ES2140563T5 - TISSUE CONDITIONING COMPOSITION. - Google Patents
TISSUE CONDITIONING COMPOSITION.Info
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- ES2140563T5 ES2140563T5 ES94929545T ES94929545T ES2140563T5 ES 2140563 T5 ES2140563 T5 ES 2140563T5 ES 94929545 T ES94929545 T ES 94929545T ES 94929545 T ES94929545 T ES 94929545T ES 2140563 T5 ES2140563 T5 ES 2140563T5
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Classifications
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- 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
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- 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
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/94—Mixtures with anionic, cationic or non-ionic compounds
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- 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
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- 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
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/90—Betaines
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
Abstract
UNA COMPOSICION CONCENTRADA DE ACONDICIONAMIENTO DE TEJIDOS QUE CONTIENE MAS DE UN 7 % EN PESO DE UN AGENTE SUAVIZANTE CATIONICO Y UN COMPUESTO ZWITTERIONICO DE LA FORMULA (I), EN LA QUE R ES UN GRUPO ALQUILO C{SUB,7}-C{SUB,27} O ALQUENILO; R{SUP,1} Y R{SUP,2} SE SELECCIONAN INDEPENDIENTEMENTE DE GRUPOS ALQUILO C{SUB,1-14}; Z ES O O NH; A ES UN ENTERO DE 0 A 1; B Y C SE SELECCIONAN INDEPENDIENTEMENTE DE LOS ENTEROS DEL 1 AL 4; Y X{SUP,-} ES UN ANION COMPATIBLE. LA COMPOSICION PUEDE TOLERAR ALTOS NIVELES DE PERFUME Y PASA RAPIDAMENTE A UN ESTADO LIQUIDO CUANDO SE DESCONGELA.A CONCENTRATED COMPOSITION OF FABRIC CONDITIONING CONTAINING MORE THAN 7% BY WEIGHT OF A CATIONIC SOFTENING AGENT AND A ZWITTERION COMPOUND OF FORMULA (I), IN WHICH R IS A RENTING GROUP C {SUB, 7} -C {SUB , 27} OR ALKYLENE; R {SUP, 1} AND R {SUP, 2} SELECTED INDEPENDENTLY FROM GROUPS RENT C {SUB, 1-14}; Z ES O O NH; A IS A WHOLE FROM 0 TO 1; B AND C ARE SELECTED INDEPENDENTLY FROM THE ENTIRE 1 TO 4; AND X {SUP, -} IS A COMPATIBLE ANION. THE COMPOSITION CAN TOLERATE HIGH LEVELS OF PERFUME AND RAPIDLY GOES TO A LIQUID STATE WHEN DEFROSTING IT.
Description
Composición acondicionadora de tejidos.Fabric conditioning composition.
La presente invención se refiere a una composición acondicionadora de tejidos. En particular la invención se refiere a dispersiones acuosas de composiciones acondicionadoras de tejidos que comprenden un compuesto de amonio cuaternario insoluble en agua y un compuesto híbrido adecuado para composiciones suavizantes de tejidos que se añaden durante el aclarado.The present invention relates to a tissue conditioning composition. In particular the invention refers to aqueous dispersions of conditioning compositions of tissues comprising a quaternary ammonium compound insoluble in water and a hybrid compound suitable for compositions fabric softeners that are added during rinsing.
Se conocen composiciones acondicionadoras de tejidos que se añaden durante el aclarado. Típicamente dichas composiciones contienen un agente suavizante de tejidos del tipo de compuesto de amonio cuaternario insoluble en agua, disperso en agua a un nivel de agente suavizante de hasta aproximadamente 7% en peso, en cuyo caso las composiciones se consideran diluidas, o a niveles de 7% en peso a 50% en peso, en cuyo caso las composiciones se conocen como concentrados.Conditioning compositions of tissues that are added during rinsing. Typically said compositions contain a fabric softening agent of the type of water insoluble quaternary ammonium compound, dispersed in water at a softening agent level of up to about 7% by weight, in which case the compositions are considered diluted, or at levels from 7% by weight to 50% by weight, in which case the compositions are They know as concentrates.
En la patente de los Estados Unidos 4.137.180 (Lever Brothers Company) se describen diésteres catiónicos de fórmulaIn U.S. Patent 4,137,180 (Lever Brothers Company) cationic diesters of formula
en la que cada uno de R^{1}, R^{2} y R^{3} es un grupo alquilo o hidroxialquilo que contiene de 1 a 4 átomos de carbonos o un grupo bencilo, cada uno de R_{4} y R_{5} es una cadena alquílica que contiene de 11 a 23 átomos de carbono y X^{-} es un anión soluble en agua.wherein each of R 1, R 2 and R 3 it is an alkyl or hydroxyalkyl group containing from 1 to 4 atoms of carbons or a benzyl group, each of R 4 and R 5 is an alkyl chain containing 11 to 23 carbon atoms and X <-> is an anion soluble in Water.
Uno de los problemas asociados con muchas composiciones acondicionadoras de tejidos, incluidas las que contienen diésteres catiónicos como los descritos en la patente de los Estados Unidos 4.137.180, es la inestabilidad física de estos compuestos. El problema se agrava a temperaturas altas y bajas y por adición de perfume. Cuando un acondicionador de tejidos está en forma concentrada, el problema de la estabilidad está más exacerbado y, por esta razón, raramente se comercializan acondicionadores con niveles altos de perfume. Incluso cuando el perfume está encapsulado en una matriz sólida, puede haber problemas de estabilidad debido a fuga de las cápsulas.One of the problems associated with many tissue conditioning compositions, including those they contain cationic diesters such as those described in the patent of the United States 4,137,180, is the physical instability of these compounds. The problem is exacerbated at high and low temperatures and by perfume addition When a tissue conditioner is in concentrated form, the stability problem is more exacerbated and, for this reason, conditioners are rarely marketed with high levels of perfume Even when the perfume is encapsulated in a solid matrix, there may be stability problems due to leakage of the capsules.
Un problema adicional que surge en climas más fríos es que, cuando se transporta o almacena un acondicionador de tejidos en un lugar frío, el producto se gelifica formando un sólido. En algunos casos el producto no se recupera y en otros el tiempo necesario para convertirlo en un producto líquido es un par de días. Esto plantea problemas a supermercados que no pueden colocar el producto solidificado directamente en las estanterías del supermercado.An additional problem that arises in more climates cold is that when a conditioner is transported or stored tissues in a cold place, the product gels forming a solid. In some cases the product does not recover and in others the time needed to turn it into a liquid product is a couple of days. This poses problems to supermarkets that cannot place the solidified product directly on the shelves of the Supermarket.
Las patentes EP 280 550 y EP 507 478 (Unilever) describen el uso de agentes estabilizantes no iónicos seleccionados para solucionar la poca estabilidad. Sin embargo, no se menciona la inestabilidad de la formulación cuando se añade perfume.EP 280 550 and EP 507 478 (Unilever) describe the use of selected non-ionic stabilizing agents to solve the poor stability. However, the instability of the formulation when perfume is added.
La patente de los Estados Unidos 3.984.335 (Ciko et al.) describe composiciones que contienen, como agente suavizante, una amina grasa cuaternizada y un compuesto ácido graso híbrido.US Patent 3,984,335 (Ciko et al. ) Describes compositions containing, as a softening agent, a quaternized fatty amine and a hybrid fatty acid compound.
En la patente EP 0 332 270 (Unilever) se describen agentes suavizantes híbridos, como óxidos de aminas, combinados con agentes suavizantes catiónicos y una amina.In EP 0 332 270 (Unilever), describe hybrid softening agents, such as amine oxides, combined with cationic softening agents and an amine.
La patente EP 0 326 213 describe una composición para tratamiento de tejidos, que comprende uno o más materiales acondicionadores de tejidos anfóteros solubles en agua, preferiblemente un óxido de amina y un material coactivo, siendo la relación en peso de material anfótero a material coactivo de 5:1 a 50:1. El material coactivo puede ser un tensioactivo catiónico, no iónico o semipolar.EP 0 326 213 describes a composition for tissue treatment, comprising one or more materials water soluble amphoteric tissue conditioners, preferably an amine oxide and a coactive material, the weight ratio of amphoteric material to coactive material of 5: 1 a 50: 1 The coactive material may be a cationic surfactant, not ionic or semipolar.
Con la presente invención se mitiga el problema de formar un acondicionador de tejidos concentrado, con niveles relativamente bajos de perfume.With the present invention the problem is mitigated of forming a concentrated tissue conditioner, with levels relatively low perfume.
Además, la presente invención ayuda en la recuperación de un acondicionador de tejidos líquido de un estado solidificado a un líquido homogéneo.In addition, the present invention helps in the recovery of a one-state liquid tissue conditioner solidified to a homogeneous liquid.
La presente invención reivindica una dispersión acuosa de una composición acondicionadora de tejidos que comprende más de 7% en peso de un agente suavizante de tejidos no soluble en agua del tipo de compuesto biodegradable de amonio cuaternario con por lo menos un enlace éster, y entre 0,5% en peso y 3,0% en peso de un perfume, caracterizada porque la composición comprende, además, de 0.1 a 8% en peso de un compuesto híbrido de fórmula:The present invention claims a dispersion aqueous of a fabric conditioning composition comprising more than 7% by weight of a non-soluble fabric softening agent in water of the quaternary ammonium biodegradable compound type with at least one ester bond, and between 0.5% by weight and 3.0% by weight of a perfume, characterized in that the composition also includes 0.1 to 8% by weight of a hybrid compound of the formula:
R (COZ)_{a}(CH_{2})_{b}---
\melm{\delm{\para}{R ^{2} }}{N}{\uelm{\para}{R ^{1} }}^{+}--- (CH_{2})_{c}---X^{-}R (COZ) a (CH 2) b ---
\ melm {\ delm {\ para} {R 2}} {N} {\ uelm {\ para} {R 1}}}<+> --- (CH2) c --- X <->
en la que R es un grupo alquilo o alquenilo C_{7}-C_{27}, R^{1} y R^{2} se seleccionan independientemente de grupos alquilo C_{1}-C_{4}, a un número entero de 0 a 1, b y c se seleccionan independientemente de números entero de 1 a 4, Z es oxígeno o nitrógeno y X^{-} es un anión compatible.wherein R is an alkyl or alkenyl group C 7 -C 27, R 1 and R 2 are selected independently of alkyl groups C_ {1} -C_ {4}, to an integer from 0 to 1, b and c are independently selected from integers from 1 to 4, Z is oxygen or nitrogen and X - is an anion compatible.
A pH bajos, el anión puede estar protonado.At low pH, the anion may be protonated.
La invención describe también el uso de una betaína del ácido alquilamidorpopildimetilaminoacético de fórmula:The invention also describes the use of a alkylamidopopyldimethylaminoacetic acid betaine from formula:
R CONH(CH_{2})_{3}
\melm{\delm{\para}{CH _{3} }}{N}{\uelm{\para}{CH _{3} }}^{+} (CH_{2})_{3} COO Na^{+}R CONH (CH 2) 3
\ melm {\ delm {\ para} {CH 3}} {N} {\ uelm {\ para} {CH 3}}<+> (CH2) <3> COO Na <+>
en la que R es una cadena alquilíca C_{11}-C_{17} o mezclas de la misma, para estabilizar una dispersión acuosa de un acondicionador de tejidos perfumados o para formar una dispersión acuosas de acondicionador de tejidos concentrado, y entre 0,5% en peso y 3,0% en peso de un perfume, que comprende más de un 7% en peso de un agente suavizante de tejidos que es no soluble en agua del tipo de compuesto biodegradable de amonio cuaternario con por lo menos un enlace éster.in which R is an alkyl chain C 11 -C 17 or mixtures thereof, for stabilize an aqueous dispersion of a tissue conditioner scented or to form an aqueous dispersion of conditioner concentrated tissues, and between 0.5% by weight and 3.0% by weight of a perfume, which comprises more than 7% by weight of a softening agent of tissues that is not water soluble of the type of compound biodegradable quaternary ammonium with at least one bond ester.
El compuesto activo catiónico usado en la presente invención comprende un agente suavizante de tejidos catiónico insoluble en agua que comprende un material biodegradable de amonio cuaternario con por lo menos un en lace éster. Los materiales preferidos son agentes suavizantes de tejidos catiónicos insolubles en agua que comprenden un compuesto que tiene dos grupos alquilo o alquenilo C_{12}-C_{28} conectados a un nitrógeno cuaternario mediante un enlace éster.The cationic active compound used in the The present invention comprises a fabric softening agent water insoluble cationic comprising a biodegradable material of quaternary ammonium with at least one in lace ester. The Preferred materials are cationic fabric softening agents Water insoluble comprising a compound that has two groups C 12 -C 28 alkyl or alkenyl connected to a quaternary nitrogen through an ester bond.
De particular interés en la presente invención son compuestos suavizantes que tienen la fórmula:Of particular interest in the present invention They are softening compounds that have the formula:
en la que R^{1} es un grupo alquilo C_{1}-C_{4}, R^{2} y R^{3} son grupos alquilo o alquenilo C_{12}-C_{22} iguales o diferentes, T son grupos iguales o diferenteswherein R1 is an alkyl group C 1 -C 4, R 2 and R 3 are groups C 12 -C 22 alkyl or alkenyl the same or different, T are equal groups or different
---
\delm{C}{\delm{\dpara}{O}}---O
\hskip0,5cmu
\hskip0,5cm---O---
\delm{C}{\delm{\dpara}{O}}---
\hskip0,5cmu
\hskip0,5cm---O---
\delm{C}{\delm{\dpara}{O}}---O------
\ delm {C} {\ delm {\ dpara} {O}}---OR
\ hskip0,5cmor
\ hskip0,5cm---OR---
\ delm {C} {\ delm {\ dpara} {O}}---
\ hskip0,5cmor
\ hskip0,5cm---OR---
\ delm {C} {\ delm {\ dpara} {O}}---OR---
\newpage\ newpage
y X^{-} es un anión soluble en agua.and X <-> is a soluble anion in Water.
Se prefiere especialmente que le material de amonio cuaternario sea de fórmula:It is especially preferred that the material of quaternary ammonium is of formula:
en la que cada uno de R_{1}, R_{2} y R_{3} es un grupo alquilo o hidroxialquilo que contiene de 1 a 4 átomos de carbono o un grupo alquenilo con 2 a 4 átomos de carbono o un grupo bencilo, cada uno de R^{4} y R^{5} es una cadena alquílica que contiene de 8 a 28 átomos de carbono y X^{-} es un anión soluble en agua.in which each of R_ {1}, R2 and R_ {3} it is an alkyl or hydroxyalkyl group containing from 1 to 4 atoms of carbon or an alkenyl group with 2 to 4 carbon atoms or a benzyl group, each of R 4 and R 5 is a chain alkyl containing from 8 to 28 carbon atoms and X - is a soluble anion in Water.
Se prefiere además que el compuesto activo catiónico insoluble en agua sea cloruro de N,N-di(sebooxiendurecido)-N, N-trimetilamoniopropano.It is further preferred that the active compound water-insoluble cationic be chloride N, N-di (sebum-hardened) -N, N-trimethylammoniumpropane.
En la patente de los Estados Unidos 4.137.180 (Lever Brothers) se describen materiales preferidos y métodos para su preparación. Preferiblemente, estos materiales comprenden cantidades pequeñas del correspondiente monoéster descrito en la patente de los Estados Unidos 4.137.180, por ejemplo, cloruro de 1-sebo-2-hidroxitrimetilamoniopropano.In U.S. Patent 4,137,180 (Lever Brothers) described preferred materials and methods for its preparation. Preferably, these materials comprise small amounts of the corresponding monoester described in the U.S. Patent 4,137,180, for example, chloride 1-tallow-2-hydroxytrimethylammoniumpropane.
El nivel del compuesto de amonio con enlace éster está por encima del 7% en peso de la composición; más preferentemente por encima del 15% en peso de la composición; mucho más preferentemente entre el 15% y el 40% en peso de la composición.The level of the ammonium compound with ester bond it is above 7% by weight of the composition; plus preferably above 15% by weight of the composition; a lot more preferably between 15% and 40% by weight of the composition.
Es ventajoso que el material híbrido usado en la presente invención sea una betalina del ácido alquilamidopropildimetilaminoacético de fórmula:It is advantageous that the hybrid material used in the present invention be an acid betalin alkylamidopropyldimethylaminoacetic acid of the formula:
en la que R es una cadena alquílica C11-C17 o mezclas de la misma.in which R is an alkyl chain C11-C17 or mixtures of the same.
R CONH(CH_{2})_{3}
\melm{\delm{\para}{CH _{3} }}{N}{\uelm{\para}{CH _{3} }}_{+} (CH_{2})_{3} COO^{-} Na^{-}R CONH (CH 2) 3
\ melm {\ delm {\ para} {CH 3}} {N} {\ uelm {\ para} {CH 3}}+ (CH 2) 3 COO - Na -
El nivel de material hídrido es preferiblemente de 0,1% en peso a 8% en peso de la composición, más preferiblemente de 0,4% en peso a 5% en peso de la composición total.The level of hydrous material is preferably from 0.1% by weight to 8% by weight of the composition, more preferably from 0.4% by weight to 5% by weight of the total composition.
La composición acondicionadora de tejidos se puede formar en cualquier base, pero se prefiere especialmente que la base sea acuosa.The fabric conditioning composition is it can form on any base, but it is especially preferred that The base is watery.
La composición puede contener también material ácido graso de cadena larga, por ejemplo, ácidos alquílicos o alquenílicos monocarboxílicos C_{8}-C_{24} o polímeros de los mismos. Preferiblemente se usan ácidos grasos saturados, en particular ácidos grasos de sebo endurecido C_{16}-C_{18}. Preferiblemente, el ácido graso no está saponificado, más preferiblemente el ácido graso está libre, por ejemplo, ácido oleico, ácido láurico o ácido graso de sebo.The composition may also contain material long chain fatty acid, for example, alkyl acids or C 8 -C 24 monocarboxylic alkenyl or polymers thereof. Preferably fatty acids are used saturated, in particular hardened tallow fatty acids C_ {16} -C_ {18}. Preferably, the fatty acid it is not saponified, more preferably the fatty acid is free, for example, oleic acid, lauric acid or tallow fatty acid.
El nivel de material ácido graso es preferiblemente superior a 0,1%, más preferiblemente superior a 0,2% en peso. Se prefieren especialmente composiciones diluidas en los que el material ácido graso está presente en una cantidad de 0,25% en peso a 20% en peso. La relación en peso de compuesto de amonio cuaternario a material ácido graso es preferiblemente de 1:10 a 10:1.The level of fatty acid material is preferably greater than 0.1%, more preferably greater than 0.2% in weigh. Especially preferred are compositions diluted in the that the fatty acid material is present in an amount of 0.25% by weight to 20% by weight. The weight ratio of ammonium compound Quaternary to fatty acid material is preferably 1:10 to 10: 1
La composición también puede contener uno o más ingredientes opcionales seleccionados del grupo formado por disolventes no acuosos, agentes tampón del pH, vehículos de perfumes, sales inorgánicas, fluorescentes, colorantes, hidrotropos, agentes antiespumantes, agentes de antirredeposición, enzimas, blanqueantes ópticos, opacificantes, agentes antiarrugas, agentes que imparten caída, agentes antiestáticos, coadyuvantes del planchado y agentes de concentración como monoestearato de glicerol.The composition may also contain one or more optional ingredients selected from the group consisting of non-aqueous solvents, pH buffering agents, vehicles perfumes, inorganic salts, fluorescent, dyes, hydrotropes, antifoaming agents, antiredeposition agents, enzymes, optical brighteners, opacifiers, anti-wrinkle agents, agents that impart fall, antistatic agents, adjuvants of the ironing and concentrating agents such as monostearate glycerol.
También es preferible que en la composición estén presentes alcoholes grasos etoxilados. Es especialmente ventajoso que estén presentes en una cantidad de 0,5% en peso a 2% en peso de la composición total.It is also preferable that in the composition they are ethoxylated fatty alcohols present. It is especially advantageous that are present in an amount of 0.5% by weight to 2% by weight of The total composition.
El perfume puede estar encapsulado o libre. El nivel de perfume en el producto es entre 0,5% en peso y 3,0% en peso.The perfume can be encapsulated or free. The Perfume level in the product is between 0.5% by weight and 3.0% in weight.
La composición también puede contener agentes suavizantes de tejidos no iónicos, como lanolina y derivados de la misma,The composition may also contain agents. fabric softeners, such as lanolin and derivatives of the same
Es deseable que la viscosidad de estas composiciones acondicionadoras de tejidos esté en el intervalo de 15 mPa.s a 120 mPa.s a una velocidad de cizallamiento de 110 s^{-1}.It is desirable that the viscosity of these tissue conditioning compositions are in the range of 15 mPa.s at 120 mPa.s at a shear rate of 110 s -1.
Las composiciones de la invención tienen preferiblemente un pH superior a 2, más preferiblemente entre 2 y 5.The compositions of the invention have preferably a pH greater than 2, more preferably between 2 and 5.
La invención será ilustrada a continuación por los siguientes ejemplos.The invention will be illustrated below by The following examples.
En los ejemplos, todos los porcentajes se expresan en peso.In the examples, all percentages are Express in weight.
Los ejemplos comparativos se representan con una letra mientras que los ejemplos de la invención se representan con un número.Comparative examples are represented by a letter while the examples of the invention are represented by a number.
Se preparan agentes suavizantes líquidos de tejidos como sigue:Liquid softening agents are prepared from fabrics as follows:
Se premezclan el agente suavizante de tejidos catiónico y el agente estabilizante no iónico y se calientan para formar una mezcla fundida transparente. La mezcla fundida así formada se añade en un período de por lo menos un minuto a agua a temperatura ambiente, agitando constantemente, para formar una dispersión. Se añade perfume a la mezcla acuosa. La adición del material híbrido se hace:The fabric softening agent is premixed cationic and non-ionic stabilizing agent and are heated to form a clear molten mixture. The melted mixture as well formed is added in a period of at least one minute to water at room temperature, constantly stirring, to form a dispersion. Perfume is added to the aqueous mixture. The addition of Hybrid material is made:
a) al fundido oa) to melt or
b) a la mezcla acuosa antes o justo con la adición del perfume.b) to the aqueous mixture before or just with the perfume addition
Ejemplos 1, 2, 3, A, B, C, D, E y FExamples 1, 2, 3, A, B, C, D, E and F
Se prepararon los ejemplos de acuerdo con los métodos a) o b) antes mencionados.The examples were prepared according to the methods a) or b) mentioned above.
Los ejemplos A, B, E y F flocularon en 12 horas a temperatura ambiente. Los ejemplos 1, 2, y 3 permanecieron estables durante varios meses a temperatura ambiente.Examples A, B, E and F flocculated in 12 hours at room temperature. Examples 1, 2, and 3 remained stable for several months at room temperature.
Los resultados de almacenamiento de los ejemplos C y D fueron los siguientes:The storage results of the examples C and D were the following:
Ejemplos 4 y GExamples 4 and G
Tanto el ejemplo 4 como el ejemplo G flocularon al añadir perfume. Sin embargo, el ejemplo 4 necesitó, para flocular, doble cantidad de perfume que el ejemplo G.Both example 4 and example G flocculated When adding perfume. However, example 4 needed, to flocculate, double quantity of perfume than example G.
Los ejemplos 1, 2, 4, A a D, G y H solidificaron.Examples 1, 2, 4, A to D, G and H solidified.
Los ejemplos 1, 2 y el ejemplo 4 se recuperaron de la solidificación en 1 a 2 horas.Examples 1, 2 and example 4 were recovered of solidification in 1 to 2 hours.
Los ejemplos A a D y el ejemplo se recuperaron de la solidificación en 2 a 4 días.Examples A to D and the example were retrieved from Solidification in 2 to 4 days.
El ejemplo H se recuperó de la solidificación en 4 horas.Example H recovered from solidification in 4 hours.
Se demuestra así que la presencia de un material híbrido ayuda a la recuperación de la solidificación. La recuperación de la solidificación se intensifica más con materiales que contienen un enlace éster.It shows that the presence of a material hybrid helps solidification recovery. The solidification recovery is further intensified with materials that contain an ester link.
Se preparó el ejemplo I de acuerdo con el método a o b. Ocurrió floculación en 1 semana a temperatura ambiente con independencia del método de preparación usado. Se demuestra así que no todos los compuestos anfóteros son adecuados para ser usados en esta invención.Example I was prepared according to the method a or b. Flocculation occurred in 1 week at room temperature with Independence of the preparation method used. It shows that Not all amphoteric compounds are suitable for use in this invention.
Claims (9)
\melm{\delm{\para}{R ^{2} }}{N}{\uelm{\para}{R ^{1} }}^{+}--- (CH_{2})_{c}---X^{-}R (COZ) a (CH 2) b ---
\ melm {\ delm {\ para} {R 2}} {N} {\ uelm {\ para} {R 1}}}<+> --- (CH2) c --- X <->
\melm{\delm{\para}{CH _{3} }}{N}{\uelm{\para}{CH _{3} }}^{+} (CH_{2})_{3} COO^{-} Na^{-}R CONH (CH 2) 3
\ melm {\ delm {\ para} {CH 3}} {N} {\ uelm {\ para} {CH 3}}<+> (CH2) <3> COO <-> Na <->
\melm{\delm{\para}{CH _{3} }}{N}{\uelm{\para}{CH _{3} }}^{+} (CH_{2})_{3} COO^{-} Na^{-}R CONH (CH 2) 3
\ melm {\ delm {\ para} {CH 3}} {N} {\ uelm {\ para} {CH 3}}<+> (CH2) <3> COO <-> Na <->
\melm{\delm{\para}{CH _{3} }}{N}{\uelm{\para}{CH _{3} }}^{+} (CH_{2})_{3} COO^{-} Na^{-}R CONH (CH 2) 3
\ melm {\ delm {\ para} {CH 3}} {N} {\ uelm {\ para} {CH 3}}<+> (CH2) <3> COO <-> Na <->
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9323268 | 1993-11-11 | ||
GB939323268A GB9323268D0 (en) | 1993-11-11 | 1993-11-11 | Fabric comditioning composition |
Publications (2)
Publication Number | Publication Date |
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ES2140563T3 ES2140563T3 (en) | 2000-03-01 |
ES2140563T5 true ES2140563T5 (en) | 2004-10-01 |
Family
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Application Number | Title | Priority Date | Filing Date |
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ES94929545T Expired - Lifetime ES2140563T5 (en) | 1993-11-11 | 1994-10-13 | TISSUE CONDITIONING COMPOSITION. |
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EP (1) | EP0728178B2 (en) |
JP (1) | JPH09504839A (en) |
AU (1) | AU7855994A (en) |
BR (1) | BR9408021A (en) |
DE (1) | DE69422305T3 (en) |
ES (1) | ES2140563T5 (en) |
GB (1) | GB9323268D0 (en) |
TW (1) | TW284808B (en) |
WO (1) | WO1995013346A1 (en) |
ZA (1) | ZA948165B (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
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SK284220B6 (en) * | 1994-04-07 | 2004-11-03 | Unilever Nv | Fabric softening composition |
ES2128723T3 (en) * | 1994-04-07 | 1999-05-16 | Unilever Nv | SOFTENING COMPOSITION OF FABRICS. |
GB9406824D0 (en) * | 1994-04-07 | 1994-06-01 | Unilever Plc | Fabric softening composition |
US6063754A (en) * | 1995-11-07 | 2000-05-16 | Quest International B.V. | Fabric conditioning composition |
US5830845A (en) * | 1996-03-22 | 1998-11-03 | The Procter & Gamble Company | Concentrated fabric softening composition with good freeze/thaw recovery and highly unsaturated fabric softener compound therefor |
Family Cites Families (6)
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JPS5914077B2 (en) * | 1976-10-01 | 1984-04-03 | 花王株式会社 | Liquid light detergent composition |
US4556502A (en) * | 1983-04-08 | 1985-12-03 | Lever Brothers Company | Liquid fabric-softening composition |
GB2163771B (en) * | 1984-08-31 | 1989-01-18 | Colgate Palmolive Co | Wash cycle detergent-softener compositions |
EP0326213B1 (en) * | 1988-01-28 | 1994-11-09 | Unilever N.V. | A fabric treatment composition and the preparation thereof |
GB8805837D0 (en) * | 1988-03-11 | 1988-04-13 | Unilever Plc | Fabric conditioning composition |
GB8818593D0 (en) * | 1988-08-04 | 1988-09-07 | Albright & Wilson | Fabric conditioners |
-
1993
- 1993-11-11 GB GB939323268A patent/GB9323268D0/en active Pending
-
1994
- 1994-10-13 WO PCT/EP1994/003388 patent/WO1995013346A1/en active IP Right Grant
- 1994-10-13 AU AU78559/94A patent/AU7855994A/en not_active Abandoned
- 1994-10-13 ES ES94929545T patent/ES2140563T5/en not_active Expired - Lifetime
- 1994-10-13 JP JP7513550A patent/JPH09504839A/en not_active Ceased
- 1994-10-13 BR BR9408021A patent/BR9408021A/en not_active IP Right Cessation
- 1994-10-13 DE DE69422305T patent/DE69422305T3/en not_active Expired - Lifetime
- 1994-10-13 EP EP94929545A patent/EP0728178B2/en not_active Expired - Lifetime
- 1994-10-18 ZA ZA948165A patent/ZA948165B/en unknown
- 1994-11-22 TW TW083110851A patent/TW284808B/zh active
Also Published As
Publication number | Publication date |
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EP0728178A1 (en) | 1996-08-28 |
DE69422305T2 (en) | 2000-04-20 |
DE69422305D1 (en) | 2000-01-27 |
TW284808B (en) | 1996-09-01 |
AU7855994A (en) | 1995-05-29 |
ZA948165B (en) | 1996-04-18 |
WO1995013346A1 (en) | 1995-05-18 |
ES2140563T3 (en) | 2000-03-01 |
DE69422305T3 (en) | 2004-06-24 |
GB9323268D0 (en) | 1994-01-05 |
EP0728178B1 (en) | 1999-12-22 |
JPH09504839A (en) | 1997-05-13 |
BR9408021A (en) | 1996-12-10 |
EP0728178B2 (en) | 2004-01-28 |
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