CA1177586A - Method for controlling the growth of legionnaires disease bacteria in aqueous systems - Google Patents

Method for controlling the growth of legionnaires disease bacteria in aqueous systems

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Publication number
CA1177586A
CA1177586A CA000412155A CA412155A CA1177586A CA 1177586 A CA1177586 A CA 1177586A CA 000412155 A CA000412155 A CA 000412155A CA 412155 A CA412155 A CA 412155A CA 1177586 A CA1177586 A CA 1177586A
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CA
Canada
Prior art keywords
growth
ester
bacteria
systems
methanethiol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA000412155A
Other languages
French (fr)
Inventor
Oscar W. May
John D. Pera
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Buckman Laboratories International Inc
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Buckman Laboratories International Inc
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Classifications

    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/50Treatment of water, waste water, or sewage by addition or application of a germicide or by oligodynamic treatment
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W10/00Technologies for wastewater treatment
    • Y02W10/30Wastewater or sewage treatment systems using renewable energies
    • Y02W10/37Wastewater or sewage treatment systems using renewable energies using solar energy

Abstract

(109) METHOD FOR CONTROLLING THE GROWTH
OF LEGIONNAIRES DISEASE BACTERIA IN AQUEOUS SYSTEMS
Abstract of the Disclosure The 2-hydroxyethyl and 2-hydroxypropyl esters of methanethiolsulfonic acid used either alone or in combination are highly effective in controlling the growth of Legionella pneumophila bacteria in aqueous systems.

Description

BACRGROU~D OF l~E INVENTION

1. Field of the Invention This invention relates to the use of certain hydroxy-substituted esters of thiolsulfonic acids to control the growth in aqueou~ systems f ~
pneumophila, the causative bacterium for Legionnaires Dlsease. More particu-larly, the compounds 2~hydroxyethyl methanethiolsulfonate and 2-hydroxypropyl methanethiolsulfonate are useful as bactericides to inhibit the growth of Legionella Pneumophila in eommercial and industrial cooling water systems, cooling towers, evaporative condensers, air-washing systems, and other aqueous systems in which this pathogenic organism might grow.
2. Description of the Prior Art ~egionnaires Disease is a serious and sometimes fatal pneumonia-like respiratory illness. The causative organlsm for this disease was identified after an outbreak of the disease among the people ~ho attended the July 1976 American Legion Convention at the Bellevue-Stratford Hotel in Philadelphia.
; This epidemic resulted in the deaths of 29 of the 182 people who became ill.
After the 1976 epidemic among the Legionnaires who went to Philadelphia, the I U.S. Public Health Service Center for Disease Control (CDC)~ Atlanta, Georgia,initiated an intensive effort to determine the cause of this respiratory !: .
i ~ .

;l ~
.
_ , ..
~ -~

(109~ ~
1 1:L77~

illness, which has since become known as "Legionnaires Disease." Subsequently,¦
the CDC identified the causative organism as a gram-negative bacterium to which they gave the name Legioneila pneumophila. Later investigations by the ji CDC showed that L. pneumophila ~as not new but could be connected to lllnesses 'I that occurred as far back as the late 1940s. For a review of the epidemiologyof this disease, see Eickhoff, "Epidemiology of Legionnaires' Disease," Ann.
I Inter. Med., Vol. 90, pp. 499-502 (1979).
i In the course of the CDC investigations, L. pneumophila was recovered - ~' from the water ln cooling towers and evaporative condensers of air-conditioning;
~ or cooling water systems of buildings or insta11ations associated with out-breaks of Legionnaires Disease. See, for eYample, Eickhoff in the work cited in the foregoing. The epidemiological data indicated that infection may have been the result of inhaling aerosols of contaminated water generated from these sources. ~lthough the exact route of infection has not yet been defi-nitely confirmed, the CDC deems it prudent to take measures to control or prevent the growth of this pathogenic organism in the water in cooling water systems, cooling towers, evaporative condensers, air-washing systems, and other aqueous systems that might generate aerosols wh~ch may accidentally be inhaled by people in the vicinity of these systems.
It is well-known that bacteria and other microorganisms grow in cooling towers and other aqueous systems, causing slime formation, fouling of equip-ment, corrosion, odors, and other problems. Therefore it,is customary to use chemical treatments or other techniques in order to control the growth of these troublesome organisms. However, such control procedures have not usually been designed to completely eradicate the organisms but only to keep the microbial growth at a tolerable level where slime and other prpblems are mlnimal. ~n the other hand, in the case of pathogenic organisms like L.
pneumophila, it is desirable to have treatment chemicals and ~ethods that can completely eradicate ~hese organisms and still be economically feasible to apply and safe to use.

.

l' (lOg) I 1~17758~
~, i 'I Since it first became known that Legionnaires Disease was associated with I the presence of L. pneumophila in cooling water systems and other aqueous i~' systems that might generate ~erosols, studies have been made to determine the 1 efficacy of various commercial microbicides commonly used to control other 1l microorganisms in wa~er systems of these types. However, while these products j have generally been adequate for the de~ree of control required for the ¦l troublesome but usually nonpathogenic organisms that cause slime and operating I
problems, most of those tested cannot provide, at safe and economical use ~ rates, the degree of control required to eliminate L. pneumophila as a hazard in ~ater. Por most of the commonly used products, the concentration of chemical required to completely eradicate L. Pneumophila in reasonable contact times has been several times that required to control other organisms, and the ; cost of treatment at these concentrations has been economically prohibitive.
Other products that could inhibit the growth of this organism at reasonable lS concentrations have had other disadvantages such as relatively high toxicities to fish and other aquatic organisms or severe foaming tendencies. These latter properties make them hazardous to ~he enYironment or cause problems in operating the cooling systems.
For example, the product poly~oxyethylene (dimethyliminio) ethylene ~dimethyliminio) ethylene dichloride] is useful for controlling the growth of algae and bacteria in industrial water systems. See, for example, Pera et al., U.S. Pat. No. 3,771,989, ~here it is reported that 2.0 parts per million of this microbicide completely inhibited the growth of several algal and cyanobacterial species commonly encountere~ in cooling water systems. How-ever, it required 120 parts per million of this microbicide to ob~ain complete inhibition or complete kill of L. pneumophila in standar~ in vitro tests ~ith 2 hours contact time. See Hollis et al., "Resistance of Legionella pne_ ophila to Microbicides," Dev. Ind. Microbiol., Vol. 21, pp. 265-271 (1980).
Halogenated amides such as 2,2-dibromo-3-nitrilopropionamide ~DBNPA) are also useful as antimicrobials in cooling water and other aqueous systems.

(1~9~ , 1 ~ 17~8~

See, for example, Wolf, U.S. Pat. No. 3,6479610, and Wolf et al., "2,2-Dibromo-
3-nitrilopropionamide, a Compound with Slimicidal Activity," Appl. Microbiol., Vol. 24, No. 4, pp. 581-584 (1972). DBNPA has demonstrated a higher degree of lieffectiveness than many other microbicides in inhibiting the growth of L.
l pneumophila, slnce it gave a complete kill with 4 parts per million of the compound with 2 hours contact time. See Hollis e~ al. in the ~ork cited in l the foregoing. ~owever, the cost of this compound, which i8 currently manu-¦ factured and sold by The Dow Chemical Co., Midland, Michigan under the trade-t~s ~ ¦ n~es DOW Antimicrobial 72B7 (20% active DBNPA) and DOW Antimicrobial 8536 (5%
~ active DBNPA), makes lts use costly even at this concentration. In addition, this compound like many others used for cooling wa~er treatment has a rela-tively high degree of toxicity to fish.
It has been demonstrated that L. pneumo~hila is hi~hly susceptible to free chlorine. See, for example, Skaliy et al., "Laboratory Studies of Disinfectants Against Legionella pneumophila," Appl. Envir. Microbiol., Vol.
40, No. 4, pp. 697-700 (1980). These workers found that 3.3 parts per million chlorine from calcium hypochlorite gave a 100% kill of L. pneumophila.
However, as they pointed out, chlorine is especially unstable in the presence of or~anic matter, and its effects may rapidly be neutralized because of this.
To get the levels of free chlorine necessary to inhibit L. pneumophila under actual use conditions, excessive amounts of calcium hypochlorite would be required, which would result in a severely corrosive situation as ~ar as the materials of construction used in the coolins water system are concerned.
Also effluents with high chlorine residuals could be harmful to the environment.Another microbicide that is reported to be effective in controlling L.
pneumophlla i6 the combination of N-alkyl dimethyl benzyl ammonium chloride (12.5%) and bis(tri-n-butyltin) oxide (2.25%). See, for example, Grace et al.
"Susceptibility of Leglonella pneumophila to Three Cooling Tower Microbicides,"
Appl. Environ. Microbiol., Vol. 41, No. 1, pp. 233-236 (1981), where it is reported tha~ 2 parts per million of this combination provides a complete kill , :`

' (109) l ' I' . ........................................................ I
Il 1 17~8~ l' 'of L. Pneumophlla in an aqueous medium with a 3-hour contact time. Quaternary , am,monium compounds of this type, however, are ~urface active and cause fsam ; I problems in recirculating cooling water systems as well as in many other Illaqueous systems. Moreover, quaternary ammonium compounds generally have a , high toxicity to fish, and heavy metal compounds such as the organlc tin i!
'compound in this combination are not always acceptable-ln effluents going into ' lakes, streams, or other public waters.
- 1 Grace et al. in the work cited in the foregoing also tested another compound that is widely used as a cooling tower biocide, that is, methylene bis(thiocyanate). They found that the minimum lethal concentration of this comp~und against L. pneumophila was 62 parts per million at a 3-hour contact time, which makes the use of this compound economically prohibitive for the control of this organism.
In addition to the disadvantages previously outlined for prior art micro-bicides, these products also all have relatively high degrees of toxicity to fish. For example, DBNPA, which, as discussed in the foregoing9 shows rela-tively good effectiveness in inhibiting the growth of L. ~ , has 96-hour LC~o values in rainbow trout and bluegill sunfish in the range of 0.9 to 1.8 parts per million of the compound, according to the "Technical Handbook for DOW Antimicrobial 7287 and DOW Antimicrobial 8536" published by The Dow Chemical Co. (1980). This means that concentrations of the compound in this range cause a 50% kill of these fish species with a 96-hour exposure in static fish toxicity tests. Of course, since this compound is rapidly degraded and is not persistent in aqueous systems, it generally causes no fish-kill problems in actual use. However, where cooling tower water effluents flow, for example, directly into fish bearing lakes or streams without golng through a waste treatment system, it would be possible for fish kills to occurl especially ~here this microbicide or others with similarly high fish toxicities must be used in the higher concentratioDs required for the control of L. pneumophila.
~0 It is, therefore, an object of the present inventiun to provide a method ~1~9) li , 1 1~7~8~
l!
I of controlling the growth of L. pneumophila in aqueous ~ystems that obviates the disadvantages of the prior art metbods. This and oth~r objects, features, and advantages of the invention will become apparent as the description l proceeds.
' Summary of the Invention ¦, To the accomplishment of the foregoing and related ends, this invention Il then comprises the features hereinafter fully described and particularly ! pointed out in the claims, the following description setting forth in detail certain illustrative embodiments of the $nvention, these beln~ indicative, however, of but a few of the various ways in which the principles of this invention may be employed.
In brief, we have discovered that the foregoing objects and advantages are attained by employing as a bactericide 2-hydroxyethyl methanethiolsulfonate (HEMTS) or 2-hydroxypropyl methanethiolsulfonate (HPMTS), alone or in combi-nation with each other or with other microbicides. When these compounds are used to treat aqueous systems, the biocidal amount providing complete inhibi-tion (100% kill) of Legionella pneumophila bacteria is much lower than that of other microbicides used in prior art methods of controlling this organism. In addition, at least one of these two substances has been shown to be relatively nontoxic to fish. Moreover, these compounds are not corrosive to mater-lals of conseruction when used in the low concentrations required for the control of L. pneumophila.
Detailed Description of the Invention The bactericides of this invention are compounds o~ the type that may be described as 2-hydroxyalkyl esters of thiolsulfonic acids. One method for the preparation of such compounds is disclosed by Buckman et al. in U.S. Patent 3,859,322. The method of preparation comprlses reacting an alkali metal salt ¦ of a thiolsulfonic acid in the presence of an organic acid with a 1,2-epoxide.The preferred compounds of the present invention can be prepared sccording to the teachings of this patent by reacting sodium methanethiolsulfonate with ,' (109) i, ~ 1775~

ethylene oxide or propylene oxidc in the presence of acetic acld, These compounds may further be characterized by the names 2-hydroxyethyl methane-~thiolsulfonate and 2-hydroxypropyl methanethiolsulfonate, respectively, which have the following formulas:
O OH
11 1 ;
CH~- S- S - CH2- CHa . 1,,. o ~ 2-~ydroxyethyl methanethiolsulfonate O OH

2-Hydroxypropyl methanethiolsulfonate When these compounds are used to inhibit the growth of Legionella pneumophila accordin~ to the teachings of our invention, suitable quantities vary from 0.1 to 25 parts per million parts of water. Preferred quantities vary from 0.25 to 10 parts per million parts of water. It will be understood, of course, that larger quantities of the compounds may be used with no detri-mental effect, but such larger quanti~ies increase the cost of operation with limited material benefit. Both of these compounds are water-soluble and are compatible with many other water-soluble microbicides co~monly used to treat aqueous systems such as recirculating cooling ~ater systems~ Thus, they can easily be formulated wi~h other compatible bactericides, algicides, or fungi-cides to provide a broad range of microorganism control with a single formu-lated product.
One of these compounds, 2-hydroxypropyl methanethiolsulfonate, has been found to be relatively nontoxic to fish. A solution containing 80 percent of 2-hydroxypropyl methanethiolsulfonate, for example, had a 96-hour LC~o of 78 parts per m~llion in bluegill sunfish and a 96-hour LC~o greater than 56 parts per million in rainbow trout. Such concentrations ar~ much greater than those required to accomplish comple~e inhibition of L. pneumophila. Thus, the use ~109) I :l775 .
of this compound for the treatment of aqueous sy6tems presents ~ery little ~hazard to ~he aquatic environment compared to that presented by other micro-I bicides commonly used to treat ~uch systems.
Il In order to disclose the nature of the present invention still more clearly, the following illustrative examples will be given. It is understood, however, that the invention is not to be limited to the specific conditions or details set forth in these examples, except insofar as such limitations are '~pecified in the appended claims.

The effecti~eness of the compound 2-hydroxyethyl methanethiolsulfonate in inhibiting the growth of the bacterium Legionella pneumophila ~as tested by the following testing protocol. Le~ionella pneumoPhila (Philadelphia strain, Serogroup 1), provided by the Center for Disease Control, Atlanta, Georgia, to Methodist Hospita~, Memphis, Tennessee, where this work W2S performed, was grown initially and maintained on Mueller-Hinton Agar supplemented by 1%
IsoVitaleX (BBL) and 1% hemoglobin, and subsequently on FG sgar at 35C, pH
6.9, under 2.5% CO2. For the preparation of an inoculum for testing, the organism was grown on FG agar plates for 72 hours and resuspended in 0.85%
saline in distilled water at pH 6.9. The concentration of cells was adjusted to 6 x 10~/uL. A dilute stock solution of 2-hydroxyethyl methane thiolsulfo-nate was prepared fresh immediately before testing by weighing a sufficient quantity to prepare a stock solution in sterile 0.85% saline containing 1.000 mg/mL of the compound. The stock solution was added to sterile 0.85% saline so that when 1.0 mL of the inoculum was added to the contact bottle, it would contain a total of 100 mL. Tests were run with con~act times of 2 and 8 hours at a contact temperature of 24C. Then 4-mm loops from each contact bottle were streaked on FG agar plates, which were then incubated at 35C for 10 days under 2.5% C02. At the end of the lncubation perlod, the number of colonies on ~ach plate was counted. The results are summarized ~n Table 1 with the following key for interpreting the results:

'' ~109) I , , ~' ~ 17~8~; 1
4 = More than 300 colonies on recovery plate 3 = 151 to 300 c~lonies j 2 - 51 to 150 colonies ~I 1 = l to 50 colonies
5 1, 0 ~ No growth ! ! TABLE 1 I Inhibition of L. pneumophila by 2-hydroxyethyl methanethiolsulfonate ¦, Concentration, Contact Time ~ i parts per l~ million 2 Hours 8 Hours 0.25 0.5 0 0 1.0 0 o 2.0 0 o These results` show that addition of only 0.25 part per million 2-hydroxy-ethyl methanethiolsulfonate provided a high degree of inhibition of L. pneumo-phila, and 0.5 part per million of the compound gave complete inhibition even with only 2 hours contact time.
EXA~LE 2 The-compound 2-hydroxypropyl methanethiolsulfonate was evaluated for its efficacy in controlling the growth of L. pneumophila by use of the same proce-dure described in Example 1. The results are shown in Table 2. The key for the interpretation of the degree of inhibition is the same as used for Table 1.

25 Inhibition of L. pneumoDhila by 2-hydroxypropyl methanethiolsulfonate Concentration, Contact Time parts per million 2 Hours 8 Hours 0.5 1 0 l.o o o 2.0
6.0 o o _ g _ ll 1 ~ 7 7 5 ~ og) !
l~ The results of these tests show that a concentration of only 0.5 part per `million 2-hydroxypropyl methanethiolsulfonate provided a high de~ree of inhi-bition of the growth of L. pneumophila with just 2 hours contact ~ime and 1, complete inhibition ~ith 8 hours of ~ontact time~ A c~ncentration of 1.0 part l per million 2-hydroxypropyl methanethiolsulfonate provlded a 100% kill of L.
j'pneumophila with a contact time of only 2 hours.
¦I EXAMPLE 3 1 The following compounds or mixtures of compounds that are commonly used , .
in cooling water treatment were evaluated by the same procedure described in Example 1. The minimum inhibitory concentrations of each required to kill Le~ionella pneumophila with only 2 hours contact time are shown in Table 3.
The results for the compounds of this invention, 2-hydroxyethyl methanethiol-sulfonate (HEMTS) nd 2-hydroxypropyl methanethiolsulfonate (HPMTS), are included in the same table for comparison purposes.
Microbicide A: Potassium N-methyldithiocarbamate, 14.7 parts Disodi~ cyanodithioimidocarbonate, 20.3 parts Microbicide B: Potassium dimethyldithiocarbamate - Microbicide C: 2,2-Dibromo-3-nitrilopropionamide Microbicide D: Polyloxyethylene (dimethyliminio) ethylene (dimethyliminio) ethylene dichloride]

Minimum inhibitory concentrations of cooling-water microbicides required to kill L. ~neumophila in 2 hours contact time Microbicide Minimum Inhibitory C_ncentration Parts per million A 70.
~5 B 100.
C 4.0 D 120.
HE~TS 0.5 HPMTS 1.0 These tests clearly indicate the great superiority of 2-hydroxypropyl '~

(109) ¦! ~1 7758B
' I .
methanethlolsulfonate and 2-hydroxyethyl methanPthiolsulf~nate over other j commonly used microbicides in controlling the growth of Legionella pneumo-i; phila in aqueous media.
,, While particular embodiments of the in~ention have been described, it I will be understood, of course, that the invention is not limited thereto since,~ ~any modifications may be made and it is, therefore, contemplated to cover by~i the appended claims any such modifications as fall within the true spirit and I scope ~f the invention.
~ The invention having thus been described, what is claimed and desired to be secured by Letters Patent is:

, . , .

~.

- 11 ~

Claims (12)

(109) THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A method of inhibiting the growth and proliferation of Legionella pneumo-phila bacteria in an aqueous system which comprises contacting said bacteria with an ester selected from the group consisting of 2-hydroxy-ethyl methanethiolsulfonate and 2-hydroxypropyl methanethiolsulfonate in an amount sufficient to inhibit the growth and proliferation of said bacteria.
2. The method of claim 1 wherein the ester is 2-hydroxyethyl methanethiol-sulfonate.
3. The method of claim 1 wherein the ester is 2-hydroxypropyl methanethiol-sulfonate.
4. A method of inhibiting the growth and proliferation of Legionella pneumo-phila bacteria in commercial and industrial cooling water systems which comprises adding to the water in said systems an ester as defined in claim 1 in an amount sufficient to inhibit the growth and proliferation of said bacteria.
5. The method of claim 4 wherein the ester is 2-hydroxyethyl methanethiol-sulfonate.
6. The method of claim 4 wherein the ester is 2-hydroxypropyl methanethiol-sulfonate.
7. A method of inhibiting the growth and proliferation of Legionella pneumo-phila bacteria in air-washing systems which comprises adding to the water in said systems an ester as defined in claim 1 in an amount sufficient to inhibit the growth and proliferation of said bacteria.
8. The method of claim 7 wherein the ester is 2-hydroxyethyl methanethiol-sulfonate.
9. The method of claim 7 wherein the ester is 2-hydroxypropyl methanethiol-sulfonate.

(109)
10. A method of inhibiting the growth and proliferation of Legionella pneumo-phila bacteria in evaporative condensers of cooling and air-conditioning systems which comprises adding to the water in said systems an ester as defined in claim 1 in an amount sufficient to inhibit the growth and proliferation of said bacteria.
11. The method of claim 10 wherein the ester is 2-hydroxyethyl methanethiol-sulfonate.
12. The method of claim 10 wherein the ester is 2-hydroxypropyl methanethiol-sulfonate.
CA000412155A 1982-08-09 1982-09-24 Method for controlling the growth of legionnaires disease bacteria in aqueous systems Expired CA1177586A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US40659682A 1982-08-09 1982-08-09
US406,596 1982-08-09

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JP (1) JPS5884089A (en)
AR (1) AR228104A1 (en)
AT (1) AT381836B (en)
AU (1) AU8877382A (en)
BE (1) BE894714A (en)
BR (1) BR8206541A (en)
CA (1) CA1177586A (en)
DE (1) DE3234940A1 (en)
FI (1) FI823296L (en)
FR (1) FR2531314A1 (en)
GB (1) GB2125024A (en)
IT (1) IT1157230B (en)
NL (1) NL8203805A (en)
NO (1) NO823350L (en)
SE (1) SE8205446L (en)
ZA (1) ZA827118B (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3639604A (en) * 1968-03-08 1972-02-01 Buckman Labor Inc Compositions containing an organic thiocyanate and 2-hydroxy alkyl esters of organic thiosulfonic acids and processes of utilizing th same
US3859322A (en) * 1969-09-29 1975-01-07 Buckman Labor Inc Novel hydroxy substituted esters of thiolsulfonic acids and their use as microbicides
NL6919681A (en) * 1969-09-29 1971-03-31

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AR228104A1 (en) 1983-01-14
BE894714A (en) 1983-01-31
BR8206541A (en) 1984-03-20
FR2531314A1 (en) 1984-02-10
IT8249321A0 (en) 1982-10-20
AU8877382A (en) 1984-02-16
NL8203805A (en) 1984-03-01
AT381836B (en) 1986-12-10
JPS5884089A (en) 1983-05-20
NO823350L (en) 1984-02-10
SE8205446D0 (en) 1982-09-23
SE8205446L (en) 1984-02-10
FI823296L (en) 1984-02-10
FI823296A0 (en) 1982-09-24
GB2125024A (en) 1984-02-29
IT1157230B (en) 1987-02-11
ATA383482A (en) 1986-05-15
DE3234940A1 (en) 1984-02-09
ZA827118B (en) 1983-08-31
JPH0210714B2 (en) 1990-03-09

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