Technical field
[0001] The present invention is in the field of microcapsules, in particular it relates
to microcapsules having a core and a polymeric polyanion-polycation complex shell
wherein the polyanion is capable of forming a weak gel in the presence of calcium,
a process for making them, liquid detergents comprising the microcapsules and their
use for laundering, dishwashing and other purposes.
Background of the invention
[0002] Liquid detergent comprising microcapsules are very appealing to consumers. The inclusion
of microcapsules in liquid detergents is desirable not only for aesthetic reasons
but also for functional reasons such as isolation of incompatible ingredients, controlled
and/or delayed release, etc. Ideally, the microcapsules are stably suspended in the
liquid detergent and only dissolve/disintegrate in-use. This makes the design of the
microcapsules technically very challenging. In-use conditions can vary widely depending
on a number of factors, including cleaning temperature, hardness of the cleaning water,
duration of the cleaning process, etc.
[0003] The use of microcapsules in liquid detergents is known from the literature. WO 02/055649
discloses a method for the production of microcapsules containing washing and/or cleaning
substances with semi-permeable capsule shells (membranes) by means of complexing suitable
polyelectrolytes.
[0004] Semi-permeable type microcapsules known from the literature do not seem to be strong
enough to withstand the liquid detergent manufacture process and transport and at
the same time be capable of breaking in use without leaving residues. The generation
of residues is made worse under stressed use conditions, such as low temperature,
hard water and short duration cleaning.
[0005] One objective of the present invention is to provide strong microcapsules for use
in liquid detergents capable of dissolving/disintegrating under a wide variety of
conditions including stressed conditions. In particular, the microcapsules should
be suitable for use in laundry liquid detergents dissolving/disintegrating without
leaving residues even when using a heavily loaded drum, a short wash cycle, low wash
temperature and/or hard water.
Summary of the Invention
[0006] Microcapsules having a core and a polymeric polyanion-polycation complex shell for
use in liquid detergents should be designed in such a way that they are capable of
being stably suspended in the liquid matrix, withstand manufacture and transport conditions,
and dissolve/disintegrate during the wash process. The microcapsules have a semipermeable
membrane (shell) which permits the transfer of ions between the core and the liquid
or gel matrix of the detergent, by osmotic effect, until equilibrium is substantially
reached, thereby contributing to the physical stability of the microcapsules in the
matrix. Without being bound by theory, it is believed that when the detergent containing
microcapsules is introduced into fresh water, for example during a cleaning process,
the gradient of ionic strength between the wash water and the microcapsule draws water
into the core, exerting high pressure on the shell which consequently disintegrates.
This mechanism together with the shear exerted during the cleaning process contributes
to the breakage of the microcapsules in use.
[0007] It has been found that microcapsules are prone to form residues. This tendency has
been found to be more acute under stressed conditions, such as heavily loaded drum,
short cleaning cycles, low temperature and hard water conditions. The microcapsules
of the invention do not generate residues under stressed conditions.
[0008] Tap water, containing metal ions -such as calcium- is generally used for cleaning
with a liquid detergent. Liquid detergents may also include calcium ions, as part
of the cleaning ingredients and/or aqueous matrix, for instance for enzyme stability.
Without wishing to be bound by theory, it is believed that the polyanion of the microcapsule
is prone to interact, specially cross-link, with the calcium either from the cleaning
water, the liquid detergent or both. This interaction can give rise to gellation of
the polyanion. If the gel formed is too strong, it will not dissolve/disintegrate
in water leaving residues on the cleaned items.
[0009] In the case of a laundry process, the microcapsules can be exposed in the washing
liquor to a high concentration of calcium proceeding from different sources, such
as the feed water, the laundry load itself, garments which have been previously laundered
can contain calcium left behind after the evaporation of the water during the drying
step, some soils, etc. Laundry liquid detergents tend to be under built, relative
to total calcium and other hardness ions, i.e. they cannot bind all the calcium present
in the wash process, especially under stressed conditions.
[0010] According to a first aspect of the invention, there is provided a microcapsule for
use in a liquid detergent composition, the microcapsule having a core and a polymeric
polyanion-polycation complex shell. The polyanion component, in aqueous solution,
is capable of forming a weak gel in the presence of calcium. By weak gel is understood
a polyanion-calcium gel, formed from 0.05 moles/l of calcium (released in situ from
a Ca-EDTA solution, as described herein below) having a storage modulus of less than
about 150 Pa. The storage modulus is measured as detailed herein below.
[0011] A preferred polyanion for use in the microcapsules of the invention is alginate.
Alginate is the general name given to alginic acid and its salts. Alginic acid is
a linear polysaccharide consisting of (1,4) linked β-D-mannuronate (M) and its C-5
epimer α-L-guluronate (G) residues arranged in a non-regular blockwise pattern along
the linear chain. The chemical composition and sequence of the M and G blocks depend
on the biological source, growth and seasonal conditions. There are three dimmer blocks
in alginate MM, GG and MG. The ratio of mannuronic to guluronic units is known as
the M:G ratio. In preferred embodiments the polyanion is alginate having an M:G ratio
of at least about 1:1, preferably at least about 1.1:1, more preferably at least about
1.3:1 and even more preferably at least about 1.5:1. Preferably the alginate has a
fraction of GG blocks of less than about 0.5, more preferably less than about 0.4
and even more preferably less than about 0.3. Preferably the alginate has a molecular
weight of less than about 500 KDa. Again, without wishing to be bound by theory, it
is believed that divalent and multivalent cations form stronger gel with G residues,
especially blocks of G residues, than with M residues and this leads to poor dissolution/disintegration
characteristics and consequent residue formation. Divalent cations, especially calcium
ions, take part in the interchain binding between G blocks and give rise to a three-dimensional
network in the form of a gel. The binding zone between the G blocks is described by
the so-called "egg-box model".
[0012] The most preferred alginate for use in the microcapsules of the invention is that
having: i) an M:G ratio of at least about 1:1, preferably at least about 2:1, more
preferably at least about 3:1 and even more preferably at least about 4:1; ii) a fraction
of GG blocks of less than about 0.5, more preferably less than about 0.4 and even
more preferably less than about 0.3; and iii) a molecular weight of less than about
500 KDa.
[0013] In another aspect of the invention, there is provided a microcapsule for use in a
liquid detergent composition, the microcapsule having a core and a polymeric polyanion-polycation
complex shell wherein the polyanion component is alginate having a ratio of mannuronic
to guluronic units of at least about 1:1, preferably at least about 1.1:1, more preferably
at least about 1.3:1 and even more preferably at least about 1.5:1. Preferably the
alginate has a fraction of GG blocks of less than about 0.5, more preferably less
than about 0.4 and even more preferably less than about 0.3. Preferably the alginate
has a molecular weight of less than about 500 KDa.
[0014] In preferred embodiments the microcapsules are capable of withstanding a force before
bursting (measured as described herein below) of from about 20 mN to about 20,000
mN, preferably from about 50 mN to about 15,000 mN and more preferably from about
100 mN to about 10,000 mN. This strength makes them suitable for industrial handling,
including the liquid detergent making processes. They can withstand pumping and mixing
operations without significant breakage and are also stable on transport. At the same
time the microcapsules disintegrate readily in use even under stressed conditions.
The microcapsules have a wide operating window, eliminating the need to design different
microcapsules for use under different conditions.
[0015] According to a process aspect of the invention, there is provided a process for making
a microcapsule for use in a liquid detergent composition, the microcapsule having
a core and a polymeric polyelectrolyte complex shell. The microcapsule is made from
a polyanion component capable of forming a weak gel, in aqueous solution, (as described
herein above) in the presence of calcium. The process comprises the following steps:
a. forming a first solution comprising the polyanion component;
b. forming droplets of the first solution; and
c. introducing the droplets into a second solution comprising a polymeric polycation
component capable of reacting with the polyanion component to form a complex at the
surface of the droplets.
[0016] The term "solution" as used herein includes liquid or gel compositions having a main
component and at least a second component dissolved, dispersed or emulsified therein.
[0017] Preferably, the polyanion is alginate having an M:G ratio of at least about 1:1,
preferably at least about 2:1, more preferably at least about 3:1 and even more preferably
at least about 4:1. Preferably the alginate has a fraction of GG blocks of less than
about 0.5, more preferably less than about 0.4 and even more preferably less than
about 0.3. Preferably the alginate has a molecular weight of less than about 500 KDa.
[0018] According to another aspect of the invention, there is provided a liquid detergent
composition comprising the microcapsules of the invention. In a preferred embodiment
the liquid detergent composition comprises from about 0.5 to about 30%, preferably
from about 2 to about 15% by weight of the composition of detersive builder. Builders
improve the cleaning performance of the compositions herein and can include any of
the sequestering, chelating or precipitating types. Examples of such builders include
C
12-18 fatty acids and citric acid, typically neutralized by alkali metal hydroxides, amines
or alkanolamines. A preferred builder for use herein is a mixture comprising from
about 2 to about 15% by weight of the composition of C
12-18 fatty acids and citric acid in a weight ratio of from about 10:1 1 to about 1:10,
preferably from about 5:1 to about 1:5, more preferably from about 3:1 to about 1:3.
[0019] In a method aspect of the invention, there is provided a method of cleaning a soiled
item or substrate comprising contacting the item or substrate with an aqueous solution
comprising the liquid detergent composition of the invention. The method is suitable
for a variety of applications, including, hard surface cleaning -manual and automatic
dishwashing, toilet rim blocks -, laundry, etc.
[0020] The method is especially suitable for laundry. The liquid detergent compositions
of the invention when used under stressed conditions such as hard water, i.e. above
about 2 mmol/l, preferably between about 3 and 6 mmol/l and more preferably about
4 mmol/l of calcium and magnesium (preferably in a ratio of 3 to 1)-and/or low inlet
temperature -about 4-6°C- and/or low program temperature -about 30°C- and/or heavy
load, do not leave residues on the washed items.
[0021] Generally, it is not possible to accurately control in-use wash temperature conditions
in a washing machine, even though it is possible to pre-select the program temperature.
The machine is filled with water from the mains, the temperature of the inlet water
is dictated by the external conditions and widely varies depending, among other things,
on the weather. The inlet water is subsequently heated up to the desired program temperature.
A considerable difference can exist between the inlet and the program water temperature
such that the temperature of the washing liquor could be low for a considerable part
of the cycle. These conditions can contribute to the gellation of the beads. The problem
can be exacerbated when hard water is used and/or the machine drum is heavily loaded.
[0022] The current trend is to design washing machines with low energy consumption, usually
involving low temperatures, reduced agitation and longer washing times. These conditions
also contribute to the gellation of microcapsules.
[0023] In another method aspect of the invention, there is provided a method of cleaning
laundry, without leaving visible residues on the clean laundry. The cleaning takes
place in a washing machine, under hard water conditions, i.e. above about 2 mmol/l,
preferably between about 3 and 6 mmol/l and more preferably about 4 mmol/l of calcium
and magnesium (preferably in a ratio of 3 to 1). The cleaning method comprises the
step of contacting the laundry with hard water and adding a liquid detergent. The
liquid detergent preferably comprises from about 0.3% to about 3%, more preferably
from about 0.5 to about 2% and even more preferably from about 0.8 to about 1.5% by
weight of the liquid detergent of microcapsules having a core and a polymeric polyanion-polycation
complex shell. Preferably, the liquid detergent provides from about 10 to about 2000
ppm, more preferably from about 50 to about 1200 ppm and even more preferably from
500 to 900 ppm of builder in the wash liquor.
[0024] The microcapsules are such that they leave no visible residues on laundry according
to the test described below. Preferably, the polyanion component, of the microcapsules
for use in the cleaning method, is capable of forming a weak gel in aqueous solution
in the presence of calcium and has a storage modulus (measured as detailed herein
below) of less than about 150 Pa. A preferred polyanion is alginate having an M:G
ratio of at least about 1:1, preferably at least about 1.1:1, more preferably at least
about 1.3:1 1 and even more preferably at least about 1.5:1. Preferably the fraction
of GG blocks is less than about 0.5, more preferably less than about 0.4 and even
more preferably less than about 0.3. Preferably, the molecular weight is less than
about 500 KDa.
[0025] Whether a laundry process leaves visible residues on the clean garments is evaluated
according to the following test. The cotton short cycle program of a Miele Novotronic
W8810 machine is used to wash about 12 dark garments weighing, in total, about 4-4.5
kg. The water inlet temperature is about 5-6°C, the wash temperature about 30°C and
the water hardness 4 mmol/l. 180 ml of a laundry liquid detergent comprising 1% by
weight of the composition of microcapsules is placed in a dispensing ball and the
ball is placed in the middle of the drum. At the end of the program, the garments
are visually inspected. If less than 20%, preferably less than 10% and even more preferably
less than 5% of the garments present residues, it is concluded that the laundry process
leaves no visible residues.
Detailed description of the invention
[0026] The present invention envisages microcapsules (sometimes referred as beads) for use
in liquid detergents, a process for making them, liquid detergents comprising said
microcapsules and methods of cleaning using the liquid detergents. The microcapsules
do not form strong gels and therefore they dissolve/disintegrate in use without leaving
residue even under stressed conditions.
[0027] The microcapsules preferably take the form of spherical beads with a diameter of
from about 0.1 to about 10 mm, which contain a core surrounded by a membrane. The
membrane protects the core and any active within the core from the surrounding medium.
[0028] The term liquid detergent as used herein includes all flowable fluids having cleaning
properties, including liquids and gels for use in manual and automatic laundry, dishwashing,
hard surface cleaning, personal cleansing and lavatory rim-blocks.
[0029] The microcapsules of the invention are made by a process based on the reaction of
two polyelectrolytes of opposite charge (herein also referred as polyanions and polycations)
and which are capable of forming a complex. Suitable polyelectrolytes for the present
invention can be synthetic or natural polyelectrolytes.
Polyanion
[0030] Suitable polyanions for the present invention can be synthetic or natural polyanions
which fulfil the requirement of being capable of forming a weak gel in the presence
of calcium and having a storage modulus when gelled with 0.05 moles/litre of calcium
of less than about 150 Pa at an angular frequency of about 0.5 rad/s and a polyanion
concentration of about 3.8% by weight at 25°C.
[0031] Synthetic polyanions may be selected from the group consisting of polyacrylates and
polymethacrylates, polyvinyl sulphates, polystyrene sulphonates, polyphosphates and
mixtures thereof. Natural polyanions may be selected from anionic gums, including
alginates, carrageenan, gellan gum, carboxyl methyl cellulose, xanthan gum and mixtures
thereof.
[0032] Preferred polyanion for use herein is alginate, more preferably Lamitex M45 (ex.
FMC), and Manutex RM, Kelgin HV, Manucol LH, Manucol DM and Manucol DH all of them
supplied by ISP. The most preferred are Manucol DM and Manucol DH.
[0033] Preferred alginates with high levels of mannuronic acid include those derived from
the algae
Ascophyllum nodosum or the algae
Macroystis pyrifera.
Measurement of the polyanion storage modulus
[0034] The polyanion storage modulus is measured in an aqueous solution comprising 3.8%
by weight of the polyanion cross-linked with calcium and thereby forming a gel. The
calcium-polyanion gel is prepared by in situ release of calcium cations from a Ca-EDTA
solution. In this way a homogeneous polyanion gel is obtained and the problem of calcium
concentration gradient in the gel is avoided. This method is based on that developed
by X. Liu et al., Polymer, vol. 44, pp 407 - 412 (2003).
[0035] Firstly, a gluconate solution is prepared by adding 0.3 g (99% purity) of D-glucono-δ-lactone
(GDL, Sigma) to 19.7 g of water and stirring with a magnetic stirrer at 400 rpm for
2 minutes.
[0036] Secondly, a Ca-EDTA solution is prepared by adding 1 g of CaCl
2 hexahydrate (98% purity) and 44.69 g of 0.01 mol/l of an EDTA aqueous solution to
21.51 g of water. The solution is stirred at 400 rpm with a magnetic stirrer and 0.1
N NaOH aqueous solution (approximately 9 g) is slowly added until the pH becomes stable
at a value of about 7.
[0037] A polyanion solution is prepared by adding 3.8 g of polyanion, preferably alginate,
to the Ca-EDTA solution. The resulting solution is stirred with a turrax ultramixer
for 3 minutes, moving the ultramixer through the entire solution using 6,500 rpm for
the first minute, 13,500 rpm for the second minute and 21,500 for the third minute.
[0038] Thereafter a calcium polyanion solution is prepared by adding the gluconate solution
to the polyanion solution. The resulting solution is stirred under the same regime
as the polyanion solution (i.e., using 6,500 rpm for the first minute, 13,500 rpm
for the second minute and 21,500 for the third minute). The gluconate causes a decrease
in the pH of the solution with a consequent decrease in the chelation stability constant
of Ca-EDTA, thereby releasing calcium. The resulting calcium polyanion solution is
stored at 20°C for 24 h.
[0039] The storage modulus is measured with a rheometer UDS 200 Paar Physica with a cone
and plate fixture. The diameter and angle of the cone are 50 mm and 0.04 rad, respectively.
Measurements are carried out at 25 ± 0.1°C. After calibrating the apparatus (as indicated
in the manual) the strain is set up at 0.5%. A frequency sweep is performed in the
range of from 0.1 to 100 s
-1. 25 points are measured in an automatic mode. The storage modulus is plotted against
the frequency.
Measurement of the polyanion molecular weight
[0040] The molecular weight is determined via gel permeation chromatography (GPC), using
the conventional calibrated GPC technique for data processing. Molecular weights are
determined via calibration with a set of narrowly dispersed reference materials: poly
ethylene oxide (PEO) standards of molecular weights: 26, 45, 95, 170, 250, 510 and
913 kdalton (peak molecular weight).
[0041] A Waters Alliance 2695 separation module gel permeation chromatograph with a Viscotek
triple detector (using Refractive Index detection for Conventional Calibration) is
used. The control system is the Waters Empower and Viscotek triple detection software.
The detection is carried out using a Viscotek Refractive Index. The module comprises
two Waters Ultrahydrogel 300 x 7.8 mm columns, one containing Ultrahydrogel Linear
and another one containing Ultrahydrogel 102. The eluent is a 0.1 M aqueous solution
of Na
2HPO
4 0.1 M in acetonitrile in a volume ratio of 90:10. The sample injection is 100 µL
of a solution having a concentration of polyanion of 2.5 mg/ml at a flow rate of 0.8
mL/min.
[0042] Molecular weights of the unknown samples are determined by 'slicing' the chromatographic
trace along the time/volume axis and subsequently reading the slice molecular weight
for each slice from the PEO calibration curve (Log MW vs Retention time or Volume).
Weight average molecular weight is calculated based on the slice molecular weights
and their relative intensities. Calibration, slicing and calculation of molecular
weights are all performed through the GPC processing software.
Polycation
[0043] Suitable cationic synthetic polyelectrolytes may be selected from the group consisting
of poly-(N,N,N-trialkylammoniumalkyl) acrylates, poly-(N-alkylpyridinium) salts, polyethylenimines,
aliphatic ionenes, poly-(diallyldialkylammonium) salts and mixtures thereof, wherein
the alkyl is preferably short chain with from 1 to about 4 carbon atoms, preferably
methyl.
[0044] Suitable cationic natural polyelectrolytes may be selected from the group consisting
of chitosan, chitosan derivatives such as quaternarised chitosan and aminoalkylated
and quaternarised celluloses and poly-L-lysine and mixtures thereof.
[0045] Preferred for use herein are the combinations of sodium alginate (for the first solution),
preferably Manucol DH or DM, with poly-(diallyldimethylammonium) chloride, chitosan
polymer (having a molecular weight of from about 10 to 1,000 kDa, preferably from
about 50 to 500 kDa), chitosan oligomer (having a molecular weight of from about 300
to about 9,000 Da, preferably from about 500 to about 5,000 Da) or a mixture of chitosan
polymer and oligomers (for the second solution). These combinations are preferred
for there short reaction time and for the low permeability of the resulting microcapsules,
especially preferred being combinations of sodium alginate with poly-(diallyldimethylammonium)
chloride. Membrane permeability is preferably such as to allow the transfer of water
or solvent between the liquid detergent and the core of the microcapsule but to preclude
the leaching out of actives.
[0046] Measurement of force before bursting
[0047] The force before bursting that a microcapsule can withstand can be measured by using
a Dynamic Mechanical Analyser (Perkin Elmer DMA 7e). A single microcapsule is separated
from the storage liquid (0.9% NaCl) and placed on the sample plate of the analyser.
The capsule is covered with a drop of a 0.9% sodium chloride solution. To establish
the force at the bursting point, a static strain scan is performed applying an increasing
force of 20 mN/minute during the microcapsule compression. The imposed force and the
displacement of the squeezed capsule are automatically recorded. The point of bursting
corresponds to the first shoulder on the static force scan curve and in particular
the intersection point of the two tangents constructed as a best fit to the upper
and lower lateral portions of the shoulder.
[0048] Preferably, the microcapsules of the invention have a density of from about 900 to
about 1,300 Kg/m
3, preferably from about 950 to about 1,200 Kg/m
3 and more preferably from about 980 to about 1,100 Kg/m
3 at 25°C.
[0049] The density of the microcapsules is measured using a Helium Pycnometer (Micromeritics
AccuPyc 1330) at 21°C and 25 psi. A microcapsule is taken from a 0.9% sodium chloride
storage solution and gently patted with paper tissue to remove excess liquid before
the measurement is taken.
[0050] The microcapsules of the invention are preferably essentially spherical in shape,
especially when they are suspended in a liquid detergent. In addition the microcapsules
preferably have a diameter (measured as equivalent circle diameter) in the range from
about 0.2 to about 8 mm, preferably from about 0.5 to about 5 mm and more preferably
from about 0.7 to about 4 mm, these ranges being preferred from the viewpoint that
the microcapsules can be visualised with the naked eye and from ease of manufacture.
[0051] The size and shape of the microcapsules can be characterized using an optical microscope
(Leica MZ8) and image analysis system (Leica Q500MC, Quips, UK). Before running the
analysis the capsules are taken from a 0.9% sodium chloride solution and placed on
the microscope table. During the measurement the capsules are kept wet using a 0.9%
sodium chloride solution. Prior to processing of the images, it should be checked
that all capsules are detected as single entities. The equivalent circle diameter
is the diameter of a circle of an equivalent cross sectional area to that of the particle.
[0052] Preferably the microcapsules have a degree of elasticity at 25°C of at least about
30%, more preferably at least about 50% and especially at least about 70%. The elasticity
can be calculated using the Dynamic Mechanical Analyser described hereinabove. Elasticity
is herein defined as the deformation of the capsule in the direction of movement of
the plate before bursting as a percentage of the corresponding undeformed capsule
dimension. The elasticity of the microcapsules contribute to their mechanically stability
in liquid detergents.
[0053] Preferably, the core of the microcapsules includes an active material. Optionally,
the shell can also include an active material. Preferably the active material is selected
from hydrophobic materials and non-hydrophobic materials having a molecular weight
higher than about 12,000. By "hydrophobic material" is herein understood a material
having an octanol water partition coefficient at 25°C higher than about 1, preferably
higher than about 1.2 and more preferably higher than about 1.5. The octanol water
coefficient partition of a material is defined as the ratio of the concentration of
the material in the octanol phase to its concentration in the water phase at 25°C.
Preferred hydrophobic materials for use herein include perfume oils, silicone fluids
and gums, surfactants and vitamin oils. Preferred non-hydrophobic materials having
a molecular weight higher than about 12,000 for use herein include enzymes. Other
suitable actives include materials set out herein below. The microcapsules can provide
protection for the active materials reducing or avoiding interaction between the active
material in the core and materials in the liquid matrix of the liquid detergent, thereby
improving the chemical stability of sensitive materials such as enzymes and perfumes.
The retention of actives in the core of the microcapsules of the invention is higher
than that for microcapsules produced by polymeric crosslinking, for example using
calcium as crosslinking agent.
[0054] Preferably the core of the microcapsules of the invention includes a density modifier
in a level such as to reduce the density of the microcapsules by at least about 10%,
more preferably at least about 15% at 25°C. The density modifier helps to generate
microcapsules of predetermined density which can be suspended in liquid detergents
without or with low levels of structuring or thickening agents. By "low level" is
meant less than about 5%, preferably less than about 1% and more preferably less than
about 0.2% of structuring or thickening agent by weight of the detergent matrix. The
density reduction is evaluated by comparing two similar microcapsules, the first one
made from a solution containing a given level of density modifier and the second one
from a solution wherein the density modifier has been substituted by the same weight
of water. Density modifiers suitable herein preferably have a density of less than
about 1,000 Kg/m
3, more preferably less than about 990 Kg/m
3 and higher than about 700 Kg/m
3, and especially higher than about 800 Kg/m
3. Suitable density modifiers include hydrophobic materials and materials having a
molecular weight higher than about 12,000. Preferably the density modifier is insoluble
but dispersible either with or without the aid of a dispersant agent, in water. Active
materials can play the role of density modifiers if they fulfil the aforementioned
requirements. Preferred density modifiers for use herein are selected from the group
consisting of silicone oils, petrolatums, vegetable oils, especially sunflower oil
and rapeseed oil, and hydrophobic solvents having a density of less than about 1,000
Kg/m
3 at 25°C, such as limonene and octane.
Process
[0055] The process of the present invention involves the complexation reaction of a polyanion
and a polycation. Droplets of a first solution comprising a polyanion are dropped
into a second solution comprising a polycation. The polyanion, when is in aqueous
solution, fulfil the requirement of having a storage modulus of less than 150 Pa,
under the conditions defined herein above.
[0056] Preferably, a density modifier is present in the first solution in a level of from
about 5% to about 50%, preferably from about 10% to about 30% by weight.
[0057] The first and/or second solutions can comprise any solvent, including water and organic
solvents. Preferably, the first and second solutions are aqueous, making the resulting
microcapsules easily compatible with the majority of liquid detergents, which are
usually aqueous. Preferably, the first and second solutions are aqueous compositions
having the polyelectrolytes of opposite charge dissolved therein.
[0058] The process of the invention is preferably undertaken at ambient temperature thereby
reducing the operating costs and allowing the encapsulation of heat sensitive materials.
[0059] The process of the invention is quick, simple, versatile, capable of high output
and therefore suitable for large-scale production.
[0060] The droplets of the first solution can be generated by means of jet cutting. Jet
cutting allows a high production rate and a narrow distribution of droplet size and
permits the handling of solutions of high viscosity, i.e. solutions having viscosity
of more than about 200 mPa s, preferably more than about 1,000 mPa s and more preferably
more than about 2,000 mPa s as measured at 1 s
-1 and 25°C. Jet cutting can also handle solutions of complex rheology, for example
shear thinning fluids.
[0061] Preferably, the jet of the first solution is formed by passing the solution through
a nozzle having a diameter of from about 0.2 mm to about 8 mm, more preferably from
about 0.5 mm to about 4 mm and a through put rate of from about 0.5 g/s to about 20
g/s, more preferably from about 1g/s to about 6 g/s.
[0062] The jet is preferably cut by mechanical means, especially preferred being rotating
cutting wires having a diameter of from about 10 µm to about 1,000 µm, more preferably
from about 50 µm to about 500 µm, and a cutting speed of from about 500 rpm to about
10,000 rpm, more preferably from about 1,000 rpm to about 6,000 rpm.
[0063] Preferably, the first solution comprises the first polyanion in a level of from about
1% to about 15%, more preferably from about 2% to about 10%, especially from about
3% to about 8% by weight of the solution, this level being preferred for both the
strength and the low permeability of the resulting microcapsules. Preferably the first
polyelectrolyte has a viscosity of at least 100 mPa s, more preferably of at least
300 mPa s as measured at a shear rate of 1 s
-1 at 25°C and at a concentration of 1% by weight, this viscosity being preferred for
the high strength of the resulting microcapsules. Preferred for the process of the
invention are first solutions comprising from about 2% to about 7%%, more preferably
from about 3% to about 6%, especially from about 3.5% to about 5% by weight of sodium
alginate, said sodium alginate having a viscosity of at least 100 mPa s, preferably
of at least 300 mPa s as measured at a shear rate of 1 s
-1 at 25°C and at a concentration of 1% by weight.
[0064] The solutions used in the process of the invention can be prepared by using any solvent,
however aqueous solutions are preferred for reasons of availability and environmental
profile and because of the compatibility of water with the majority of active substances
and liquid detergents. The process is preferably carried out at ambient temperature,
this being advantageous when dealing with heat sensitive materials such as perfumes
and enzymes. However, if non-heat sensitive materials are encapsulated the solutions
of the process can be heated in order to speed the kinetics of the complexation reaction.
[0065] The first solution preferably comprises a density modifier and/or an active material,
dissolved, suspended or emulsified therein. The first solution can also comprise a
dispersant or emulsifier, especially if the active material is hydrophobic, in order
to facilitate the suspension or emulsification process, preferred dispersants for
use herein being polymers, especially polyvinyl alcohol. Preferred emulsifiers for
use herein are surfactants. Dispersants and/or emulsifiers are usually used in low
levels, suitable levels for use herein being from about 0.1 to about 5%, preferably
from about 0.2 to about 3% by weight of the first solution.
[0066] Actives suitable for use herein include any substance that contribute to the cleaning
process such as surfactants, enzymes, builders and bleaching agents; and substances
that provide additional benefits, such as suds suppressers, perfumes, especially perfume
oils, vitamins, anti-microbial agents, colour protection agent, care additives, finishing
agents, especially fabric softening, drying and shine additives.
[0067] The microcapsules are preferably coloured comprising dyes and/or pigments so they
can be readily visualised when placed in liquid detergents.
[0068] Droplets can be formed by any known method. Preferably the droplets are formed by
extruding the first solution through a nozzle into a coherent jet and cutting the
jet, by cutting means, into cylindrical segments, which then form droplets, due to
surface tension, on their way to the second solution. Preferred cutting means include
rotating cutting wires. Suitable methods and devices for forming the droplets are
described in DE 44 24 998 and WO 00/48722.
[0069] Usually the volume of second solution is at least 10 times, preferably at least 100
times and more preferably at least 1,000 times larger than that of a droplet, therefore,
the amount of the second polyelectrolyte is well in excess over that of the first
polyelctrolyte, thus the concentration of the polyelectrolyte in the second solution
is not critical. Preferably the concentration of the second polyelectrolyte is from
about 0.5% to about 5%, more preferably from about 0.8% to about 2% by weight of the
solution. The pH of the second solution is selected according to the pH conditions
for dissolution of the second polyelectrolyte. The residence time of the droplets
is adjusted according to the desired shell thickness. Usually the reaction takes place
under agitation conditions.
[0070] The liquid detergents of the invention comprise from about 0.5 to about 30%, preferably
from about 0.7 to about 10%, more preferably from about 0.8 to about 2% microcapsules
by weight of the composition. Suitable surfactants for use in the liquid detergents
of the invention are well known and can be selected from anionic, nonionic, amphoteric
and cationic surfactants, depending on the specific application of the detergent.
[0071] Builders suitable for use in the liquid detergents of the invention include builders
that form water-soluble hardness ion complexes (sequestering builder) such as citrates
and polyphosphates e.g. sodium tripolyphosphate and sodium tripolyphosphate hexahydrate,
potassium tripolyphosphate and mixed sodium and potassium tripolyphosphate salts;
and builders that form hardness precipitates (precipitating builder) such as carbonates
e.g. sodium carbonate. Chelating agents can be selected from the acid or salt forms
of organic phosphonates and aminophosphonates, aminocarboxylates, polyfunctionally-substituted
aromatic compounds, and mixtures thereof. Also suitable for use herein are precipitating
builders such as fatty soaps (fatty acids neutralized by Na or K hydroxides, or alkanolamines).
[0072] The detergent compositions herein can additionally comprise one or more detergent
active or auxiliary components. Detergent actives may be selected from traditional
detergent ingredients such as bleaching systems (including bleaching agents and bleach
activators), alkalinity sources, enzymes, etc. Detergent auxiliaries may be selected
from finishing agents and care agents. Some of these ingredients can be used in either
or both of the microcapsules and the matrix of the liquid detergent.
[0073] Preferably, the detergent matrix is transparent or translucent, more preferably transparent,
containing colored microcapsules and packaged in a clear, transparent or see through
package.
Examples
Example 1
[0074] 380 grams of sodium alginate from brown algae (Manucol DM ex ISP -having a MG ratio
of about 61/39, a GG fraction of about 0.21 and a molecular weight of about 448 KDa)
and 40g of titanium dioxide (ex Sigma Aldrich product code T8141) was added to 9580
grams and mixed to form a solution.
[0075] The above solution was extruded at throughput of 5.20 g/s through a 1.0 mm nozzle
and cut using a rotational cutting tool (JetCutter from GeniaLab) containing 24 wires
of 200 micron thickness with a cutting speed of 3400 rpm to form spherical droplets
with a diameter between 1750 and 2250 microns. The droplets were allowed to fall into
an agitated hardening bath that contained 75 litres of a 1% chitosan solution (Chitoclear
ex Primex) brought to pH 1.5 with HCl.
[0076] After a hardening time of 15 minutes, the microcapsules were separated from the chitosan
solution via filtration, washed with plenty of water and stored in a 1.0% NaCl solution.
Example 2
[0077] Filtered microcapsules of Example 1 were stirred into the laundry liquid detergent
prepared as described hereinbelow. The microcapsules remained homogeneously suspended
in the liquid detergent.
[0078] A structured liquid detergent matrix is prepared by combining an aqueous premix of
conventional heavy duty liquid (HDL) detergent composition components with a structuring
agent premix. Each of these two premixes is prepared as follows:
HDL premix
[0079] The HDL components premix is prepared by combining HDL components with water in a
suitable vessel under suitable agitation. The resulting premix has the composition
shown in Table I.
TABLE I HDL Components Premix
Component |
Concentration (Wt%) |
C12LAS |
7.5 |
C14-15E08 Alcohol Ethoxylate |
5.2 |
C12-14 Amine Oxide |
2.9 |
Citric acid |
4.3 |
C12-18 Fatty Acid |
5.2 |
Enzymes (Protease, Amylase, Mannanase) |
0.6 |
MEA-Borate |
2.4 |
DTPMP1 Chelant |
0.6 |
Ethoxylated Polyamine Dispersants |
1.5 |
Silicone/Silica Suds Suppressor |
0.02 |
Ethanol |
1.4 |
Propane Diol |
3.6 |
NaOH |
6.1 |
Perfume, Brightner, Hydrotrope, Colorant, Others Minors |
4.2 |
Water |
Balance to 100% |
1Sodium diethylene triamine penta (methyl phosphonate) |
Structuring agent premix
[0080] The structuring agent premix is prepared by combining hydrogenated castor oil and
the other structuring agent premix ingredients shown in Table II with water under
certain conditions. In particular, the Table II components except for the hydrogenated
castor oil are combined and the resulting mixture is heated to 90°C. The hydrogenated
castor oil is then added and the mixture is maintained under agitation until all of
the hydrogenated castor oil has been emulsified. After full emulsification, the mixture
is flash cooled to 70°C and left at this temperature until all of the hydrogenated
castor oil is re-crystallized. At this point the structuring agent premix is allowed
to cool down slowly to ambient temperature. The resulting structuring agent premix
has the composition shown in Table II.
TABLE II Structuring Agent Premix
ComponentConcentration (Wt %) |
|
Hydrogenated Castor Oil |
4.0 |
C12HLAS |
16.0 |
Sodium Metaborate |
1.5 |
NaOH |
3.5 |
Water |
Balance to 100% |
HDL
[0081] As a next step, 2.5 parts of the structuring agent premix of Table II are added slowly
to 96.5 parts of the HDL components premix of Table I under slow agitation forming
the structured detergent matrix.
[0082] The microcapsules which are formed in accordance with the procedure of Example 1
are combined with the structured aqueous liquid detergent composition matrix. This
is accomplished by slowly adding the microcapsules to the structured liquid matrix
while it is maintained under gentle agitation. Enough microcapsules are added to constitute
1% by weight of the composition which is formed. The resulting heavy duty liquid laundry
detergent product has the composition shown in Table III.
TABLE III Microcapsule-Containing Liquid Laundry Detergent
Component |
Concentration (Wt %) |
C12LAS |
7.9 |
C14-15E08 Alcohol Ethoxylate |
5.7 |
C12-14Amine Oxide |
1.0 |
Citric Acid |
2.0 |
C12-18 Fatty Acid |
5.2 |
Enzymes (Protease, Amylase, Mannanase) |
0.6 |
MEA-Borate |
1.5 |
DTPMP1 Chelant |
0.2 |
Ethoxylated Polyamine Dispersants |
1.2 |
Silicone/Silica Suds Suppressor |
0.002 |
Ethanol |
1.4 |
Propane Diol |
5.0 |
NaOH |
3.2 |
Hydrogenated Castor Oil |
0.1 |
Microcapsules from Example 1 |
1.0 |
Perfume, Brightner, Hydrotrope, Colorant, Other Minors |
4.2 |
Water |
Balance to 100% |
[0083] 180 ml of the microcapsules-containing liquid detergent was placed in a dosing ball.
A wash load of 4-4.5 Kg dark garments was placed into a Miele Novotronic W8810 and
the cotton short cycle at 30°C was used. The temperature of the incoming water was
cooled to a temperature of 5-6°C. The dosing ball was placed in approximately the
middle of the washing load. The hardness of the water was 4 mmol/l. At the end of
the cycle the washed garments were visually examined. No residues were found.