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
  • C11D3/001—Softening compositions
  • C11D3/0015—Softening compositions liquid
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
  • C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
  • C07C213/06—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton from hydroxy amines by reactions involving the etherification or esterification of hydroxy groups
• • 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
  • C11D1/62—Quaternary ammonium 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
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/20—Organic compounds containing oxygen
  • C11D3/2075—Carboxylic acids-salts thereof
  • C11D3/2079—Monocarboxylic acids-salts thereof
• • 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
  • C11D3/16—Organic compounds
  • C11D3/20—Organic compounds containing oxygen
  • C11D3/2093—Esters; Carbonates
• • 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
  • C11D3/16—Organic compounds
  • C11D3/26—Organic compounds containing nitrogen
  • C11D3/30—Amines; Substituted amines ; Quaternized amines
• • 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
  • C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
  • C11D7/22—Organic compounds
  • C11D7/32—Organic compounds containing nitrogen
  • C11D7/3209—Amines or imines with one to four nitrogen atoms; Quaternized amines
• • 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
  • C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
  • C11D2111/10—Objects to be cleaned
  • C11D2111/12—Soft surfaces, e.g. textile

Definitions

• the present invention relates to fabric treatment compositions and methods of using and making the same.
• WO2007/092020 also teaches that the iodine value (IV) of the feed used to provide the alkyl chains should be 20 or below - in general, the lower the IV of the feed, the worse the storage stability of liquid compositions made from fabric softener actives utilizing that feed, since the more saturated the fatty acids that hydrolyze (especially at elevated temperatures of the liquid fabric softener composition), the more they will crystallize and increase viscosity.
• IV iodine value
• the present technology provides a liquid fabric softening composition
• a liquid fabric softening composition comprising from 0.5% to 12% by weight of a fabric softening active containing an esterquat mixture of quaternized mono-, di- and tri-ester alkanolamines, in which the tri-esterquat content of the esterquat mixture is greater than 25% by weight of the mixture; and water; wherein, when the fabric softening active is made from a 50% by weight hard, 50% by weight soft tallow fatty acid mixture, the initial viscosity of a 4% dispersion of the composition is greater than 304 cPs; and the fabric softening active contains greater than1 % free fatty acid.
• the present technology is directed to a method for conditioning textiles comprising, in no particular order, the steps of:
• A. providing a laundry detergent or fabric softener composition comprising water, at least one anionic surfactant, and from 0.5% to 12% by weight of a fabric softening active containing an esterquat mixture of quaternized mono-, di-, and tri- ester alkanolamines, in which the tri-esterquat content of the esterquat mixture is greater than 25% by weight of the mixture, in a ratio and concentration to effectively soften and condition fabrics under predetermined laundering conditions;
• the present technology is directed to a fabric softening active composition
• a fabric softening active composition comprising: a mixture of quaternized mono-, di- and tri-ester alkanolamines
• the combined diester quat and triester quat is greater than 78% by weight of the total esterquat mixture; the triester quat is greater than 25% by weight of the total esterquat mixture; and, the fabric softening active contains greater than 1 % by weight free fatty acid.
• the molar ratio of fatty acid/fat to alkanolamine used to make the esterquat mixture is greater than 1 .94:1 , and the reaction time required to produce the esteramine which yields a triester quat content of greater than 25% and combined diester quat and triester quat content of greater than 78% after quatting is less than 6 hours and 40 minutes when the reaction is run at 1 90°C and the zero time of the reaction is set at when the reaction mixture first reaches 190 ⁇ .
• the fabric conditioning active material of the present invention is useful, for example, in formulating liquid fabric conditioning and antistatic compositions used, for example, in a laundering process.
• the fabric conditioning active material of the present invention comprises an esterquat mixture of quaternized mono-ester, di-ester, and tri-ester components wherein the tri-esterquat component is greater than 25% by weight of the total esterquat mixture, up to about 55%, alternatively up to 50%, alternatively up to 45% by weight of the total esterquat mixture.
• the combined di-ester quat and tri-ester quat components is greater than 78% by weight of the total esterquat mixture, up to about 98%, alternatively up to 95%, alternatively up to 93% by weight of the total esterquat mixture. (The sum of the weights of mono-esterquat, di- esterquat, and tri-esterquat is 100% by weight of the esterquat mixture.)
• esterquat conditioning material comprises, respectively, a mono-esterquat (an esterquat compound comprising a single ester link with a fatty hydrocarbyl chain attached thereto), a di-esterquat (an esterquat compound comprising two ester links each of which has a fatty hydrocarbyl chain attached thereto), and a tri-esterquat (an esterquat compound comprising three ester links each of which has a fatty hydrocarbyl chain attached thereto).
• a "fatty hydrocarbyl chain” such as “FT in the amine and esterquat structures in this specification, is the alkyl or alkenyl moiety of a fatty acid, having one less carbon atom than the corresponding complete fatty acid. (The final carbon atom of the complete fatty acid is the acyl carbon of the ester linkage.)
• stearic acid has 18 carbon atoms, arranged in the molecular formula:
• the corresponding fatty hydrocarbyl chain is CH 3 (CH 2 ) i 6-, alternatively referred to here as a C17 alkyl moiety. If unsaturated (for example, the fatty hydrocarbyl chain of oleic acid - a monounsaturate), it would be a Ci 7 alkenyl moiety.
• the average chain length of the alkyl or alkenyl moiety is at least Ci 3 , alternatively at least C15. In one contemplated embodiment, at least 80% of the chains have a length of Ci 5 Ci 7 combined. [18] It is contemplated in one embodiment that the alkyl or alkenyl chains can be predominantly linear.
• the fatty acid hydrocarbyl chain can be contributed by various starting materials, for example free fatty acids, either separately or in combinations, such as fatty acid mixtures characteristic of the fatty acid constituents of glyceride esters in natural tallow, palm oil, palm kernel oil, lard, corn oil, soybean oil or other suitable feedstocks or mixtures thereof.
• Other contemplated starting materials are glyceride mono-, di-, or tri-esters of fatty acids (for example, tallow or palm kernel oil), lower alkyl esters of fatty acids (for example methyl esters), acid chlorides corresponding to fatty acids, and other compounds, as is well known in the art.
• these fatty acid derivatives may be made from a single fatty acid or mixtures of fatty acids, such as those derived from natural fatty acid feedstocks.
• the fatty acid feedstocks contain predominately (for example 80% or more) C16 and C18 fatty acids and/or methyl esters.
• alkanolamines useful in preparing the fabric softening active generally correspond to the following general formula:
• Suitable alkanolamines include triethanol amine (TEA), tripropanol amine, dimethyl amino-N-(2,3-propanediol), diethylamino-N-(2,3-propanediol), methylamino- N-2-ethanol-N-2,3-propanediol, and ethylamino-N-2-ethanol-N-2,3-propanediol, and mixtures thereof.
• the molar ratio of fatty acid/fat to alkanolamine is greater than 1 .94:1 , preferably equal to or greater than 2.0:1 , up to about 2.7:1 , alternatively 2.5:1 .
• Preferred esterquats are the TEA-based esterquats.
• Each R is independently selected from a C5-35 alkyl or alkenyl group, optionally a C7-21 alkyl or alkenyl group, optionally a Cn-21 alkyl or alkenyl group, optionally an at least predominantly C13-17 alkyl or alkenyl group.
• R 1 represents a Ci- 4 alkyl or hydroxyalkyl group or a C 2 - 4 alkenyl group,
• O O T is — O— C— or — C— O—
• n is 0 or an integer selected from 1 to 4, optionally selected from 2 to 4; m is 1 for an mono-esterquat, 2 for an di-esterquat, or 3 for an tri-esterquat, and denotes the number of moieties to which it refers that pend directly from the N atom, and X " is an anionic group, such as a halide or alkyl sulphate, for example, a Ci- 4 alkyl or hydroxyalkyl sulfate or a C 2 - 4 alkenyl sulfate.
• anionic groups include chloride, methyl sulphate or ethyl sulphate.
• Contemplated materials within this class are esters of triethanolammonium methyl sulphate, particularly tallow or hardened tallow esters.
• the tri-esterquat content of the fabric conditioning material is greater than 25% by weight.
• This tri-esterquat content can be provided in a variety of ways, as by using a relatively high ratio of the fatty acid to the starting alkanolamine in the reaction mixture, using an optimal amount of a suitable catalyst in the reaction mixture for promoting triester formation, raising the temperature of the reaction mixture relatively slowly, and other expedients known to the skilled person.
• the contemplated di-esterquat content of the esterquat mixture is at most 70%, optionally at most 60%, optionally at most 53%, by weight of the esterquat mixture such that the combination of di-ester quat and tri-esterquat is greater than 78% by weight of the esterquat mixture.
• the weight percentages of the mono-, di-, and tri-esterquats in the esterquat mixture are reported on the basis of the total weight of the three. Thus, the sum of these three percentages is 100%.
• the weight percentages of free amine and fatty acid in the esterquat mixture are also stated here based on the total weight of mono-, di-, and tri-esterquats in the esterquat mixture.
• compositions should contain greater than 1 % by weight of free fatty acid based on the fabric conditioning material.
• a free fatty acid content of greater than 1 % can be provided, for example, by reacting a fatty acid or a parent fatty acyl compound (such as a glyceride, alkyl ester, or acid chloride) and trialkanolamine at a reaction temperature of about 190°C or less and at a reaction time of less than 6 hours and 40 minutes when the reaction temperature is 190°C.
• the free fatty acid content can be up to 10%, alternatively up to 8% based on the weight of the fabric conditioning active.
• the iodine value of the parent fatty acyl compound or acid from which the esterquat fabric conditioning material is formed is from 1 to 1 00, preferably from 5 to 80, alternatively from 1 0 to 60, alternatively from 15 to 55, alternatively from 20 to 50. It is therefore contemplated that the alkyl or alkenyl carbon chains contain at least some unsaturation.
• the iodine value represents the mean iodine value of the parent fatty acyl compounds or fatty acids of all of the esterquat materials present.
• the iodine value of the parent fatty acyl compound or acid, from which the fabric conditioning material is formed is defined as the number of grams of iodine which react with 100 grams of the parent compound.
• the method for calculating the iodine value of a parent fatty acyl compound/acid is known in the art and comprises dissolving a prescribed amount (from 0.1 -3g) into about 1 5ml chloroform.
• the dissolved parent fatty acyl compound/fatty acid is then reacted with 25 ml of iodine monochloride in acetic acid solution (0.1 M). To this, 20ml of 10% potassium iodide solution and about 150 ml deionized water are added. After addition of the halogen has taken place, the excess of iodine monochloride is determined by titration with sodium thiosulfate solution (0.1 M) in the presence of a blue starch indicator powder. At the same time a blank is determined with the same quantity of reagents and under the same conditions. The difference between the volume of sodium thiosulfate used in the blank and that used in the reaction with the parent fatty acyl compound or fatty acid enables the iodine value to be calculated.
• the conditioning active compositions of the present invention are made by combining a fatty acid source and an alkanolamine, typically at a starting temperature at which the fatty acid source is molten, optionally adding a catalyst, then heating the reaction mixture while drawing vacuum until the desired endpoint(s), such as acid value and final alkalinity value, are reached.
• a typical acid value endpoint is in the range of about 0.05 to about 0.06 meq/g.
• a desired alkalinity value will depend upon the ratio of fatty acid/fat to alkanolamine, but typically will be about 1 .30 to about 1 .90 meq/g.
• the resulting esteramine intermediate is then quaternized using an alkylating agent, yielding an esterquat product.
• the esterquat product is a mixture of quaternized monoester, diester, and triester components and optionally some amount of one or more reactants, intermediates, and byproducts, including but not limited to free amine and free fatty acid or parent fatty acyl compounds.
• the fabric conditioning active compositions of the present invention can be formulated with water and other ingredients to provide fabric conditioner compositions for use in the rinse cycle of a domestic or commercial laundry process. Additional ingredients useful in formulating fabric conditioner compositions are known to those of skill in the art. Some examples of other ingredients can be found in WO2007/092020, which is herein incorporated by reference.
• the fabric conditioner compositions can optionally further comprise a liquid carrier.
• the liquid carrier employed in the instant compositions is preferably water due to its low cost, relative availability, safety, and environmental compatibility.
• the level of water in the liquid carrier is more than about 50%, optionally more than about 80%, alternatively more than about 85%, by weight of the carrier.
• the level of liquid carrier is greater than about 50%, optionally greater than about 65%, alternatively greater than about 70%.
• Mixtures of water and a low molecular weight, for example ⁇ 100, organic solvent, for example a lower alcohol such as ethanol, propanol, isopropanol or butanol are useful as the carrier liquid.
• Low molecular weight alcohols including monohydric, dihydric (glycol, etc.) trihydric (glycerol, etc.), and polyhydric (polyols) alcohols are also suitable carriers for use in the compositions of the present invention.
• Adjunct ingredients may be added to the compositions of the present technology.
• the term "adjunct ingredient” includes: perfumes, dispersing agents, stabilizers, pH control agents, metal ion control agents, colorants, brighteners, dyes, odor control agent, pro-perfumes, cyclodextrin, perfume, solvents, soil release polymers, preservatives, antimicrobial agents, chlorine scavengers, anti-shrinkage agents, fabric crisping agents, spotting agents, anti-oxidants, anti-corrosion agents, bodying agents, drape and form control agents, smoothness agents, static control agents, wrinkle control agents, sanitization agents, disinfecting agents, germ control agents, mold control agents, mildew control agents, antiviral agents, antimicrobials, drying agents, stain resistance agents, soil release agents, malodor control agents, fabric refreshing agents, chlorine bleach odor control agents, dye fixatives, dye transfer inhibitors, color maintenance agents, color restoration, rejuvenation agents, anti-fading agents,
• the liquid fabric softening compositions of the present technology achieve a high initial viscosity when the fabric softening active is present in an amount from 0.5 to 12%, preferably 1 .5% to 10%, more preferably 2% to 8%, most preferably 3% to 6% by weight of esterquat material (active ingredient) based on the total weight of the composition.
• the initial viscosity is determined by taking viscosity measurements of the liquid fabric softener compositions after 24 hours on a Brookfield DV-II+ Pro Viscometer with an RVT spindle #4 at 50 rpm at 70 °F.
• the initial viscosity is greater than 304 cPs, alternatively, greater than 310 cPs, alternatively greater than 325 cPs, alternatively greater than 350 cPs.
• the initial viscosity is less than 304 cPs
• the initial viscosity is greater than 304 cPs.
• the initial viscosities can range up to about 5000 cPs, alternatively up to 4000 cPs, alternatively up to 3000 cPs, alternatively up to 2000 cPs.
• liquid fabric softening compositions have good storage stability, even under elevated temperature conditions, and provide good fabric softening properties.
• Making the liquid fabric softener composition entails slowly mixing the molten quat which is at 80°C or less into the liquid, preferably water, which has been heated to 70 °C or less with agitation. The dispersion is then mixed for several minutes more while it is allowed to cool to room temperature.
• the approach described here is not intended to be limiting as to how the dispersion can be made. Dispersion production can follow many approaches and is well known to those skilled in the art. As the temperature of the fabric softener active system is increased, viscosity decreases. Therefore, 80 °C will be the point of lowest viscosity yet at the maximum temperature which will still minimize chemical degradation in storage.
• the fabric softening compositions of the present technology are suitable for use in the rinse cycle of a laundry process, in particular, the rinse cycle of a domestic or industrial automatic laundry washing machine or a hand washing laundry rinse basin.
• the fabric softening composition can be dispensed from a fabric softener dispenser that is integral to the automatic laundry washing machine at the appropriate time during the laundry process.
• the fabric softening composition is added to the dispenser in an amount effective to soften and condition fabric articles under predetermined laundering conditions.
• the fabric softening composition is dispensed from the dispenser and contacts the fabric articles to soften and condition the fabrics. Following the laundering process, the fabric articles are allowed to dry or are mechanically tumbled dry.
• the fabric softening composition can be used in a hand washing laundry process wherein the fabric softening composition is added to one or more rinse bath solutions for manually rinsing fabric articles in a hand washing laundry process.
• the fabric softening composition is added to the rinse bath solution in an amount effective to soften and condition the fabric articles. Following the laundering process, the fabric articles are allowed to dry or are mechanically tumbled dry.
• Antioxidant 101 a tetrakis [methylene-3 (3',5'-di-tert-butyl-4- hydroxyphenyl)propionate] methane (commercially available from Mayzo, Inc. Suwanee, GA) and phosphorous acid were added. TEA was added at the desired amount. Nitrogen was regulated and sub-surface sparged at a rate of 150 mL/min. The mixture was heated until a temperature of 190°C was reached. As water distilled, the reaction mixture was tested for residual fatty acid using 0.1 N KOH in methanol until the target amount of free fatty acid was achieved.
• the produced ester amine mixture was then added to a flask equipped with nitrogen blanketing, mechanical stirring and a reflux condenser.
• the quatting agent dimethyl sulfate
• Methyl chloride can also be used as the quatting agent.
• Isopropanol was added to the flask, and the reaction was cooled to 72 °C.
• Sodium chlorite was added to the flask at the desired amount for bleaching followed by butylated hydroxytoluene as an antioxidant and citric acid monohydrate as a pH control agent.
• Palm Fatty Acid-Based Esterquat Synthesis The desired amount of palm fatty acid was placed into a 2-liter glass reactor equipped with mechanical stirring, a distillation column and nitrogen blanketing. Fabric softener actives 2 and 9were made with a 50:50 weight percent mixture of fully hardened ("hard”) and, "as is", non- hydrogenated ("soft") palm fatty acid. Antioxidant 101 0 and phosphorous acid were added. TEA was added at the desired amount. Nitrogen was regulated and subsurface sparged at a rate of 150 mL/min. The mixture was heated until a temperature of 175 °C was reached.
• the reaction mixture was tested for residual fatty acid using 0.1 N KOH in methanol until the target amount of free fatty acid was achieved.
• the produced esteramine mixture was then added to a flask equipped with nitrogen blanketing, mechanical stirring and a reflux condenser.
• the quatting agent dimethyl sulfate
• Methyl chloride can also be used as the quatting agent.
• Isopropanol was added to the flask, and the reaction was cooled to 72 °C.
• Sodium chlorite was added to the flask at the desired amount for bleaching followed by butylated hydroxytoluene as an antioxidant and citric acid monohydrate as a pH control agent.
• Esterquat weight percent method Dilute esterquat solutions were prepared by dissolving around 100 mg of esterquat in about 2ml_ of a 2:1 mixture of acetone- d6 and chloroform-d for analyzing FSAs 1 -10; a 1 :1 mixture of acetone-d6 and chloroform-d was used to analyze FSAs 1 1 -14. Proton NMR spectra of the solutions are collected using standard proton acquisition parameters with a 15 second relaxation delay. The esterquat peaks are identified and the spectrum is integrated. The normalized weight percents of the MEQ, DEQ and TEQ are calculated from their integrated areas.
• Free fatty acid determination in the fabric softener active composition a.
• the Acid Value is determined for the esteramine using a colorimetric titration to a pink endpoint using phenolphthalein indicator b.
• the Free Fatty Acid % is determined for the esteramine using the Molecular Weight for the Fatty Acid (i.e. 272 g/mol)
• Esteramine Free Fatty Acid % Acid Value meq/g * (MW Fatty Acid/10)
• the Free Fatty Acid % for the esterquat is determined using the percentage of esteramine in the esterquat formulation (i.e. 72%)
• Esterquat Free Fatty Acid % Esteramine Free Fatty Acid % * Percentage of esteramine in esterquat.
• liquid fabric softener compositions were made by heating water from 35 °C to 55 °C in a glass beaker equipped with an Ika Eurostar mixer and blade with a 2.5" diameter and then slowly adding the molten FSA while agitating between 1 00 - 600 rpm. After all the FSA was added, agitation was continued for another 20 minutes.
• fabric softener actives 1 and 2 afford only very low viscosity 4% aqueous dispersions.
• Fabric softener actives 1 and 2 and Formulations 1 and 2 are examples of compositions which fall outside the scope of this invention.
• Example 2 is
• Fabric softener active 3 has a long reaction time relative to fabric softener active 4 and both afford about the same level of TEQ and combined DEQ and TEQ.
• Fabric softener active 4 utilizes more biorenewable ingredient (fatty acid) relative to the petroleum-based amine hub (TEA) than does fabric softener active 3. Even though both Formulations are based on fabric softener actives with similar TEQ and DEQ levels, Formulation 4 has higher viscosity than Formulation 3.
• Fabric softener active 3 and Formulation 3 are examples of compositions which fall outside the scope of this invention.
• Fabric softener active 4 and Formulation 4 are examples of compositions which fall within the scope of this invention.
• Example 3 is
• Fabric softener active 5 has a long reaction time relative to fabric softener active 6 and both afford about the same level of TEQ and combined DEQ and TEQ.
• Fabric softener active 6 utilizes more biorenewable ingredient (fatty acid) relative to the petroleum-based amine hub (TEA) than does fabric softener active 5.
• TAA petroleum-based amine hub
• Formulation 6 has higher viscosity than Formulation 5.
• Formulation 6 also retains its viscosity better than Formulation 5 after extended storage at elevated temperature.
• Fabric softener active 5 and Formulation 5 are examples of compositions which fall outside the scope of this invention.
• Fabric softener active 6 and Formulation 6 are examples of compositions which fall within the scope of this invention.
• Fabric softener active 7 and Formulation 7 are examples of compositions which fall outside the scope of this invention.
• Fabric softener actives 8 and 9 and Formulations 8 and 9 are examples of compositions which fall within the scope of this invention.
• Example 6
• Fabric softener active 10 is an example of a composition which falls outside the scope of this invention.
• FSA 1 1 and Formulations 10 and 12 are examples of compositions which fall within the scope of this invention.
• FSA 13 and Formulation 14 are examples of compositions which fall within the scope of this invention.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Wood Science & Technology (AREA)
• Health & Medical Sciences (AREA)
• Emergency Medicine (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Priority Applications (11)

Applications Claiming Priority (2)

Related Child Applications (1)

Publications (1)

Family

ID=51537433

Family Applications (1)

Country Status (10)

Cited By (5)

Families Citing this family (2)

Citations (5)

Family Cites Families (15)

• 2013
  • 2013-10-17 WO PCT/US2013/065477 patent/WO2014143182A1/en not_active Ceased
  • 2013-10-17 EP EP13877679.4A patent/EP2970827B1/en active Active
  • 2013-10-17 MX MX2015012784A patent/MX362992B/es unknown
  • 2013-10-17 MY MYPI2015002381A patent/MY189487A/en unknown
  • 2013-10-17 AU AU2013381757A patent/AU2013381757B2/en active Active
  • 2013-10-17 CA CA2907001A patent/CA2907001C/en active Active
  • 2013-10-17 CN CN201380076525.7A patent/CN105209589B/zh active Active
  • 2013-10-17 BR BR112015023490-9A patent/BR112015023490B1/pt active IP Right Grant
  • 2013-10-17 MX MX2018015425A patent/MX370999B/es unknown
  • 2013-10-17 JP JP2016500101A patent/JP6397883B2/ja active Active
• 2015
  • 2015-09-14 US US14/853,500 patent/US20160010029A1/en not_active Abandoned
• 2016
  • 2016-06-03 US US15/173,188 patent/US10011807B2/en active Active

Patent Citations (5)

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events