GB1569636A - Sweetening composition and method for the preparation thereof - Google Patents
Sweetening composition and method for the preparation thereof Download PDFInfo
- Publication number
- GB1569636A GB1569636A GB12722/77A GB1272277A GB1569636A GB 1569636 A GB1569636 A GB 1569636A GB 12722/77 A GB12722/77 A GB 12722/77A GB 1272277 A GB1272277 A GB 1272277A GB 1569636 A GB1569636 A GB 1569636A
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- compound
- particles
- sweetening
- composition
- water
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- 239000000203 mixture Substances 0.000 title claims description 42
- 238000000034 method Methods 0.000 title claims description 25
- 238000002360 preparation method Methods 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 72
- 239000002245 particle Substances 0.000 claims description 67
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- 239000002002 slurry Substances 0.000 claims description 23
- 239000013078 crystal Substances 0.000 claims description 15
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims description 14
- 238000001035 drying Methods 0.000 claims description 11
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 claims description 10
- 229960005261 aspartic acid Drugs 0.000 claims description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 10
- 238000009826 distribution Methods 0.000 claims description 10
- 235000012054 meals Nutrition 0.000 claims description 10
- CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 claims description 9
- CKLJMWTZIZZHCS-UWTATZPHSA-N L-Aspartic acid Natural products OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 0.000 claims description 9
- 239000008122 artificial sweetener Substances 0.000 claims description 8
- 235000021311 artificial sweeteners Nutrition 0.000 claims description 8
- 230000009969 flowable effect Effects 0.000 claims description 8
- 235000013305 food Nutrition 0.000 claims description 8
- 239000007921 spray Substances 0.000 claims description 8
- 238000001694 spray drying Methods 0.000 claims description 8
- 235000013361 beverage Nutrition 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 7
- -1 L-aspartic acid derivative compound Chemical class 0.000 claims description 6
- 230000004523 agglutinating effect Effects 0.000 claims description 5
- 125000005907 alkyl ester group Chemical group 0.000 claims description 5
- 239000008346 aqueous phase Substances 0.000 claims description 5
- 239000000796 flavoring agent Substances 0.000 claims description 4
- 238000003801 milling Methods 0.000 claims description 4
- 238000010079 rubber tapping Methods 0.000 claims description 4
- 235000019634 flavors Nutrition 0.000 claims description 3
- 238000000227 grinding Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000007493 shaping process Methods 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 238000004220 aggregation Methods 0.000 claims description 2
- 230000002776 aggregation Effects 0.000 claims description 2
- 229960004543 anhydrous citric acid Drugs 0.000 claims description 2
- 238000013459 approach Methods 0.000 claims description 2
- 229960004106 citric acid Drugs 0.000 claims description 2
- 238000006073 displacement reaction Methods 0.000 claims description 2
- 239000012530 fluid Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000008399 tap water Substances 0.000 claims description 2
- 235000020679 tap water Nutrition 0.000 claims description 2
- YZQCXOFQZKCETR-UWVGGRQHSA-N Asp-Phe Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 YZQCXOFQZKCETR-UWVGGRQHSA-N 0.000 claims 2
- 230000004931 aggregating effect Effects 0.000 claims 1
- 235000003599 food sweetener Nutrition 0.000 description 6
- 239000003765 sweetening agent Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- 238000004040 coloring Methods 0.000 description 3
- 108010016626 Dipeptides Proteins 0.000 description 2
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 239000002178 crystalline material Substances 0.000 description 2
- HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical class OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 2
- 229940081974 saccharin Drugs 0.000 description 2
- 235000019204 saccharin Nutrition 0.000 description 2
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 2
- UKZZLYXCJLZNAP-WPRPVWTQSA-N (3s)-3-amino-4-[[(s)-carboxy(phenyl)methyl]amino]-4-oxobutanoic acid Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(O)=O)C1=CC=CC=C1 UKZZLYXCJLZNAP-WPRPVWTQSA-N 0.000 description 1
- QDGAVODICPCDMU-UHFFFAOYSA-N 2-amino-3-[3-[bis(2-chloroethyl)amino]phenyl]propanoic acid Chemical compound OC(=O)C(N)CC1=CC=CC(N(CCCl)CCCl)=C1 QDGAVODICPCDMU-UHFFFAOYSA-N 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 229940109275 cyclamate Drugs 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000002036 drum drying Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 235000007983 food acid Nutrition 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 125000003630 glycyl group Chemical class [H]N([H])C([H])([H])C(*)=O 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 238000000643 oven drying Methods 0.000 description 1
- 229960005190 phenylalanine Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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
- A23L27/30—Artificial sweetening agents
- A23L27/31—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives
- A23L27/32—Artificial sweetening agents containing amino acids, nucleotides, peptides or derivatives containing dipeptides or derivatives
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Seasonings (AREA)
Description
(54) SWEETENING COMPOSITION AND METHOD FOR THE
PREPARATION THEREOF
(71) We, GENERAL FOODS CORPORATION, a Corporation organised and existing under the laws of the State of Delaware, United States of America, of 250 North
Street, White Plains, State of New York, 10625, United States of America, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement.
The present invention relates to a process for the preparation of artificially sweetened comestibles and, more particularly, to a process whereby the class of L-aspartic acid derivatives that are sweet are effectively converted to a free flowing mixable and highly soluble sweetening composition.
The members of the sweetening class of L-aspartic acid derivatives such as the dipeptide
L-aspartic acid ester of L-phenylalanine, i.e., APM aforesaid, are characteristically less soluble than would be prepared for a so-called "instant" comestible like a beverage mix containing the artificial sweetener. Accordingly, attempts have been made to render the compounds in this class more readily dispersible and soluble such as by subdividing them and thus improving their rate of solubility, as well as their rate of dispersibility. Attempts at subdivision of the crystalline particles of such compounds to enhance the rate of solubility have not been too successful and alternative means have been employed to effectively improve the rate of dispersion and hence the overall rate of solubility. One common problem of such compounds appears to be their electrostatic properties; as recovered in crystalline form, they possess an inherent zwitterion capacity; indeed as long as the compounds retain their identity as sweeteners it appears that they possess this capacity.
Comestibles such as beverage mixes containing food acids, and powdered flavouring and/or colouring agents, when commingled with the artificial sweetener will have erratic flow properties due to the electrostatic properties of the sweetener. Also, such mixes are prone to dusting and are not free flowing compared to the more flowable active ingredients which characterize the mix; the consequences are irregularities or even useless beverage and other comestible recipes. Attempts at ameliorating these effects such as by screening are not effective since such attempts at subdivision are not permanent since the sweetening compound particles reaggregate under the influence of their inherent electrostatic charges.
It would be desirable to have a form of L-aspartic acid-derived sweetener which is readily blendable and flowable and which has a high rate of solubility and dispersibility. Preferably, such a compound should be blendable with flavouring and colouring ingredients, or should itself impart flavouring and colouring while at the same time being a stable sweetener.
We have now developed a process whereby discrete crystals of L-aspartic acid derivative sweetening compounds meeting the foregoing requisites are produced by employing a minor amount of the compound per se in solution as a medium to aggregate the crystals thereof in an immobilized state, the crystals being assembled randomly at spaced points of contact by the dried solution of the sweetening compound.
Accordingly, the present invention provides a process for producing a flowable dry sweetening composition which comprises admixing crystalline particles of an L-aspartic acid-derived sweetening compound with an amount of water sufficient either (c) to form a mixture of undissolved compound particles therewith and to cause a minor amount of the compound particles to be dissolved by the water to form an agglutenating solute, milling the compound particles admixed with water to a uniform, cluster-free slurry, causing the resulting solute solution to be distributed throughout the remaining undissolved compound particles while causing the particles to arrange themselves randomly with respect to one another, and drying the solution to immobilize the particles in the random arrangement thereof at spaced points of contact through the intermediation of the redried compound, the sweetening composition consisting essentially of the particles immobilized by the redried compound, or (b) to form a semi-moist meal or dough and to cause a minor amount of the compound particles to be dissolved by the water to form an agglutinating solute which enables the moist mixture of crystalline solids to be converted into a handle able mass, shaping and subsequently drying and grinding the mass to immobilize the particles in the random arrangement thereof at spaced points of contact through the intermediation of the redried compound, the sweetening composition consisting essentially of the particles immobilized by the redried compound.
In carrying out the process of the invention according to alternative (a) the sweetening compound crystals are preferably subdivided by hydro-milling them to a uniform particle size upon which some crystals will be dissolved and form agglutinating solutes. This hydromilled slurry, preferably at a reduced temperature at which solution is minimized, is then dried such as by spray drying droplets produced by pumping the slurry through an atomizing nozzle; the droplets advantageously dry in a form whereby the subdivided discrete crystals nest with one another while a part of the droplet and are permanently bound to one another by the solute sweetening compound at their points of contact, so that when the droplet is recovered as a dry powder a permanent agglomerate of sweetening compound in a free flowing, rounded form is obtained.
In alternative (b) the sweetening compound is converted into a semi-moist meal or dough consistency produced by combining limited quantities of water and the sweetening compound in crystalline form, whereby the water partially dissolves a portion of the sweetening compound forming an agglutinating solute which enables the moist mixture of crystalline solids to be converted into a handleable mass, as by extruding at room temperature, which extrudate or otherwise-shaped mass can be dried and subsequently ground; the aggregated particles will possess the same characteristic random nesting of crystalline sweetening compounds adhering at their spaced points of contact through the intermediation of redried sweetening compound acting to bridge the crystalline particles into immobilized granules.
In this aspect of the invention the compound particles are preferably distributed in an amount of water which forms a doughy, shape-retaining meal having the solution of sweetening compound distributed therethrough to agglutinate the particles in the random arrangement. More preferably, the meal is shaped and sub-divided.
The alternative embodiments of the process of this invention and the product produced thereby, will be chosen dependent upon the intended use of the product. The preferred spray dried form of particles having a very free blowing, high rate of solubility are preferred for beverage uses, whereas in other applications it may be practical to resort to the dough-forming techniques to be hereinafter described wherein a more granular form of particulate structure will be suitable.
The invention may be used in the production of sweetening compositions from a broad class of L-aspartic acid derivatives which will be categorized as follows:
(1) The methyl esters of L-aspartyl-2, 5-Dihydro-L-phenylalanine; L-aspartyl-L-(1cyclohex-1-en)-alanine; L-aspartyl L-phenylglycine; L-aspartyl-L-2, 5-dihydrophenylglycine;
(2) methyl-L-aspartyl-L-alpha-phenylglycinase and its salts.
(3) Lower alkyl esters of L-aspartyl-L-(beta-cyclohexyl)-alanine disclosed in South
Africa Patent No. 6,695,910;
(4) Those alkyl esters classed as alpha-L-or DL-aspartyl-L or DL-substituted glycines described in Netherlands Patent No. 7,007,176;
(5) Those hydrogenated dipeptide ester sweeteners such as L-asparagio-O-etherified serine methyl esters described in French Patent No. 2,105,896;
(6) Those aspartic acid peptide esters having the formula:
H2CC(CH2COOH)HCONHC (Rl)(R2)COOR where R and R1 and CH3 or QH5 and R2 is C4-7 alkyl having the stereo chemical form L-L,
DL-L, L-DL, or DL-DL;
(7) Those sweetening agents having the formula: H2N- CR - CONH-CH - COOR bH2 CH2 COOH pH shown in British Patent 1,339,101; wherein R is a lower alkyl such as methyl and is prepared by reacting an N-protected-L-aspartic anhydride with L-phenylalanine lower alkyl esters, and
(8) Those sweetening preparations having the formula L-aspartyl-L-1, 4-dimethylpentyl amide disclosed in German Patent No. 2,306,909.
In the preferred spray drying process, the L-aspartic acid derivative crystal solids at a minor weight percent are admixed with water and converted into a slurry maintained at a temperature much below 1500F and typically at ambient room temperature conditions, whereby a minimum of the sweetening compound is allowed to go into solution, the vast majority of the derivative crystalline materials being undissolved and at most hydrated.
This slurry is thereafter subjected to a hydromill processing wherein it will be force hydromilled or otherwise colloidally milled under pressure between a narrow orifice operative to sub-divide the crystalline material to a uniform particle size distribution as by passage between a mill having an opening less than 125 microns intermediate the working mill faces.
The hydromilled slurry is thereafter spray dried into the intended form. The partial solution of the sweetening compound will be just sufficient to provide the agglutenating adhesion intermediate the undissolved crystalline sweetening compound solids whereby when a droplet is caused to undergo evaporation the crystals will be randomly aggregated at their spaced points of contact through the intermediation of the re-dried compounds per se.
As indicated, the slurry may be dried by means other than spray drying, spray drying being most preferred in that by the formation of a droplet and the surface tension effects produced thereby the crystals are caused to be assembled into a spherical aggregated
condition whence they may be permanently bonded to one another in the structure
intended to provide a substantial immobilization and reduction of the effects of the
electrostatic charges thereof. A slurry may be dried by any one of a number of well known drying methods of use in accordance with the foods arts such as drum drying, oven drying, freeze drying, etc.; in all of these applications, a slurry form that is relatively cool will be employed and if the slurry is dried in this unitary condition en masse, it will be subsequently
subdivided into the granular state of use.
In lieu of a slurry form, a dough may be produced which takes advantage of the glutinous
character of the peptide and equivalent hydrated crystals which is generated by the addition
of a minor weight percent of water thereto, whence a suitable dough or meal that is moist will be produced and converted into a shape-retaining form as by the preferred step of extrusion subsequent to which the shape will be redried and incident to which redrying the individual crystals will be permanently bonded to one another through the intermediation of the redried dissolved sweetening compounds.
The slurry or dough practices do not preclude the presence in the aqueous phase of compatible inert or adjunctive agents such as colors and even flavors provided they are sufficiently incapable of entering into unstabilizing reactions with the L-aspartic acid derivative; thus, the aqueous medium used to produce the slurry or meal may have the coloring matter dissolved in the aqueous solvent; e.g. a spray dried form can be advantageously colored requiring no blending for this purpose. Likewise, water insoluble materials may be emulsified or homogenized in the aqueous medium forming a slurry or the dough for efficacious combination with the sweetening compound, the remaining water present being operative to effect the partial dissolution of the compound and form the agglutenating bridging solution.
Moreover, other artificial sweeteners such as saccharin and/or cyclamates may be blended at minor weight percents of the total composition to provide a balanced organoleptic sweetening impact by force of the uniformity of their distribution throughout
the slurry or dough matrices depending upon the particular process employed; in this application, it will be desired to employ the cyclamate at a very minor weight percent of the saccharin which in turn will be a very minor weight percent of the total L-aspartic acid compound solids used whereby a preferred balanced organoleptic sweetness will be afforded when the total sweetening compounds are rendered soluble and used in beverage or other food applications. In these applictions, the artificial sweeteners may be either dissolved in the aqueous phase or dry blended in the non-aqueous phase and will be effectively fixed through the random aggregation of the crystalline L-aspartic acid derivative compound per se.
All of these applications will produce a most flowable and blendable, stable, highly soluble composition which avoids the disadvantages stemming from the electrostatic properties still possessed by the compound itself.
The invention will now be more fully understand by reference to the following Example.
Example
APM crystals (30%) and room temperature tap water (70%) are admixed; the admixture is then charged to a Fryma mill wherein the particles are caused to pass an opening having a gap setting of about 75 microns operative to reduce the particle size of the APM crystals and subdivide any clusters thereof resulting in a fluid, pumpable, creamy slurry which at room temperature is pumped to a spray drying, atomizing nozzle which charges, under a spray pressure of 425 psig, the droplets into a vertical, spray drying tower having an inlet drying air temperature of 410"F and an outlet air temperature of about 235"F with an air flow of approximately 2600 cubic feet per minute. The dried droplets charge was recovered at a moisture content of 1.07% and a density of 0.248 grams per cc and 0.304 grams per cc packed - the density resulting from tapping a charge of the material until it approaches asymptotic density reduction under the influence of tapping per se with no overt positive mechanical displacement force.
The dried particles had the following particle size distribution:
Sieve Number (U.S.S.) % on Sieve + 60 0.60 - 60,+ 70 25.4 - 17,+120 58.03 -120,+140 11.80 -140,+200 3.80 -200,+300 0.30 -300 0.07
The dried product will be noted to have a very uniform particle size distribution wherein 99% of the particles are between 60-200 mesh size; advantageously the composition has a narrow particle size distribution such that the particles are an amount of 1.10 grams of the spray dried APM agglomerates, dry blended with 3.60 grams of anhydrous citric acid can be spoon-stirred in 1892 milimeters of water at 45"F for 40 seconds and will form a complete solution; a like mixture of APM-acid mix that is unprocessed will take between 60 and 90 seconds to go into solution depending upon particle distribution and size of the sweetening compound therein.
A complete beverage mix of colour, flavour and citric acid, blended with the processed
APM particles of this invention, had a free flow capacity which was quite acceptable to food manufacturing processes.
We are aware of the Food Regulations 1969 and in so far as the present invention relates to the use of artificial sweeteners which are governed by these regulations, we make no claim to the use of the invention in contravention of these regulations.
WHAT WE CLAIM IS:
1. A process for producing a flowable dry sweetening composition which comprises admixing crystalline particles of an L-aspartic acid-derived sweetening compound with an amount of water sufficient either (a) to form a mixture of undissolved compound particles therewith and to cause a minor amount of the compound particles to be dissolved by the water to form an agglutenating solute, milling the compound particles admixed with water to a uniform, cluster-free slurry, causing the resulting solute solution to be distributed throughout the remaining undissolved compound particles while causing the particles to arrange themselves randomly with respect to one another, and drying the solution to immobilize the particles in the random arrangement thereof at spaced points of contact through the intermediation of the redried compound, the sweetening composition consisting essentially of the particles immobilized by the redried compound, or (b) to form a semi-moist meal or dough and to cause a minor amount of the compound particles to be dissolved by the water to form an agglutinating solute which enables the moist mixture of crystalline solids to be converted into a handleable mass, shaping and subsequently drying and grinding the mass to immobilize the particles in the random arrangement thereof at
**WARNING** end of DESC field may overlap start of CLMS **.
Claims (18)
1. A process for producing a flowable dry sweetening composition which comprises admixing crystalline particles of an L-aspartic acid-derived sweetening compound with an amount of water sufficient either (a) to form a mixture of undissolved compound particles therewith and to cause a minor amount of the compound particles to be dissolved by the water to form an agglutenating solute, milling the compound particles admixed with water to a uniform, cluster-free slurry, causing the resulting solute solution to be distributed throughout the remaining undissolved compound particles while causing the particles to arrange themselves randomly with respect to one another, and drying the solution to immobilize the particles in the random arrangement thereof at spaced points of contact through the intermediation of the redried compound, the sweetening composition consisting essentially of the particles immobilized by the redried compound, or (b) to form a semi-moist meal or dough and to cause a minor amount of the compound particles to be dissolved by the water to form an agglutinating solute which enables the moist mixture of crystalline solids to be converted into a handleable mass, shaping and subsequently drying and grinding the mass to immobilize the particles in the random arrangement thereof at
spaced points of contact through the intermediation of the redried compound, the sweetening composition consisting essentially of the particles immobilized by the redried compound.
2. A process as claimed in claim 1 wherein the compound particles are milled in step (a) to a particle size less than 125 microns.
3. A process as claimed in claim 1 or claim 2 wherein the amount of water in step (a) is a major percent by weight of the admixture of compound and water.
4. A process as claimed in any one of the preceding claims wherein the slurry in step (a) is maintained below 1500F prior to drying.
5. A process as claimed in claim 4 wherein the slurry in step (a) is maintained at ambient temperature prior to drying.
6. A process as claimed in any one of the preceding claims wherein the slurry in step (a) is hydromilled.
7. A process as claimed in claim 6 wheren the slurry in step (a) is spray dried.
8. A process as claimed in claim 1 wherein in step (b), the compound particles are distributed in an amount of water which forms a doughy, shape-retaining meal having the solution of sweetening compound distributed therethrough to agglutinate the particles in the random arrangement.
9. A process as claimed in claim 8 wherein the meal is shaped and subdivided.
10. A process as claimed in any one of the preceding claims wherein the compound is an alkyl ester of L-aspartyl-L-phenylalanine.
11. A process as claimed in claim 1 substantially as hereinbefore described with reference to the Example.
12. A free-flowing water soluble powdery sweetening composition which comprises immobilized crystalline particles of an L-aspartic acid-derived sweetening compound aggregated to one another at spaced points of contact through intermediate aggregating bonds formed by redried quantities of the compound, the dissolved and redried form of the compound at the spaced contact points being a minor amount of the L-aspartic acid sweetening compound present, the sweetening composition consisting essentially of the
L-aspartic acid sweetening compound particles immobilized by the redried compound.
13. A composition as claimed in claim 12 wherein the compound is an alkyl ester of L-aspartyl-L-phenylalanine.
14. A composition as claimed in claim 13 wherein the compound is L-aspartyl
L-phenylalanine methyl ester.
15. A composition as claimed in any one of claims 12 to 14 wherein the sweetening composition contains minor quantities by weight of the total composition of other artificial sweeteners.
16. A composition as claimed in claim 12 substantially as hereinbefore described with reference to the Examples.
17. A flowable dry sweetening composition when prepared by a process as claimed in any one of claims 1 to 11.
18. A comestible when sweetened using a sweetening composition as claimed in any one of claims 12 to 17.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB12722/77A GB1569636A (en) | 1977-03-25 | 1977-03-25 | Sweetening composition and method for the preparation thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB12722/77A GB1569636A (en) | 1977-03-25 | 1977-03-25 | Sweetening composition and method for the preparation thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1569636A true GB1569636A (en) | 1980-06-18 |
Family
ID=10009908
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12722/77A Expired GB1569636A (en) | 1977-03-25 | 1977-03-25 | Sweetening composition and method for the preparation thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1569636A (en) |
-
1977
- 1977-03-25 GB GB12722/77A patent/GB1569636A/en not_active Expired
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