This application is the National Phase entry of International Application No. PCT/FI2013/051145, filed on Dec. 5, 2013, which claims priority to Finnish Application No. 20126279, filed on Dec. 7, 2012, both of which are incorporated herein by reference in their entireties.
The invention relates to a method for making a physiologically beneficial nutrient salt that contains sodium, potassium and magnesium. In its basic form, the product contains metal chlorides only. The method is characterized by a low energy requirement and a fast manufacturing process.
Preparation of the above described salt products that contain potassium magnesium chloride hydrate, i.e. carnallite, or ammonium substituted carnallites, has been described in patent publications U.S. Pat. No. 6,787,169 B1 and EP 1 150 578 B1, and in application WO 2009117702 (A2) derived from these. In the above mentioned documents, carnallite, in this case potassium carnallite, is made by adding equivalent amounts of magnesium chloride hexahydrate and potassium chloride to water, whose amount is typically 120 to 140 ml per mole. The mixture is heated to boiling point (about 120° C.) and cooled down when all the material is in dissolved form: The formed crystals are isolated, dried, ground, and used in addition to sodium chloride and potassium chloride as a component of a food salt mixture in desired ratios. The documents also present buffering methods for compensating changes taking place in magnesium chloride solutions at said temperatures.
When contemplating possibilities of preparing the above described salt mixtures in a simpler way, one has to recognize that the solubility of potassium chloride in water is relatively low. Thus, for dissolving one gram of potassium chloride, 2.8 ml of water (20° C.) and 1.8 ml of boiling water is required. Furthermore, it has to be taken into account that carnallite is formed as a real double salt at high ionic strengths only, and that it is characteristic of potassium chloride to crystallize out of the solution in the presence of other salts, such as magnesium chloride.
In our studies, it was surprisingly found that the desired salt mixture can be advantageously prepared by adding an equivalent or close to an equivalent amount of magnesium chloride to a warm, almost saturated solution of potassium chloride. After the solution has been formed, a desired quantity of potassium chloride is still added to this solution under agitation, and finally the sodium chloride. The addition of the salts will quickly increase the ionic strength and simultaneously cool the mixture, and the carnallite (KCl.MgCl2.6H2O) will precipitate. The formed dryish crystal mass is allowed to stand overnight, after which it is dried e.g. in a vacuum. Allowing the mixture to stand, or possible turning over of the mixture, is advantageous because the size of the carnallite crystals will increase. An alternative is naturally to precipitate carnallite partly from the solution and then perform the above described salt additions for precipitating the carnallite.
The carnallite solution can be prepared advantageously in the temperature range from 20 to 100° C. Taking into account the above mentioned values relating to the solubility of potassium chloride, the salt product can be provided with a lo magnesium content higher than normal by preparing the carnallite solution at the temperature of, for example, 100° C. The amount of water applied in preparing the concentrated carnallite solution can be 10 to 20 ml, advantageously 10 ml per 100 g of the final salt product. The relatively low moisture content in the salt product will facilitate and thereby reduce the duration of the drying process. The finished dried product contains crystal water which is typical for carnallite.
In the method, after first preparing a sufficiently concentrated aqueous solution of potassium chloride, all the other salts can be added in solid state.
Taking into account the needs of food industry, the salt product can also be brought to a completely soluble form before it is dried to sprinklable form.
It is noteworthy that the method does not involve any filtering. Consequently, no salt solutions are formed which should be subjected to further processing or recirculated in the process. The low temperature is also advantageous in view of the handling of magnesium chloride, because it starts to decompose partly above the temperature of 105° C., producing small amounts of hydrogen chloride. Prepared by this method, the product does not contain free magnesium chloride, which would result in problems of water absorption. The dried product is pleasant in taste, easily flowable, and meets the requirements set for low hygroscopicity.
The invention is also characterized in that for preparing the product, it is possible to use fine-grained sea salt or table salt products derived from sea salt instead of purified sodium chloride. In the case of pure sodium chloride, the product obtained only consists of an equivalent amount of chlorides in addition to sodium, potassium and magnesium ions. The use of sea salt or a product derived from sea salt as the sodium source may also introduce low contents of other substances, such as micronutrients, into the product.
It is naturally possible to include additives that primarily improve the taste, for example ammonium chloride, carbohydrates, spices, refined plants or their fruit, nut powder, acidity regulators, glutamates, amino acids, their oligomers, or the like, in the finished product.
Advantageously, iodine is also added to the salt by the same methods and in the same contents as table salt is iodized.
The product can be made to a solid salt product which has suitable grain size or grain size distribution and can be sprinkled. This salt product can be packed in sales packages which can be consumer packages to be used in households, or large-scale consumer packages for professional use (food industry, restaurants, institutional kitchens).
In the following, the invention will be described in more detail with reference to examples and the appended drawings, in which
The heterogeneous product shown in
The dissolution of the salt fractions, for example in the mouth of a tasting person, is likely to take place primarily in relation to their mutual specific areas. Thus, in tasting tests, heterogeneous mixtures have been found to evoke, as the first taste, the specific taste of the carnallite type in question, whereas a product made by the method according to the invention, in which the fine-grained fraction is missing, will give a taste almost resembling that of sodium chloride. It can also be assumed that in the product made by the method, even the smallest crystals are a mixture of carnallite and sodium chloride.
It is not a mixture of crystals of different salts but a product in which sodium chloride (NaCl) and carnallite (KCl.MgCl2.6H2O) have been crystallized together in the same crystals when dissolution and recrystallization of salts repeatedly takes place in the moist crystal mass being formed.
As shown in
Consequently, the finished solid salt product has been found to have a homogeneous physical structure; in other words, it is equigranular in its crystal structure. It is not a mixture of crystals of different salts but a product in which sodium chloride (NaCl) and carnallite (KCl.MgCl2.6H2O) have been crystallized together in the same crystals when dissolution and recrystallization of salts repeatedly takes place in the moist crystal mass being formed.
The salt product is used by adding it to food for improving the taste and/or preservability. In this context, the food should be understood in a wide sense. The addition can be made to finished food or to its raw material during the preparation.
The invention will be described in more detail in the following examples.
3.73 g (0.05 mol) of potassium chloride was dissolved in 10 ml of water at a temperature of about 40° C. 10.1 g (about 0.05 mol) of magnesium chloride hexahydrate was added to the mixture. The vessel was heated for compensating the heat of dissolution, and agitated. 16.3 g of potassium chloride and, after about 5 min, 70 g of sodium chloride were added to the solution which was slightly turbid. A moist well mixable salt mass was formed, which was allowed to stand for about 16 h in a closed vessel at intermittent stirring. The product was dried at about 30° C. The product was even-grained and fluffy.
The product contains: 27.5 wt % Na
The procedure according to Example 1 was repeated by adding 21.3 g of solid potassium chloride and 65 g of sodium chloride to the cooled carnallite solution. The crystal mass was then processed as described above.
The metal ion composition of the product is: 25.6 wt % Na
The example describes a process in which a carnallite solution is prepared at a higher temperature than in the above examples and in which fine-grained sea salt is used instead of pure sodium chloride for introducing the sodium chloride fraction.
5.22 g (0.07 mol) of potassium chloride was added to 10 ml of water. The mixture was heated close to the boiling point, and 14.2 g of magnesium chloride hexahydrate was added to the slightly turbid solution formed. The mixture was heated under continued agitation until a solution was formed.
The mixture was allowed to cool to about 50° C., and 15.6 g of solid potassium chloride and, after about 5 min, 65 of fine-grained sea salt were added under agitation. The mixture was homogenized and allowed to stand for about 16 h in a closed vessel at intermittent stirring. The dryish crystal mass was finally dried at about 30° C. The product was even-grained and fluffy.
The metal ion composition of the product is: 25.6 wt % Na
In the examples, the rest of the salt consists of chloride ions. As mentioned above, due to the salt raw materials used, the product may also contain traces of other cations and anions, but these do not affect the physical structure of the product, which is determined by the crystal system formed by carnallite and sodium chloride.
Number | Date | Country | Kind |
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20126279 | Dec 2012 | FI | national |
Filing Document | Filing Date | Country | Kind |
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PCT/FI2013/051145 | 12/5/2013 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2014/087056 | 6/12/2014 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
1875013 | Kaselitz | Aug 1932 | A |
3312607 | Goodenough et al. | Apr 1967 | A |
3337432 | Belski | Aug 1967 | A |
3798314 | Suzukawa et al. | Mar 1974 | A |
4775546 | Higurashi | Oct 1988 | A |
6787169 | Maki | Sep 2004 | B1 |
20120308487 | Stachiw | Dec 2012 | A1 |
20130164424 | Einarsson | Jun 2013 | A1 |
Number | Date | Country |
---|---|---|
1567937 | Oct 1970 | DE |
3008171 | Sep 1981 | DE |
10304315 | Aug 2004 | DE |
1150578 | Mar 2005 | EP |
351845 | Jul 1931 | GB |
1308084 | Feb 1973 | GB |
H01181762 | Jul 1989 | JP |
WO 9000522 | Jan 1990 | WO |
WO-9216117 | Oct 1992 | WO |
WO-9318668 | Sep 1993 | WO |
WO 9318668 | Sep 1993 | WO |
WO 9507630 | Mar 1995 | WO |
WO 0044245 | Aug 2000 | WO |
WO 2009117702 | Sep 2009 | WO |
WO 2012166854 | Dec 2012 | WO |
WO-2014087056 | Jun 2014 | WO |
Entry |
---|
International Search Report dated Apr. 7, 2014 issued in PCT/FI2013/051145. |
International Preliminary Report on Patentability dated Mar. 30, 2015 issued in PCT/FI2013/051145. |
Number | Date | Country | |
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20150305377 A1 | Oct 2015 | US |