Abstract: A demulsifying agent may comprise the structure R1 may be a hydrocarbyl group or heterohydrocarbyl group comprising from 1 to 20 carbon atoms. m may be from 2 to 10, n may be from 5 to 20, and p may be from 2 to 15. R2 may comprise a residue of propylene oxide. R3 may comprise a residue of glycidol. Embodiments of the present disclosure may further comprise methods of making the demulsifying agent and methods of using the demulsifying agent to demulsify a hydrocarbon emulsion.

Abstract: An acid mixture includes hydrochloric acid, a monoamine corrosion inhibitor, and at least one of a diamine corrosion inhibitor and an acid additive. A method for inhibiting corrosion in an acid treatment operation includes introducing an acid mixture comprising hydrochloric acid and a monoamine corrosion inhibitor into at least one of a subterranean formation and subterranean wellbore. The method also includes maintaining the amount of the monoamine corrosion inhibitor in the acid mixture in the subterranean formation and/or the subterranean wellbore in a range of 10 ppm to 400 ppm for the duration of the acid treatment operation. The corrosion rate of steel parts of an acidic fluid circulation system in the acid mixture may be within an acceptable corrosion rate in a temperature range of 20° C. to 135° C.

Abstract: An acid mixture includes hydrochloric acid, a monoamine corrosion inhibitor, and at least one of a diamine corrosion inhibitor and an acid additive. A method for inhibiting corrosion in an acid treatment operation includes introducing an acid mixture comprising hydrochloric acid and a monoamine corrosion inhibitor into at least one of a subterranean formation and subterranean wellbore. The method also includes maintaining the amount of the monoamine corrosion inhibitor in the acid mixture in the subterranean formation and/or the subterranean wellbore in a range of 10 ppm to 400 ppm for the duration of the acid treatment operation. The corrosion rate of steel parts of an acidic fluid circulation system in the acid mixture may be within an acceptable corrosion rate in a temperature range of 20° C. to 135° C.

Abstract: Methods for preparing alkenylphenone corrosion inhibiting compositions may include providing an arylacetone and reacting the arylacetone with formaldehyde in the presence of a strong base catalyst. Corrosion inhibiting compositions may include an alkenylphenone, which may be prepared by a method including providing an arylacetone and reacting the arylacetone with formaldehyde in the presence of a strong base catalyst. Methods of inhibiting corrosion of a steel surface of an oilfield equipment component may include contacting the steel surface with an aqueous solution comprising a corrosion inhibitor. The corrosion inhibitor may include a composition containing an alkenylphenone prepared by reacting an arylacetone with formaldehyde in the presence of a strong base catalyst.

Abstract: Copolymers having General Formula (I): in which R1 and R3 are chosen from divalent C4-C7 aliphatic groups and divalent C4-C7 heteroaliphatic groups, optionally substituted with one or more C1-C6 aliphatic groups, heteroatoms independently chosen from O, N, and S, or combinations thereof, where the divalent C4-C7 heteroaliphatic groups of R1 and R3 include one or two heteroatoms independently chosen from O, N, and S, and the maximum number of heteroatoms in R1 or R3 is two, R2 is chosen from Q1 and Q2, x is a molar fraction range chosen from 0.1 to 0.9, y is a molar fraction range chosen from 0.1 to 0.9, and z is a molar fraction range chosen from 0 to 0.8, where the summation of x, y, and z equals 1. Methods for inhibiting formation of clathrate hydrates include contacting a fluid with at least one copolymer of General Formula (I).

Abstract: Copolymers having General Formula (I): in which R1 is chosen from divalent C4-C7 aliphatic groups and divalent C4-C7 heteroaliphatic groups, optionally substituted with one or more C1-C6 aliphatic groups, heteroatoms independently chosen from O, N, and S, or combinations thereof, where: the divalent C4-C7 heteroaliphatic groups include one or two heteroatoms independently chosen from O, N, and S, and the maximum number of heteroatoms in R1 is two; x is a molar fraction range chosen from 0.05 to 0.95; and y is a molar fraction range chosen from 0.05 to 0.95, where the summation of x and y equals 1. Methods for inhibiting formation of clathrate hydrates in a fluid capable of forming the clathrate hydrates. The methods include contacting the fluid with at least one copolymer of General Formula (I) under conditions suitable for forming the clathrate hydrates.

Abstract: Copolymers having General Formula (I): in which R1 is chosen from divalent C4-C7 aliphatic groups and divalent C4-C7 heteroaliphatic groups, optionally substituted with one or more C1-C6 aliphatic groups, heteroatoms independently chosen from O, N, and S, or combinations thereof, where: the divalent C4-C7 heteroaliphatic groups include one or two heteroatoms independently chosen from O, N, and S, and the maximum number of heteroatoms in R1 is two; x is a molar fraction range chosen from 0.05 to 0.95; and y is a molar fraction range chosen from 0.05 to 0.95, where the summation of x and y equals 1. Methods for inhibiting formation of clathrate hydrates in a fluid capable of forming the clathrate hydrates. The methods include contacting the fluid with at least one copolymer of General Formula (I) under conditions suitable for forming the clathrate hydrates.

Abstract: Copolymers having General Formula (I): in which R1 and R3 are chosen from divalent C4-C7 aliphatic groups and divalent C4-C7 heteroaliphatic groups, optionally substituted with one or more C1-C6 aliphatic groups, heteroatoms independently chosen from O, N, and S, or combination thereof, where the divalent C4-C7 heteroaliphatic groups of R1 and R3 include one or two heteroatoms independently chosen from O, N, and S, and the maximum number of heteroatoms in R1 or R3 is two, R2 is chosen from Q1 and Q2, x is a molar fraction range chosen from 0.1 to 0.9, y is a molar fraction range chosen from 0.1 to 0.9, and z is a molar fraction range chosen from 0 to 0.8, where the summation of x, y, and z equals 1. Methods for inhibiting formation of clathrate hydrates include contacting a fluid with at least one copolymer of General Formula (I).

Abstract: Copolymers having General Formula (I): in which R1 and R3 are chosen from divalent C4-C7 aliphatic groups and divalent C4-C7 heteroaliphatic groups, optionally substituted with one or more C1-C6 aliphatic groups, heteroatoms independently chosen from O, N, and S, or combination thereof, where the divalent C4-C7 heteroaliphatic groups of R1 and R3 include one or two heteroatoms independently chosen from O, N, and S, and the maximum number of heteroatoms in R1 or R3 is two, R2 is chosen from Q1 and Q2, x is a molar fraction range chosen from 0.1 to 0.9, y is a molar fraction range chosen from 0.1 to 0.9, and z is a molar fraction range chosen from 0 to 0.8, where the summation of x, y, and z equals 1. Methods for inhibiting formation of clathrate hydrates include contacting a fluid with at least one copolymer of General Formula (I).

Abstract: Copolymers having General Formula (I): in which R1, R2, and R3 are chosen from C1 to C30 aliphatic groups, R4 is chosen from divalent C4 to C7 linear aliphatic groups and divalent C4 to C7 linear heteroaliphatic groups, optionally substituted with one or more C1-C6 linear aliphatic groups, C1-C6 branched aliphatic groups, or combination thereof, R5, R6, and R7 are each independently chosen from methyl or hydrogen, x is chosen from 0 to 0.8, y is chosen from 0 to 0.8, when y is 0, x is greater than 0, and when x is 0, y is greater than 0, and z is chosen from 0.1 to 0.9. The summation of x, y, and z equals 1. Methods for inhibiting formation of clathrate hydrates in a fluid capable of forming the clathrate hydrates, including contacting the fluid with at least one copolymer of General Formula (I).

Abstract: Cross-linked tetrapolymers made up of different diallyl zwitterionic diallyl quaternary ammonium salt monomers, with one of them functioning as a cross-linking monomer. The cross-linked terpolymers include a repeating unit with multiple ligand centers that different metal ions can bind to. The cross-linked tetrapolymers are cationic, zwitterionic and anionic, and can be in either an acidic form or a basic form. A method of removing metal ions from an aqueous solution with these cross-linked tetrapolymers is also described.

Abstract: Cross-linked tetrapolymers made up of different diallyl zwitterionic diallyl quaternary ammonium salt monomers, with one of them functioning as a cross-linking monomer. The cross-linked terpolymers include a repeating unit with multiple ligand centers that different metal ions can bind to. The cross-linked tetrapolymers are cationic, zwitterionic and anionic, and can be in either an acidic form or a basic form. A method of removing metal ions from an aqueous solution with these cross-linked tetrapolymers is also described.

Abstract: An aminoalkyl imidazolines of the formula: having p-octyloxy-, p-dodecyloxy-, or p-octadecyloxy-phenyl pendants as hydrophobes, for use to mitigate mild steel corrosion. An electron-rich aromatic ring, in conjugation with an amidine motif, imparts increasing corrosion inhibition efficiencies with an increasing hydrophobe chain length. X-ray photoelectron spectroscopy confirms the formation of an aminoalkyl imidazoline film on a metal surface prior to reaching a critical molar concentration.

Abstract: Cross-linked cyclopolymeric resins from N,N-diallyl quaternary ammonium monomers and tetrallylpiperazinium cross-linking monomer or salts, solvates, tautomers or stereoisomers as adsorbent materials for the removal of heavy metals from aqueous solution. A process for producing the cross-linked cyclopolymeric resins by Butler cyclocopolymerization of the monomers with a free radical initiator. The cross linked cyclopolymeric resins are polyzwitterionic or polyzwitterionic and dianionic and feature repeating units with multiple chelating centers that heavy metal ions can bind to. In addition, a method for removing heavy metals from aqueous solution via contacting and treatment with the cross-linked cyclopolymeric resins.

Abstract: An aminoalkyl imidazolines of the formula: having p-octyloxy-, p-dodecyloxy-, or p-octadecyloxy-phenyl pendants as hydrophobes, for use to mitigate mild steel corrosion. An electron-rich -aromatic ring, in conjugation with an amidine motif, imparts increasing corrosion inhibition efficiencies with an increasing hydrophobe chain length. X-ray photoelectron spectroscopy confirms the formation of an aminoalkyl imidazoline film on a metal surface prior to reaching a critical molar concentration.

Abstract: An aminoalkyl imidazolines of the formula: having p-octyloxy-, p-dodecyloxy-, or p-octadecyloxy-phenyl pendants as hydrophobes, for use to mitigate mild steel corrosion. An electron-rich aromatic ring, in conjugation with an amidine motif, imparts increasing corrosion inhibition efficiencies with an increasing hydrophobe chain length. X-ray photoelectron spectroscopy confirms the formation of an aminoalkyl imidazoline film on a metal surface prior to reaching a critical molar concentration.

Abstract: Copolymers having General Formula (I): in which R1 and R3 are chosen from divalent C4-C7 aliphatic groups and divalent C4-C7 heteroaliphatic groups, optionally substituted with one or more C1-C6 aliphatic groups, heteroatoms independently chosen from O, N, and S, or combination thereof, where the divalent C4-C7 heteroaliphatic groups of R1 and R3 include one or two heteroatoms independently chosen from O, N, and S, and the maximum number of heteroatoms in R1 or R3 is two, R2 is chosen from Q1 and Q2, x is a molar fraction range chosen from 0.1 to 0.9, y is a molar fraction range chosen from 0.1 to 0.9, and z is a molar fraction range chosen from 0 to 0.8, where the summation of x, y, and z equals 1. Methods for inhibiting formation of clathrate hydrates include contacting a fluid with at least one copolymer of General Formula (I).

Abstract: Methods for synthesizing acryloyl-based copolymers. The methods include providing a free radical initiator with a solution including monomeric repeating units, a chain transfer agent, and an organic solvent to form a reaction mixture, in which the monomeric repeating units include a first monomeric repeating unit having formula (1a), a second monomeric repeating unit having formula (1b) or (1d), and optionally a third monomeric repeating unit having formula (1c): in which the organic solvent is chosen from monoethylene glycol, ethanol, toluene, or combination thereof; and (B) initiating a polymerization reaction in the reaction mixture to polymerize the monomeric repeating units, thereby synthesizing the acryloyl-based copolymer. Methods for inhibiting formation of clathrate hydrates include contacting a fluid with the acryloyl-based copolymer synthesized in the reaction mixture.

Abstract: Copolymers having General Formula (I): in which R1 is chosen from divalent C4-C7 aliphatic groups and divalent C4-C7 heteroaliphatic groups, optionally substituted with one or more C1-C6 aliphatic groups, heteroatoms independently chosen from O, N, and S, or combinations thereof, where: the divalent C4-C7 heteroaliphatic groups include one or two heteroatoms independently chosen from O, N, and S, and the maximum number of heteroatoms in R1 is two; x is a molar fraction range chosen from 0.05 to 0.95; and y is a molar fraction range chosen from 0.05 to 0.95, where the summation of x and y equals 1. Methods for inhibiting formation of clathrate hydrates in a fluid capable of forming the clathrate hydrates. The methods include contacting the fluid with at least one copolymer of General Formula (I) under conditions suitable for forming the clathrate hydrates.

Abstract: Copolymers having General Formula (I): in which R1, R2, and R3 are chosen from C1 to C30 aliphatic groups, R4 is chosen from divalent C4 to C7 linear aliphatic groups and divalent C4 to C7 linear heteroaliphatic groups, optionally substituted with one or more C1-C6 linear aliphatic groups, C1-C6 branched aliphatic groups, or combination thereof, R5, R6, and R7 are each independently chosen from methyl or hydrogen, x is chosen from 0 to 0.8, y is chosen from 0 to 0.8, when y is 0, x is greater than 0, and when x is 0, y is greater than 0, and z is chosen from 0.1 to 0.9. The summation of x, y, and z equals 1. Methods for inhibiting formation of clathrate hydrates in a fluid capable of forming the clathrate hydrates, including contacting the fluid with at least one copolymer of General Formula (I).