synthesis of compounds comprising at least one poly functional substitution on iminodisuccinic acid having the following formula and the ability to donate at least five nonbonded pairs of electrons without hindrance or bond strain:
where X is H, alkali, alkaline earth, ammonium-substituted radical, ammonium or transition metal; n is 1 to 10, and R is a Lewis base capable of donating a nonbonded pair of electrons, wherein said synthesis comprises the steps of:
(a) adding an acid anhydride or lactone to a monoethanolamine, and allowing same to react to form a N-polyfunctional acid common name amide; and
(b) adding water, alkali metal hydroxide, and a polyfunctional amine to said N— polyfunctional acid common name amide and allowing same to react to form an imino di N-polyfunctional acid common name amide; and
wherein said synthesis occurs in a single vessel, at ambient pressure, and without the addition of heat.
8. The synthesis of compounds comprising at least one poly functional substitution on iminodisuccinic acid having the following formula and the ability to donate at least five nonbonded pairs of electrons without hindrance or bond strain:
where X is H, alkali, alkaline earth, ammonium-substituted radical, ammonium or transition metal salts, n is 1 to 10, and R is a Lewis base capable of donating a nonbonded pair of electrons, wherein said synthesis comprises the steps of:
(a) adding an acid anhydride or lactone to monoethanolamine, and allowing same to react to form a N-polyfunctional acid common name amide; and
(b) adding to said N— polyfunctional acid common name amide, water, a polyfunctional amine, an acid anhydride or lactone, a alkali metal hydroxide, and allowing same to react to form said compounds, and
wherein said synthesis occurs in a single vessel, at ambient pressure, and without the addition of heat.
9. The synthesis of compounds comprising at least one poly functional substitution on iminodisuccinic acid having the following formula and the ability to donate at least five nonbonded pairs of electrons without hindrance or bond strain:
where X is H, alkali, alkaline earth, ammonium-substituted radical, ammonium or transition metal salts, where n is 1 to 10; where R is a Lewis base capable of donating a nonbonded pair of electrons, wherein said synthesis comprises the steps of: adding maleic anhydride or malic acid to alkali metal hydroxide+monoethanolamine+water, and allowing same to react to form the N,N-disuccinicamino(:functional group), and wherein said synthesis occurs in a single vessel, at ambient pressure, and without the addition of heat.
10. The synthesis of compounds comprising at least one poly functional substitution on iminodisuccinic acid having the following formula and the ability to donate at least five nonbonded pairs of electrons without hindrance or bond strain:
where X is H, alkali, alkaline earth, ammonium-substituted radical, ammonium or transition metal salts; where n is 1 to 10, where R is a Lewis base capable of donating a nonbonded pair of electrons; wherein said synthesis comprises the steps of:
(a) adding acid anhydride or lactone to monoethanolamine and allowing same to react to form a N-polyfunctional acid common name amide;
(b) adding to said N-polyfunctional acid common name amide, water+ammonia+alkali metal hydroxide, and allowing same to react to form an N,N-amino polyfunctional acid common name amide; and
wherein said synthesis occurs in a single vessel, at ambient pressure, and without the addition of heat.
11. The synthesis of compounds comprising at least one poly functional substitution on iminodisuccinic acid having the following formula and the ability to donate at least five nonbonded pairs of electrons without hindrance or bond strain:
where X may be H, alkali, alkaline earth, ammonium-substituted radical, ammonium or transition metal; where n may be 1 to 10; where R may be a lewis base capable of donating a nonbonded pair of electrons; wherein said synthesis comprises the steps of:
(a) adding an acid anhydride or lactone to a monoethanolamine and allowing same to react to form an N-polyfunctional acid common name amide;
(b) adding to said N— polyfunctional acid common name amide, water, ammonia+maleic anhydride or maleic acid (salt) and allowing same to react to form said compounds; and
wherein said synthesis occurs in a single vessel, at ambient pressure, and without the addition of heat.