AU711548B2

AU711548B2 - Acrolein-releasing copolymers

Info

Publication number: AU711548B2
Application number: AU14844/97A
Authority: AU
Inventors: Hans-Peter Krimmer; Franz-Rudolf Kunz; Martin Trageser; Peter Werle
Original assignee: Degussa GmbH
Current assignee: Evonik Operations GmbH
Priority date: 1996-02-22
Filing date: 1997-02-21
Publication date: 1999-10-14
Anticipated expiration: 2017-02-21
Also published as: JP3311629B2; ATE201218T1; EP0792895B1; ES2157025T3; EP0792895A1; CA2198158C; AU1484497A; CA2198158A1; JPH09235340A; SG72728A1

Abstract

Novel acrolein (AL)-releasing copolymers (I), prepared from AL and one or more polyhydric alcohols, release monomeric AL in aqueous media (preferably with pH value above 7) and thus provide long-lasting activity against microorganisms.

Description

S F Ref: 368384

AUSTRALIA

PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT

ORIGINAL

0

OW*.

*500 a 4.

A 4 a.

Name and Address of Applicant: Actual Inventor(s): Address for Service: Invention Title: Degussa Aktiengesellschaft Welssfrauenstrasse 9 D-60311 Frankfurt

GERMANY

Peter Werle, Hans-Peter Krimmer, Martin Trageser and Franz-Rudolf Kunz Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Acrolein-releasing copolymers The following statement is a full description of this invention, including the best method of performing it known to me/us:- 5845

I

950098 AC/i.P.

Acrolein-releasing copolymers The invention relates to acrolein-releasing copolymers, the process for the preparation thereof, and to their use as a biocide.

It is known to use monomeric acrolein (2-propenal) as a very effective biocide in the treatment of water channels in order to suppress unwanted algae and plant growth.

10 Similarly, it may be used to combat sulphate-reducing 99*o bacteria in petroleum exploration.

oo* Until now, no other fields of application have been opened up for the biocidal action of monomeric acrolein in view of 15 its high reactivity. Investigations have shown that acrolein is subject to rapid changes in aqueous systems such as, for example, hydration or polymerisation, depending on the pH (see Figure Consequently, it has also been impossible hitherto to use acrolein as a 20 preservative with a prolonged effect. Due to its tendency to polymerise spontaneously and possibly in an explosive manner if treated incorrectly, it can be handled only by taking special safety measures. It has a strong irritant effect on the respiratory organs and the eyes. Even in the stabilised form, acrolein may be stored only for a limited period.

It is known to use copolymers of acrolein with formaldehyde, which were prepared by condensation of acrolein and formaldehyde in a molar ratio between 1 1 950098 AC/i.P.

2 and 1 10 in the presence of a basic catalyst, as biocides for aqueous systems (DE-B 32 05 484). The known copolymers of acrolein with formaldehyde have the disadvantage that they contain about 15% of free, unreacted formaldehyde.

It is known to use homopolymers of acrolein as biocides (EP-A 0 339 044). Polymerisation is carried out predominantly with radicals. The polyaldehyde structures forming during this process are said to be vehicles of the 10 biocidal action (structural similarity with glutaraldehyde). The formation of free acrolein is not mentioned. The homopolymers of acrolein produced by radical polymerisation have the disadvantage of being insoluble in organic media or in water and, in the form of 15 an aqueous suspension, exhibit only a very low biological activity.

The preparation of polyacroleins described in German patent application P 44 04 404 is problematic because the yields 20 from the reaction of acrolein with NaOH in the aqueous system are only 75 80% of polymer material. Mother liquor and wash water which contain organic substances and must therefore be disposed of at great expense are thus obtained.- Recycling is not possible because of the negative effect on the polymer properties. These polymers, too, are virtually insoluble in water.

Acrolein polymers or copolymers which act as an acrolein depot have not been described hitherto. The monomeric acrolein released continuously in small quantities under 950098 AC/i.P.

3 suitable conditions was said to act as a biocidal active Ssubstance which is formed repeatedly from the polymer or copolymer over a long period.

The object of the present invention was to develop such products and to show a technically simple process for the preparation thereof.

The object was, therefore, to prepare acrolein polymers which have a good biocidal activity and are easy to handle.

*0 :i The present invention provides acrolein-releasing *0* S" copolymers prepared from acrolein and one or more polyhydric alcohols, which are characterised by: Release of monomeric acrolein in aqueous systems, preferably with a pH of >7 and hence a prolonged effect on microorganisms.

The invention also provides a process for the preparation of acrolein-releasing copolymers, which is characterised in that acrolein is added to the polymerisable reaction medium in which the catalyst required for copolymerisation is dissolved, and the temperature of the reaction medium is not allowed to rise above 50 0 C. The ratio of acrolein to catalyst may lie in the range from 1 0.001 to 1 0.05.

The post-agitation time to be maintained after all the acrolein has been introduced may be 0.5 3 h, preferably 1 2 h. If necessary, small residual quantities of 950098 AC/i.P.

4 monomeric acrolein (conversion normally may be removed by applying a vacuum for a short period. The reaction solution is neutralised by the addition of acid.

The invention provides acrolein polymers which are watersoluble or which become water-soluble or water-dispersible in the presence of an emulsifier and which release monomeric acrolein in an aqueous medium, which polymers are characterised in that acrolein is reacted with a polyhydric 10 alcohol to form said polymers and the alcohol used is incorporated at least proportionally in the polymer structure.

The reaction medium is substantially water-free. Both one 15 or more polyhydric alcohols such as ethane 1,2-diol, propane 1,3-diol, propane 1,2-diol, butane 1,4-diol, .glycerol, cyclohexane diols and/or polyethylene glycols may be used as a reaction medium suitable for copolymerisation.

Dihydric alcohols of the aliphatic series may be used in 20 preference. The reaction in ethylene glycol or propane 1,2-diol is particularly preferred.

The catalyst used may be compounds from the group comprising alkali- and/or alkaline earth hydrogen sulphites, basic inorganic compounds and/or basic organic compounds. The basic catalyst used may be alkali hydroxides, such as e.g. sodium hydroxide, alkali alcoholates or organic bases such as, for example, piperidine, guanidine, piperazine etc.

950098 AC/i.P.

Surprisingly, copolymerisation may also be carried out in a weakly acid medium with hydrogen sulphite salts, MeHSO 3 (M=Li, Na, K, NH 4 Rb, Cs) of alkali- and/or alkaline earth metals as catalyst. Completely colourless polymers are obtained in this case.

The colourless or pale yellow-coloured viscous solutions formed by the reaction contain virtually no free acrolein.

They are copolymers of acrolein with the solvent.

Using GPC-MALLS analysis (Multi Angle Laser Light Scattering (MALLS), Wyatt MiniDAWN and RI detection after chromatography with tetrahydrofuran on an SDV-5 1 -100A phase), the average molecular weights determined for the 15 products are 3000 6000 g/mol in a range from 1000 10000 g/mol (see Example The alcohol and water contents may be adjusted in a variable manner by controlling the reaction, and amount to approx. 40 50% in total.

20 In the case of the copolymer of propylene 1,2-glycol and acrolein, double bonds of the R-CH=CH 2 type and aldehyde functions are detected in the 13 C-NMR spectrum (125 MHz, DMSO-d 6 /303 K) as a broad signal on a very small scale: 8117

(=CH

2 6136 and 6200 In addition, the spectra contain the following structural data: 616.7/20.1

(-CH

3 863-77 (OCH 2 and OCH groups) and 690-100 (acetal) The H,C-COSY correlation experiment shows practically no signal intensity for aliphatic CH groups (weak signal at 950098 AC/i.P.

6 843) of the kind expected for a polyacrolein which is polymerised via the double bond.

On the whole, the spectroscopic data are consistent with a polyacrolein having the following structure (y x 1): *X "V

OH

15 The copolymer obtained has only limited miscibility with water (about In the case of relatively high dilutions, milky emulsions are formed from which a part of the copolymer separates on standing as a greasy, viscous liquid. This behaviour makes it difficult to handle the .i 20 copolymer according to the invention because, for example, containers cannot be cleaned simply by rinsing with water.

Surprisingly, it was found that complete miscibility of the copolymer in water is obtained by adding an emulsifier, and, in particular, that even high dilutions do not exhibit any turbidity or Tyndall effects whatsoever, behaving instead as physically true solutions. The emulsifier is usually used in quantities of 0.5 preferably 0.75 based on the total weight of the copolymer solution.

950098 AC/i.P.

7 The emulsifier used is preferably alkali salts of sulphosuccinic acid esters having the general formula

OR

R-O-C-CH

2 -CH-C with R alkyl; C >6 0 SO3Na 0 The diethylhexyl ester is particularly preferred.

The addition may take place during or after copolymerisation.

The alcohol acrolein ratio may vary widely and is often 15 limited by the ease of handling of the solutions which become highly viscous as the acrolein concentration increases. For ethylene glycol or propane 1,2-diol, weight ratios of up to 1 1, that is, 50 wt.% solutions of polymerised acrolein, may be prepared. Higher S 20 concentrations have only limited free-flow properties. In preference, reactions are carried out with a ratio of polyhydric alcohols to acrolein of about 1 0.4 to 1 0.7. In order to reduce the viscosity of the products, water may be introduced into the system during the addition of acrolein without precipitation of polymeric acrolein occurring.

The acrolein polymers according to the invention are effective preservatives because of their ability to release

I

950098 AC/i.P.

8 acrolein continuously over a long period in aqueous systems, preferably at pH values greater than seven.

The invention also provides a process for the preservation of substances, which is characterised in that the acrolein copolymers according to the invention are added as monomeric acrolein-releasing substances to aqueous systems or aqueous dispersions or suspensions.

10 For example, the following substances may be preserved with o o the acrolein copolymers according to the invention: Plastics dispersions, wall coatings, dye pastes, sealing compounds, distempers, wood preserving paints, adhesive 15 emulsions, skin and leather glues, bone glues, starch glues, casein glues, dextrin adhesives, salted hides, pickling solutions, dry hides, tanning liquors, wet chrome leather, finished leather, spinning baths, wax emulsions, i wax raw materials, textile finishing, textile finishes, 20 paper/board, PVC coating, drilling and cutting oils (diluted), drilling and cutting oils (concentrated), wood preservation, cellulose fibres (to prevent rotting), jointing cement, marine paints, liquid cleaning agents.

The acrolein copolymers according to the invention may be added to the substances in quantities of 0.01 A particularly preferred embodiment of the invention is the copolymer of acrolein and ethylene glycol or propane 1,2diol. Due to its good algicidal effect, the former may also be used to control algae growth in cooling circuits.

950098 AC/i.P.

9 Moreover, it also controls higher water weeds. The activity is based on the fact that the copolymers according to the invention split off acrolein in the aqueous phase.

Cleavage is dependent on the pH of the aqueous solution and on the polyhydric alcohol used. The release of acrolein as a function of time at a pH of 9 is shown by way of the graph in Figure 2.

e 950098 AC/i.P.

Examples Example 1 A charge of 270 ml of ethylene glycol and 2.5 ml of 1 N NaOH is prepared. 237 ml of acrolein are added with cooling at 5 25 0 C (final temperature). Stirring is continued for 1 h at room temperature and the mixture is neutralised with 2.5 ml of 1 N HC1.

Yield: 500 g of an almost colourless, pale yellow viscous liquid. The unreacted ethylene glycol content is 35% (95 ml). 0.025% of free acrolein was found.

15 Example 2 The same procedure as described in Example 1 is followed except that piperazine is used as catalyst. A pale yellow liquid with 0.08% of free acrolein is obtained.

Example 3 A charge of 207 ml of ethylene glycol together with 1.0 g of NaHSO 3 is prepared. 200 ml of acrolein are added at 20 40 0 C. Stirring is continued for 3 h. The copolymer is obtained as a viscous, completely clear solution.

950098 AC/i.P.

11 Example 4 A charge of 725 ml of propylene 1,2-glycol and 10 ml of IN NaOH is prepared in a flask and 610 ml of acrolein are added at 10 0 C with cooling. The mixture is kept in the temperature range of up to 35 0 C and stirring is continued for about 1 h at 40 0 C. The viscous yellow solution is neutralised by the addition of hydrochloric acid. The residual content of unreacted acrolein is about 0.01%.

The microbicidal action of the preparations prepared is determined with the so-called time-kill test (TKT). In this test carried out in accordance with the recommendations of the American Petroleum Institute (API, *nd RP 38 2nd ed., Dec. 1965), the desired quantity of biocide is added to a highly enriched bacterial suspension (bacterial count 106 to 108) and incubated for 24 hours at e. 25 0 C. The suspension is then inactivated and a geometric dilution series to 6 is carried out; 1 ml of each is mixed 20 with 10 ml of nutrient agar on plates and incubated for 48 hours at 37 0 C. The kill rate is determined from the colony count. The biocide concentration is based on the acrolein content.

Evaluation: The arithmetic mean of 2 values (double determination) is formed. The bacterial reduction count Br t per unit of time 950098 AC/i.P.

12 in the TKT (24 hours), also called the evaluation number, is calculated with the equation: Br t log CFU(control) log CFU(D) CFU(control the number of CFU/ml without the action of the preparation (also the O sample) CFU(D) the number of CFU/ml after the action of the preparation.

Reductions of at least 5 log stages must be obtained for a good effect.

S.

S S

S.

S

S 950098 AC/i.P.

.0e* .r a. 0 a Type of bacteria: Pseudomonas aeruginosa ATCC 15442 Test no. Temp. pH Time Conc. Br t oC (ppm) 1 25 6.5 24 100 4.4 1 25 6.5 24 250 >7.2 1 9 24 100 7.2 2 25 6.5 24 250 >7.2 3 25 6.5 24 500 >7.3 Test no. 1 Type of Temp. pH Time cone. Br t bacteria °C (ppm) E. coli 25 6.5 24 100 >7.3 9.0 24 50 >7.3 Staph. aureus 25 6.5 24 50 >7.3 9.0 24 25 >7.3 9.0 24 10 4 The effectiveness of the copolymers according to the invention as preserving agents may be demonstrated convincingly in a preservative loading test.

950098 AC/i.P.

14 Preservative loading test: g of an unpreserved, freshly prepared emulsion paint are introduced into a 100 ml polyethylene beaker. The substances to be tested are then weighed out and dispersed homogeneously. An unpreserved paint sample is used as the control.

The sample beakers are stored in a refrigerated incubator for the remaining period at 25 0 C and 65% relative humidity.

Three days after the addition of the preservatives, the samples are inoculated with 0.5 ml of a bacterial mixture composed of Alcaligenes denitrificans, E. coli, Klebsiella 15 pneumoniae, Proteus mirabilis, Proteus vulgaris, Pseudomonas aeruginosa, Pseudomonas putida, Serratia •o ~marcescens, Staphylococcus aureus and stirred in with a spatula. Inoculation is carried out seven times altogether at weekly intervals. After thorough mixing of the sample 20 beakers, smears are made on CASO agar after 3 and after 7 days. Readings of the smears are taken after three days' incubation at 25 to 30 0 C in the incubator. Negative smears are observed for another two days for safety's sake, and assessed once again.

The growth is assessed according to the following scheme: 0 no bacteria 0 1 up to 10 bacteria/CFU 950098 AC/i.P.

1 2 3 3 -4 4 6 up to 30 bacteria/CFU up to 100 bacteria/CFU up to 250 bacteria/CPU up to 500 bacteria/CPU up to 1000 bacteria/CFU 85% of the smear covered with growth smear completely covered; thick growth 0S~S 0* 0e 0 0004

C

S 0* 0 0* 00 0 000000 0* 0 0* 0 00 CPU colony-forming units 950098 AC/i.P.

Sbbt 9*b*

C.

C. C

C

C. CeeC

C

S.

be..

S C C. C

C

C.

*9#C C C. C

C.

Week/ 1 2 3 4 5 6 7 inoculation Smears 3d 7d 3d 7d 3d 7d 3d 7d 3d 7d 3d 7d 3d 7d conc. 2.7 x 10' 4.2 x 10 3.7 x 10' 4.0 x 10' 4.0 x 10' 4.0 x 10' x CFU/ml Date 14.11.95 21.11.95 28.11.95 05.12.95 12.12.95 19.12.95 03.01.96 O sample 3-4 2 4 4 6 6 6 6 6 6 6 6 6 6 Polymer 0 0 0 0 0 0 0 0 0 0 0 0 0 0 from Example 1 0.05% Polymer 0 0 0 0 0 0 0 0 0 0 0 0 0 0 from Example 4 0.05% Polymer 0 0 0 0 0 0 0 0 0 0 0 0 0 0 from Example 1 0.025% Polymer 0 0-1 0-1 0 0-1 0 0 0 0-1 0 0-1 0 0-1 0 from Example 4 0.025% Polymer 0 0-1 0-1 0 0-1 0 0-1 0 0-1 0 0-1 0 0-1 0 from Example 1 0.01% After 5 months, 6 ppm of free acrolein can be detected by high pressure liquid chromatography in an emulsion paint to which 0.1% has been added.

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950098 AC/i.P.

17 Acrolein cleavage from product according to Example 1 and Example 4 in buffer solutions at pH 9 Solutions used: Example 1: Merck Example 4: 2% polymer in buffer solution pH 9 from 2% polymer in buffer solution pH 9 from Merck es..

900@ 0* o

S*

0S*r 0b 0

S

4*

SS

Table of measured values Residence time Acrolein released Acrolein released (ppm) (ppm) Example 1 Example 4 0 216 2 1416 490 5 2035 680 7 2190 750 24 1773 650 48 1354 500 72 977 462 100 812 404 These values are shown in a graph in Figure 2.

Claims

1. Acrolein-releasing copolymers prepared from acrolein and one or more polyhydric alcohols, characterised by release of monomeric acrolein in aqueous systems, preferably with a pH value of 7 and hence a prolonged effect on microorganisms.

2. Acrolein-releasing copolymers prepared from acrolein and one or more polyhydric alcohols, substantially as hereinbefore described with reference to any one of the examples.

3. A process for the preparation of the acrolein-releasing copolymer according to claim 1, characterised in that acrolein is added to the polymerisable reaction medium in which the catalyst required for copolymerisation is dissolved, and the temperature of the reaction medium is not allowed to rise about

4. A process for the preparation of acrolein-releasing copolymers prepared from acrolein and one or more polyhydric alcohols, substantially as hereinbefore described with reference to any one of the examples. 15

5. The use of the acrolein-releasing copolymer according to claim 1 as acrolein- releasing compounds in water-containing systems for biocidal purposes.

6. A process for preserving substances, characterised in that the acrolein- releasing copolymer according to claim 1 or claim 2 is added to the substances as a biocide. 20 Dated 17 February, 1997 Degussa Aktiengesellschaft Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON **el [n:\libc]01765:MEF