US2979528A - Nitrogen-containing polyoxyalkylene detergent compositions - Google Patents

Nitrogen-containing polyoxyalkylene detergent compositions Download PDF

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US2979528A
US2979528A US70573057A US2979528A US 2979528 A US2979528 A US 2979528A US 70573057 A US70573057 A US 70573057A US 2979528 A US2979528 A US 2979528A
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reactive hydrogen
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oxypropylene
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Lester G Lundsted
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Wyandotte Chemicals Corp
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D19/00Degasification of liquids
    • B01D19/02Foam dispersion or prevention
    • B01D19/04Foam dispersion or prevention by addition of chemical substances
    • B01D19/0404Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance
    • B01D19/0413Foam dispersion or prevention by addition of chemical substances characterised by the nature of the chemical substance compounds containing N-atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL AND VEGETABLE OILS, FATS, FATTY SUBSTANCES AND WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/42Amino alcohols or amino ethers
    • C11D1/44Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines
    • 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
    • Y10S516/07Organic amine, amide, or n-base containing

Description

United States Patent NITROGEN-CONTAINING POLYOXYALKYLENE 1 DETERGENT COMPOSITIONS Lester G. Lnndsted, Grosse lle, Mich., assignor to Wyantlotte Chemicals Corporation, Wyandotte, Mich., a corporation of Michigan I No Drawing. Filed Dec. 30, 1957, Ser. No. 705,730

Claims. c1. 260-584) ice known alkylarylsulfonates. Thus, it is desirable that compositions be found which have the highest detergency effectiveness and, particularly, it is desirable that compositions be found which are superior to other synthetic detergents with respect to detergency effectiveness.

In industrial laundering practice, two general temperature ranges are employed depending on the type of fabric and dyes involved. For white cottons and fast-colored cotton, the temperature of the detergent solution is usually'about 140-160 F. On the other hand, for woolens, delicate synthetic fabrics and fabrics containing dyes which tend to run at 140-160 F., the laundering process is usually carried out at about 90-95 F. It is under the tion Serial No. 316,984 was a continuation-in-part of my application Serial No. 153,946, filed April 4, 1950, now abandoned.

A basically new approach for the chemical structure of a polyoxyalkylene nonionic surface active agent is dis- 1 closed in U.S. 2,674,619. Prior to the disclosure of U.S. 2,674,619, polyoxyalkylene nonionic surface active agents were known which were composed of a long hydrocarbon chain or alkyl-substituted ring compound, e.g., nonylphenol, and a water-solubilizing polyoxyethylene chain.

The compositions disclosed in U.S. 2,674,619 depart from of ethylene oxide condensed with the polyoxypropylene chain. The compositions of US. 2,674,619 are initially prepared by condensing the required amount of propylene oxide with a lower molecular weight reactive hydrogen compound, followed by condensation with ethylene oxide so as to produce water solubility and introduce surface active properties. The disclosure of U.S. 2,674,619 teaches thatany of a broad group of reactive hydrogen compounds can be used which have at least two reactive hydrogen atoms and are relatively low molecular weight materials which arenot hydrophobic in and of themselves. It is indicated that, ordinarily, the reactive hydrogen compound constitutes such a relatively small proportion of the block polymer surfactant composition that the reactive hydrogen compound has little or no material effect on the properties of the final detergent composition.

Although such nonionic surface active agents have important "and unique chemical and physical properties,

many uses of these compounds are based on their effective- 1 ness as detergents and in many cases the polyoxyalkylene nonionic surface active agents are in direct competition with Other different synthetic detergents, such as the welllatter condition that the compositions of this invention,

as aspecifal class, are unusually superior to those generally disclosed'in U.S. 2,674,619.

An object of this invention is, therefore, to provide polyoxyalkylene nonionic surface active agents which have improved effectiveness as detergents.

which is, therefore, a specific improvement over the general' class of such detergents disclosed in U.S. 2,674,619.

I'have found that the foregoing objectives and others to be indicated herein are attained by polyoxyalkylene nonionic surface active agents of the general class disclosed in U.S. 2,674,619 but where the reactive hydrogen compound employed is one of a specific class of reactive hydrogen compounds, i.e., nitrogen-containing reactive hydrogen compounds. The polyoxyalkylene nonionic detergent compositions of this invention constitute a superior classof detergents in several respects when compared to the polyoxyalkylene nonionic detergent compositions of U.S. 2,674,619 as exemplified by those prepared with propylene glycol as the reactive hydrogen compound. Specifically, nitrogen-containing polyoxyalkylene nonionic detergent compositions of this invention can be prepared which produce higher detergency effectiveness than that of other propylene glycol-based compositions disclosed in U.S. 2,674,619 regardless of the proportions of propylene oxide and ethylene oxide employed in preparing the latter. The nitrogen-containing compositions of this invention have unusually superior detergency effectiveness in relatively cold water, i.e., at F. Thus, nitrogen-containing polyoxyalkylene compositions of this invention can be and have been prepared which are better detergents "at 90 F. than can be prepared using propylene'glycol or other reactive hydrogen compounds disclosed in U.S. 2,674,619 regardless of the proportions of propylene oxide and ethylene oxide used inthe latter. Furthermore, the compositions of this invention are at least as efiective at F., and usually more effective, detergents than are such compositions of U.S. 2,674,619.

Thus, the compositions of this invention constitute a specific class of compositions within the scope of the disclosure of U.S. 2,674,619 but possessing unusually superior detergency properties when compared to other compositions of the broad class disclosed in the patent.

The compositions of this invention possess a still further unique and characterizing feature when compared to the glycol-based surfactants disclosed in U.S. 2,674,619

of this invention and which greatly reduce undesirable lime soap formation by maintaining the lime soap curds in a dispersed condition.

It will be recognized from the foregoing that the significant and characterizing feature of the compositions of this invention is the class of reactive hydrogen compounds that is employed. The reactive hydrogen compound must contain at least one nitrogen atom and contain at least two reactive hydrogen atoms and not more than about six reactive hydrogen atoms. Usually, at least one of the reactive hydrogen atoms is attached to a nitrogen atom. An exception is in the case where the reactive hydrogen compound is derived from a reactive hydrogen compound in which one or more reactive hydrogen atoms were attached to a nitrogen atom. Triisopropanolamine, derived from ammonia and propylene oxide, is an example of the latter. The expression reactive hydrogen atom is well known to those skilled in the art of alkylene oxide chemistry. It may be stated, however, that the expression reactive hydrogen atom. is used in this application to mean that the compound contains a hydrogen atom which is sufiiciently labile to open the epoxide ring of 1,2-propylene oxide and will react with methyl magnesium iodide to liberate methane in the classical Zerewitinofii reaction (see Niederl and Niederl, Micromethods of Quantitative Organic Analysis, page 263, John Wiley & Sons, New York City, 1946).

An equally important characteristic of the class of nitrogen-cntaining reactive hydrogen compounds is that the compounds used must be relatively lower molecular weight compounds which are not essentially hydrophobic in and of themselves. By this is meant that the condensation product of the reactive hydrogen compound with ethylene oxide alone would not yield a detergent having a carbon soil removal value of 100 by the procedure for determining the carbon soil removal value set forth in U.S. 2,674,619, column-6, lines 11-75 and column 7, lines 1-49. Thus, the nitrogen-containing reactive hydrogen compound used is one which is not sufliciently hydrophobic so that it could serve as the hydrophobic element of a nonionic surfactant and the latter must be provided by the defined oxypropylene chains in the compositions. Generally, the nitrogen-containing reactive hydrogen compound has up to about six, in-- elusive, carbon atoms. When the nitrogen-containing reactive hydrogen compound is so defined, there still remains a reasonably broad group of such compounds which can be used. Ammonia, primary amines, alkylene polyamines, alkanolamines, heterocyclic nitrogen compounds are examples of the classes of nitrogen-containing reactive hydrogen compounds which can be used.

Thus, primary amines having not over six carbon atoms such as methylamine, ethylamine, propylamine, butylamine, amylamine, hexylamine and aniline are satisfactory. Alkylene polyamines, especially aliphatic primary diamines, having not over six carbon atoms are the preferred reactive hydrogen compounds since the highest detergency values have been obtained when these were used. These include ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, hexamethylenediamine, phenylenediamine and the like. Alkanolamines having not over six carbon atoms can be used such as monoethanolarnine, diethanolamine, triethanolamine, isopropanolamine, tri(2-propanol)a mine, Z-aminol-butanol, N-butyl-di(2-propanol)amine and the like. Furthermore, heterocyclic nitrogen compounds containing a hetero N atom can be employed, such as piperazine, Z-methylpiperazine, 2,5-dimethylpiperazine, imidazimidazole, pyrazolidine, pyrazolidone, hydantoin, dimethylhydantoin and the like. Hydroxyl amine and the hydroxylamine derivatives and aminophenol and aminophenol derivatives can also be used.

The compositions of this invention are surface active mixtures of conjugated polyoxypropylene-polyoxyethylene compounds based on the nitrogen-containing reactive 5 harness a p ,--.a

hydrogen compound wherein chains of oxypropylene groups having a defined molecular weight are attached to the nucleus of the reactive hydrogen compound at the sites of the reactive hydrogen atoms and wherein chains of oxyethylene groups are attached to the ends of the oxypropylene chains. The compositions are prepared by condensing propylene oxide with the nitrogen-containing reactive hydrogen compound and subsequentlycondensing ethylene oxide with the propylene oxide-reactive hydrogen compound condensate.

The collective molecular weight of the oxypropylene chains attached to the nitrogen-containing reactive hydrogen compound must be at least about 900 and can range up to about 25,000 or higher. Since the reactive hydrogen compound employed is one having not more than about six carbon atoms, it is not sufficiently hydrophobic in and of itself so that a detergent would be obtained by simply condensing ethylene oxide with the reactive hydrogen compound. Therefore, the hydrophobic element of the surface active compositions of the invention necessarily is found in the defined oxypropylene chains. This significant feature distinguishes the compositions from those known in the art prior to U.S. 2,674,619 wherein propylene oxide and ethylene oxide were treated as comparable materials and condensed with long carbon chain reactive hydrogen compounds in order to introduce water solubility. The compositions of this invention rely on the hydrophobic oxypropylene chain just as do the compositions of U.S. 2,674,619, but distinguish over the general broad class of compositions disclosed in U.S. 2,674,619 by virtue of the specific class of reactive hydrogen compounds here employed. The advantages for the compositions of this invention set forth hereinabove are obtained when the compositions have oxypropylene chains having a molecular weight of at least about 900 and up to 25,000. The best detergent compositions are obtained, however, when the molecular weight of the oxypropylene chains is in the range of about 1000 to 15,000. The molecular weight stated and that reported in the examples to follow is for the molecular weight of the oxypropylene chains themselves and does not include the molecular weight of the particular reactive hydrogen compound employed.

It is to be noted that it is not necessary to use pure propylene oxide in producing the oxypropylene chains of the detergent compositions, although this is preferred. Small amounts, for example up to about 5 weight percent, of ethylene oxide can be included in the propylene oxide employed to prepare the hydrophobic reactive hydrogen compound-propylene oxide condensate without significant alteration of the detergent properties of the final composition. In this connection, the ethylene oxide subsequently condensed with the hydrophobic propylene oxide-reactive hydrogen compound condensate can also contain small amounts, such as up to about 5 weight percent, of propylene oxide without significant alteration of the detergent properties of the compositions of the invention.

It is further to be noted that when molecular weight is stated in this specification and claims, unless otherwise noted, there is meant the average theoretical molecular weight which equals the total of the grams of the propylene oxide employed per mol of reactive hydrogen compound. It is well recognized in the field of alkylene oxide chemistry that the polyoxyalkylene compositions one obtains by condensing an alkylene oxide with a reactive hydrogen compound are actually mixtures of compounds rather than a single molecular compound. The mixture contains closely related homologues wherein the statistical average number of oxyalkylene groups equals the number of mols of the alkylene oxide employed and the individual members in the mixture contain varying numbers of oxyalkylene groups. Thus, the compositions of this invention are mixtures of compounds which are defined by molecular weight of the polyoxypropylene chains and weight percent of oxyethylene groups.

As has been noted above, the compositions of the invention contain chains of oxyethylene groups attached to the oxypropylene chains. formed by condensing ethylene oxide with the propylene oxide-reactive hydrogen compound condensate. The ;amount of ethylene oxide employed is such that the oxyethylene groups constituteabout 20 to 90weight percent of the final composition. Compositions having outstanding detergent properties are obtained when the weight percent of oxyethylene groups falls within this range. The very highest detergency values at 90 F." have been obtained in compositions of the invention having from about 25 to 55 weight percent of oxyethylene groups. The condensation of propylene oxide with the nitrogencontaining reactive hydrogen compound and the subse- .quent condensation of ethylene oxide therewith are carried out in the known manner for condensing alkylene oxides with reactive hydrogen compounds. The process is normally carried out at elevated temperatures and pressures in the presence of alkaline catalysts, such as sodium hydroxide, potassium hydroxide, sodium alkoxide, qua- Zternary ammonium bases, and thelike. The condensation reactions can also be carried out in the presence of acidcatalysts. The manipulative steps will vary to some extent depending'upon the normal'physical state of the reactive hydrogen compound. Certain of these compounds are normally gases, e.g., ammonia and methylamine, and propylene oxide can be condensed with these compounds by carrying out the reaction under sufficient pressure to liquefy the nitrogen-containing reactive hydrogen compound, or the normally gaseous nitrogencontaining reactive hydrogen compound can be dissolved in an inert solvent. Similarly, if the reactive hydrogen compound is a solid at reaction temperatures, ,it is normally dissolved in an inert solvent. After a few mols of propylene oxide havebeen condensed with the reactive Yhydrogen compound, the adduct becomes a liquid and the inert solvent can be removed by distillation. Thereafter, it is preferred to simply add the propylene oxide to ,the liquid reaction mixture without the use of a solvent. Although the reaction of propylene oxide with the reactive hydrogen compound can be carried out by simply heating a mixture of the reactants under pressure at a sufiiciently high temperature, this method is not ordifnarily used as the temperatures and pressure required are excessive and control of the reaction is difiicult. The preferred method is to add the propylene oxide to' a stirred and heated mixture of the desired nitrogen-containing reactive hydrogen compound and an alkaline catalyst'in' a sealed reaction vessel. By adding the propylene oxide "to the reaction vessel at such a rate that it reacts as rapidly, as added, an excess of propylene oxide is avoided and control of the reaction is simplified. The condensation of ethylene oxide with the propylene oxide-reactive hydrogen compound condensateis carried out in an analogousmanner.

" l EXAMPLES A series of compositions according to this invention was prepared using exemplary nitrogen-containing reacgive". hydrogen compounds and varying amounts of propylene oxide and ethylene oxide. The procedure by .which these compositions were made is that generallyset forthin U.S. 2,674,619. The initial reaction of the The oxyethylene chains are I.

nitrogen-containing reactive hydrogen compound with propylene oxide was carried out in two or three stages ,due to volume limitations imposedby the reactors employed. Due to the basic nature of the nitrogen-conitaining reactive hydrogen compounds, the first stage re- ,action. with propylene oxide was carried out in the presence of about 10 weight percent of water and sub- ;Seqirhtcondensations with propylene oxide and ethylene [oxide were carried out with added potassium or sodium "hydroxide as the catalyst. I

1. Ethylenediamine...;

Each composition was thus prepared by condensin g propylene oxide with the indicated reactive hydrogen compound and subsequently condensing ethylenev oxide with the previously formed reactive hydrogen compoundpropylene oxide condensate. a 1

These compositions are summarized below in Table I together with the results of detergency tests in terms of carbon soil removal values at F. The compositions are characterized by the molecular weight of the oxypropylene chains and weight percent or the oxyethylene chains. The molecular weight of the oxypropylene chains is the theoretical molecular weight based on the weight in grams of propylene oxide used per mol of reactiveihy- 'drogen compound and the weight percent of oxyethylene chains is based on the weight of the total composition.

The carbon soil removal values were obtained by the procedure set forth in U.S. 2,674,619, previouslycited, except that the test solutions were 0.10% oncentration instead of 0.25% concentration as set' forth in U.S. 2,674,619.

I Table I COMPOSITIONS OF INVENTION a Carbon Soil Weight Removal. Weight of Percent of Value, Oxypropyl- Oxyethyl- 0.1% Conene Chains ene Chains centration at 90. F.

. Molecular Ex. Reactive Hydrogen No. Compound The foregoing results show how very effective the compositions of this invention are as detergents at 90 F. Higher carbon soil removal values at 90 F. canbe obtained when a nitrogen-containing reactive hydrogen .compound is employed in accordance with this invention than can be obtained when other reactive hydrogen compounds of the classes disclosed in U.S. 2,674,619 are used. For example, when propylene glycol is employed as the reactive hydrogen compound, the highest carbon soil removal value at 90 F. that has been obtained is Ireported in U.S. 2,674,619, column 8, Table II, run No.

4, where a propylene g1ycol-polyoxypropylene-polyoxyjethylene condensate having a molecular weight, based on the hydroxyl number test, in the oxypropylene chains of 2320 and having 44 weight percent of oxyethylene chains 7 hainsins'uch compositions. 'ComparisoneXamples which bear-this outare set 'forth below. It should be .noted tha'tExample No. 37 having o'xypr'opylene chains with a "molecular weight ersrso has the highest oxypropylen'e chain molecular weight which has been made and tested.

Table II COMPOSITIONS F us. 2,674,619

Carbon Soil Molecular Weight Ex 1 'ReaetlveHydrogen Weightof Percent of '.Particular attention is called to Examples 1, 2, 5, 6, 9,

l0, 13, 14,18 and '19 in Table I wherein compositions employinga nitrogen-containing reactive hydrogen com- :pound which far exceed the best thatcan beobtained at this temperature when other reactive hydrogen compounds, such as propylene glycol, are used. Furthermore, it will be observed that thehighest carbon soil .removal values at F. were obtained when theweight percent ofoxyethylenechains was "in therange of'2'5 55. Compositions of thisinvention-having this proportion of oxyethylene chains are speciallypreferred, therefore.

Reactive hydrogen compounds 'of the general classes "disclosed in U.S. 2,674,619 otherthan those of this invention and other than propylene glycol haveshown similar carbon soil removal values at 90 F. Those which have been prepared and tested are set forth below in Table III.

. Table III fooMP'osrmoNs or-Us. 2,674,619

Carbon Soil 1 Molecular Weight Removal -Ex. Reactive Hydrogen Weight of Percent 01 Value, No. Compound Oxypropyl- Oxyethyl- 0.10% Conene Chains ene Chains 'centration at 90F.

Glycerl.ue.-.-.. 4, 000 46. 0 172 Trimeth ylolpropaneu -'5, 000 66.1 Pentserythritoln 9, 500' 33. 2, 33. 0 144 1,5-Pentanedl0l 6, 000

Table IV A Molecular Weight Ex.'No. Reactive'Hydrogen Weight Percent Compound Oxypropyl- 0xyethylone Chains eno Chains .42 Ethylenediamiue 1,860 '43. 1,860 44 1, 860i 3, 965 64 Triisopropanolaminc 1, 716 65- .1, 716. 66 do 1, 716 75. 67 n-Butylamine 2. 969 25. B8 .2. 069 50. 69- do 2, 969 75.

, 1 Based on hydroxyl number procedure, OGG ct 211, Industrial and Engineering Chemistry, Analytical Edition, vol. 17,1). 395 (1945).

In testing the compositions of the invention set forth in'Table IV asExamriles 42 69, dilute solutions (03%) of-afformulate'd medium titer alkali metal fatty acid'soap wierepreparedin 180 p.p.m. hard water (as CaCO and coritainingafZ/l mol ratio of Ca to'Mg'). The formulatedtsoap was a proprietary ,product comprising 60% medium titer .soap,.approximately 30% builders .(phosphates, silicates and sodaash) and 10% moisture. The soap ingredient was asodium soap, 38 C. titer, having anacid number of 227 and being derived from a mixture'of approximately-10 parts tallow and 1 part coconut oil. A smalLproportion (0.02%) of the lime soap 'clispersant Wasadded-tO the above prepared soap solutions. .T his quantity of lime soap dispersant constituted 10 Weight percent of' the actual soap present in the proprietary formulation. One .part of each of the soap .solutions containinga lime soap dispersant .was then diluted with nine parts of 180 ppm. hard water. The resulting solutions ,were maintained at 120 .F. for twenty minutes and werestirred with-a mechanical stirrer at 80..r.p.m. After this period of time, the. solutions wereexamined visually fortthe ipresencetof lime soapcurds.

.All of. the solutions containing the lime soapdispersant -were r essentially free of insoluble soap curds, -or at .most contained only a slight trace .of.flocculated material. Moreover,xthe:solutions :were opalescent, thus indicating thatzthe .lime .soap was highly dispersed throughout the solutionrasza colloid. .In contrast to these results, acontrol solution prepared as stated above but containing .no'lime soap dispersant contained copious quantities of lime soap curds.

'Similarlresults were obtained when theiproportion of .lime soap dispersant was varied from 4 to 25 Weight percent of..the soap present in the ,properietary formulation.

Thus, the compositions of'this invention have thesignificant property offdispersinglime soaps as Well as'outstanding. detergencyin relatively cold water,i'.e., at 90F.

I claim:

.1. A.surface active mixture of conjugatedpolyoxyalkylene compounds consisting of oxypropylenegroups, oxye'thylene ggroups and'thenucleus of a nitrogen-cont-aining .-reactive hydrogen compound having notmore than 6 carbon atoms ,per molecule and being selected from :the group consisting of ammonia, primary Zalkyl .75 amines, alkylene polyamines, alkanolamines, piperaiirie CRT and aminophenol, the structure of the compounds being such that all of the oxypropylene groups are present in oxypropylene chains that are attached to the reactive hydrogen compound at the sites of the reactive hydrogen atoms, and all of the oxyethylene groups are present in oxyethylene chains that are attached to the ends of the oxypropylene chains, the average molecular weight of the oxypropylene chains being at least about 900 and to about 25,000, and the oxyethylene groups being present in an amount so as to constitute from 20 to 90 weight percent of the mixture of compounds.

2. A surface active mixture of conjugated polyoxyalkylene compounds according to claim 1 wherein said reactive hydrogen compound is ammonia.

3. A surface active mixture of conjugated polyoxyalkylene compounds ac-cording to claim 1 wherein said reactive hydrogen compound is a primary alkyl amine.

4. A surface active mixture of conjugated polyoxyalkylene compounds according to claim 1 wherein said reactive hydrogen compound is an alkylene polyamine.

' 5. A surface active mixture of conjugated polyoxyalkylene compounds according to claim 1 wherein said reactive hydrogen compound is an alkanolamine.

6. A surface active mixture of conjugated polyoxyalkylene compounds according to claim 1 wherein the molecular weight of the oxypropylene chains is in the range of 1000 to 10,000.

7. A surface active mixture of conjugated polyoxyalkylene compounds according to claim 1 wherein the weight percent of oxyethylene groups is in the range of 25-55.

8. A surface active mixture of conjugated polyoxyalkylene compounds consisting of oxypropylene groups, oxyethylene groups and the nucleus of ethylenediamine as a reactive hydrogen compound, the structure of the compounds being such that all of the oxypropylene groups are present in oxypropylene chains that are attached to the nucleus of the ethylenediamine at the sites of its reactive hydrogen atoms and all of the oxyethylene groups are present in oxyethylene chains that are attached to the ends of the oxypropylene chains, the molecular weight of the oxypropylene chains being at least about 900 and up to about 25,000 and the oxyethylene groups being present in an amount so as to constitute 20-90 weight percent of the mixture of compounds.

9. A surface active mixture of conjugated polyoxyalkylene compounds consisting of oxypropylene groups, oxyethylene groups and the nucleus of triethylenetetramine as a reactive hydrogen compound, the structure of the compounds being such'that all of the oxypropylene groups are present in oxypropylene chains that are attached to the nucleus of the triethylenetetramine at the sites of its reactive hydrogen atoms and all of the oxyethylene groups are present in oxyethylene chains that are attached to the ends of the oxypropylene chains, the molecular weight of the oxypropylene chains being at least about 900 and up to about 25,000 and the oxyethylene groups being present in an amount so as to constitute 20-90 weight percent of the mixture of compounds.

10. A surface active mixture of conjugated polyoxyalkylene-compounds consisting of oxypropylene groups, oxyethylene groups and the nucleus of n-butylamine as a reactive hydrogen compound, the structure of the compounds being such that all of the oxypropylene groups are present in oxypropylene chains that are attached to the nucleus of the n-butylamine at the sites of its reactive hydrogen atoms and all of the oxyethylene groups are present in oxyethylene chains that are attached to the ends of the oxypropylene chains, the molecular weight of the oxypropylene chains being at least about 900 and up to about 25,000 and the oxyethylene groups being present in an amount so as to constitute 20-90 weight percent of the mixture of compounds.

References Cited in the file of this patent UNITED STATES PATENTS 2,174,762 Schuette et al. Oct. 3, 1939 2,220,147 Dreyfus Nov. 5, 1940 2,552,530 De Groote May 15, 1951 2,552,534 De Groote May 15, 1951 2,589,199 Monson Mar. 11, 1952 2,674,619 Lundstead Apr. 6, 1954 2,677,700 Jackson May 4, 1954 2,742,455 Sundberg Apr. 17, 1956 2,786,080 Patton Mar. 19, 1957 2,792,367 De Groote et al. Mar. 14, 1957 2,792,369 Dickson May 14, 1957 FOREIGN PATENTS 297,484 Great Britain Sept. 24, 1924

Claims (2)

1. A SURFACE ACTIVE MIXTURE OF CONJUGATED POLYOXYALKYLENE COMPOUNDS CONSISTING OF OXYPROPYLENE GROUPS, OXYETHYLENE GROUPS AND THE NUCLEUS OF A NITROGEN-CONTAINING REACTIVE HYDROGEN COMPOUND HAVING NOT NORE THAN 6 CARBON ATOMS PER MOLECULE AND BEING SELECTED FROM THE GROUP CONSISTING OF AMMONIA, PRIMARY ALKYL AMINES, ALKYLENE POLYAMINES, ALKANOLAMINES, PIPERAZINE AND CARBON-SUBSTITUTED ALKYLPIPERAZINES, HYDROXYLAMINE AND AMINOPHENOL, THE STRUCTURE OF THE COMPOUNDS BEING SUCH THAT ALL OF THE OXYPROPYLENE GROUPS ARE PRESENT IN OXYPROPYLENE CHAINS THAT ARE ATTACHED TO THE REACTIVE HYDROGEN COMPOUND AT THE SITES OF THE REACTIVE HYDROGEN ATOMS, AND ALL OF THE OXYETHYLENE GROUPS ARE PRESENT IN OXYETHYLENE CHAINS THAT ARE ATTACHED TO THE ENDS OF THE OXYPROPYLENE CHAINS, THE AVERAGE MOLECULAR WEIGHT OF THE OXYPROPYLENE CHAINS BEING AT LEAST ABOUT 900 AND TO ABOUT 25,000, AND THE OXYETHYLENE GROUPS BEING PRESENT IN AN AMOUNT SO AS TO CONSTITUTE FROM 20 TO 90 WEIGHT PERCENT OF THE MIXTURE OF COMPOUNDS.
4. A SURFACE ACTIVE MIXTURE OF CONJUGATED POLYOXYALKYLENE COMPOUNDS ACCORDING TO CLAIM 1 WHEREIN SAID REACTIVE HYDROGEN COMPOUND IS AN ALKYLENE POLYAMINE.
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US3287145A (en) * 1965-08-10 1966-11-22 Union Carbide Corp Chemical admixture for hydraulic cementitious mixtures
US3337463A (en) * 1963-10-18 1967-08-22 Wyandotte Chemicals Corp Foaming detergent compositions
DE2440531A1 (en) * 1973-08-24 1975-03-06 Cooper & Co Ltd Edwin Lubricant mixture, its use as hydraulic fluid and additive concentrate on his production
US3905932A (en) * 1973-03-29 1975-09-16 Toyo Soda Mfg Co Ltd Process for preparing polychloroprene latex
US3923707A (en) * 1973-06-20 1975-12-02 Huels Chemische Werke Ag Process for the production of pourable, pulverulent rubbers
US3929707A (en) * 1973-06-28 1975-12-30 Huels Chemische Werke Ag Process for the production of pourable, pulverulent rubber-filler mixtures
US3932659A (en) * 1970-07-24 1976-01-13 Beecham Group Limited Biologically active substance
US3945978A (en) * 1973-05-12 1976-03-23 Chemische Werke Huels Aktiengesellschaft Process for the production of pourable, pulverulent filler mixtures containing plasticizer oils
US4043972A (en) * 1975-10-06 1977-08-23 Phillips Fibers Corporation Stabilizing polyamide antistatic compositions
US4049557A (en) * 1972-07-17 1977-09-20 Colgate-Palmolive Company Fabric conditioning compositions
US4075130A (en) * 1976-08-30 1978-02-21 Texaco Development Corporation Polyoxypropylene polyamine derivatives as defoamers
US4218218A (en) * 1977-10-08 1980-08-19 Basf Aktiengesellschaft Stable finely dispersed aqueous formulations of disperse dyes and optical brighteners, and their use
US4244832A (en) * 1979-07-27 1981-01-13 Basf Wyandotte Corporation Phosphate-free machine dishwashing detergents useful at low temperatures
US4294581A (en) * 1978-11-30 1981-10-13 Basf Aktiengesellschaft Uniformly dyed water-swellable cellulosic fibers
US4305835A (en) * 1979-12-14 1981-12-15 Ethyl Corporation Lubricating composition containing emulsion-sludge inhibitors
US4305834A (en) * 1980-01-02 1981-12-15 Ethyl Corporation Lubricating composition containing emulsion-sludge inhibitors
US4351753A (en) * 1980-10-24 1982-09-28 Basf Wyandotte Corporation Liquified normally solid polyoxyalkylene block copolymers
EP0078483A2 (en) * 1981-11-02 1983-05-11 Basf Wyandotte Corporation Coal-oil slurries containing a surfactant
US4445908A (en) * 1980-12-01 1984-05-01 The United States Of America As Represented By The United States Department Of Energy Extracting alcohols from aqueous solutions
US4456543A (en) * 1982-06-17 1984-06-26 The Buckeye Cellulose Corporation Bisbiguanide based antibacterial cleansing products
US4464193A (en) * 1980-02-19 1984-08-07 Basf Wyandotte Corporation Anionic biocide emulsions in aqueous solutions of strongly ionizable salts
FR2541908A1 (en) * 1983-03-04 1984-09-07 Ugine Kuhlmann Antifoam composition, process for its manufacture and its application
US4474752A (en) * 1983-05-16 1984-10-02 Merck & Co., Inc. Drug delivery system utilizing thermosetting gels
US4474753A (en) * 1983-05-16 1984-10-02 Merck & Co., Inc. Topical drug delivery system utilizing thermosetting gels
US4474751A (en) * 1983-05-16 1984-10-02 Merck & Co., Inc. Ophthalmic drug delivery system utilizing thermosetting gels
US4478602A (en) * 1982-02-12 1984-10-23 Diamond Shamrock Chemicals Company Carbonaceous oil slurries stabilized by binary surfactant mixtures
US4478822A (en) * 1983-05-16 1984-10-23 Merck & Co., Inc. Drug delivery system utilizing thermosetting gels
US4534959A (en) * 1983-08-22 1985-08-13 Basf Wyandotte Corporation Aerosol gel
US4548744A (en) * 1983-07-22 1985-10-22 Connor Daniel S Ethoxylated amine oxides having clay soil removal/anti-redeposition properties useful in detergent compositions
US4551506A (en) * 1982-12-23 1985-11-05 The Procter & Gamble Company Cationic polymers having clay soil removal/anti-redeposition properties useful in detergent compositions
US4659802A (en) * 1982-12-23 1987-04-21 The Procter & Gamble Company Cationic compounds having clay soil removal/anti-redeposition properties useful in detergent compositions
US4661288A (en) * 1982-12-23 1987-04-28 The Procter & Gamble Company Zwitterionic compounds having clay soil removal/anti/redeposition properties useful in detergent compositions
US4661275A (en) * 1985-07-29 1987-04-28 The Lubrizol Corporation Water-based functional fluid thickening combinations of surfactants and hydrocarbyl-substituted succinic acid and/or anhydride/amine terminated poly(oxyalkylene) reaction products
US4664834A (en) * 1985-07-29 1987-05-12 The Lubrizol Corporation Hydrocarbyl-substituted succinic acid and/or anhydride/amine terminated poly(oxyalkylene) reaction products, and aqueous systems containing same
US4664848A (en) * 1982-12-23 1987-05-12 The Procter & Gamble Company Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties
US4676921A (en) * 1982-12-23 1987-06-30 The Procter & Gamble Company Detergent compositions containing ethoxylated amine polymers having clay soil removal/anti-redeposition properties
US4726909A (en) * 1985-12-23 1988-02-23 Basf Corporation Low odor surfactant
WO1988001272A2 (en) 1986-08-14 1988-02-25 The Lubrizol Corporation Borated amine salts of monothiophosphoric acids
WO1988001873A1 (en) * 1986-09-22 1988-03-24 Emory University Vaccine and method of preparation
WO1989004653A1 (en) * 1987-11-20 1989-06-01 S.C. Johnson & Son, Inc. Composition and method for hot curling hair treatment
US4859358A (en) * 1988-06-09 1989-08-22 The Procter & Gamble Company Liquid automatic dishwashing compositions containing metal salts of hydroxy fatty acids providing silver protection
US4988452A (en) * 1988-06-09 1991-01-29 The Procter & Gamble Company Liquid automatic dishwashing detergent compositions containing bleach-stable nonionic surfactant
US4995944A (en) * 1988-09-16 1991-02-26 Dearborn Chemical Company Ltd. Controlling deposits on paper machine felts using cationic polymer and cationic surfactant mixture
US5034508A (en) * 1988-08-31 1991-07-23 Dai-Ichi Kogyo Seiyaku Co., Ltd. Dispersant for nonaqueous systems
US5082498A (en) * 1989-06-21 1992-01-21 Basf Aktiengesellschaft Highly concentrated solid pigment formulations
US5116897A (en) * 1990-06-27 1992-05-26 Basf Corporation Antistatic composition
US5126068A (en) * 1989-05-05 1992-06-30 Burke John J Hard surface cleaning composition containing polyacrylate copolymers as performance boosters
US5130043A (en) * 1988-06-09 1992-07-14 The Procter & Gamble Company Liquid automatic dishwashing compositions having enhanced stability
US5298260A (en) * 1990-05-01 1994-03-29 Mediventures, Inc. Topical drug delivery with polyoxyalkylene polymer thermoreversible gels adjustable for pH and osmolality
EP0594479A1 (en) * 1992-10-23 1994-04-27 Institut Francais Du Petrole Process to reduce the tendency to agglomerate of hydrates in production effluents
US5346703A (en) * 1990-08-07 1994-09-13 Mediventures, Inc. Body cavity drug delivery with thermo-irreversible polyoxyalkylene and ionic polysaccharide gels
US5366735A (en) * 1988-11-16 1994-11-22 Mediventures, Inc. Method and composition for post-surgical adhesion reduction
US5466445A (en) * 1985-06-18 1995-11-14 Emory University Methods for reducing salmonella in chickens
US5494660A (en) * 1985-06-18 1996-02-27 Emory University Method for inhibiting microbial binding to surfaces
US5498355A (en) * 1994-09-20 1996-03-12 Ethyl Corporation Lubricant compositions of enhanced performance capabilities
US5505878A (en) * 1993-08-16 1996-04-09 Exxon Chemical Patents Inc. Method of demulsifying water-in-oil emulsions
EP0713907A2 (en) 1994-09-26 1996-05-29 Ethyl Petroleum Additives Limited Zinc additives of enhanced performance capabilities
US5554372A (en) * 1986-09-22 1996-09-10 Emory University Methods and vaccines comprising surface-active copolymers
US5612305A (en) * 1995-01-12 1997-03-18 Huntsman Petrochemical Corporation Mixed surfactant systems for low foam applications
US5622649A (en) * 1991-06-27 1997-04-22 Emory University Multiple emulsions and methods of preparation
US5648071A (en) * 1986-05-15 1997-07-15 Emory University Method of treating tumors
US5674911A (en) * 1987-02-20 1997-10-07 Cytrx Corporation Antiinfective polyoxypropylene/polyoxyethylene copolymers and methods of use
US5696298A (en) * 1991-03-19 1997-12-09 Cytrx Corporation Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
US5800711A (en) * 1996-10-18 1998-09-01 Mdv Technologies, Inc. Process for the fractionation of polyoxyalkylene block copolymers
US5811088A (en) * 1987-02-20 1998-09-22 Emory University Antiinfective compounds and methods of use
US5824322A (en) * 1995-08-21 1998-10-20 Cytrx Corporation Compositions and methods for growth promotion
US5843470A (en) * 1995-10-06 1998-12-01 Mdv Technologies, Inc. Method and composition for inhibiting post-surgical adhesions
US5958859A (en) * 1997-07-29 1999-09-28 Basf Corporation Aqueous based solvent free cleaner compositions containing a blend of polyoxyalkylene block copolymers
US5990241A (en) * 1991-03-19 1999-11-23 Cytrx, Corporation Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
US6060531A (en) * 1995-10-16 2000-05-09 Basf Aktiengesellschaft Production of low-fogging polyurethane foams, and specific polyoxyalkylene-polyols which can be used for this purpose
US6123740A (en) * 1996-12-02 2000-09-26 Basf Aktiengesellschaft Dye preparations containing methine dyes
US6171445B1 (en) 1999-07-30 2001-01-09 Hercules Incorporated Process for controlling deposit of sticky material
US6280745B1 (en) 1997-12-23 2001-08-28 Alliance Pharmaceutical Corp. Methods and compositions for the delivery of pharmaceutical agents and/or the prevention of adhesions
US6294592B1 (en) 1997-06-30 2001-09-25 Basf Aktiengesellschaft Pigment preparations with radiation curable binder suitable for ink jet printing method
US6332943B1 (en) 1997-06-30 2001-12-25 Basf Aktiengesellschaft Method of ink-jet printing with pigment preparations having a dispersant
US6436425B1 (en) 1988-11-16 2002-08-20 Mdv Technologies, Inc. Method and non-gelling composition for inhibiting post-surgical adhesions
US6537331B1 (en) 1997-12-05 2003-03-25 Basf Aktiengesellschaft Dye preparations containing azo dyes
US6607565B1 (en) 1997-11-26 2003-08-19 Basf Aktiengesellschaft Colorant preparations
USRE38558E1 (en) 1991-03-19 2004-07-20 Cytrx Corporation Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
US6790816B2 (en) 1999-09-24 2004-09-14 Bausch & Lomb Incorporated High osmolyte cleaning and disinfection method and solution for contact lenses
US20040214735A1 (en) * 2000-10-06 2004-10-28 Groemminger Suzanne F. Cleaner for contact lens
US20040248833A1 (en) * 1991-03-19 2004-12-09 Emanuele R Martin Therapeutic delivery compositions and methods of use thereof
US20050131095A1 (en) * 2002-08-02 2005-06-16 Jianming Yu Novel polyols
US6933286B2 (en) 1991-03-19 2005-08-23 R. Martin Emanuele Therapeutic delivery compositions and methods of use thereof
US7202225B1 (en) 1993-10-15 2007-04-10 Emanuele R Martin Therapeutic delivery compositions and methods of use thereof

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB297484A (en) * 1927-05-23 1928-09-24 Ig Farbenindustrie Ag Improvements in the manufacture and production of amines of the hydroaromatic-aliphatic series
US2174762A (en) * 1935-04-13 1939-10-03 Ig Farbenindustrie Ag Condensation products derived from amines and method of producing them
US2220147A (en) * 1936-09-19 1940-11-05 Dreyfus Henry Manufacture of alkylolamines
US2552530A (en) * 1949-07-28 1951-05-15 Petrolite Corp Process for breaking petroleum emulsions
US2552534A (en) * 1950-03-04 1951-05-15 Petrolite Corp Processes for breaking petroleum emulsions
US2589199A (en) * 1950-08-26 1952-03-11 Petrolite Corp Process for breaking emulsions of the oil-in-water class
US2674619A (en) * 1953-10-19 1954-04-06 Wyandotte Chemicals Corp Polyoxyalkylene compounds
US2677700A (en) * 1951-05-31 1954-05-04 Wyandotte Chemicals Corp Polyoxyalkylene surface active agents
US2742455A (en) * 1951-09-24 1956-04-17 Gen Aniline & Film Corp Production of n, n-polyoxyethylated rosin amines
US2786080A (en) * 1953-11-25 1957-03-19 Wyandotte Chemicals Corp Stabilized polyoxyalkylene compositions
US2792367A (en) * 1953-10-05 1957-05-14 Petrolite Corp Process for breaking petroleum emulsions employing certain oxyalkylation products derived in turn from reactive nitrogen containing compounds
US2792369A (en) * 1954-09-15 1957-05-14 Petrolite Corp Process for breaking petroleum emulsions employing certain oxyalkylated diethylene triamines

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB297484A (en) * 1927-05-23 1928-09-24 Ig Farbenindustrie Ag Improvements in the manufacture and production of amines of the hydroaromatic-aliphatic series
US2174762A (en) * 1935-04-13 1939-10-03 Ig Farbenindustrie Ag Condensation products derived from amines and method of producing them
US2220147A (en) * 1936-09-19 1940-11-05 Dreyfus Henry Manufacture of alkylolamines
US2552530A (en) * 1949-07-28 1951-05-15 Petrolite Corp Process for breaking petroleum emulsions
US2552534A (en) * 1950-03-04 1951-05-15 Petrolite Corp Processes for breaking petroleum emulsions
US2589199A (en) * 1950-08-26 1952-03-11 Petrolite Corp Process for breaking emulsions of the oil-in-water class
US2677700A (en) * 1951-05-31 1954-05-04 Wyandotte Chemicals Corp Polyoxyalkylene surface active agents
US2742455A (en) * 1951-09-24 1956-04-17 Gen Aniline & Film Corp Production of n, n-polyoxyethylated rosin amines
US2792367A (en) * 1953-10-05 1957-05-14 Petrolite Corp Process for breaking petroleum emulsions employing certain oxyalkylation products derived in turn from reactive nitrogen containing compounds
US2674619A (en) * 1953-10-19 1954-04-06 Wyandotte Chemicals Corp Polyoxyalkylene compounds
US2786080A (en) * 1953-11-25 1957-03-19 Wyandotte Chemicals Corp Stabilized polyoxyalkylene compositions
US2792369A (en) * 1954-09-15 1957-05-14 Petrolite Corp Process for breaking petroleum emulsions employing certain oxyalkylated diethylene triamines

Cited By (97)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3123559A (en) * 1964-03-03 Hccjhio
US3239381A (en) * 1962-05-21 1966-03-08 Monsanto Co Battery separator impregnated with a phenol-aldehyde resin composition
US3337463A (en) * 1963-10-18 1967-08-22 Wyandotte Chemicals Corp Foaming detergent compositions
US3287145A (en) * 1965-08-10 1966-11-22 Union Carbide Corp Chemical admixture for hydraulic cementitious mixtures
US3932659A (en) * 1970-07-24 1976-01-13 Beecham Group Limited Biologically active substance
US4049557A (en) * 1972-07-17 1977-09-20 Colgate-Palmolive Company Fabric conditioning compositions
US3905932A (en) * 1973-03-29 1975-09-16 Toyo Soda Mfg Co Ltd Process for preparing polychloroprene latex
US3945978A (en) * 1973-05-12 1976-03-23 Chemische Werke Huels Aktiengesellschaft Process for the production of pourable, pulverulent filler mixtures containing plasticizer oils
US3923707A (en) * 1973-06-20 1975-12-02 Huels Chemische Werke Ag Process for the production of pourable, pulverulent rubbers
US3929707A (en) * 1973-06-28 1975-12-30 Huels Chemische Werke Ag Process for the production of pourable, pulverulent rubber-filler mixtures
DE2440531A1 (en) * 1973-08-24 1975-03-06 Cooper & Co Ltd Edwin Lubricant mixture, its use as hydraulic fluid and additive concentrate on his production
US4043972A (en) * 1975-10-06 1977-08-23 Phillips Fibers Corporation Stabilizing polyamide antistatic compositions
US4075130A (en) * 1976-08-30 1978-02-21 Texaco Development Corporation Polyoxypropylene polyamine derivatives as defoamers
US4218218A (en) * 1977-10-08 1980-08-19 Basf Aktiengesellschaft Stable finely dispersed aqueous formulations of disperse dyes and optical brighteners, and their use
US4294581A (en) * 1978-11-30 1981-10-13 Basf Aktiengesellschaft Uniformly dyed water-swellable cellulosic fibers
US4244832A (en) * 1979-07-27 1981-01-13 Basf Wyandotte Corporation Phosphate-free machine dishwashing detergents useful at low temperatures
US4305835A (en) * 1979-12-14 1981-12-15 Ethyl Corporation Lubricating composition containing emulsion-sludge inhibitors
US4305834A (en) * 1980-01-02 1981-12-15 Ethyl Corporation Lubricating composition containing emulsion-sludge inhibitors
US4464193A (en) * 1980-02-19 1984-08-07 Basf Wyandotte Corporation Anionic biocide emulsions in aqueous solutions of strongly ionizable salts
US4351753A (en) * 1980-10-24 1982-09-28 Basf Wyandotte Corporation Liquified normally solid polyoxyalkylene block copolymers
US4445908A (en) * 1980-12-01 1984-05-01 The United States Of America As Represented By The United States Department Of Energy Extracting alcohols from aqueous solutions
EP0078483A2 (en) * 1981-11-02 1983-05-11 Basf Wyandotte Corporation Coal-oil slurries containing a surfactant
EP0078483A3 (en) * 1981-11-02 1984-10-17 Basf Wyandotte Corporation Coal-oil slurries containing a surfactant
US4478602A (en) * 1982-02-12 1984-10-23 Diamond Shamrock Chemicals Company Carbonaceous oil slurries stabilized by binary surfactant mixtures
US4456543A (en) * 1982-06-17 1984-06-26 The Buckeye Cellulose Corporation Bisbiguanide based antibacterial cleansing products
US4551506A (en) * 1982-12-23 1985-11-05 The Procter & Gamble Company Cationic polymers having clay soil removal/anti-redeposition properties useful in detergent compositions
US4664848A (en) * 1982-12-23 1987-05-12 The Procter & Gamble Company Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties
US4676921A (en) * 1982-12-23 1987-06-30 The Procter & Gamble Company Detergent compositions containing ethoxylated amine polymers having clay soil removal/anti-redeposition properties
US4661288A (en) * 1982-12-23 1987-04-28 The Procter & Gamble Company Zwitterionic compounds having clay soil removal/anti/redeposition properties useful in detergent compositions
US4659802A (en) * 1982-12-23 1987-04-21 The Procter & Gamble Company Cationic compounds having clay soil removal/anti-redeposition properties useful in detergent compositions
FR2541908A1 (en) * 1983-03-04 1984-09-07 Ugine Kuhlmann Antifoam composition, process for its manufacture and its application
US4474753A (en) * 1983-05-16 1984-10-02 Merck & Co., Inc. Topical drug delivery system utilizing thermosetting gels
US4474752A (en) * 1983-05-16 1984-10-02 Merck & Co., Inc. Drug delivery system utilizing thermosetting gels
US4474751A (en) * 1983-05-16 1984-10-02 Merck & Co., Inc. Ophthalmic drug delivery system utilizing thermosetting gels
US4478822A (en) * 1983-05-16 1984-10-23 Merck & Co., Inc. Drug delivery system utilizing thermosetting gels
US4548744A (en) * 1983-07-22 1985-10-22 Connor Daniel S Ethoxylated amine oxides having clay soil removal/anti-redeposition properties useful in detergent compositions
US4534959A (en) * 1983-08-22 1985-08-13 Basf Wyandotte Corporation Aerosol gel
US5466445A (en) * 1985-06-18 1995-11-14 Emory University Methods for reducing salmonella in chickens
US5494660A (en) * 1985-06-18 1996-02-27 Emory University Method for inhibiting microbial binding to surfaces
US4661275A (en) * 1985-07-29 1987-04-28 The Lubrizol Corporation Water-based functional fluid thickening combinations of surfactants and hydrocarbyl-substituted succinic acid and/or anhydride/amine terminated poly(oxyalkylene) reaction products
US4664834A (en) * 1985-07-29 1987-05-12 The Lubrizol Corporation Hydrocarbyl-substituted succinic acid and/or anhydride/amine terminated poly(oxyalkylene) reaction products, and aqueous systems containing same
US4726909A (en) * 1985-12-23 1988-02-23 Basf Corporation Low odor surfactant
US5648071A (en) * 1986-05-15 1997-07-15 Emory University Method of treating tumors
WO1988001272A2 (en) 1986-08-14 1988-02-25 The Lubrizol Corporation Borated amine salts of monothiophosphoric acids
US4861583A (en) * 1986-09-04 1989-08-29 S. C. Johnson & Son, Inc. Hot curling hair treatment
WO1988001873A1 (en) * 1986-09-22 1988-03-24 Emory University Vaccine and method of preparation
US5554372A (en) * 1986-09-22 1996-09-10 Emory University Methods and vaccines comprising surface-active copolymers
US5811088A (en) * 1987-02-20 1998-09-22 Emory University Antiinfective compounds and methods of use
US5674911A (en) * 1987-02-20 1997-10-07 Cytrx Corporation Antiinfective polyoxypropylene/polyoxyethylene copolymers and methods of use
WO1989004653A1 (en) * 1987-11-20 1989-06-01 S.C. Johnson & Son, Inc. Composition and method for hot curling hair treatment
US4988452A (en) * 1988-06-09 1991-01-29 The Procter & Gamble Company Liquid automatic dishwashing detergent compositions containing bleach-stable nonionic surfactant
US5130043A (en) * 1988-06-09 1992-07-14 The Procter & Gamble Company Liquid automatic dishwashing compositions having enhanced stability
US4859358A (en) * 1988-06-09 1989-08-22 The Procter & Gamble Company Liquid automatic dishwashing compositions containing metal salts of hydroxy fatty acids providing silver protection
US5034508A (en) * 1988-08-31 1991-07-23 Dai-Ichi Kogyo Seiyaku Co., Ltd. Dispersant for nonaqueous systems
US4995944A (en) * 1988-09-16 1991-02-26 Dearborn Chemical Company Ltd. Controlling deposits on paper machine felts using cationic polymer and cationic surfactant mixture
US6436425B1 (en) 1988-11-16 2002-08-20 Mdv Technologies, Inc. Method and non-gelling composition for inhibiting post-surgical adhesions
US5366735A (en) * 1988-11-16 1994-11-22 Mediventures, Inc. Method and composition for post-surgical adhesion reduction
US5126068A (en) * 1989-05-05 1992-06-30 Burke John J Hard surface cleaning composition containing polyacrylate copolymers as performance boosters
US5082498A (en) * 1989-06-21 1992-01-21 Basf Aktiengesellschaft Highly concentrated solid pigment formulations
US5298260A (en) * 1990-05-01 1994-03-29 Mediventures, Inc. Topical drug delivery with polyoxyalkylene polymer thermoreversible gels adjustable for pH and osmolality
US5116897A (en) * 1990-06-27 1992-05-26 Basf Corporation Antistatic composition
US6346272B1 (en) 1990-08-07 2002-02-12 Mdv Technologies, Inc. Body cavity drug delivery with thermo-irreversible polyoxyalkylene and ionic polysaccharide gels
US5346703A (en) * 1990-08-07 1994-09-13 Mediventures, Inc. Body cavity drug delivery with thermo-irreversible polyoxyalkylene and ionic polysaccharide gels
US6359014B1 (en) 1991-03-19 2002-03-19 Cytrx Corporation Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
US20040248833A1 (en) * 1991-03-19 2004-12-09 Emanuele R Martin Therapeutic delivery compositions and methods of use thereof
US5990241A (en) * 1991-03-19 1999-11-23 Cytrx, Corporation Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
US6933286B2 (en) 1991-03-19 2005-08-23 R. Martin Emanuele Therapeutic delivery compositions and methods of use thereof
US5696298A (en) * 1991-03-19 1997-12-09 Cytrx Corporation Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
US6747064B2 (en) 1991-03-19 2004-06-08 Cytrx Corporation Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
USRE38558E1 (en) 1991-03-19 2004-07-20 Cytrx Corporation Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
US5622649A (en) * 1991-06-27 1997-04-22 Emory University Multiple emulsions and methods of preparation
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US5426258A (en) * 1992-10-23 1995-06-20 Institut Francais Du Petrole Process for reducing the agglomeration tendency of hydrates in the production effluent
US5505878A (en) * 1993-08-16 1996-04-09 Exxon Chemical Patents Inc. Method of demulsifying water-in-oil emulsions
US7202225B1 (en) 1993-10-15 2007-04-10 Emanuele R Martin Therapeutic delivery compositions and methods of use thereof
US5498355A (en) * 1994-09-20 1996-03-12 Ethyl Corporation Lubricant compositions of enhanced performance capabilities
EP0713907A2 (en) 1994-09-26 1996-05-29 Ethyl Petroleum Additives Limited Zinc additives of enhanced performance capabilities
US5612305A (en) * 1995-01-12 1997-03-18 Huntsman Petrochemical Corporation Mixed surfactant systems for low foam applications
US5824322A (en) * 1995-08-21 1998-10-20 Cytrx Corporation Compositions and methods for growth promotion
US6034088A (en) * 1995-10-06 2000-03-07 Mdv Technologies, Inc. Method and composition for inhibiting post-surgical adhesions
US5843470A (en) * 1995-10-06 1998-12-01 Mdv Technologies, Inc. Method and composition for inhibiting post-surgical adhesions
US6060531A (en) * 1995-10-16 2000-05-09 Basf Aktiengesellschaft Production of low-fogging polyurethane foams, and specific polyoxyalkylene-polyols which can be used for this purpose
US20030108610A1 (en) * 1996-02-09 2003-06-12 Flore Stephen G. Methods and compositions for the delivery of pharmaceutical agents and/or the prevention of adhesions
US5800711A (en) * 1996-10-18 1998-09-01 Mdv Technologies, Inc. Process for the fractionation of polyoxyalkylene block copolymers
US6123740A (en) * 1996-12-02 2000-09-26 Basf Aktiengesellschaft Dye preparations containing methine dyes
US6294592B1 (en) 1997-06-30 2001-09-25 Basf Aktiengesellschaft Pigment preparations with radiation curable binder suitable for ink jet printing method
US6332943B1 (en) 1997-06-30 2001-12-25 Basf Aktiengesellschaft Method of ink-jet printing with pigment preparations having a dispersant
US5958859A (en) * 1997-07-29 1999-09-28 Basf Corporation Aqueous based solvent free cleaner compositions containing a blend of polyoxyalkylene block copolymers
US6607565B1 (en) 1997-11-26 2003-08-19 Basf Aktiengesellschaft Colorant preparations
US6669740B2 (en) 1997-12-05 2003-12-30 Basf Aktiengesellschaft Dye preparations comprising azo dyes
US6537331B1 (en) 1997-12-05 2003-03-25 Basf Aktiengesellschaft Dye preparations containing azo dyes
US6280745B1 (en) 1997-12-23 2001-08-28 Alliance Pharmaceutical Corp. Methods and compositions for the delivery of pharmaceutical agents and/or the prevention of adhesions
US6171445B1 (en) 1999-07-30 2001-01-09 Hercules Incorporated Process for controlling deposit of sticky material
US6790816B2 (en) 1999-09-24 2004-09-14 Bausch & Lomb Incorporated High osmolyte cleaning and disinfection method and solution for contact lenses
US20040214735A1 (en) * 2000-10-06 2004-10-28 Groemminger Suzanne F. Cleaner for contact lens
US6872695B1 (en) 2000-10-06 2005-03-29 Bausch & Lomb Incorporated Method for in-eye cleaning of contact lens comprising polymeric beads
US20050131095A1 (en) * 2002-08-02 2005-06-16 Jianming Yu Novel polyols

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