Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
  • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
  • C07C217/50—Ethers of hydroxy amines of undetermined structure, e.g. obtained by reactions of epoxides with hydroxy amines
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
  • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
  • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
  • C07C217/28—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having one amino group and at least two singly-bound oxygen atoms, with at least one being part of an etherified hydroxy group, bound to the carbon skeleton, e.g. ethers of polyhydroxy amines
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
  • C09D5/02—Emulsion paints including aerosols
  • C09D5/024—Emulsion paints including aerosols characterised by the additives
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/002—Surface-active compounds containing sulfur
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/38—Cationic compounds
  • C11D1/42—Amino alcohols or amino ethers
  • C11D1/44—Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines

Definitions

• This invention relates to surfactants and defoaming agents useful in both aqueous and nonaqueous compositions.
• Surface active foam control agents and detergency enhancement agents are widely used in both aqueous and nonaqueous compositions. However, these agents vary in their effectiveness and ecotoxicity, and new and more effective agents with low ecotoxicity are in constant demand.
• the present invention relates to compounds useful as surfactants, and/or foam control agents, and/or rheology modifiers. These compounds are compounds of formula I given below:
• R 1 and R 2 can be independently a substituted or unsubstituted, saturated or unsaturated C ⁇ -C 36 hydrocarbon group, or a -RX(AO) favor-R 4 group in which R is a C 6 - C 10 arylene group, a straight or branched chain C 2 -C 20 alkylene group, optionally containing an arylene group, or a C 4 -C 20 straight chain alkylene group containing one or more -NH- groups in the alkylene chain, X is -O-, -S-, or -NR 5 - where R 5 is hydrogen or Ci-C ⁇ alkyl, each AO group is independently an ethyleneoxy (EO), a 1,2- propyleneoxy (PO), or a 1,2-butyleneoxy (BO) group, n is a number of from 1 to 100, and the R 4 group is a C ⁇ -C 36 organic group; and the R 3 group is an -RX(
• Figure 1 is a graph showing the foam behavior of surfactants, including combinations thereof, in aqueous solutions.
• Figure 2 is a graph showing the % soil removal obtained by the aqueous surfactant solutions of Figure 1.
• R 1 and/or R 2 are hydrocarbon groups
• such groups include linear or branched alkyl groups having from 1 to 36 carbon atoms, preferably from 4 to 22 carbon atoms, more preferably from 4 to 12 carbon atoms, and most preferably from 8 to 10 carbon atoms; linear or branched alkenyl or alkynyl groups having from 2 to 36 carbon atoms, preferably from 4 to 22 carbon atoms, aryl groups having from 6 to 22 carbon atoms, e.g.
• R 1 and/or R 2 groups can also be saturated carbocyclic groups, unsaturated carbocyclic groups having one or more multiple bonds, saturated heterocyclic groups, e.g. piperidino, morpholino, thiomorpholino, pyrrolidino, and the like, or unsaturated heterocyclic groups, such as the above groups having one or more multiple bonds.
• any of the above groups can be substituted groups, i.e. the substituent groups can be single or multiple substituents such as a sulfur functionality, e.g. a mercaptan or thio group; a nitrogen functionality such as an amine or amide functionality; an alcohol functionality; a silicon functionality, e.g., a siloxane; an ether functionality, e.g. a C ⁇ -C 6 alkoxy group; or any combination thereof.
• the AO groups are preferably all ethyleneoxy groups, n is preferably a number of from 4 to 50, and the R 4 group can be
• Cis saturated or unsaturated, substituted or unsubstituted, hydrocarbon group e.g. alkyl, alkenyl, cycloalkyl, arenyl, or aryl, optionally containing one or more of the substituents described above.
• the compounds of the invention preferably have the following structure II: ⁇ - RX(AO) n -R 4
• R, X, AO, n, and R 4 have the meanings given in Formula I, and m and p are independently a number of from 1 to 100, provided that the sum of n, m, and p is from 3 to 100, preferably from 4 to 50.
• the AO groups are preferably at least mostly ethyleneoxy groups, and the R 4 groups are preferably all independently C ⁇ -C 36 hydrocarbon groups.
• R is a straight or branched chain C 2 -C 10 alkylene group
• X has the meamng given in formula I
• AO has the meaning given in formula I, but preferably all AO groups are ethyleneoxy groups, the sum of n, m, and p is from 6 to 27, preferably from 6 to 18, and more preferably from 6 to 12, and each R 8 group is independently a
• R 9 is a Ci-Cis straight or branched chain, saturated or unsaturated hydrocarbon group.
• R 7 groups are all ethylene groups; the X groups are all -O-; the AO groups are all ethyleneoxy groups; n, m, and p total from 6 to 18, preferably from 6 to 12; and R 9 is a C 4 -C 12 alkyl group.
• the most preferred compound of the invention is the reaction product of (a) triethanolamine ethoxylated with an average of 9 moles of ethylene oxide and (b) about 3 moles of epoxylated 1-decene.
• the reaction mixture resulting therefrom will contain the following compound of formula IV: . CH 2 CH 2 O(EO) 3 CH 2 CH-C 8 H 17
• the compounds of formulae I, II, III, and IV can be prepared by (a) reacting a tertiary amine having at least one hydrogen atom which will react with an alkylene oxide, with a C 2 -C 4 alkylene oxide, and (b) reacting the reaction product from step (a) with either (i) a C ⁇ -C 36 organic halide, preferably a chloride or bromide, (ii) a Cs-C 2 o epoxy compound or (iii) a C 2 -C 19 carboxylic acid-based esterifying agent e.g. R 6 COH, R° X, where X is a halogen atom, or RR 6 ⁇ COR where R is a C ⁇ -C 6 alkyl group and R has the meaning given above.
• the epoxy compound preferably has the formula CCHH ⁇ 2 -CCHH--RR 9 " w'he ⁇ r-e R has the meaning given above in formula III.
• epoxy compounds in which the epoxy group is not in the alpha position can also be used herein.
• Reaction conditions for carrying out the above reactions will depend on the particular reactants employed and can be readily determined by those skilled in the art, especially since alkoxylation reactions, organic halide reactions, reactions with epoxy compounds, and esterification reactions are known reaction types.
• the amines in step (a) prior to alkoxylation containing an -SH or -NR 5 H group can be readily prepared from the corresponding alcohols.
• the corresponding alcohol can be subjected to a catalyzed ammoniation (with ammonia, or a lower alkylamine) for replacement of the hydroxyl, or to a capping of the hydroxyl with epichlorohydrin followed by ammoniation (with ammonia, or a lower alkylamine) of the resulting glycidal group.
• X is -SH
• the corresponding alcohol can be converted to the mercaptan by methods well known to the art, e.g. by converting the alcohol to a halide and reacting the halide with sodium hydrosulfide.
• the compounds of the invention can be used as surfactants and/or foam control agents and/or rheology modifying agents in both aqueous and nonaqueous compositions, and are particularly useful in minimizing or eliminating foaming in aqueous compositions containing high foaming surfactants, such as alkyl polyglycosides and anionic surfactants such as alcohol sulfates.
• high foaming surfactants such as alkyl polyglycosides and anionic surfactants such as alcohol sulfates.
• reaction products can be used in aqueous cleaning compositions, in emulsion polymer latex compositions such as latex paints, in inks, in adhesives, in metal working compositions, and in other aqueous and nonaqueous compositions in which surfactants and/or defoaming agents and/or rheology modifying agents are advantageously present.
• reaction products of the invention are biodegradable, can act as surfactants, defoaming agents, and rheology modifying agents at the same time, contain no organic solvents, and do not adversely affect the detergency of other surfactants that may be present in compositions in which they are used since they are themselves surfactants. In addition, they do not contain any organically bound chlorine or other halides, i.e. they have a very low eco-toxicity.
• the degree of hydrophilic and hydrophobic properties of the compounds of the invention can be readily controlled by controlling the type and number of alkyleneoxy groups and the carbon content of the hydrophobic groups. For example, the greater the number of ethyleneoxy groups present, the greater the water solubility, while the presence of 1,2-propyleneoxy groups and/or 1,2-butyleneoxy groups will decrease water solubility.
• the compounds of the invention can be added to the above aqueous and nonaqueous compositions in a surfactant-effective and/or defoaming-effective quantity, and/or rheology modifying-effective quantity, usually from 0.01 to 20% by weight, preferably from 0.1 to 10% by weight, based on the weight of solids in the composition.
• the compounds of the invention are particularly useful as a defoaming agent component of aqueous solutions containing one or more alkyl polyglycosides.
• Alkyl polyglycosides are a class of nonionic surfactants that exhibit significantly higher foaming profiles than other nonionic surfactants, such as alcohol ethoxylates.
• foaming tendencies of alkyl polyglycosides more closely resemble those of anionic surfactants, such as alcohol sulfates, than the foaming tendencies of other nonionic surfactants.
• This higher foaming tendency makes the use of alkyl polyglycosides undesirable for many applications, e.g. cleaning-in-place for food processing plants, high pressure spray cleaning, bottle washing, floor cleaners and automatic dishwashing, wherein high levels of foam interfere with the cleaning and rinsing operation and reduce the efficiency of the operation.
• a defoaming-effective amount is an amount effective to eliminate or decrease the foam generated by the alkyl polyglycoside as a result of some type of mechanical action such as mixing, pouring, and/or shaking.
• the amount required to eliminate and/or decrease foam will vary from one instance to another depending upon the nature of the alkyl polyglycoside surfactant or mixture of surfactants and the defoaming effect desired.
• a defoaming effective amount will be readily determinable by one of ordinary skill in the art.
• the defoaming effective amount will typically vary from a weight ratio of alkyl polyglycoside/defoamer of 4.0/1.0 to about 1.0/1.0.
• Alkyl polyglycosides include those having formula IV below:
• Ri is a monovalent organic radical having from 6 to 30 carbon atoms, preferably from 6 to 16 carbon atoms;
• R 2 is a divalent alkylene radical having from 2 to 4 carbon atoms;
• Z is a saccarhide residue having 5 or 6 carbon atoms;
• b is a number having a value from 0 to 12;
• a is a number having a value from 1 to 6, preferably from 1.2 to 2.2, and more preferably from 1.4 to 1.7.
• Preferred alkyl polyglycosides which can be used in the compositions according to the invention have the formula I wherein Z is a glucose residue and b is zero.
• alkyl polyglycosides are commercially available, for example, as APG®, GLUCOPON®, or PLANTAREN® surfactants from Cognis Corporation, Ambler, PA, 19002.
• surfactants include but are not limited to:
• GLUCOPON® 225 DK Surfactant an alkyl polyglycoside in which the alkyl group contains 8 to 10 carbon atoms and having an average degree of polymerization of 1.7
• GLUCOPON® 425N Surfactant an alkyl polyglycoside in which the alkyl group contains 8 to 16 carbon atoms, having an average of 10.3 carbon atoms, and having an average degree of polymerization of 1.5.
• APG® 325N Surfactant an alkyl polyglycoside in which the alkyl group contain 9 to 11 carbon atoms and having an average degree of polymerization of 1.5.
• GLUCOPON® 600UP Surfactant - an alkyl polyglycoside in which the alkyl group contains 12 to 16 carbon atoms and having an average degree of polymerization of 1.4.
• PLANTAEREN® 2000 Surfactant - a C 8 -C 16 alkyl polyglycoside in which the alkyl group contains 8 to 16 carbon atoms and having an average degree of polymerization of 1.5.
• PLANTAEREN® 1300 Surfactant - a C 12 -C 16 alkyl polyglycoside in which the alkyl group contains 12 to 16 carbon atoms and having an average degree of polymerization of 1.6.
• GLUCOPON® 220N Surfactant - an alkyl polyglycoside in which the alkyl group contains 8 to 10 carbon atoms and having an average degree of polymerization of 1.5.
• alkyl polyglycoside surfactant compositions which are comprised of mixtures of compounds of formula I wherein Z represents a moiety derived from a reducing saccharide containing 5 or 6 carbon atoms; a is a number having a value from 1 to about 6; b is zero; and Ri is an alkyl radical having from 8 to 20 carbon atoms.
• compositions are characterized in that they have increased surfactant properties and an HLB in the range of about 10 to about 16 and a non-Flory distribution of glycosides, which is comprised of a mixture of an alkyl monoglycoside and a mixture of alkyl polyglycosides having varying degrees of polymerization of 2 and higher in progressively decreasing amounts, in which the amount by weight of polyglycoside having a degree of polymerization of 2 or mixtures thereof with the polyglycoside having a degree of polymerization of 3 predominate in relation to the amount of monoglycoside, said composition having an average degree of polymerization of about 1.8 to about 3.
• compositions also known as peaked alkyl polyglycosides
• the relative distribution of the various components, mono- and poly- glycosides, in the resulting product changes and the concentration in the product of the polyglycosides relative to the monoglycoside increases as well as the concentration of individual polyglycosides to the total, i.e.
• TW is POE(9) triethanolamine tris-(2-hydroxydecyl) ether prepared in Example 1.
• 2 - DEHYPOUND® ST-15 is a commercial highly effective foam control agent produced by the base- catalyzed reaction between epichlorohydrin and n-octyl/n-decyl (45:55) alcohol ⁇ 4EO (mole ratio 1:0.65).
• the above surfactant compositions were further diluted by adding 10 grams of the composition to 400 grams of soft water, resulting in 0.1% total active solutions. The 0.1% active solutions were transferred to a dynamic foam cell and circulated for a total of 8 minutes.
• the foam cell consisted of a 2-liter jacketed graduate, peristaltic pump with variable voltage controller, and silicone and glass tubing.
• test mixture was circulated at a constant temperature and flow rate; and fell from a constant height of 30 cm back into itself, creating foam.
• the tests were run under the following set of conditions: a 0.1% active solution of the test surfactant in soft (10-15 ppm) water was circulated at 25°C and the foam volume was read every 30 seconds.
• the results obtained are set forth in Table 1 below:
• Example 1 is a more effective foam control agent than the commercial product DEHYPOUND® ST-15 since 1 part of DEHYPOUND® ST-15 for every 4.5 parts of actives in GLUCOPON® 425N is required to obtain satisfactory foam control, while only 1 part of the compound of Example 1 is needed for every 5.75 parts of actives in GLUCOPON® 425N to achieve even better foam control results.
• Example 3 is a more effective foam control agent than the commercial product DEHYPOUND® ST-15 since 1 part of DEHYPOUND® ST-15 for every 4.5 parts of actives in GLUCOPON® 425N is required to obtain satisfactory foam control, while only 1 part of the compound of Example 1 is needed for every 5.75 parts of actives in GLUCOPON® 425N to achieve even better foam control results.
• aqueous surfactant compositions prepared in Example 2 were tested for hard surface detergency according to the following procedure:
• the test soil used had the following composition: Composition Parts bv weight
• the cleaning operation was carried out as follows, after first measuring the reflectance of the soiled tiles:
• test solution 200 ml were added to the wash tray, and left for one minute.
• test panels were scrubbed with a synthetic sponge for 16 cycles, rotating panels 90°after 8 cycles.
• the total number of cycles can be varied from 8 to 40, provided the same number is used for each test solution.
• Steps 1-4 were repeated for a total of four panels for each test solution. The reflectance of the washed panels were measured after the drying period, and averaged for each test solution. Calculation:
• compositions containing the compounds of the invention are more effective hard surface detergents than both GLUCOPON® 425N alone (composition a)), and composition d) containing DEHYPOUND® ST-15 even though DEHYPOUND® ST-15 is present in composition d) in greater quantity than the compound of Example 1 in compositions b) and c).

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Wood Science & Technology (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Materials Engineering (AREA)
• Dispersion Chemistry (AREA)
• Crystallography & Structural Chemistry (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Detergent Compositions (AREA)
• Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
• Degasification And Air Bubble Elimination (AREA)
• Paints Or Removers (AREA)
• Inks, Pencil-Leads, Or Crayons (AREA)
• Adhesives Or Adhesive Processes (AREA)

Priority Applications (4)

Applications Claiming Priority (4)

Publications (2)

Family

ID=26950891

Family Applications (1)

Country Status (6)

Families Citing this family (7)

Family Cites Families (32)

• 2002
  • 2002-10-04 US US10/265,004 patent/US7247606B2/en not_active Expired - Fee Related
  • 2002-10-31 ES ES02791198T patent/ES2404892T3/es not_active Expired - Lifetime
  • 2002-10-31 EP EP02791198A patent/EP1441827B1/en not_active Expired - Lifetime
  • 2002-10-31 WO PCT/US2002/034844 patent/WO2003040277A2/en not_active Ceased
  • 2002-10-31 AU AU2002363470A patent/AU2002363470A1/en not_active Abandoned
  • 2002-10-31 JP JP2003542316A patent/JP2005508392A/ja active Pending

Also Published As

Similar Documents

Legal Events