WO2019055082A1 - LOW SODIUM SALT SUBSTITUTE COMPRISING POTASSIUM CHLORIDE - Google Patents

LOW SODIUM SALT SUBSTITUTE COMPRISING POTASSIUM CHLORIDE Download PDF

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Publication number
WO2019055082A1
WO2019055082A1 PCT/US2018/037857 US2018037857W WO2019055082A1 WO 2019055082 A1 WO2019055082 A1 WO 2019055082A1 US 2018037857 W US2018037857 W US 2018037857W WO 2019055082 A1 WO2019055082 A1 WO 2019055082A1
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WO
WIPO (PCT)
Prior art keywords
salt substitute
salt
precursor
acid
chloride
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2018/037857
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English (en)
French (fr)
Inventor
James S. Brophy
Frank E. Davis
Sambasiva Rao Chigurupati
Chris TROTTER
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S & P Ingredient Development LLC
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S & P Ingredient Development LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by S & P Ingredient Development LLC filed Critical S & P Ingredient Development LLC
Priority to MX2020002891A priority Critical patent/MX2020002891A/es
Priority to CN201880060235.6A priority patent/CN111093391A/zh
Priority to US16/347,288 priority patent/US11051539B2/en
Priority to JP2020515972A priority patent/JP7274462B2/ja
Priority to AU2018332654A priority patent/AU2018332654B2/en
Priority to CA3075623A priority patent/CA3075623C/en
Priority to ES18855922T priority patent/ES2995057T3/es
Priority to EP18855922.3A priority patent/EP3684196B1/en
Priority to PL18855922.3T priority patent/PL3684196T3/pl
Priority to BR112020005285-0A priority patent/BR112020005285B1/pt
Publication of WO2019055082A1 publication Critical patent/WO2019055082A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
    • A23L27/40—Table salts; Dietetic salt substitutes
    • A23L27/45—Salt substitutes completely devoid of sodium chloride
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
    • A23L29/294—Inorganic additives, e.g. silica
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
    • A23L27/40—Table salts; Dietetic salt substitutes
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/16—Inorganic salts, minerals or trace elements
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs

Definitions

  • the present disclosure is related to a low sodium salt substitute with potassium chloride.
  • Salt or sodium chloride (NaCl)
  • NaCl sodium chloride
  • salt substitutes there are a variety of salt substitutes on the market.
  • One approach to production of salt substitutes involves combining sodium and potassium salts, or occasionally magnesium salts, in various ratios and adding a wide variety of other additives to this mix.
  • the other additives are typically added to mask or at least partially reduce the metallic or bitter taste of potassium that has been
  • a salt substitute precursor includes a mixture of water, potassium chloride, a food grade acid, and an anticaking agent.
  • a pH of the salt substitute precursor is between 2 and 4, and the salt substitute precursor is a saturated or supersaturated solution, a suspension, or a slurry.
  • Implementations of the first general aspect may include one or more of the following features.
  • the food grade acid may be citric acid.
  • the anticaking agent may include at least one of sodium aluminosilicate, sodium ferrocyanide, potassium ferrocyanide, calcium carbonate, magnesium carbonate, tricalcium phosphate, and silicon dioxide.
  • the mixture may include sodium chloride.
  • the salt substitute precursor is a homogeneous solution.
  • a pH of the salt substitute precursor is typically in a range between 3 and 4.
  • the salt substitute precursor may include less than 80 wt% water, less than 70 wt% water, less than 65 wt% water, or less than 60 wt% water.
  • a salt substitute in a second general aspect, includes potassium chloride or solvated portions thereof, citric acid or solvated portions thereof, and an anticaking agent or solvated portions thereof.
  • the salt substitute includes at least 1 wt% citric acid.
  • Implementations of the second general aspect may include one or more of the following features.
  • the salt substitute may include at least 96 wt%, at least 97 wt%, at least 98 wt%, or less than 99 wt% potassium chloride.
  • the salt substitute may include 0.1 wt% to 2 wt% of the anticaking agent.
  • the salt substitute may include 0.1 wt% to 5 wt% citric acid.
  • the salt substitute may include sodium chloride.
  • making a salt substitute includes forming a salt substitute precursor including a mixture of water, potassium chloride, a food grade acid, and an anticaking agent.
  • a pH of the salt substitute precursor is between 2 and 4
  • the salt substitute precursor is a saturated or supersaturated solution, a suspension, or a slurry
  • a temperature of the salt substitute precursor is less than 240 °F.
  • the third general aspect further includes providing the salt substitute precursor to a centrifuge, and centrifuging the salt substitute precursor to yield a salt substitute in the form of a solid and a centrate.
  • Implementations of the third general aspect may include one or more of the following features.
  • the salt substitute may be a homogeneous composition.
  • the salt substitute may include less than 5 wt% water.
  • Some implementations include washing the salt substitute with the centrate and drying the salt substitute to yield a dried salt substitute, wherein the dried salt substitute comprises less than 1.5 wt% water.
  • a salt substitute precursor includes water, a chloride salt, a food grade acid, and an anticaking agent.
  • the chloride salt includes potassium chloride.
  • a pH of the salt substitute precursor is between 2 and 4, and the salt substitute precursor is a saturated or supersaturated solution, a suspension, or a slurry.
  • Implementations of the fourth general aspect may include one or more of the following features.
  • the food grade acid may include at least one of acetic acid, ascorbic acid, benzoic acid, citric acid, fumaric acid, lactic acid, malic acid, tartaric acid, lemon juice, hydrochloric acid, and phosphoric acid.
  • the anticaking agent may include at least one of sodium aluminosilicate, sodium ferrocyanide, potassium ferrocyanide, calcium carbonate, magnesium carbonate, tricalcium phosphate, and silicon dioxide.
  • the chloride salt may further include sodium chloride.
  • the salt substitute precursor is typically free of a carrier.
  • a pH of the salt substitute precursor is typically between 3 and 4.
  • the salt substitute precursor is a homogeneous solution. Water may comprise less than 80 wt%, less than 70 wt%, less than 50 wt%, or less than 25 wt% of the salt substitute precursor.
  • a salt substitute in a fifth general aspect, includes a chloride salt, a food grade acid, and an anticaking agent.
  • the salt substitute includes potassium chloride, and is in the form of a crystalline solid including at least 95 wt% of the chloride salt, up to 1 wt% of the food grade acid, and up to 1 wt% of the anticaking agent.
  • Implementations of the fifth general aspect may include one or more of the following features.
  • the salt substitute includes at least 98 wt% of the chloride salt, up to 1 wt% of the food grade acid, and up to 1 wt% of the anticaking agent.
  • the salt substitute includes at least 99 wt% of the chloride salt, up to 0.1 wt% of the food grade acid; and up to 0.1 wt% of the anticaking agent.
  • the chloride salt includes at least 99 wt% potassium chloride.
  • the chloride salt further includes sodium chloride, and the salt substitute is in the form of a particulate combined crystalline solid, where each particle of the combined crystalline solid includes a region consisting essentially of potassium chloride in direct contact with a region consisting essentially of sodium chloride.
  • the chloride salt includes 1 wt% to 90 wt% sodium chloride and 10 wt% to 99 wt% potassium chloride.
  • the food grade acid may include at least one of acetic acid, ascorbic acid, benzoic acid, citric acid, fumaric acid, lactic acid, malic acid, tartaric acid, succinic acid, lemon juice, hydrochloric acid, and phosphoric acid.
  • the salt substitute includes at least 0.01 wt% of the food grade acid (e.g., 0.01 wt% to 0.5 wt% of the food grade acid, or 0.01 wt% to 0.1 wt% of the food grade acid).
  • the anticaking agent typically includes at least one of sodium aluminosilicate, sodium ferrocyanide, potassium ferrocyanide, calcium carbonate, magnesium carbonate, tricalcium phosphate, and silicon dioxide.
  • the salt substitute may include at least 0.001 wt% or at least 0.01 wt% of the anticaking agent.
  • An aqueous solution formed by dissolving the salt substitute in water having a pH of 7 yields a solution having a pH between 4 and 5.
  • the salt substitute is substantially free of a metallic taste.
  • making a salt substitute includes forming a salt substitute precursor, providing the salt substitute precursor to a centrifuge, and centrifuging the salt substitute precursor to yield a salt substitute in the form of a solid and a centrate.
  • the salt substitute precursor includes a mixture of water, a chloride salt, a food grade acid, and an anticaking agent.
  • the chloride salt includes potassium chloride.
  • the salt substitute precursor is a saturated or supersaturated solution, a suspension, or a slurry, and a pH of the salt substitute precursor is between 2 and 5.
  • Implementations of the sixth general aspect may include one or more of the following features.
  • the salt substitute may be washed with the centrate.
  • the chloride salt may further include sodium chloride.
  • the salt substitute is typically in the form of a combined crystalline solid including particles, wherein each particle of the combined crystalline solid includes a region consisting essentially of potassium chloride in direct contact with a region consisting essentially of sodium chloride.
  • a temperature of the salt substitute precursor provided to the centrifuge is typically less than 240 °F.
  • a pH of the salt substitute precursor is typically between 2 and 4.
  • FIG. 1 is a flowchart showing a process for preparing a salt substitute with potassium.
  • FIGS. 2A and 2B show energy dispersive X-ray spectroscopy (EDS) and scanning electron microscopy (SEM) images, respectively, of the salt substitute prepared as described in Example 1.
  • EDS energy dispersive X-ray spectroscopy
  • SEM scanning electron microscopy
  • FIGS. 3A and 3B show EDS and SEM images, respectively, of the salt substitute prepared as described in Example 2.
  • FIGS. 4A and 4B show EDS and SEM images, respectively, of the comparative salt substitute prepared as described in Comparative Example 1.
  • FIG. 1 shows process 100 for preparing a salt substitute with potassium.
  • a salt substitute precursor is formed.
  • the salt substitute precursor includes water, a chloride salt, a food grade acid, and an anticaking agent.
  • the chloride salt includes potassium chloride, and may also include sodium chloride.
  • the salt substitute precursor may be formed by combining components including water, a chloride salt, a food grade acid, and an anticaking agent.
  • Suitable food grade acids include organic acids and mineral acids. Examples of suitable organic food grade acids include acetic acid, ascorbic acid, benzoic acid, citric acid, fumaric acid, lactic acid, succinic acid, malic acid, tartaric acid, and compositions such as lemon juice that include one or more organic acids. Examples of suitable mineral acids include hydrochloric acid and phosphoric acid.
  • Suitable anticaking agents include sodium aluminosilicate, sodium ferrocyanide, potassium ferrocyanide, calcium carbonate, magnesium carbonate, tricalcium carbonate, and silicon dioxide.
  • the salt substitute precursor consists of or consists essentially of a mixture of water, potassium chloride, a food grade acid, and an anticaking agent.
  • these components make up at least 99 wt% of the salt substitute precursor.
  • the salt substitute precursor includes sodium, and the salt substitute precursor is formed by combining sodium chloride with other salt substitute precursor components.
  • the salt substitute precursor consists of or consists essentially of a mixture of water, potassium chloride, sodium chloride, a food grade acid, and an anticaking agent.
  • the salt substitute precursor is free or substantially free of a carrier.
  • carrier generally refers cereal flours or starches (such as wheat flour and rice flour), fruit flour or starches (such as banana flour), root flours or starches (such as potato flour and tapioca flour),
  • the salt substitute precursor may include one or more additional components, such as one or more mineral salts.
  • suitable mineral salts include magnesium chloride and calcium chloride.
  • Forming the salt substitute precursor includes mixing the components of the salt substitute precursor to yield a homogenous solution or a mixture including suspended solids. Mixing the components of the salt substitute precursor may occur at any temperature above a freezing point and below a boiling point of the salt substitute precursor. In some cases, mixing the components of the salt substitute precursor occurs at a temperature between ambient temperature and 240 °F. In some examples, mixing the components of the salt substitute precursor occurs at a temperature between 20 °F and 240 °F, between 80 °F and 180 °F, or between 100 °F and 160 °F
  • Forming the salt substitute precursor typically includes heating the components of the salt substitute precursor.
  • the salt substitute precursor may be heated to a boiling temperature of the salt substitute precursor. In some cases, the salt substitute precursor is heated to a temperature of at least 50 °F or at least 120 °F. In certain cases, the salt substitute precursor is heated to a temperature of at least 140 °F, at least 160 °F, or at least 240 °F.
  • the salt substitute precursor may be heated to a temperature suitable to achieve a total dissolved and suspended solids content of 25 wt% to 50 wt%, 20 wt% to 80 wt%, 40 wt% to 80 wt%, or 45 wt% to 75 wt% total solids.
  • Mixing the salt substitute precursor, heating the salt substitute precursor, or mixing and heating the salt substitute precursor typically occurs for a length of time sufficient to form a homogenous solution, a suspension, or a slurry.
  • the salt substitute precursor is heated and mixed for a length of time in a range between 1 and 100 minutes, between 10 and 90 minutes, between 15 minutes and 80 minutes, between 20 minutes or 40 minutes, or between 20 minutes and 60 minutes.
  • the salt substitute precursor may include 0.1 wt% to 5 wt%, 0.1 wt% to 4 wt%, 0.1 wt% to 3 wt%, 0.1 wt% to 2 wt%, or 0.1 wt% to 1 wt% food grade acid.
  • the salt substitute precursor includes 0.1 wt% to 5 wt%, 0.1 wt% to 4 wt%, 0.1 wt% to 3 wt%, 0.1 wt% to 2 wt%, or 0.1 wt% to 1 wt% anticaking agent.
  • a pH of the salt substitute precursor may be less than 7, less than 6, less than 5, or less than 4. In some cases, a pH of the salt substitute precursor is between 2 and 4, between 2 and 5, between 3 and 6, between 4 and 6, between 3 and 5, between 3.5 and 5.5, between 3 and 4, or between 4 and 5.
  • the salt substitute precursor may be a homogeneous solution, or may include suspended solids. In some cases, the salt substitute precursor is a saturated or supersaturated solution. In one example, the solids content of the salt substitute precursor exceeds the saturation point by at least 10 wt%.
  • the salt substitute precursor may include 20 wt% to 80 wt%, 40 wt% to 80 wt%, or 45 wt% to 75 wt% total solids.
  • the salt substitute precursor includes 30 to 45 wt% total solids.
  • the salt substitute precursor typically includes less than 80 wt% water.
  • the salt substitute precursor includes less than 75 wt%, less than 70 wt%, less than 65 wt%, or less than 60 wt% water.
  • the salt substitute precursor includes 5 wt% to 25 wt% water.
  • a salt substitute precursor including, consisting of, or consisting essentially of a mixture of water, potassium chloride, a food grade acid, and an anticaking agent
  • suitable amounts of these components include 20 wt% to 75 wt% water, 20 wt% to 75 wt% potassium chloride, 0.1 wt% to 5 wt% food grade acid, and 0.1 wt% to 5 wt% anticaking agent.
  • embodiments include all combinations of various component ranges disclosed herein.
  • a salt substitute precursor including, consisting of, or consisting essentially of a mixture of water, potassium chloride, sodium chloride, a food grade acid, and an anticaking agent
  • suitable amounts of these components include 20 wt% to 95 wt% water, 2 wt% to 75 wt% potassium chloride, 2 wt% to 75 wt% sodium chloride, 0.1 wt% to 5 wt% food grade acid, and 0.1 wt% to 5 wt% anticaking agent.
  • embodiments include all combinations of various component ranges disclosed herein.
  • the salt substitute precursor from 102 is centrifuged to yield a centrate and a salt substitute in the form of a solid.
  • the salt substitute precursor may be provided to the centrifuge continuously or intermittently via a conduit.
  • a temperature of the salt substitute precursor provided to the centrifuge is typically above 20 °F and up to 240 °F. In some cases, the salt substitute precursor is at ambient temperature before centrifuging.
  • Suitable centrifuges include but are not limited to pusher centrifuges, disc stack centrifuges, decanter centrifuges, and basket centrifuges.
  • the salt substitute may be in the form of a solid cake or in particulate form.
  • the salt substitute typically includes at least 90 wt% total solids or at least 99 wt% total solids. In some cases, the salt substitute includes 90 wt% to 95 wt% total solids.
  • a water content of the salt substitute is typically less than 10 wt%, less than 5 wt%, or less than 2 wt%.
  • the salt substitute with less than 10 wt%, less than 5 wt%, or less than 2 wt% water can be prepared from the salt substitute precursor without the addition of heat to remove the water.
  • the centrate from 104 typically has a solids content between 20 wt% and 50 wt%, or between 30 wt% and 40 wt%.
  • a pH of the centrate is typically in a range between 2 and 4 or between 2 and 5, for example, between 2 and 3, or between 3 and 4.
  • the salt substitute is washed. Washing the salt substitute typically includes contacting the salt substitute with a wash liquid including water, with or without one or more other solvents.
  • the wash liquid may include one or more additives.
  • the wash liquid includes a food grade acid, such as citric acid.
  • the centrate is collected and used as the wash liquid.
  • salt substitute precursor components remaining in the centrate may be added to the salt substitute, thereby increasing recovery of the components in the salt substitute precursor.
  • the salt substitute formed during 104 may be washed while the salt substitute is being formed. That is, 104 and 106 may occur at the same time.
  • the salt substitute is dried to yield a dry salt substitute.
  • Drying the salt substitute may include heating the salt substitute to reduce a water content of the salt substitute to less than 5 wt%, less than 4 wt%, less than 3 wt%, less than 2 wt%, or less than 1 wt%.
  • suitable dryers include fluid bed dryers, rotary dryers, flash dryers, belt dryers, microwave dryers, and tray dryers.
  • the salt substitute is milled. Milling may include forming particles or reducing a particle size of the salt substitute.
  • the salt substitute is sifted.
  • the salt substitute is packaged.
  • the salt substitute is in crystalline form.
  • the salt substitute includes, consists of, or consists essentially of a chloride salt, a food grade acid, and an anti caking agent.
  • the salt substitute may be a chemically homogeneous composition that includes, consists of, or consists essentially of potassium chloride or ionic components thereof (e.g., potassium ions and chloride ions), citric acid or ionic components thereof (e.g., citrate and hydrogen ions), and an anticaking agent or ionic components thereof (e.g., anions, cations, conjugate acids, or conjugate bases of the anticaking agent).
  • the salt substitute includes, consists of, or consists essentially of potassium chloride or ionic components thereof, sodium chloride or ionic components thereof (e.g., sodium ions and chloride ions), citric acid or ionic components thereof, and an anticaking agent or ionic components thereof.
  • the salt substitute is typically a combined crystalline solid in the form of particles, where each particle includes a region consisting of or consisting essentially of potassium chloride in direct contact with a region consisting of or consisting essentially of sodium chloride.
  • a component is understood to include its ionic and nonionic forms.
  • potassium chloride is understood to include any combination of potassium chloride, potassium ions, and chloride ions
  • citric acid is understood to include any combination of citric acid and its conjugate base(s) (e.g., citrate) and hydrogen or hydronium ions
  • sodium chloride is understood to include any combination of sodium chloride, sodium ions, and chloride ions
  • antagonisticaking agent is understood to include any combination of the anticaking agent, and its nonionic and ionic forms, including its conjugate acid(s), base(s), or both.
  • the salt substitute includes at least 1 wt% citric acid. In one example, the salt substitute includes 0.8 wt% to 5 wt% citric acid. In some examples, the salt substitute includes 0.01 wt% to 2 wt%, 0.01 wt% to 1 wt%, 0.01 wt% to 0.5 wt%, 0.01 wt% to 0.4 wt%, 0.01 wt% to 0.3 wt%, 0.01 wt% to 0.2 wt%, or 0.01 wt% to 0.1 wt% citric acid.
  • the salt substitute includes at least 96 wt%, at least 98 wt%, or at least 99 wt% potassium chloride.
  • the salt substitute may include 0.1 wt% to 1 wt%, 0.1 wt% to 2 wt%, 0.1 wt% to 3 wt%, 0.1 wt% to 4 wt%, or 0.1 wt% to 5 wt% of the anticaking agent.
  • the salt substitute includes, consists of, or consists essentially of potassium chloride, food grade acid, an anticaking agent, and sodium chloride.
  • the salt substitute typically includes up to 1 wt% or up to 0.1 wt% food grade acid.
  • up to refers to "up to and including.”
  • up to 0.1 wt% includes values of 0.1 wt% and less.
  • the salt substitute can include up to 0.1 wt%, up to 0.2 wt%, up to 0.3 wt%, up to 0.4 wt%, up to 0.5 wt%, up to 1 wt%, or up to 2 wt% food grade acid.
  • an amount of food grade acid in the salt substitute is 10% or less or 5% or less of the food grade acid in the salt substitute precursor.
  • the chloride salt may include 10 wt% to 99 wt% potassium chloride and 1 wt% to 90 wt% sodium chloride, or 20 wt% to 99 wt% potassium chloride and 0 wt% to 80 wt% sodium chloride.
  • the salt substitute may include 0.1 wt% to 5 wt% of the anticaking agent.
  • the salt substitute typically has a particle size in a range of 25 ⁇ to 1000 ⁇ . The particle size can be adjusted by altering processing conditions or milling the salt substitute to achieve a size desired for an intended application.
  • a density of the salt substitute is typically in a range between 58 pounds/cubic foot (0.8 grams/cubic centimeter) and 72 pounds/cubic foot (1.2 grams/cubic centimeter).
  • the salt substitute when dissolved in water having a pH of 7, typically yields a solution having a pH between 2 and 5, between 3 and 5, or between 4 and 5.
  • one or more of the operations in FIG. 1 may be omitted. That is, one or more of the operations in FIG. 1 may be optional. In some examples, 1 10, 1 12, 1 14, or any combination thereof may be omitted. In certain cases, one or more of the operations depicted in FIG. 1 is replaced or combined with another operation, the order of one or more the operations is interchanged, two or more operations occur simultaneously or continuously, an additional operation is added, or any combination thereof.
  • the salt substitute described herein may be used as a substitute for salt (i.e., sodium chloride), or in addition to or blended with sodium chloride.
  • the salt substitute is advantageously substantially free of a metallic taste.
  • the salt substitute described herein may be used in a variety of applications as table salt, inclusion in processed foods such as snack foods, baked goods, to season meats and poultries, and for other food items that have included salt.
  • Example 1 In this example, 121 gallons of water was added to a batching tank. The water was 180.0 °F when added. 500 pounds of potassium chloride was added to the water to yield a slurry. 2.5 pounds of magnesium carbonate was added to the slurry. 8.0 pounds of citric acid was added to the slurry. The pH was tested to be 3.79. The slurry was held for 1 hour, during which time the temperature fell to between 110 °F and 120 °F. After 1 hour hold time, 500 pounds of sodium chloride was added to the slurry, and the pH was retested and found to be 3.40. The slurry was 51.30 wt% solids. The slurry was then provided to a pusher centrifuge (BP Littleford, Model S-200 Centrifuge) and dried.
  • BP Littleford, Model S-200 Centrifuge BP Littleford, Model S-200 Centrifuge
  • FIGS. 2A and 2B show energy dispersive X-ray spectroscopy (EDS) and scanning electron microscopy (SEM) images, respectively, of the salt substitute of Example 1.
  • the salt substitute is in the form of a combined crystalline solid comprising particles 200.
  • red portions 202 of particles 200 correspond to potassium
  • green portions 204 of particles 200 correspond to sodium.
  • particles 200 include regions 202 consisting essentially of potassium chloride and regions 204 consisting essentially of sodium chloride, with regions 202 and 204 in direct contact.
  • the scale bars in FIGS. 2A and 2B are 100 ⁇ and 500 ⁇ , respectively.
  • the magnification in FIG. 2B is 150x.
  • Example 2 In this example, 121 gallons of water was added to a batching tank. The water was 177.4 °F when added. 500 pounds of potassium chloride, which included 0.005 wt% or 2.5 pounds of magnesium carbonate, was added to the water to yield a slurry. 8.0 pounds of citric acid was added to the slurry. The pH was tested to be 2.98. The slurry was held for 1 hour, during which time the temperature fell to 1 18 °F. After 1 hour hold time, 500 pounds of sodium chloride was added to the slurry, and the pH was retested and found to be 2.64. The slurry was 53.78 wt% solids. The slurry was then provided to a pusher centrifuge (BP Littleford, Model S-200
  • FIGS. 3A and 3B show EDS and SEM images, respectively, of the salt substitute of Example 2.
  • the salt substitute is in the form of a combined crystalline solid comprising particles 200.
  • red portions 302 of particles 300 correspond to potassium
  • green portions 304 of particles 300 correspond to sodium.
  • particles 300 include regions 302 consisting essentially of potassium chloride and regions 304 consisting essentially of sodium chloride, with regions 302 and 304 in direct contact.
  • the scale bars in FIGS. 3A and 3B are 100 ⁇ and 500 ⁇ , respectively.
  • the magnification in FIG. 3B is 150x.
  • Example 3 In this example, 665 lbs of potassium chloride, 3.325 lbs of magnesium carbonate, and 6.65 lbs of citric acid were mixed in 766 lbs of water and blended at 120 °F to yield a slurry.
  • the slurry contained 46.8% solids, and the pH was 3.25.
  • the slurry was held in suspension by tank agitation.
  • the slurry was fed to a pusher centrifuge at 216.2 lb/min, and a solid cake was created at 52.2 lb/min and 2.5 wt% moisture. The cake was further dried in an infrared oven to reduce the moisture content to less than 1 wt%.
  • the salt substitute was sampled for taste, and reflected a clean profile with little to no metallic aftertaste.
  • Example 4 In this example, 325 lbs of potassium chloride, 325 lbs of sodium chloride, 3.25 lbs of magnesium carbonate, and 6.5 lbs of citric acid were mixed in 766 lbs of water and blended at 120 °F.
  • the slurry contained 46.3 wt% solids, and the pH was 3.2.
  • the slurry was held in suspension by tank agitation.
  • the slurry feed rate to the pusher centrifuge was 171.2 lb/min, and a solid cake was created at 49 lb/min at 2.89% moisture.
  • the cake was further dried in an infrared oven to reduce the moisture content to less than 1 wt%.
  • the salt substitute was sampled for taste, and reflected a clean profile with little to no metallic aftertaste.
  • Table 1 A lists components used to prepare Salt Substitutes A-O, as well as properties of the salt substitute precursor, the salt substitute, and the centrate.
  • Examples 1 and 2 correspond to Tests D and E, respectively, in Table 1.
  • Table IB lists components used to prepare Salt Substitutes P-U, as well as properties of the salt substitute precursor, the salt substitute, and the centrate.
  • the procedure used to prepare Salt Substitutes A-U generally corresponds to procedures described in Examples 1-4.
  • Salt Substitutes A-O the salt substitute precursor was held for 1 hour between 105 °F and 125 °F before centrifugation.
  • Salt Substitutes L1-L3 differed by the temperature of the slurry provided to the centrifuge, with temperatures of 75 °F, 85 °F and 95 °F, respectively.
  • Salt Substitutes P1-P9 differed by the length of the hold time in the slurry before centrifugation.
  • the amount of citric acid (i.e., citric acid plus citrate) in Salt Substitutes N, O, and S was measured three times, with the average result being 400 ppm by weight (0.04 wt%), 1003 ppm by weight (0.10 wt%), and 684 ppm (0.07 wt%), respectively.
  • Table 2 lists RO-TAP test results (particle size distribution by weight in US20-US200 Mesh) for 100 grams of Salt Substitutes M and O.
  • Table 3 lists RO-TAP test results (particle size distribution by weight in US20-US400 Mesh) for 100 grams of Salt Substitutes P-T.
  • Table 4 lists average bulk density (tapped and untapped) for 100 g of Salt Substitutes P-T in g/cm 3 and lb/ft 3 .
  • the bulk density ranges from about 60 lb/ft 3 to about 80 lb/ft 3 (tapped and untapped) for these samples, which is similar to the reported ranges of various types of commercially available sodium chloride.
  • Comparative Example 1 Water (35 pounds, 15.9 kg) was heated to 180 °F (82 °C) in a stirred, jacketed kettle. To the heated water, potassium chloride (6 pounds, 2.7 kg) and sodium chloride (9 pounds, 4.1 kg) were added, stirred, and dissolved. Next, citric acid (0.22 pounds, 100 g) was added followed by the slow addition of maltodextrin (6 pounds, 2.7 kg) in small amounts, which dissolved slowly into the solution. The pH of the formulation was measured at 2.16. The completed solution was then transferred to a stainless steel vessel, through which it was pumped into the spray dryer. The spray-dried formulation was packed and stored in plastic, resealable bags.
  • FIGS. 4A and 4B show EDS and SEM images, respectively, of the salt substitute of Comparative Example 1.
  • the salt substitute is in the form of
  • homogenous particles 400 where red portions of particles 400 correspond to potassium, and green portions of particles 400 correspond to sodium.
  • Particles 400 do not include regions consisting essentially of potassium chloride and regions consisting essentially of sodium chloride in direct contact.
  • the scale bars in FIGS. 4A and 4B are 90 ⁇ and 200 ⁇ , respectively.
  • the magnification in FIG. 4B is 150x.

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PCT/US2018/037857 2017-09-18 2018-06-15 LOW SODIUM SALT SUBSTITUTE COMPRISING POTASSIUM CHLORIDE Ceased WO2019055082A1 (en)

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MX2020002891A MX2020002891A (es) 2017-09-18 2018-06-15 Sustituto de sal bajo en sodio con cloruro de potasio.
CN201880060235.6A CN111093391A (zh) 2017-09-18 2018-06-15 含氯化钾的低钠食盐代用品
US16/347,288 US11051539B2 (en) 2017-09-18 2018-06-15 Low sodium salt substitute with potassium chloride
JP2020515972A JP7274462B2 (ja) 2017-09-18 2018-06-15 塩化カリウムを有する低ナトリウム塩代替物
AU2018332654A AU2018332654B2 (en) 2017-09-18 2018-06-15 Low sodium salt substitute with potassium chloride
CA3075623A CA3075623C (en) 2017-09-18 2018-06-15 Low sodium salt substitute with potassium chloride
ES18855922T ES2995057T3 (en) 2017-09-18 2018-06-15 Low sodium salt substitute with potassium chloride
EP18855922.3A EP3684196B1 (en) 2017-09-18 2018-06-15 Low sodium salt substitute with potassium chloride
PL18855922.3T PL3684196T3 (pl) 2017-09-18 2018-06-15 Niskosodowy substytut soli z chlorkiem potasu
BR112020005285-0A BR112020005285B1 (pt) 2017-09-18 2018-06-15 Precursor de substituto de sal e método para produzir substituto de sal

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021175658A1 (en) * 2020-03-03 2021-09-10 Omya International Ag Anticaking agent

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117122040A (zh) * 2023-08-15 2023-11-28 中盐安徽润华强旺盐业有限公司 鲜咸合一低钠调味盐及其制备方法
GB2635182A (en) * 2023-11-01 2025-05-07 Frito Lay Trading Co Gmbh Salt substitute compositions

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US82A (en) 1836-11-17 Spiral bit with countersink for setting screws
US3505A (en) 1844-03-26 Mill-btjsh
EP0124254A1 (en) 1983-03-30 1984-11-07 NABISCO BRANDS, Inc. Salt substitute composition
US5626904A (en) * 1992-03-19 1997-05-06 Hitavejta Sudurnesja Salt product and a method for the preparation thereof
US20030143152A1 (en) * 2002-01-31 2003-07-31 Vohra Rajinder Nath Process for recovery of low sodium salt from bittern
US20040047976A1 (en) * 2000-08-14 2004-03-11 Narayan Anantha Subramony Granulation process
US20130243924A1 (en) * 2005-09-14 2013-09-19 Pratik N. Bhandari Low Sodium Salt Composition
US20140044846A1 (en) 2006-10-05 2014-02-13 S & P Ingredient Development, Llc Low sodium salt composition
US20140255589A1 (en) 2012-11-21 2014-09-11 S&P Ingredient Development Llc Compositions of low sodium salt and methods of making and using
US20150056338A1 (en) * 2013-08-20 2015-02-26 S&P Ingredient Development Llc Salt compositions and methods of making and using
US9247762B1 (en) * 2014-09-09 2016-02-02 S & P Ingredient Development, Llc Salt substitute with plant tissue carrier

Family Cites Families (176)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB312088A (en) 1928-05-19 1930-05-08 Chemisch Pharmazeutische Ag Ba A process for preparing substitutes for table salt suitable for flavouring purposes
US1874055A (en) 1928-05-19 1932-08-30 Firm Chemisch Pharmazeutische Process for preparing suitable substitutes for table salt for flavoring purposes
US1978040A (en) 1931-09-14 1934-10-23 Firm Daitz Patents Foundation Process for maintaining the sprinkling capability of finely granular table salt
US2500919A (en) 1948-12-03 1950-03-21 Louis Milani Foods Inc Sodium-free flavoring compositions
US2601112A (en) 1950-03-31 1952-06-17 Us Vitamin Corp Saline composition
US2596333A (en) 1951-04-03 1952-05-13 Fougera & Co Inc E Dietary salt substitute
GB713803A (en) 1951-04-03 1954-08-18 Fougera & Co Inc E Dietary salt substitute
US2742366A (en) 1952-10-18 1956-04-17 Little Inc A Salt substitute and method of preparing the same
US2829056A (en) 1956-01-24 1958-04-01 Mead Johnson & Co Dietary seasoning composition
US2824008A (en) 1956-03-12 1958-02-18 Giulio C Perri Salt substitute
US2874027A (en) 1956-05-07 1959-02-17 Int Minerals & Chem Corp Preparation of alkali metal phosphates
US2900268A (en) 1956-11-15 1959-08-18 John C Rankin Process for preparing hydroxyalkylated cereal flour
US2968566A (en) 1959-01-07 1961-01-17 Pharmacodynamics Inc Composition useful with comestibles
GB911130A (en) 1959-11-10 1962-11-21 Dominion Tar & Chemical Co Salt production
US3514296A (en) 1967-01-16 1970-05-26 Morton Int Inc Salt substitute
US3505082A (en) * 1967-06-12 1970-04-07 Morton Int Inc Salt substitute composition
US3860732A (en) 1970-03-30 1975-01-14 Cumberland Packing Corp Salt substitute
US3782974A (en) 1971-08-02 1974-01-01 J Lontz Dietetic salt substitute composition
FR2196151A1 (en) 1972-08-18 1974-03-15 Grimberg George Dietetic sodium-free salt mixture - for use by patients with renal insuffic--iency or hypertension
IL45392A (en) 1974-08-02 1977-07-31 Cumberland Packing Corp Table salt substitute
US4076846A (en) 1974-11-22 1978-02-28 Sumitomo Bakelite Company Limited Protein-starch binary molding composition and shaped articles obtained therefor
US4066799A (en) 1975-12-22 1978-01-03 Miles Laboratories, Inc. Sodium chloride flavor substitute composition and use thereof
US4068006A (en) 1976-10-07 1978-01-10 Akzona Incorporated Salt seasoning mixture
US4216244A (en) 1978-09-19 1980-08-05 Allen Alfred E Jr Low sodium salt seasoning
US4243691A (en) 1979-05-18 1981-01-06 The Procter & Gamble Company Sodium-free salt substitute
US4297375A (en) 1979-09-21 1981-10-27 Standard Oil Company (Indiana) Salt substitutes having reduced bitterness
DE3021298A1 (de) 1980-06-06 1982-01-07 Basf Ag, 6700 Ludwigshafen Streng natriumarmes diaetsalz und dessen herstellung
US4293535A (en) 1980-08-22 1981-10-06 General Electric Company Molten salt synthesis of alkaline zirconate powder
DE3107800A1 (de) 1981-02-28 1982-09-16 Merck Patent Gmbh, 6100 Darmstadt Salzgemisch, verfahren zu seiner herstellung und verwendung
JPS57186460A (en) 1981-05-14 1982-11-16 Tanpei Seiyaku Kk Low sodium salt substitute and food containing the same
WO1983000081A1 (en) 1981-07-13 1983-01-20 Stuart Mccornack Oliver Flavoring system for sodium reduced foods
CA1155330A (en) 1981-10-20 1983-10-18 John R. Shackelford Salt substitutes having reduced bitterness
US4473595A (en) 1982-01-04 1984-09-25 Rood Robert P Low-sodium salt substitute
US5064663A (en) 1982-08-23 1991-11-12 Burns Philp Food, Inc. Sodium chloride substitute containing autolyzed yeast and ammonium chloride
US4451494A (en) 1982-09-10 1984-05-29 Roan Iii Charles F Sodium-free salt substitute
US4556567A (en) 1983-06-30 1985-12-03 Mallinckrodt, Inc. Salt substitute containing potassium chloride coated with maltodextrin and method of preparation
US4556568A (en) 1983-06-30 1985-12-03 Mallinckrodt, Inc. Salt substitute containing potassium chloride coated with a mixture including maltodextrin and potassium bitartrate and method of preparation
US4556577A (en) 1983-06-30 1985-12-03 Mallinckrodt, Inc. Admixture of potassium chloride and maltodextrin as salt substitute and method of preparation
US4560574A (en) 1983-06-30 1985-12-24 Mallinckrodt, Inc. Salt substitute containing potassium chloride, maltodextrin and sodium chloride and method of preparation
US4556566A (en) 1983-06-30 1985-12-03 Mallinckrodt, Inc. Salt substitute containing potassium chloride coated with a mixture of maltodextrin and sodium chloride and method of preparation
DE3466466D1 (en) 1983-06-30 1987-11-05 Mallinckrodt Inc Salt substitute blends of potassium chloride and maltodextrin and method of preparation
US4556578A (en) 1983-06-30 1985-12-03 Mallinckrodt, Inc. NaCl-Free salt substitute containing potassium chloride, maltodextrin and potassium bitartrate and method of preparation
US4486456A (en) 1983-09-19 1984-12-04 Thompson Jerome B Sodium-reduced baked dough products and method
FI834309A7 (fi) 1983-11-24 1985-05-25 Pharmaconsult Oy Suolaseos.
DK148784D0 (da) 1984-02-29 1984-02-29 Nexus Aps Pulverprodukt
DE3418644A1 (de) 1984-05-18 1985-11-28 Diamalt AG, 8000 München Natriumarmes, als kochsalzsubstitut geeignetes salzgemisch
GB8507977D0 (en) * 1985-03-27 1985-05-01 Howard Foundation Culinary seasoning compositions
GR861162B (en) 1985-05-06 1986-09-01 Unilever Nv Improved protein hydrolysate
DE3541802A1 (de) 1985-11-22 1987-05-27 Diamalt Ag Diaetetische speisewuerze
US4734290A (en) 1985-12-12 1988-03-29 Mallinckrodt, Inc. Process for preparing a coated-particle salt substitute composition
JPH0622458B2 (ja) 1986-01-18 1994-03-30 株式会社味食研 食塩代用品
SU1375237A1 (ru) 1986-04-18 1988-02-23 Ивановский государственный медицинский институт им.А.С.Бубнова Заменитель поваренной соли,обладающий антигипертензивным действием
DK273888A (da) 1987-05-20 1988-11-21 Chugai Pharmaceutical Co Ltd Salterstatning og krydderier med et indhold deraf
SE465669B (sv) 1988-07-15 1991-10-14 Hanson & Moehring Ab Salt foer livsmedelsaendamaal samt foerfarande foer dess framstaellning
US5034378A (en) 1988-12-15 1991-07-23 James P. Cox Synergistic flavor enhancement nutritional compositions and methods
US5094862A (en) 1989-08-25 1992-03-10 Warner-Lambert Company Salt substitute granule and method of making same
AT403237B (de) 1989-09-08 1997-12-29 Salinen Austria Ges M B H Natriumreduziertes speisesalz
US5098723A (en) 1989-09-15 1992-03-24 Dubois Grant E Low sodium salt composition and method of preparing
US5098724A (en) 1989-09-15 1992-03-24 Dubois Grant E Low sodium salt composition and method of preparing
GB2237720B (en) 1989-11-08 1993-12-15 Patrick Hylton Heron Potassium-enriched dietary salt substitute
US5106632A (en) 1990-01-23 1992-04-21 Warner-Lambert Company Enhanced sweetness of acesulfame-k in edible compositions
US5213838A (en) 1991-01-23 1993-05-25 Morris Sheikh Sodium-free salt substitute containing citrates and method for producing the same
DK44891D0 (da) 1991-03-12 1991-03-12 Gunnar Olof Sundien Partikelformet mineralsaltkomposition og fremgangsmaade til fremstilling af samme
US5447543A (en) 1991-06-10 1995-09-05 Exportadora De Sal, S.A. De C.V. Process for crystallizing inorganic salts
US5173323A (en) 1991-07-22 1992-12-22 Omari Yunis J Process for removing the bitterness from potassium chloride
DE4133094A1 (de) 1991-10-05 1993-04-08 Solvay Deutschland Verfahren zur molkenpermeataufarbeitung
US5288510A (en) 1992-05-18 1994-02-22 George Gregory Palatable low salt substitutes
US5370882A (en) 1993-01-26 1994-12-06 Nestec S.A. Taste-enhancement of sodium chloride-reduced compositions
DE9302125U1 (de) 1993-02-15 1993-04-22 BHS-Bayerische Berg-, Hütten- und Salzwerke AG, 8000 München Als Kochsalzersatz geeignetes Salzgemisch
US5562942A (en) 1993-10-05 1996-10-08 Koh; Hen-Sik Salt compositions
WO1995018546A1 (en) 1994-01-11 1995-07-13 George Gregory Palatable low salt substitutes
TW287090B (enExample) 1994-12-07 1996-10-01 Fujisawa Yakusin Kogyo Kk
US5897908A (en) 1995-01-23 1999-04-27 Board Of Trustees Operating Michigan State University Composition and method for producing a salty taste
HU212837B (en) 1995-10-06 1997-02-28 Farsang Sodium-poor, containing, magnesium and potassimum vegetables and spice mixture repast salt mixture
GB9520923D0 (en) 1995-10-12 1995-12-13 Procter & Gamble Detergent compositions
JP2887105B2 (ja) 1996-04-24 1999-04-26 幸子 林 飲料水および塩の製造方法および製造装置
US6090419A (en) 1996-05-02 2000-07-18 Mccormick & Company, Inc. Salt compositions and method of preparation
IL118460A (en) 1996-05-28 1999-09-22 Dead Sea Works Ltd Edible salt mixture
BR9702500A (pt) 1996-06-21 1998-09-15 Fernando Horacio Garcia Sal marinho comestível líquido de baixo teor de sódio e processo para obtê-lo
ES2206730T3 (es) 1996-07-15 2004-05-16 Fujisawa Pharmaceutical Co., Ltd. Composiciones funcionales de cloruro de sodio.
US5871803A (en) 1997-05-30 1999-02-16 Campbell Soup Company Salt flavor enhancing compositions, food products including such compositions, and methods for preparing such products
FI973929L (fi) 1997-10-10 1999-04-11 Itara H K Ab Oy WOF inhibiittori
AR011559A1 (es) 1998-01-22 2000-08-30 Cohen Gloria Virginia Sustituto de la sal de mesa en base a sales de potasio
FR2773955B1 (fr) 1998-01-26 2000-04-07 Sanofi Sa Composition dietetique sous forme d'un sel de substitution du sel de table
FI104783B (fi) 1998-02-12 2000-04-14 Valio Oy Herasuolajauhe, menetelmä sen valmistamiseksi ja sen käyttö
US6541050B1 (en) 1998-11-27 2003-04-01 Campbell Soup Company Salt flavor enhancing compositions, food products including such compositions, and methods for preparing such products
US20030008046A1 (en) 1998-12-18 2003-01-09 Paula A. Gerlat Use of n-neohexyl-a-aspartyl-l-phenylalanine methyl ester as a flavor modifier
DE19902395C2 (de) 1999-01-22 2001-05-03 Kali & Salz Ag Verfahren zur Verengung des Kornspektrums von Kalium- und Natriumchloridkristallisaten zur Verbesserung der Rieseleigenschaften
FI110474B (fi) 1999-01-27 2003-02-14 Modulpo Salts Oy Ravintofysiologinen suolatuote, sen käyttö ja menetelmä sen valmistamiseksi
JP4182644B2 (ja) 2001-02-09 2008-11-19 味の素株式会社 調味料組成物およびそれを用いてなる食品の製造方法
PT1404615E (pt) * 2001-07-09 2005-05-31 Akzo Nobel Nv Processo para produzir sal humido de elevada pureza, sal humido assim obtido e sua utilizacao num processo electrolitico
US6632467B1 (en) 2001-09-19 2003-10-14 Mafalda Salvi Solid condiment comprising a solid and a liquid
US6753023B2 (en) 2001-10-12 2004-06-22 California Natural Products Rice-flour hydrolysates fat substitute
US6743461B1 (en) 2001-11-09 2004-06-01 Ecosalt Corporation Salt substitute compositions
FR2833466B1 (fr) 2001-12-17 2004-08-06 Larena Sa Composition de sel pauvre en chlorure de sodium et riche en sel organique de potassium et ses utilisations
TWI261521B (en) 2002-02-05 2006-09-11 Shiang-Kuen Mau Composition for reducing or removing nitrosamine resulting from chewing betel quid
US6926918B2 (en) 2002-03-11 2005-08-09 Ocean Nutrition Canada Limited Fish hydrolysates as salt replacement
JP2004052449A (ja) 2002-07-23 2004-02-19 Yonekyu Corp 地層からの海洋深層水の採取方法およびそれを用いた食用塩の製造方法
GB0230274D0 (en) 2002-12-30 2003-02-05 Vivotec Ltd Composition
US7402328B2 (en) 2003-12-08 2008-07-22 Ramon Efrain Vasquez Stable sodium-free or low-sodium aqueous solution of agreeable saltiness taste
US7220435B2 (en) * 2003-12-23 2007-05-22 Council Of Scientific & Industrial Research Process for the production of glycine enriched NaCI crystals with improved flow
US20050142219A1 (en) 2003-12-26 2005-06-30 Diversified Natural Products, Inc. Essentially sodium-free potassium salt derived from seaweed
WO2005094615A1 (en) 2004-03-03 2005-10-13 Ecosalt Corporation Non-bitter sodium-free or low-sodium salt composition
CN1559436A (zh) 2004-03-12 2005-01-05 杨理林 一种口服补液盐闪溶片剂及其制备方法
EP1734838A2 (en) 2004-03-15 2006-12-27 TVD Taste Virtual Dimensions, Inc. Salt substitute comprising biocompatible polymer
US7208189B2 (en) 2004-04-06 2007-04-24 Council Of Scientific And Industrial Research Low sodium salt of botanic origin
US20060024422A1 (en) 2004-07-30 2006-02-02 Cumberland Packing Corp. Salt substitute compositions having N-neohexyl-a-aspartyl-l- phenylalanine methyl ester for modifying flavor and methods of manufacturing the same
WO2006013997A1 (ja) 2004-08-03 2006-02-09 Ajinomoto Co., Inc. 調味料組成物、調味料素材、およびそれらを用いた食品の製造方法
US8231925B2 (en) 2004-08-20 2012-07-31 Cargill, Incorporated Ingredient systems comprising trehalose, food products containing trehalose, and methods of making same
WO2006023812A1 (en) 2004-08-20 2006-03-02 Cargill Incorporated Ingredient systems comprising trehalose, food products containing trehalose, and methods of making same
US7427421B2 (en) 2004-09-10 2008-09-23 International Flavors & Fragrances Inc. Saturated and unsaturated N-alkamides exhibiting taste and flavor enhancement effect in flavor compositions
US7666409B2 (en) 2004-11-16 2010-02-23 Kao Corporation Low salt liquid seasoning with antihypertensive activity
US7452563B2 (en) 2005-06-20 2008-11-18 Redpoint Bio Corporation Compositions and methods for producing flavored seasonings that contain reduced quantities of common salt
US7455872B2 (en) 2005-06-20 2008-11-25 Redpoint Bio Corporation Compositions and methods for producing a salty taste in foods or beverages
DE602005020046D1 (de) 2005-09-05 2010-04-29 Immatics Biotechnologies Gmbh Tumor-assoziierte Peptide, welche an unterschiedliche menschliche Leukozytenantigene der Klasse II binden
US20070059428A1 (en) 2005-09-14 2007-03-15 Chigurupati Sambasiva R Low-sodium salt composition
US20080193591A1 (en) 2005-12-26 2008-08-14 Yaizu Suisankagaku Industry Co., Ltd. Taste Improving Agent for Food and Beverage Containing Potassium Chloride, Process for Producing Food and Beverage Containing Potassium Chloride and Food and Beverage Containing Potassium Chloride Produced by the Process
KR100759090B1 (ko) 2006-02-16 2007-09-17 박상영 알칼리성분이 풍부한 식품첨가제 및 그 제조방법
EP2007226B1 (de) 2006-04-11 2010-07-07 Jungbunzlauer Austria AG Salzersatzmischung mit vermindertem nacl-gehalt
FR2900799A1 (fr) 2006-05-15 2007-11-16 Lesaffre & Cie Nouvel agent substitut du sel naci, son utilisation et produits en contenant
US20070292592A1 (en) 2006-06-15 2007-12-20 Mccormick & Company Salt replacing composition, process for its preparation and food systems containing such composition
JP5265142B2 (ja) 2006-06-21 2013-08-14 株式会社Ａｄｅｋａ 塩味強化剤を含有する食塩組成物
US7867520B2 (en) 2006-06-21 2011-01-11 Adeka Corporation Flavor improving agent
US20080003339A1 (en) 2006-06-30 2008-01-03 Clinton Johnson Seasoning and method for seasoning a food product utilizing small particle sea salt
US20080038411A1 (en) 2006-06-30 2008-02-14 Michael Jensen Seasoning and method for enhancing and potentiating food flavor
US20080008790A1 (en) 2006-06-30 2008-01-10 Michael Jensen Seasoned food, seasoning, and method for seasoning a food product
US7923047B2 (en) 2006-06-30 2011-04-12 Conagra Foods Rdm, Inc. Seasoning and method for seasoning a food product while reducing dietary sodium intake
US7989016B2 (en) 2006-10-05 2011-08-02 Sambasiva Rao Chigurupati Method for producing a low sodium salt composition
WO2008074770A1 (en) 2006-12-19 2008-06-26 Dsm Ip Assets B.V. Reduced-salt dairy product with improved taste
FI20075086A7 (fi) 2007-02-07 2008-08-08 Slk Found Aromikoostumus
US20080199595A1 (en) 2007-02-15 2008-08-21 Mccormick & Company Salt replacing composition, process for its preparation and food systems containing such composition
US7854956B2 (en) 2007-03-07 2010-12-21 Exportadora De Sal, S.A. De C.V. Low sodium salt compositions and methods of preparation and uses thereof
US7820225B2 (en) 2007-03-07 2010-10-26 Exportadora De Sal, S.A. De C.V. Low sodium salt compositions and methods of preparation and uses thereof
JP2010521974A (ja) 2007-03-22 2010-07-01 エコソルト コーポレーション 苦味のないナトリウム不含または低ナトリウム塩組成物
WO2008120726A1 (ja) 2007-03-30 2008-10-09 Hiroshima University 塩味増強剤、飲食品、および飲食品の製造方法
JP4824628B2 (ja) 2007-05-25 2011-11-30 日清食品ホールディングス株式会社 食塩代替物、及び減塩加工食品とその製造方法
JP5251019B2 (ja) 2007-05-31 2013-07-31 味の素株式会社 塩類の固結防止方法
CL2007002915A1 (es) 2007-10-10 2008-04-25 Cox Y Compania S A Composicion para alimentos, suplementos nutritivos, productos nutraceuticos u otros de consumo humano que comprende cloruro de sodio, cloruro de potasio, acidos y edulcorantes, donde las proporciones de dichos componentes confieren a la composicion p
US20090104330A1 (en) 2007-10-19 2009-04-23 Mccormick & Company, Inc. Reduced sodium salty taste composition, process for its preparation and food systems containing such composition
FR2922728B1 (fr) 2007-10-26 2011-06-24 Lesaffre & Cie Nouvel agent substitut du sel nacl, son utilisation et produits en contenant.
MX352695B (es) 2008-02-06 2017-12-05 Campbell Soup Co Metodos y composiciones para reducir el contenido de sodio en productos alimenticios.
US8409653B2 (en) 2008-03-14 2013-04-02 Nippon Suisan Kaisha, Ltd. Salty taste enhancer and food or drink containing the same
WO2009116050A1 (en) 2008-03-19 2009-09-24 Greensalt Ltd. Salt substitute
UY31725A (es) 2008-03-21 2009-11-10 Smart Salt Inc Sales alimenticias tipo carnalita y productos de las mismas
CN101977516B (zh) 2008-03-24 2016-12-07 日本水产株式会社 咸味增强剂及含有该咸味增强剂的饮食品
KR20090105762A (ko) 2008-04-03 2009-10-07 전남대학교산학협력단 대체염을 이용한 저염 오이지의 제조 기술
GB0807919D0 (enExample) 2008-05-01 2008-06-04 Moorlodge Biotech Ventures Ltd
DE102008024206A1 (de) 2008-05-14 2009-11-19 Symrise Gmbh & Co. Kg Aromakompositionen und Zubereitungen umfassend Nα-β-Alanyl-Dipeptide
JP5452893B2 (ja) 2008-06-25 2014-03-26 小川香料株式会社 カリウム塩又はカリウム塩含有飲食品の呈味改善剤
US20100227023A1 (en) 2009-03-06 2010-09-09 Danisco A/S Seasoning blend
US20100239740A1 (en) 2009-03-17 2010-09-23 Meyer Richard S Low sodium salt substitute compositions
GB0906379D0 (en) 2009-04-14 2009-05-20 Kencryst Ltd Reduced sodium salt
WO2011040505A1 (ja) 2009-10-02 2011-04-07 ハウス食品株式会社 塩味が補強又は増強された食品組成物及び異味が抑制された塩化カリウム含有組成物
US20120232166A1 (en) 2009-10-12 2012-09-13 Finley John W Masking Bitter Flavors
CN102187990A (zh) * 2010-03-09 2011-09-21 中盐国本盐业有限公司 一种食用盐
MY174578A (en) 2010-08-06 2020-04-28 Matsutani Kagaku Kogyo Kk Method for improving salty taste of food or beverage and salty taste improving agent
US20120128830A1 (en) 2010-11-18 2012-05-24 Sambasiva Rao Chigurupati Novel low sodium salt composition
US20120164287A1 (en) 2010-12-23 2012-06-28 Pamela Lynn Lundberg Pasta Product Having Reduced Sodium Anti-Boil-Over Composition With Enhanced Cheese Flavor Notes
MY160447A (en) 2011-01-06 2017-03-15 Holista Biotech Sdn Bhd Reduced sodium composition
MX350838B (es) * 2011-02-11 2017-09-18 Grain Proc Corporation * Composicion de sal.
FR2973989A1 (fr) 2011-04-15 2012-10-19 Nutrionix Nouvel agent substitut du sel nacl, son utilisation et produits en contenant
BR112013030729A2 (pt) 2011-06-03 2016-12-06 Icl Performance Products Lp preparação de carnalita e usos da mesma em aplicações comestíveis
EP2747583B1 (en) 2011-08-25 2018-12-26 Working Bugs, LLC An improved sodium-free salt substitute
JP6022463B2 (ja) 2011-09-30 2016-11-09 理研ビタミン株式会社 呈味改善剤
MX355775B (es) 2011-10-20 2018-04-30 Chromocell Corp Compuestos, composiciones y metodos para reducir o eliminar el sabor amargo.
CN109259179A (zh) 2011-12-06 2019-01-25 日本水产株式会社 味道改善剂、含有其的食盐替代物、以及用于食品的味道改善方法
WO2013085858A2 (en) 2011-12-08 2013-06-13 Dow Global Technologies Llc Salt composition
WO2013085859A1 (en) 2011-12-08 2013-06-13 Dow Global Technologies Llc Salt composition
US8999425B2 (en) 2012-01-04 2015-04-07 Jcr Technologies Llc Low sodium salt substitute compositions
US20130196001A1 (en) 2012-01-30 2013-08-01 Health & Science, LLC Salt replacement compositions and methods of using same
FR2989556B1 (fr) 2012-04-24 2014-05-23 Midi & Salines Est Salins Substitut de sel
KR102040743B1 (ko) * 2012-07-12 2019-11-05 아크조 노벨 케미칼즈 인터내셔널 비.브이. 증발 결정화에 의해 제조된 자유 유동성 염 조성물
WO2014071394A1 (en) 2012-11-05 2014-05-08 S & P Ingredient Development, Llc A low sodium salt composition
WO2014127003A2 (en) 2013-02-13 2014-08-21 The Trustees Of Columbia University In The City Of New York Modulation of salty taste perception by altering the function of bitter- or pkd2l1-expressing taste receptor cells
FR3012293A1 (fr) 2013-10-31 2015-05-01 Setalg Ingredient alimentaire d'origine algale et son utilisation comme substitut de sel et exhausteur de gout
JP2017158543A (ja) 2016-03-04 2017-09-14 味の素株式会社 塩味増強組成物

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US82A (en) 1836-11-17 Spiral bit with countersink for setting screws
US3505A (en) 1844-03-26 Mill-btjsh
EP0124254A1 (en) 1983-03-30 1984-11-07 NABISCO BRANDS, Inc. Salt substitute composition
US5626904A (en) * 1992-03-19 1997-05-06 Hitavejta Sudurnesja Salt product and a method for the preparation thereof
US20040047976A1 (en) * 2000-08-14 2004-03-11 Narayan Anantha Subramony Granulation process
US20030143152A1 (en) * 2002-01-31 2003-07-31 Vohra Rajinder Nath Process for recovery of low sodium salt from bittern
US20130243924A1 (en) * 2005-09-14 2013-09-19 Pratik N. Bhandari Low Sodium Salt Composition
US20140044846A1 (en) 2006-10-05 2014-02-13 S & P Ingredient Development, Llc Low sodium salt composition
US20140255589A1 (en) 2012-11-21 2014-09-11 S&P Ingredient Development Llc Compositions of low sodium salt and methods of making and using
US20150056338A1 (en) * 2013-08-20 2015-02-26 S&P Ingredient Development Llc Salt compositions and methods of making and using
US9247762B1 (en) * 2014-09-09 2016-02-02 S & P Ingredient Development, Llc Salt substitute with plant tissue carrier

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP3684196A4

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021175658A1 (en) * 2020-03-03 2021-09-10 Omya International Ag Anticaking agent
CN115038342A (zh) * 2020-03-03 2022-09-09 欧米亚国际集团 抗结块剂
CN115038342B (zh) * 2020-03-03 2024-02-02 欧米亚国际集团 抗结块剂

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