Background
[0001] Succinic acid and its salts are known ingredients of detergent compositions. They
are used for their surface active and hydrotropic properties as well as calcium and
magnesium binding capacity.
[0002] They are easily processed directly into a detergent liquid or slurry by in situ hydrolysis
of the corresponding succinic anhydride, and subsequent neutralisation.
[0003] This hydrolysis typically requires a considerable excess of water and the presence
of solvents (eg. lower alcohols), in an alkaline environment in order to make the
hydrolysis reaction move rapidly to completion.
[0004] There is now a trend to more concentrated detergents containing very little water.
As the water level is decreased in the hydrolysis step the rate of reaction decreases
and undesirable side reactions between the anhydride and the solvents forming, for
example esters, start to become significant.
[0005] Various prior art has dealt with detergent compositions containing succinic acid.
These applications are in general, dilute.
[0006] GB-A-2 049 723, published December 31, 1980, discloses a composition containing partly
neutralised succinic acid with one of its salts such that the pH is in the range from
5.5 to 8.0. It describes liquid compositions containing 3%-50% by weight of the partly
neutralised succinic acid.
[0007] EP 0 028 850, published May 5, 1981, discloses a liquid detergent composition containing
succinates and a low level of alkyl benzene sulphonate, for improved storage stability.
The application mentions the neutralisation of the acid or anhydride in situ, but
there is no mention of high active compositions.
[0008] GB 1 285 582, published August 16, 1972, discloses a composition substantially containing
25-90% succinic acid, which may be derived from the anhydride, and 10-75% nonionic
surfactant. There is no disclosure of a suitable process for making such compositions.
[0009] However, none of the prior art deals with the problem of making a highly concentrated
solution of succinic acid which is suitable for further processing into a concentrated
liquid detergent. There is a need for a process of hydrolysis of succinic anhydrides
which can be carried out effectively in an environment in which very little water
is present.
[0010] The present invention provides a new process for hydrolysis of the succinic anhydride
to yield a solution of at least 85% by weight of partly neutralised succinic acid.
The process can be carried out in situ, continuously or batch-wise, and offers a flexible
process for making a concentrated liquid detergent.
Summary of the Invention
[0011] A process for making a concentrated liquid detergent composition which comprises
(A) succinic acid

where R is an alk(en)yl moity with C10-C20 X,Y are independently H,Na,K, alkanolamine
and (B) water,
characterised in that succinic anhydride, water and an alkaline catalyst are:
i) mixed in a ratio of succinic anhydride to water (B) of not less than 4:1 in order
to start an exothermic hydrolysis reaction
ii) held in a buffer tank, and
iii) mixed with other detergent ingredients.
Detailed Description of the Invention
[0012] The present invention provides a process for the hydrolysis of succinic anhydride
to succinic acid in the presence of a small excess of water. The process takes place
in the presence of an alkali which catalyses the reaction and partly neutralises the
succinic acid. Firstly the succinic anhydride, water and alkali are intimately mixed,
either by passing through static mixers, or, preferably, in a high shear mixer. The
mixture is then stored in a buffer tank (which may be in-line in a continuous process)
until the exothermic hydrolysis reaction is substantially completed. The resulting
high active partly neutralised succinic acid may then be stored or transferred directly
into a batch tank or continuous process for further processing to a concentrated liquid
detergent.
THE SUCCINIC ANHYDRIDE
[0013] Any succinic anhydride of the general formula:

is suitable for use in the present invention. The choice of R will be made by the
detergent formulator.
A particularly preferred chain is when:
R is CH3-(CH2)n-CH=CH-CH2- and n=8-10 or mixtures thereof.
THE ALKALI
[0014] Any suitable alkali may be used including sodium hydroxide, potassium hydroxide,
monoethanolamine and ammonia. Preferred are sodium hydroxide and potassium hydroxide.
The ratio of hydroxide present : hydroxide needed for stoichiometric neutralisation,
should be 0.15 or less.
[0015] The alkali may be added to the succinic acid in the form of a solution (typically
50% aqueous solution of either sodium or potassium hydroxide). Extra water may also
be added in order to ensure complete hydrolysis by the following reaction:

However total water which is present (both added and with the aqueous alkali) should
be limited in order to avoid diluting the final composition, and to avoid an excessively
long reaction time. It has been found that the ratio of succinic anhydride to water
should be not less than 4:1 by weight.
THE HYDROLYSIS PROCESS
[0016] The reactants are brought together and mixed, preferably in a high shear mixer. Suitable
mixers include Pentax (trade name), supplied by Bran and Luebbe, Germany; Dispax (trade
name), supplied by Janke and Kunkel, and mixers supplied by Karg and Fryma. This mixture
is then pumped into buffer tank where the hydrolysis reaction will proceed. Preferably
the buffer tank already contains an amount of succinic acid which itself promotes
rapid hydrolysis of the mixture. In a most preferred embodiment, the buffer tank is
in-line in a continuous process and gives a residence time sufficient for hydrolysis
to be substantially completed. In this embodiment of the invention the buffer tank
contains at all times a mixture of succinic acid, water, alkali and partly neutralised
succinic anhydride. The hydrolysis reaction is exothermic, and the temperature rises,
preferably to about 90°C.
The buffer tank should be gently stirred or agitated in order to keep the reactants
mixed. In the case of a continuous process the buffer tank should be designed to give
a residence time of from 2 to 30 minutes, preferably from 5 to 20 minutes.
[0017] The high active succinic acid made according to the above ratios and process has
a pH of less than 5.5, preferably about pH4.5 when it is diluted to a 0.5% aqueous
solution. Furthermore, after hydrolysis the ratio of partly neutralised succinic acid
to water will not be less than about 6:1 by weight.
START-UP AND SHUT-DOWN PROCEDURE
[0018] When a continuous process is in use as described hereinabove, the process is shutdown
by firstly closing the supply of water and alkali to the mixer. The supply of succinic
anhydride is allowed to continue until all water and alkali have been flushed through
the mixer then this supply is also shut-down. This procedure ensures that no hydrolysis
continues in the mixer whilst not in use.
Preferably not all of the succinic acid is flushed through the buffer tank. This means
that when the supplies of succinic anhydride, water and alkali are switched on for
start-up, there is still some acid in the buffer tank to "seed" the hydrolysis reaction.
During the period that the process is not operating, the buffer tank should be maintained
at an elevated temperature (typically 60-80°C) in order to prevent solidification
of the succinic acid/anhydride mix.
FURTHER PROCESSING
[0019] The highly active, partly neutralised succinic acid made by the present invention
may subsequently be added to other detergent ingredients including surfactants, builders,
chelants, enzymes and softening clays, in order to make a finished liquid detergent
composition. An example of this is given hereinbelow.
Preferably the high active succinic acid is mixed with compatible detergent ingredients
which allow its temperature to be reduced below 60°C, before it is mixed with lower
alcohols. Such short chain alcohols may be present in the final formulation as solvents,
examples include ethanol, propanol, propane diol and glycerol. If the succinic acid
and such solvents are present at temperatures in excess of 60°C, then undesirable
side products such as esters may be formed. An intermediate composition may be formed
which is a stable, pumpable liquid at temperatures below 60°C. This intermediate composition
preferably consists of at least 40% by weight of partly neutralized succinic acid.
Example 1
[0020]
| Dodecyl/tetradecyl succinic anhydride |
300 kg/hour |
| Potassium hydroxide (50% aq. soln.) |
20 kg/hour |
| Water |
40 kg/hour |
Succinic anhydride, potassium hydroxide solution and water are supplied at ambient
temperature from metering pumps at the rates described above, into a Pentax KMF8 (Trade
Mark) high shear mixer.
[0021] This mixture is transferred directly from the outlet port of this mixer into the
bottom of a buffer tank. The buffer tank has a diameter of about 0.4m and a height
of about 0.8m, giving a residence time of about 17 minutes. The temperature in the
buffer tank rises to 92°C as the exothermic hydrolysis reaction takes place.
The reacted material leaving from the top of the buffer tank has a composition of:
| Dodecyl/tetradecyl succinic acid (partly neutralised) |
90% |
| Water |
10% |
and, when diluted to give a aqueous solution of 0.5% by weight, has a pH of 4.5.
In this example, the high active, partly neutralised succinic acid is mixed with a
nonionic surfactant in the ratio of 1:1. The surfactant is supplied at ambient temperature
and the resulting mix has a temperature of 55°C. The resulting mixture is a stable,
pumpable intermediate composition at this temperature.
A finished composition is made by mixing the acid/ surfactant mixture with other detergent
ingredients as follows (all given as % by weight):
| Succinic acid/nonionic surfactant |
18 |
| Ethanol & 1,2 propane diol |
12 |
| Sodium hydroxide |
9* |
| Alkyl benzene sulphonic acid |
12 |
| Sodium alkyl sulphate |
2 |
| Citric acid |
7 |
| Enzymes and minors |
1 |
| Miscellaneous (suds suppressor, perfume etc. ) |
1 |
| Water |
to balance to 100% |
| *Level of sodium hydroxide may be varied in order to give finished pH8 |
1. A process for making a concentrated liquid detergent composition which comprises
(A) succinic acid

where R is an alk(en)yl moity with C10-C20
X,Y are independently H,Na,K, alkanolamine
and (B) water,
characterised in that succinic anhydride, water and an alkaline catalyst are:
i) mixed in a ratio of succinic anhydride to water (B) of not less than 4:1 in order
to start an exothermic hydrolysis reaction
ii) held in a buffer tank, and
iii) mixed with other detergent ingredients.
2. A process according to claim 1 which is continuous and in which the reactants have
a residence time of at least 5 minutes in the buffer tank.
3. A process according to claim 1 or 2 characterised in that the alkaline catalyst is
sodium hydroxide or potassium hydroxide, in a ratio of:
hydroxide present : hydroxide needed for stoichiometric neutralisation,
of 0.15 or less.
4. A process according to any of claims 1 to 3 where:
R is CH3-(CH2)n-CH=CH-CH2- and n=8-10 or mixtures thereof.