AU621564B2 - Creación de Inventos y Patentes con Inteligencia Artificial

AU621564B2 – Process for controlling calcium oxalate scale over a wide ph range
– Google Patents

AU621564B2 – Process for controlling calcium oxalate scale over a wide ph range
– Google Patents
Process for controlling calcium oxalate scale over a wide ph range

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Publication number
AU621564B2

AU621564B2
AU24183/88A
AU2418388A
AU621564B2
AU 621564 B2
AU621564 B2
AU 621564B2
AU 24183/88 A
AU24183/88 A
AU 24183/88A
AU 2418388 A
AU2418388 A
AU 2418388A
AU 621564 B2
AU621564 B2
AU 621564B2
Authority
AU
Australia
Prior art keywords
calcium oxalate
component
precipitation
weight
aqueous system
Prior art date
1987-10-23
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.)

Ceased

Application number
AU24183/88A
Other versions

AU2418388A
(en

Inventor
Kevin J. Hipolit
Gloria D. Sinkovitz
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.)

Calgon Corp

Original Assignee
Calgon Corp
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.)
1987-10-23
Filing date
1988-10-21
Publication date
1992-03-19

1988-10-21
Application filed by Calgon Corp
filed
Critical
Calgon Corp

1989-04-27
Publication of AU2418388A
publication
Critical
patent/AU2418388A/en

1992-03-19
Application granted
granted
Critical

1992-03-19
Publication of AU621564B2
publication
Critical
patent/AU621564B2/en

1994-11-10
Assigned to CALGON CORPORATION
reassignment
CALGON CORPORATION
Alteration of Name(s) in Register under S187
Assignors: CALGON CORPORATION

2008-10-21
Anticipated expiration
legal-status
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Status
Ceased
legal-status
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Classifications

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

C02F5/105—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 combined with inorganic substances

Abstract

This invention is directed to the use of an improved composition for inhibiting the precipitation of calcium oxalate in aqueous systems. The composition contains: (a) a water soluble phosphate; and (b) a water soluble polycarboxylate having a weight average molecular weight of about 7,000 to about 9,000; wherein the ratio of component (a) to component (b) ranges from 10:1 to 1:10.

Description

^1_1 6 2156 4 S F Re: 7259G FORM COMMONWEALTH OF AUSTRALIA PATENTS ACT 1952 COMPLETE SPECIFICATION
(ORIGINAL)
FOR OFFICE USE: Clasc Int Class Complete Specification Lodged: Accepted: Published: 4 t Priority: Related Art: tr Name and Address of Applicant: Address for Service: Calgon Corporation Route 60 Campbell’s Run Road Robinson Township Pennsylvania UNITED STATES OF AMERICA SprLson Fergussr, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia if ft Complete Specification for the invention entitled: ri; I 4p @4
I
I
Process For Controlling Calcium Oxalate Scale Over a Wide pH Range The following statement is a full description of this invention, including the best method of performing it known to me/us 5845/3 C- 1464 TITLE OF THE INVENTION 0 00 «AN IMPROVED PROCESS FOR CONTROLLING CALCIUM OXALATE .09000of 0 *SCALE OVER A WIDE pH RANGE» 00 0 ABSTRACT OF THE DISCLOSURE This invention is directed to the use of an 00 improved composition for inhibiting the precipitation of calcium oxalate in aqueous systems. The t~omposition contains: a wate,,, soluole phosphate; and a water soluble polycarboxylate having a 0:001weight average molecular weight of about 7,000 to about 9,000; wherein the ratio of component to component ranges from 10:1 to 1:10.
I b» C-1464 0 i TITLE OF THE INVENTION It
I.
I II I-t i:
I-
I-It «AN IMPROVED PROCESS FOR CONTROLLING CALCIUM OXALATE SCALE OVER A WIDE pH RANGE» BACKGROUND OF THE INVENTION Most commercial water contains alkaline earth metal cations, such as calcium, magnesium, 5 etc., and anions such as carbonate and oxalate. When combinations of these anions and cations are present in concentrations which exceed the solubility of their reaction products, precipitates form until their product solubility concentrations are no longer exceeded. For example, when the concentrations of calcium ion and oxalate ion exceed the solubility of the calcium oxalate reaction product, a solid phase of calcium oxalate will form as a precipitate.
Solubility product concentrations are exceeded for various reasons, such as evaporation of the water phase, change in pH, pressure or
U
2 C-1464 temperature, and the introduction of additional ions which can form insoluble compounds with the ions already present in the solution. As these reaction products precipitate on the surfaces of a water carrying system, they form scale. Scale prevents effective heat transfer, interferes with fluid flow, facilitates corrosive processes, and harbors bacteria. Scale is an expensive problem in many industrial water systems, causing delays and shutdowns for cleaning and removal.
Calcium oxalate is a ommon substituent of scale which forms on the surfaces of apparatuses used for thermal treatment of aqueous solutions and suspensions. It is known that calcium oxalate scale can be removed by washing pipes, tubes, or other metallic surfaces upon which calcium oxalate deposits have form with dilute aqueous acid solutions, such as hydrochloric acid or nitric acid solutions.
,i 20 However, due to the limited solubility of calcium oxalate in these acids, repeated washings are necessary. Thus, acid washing constitutes a costly and time-consuming operation. Acid washing also deteriorates equipment.
U.S. Patent 4,108,680 discloses a process SII ^for removing calcium oxalate scale from metallic surfaces comprising contacting the scale with an aqueous suspension containing nitric acid and manganese dioxide at a temperature between 20 and PC. This process, like the acid washing process previously discussed, is directed to removal of calcium oxalate which has formed on metallic L W1 3 C-1464 surfaces. These processes are not directed to prevention or inhibition of calcium oxalate precipitation.
U.S. Paten-: ,575,425 discloses the use of phosphate/polycarboxylate compositions to inhibit calcium oxalate precipitation. The instant invention represents an improvement over the method of the ‘425 patent.
Polyphosphates, such as a product which is 1.1 Na20:1.0 P 5 can control calcium oxalate .o 2 scales up to a pH of approximately 4. However, o calcium oxalate scale is diff cult to control as the pH increases above 4. Since acrylates control 0 0 o0o° 15 calcium oxylate precipitation at pH’s above 6.0, the 00ooo0 0 a most critical range for control is a pH of about °0 0 through a pH of about 6.0. The inventors have discovered that polyacrylates having a weight average molecular weight ranging between 7,000 and 9,000 are S00 Soo 20 especially effective (in combination with a phosphate) for controlling calcium oxalate scaling.
ooo 000 0000: It is an object of this invention to provide an improved composition and process for the 25 inhibition of calcium oxalate precipitation at pH’s o. greater than or equal to 2.0, especially at pH’s ranging from 4.0 to These and other objects of the instant invention are accomplished by a process in which an effective amount of an admixture comprising: a compound selected from the group consisting of water soluble phosphates and a polyacrylic acid or salt
I
-4thereof having a weight average molecular weight of about 7,000 to about 9,000, preferably about 8,000, is added to an aqueous system, thereby preventing the deposition and precipitation of calcium oxalate scale on metallic surfaces in contact with the aqueous system over a wide pH range.
DETAILED DESCRIPTION OF THE INVENTION According to a broad form of the invention there is provided a method of inhibiting the precipitation and deposition, as herein defined, of calcium oxalate scale in an aqueous system, as herein defined, comprising adding to said system 0.1 to 1000 ppm based on the weight of said aqueous system of a compound selected from the group consisting of water soluble phosphates and a water soluble homopolymer of acrylic acid, or salt thereof, having a weight average molecular weight of from 7,000 to 9,000, wherein the ratio of component to component ranges from 10:1 to 1:10, by weight, and wherein the pH of said aqueous system ranges from 4,0 to The instant invention is directed to an improved method of inhibiting the precipitation and deposition of calcium oxalate scale in an aqueous system comprising adding to said system an effective amount of an admixture comprising: a compound selected from the group consisting of water soluble phosphates and a polyacrylic acid or salt thereof having a weight average molecular weight of about 7,000 ‘o about 9,000, preferably about 8,000, wherein the ratio of component to component ranges from 10:1 to 1:10 by weight, and wherein the pH of said aqueous system is greater than or equal to The instant invention Is further directed to a composition comprising: a compound selected from the group consisting of wate, i;oluble phosphates and a polyacrylic acid or salt thereof having a weight average molecular weight of about 7,000 to about 9,000, preferably abcut 8,000, wherein said composition is useful in inhibiting or i 30 preventing the precipitation and deposition of calcium oxalate scale on metallic surfaces in contact with aqueous systems over a wide pH range.
5 C-1464 Any water soluble phosphate can be used as component in the compositions of the present invention. Preferred phosphates are «molecularly dehydrated phosphates», by which is meant any phosphate which can be considered as derived from a monobasic or dibasic orthophosphate or from orthophosphoric acid, or from a mixture of any to of these by elimination of water of constitution therefrom. There may be employ d alkaline metal tripolyphosphates, or pyrophosph tes, or the metaphosphate which is often designated as hexametaphosphate. Any molecularly dehydrated phosphate may be employed, but it is preferred to use those which have a molar ratio of alkaline metal to phosphorous methoxide from about 0.9:1 to about 2:1, the latter being the alkaline metal pyrophosphate.
While it is preferred to use the metaphosphates, pyrophosphates, or polyphosphates of sodium, because they are the least expensive and most readily 2 available, it is also possible to use the molecularly dehydrated phosphates of other metals such as a4 t potassium, lithium, cesium, or rhobidium or the ammonium molecularly dehydrated phosphates, which in many instances are classified as being elkaline metal phosphates, or the alkaline earth metal molecularly dehydrated phosphates such as those as calcium, barium, or strontium, or mixtures of alkaline metal 2t and alkaline earth molecularly dehydrated phosphates.
Additional examples of acceptable water soluble phosphates include phosphate esters; organophosphate esters, such as the lower alkyl mono-, di- and trialkyl phosphates. The alkyl group i* L
__MWA
6 C-1464 is selected from C 1 to C and may be branched or unbranched. The alkyl group may be substituted with hydroxy, amino, halide, sulfate or sulfonate, alone or in combination.
The most preferred water soluble phosphate is sodium hexametaphosphate, such as «Calgon», available from Calgon Corporation, Pittsburgh, Pa., which may be described as 1.1 Na02:l P 2 0 5 The second component of the instant synergistic admixtures is a water-soluble homopolymer of acrylic acid, or salt thereof, having a weight 0, average molecular weight of about 7,000 to about 9,000, preferably about 8,000.
The inventors have found that, in the o above-defined molecular weight range, polyacrylic acid effectiveness is substantially improved.
S 2 The instant homopolymers of acrylic acid, o. and salts thereof, may optionally contain up to by weight, of one or more random unsaturated, polymerizable monomer(s).
p eciP-f-aiorn ond The phrase «inhibiting the 4-pe-ion oro(epesi r\ _eoipi4tIIn» is meant to include threshold 0 inhibition, dispersion and/or solubilization of 6 calcium oxalate scale.
0 7 C-1464 The phrase «aqueous system» is meant to include any system containing water; including, but not limited to, cooling water systems, boilers, desalination systems, gas scrubbers, blast furnaces, sewage sludge thermal conditioning equipment, reverse osmosis systems, sugar evaporators, paper processing circuits, mining circuits and the like.
The weight ratio of component to component should be about 10:1 to about 1:10, preferably 1,5:1 to 1:1.5.
An effective amount of the calcium oxalate inhibitor disclosed herein means that level of inhibitor necessary to prevent deposition or precipitation of calcium oxalate in the system being treated. Treatment levels can be as high as 1,000 ppm. The preferred treatment level is from 0.1 to ppm.
44 7 44 1 4 4 4r 4 f t Unexpectedly, the instant compositions It provide enhanced control of calcium oxalate scaling It Cwhen compared to the compositions described in U.S.
Patent 4,575,425. Thus, the instant compositions are substantially more effective as calcium oxalate scale inhibitors at pH’s greater than or equal to These inhibitors are especially effective as scale 0 inhibitors in the pH range of 4.0 to 6.0. It is noteworthy that polyphosphonates alone can control scales up to a pH of approximately 4 and that polyacrylates alone can control calcium oxalate precipitation at pH’s in excess of 6. Thus, the critical range for complete control of nalcium *rr i hrCi;L 8 C-1464 oxalate precipitation includes pH’s from approximately 4.0 through approximately 6.0. Calcium ;oxalate precipitation is not controlled throughout i this range by components or of the instant admixtures individually.
The preferred compositions comprise sodium hexametaphosphate and a homopolymer of acrylic acid having a weight average molecular weight of from about 7,000 to about 9,000, and salts of these polymers.
These preferred compositions are effective inhibitors over a pH range of from 2.0 to 12.0.
The temperature of the system oeing treated is not critical to the effectiveness of the instant inhibitors, if below the temperature at which the individual components employed thermally destruct.
20 Though it is preferred to treat aqueous t I systems with admixtures comprising components and as described earlier, these components may be added separately to the system being treated without departing prom the spirit of this invention.
tE Examples t The following examples illustrate the present invention in greater detail. It should be understood that the invention is not in any way limited by these examples.
-I
9 C-1464 The following abbreviations and product names are used in the examples and are defined as indicated: PAA-L polyacrylic acid, (Mw) of approximately 2,000 as determined by gel permeation chromatography, partially neutralized to pH PAA-H polyacrylic acid, (Mw) of approximately 8,000 as determined by gel permeation chromatography, neutralized to pH o ct PP polyphosphete; this product, which is manufactaured by Calgon Corporation, Pittsburgh, Pa., under the tradename Calgon, is defined as 1.1 Na20:1 P205.
Examples 1-20 Threshold inhibition flask tests were run for calcium oxalate. Due to the increased solubility of oxalate at pH’s less than 4, a 3.5 millimole concentrate of calcium and oxalate ions was used ti induce scaling, Solution pH was adjusted to within 0.2 units of the desired test pH prior to additon of inhibitor being treated. After addition of the inhibitor, the catLon (CACX 2 was added and the pH was adjusted to within 0.05 units of the desired pH.
The flasks were then loosely capped and incubated for 24 hours at 62 0 C. Before titration, to determine the ppm of Ca remaining in solution, precipitated calcium oxalate was removed by filtering aliquots of all solution through a 0.45 um membrane. Final pH of the unfiltered test solution was considered to be the actual test pH. All inhibitor concentrations were calculated on an active basis.
i7i=;iflirnrli=»=~~l~ 10 C-1464 Table 1, below, shows the results of examples 1-20. In examples 1-7 polyacrylic acid (PAA) alone was used as the inhibitor. In examples 8-13 polyphosphate (PP) was used as the sole inhibitor. In examples 17-20 a 1:1 combination by weight of a low molecular weight polyacrylic acid and polyphosphate was used as the inhibitor.
#f t Ir I I I
I
It
II
I I
I
I
TA~BLE I C-1464 Calcium Oxylate Inhibition at Designated Dosage (ppm of Inhibitor In Solution, Weight basis) In h i b Itor (weight Example ratio) (I ppm) (3 ppm) @1 4t q e t S I I I
PAA-L
PAA-L
PAA-L
PAA-L
4.0 5.0 6.0 7.0 22.0 35 .0* 75.0 97.0 26.0 74 .8* 94 .0 94.0 (5 ppm) 35.0 77 .0* 97.0 96.0 (15 ppm) 82.5* 84,.5 (1 ppm) L5_2em)
A
~f It C I It I I I C I I.
C
I
PAAP-L
PAAP-L
8.5 10.0 66.0* 81.0 67. 5* 75 .5 (20 ppm) (50 ppm) 100 PPM) I t
PAA-L
PP
pp pp
PP
PP
pp 11.3 2,~0 3.0 4. 0 4.5 5.0 6.0 100.0 100.0 98.0 85.0 9.5* No inhibition 100.0 100.0 98.0 93 .5* 6C. .0* 45.0 100.0 100 .0 97 93.** 6
I.
12 C- 1464 TABLE I (Continued): Inhibitor (weight Example ratio) Calcium Oxylate Inhibition at Designated Dosage (ppm of Inh~ibitor In Solution, Weight basis) (1 ppm) (5 ppm) 33Q0* 1.5* 53.5* 11.5* 20.0* 97.0 98.0 (15 ppm)
PP/PP
1
A-L
1:1 PF/ P A A-L (1:1) PF/ PAA-L (1 1)
PP/PA.-L
(1:1) .0.0 4.0 5.0 51.0* 6 9 .0* 100.0 97.0 87.0 87.0 98.0 89.0 98.0 98.0 6.0 9510 repreqents an average of 2 data points 0 0 OOt) tao~. .4 a a v -I
L
13 C-1464 Example 21 Supersaturated solutions of calcium txalate containing 110 mg/L oxalate ion and 20 mg/L calcium ion were prepared. Papermill water was synthesized which contained 2,000 mg/L sodium, 3,100 mg/L chloride and 200 mg/L sulfate ions. The supersaturated oxalate solutions were combined with synthesized mill water to conduct these tests.
00 o0 S° 10 1 Standard calcium oxalate flask tests were then run, in accordance with the procedure described for Examples 1-20, for high and low molecular weight polyacrylic acid/polyphosphate inhibitors to compare the performance of these inhibitors. The results are shown in Table II.
14 TABLE II Actrive Dosage 4Z5 S 0t 5 .j 6.0 6.
SAM
A) PP/PAA-L 0.5 10.0 2. 0 14.0 78 86 90 94 98 65, 80, 68, 61 100, 98 100 62, 78 100 71.
100 13) PP/PAA-1R (1:i1) 0.5 240 82 100 75, 31L 100, 1.00 67 90 100 100 2.00 100, 90 100, 1.00 84, 100 1.00

Claims (4)

1. A method of inhibiting the precipitation and deposition, as herein defined, of calcium oxalate scale in an aqueous system, as herein defined. comprising adding to said system 0.1 to 1000 ppm based on the weight of said aqueous system of a compound selected from the group consisting of water soluble phosphates and a water soluble homopolymer of acrylic acid, or salt thereof, having a weight average molecular weight of from 7,000 to 9,000, wherein the ratio of component to component ranges from 10:1 to 1:10, by weight, and wherein the pH of said aqueous system ranges from 4,0 to

2. The method of Claim 1, wherein said ratio of component to component is from 1.5:1 to 1:1.5.

3. The method of Claim 1 or Claim 2, wherein said water soluble phosphate is sodium hexametaphosphate. S 15

4. A method of inhibiting the precipitation and deposition, as herein defined, of calcium oxalate scale in an aqueous system, as herein defined, which method is substantially as herein described with reference to Example 218. An aqueous system whenever inhibited from precipitation and deposition, as herein defined, of calcium oxalate scale by a method of any one of Claims 1 to 4. i DATED this TWENTY-THIRD day of DECEMBER 1991 t Calgon Corporation Oatent Attorneys for the Applicant SPRUSON FERGUSON KEH/337f

AU24183/88A
1987-10-23
1988-10-21
Process for controlling calcium oxalate scale over a wide ph range

Ceased

AU621564B2
(en)

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Priority Date
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Title

US111948

1987-10-23

US07/111,948

US4804476A
(en)

1987-10-23
1987-10-23
Process for controlling calcium oxalate scale over a wide pH range

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AU2418388A

AU2418388A
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1989-04-27

AU621564B2
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AU621564B2
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1992-03-19

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AU24183/88A
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AU621564B2
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1987-10-23
1988-10-21
Process for controlling calcium oxalate scale over a wide ph range

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US4804476A
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EP0313157B1
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JPH01143700A
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AT
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ATE76857T1
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AU621564B2
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DE
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DE3871713T2
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US5279827A
(en)

1991-01-16
1994-01-18
Allegheny-Singer Research Institute
Extract and pharmaceutical composition for treatment of calcium oxalate stone disease and viral infections

US5137722A
(en)

1991-01-16
1992-08-11
Allegheny-Singer Research Institute
Extract and pharmaceutical composition for treatment of calcium oxalate stone disease

US5320757A
(en)

1993-04-05
1994-06-14
Betz Laboratories, Inc.
Method of inhibiting calcium oxalate scale deposition

ATE205460T1
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1993-06-14
2001-09-15
Solutia Europ Nv Sa

METHOD FOR PREVENTING OXALATE DEPOSIT

AU701456B2
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1994-09-12
1999-01-28
Rohm And Haas Company
Method of inhibiting sulfate scale in aqueous systems

US6096197A
(en)

1997-12-11
2000-08-01
Hughes; Douglass E.
Shower filter for chlorine removal and scale deposit prevention

KR100308522B1
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1999-06-10
2001-11-05
선우 영석
Calcium oxalate scale remover

ES2272191B1
(en)

2005-10-14
2008-04-01
Universitat De Les Illes Balears

USE OF FITATE FOR WATER TREATMENT.

JP5615049B2
(en)

2010-06-07
2014-10-29
伯東株式会社

Barium sulfate scale prevention method

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not_active
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1988

1988-10-14
DE
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patent/DE3871713T2/en
not_active
Expired – Fee Related

1988-10-14
ES
ES198888202304T
patent/ES2031584T3/en
not_active
Expired – Lifetime

1988-10-14
AT
AT88202304T
patent/ATE76857T1/en
not_active
IP Right Cessation

1988-10-14
EP
EP88202304A
patent/EP0313157B1/en
not_active
Expired – Lifetime

1988-10-20
JP
JP63263022A
patent/JPH01143700A/en
active
Pending

1988-10-21
AU
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not_active
Ceased

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Calgon Corporation
Synergistic scale and corrosion inhibiting admixtures containing carboxylic acid/sulfonic acid polymers

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EP0313157A3
(en)

1989-09-27

US4804476A
(en)

1989-02-14

ES2031584T3
(en)

1992-12-16

JPH01143700A
(en)

1989-06-06

DE3871713T2
(en)

1992-12-10

AU2418388A
(en)

1989-04-27

EP0313157A2
(en)

1989-04-26

DE3871713D1
(en)

1992-07-09

EP0313157B1
(en)

1992-06-03

ATE76857T1
(en)

1992-06-15

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