Abstract: This disclosure provides a chelating composition having a pH of at least about 9 and comprising: water; and the tetrasodium salt of glutamic acid N,N-diacetic acid present in an amount of at least about 50 weight percent based on a total weight of the chelating composition as determined using an Fe-Total Sequestering Value, wherein the chelating composition has a viscosity of less than about 1350 mPa·s measured at about 5° C., or less than about 350 mPa·s measured at about 20° C., each using a Brookfield DV II plus viscometer with spindle S18 and a temperature controlled bath.

Abstract: A method includes combining monosodium glutamate and/or glutamic acid with formaldehyde to form a first combination; adding hydrogen cyanide to form a second combination comprising a monosodium salt of glutamic acid diacetonitrile, a cyclic GLMN, and a sodium salt of glutamic acid N-monoacetonitrile, maintaining a temperature of the second combination at less than about 16° C. and a pH of less than about 7; converting nitrile groups to carboxylate groups thereby forming a third combination comprising water and at least about 47 weight percent of the tetrasodium salt of GLDA, wherein a reaction yield is at least about 91%; providing a fourth combination comprising water and the tetrasodium salt of GLDA and having a pH of less than about 7; and combining the third and fourth combinations to form the chelating composition.

Abstract: A method of forming a chelating composition includes the steps of: providing a first mixture comprising water and a tetrasodium salt of glutamic acid N,N-diacetic acid and having a pH of greater than about 10; and acidifying the first mixture via ion exchange and/or bipolar membrane electrodialysis to reduce a pH of the chelating composition to a pH of at least about 9; wherein the chelating composition comprises the tetrasodium salt of glutamic acid N,N-diacetic acid in an amount of at least about 50 weight percent based on a total weight of the chelating composition as determined using an Fe-Total Sequestering Value; and wherein the chelating composition has a viscosity of less than about 1350 mPa·s measured at about 5° C., or less than about 350 mPa·s measured at about 20° C., each using a Brookfield DV II plus viscometer with spindle S18 and a temperature controlled bath.

Abstract: A two-step process to produce oil or gas from a subterranean formation wherein in a first step the subterranean formation is treated with an aqueous composition containing a chelating agent selected from the group of glutamic acid N,N-diacetic acid or a salt thereof (GLDA), aspartic acid N,N-diacetic acid or a salt thereof (ASDA), methylglycine N,N-diacetic acid or a salt thereof (MGDA), and N-hydroxyethyl ethylenediamine N,N?,N?-triacetic acid or a salt thereof (HEDTA) and wherein, in a next step, in the outlet streams from the subterranean formation the aqueous phase is separated from the non-aqueous phase.

Abstract: The present invention relates to a foam containing water, between 5 and 30 wt % on total weight of the foam of a chelating agent selected from the group of glutamic aid N,N-diacetic acid or a salt thereof (GLDA), aspartic acid N,N-diacetic acid or a salt thereof (ASDA), methylglycine N,N-diacetic acid or a salt thereof (MGDA), N-hydroxyethyl ethylenediamine-N,N?,N?-triacetic acid or a salt thereof (HEDTA), a foaming agent, and at least 25 vol % on total volume of the foam of a gas, and having a pH of between 2 and 5, to a viscosified composition containing water, between 5 and 30 wt % on total volume of the composition of a chelating agent selected from the group of glutamic aid N,N-diacetic acid or a salt thereof (GLDA), aspartic acid N,N-diacetic acid or a salt thereof (ASDA), methylglycine N,N-diacetic acid or a salt thereof (MGDA), N-hydroxyethyl ethylenediamine-N,N?,N?-triacetic acid or a salt thereof (HEDTA), and at least 0.

Abstract: The present invention relates to a process for treating a subterranean formation wherein a fluid containing an ammonium salt of glutamic acid N,N-diacetic acid (GLDA) or methylglycine N,N-diacetic acid (MGDA) is introduced into the formation.

Abstract: The present invention relates to a chelating agent precursor that contains glutamic acid N,N-diacetic acid (GLDA) and/or methylglycine N,N-diacetic acid (MGDA) wherein at least one of the carboxylic acid groups is present as a carboxylic acid derivative selected from the group of amides, anhydrides, and esters, combinations thereof, and salts thereof, provided that it is not the triethyl ester of GLDA, the triethyl mono-t-butyl ester of GLDA, the tri-t-butyl ester of GLDA, the monobenzyl tri-t-butyl ester of GLDA, any ester or amide that contains azacycloalkane groups, any amide that contains biotin groups, any amide that contains minoethylcarbamoyl based amide groups, (S)-diethyl 2,2?-(1-benzyloxy)-1,5-dioxo-5-(prop-2-ynylamino)pentan-2-ylazanediyl-diacetate, diethyl 2,2?-(5-(3-azidopropylamino)-1-(benzyloxy)-1,5-dioxo-pentan-2-ylazanediyl-diacetate, the trimethyl ester of MGDA, the monomethyl ester dimethylamide of MGDA, the dibenzyl ester of MGDA, the dibenzyl mono t-butyl ester of MGDA, the di t-butyl est

Abstract: The present invention relates to a two-step process to produce oil or gas from a subterranean formation wherein in a first step the subterranean formation is treated with an aqueous composition containing a chelating agent selected from the group of glutamic acid N,N-di-acetic acid or a salt thereof (GLDA), aspartic acid N,N-diacetic acid or a salt thereof (ASDA), methylglycine N,N-diacetic acid or a salt thereof (MGDA), and N-hydroxyethyl ethylenediamine N,N?,N?-triacetic acid or a salt thereof (HEDTA) and wherein, in a next step, in the outlet streams from the subterranean formation the aqueous phase is separated from the non-aqueous phase.

Abstract: The present invention relates to a foam containing water, between 5 and 30 wt % on total weight of the foam of a chelating agent selected from the group of glutamic aid N,N-diacetic acid or a salt thereof (GLDA), aspartic acid N,N-diacetic acid or a salt thereof (ASDA), methylglycine N,N-diacetic acid or a salt thereof (MGDA), N-hydroxyethyl ethylenediamine-N,N?,N?-triacetic acid or a salt thereof (HEDTA), a foaming agent, and at least 25 vol % on total volume of the foam of a gas, and having a pH of between 2 and 5, to a viscosified composition containing water, between 5 and 30 wt % on total volume of the composition of a chelating agent selected from the group of glutamic aid N,N-diacetic acid or a salt thereof (GLDA), aspartic acid N,N-diacetic acid or a salt thereof (ASDA), methylglycine N,N-diacetic acid or a salt thereof (MGDA), N-hydroxyethyl ethylenediamine-N,N?,N?-triacetic acid or a salt thereof (HEDTA), and at least 0.

Abstract: The present invention relates to a chelating agent precursor that contains glutamic acid N,N-diacetic acid (GLDA) and/or methylglycine N,N-diacetic acid (MGDA) wherein at least one of the carboxylic acid groups is present as a carboxylic acid derivative selected from the group of amides, anhydrides, and esters, combinations thereof, and salts thereof, provided that it is not the triethyl ester of GLDA, the triethyl mono-t-butyl ester of GLDA, the tri-t-butyl ester of GLDA, the monobenzyl tri-t-butyl ester of GLDA, any ester or amide that contains azacycloalkane groups, any amide that contains biotin groups, any amide that contains minoethylcarbamoyl based amide groups, (S)-diethyl 2,2?-(1-benzyloxy)-1,5-dioxo-5-(prop-2-ynylamino)pentan-2-ylazanediyl-diacetate, diethyl 2,2?-(5-(3-azidopropylamino)-1-(benzyloxy)-1,5-dioxo-pentan-2-ylazanediyl-diacetate, the trimethyl ester of MGDA, the monomethyl ester dimethylamide of MGDA, the dibenzyl ester of MGDA, the dibenzyl mono t-butyl ester of MGDA, the di t-butyl est

Abstract: The present invention relates to a process for treating a subterranean formation wherein a fluid containing an ammonium salt of glutamic acid N, N-diacetic acid (GLDA) or methylglycine N, N-diacetic acid (MGDA) is introduced into the formation.