Geopolymer compositions and methods
Geopolymeric compositions are presented that are useful for cementing subterranean wells. The compositions may contain an aluminosilicate source, a metal silicate, an alkali activator and a slurry density modifier that may contain uintaite, vitrified shale, petroleum coke or coal or combinations thereof. Methods for placing the geopolymeric compositions in subterranean wells are also presented.
1 . A method, comprising:
preparing a geopolymer precursor comprising an aluminosilicate source, a metal silicate, an alkali or alkaline earth activator, a carrier fluid including water, slurry density modifier particles, and a viscosifier, the viscosifier including diutan gum having a molecular weight greater than 1,000,000 g/mol, the viscosifier having a viscosifier concentration of between 0.14 g/L and 1.4 g/L, wherein the geopolymer precursor is pumpable and has a solids volume fraction of 35% to 75%;
placing the geopolymer precursor in a subterranean well; and
hardening the geopolymer precursor into a solid geopolymer.
2 . The method of claim 1 , wherein the slurry density modifier particles comprise hollow glass or ceramic microspheres, plastic particles, uintaite, vitrified shale, petroleum coke or coal, hematite, barite, ilmenite, silica, manganese tetroxide, or combinations thereof.
3 . The method of claim 1 , wherein the slurry density modifier particles have a particle size of 0.3 μm to 3350 μm.
4 . The method of claim 1 , wherein the geopolymer precursor further comprises a fluid-loss control agent comprising an alkali-swellable latex present in the geopolymer precursor at a latex concentration of 0.02 L/L to 0.3 L/L.
5 . The method of claim 1 , wherein the metal silicate comprises sodium metasilicate.
6 . The method of claim 5 , wherein the sodium metasilicate is present in the geopolymer precursor at a metal silicate concentration of 0.01 kg/L to 0.2 kg/L.
7 . The method of claim 1 , wherein the geopolymer precursor further comprises calcium sulfate hemihydrate.
8 . The method of claim 1 , wherein the geopolymer precursor further comprises an additive including at least one of glucoheptonic acid, a soluble salt of glucoheptonic acid, tartaric acid, a soluble salt of tartaric acid, citric acid, a soluble salt of citric acid, glycolic acid, a soluble salt of glycolic acid, lactic acid, a soluble salt of lactic acid, formic acid, a soluble salt of formic acid, acetic acid, a soluble salt of acetic acid, propionic acid, a soluble salt of propionic acid, oxalic acid, a soluble salt of oxalic acid, malonic acid, a soluble salt of malonic acid, succinic acid, a soluble salt of succinic acid, adipic acid, a soluble salt of adipic acid, malic acid, a soluble salt of malic acid, nicotinic acid, a soluble salt of nicotinic acid, benzoic acid, a soluble salt of benzoic acid, ethylenediamine tetraacetic acid, a soluble salt of ethylenediamine tetraacetic acid, phosphoric acid, or a soluble salt of phosphoric acid.
9 . The method of claim 1 , wherein the aluminosilicate source comprises granulated blast furnace slag, a fly ash, volcanic ash, calcined clay, aluminum-containing silica fume, natural aluminosilicate, synthetic aluminosilicate glass powder, zeolite, scoria, allophone, bentonite, red mud, pumice, or a combination thereof.
10 . The method of claim 1 , wherein the alkali or alkaline earth activator comprises alkali metal hydroxide, alkaline earth metal hydroxide, alkali salts, or combinations thereof.
11 . A geopolymer precursor, comprising:
an aluminosilicate source, a metal silicate, an alkali or alkaline earth activator, a carrier fluid including water, slurry density modifier particles, and a viscosifier, the viscosifier including diutan gum having a molecular weight of at least 1,000,000 g/mol, the viscosifier having a viscosifier concentration of between 0.14 g/L and 1.4 g/L, wherein the geopolymer precursor is pumpable and has a solids volume fraction of 35% to 75%.
12 . The geopolymer precursor of claim 11 , wherein the slurry density modifier particles comprise hollow glass or ceramic microspheres, plastic particles, uintaite, vitrified shale, petroleum coke or coal, hematite, barite, ilmenite, silica, manganese tetroxide, or combinations thereof.
13 . The geopolymer precursor of claim 11 , wherein the slurry density modifier particles have a particle size of 0.3 μm to 3350 μm.
14 . The geopolymer precursor of claim 11 , further comprising an additive including at least one of glucoheptonic acid, a soluble salt of glucoheptonic acid, tartaric acid, a soluble salt of tartaric acid, citric acid, a soluble salt of citric acid, glycolic acid, a soluble salt of glycolic acid, lactic acid, a soluble salt of lactic acid, formic acid, a soluble salt of formic acid, acetic acid, a soluble salt of acetic acid, propionic acid, a soluble salt of propionic acid, oxalic acid, a soluble salt of oxalic acid, malonic acid, a soluble salt of malonic acid, succinic acid, a soluble salt of succinic acid, adipic acid, a soluble salt of adipic acid, malic acid, a soluble salt of malic acid, nicotinic acid, a soluble salt of nicotinic acid, benzoic acid, a soluble salt of benzoic acid, ethylenediamine tetraacetic acid, a soluble salt of ethylenediamine tetraacetic acid, phosphoric acid, or a soluble salt of phosphoric acid.
15 . A method, comprising:
obtaining a pumpable geopolymer precursor comprising an aluminosilicate source, a metal silicate, an alkali or alkaline earth activator, a carrier fluid including water, slurry density modifier particles, and a viscosifier, the viscosifier including diutan gum having a molecular weight of at least 1,000,000 g/mol, the viscosifier having a viscosifier concentration of between 0.14 g/L and 1.4 g/L, wherein the pumpable geopolymer precursor has a solids volume fraction of 35% to 75%;
placing the pumpable geopolymer precursor in a subterranean well, and hardening the pumpable geopolymer precursor into a solid geopolymer.
16 . The method of claim 15 , wherein the slurry density modifier particles comprise hollow glass or ceramic microspheres, plastic particles, uintaite, vitrified shale, petroleum coke or coal, hematite, barite, ilmenite, silica, manganese tetroxide, or combinations thereof.
17 . The method of claim 16 , wherein the slurry density modifier particles have a particle size of 0.3 μm to 3350 μm.
18 . The method of claim 15 , wherein the pumpable geopolymer precursor further comprises an additive including at least one of glucoheptonic acid, a soluble salt of glucoheptonic acid, tartaric acid, a soluble salt of tartaric acid, citric acid, a soluble salt of citric acid, glycolic acid, a soluble salt of glycolic acid, lactic acid, a soluble salt of lactic acid, formic acid, a soluble salt of formic acid, acetic acid, a soluble salt of acetic acid, propionic acid, a soluble salt of propionic acid, oxalic acid, a soluble salt of oxalic acid, malonic acid, a soluble salt of malonic acid, succinic acid, a soluble salt of succinic acid, adipic acid, a soluble salt of adipic acid, malic acid, a soluble salt of malic acid, nicotinic acid, a soluble salt of nicotinic acid, benzoic acid, a soluble salt of benzoic acid, ethylenediamine tetraacetic acid, a soluble salt of ethylenediamine tetraacetic acid, phosphoric acid, or a soluble salt of phosphoric acid.
19 . The method of claim 15 , wherein the metal silicate comprises sodium metasilicate.
20 . The method of claim 15 , wherein the pumpable geopolymer precursor further comprises calcium sulfate hemihydrate.