Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing
Reexamination Certificate
2000-09-06
2003-01-07
Sergent, Rabon (Department: 1711)
Organic compounds -- part of the class 532-570 series
Organic compounds
Oxygen containing
C528S486000, C528S487000, C528S490000, C528S499000, C568S620000
Reexamination Certificate
active
06504062
ABSTRACT:
The present invention relates to a process for the preparation of substantially odour-lean polyether polyols from a polyether polyol starting product, which has been obtained by polymerizing at least one alkylene oxide in the presence of a suitable polymerization catalyst.
Methods for preparing polyether polyols, also sometimes referred to as poly(alkylene oxide) polyols, are well known in the art. Typically, such methods involve reacting a starting compound having a plurality of active hydrogen atoms with one or more alkylene oxides, such as ethylene oxide, propylene oxide, butylene oxide or mixtures of two or more of these. Suitable starting compounds include polyfunctional alcohols, generally containing 2 to 6 hydroxyl groups. Examples of such alcohols are glycol, such as diethylene glycol, dipropylene glycol, glycerol, di- and polyglycerols, pentaerythritol, trimethylolpropane, triethanolamine, sorbitol, mannitol, etc. Usually a strong base like potassium hydroxide is used as a catalyst in this type of reaction.
The polyether polyols obtained from the type of process described above as well as polyurethane foams manufactured from these polyether polyols usually suffer from a rather unpleasant odour. Although this odour does not adversely affect the chemical properties of the polyether polyol in any way, it would be desirable when polyether polyols could be provided not having such unpleasant odour. Since consumers have become more and more critical over the years, there is an increasing need for providing odour-lean products. Particularly in those applications where people come in close contact with polyurethane foams (e.g. in mattresses and pillows), the odour of the foam could be a problem. Since relatively large amounts of polyols are used in the manufacture of flexible polyurethane foams, it could be expected that at least some of the unpleasant odour of the polyurethanes stems from the polyols.
The present invention therefore aims to provide a method for reducing the odour of polyether polyols manufactured as alkylene adducts of polyfunctional alcohols, substantially as described above.
Accordingly, the present invention relates to a process for the preparation of an odour-lean polyether polyol from an unneutralised polyether polyol starting product which is obtained by reacting a starting compound having a plurality of active hydrogen atoms with one or more alkylene oxides, which process consists of the steps of:
(a) contacting the unneutralised polyether polyol product with an excess of an acid having a pKa of less than 5, at a temperature of 80 to 130° C.,
(b) contacting the reaction mixture with water at a temperature of 80 to 130° C., and
(c) recovering the odour-lean polyether polyol,
wherein the acid-is added in step (a) in such an excess so as to impart sufficient acidity to the reaction medium to allow the hydrolysis-reactions in steps (a) and (b) to proceed.
Without wishing to be bound by any particular theory it is believed that components which are for a large part responsible for the short term chemical odour of polyether polyols are aldehydes, present as such or in a latent form as alkenyl ether endgroups of the polyether polyol, while the long term musty odour of polyurethane foams is due to ether-like compounds -presumably cyclic ethers- formed during the polyol manufacturing, i.e. during the alkoxylation (so normally under basic conditions). Examples of such cyclic ethers could be 2-ethyl-4,7-dimethyl-1,3,6-trioxacyclo-octane and 2,5,8-trimethyl-1,4,7-trioxacyclononane. In the case of propylene oxide, for instance, the short term chemical odour is considered to be caused by propionaldehyde and propenylether end groups of the polyether polyol. For the sake of convenience, the odour causing compounds in case propylene oxide is used as the alkylene oxide will be further referred to in this patent application. It will, however, be understood that if other alkylene oxides are used, the odour-causing compounds will vary accordingly.
In step (a) of this process the propenylether end groups are removed from the unneutralised (i.e. the polyol end product as it leaves the reactor prior to working-up) polyether polyol by hydrolysis, thus resulting in propionaldehyde and a hydroxyl end group in the polyether polyol. In subsequent or simultaneous step (b) water is added in order to hydrolyse the cyclic ethers present, e.g. into propionaldehyde and dipropylene glycol. In step (c), finally, the odour-lean polyol is recovered. This recovery suitably involves several treatments, including dewatering and steam or nitrogen stripping to remove the propionaldehyde formed as one of the hydrolysis products in steps (a) and (b), as will be discussed hereinafter.
It is preferred within the context of the present invention that the polyether polyol starting product is obtained by polymerizing propylene oxide and optionally ethylene oxide. Nevertheless, other alkylene oxides may be used as well.
The acid to be used in step (a) of the present process in principle may be any water-soluble acid having a pKa less than 5, preferably of less than 3. The acid may be an organic or mineral acid. Examples of suitable organic acids are para-toluene sulphonic acid and acetic acid. Examples of suitable mineral acids include sulphuric acid, hydrochloric acid, nitric acid and phosphoric acid. It has been found particularly useful to use para-toluene sulphonic acid or phosphoric acid (H
3
PO
4
). A combination of both acids may also be suitably used. Para-toluene sulphonic acid was found to be particularly suitable when steps (a) and (b) are carried out simultaneously, whereas phosphoric acid is advantageously used when carrying out steps (a) and (b) successively.
If step (a) is carried out before step (b), the acid is suitably added in the form of a concentrated solution in water, for instance in a concentration of 50-90%. In addition, further water may also be added. The acid should be used in such amount so as to impart sufficient acidity to the reaction medium to allow the hydrolysis reactions in steps (a) and (b) to proceed. In practice the term “excess” in relation to the acid added in step (a) refers to such amount of acid that the amount of free acid will be between 0.001 and 0.5 mole acid per kg polyether polyol, preferably between 0.005 and 0.2 mole acid per kg polyether polyol. The expression “free acid” as used herein refers to the acid which has not reacted with any component present in the reaction medium. For instance, if unneutralised polyether polyol is used as the starting material in step (a) of the present process, potassium ions from the KOH initiator will be present in the polyol. The anion of the acid added will then first react with the potassium ions. Only after the potassium ions have been “neutralised”, any acid added will be present as free acid.
The conditions under which the hydrolysis in step (a) is carried out may vary within wide limits. In general, the hydrolysis conditions can be varied within limits known by the person skilled in the art. It has been found particularly advantageous to carry out step (a) at a temperature of 80 to 130° C., preferably 100 to 120° C., at any arbitrary pressure ranging from essentially 0 bar up to 15 bar, preferably from 0.1 to 5 bar. If step (a) is carried out in vacuo, then the vacuum should be broken once step (a) is finished. The time necessary to carry out the reaction in step (a) may also vary within wide limits. Depending on the amount of excess acid used and the temperatures applied, the length of step (a) if carried out before step (b) will normally vary from several minutes to several hours, suitably from 10 minutes to 5 hours. It is preferred that while step (a) is carried out continuous mixing of the components takes place to ensure optimum contact between the reactants.
In step (b) of the present process water is added to the reaction mixture. The water is necessary to hydrolyse the cyclic ethers. Water can be added either in excess or in an equivalent or even lower amount. The term “excess” as used in this connecti
Brons Henricus Maria Johannes
De Vos Hans
Sergent Rabon
Shell Oil Company
Tsang Y. Grace
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