Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing
Patent
1995-05-16
1997-03-04
Mullis, Jeffrey C.
Organic compounds -- part of the class 532-570 series
Organic compounds
Oxygen containing
C07C 4311, C11D 172
Patent
active
056081189
DESCRIPTION:
BRIEF SUMMARY
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to an alkoxylate of 2-propyl heptanol. The alkoxylate exhibits high detergent power on textile materials and low foaming compared with similar compounds having a hydrophobic group of approximately the same size and approximately the same HLB-value. The alkoxylate may advantageously be used as a surface-active component in detergent compositions for textile materials.
2. Description of the Related Art
It has long been known to alkoxylate alcohols for obtaining non-ionic surface-active compounds. These compounds have been used in detergent compositions because of their wetting and dispersing properties. In a number of applications, alkoxylates of C.sub.8-11 alcohols have however been found to be too high-foaming and/or not to have the desired detergent power. For example, ethoxylates based on branched C.sub.8 alcohols often exhibit acceptable foaming but too low a detergent power, whereas ethoxylates based on straight or branched alcohols having a larger hydrocarbon chain often show an acceptable surface activity but too high foaming. Thus, there is a need for new alkylene oxide adducts with an improved ratio of foaming to detergent power.
SUMMARY OF THE INVENTION
It has now been found that an alkoxylate based on 2-propyl heptanol has good detergent and wetting properties as well as low foaming as compared with other alcohols having substantially the same chain length. In addition, it has been found that the alkoxylate is easily degradable and has a surprisingly low biotoxicity. In tests, no skin-irritant effect has been noted.
The alkoxylate according to the invention can be illustrated by the formula O).sub.p H (I) is 1-6. Preferably, p is 2-8 and r is 1-4. In these compounds, the hydrophobic properties of the hydrocarbon chain have been enhanced by adding hydrophobic alkyleneoxy groups closest to the alcohol. The compounds have a good detergent power on textile materials while at the same time showing slightly lower foaming in relation to compounds having a hydrophobic group of approximately the same hydrophobicity and approximately the same HLB-value.
The alkoxylates according to the invention described above can be prepared by adding in a conventional manner in the presence of a conventional alkali catalyst, such as potassium hydroxide or sodium hydroxide, the above-mentioned amounts of alkylene oxide to 2-propyl heptanol, which is a so-called Guebert alcohol. According to a preferred mode of execution, the addition of ethylene oxide is performed using a conventional catalyst which gives a narrower distribution of added ethylene oxide than any alkali catalyst, such as NaOH or KOH. Thus prepared alkoxylates according to the invention have very low foaming. Examples of conventional catalysts giving a narrow distribution of added alkylene oxide are Ca(OH).sub.2, Ba(OH).sub.2, Sr(OH).sub.2 and hydrotalcite. The reaction is preferably conducted in the absence of free water to reduce the amount of by-products and usually at a temperature of 70.degree.-180.degree. C.
Textile-cleaning compositions including the alkoxylate according to the invention may also contain other surface-active compounds, such as anionic ones. Examples hereof are alkyl sulphate, alkyl ether sulphate, alkyl benzene sulphonate, .alpha.-olefin sulphonate and alkyl glyceryl sulphonate. Other commonly occurring components solubilizing additives, complexing agents and/or pH-adjusting agents, enzymes, bactericides and perfumes. The compositions are usually aqueous and in the form of emulsions, microemulsions or solutions.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The invention will be further illustrated by the following Examples.
EXAMPLE 1
An alkoxylate according to the invention are prepared by alkoxylating 2-propyl heptanol with the amounts of alkylene oxide appearing from the Table below in the presence of potassium hydroxide as catalyst. For reference purposes, two alkoxylates were prepared using a C.sub.9-11 alcohol (Dobanol 91 Shell) as hydropho
REFERENCES:
patent: 2508036 (1950-03-01), Kosmin
patent: 3340309 (1967-09-01), Weipert et al.
patent: 3567784 (1971-03-01), Tsatsos et al.
patent: 3862243 (1975-01-01), Bellos
Bergstr om Karin
Dahlgren Lennart
Berol Nobel AB
Mullis Jeffrey C.
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