OA18403A - Modified amines useful as scale inhibitors in wet process phosphoric acid production. - Google Patents

Abstract

Processes for inhibiting scale produced during wet process phosphoric acid production by adding a scale inhibiting amount of a reagent having at least one amine portion including at least one primary amine, and at least one hydrocarbyl portion having an insolubilizing group attached thereto to at least one stage of a wet process phosphoric acid production process are provided herein.

Description

MODIFIED AMINES USEFUL AS SCALE INHIBITORS IN WET PROCESS PHOSPHORIC ACID PRODUCTION

BACKGROUND OF THE INVENTION [0001] Field ofthe Invention.

[0002] The présent invention generally relates to the inhibition of scale in industrial process streams. More particularly, the présent invention relates to inhibiting scale (e.g., reducing or preventing the nucléation and/or growth of minerai scale solids) produced during operation of wet process phosphoric acid (WPA) production streams by addition of chemical reagents.

[0003] Description of the Related Art.

[0004] About 90 % of the world’s phosphoric acid is produced according to the wet process, which is conventionally prepared by acidulating phosphate rock (which contains calcium phosphate) with sulfuric acid to yield a crude wet-process phosphoric acid (WPA) and insoluble calcium sulfate (gypsum).

[0005] The manufacture of phosphoric acid is well known and is the subject of numerous text books. An overall view of the manufacture of phosphates and phosphoric acid is treated by Becker in Phosphates and Phosphoric Acids, Marcel Dekker, Inc. 1989; and by Slack in Phosphoric Acid, Part 1 and Part 2, Marcel Dekker, Inc. 1968. In the process, calcium phosphate rocks are cleaned in the wash plant and ground in the Bail mill before being fed into a sériés of reactors for digestion with sulfuric acid along with recycled phosphoric acid from the process. After digestion, the reaction slurry is filtered to separate phosphoric acid from gypsum.

[0006] The filtered, crude WPA is then sent to clarifiers and evaporators for further purification and concentration. The purified phosphoric acid is either sent out as Merchant Grade Acid (MGA) or continued to make 69% P2O5 Super Phosphoric Acid (SPA), where it can be converted to many end products ranging from a chemical reagent, rust inhibitor, food additive, dental and orthopaedic etchant, electrolyte, flux, dispersing agent, industrial etchant, fertilizer feedstock, and component of home cleaning products. For example, crude phosphoric acid is concentrated to 54% (P2O5) before sent for Monoammonium Phosphate (MAP), Diammonium Phosphate (DAP), or ammonium phosphate-sulfate (APS) production.

[0007] As noted in U.S. Patent No. 5,080,801 to Molter et al. (1992), which teaches various mixed polymère for preventing scale in minerai process waters from a variety of processes, due to the highly acidic environment which is inhérent to phosphoric acid production (pH 1>), these plants expérience sealing problems unique to this industry. Accordingly, solutions that may be useful for reducing or preventing scale in some industrial processes frequently do not prove suitable for use in the phosphoric acid production stream. U.S. Patent No. 5,456,767 to Shah et al. (1995) describes a similar sentiment with regard to the use of corrosion inhibitore in refînery overheads (noting that because the refînery overhead environment is extremely acidic, the corrosion inhibitore generally used in other oil field environments are not generally suitable for use with the refînery overheads).

[0008] Crude WPA contains significant amounts of dissolved impurities including carbonaceous matter, silica, and many metallic contaminants. Due to the supereaturated nature of the acid and the impurities in the phosphate ores, the concentration steps with respect to P2O5 render several side reactions, causing scale formation and/or déposition in 25 and/or on the equipment in contact with the WPA at different stages of the phosphoric acid production process.

[0009] For example, scale from the phosphoric acid production process forms on filter cloth and pipes, heat exchangers, evaporators, concentratore, valves, and pipes during the répétitive flashing/cooling/concentrating process ofthe phosphoric acid production 30 process. Twelve to fïfteen different types of sealing species can usually be found throughout the phosphoric acid production process and they pose significant challenges for the industry. Moreover, different phosphoric acid production plants expérience different types of scale. Even within one plant, the type of scale can differ greatly

between steps in the process or even between phosphate ore composition. Plants normally hâve to shut down production every few weeks to physically remove the scale using high-pressure water and/or mechanical means. Valuable operating time is lost during this descaling phase resulting in reduced process capacity and ultimately reduced profits.

[00101 While some proposed solutions hâve focused on physical means to remove scale formation and/or déposition on equipment surfaces in the phosphoric acid production process, most hâve tried to solve the problem by developing a chemical-based reagent. This is the preferred approach because it requires a limited amount of capital investment 10 and does not alter the existing process in the phosphoric acid plants. It also does not require a large amount of reagent and is therefore considered both environmental, and to hâve a minimal downstream impact. However, due to the complexity of the scale forming issues (e.g., processes of nucléation, crystal growth, and déposition), it is a great challenge to develop reagents useful for inhibition of scale formation and/or déposition on 15 surfaces in contact with digested phosphate rock.

[0011] Numerous patents hâve attempted to address the sealing problem in the phosphoric acid production process. Some of these patents include, for example, U.S. Patent Nos. 3,972,981,4,221,769, and 5,120,519; Chinese Patent Nos. 1762857, and 1724965; and GB Patent Nos. 1,406,884, and 1,433,123.

[0012] Sealing in the WPA production process has also been addressed by U.S. Published

Application Nos. 2011/0076218,2011/0076219, 2012/0244058, which work has resulted in PHOSFLOW® Scale Inhibitor (commercially available from Cytec Industries Inc., Woodland Park, NJ), as weil as addressed by U.S. Provisional Application No. 61/938,235.

[0013] The économie impact for the scale-related issues is substantial, and the industry is in need of a more efficient scale prévention technology than the existing physical means of post-scale formation removal. Furthermore, while various chemical-based reagents may hâve some merits and applicability in scale inhibition for wet process phosphoric acid production, they are not currently in widespread use. Accordingly, the compositions and methods presently available for inhibiting the nucléation and/or growth of minerai scale solids in the phosphoric acid production process require further improvement.

[0014] Processes that employ reagent compositions and formulations that effectively inhibit the nucléation and/or growth of minerai scale solids on equipment surfaces in

contact with scale-forming ions released from digested phosphate rock, thereby enabling the phosphoric acid production plant to run longer without shutting down to physically remove scale, would be a useful advance in the art and could find rapid acceptance in the industry.

SüMMARY OF THE INVENTION [0015] The foregoing and additional objects are attained in accordance with the principles of the invention wherein the inventors detail the surprising discovery that small molécule amines as described and characterized herein are useful for preparing reagents effective 10 for inhibiting scale produced during the wet process phosphoric acid production process.

[0016] Accordingly, in one aspect the présent invention provides processes for inhibiting scale produced during wet process phosphoric acid production by adding a scale inhibiting amount of a reagent to at least one stage of a wet process phosphoric acid production process, wherein the reagent includes a reaction product formed from reacting 15 Reactant A and Reactant B, and having an average molecular weight < 1,000 Da and at least one primary amine. Reactant A includes a polyamine or polyether amine, and Reactant B includes a hydrocarbyl radical having 1 to 22 carbon atoms including an amine reactive group, wherein one or more of the carbon atoms is optionally replaced by a hetero atom, and/or optionally substituted at one or more substitutable position with a 20 moiety as further described herein. The reagent comprising the reaction product is thereby useful in reducing or preventing scale in the wet process phosphoric acid production process. The reaction product can be further characterized as being substantially oil-free and being less soluble in an aqueous solution of the wet process phosphoric acid production process than Reactant A alone, by virtue of Reactant A being 25 modified by/reacted with Reactant B.

[0017] In another aspect, the invention can be characterized as a process for inhibiting scale produced during wet process phosphoric acid production by adding a scale inhibiting amount of a reagent to at least one stage of the wet process phosphoric acid production stream, wherein the reagent includes a compound having at least one amine 30 portion having at least one primary amine, and at least one hydrocarbyl portion that is part of the backbone of the compound or a pendant group attached to the backbone and/or amine portion and which includes a sufficient number of carbon atoms, or which is multiply présent in sufficient number so as to reduce the solubility of the compound in an

aqueous solution ofthe wet process phosphoric acid production stream. The compound can be further characterized as having an average molecular weight of < 1,000 Daltons, and the reagent is further characterized as being substantially oil-free.

[0018] The effective or threshold amount of reagent useful for achieving scale inhibition in the wet process phosphoric acid production process is generally from 0.5 g per ton to 5000 g per ton of phosphoric acid.

[0019] These and other objects, features and advantages of this invention will become apparent from the following detailed description ofthe various embodiments ofthe invention taken in conjunction with the accompanying Examples.

Detailed Description of Certain Embodiments of the Invention [0020] The formation of scale in wet process phosphoric acid production results from the release of scale-forming ions from crushed and digested phosphate rock. Scale déposition on equipment surfaces in contact with the digested phosphate rock is problematic and eventually nécessitâtes shut down of the production process for cleaning and/or descaling the equipment. Controlling scale via a réduction of scale formation and/or déposition on surfaces in contact with scale-forming ions released from digested phosphate rock translates to greater time between shut downs, which in tum provides greater efïïciency and production capacity.

[0021] As summarized above, the présent invention is based at least in part on the discovery that small molécule amines (i.e., amine compounds having an average molecular weight < 1,000 Daltons) having a primary amine functionality are useful as scale inhibitors in the wet process phosphoric acid production process when the small molécule amine is modified at one or more substitutable position with one or more hydrocarbyl radical to effectively reduce the amine compound’s solubility in an aqueous solution as compared to its native (i.e., unsubstituted) form. The compound resulting from reacting the small molécule amine with the hydrocarbyl radical is generally < 1,000 Daltons and maintains the functionality of at least one primary amine.

[0022] The successful application of such compounds in the delayed nucléation and/or retardation (i.e., inhibition) of various scale species formed in the phosphoric acid process stream, particularly in dihydrate (“DH”) or hemihydrate (“HH”) plants, was surprising given that the native small molécule amine itself performed poorly as an anti-scalant, and

because it was also believed by the inventors at the time of invention that to be a successful reagent a threshold amount or ratio of primary amines was required. [0023] As will be more fùlly described below, while the reagents useful as anti-scalants vary in composition, they are similar in that the compounds comprising the reagents ail hâve an average molecular weight of < 1,000 Daltons (Da), they contain at least one primary amine, and their solubility in an aqueous solution is lower than that of the unmodified compound so as to be usefùl as a scale inhibitor. Additionally, while the reagents described herein may include a single compound or mixture of compounds described herein, ail the reagents are substantially oil-free.

[0024] As employed throughout the dîsclosure of the invention, the following terms are provided to assist the reader. Unless otherwise defined, ail terms of art, notations and other scientific or industrial terms or terminology used herein are intended to hâve the meanings commonly understood by those of skill in the chemical arts. In some cases, terms with commonly understood meanings are defined herein for clarity and/or for ready reference, and the inclusion of such définitions herein should not necessarily be construed to represent a substantial différence over the définition of the term as generally understood in the art unless otherwise indicated. As used herein and in the appended claims, the singular forms include plural referents unless the context clearly dictâtes otherwise.

[0025] Throughout this spécification, the terms and substituents retain their définitions.

A comprehensive list of chemical abbreviations commonly utilized in the field appears in the first issue of each volume of the Journal of Organic Chemistrv. The list, which is typically presented in a table entitled “Standard List of Abbreviations,” is incorporated herein by reference.

[0026] The terms “hydrocarbon” or hydrocarbyl are broad terms that are used herein in their ordinary sense as understood by those skilled in the art, and include aliphatic, alicyclic, and aromatic organic compounds, fragments, or radicals having an all-carbon backbone and consisting of carbon and hydrogen atoms. Such moieties can be saturated, or be mono-, or poly-unsaturated. Examples of these moieties include alkyl, cycloalkyl, alkenyl, alkynyl, and aryl ranging from 1 to 36 carbon atoms, wherein moieties having from 1 to 22 carbon atoms are preferred. Such moieties can be substituted at one or more substitutable positions by a substituent defined herein. Spécifie examples of hydrocarbyl include any individual value or combination of values selected from Ci through C36.

[0027] As used herein, the term alkyl means a straight or branched chain hydrocarbon generally containing from 1 to 36 carbon atoms. Alkyl groups having from 1 to 22 carbon atoms are preferred, with alkyl groups having 1 to 18 carbon atoms being most preferred. “Lower alkyl” refers to alkyl groups of from 1 to 6 carbon atoms. While particular examples include any individual value or combination of values selected from Ci through C36, preferred représentative examples of alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, n-heptyl, n-octyl, tert-octyl, n-nonyl, n-decyl, etc. Examples of lower alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, s-and t10 butyl and the like.

[0028] The term alkenyl means a straight or branched chain hydrocarbon radical containing from 2 to 36 carbons, with 2-22 carbon atoms being preferred, and containing at least one carbon-carbon double bond formed by the removal of two hydrogens. Représentative examples of alkenyl include, but are not limited to, ethenyl, propylenyl, 15 buten-l-yl, isobutenyl, penten-l-yl, 2-methylbuten-l-yl, 3-methylbuten-l-yl, hexen-l-yl, hepten-l-yl, and octen-l-yl, and the like.

[0029] “Aryl” (carbocyclic aryl) refers to a 5- or 6-membered aromatic carbocycle ring system; a bicyclic 9- or 10-membered aromatic ring system; or a tricyclic 13- or 14membered aromatic ring system. The aromatic 6- to 14-membered carbocyclic rings include, for example, phenyl groups, benzene, naphthalene, indane, tetralin, and fluorene. [0030] “Halides” refer to ionic compounds containing a halogen (e.g., fluorine, chlorine, bromine or iodine).

[0031] The term “substituted” is used herein in its ordinary sense as understood by those skilled in the art and, thus, includes replacement of one or more hydrogen or other suîtable atom (i.e., substitutable position) in a compound, structure, or fragment of said compound or structure, with one or more organic moiety or fiinctionality that may be the same or different. Such moiety that replaces the hydrogen or other suîtable atom is referred to herein as a “substituent”. As one of skill in the art would appreciate, these terms can also refer to, in certain contexts, the replacement of one or more carbon atoms in a hydrocarbon chain by a heteroatom (e.g., N, S, or O). In either case, the substituent does not interfère with the intended purpose of the compound or structure on which the substituent is incorporated. As used herein, the term “optionally substituted” just means that the referenced compound or fragment of compound can be substituted in certain

embodiments at one or more substitutable positions, or remain unsubstituted in other embodiments.

[0032] Exemplary substituent groups that can be present at one or more substitutable positions of a compound, structure, or fragment of said compound or structure include, but are not limited to, OH; C1-C12 alkyl; C1-C12 alkenyl; allyl; halogen; C1-C12 haloalkyl; C1-C12 alkoxy; hydroxy C1-C12 alkyl; carboxy; C1-C12 alkoxycarbonyl; C1-C12 carboxyalkoxy; C1-C12 carboxamido; cyano; formyl; C1-C12 açyl; C2-C12 alkyl ester or alkylhydroxy ester; C6-C12 aryl ester; nitro; amino; C1-12 alkylamino; Ci-ndialkylamino; anilino; mercapto; C1-12 alkylthio; sulfoxide; sulfone; C1-12 acylamino; amidino; aryloxy;

arylamino; amido; epoxy; carbonyl; alkoxycarbonyl (ester); nitrile; ureido; silanol; phenyl; benzyl; heteroaryl; heterocycle; phenoxy; benzoyl; benzoyl substituted with amino, hydroxy, methoxy, methyl or halo; benzyloxy and heteroaryloxy. When the group that is substituted contains an alkyl segment, two hydrogen atoms on the same carbon atom may be replaced by a single substituent double bonded to the carbon atom (e.g., =O).

[0033] As used herein, the term “small molécule amine” refers to any amine containing compound that is < 1,000 Da. As described more fully below such compounds can include, for example, aliphatic amines/diamines, cycloaliphatic and aromatic amines/diamines, oligoamines, and ether amines/diamines. The term “modified amine” 20 just refers to the small molécule amine being substituted at one or more substitutable positions with one or more organic moieties, which may themselves be substituted or unsubstituted.

[0034] The term “scale” as used herein in reference to the wet process phosphoric acid production process refers to numerous species of minerai solids that are primarily or 25 completely inorganic in composition and become supersaturated during the processing of phosphate ore.

[0035] As used herein, the term “oligomer” or “oligomeric” refers to a compound (e.g., a small molécule amine) containing a moiety that repeats two or more times, but not more than would cause the compound to be greater than 1,000 Da for purposes of the present 30 invention. Typically, the moiety repeats from 2 to 10 times. The terms “oligoamine” or “polyamine” can be used interchangeably to refer to small molécule amines that hâve an amine moiety that repeats two or more times, but not more than would cause the small molécule amine to be greater than 1,000 Da. Similarly, the term “polyetheramine” as

used herein just refers to small molécule amines that hâve an ether amine moiety that repeats two or more times, such that does not cause the small molécule amine to be greater than 1,000 Da.

[0036] Terms used to describe the reagents referred to herein, such as “anti-scalant” or “scale inhibitor,” refer to chemical compounds, including salts thereof, and/or mixtures thereof, that are effective for delaying or preventing (i.e., inhibiting) nucléation or supersaturation of minerai scale species, or for reducing, removing, and/or eliminating existing scale in the phosphoric acid process stream. The term “scale inhibiting amount” in the context of describing the amount of reagent added to the process stream is an acceptable term to those ordinarily skilled in the art and is understood to mean an amount that is necessary to achieve any of those outcomes (preventing, reducing, or eliminating). As those skilled in the art will appreciate, the amount of reagent to be added to the process will dépend on the type and/or saturation of scale being produced, as well as the outcome desired (e.g., élimination of existing scale vs. prévention of scale).

[0037] The terms “substantially free.ofoil” or “substantially oil-free” as used herein are interchangeable and refer to a reagent that contains less than 50 % by weight of an oil, such as, but not Iimited to, an organic petroleum distallate. Preferably, reagents that are substantially free of oil contain less than 25 wt. % of oil; more preferably less than 10 wt. %; and more preferably still are “essentially free of oil,” or “essentially oil-free,” which are interchangeable terms and as used herein are taken to mean reagents containing less than 1 wt. % of oil.

[0038] The term “aqueous solution” is used herein in its ordinary sense and refers to solutions wherein the solvent is water or primarily water. The solution can simply be distilled water, for example, or can include an acidic aqueous solution from the wet process phosphoric acid stream. The term “insolubilizing group” as used herein refers to a group, substructure, or moiety on a molécule or compound that includes a sufficient number of carbon atoms, or is multiply présent in a sufficient number or quantity so as to decrease the molecule’s or compound’s solubility in an aqueous solution. The hydrocarbyl portion of a compound that also includes an amine portion is an example of 30 such an insolubilizing group.

[0039] Accordingly, one aspect of the invention provides processes for inhibiting scale produced during wet process phosphoric acid production, by adding a scale inhibiting amount of a reagent to at least one stage of a wet process phosphoric acid production

process, wherein said reagent includes a compound having a portion that includes a small molécule amine with at least one primary amine, and at least one hydrocarbyl portion that can be part of the backbone of the compound, or can be a pendant group attached (directly or indirectly) to the backbone, and which includes at least one insolubilizing group, thereby inhibiting (i.e., preventing, reducing, or eliminating) scale in the wet process phosphoric acid production process.

[0040) While ail of the reagents described herein are substantially oil-free, in preferred embodiments the reagent contains less than 25 wt. % oil, and more preferably less than 10 wt. % oil. In other embodiments, the reagents useful as anti-scalants are essentially oil10 free and contain less than 1 wt. % of oil based on the weight of the reagent.

[0041) Any amine that is less than 1,000 Daltons and contains at least one primary amine are suitable for use as the amine portion of the compound. In certain embodiments, the amine portion ofthe compound can be derived from a polyamine or a polyetheramine, the structure of which can include, for example, those disclosed in col. 7, lines 10-28 in U.S.

Patent No. 7,999,065, which is incorporated herein by reference. When the amine portion of the compound is derived from a polyamine, for example, in certain embodiments the amine portion can be derived from polyallylamine. In other embodiments, the polyamine can be derived from polyvinylamine.

)0042) In the same or other embodiments, the hydrocarbyl portion of the compound includes an insolubilizing group having 1 to 22 carbon atoms, wherein one or more carbon atoms is optionally replaced by a hetero atom, and/or optionally substituted at one or more substitutable positions with a substituent selected from the group consisting of OH; C1-C12 alkyl; C1-C12 alkenyl; allyl; halogen; C1-C12 haloalkyl; C1-C12 alkoxy; hydroxy C1-C12 alkyl; carboxy; C1-C12 alkoxycarbonyl; C1-C12 carboxyalkoxy; C1-C12 carboxamido; cyano; formyl; C1-C12 acyl; C2-C12 alkyl ester or alkylhydroxy ester; C6-C12 aryl ester, nitro; amino; Ci.i2alkylamino; Ci-ndialkylamino; anilino; mercapto; C1-12 alkylthio; sulfoxide; sulfone; C1-12 acylamino; amidino; aryloxy; arylamino; amido; epoxy; carbonyl; alkoxycarbonyl (ester); nitrile; ureido; silanol; phenyl; benzyl; heteroaryl; heterocycle; phenoxy; benzoyl; benzoyl substituted with amino, hydroxy, methoxy, methyl or halo; benzyloxy; and heteroaryloxy.

)0043) As indicated above, the purpose of the insolubilizing group is to decrease the solubility of the small molécule amine in an aqueous solution, such as distilled water, for example. Accordingly, those skilled in the art will appreciate that the hydrocarbyl portion of the compound can be chosen accordingly so as to ensure that either a sufficient number of carbon atoms are included in the insolubilizing group, or that the hydrocarbyl portion is multiply présent in a sufficient number or ratio as compared to the amines in the amine portion of the compound that the solubility of the compound in an aqueous solution is decreased (as compared to the compound without the insolubilizing group(s)).

[0044] In some embodiments, the compound having at least one amine portion containing at least one primary amine, and at least one hydrocarbyl portion having an insolubilizing group that is part of the backbone of the compound and/or a pendant group attached to the backbone is a compound according to Formula (IV):

(IV), or salts thereof wherein [0045] each of R⁸ and R¹⁰ is independently chosen from H or a hydrocarbyl radical having 1 to 22 carbon atoms, wherein one or more carbon atoms is optionally replaced by a hetero atom, and/or optionally substituted at one or more substitutable position with a substituent selected from the group consisting of OH; C1-C12 alkyl; C1-C12 alkenyl; allyl; halogen; C1-C12 haloalkyl; C1-C12 alkoxy; hydroxy C1-C12 alkyl; carboxy; C1-C12 alkoxycarbonyl; C1-C12 carboxyalkoxy; C1-C12 carboxamido; cyano; formyl; C1-C12 acyl; C2-C12 alkyl ester or alkylhydroxy ester; C6-C12 aryl ester; nitro; amino; C1.12 alkylamino; Ci-ndialkylamino; anilino; mercapto; C1-12 alkylthio; sulfoxide; sulfone; C1-12 acylamino; amidino; aryloxy; arylamino; amido; epoxy; carbonyl; alkoxycarbonyl (ester); nitrile; ureido; silanol; phenyl; benzyl; heteroaryl; heterocycle; phenoxy; benzoyl; benzoyl substituted with amino, hydroxy, methoxy, methyl or halo; benzyloxy; and heteroaryloxy; [0046] R⁹ is chosen from H or a Ci-Cô alkyl;

[0047] L is an optionally substituted hydrocarbyl fragment having 1 to 20 carbon atoms;

[0048] p is an integer chosen from 2 to 4; and [0049] t is an integer from 0 to 10, [0050] with the proviso that at least one ofR⁸, R¹⁰, or L includes the hydrocarbyl portion of the compound that includes an insolubilization group.

[0051] In the same or other embodiments, the compound having at least one amine portion containing at least one primary amine, and at least one hydrocarbyl portion having an insolubilizing group that is part of the backbone of the compound and/or a pendant group attached to the backbone is a compound according to Formula (V):

¹²fe

nh₂ (V), or salts thereof wherein [0052] R¹¹ is chosen from H or a hydrocarbyl radical having 1 to 22 carbon atoms, wherein one or more carbon atoms is optionally replaced by a hetero atom, and/or optionally substituted at one or more substitutable position with a substituent selected from the group consisting of OH; C1-C12 alkyl; C1-C12 alkenyl; allyl; halogen; C1-C12 haloalkyl; C1-C12 alkoxy; hydroxy C1-C12 alkyl; carboxy; C1-C12 alkoxycarbonyl; C1-C12 carboxyalkoxy; C1-C12 carboxamido; cyano; formyl; C1-C12 acyl; C2-C12 alkyl ester or alkylhydroxy ester; C6-C12 aryl ester; nitro; amino; C1-12 alkylamino; Ci-udialkylamino;

anilino; mercapto; C1-12 alkylthio; sulfoxide; sulfone; C1.12 acylamino; amidino; aryloxy; arylamino; amldo; epoxy; carbonyl; alkoxycarbonyl (ester); nitrile; ureido; silanol; phenyl; benzyl; heteroaryl; heterocycle; phenoxy; benzoyl; benzoyl substituted with amino, hydroxy, methoxy, methyl or halo; benzyloxy; and heteroaryloxy;

[0053] R¹² is chosen from H or a C1-C4 alkyl;

[0054] Y is L as defined for Formula (IV) (i.e., an optionally substituted hydrocarbyl fragment having 1 to 20 carbon atoms);

[0055] w is an integer from 2 to 4; and [0056] z is an integer from 1 to 10, [0057] with the proviso that at least one of R¹¹ or Y includes the hydrocarbyl portion of the compound that includes an insolubilization group.

[0058] In certain embodiments, each of L and Y can be independently chosen from (CHR )_q , _wft_ere r’j_s chosen from H or Ci-Cô alkyl, and q is an integer chosen from to 5.

[0059] In various embodiments, the reagent for use in the processes of the présent invention can also be characterized as a reaction product between a small molécule amine (as Reactant A), and an optionally substituted hydrocarbyl radical of 1 to 22 carbon atoms having an amine reactive group, and which acts as an insolubilizing group (Reactant B).

While those skilled in the art will appreciate that any small molécule amine is suitable for use as Reactant A, in certain embodiments it can be advantageous for Reactant A to be a polyamine or polyetheramine. In the same or other embodiments, one or more carbon atoms of Reactant B can be replaced by a hetero atom, and/or substituted at one or more substitutable position with a substituent selected from the group consisting of OH; C1-C12 10 alkyl; C1-C12 alkenyl; allyl; halogen; C1-C12 haloalkyl; C1-C12 alkoxy; hydroxy C1-C12 alkyl; carboxy; C1-C12 alkoxycarbonyl; C1-C12 carboxyalkoxy; C1-C12 carboxamido; cyano; formyl; C1-C12 acyl; C2-C12 alkyl ester or alkylhydroxy ester; C6-C12 aryl ester; nitro; amino; C1-12 alkylamino; C1-12 dialkylamino; anilino; mercapto; Ci-ualkylthio; sulfoxide; sulfone; C1-12 acylamino; amidino; aryloxy; arylamino; amido; epoxy;

carbonyl; alkoxycarbonyl (ester); nitrile; ureido; silanol; phenyl; benzyl; heteroaryl; heterocycle; phenoxy; benzoyl; benzoyl substituted with amino, hydroxy, methoxy, methyl or halo; benzyloxy; and heteroaryloxy.

[0060] In certain embodiments, Reactant A can include a small molécule amine compound according to Formula (I) ₂₀ H₂N-(CRR>) —nr²r³ _ω wherein m is an integer from 1 to 20; (more preferably an integer from 1 to 10) each instance of R and R* is independently chosen from H, or an optionally substituted hydrocarbyl fragment having 1 to 20 carbon atoms; (more preferably a C1-C4 25 alkyl, or C2-C6 alkenyl); and each of R² and R³ is independently chosen from H, C1-C12 alkyl, or C1-C12 alkylamine.

[0061] Représentative compounds according to Formula (I) where m is from 1 to 20 are specifically contemplated as if recited herein. In certain embodiments, m is at least 2. In other embodiments m is at least 3. Similarly, each value of R-R³ is specifically contemplated as if recited herein, including ail permutations. In some embodiments each of R and R* are H in each instance. In other embodiments, each of R and R¹ can be H in some instances and C1-C4 alkyl in other instances. In certain embodiments, in at least one instance of R and R¹, one of R or R¹ can be C1-C4 alkyl, and the other is H.

[0062] In the same or other embodiment, each ofR² and R³ can be H. In some embodiments, one of R² or R³ can be H and the other can be a C1-C12 alkyl or alkylamine. In still other embodiments, each of R² and R³ can be chosen from a C1-C12 alkyl. In certain embodiments where each of R² and R³ are C1-C12 alkyl, C1-C4 alkyl is preferred.

[0063] In other embodiments, Reactant A can include a small molécule amine compound according to Formula (II):

H₂N—[(CHR⁴)^—NR^sJçj-X—NH₂ (ID.

wherein each instance of R⁴ is independently chosen from H or Ci-Cô alkyl; (more preferably from C1-C4 alkyl) each instance of R⁵ is independently chosen from H or C1-C4 alkyl;

p is an integer from 2 to 4;

n is an integer from 0 to 20 (more preferably from ί to 10);

X is an optionally substituted hydrocarbyl fragment having 1 to 20 carbon atoms (and more preferably is chosen from (CHR )_q > _wh_ere r’ j_s chosen from H or C1-C6 alkyl, and q is an integer chosen from 1 to 5).

[0064] In certain embodiments where Reactant A is a small molécule amine according to

Formula (II), each instance of the fragment in brackets can be

where p can be at least 2, and X is (CHR )_q , _wfr_ere q _can |,_e f_rom 2 to 3.

[0065] In the same or other embodiments, n can be from 2 to 3. In another embodiment, R⁴ can be C1-C4 alkyl in at least one instance.

[0066] In still other embodiments, Reactant A can be chosen from a small molécule amine compound according to Formula (III):

h₂n-Rchr⁷)-o

-τ—nh₂ ^z (HD, wherein each instance of R⁷ is independently chosen from H or C1-C4 alkyl;

T = X as defined for Formula (II) (i.e., an optionally substituted hydrocarbyl fragment having 1 to 20 carbon atoms (and more preferably is chosen from ¹ , where R is chosen from H or Ci-Cô alkyl, and q is an integer chosen from to 5);

w is an integer from 2 to 4; and z is an integer from 1 to 10.

[0067] In certain embodiments where Reactant A is a small molécule amine compound according to Formula (III), z can be at least 2, each instance of w can be from 2 to 4, and T is (CHR )q _f where q is at least 3.

[0068] Again, while any amine compound having an average molecular weight < 1,000 Da and at least one primary amine is suitable for use as Reactant A, some may be more advantageous to use than others depending on the type of scale being produced in the process, or the availability and/or type of reactants as Reactant B. Particularly preferred small molécule amines suitable for use as Reactant A can include, but are not limited to, polyethyleneimine; diethylenetriamine; triethylenetetramine; tetraethylenepentamine; dipropylene triamine; diaminoalkanes (including, but not limited to, 1,2-diaminoethane; 1,3-diaminopropane; 1,4-diaminobutane; 1,5 diaminopentane; 1,5-diaminohexane; 1,8diaminooctane); dimethylaminopropylamine; diethylaminopropylamine; bis(3aminopropyl)-methylamine; 3-(2-aminoethyl)amino-propylamine; N,N’-bis(3aminopropyl)-ethylenediamine; neopentanediamine; isophorone diamine; aminoaniline; aminomethylbenzylamine; 4,4’-diamino-dicyclohexylmethane; 3,3’dimethyl-4,4’diamino-dicyclohexylmethane; 3-cyclohexylamino-propylamine; 4,7-dioxadecane-l ,10diamine; and 4,9-dioxadodecane-l,12-diamine.

[0069] In certain embodiments, Reactant A can include polyallylamine or polyvinylamine oligomers of less than 1,000 Da, or mixtures thereof. In still another embodiment, the small molécule amine can be a branched ethyleneimine oligomer, or salts thereof. Such

branched ethylenimine oligomers are commercially available as EPOMIN SP-003 (MW = 300 Da) or EPOMIN SP-006 (MW = 600 Da) from Nippon Shokubai. In other embodiments, Reactant A can advantageously include mixtures of branched polyethyleneimine oligomers of less than 1,000 Da.

[0070] In another embodiment, the small molécule amine of Reactant A can be a linear or branched etheramine oligomer, or salts thereof. In some embodiments, the etheramine oligomer can hâve the general structure of NH2CH(CH3)CH2-(OCH2CH(CH3))w—NH2, wherein w is an integer of at least 1, but not higher than would place the molecular weight of the compound above 1,000 Da. Such etheramine oligomers are commercially available 10 from BASF Corp. or Huntsman Corp.

[0071] In the same embodiments pertaining to Reactant A, Reactant B can advantageously include a substituted hydrocarbyl fragment having 8 to 22 carbon atoms selected from the group consisting of alkyl halides; alkenyl halides; aralkyl halides; alkyl sulfates; compounds containing at least one epoxide group; and compounds containing at 15 least one anhydride group. Again, compounds having an amine reactive portion (or “nitrogen-reactive compounds”) that are suitable for use as Reactant B in the processes according to the invention are well known to those skilled in the art and hâve been previously disclosed at least in U.S. Patent No. 7,999,065 at col. 7, line 51 through col. 8, line 9, which portion is specifically incorporated herein by reference as if explicitly 20 written herein.

[0072] Particularly preferred compounds suitable for use as Reactant B for processes according to the invention can include, but are not limited to, one or more members ofthe group consisting of octyl chloride; dodecyl bromide; chlorohexane; benzyl chloride; dimethylsulfate; epichlorohydrin; glycidyl 4-nonylphenylether; butyl glycidyl ether; 225 ethylhexyl glycidyl ether; phenyl glycidyl ether; Cs-Cm alkyl glycidyl ethers; cresyl glycidyl ether; tall oil fatty acids; C12-C18 tallow alkyls; octenylsuccinic anhydride; and octadecenylsuccinic anhydride.

[0073] In preferred embodiments, the reagents useful as scale inhibitors in the wet process phosphoric acid production processes according to the invention can include at 30 least one reaction product formed between Reactant A and Reactant B, wherein Reactant

A includes one or more member selected from the group consisting of triethylenetetramine; tetraethylenepentamine; dipropylene triamine; and mixtures of branched polyethyleneimine; and wherein Reactant B includes one or more member

selected from the group consisting of octyl chloride; dodecyl bromide; oleyl; mixtures of octyl glycidal ethers and decyl glycidal ethers; 2-ethylhexyl glycidyl ether; mixtures of Cu, Ci6, and Ci8 saturated carbon chains derived from tallow; and tail oil fatty acids. [0074] In certain embodiments, it may be preferred that the reagent include a mixture of reaction products between the small molécule amine compounds of Reactant A and the hydrocarbyl radicals of Reactant B, which contain an insolubilizing group. Indeed, those skilled in the art will recognize that any ofthe reagents as described herein and useful as an anti-scalant for inhibiting scale in the WPA production stream can also include mixtures of any one or more reagents, which mixtures can be added as separate reagents 10 to the process stream at one or more stage of the phosphoric acid production process, or added as mixtures, or separately in sequence, in reverse order, or simultaneously to one or more stage of the process stream.

[0075] According to certain embodiments of the processes of the invention, the reagent as described herein can be added to any stage (including multiple stages) of a wet process phosphoric acid production stream (e.g., one or more of the milling stage, digesting stage, filtering stage, clarifying stage, or evaporator stage). While the reagent may be added at any one or more of these stages, in certain embodiments it is more preferably added to the phosphoric acid stream going to the filters or evaporators as this is where the most prévalent sealing problems occur.

[0076] In still other embodiments, the reagent can be added to any of the piping connecting the various stages of the phosphoric acid production process plant. This is sometimes referred to in the field as the “interstitial piping” or “process fiow pipeline”. [0077] The reagents described herein are effective against various species of scaleforming ions most commonly found in the wet process phosphoric acid production stream. Accordingly, in certain embodiments, the reagent is useful in treating or inhibiting scale that includes, but are not limited to, at least one species of scale-forming ion chosen from Na₂SiF6; K₂SiF6; CaSÛ4+ 2 H2O; CaSÛ4 + V2 H₂O; CaSÛ4; MgSiFô+ 6 H₂O; Ca3(PO4)₂; CaHPO»; Si₂F6; CaSiFô+ 2 H₂O; CaF₂; MgF₂; Mgo.8Ali.5F6+ X H₂O, wherein X is an integer ranging from 2 to 10; MglfrPôCh; A1(PÛ3)3; NaK2AlFô;

Ca3(AlF6)₂+ 4 H₂O; MgNaAlFô+ 2 H₂O; or Ca4SO4AlSiFi3+ 10 H₂O. As will be appreciated by those skilled in the art, the typical phosphoric acid process stream contains numerous species of scale-forming ions, which gives rise to the difficulty in inhibiting scale formation and/or déposition in the first place.

[0078] As will further be appreciated by those skilled in the art, the amount or dosage of reagent required to effectively inhibit scale (i.e., a scale inhibiting amount) will vary depending upon the particular reagent used and/or the severîty of the scaling problem encountered, the species of scale-forming ions présent, as well as the concentration or saturation of scale-forming ions.

[0079] As a general rule, the dosage is based on active reagent to the weight of phosphoric acid solution, and can range from between 0.5 g/ton to 5000 g/ton of phosphoric acid. In certain embodiments, the dosage of active reagent can be from 0.5 g/ton to 1000 g/ton of phosphoric acid solution, and preferably from 0.5 g/ ton to 500 g/ ton of phosphoric acid solution. In other embodiments, the dosage of active reagent is at least 100 g/ton of phosphoric acid solution, or at least 500 g/ton of phosphoric acid solution. Those skilled in the art will recognize that the contemplated dosage range includes the lower dose value and higher dose value, as well as any spécifie dose value there between (e.g., 0.5 g/ton, 0.6 g/ton, 0.7 g/ton, et seq. up to and including 5000 g/ton of phosphoric acid).

[0080] The scale inhibiting reagents described herein can be in liquid form (such as with water, oil and/or alcohol diluents) and may be formulated in various ways, e.g., the solid reagent may be suspended (e.g., colloïdal suspension), dispersed and/or slurried in the liquid, and/or the reagent may be suspended, dispersed, slurried and/or dissolved in the liquid.

[0081] The scale inhibiting reagents described herein can be intermixed with the phosphoric acid liquor in various ways, e.g., in a single stage, in multiple stages, or if various mixtures of reagent are added, then sequentially, in reverse order, or simultaneously. For example, in one embodiment, the scale inhibiting reagent is added to diluent to form a pre-mix, and then intermixed with the phosphoric acid liquor. In another embodiment, the reagent can be added directly to the process stream. Various modes of addition will be found to be effective and can be adjusted using no more than routine expérimentation.

[0082] In certain embodiments of the processes described herein, one or more other industrial additives can also be added. Such additives include, for example, other antiscalants, biocides, corrosion inhibitors, or dispersants. The prior art is replete with such industrial treatment additives and these are generally known to those skilled in the art. Furthermore, such additives can also be added in a single stage or multiple stages of the

phosphoric acid production process along with the reagents described herein. It will be appreciated that the additives can be added in the same stage or different stage as the reagent, or sequentially, in reverse order, or simultaneously.

[0083] This new type of anti-scalant effective for use in the wet process phosphoric acid production stream is unexpected because the small molécule amines by themselves (i.e., not containîng an insolubilizing group) were previously known to be poor performers of scale inhibition as determined by the inventors’ in-house testing method (Turbidity Test). A potential advantage of this new class of reagent could be a lower effective treatment cost, as compared to presently available commercial products.

[0084] While certain embodiments of the reagent suitable for use as a scale inhibitor with processes according to the invention hâve been provided herewith, those skilled in the art will appreciate that others not specifically discussed will also be encompassed by these teachings and are, thus, within the spirit and scope of the invention.

[0085] Examples [0086] The following examples are provided to assist one skilled in the art to further understand certain embodiments of the présent invention. These examples are intended for illustration purposes and are not to be construed as limiting the scope of the appended claims.

[0087] Example 1 - General Synthesis of Alkylamine Reagents:

[0088] Excepting those reagents that are commercially available, such as TRIAMEEN® T and DUOMEEN® O (available from Akzo Nobel Chemicals B.V.), the general synthetic procedure for the various reagents suitable for use with the présent invention includes filling an appropriate vessel with some quantity of solvent allowing for a reaction to proceed between the small molécule amine, such as ethylenediamine or other aliphatic oligoamines (e.g., H2N(-CH2-CH2-NH-)_XCH2CH2NH2, or H2N(-CH2-CH2-CH2-NH-)yCH2CH2NH2, where x and y is an integer from 1-10), or NH2(CH2-CH2-O-)n CH2CH2NH2, where n = 8-25), or etheramines or ethyleneimine oligomers, and any one or more organic moiety containîng as its major constituent a hydrocarbon chain that may be saturated, monounsaturated, polyunsaturated or branched, along with a minor constituent which may contain any atoms to achieve a reactive product, which minor constituent will be readily known to those skilled in the art.

[0089] The combined mixture is stirred and warmed as needed to a température from 50160 °C, preferably from 75-85 °C for reactions between amines and glycidyl ethers or

amines and alkylhalides, or from 130-140 °C with azeotropic removal of water, molecular sieve removal of water, or other appropriate method for removal of water for reactions between amines and tall oil fatty acids. The reaction time period may range from 0-72 hours but more typically is from 0-8 hours, and more typically still from 1-3 hours. The solvent may be used as the final diluent, evaporated with heat or under reduced pressure, or both, to concentrate or to further isolate the active reagent.

[0090] Example 2 - Reaction product of tetraethylenepentamine and octyl-, decyl-glycidyl ether:

[0091] To a 100 mL round-bottomed flask charged with 13 mL acetonitrile, tetraethylenepentamine (“ΤΕΡΑ”) (MW 189.3; 1 g, 5.2 mmol) is added and dissolved with continuous stirring, followed by addition of half an équivalent of octyl-,decyl-glycidyl ether (MW -172; 0.86 g, 5 mmol) (available as ERISYS™ GE-7 from Emerald Performance Materials) by dropper. The combined mixture is stirred and heated to reflux (80 °C) for 2 hrs. The solvent is evaporated under reduced pressure and the crude is dried under vacuum (300 mTorr) to give a clear oil (Reaction Product B of Table 1).

[0092] Example 3 - Reaction product of a mixture of oligoamines from distillation bottoms of ethyleneimine and tall oil fatty acid:

[0093] To a 100 mL round-bottomed flask equipped with a Dean-Stark trap, reflux condenser and a heat source and further charged with 75 mL xylenes purged with nitrogen, 20 is added activated 4 angstrom molecular sieves followed by a mixture of oligoamines from distillation bottoms of ethyleneamine (MW -266; 3 g, 11 mmol) (available as E-100 from Huntsman), and tall oil fatty acid (MW -285; 1.6 g, 5.6 mmol) (available as XTOL® 100 from Georgia-Pacific Chemical), over 2 minutes. The combined mixture is stirred and heated to reflux (138.5 °C) for 2.5 hours. The solvent is evaporated under reduced pressure 25 and the crude is dried under vacuum (200 mTorr) to give a yellow oil (Reaction Product I ofTable 1).

[0094] Other reaction products are prepared similarly as described by Examples 1, 2, or 3, wherein the reactants and ratios are provided by reaction products A and C-H ofTable 1.

[0095] Example 4 - Evaluation of the relative performance of reagents for inhibiting scale:

[0096] The performance of substituted oligoamines or fatty acid amines, which hâve reduced solubility in an aqueous environment as compared to their unsubstituted forms,

and which are thus useful as reagents for inhibiting scale in wet process phosphoric acid production is measured via a turbidity test (based on supersaturation-precipitation process). This method is useful to evaluate whether the reagent can control the précipitation of calcium sulfate and fluorosilicate type scales from process phosphoric 5 acid solutions that hâve been supersaturated via évaporation and cooling. The general procedure for the test is outlined below, which is based on the génération of 16 individual samples. Those skilled in the art will appreciate that different starting and ending volumes may be used to generate greater or fewer samples. The acid may also be concentrated to a greater or lesser degree.

[0097] In a ventilated hood, 600 g of 28 wt % process phosphoric acid (P2O5) is added to a IL Teflon beaker. The total weight of the acid and beaker is recorded. The acid is reduced in weight to approx. 400 g (i.e., concentrated to approx. 42 wt % P2O5) by heating on a hot plate (Thermo Scientific Cimarec) set at 120 °C with moderate stirring (set at 6). Concentration of the phosphoric acid to this level typically occurs after 20-24 hours and can be performed ovemight.

[0098] For 100 ppm dosage of reagent, 0.2 g of 1 wt % (based on active dry component) solutions of the reagents of interest are added to 4 oz. glass vials using an analytical balance. 0.2 g of water is added to the control vials. 19.8 g of hot concentrated phosphoric acid is added to each vial using a plastic syringe with a 0.2 micron syringe filter. The vials are shaken to form a homogenous mixture and left to sit at room température, without agitation, for 30 min. to 24 hours.

[0099] Turbidity is measured with a HACH® 2100Q portable turbidimeter (nephelometer), or other équivalent, which is calibrated and used according to directions in the instruction manual. Each glass vial is shaken gently to loosen attached scales from 25 sidewall and bottom of vials. The contents of the vial are emptied into the turbidity meter test cell, and the measurement is taken after 10-30 seconds. The test cell is flipped back and forth 5 times and the measurement is taken again after 10-30 seconds. The testing cell is emptied and rinsed with deionized water and dried with an air or nitrogen stream and the remaining samples are measured in the same way. Units of measurement are given as Nephelometric Turbidity Units (NTUs), with lower NTUs representing less particles suspended in the sample solution. HACH® 2100Q portable turbidimeter has an upper limit reading of 1000 NTUs. For purposes of the invention a lower NTU is

désirable and indicates less scale particles and is prédictive of the reagent being more effective as a scale inhibitor for wet process phosphoric acid productions streams. [0100] Example 5 - Evaluation of the reaction product of triethylenetetramine and octyl-, decyl-glycidyl ether:

[0101] A reaction product (A) is prepared as described in Example 2, except that triethylenetetramine is substituted for the tetraethylenepentamine and an équivalent amount of octyl-, decyl-glycidyl ether is used. The performance of the reaction product as a reagent for phosphoric acid anti-scalant is measured in the turbidity test as described in Example 4, wherein 100 ppm dose of reagent is applied to a phosphoric acid liquor of 10 42 % phosphoric acid. The results are summarized in Table 1 below.

[0102] Example 6 - Evaluation of the reaction product of tetraethylenepentamine and octyl-, decyl-glycidyl ether:

[0103] A reaction product (B) is prepared as described in Example 2. Reaction products (C) and (D) are also prepared according to Example 2, except that the reactants are présent at a 1:1 and a 1:2 ratio, respectively. The performance of the reaction products as suitable reagents for phosphoric acid anti-scalant are measured in the turbidity test as described in Example 4, wherein 100 ppm dose of reagent is applied to a phosphoric acid liquor of 40 % phosphoric acid. The results are summarized in Table 1 below.

[0104] Example 7 - Evaluation of the reaction product of tetraethylenepentamine and an alkylhalide:

[0105] Reaction products (E) and (F) are prepared as described in Example 2, except the hydrocarbon chain is octylchloride and dodecylbromide, respectively. The performance of the reaction products as suitable reagents for phosphoric acid anti-scalant are measured in the turbidity test as described in Example 4, wherein 100 ppm and 500 ppm dose of reagent, respectively is applied to a phosphoric acid liquor of 42 % phosphoric acid. The results are summarized in Table 1 below.

[0106] Example 8 - Evaluation of the reaction product of tetraethylenepentamine and 2ethylhexyl glycidyl ether:

[0107] A reaction product (G) is prepared as described in Example 2, except that half an équivalent of 2-ethylhexyl glycidyl ether is used in place of octyl-, decyl-glycidyl ether. The performance of the reaction product as a suitable reagent for phosphoric acid antiscalant is measured in the turbidity test as described in Example 4, wherein 500 ppm dose

of reagent is applied to a phosphoric acid liquor of 42 % phosphoric acid. The results are summarized in Table 1 below.

[0108] Example 9 - Evaluation of the reaction product of mixture of oligoamines from distillation bottoms of ethyleneamines and octyl-, decyl-glycidyl ether:

[0109] A reaction product (H) is prepared as described in Example 2, except that équivalent amounts of reactants are used and E-100 from Huntsman (mixture of oligoamines from distillation bottoms of ethyleneamine) is substituted for the tetraethylenepentamine. The performance of the reaction product as a suitable reagent for phosphoric acid anti-scalant is measured in the turbidity test as described in Example 4, wherein 100 ppm dose of reagent is applied to a phosphoric acid liquor of 42 % phosphoric acid. The results are summarized in Table 1 below.

[0110] Example 10 - Evaluation of the reaction product of a mixture of oligoamines from distillation bottoms of ethyleneamines and tall oil fatty acid:

[0111] A reaction product (I) is prepared as described in Example 3. The performance of 15 the reaction product as a suitable reagent for phosphoric acid anti-scalant are measured in the turbidity test as described in Example 4, wherein 100 ppm dose of reagent is applied to a phosphoric acid liquor of 42 % phosphoric acid. The results are summarized in Table 1 below.

[0112] Example 11 - Evaluation of N-tallowalkyl dipropylene triamines (commercially 20 available as TRIAMEEN® T from AkzoNobel):

[0113] TRIAMEEN® T is a mixture of compounds of dipropylene triamine substituted with a mixture of hydrocarbon chains derived from tallow. The performance of the reaction product as a suitable reagent for phosphoric acid anti-scalant are measured in the turbidity test as described in Example 4, wherein 100 ppm dose of reagent is applied to a 25 phosphoric acid liquor of 45 % phosphoric acid. The results are summarized in Table 1 below.

[0114] Example 12 - Evaluation ofN-oleyl-l,3-diaminopropane (commercially available as DUOMEEN® O from AkzoNobel):

[0115] DUOMEEN® O is an oleylpropylene diamine (diaminopropane substituted with 30 an oleyl hydrocarbon chain). The performance of the reaction product as a suitable reagent for phosphoric acid anti-scalant are measured in the turbidity test as described in Example 4, wherein 1000 ppm dose of reagent is applied to a phosphoric acid liquor of 44 % phosphoric acid. The results are summarized in Table 1 below.

[0116] Example 13 - Evaluation of the reaction product of ethyleneimine oligomers of MW 300 and 600 with octyl-, decyl-glycidyl ether:

[0117] Reaction products (J-P) are prepared as described in Example 2, except that ethyleneimine oligomers are replaced with tetraethylenepentamine. Ethyleneimine oligomers of the indicated molecular weights are commercially available as EPOMIN SP003 and EPOMIN SP-006 from Nippon Shokubai. The moles of reactants are varied. The performance of the reaction product as a suitable reagent for phosphoric acid antiscalant is measured in the turbidity test as described in Example 4, wherein various doses (from 10 ppm to 100 ppm) of each reagent is applied to a phosphoric acid liquor of 42 % phosphoric acid. The results are summarized in Table 1 below, where the NTU of the reaction product is provided as a négative number to indicate how much lower the NTU of the reaction product was than the NTU of the control.

[0118] Table 1. Summary of Evaluai ion of Examples 6-12, wherein Reactant A is the small molécule amine and Reactant B is the compound from which the organic moiety 15 or moieties (T) is derived. Time is given in minutes and dose in part per million (ppm)

Reaction Product	Reactant A	Reactant B	Moles A	Moles B	NTU Blank	NTU Prod.	NTU time	Dose (PPm)
A	TETA	GE-7	1	1	758	123	300’	100
B	ΤΕΡΑ	GE-7	2	1	1000	54	120’	100
C	ΤΕΡΑ	GE-7	1	1	1000	142	120’	100
D	ΤΕΡΑ	GE-7	1	2	1000	334	120’	100
E	ΤΕΡΑ	Octyl-Cl	2	1	173	162	40’	100
F	ΤΕΡΑ	Dodecyl-Br	2	1	852	93	70’	500
G	ΤΕΡΑ	2-EHGE	2	1	852	80	70’	500
H	Ε-100	GE-7	1	1	1000	161	45’	100
I	Ε-100	TOFA (XTOL)	2	1	900	22	60’	100
TRIAMEEN-T	DPTA	TA	N/A	N/A	921	477	330’	100
DUOMEEN-O	PDA	oleyl	N/A	N/A	667	137	300’	1000
J	EPOMIN SP-003 (MW 300)	GE-7	1	1		-221	150	10
K	U	66	1	2	—	-217	150	10
L	66	66	1	1	—	-457	150	50
M	66	66	1	1	—	-238	1200	100
N	EPOMIN SP-006 (MW 600)	GE-7	1	1		-157	150	10
O	66	66	1	1	—	-471	150	50
P	66	66	1	1	-	-239	1200	100

“TETA” = triethylenetetramine.

“ΤΈΡΑ” = tetraethylenepentamine.

“E-100” = a mixture of oligoamines from distillation bottoms of ethyleneimine as sold by Huntsman.

“GE-7” = a mixture of octyl-, decyl- glycidyl ethers as sold by Emerald Performance

Materials and marketed as ERISYS® GE-7.

“2-EHGE” = 2-ethylhexyl glycidyl ether commercially available from Sigma Aldrich. “DPTA” = dipropylene triamine.

“TA” = tallow-alkyl, a mixture of Cl4, Cl6 and Cl8 chains, saturated and containing one or more unsaturations as derived from tallow.

“PDA”= 1,3-propanediamine.

“oleyl” = a monounsaturated oleyl carbon chain.

“TOFA” = tall oil fatty acid and is either XTOL® 100 sold by Georgia-Pacific Chemicals or SYLFAT™ FA2 sold by Arizona Chemical.

DUOMEEN® O is a diaminopropane substituted with an oleyl hydrocarbon chain (oleylpropylene diamine) and is commercially available from AkzoNobel.

TRIAMEEN® T is a mixture of dipropylene triamines substituted with various lengths of hydrocarbon chains derived from tallow and is commercially available from AkzoNobel.

EPOMIN SP-003 and SP-006 are ethyleneimine oligomers of MW 300 and 600, respectively, and are commercially available from Nippon Shokubai [0119] In view of the above description and the examples, one of ordinary skill in the art will be able to practice the disclosure as claimed without undue expérimentation.

[0120] While typical embodiments hâve been set forth for the purpose of illustrating the fondamental novel features of the présent invention, the foregoing descriptions should not be deemed to be a limitation on the scope herein. Accordingly, various modifications, adaptations, and alternatives can occur to one skilled in the art without departing from the spirit and scope of the invention described herein, and the scope of the invention should be defined by the appended claims. While the claims below are presented as singly dépendent for purposes of convention and cost, those skilled in the art will understand from reading the detailed description that multiply dépendent embodiments are also contemplated by the inventors and that any of the claims below can be written as such.

Claims (24)

1. Claims

   We claim:

   5 1. A process for inhibiting scale produced during wet process phosphoric acid production, the process comprising adding a scale inhibiting amount of a reagent to at least one stage of a wet process phosphoric acid production process, said reagent comprising a reaction product having a weight average molecular weight < 1 kDa and at least one primary amine, and wherein said 10 reaction product is further characterized as the product between Reactant A and Reactant B, wherein Reactant A comprises a polyamine or polyether amine; and wherein Reactant B comprises a hydrocarbyl radical having 1 to 22 carbon atoms that includes an amine reactive group, wherein one or more carbon atoms is optionally replaced by a hetero atom, and/or optionally substituted at one or more substitutable position with a 15 substituent selected from the group consisting of OH; C1-C12 alkyl; C1-C12 alkenyl; allyl;

   halogen; C1-C12 haloalkyl; C1-C12 alkoxy; hydroxy C1-C12 alkyl; carboxy; C1-C12 alkoxycarbonyl; C1-C12 carboxyalkoxy; C1-C12 carboxamido; cyano; formyl; C1-C12 acyl; C₂C12 alkyl ester or alkylhydroxy ester; C6-C12 aryl ester; nitro; amino; C1-12 alkylamino; C1.12 dialkylamino; anilino; mercapto; C1-12 alkylthio; sulfoxide; sulfone; C1.12 acylamino;

   20 amidino; aryloxy; arylamino; amido; epoxy; carbonyl; alkoxycarbonyl (ester); nitrile; ureido; silanol; phenyl; benzyl; heteroaryl; heterocycle; phenoxy; benzoyl; benzoyl substituted with amino, hydroxy, methoxy, methyl or halo; benzyloxy; and heteroaryloxy, provided that Reactant B includes at least 4 carbon atoms, which can be cyclic, linear, or branched, with the proviso that said reagent is substantially free of oil.
2. 2. A process according to claim 1, wherein Reactant A is chosen from:

   i) Formula (I)

   H₂N-(CRR')— nr²r³ _(ΐλ wherein m is an integer from 1 to 20;

   >

   each instance of R and R¹ is independently chosen from H, optionally substituted hydrocarbyl fragment having 1 to 20 carbon atoms; and each of R² and R³ is independently chosen from H, C1-C12 alkyl, or CiC12 alkylamine;

   ii) Formula (II) h₂n )_P~NR⁵ x-nh₂ (ID.

   wherein each instance of R^{3 4} is independently chosen from H or Ci-Cô alkyl; each instance of R^{5 *} is independently chosen from H or C1-C4 alkyl; p is an integer from 2 to 4;

   n is an integer from 0 to 20;

   X is an optionally substituted hydrocarbyl fragment having 1 to 20 carbon atoms; or iii) Formula (III)

   HzN-RcHRVÔI-T-NHz ^L -*^z (ΙΠ), wherein each instance of R⁷ is independently chosen from H or C1-C4 alkyl; T = X as defined for Formula (II);

   w is an integer from 2 to 4; and z is an integer from 1 to 10.
3. 3. A process according to claim 1 or claim 2, wherein Reactant A is selected from the group consisting of polyethyleneimine; diethylenetriamine; triethylenetetramine;

   tetraethylenepentamine; dipropylene triamine; diaminoalkanes; dimethylaminopropylamine;

   diethylaminopropylamine; bis(3-aminopropyl)-methylamine; 3-(2-aminoethyl)amino18403 propylamine; N,N’-bis(3-aminopropyl)-ethylenediamine; neopentanediamine; isophorone diamine; aminoaniline; aminomethylbenzylamine; 4,4’-diamino-dicyclohexylmethane; 3,3’dimethyl-4,4’-diamino-dicyclohexylmethane; 3-cyclohexylamino-propylamine; 4,7dioxadecane-l,10-dÎamine; and 4,9-dioxadodecane-l,12-dÎamine.
4. 4. A process according to any ofclaims 1 to 3, wherein Reactant A includes mixtures of branched polyethyleneimine.
5. 5. A process according to any of claims 1 to 4, wherein Reactant B includes 8 to 22

   10 carbon atoms and is selected from one or more members of the group consisting of alkyl; alkyl halides; alkenyl halides; aralkyl halides; alkyl sulfates; compounds containing at least one epoxide group; and compounds containing at least one anhydride group.
6. 6. A process according to any of claims 1 to 5, wherein Reactant B is selected from one 15 or more members of the group consisting of oleyl; octyl chloride; dodecyl bromide;

   chlorohexane; benzyl chloride; dimethylsulfate; epichlorohydrin; glycidyl 4nonylphenylether; butyl glycidyl ether; 2-ethylhexyl glycidyl ether; phenyl glycidyl ether; CsCu alkyl glycidyl ethers; cresyl glycidyl ether; tall oil fatty acids; C12-C18 tallow alkyls; octenylsuccinic anhydride; and octadecenylsuccinic anhydride.
7. 7. A process according to any of claims 1 to 6, wherein the reagent includes at least one reaction product formed from a reaction between Reactant A and Reactant B, wherein Reactant A includes one or more member selected from the group consisting of triethylenetetramine; tetraethylenepentamine; dipropylene triamine; and mixtures of branched

   25 polyethyleneimine; and wherein Reactant B includes one or more member selected from the group consisting of octyl chloride; dodecyl bromide; oleyl; mixtures of octyl glycidal ethers and decyl glycidal ethers; 2-ethylhexyl glycidyl ether; mixtures of Cu, Ci6, and Cis saturated carbon chains derived from tallow; and tall oil fatty acids.

   30
8. 8. A process according to any of claims 1 to 7, wherein the reagent is a mixture of reaction products.
9. 9. A process according to claim 8, wherein the reagent is a mixture that includes (Z)-N18403

   9-octadecenyl-l,3-propanediamîne and oleylamine.
10. 10. A process according to any of claims 1 to 9, wherein the reaction product of Reactant A and Reactant B is less soluble in an aqueous solution of the wet process phosphoric acid

    5 production stream than Reactant A alone.
11. 11. A process for inhibiting scale produced during wet process phosphoric acid production, the process comprising, adding a scale inhibiting amount of a reagent to at least one stage of the wet process 10 phosphoric acid production process, wherein the reagent comprises a compound comprising at least one amine portion having at least one primary amine; and at least one hydrocarbyl portion that is part of the backbone of the compound or a pendant group attached to the backbone and which includes a sufficient number of carbon atoms, or is multiply présent in sufficient number so as to reduce 15 the solubility of the compound in an aqueous solution of the wet process phosphoric acid production stream, with the proviso that the weight average molecular weight ofthe compound is < 1,000 Da, and that the reagent is substantially free of oil.

    20
12. 12. A process according to any of claims 1 to 11, wherein the reagent contains less than

    25 % oil by volume.
13. 13. A process according to claim 12, wherein the reagent contains less than 10 % oil by volume.
14. 14. A process according to claim 12, wherein the reagent is essentially oil free and contains less than 1 % of oil by volume.
15. 15. A process according to any of claims 11 to 14, wherein the amine portion of the

    30 compound is derived from a polyamine or a polyetheramine.
16. 16. A process according to claim 15, wherein the amine portion is a polyamine chosen from polyallylamine or polyvinylamine.
17. 17. A process according to any of claims 11 to 16, wherein the hydrocarbyl portion includes 1 to 22 carbon atoms, wherein one or more carbon atoms is optionally replaced by a hetero atom, and/or optionally substituted at one or more substitutable position with a substituent selected from the group consisting of OH; C1-C12 alkyl; C1-C12 alkenyl; allyl; halogen; C1-C12 haloalkyl; C1-C12 alkoxy; hydroxy C1-C12 alkyl; carboxy; C1-C12 alkoxycarbonyl; C1-C12 carboxyalkoxy; C1-C12 carboxamido; cyano; formyl; C1-C12 acyl; C2C12 alkyl ester or alkylhydroxy ester; C6-C12 aryl ester; nitro; amino; Ci-ualkylamino; C1-12 dialkylamino; anilino; mercapto; Ci-ualkylthio; sulfoxide; sulfone; C1-12 acylamino; amidino; aryloxy; arylamino; amido; epoxy; carbonyl; alkoxycarbonyl (ester); nitrile; ureido; silanol; phenyl; benzyl; heteroaryl; heterocycle; phenoxy; benzoyl; benzoyl substituted with amino, hydroxy, methoxy, methyl or halo; benzyloxy; and heteroaryloxy, provided that hydrocarbyl portion includes at least 4 carbon atoms.
18. 18. A process according to any of claims 11 to 15, wherein the compound is according to a formula selected from the group consisting of:

    i) Formula (IV):

    (IV), or salts thereof wherein each of R⁸ and R¹⁰ is independently chosen from H or a hydrocarbyl radical having 1 to 22 carbon atoms, wherein one or more carbon atoms is optionally replaced by a hetero atom, and/or optionally substituted at one or more substitutable position with a substituent selected from the group consisting of OH; C1-C12 alkyl; C1-C12 alkenyl; allyl; halogen; C1-C12 haloalkyl; C1-C12 alkoxy; hydroxy C1-C12 alkyl; carboxy; C1-C12 alkoxycarbonyl; C1-C12 carboxyalkoxy; C1-C12 carboxamido; cyano; formyl; C1-C12 acyl; C2-C12 alkyl ester or alkylhydroxy ester; C6-C12 aryl ester; nitro; amino; Ci-nalkylamino; C1-12 dialkylamino; anilino; mercapto; C1-12 alkylthio; sulfoxide; sulfone; C1-12 acylamino; amidino; aryloxy; arylamino; amido; epoxy; carbonyl; alkoxycarbonyl (ester); nitrile; ureido; silanol; phenyl; benzyl; heteroaryl;

    heterocycle; phenoxy; benzoyl; benzoyl substituted with amino, hydroxy, methoxy, methyl or halo; benzyloxy; and heteroaiyloxy;

    R⁹ is chosen from H or a Ci-Cô alkyl;

    L is an optionally substituted hydrocarbyl fragment having 1 to 20 carbon atoms;

    p is as defined for Formula (II); and t is an integer from 0 to 10, with the proviso that at least one of R⁸, R¹⁰, or L includes the hydrocarbyl portion of the compound that reduces solubility of the compound; or ii) Formula (V):

    (V), or salts thereof wherein

    R¹¹ is chosen from H or a hydrocarbyl radical having 1 to 22 carbon atoms, wherein one or more carbon atoms is optionally replaced by a hetero atom, and/or optionally substituted at one or more substitutable position with a substituent selected from the group consisting ofOH; C1-C12 alkyl; C1-C12 alkenyl; allyl; halogen; C1-C12 haloalkyl; C1-C12 alkoxy; hydroxy C1-C12 alkyl; carboxy; C1-C12 alkoxycarbonyl; C1-C12 carboxyalkoxy; C1-C12 carboxamido; cyano; formyl; C1-C12 acyl; C2-C12 alkyl ester or alkylhydroxy ester; C6-C12 aryl ester; nitro; amino; C1-12 alkylamino; Ci-udialkylamino; anilino; mercapto; C1-12 alkylthio; sulfoxide; sulfone; C1-12 acylamino; amidino; aryloxy; arylamino; amido; epoxy; carbonyl; alkoxycarbonyl (ester); nitrile; ureido; silanol; phenyl; benzyl; heteroaryl; heterocycle; phenoxy; benzoyl; benzoyl substituted with amino, hydroxy, methoxy, methyl or halo; benzyloxy; and heteroaryloxy;

    R¹² is chosen from H or a C1-C4 alkyl;

    Y is L as defined for Formula (IV); w is p as defined for Formula (II); and z is an integer from 1 to 10, with the proviso that at least one of R¹¹ or Y includes the hydrocarbyl portion of the compound that reduces solubil ity of the compound.
19. 19. A process according to any of claims 1 to 18, wherein the scale includes at least one

    5 species of scale-forming ion selected from the group consisting of NaiSiFô; K2S1F6; CaSÛ4+ 2 H2O; CaSÛ4 + V2 H2O; CaSCh; MgSiFô+ 6 H2O; Ca3(PO4)2î CaHPÛ4; S12F6; CaSiFô+ 2 H2O; CaF2î MgF2î Mgo.8Ali.5F6+X H2O, wherein X is an integer ranging from 2 to 10; MgffrPôCh; A1(PO₃)3; NaK₂AlF₆; Ca₃(AlF6)2+ 4 H2O; MgNaAlF₆+ 2 H2O; and Ca4SC>4AlSiFi3+ 10 H2O.
20. 20. A process according to any of claims 1 to 19, wherein said at least one stage of the phosphoric acid production process to which the reagent is added is selected from the group consisting of the milling stage; the digesting stage; the filtering stage; the évaporation stage; and the clarifying stage.
21. 21. A process according to claim 20, wherein the stage to which the reagent is added is the filtering stage, évaporation stage, or both.
22. 22. A process according to any one of claims 1 to 21, wherein the reagent is added to any

    20 of the interstitial piping or process fiow pipeline of the phosphoric acid production process.
23. 23. A process according to any of claims 1 to 22, wherein the scale-inhibiting amount of reagent added to the wet process phosphoric acid production process is from 0.5 g per ton to 5000 g per ton of phosphoric acid.
24. 24. A process according to claim 23, wherein the scale-inhibiting amount of reagent added to the wet process phosphoric acid production process is from 0.5 g per ton to 1000 g per ton of phosphoric acid.

    30 25. A process according to claim 24, wherein the scale-inhibiting amount of reagent added to the wet process phosphoric acid production process is from 1.0 g per ton to 500 g per ton of phosphoric acid.