AU615800B2 - Creación de Inventos y Patentes con Inteligencia Artificial

AU615800B2 – Polymeric compounds
– Google Patents

AU615800B2 – Polymeric compounds
– Google Patents
Polymeric compounds

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Publication number
AU615800B2

AU615800B2
AU41719/89A
AU4171989A
AU615800B2
AU 615800 B2
AU615800 B2
AU 615800B2
AU 41719/89 A
AU41719/89 A
AU 41719/89A
AU 4171989 A
AU4171989 A
AU 4171989A
AU 615800 B2
AU615800 B2
AU 615800B2
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AU
Australia
Prior art keywords
formula
compound
weight
aqueous
compounds
Prior art date
1988-09-21
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.)

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Application number
AU41719/89A
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AU4171989A
(en

Inventor
Barry Cook
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

FMC Technologies Ltd

Original Assignee
Ciba Geigy AG
Priority date (The priority date 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 date listed.)
1988-09-21
Filing date
1989-09-21
Publication date
1991-10-10

1989-09-21
Application filed by Ciba Geigy AG
filed
Critical
Ciba Geigy AG

1990-03-29
Publication of AU4171989A
publication
Critical
patent/AU4171989A/en

1991-10-10
Application granted
granted
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1991-10-10
Publication of AU615800B2
publication
Critical
patent/AU615800B2/en

1994-09-15
Assigned to FMC CORPORATION (UK) LIMITED
reassignment
FMC CORPORATION (UK) LIMITED
Alteration of Name(s) in Register under S187
Assignors: CIBA-GEIGY AG

2009-09-21
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Classifications

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS

C08F2/00—Processes of polymerisation

C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation

C—CHEMISTRY; METALLURGY

C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE

C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE

C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents

C02F5/08—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents

C02F5/10—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances

C02F5/14—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances containing phosphorus

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM

C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System

C07F9/02—Phosphorus compounds

C07F9/28—Phosphorus compounds with one or more P—C bonds

C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)

C07F9/3804—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se) not used, see subgroups

C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM

C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System

C07F9/02—Phosphorus compounds

C07F9/28—Phosphorus compounds with one or more P—C bonds

C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)

C07F9/40—Esters thereof

C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic

C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl

Description

U Our. Ref: 289670 615 0 FORM
AUSTRALIA
Patents Act COMPLETE SPECIFICATION
(ORIGINPT
00 o 00 00 0 000000 o r 00 o o o 000 0 0~ ~04 o 0 0000 0 o 0,0′ 0 Application Number: Lodged: Complete Specification Lodged: Accepted: Published: Priority: Related Art: 0 0 0 0 0 Applicant(s): Address for Service: CIBA-GEIGY AG Klybeckstrasse 141, 4002 Basle, Switzerland ARTHUR S. CAVE CO.
Patent Trade Mark Attornerys Level 10, 10 Barrack Street SYDNEY NSW 2000 0 000000 4 0 04 0 0 00 0 00 Complete specificatic.. for the invention entitled 0 Gc) \c The following stat~ment is a full description of this invention, including the best method of perfo-wing it known to me: %T 0/ 1 la- A-17230/=/MA 1939 Teleme ee- pound The present invention relates to new compounds, to their production and to their use in the treatn ent of aqueous systems, in particular to inhibit scale deposition from the aqueous system and/or to prevent fouling of the aqueous system and/or to inhibit corrosion of S metals in contact with the aqueous system.
In our British Patent Specification No. 1458235, there is described and claimed a method of inhibiting the precipitation of the scale forming salts of clacium, magnesium, barium and strontium from aqueous systems over a wide temperature range, comprising adding to the aqueous system a minor proportion of a product comprising a telomeric compound of the formula:
R-P-(CH
2 CR»)n- CH 2
CHR»CO
2
H
R’ CO 2
H
and salts thereof, wherein R» is hydrogen or a methyl or ethyl resicdue, R is hydrogen, a Sstraight- or branched alkyl residue, having from 1 to 18 carbon r.coms, a cycloalkyl residue 0 having from 5 to 12 carbon atoms, an aryl residue, an aralkyl residue, a residue of formula:
-(CH
2 CR»)m- CH 2
CHR»CO
2
H
CO 2
H
wherein R» has its previous significance and the sum n m is an integer of at the most 100, or a residue -OX wherein X is hydrogen or a straight- or branched alkyl residue having from 1 to 4 carbon atoms and R’ is a residue -OX wherein X has its previous significance.
We have now found that certain new compounds which, unexpectedly, have superior activity in the inhibition of scale deposition from aqueous systems and additionally have superior activity in the control of corrosion of metals in contact with aqueous systems. V -c -2- Accordingly, the present invention provides compounds having the formula I: Or
R,
MyO P CH 2
CH
2
CH(R
1 )CO2M 3
I
M
2 0I C0 2
M
3 p wherein M 1
M
2
M
3 independently, are hydrogen, C 1
-C
4 alkyl, phenyl, a monovalent or an equivalent of a polyvalent metal atom, ammonium or a substituted ammonium ion; 00 R is C 1
-C
4 alkyl substituted by one or more hydroxy or carboxyl groups and p is an 0 0 oa integer.
0 S E.g. one or more of preferably all three of M 1
M
2 and M 3 are hydrogen, a monovalent or o an equivalent of a polyvalent metal atom, ammonium or a substituted ammonium ion.
0 0 p is an integer ranging e.g. from 1 to 1000, preferably ranging from 1 to 99 and most preferred ranging from 1 to When one or more of M 1
M
2 and M 3 is a metal atom, they may be e.g. an alkali metal S atom or an alkaline earth metal. Typical alkali metal atoms are e.g. sodium and potassium atoms and typical alkaline earth metal atoms are e.g. calcium, barium and strontium atoms. Substituted ammonium ions include e.g. trimethylammonium, triethylaminonium, bis(2-hydroxyethyl) ammonium, tris(2-hydroxyethyl) ammonium and bis(2-hydroxyethyl)-(2-hydroxy-3-p-nonylphenoxy propyl ammonium ions.
S When one or more of M 1
M
2 and M 3 is a C 1 -C4alkyl residue, they may be e.g. methyl, S ethyl, n-propyl, i-propyl, n-butyl, i-butyl or tert-butyl.
When R 1 is C 1
-C
4 alkyl substituted by one or more hydroxy or carboxyl groups, it may be e.g. hydroxymethyl, 2-hydroxypropyl, carboxymethyl, carboethoxylmethyl, 2-carboxyethyl, 2-carboethoxyethyi, 1,2-dicarboxyethyl, 1,2-dicarbomethoxyethyl, 2,4-dicarboxybutyl or 2,4-di-carbomethoxybutyl. Preferred for R 1 are carboxymethyl, carboxyethyl and 1,2-dicarboxyethyl.
The new compounds of formula I may be produced by reacting p+l moles of a compound of formula II: i
CH
2 =C(Rl)-CO2-R 3 and one mole of a compound having the formula III: 0 0 00 0 0 0 0 00 C 0 0 0 0
O
O R 4 Ill
H-P
OR
wherein R 1 has its previous significance, and R 3
R
4 and R 5 independently, are hydrogen,
C-C
4 alkyl, phenyl, a monovalent or an equivalent of a polyvalent metal ion, ammonium or a substituted ammonium ion, or R 4 and R 5 may be linked by a -CH- 2
CH
2 residue to form a cyclic ring structure.
Typical metal ions R 3
R
4 and R 5 and optionally substituted ammonium ions R 3
R
4 and
R
5 respectively, are those previously indicated under the defintion of M 1
M
2 and M 3 The reaction may be effected, in the presence or absence of a solvent, and in the presence S of a free radical initiator e.g. organic peroxides such as di-tert.butyl peroxide, benzoyl peroxide, bigazoisobutyronitrile, hydrogen peroxide, sodium peroxide and sodium S perborate. If a solvent is used, this may be e.g. water, an aromatic hydrocarbon such as toluene; dioxan; a ketone such as 2-butanone; or an alcohol e.g. isopropanol; each optionally in admixture with water.
0 0 0 0 0 0 0 00 The products of the process according to the present invention are water-soluble. When, a reactant of formula II or III is used which contains a group R 3
R
4 or R 5 which is
C
1
-C
4 alkyl or phenyl, such groups may be partially or fully hydrolysed to subsequently produce a compound of formula I containing the corresponding groups M 1
M
2 and M 3 wherein M 1
M
2 and M 3 have their previous significance. Such compounds of formula I are produced by the said hydrolysis followed by substitution of some or all of the acidic hydrogen atoms so obtained, by cations of the salt-forming bases, hereinbefore defined.
Reactants of formula II include itaconic acid, di-methyl itaconate, but-1-en-2,4-dicarboxylic acid, diethyl but-1-ene-2,4-dicarboxylate, hex-1-en-2,4,6-tri-carboxylic acid, triethyl-hex-l-en-2,4,6-tricarboxylate, but-l-en-2,3,4-tricarboxylic acid, trimeth but-l-en-1,3,4-tricarboxylate, 2-hydroxymethyl acrylic acid and 2-hydroxyethyl acrylic IM A -4acid.
Reactants of formula III include phosphorous acid, di-ethyl phosphite, di-methyl phosphite, di-butyl phosphite, di-phenyl phosphite, ethylene phosphite and sodium hydrogen phosphite.
The compounds of formula I are effective in inhibiting deposition of scale and precipitation of salts from aqueous solutions. The compounds are particularly effective in combatting scale-forming salts derived from calcium, magnesium, barium, or strontium cations and anions such as sulphate carbonate, hydroxide, phosphate or silicate. The 0 compounds of formula I are especially effective in inhibiting deposition of calcium sulphate, magnesium hydroxide, calcium phosphate and calcium carbonate scale.
a The compounds of formula I also function as dispersing agents and/or antifoulants towards S common deposits found in water used in commercial plants e.g. industrial boilers, cooling water systems, gas scrubbing plants and aqueous slurries found in china clay operations.
Examples of such deposits are iron oxides, calcium and magnesium deposits e.g. their carbonates, sulphates, oxalates and phosphates, and silt, alumina, silicates and clays.
0 0 The compounds of formula I also provide excellent inhibition against corrosion of metals, especially ferrous metals, in contact with water.
Still further, the compounds of formula I are useful for inhibiting the thick velvety coating (sealing smut) which can be deposited over the surface of aluminium during the sealing of S anodically produced oxide layers on the aluminium, using hot or boiling water.
The products of the process of the present invention are obtained as solutions. For the purpose of isolation they may be subjected to partial or complete evaporation under reduced pressure. The reaction products may be used as the telomeric products in the method of the invention as described hereinafter.
Salt forms of the compounds of formula I in which some or all of the acidic hydrogens in the compounds of formula I have been replaced by the cations derived from the salt forming bases hereinbefore defined, may be prepared by mixing an aqueous or alcoholic solution of the compound of formula I with an aqueous or alcoholic solution of the compound of formula I with an aqueous or alcoholic solution containing an amount of the requisite base in excess of, equal to or less than the stoichiometric requirement. The solvent may then be removed by evaporation. In many of the water-containing systems where inhibitors of this invention would prove useful, the water is sufficiently alkaline to effect neutralisation and only the product of the invention need be added.
The present invention also provides a method of treating an aqueous system comprising adding to the system a telomer compound of formula I.
In practice, the amount of the compound of formula I used to treat the aqueous system So o may vary according to the protective function which the compound is required to perform.
o For example, for corrosion-inhibiting protective treatments, optionally with simultaneous 03′ 0°I scale-inhibiting treatments, the amount of the compound of formula I added to the aqueous «0 0- system may range from 0.1 to 50’000 ppm (0.00001 to 5 by weight), preferably from 1 to 500 ppm (0.0001 to 0.05 by weight), based on the weight of the aqueous system.
For solely anti-scale treatments, the amount of the compound of formula I added is conveniently from 1 to 200, preferably 1 to 30 ppm, based on the aqueous system. For o’°o most relatively dilute aqueous dispersions to be treated, the amount of compound of o formula I to be added as dispersant/antifoulant is conveniently from 1 to 200 ppm, o o0 preferably 2 to 20 ppm by weight. Aqueous slurries to be treated, however, may require So much higher levels of compound of formula I e.g. from 0.1 to 5 by weight on total 00 0 solids which can be as high as 70 by weight of the total aqueous system.
When used to inhibit the deposition of scale and the precipitation of salts from aqueous 0, Oo solutions, the compounds of formula I, or salts thereof, are particularly effective in inhibiting deposition of scale-forming salts derived from calcium, magnesium, barium or strontium cations, and anions such as sulphate, carbonate, hydroxide, phosphate and silicate.
With respect to aqueous system which may be treated according to the present invenion, of particular interest with respect to combined corrosion inhibition and anti-scale treatments are cooling water system, steam generating systems, sea-water evaporators, reverse osmosis equipment, paper manufacturing equipment, sugar evaporator equipment, soil irrigation systems, hydrostatic cookers, gas scrubbing systems, closed circuit heating systems, aqueous-based refrigeration systems and down-well systems; for corrosion k\ -6inhibition treatments alone, aqueous systems of particular interest include aqueous machining fluid formulations for use in boring, milling, reaming, broaching, drawings, spinning, turning, cutting, sawing, grinding, and thread-cutting operations or in non-cutting shaping in drawing or rolling operations) aqueous scouring systems, engine coolants including aqueous glycol antifreeze systems, water/glycol hydraulic fluids; and aqueous based polymer surface-coating systems/or solvent-based polymer systems, e.g.
those containing tetrahydrofuran, ketones or alkoxyalkanols.
The inhibitor compound of formula I used according to the invention may be used alone, or in conjunction with other compounds known to be useful in the treatment of aqueous systems.
S’.o In the treatment of systems which are completely aqueous, such as cooling water systems, o c air-conditioning systems, steam-generating systems, sea-water evaporator systems, 0 hydrostatic cookers, and closed circuit heating or refrigerant systems, further corrosion inhibitors may be used such as, for example, water soluble zinc salts; phosphates; polyphosphates; phosphonic acids and their salts, for example, hydroxyethyl diphosphonic acid (HEDP), nitrilotris methylene phopshonic acid and methylamino dimethylene «o phosphonocarboxylic acids and their salts, for example, those described in German Co o Offenlegungsschrift 2632774, hydroxyphosphonoacetic acid, 2-phosphonobutane-1,2,4tri-carboxlyic acid and those disclosed in GB 1572406; nitrates, for example, sodium nitrate; nitrites, e.g. sodium nitrite; molybdates, e.g. sodium molybdate, tungstates; silicates, e.g. sodium silicate; benzotriazole, bis-benzotriazole or copper deactivating benzotriazole or tolutriazole derivatives or their Mannich base derivatives; ,o 000 mercaptobenzotriazole; N-acyl sarcosines; N-acylimino diacetic acids; ehtanolamines; o o fatty amines; and polycarboxylic acids, for example, polymaleic acid and polyacrylic acid, as well as their respective alkali metal salts, copolymers of maleic anhydride, e.g.
copolymers o maleic anhydride and sulfonated styrene, copolymers of acrylic acid, e.g.
copolymers of acrylic acid an hydroxyalkylated acrylic acid, and substituted derivatives of polymaleic and polyacrylic acids and their copolymers. Moreover, in such completely aqueous systems, the inhibitor used according to the invention may be used in conjunction with further dispersing and/or threshold agents, e.g. polymerised acrylic acid (or its salts), phosphino-polycarboxylic acids (as described and claimed in British Patent 1458235), the cotelomeric compounds described in European Pa’-,nt Application No. 0150706, hydrolysed polyacrylonitrile, polymerised meth-acrylic acid and its salts, polyacrylamide and copolymers thereof from acrylic and methacrylic acids, lignin sulphonic acid and its -7salts, tannin, naphthalene sulphonic acid/formaldehyde condensation products, starch and its derivatives, cellulose, acrylic acid/lower alkyl hydroxy-acrylate copolymers, e.g. those.
described in US Patent Specification No. 4029577, styrene/maleic anhydride copolymers and sulfonated styrene homopolymers, e.g. those described in US Patent Specification No. 4374733 and combinations thereof. Specific threshold agents, such as for example, 2-phosphono-butane-1,2,4-tri-carboxylic acid (PBSAM), hydroxyethyl diphosphonic acid (HEDP), hydrolysed polymaleic anhydride and its salts, alkyl phosphonic acids, hydroxyphosphonoacetic acid, 1-aminoalkyl-l,l-diphosphonic acids and their salts, and alkali metal polyphosphates, may also be used.
a e Particularly interesting additive packages are those comprising compounds of formula I S with one or more of polymaleic acid or polyacrylic acid or their copolymers, or substituted 0 2 copolymers, hydroxyphosphonoacetic acid, HEDP, PBSAM, triazoles such as tolutriazole, S molybdates and nitrites.
Precipitating agents such as alkali metal orthophosphates, carbonates; oxygen scavengers such as alkali metal sulphites and hydrazines; sequestering agents such as nitrilotriacetic acid and its salts; antifoaming agents such as silicones, e.g. polydimethylsiloxanes, aon distearylsebacamide, distearyl adipamide and related products derived from ethylene oxide and/or propylene oxide condensation, in addition to fatty alcohols, such as capryl alcohols and their ethylene oxide condenstes; and biocides, e.g. amines, quaternary o ammonium compounds, chlorophenols, sulphur-containing compounds such as sulphones, methylene bis thiocyanates and carbamates, isothiazolones, brominated propionamides, triazines, phosphonium compounds, chlorine and chlorine-release agents and o oo organometallic compounds such as tributyl tin oxide, may be used.
If the system to be treated by the method of the invention is not completely aqueous, e.g.
an aqueous machining fluid formulation, it may be e.g. a water dilutable cutting or grinding fluid.
The aqueous maching fluid formulations of the invention may be, e.g. metal working formulations. By «metal working», we mean reaming, broaching, drawing, spinning, cutting, grinding, boring, milling, turning, sawing, non-cutting shaping or rolling.
Examples of water-dilutable cutting or grinding fluids into which tlh corrosion inhibiting combination may be incorporated include: a) aqueous concentrates of one or more corrosion inhibitors, and optionally one or more ,4 A -8anti-wear additives, used at dilutions of 1:50 to 1:100, which are usually employed as grinding fluids; b) polyglycols containing biocides, corrosion inhibitors and anti-wear additives which are used at dilutions of 1:20 to 1:40 for cutting operations and 1:60 to 1:80 for grinding; c) semi-synthetic cutting fluids similar to but containing in addition 10 to 25 oil with sufficient emulsifier to render the water diluted product translucent; d) an emulsifiable mineral oil concentrate containing, for example, emulsifiers, corrosion inhibitors, extreme pressure/anti-wear additives, biocides, anti-foaming agents, coupling agents etc; they are generally diluted from 1:10 to 1:50 with water to a white opaque 4, emulsion; o e) a product similar to containing less oil and more emulsifier which on dilution to the a a ao range 1:50 to 1:100 gives a translucent emulsion for cutting or grinding operations.
V 0 For those partly-aqueous systems in which the aqueous system component is an aqueous machining fluid formulation the inhibitor of formula I used according to the invention may be used singly, or in admixture with other additives, e.g. known further corrosion inhibitors and/or extreme-pressure additives.
Examples of other corrosion inhibitors which may be used in these aqueous systems, in addition to the inhibitor composition used according to the invention, include the following groups: a) Organic acids, their esters or ammonium, amine, alkanol-amine and metal salts, for example, berzoic acid, p-tert-butyl benzoic acid, disodium sebacate, triethanolamine laurate, isononanoic acid, triethanolamine salt of (p-toluene sulphonamido caproic acid), S triethanolamine salt of benzene sulphonamido caproic acid, triethanolamine salts of 5-ketocarboxylic acid derivatives as described in European Patent No. 41927, sodium N lauroyl sarcosinate or nonyl phenoxy acetic acid; b) Nitrogen-containing materials such as the following types: fatty acid alkanolamides; imidazolines, for example, 1-hydroxy-ethyl-2-oleyl-imidazolines, oxazolines; triazoles for example, benzotriazoles; or their Mannich base derivatives, triethanolamines; fatty amines; inorganic salts, for example, sodium nitrate; and the carboxy-triazine compounds described in European Patent Application No. 46139; c) Phosphorus containing materials such as the following types: amine phosphates, phosphonic acids or inorganic salts, for example, sodium dihydrogen phosphate or zinc phosphate; d) Sulphur containing compounds such as the following types: sodium, calcium or barium -9petroleum sulphonates, or heterocyclics, for example, sodium mercaptobenzothiazole.
Nitrogen containing materials, particularly triethanolamine, are preferred.
Examples of extreme pressure additives which may be present in the systems treated according to the present invention include sulphur and/or phosphorus and/or halogen containing materials, for instance, sulphurised sperm oil, sulphurised fats, tritolyl phosphate, chlorinated paraffins or ethoxylated phosphate esters.
0o». When triethanolamine is present in the aqueous systems treated according to the present e0oo? invention, it is preferably present in an amount such that the ratio of inhibitor composition 0 0 to triethanolamine is from 2:1 to 1:20.
0 The partly-aqueons systems treated by the method of the present invention may also be S aqueous surface-coating compositions, e.g. emulsion paints and aqueous powder coatings for metallic substrates.
The aqeous surface-coating composition may be, e.g. a paint such as a styrene-acrylic copolmyer emulsion paint, a resin, latex, or other aqueous based polymer surface-coating systems, to coat a metal substrate. The inhibitor composition used according to the invention may be employed to prevent flash rusting of the metal substrate during application of the surface coating and to prevent subsequent corrosion during use of the coated metal.
In aqueous surface-coating compositions treated by the method of the invention the inhibitor composition may be used singly, or in admixture with other additives, e.g. known corrosion inhibitors, biocides, emulsifiers and/or pigments.
The further known corrosion inhibitors which may be used are, e.g. those of classes b), c) and d) hereinbefore defined.
Examples of biocides which may be used in these aqueous systems, in addition to the compound of formula I, include the following: Phenols, and alkyl- and halogenated phenols, for example, pentachlorophenol, o-phenylphenol, o-phenoxyphenol and chlorinated o-phenoxyphenol, and salicylanilides, diamines, triazines and organometallic compounds such as organomercury compounds and organotin compounds.
Examples of emulsifiers for aqueous surface coatings include alkyl sulfates, alkyl I sulfonates, ether-alcohol sulphonates, di-n-alkyl sulphosumates and polyoxyethylen i nonylphenyl ethers.
Examples of pigments which may be used in these aqueous systems, in addition to the compound of formula I, include titanium dioxide, zinc chromate, iron oxide and organic ,T pigments such as the phthalocyanines.
I ,a As already indicated compounds of formula I also function as dispersing agents and/or antifoulants towards common deposits, e.g. iron oxides and/or iron salts, calcium and magnesium deposits, e.g. their carbonates, sulphates, oxalates and phosphates, and silt, alumina, silicates and clays found in such waters.
In particular, the method of the present invention may be applied to disperse deposits in an aqueous system containing 5 to 1500 ppm by weight of calcium ion as well as suspended solids. This aspect of the present invention finds particular use in the china clay industry in which it is important to obtain slurries which will not appreciably separate out during transportation from the clay pits to the user. At high concentrations of suspended solids in these slurries, the compounds of formula I have been found to disperse china clay and to be of value as «in-process» dispersants and as grinding aids.
The following Examples further illustrate the present invention. All parts and percentages are by weight, unless stated otherwise.
Example 1: To 12.1 parts by weight of di-ethylpiosphite are added, separately, 70 parts by weight of diethyl but-l-en-2,4-dicarboxylate and 5.75 parts by weight of di-tert-butylperoxide, dropwise, over 3 hours, with stirring at 140 0 C. The temperature is maintained at 140 0 C for a further 2 hours after the additions are complete. Unreacted di-ethyl-phosphite is removed by distillation under reduced pressure up to 2000/130 Pa and the residual liquid is suspended in 400 parts by weight of concentrated hydrochloric acid, and the mixture heated under reflux conditions for 18 hours.
The resulting solution is evaporated to dryness under reduced pressure at 100°C/1600 Pa
I
11 to give 53 parts by weight of a solid polymer having a molecular weight of 1430.
The absence of phosphorous acid and the presence of the phosphonic acid telogen is proven be 31 P nmr analysis (multiple signals at 28 ppm).
Example 2: Following the procedure described in Example 1, from 23 parts by weight of diethylphosphite, 52.7 parts by weight of di-methyl itaconate ad 5.3 parts by weight of di-tert-butyl-peroxide there are obtained 44.5 parts by weight of a polymer having a molecular weight of 590 and a 31 P multiple spectrum around 25-30 ppm.
Example 3: Calcium carbonate (cooling water) threshold test o Test Conditions S Test temperature 70 0
C
Test duration 30 minutes Aeration rate 500 cc/min (per 100 ml) Calcium 150 ppm as Ca 2 Magnesium 45 ppm as Mg 2 Carbonate 51 ppm as CO32″ Bicarbonate 269 ppm as -HC0 3 Test additive 1 ppm The test is designed to assess the ability of an additive to inhibit the precipitation of CaCO 3 The water composition simulates cooling water and the high temprature represents the conditions which exist close to a heat exchanger. Air bubbling is used to increase the severity of the test conditions.
A volume of solution containing sodium carbonate and sodium bicarbonate is mixed with an equal volume of a solution containing calcium chloride and magnesium chloride which i already contains the test additive. The resulting test solution, through which air is bubbled at a contant rate, is stored at 70 0 C for 30 minutes. After this time, the solution is filtered and the calcium remaining in the filtrate is determined by EDTA titration.
Each test is carried out in duplicate, and the first test is a standard test which determines the actual Ca 2 concentration in the test.
I
12 titre of test-titre of blank CaC3 inibiton =titre of standard-titre of The standard and blank titres are usually 15-16 ml and 5-6 ml, respectively.
The product of Example 1, at 1 ppm level of addition, gave a CaCO 3 inhibition of 63.
44 4
I

Claims (2)

1. Compounds having the formula I: O R, M 2 0 C0 2 M 3 p o wherein M 1 M 2 M 3 independently, are hydrogen, C 1 -C 4 alkyl, phenyl, a monovalent or S an equivalent of a polyvalent metal atom, ammonium or a substituted aminonium ion; a, R 1 is C 1 -C 4 alkyl substituted by one or more hydroxy or carboxyl groups and p is an integer. 0 0 ,o 2. Compounds according to claim 1 wherein p is an integer within the range of from 1 to

99. 3. Compounds according to claim 1 wherein p is an integer within the range from 1 to o 0″ 4. Compounds according to claim 1 wherein all three of M1, M 2 and M 3 are hydrogen, a monovalent or an equivalent of a polyvalent metal atom, ammonium or a substituted S0 ammonium ion. Process for the production of compounds of formula I, as defined in claim 1, comprising reacting p+1 moles of a compound of formula II: 0 o o I CH 2 =C(R 1 )-C0 2 R 3 II and one mole of a compound having the formula III: i: 0 OR 4 H-P OR wherein R 1 has the significance given in claim 1, and R 3 R 4 and R 5 independently, are hydrogen, C 1 -C 4 alkyl, phenyl, a monovalent or an equivalent of a polyvaleint metal ion, L. -14- ammonium or a substituted ammonium ion. 6. Process according to claim 5 wherein the process is effected in the presence of a free radical initiator. 7. Method of treating an aqueous system comprising adding to the system a compound of formula I as defined in claim 1. 8. Method according to claim 7 wherein the system is treated to provide a corrosion- inhibiting treatment, or a corrosion-inhibiting with simultaneous scale-inhibiting treatments, ald the compound of formula I is added in amount of from 0.1 to 50’000 ppm by weight, based on the weight of the aqeuous system. 9. Method according to claim 8 whereir. the compound of formula I is added in amount of 1 to 500 ppm by weight, based on the aqueous system. Method according to claim 7 wherein the system is treated to provide solely an anti-scale treatment and the compound of formula I is added in amount of 1 to 200 ppm by weight, based on the aqueous system. 11. Method according to claim 10 wherein the compound of formula I is added in amount of 1 to 30 ppm by weight, based on the aqueous system. 12. Method ,-cording to claim 7 wherein the system is treated to provide a dispersant/anti- foulant treatment and the amount of compound of formula I added is from 1 to 200 ppm by weight based on the aqueous system. 13. Method according to claim 12 wherein the compound of formula I is added in amount of 1 to 30 ppm by weight, based on the aqueous system. 14. Method according to claim 7 wherein the compound of formula I is added in conjunction with other compounds known to be useful in the treatment of aqueous systems. Method according to claim 14 wherein the compound of formula I is used in conjunction with one or more of polymaleic or polyacrylic acid or their copolymers, or 1/ 1 15 substituted copolymers; hydroxyphosphonoacetic acid, HEDP; PBSAM; triazoles such as tolutriazole; molybdates; and nitrites. 16. A compound of formula I as shown in claim 1, said compound substantially as herein described with reference to Examples 1 or 2. 17. A method of treating an aqueous system substantially as herein described and with reference to Example 3. DATED this 23rd day of July, 1991. ep~o r, o a u it aa posD,,r o r i i CIBA-GEIGY AG By Their Patent Attorneys ARTihUR S. CAVE CO. 1 ti 4112U/VMJ 1

AU41719/89A
1988-09-21
1989-09-21
Polymeric compounds

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AU615800B2
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1988-09-21

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1990-03-29

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1991-10-10

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1988-09-21
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Polymeric compounds

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EP0360747B1
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JP
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JP2939754B2
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AU615800B2
(en)

BR
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BR8904716A
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CA
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CA1339536C
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DE68924632T2
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Families Citing this family (24)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US5629396A
(en)

1989-01-17
1997-05-13
The Dow Chemical Company
Latex containing oxazoline for industrial coatings

GB9024470D0
(en)

1990-11-10
1991-01-02
Ciba Geigy Ag
Corrision inhibition

AU667295B2
(en)

1990-12-18
1996-03-21
Albright & Wilson Uk Limited
Water treatment agent

US5386038A
(en)

1990-12-18
1995-01-31
Albright & Wilson Limited
Water treatment agent

US5256746A
(en)

1991-04-25
1993-10-26
Rohm And Haas Company
Low molecular weight monoalkyl substituted phosphinate and phosphonate copolymers

GB9111704D0
(en)

1991-05-31
1991-07-24
Ciba Geigy
Telomers

US5681479A
(en)

1991-05-31
1997-10-28
Fmc Corporation (Uk ) Limited
Phosphonic cotelomers and method of use

US6063288A
(en)

1998-06-30
2000-05-16
Betzdearborn Inc.
Inhibition of silica and silicate deposition using imidazolines

US6077440A
(en)

1998-06-30
2000-06-20
Betzdearborn Inc.
Inhibition of silica and silicate deposition

US6585933B1
(en)

1999-05-03
2003-07-01
Betzdearborn, Inc.
Method and composition for inhibiting corrosion in aqueous systems

US6989035B2
(en)

2001-10-18
2006-01-24
The Procter & Gamble Company
Textile finishing composition and methods for using same

US7169742B2
(en)

2001-10-18
2007-01-30
The Procter & Gamble Company
Process for the manufacture of polycarboxylic acids using phosphorous containing reducing agents

US7008457B2
(en)

2001-10-18
2006-03-07
Mark Robert Sivik
Textile finishing composition and methods for using same

US7018422B2
(en)

2001-10-18
2006-03-28
Robb Richard Gardner
Shrink resistant and wrinkle free textiles

US6841198B2
(en)

2001-10-18
2005-01-11
Strike Investments, Llc
Durable press treatment of fabric

US7144431B2
(en)

2001-10-18
2006-12-05
The Procter & Gamble Company
Textile finishing composition and methods for using same

US7727420B2
(en)

2005-05-17
2010-06-01
Ppt Research
Corrosion inhibiting compositions

US8021607B2
(en)

2008-10-31
2011-09-20
General Electric Company
Methods for inhibiting corrosion in aqueous media

US8025840B2
(en)

2008-10-31
2011-09-27
General Electric Company
Compositions and methods for inhibiting corrosion in aqueous media

MX2011010890A
(en)

2009-04-21
2011-11-02
Ecolab Usa Inc
Methods and apparatus for controlling water hardness.

US9193610B2
(en)

2011-08-10
2015-11-24
Ecolab USA, Inc.
Synergistic interaction of weak cation exchange resin and magnesium oxide

CN102898574B
(en)

2012-10-25
2014-06-25
南京大地冷冻食品有限公司
Preparation method of novel environment-friendly high-efficiency detergent

EP2813524A1
(en)

2013-06-10
2014-12-17
Basf Se
Phosphorylated polymers

BR102014027956B1
(en)

2013-11-22
2020-11-17
Rohm And Haas Company

COPOLYMER COMPOSITION AND METHOD TO PRODUCE A TELOMERIC COPOLYMER COMPOSITION

Family Cites Families (10)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
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CA509034A
(en)

1955-01-11
Dominion Rubber Company
Organo-phosphorus compounds and process of making same

NL76613C
(en)

1948-07-01

GB660169A
(en)

1948-07-10
1951-10-31
Us Rubber Co
Improvements in organo-phosphorus compounds and process of making same

GB694772A
(en)

1948-07-10
1953-07-29
Us Rubber Co
Improvements in phosphonic acid esters

US3048613A
(en)

1948-07-10
1962-08-07
Us Rubber Co
Organo-phosphorus compounds and process of making same

US4127483A
(en)

1974-06-11
1978-11-28
Ciba Geigy (Uk) Limited
Treatment of aqueous systems

US4159946A
(en)

1974-06-11
1979-07-03
Ciba Geigy (Uk) Limited
Treatment of aqueous systems

GB1458235A
(en)

1974-06-11
1976-12-08
Ciba Geigy Uk Ltd
Inhibiting scale formation in aqueous systems

JPS5998150A
(en)

1982-11-26
1984-06-06
Adeka Argus Chem Co Ltd
Halogen-containing resin composition

JPS6011566A
(en)

1983-06-30
1985-01-21
Pentel Kk
Ball point water ink

1988

1988-09-21
GB
GB888822144A
patent/GB8822144D0/en
active
Pending

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1989-09-12
DE
DE68924632T
patent/DE68924632T2/en
not_active
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1989-09-12
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1990-05-01

CA1339536C
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1997-11-11

AU4171989A
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1990-03-29

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1990-05-29

EP0360747B1
(en)

1995-10-25

EP0360747A2
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1990-03-28

DE68924632T2
(en)

1996-06-05

US5073299A
(en)

1991-12-17

JP2939754B2
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1999-08-25

DE68924632D1
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1995-11-30

GB8822144D0
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1988-10-26

EP0360747A3
(en)

1991-05-02

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