CA1239000A - Process for producing granular, water-swellable crosslinked acrylic copolymer, and its use - Google Patents

Abstract

Abstract of the Disclosure A process for producing a granular, water-swel-lable crosslinked acrylic copolymer, which comprises copolymerizing in an aqueous medium in the presence of a radical polymerization initiator a monomeric mixture comprising (a) at least one acrylic amide monomer selected from the group consisting of acrylamide, methacrylamide and N-methyl substitution products of these amides and (b) at least one acrylic crosslinkable comonomer selected from the group consisting of N,N'-alkylene- or arylene-bis-acrylamides, N,N'-alkylene-bismethacrylamides, alkylene-bisacrylates, alkylene-bismethacrylates, alkylene glycol-bisacrylates, polyalkylene glycol-bisacrylates, alkylene glycol-bismethacrylates and polyalkylene glycol-bismeth-acrylates, the proportion of the comonomer (b) being 0.01 to 5 moles per 100 moles of the acrylic amide monomer (a), and forming a granular copolymer; and (i) drying the resulting granular copolymer at a temperature of 105 to 150°C, or (ii) heat-treating the resulting granular copolymer in the presence of moisture under substantially sealed conditions at a temperature of 100 to 160°C; and a method of hydroponically growing a plant, which com-prises growing the plant in artificial soil composed of a granular, water-swellable crosslinked acrylic copolymer.

Description

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This invention relates to a process for product in a granular, water-s~7ellable cross linked acrylic co-polymer, and its use. Particularly, this invention no-fates to a process for producing a granular, water-s~el-fable cross linked acrylic copolymer which has excellent water sealability, shape retention (water insolubility) and transparency, shows excellent performance in its use as artificial soil in regard to water retention, root holding property, air holding property and ornamental property, and is particularly useful as artificial soil in hydroponics; and to its use as artificial soil.
More specifically, this invention pertains to a process for producing a granular, water-swellable cross-linked acrylic copolymer, which comprises copolymerizing in an aqueous medium in the presence of a radical polyp merization initiator a monomeric mixture comprising (a) at least one acrylic aside monomer selected from the group consisting of acrylamide, methacrylamide and N-methyl substitution products of these asides and (b) at least one acrylic crosslinkable comonomer selected from the group consisting of N,N'-alkylene- or arylene-bisacrylamides, N,N'-alkylene-bismethacrylamides, alkylene-bisacrylates, alkylene-bismethacrylates, alkaline glycol-bisacrylates, polyalkylene glycol-bisacrylates, alkaline glycol-bis-methacrylates, and polyalkylene glycol-bismethacrylates, the proportion of the comonomer (b) being 0.01 to 5 moles per 100 moles of the acrylic aside monomer (a), and form-in a granular copolymer; and (i) drying the resulting granular copolymer at a temperature of 105 to 150C, or (ii) heat-treating the resulting granular copolymer in the presence of moisture under substantially sealed conditions at a temperature of 100 to 160C.
This invention also pertains to the use of the 1239~0 resulting granular, water-swellable cross linked acrylic copolymer as artificial toil, particularly for hydra-ponies.
Granular water-swellable cross linked acrylic copolymers derived from acrylic aside monomers and acrylic crosslinkable comonomers have been used, for example, as artificial soil, such as artificial soil in hydroponics, a soil conditioner, etc. In any of these applications, the copolymers are required to have good water sealability.
or use as artificial soil in hydroponics, they are also required to have high transparency to provide ornamental characteristics.
Japanese Laid-Open Patent Publication No.
145908/1981 plaid open on November 13, 1981) relates to a water-exchangeable nontoxic polymeric material derived from an acrylic aside monomer and an acrylic crosslinkable comonomer and a process for its production. The polymeric material is stated to be useful as artificial soil which, for example, serves to make barren lands such as desert or to stabilize soil used for concentrated cultivation, for example soil in greenhouses and pots for flower and other plants.
This Japanese patent document discloses a pro-cuss for producing a water-exchangeable nontoxic water-insoluble polymeric material by copolymerizing acrylamideand N,N'-methylene-bisacrylamide under controlled con-dictions, which comprises (1) dissolving acrylamide and N,N'-methylene-bisacrylamide together in water with the maximum weight ratio of the monomers to water being kept I at 2:8, (2) optionally adding an N-substituted acrylamide monomer further so that the weight ratio of the monomers to water does not exceed said maximum ratio, I adding at least one finely pulverized polymerization initiator, suspended and/or dissolved, while stirring the resulting aqueous solution, (4) copolymerizing the monomers at a temperature higher than 50C, (5) granulating the ~2~90~

resulting gel and washing the granules to a maximum acryl-aside monomer content of not more than 0.1% by weight based on the weight of the final product, and (6) drying the granules at a temperature lower than 100C to a maximum moisture content of 12% by weight based on the final product, and thus completely copolymerizing and curing the granules. The weight ratio of the acrylamide to N,N'-methylene-bisacrylamide exemplified is from 9:1 to 9 9 : 1 .
lot air drying at 95 + 5C is recommended in the above patent document, but the patent document does not refer to drying at more than 100C and is completely silent on heat treatment in the presence of water under substantially sealed conditions.
The water sealability of the granular, water-syllable cross linked acrylic copolymer obtained by the process of this Japanese patent document is not high enough to be satisfactory, and is still desired to be improved. Particularly, the product of this prior art does not have fully satisfactory performance as artificial soil, especially for hydroponics.
The present inventors made extensive invest-gallons in order to provide a granular, water-swellable cross linked acrylic copolymer derived from an acrylic aside monomer and an acrylic crosslinkable comonomer which is useful as artificial soil and can overcome the dip-faculties of the prior acrylic copolymers discussed above.
These investigations have led to the discovery that a granular, water-swellable cross linked acrylic copolymer which is free from the aforesaid difficulties, has excel-lent water-swellability, shape retention and transparency, and shows excellent performance as artificial soil, en-specially for hydroponics, with regard to water holding property, root holding property, air holding property and ornamental characteristics can be provided by Capella-meriting a monomeric mixture comprising 100 moles of (a) an acrylic aside monomer and 0.01 to 5 moles of (b) an acrylic erosslinkable eomonomer in an aqueous medium in the presence of a radical polymerization initiator, form-in a granular product by, for example, granulating the resulting eopolymer into a desired granular form after the eopolymerization or by performing the eopolymerization under such conditions as to form the desired granular eopolymer, and thereafter either (i) drying the granules at a temperature of 105 to 150C (under non-sealed conditions), or (ii) heat-treating the granules in the presence of moisture at 100 to 160C under substantially sealed conditions and as desired, further drying the product at a temperature of, for example, 40 to 150C
(under non-sealed conditions).
It is an object of this invention therefore to provide a process for producing an improved granular, water-swellable erosslinked acrylic eopolymer.
Another object of this invention is to provide the use of the resulting granular, water-swellable cross-linked acrylic copolymer as artificial soil.
The above and other objects and advantages of this invention will become apparent from the following description.
According to the process of this invention, a monomeric mixture composed of (a) at least one acrylic aside monomer selected from the group consisting of acrylamide, methacryliamide and N-methyl substitution products of these asides and (b) at least one acrylic Crosslinkable comonomer selected from the group consist-in of N,~1'-alkylene-bis-acryl- or methacryl-amicies, alkylene-bis-acrylates or methacrylates and (poly)alkylene glycol-bis-acrylates or methacrylates is copolymerized in an aqueous medium in the presence of a radical polymeric ration initiator.
Specific examples of the monomer (A) include aerylamide, methacrylamide and such N-methyl substitution I

products thereof as N-methylacrylamide, N,N-diethylacryl-aside, N-methylmethacrylamide and N,N-dimethylmethacryl-aside. The use of acrylamide and/or methacrylamide is preferred as the monomer (a).
Specific examples of the comonomer (b) include N,N'-~Cl-C6)alkylene- or (C6)arylene-bisacryl- or bismuth-acryl-amides such as N,N'-methylenebis(meth)acrylamide, N,N'-ethylenebis(meth)acrylamide, N,N'-propylenebis(meth)-acrylamide, N,N'-hexamethylenebis~meth)acrylamide and lo N,N'-phenylenebis(meth)acrylamide; (C2-C6)alkylene-bis-acrylates or bismethacrylates such as ethylenebis(meth)-acrylate, propylenebis(meth)acrylate and hexamethylenebis-(meth)acrylate; and polyalkylene glycol-bisacrylates or bismethacrylates having a molecular weight of 214 to 5,000, such as diethylene glycol bis(meth)acrylate, in-ethylene glycol bis(meth)acrylate and polyethylene glycol bis(meth)acrylate.
Of these, N,N'-methylene-bis(meth)acrylamide, N,N'-methylene-bisacrylate and N,N'-methylene-bismeth-acrylate are preferred.
In the present invention, the aforesaid moo-metric mixture may contain a minor amount of (c) an us-saturated monomer copolymerizable with the monomer (a) and the comonomer (by. Examples of the other monomer (c) are acrylic acid, methacrylic acid, malefic acid, functional derivatives of these acids such as their acid androids, salts and esters (e.g., lower alkyd esters), vinyl acetate, styrenes methylstyrene and vinyltoluene. The monomeric units of this type may also be introduced by other means than coplymerization, or example by hydra-louses.
In order to impart protection from algae, mold-profanes and coloration to the granular, water-swellable Cross linked acrylic copolymer obtained in this invention, it is possible to add (d) an unsaturated monomer come potent, such as an anti-algal unsaturated monomer (e.g., owe a vinyl bond-containilng tria7ine-type derivative and a vinyl bond containing organotin compound, a mold proof unsaturated monomer or a coloring unsaturated monomer.
Specific examples of the monomer (d) include 4-(~-acryloyl-5 N-ethyl)amino-6-isopropylamino-2-methylthio-s-triaamine, 4-(N-acryloyl-~-ethyl)amino-2-chloro-6-s-triazine,, 4-(N-acryloyl-N-ethyl)amino-2-chloro-6-isopropylamminors-treason, chlorodibutyltin acrylate, tributyltin acrylate, 6-methylamino-5-[4-~-bromoacryloylamino-2-sulfo]azzoo naphthalene-2-sulfonic acid, 4-(3-acryloylamino-phenyl-amino)-l-amino-anthraquinone-2-sulfonic acid, l-acryloyl-amino-4-phenylaminoanthraquinone, and 1-acryloylamino-4-phenylamimidoanthraquinone.
In the monomeric mixture to be copolymerized by the process of this invention, the proportion of the acrylic crosslinkable comonomer (b) is 0.01 to 5 moles, preferably 0.05 to 3 moles, per 100 moles of the acrylic aside monomer (a). If the proportion of the comonomer by is smaller than the lower limit specified above, the resulting water-swellable cross linked acrylic copolymer becomes too soft. When such a copolymer is used as anti-filial soil particularly for hydroponics, its ability to hold plants is reduced. On the other hand, too large a proportion of the comonomer (b) beyond the upper limit specified reduces the transparency of the resulting water-syllable cross linked acrylic copolymer and degrades its ornamental characteristics.
The amount of the monomer (c) which may further be included in the monomeric mixture is up to 60 moles, for example 0.01 to 60 moles, preferably up to I moles, for example 1 to I moles, per 100 moles of the monomer (a). The amount of the monomer (d) which may further be included in the monomeric mixture is up to 15 moles, for example 0.01 to 15 moles, preferably up to 10 moles, for example 0.01 to 10 moles.
In the present invention, the monomeric mixture owe comprising the acrylic aside monomer (a) and the acrylic crosslinkable monomer IBM an if required, the monomer (c) and/or the monomer (d) is copolymerized in an aqueous medium in the presence of a radical polymerization in-shutter.
The radical polymerization initiator may be a water-soluble radical polymerization initiator such as ammonium per sulfate, potassium per sulfate and sodium persulfateO Two or more of these initiators may be used in combination. The amount of the radical polymerization initiator may be properly selected. For example, it is about 0.001 to about 10 moles, preferably about 0.01 to about 5 moles, per 100 moles of the monomer (a). As required, an amine may be used in combination with the radical polymerization initiator in accordance with a technique known Per so. Examples of such amine are triethanolamine and 3-dimethylaminopropionitrile. The amount of the amine is, for example, 0.1 to 30 moles per mole of the radical polymerization initiator.
The copolymerization reaction may be carried out while the monomeric mixture is in the form of an aqueous solution, or while forming an aqueous dispersion by stir-ring a mixture of an aqueous solution of the monomeric mixture and a solvent inducing phase separation from the aqueous solution under the polymerization conditions. An oil-soluble polymerization initiator such as azobisiso-butyronitrile or ensoul peroxide may also be used as the polymerization initiator in the above process. The "co-polymerization in an aqueous medium", as referred to in the present invention, is meant to include copolymeri-ration in the above-exemplified aqueous dispersion.
The amount of water may be properly selected in performing the copolymerization reaction, and may be any desired amount capable of forming an aqueous solution of the monomeric mixture. For example, it is 100 to 5,000 parts by weight, preferably 200 to 5,000 parts by weight, owe per 100 parts by weight of the monomeric mixture. The polymerization temperature may be properly selected, and is, for example, 10 to 150C, preferably 50 to 100C.
The polymerization time may be properly chosen, and is, for example, 1 to 600 minutes, preferably 3 to 300 minutes.
In the process of this invention, granules in the desired shape are formed by, for example, granulating the resulting copolymer into the desired shape after the copolymerization, or by performing the copolymerization under such conditions as to form a copolymer of a desired granular shape. The granules may be in the shape ox a solid cylinder, a prism (a regular prism, a right prism, a triangular prism, a tetragonal prism, a pentagonal prism, a hexagonal prism, etc.), a cone, a pyramid, a sphere, a hollow cylinder, or a hollow prism.
The granules may be formed by using suitable methods which can give granules of the desired shapes.
Some of the examples are given below.
(1) method which comprises polymerizing a starting aqueous solution containing the monomeric mixture and the radical polymerization initiator by passing it through a tube of a desired shape under heat, extruding the resulting water-s~7ellable gel-like cross linked co-polymer, and cutting the polymer with a cutter to give granules having various prismatic shapes. The surface of the cutter and the inside surface of the polymerization tube may be coated with a fluorine-containing resin such as polyfluoroethylene polymers in order to improve the lubricity of the gel-like cross linked copolymer.

(2) A method which comprises polymerizing the starting aqueous solution by passing it through the tube, extruding the resulting water-swellable gel-like cross-linked copolymer through a Michelle blade of the desired shape to obtain prismatic granules, and cutting the granules with a cutter to obtain granules of various _ 9 prismatic shapes. The surface of the mesh-like blade and the inside surface of the polymerization tube may be coated as in (1).

(3) A method comprising polymerizing the start-in aqueous solution in bulk, and cutting the resulting ingot to form granules of the desired shape.

(4) A method which comprises polymerizing the starting aqueous solution into a plate form, and cutting it by a mesh e blade or a cutter to obtain the desired shape.

(5) A method which comprises polymerizing the starting aqueous solution on a belt conveyor having a polymerization mold of the desired shape.

(6) A method which comprises stirring a mixture composed of the starting aqueous solution and a solvent capable of inducing phase separation from the aqueous solution under the polymerization conditions, thereby to obtain nearly spherical granules. The shape and size of the water-swellable gel-like cross linked copolymer may be varied by changing the type and amount of the solvent, the stirring conditions, the temperature, etc.
In addition, the resulting water-swellable gel-like cross linked copolymer is pulverized to form a powdery or granular polymer according to the purpose of use.
The granular copolymer, as referred to in this invention, is meant to denote all products obtained by the techniques exemplified above.
In the present invention, the resulting granules may be (i) dried (under non-seale~l conditions) at a temperature of 105 to 150C, or (ii) heat-treated at 100 to 160C under sub Stan-tidally sealed conditions in the presence of water. As desired, the heat-treated granules may further be dried (under non-sealed conditions) at a temperature of, for owe it I; ;

example, 40 to 150C.
In the embodiment (i), it is desirable to in-crease the conversion in the copolymerization reaction in order to obtain a cross linked copolymer having excellent S water sealability and transparency. Preferably, there is used a copolymer obtained by performing the copolymeri-ration until the polymerization conversion reaches pro-fireball at least 80%, especially preferably at least 85%.
In the embodiment (i), the water-swellable gel-like cross linked copolymer is cried at a temperature of 105 to 150C, preferably 110 to 15Q C, more preferably 110 to 140C. If the drying temperature is too low beyond the above-temperature range (for example, when it is 100C or less), the water sealability of the polymer is reduced. If it is too high, the transparency of the polymer is very much reduced. Accordingly, the tempera-lure specified above is employed.
The drying treatment may be carried out at a temperature of 105 to 150C by any desired means capable of producing a drying effect. For example, known drying means such as hot air drying and infrared ray drying may be properly carried out. The drying is carried out under non-sealed conditions in which drying is effected.
In the embodiment (ii), the water-swellable gel-like cross linked copolymer is heat-treated at a temperature of 100 to 160C, preferably 110 to 150C, under substantially sealed conditions in the presence of moisture. If the heat-treatment in the presence of water is carried out at a temperature lower than the above-specified limit, no satisfactory improvement in water sealability is obtained. If, on the other hand, the temperature is higher than the upper limit specified, the copolymer is degenerated considerably and becomes sunsuit-able for use as artificial soil in hydroponics.
The heat-treatment in the presence of moisture can be carried out by suitable means which do not produce owe a dry condition with a substantial loss of moisture. Some examples are shown below.
(1) method which comprises heat-treating the water-swellable gel-like cross linked copolymer in the swollen state under substantially sealed conditions in a container.
(2) A method which comprises partially dehydrate in and drying the water-swellable gel-like cross linked copolymer and thereafter heat-treating it under sub Stan-tidally sealed conditions in a container.
(3) method which comprises completely Dodd-rating and drying the water-swellable gel-like cross linked copolymer to give a water-swellable cross linked copolymer, adding water, and then heat-treating the copolymer under substantially sealed conditions in a container.
In any of such methods, the heat-treatment may be carried out under such conditions that moisture is not lost from the vapor or liquid phase. According to the methods (1) and (2), the gel-like cross linked copolymer may be directly heat-treated because it contains water.
As a matter of course, the heat-treatment may be carried out after adding water. According to the method (3), water is adder to the water-swellable cross linked co-polymer prior to heat-treatment. The amount of water to be present may be at least about 0.1 part by weight, per 100 parts by weight of the water-swellable cross linked copolymer in the dry state.
The heat-treatment may be carried out under such substantially sealed conditions that moisture contained in the water-swellable gel-like copolymer is not lost in substantial amounts by evaporation, for example in a sealed vessel such as a sealed tube or autoclave. At this time, the heat-treament may also be carried out in such an atmosphere as argon, helium, carbon dioxide gas, steam, etc. The heat-treatment time can be properly selected, and is, for example, about 3 to about 600 minutes, ~;390~

preferably about 10 to about 300 minutes.
In the heat-treatment method (2), the tempera-lure at which the partial dehydration and drying is carried out before the heat-treatment is not particularly limited, and may, for example, be about 40 to about 150C, preferably 60 to 140C.
As required, the heat-treated water-swellable cross linked polymer may be dried. The drying temperature at this time is usually 40 to 150C, preferably 60 to 140C.
The water-swellable cross linked polymer obtained by the process of this invention has excellent water sealability, shape retention and transparency and can be used in various applications in the shapes exemplified hereinabove. Depending upon its end uses, it may be pulverized in a powdery or granular form after the drying treatment.
The water-swellable cross linked acrylic co-polymer which can be produced as above has a water swell lying ratio of usually at least 65, preferably 70 to ~00.
The water swelling ratio, as used herein, is determined as follows:-A fixed weight owl g) of the dry copolymer is sampled, and immersed in deionized water at 2~C for 24 hours. Then, the copolymer is poured onto a wire gauze having a size of 100 mesh to remove the excess of water.
Then, the weight (We g) of the swollen gel-like polymer is measured. The water swelling ratio is calculated in accordance with the following equation W - W
We The water-swellable cross linked acrylic Capella-men in granular form obtained by the process of this invention is especially useful as artificial soil in agriculture and horticulture, and above all as artificial 1~9~0~

soil in hydroponics.
Thus, according to this invention, there is also provided a method of hydroponically growing a plant, which comprises growing the plant in artificial soil composed of a granular, water-swellable cross linked acrylic copolymer, said acrylic copolymer being obtained by copolymerizing in an aqueous medium in the presence of a radical polymer ration initiator a monomeric mixture comprising (a) at least one acrylic aside monomer selected from the group consisting of acrylamide, methacrylamide and N-methyl substitution products of these asides and (b) at least one acrylic crosslinkable comonomer selected from the group consisting of N,N'-alkylene- or arylene-bisacrylamides, N,N'-alkylene-bismethacrylamides, alkylene-bisacrylates, alkylene-bismethacrylates, (poly)alkylene glycol-bis-acrylates and (poly)alkylene glycol-bismethacrylates, the proportion of the comonomer (b) being 0.01 to 5 moles per 100 moles of the acrylic aside monomer (a), and forming a granular copolymer; and (i) drying the resulting granular copolymer at a temperature of 105 to 150C, or (ii) heat-treating the resulting granular copolymer in the presence of moisture under substantially sealed conditions at a temperature of 100 to 160C.
The artificial soil for hydroponics in accord-ante with this invention is suitable for growing various plants, particularly ornamental plants, because it has good transparency, air holding property, water holding property and root holding property. Furthermore, since it permits good observation of the state of growth of roots, it is also suitable for growing plants in order to test an observing germination and growth of plants, the growing of roots, etc. Suitably, hydroponics on this artificial soil may be practiced in transparent pots, planters and other suitable receptacles made of glass, polystyrene, polyp methyl methacrylate, polyphonies, etc.
The hydroponically technique itself is well known, ~,23900~

and may be practiced in this invention except that the artificial soil of this invention is used. For example, it is possible to sow seeds, plant bulbs and tubers, or transplant seedlings or grow plants in the artificial soil of this invention swollen with water. As required, water used for this purpose may contain suitable amounts and suitable concentrations of fertilizer components such as N, PLY and K. For example, the Holland solution may be dissolved in the water used. At times, a coloring agent may be dissolved in water to provide a greater ornamental effect.
The following examples illustrate the present invention more specifically.
Examples 1 to 8 In each run, a uniform starving solution of the composition shown in Table 1 was continuously fed into a tubular polymerization device of Teflon having an inside diameter of 7 mm and a length of 300 mm, and polymerized at a temperature of 90C for a period of 8 minutes. The resulting water-swollen gel-like cross linked copolymer in the form of a strand having a diameter of 7 mm was con-tenuously cut to a length of 7 mm. The pellets of the copolymer were washed in flowing water for 8 hours to remove the monomers remaining in the copolymer. The washed pellets of the copolymer were dried for 8 hours in a hot air dryer kept at each of the temperatures indicated in Table 1. The physical properties of the resulting semi-transparent poulticed water-swellable cross linked copolymer are shown in Table 1.
The pellets of the copolymer were dipped in water containing a diluted liquid fertilizer (Holland solution) to obtain a transparent water-swollen gel-like cross linked copolymer containing the fertilizer. The swollen gel-like cross linked copolymer (400 ml) was put in US a glass bowl with a diameter of 130 mm and a height of 140 mm, and about 10 cm tall seedlings of begonia and l~?ff(;O

saintpaulia were transplanted in the swollen copolymer in the bowl. They were grown in a well sunlit room while occasionally supplying a diluted aqueous solution of the liquid fertilizer. Four months later, these plants were growing in good condition.

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Examples 9 to 16 In each run, a uniform starting solution of the composition indicated in Table 2 was polymerized, washed in flowing water for 8 hours, and dried for 8 hours in a 5 hot air dryer kept at each of the temperatures shown in Table 2 in the same way as in Example 1. The physical properties of the resulting semi-transparent poulticed water-swellable cross linked polymer are summarized in Table 2.
Examples 17 to 19 In each run, a uniform starting solution of the composition shown in Table 3 was polymerized, washed in flowing water for 8 hours, and dried at 160C for 8 hours in a hot air dryer in the same way as in Example 1.
The polymer, however, foamed in popcorn form. When imp messed in water, the popcorn-like water-swe~lable cross-linked polymer absorbed water and became a water-swollen gel-like cross linked polymer. But this gel became whitely turbid over a broad range, and contained many bubbles.
Its appearance was therefore markedly impaired. The water swelling ratio of the water-swollen cross linked polymer is shown in Table 3.

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crylamide (88 g), 3 g of acrylic acid and 2.0 g of N,N-methylene-bisacrylamide were dissolved in 900 g of water, and 0.1 g of ammonium per sulfate was dissolved in it to form a uniform solution. The solution was continue ouzel fed into a tubular polymerization device of Teflon having an inside diameter of 7 mm and a length of 300 mm, and polymerized at 90C for 10 minutes. The resulting water-swollen gel-like cross linked polymer in the form of a strand having a diameter of 7 mm was cut continuously to a length of 7 mm. The resulting water-swollen gel-like Cross linked polymer was washed in flowing water for 8 hours to remove the monomers remaining in the copolymer.
After washing, the water-swollen gel-like cross linked 15 polymer was dried at 125C for 15 hours in a hot air dryer. The resulting semi-transparent poulticed water-syllable cross linked polymer had a water swelling ratio of 120.
Example 21 A uniform starting solution having the same come position as in Example 20 was polymerized in the same way as in Example 20, washed in flowing water for 8 hours, and then dried at 60C in a hot air dryer. The resulting semi-transparent poulticed water-swellable cross linked 5 polymer had a water swelling ratio of 80.
Examples 22 to 24 In each run, a uniform starting solution of the composition shown in Table 4 was continuously fed into a tubular polymerization device of Teflon having an inside diameter of 7 mm and a length of 300 mm, and polyp merited at ~0C for 8 minutes. The resulting water-swollen cross linked polymer in the form of a strand having a diameter of 7 mm was continuously cut to a length of 7 mm. The resulting pellets of the water-swollen gel-like cross linked copolymer were washed in flowing water for 8 hours to remove the monomers remaining in the water-owe swollen gel-like cross linked copolymer. After washing, 30 g of the water-swollen gel-like cross linked copolymer was put in a stainless steel sealed tube having a capacity of 50 ml and heat-treated in an oil bath kept at each of the temperatures shown in Table 4 for 5 hours. It was then dried to a constant weight in a hot air dryer at 100C.
The physical properties of the resulting semi-transparent poulticed water-swellable cross linked polymer are shown in Table 4.
The pellets of the copolymer were dipped in water containing a diluted liquid fertilizer (Holland solution) to obtain a transparent water-swollen gel-like cross linked copolymer containing the fertilizer. The swollen gel-like cross linked copolymer (400 ml) was put in a glass bowl with a diameter of 130 mm and a height of 140 mm, and about 10 cm tall seedlings of begonia and saint-Paula were transplanted in the swollen copolymer in the bowl. They were grown in a well sunlit room while ox-casionally supplying a diluted aqueous solution of the liquid fertilizer. your months later, these plants were growing in good condition.

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- I -Example 25 uniform starting solution having the same composition as in Example 10 was polymerized in the same way as in Example 22, washed in flowing water for 8 hours, and dried at 60C in a hot air dryer until its water content became 100~ of its own weight. Thirty grams of the resulting semi-transparent poulticed water-swollen cross linked copolymer was put in a 50 ml stainless steel sealed tube, and heat-treated in an oil bath at 140C
for 5 hours. It was then dried in a hot air dryer at 100 C until its weight became constant. The resulting semi-transparent pullets water-swollen cross lined copolymer had a density of 1.30 g/cm3 and a water swell lying ratio of 121.
The pellets of the copolymer were dipped in water containing a diluted liquid fertilizer (Holland solution to obtain a transparent water-swollen gel-like cross linked copolymer containing the fertilizer. The swollen gel-like cross linked copolymer (400 ml) was put in a glass bowl with a diameter of 130 mm and a height of 140 mm, and about 10 cm tall seedlings of begonia and saint-Paula were transplanted in the swollen copolymer in the bowl. They were grown in a well sunlit room while ox-casionally supplying a diluted aqueous solution of the liquid fertilizer. Four months later, these plants were growing in good condition.
example 26 A uniform starting solution of the same come position as in Example 22 was polymerized in the same way as in example 22, and then washed in flowing water fox 8 hours. Thirty grams of the resulting water-swollen gel-like cross linked copolymer was put in a 50 ml stainless steel sealed tube, and heat-treated in an oil bath at 90C for 5 hours, followed by drying to a constant weight in a hot air dryer at 100C. The resulting semitransparent poulticed water-swellable cross linked Jo.

copolymer had a density of 1.30 g/cm3 and a water swell lying ratio of 35.
Example 27 uniform starting solution having the same composition as in Example 22 was polymerized in the same way as in Example 10, and washed in flowing water for 8 hours. Thirty grams of the resulting water-swollen vet-like cross linked copolymer was put in a 50 ml stainless steel sealed tube, and heat-treated in an oil bath at 180C for 5 hours. The polymer consequently became water-soluble and could not be used for the intended application.
Example 28 Acrylamide (88 g), 3 g of acrylic acid and 2.0 g of ~l,N-methylene-bisacrylamide were dissolved in 900 g of water and 0.1 9 of ammonium per sulfate was dissolved to form a uniform solution. The solution was continuously fed into a tubular polymerization device of Teflon having an inside diameter of 7 mm and a length of 300 mm, and polymerized at 90C for 8 minutes. The resulting water-swollen gel-like cross linked copolymer in the form of a strand having a diameter of 7 mm was continuously cut to a length of 7 mm. The resulting water-swollen gel-like cross linked copolymer was washed in flowing water for 8 hours to remove the monomers remaining in the copolymer.
After washing, 30 g of the water-swollen gel-like cross-linked copolymer was put in a 50 ml stainless steel sealed tube and heat-treated in an oil bath at 120C for 1 hour, and then dried in a hot air dryer at 60C for 48 hours.
The resulting semitransparent poulticed water-syllable cross linked polymer had a water swelling ratio of 150.
Example 29 uniform starting solution of the same come position as in Example 10 was polymerized in the same way as in Example 10, washed in flowing water for hours, and owe dried in a hot air fryer at 60C for 48 hours. The resulting semitransparent poulticed w~ter-swollen cross-linked copolymer had a water swelling ratio of 80.

Claims (4)

What is claimed is:

1. A process for producing a granular, water-swel-lable crosslinked acrylic copolymer, which comprises copolymerizing in an aqueous medium in the presence of a radical polymerization initiator a monomeric mixture comprising (a) at least one acrylic amide monomer selected from the group consisting of acrylamide, methacrylamide and N-methyl substitution products of these amides and (b) at least one acrylic crosslinkable comonomer selected from the group consisting of N,N'-alkylene- or arylene-bis-acrylamides, N,N'-alkylene-bismethacrylamides, alkylene-bisacrylates, alkylene-bismethacrylates, alkylene glycol-bisacrylates, polyalkylene glycol-bisacrylates, alkylene glycol-bismethacrylates and polyalkylene glycol-bismeth-acrylates, the proportion of the comonomer (b) being 0.01 to 5 moles per 100 moles of the acrylic amide monomer (a), and forming a granular copolymer; and (i) drying the resulting granular copolymer at a temperature of 105 to 150°C, or (ii) heat-treating the resulting granular copolymer in the presence of moisture under substantially sealed conditions at a temperature of 100 to 160°C.

2. The process of claim 1 wherein the granular water-swellable crosslinked acrylic copolymer had a water swelling ratio of at least 65.

3. The process of claim 1 wherein the resulting granular copolymer is (i) dried at 110 to 150°C, or (ii) heat-treated at 110 to 150°C in the presence of moisture under substantially sealed conditions.

4. A method of hydroponically growing a plant, which comprises growing the plant in artificial soil composed of a granular, water-swellable crosslinked acrylic copolymer, said acrylic copolymer being obtained by copolymerizing in an aqueous medium in the presence of a radical polymerization initiator a monomeric mixture comprising (a) at least one acrylic amide monomer selected from the group consisting of acrylamide, methacrylamide and N-methyl substitution products of these amides and (b) at least one acrylic crosslinkable comonomer selected from the group consisting of N,N'-alkylene- or arylene-bisacryl-amides, N,N'-alkylene-bismethacrylamides, alkylene-bis-acrylates, alkylene-bismethacrylates, alkylene glycol-bis-acrylates, polyalkylene glycol-bisacrylates, alkylene glycol-bismethacrylates and polyalkylene glycol-bismeth-acrylates, the proportion of the comonomer (b) being 0.01 to 5 moles per 100 moles of the acrylic amide monomer (a), and forming a granular copoymer; and (i) drying the re-sulting granular copolymer at a temperature of 105 to 150°C, or (ii) heat-treating the resulting granular copolymer in the presence of moisture under substantially sealed conditions at a temperature of 100 to 160°C.