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US4603006A Expired / Lapsed US ⏱️ 0.0 years remaining

Inhibition of inorganic or biological CaCO3 deposition by synthetic polysaccharide derivatives

Assignee: University of South Alabama
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Filing: 1983-12-19
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Granted: 1986-07-29
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Expires: 2003-12-19
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Abstract

Abstract The present invention relates to a method of inhibiting the formation of calcium carbonate-containing deposits on a surface by applying a composition comprising an anticalcification-effective amount of a polysaccharide or derivative thereof. The present method is useful for the prevention and/or retardation (inhibition) of inorganic scaling, as well as, for the inhibition of fouling by plant or animal organisms.

Inventors

  • 👤 C. Steven Sikes
  • 👤 A. P. Wheeler

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 18:07
CPC Classifications
A; A01; A01N; A01N43/00; A01N43/02; A01N43/04; A01N43/14; A01N43/16; A01N43/06; A01N43/08; A01N57/00; A01N57/10; A01N57/16; A01N57/26; A01N57/32; C; C02; C02F; C02F1/00; C02F1/50; C02F5/00; C02F5/08; C02F5/10; C02F5/12; C02F5/14

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 330 words
A method of inhibiting the formation of CaCO 3 -containing deposits on a surface, comprising applying to said surface an anticalcifying composition, comprising: a substoichiometric amount of a monosaccharide or disaccharide polymer of at least 500 MW of the formula Poly (X.sub.n Y.sub.m) wherein the polymer is formed by glycosidic linkages between adjacent monomers; wherein each X independently, is the radical of a monomer selected from the group consisting of furanosic monosaccharides, pyranosic monosaccharides and disaccharides containing 5 to 12C atoms and one group of the formula: ##STR2## attached to a C-atom thereof, wherein each R 2 , independently is H, C 1 -C 4 alkyl, C 1 -C 4 alkenyl, C 1 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkenyl, C 1 -C 4 haloalkynyl, halogen, OH, C 1 -C 4 ether of C 1 -C 4 amine; r is 0-4; each R 3 , independently, is COOH, CONH 2 , COR 4 , COOR 4 , COOM, SO 4 H, SO 3 HNH 2 , SO 3 R 4 , SO 4 M, PO 4 H 2 , PO 3 HNH 2 , PO 4 HR 4 , PO 2 H(OR 4 ) 2 or PO 4 R 2 4 ; wherein each R 4 , independently, is C 1 -C 4 alkyl, C 1 -C 4 alkenyl, C 1 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkenyl, or C 1 -C 4 haloalkynyl; and M is Na, K, 1/2 Ca or 1/2 Ba; each Y, independently, is X wherein R 3 further is H, C 1 -C 4 alkyl, C 1 -C 4 alkenyl, C 1 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkenyl, C 1 -C 4 haloalkynyl, OH, C 1 -C 4 amine, C 1 -C 4 alkanol or phenyl; and m/n varies from 1 to 10; in an amount effective for inhibiting the formation of CaCO 3 -containing deposits.
Claim 2
Independent Claim 330 words
A method of inhibiting the formation of CaCO 3 -containing deposits on a surface, comprising applying to said surface an anticalcifying composition, comprising: a substoichiometric amount of a monosaccharide or disaccharide polymer of at least 500 MW of the formula Poly (X.sub.n Y.sub.m) wherein the polymer is formed by glycosidic linkages between adjacent monomers; wherein each X independently, is the radical of a monomer selected from the group consisting of furanosic monosaccharides, pyranosic monosaccharides and disaccharides containing 5 to 12C atoms and one group of the formula: ##STR2## attached to a C-atom thereof, wherein each R 2 , independently is H, C 1 -C 4 alkyl, C 1 -C 4 alkenyl, C 1 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkenyl, C 1 -C 4 haloalkynyl, halogen, OH, C 1 -C 4 ether of C 1 -C 4 amine; r is 0-4; each R 3 , independently, is COOH, CONH 2 , COR 4 , COOR 4 , COOM, SO 4 H, SO 3 HNH 2 , SO 3 R 4 , SO 4 M, PO 4 H 2 , PO 3 HNH 2 , PO 4 HR 4 , PO 2 H(OR 4 ) 2 or PO 4 R 2 4 ; wherein each R 4 , independently, is C 1 -C 4 alkyl, C 1 -C 4 alkenyl, C 1 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkenyl, or C 1 -C 4 haloalkynyl; and M is Na, K, 1/2 Ca or 1/2 Ba; each Y, independently, is X wherein R 3 further is H, C 1 -C 4 alkyl, C 1 -C 4 alkenyl, C 1 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkenyl, C 1 -C 4 haloalkynyl, OH, C 1 -C 4 amine, C 1 -C 4 alkanol or phenyl; and m/n varies from 1 to 10; in an amount effective for inhibiting the formation of CaCO 3 -containing deposits.
Claim 3
Dependent Claim 13 words
The method of claim 1 wherein the polymer has a 2,000-10 7 MW.
Claim 4
Dependent Claim 15 words
The method of claim 2 wherein the polymer has a MW of 2,000-10 6 .
Claim 5
Dependent Claim 13 words
The method of claim 3 wherein the polymer has a MW of 2,500-20,000.
Claim 6
Dependent Claim 13 words
The method of claim 4 wherein the polymer has a MW of 3,500-10,000.
Claim 7
Dependent Claim 38 words
The method of claim 1 wherein the surface whereto the polysaccharide is applied is made of a material selected from the group consisting of wood, glass, ceramic, metal, synthetic polymers and copolymers, and painted or otherwise coated surfaces.
Claim 8
Dependent Claim 30 words
The method of claim 1 wherein said polymer is applied in admixture with a carrier in the form of a powder, solution, suspension, gel, oil, aerosol, paste or viscous colloid.
Claim 9
Dependent Claim 17 words
The method of claim 1 wherein the CaCO 3 -containing deposit comprises a CaCO 3 -forming organism.
Claim 10
Dependent Claim 24 words
The method of claim 1 wherein at least 10 -4 μg/ml of the polymer are added to a liquid in contact with said surface.
Claim 11
Dependent Claim 18 words
The method of claim 8 wherein 0.001%-90% by weight of the monosaccharide polymer is applied to said surface.
Claim 12
Dependent Claim 18 words
The method of claim 9 wherein about 0.001-1,000 μg/ml of the monosaccharide polymer are added to said liquid.
Claim 13
Dependent Claim 11 words
The method of claim 7 wherein the carrier is a paint.
Claim 14
Dependent Claim 31 words
The method of claim 1 wherein the polymer is formed from a monosaccharide selected from the group consisting of glucuronic acid, galacturonic acid, mannuronic acid, methyl esters thereof and mixtures thereof.
Claim 15
Dependent Claim 46 words
The method of claim 1 wherein the polymer is formed from at least one monosaccharide selected from the group consisting of glucuronic acid, galacturonic acid, mannuronic acid in combination with at least one other monosaccharide selected from the group consisting of arabinose, ribose, xylose, and rhamnose.
Claim 16
Dependent Claim 59 words
The method of claim 14 wherein the monosaccharide polymer is selected from the group consisting of polygalacturonic acid, polyglucuronic acid, polymannuronic acid, poly (mannuronic acidarabinose), poly (mannuronic acid-ribose), poly (mannuronic acid-xylose), poly (mannuronic acidrhamnose), poly (glucuronic acid-arabinose), poly (glucuronic acid-ribose), poly (glucuronic acidxylose), poly (glucuronic acid-rhamnose), poly (galacturonic acid-arabinose), poly (galacturonic acidribose), poly (galacturonic acid-xylose) and poly (galacturonic acid-rhamnose).
Claim 17
Dependent Claim 35 words
The method of claim 1 wherein the polymer is formed from at least one disaccharide formed form two monosaccharides selected from the group consisting of hexoses, deoxyhexoses, pentoses, and deoxypentoses, wherein R 3 is --COOH.
Claim 18
Dependent Claim 33 words
The method of claim 16 wherein at least one disaccharide is combined with at least one monosaccharide selected from the group consisting of hexoses deoxyhexoses, pentoses and deoxypentoses, wherein R 3 is --COOH.

References Cited (Backward Citations)

US2678303A Cited
US3188289A Cited
US3541009A Cited
US3791978A Cited
US4087371A Cited
US4061585A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-07-28 1990-01-27 1990-07-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-07-28 1994-01-27 1994-07-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-07-28 1998-01-27 1998-07-29 $7700.00 Window Closed / Lapsed

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