A POLYMERIC MATERIAL COMPOSITION

Abstract

The present invention provides a polymeric material composition comprising: (a) at least one superabsorbent polymer; and (b) 0.1% w/w to 2% w/w microporous silicon dioxide; wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the polymeric material composition at room temperature. The present invention further provides process of preparing said polymeric composition and method of its application.

Claims

1. A combination comprising: (a) at least one superabsorbent polymer; and (b) a microporous silicon dioxide; wherein the superabsorbent polymer absorbs less than 15% w/w moisture by its weight at room temperature.

2. A polymeric material composition comprising: (a) at least one superabsorbent polymer; and (b) 0.1% w/w to 2.5% w/w microporous silicon dioxide; wherein said composition has a moisture content lesser than 15% w/w of the total weight of said composition at room temperature.

3. The polymeric material composition as claimed in claim 2 wherein said superabsorbent polymer is a starch based superabsorbent polymer.

4. The polymeric material composition as claimed in claim 3 wherein said starch based superabsorbent polymer is selected from the group comprising starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt, starch-g-poly (2-propenamide-co-2-propenoic acid) sodium salt, starch-g-poly (propenoic acid) sodium salt and starch-g-poly (propenoic acid) potassium salt.

5. The polymeric material composition as claimed in claim 2 wherein said superabsorbent polymer has a particle size ranging from about 2380 ?m to about 149 ?m.

6. The polymeric material composition as claimed in claim 2 wherein said superabsorbent polymer is in the form of granules or powder.

7. The polymeric material composition as claimed in claim 2 wherein said superabsorbent polymer has a water absorption capacity from about 300 times to about 1000 times its weight.

8. The polymeric material composition as claimed in claim 2 wherein said microporous silicon dioxide is selected from amorphous silica and precipitated silica.

9. The polymeric material composition as claimed in claim 2 wherein said polymeric material composition exhibits non-hygroscopic characteristics with moisture content lesser than 15% w/w of the total weight of said composition at room temperature in humidity ranging from 80-90%.

10. The polymeric material composition as claimed in claim 2 wherein said composition comprises starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt and 0.1% w/w to 2% w/w microporous silicon dioxide; and wherein said composition has a moisture content lesser than 15% w/w of the total weight of said composition at room temperature in humidity ranging from 80-90%.

11. A process of preparing a polymeric material composition comprising a superabsorbent polymer; and 0.1% w/w to 2% w/w microporous silicon dioxide; wherein the polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of said composition at room temperature and in humidity ranging from 80-90%; and wherein process comprises the steps of: 1. contacting at least one superabsorbent polymer and microporous silicon dioxide in a mixing vessel; and 2. blending the contents of step (1) to obtain the polymeric material composition.

12. A method of treating soil, plants and plant propagation material by applying to their locus, a polymeric material composition comprising: at least one superabsorbent polymer; and 0.1% w/w to 2% w/w microporous silicon dioxide wherein said polymeric material composition exhibits non-hygroscopic characteristics with moisture content lesser than 15% w/w of the total weight of said composition at room temperature and in humidity ranging from 80-90%.

13. The method as claimed in claim 12 wherein said polymeric material composition comprises starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt; and 0.1% w/w to 2% w/w microporous silicon dioxide wherein said polymeric material composition exhibits non-hygroscopic characteristics with moisture content lesser than 15% w/w of the total weight of said composition at room temperature and in humidity ranging from 80-90%.

14. Use of the polymeric material composition as claimed in claim 2 for water retention.

15. The polymeric material composition as claimed in claim 9 wherein said composition comprises starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt and 0.1% w/w to 2% w/w microporous silicon dioxide; and wherein said composition has a moisture content lesser than 15% w/w of the total weight of said composition at room temperature in humidity ranging from 80-90%.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0043] Surprisingly, inventors of the present invention found that a polymeric material composition of starch-grafted SAPs with enhanced non-hygroscopic characteristics can be obtained by combining 0.1% w/w to 2% microporous silicon dioxide with starch grafted superabsorbent polymers. Addition of microporous silicon dioxide below 2% exhibited marked improvement in caking tendency of starch grafted SAPs by effectively controlling inherent moisture of superabsorbent polymer as well as by providing suitable barrier from surrounding moisture. The polymeric material composition developed according to the present invention do not agglomerate when exposed to a humid environment, i.e., it comprises preferably about 90% or more free-flowing particles and moisture content lesser than 15% at room temperature and in humidity ranging from 80-90%.

Advantages of the Present Invention

[0044] The polymeric composition can be stored and shipped, even in hot, humid locations with little or no caking problems.

[0045] The polymeric composition retains the regular particle size distribution.

[0046] The polymeric composition offers dust reduction and remain intact while shipping and storage.

[0047] Some of the objects and advantages of the invention having been stated, other objects and advantages will become evident as the description proceeds.

[0048] Within the context of this specification, the terms superabsorbent polymer or SAP or polymer gel refer to water swellable polymers that can absorb water many times their weight in an aqueous solution. Without wishing to be bound by theory, the term superabsorbent polymers also apply to polymers that absorb water as well as de-sorb the absorbed water.

[0049] The superabsorbent polymer may be selected from but not limited to water-swellable or water absorbing or water-retentive polymers such as cross-linked polymers that swell without dissolving in the presence of water, and may, absorb at least 10, 100, 1000, or more times their weight in water.

[0050] Accordingly, in an embodiment of the present invention, provided is a polymeric material composition comprising: [0051] (a) at least one superabsorbent polymer; and [0052] (b) 0.1% w/w to 2% w/w microporous silicon dioxide;
wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature.

[0053] According to an embodiment of the present invention, there is provided a polymeric material composition comprising: [0054] (a) at least one superabsorbent polymer, and [0055] (b) 0.1% w/w to 2% w/w microporous silicon dioxide;
wherein said composition has a moisture content lesser than 15% w/w of the total weight of the composition at room temperature.

[0056] According to an embodiment, the superabsorbent polymers of the polymeric material composition is selected from, but not limited to, copolymer of acrylamide and sodium acrylate, copolymer of acrylamide and potassium acrylate; hydrolyzed starch-polyacrylonitrile; 2-propenenitrile homopolymer) or poly(2-propenamide-co-2-propanoic acid, sodium salt); starch-g poly(2-propenamide-co-2-propanoic acid, mixed sodium and aluminium salts); starch g-poly(2-propenamide-co-2-propanoic acid, potassium salt); poly(2-propenamide-co-2-propanoic acid, sodium salt); Starch-g-poly (propenoic acid) sodium salt, Starch-g-poly(propenoic acid) potassium salt, poly-2-propanoic acid, sodium salt; starch-g poly(acrylonitrile) or poly(2-propenamide-co-sodium acrylate); starch/acrylonitrile copolymer; crosslinked copolymers of acrylamide and sodium acrylate; crosslinked polymers of acrylamide and sodium polyacrylate; anionic polyacrylamide; starch grafted sodium polyacrylates; crosslinked copolymers of potassium polyacrylate and polyacrylamide; sodium polyacrylate; superabsorbent polymer laminates and composites; partial sodium salt of crosslinked polypropenoic acid; potassium polyacrylate, lightly crosslinked; sodium polyacrylate, lightly crosslinked; poly(sodiumacrylate) homopolymer; polyacrylamide polymers, carrageenan, agar, alginic acid, guar gums and its derivatives, and gellan gum.

[0057] According to a preferred embodiment of the present invention, the superabsorbent polymers are selected from starch-based superabsorbent polymer that includes a monomer graft polymerized onto starch in the presence of an initiator to form a starch graft copolymer.

[0058] According to a preferred embodiment of the present invention, the superabsorbent polymers are selected from group comprising of copolymers of hydrolyzed starch-polyacrylonitrile; 2-propenenitrile homopolymer, hydrolyzed, sodium salt or poly(acrylamide co-sodium acrylate) or poly(2-propenamide-co-2-propanoic acid, sodium salt); starch-g-poly(2propenamide-co-2-propanoic acid, mixed sodium and aluminium salts); starch-g-poly(2-propenamide-co-2-propanoic acid, potassium salt); poly(2-propenamide-co-2-propanoic acid, sodium salt); poly-2-propanoic acid, sodium salt; starch-g-poly(acrylonitrile) or poly(2-propenamide-co-sodium acrylate).

[0059] In a preferred embodiment, the superabsorbent polymers are selected from the group comprising starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt, starch-g-poly(2-propenamide-co-2-propenoic acid) sodium salt, starch-g-poly (propenoicacid) sodium salt, starch-g-poly (propenoic acid) potassium salt, sodium polyacrylamide and potassium polyacrylamide.

[0060] According to preferred embodiment of the present invention, the superabsorbent polymer is starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt or crosslinked polyacrylic acid potassium salt.

[0061] According to another embodiment of the present invention, particle size of the superabsorbent polymers is in the range from about 2380 ?m to about 149 ?m (equivalent to 8-100 mesh).

[0062] According to another embodiment of the present invention, superabsorbent polymers comprise from about 0.1% w/w to about 99.9% w/w and preferably from about 50% w/w to about 99.5% w/w of the total weight of the composition.

[0063] In a preferred embodiment of the present invention superabsorbent polymers comprises from about 80% w/w to about 99% w/w of the total weight of the composition.

[0064] According to an embodiment of the present invention superabsorbent polymers have inherent moisture content ranging from 5% w/w to 15% w/w.

[0065] According to an embodiment of the present invention superabsorbent polymers have inherent moisture content less than 12% w/w.

[0066] According to an embodiment of the present invention superabsorbent polymers have inherent moisture content less than 10% w/w.

[0067] According to an embodiment of the present invention superabsorbent polymer has the water absorption capacity from about 300 times to about 1000 times its weight.

[0068] According to an embodiment of the present invention superabsorbent polymers have the water absorption capacity from about 500 times to about 800 times its weight.

[0069] According to an embodiment of the present invention superabsorbent polymers are in the form of powder and granules.

[0070] According to an embodiment of the present invention superabsorbent polymers are in the form of powder.

[0071] According to an embodiment of the present invention superabsorbent polymers are in the form of granules.

[0072] According to an embodiment of the present invention superabsorbent polymers of the polymeric material composition are biodegradable.

[0073] According to an embodiment of the present invention starch grafted superabsorbent polymers of the polymeric material composition are biodegradable.

[0074] According to an embodiment of the present invention, the polymeric material composition exhibits anti-caking characteristics in that more than about 90% of the composition particles, by weight, will pass through a U.S. Standard 12 mesh sieve with 1700 micrometer openings after at least 3 hours at about 36?3? C. and about 77?3% relative humidity.

[0075] According to an embodiment of the present invention the polymeric material composition comprises of microporous silicon dioxide.

[0076] According to an embodiment of the present invention the polymeric material composition comprises of microporous silicon dioxide selected from fumed silica and precipitated silica.

[0077] According to an embodiment of the present invention the polymeric material composition comprises the microporous silicon dioxide in an amount less than about 2.5% of the total weight of the composition.

[0078] According to an embodiment of the present invention the polymeric material composition comprises the microporous silicon dioxide in an amount less than about 2.0% of the total weight of the composition.

[0079] According to an embodiment of the present invention the polymeric material composition comprises the microporous silicon dioxide in an amount less than about 1.5% of the total weight of the composition.

[0080] According to an embodiment of the present invention the polymeric material composition comprises from about 0.1% w/w to about 2% w/w microporous silicon dioxide of the total weight of the composition.

[0081] According to an embodiment of the present invention the polymeric material composition comprises from about 0.1% w/w to about 1% w/w microporous silicon dioxide of the total weight of the composition.

[0082] In an embodiment of the present invention, there is provided a combination comprising: [0083] (a) at least one superabsorbent polymer; and [0084] (b) microporous silicon dioxide.

[0085] According to an embodiment of the present invention, there is provided a polymeric material composition comprising: [0086] (a) at least one superabsorbent polymer; and [0087] (b) 0.1% w/w to 2% w/w microporous silicon dioxide;
wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0088] According to an embodiment of the present invention, there is provided a polymeric material composition comprising: [0089] (a) at least one superabsorbent polymer; and [0090] (b) 0.1% w/w to 2% w/w microporous silicon dioxide;
wherein said composition has a moisture content lesser than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0091] According to an embodiment of the present invention, the polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0092] According to an embodiment of the present invention, the polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 12% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0093] According to an embodiment of the present invention, the polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 10% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0094] According to an embodiment of the present invention, the polymeric material composition has a moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0095] According to an embodiment of the present invention, the polymeric material composition has a moisture content less than 12% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0096] According to an embodiment of the present invention, the polymeric material composition has a moisture content less than 10% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0097] According to an embodiment of the present invention the polymeric material composition comprises of at least one starch grafted superabsorbent polymer and 0.1% w/w to 2% w/w microporous silicon dioxide wherein said polymeric material composition has a moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0098] According to an embodiment of the present invention, the polymeric material composition comprises of starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt and 0.1% w/w to 2% w/w precipitated silica wherein said polymeric material composition has a moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0099] According to an embodiment of the present invention the polymeric material composition comprises starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt and 0.1% w/w to 2% w/w fumed silica wherein said polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0100] According to an embodiment of the present invention, a process of preparing a polymeric material composition comprising a superabsorbent polymer and 0.1% w/w to 2% w/w microporous silicon dioxide; wherein said polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%; and wherein said process comprises steps of: [0101] 1. contacting the superabsorbent polymer and microporous silicon dioxide in a mixing vessel; and [0102] 2. blending the contents of step (1) to obtain the polymeric material composition.

[0103] According to an embodiment of the present invention the process of preparing polymeric material composition comprising at least one superabsorbent polymer and 0.1% w/w to 2% w/w microporous silicon dioxide; wherein said polymeric material composition has a moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%; and wherein said process comprises the steps of: [0104] 1. contacting superabsorbent polymers and microporous silicon dioxide in a mixing vessel; [0105] 2. blending the contents of step (1) to obtain polymeric material composition.

[0106] According to an embodiment of the present invention the process of preparing a polymeric material composition comprising a starch grafted superabsorbent polymer and 0.1% w/w to 2% w/w microporous silicon dioxide; wherein said polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%; and wherein process comprises the steps of: [0107] 1. contacting the starch grafted superabsorbent polymer and microporous silicon dioxide in a mixing vessel; and [0108] 2. blending the contents of step (1) to obtain polymeric material composition.

[0109] According to an embodiment of the present invention the process of preparing a polymeric material composition comprising at least one starch grafted superabsorbent polymer and 0.1% w/w to 2% w/w microporous silicon dioxide; wherein polymeric material composition has a moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%; and wherein the process comprises the steps of: [0110] 1. contacting at least one starch grafted superabsorbent polymer and microporous silicon dioxide in a mixing vessel; and [0111] 2. blending the contents of step (1) to obtain the polymeric material composition.

[0112] According to an embodiment of the present invention, blending of superabsorbent polymer and microporous silicon dioxide is carried out in suitable mixing equipment such as ribbon blender, plough mixer, and horizontal non-gravity mixer.

[0113] According to an embodiment of the present invention, blending of superabsorbent polymer and microporous silicon dioxide is carried out from about 5 min to about 30 min to obtain a homogeneous polymeric material composition.

[0114] According to an embodiment of the present invention, provided is a method of treating plants and plant propagation material by applying to their locus, a polymeric material composition comprising: at least one superabsorbent polymer and 0.1% w/w to 2% w/w microporous silicon dioxide wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0115] According to an embodiment of the present invention, the method of treating plants and plant propagation material comprises applying to their locus, a polymeric material composition comprising: at least one superabsorbent polymer; and 0.1% w/w to 2% w/w microporous silicon dioxide wherein said polymeric material composition exhibits non-hygroscopic characteristics with moisture content lesser than 15% w/w of the total weight of said composition at room temperature and in humidity ranging from 80-90%.

[0116] According to an embodiment of the present invention, the method of treating plants and plant propagation material comprises applying to their locus, a polymeric material composition comprising: at least one starch grafted superabsorbent polymer and 0.1% w/w to 2% w/w microporous silicon dioxide wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0117] According to an embodiment of the present invention, the method of treating plants and plant propagation material comprises applying to their locus, a polymeric material composition comprising: at least one starch grafted superabsorbent polymer and 0.1% w/w to 2% w/w microporous silicon dioxide wherein polymeric material composition has a moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0118] According to an embodiment of the present invention, the method of treating plants and plant propagation material comprises applying to their locus, a polymeric material composition comprising starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt and 0.1% w/w to 2% w/w precipitated silica wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0119] According to an embodiment of the present invention, the method of treating plants and plant propagation material comprises applying to their locus, a polymeric material composition comprising starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt and 0.1% w/w to 2% w/w fumed silica wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0120] According to an embodiment of the present invention, polymeric material composition is used for fluid retention.

[0121] According to an embodiment of the present invention, polymeric material composition is used in agriculture for soil application for water retention.

[0122] According to an embodiment of the present invention, polymeric material composition is used in agriculture for soil application along with other agriculturally relevant substances such as agrochemicals and fertilizers.

[0123] According to an embodiment of the present invention, the polymeric material composition comprises from about 90% w/w to about 99.9% w/w superabsorbent polymer(s) and from about 0.1% w/w to about 2% w/w microporous silicon dioxide; wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0124] According to an embodiment of the present invention the polymeric material composition comprises superabsorbent polymer(s) and 0.1% w/w to 2% w/w microporous silicon dioxide; wherein said composition has a moisture content lesser than 15% w/w of the total weight of the composition at room temperature in humidity ranging from 80-90%.

[0125] According to an embodiment of the present invention the polymeric material composition comprises starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt and 0.1% w/w to 2% w/w precipitated silica; and wherein said composition has a moisture content lesser than 15% at room temperature in humidity ranging from 80-90%.

[0126] According to an embodiment of the present invention the polymeric material composition comprises starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt and 0.1% w/w to 2% w/w fumed silica; and wherein said composition has a moisture content lesser than 15% at room temperature in humidity ranging from 80-90%.

[0127] According to an embodiment of the present invention, the polymeric material composition comprises from about 98% w/w to about 99.9% w/w superabsorbent polymers and from about 0.1% w/w to about 1% w/w microporous silicon dioxide; wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%.

[0128] According to an embodiment of the present invention, the polymeric material composition comprises from about 98% w/w to about 99.9% w/w superabsorbent polymer of 8 mesh to 60 mesh and from about 0.1% w/w to about 1% w/w precipitated silica; wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%; and wherein said polymeric material composition is in the form of coarse granules.

[0129] According to an embodiment of the present invention, the polymeric material composition comprises from about 98% w/w to about 99.9% w/w superabsorbent polymer of 100 mesh and from about 0.1% w/w to about 1% w/w precipitated silica; wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%; and wherein said polymeric material composition is in the form of fine powder.

[0130] According to an embodiment of the present invention, the polymeric material composition comprises from about 98% w/w to about 99.9% w/w superabsorbent polymer of 8 mesh to 60 mesh and from about 0.1% w/w to about 1% w/w fumed silica; wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%; and wherein said polymeric material composition is in the form of coarse granules.

[0131] According to an embodiment of the present invention, the polymeric material composition comprises from about 98% w/w to about 99.9% w/w superabsorbent polymer of 100 mesh and from about 0.1% w/w to about 1% w/w fumed silica; wherein polymeric material composition exhibits non-hygroscopic characteristics with moisture content less than 15% w/w of the total weight of the composition at room temperature and in humidity ranging from 80-90%; and wherein said polymeric material composition is in the form of fine powder.

[0132] In an embodiment of the present invention, the polymeric material composition may further comprise one or more agrochemicals, antifreeze agent, wetting agents, fillers, surfactants, anticaking agents, pH-regulating agents, preservatives, biocides, antifoaming agents, colorants and other formulation aids.

[0133] According to an embodiment of the present invention, the polymeric material composition is used in agricultural and horticultural applications.

[0134] According to an embodiment of the present invention, the polymeric material composition application to soil in agricultural settings have resulted in earlier seed germination and/or blooming, decreased irrigation requirements, increased propagation, increased crop growth and production, increased crop quality, decreased soil crusting, increased yield and decreased time of emergence.

[0135] According to an embodiment of the present invention, the polymeric material composition application is used as carrier for applying active ingredients with the purpose of controlling pests and weeds.

[0136] According to an embodiment of the present invention, the polymeric material composition application is used as carrier for micronutrients or fertilizers with the purpose of providing nutrition to the plants.

[0137] It will be understood that the specification and examples are illustrative but not limitative of the present invention and that other embodiments within the spirit and scope of the invention will suggest themselves to those skilled in the art. Other embodiments can be practiced that are also within the scope of the present invention. The following examples illustrate the invention, but by no means intend to limit the scope of the invention.

Example 1: 99.9% w/w Polyacrylamide Coarse Granules

[0138]

TABLE-US-00001 Ingredients Quantity (% w/w) Polyacrylamide polymer (8 to 60 mesh) 99.9 Precipitated silica 0.1 Total 100

[0139] 99.9 g polyacrylamide polymer (8 to 60 mesh) was mixed with 0.1 g silica in a ribbon blender and blended for about 30 minutes. The blended mixture thus obtained was send to quality check to analyse moisture content and packed.

Example 2: 99.9% w/w Polyacrylamide Coarse Granules

[0140]

TABLE-US-00002 Ingredients Quantity (% w/w) Polyacrylamide polymer (8 to 60 mesh) 99.9 Fumed silica 0.1 Total 100

[0141] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (8 to 60 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 3: 99.5% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Coarse Granules

[0142]

TABLE-US-00003 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 99.5 propenoic acid) potassium salt (8 to 60 mesh) Precipitated silica 0.5 Total 100

[0143] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (8 to 60 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 4: 99.4% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Coarse Granules

[0144]

TABLE-US-00004 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 99.4 propenoic acid) potassium salt (8 to 60 mesh) Precipitated silica 0.6 Total 100

[0145] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (8 to 60 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 5: 99% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Coarse Granules

[0146]

TABLE-US-00005 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 99 propenoic acid) potassium salt (8 to 60 mesh) Precipitated silica 1 Total 100

[0147] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (100 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 6: 98.5% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Powder

[0148]

TABLE-US-00006 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 98.5 propenoic acid) potassium salt (8 to 60 mesh) Precipitated silica 1.5 Total 100

[0149] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (8 to 60 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 7: 99.4% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Powder

[0150]

TABLE-US-00007 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 99.4 propenoic acid) potassium salt (100 mesh) Precipitated silica 0.6 Total 100

[0151] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (100 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 8: 99% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Powder

[0152]

TABLE-US-00008 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 99 propenoic acid) potassium salt (100 mesh) Fumed silica 1 Total 100

[0153] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (100 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 9: 98.5% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Powder

[0154]

TABLE-US-00009 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 98.5 propenoic acid) potassium salt (100 mesh) Precipitated silica 1.5 Total 100

[0155] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (100 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 10: 98.5% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Powder

[0156]

TABLE-US-00010 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 98.0 propenoic acid) potassium salt (8 to 60 mesh) Precipitated silica 2.0 Total 100

[0157] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (8-60 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 11: 97.5% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Powder (Comparative Example)

[0158]

TABLE-US-00011 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 97.5 propenoic acid) potassium salt (100 mesh) Precipitated silica 2.5 Total 100

[0159] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (100 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 12: 97.5% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Powder (Comparative Example)

[0160]

TABLE-US-00012 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 97.5 propenoic acid) potassium salt (8 to 60 mesh) Precipitated silica 2.5 Total 100

[0161] Starch-g-poly (2-propenamide-co-2-propenoic acid) potassium salt (8 to 60 mesh) and silica were mixed in above mentioned quantity and processed as per the process given in Example-1.

Example 13: 100% w/w Starch-g-Poly (2-propenamide-co-2-propenoic acid) Potassium Salt Powder (Comparative Example)

[0162]

TABLE-US-00013 Ingredients Quantity (% w/w) Starch-g-poly (2-propenamide-co-2- 100 propenoic acid) potassium salt (8 to 60 mesh) Total 100
Comparative Study of Polymeric Material Composition with Normal Starch-Based Superabsorbent Polymers

[0163] The polymeric material composition prepared according to the present invention was analysed for moisture content and water absorption capacity. It was observed that the compositions of Example-2, 3, 5 and 6 prepared according to the present invention did not suffer decline in absorption capacity. Also, moisture content of the compositions of Example-2, 3, 5 and 6 remain controlled within 15%. The optimum concentration of silica from 0.5% to 1.5% found best to control moisture under 10%. However, the composition of Example-13 deprived of silica became lumpy when kept for 48 hours at room temperature and in humidity ranging from 80-90% and hence was not found suitable for further study. (Table 1 and Table 1A).

TABLE-US-00014 TABLE 1 Example-13 Example-2 Example-3 Sample Sample Sample Kept at 90% Kept at 90% Kept at 90% Humidity Humidity Humidity and 25? C. and 25? C. and 25? C. 0 day for 48 hrs. 0 day for 48 hrs. 0 day for 48 hrs. Physical form/ Flowable Become Flowable Flowable Flowable Flowable Appearance granules Lumpy granules granules granules granules Water absorption in 405 385 409 397 407 412 gm/gm of polymer/ composition Moisture content 5.92 16.33 5.68 13.97 5.52 9.87 (% w/w)

TABLE-US-00015 TABLE 1A Example-5 Example-6 Sample Sample Kept at Kept at 90% 90% Humidity Humidity and 25? C. and 25? C. 0 day for 48 hrs. 0 day for 48 hrs. Physical Flowable Flowable Flowable Flowable form/ granules granules granules granules Appear- ance Water 408 406 405 410 absorption in gm/gm of polymer/composition Moisture content 5.25 8.94 5.11 7.56 (% w/w)

Study of Optimization of Microporous Silicon Dioxide

[0164] Study was conducted to identify most suitable range of microporous silicon dioxide in the polymeric material composition. Several compositions were prepared by incorporating various amounts of microporous silicon dioxide ranging from 0.1% to 2.5%.

[0165] It was observed that the compositions of Example-4 with 0.6% microporous silica and starch based superabsorbent polymer of 8 to 60 mesh size (FIG. 1) remained intact without dusting or separation of microporous silicon dioxide from superabsorbent polymer material. Upon increasing the concentration of microporous silicon dioxide from 0.6% to 2.5% (Example-12 and FIG. 2), clear cut separation of superabsorbent polymer and microporous silicon dioxide was observed.

[0166] Similarly, it was observed that the compositions of Example-7 with 0.6% microporous silica and starch based superabsorbent polymer of 100 mesh size (FIG. 3) remained intact without dusting or separation of microporous silicon dioxide from superabsorbent polymer material. Upon increasing the concentration of microporous silicon dioxide from 0.6% to 2.5% (Example-11 and FIG. 4), clear cut separation of superabsorbent polymer and microporous silicon dioxide was observed.

Real Time Stability Study

[0167] The polymeric material composition prepared according to the present invention was analysed for moisture content and water absorption capacity in real time after keeping the composition intact in trilaminated aluminium pouch for 18 months. It was observed that the compositions of Example-2, 3, 5 and 6 prepared according to the present invention did not suffer decline in absorption capacity even after storing it for 18 months under real time study in trilaminated pouch at ambient conditions. Also, moisture content of the compositions of Example-2, 3, 5 and 6 remain controlled within 15% w/w of the total weight of the polymeric material composition. The optimum concentration of silica from 0.5% w/w to 1.5% w/w was found best to control moisture under 10% w/w of the total weight of the composition. (Table 2).

TABLE-US-00016 TABLE 2 18-months shelf-life storage in trilaminated pouch at ambient conditions Example-2 Example-3 Example-5 Example-6 Example-10 Physical Flowable Flowable Flowable Flowable Flowable form/ granules granules granules granules granules Appear- ance Water 402 408 404 389 380 absorption in gm/gm of SAP Moisture 5.30 6.48 5.78 6.24 6.90 content (% w/w)

[0168] It is clear from the experimental data, as described above, the polymeric material composition of the present invention found to have controlled moisture with free-flowing characteristics. Microporous silicon dioxide within 0.1% w/w to 2% w/w found to control inherent moisture content of starch-based polymers and reduce caking of the polymeric material composition. The polymeric material composition of the present invention found to be very useful in agriculture applications for fluid or water retention. The composition remained quite stable during transport and shelf life. The process described is simple, convenient to perform and does not require any heavy instruments. As such, the spirit and scope of the disclosure should not be limited to the description of the preferred embodiment contained therein.