US3916003A - Surface active agents - Google Patents

Surface active agents Download PDF

Info

Publication number
US3916003A
US3916003A US422146A US42214673A US3916003A US 3916003 A US3916003 A US 3916003A US 422146 A US422146 A US 422146A US 42214673 A US42214673 A US 42214673A US 3916003 A US3916003 A US 3916003A
Authority
US
United States
Prior art keywords
surface active
active agents
fatty acid
rust
properties
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US422146A
Inventor
Hiroshi Suzuki
Yoshiro Tsutsui
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to US422146A priority Critical patent/US3916003A/en
Application granted granted Critical
Publication of US3916003A publication Critical patent/US3916003A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S516/00Colloid systems and wetting agents; subcombinations thereof; processes of
    • Y10S516/01Wetting, emulsifying, dispersing, or stabilizing agents
    • Y10S516/06Protein or carboxylic compound containing

Definitions

  • non-ionic surface active agents are generally low in toxicity they are commonly used as additives in pharmaceuticals, cosmetics, foodstuffs, etc. However, nonionic surface active agents which exhibit antimicrobial action or rust-inhibiting property have not hitherto been known.
  • the present invention uses hydroxy-fatty acid amide polyoxyalkylene ether, as the active ingredients. As this substance is superior in antimicrobial action and rust-inhibiting property, the surface active agents manufactured according to the present invention exhibit not only the superior properties inherent in the conventional surface active agents, e.g., emulsifying and dispersing power, but also superior rustinhibiting property and antimicrobial action. Further, if metal soap is added to the surface active agents, the aforementioned properties become more conspicuous.
  • this invention relates to non-ionic surface active agents comprising, as active ingredients, hydroxy-fatty acid amide polyoxyalkylene ethers which exhibit excellent dispersing, rust-inhibiting, antimicrobial and emulsifying properties, and to surface active compositions comprising said ethers and metal soaps which exhibit further improved dispersing, rust-inhibiting, antimicrobial, emulsifying and other general properties.
  • surface active agents having rust-inhibiting and antimicrobial properties have been known and the examples of such agents are amine-type cation surface active agents and some of the amphoteric surface active agents.
  • these known agents are strongly toxic and, in addition, the activity of these agents in solution is readily affected by the pH value of the solution. Further, these known agents tend, at low temperatures, to decrease in their ability to solubilize other materials to be dissolved and to decrease their own solubility in a medium and thus these agents have the limited utilities.
  • non-ionic surface active agents now available are generally less toxic and, therefore, are often acceptable as additives to pharmaceuticals, cosmetics as well as foodstuffs.
  • the non-ionic surface active agents are not useful for the bacteriocidal or germicidal purposes since they generally exhibit no such antimicrobial properties and are on the contrary known to have a growth promoting property with respect to the microorganisms.
  • the primary object of this invention is to provide amide-type non-ionic surface active agents which are highly effective as dispersing, rust-inhibiting, antimicrobial and emulsifying agents, as well as surface active compositions containing, as active ingredients, said amide-type non-ionic surface active agents.
  • the present inventors searched for surface active agents suitable for the above purposes and found that hydroxy-fatty acid amide polyoxyalkylene ethers, one of the amide-type non-ionic surface active agents, have excellent antimicrobial and rust-inhibiting properties, and further that these properties are effectively improved by combining said ethers with metal soaps.
  • the improved activities obtainable by the surface active agents of this invention are the outstanding features of the present invention in view of the fact that the conventional non-ionic surface active agents generally have no rust-inhibiting property and the fact that, when they are combined with the metal soaps, the rustinhibiting property inherent to metal soaps is generally 2 lowered by the corrosive action due to the presence of the non-ionic surface active agents.
  • R is a hydrocarbon radical having 7 to 21 carbon atoms; R is selected from the group consisting of hydrogen and a lower alkyl group; y is an integer between 1 and 50; and z is an integer not less than 1.
  • the surface active composition of this invention comprises the above hydroxyfatty acid amide polyoxyalkylene ethers and the metal soaps which have as their main component a substance represented by the formula (RCOO),M
  • R represents a hydrocarbon radical having 2 to 21 carbon atoms
  • x is an integer between 1 and 5 equivalent to the atomic valence of the metal M
  • M represents a metal, the amount of the metal soaps used being in the range of from equivalent weight to l/ 1000 by weight, preferably from equivalent weight to 1/100 on the basis of said ethers.
  • novel hydroxy-fatty acid amide polyalkylene ethers of the present invention can be prepared, for example, by reacting a monoor polyhydroxy-fatty acid ester such as castor oil, hydrogenated castor oil, methyl ricinolate, l2-hydroxy-stearic acid ester, tetrahydroxy stearic acid ester and the like with an alkylene oxide such as ethylene oxide and propylene oxide to obtain a hydroxy-fatty acid ester polyoxyalkylene ether followed by ammonolysis with liquid ammonia, or by subjecting the above hydroxy-fatty acid ester to ammonolysis to obtain the corresponding acid amide which is then reacted with an alkylene oxide.
  • a monoor polyhydroxy-fatty acid ester such as castor oil, hydrogenated castor oil, methyl ricinolate, l2-hydroxy-stearic acid ester, tetrahydroxy stearic acid ester and the like
  • an alkylene oxide such as ethylene oxide and propylene oxide
  • hydroxy-fatty acid amide polyoxyalkylene ethers examples include castor oil fatty acid amide polyoxyethylene ether, ricinoleic acid amide polyoxypropylene ether, hydrogenated castor oil fatty acid amide polyoxyethylene ether, etc.
  • the surface active agents of this invention contain free amide radicals having high hydrogen-bonding strength and hydrophilic radicals in the side chains and, therefore they are excellent in emulsifying, dispersing, wetting and antistatic properties.
  • Non-ionic surface active agents are, as previously mentioned, generally less toxic, but some of the agents such as alkylphenyl derivatives show a low LD value.
  • polyoxyethylene-(9,7 )-p-tert-octylphenyl ether is said to have a [D value of 1.7 ml/kg (acute toxicity in rat, Handbook p267 (1968) issued by Nikko Chemicals Co., Ltd.).
  • the surface active agents of this invention were found to have low toxicity as evidenced by the LD value of 20 ml/kg (acute toxicity in mice) shown by castor oil fatty acid amide polyoxyethylene ether (6 mole addition product).
  • the LD value has been found to be 22 ml/kg, indicating that the toxicity is practically negligible.
  • the surface active agents of this invention give rise to almost no skin irritability or oversensi tivity.
  • Mixtures formed by separately combining the 7 and 21 mole product of the above ether with a magnesium salt of castor oil fatty acid (5:1 molar ratio) were diluted to form a 30% water solution and applied to rabbits once daily over a period of ten days. At the end of the test period absolutely no abnormalty could be found either by the naked eye or by microscopic inspection of the tissue in either case.
  • a further test was conducted wherein the same solutions were applied to marmots twice daily over a 3 day period. Neither an examination of either animals reactions nor a microscopic examination of its tissue showed any abnormalty.
  • the metal soaps used in the composition of this invention are well known metal salts of hydroxy-fatty acids of saturated or unsaturated and straight or branched chain containing 2 to 21 carbon atoms or of naphthenic acid or resin acid.
  • the metal useful as the metal salts includes those of I to V valences in the Periodic Table, i.e., Group la (Li, Na, K, etc.), Group Ila (Mg, Ca, Ba, etc.), Group Illa (B, Al, etc.), Group IVb (Si, Sn, Pb, etc.), Group Vb (As, Sb, Bi), Group lb (Cu, Ag, etc.), Group Ilb (Zn, Cd, Hg), Group lVa (Ti, Zr, etc.), Group Va (V, etc.), Group Vla (Cr, Mo, W, etc.), Group VIla (Mn, etc.), Group VIII (Fe, Co, Ni, etc.), and the like.
  • the surface active composition of this invention can be obtained by blending the amide-type non-ionic surface active agent and the metal soap in a proportion of 1:1 to 1:1/l000 by weight. This can be accomplished either by adding the metal soap to an aqueous solution of the amide-type non-ionic surface active agent or by merely blending together the two components. Since the amide-type non-ionic surface active agents of this invention are highly soluble in water and, in addition, have an excellent ability to dissolve a wide variety of metal soaps, it is possible to obtain a composition containing high concentrations of both the surface active agent and the metal soap.
  • the properties of the surface active agent and the composition according to the present invention can be controlled by changing the addition molar numbers of alkylene oxide in the amide-type surface active agent or by changing a proportion of the amide-type surface active agent and the metal soap.
  • the various properties of the hydroxy-fatty acid amide polyoxyethylene ether of the present invention are as follows: its solubility in petroleum solvents and ethyl ether is a little low, but it is easily soluble in most of the other solvents; the agents in which more than about 7 moles of ethylene oxide are added give a clear aqueous solution; the optimum chain length of polyoxyethylene group (POE) for the emulsifying, solubilizing, and antistatic properties varies depending upon the type of substances for which such properties are utilized; the agents having relatively short chains are superior in lowering of surface tension, in wetting, rustinhibiting and antimicrobial properties and in wettability; and the agents having relatively long chains are su- 4 perior in the dispersing, cleaning and foaming properties. Hydroxy-fatty acid amide polyoxypropylene ether has lower water-solubility than that of POE ether and has, in some instances, a solubilizing activity inferior to POE ether.
  • the metal soap as one of the additives of the surface active composition of this invention shows the following tendency.
  • the order of higher solubility of the soap is K, Na Li, Mg Ba, Mn, Co Zn, Cd Pb, Fe, and, in the metal soap comprising a different fatty acid and a given metal, the shorter the chain length, the higher the unsaturation and the more branched chains, the higher the solubility.
  • hydroxylic acids are particularly soluble at a low temperature.
  • the activity of the metal soap is generally superior when the metal is an alkali earth metal, manganese or cobalt, but the metal soaps comprising other metals have also specific characteristics.
  • a potassium and sodium soap and a lithium salt of a hydroxylic acid exhibit an increased solubility in water, and a mixture of one of the above soaps and a hydroxy-fatty acid amide polyalkylene ether (y 0-3) having a short POE chain or a hydroxy-fatty acid amide polyoxypropylene ether give a clear aqueous solution, and is often superior in cleaning and dispersing properties. Further, superior antimicrobial properties are exhibited by silver, lead and bismuth soaps, superior dispersing properties by zinc, zirconium and vanadium soaps, superiro emulsifying properties by chrome soap and superior rust-inhibiting and other properties by aluminum soap.
  • the surface active agent of this invention is further characterized by the fact that its activity is not adversely affected by the changes of pH value. Soaps are generally decomposed and precipitated at acidic pH values thereby losing their surface activity, and other ionic surface active agents are also precipitated more or less in an acidic or alkaline solution, resulting in decrease or loss of their surface activity.
  • the surface active composition of this invention shows less decomposition and precipitation over a wide range of pH values because the composition is a solubilized system of the metal soap with the hydroxy-fatty acid amide polyoxyalkylene ether, and, accordingly, the activity of the composition is not significantly lowered in either at acidic or alkaline pH values and is, rather, improved in some instances.
  • the increase in the cloud point due to the dissociation of the soap is observed in any cases when, of course, the soap is an alkali soap and even when the soap is a water-insoluble metal soap.
  • a castor oil fatty acid amide polyoxyethylene ether (6 mole addition product; cloud point, 470C) is combined with magnesium ricinolate at a molar ratio of 5:1, the cloud point rises more than 10C. This means that the temperature range within which the composition is effective can be broaden, and this is very advantageous in practical use.
  • hydroxy-fatty acid amide polyoxyalkylene ethers of this invention can be combined with other substances than the metal soaps as illustrated above.
  • the surface active agents of this invention are incorporated into various surface active agents, the emulsifying, dispersing, cleaning, solubilizing, rust-inhibiting,
  • solubility and foaming properties of the resulting blend are strengthened synergistically depending upon the length of the polyoxyalkylene chain in the former agents.
  • chain length is relatively short, foam stability, sustained cleaning and wetting properties are significantly improved.
  • the hydroxy-fatty acid amide polyoxyalkylene ethers of this invention exhibit an excellent solubilizing property.
  • those containing a relatively short chain exhibit a potent antimicrobial property. Such properties are useful when, for example, the product is used for dissolving iodine in water thereby preparing an aqueous iodine solution which has excellent antimicrobial property and low toxicity.
  • the activities of the surface active agent and composition can often be increased by adding thereto various builders.
  • wetting, rust-inhibiting, emulsifying, cleaning and other properties, in particular at acidic pH values, of the 5:1 mole mixture of hydroxyfatty acid amide polyoxyethylene ether and a magnesium salt of castor oil fatty acid can be increased by incorporating sodium tripolyphosphate in an amount ranging from equimolar to one-fifth mole on the basis of said ether.
  • Suitable builders include a wide variety of phosphates, sulphates, nitrite, carbonates, borates silicates and ethanolamines and CMC, urea, EDTA, sodium nitrilotriacetate, sodium toluene sulfonate and the like which are known to those skilled in the art.
  • the hydroxy-fatty acid amide polyoxyalkylene ethers of this invention are easily dispersible or soluble in various organic solvents, and a dispersion or solution in such solvent as benzene, toluene, carbon tetrachloride, trichloroethane, trichloroethylene, iso-propyl alcohol, kerosene, etc. is highly effective in enhancing the cleaning, dispersing, emulsifying, solubilizing, wetting, rust-inhibiting and antistatic properties.
  • the mixture of the ether and the metal soap is also soluble in a wide variety of organic solvents, and a solution of the mixture in benzene, toluene, carbon tetrachloride, cottonseed oil, trichloroethane, trichloroethylene, iso-propanol, kerosene or the like often shows excellent cleaning, dispersing, emulsifying, solubilizing, wetting, rust-inhibiting, antimicrobial and antistatic properties.
  • the surface active agents of this invention are non-ionic surface active agents being by nature of relatively low toxicity, but exhibiting an antimicrobial property on some species of the microorganism comparable to that of the cationic surface active agents. Also, the surface active agents of this invention are characterized in that they are useful rust-inhibiting agents with respect to aluminum, iron, copper, etc. Further, the surface active properties of the agents can be improved by incorporating metal soaps and/or other additives.
  • EXAMPLE 1 The various properties of the known surface active agents were compared with those of the castor oil fatty acid amide polyoxyethylene ethers (8 and 25 mole addition products) at a temperature of 30C and a concentration of 0.02 mol/l. The results obtained as shown in Table 1. The numerical values in Table 1 were determined according to methods reported by one of the inventors [H. Suzuki, Yukagaku, 15, 475 (1966); ibid, 16, 667 (1967); ibid, 18, 136 (1969); H. Suzuki Kogyokagaku Zasshi, 72, 2253 (1969); ibid, Yukagaku, 19, 125 (1970)].
  • EXAMPLE 2 The comparative test for various surface active properties was conducted at a temperature of C using each of the compositions consisting of a typical surface active agent and a magnesium salt of castor oil fatty acid in a molar ratio of 0.02 0.004 per liter. The results obtained are as shown in Table 2.
  • the compositions used in the above test were prepared in the following manner: 1.30 g castor oil fatty acid amide polyadded to a portion of the solution (1), and the mixture was heated with shaking to dissolve the salt. After cooling, the total volume of the solution was made up to 100 ml with water to produce an aqueous solution (2) of the surface active composition of this invention [the molar ratio of 5 l, 0.05 0.01 (m0l/l)]. The various surface activities of the resulting aqueous solution (1) and (2) at a temperature of 15C were determined and compared with each other. The results obtained are as shown in Table 3.
  • oxyethylene ether (8 mole addition product) was dis- Table 3 solved in ml of water and 0.248 g of a magnesium salt of castor oil fatty acid was added to the solution 30 Pro "y and the mixture was heated with shaking to dissolve the pe salt. After cooling, the volume of the resulting solution 2 was made up to 100 ml with water [the molar ratio of Rusplnhibiting Brass C B 5 l, 0.02 0.004 (mol/l)].
  • Example *1 The value indicates the molar number of ethylene oxide.
  • Kerosene Nylon-Fabric Foaming Emulsifying Surface Tension (dyne/cm) (dyne/cm) Antistatic 1 Solution of castor oil fatty acid amide polyoxyethylenen other.
  • aque- )us solutions comprising 1) various addition products )f a castor oil fatty acid amide-type non-ionic surface ictive agent and ethylene oxide in different molar raios and (2) various metal soaps in different amounts 5 vere prepared, and surface activities were determined 1nd compared with those of the aqueous solutions conaining only the corresponding addition products.
  • the 'esults obtained are as shown in Table 5.
  • Table 1 shows the composition of the example aqueous soluions shown in Table 5.
  • the volume of each aqueous olution in Table 4 is ml.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Detergent Compositions (AREA)

Abstract

As non-ionic surface active agents are generally low in toxicity they are commonly used as additives in pharmaceuticals, cosmetics, foodstuffs, etc. However, non-ionic surface active agents which exhibit antimicrobial action or rust-inhibiting property have not hitherto been known. The present invention uses hydroxy-fatty acid amide polyoxyalkylene ether, as the active ingredients. As this substance is superior in antimicrobial action and rust-inhibiting property, the surface active agents manufactured according to the present invention exhibit not only the superior properties inherent in the conventional surface active agents, e.g., emulsifying and dispersing power, but also superior rust-inhibiting property and antimicrobial action. Further, if metal soap is added to the surface active agents, the aforementioned properties become more conspicuous.

Description

United States Patent [191 Suzuki et al.
[ SURFACE ACTIVE AGENTS [75] Inventors: Hiroshi Suzuki; Yoshiro Tsutsui,
both of Tokyo, Japan [73]- Assignee: Agency of Industrial Science &
Technology, Tokyo, Japan [22] Filed: Dec. 5, 1973 [21] Appl. No.: 422,146
Related US. Application Data [62] Division of Ser. No. 119,845, March 1, 1971, Pat.
[52] US. Cl 260/404; 252/356 [51] Int. Cl. C07C 103/175 [58] Field of Search 260/404 [56] References Cited UNITED STATES PATENTS 2,520,381 8/1950 Carnes 260/404 2,677,700 5/1954 Jackson et al. 260/404 X 3,264,281 8/1966 Applewhite et al... 260/404 X 3,417,114 12/1968 Kuceski 260/404 3,539,603 11/1970 Clough 260/404 X OTHER PUBLICATIONS Motoyasu et al., C.A., Vol. 72 (1970), l0l427m.
[451 Oct. 28, 1975 Schwartz et al., Surface Active Agents, pub. by Interscience Pub., Inc., N.Y., NY. (1949) Vol. 1, p. 205.
Primary Examiner-Patrick P. Garvin [57] ABSTRACT As non-ionic surface active agents are generally low in toxicity they are commonly used as additives in pharmaceuticals, cosmetics, foodstuffs, etc. However, nonionic surface active agents which exhibit antimicrobial action or rust-inhibiting property have not hitherto been known. The present invention uses hydroxy-fatty acid amide polyoxyalkylene ether, as the active ingredients. As this substance is superior in antimicrobial action and rust-inhibiting property, the surface active agents manufactured according to the present invention exhibit not only the superior properties inherent in the conventional surface active agents, e.g., emulsifying and dispersing power, but also superior rustinhibiting property and antimicrobial action. Further, if metal soap is added to the surface active agents, the aforementioned properties become more conspicuous.
1 Claim, No Drawings SURFACE ACTIVE AGENTS amide polyoxyalkylene ethers. More particularly, this invention relates to non-ionic surface active agents comprising, as active ingredients, hydroxy-fatty acid amide polyoxyalkylene ethers which exhibit excellent dispersing, rust-inhibiting, antimicrobial and emulsifying properties, and to surface active compositions comprising said ethers and metal soaps which exhibit further improved dispersing, rust-inhibiting, antimicrobial, emulsifying and other general properties.
Heretofore, surface active agents having rust-inhibiting and antimicrobial properties have been known and the examples of such agents are amine-type cation surface active agents and some of the amphoteric surface active agents. However, many of these known agents are strongly toxic and, in addition, the activity of these agents in solution is readily affected by the pH value of the solution. Further, these known agents tend, at low temperatures, to decrease in their ability to solubilize other materials to be dissolved and to decrease their own solubility in a medium and thus these agents have the limited utilities.
The non-ionic surface active agents now available are generally less toxic and, therefore, are often acceptable as additives to pharmaceuticals, cosmetics as well as foodstuffs. However, the non-ionic surface active agents are not useful for the bacteriocidal or germicidal purposes since they generally exhibit no such antimicrobial properties and are on the contrary known to have a growth promoting property with respect to the microorganisms. Further, there are many non-ionic surface active agents which are corrosive in nature, but the agents having rust-inhibiting properties are almost unknown. Accordingly, surface active agents which are both suitable for application to the apparatus, instruments, packages, etc. employed particularly in industries requiring a high degree of sanitation such as the foodstuff, cosmetic and pharmaceutical industries and which also have cleaning, preserving and rust-inhibiting properties were hitherto unknown.
The primary object of this invention is to provide amide-type non-ionic surface active agents which are highly effective as dispersing, rust-inhibiting, antimicrobial and emulsifying agents, as well as surface active compositions containing, as active ingredients, said amide-type non-ionic surface active agents.
The present inventors searched for surface active agents suitable for the above purposes and found that hydroxy-fatty acid amide polyoxyalkylene ethers, one of the amide-type non-ionic surface active agents, have excellent antimicrobial and rust-inhibiting properties, and further that these properties are effectively improved by combining said ethers with metal soaps.
The improved activities obtainable by the surface active agents of this invention are the outstanding features of the present invention in view of the fact that the conventional non-ionic surface active agents generally have no rust-inhibiting property and the fact that, when they are combined with the metal soaps, the rustinhibiting property inherent to metal soaps is generally 2 lowered by the corrosive action due to the presence of the non-ionic surface active agents.
The surface active agents of this invention are represented by the formula wherein R is a hydrocarbon radical having 7 to 21 carbon atoms; R is selected from the group consisting of hydrogen and a lower alkyl group; y is an integer between 1 and 50; and z is an integer not less than 1.
The surface active composition of this invention comprises the above hydroxyfatty acid amide polyoxyalkylene ethers and the metal soaps which have as their main component a substance represented by the formula (RCOO),M
wherein R represents a hydrocarbon radical having 2 to 21 carbon atoms; x is an integer between 1 and 5 equivalent to the atomic valence of the metal M; and M represents a metal, the amount of the metal soaps used being in the range of from equivalent weight to l/ 1000 by weight, preferably from equivalent weight to 1/100 on the basis of said ethers.
The novel hydroxy-fatty acid amide polyalkylene ethers of the present invention can be prepared, for example, by reacting a monoor polyhydroxy-fatty acid ester such as castor oil, hydrogenated castor oil, methyl ricinolate, l2-hydroxy-stearic acid ester, tetrahydroxy stearic acid ester and the like with an alkylene oxide such as ethylene oxide and propylene oxide to obtain a hydroxy-fatty acid ester polyoxyalkylene ether followed by ammonolysis with liquid ammonia, or by subjecting the above hydroxy-fatty acid ester to ammonolysis to obtain the corresponding acid amide which is then reacted with an alkylene oxide. Examples of the hydroxy-fatty acid amide polyoxyalkylene ethers include castor oil fatty acid amide polyoxyethylene ether, ricinoleic acid amide polyoxypropylene ether, hydrogenated castor oil fatty acid amide polyoxyethylene ether, etc. In contrast to the conventional substituted amidetype non-ionic surface active agents, the surface active agents of this invention contain free amide radicals having high hydrogen-bonding strength and hydrophilic radicals in the side chains and, therefore they are excellent in emulsifying, dispersing, wetting and antistatic properties. They also exhibit a potent antimicrobial property and a rust-inhibiting properties on a wide variety of metals and alloys such as iron, aluminum, copper, zinc, nickel, lead, tin, brass, bronze, solder, phosphorus bronze and the like because of their good affinity to the surface of the metals.
Non-ionic surface active agents are, as previously mentioned, generally less toxic, but some of the agents such as alkylphenyl derivatives show a low LD value. For example, polyoxyethylene-(9,7 )-p-tert-octylphenyl ether is said to have a [D value of 1.7 ml/kg (acute toxicity in rat, Handbook p267 (1968) issued by Nikko Chemicals Co., Ltd.). The surface active agents of this invention were found to have low toxicity as evidenced by the LD value of 20 ml/kg (acute toxicity in mice) shown by castor oil fatty acid amide polyoxyethylene ether (6 mole addition product). Also, in the mixture of said ether and a metal soap, for example, a mixture of the above ether and a magnesium salt of castor oil fatty acid (:1 molar ratio), the LD value has been found to be 22 ml/kg, indicating that the toxicity is practically negligible.
The surface active agents of this invention give rise to almost no skin irritability or oversensi tivity. Mixtures formed by separately combining the 7 and 21 mole product of the above ether with a magnesium salt of castor oil fatty acid (5:1 molar ratio) were diluted to form a 30% water solution and applied to rabbits once daily over a period of ten days. At the end of the test period absolutely no abnormalty could be found either by the naked eye or by microscopic inspection of the tissue in either case. A further test was conducted wherein the same solutions were applied to marmots twice daily over a 3 day period. Neither an examination of either animals reactions nor a microscopic examination of its tissue showed any abnormalty.
The metal soaps used in the composition of this invention are well known metal salts of hydroxy-fatty acids of saturated or unsaturated and straight or branched chain containing 2 to 21 carbon atoms or of naphthenic acid or resin acid. The metal useful as the metal salts includes those of I to V valences in the Periodic Table, i.e., Group la (Li, Na, K, etc.), Group Ila (Mg, Ca, Ba, etc.), Group Illa (B, Al, etc.), Group IVb (Si, Sn, Pb, etc.), Group Vb (As, Sb, Bi), Group lb (Cu, Ag, etc.), Group Ilb (Zn, Cd, Hg), Group lVa (Ti, Zr, etc.), Group Va (V, etc.), Group Vla (Cr, Mo, W, etc.), Group VIla (Mn, etc.), Group VIII (Fe, Co, Ni, etc.), and the like.
As previously described, the surface active composition of this invention can be obtained by blending the amide-type non-ionic surface active agent and the metal soap in a proportion of 1:1 to 1:1/l000 by weight. This can be accomplished either by adding the metal soap to an aqueous solution of the amide-type non-ionic surface active agent or by merely blending together the two components. Since the amide-type non-ionic surface active agents of this invention are highly soluble in water and, in addition, have an excellent ability to dissolve a wide variety of metal soaps, it is possible to obtain a composition containing high concentrations of both the surface active agent and the metal soap. Further, for various applications, the properties of the surface active agent and the composition according to the present invention can be controlled by changing the addition molar numbers of alkylene oxide in the amide-type surface active agent or by changing a proportion of the amide-type surface active agent and the metal soap.
The various properties of the hydroxy-fatty acid amide polyoxyethylene ether of the present invention are as follows: its solubility in petroleum solvents and ethyl ether is a little low, but it is easily soluble in most of the other solvents; the agents in which more than about 7 moles of ethylene oxide are added give a clear aqueous solution; the optimum chain length of polyoxyethylene group (POE) for the emulsifying, solubilizing, and antistatic properties varies depending upon the type of substances for which such properties are utilized; the agents having relatively short chains are superior in lowering of surface tension, in wetting, rustinhibiting and antimicrobial properties and in wettability; and the agents having relatively long chains are su- 4 perior in the dispersing, cleaning and foaming properties. Hydroxy-fatty acid amide polyoxypropylene ether has lower water-solubility than that of POE ether and has, in some instances, a solubilizing activity inferior to POE ether.
The metal soap as one of the additives of the surface active composition of this invention shows the following tendency. In the metal soap comprising a different metal and a given fatty acid, the order of higher solubility of the soap is K, Na Li, Mg Ba, Mn, Co Zn, Cd Pb, Fe, and, in the metal soap comprising a different fatty acid and a given metal, the shorter the chain length, the higher the unsaturation and the more branched chains, the higher the solubility. Also, hydroxylic acids are particularly soluble at a low temperature. The activity of the metal soap is generally superior when the metal is an alkali earth metal, manganese or cobalt, but the metal soaps comprising other metals have also specific characteristics. A potassium and sodium soap and a lithium salt of a hydroxylic acid exhibit an increased solubility in water, and a mixture of one of the above soaps and a hydroxy-fatty acid amide polyalkylene ether (y 0-3) having a short POE chain or a hydroxy-fatty acid amide polyoxypropylene ether give a clear aqueous solution, and is often superior in cleaning and dispersing properties. Further, superior antimicrobial properties are exhibited by silver, lead and bismuth soaps, superior dispersing properties by zinc, zirconium and vanadium soaps, superiro emulsifying properties by chrome soap and superior rust-inhibiting and other properties by aluminum soap.
The surface active agent of this invention is further characterized by the fact that its activity is not adversely affected by the changes of pH value. Soaps are generally decomposed and precipitated at acidic pH values thereby losing their surface activity, and other ionic surface active agents are also precipitated more or less in an acidic or alkaline solution, resulting in decrease or loss of their surface activity. In contrast, the surface active composition of this invention shows less decomposition and precipitation over a wide range of pH values because the composition is a solubilized system of the metal soap with the hydroxy-fatty acid amide polyoxyalkylene ether, and, accordingly, the activity of the composition is not significantly lowered in either at acidic or alkaline pH values and is, rather, improved in some instances. In aqueous solutions of nonionic surface active agents, the shorter the polyoxyethylene chain the lower the cloud point, and their activity sharply decreases at a temperature above the cloud point. However, in the surface active composition of this invention, the increase in the cloud point due to the dissociation of the soap is observed in any cases when, of course, the soap is an alkali soap and even when the soap is a water-insoluble metal soap. For example, when a castor oil fatty acid amide polyoxyethylene ether (6 mole addition product; cloud point, 470C) is combined with magnesium ricinolate at a molar ratio of 5:1, the cloud point rises more than 10C. This means that the temperature range within which the composition is effective can be broaden, and this is very advantageous in practical use.
The hydroxy-fatty acid amide polyoxyalkylene ethers of this invention can be combined with other substances than the metal soaps as illustrated above. When the surface active agents of this invention are incorporated into various surface active agents, the emulsifying, dispersing, cleaning, solubilizing, rust-inhibiting,
solubility and foaming properties of the resulting blend are strengthened synergistically depending upon the length of the polyoxyalkylene chain in the former agents. When the chain length is relatively short, foam stability, sustained cleaning and wetting properties are significantly improved. The hydroxy-fatty acid amide polyoxyalkylene ethers of this invention exhibit an excellent solubilizing property. Also, those containing a relatively short chain exhibit a potent antimicrobial property. Such properties are useful when, for example, the product is used for dissolving iodine in water thereby preparing an aqueous iodine solution which has excellent antimicrobial property and low toxicity.
The activities of the surface active agent and composition can often be increased by adding thereto various builders. For example, wetting, rust-inhibiting, emulsifying, cleaning and other properties, in particular at acidic pH values, of the 5:1 mole mixture of hydroxyfatty acid amide polyoxyethylene ether and a magnesium salt of castor oil fatty acid can be increased by incorporating sodium tripolyphosphate in an amount ranging from equimolar to one-fifth mole on the basis of said ether. Other suitable builders include a wide variety of phosphates, sulphates, nitrite, carbonates, borates silicates and ethanolamines and CMC, urea, EDTA, sodium nitrilotriacetate, sodium toluene sulfonate and the like which are known to those skilled in the art.
The hydroxy-fatty acid amide polyoxyalkylene ethers of this invention are easily dispersible or soluble in various organic solvents, and a dispersion or solution in such solvent as benzene, toluene, carbon tetrachloride, trichloroethane, trichloroethylene, iso-propyl alcohol, kerosene, etc. is highly effective in enhancing the cleaning, dispersing, emulsifying, solubilizing, wetting, rust-inhibiting and antistatic properties. The mixture of the ether and the metal soap is also soluble in a wide variety of organic solvents, and a solution of the mixture in benzene, toluene, carbon tetrachloride, cottonseed oil, trichloroethane, trichloroethylene, iso-propanol, kerosene or the like often shows excellent cleaning, dispersing, emulsifying, solubilizing, wetting, rust-inhibiting, antimicrobial and antistatic properties.
As set forth above, the surface active agents of this invention are non-ionic surface active agents being by nature of relatively low toxicity, but exhibiting an antimicrobial property on some species of the microorganism comparable to that of the cationic surface active agents. Also, the surface active agents of this invention are characterized in that they are useful rust-inhibiting agents with respect to aluminum, iron, copper, etc. Further, the surface active properties of the agents can be improved by incorporating metal soaps and/or other additives.
The following examples illustrate the surface active agents of this invention comprising hydroxy-fatty acid amide polyoxyethylene ether, and the surface active composition comprising said ethers and the metal soaps, but these examples are given for illustrative purpose only and are not to be construed as limiting the scope of this invention.
EXAMPLE 1 The various properties of the known surface active agents were compared with those of the castor oil fatty acid amide polyoxyethylene ethers (8 and 25 mole addition products) at a temperature of 30C and a concentration of 0.02 mol/l. The results obtained as shown in Table 1. The numerical values in Table 1 were determined according to methods reported by one of the inventors [H. Suzuki, Yukagaku, 15, 475 (1966); ibid, 16, 667 (1967); ibid, 18, 136 (1969); H. Suzuki Kogyokagaku Zasshi, 72, 2253 (1969); ibid, Yukagaku, 19, 125 (1970)]. That is to say, surface tension was determined by the ring method, wetting power for felt and cotton by the disk method, foaming power by the semi-micro improved T-K method and in each of these cases the temperature was 30C. The results obtained in respect of emulsifying property is that obtained after 2 hours after shaking at C. Dispersing power was determined from the cloudiness after the solution had stood 4 hours after shaking and the antimicrobial action is expressed as the minimum inhibitory concentration obtained by the plate culture method after 3 days at 30C. The rust-inhibiting property is expressed in terms of change in weight of the metal plate after soaking 10 days at 30C. The other results are represented in terms of A to E in the order better to poorer results.
Table 1 Surface Products of Active This invention Anionic Cationic Non-ionic Agent *1 *2 *3 *4 *5 *6 *7 Property COAd-8 COAd-25 ABS DPC T-20 NP- 1 5 StAdl 5 Remarks *8 Rust-Inhibiting Soft Iron 5.2 17.0 22.7 85.0 19.1 77.0 81.5 "'1 l (mg/dm 10 days) Aluminum B C E E D D D Brass C C E E C D C *9 Penicillium 1000 500 5 2000 2000 1000 *1 1 Antimicrobial Citrinum (moI/l X 10") Bacillus C D D A E E E *12 Subitilis Manganese 41.0 46.2 37.2 2.6 2.2 3.3 26.5 Dispersing Dioxide Carbon Black C A B E A C D Wetting Felt 13.1 253 16.3 16.4 260 320 180 *1 1 (sec) Cotton 75.1 500 7.5 500 500 500 500 *11 (ml) Foam Volume 240 262 113 242 151 Foaming 10 Stability 25 19 5 92 46 75 21 Emulsifying Kerosene 75 89 90 0 84 90 85 *12 Surface Tension 35.5 41.4 36.1 45.2 37.7 42.0 40.7 11
( dyne/cm) Table l-continued Surface Products of Active This Invention Anionic Cationic Non-ionic Agent *1 *2 *3 *4 *5 *6 *7 Property COAd-8 COAd-25 ABS DPC T- NP- 1 5 StAdl 5 Remarks Antistatic Nylon-Fabric B B D D E E C 1 Castor oil fatty acid amide polyoxyethylene ether (8 mole addition product). '2 Castor oil fatty acid amide polyoxyethylene ether mole addition product). *3 Sodium alkylbenzene sulfonate.
4 Dodecylpyridinium chloride.
5 Tween 20.
6 Polyoxyethylcne nonylphenyl ether 15 mole addition product).
7 Stcaric acid amide polyoxyethylene addition product 15 mole addition product).
'8 Determined as difference in weight. *9 Minimum Inhibitory Concentration.
10 Foam breaking ratio (determined after one minute); the smaller the more stable.
I l the smaller the better. '12 the larger the better.
EXAMPLE 2 The comparative test for various surface active properties was conducted at a temperature of C using each of the compositions consisting of a typical surface active agent and a magnesium salt of castor oil fatty acid in a molar ratio of 0.02 0.004 per liter. The results obtained are as shown in Table 2. The compositions used in the above test were prepared in the following manner: 1.30 g castor oil fatty acid amide polyadded to a portion of the solution (1), and the mixture was heated with shaking to dissolve the salt. After cooling, the total volume of the solution was made up to 100 ml with water to produce an aqueous solution (2) of the surface active composition of this invention [the molar ratio of 5 l, 0.05 0.01 (m0l/l)]. The various surface activities of the resulting aqueous solution (1) and (2) at a temperature of 15C were determined and compared with each other. The results obtained are as shown in Table 3.
oxyethylene ether (8 mole addition product) was dis- Table 3 solved in ml of water and 0.248 g of a magnesium salt of castor oil fatty acid was added to the solution 30 Pro "y and the mixture was heated with shaking to dissolve the pe salt. After cooling, the volume of the resulting solution 2 was made up to 100 ml with water [the molar ratio of Rusplnhibiting Brass C B 5 l, 0.02 0.004 (mol/l)]. Penicillwm Table 2 Surface Products of Non-ionic Cationic Anionic Active This Invention Surfactant Surfactant Surfactant Property Agent COAd-8 NP- 1 5 DPC ABS Rust-Inhibiting Soft Iron 0 3.0 27.0 -8.2 (mg/dml 10 days) Aluminum A B B B Brass B C C C Antimicrobial Penicillium 100 2000 l 2000 Citrinum (mol/lX 10) Bacillus C E A D Subitilis Dispersing Manganese 57.5 41.5 40. 3 50. 3
Dioxide Carbon Black B A C B Wetting Felt 1.3 15 .2 2.2 2.7 (sec) Cotton 6.1 2.9 13.5 2.4 (ml) Foam Volume 220 255 194 152 Foaming Stability 30 64 12 23 Emulsifying Kerosene 9 1 92 61 95 Surface Tension 33.4 35.1 32.0 30.3 (dyne/cm) Antistatic Nylon-Fabric A B B B As is clear from the results shown in Table 2, the composition of this invention exhibits the best activity C i C A in the rust-inhibiting of the metal and the best antimi- 3311;: E C crobial action second to the cation surface active agent Manganese which is toxic in nature, as well as the best antistatic gj Black 3- 2 property, the best dispersing power for manganese di- Wetting Felt 3.5 2,0 oxide and the best wetting power into the felt. (sec) Cotton 3.0 1.3
Foam Volume 13 A Foaming Stability B A EXAMPLE 3 Emulsifying Kerosene B A 3.91 g of castor oil fatty acid amide polyoxyethylene ggi g ff ether (11 mole addition product) was dissolved in Antistatic Nylon-Fabric B A water to produce 40 ml of an aqueous solution (1). 0.732 g of a barium salt of castor oil fatty acid was Table 4 Surfactant/Metal Soap Amide Type Surfactant Metal Soap (mol/l) Type Amount (g) Type Amount (g) Molar Ratio Concentration COAd- 0.589 Na 0.037 3/1 0.005/0.00l67 Laurate Ni Castor COAd-l3 4.350 Oil Fatty 0.033 100/1 0.05/0.0005 Acid Mg Castor COAd6 0.056 Oil Fatty 0.012 5/1 0.001/0.0002
Acid COAd-9 0.347 Ca Oleate 0.030 10/1 ODDS/0.0005 COAd17 1.046 Mn 0.045 10/1 0.0l/0.001
Laurate KCastor COAd4 0.237 Oil Fatty 0.135 l/0.8 0.005/0.004
Acid COAd-l4 0.914 Co 0.076 6/1 0.01/0.00l67 Laurate Table 5 *2 Sol. Mix. Sol. Mix. Sol. Mix. Sol Mix. Sol. Mix. Sol. Mix. Sol. Mix.
EXAMPLES 4 TO 10 Example *1 The value indicates the molar number of ethylene oxide.
Example Temperature of Solution (C) Solution Property AABB BBCD
AABA
BCCA
AABA
CCCC
ABBA
BBCB
AA A
CBCA
BABA
CBCB
ABBC
C C C D Rust-lnhibiting Bacillus Subitilis Manganese Dioxide Antimicrobial ACA BCB
BBB
CCD
ABA
BBC
BCB
CCC
ACC
CCD
AAC
BBD
BBD
B C E Carbon Black Felt Dispersing Cotton Foam Volume Stability Wetting What is claimed is: l. A surface active agent of the formula IIRCONHZ ?(cHcH20),,H RI wherein R is an alphatic hydrocarbon radical having 17 carbon atoms, and the polyoxyalkylene chain is attached at the No. 12 carbon atom of said RCONHz R is selected from the group consisting of hydrogen and a1 and a lower alkyl group, and y is an integer of from 1 to 50.
Kerosene Nylon-Fabric Foaming Emulsifying Surface Tension (dyne/cm) (dyne/cm) Antistatic 1 Solution of castor oil fatty acid amide polyoxyethylenen other.
*2 Solution of said ether plus barium salt of castor oil fatty acid.
In the same manner as set forth in Example 2, aque- )us solutions comprising 1) various addition products )f a castor oil fatty acid amide-type non-ionic surface ictive agent and ethylene oxide in different molar raios and (2) various metal soaps in different amounts 5 vere prepared, and surface activities were determined 1nd compared with those of the aqueous solutions conaining only the corresponding addition products. The 'esults obtained are as shown in Table 5. Further, Table 1 shows the composition of the example aqueous soluions shown in Table 5. The volume of each aqueous olution in Table 4 is ml.

Claims (1)

1. A SURFACE ACTIVE AGENT OF THE FORMULA
US422146A 1971-03-01 1973-12-05 Surface active agents Expired - Lifetime US3916003A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US422146A US3916003A (en) 1971-03-01 1973-12-05 Surface active agents

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11984571A 1971-03-01 1971-03-01
US422146A US3916003A (en) 1971-03-01 1973-12-05 Surface active agents

Publications (1)

Publication Number Publication Date
US3916003A true US3916003A (en) 1975-10-28

Family

ID=26817768

Family Applications (1)

Application Number Title Priority Date Filing Date
US422146A Expired - Lifetime US3916003A (en) 1971-03-01 1973-12-05 Surface active agents

Country Status (1)

Country Link
US (1) US3916003A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4307079A (en) * 1975-10-23 1981-12-22 L'oreal Condensation product of glycidol on fatty chain-containing diglycolamides and cosmetic compositions containing the same
US4650360A (en) * 1984-09-27 1987-03-17 Dennison Manufacturing Company Antistatic marking
EP0631722A1 (en) * 1993-06-28 1995-01-04 Iwao Hishida Method for exterminating microbes for disinfection and deodorization
US5489393A (en) * 1993-09-09 1996-02-06 The Procter & Gamble Company High sudsing detergent with n-alkoxy polyhydroxy fatty acid amide and secondary carboxylate surfactants
US5500150A (en) * 1993-09-09 1996-03-19 The Procter & Gamble Company Solidified detergent additive with n-alkoxy polyhydroxy fatty acid amide and alkoxylated surfactant
US5510049A (en) * 1993-09-09 1996-04-23 The Procter & Gamble Company Bar composition with N-alkoxy or N-aryloxy polyhydroxy fatty acid amide surfactant
US7847123B2 (en) 2006-11-14 2010-12-07 Evonik Goldschmidt Gmbh Antimicrobial compositions
US20130338420A1 (en) * 2012-06-19 2013-12-19 The Procter & Gamble Company Surfactant Composition and Method for Decontamination

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2520381A (en) * 1946-06-18 1950-08-29 American Cyanamid Co Condensation of ethylene oxide with carboxylic acid amides
US2677700A (en) * 1951-05-31 1954-05-04 Wyandotte Chemicals Corp Polyoxyalkylene surface active agents
US3264281A (en) * 1963-04-23 1966-08-02 Thomas H Applewhite Preparation of amides
US3417114A (en) * 1965-07-20 1968-12-17 C P Hall Company Of Illinois Method of making amides from moisture and acid-gas containing esters
US3539603A (en) * 1965-03-18 1970-11-10 Atlantic Richfield Co Addition polymerization process

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2520381A (en) * 1946-06-18 1950-08-29 American Cyanamid Co Condensation of ethylene oxide with carboxylic acid amides
US2677700A (en) * 1951-05-31 1954-05-04 Wyandotte Chemicals Corp Polyoxyalkylene surface active agents
US3264281A (en) * 1963-04-23 1966-08-02 Thomas H Applewhite Preparation of amides
US3539603A (en) * 1965-03-18 1970-11-10 Atlantic Richfield Co Addition polymerization process
US3417114A (en) * 1965-07-20 1968-12-17 C P Hall Company Of Illinois Method of making amides from moisture and acid-gas containing esters

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4307079A (en) * 1975-10-23 1981-12-22 L'oreal Condensation product of glycidol on fatty chain-containing diglycolamides and cosmetic compositions containing the same
US4650360A (en) * 1984-09-27 1987-03-17 Dennison Manufacturing Company Antistatic marking
EP0631722A1 (en) * 1993-06-28 1995-01-04 Iwao Hishida Method for exterminating microbes for disinfection and deodorization
US5489393A (en) * 1993-09-09 1996-02-06 The Procter & Gamble Company High sudsing detergent with n-alkoxy polyhydroxy fatty acid amide and secondary carboxylate surfactants
US5500150A (en) * 1993-09-09 1996-03-19 The Procter & Gamble Company Solidified detergent additive with n-alkoxy polyhydroxy fatty acid amide and alkoxylated surfactant
US5510049A (en) * 1993-09-09 1996-04-23 The Procter & Gamble Company Bar composition with N-alkoxy or N-aryloxy polyhydroxy fatty acid amide surfactant
US7847123B2 (en) 2006-11-14 2010-12-07 Evonik Goldschmidt Gmbh Antimicrobial compositions
US20130338420A1 (en) * 2012-06-19 2013-12-19 The Procter & Gamble Company Surfactant Composition and Method for Decontamination
US9295865B2 (en) * 2012-06-19 2016-03-29 TOA Research, Inc. Surfactant composition and method for decontamination

Similar Documents

Publication Publication Date Title
AU721966B2 (en) Germicidal dishwashing detergent compositions
US3539520A (en) Compositions comprising quaternary ammonium germicides and nonionic surfactants
US4207421A (en) Biodegradable, alkali stable, non-ionic surfactants
US3281365A (en) Antiseptic detergent compositions
US3850854A (en) Novel detergent composition
US3916003A (en) Surface active agents
DE69632359T2 (en) Machine dishwashing detergent compositions containing bleach activators which form polybasic percarboxylic acids
US3574100A (en) Water-soluble lubricating agents for continuously moving conveyor systems
WO1997045508A1 (en) Alkyl ether amine conveyor lubricant
DE3008983C2 (en)
US3382285A (en) Liquid nonionic polyoxyalkylene surface-active materials
US3438905A (en) Iodine-containing nonionic surfactant compositions
US3812046A (en) Germicidal liquid cleaner
US3445398A (en) Synergistic antibacterial compositions
WO1996039839A1 (en) Iodine complex of alkyl polyglycosides
US3717579A (en) Biocidal preparation
JPH0819082B2 (en) Surfactants derived from sulfosuccinates
US3781218A (en) Hydroxy-fatty acid amide polyoxy-alkylene ether:soap compositions
US3364142A (en) Composition for reconstituting frozen aqueous systems and method for making
KR20010015752A (en) Acid cleaning compositions containing alkoxylated amines and their use
US4759931A (en) Novel liquid iodophors
GB1562961A (en) Germicidal compositions
US2831814A (en) Acid pickling of metals and compositions therefor
GB1561274A (en) Compositions containing beta subsituted acrylic acid amides as preservatives
GB2031941A (en) Concentrated aqueous surfactant compositions