Temperature-stable paraffin inhibitor compositions
US-2017292657-A1 · Oct 12, 2017 · US
US10889677B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10889677-B2 |
| Application number | US-201815879245-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 24, 2018 |
| Priority date | Jan 25, 2017 |
| Publication date | Jan 12, 2021 |
| Grant date | Jan 12, 2021 |
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This invention relates to compositions and a process for stabilizing or solubilize a phenolic resin containing a mixture of linear phenolic resins and calixarenes. The process comprises contacting the phenolic resin with an epoxide, to at least partially alkoxylate the phenolic hydroxyl groups of the calixarenes. This process forms a stabilized or solubilized phenolic resin with an increased solubility in a hydrocarbon solvent.
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We claim: 1. A resin solution of a phenolic resin, comprising one or more modified calixarene compounds, each calixarene compound comprising 4-20 units of formula (I′) and/or formula (II): wherein: each X is independently the same or different moiety, each moiety having a structure of each R 1 is independently a H, C 1 to C 30 alkyl, phenyl, or arylalkyl; each R 2 is independently a H, C 1 to C 20 branched or unbranched alkyl which may optionally be substituted with one or more glycidyl ether units of the formula C 2 to C 10 alkenyl, or C 5 to C 10 aryl; each L is independently selected from the group consisting of —CH 2 —, —C(O)—, —CH(R 3 )—, —(CH 2 ) n —O—(CH 2 ) n —, —C(R 3 ) 2 —, and —S—; each R 3 is independently a C 1 -C 6 alkyl; each m is independently an integer from 0 to 10; provided that when m is 0, each R 2 is independently a C 5 to C 10 aryl; each n is independently an integer from 1 to 2; each q is independently an integer from 1 to 100; each A 1 represents a direct covalent bond to an adjacent unit of formula (I′) or formula (II) such that there is one L group between adjacent units, whereby the total units in the calixarene compound form a ring; and wherein units of formula (I′) make up from about 35% to 100% of the overall units present in the calixarene compound, and wherein the phenolic resin is soluble in a hydrocarbon solvent having a concentration of about 50 wt % to about 75 wt %. 2. The resin solution of claim 1 , wherein each m is 0 or 1. 3. The resin solution of claim 2 , wherein each R 2 is independently selected from the group consisting of hydrogen, methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, allyl, ethylhexyl, octyl, nonyl, decyl, phenyl, nonylphenyl, and hexadecyl; or is independently a C 1 to C 20 branched or unbranched alkyl substituted with one or more glycidyl ether units of the formula 4. The resin solution of claim 3 , wherein each R 2 is n-butyl or 5. The resin solution of claim 2 , wherein each R 1 is independently a C 4 to C 12 alkyl or C 24 to C 28 alkyl. 6. The resin solution of claim 2 , wherein the total number of units in the calixarene compounds is from 4 to 8. 7. The resin solution of claim 1 , wherein q is 1 in one or more units in the modified calixarene compounds. 8. The resin solution of claim 1 , wherein the one or more modified calixarene compounds have one or more units of formula (I′) represented by the structure of wherein: each R 1 is independently a C 4 to C 12 alkyl; each L is independently selected from the group consisting of —CH 2 —, —C(O)—, —CH(R 3 )—, —(CH 2 ) n —O—(CH 2 ) n —, and —C(R 3 ) 2 —; each R 3 is independently a C 1 -C 6 alkyl; each n is independently an integer from 1 to 2; and the total number of units in the calixarene compounds is from 4 to 8. 9. The resin solution of claim 8 , wherein each R 1 is independently tert-butyl, nonyl, or tert-octyl. 10. The resin solution of claim 1 , wherein the hydrocarbon solvent is an aromatic hydrocarbon solvent selected from the group consisting of toluene, xylene, tetralin, a C 9 -C 10 aromatic hydrocarbon solvent, and a C 10 -C 12 aromatic hydrocarbon solvent. 11. A resin with an increased solubility in a hydrocarbon solvent, comprising one or more modified calixarene compounds, each calixarene compound comprising 4-20 units of formula (I′) and/or formula (II): wherein: each X is independently the same or different moiety, each moiety having a structure of each R 1 is independently a H, C 1 to C 30 alkyl, phenyl, or arylalkyl; each R 2 is independently a H, C 1 to C 20 branched or unbranched alkyl which may optionally be substituted with one or more glycidyl ether units of the formula C 2 to C 10 alkenyl, or C 5 to C 10 aryl; each L is independently selected from the group consisting of —CH 2 —, —C(O)—, —CH(R 3 )—, —(CH 2 ) n —O—(CH 2 ) n —, —C(R 3 ) 2 —, and —S—; each R 3 is independently a C 1 -C 6 alkyl; each m is independently an integer from 0 to 10; provided that when m is 0, each R 2 is independently a C 5 to C 10 aryl; each n is independently an integer from 1 to 2; each q is independently an integer from 1 to 100; each A 1 represents a direct covalent bond to an adjacent unit of formula (I′) or formula (II) such that there is one L group between adjacent units, whereby the total units in the calixarene compound form a ring; and wherein units of formula (I′) make up from about 35% to 100% of the overall units present in the calixarene compound, and wherein the solubility of the resin is increased by at least 20% compared to a resin comprising calixarene compounds containing units of formula (II) but no units of formula (I′). 12. A method of resolving a water-in-oil or oil-in-water emulsion, comprising: adding to a water-in-oil or oil-in-water emulsion an effective demulsifying amount of the resin solution of claim 1 .
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