CA2014085A1 - Surfactant composition, degreasing composition and degreasing bath - Google Patents
Surfactant composition, degreasing composition and degreasing bathInfo
- Publication number
- CA2014085A1 CA2014085A1 CA 2014085 CA2014085A CA2014085A1 CA 2014085 A1 CA2014085 A1 CA 2014085A1 CA 2014085 CA2014085 CA 2014085 CA 2014085 A CA2014085 A CA 2014085A CA 2014085 A1 CA2014085 A1 CA 2014085A1
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- degreasing
- composition
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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
- C11D3/0026—Low foaming or foam regulating compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/825—Mixtures of compounds all of which are non-ionic
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
- C23G1/14—Cleaning or pickling metallic material with solutions or molten salts with alkaline solutions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/78—Neutral esters of acids of phosphorus
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Detergent Compositions (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
The degreasing composition comprises a surfactant composition comprising a compound (a) represented by the general formula:
R1O(AO)nH, wherein R1 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is 5 mol or more per 1 mol of R1, and that the ethylene group is 50 mol % or more per 100 mol % of the A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
(R2O)x?(O(EO)n)yH, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5, and further comprises an alkali builder in a weight ratio [(compound (a) +
compound (b))/alkali builder] of 1:0.1 - 1:2,000.
The degreasing composition comprises a surfactant composition comprising a compound (a) represented by the general formula:
R1O(AO)nH, wherein R1 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is 5 mol or more per 1 mol of R1, and that the ethylene group is 50 mol % or more per 100 mol % of the A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
(R2O)x?(O(EO)n)yH, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5, and further comprises an alkali builder in a weight ratio [(compound (a) +
compound (b))/alkali builder] of 1:0.1 - 1:2,000.
Description
20~40~5 BACKGROUND OF THE INVENIION
The present invention relates to a surfactant composition, and a degreasing composition and a degreasing bath containing the surfactant 5 composition, and more particularly to a surfactant composition suitable for a degreasing composition having excellent detergency and antifoaming properties at room temperature, and a degreasing composition and a degreasing bath containing such surfactant composition.
In the chemical coating of metal surfaces, degreasing is usually conducted to remove oil substances (mineral oils, animal or vegetable fats and oils, etc.) from the surfaces of metal members to be formed with chemical coatings.
Degreasing detergents used for degreasing treatments contain 15 as main components builders based on acids or alkalis and nonionic surfactants, and they are used in the form of aqueous solutions by a spraying method or an immersion method at 40 - 70C for 1 - 10 minutes.
However, in view of the recent demands of saving energy, 2 0 detergents capable of removing oils at lower temperatures such as S
40C are desired.
As such detergents, Japanese Patent Laid-Open No. 61-60892 discloses an alkali detergent usable at room temperature which contains polyoxyalkylene alkyl ether as a surfactant. The polyoxyalkylene alkyl 25 ether in this detergent has the following general formula:
RO(EO)m(PO)nH, wherein R: Alkyl group, E 0: Ethylene oxide group, 2~14085 PO: Propylene oxide group, and m,n: Moles.
However, although this detergent has improved detergency at room Itemperature, the level of detergency is still insufficient.
OBJECTS AND SUMMAR~ OF THE INVENTION
Accordingly, an object of the present invention is to provide a surfactant composition having excellent detergency at room temperature which is equal to or even higher than under heated conditions (40C or 10 higher), with little foaming.
Another object of the present invention is to provide a degreasing composition having excellent detergency at room temperature which is equal to or even higher than under heated conditions (40C or higher), with little foaming.
A further object of the present invention is to provide a degreasing bath having excellent detergency at room temperature which is equal to or even higher than under heated conditions (40C or higher), with little foaming.
A still further object of the present invention is to provide a 2 0 degreasing composition and a degreasing bath showing excellent detergency even when oil materials are accumulated.
As a result of intense research in view of the above objects, the inventors of the present invention have found that a surfactant composition obtained by mixing a polyoxyalkylene ether-type nonionic 2 5 surfactant containing a predetermined amount of ethylene group with a phosphate-polyethylene oxide adduct shows excellent detergency and antifoaming properties at room temperature when combined with an alkali builder. The present invention is based upon this finding.
Thus, the surfactant composition according to the present invention comprises a compound (a) represented by the general formula:
R1O(AO)nH, wherein R I is a substituted or unsubstituted hydrocarbon group having 6 S or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is S mol or more per 1 mol of Rl, and that the ethylene group is 50 mol % or more per 100 mol % of the A; and n is an integer of 5 - 50; and 10 a compound (b) represented by the general formula:
O
(R )x P(O(EO)n)y H, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 15 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x ~ y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5.
The degreasing composition according to the present invention comprises a compound (a) represented by the general formula:
2 0 RlO(AO)nH, wherein Rl is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is S mol or more 2~ per 1 mol of Rl, and that the ethylene group is 50 mol % or more per 100 mol % of the A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
2 ll (R )x P(O(EO)n) y H, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 5 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/S, and further comprising an allcali builder in a weight ratio [(compound (a) +
compound (b)3/alkali builder] of 1:0.1 - 1:2,000.
The degreasing bath according to the present invention comprises:
(1) 0.005 - 0.5 weight % of a surfactant composition comprising:
a compound (a) represented by the general formula:
RlO(AO),~H, wherein Rl is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is S mol or more per 1 mol of Rl, and that the ethylene group is 50 mol % or more per 100 mol % of the A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
o (R2 )X P(O~EO)n) y H, ~
wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integerofl -20,xandyarel or2,andx+y=3, ~ 014085 in a weight ratio of compound (a~/compound (b) - lO/90 - 95/5;
and (2) 0.05 - lO weight % of an alkali builder.
5 DETArLl~D DESCRIPTION OF THE lNVENTION
The compound (a) used in the pIesent invention is represented by the following general formula (l):
RlO(AO)nH, ... (1) wherein n is an integer of 5 - 50.
l O In the above general formula (l), Rl is, as described below in detail, a hydrocarbon group having 6 or more carbon atoms. When the number of carbon atoms is 5 or less, sufficient surfactant activity cannot be obtained, failing to provide good detergency.
"A" in the above general formula (l) is at least one group l 5 selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group. Incidentally, the number of the ethylene group in "A" is 5 mol or more per l mol of Rl. When the ethylene group is less than 5 mol, the resulting surfactant composition does not have sufficient detergency. Further, the proportion of the 20 ethylene group in "A" is 50 mol % or more per lOO mol % of "A." When the proportion of the ethylene group is lower than 50 mol %, the resulting surfactant composition does not show sufficient detergency. Incidentally, the antifoaming properties of the surfactant composition according to the present invention can be freely adjusted by changing the proportion of 25 the ethylene group relative to lOO mol % of "A" in the compound (a) within the above range.
The number (n) of an AO group in the compound (a) is 5 - 50.
When the number (n) of the AO group is less than 5, sufficient ;~0~4085 detergency cannot be obtained. On the other hand, when n exceeds SO, detergency also becomes insufficient.
Thus, for instance, when n = 5, "A" is completely composed of an eth~lene group. And when n is 6 or more, a portion exceeding 5 may 5 be a group other than the ethylene group. In this case, the ethylene group should be 50 mol % or more based on the total "A."
Incidentally, as long as the content of an oxyethylene group meets the above requirement, the AO group may be contained in the compound (a) in the form of random addition, block addition or a mixture 10 of block addition and random addition.
The compound (b) used in the present invention is represented by the following general formula:
O
1 5 (R )x P(O(EO)n)y H, ,- (2) wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3.
In the above general formula (2), R2 is a hydrocarbon group 20 having 6 or more carbon atoms. When the number of carbon atoms is 5 or less, good detergency canno~ be obtained.
The mole number (n) of an oxyethylene group represented by EO is 1 - 20. When there is no oxyethylene group or when the oxyethylene group exceeds 20 mol, sufficient detergency cannot be 2 5 obtained.
Incidentally, Rl and R2 in the compound (a) and the compound (b) used in the present invention may be the same or different from each other, and as long as they are hydrocarbon groups having 6 or Z0~4085 more carbon atoms, they may be substituted or unsubstituted. Typical examples of Rl and R2 are alkyl groups such as a hexyl group, an octyl group, a decyl group, a dodecyl group, a stearyl group; alkenyl groups such as an oleyl group; cycloalkyl groups such as a cyclohexyl group;
S alkyl-substituted or phenyl-substituted phenyl groups such as a xylene group, an octyl phenyl group, a nonyl phenyl group, a dodecyl phenyl group, a dinonyl phenyl group, a paracumyl phenyl group, a styrene-added phenyl group; an unsubstituted phenyl group, etc.
In the surfactant composition of the present invention, the 10 compound (a) and the compound (b) may be used in combination.
With respect to the weight ratio of the compound (a) to the compound (b) in the surfactant composition of the present invention, compound (a)/compound (b) is 10/90 - 95/5, preferably 25/75 - 75/25.
When the weight ratio of the compound (a) to the compound (b) is lower 15 than 10/90 or larger than 95/5, sufficient detergency cannot be obtained.
Next, the degreasing composition of the present invention will be described below.
The degreasing composition of the present invention comprises the above surfactant composition containing the compound (a) 20 and the compound (b) in a weight ratio of compound (a)/compound (b) -10/90 - 95/5 and an alkali builder.
The alkali builders which may be used in the present invention include alkali metal salts, alkali phosphate, alkali carbonates, alkali silicates, alkali nitrites, alkali borates, etc., and they may be used 2 5 alone or in combination.
In the degreasing composition of the present invention, a proportion of the alkali builder to the surfactant composition [wei~ht ratio of (compound (a) + compound (b))/alkali builder] is 1:0.1 - 1:2000, 2~
preferably 1:1 - 1:100.
When the weight ratio of [(compound (a) + compound (b))/alkali builder] is less than 1:0.1, the decrease in detergency does not substantially take place, but it is dif~lcult to maintain a pH for suppressing the corrosion of metal members to be treated. On the other hand, when the weight ratio exceeds 1:2000, the concentration of the surfactant composition in the degreasing detergent ccomposition becomes too low, resulting in insufficient detergency.
Incidentally, depending upon degreasing facilities, the degreasing composition of the present invention may further contain 5-100 parts by weight of an antifoaming agent per 100 parts by weight of the surfactant composition. When the amount of the antifoaming agent is less than 5 parts by weight, sufficient improvement of antifoaming properties cannot be obtained, and when it exceeds 100 parts by weight, the detergency of the degreasing composition decreases.
The antifoaming agents include higher alcohols, higher ethers, higher aliphatic acids, higher aliphatic acid esters, and alkyl alkylates or alkyl phenol alkylates having HLB values of 10 or less, polypropylene glycolsJpolyethylene glycol ethers, etc. having cloud points of 40C or lower, and they may be used alone or in combination.
Next, the degreasing bath of the present invention will be described.
The degreasing bath of the present invention contains the above surfactant composition and the alkali builder.
The amount of the surfactant composition is 0.005 - 0.5 weight %, preferably 0.05 - 0.3 weight %. When the amount of the surfactant composition is lower than 0.005 weight %, sufficient degreasing activity cannot be obtained. When it exceeds 0.5 weight %, ~ 0~4085 further increase in degreasing activity cannot be achieved.
The amount of the alkali builder is 0.05 - 10 w~ight %, preferably 1 - 5 weight %. When the amount of the alkali builder is less than 0.05 weight %, the degreasing detergent solution has a low pH, 5 making it likely that the metal members to be treated are rusted, and making it difficult to emulsify oil materials removed from the metal members being treated. On the other hand, when the amount of the alkali builder exceeds 10 weight %, it is difficult to dissolve the alkali builder, deteriorating operability.
The composition of the degreasing bath of the present invention can be adjusted by introducing the surfactant composition and the alkali builder separately into a degreasing bath (hereinaft~r called "separate system") or by mixing them in advance and then introducing the resulting mixture into the degreasing bath (hereinafter called 1 5 "premixed system").
As far as the operability is concerned, the premixed system is preferable, but from the viewpoint of stability with time, the separa~e system is preferable. In the case of the premixed system, the amount of the alkali builder is preferably 80 weight % or more based on the 2 0 surfactant composition to avoid swelling.
As described above, the surfactant composition of the present invention comprises the compound (a) which is a particular polyoxyalkylene ether-type nonionic surfactant, and the compound (b) which is a phosphate-ethylene oxide adduct in a particular proportion.
25 The compound (a) itself does not have sufficient detergency at room temperature, and the compound (b) itself does not have detergency at all.
Nevertheless, a combination of the compound (a) and the compound (b) provides a degreasing detergent with good detergency. The reason g 20~408~;
therefor is not necessarily clear, but it may be considered that a synergistic effect between the compound (a) and the compound (b) serves to increase the detergency of the compound (a), while providing the degreasing detergent with good antifoaming properties.
Further, the degreasing bath of the present invention utilizing the synergistic effect of the compound (a) and the compound (b) can maintain degreasing detergency and antifoaming properties equally at start and even after oil accumulation in the bath.
The present invention will be described in further detail by means of the following Examples.
SYnthesis of Compound (a) As the compound (a), the following compounds Al - A9 are synthesized by adding alkylene oxides to various alcohols and phenols having various Rl groups in the general formula (1), in the presence of an alkali catalyst by a usual method.
Al: 7.5 mol of ethylene oxide added to lauryl alcohol.
A2: 10 mol of ethylene oxide added to lauryl alcohol.
A3: 20 mol of ethylene oxide added to lauryl alcohol.
A4: 8 mol of ethylene oxide added to octyl alcohol.
A5: 10 mol of ethylene oxide added to nonyl phenol.
A6: 15 mol of ethylene oxide added to styrene-added phenol.
A7: 10 mol of ethylene oxide block and 3 mol of propylene oxide block added to nonyl phenol.
A8: 10 mol of ethylene oxide and 7 mol of propylene oxide added to nonyl phenol in random.
A9: 10 mol of ethylene oxide block and 2 mol of propylene oxide block added to nonyl phenol.
Svnthesis of Com~ound (b) 201A0~3S
As the compound (b), the following compounds B1 - B6 are synthesized by preparing phophates of various alcohols and phenols having R2 groups in the fomula (2) using phosphorus pentoxide by a usual method, and then adding ethylene oxide thereto in the presence of 5 an alkali catalyst by a usual method.
B 1: 3 mol of ethylene oxide added to lauryl alcohol phosphate.
B2: 5 mol of ethylene oxide added to lauryl alcohol phosphate.
B3: 12 mol of ethylene oxide added to lauryl alcohol phosphate.
B4: 5 mol of ethylene oxide added to octyl alcohol phosphate.
o B5: 10 mol of ethylene oxide added to nonyl phenol phosphate.
B6: 9 mol of ethylene oxide added to paracumyl phenol phosphate.
Svnthesis of Compound (c~
For comparison with the compound (b), the following compound C1 is synthesized by adding 10 mol of ethylene oxide to 1 mol of nonyl phenyl having an R2 group in the general formula (2) in the presence of an alkali catalyst by a usual method, and preparing a phosphate thereof by using phosphorus pentoxide by a usual method.
C1: Phosphate of a nonyl phenol -10 mol ethylene oxide adduct.
Examples_1 - 17. Comparative Examples 1 - 16 Each of surfactant compositions containing the above compounds A1 - A9, B1 - B6 and C1 as shown in Table 1 is mixed with an alkali builder in a proportion shown in Table 2 to prepare each degreasing composition.
2 parts by weight of each degreasing composition is mixed with 98 parts by weight of water to prepare each degreasing detergent solution bath.
Evaluation of Deter~encv With respect to each degreasing detergent solution, detergency is evaluated at start (fresh composition) and after oil accumulation in the bath.
(l! Deter~ency at Start Each degreasing detergent solution is introduced into a 50.0 ml-beaker and kept at 15C. A steel test piece (JIS G-3141) is immersed in the solution, and the solution is stirred at 200 rpm for 10 minutes.
Thereafter, the steel test piece is removed and rinsed by running water for 30 seconds to measure water wettability of the steel test piece surface. This is regarded as detergency at start. Incidentally, the detergency is regarded as 100% when the entire surface of the steel test piece is still wet with water 30 seconds after the removal from the bath, and the water wettability is expressed by percentage of surface area wet with water observed by the naked eye.
(2! Deter~encv after 0i2 Accumulation With respect to the above degreasing composition mixed with 2000 ppm of an anti-corrosion oil ("Anti-rust P1400," manufactured by Nippon Oil Co., Ltd.), a water wettability is measured on the steel test piece surface in the same method as in the detergency at start, and it is 2 0 evaluated as detergency after oil accumulation.
The evaluation results of each detergency are shown in Table 1.
2s 2~)~14~35 Table 1 Detergencv (%) Composition of E,xample Surfactant After Oil _ No. (Weight Ratio)At StartAccumulation 1 Al/B5 = 75/25 1 00 1 00 2 Al/B5 = 50/50 100 100 3 Al/B5 = 25/75 9 5 9 0 4 A2/B5 = 50/50 1 00 1 00 A3/B5 = 50/50 9 0 8 5 1 0 6 ~4/B5 = 50/50 9 0 8 0 7 A5/B5 = 50/50 1 00 9 0 8 A6/B5 = 50/50 9 0 9 0 9 A7/B5 = 50l50 1 0 0 9 5 1 0 A8/B5 = 50/50 9 5 9 0 1 5 1 1 A9/B5 = 50t50 9 5 9 0 1 2 Al/Bl = 50/50 90 90 1 3 Al/B2 = 50/50 1 00 1 00 1 4 Al/B3 = 50/50 9 5 9 0 1 5 Al/B4 = 50/50 9 5 9 0 2 0 1 6 Al/B5 = 50/50 9 0 8 0 1 7 Al/B6 - 50/50 9 5 9 0 20~40~35 Table 1 (Continued) .
Deter~encv (%3 Comparative Composition of ~xample Surfactant After Oil No. (Weight Ratio~At StartAccumulation 1 Only Al 50 0 2 Only A2 70 20 3 Only A3 40 0 4 Only A4 30 0 Only A5 75 20 6 Only A6 30 0 7 Only A7 60 0 8 Only A8 40 0 9 Only A9 0 0 Only Bl 0 0 1 1 Only B2 0 0 12 On1y B3 0 0 13 Only B4 0 0 14 Only B5 0 0 Only Cl 10 0 2 0 1 6 Al/Cl = 50/50 5 0 0 Table 2 Composition Parts bY Wei~ht Surfactant Composition 10 Alkali Builder Sodium Metasilicate SH20 45 Anhydrous Sodium 18 Carbonate Sodium Phosphate 18 Sodium ~itrite 9 ~ .
~ 25:
As is clear from Table 1, the degreasing composition of the present invention are much better than those of Comparative Examples I - 16 both at start and after oil accumulation.
;~amples 18 - 21. Comparative Examples 17 - 19 5 l~valuation of ~ntifoamin~ Properties Various compounds (a) and compounds (b) are mixed in proportions shown in Table 3 to prepare surfactant compositions, and each surfactant composition is mixed with an alkali builder in a proportion shown in Table 2 to prepare a degreasing composition.
10 Next, 2 parts by weight of each degreasing composition is mixed with 98 parts by weight of water to prepare a degreasing detergent solution.
The evaluation of antifoaming properties is conducted on the resulting degreasing detergent solution by a Ross-Miles Test 15 Method. Specifically, 200 ml of the degreasing composition solution is dropped from a height of 90 cm onto a 50 ml of degreasing composition solution contained in a glass cylinder of 50 mm in inner diameter at 25C for 30 seconds to measure the height (mm) of a foam generated immediately after dropping and the height (mm) 5 20 minutes after dropping. The height of a foam is expressed as a level of foaming.
The evaluation results of antifoaming properties are shown in Table 3.
20~4085 Table 3 Foamin g Level (mm~
Composition of Immediately 5 Minutes Surfactant After After No._ (Wei,~ht Ratio) Foaming Foamin~
Example 1 8 A1/B1 = 50/50 5 0 3 5 19 A1/B2 = 50/50 6 0 4 3 2 0 A2/B 1 = 50/50 6 5 5 0 2 1 A5/B 1 = 50/50 6 8 4 4 Comparative Example 17 Only A-1 120 75 1 8 Only A-2 140 117 19 Only A-5 13 3 104 20140~5 As is clear from Table 3, the degreasing composition solution of the present invention is more excellent in antifoaming properties than those containing conventional surfactants in Compartive Examples 17-19.
Examples 22. 23, Com~arative Examp~es 20 and 21 AS and Bl are selected as the compound (a) and the compound (b), and mixed in a weight ratio of 50/S0 to prepare a surfactant composition, and the surfactant composition is mixed with an alkali builder in the proportion shown in Table 4 to prepare a degreasing composition. Next, each degreasing composition is mixed with water in a proportion shown in Table 4 to prepare a degreasing composition solution. The resulting degreasing composition solution is evaluated with respect to detergency and antifoaming properties in the same method as above. The evaluation results are shown in Table lS 4.
2~:14085 Table 4 Comparative Example No. Example No.
5 Composition of Degreasing Detergent Solution (Parts bv Weight~
Surfactant (X) 2 2 0.04 Alkali 2 2 0 0 1 0 0 0 . 1 Builder (Y) Water (Z) 980 1798 900 980 X/Y 1/1 1/100 1/2500 1/0.1 ~X/(X+Y+Z)] x 1000.2 0.1 0.004 0.1 (weight %) 1 5 [Y/(X+Y+Z)] x 1000.2 1 0 1 0 0.01 (weight %) Deter~ency (%) At Start 100 100 1 0 lO0*
After Oil 95 100 0 70*
2 0 Accumulation Foamin~ Level (mm~
Immediately7 0 6 7 5 After Foaming 5 Minutes 4 0 4 2 2 2 5 After Foaming Note *: Steel test piece was rusted.
~)14085 As is clear from ~able 4, the degreasing composition solutions in Examples 22 and 23 are much better in detergency than that of Comparative Example 20 in which the proportion of the surfactant composition to the alkali builder is less in detergency than 5 l/2G00~ In addition, in Comparative Example 22, in which the content of the alkali builder in the degreasing composition solution is less than 0.05 weight %, the steel test piece is rusted in the evaluation process of detergency. Therefore, a proper amount of the alkali builder is important to adjust pH, thereby achieving the object of the present 1 0 invention.
As described above in detail, since the surfactant composition of the present invention contains the compound (a) and the compound (b) in a weight ratio [compound (a)/compound (b)] of lO/90 - 95/5, the degreasing composition and degreasing lS bathcontaining such surfactant composition and an alkali builder are excellent in detergency and antifoaming properties at room temperature .
The degreasing detergent of the present invention can advantageously maintain detergency and antifoaming properties even 20 after oil accumulation in the bath on an equal level to that at start.
The present invention relates to a surfactant composition, and a degreasing composition and a degreasing bath containing the surfactant 5 composition, and more particularly to a surfactant composition suitable for a degreasing composition having excellent detergency and antifoaming properties at room temperature, and a degreasing composition and a degreasing bath containing such surfactant composition.
In the chemical coating of metal surfaces, degreasing is usually conducted to remove oil substances (mineral oils, animal or vegetable fats and oils, etc.) from the surfaces of metal members to be formed with chemical coatings.
Degreasing detergents used for degreasing treatments contain 15 as main components builders based on acids or alkalis and nonionic surfactants, and they are used in the form of aqueous solutions by a spraying method or an immersion method at 40 - 70C for 1 - 10 minutes.
However, in view of the recent demands of saving energy, 2 0 detergents capable of removing oils at lower temperatures such as S
40C are desired.
As such detergents, Japanese Patent Laid-Open No. 61-60892 discloses an alkali detergent usable at room temperature which contains polyoxyalkylene alkyl ether as a surfactant. The polyoxyalkylene alkyl 25 ether in this detergent has the following general formula:
RO(EO)m(PO)nH, wherein R: Alkyl group, E 0: Ethylene oxide group, 2~14085 PO: Propylene oxide group, and m,n: Moles.
However, although this detergent has improved detergency at room Itemperature, the level of detergency is still insufficient.
OBJECTS AND SUMMAR~ OF THE INVENTION
Accordingly, an object of the present invention is to provide a surfactant composition having excellent detergency at room temperature which is equal to or even higher than under heated conditions (40C or 10 higher), with little foaming.
Another object of the present invention is to provide a degreasing composition having excellent detergency at room temperature which is equal to or even higher than under heated conditions (40C or higher), with little foaming.
A further object of the present invention is to provide a degreasing bath having excellent detergency at room temperature which is equal to or even higher than under heated conditions (40C or higher), with little foaming.
A still further object of the present invention is to provide a 2 0 degreasing composition and a degreasing bath showing excellent detergency even when oil materials are accumulated.
As a result of intense research in view of the above objects, the inventors of the present invention have found that a surfactant composition obtained by mixing a polyoxyalkylene ether-type nonionic 2 5 surfactant containing a predetermined amount of ethylene group with a phosphate-polyethylene oxide adduct shows excellent detergency and antifoaming properties at room temperature when combined with an alkali builder. The present invention is based upon this finding.
Thus, the surfactant composition according to the present invention comprises a compound (a) represented by the general formula:
R1O(AO)nH, wherein R I is a substituted or unsubstituted hydrocarbon group having 6 S or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is S mol or more per 1 mol of Rl, and that the ethylene group is 50 mol % or more per 100 mol % of the A; and n is an integer of 5 - 50; and 10 a compound (b) represented by the general formula:
O
(R )x P(O(EO)n)y H, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 15 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x ~ y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5.
The degreasing composition according to the present invention comprises a compound (a) represented by the general formula:
2 0 RlO(AO)nH, wherein Rl is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is S mol or more 2~ per 1 mol of Rl, and that the ethylene group is 50 mol % or more per 100 mol % of the A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
2 ll (R )x P(O(EO)n) y H, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 5 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/S, and further comprising an allcali builder in a weight ratio [(compound (a) +
compound (b)3/alkali builder] of 1:0.1 - 1:2,000.
The degreasing bath according to the present invention comprises:
(1) 0.005 - 0.5 weight % of a surfactant composition comprising:
a compound (a) represented by the general formula:
RlO(AO),~H, wherein Rl is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is S mol or more per 1 mol of Rl, and that the ethylene group is 50 mol % or more per 100 mol % of the A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
o (R2 )X P(O~EO)n) y H, ~
wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integerofl -20,xandyarel or2,andx+y=3, ~ 014085 in a weight ratio of compound (a~/compound (b) - lO/90 - 95/5;
and (2) 0.05 - lO weight % of an alkali builder.
5 DETArLl~D DESCRIPTION OF THE lNVENTION
The compound (a) used in the pIesent invention is represented by the following general formula (l):
RlO(AO)nH, ... (1) wherein n is an integer of 5 - 50.
l O In the above general formula (l), Rl is, as described below in detail, a hydrocarbon group having 6 or more carbon atoms. When the number of carbon atoms is 5 or less, sufficient surfactant activity cannot be obtained, failing to provide good detergency.
"A" in the above general formula (l) is at least one group l 5 selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group. Incidentally, the number of the ethylene group in "A" is 5 mol or more per l mol of Rl. When the ethylene group is less than 5 mol, the resulting surfactant composition does not have sufficient detergency. Further, the proportion of the 20 ethylene group in "A" is 50 mol % or more per lOO mol % of "A." When the proportion of the ethylene group is lower than 50 mol %, the resulting surfactant composition does not show sufficient detergency. Incidentally, the antifoaming properties of the surfactant composition according to the present invention can be freely adjusted by changing the proportion of 25 the ethylene group relative to lOO mol % of "A" in the compound (a) within the above range.
The number (n) of an AO group in the compound (a) is 5 - 50.
When the number (n) of the AO group is less than 5, sufficient ;~0~4085 detergency cannot be obtained. On the other hand, when n exceeds SO, detergency also becomes insufficient.
Thus, for instance, when n = 5, "A" is completely composed of an eth~lene group. And when n is 6 or more, a portion exceeding 5 may 5 be a group other than the ethylene group. In this case, the ethylene group should be 50 mol % or more based on the total "A."
Incidentally, as long as the content of an oxyethylene group meets the above requirement, the AO group may be contained in the compound (a) in the form of random addition, block addition or a mixture 10 of block addition and random addition.
The compound (b) used in the present invention is represented by the following general formula:
O
1 5 (R )x P(O(EO)n)y H, ,- (2) wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3.
In the above general formula (2), R2 is a hydrocarbon group 20 having 6 or more carbon atoms. When the number of carbon atoms is 5 or less, good detergency canno~ be obtained.
The mole number (n) of an oxyethylene group represented by EO is 1 - 20. When there is no oxyethylene group or when the oxyethylene group exceeds 20 mol, sufficient detergency cannot be 2 5 obtained.
Incidentally, Rl and R2 in the compound (a) and the compound (b) used in the present invention may be the same or different from each other, and as long as they are hydrocarbon groups having 6 or Z0~4085 more carbon atoms, they may be substituted or unsubstituted. Typical examples of Rl and R2 are alkyl groups such as a hexyl group, an octyl group, a decyl group, a dodecyl group, a stearyl group; alkenyl groups such as an oleyl group; cycloalkyl groups such as a cyclohexyl group;
S alkyl-substituted or phenyl-substituted phenyl groups such as a xylene group, an octyl phenyl group, a nonyl phenyl group, a dodecyl phenyl group, a dinonyl phenyl group, a paracumyl phenyl group, a styrene-added phenyl group; an unsubstituted phenyl group, etc.
In the surfactant composition of the present invention, the 10 compound (a) and the compound (b) may be used in combination.
With respect to the weight ratio of the compound (a) to the compound (b) in the surfactant composition of the present invention, compound (a)/compound (b) is 10/90 - 95/5, preferably 25/75 - 75/25.
When the weight ratio of the compound (a) to the compound (b) is lower 15 than 10/90 or larger than 95/5, sufficient detergency cannot be obtained.
Next, the degreasing composition of the present invention will be described below.
The degreasing composition of the present invention comprises the above surfactant composition containing the compound (a) 20 and the compound (b) in a weight ratio of compound (a)/compound (b) -10/90 - 95/5 and an alkali builder.
The alkali builders which may be used in the present invention include alkali metal salts, alkali phosphate, alkali carbonates, alkali silicates, alkali nitrites, alkali borates, etc., and they may be used 2 5 alone or in combination.
In the degreasing composition of the present invention, a proportion of the alkali builder to the surfactant composition [wei~ht ratio of (compound (a) + compound (b))/alkali builder] is 1:0.1 - 1:2000, 2~
preferably 1:1 - 1:100.
When the weight ratio of [(compound (a) + compound (b))/alkali builder] is less than 1:0.1, the decrease in detergency does not substantially take place, but it is dif~lcult to maintain a pH for suppressing the corrosion of metal members to be treated. On the other hand, when the weight ratio exceeds 1:2000, the concentration of the surfactant composition in the degreasing detergent ccomposition becomes too low, resulting in insufficient detergency.
Incidentally, depending upon degreasing facilities, the degreasing composition of the present invention may further contain 5-100 parts by weight of an antifoaming agent per 100 parts by weight of the surfactant composition. When the amount of the antifoaming agent is less than 5 parts by weight, sufficient improvement of antifoaming properties cannot be obtained, and when it exceeds 100 parts by weight, the detergency of the degreasing composition decreases.
The antifoaming agents include higher alcohols, higher ethers, higher aliphatic acids, higher aliphatic acid esters, and alkyl alkylates or alkyl phenol alkylates having HLB values of 10 or less, polypropylene glycolsJpolyethylene glycol ethers, etc. having cloud points of 40C or lower, and they may be used alone or in combination.
Next, the degreasing bath of the present invention will be described.
The degreasing bath of the present invention contains the above surfactant composition and the alkali builder.
The amount of the surfactant composition is 0.005 - 0.5 weight %, preferably 0.05 - 0.3 weight %. When the amount of the surfactant composition is lower than 0.005 weight %, sufficient degreasing activity cannot be obtained. When it exceeds 0.5 weight %, ~ 0~4085 further increase in degreasing activity cannot be achieved.
The amount of the alkali builder is 0.05 - 10 w~ight %, preferably 1 - 5 weight %. When the amount of the alkali builder is less than 0.05 weight %, the degreasing detergent solution has a low pH, 5 making it likely that the metal members to be treated are rusted, and making it difficult to emulsify oil materials removed from the metal members being treated. On the other hand, when the amount of the alkali builder exceeds 10 weight %, it is difficult to dissolve the alkali builder, deteriorating operability.
The composition of the degreasing bath of the present invention can be adjusted by introducing the surfactant composition and the alkali builder separately into a degreasing bath (hereinaft~r called "separate system") or by mixing them in advance and then introducing the resulting mixture into the degreasing bath (hereinafter called 1 5 "premixed system").
As far as the operability is concerned, the premixed system is preferable, but from the viewpoint of stability with time, the separa~e system is preferable. In the case of the premixed system, the amount of the alkali builder is preferably 80 weight % or more based on the 2 0 surfactant composition to avoid swelling.
As described above, the surfactant composition of the present invention comprises the compound (a) which is a particular polyoxyalkylene ether-type nonionic surfactant, and the compound (b) which is a phosphate-ethylene oxide adduct in a particular proportion.
25 The compound (a) itself does not have sufficient detergency at room temperature, and the compound (b) itself does not have detergency at all.
Nevertheless, a combination of the compound (a) and the compound (b) provides a degreasing detergent with good detergency. The reason g 20~408~;
therefor is not necessarily clear, but it may be considered that a synergistic effect between the compound (a) and the compound (b) serves to increase the detergency of the compound (a), while providing the degreasing detergent with good antifoaming properties.
Further, the degreasing bath of the present invention utilizing the synergistic effect of the compound (a) and the compound (b) can maintain degreasing detergency and antifoaming properties equally at start and even after oil accumulation in the bath.
The present invention will be described in further detail by means of the following Examples.
SYnthesis of Compound (a) As the compound (a), the following compounds Al - A9 are synthesized by adding alkylene oxides to various alcohols and phenols having various Rl groups in the general formula (1), in the presence of an alkali catalyst by a usual method.
Al: 7.5 mol of ethylene oxide added to lauryl alcohol.
A2: 10 mol of ethylene oxide added to lauryl alcohol.
A3: 20 mol of ethylene oxide added to lauryl alcohol.
A4: 8 mol of ethylene oxide added to octyl alcohol.
A5: 10 mol of ethylene oxide added to nonyl phenol.
A6: 15 mol of ethylene oxide added to styrene-added phenol.
A7: 10 mol of ethylene oxide block and 3 mol of propylene oxide block added to nonyl phenol.
A8: 10 mol of ethylene oxide and 7 mol of propylene oxide added to nonyl phenol in random.
A9: 10 mol of ethylene oxide block and 2 mol of propylene oxide block added to nonyl phenol.
Svnthesis of Com~ound (b) 201A0~3S
As the compound (b), the following compounds B1 - B6 are synthesized by preparing phophates of various alcohols and phenols having R2 groups in the fomula (2) using phosphorus pentoxide by a usual method, and then adding ethylene oxide thereto in the presence of 5 an alkali catalyst by a usual method.
B 1: 3 mol of ethylene oxide added to lauryl alcohol phosphate.
B2: 5 mol of ethylene oxide added to lauryl alcohol phosphate.
B3: 12 mol of ethylene oxide added to lauryl alcohol phosphate.
B4: 5 mol of ethylene oxide added to octyl alcohol phosphate.
o B5: 10 mol of ethylene oxide added to nonyl phenol phosphate.
B6: 9 mol of ethylene oxide added to paracumyl phenol phosphate.
Svnthesis of Compound (c~
For comparison with the compound (b), the following compound C1 is synthesized by adding 10 mol of ethylene oxide to 1 mol of nonyl phenyl having an R2 group in the general formula (2) in the presence of an alkali catalyst by a usual method, and preparing a phosphate thereof by using phosphorus pentoxide by a usual method.
C1: Phosphate of a nonyl phenol -10 mol ethylene oxide adduct.
Examples_1 - 17. Comparative Examples 1 - 16 Each of surfactant compositions containing the above compounds A1 - A9, B1 - B6 and C1 as shown in Table 1 is mixed with an alkali builder in a proportion shown in Table 2 to prepare each degreasing composition.
2 parts by weight of each degreasing composition is mixed with 98 parts by weight of water to prepare each degreasing detergent solution bath.
Evaluation of Deter~encv With respect to each degreasing detergent solution, detergency is evaluated at start (fresh composition) and after oil accumulation in the bath.
(l! Deter~ency at Start Each degreasing detergent solution is introduced into a 50.0 ml-beaker and kept at 15C. A steel test piece (JIS G-3141) is immersed in the solution, and the solution is stirred at 200 rpm for 10 minutes.
Thereafter, the steel test piece is removed and rinsed by running water for 30 seconds to measure water wettability of the steel test piece surface. This is regarded as detergency at start. Incidentally, the detergency is regarded as 100% when the entire surface of the steel test piece is still wet with water 30 seconds after the removal from the bath, and the water wettability is expressed by percentage of surface area wet with water observed by the naked eye.
(2! Deter~encv after 0i2 Accumulation With respect to the above degreasing composition mixed with 2000 ppm of an anti-corrosion oil ("Anti-rust P1400," manufactured by Nippon Oil Co., Ltd.), a water wettability is measured on the steel test piece surface in the same method as in the detergency at start, and it is 2 0 evaluated as detergency after oil accumulation.
The evaluation results of each detergency are shown in Table 1.
2s 2~)~14~35 Table 1 Detergencv (%) Composition of E,xample Surfactant After Oil _ No. (Weight Ratio)At StartAccumulation 1 Al/B5 = 75/25 1 00 1 00 2 Al/B5 = 50/50 100 100 3 Al/B5 = 25/75 9 5 9 0 4 A2/B5 = 50/50 1 00 1 00 A3/B5 = 50/50 9 0 8 5 1 0 6 ~4/B5 = 50/50 9 0 8 0 7 A5/B5 = 50/50 1 00 9 0 8 A6/B5 = 50/50 9 0 9 0 9 A7/B5 = 50l50 1 0 0 9 5 1 0 A8/B5 = 50/50 9 5 9 0 1 5 1 1 A9/B5 = 50t50 9 5 9 0 1 2 Al/Bl = 50/50 90 90 1 3 Al/B2 = 50/50 1 00 1 00 1 4 Al/B3 = 50/50 9 5 9 0 1 5 Al/B4 = 50/50 9 5 9 0 2 0 1 6 Al/B5 = 50/50 9 0 8 0 1 7 Al/B6 - 50/50 9 5 9 0 20~40~35 Table 1 (Continued) .
Deter~encv (%3 Comparative Composition of ~xample Surfactant After Oil No. (Weight Ratio~At StartAccumulation 1 Only Al 50 0 2 Only A2 70 20 3 Only A3 40 0 4 Only A4 30 0 Only A5 75 20 6 Only A6 30 0 7 Only A7 60 0 8 Only A8 40 0 9 Only A9 0 0 Only Bl 0 0 1 1 Only B2 0 0 12 On1y B3 0 0 13 Only B4 0 0 14 Only B5 0 0 Only Cl 10 0 2 0 1 6 Al/Cl = 50/50 5 0 0 Table 2 Composition Parts bY Wei~ht Surfactant Composition 10 Alkali Builder Sodium Metasilicate SH20 45 Anhydrous Sodium 18 Carbonate Sodium Phosphate 18 Sodium ~itrite 9 ~ .
~ 25:
As is clear from Table 1, the degreasing composition of the present invention are much better than those of Comparative Examples I - 16 both at start and after oil accumulation.
;~amples 18 - 21. Comparative Examples 17 - 19 5 l~valuation of ~ntifoamin~ Properties Various compounds (a) and compounds (b) are mixed in proportions shown in Table 3 to prepare surfactant compositions, and each surfactant composition is mixed with an alkali builder in a proportion shown in Table 2 to prepare a degreasing composition.
10 Next, 2 parts by weight of each degreasing composition is mixed with 98 parts by weight of water to prepare a degreasing detergent solution.
The evaluation of antifoaming properties is conducted on the resulting degreasing detergent solution by a Ross-Miles Test 15 Method. Specifically, 200 ml of the degreasing composition solution is dropped from a height of 90 cm onto a 50 ml of degreasing composition solution contained in a glass cylinder of 50 mm in inner diameter at 25C for 30 seconds to measure the height (mm) of a foam generated immediately after dropping and the height (mm) 5 20 minutes after dropping. The height of a foam is expressed as a level of foaming.
The evaluation results of antifoaming properties are shown in Table 3.
20~4085 Table 3 Foamin g Level (mm~
Composition of Immediately 5 Minutes Surfactant After After No._ (Wei,~ht Ratio) Foaming Foamin~
Example 1 8 A1/B1 = 50/50 5 0 3 5 19 A1/B2 = 50/50 6 0 4 3 2 0 A2/B 1 = 50/50 6 5 5 0 2 1 A5/B 1 = 50/50 6 8 4 4 Comparative Example 17 Only A-1 120 75 1 8 Only A-2 140 117 19 Only A-5 13 3 104 20140~5 As is clear from Table 3, the degreasing composition solution of the present invention is more excellent in antifoaming properties than those containing conventional surfactants in Compartive Examples 17-19.
Examples 22. 23, Com~arative Examp~es 20 and 21 AS and Bl are selected as the compound (a) and the compound (b), and mixed in a weight ratio of 50/S0 to prepare a surfactant composition, and the surfactant composition is mixed with an alkali builder in the proportion shown in Table 4 to prepare a degreasing composition. Next, each degreasing composition is mixed with water in a proportion shown in Table 4 to prepare a degreasing composition solution. The resulting degreasing composition solution is evaluated with respect to detergency and antifoaming properties in the same method as above. The evaluation results are shown in Table lS 4.
2~:14085 Table 4 Comparative Example No. Example No.
5 Composition of Degreasing Detergent Solution (Parts bv Weight~
Surfactant (X) 2 2 0.04 Alkali 2 2 0 0 1 0 0 0 . 1 Builder (Y) Water (Z) 980 1798 900 980 X/Y 1/1 1/100 1/2500 1/0.1 ~X/(X+Y+Z)] x 1000.2 0.1 0.004 0.1 (weight %) 1 5 [Y/(X+Y+Z)] x 1000.2 1 0 1 0 0.01 (weight %) Deter~ency (%) At Start 100 100 1 0 lO0*
After Oil 95 100 0 70*
2 0 Accumulation Foamin~ Level (mm~
Immediately7 0 6 7 5 After Foaming 5 Minutes 4 0 4 2 2 2 5 After Foaming Note *: Steel test piece was rusted.
~)14085 As is clear from ~able 4, the degreasing composition solutions in Examples 22 and 23 are much better in detergency than that of Comparative Example 20 in which the proportion of the surfactant composition to the alkali builder is less in detergency than 5 l/2G00~ In addition, in Comparative Example 22, in which the content of the alkali builder in the degreasing composition solution is less than 0.05 weight %, the steel test piece is rusted in the evaluation process of detergency. Therefore, a proper amount of the alkali builder is important to adjust pH, thereby achieving the object of the present 1 0 invention.
As described above in detail, since the surfactant composition of the present invention contains the compound (a) and the compound (b) in a weight ratio [compound (a)/compound (b)] of lO/90 - 95/5, the degreasing composition and degreasing lS bathcontaining such surfactant composition and an alkali builder are excellent in detergency and antifoaming properties at room temperature .
The degreasing detergent of the present invention can advantageously maintain detergency and antifoaming properties even 20 after oil accumulation in the bath on an equal level to that at start.
Claims (3)
1. A surfactant composition comprising:
a compound (a) represented by the general formula:
R1O(AO)nH, wherein R1 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is 5 mol or more per 1 mol of R1, and that the ethylene group is 50 mol % or more per 100 mol % of said A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
(R2O)x?(O(EO)n)yH, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 -20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5.
a compound (a) represented by the general formula:
R1O(AO)nH, wherein R1 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is 5 mol or more per 1 mol of R1, and that the ethylene group is 50 mol % or more per 100 mol % of said A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
(R2O)x?(O(EO)n)yH, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 -20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5.
2. A degreasing composition comprising:
a compound (a) represented by the general formula:
R1O(AO)nH, wherein R1 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group-consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is 5 mol or more per 1 mol of R1, and that the ethylene group is 50 mol % or more per 100 mol % of said A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
(R2O)x?(O(EO)n)yH, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5, and further comprising an alkali builder in a weight ratio [(compound (a) + compound (b))/alkali builder] of 1:0.1 - 1:2,000.
a compound (a) represented by the general formula:
R1O(AO)nH, wherein R1 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group-consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that an ethylene group in A is 5 mol or more per 1 mol of R1, and that the ethylene group is 50 mol % or more per 100 mol % of said A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
(R2O)x?(O(EO)n)yH, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5, and further comprising an alkali builder in a weight ratio [(compound (a) + compound (b))/alkali builder] of 1:0.1 - 1:2,000.
3. A degreasing bath comprising:
(1) 0.005 - 0.5 weight % of a surfactant composition comprising:
a compound (a) represented by the general formula:
R1O(AO)nH, wherein R1 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that is an ethylene group in A is 5 mol or more per 1 mol of R1, and that the ethylene group is 50 mol % or more per 100 mol % of said A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
(R2O)x?(O(EO)n)yH, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5;
and (2) 0.05 - 10 weight % of an alkali builder.
(1) 0.005 - 0.5 weight % of a surfactant composition comprising:
a compound (a) represented by the general formula:
R1O(AO)nH, wherein R1 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms; A is at least one group selected from the group consisting of an ethylene group, a propylene group, a butylene group and a styrene group, provided that is an ethylene group in A is 5 mol or more per 1 mol of R1, and that the ethylene group is 50 mol % or more per 100 mol % of said A; and n is an integer of 5 - 50; and a compound (b) represented by the general formula:
(R2O)x?(O(EO)n)yH, wherein R2 is a substituted or unsubstituted hydrocarbon group having 6 or more carbon atoms, E is an ethylene group, n is an integer of 1 - 20, x and y are 1 or 2, and x + y = 3, in a weight ratio of compound (a)/compound (b) = 10/90 - 95/5;
and (2) 0.05 - 10 weight % of an alkali builder.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1091504A JP2578367B2 (en) | 1989-04-11 | 1989-04-11 | Surfactant composition, degreasing detergent composition using the same, and degreasing cleaning bath |
| JP1-91504 | 1989-04-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2014085A1 true CA2014085A1 (en) | 1990-10-11 |
Family
ID=14028244
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2014085 Abandoned CA2014085A1 (en) | 1989-04-11 | 1990-04-06 | Surfactant composition, degreasing composition and degreasing bath |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0392394B1 (en) |
| JP (1) | JP2578367B2 (en) |
| CA (1) | CA2014085A1 (en) |
| DE (1) | DE69000812T2 (en) |
| ES (1) | ES2054135T3 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5501816A (en) * | 1994-07-12 | 1996-03-26 | Basf Corporation | Aqueous based solvent free degreaser composition |
| US6492317B1 (en) | 2000-05-19 | 2002-12-10 | Basf Corporation | High forming hard surface cleaning formulations |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4247424A (en) * | 1979-10-11 | 1981-01-27 | The Procter & Gamble Company | Stable liquid detergent compositions |
| US4539134A (en) * | 1982-12-02 | 1985-09-03 | Halliburton Company | Methods and cleaning compositions for removing organic materials from metallic surfaces |
| US4552673A (en) * | 1983-10-24 | 1985-11-12 | Olin Corporation | Blend of alkyl phenol ethoxylates and alkyl phenol glycoxylates and their use as surfactants |
-
1989
- 1989-04-11 JP JP1091504A patent/JP2578367B2/en not_active Expired - Lifetime
-
1990
- 1990-04-06 EP EP19900106663 patent/EP0392394B1/en not_active Expired - Lifetime
- 1990-04-06 ES ES90106663T patent/ES2054135T3/en not_active Expired - Lifetime
- 1990-04-06 CA CA 2014085 patent/CA2014085A1/en not_active Abandoned
- 1990-04-06 DE DE1990600812 patent/DE69000812T2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2578367B2 (en) | 1997-02-05 |
| EP0392394A1 (en) | 1990-10-17 |
| DE69000812T2 (en) | 1993-07-15 |
| DE69000812D1 (en) | 1993-03-11 |
| JPH02269799A (en) | 1990-11-05 |
| EP0392394B1 (en) | 1993-01-27 |
| ES2054135T3 (en) | 1994-08-01 |
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