Akzo Nobel Chemicals International B.v.

Nouryon Chemicals International B.v.

Edwin Rudolf Antony Bang

Cornelia Adriana De Wolf

Hisham Nasr-El-Din

James N LePage

Boen Ho O

Adrianus Maria Reichwein

Axel Carstens

Mohamed Ahmed Nasr-El-Din Mahmoud

Johanna Hendrika Bemelaar

Conrardus Hubertus Joseph Theeuwen

Estevao De Oliveira Barra

Jozef Johannes Maria Baltussen

Theodor Johannes Stanitzek

Guanqun Wang

Josef Johannes Maria Baltussen

Marcel Cornelis Paulus Van Eijk

Noble Thekkemelathethil George

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&#x2032;-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.

Process to produce oil or gas from a subterranean formation using a chelating agent

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&#x2032;-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&#x2032;,N&#x2032;-triacetic acid or a salt thereof (HEDTA), and at least 0.01 wt % on total weight of the composition of a viscosifying agent, and having a pH of between 2 and 5, and to a process for treating a subterranean formation comprising introducing the above foam or viscosified composition into the formation.

Foam or viscosified composition containing a chelating agent

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. The invention also covers a fluid containing an ammonium salt of GLDA and/or MGDA and at least one component from the group of seawater, mutual solvents, anti-sludge agents, (water-wetting or emulsifying) surfactants, foaming agents, corrosion inhibitors corrosion inhibitor intensifiers, viscosifiers, wetting agents, diverting agents, oxygen scavengers, carrier fluids, fluid loss additives, friction reducers, stabilizers, rheology modifiers, gelling agents, scale inhibitors, breakers, salts, brines, pH control additives, bactericides/biocides, particulates, crosslinkers, salt substitutes (such as tetramethyl ammonium chloride), relative permeability modifiers, sulfide scavengers, fibres, nanoparticles, and consolidating agents, and covers an ammonium salt of the formula M(NH)H-GLDA or the formula M(NH)H-MGDA, wherein M is an alkalimetal cation, x is at least 0.1, y is at least 0.1 and x+y+z=4 for GLDA and x+y+z=3 for MGDA.

Ammonium salts of chelating agents and their use in oil and gas field applications

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&#x2032;-(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 ester of MGDA, the di-t-butyl-monobenzyl ester of MGDA, N,N-bis(benzyloxycarbonylmethyl)-N&#x2032;-methoxycarbonyl-methyl-alanine amide, or N,N-bis(tert-butoxycarbonyl)-N&#x2032;-methoxycarbonylmethyl-alanine amide, and esters of GLDA immobilized on a gel, and that the amide is not the amide of ammonia, to a fluid containing the above chelating precursor and a liquid, and to the use of a chelating agent precursor of MGDA and GLDA and fluids containing them in an application wherein delayed acidity or the chelating capacity is useful, such as in descaling, bleaching, cleaning, and treating oil and/or gas-containing subterranean formations.

Chelating agent precursors, fluids containing them, and their use

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Arnhem, Netherlands

Edwin Rudolf Antony Bang