Classifications

• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/0005—Other compounding ingredients characterised by their effect
  • C11D3/0094—High foaming compositions
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/83—Mixtures of non-ionic with anionic compounds
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/86—Mixtures of anionic, cationic, and non-ionic compounds
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/02—Anionic compounds
  • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
  • C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/38—Cationic compounds
  • C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
  • C11D1/523—Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/662—Carbohydrates or derivatives

Definitions

• This invention relates to light duty liquid detergents having particular utility in the hand washing of dishware, including dishes, pots, pans, glassware and silver/flatware. More particularly, it relates to a liquid dishwashing detergent composition which provides stable, persistent foaming characteristics combined with effectiveness in removing greasy soils from dishes under ambient, i.e. low water temperature, conditions.
• Foam generation by detergent compositions is associated by the consumer with good detersive ability. However, it is apparent that long lasting foam, whether considered copious or medium to low-medium foam content is, by itself, not a sufficient measure of cleaning ability. Nevertheless, much effort has been extended to optimize foaming characteristics, without necessarily improving cleaning ability.
• Greasy soils are generally considered to be one of the most difficult soil types to be removed by hand washing. Effective grease removal is nearly always associated with requiring high temperature water to help dissolve and remove the grease.
• compositions which accomplish this objective.
• the compositions - although prepared from otherwise known ingredients, but in unique combinations and proportions, is capable of achieving a new and beneficial result.
• the liquid dishwashing detergent composition comprises, as essential ingredients: (A) from about 30 to 50% of a surfactant system comprising (1) from about 35 to 65% of a magnesium salt of a C 10 -C 15 alkyl benzene sulfonate anionic surfactant; (2) from 0 to 15% of an alkali metal salt of a 10 -C 16 alkyl benzene sulfonate anionic surfactant; and (3) from about 35 to 65% of an alkyl mono- or polyglucoside having from 9 to 13 carbon atoms, on average, in the alkyl chain, and an average degree of polymerization in the range of from about 1 to 3; and (B) from about 0.5 to 6% of a foam stabilization system comprising at least one lower alkanolamide of higher alkanoic acid, the balance water.
• a surfactant system comprising (1) from about 35 to 65% of a magnesium salt of a C 10 -C 15 alkyl benzene sulfonate ani
• (E) other adjuvants such as, chelating or sequestering agents, coloring agents, dyes, perfumes, bactericides, fungicides, preservatives, sunscreening agents, pH modifiers, pH buffering agents, opacifiers, antioxidants, thickeners, proteins, and the like, up to about 20%, in total, with a maximum of any individual component being about 10%.
• the first essential surfactant ingredient is the anionic magnesium salt of an alkyl benzene sulfonic acid, preferably a linear C 10 to C 16 alkyl benzene sulfonate.
• the linear alkyl group more preferably averages from 10 to 12 carbon atoms, and most preferably averages 12 carbon atoms.
• the most preferred Mg alkyl benzene sulfonate is the magnesium salt of linear dodecylbenzene sulfonic acid.
• the magnesium salt may be, for example, a magnesium oxide neutralized linear dodecyi benzene sulfonic acid, or alternatively, the magnesium salt may be formed by adding a magnesium salt, such as magnesium chloride, magnesium sulfate, etc. to sodium dodecyi benzene sulfonate. In the latter alternative, any excess of the magnesium salt electrolyte will raise the cloud/clear point of the composition. This undesirable effect can, however, be compensated for by addition of hydrotrope, as described below.
• the Mg salt anionic surfactant (1) is present in an amount of from about 15% to about 25%, based on the total composition, or in an amount of from about 35 to 65%, based on the total surfactants (A) (1) , (2) and (3) .
• the more preferred range of amounts of the anionic magnesium salt surfactant is from about 15 to 22%, especially about 20 to 21%, based on the total composition, or about 37 to 58%, especially about 48 to 54%, based on the sum of the surfactants (A) (l) , (2) and (3).
• the surfactant system may also include a small amount, up to about 5% of the total composition, or up to about 15% of the total surfactant component, of an alkali metal salt of a linear C 1Q -C 15 alkyl benzene sulfonic acid anionic surfactant.
• the preferred amounts are up to about 3% (total) or about 8% (surfactant) , respectively, such as about 0.5, 1.0, 1.5, 2.0, or 3.0 percent, of the total composition.
• the alkali metal may be sodium or potassium, preferably sodium.
• the linear alkyl group preferably contains from 10 to 12 carbon atoms, especially 12 carbon atoms, on average, e.g. sodium linear dodecyi benzene sulfonate.
• the sodium salt anionic is generally considered to be a milder detergent than the magnesium salt but is less effective for greasy soil removal and is also less effective in generating foam, especially in the presence of soil and, therefore, its presence in the composition will be minimized or
• magnesium salt anionic is obtained by reacting an electrolyte magnesium salt with sodium alkyl benzene sulfonate, it is not generally necessary to remove any remaining sodium ion and, in fact, this is a convenient means for introducing the magnesium salt into the composition when its presence is desired.
• Another essential surfactant in the invention composition is an alkyl glucoside, preferably an alkyl polyglucoside, although alkyl monoglucoside can also be used.
• alkyl mono- and polysaccharides have received much attention recently for their beneficial detergent, foaming and viscosity modifying properties.
• Examples of patent literature relating to light duty liquid compositions containing alkyl monosaccharides include U.S. Patents 4,732,704 and 4,732,696.
• the alkyl polysaccharides are used in the liquid detergent compositions disclosed in U.S. Patents 4,396,520, 4,536,318, 4,565,647, 4,599,177, 4,663,069, and 4,668,422 (including monoglucosides), as well as many of the patents and literature cited in these patents.
• the alkyl glycosides used in this invention are those having an alkyl group of from 9 to 13 carbon atoms, preferably 9 to 11 carbon atoms, on average, and a glucoside hydrophilic group containing from 1 to about 3, and most preferably from about 1.2 to about 3, glucoside units, such as 1.3, 1.4, 1.5, 2.0 or 2.8 glucoside units.
• the number of glucoside units in any particular surfactant molecule will be a whole number (i.e. an integer) , however, for any actual physical sample of alkyl glucoside surfactants there will, in general, be a range of glucoside units, and it is the average value which characterizes a particular surfactant product, "
• the alkyl group is preferably attached at the 1-position of the sugar molecule, but may be attached at the 1-, 3-, or 4-po ⁇ itions, thus giving a glucosyl rather than a glucoside. Furthermore, in the polyglucosides, the additional glucoside units are predominantly attached to the previous glucoside at the 2-position, but attachment at the 3-, 4- and 6-positions can also occur.
• polyalkylene oxide chain e.g. polyethylene oxide joining the alkyl moiety and the glucoside units
• the preferred alkyl polyglucosides have the formula
• Z is derived from glucose
• R 2 is an alkyl group containing from about 9 to about 11 carbons
• n is 2 or 3, preferably 2
• t is from 0 to about 6, preferably 0,
• x is from l to 3, preferably from 1.2 to 3, most preferably from 1.3 to 2.7.
• R OH long chain alcohol
• the short chain alkyl glucoside content of the final alkyl polyglucoside material should be less than 50%, preferably less than 10%, more preferably less than 5%, most preferably 0% of the alkyl polyglucoside.
• the amount of unreacted alcohol (the free fatty alcohol content) in the desired alkyl polyglucoside surfactant is preferably less than about 2%, more preferably less than about 0.5% by weight of the total of the alkyl polyglucoside plus unreacted alcohol.
• the amount of alkyl monoglucoside is preferably about 20% to about 70%, more preferably 30% to 60%, most preferably 30% to 50% by weight of the total of the alkyl polyglucoside. For some uses it is desirable to have the alkyl monoglucoside content less than about 10%.
• the amount of the alkyl glycoside surfactant to achieve the desired foam and detersive properties is in the range of from about 15 to 25% of the total composition, or from about 35 to 65% of the sum of the surfactants (A) (1) , (2) and (3) .
• the preferred amounts range from 16 to 22%, especially from 18 to 20%, based on the total composition, or from about 40 to 60%, especially from 45 to 55%, based on the total surfactant content.
• the relative amounts of the magnesium alkyl benzene sulfonate surfactant and alkyl mono- or polyglucoside surfactant is not particularly critical, but will generally be within the range of from about 1.3:1 to 1:1.3, more preferably from about 1.2:1 to 1:1.2.
• the total amount of active surfactant components will be in the range of from about 30% to 50% of the total composition, preferably from about 33% to 42%, such as 35%, 36%, 38%,
• the foam stabilization system which may also itself contribute to the foaming capacity as well as foam stabilizing effect is comprised of the lower alkanolamide of higher alkanoic acid which is the reaction product of a lower alkanol of 2 to 3 carbon atoms and an alkanoic acid of 10 to 16 carbon atoms, preferably with 80% or more of the lower alkanol being ethanol and a similar proportion of the alkanoic acid being of 12 to 14 carbon atoms.
• Other lower alkanols that are also useful are n-propanol and isopropanol.
• the preferred alkanoic acid is a mixture of lauric and yristic acids, generally in proportions of 1:2 to 2:1, with about 50% of each being preferable.
• coconut oil or hydrogenated coconut oil may be used as a source of the alkanoic acids.
• Suitable alkanoic acid alkanolamides include the monoethanolamides, diethanolamides and the monoisopropanolamides.
• Specific examples include mixed lauric/myristic diethanolamide, lauric/myristic monoethanolamide, lauric monoethanolamide, lauric diethanolamide, coco diethanolamide, coco monoethanolamide, and the like.
• trialkyl amine oxides or lower alkoxylated alkanoic acid alkanolamides may be employed.
• the amine oxides are usually dilower alkyl higher alkyl amine oxides wherein the lower alkyls are of 1 to 3 carbon atoms and the higher alkyls contain from 10 to 16, preferably 12 to 14 carbon atoms.
• the alkoxylated alkanoic acid alkanolamide has from 1 to 10, preferably 2 to 4 ethoxy groups in the molecule.
• the alkanol and the fatty acid are the same as for the present alkanoic acid alkanolamides.
• the replacement of alkanolamide will be to the extent of only 5 to 40% by weight of the proportions thereof given above. While the alkanolamide may, for some uses, be completely replaced by the amine oxide, ethoxylated alkanolamide or mixture thereof, such complete replacement is not preferred. Most preferably, none of the alkanoic acid alkanolamide content is replaced by the amine oxides.
• the amount of the alkanoic acid alkanolamide may be up to about 6% of the composition, such as 0.5 to 6%, preferably 1 to 6%, more preferably 1 to 5%, such as 2, 3 or 4%, of the composition.
• compositions of this invention which include the magnesium salt surfactant, alkyl polyglucoside and foam stabilization system, in the specified proportions, as essential ingredients are formulated in an aqueous carrier to provide mild, stable foaming liquid compositions especially effective in cleaning, by hand washing, dishware, such as dishes, glasses, flatware, pots, pans, etc., at ambient wash water temperature, as well, of course, at warm or hot wash water temperatures.
• dishware such as dishes, glasses, flatware, pots, pans, etc.
• ambient wash water temperature as well, of course, at warm or hot wash water temperatures.
• the invention formulations are mild to the hands and are clear and homogeneous. Clarity and homogeneity may often, however, be improved by inclusion of, for example, organic solvents and/or hydrotropes, and these and other optional additives may also be included in the compositions in amounts which do not adversely influence the desirable properties.
• C Organic Solvent
• Cosmetically acceptable organic solvents usually lower alcohols, such as ethanol, propanol, isopropanol, propylene glycol, or mixtures thereof, may be included in the composition for its thinning effect, lowering of clear point, and for 2 .- _ lubilizing effect for any components which may not be readily soluble in the main aqueous medium.
• the amount of solvent, when present, will usually be limited to about 10%, preferably 8%, especially about no more than 6% of the composition, such as from 2 to 5%. Ethanol is the preferred organic solvent.
• hydrotropes include primarily urea and the lower alkyl aryl sulfonate salts, such as sodium xylene sulfonate, potassium xylene sulfonate, sodium cumene sulfonate, ammonium xylene sulfonate, and the like. Mixtures of two or more hydrotropes may also be used.
• the hydrotrope when used, is generally present in amounts below about 8%, preferably below about 6%, such as from 1 or 2 to 6%.
• opacifying agents e.g. behenic acid
• a pearlescent or pearlizing composition such as an approximately equal mixture of high fatty acid ester of polyethoxy ethanol, coconut oil fatty acid alkanolamide and sodium lauryl ether sulfate.
• the higher fatty acid will usually be of 10 to 18 carbon atoms and the polyethoxy content will be of 1 to 20, preferably 1 to 10 ethoxy groups.
• the alkanolamide will preferably by ethanola ide, but can be mixed with isopropanola ide, too.
• Additional adjuvant components of the present compositions include perfumes; sequestrants, e.g. monohydrogen ethylene dia ine tetraacetate, tetrasodium ethylene diamine tetraacetate, trisodium nitrilotriacetate; bactericides, e.g. trichlorocarbanilide, tetrachlorosalicylanilide, hexachlorophene, chlorobromosalicylanilide; antioxidants; thickeners, e.g. sodium carboxymethyl cellulose, polyacrylamide, Irish moss; dyes; water dispersible pigments; salts, e.g. sodium sulfate, magnesium sulfate, as the heptahydrate or anhydrous, sodium chloride; preservatives, such as formaldehyde or hydrogen peroxide, pH modifiers, etc.
• sequestrants e.g. monohydrogen ethylene dia ine tetraacetate, t
• the total amount of the additional additives is usually no more than about 20% of the composition, preferably not exceeding 15%, while the amount of any individual ingredient will not generally exceed 10%, especially 5%, and usually no more than 2 or 3%.
• compositions of this invention and the various adjuvants employable therein, and in the claims, although individual constituents are mentioned for various classes or types of components it is within the invention that mixtures thereof be employed, such as mixtures of two or three anionic detergents or mixtures with the nonionic detergents, both possibly with other anionic and nonionic detergents known in the art, mixtures of skin treating materials and mixtures of solvents, among others.
• paraffin sulfonate surfactants such as sodium or magnesium (C 12 -C 18 ) paraffin sulfonate
• C 12 -C 18 paraffin sulfonate usually together with minor amounts of 10 -C 18 alkyl ether ethyleneoxy sulfates of the formula R(OC 2 H 4 ) n OS0 3 M wherein n is 1-10, preferably 1-5, such as 2 or 3,
• R is alkyl containing 10 to 18 carbon atoms, preferably 12 to 15 carbon atoms
• M is a cation, preferably sodium, potassium or ammonium, or magnesium
• an amine oxide nonionic foam stabilizer preferably mono g-C 18 alkyl di-(C 1 -C 4 alkyl or C 1 -C 2 alkanolamine) oxides
• an amine oxide nonionic foam stabilizer preferably mono g-C 18 alkyl di-(C 1 -C 4 alkyl or C 1 -C 2 alkanolamine)
• compositions containing from 13 to 18% paraffin sulfonate, 4 to 6% magnesium sulfate heptahydrate, 2 to 4% amine oxide, 9 to 13% of alkyl polyglucoside (Cg-C- ⁇ alkyl polyglucoside with 1.2 to 3 glycoside units), and 0 to 8% of the alkyl ether sulfate are especially effective.
• the viscosities of the detergent compositions may be further varied by the addition of thickening agents, such as gums and cellulose derivatives.
• the product viscosity and flow properties should be such as to make it pourable from a bottle and not so thin as to tend to splash or pour too readily, since usually only small quantities of the liquid detergent are to be utilized in use.
• Viscosities from 20 to 1000 centipoise (Brookfield Viscometer spindle no. 1, 12 r.p. .) are found useful with those from 100 to 500 cps. being preferred and a viscosity of about 200 centipoise being considered best by most consumers, although at somewhat lower viscosities, e.g. 100 cps., consumer acceptance is almost the same.
• the detergent constituents usually it is preferred to heat the detergent constituents to a somewhat elevated temperature, e.g. 40° to 50°C and then admix them with the water and, optionally, all or a portion of the ethanol. Thereafter, other anionic and nonionic detergents, urea, amide, protein and other adjuvants are added with the more volatile materials, such as perfumes, preferably being added last and after cooling of the composition to about room temperature. Normally when making opaque or pearly detergents, the pearlizing mixture will also be added near last at about room temperature.
• various other known techniques may also be employed, depending upon the particular detergent composition.
• the pH of the formulation will generally be near neutral, e.g. about 6 to 8, preferably about 6.5 to 7.5.
• Example 1 The following representative non-limiting examples will help to further understand the present invention.
• compositions are prepared: Component Run No.
• Mg linear dodecyi benzene sulfonate [Mg(LDBS) 2 ]
• LMEA Lauric/myristic monoethanolamide
• HEDTA Monohydrogen ethylene diamine tetraacetate, trisodium salt
• the emulsification stability of corn oil in a 1% surfactant solution at 50 ppm hardness (Ca:Mg 2:1), 100 ppm HC0 3 -.
• 0.20 g of Mazola corn oil is added to 19.80 g of the diluted (1%) surfactant solution and placed in a vial.
• the vial is inverted 25 times by hand and allowed to stand 5.0 min.
• the turbidity is read both before and after the test on a Hach turbidimeter and the change in turbidity (NTU) is calculated. The higher the turbidity the better the emulsion stability.
• a diluted (0.1% test solution is titrated with Crisco (hydrogenated cotton seed) soil to a foam end point under constant agitation in 50 ppm hardness water. This test measures the total number of plates which can be washed with the detergent composition until the foam is killed, i.e., before there is no longer the appearance of foam on top of the wash water.
• test solution A diluted (0.1%) test solution is agitated in a standard tergotometer while planchets filled with lard (Armour) are periodically added. The number of planchets required to reduce the foam height to 50 ml is measured.
• Control No. 1 Leading commercial brand of hand dishwashing composition containing anionic surfactant; foam booster; hydrotropes; inorganic salts; ethanol; water.
• composition wt.
• This test measures amount of greasy soil (lard) removal from the surface of a plastic beaker.
• 0.55 to 0.60 g of lard is spread on the walls of a 250 ml plastic beaker and the beaker is then filled with 250 grams of a 1% diluted solution of the test composition.
• the test composition is mechanically agitated with a stirrer at 200 rpm for 5 minutes.
• the percent trans ittance (%T) is measured by a fiber optic probe at 490 ran light using a Brinkman PC 800 colorimeter. The lower the value of %T as time progresses the better is the greasy soil removal capability of the test composition.
• This test is only valid for compositions that are initially clear enough to be standardized at zero absorbance with the PC 800 colorimeter.
• the procedure described for the grease removal test (5) is modified by using hamburger grease as the soil and tap water at 105°F for dilution.
• This test also measures the ability of a diluted (1%) solution in 50 ppm or 150 ppm hardness water to remove a greasy soil (lard) from a test surface (a cleaned glass slide 2.5 cm x 0.1 cm) .
• the soil is applied by spreading about 0.2 to about 0.3 gram lard onto each cleaned glass slide.
• the soiled slides are cleaned in a 1% product solution by dipping the soiled slide into the solution 600 times.
• the solution is maintained at ambient temperature (75°F) .
• the slides are dried in a desiccator for two hours.
• the difference in weight of the lard before and after the cleaning process is taken as a measure of grease removal, the greater the difference the more effective is the detergent composition.

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• Oil, Petroleum & Natural Gas (AREA)
• Wood Science & Technology (AREA)
• Organic Chemistry (AREA)
• Detergent Compositions (AREA)

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• 1989
  • 1989-08-07 NZ NZ230239A patent/NZ230239A/en unknown
  • 1989-08-08 ZA ZA896048A patent/ZA896048B/xx unknown
  • 1989-08-11 GR GR890100505A patent/GR1000487B/el unknown
  • 1989-08-14 EP EP89909976A patent/EP0431050A1/de not_active Withdrawn
  • 1989-08-14 KR KR1019900700790A patent/KR920002113B1/ko not_active IP Right Cessation
  • 1989-08-14 BR BR898907611A patent/BR8907611A/pt unknown
  • 1989-08-14 WO PCT/US1989/003469 patent/WO1990002164A1/en not_active Application Discontinuation
  • 1989-08-14 AU AU41970/89A patent/AU634489B2/en not_active Ceased
  • 1989-08-16 EG EG397/89A patent/EG18567A/xx active
  • 1989-08-16 MX MX017219A patent/MX169917B/es unknown
  • 1989-08-17 MY MYPI89001122A patent/MY104167A/en unknown
  • 1989-08-17 PT PT91475A patent/PT91475B/pt not_active IP Right Cessation
  • 1989-08-18 ES ES8902896A patent/ES2016055A6/es not_active Expired - Lifetime
• 1991
  • 1991-02-18 FI FI910764A patent/FI910764A0/fi not_active Application Discontinuation
  • 1991-02-19 DK DK028491A patent/DK28491D0/da not_active Application Discontinuation

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