US2596014A - Preparing wet strength paper using polyarylbiguanide-urea resin - Google Patents

Description

Patented May 6, 1952 PREPARING WET STRENGTH PAPER USING POLYARYLBIGUANIDE-UREA RESIN James R. Dudley, Darien, and John A. Anthes,

Springdale, Conn., assignors to American Cyanamid Company, New York, N. Y., a corporation of Maine No Drawing. Application March 5, 1947, Serial No. 732,660

12 Claims. 1

It has been known for some time that the wet A tensile strength and the bursting strength of paper can be increased by soaking the formed paper in strong solutions of ureaformaldehyde resin, followed by heating the paper to evaporate the water and cure the resin. In some paper mills the urea-formaldehyde resin solution has been applied by spraying the solution onto a moving web of paper, followed by passing the paper over or between heated drying rolls. However, experience has shown that the impregnation of a formed sheet of paper with a resin solution, followed by curing the resin, causes brittleness in the paper with a corresponding reduction in its folding endurance. Moreover, the evaporation of the additional water introduced with the resin requires a second heating of the paper if it has first been dried, or, if the paper is impregnated while it is still wet, a material reduction in the speed of the drying drums. Despite these objections, however, the so-called tub treatment of preformed paper with relatively concentrated aqueous solutions of synthetic resins is still used in some paper mills for special purposes, and the thermosetting resins hereinafter described may be applied by this method within the broader scope of the present invention if desired.

It is a principal object of the present invention to provide paper-making fibers and paper impregnated with a thermosetting urea-formaldehyde resin capable of imparting wet strength thereto, which resin can be applied to the water suspension of hydrated paper stock in the beater, stock chest, head box or at any other suitable point ahead of the paper-forming step. Certain practical advantages are obtained by applying urea-formaldehyde resins, notably the problem of broke recovery is greatly simplified when a ureaaldehyde resin is used.

We have found that the above and. other objects are accomplished by applying to fibrous cellulosic material such as paper pulp certain uncured thermosetting cationic resinous compositions comprising a urea-formaldehyde resin having intercondensed therein water-soluble product of reaction of 1) dicyandiamide with (2) the product of reaction, under acid conditions, of formaldehyde and an amine selected from the class consisting of primary aromatic monoamines and secondary monoamines having at least one monovalent aromatic radical attached to the amine nitrogen atom. In preparing the water-soluble reaction products the formaldehyde and the monoamine are employed in the ratio of from about 0.5 to about 1.5 mols of formaldehyde per mol of the amine, while the dicyandiamide is employed in an amount corresponding to at least about 0.9 mol thereof per mol of the monoamine used in forming the reaction product thereof with formaldehyde.

The water-soluble reaction products used in practicing our invention, which are sometimes referred to herein for purpose of brevity as polyarylbiguanides, are preferably prepared by effecting reaction under acid conditions between 1) dicyandiamide and (2) the product of reaction, under acid conditions, of formaldehyde (including compounds engendering formaldehyde) and either a primary aromatic monoamine, e. g., aniline, or a secondary monoamine having at least one aromatic radical attached to the amine nitrogen atom, e. g., N-methylaniline. In preparing the reaction product of (2) the formaldehyde and the amine are employed in the ratio of from about 0.5 to about 1.5 mols, more particularly from about 0.6 to about 1.3 mols, of the former per mol of the latter. The dicyandiamide is used in an amount corresponding to at least about 0.9 mol thereof, more particularly from about 1 to about 1.3 mols thereof, for each mol of the amine used in forming the reaction product of (2).

The water-soluble reaction product or polyarylbiguanide is caused to react or condense with a urea-formaldehyde partial reaction product, e. g., dimethylol urea or thiourea or similar primary or substantially monomeric urea-formaldehyde reaction or condensation product obtained by effecting reaction or condensation under neutral conditions, or preferably, under slightly alkaline conditions between formaldehyde and a urea reactive therewith, e. urea itself, thiourea, etc. In preparing the cationic, modified ureaformaldehyde resins of this invention, the reaction between the cationic additive or polyarylbiguanide and the urea-formaldehyde partial reaction product is effected under acid conditions, suflicient acid being added to the mixture of reactants, if the pH of the mixture is not initially sufliciently low, to reduce the pH (measured after the reaction has proceeded for some 3 time) to below about 4.5, e. g., about 1.0 to 4.0, and preferably about 1.0 to 2.0 or 2.5.

It is an important feature of the cationic, modified urea-formaldehyde resins of our invention that only relatively small proportions of the polyarylbiguanide need be used to impart the desired catonic properties to the final resin. The importance of using only a relatively small quantity of the polyarylbiguam'de in such resins is one which not only involves cost factors but also the practical usefulness of the resin, since relatively large quantities have a tendency to solubilize the cured resin and thus prevent the formation of a water-insoluble bond between the fibrils of the paper. In general, resins containing a larger quantity of polyarylbiguanide than of urea on a weight basis possess little or no ability to impart wet-strength characteristics to paper. Resins containing a smaller quantity of polyarylbiguanide than of urea, on the other hand, will impart wet strength to the paper, the wet tensile strength ordinarily increasing steadily as the ratio of polyarylbiguanide is decreased to the point Where the resin syrup becomes hydrophobic in character and precipitates upon dilution with water. Accordingly, the preferred resins of our invention are those in which the polyarylbiguanide is employed in an amount corresponding to from about 2 to about 30%, more particularly about 6 to about by weight of the urea component of the urea-formaldehyde resin. Optimum results have been obtained when the polyarylbiguanide constituted about 8 to about 12%, and specifically approximately 10%, by weight of the urea used in making the cationic urea-formaldehyde resin.

In the application of the resins of this invention to paper stock for increasing its wet strength characteristics, the degree of reaction or polymerization of the resin is important.

Tests have shown that much greater wet strength of paper is obtained when the resin is polymerized or advanced in cure to a stage wherein a definite increase in its viscosity has been obtained, e. g., when the reaction has continued until the water-soluble thermosetting resin has so advanced in cure that a 35-40% (more particularly approximately 38%), by weight, aqueous solution thereof (that is, an aqueous solution containing 35-40% by weight of resin solids) has a viscosity at 25 C. of at least about 100 centipoises. Accordingly, we prefer to continue the reaction or polymerization of the resin, e. g., by holding the acidified syrup within an appropriate temperature range, until a viscosity of the order of 100 centipoises or higher at 25 C. has been obtained. The syrup is then preferably neutralized to a pI-I of about 6.5 to 7.5, more particularly 6.75 to 7.25, in order to obtain a product which has optimum stability on storage. In this way resin syrups are obtained that are both water-soluble and water-dilutable. Such liquid resins may be evaporated to dryness and redissolved in water without substantial reduction in their water solubility or in their utility for the production of wet-strength paper.

As has been stated, the cationic, modified ureaformaldehyde resins of this invention can be applied to paper or other felted cellulosic products by tub application methods if desired. Thus, for example, performed and completely or partially dried paper prepared from a chemical pulp such as sulfite, neutral sulfite, rag soda or sulfate, or a mechanical pulp such as ground wood or any mixture thereof may be immersed in a 1% to 10% aqueous solution of the resin and impregnated with about 50 to about by weight thereof, based on the weight of the paper. The paper is then heated for about 1 to 4 minutes at 212 to 300 F. or thereabouts, or for a shorter period of time at higher temperatures, whereby the paper is dried and the resin is cured to a Water-insoluble condition. The resulting paper has greatly increased wet strength as compared with the untreated paper. The method is well suited for the impregnation of paper such as is used in the production of paper towels, absorbent tissues and the like, as well as heavier paper stock such as wrapping paper, bag paper, and the like to impart wet-strength characteristics thereto. a

The cationic resins of this invention are especially adapted for use in processes wherein the resin in its heat-curable (heat-convertible) and hydrophilic or water-dilutable condition is added to an aqueous suspension of the paper stock, such as any of those mentioned hereinbefore, in the beater, stock chest, Jordan engine, fan pump, head box or at any other suitable point ahead of the paper making wire or screen, followed by forming the treated fibers into a felted product on the Wire or cylinder. The quantity of liquid resin which is added to the aqueous stock suspension will depend on such influencing factors as, for example, the degree of dry and wet strength desired in the finished product, the percent of resin retained by the paper fibers, etc. Ordinarily, however, the liquid resin in an amount corresponding to about 0.5% to 5% or more by weight of resin solids is added in this manner, although in some cases as little as 0.1% (calculated as resin solids) may be employed and, for special purposes, as much as 8 to 10% (also calculated as resin solids). The aforesaid percentage figures are based on the weight of the dry paper stock. The felted paper is then dried in the usual manner to dry the paper or board, thereby curing or convertin the resin to a water-insoluble condition and imparting a substantial degree of wet strength to the paper or other product formed of felted cellulosic fibers which has been treated with our new cationic resin. The resin not adsorbed or absorbed by the paper stock may be roused by employing a circulating white-water system; that is, by using a part or all of the white water from the papermaking machine for preparing further batches of paper-pulp suspensions.

The heat-curable resin contained in the paper, whether introduced as a tub size or combined with the cellulosic fibers prior to sheet forma tion by adsorption or absorption in aqueous suspension, can be cured under neutral or acid conditions by subjecting the paper to heat treatment. However, the fastest cure and the highest wet strength are obtained by curing the resin under slightly acid conditions. Hence, it is preferable to acidify the paper stock before, during or after the resin addition thereto. In most cases this acidification can be advantageously accomplished by the addition of about 1 to 3% by weight of aluminum sulfate (alum), based on the weight of the dry paper stock. Since alum is frequently used for the purpose of fixing rosin or wax sizes in the paper, its use therefore involves no added expense. Under these conditions, the desired wet strength is imparted to the paper by a cure of 1 to 2 minutes at about -:'230 to about 260 F., or for shorter periods at higher temperatures. The degree of wet strength is frequently increased by longer heating at lower temperatures, e. g., by storing the finished paper from the drier section in rolls, whereby the heat held by the paper is utilized tocure the resin.

PREPARATION OF CATIONIC ADDITIVE The cationic additive .or polyarylbiguanide is prepared .by eifecting reaction under acid conditions between formaldehyde or a compound en- The reaction between the formaldehyde and the monoamine may be effected at various temperatures ranging, for example, from 40 or 50 C. up to the refiux or boiling temperature of a solution, more particularly an aqueous solution, of the reactants. The time of reaction will vary depending, for instance, upon the particular reactants and proportions thereof employed, the kind of acid used, the pH of the reaction mixture, the temperature employed, etc. When other influencing factors are the same, the time of reaction is longer at the lower temperatures than at the higher temperatures. In order to avoid or lessen the possibility of precipitation, the formaldehyde preferably is added slowly to the monoamine dissolved in an aqueous solution of the acid employed, that is, to an aqueous solution of the monoamine salt. Ordinarily the desired degree of reaction is obtained by heating an acidified aqueous solution of the monoamine under reflux at the boiling temperature of the mass, while slowly adding an aqueous solution of formaldehyde thereto, over a period of from about A; to about 2 /2 hours. In some cases the aqueous formaldehyde may be added rapidly to the acidified solution -of the monoamine and the resulting mixture heated under reflux until any precipitate which forms has redissolved.

The molar proportions of formaldehyde and monoamine are important. If substantially less than about 0.5 mol of formaldehyde per mol of monoamine be employed, the resulting reaction product is too low in molecular weight to provide, upon reaction with dicyandianiide, a satisfactory cationic modifier of urea-formaldehyde resin. If more than about 1.5 mols of formaldehyde per mol of monoamine be used, the product gels and, upon reaction with dicyandiamide, yields a product which, depending upon the amount of formaldehyde employed, either is not water-so1uble or does not form a stable aqueone solution. We prefer to use the formaldehyde and the monoamine in the ratio of from about 0.6 to about 1.3 mole of the former per mol of the latter, g., from 0.7 to 1.2 mols of formaldehyde per mol of the monoamine, e. g., aniline, N-methylaniline, etc. With aniline and an N lower alkyl aniline, more particularly .N-

methylaniline, optimum results have been obtained using about 0.75 mol of an aqueous .solution of formaldehyde per mol of aniline :or N -methylani1ine. With such a cationic additive a modified urea-formaldehyde liquid resin having optimum water solubility can be produced.

The reaction between the formaldehyde and the monoamine is effected under acid conditions, usually strongly acid conditions, e. g., at a pH between 0.5 and 4. Ordinarily the reaction is effected under heat at a pH not substantially exceeding about ,3, more particularly at a pH of 2 or less, e. g., from 0.5 to 2.

Any suitable organic or inorganic acid may be used in obtaining the desired acid conditions for effecting reaction between the formaldehyde and the monoamine. Illustrative examples of acids that may be employed are the inorganic acids, e. g., hydrochloric, hydrobromic, sulfuric, phosphoric, etc., and the organic acids, e. g., formic, acetic, oxalic, tartaric, malic, citric, lactic, benzoic, etc. We prefer to use a strong mineral acid such,f.or example, as hydrochloric acid.

The amount of dicyanidiamide which is reacted with the monoamine-formaldehyde reaction or condensation product is important in so faras the minimum amount thereof is concerned. The dicyandiamide should be employed in an amount corresponding to at least about 0.9 mol thereof 'for each mol of the monoamine used in forming the amine-formaldehyde reaction product. No particular advantage ordinarily accrues from using more than about 1.2 mols of dicyandiamide per mol of the monoamine reactant, although more may be used if desired, for example, 1.5 or more mols of dicyandiamide for each mol of the monoamine employed. When the dicyandiamide is used in an amount above about 1 mol thereof per mol of the monoamine, the excess dicyandiamide above 1 mol is merely present in the final product as unreacted dicyandiamide or as a hydrolysis product thereof. We prefer to use the dicyandiamide in a molar amount approximately equal to the molar amount of monoamine employed or to use a slight molar excess of dicyandiamide, e. g., from 1.05 to 1.15 mols of dicyandiamide per mol of the monoamine employed in forming the amine-formaldehyde reaction product.

The reaction between the dicyandiamide and the amine-formaldehyde reaction product is pref erably efiected or at least initiated under acid conditions. The acidity .of the amine-formaldehyde reaction product .or aqueous solution thereof may be adjusted as desired or as may be required prior to the addition of the .dicyandiamide. For example, if the pH of the aqueous amineformaldehyde reaction product is less than 2, it may be increased by adding a suitable alkaline substance (that is, a substance which gives an alkaline reaction in water) thereto, for instance, a hydroxide or carbonate of an alkali metal (e. g., sodium or potassium hydroxide or carbonate), calcium hydroxide, barium hydroxide, etc. In this way the pH may be increased to, for example, 3 or 4 or more prior to adding the dicyandiamide. As the reaction between the .dicyandiamide and amine-formaldehyde reaction product proceeds, the pH of the reaction mass ordinarily increases. Thus, depending upon the pH of the aqueous reaction product prior to adding the dicyandiamide, it may increase (depending upon the conditions of reaction including the amount of dicyandiamide employed) to from about 4.5 to about 6.5 toward the end of :the reaction period. We .pre-a 7 fer that the pH of the final product, especially when it is to be used as a cationic modifier of a urea-formaldehyde resin, be acid at the end of the reaction period, e. g., a pH of 4.5 to 6.

The amine-formaldehyde reaction product may be diluted with additional water, if desired, prior to adding the dicyandiamide thereto.

The dicyandiamide and amine-formaldehyde reaction product are caused to react at a suitable temperature, for instance, under temperature bonditions such as above described with reference to the production of the amine-formaldehyde reaction product. The time of reaction may vary considerably, the end of the reaction ordinarily being indicated by a substantial change in the color of the original reaction mass. Generally the reaction is completed by heating the reaction mass under reflux at boiling temperature for a period of the order of A to 3 or 4 hours, more particularly for about 1 to 3 hours.

The final aqueous solution of the water-soluble resinous of polymeric reaction product may be diluted or concentrated to obtain a liquid resinous composition of a particularviscosity or a particular concentration of solids. If desired, the product may be substantially completely dehydrated, for example, by heating, preferably under reduced pressure, to obtain a solid, water-soluble, non-crystalline or resinous reaction product. If desired, the reaction product may be precipitated as the free base by adding an aqueous solution of an alkali-metal hydroxide (e. g., sodium hydroxide) thereto, which product then is filtered off and dried. The dried product may be redissolved in an aqueous acid solution. The watersoluble reaction product is essentially polymeric in structure. When aniline is the amine employed in the preparation of the amine-formaldehyde reaction product, the polymer (linear polymer) is believed to correspond substantially to the for- 1 mula where 'nHX represents the acid and amount thereofwhich is combined in the form of a salt with the reaction product of (1) dicyandiamide with (2) the amine-formaldehyde reaction prodnot and it represents a number which is at least 2 and may be as high as 20 or 30 or more.

In order that those skilled in the art better may understand how the present invention may be carried into effect the following examples are given by way of illustration and not by way of limitation. All parts are by weight.

Example 1 Approx. Parts Molar Ratio Aniline 93 1.0 Concentrated hydrochloric acid (approx. 38%

HO] 120 1.25 Aqueous formaldehyde (approx. 37% ECHO)... 60 0.75 Dieyandiamide 84 l. 0 Water The aniline, hydrochloric acid and water were mixed in a reaction vessel provided with a stirrer and a reflux condenser, and the mixture was heated to boiling. The aqueous formaldehyde was added slowly to the stirred, refluxing mixture over a period of /2 hour. A bright red color developed. Refluxing was continued for an additional hour, after which 7 parts of solid sodium' Example 2 Same as Example 1 with the exception that 72 parts instead of 60 parts of aqueous formaldehyde was employed. The resulting solution was darker colored than the product of Example 1 and, on cooling, a second phase separated. The separated phase redissolved upon adding 2.38 parts of concentrated hydrochloric acid to the reaction mass.

Example 3 Approx. Parts Molar Ratio Analine 93 1.0 Concentrated hydrochloric acid (approx. 38%

The aqueous formaldehyde was added rapidly to the stirred mixture of aniline and hydrochloric 7 acid (solution of aniline hydrochloride), yielding a thick, yellow slurry which was heated to boiling with stirring. After heating for about 30 minutes a clear, bright red solution was obtained. The above-stated amount of dicyandiamide was then added all at once, and the resulting mixture was stirred and refluxed for 1%; hours, yielding an orange-colored solution of the reaction product.

Example 4 The same formulas in Example 3 with the exception that in this case 81 parts of 37% aqueous formaldehyde was employed. The aqueous formaldehyde was added slowly over a period of 20 minutes to the refluxing aniline hydrochloride solution. Thereafter 5 parts of solid sodium hydroxide was added in order partly to neutralize the excess hydrochloric acid. The dicyandiamide was added all at once, and the resulting mixture was heated with stirring under reflux at the boiling temperature of the mass for 2 hours, yielding a solution of the reaction product which was somewhat lighter in color than any of the products of the prior examples.

The same general precedure was followed as described under Example 1 with the exception that the excess hydrochloric acid was not neutralized. The addition of formaldehyde was continued until particles of gel began to form around the point of addition, the amount added being Example 6 Approx. Molar Ratio Aniline C(fiigfiitratod hydrochloric acid (approx. 38% Aques rt'rrhhlliiiyli (551 2 65 assess) "I I Dicyandiamide Te concentrated hydrochloric acid was added to the aniline and the resulting solution was: heated with stirring under reflux to boiling. The aqueous formaldehyde was added slowly to the stirred, refluxing solution over a. period of 1% hours. The dicyandiamide was thenadded. all at once, and refluxing and stirring were continued for 1 hours, yielding alight orangecolored solution of the reaction product. Sufiicient Water was added to this solution to provide a solution containing 50%- of solids (calculated as the free base) and having a pH of 5.0. Thesolution of this example was lighter in color than the products ofany of the prior examples.

Example 7 Approx. Molar Parts" Ratio N-methylaniline C(glgintmted hydrochloric and (approx. 38% Aques Manama e lb'ihiiit'v'dg 56136511 I I The N-methylaniline was dissolved in the concentrated hydrochloric acid, and the resulting solution of N-methylaniline hydrochloride was heated with stirring under reflux to boiling. The aqueous formaldehyde was added slowly' to the stirred, refluxing solution over' a period of 1 hour, yielding an orange-coloredsolution. of the N-methylaniline-formaldehyde reaction product- The solution was diluted with waterIto 40% of solids (calculated as the free base)... The dicyandiamide was addedall at once to the. diluted solution, after which the mixture was heated with stirring under reflux at. the boiling temperature of the mass for 2 hours. The color of the solution became lighter anditsviscosity increased toward the end of the reaction period.

The solid, water-soluble product ofv the reaction, which is in solution in the-water, is essentially polymeric in structure. The polymer (linear polymer) is believed to correspond substantially to the formula ILJLH NH 12 where n represents a. number which is atleast 2 and may be as high as 2001' 30 or more- Sufiicient water wasiaddedi to the solutidn.1pre'- pared as above described to provide a" solution containing of solids calculated as the free base.

PREPARATIONOF PoLY R L IGUAmn MODIFIED UREA-FORMALDEHYDE RESIN Our new modified urea-formaldehyde'- resins 10 are preferably prepared by first reacting a reactive urea, specifically urea itself, with an active methylene-containing or yielding substance, e. g., formaldehyde, paraformaldehyde, trioxane, etc., in known manner to form a primary urea; formaldehyde reaction of condensation product, which is usually designated by resin chemists as dimethylol urea and which, regardless of the specific name by which it is designated, is a partial reaction product of urea and formaldehdye. This partial reaction product is prefer;- ably' formed under neutral or slightly alkaline conditions, the latter being obtained by the addition of a small amount of a basic material, that is, a material which gives an alkaline reaction in an aqueous solution, for instance, an alkali-metal hydroxide or carbonate (e. g.,- sodium or potassium hydroxide or carbonate, etc.), an amine, preferably a tertiary amine, e. g., trimethylamine, triethylamine, triethanolamine, etc. A suitable quantity of the polyarylbiguanide is then added, and the resin solution is acidified by the addition of an acid substance, that is, a substance which gives an acid reaction in an aqueous solution, preferably a strong acid, e. g., hydrochloric acid,

- hydrobromic acid, nitric acid, ph0sphoric acid or other strongly acidic material, thereby to reduce the pH of the reaction mass to the desired point, that is, to a pH below about 4.5, e. g., from about 1.0 to 4.0, and preferably 1.0 to 2.0 or 2.5. The reaction between the polyarylbiguanide and the urea-formaldehyde partial reaction product is then caused to proceed under heat, e. g., at temperatures above 40 C., and preferably at elevated temperatures of the order of 70 to 90C., thereby resulting in intercondensation between the reactants.

In order that those skilled in the art better may understand how the present invention may be carried into effect the following examples of the preparation of modified urea-formaldehyde resins embraced by this invention are given by way of illustration and not by way of limitation. All parts are by weight.

The urea was dissolved in the aqueous formaldehyde containing the aqueous triethanolamine, yielding a solution having a pH of 8.5. This solution was heated to 70 C. for 15 minutes to effect partial reaction between the urea and formaldehyde. Thereafter the solution of the cationic additive' was added, followed by 2.38 parts of concentrated hydrochloric acid. I The resulting reaction mass had a pH of 2. The temperature rose on adding the acid to 85 C. The solution was" stirred at -85 C. until a marked increase in viscosity was apparent (about 5 minutes), then adjusted to a pH of about 65-70 with a dilute aqueous solution of sodium hydroxide. The color of the liquid resin was very pale yellow.

Cationic additive as used in this and other examples has reference to the solid reaction product on a net'dry basis.

Example 9 Same as Example 8 with the exception that 202 parts of an approximately 37 aqueous solution of formaldehyde was employed, that is, in the ratio of about 2.5 mols of formaldehyde per mol of urea. The cationic additive was reacted under acid conditions with the urea-formaldehyde partial reaction product for 12 minutes at 80-85 C. or until the viscosity of the product was about the same as the product of Example 8, and was then adjusted to a pH of about 6.5-7.0 with an aqueous NaOH solution. The liquid resin was more water-soluble than the product of Example 8, being dilutable with water in all proportions. Its color was a very pale yellow.

Example 10 Same as Example 8 with the exception that only 7.5 parts of the 40% aqueous solution of the cationic additive of Example 1 was used. Stirring and heating for only 3 minutes at 80-85 C. resulted in a liquid resin having approximately the same viscosity as that of the resins of Examples 8 and 9. The resin was adjusted to a pH of about 6.5-7.0 with an aqueous NaOI-I solution. It was soluble in water in concentrations of less than about 3% and more than about 30% resin solids. It had a barely perceptible yellow color.

Example 11 Same as Example 8 with the exception that 15 parts of a 40% aqueous solution of the cationic additive of Example 2 was used. The liquid resin was a deeper yellow in color than that of the liquid resins of Examples 8, 9, and 10.

Example 12 Same as Example 11 with the exception that 7.5 parts of a 40% aqueous solution of the cationic additive of Example 2 was used. Stirring and heating for only 3 minutes at 80-85 C. resulted in a liquid resin having approximately the same viscosity as that of the preceding examples. It was soluble in very dilute aqueous solutions. The addition of a small amount of acetone increased the solubility characteristics at concentrations between about and 20%.

Earample 13 Same as Example 8 with the exception that parts of a 40% aqueous solution of the cationic additive of Example 4 was used, and the mixture of additive and urea-formaldehyde partial reaction product was stirred at 70 C. until a marked increase in viscosity was noted (about 5 minutes) then adjusted to a pH of about 6.5-7.0 with dilute aqueous NaOH. The liquid resin, which had about the same water solubility as the liquid resin of Example 12, was pale yellow is color.

Example 14 Same as Example 13 with the exception that there were used 7.5 parts of a 40% aqueous solution of the cationic additive of Example 4 and 202 parts of an approximately 37% aqueous solution of formaldehyde, that is, in the ratio of about 2.5 mols of formaldehyde per mol of urea. In this example the reaction period between the cationic additive and the urea-formaldehyde partial reaction product was about 7 minutes at 70 C. The appearance and the water solubility of the liquid resin were about the same as that of the resin of the preceding example.

Example Same as Example 8 with the exception that 15 parts of a 40% aqueous solution of the cationic additive of Example 4 was used. The liquid resin had about the same appearance and water solubility as the resins of Examples 13 and 14.

Example 16 Same as Example 8 with the exception that there were used 30 parts of a 40% aqueous solution of the cationic additive of Example 4 and 194 parts of an approximately 37% aqueous solution of formaldehyde, that is, in the ratio of about 2.4 mols of formaldehyde per mol of urea. The liquid resin was medium yellow in color and was miscible with water in all proportions.

Example 17 Same as Example 13 with the exception that 202 parts instead of 186 parts of aqueous formaldehyde (approx. 37% HCHO) was used, and the mixture of cationic additive and urea-formaldehyde partial reaction product was adjusted to a pH of about 3.0-3.5 instead of the usual 2; also, the reaction mass was stirred and heated for 60minutes at C. instead of about 5 minutes as in Example 13. The liquid resin was pale yellow in color. It was miscible with water but gave cloudy solutions in concentrations of about 10% by weight of resin.

Example 18 Same as Example 8 with the exception that 12 parts of a 50% aqueous solution of the cationic additive of Example 5 and 202' parts of aqueous formaldehyde (approx. 37% HCHO) were used. The acidified reaction mass was stirred and heated for 10 minutes at 70-80 C. The addition of a small amount of acetone increased the .water solubility of the liquid resin at concentrations of about 10% by weight of resin.

Example 19 Same as Example 18 with the exception that about 162 parts instead of 202 parts of aqueousformaldehyde (approx. 37% HCHO) was used, that is, in the ratio of about 2 mols of formaldehyde per mol of urea. The reaction mass was acidified with dilute HCl to a pH of only 4 instead of 2, as in Examples 8-16 and 18, after adding the cationic additive. After stirring and heating for about 3 minutes at 70-80 C. a marked increase in the viscosity of the mass occurred, after which it was adjusted to a pH of about 6.5-7 with 10% aqueous NaOH solution. The water solubility of the liquid resin of this example was about the same as the resin of the preceding example with the exception that slightly more acetone was required to keep the resin in solution in concentrations of about 10% by weight-of resin. No acetone was necessary when the resin concentration in water was about 1% or less. The liquid resin was light yellow in color and slightly cloudy.

Example 20 Same as Example 18 with the exception that 227 parts instead of 202 parts of aqueous formaldehyde (approx. 37% HCHO) was used, that is,

in the ratio of about 2.8 mols of formaldehyde per mol of urea. The reaction mass was acidified I with concentrated HCl to a pH of 2 after adding 13 a pH. of 7.2 by adding a dilute aqueous NaOH. solution. It was clear, pale yellow in color and soluble in water. in concentrations. of less than about 3% and. more. than about 30%. of. resin solids. The liquid resin had. a calculated concentration of about 33% by weight of. resin solids.

Example 21 Same as Example 18 with the exception that 178 parts insteado'i 202 parts of aqueous formaldehyde (approx; 37% I-ICHO) was used, that is; in the ratio of about 2.2. mols of formaldehyde per mol of urea, and the acidified urea-formaldehyde partial reaction product was stirred and heated for about 3 minutes at 70-80 C. It was adjusted to a pH of about 6.5-7.0 by adding a dilute aqueous NaOH solution. The addition of a small amount of acetone. improved; its water-' partial reaction product was about 10 minutes.

at 70 F. Thereafter the liquid resin was adjusted to a pH of 6.85 by adding dilute aqueous NaOH solution. The liquid resin was dilutable with water in all proportions when first made, but

had limited solubility characteristics after standing. for about 48 hours.

Example 23 Approx. Parts Molar Ratio Urea 120 1; Aqueous formaldehyde (approx. 37% HOHO)... 404 2. 5' 50% aqueous solution of cationic additive of Example 6 24 The urea and aqueous formaldehyde were caused to react by heating the mixture thereof, to which had been added sufficient aqueous NaOH solution to impart to the reaction mass a pH of 8.5, for minutes at 70 C. Ihe resulting liquid urea-formaldehyde partial reaction product was acidified with about 6 parts of concentrated hydrochloric acid and the cationic. additive then added immediately thereafter. The pH of the reaction mass after adding. the cationic additive was 1.5. Samples of approximately 50 parts each were withdrawn at intervals of 1, 3, 5, 7 and 9 minutes after the addition of the acid, the reaction mass being heated during this period at 70-80 C. Each sample was adjusted to a pH of about 6.5-7, after which their v-iscosities were determined at C., using an Ostwald viscosimeter. The results were as follows:

Rleactign Viscosity (BT10 1!].

Sample N0 in Centipoises' Minutes at 25 C.

14. Example 24 Same as Example 23 with the exception that partialreaction between the urea and the formal;- dehyde was effected at a pH of about 8.5 obtained by adding about 8.6 parts of a 50% aqueous solution of triethanolamine'. The cationic additive and about 7.2 parts of concentrated HCl. were added; The reaction between the additive and.

the urea-formaldehyde partial reaction product was effected at a pH of about 1.5-2 by heating for 5 minutes at 70 to 80 C. The resulting liquid resin was adjusted to a pH of about 6.5-7 by adding a dilute aqueous NaOH. solution. The

. viscosity of the resinwas 96 centipoises at 25 C.

Eaiwmple-25 Same as Example 8 with the exception that there were used 12 parts of a 50% aqueous solution of the cationic additive of Example 7 and 202 parts of aqueous formaldehyde (approximately 37% I-ICHO), that is, in the ratio of about 2.5 mols of formaldehyde per mol of urea. Partial:

reaction between the urea and formaldehyde was effected at a pH of about 8.5, obtained by adding a 10% aqueous NaOH solution, by heating for 15 minutes at -80 C; The partial reaction product was acidified by adding 2.38 parts of concentrated hydrochloric acid followed by the cationic additive. The pH of the resultingmass was about 2. about 70 C. to effect reaction between the cationic additive and the urea-formaldehyde partial reaction product, after which it was neutralized with dilute aqueous NaOH solution to a pH of about 7.3. The liquid resin was light yellow in color, was miscible with water, and showed no change in appearance after standing for 4 months.

Example 26 Same as Example 25 with the exception that 20 parts of a 50% aqueous solution of the cationic additive of Example 7 was used. Reaction was effected between the urea and formaldehyde, which was adjusted to a pH of about 8.5 with a 10% aqueous NaOH solution, by heating the mixed reactants for 10 minutes at C. After heating the mixture of the cationic additive and the urea-formaldehyde partial reaction product for 5 minutes at about 70 0., the resulting liquid resin was adjusted to a pH of 6.5-7 with 10% aqueous NaOH solution. The liquid resin was light yellow in color and miscible with water in all proportions.

Example 27 Same as Example 26 with the exception that there were used 12 parts of a 50% aqueous solution of the cationic additive of Example 6 and 2035 parts of aqueous formaldehyde (approxi- Example 28 Same as Example 27 with the exception that to the urea-formaldehyde partial reaction prod- It was heated for 5 minutes at uct there were added 4.3 parts of triethanolamine and suflicient hydrochloric acid to bring the reaction mass containing the cationic additive to a pH of 2. The mixture was heated for 3 minutes at 70 C. The liquid resin thereby obtained was adjusted to a pH of about 6.5-7 with 10% aqueous NaOH solution. The liquid resin. was dilutable with water as initially prepared, yielding a cloudy solution. It was more difficultly soluble in water after standing for about 24 hours. The water solubility was increased by adding a small amount of acetone to aqueous solutions of the resin in concentrations of about 3 to 30% by weight of resin solids. An aqueous solution of the resin containing about 35% by weight of resin solids had a viscosity of about 500 centipoises at 25 C.

Example 29 Same as Example 27 with the exception that there was used 12 parts of a 50% aqueous solution of the cationic additive of Example '7, and the reaction mass containing the cationic additive and the urea-formaldehyde partial reaction product was heated for 3% minutes at 70 C. The liquid resin was adjusted to a pH of about 6.5-7 with 10% aqueous NaOH solution. It was miscible with water. An aqueous solution of the resin containing about 35% by weight of resin solids had a viscosity of about 125 centipoises at 25 C.

16 PRODUCTION OF WET STRENGTH PAPER Bleached kraft paper pulp was beaten in the usual manner and made into a water suspension containing about 0.6% by weight of pulp. Portions of this pulp were then treated with each of the liquid resins of Examples 8 to 29, inclusive, diluted to a concentration of 10% by Weight of resin solids. The amount of liquid resin employed in each case corresponded to 3% by weight of resin solids, based on the weight of the dry paper pulp. To the water suspension also was added 3% by weight of alum, likewise based on the weight of the dry pulp. The pH of this dilute suspension of pulp containing the resin and alum was adjusted to 4.5 by addition of hydrochloric acid or sodium hydroxide. The treated suspensions of pulp were made into hand sheets which were heated 1 minute at 220 F. to dry the paper and to cure the resin. Some of the sheets were given an additional heating of 10 minutes at 260 F. to determine the effect of a more complete cure. The sheets were then tested for dry and wet tensile strength (Schopper testing device) along with a sheetmade from the same stock but containing no resin. The values shown are, in each case, the average of 10 determinations on the particular sample. In the following table, the per cent of resin retained is based on the amount of resin added.

TABLE Strength of paper after further Strength of paper after heating for 10 heating for 1 minute at 220 F. in pounds minutes at 260 Eggggf Example N 0. per inch F. in pounds per retained men by paper Dry Wet Dry Wet Untreated paper 20 less than 0.4 8 25. 2 4. 8 26. 4 4. 6 26. 0 4. 0 26. 2 4. 4 24. 0 4. 2 23. 8 4. 4 23. 2 4. 6 23. 6 4. 4 23. 4 4. 2 25. 8 5. 0 24. 2 5. 4 28. 0 8. 2 24. 2 4.4 25. 8 6. 4 29 24. 6 4. 2 26. 2 7. 8 34 25. 6 5. 4 26. 6 7. 8 36 25. 0 5. 0 25. 4 8. O 44 24. 8 3. 4 26. 6 6. 4 38 24. 8 3. 8 24. 2 6. 4 42 25. 4 4. 0 25. 8 7. 0 41 24. 2 4. 2 25. 8 '6. 6 42 24. 4 4. 2 26. 4 7. 4 41 25. 8 4. 4 26. 2 8. 2 39 23. 8 3. 4 26. 2 6. 4 35 25. 2 4. 2 25. 8 8. 0 46 24. 6 4. 0 24. 8 6. 6 39 24. 8 4. 4 26. 4 7. 4 25. 2 4. 0 26. 2 6. 8 44 In Examples 8 to 29, inclusive, the liquid resins, unless otherwise stated, were adjusted to a calculated concentration of 35% by Weight of resin solids if they were not of that concentration as initially prepared. These solutions were subsequently diluted to about 10% by weight of resin solids prior to testing as agents for increasing the wet strength of paper. If the liquid resin was not dil-utable with water to a 10% concentration without separation of resin, suificient acetone (usually about 5% by weight of the final solution) was added to keep the resin in solution at this concentration.

- 7 amount within the range of about 2.0 to about 2.8,. more particularly. from 2.2.. to 2.6,. mols. of

formaldehyde per moltof. urea. Optimum-results.

resin containing about-35 to 40% byweight of.

resin solids has aiviscosity of 200" centipoises at 25- C. When the resin used isone havin'ga viscosity substantially above about 200 centipoises,

e.- gw, 250 to 300 centipoises' or more, the wet strength-of apaper treated with such a more viscous liquid resin is-approximately the same as that obtained using a resinhav-ing a-viscosity of 200 centipoises or less. Since reactionbetween the cationic additiveand the urea-formaldehyde partial reaction product to a point approaching gelation reduces the stabilityof the resin solution-and also its solubility,- aviscosity of the order of' 50 130200,- preferablylOO to 200,centipoises at 25 C; is thepreferred-viscosity of the resins of thisinvention when they are in' the form-ofaqueous solutions containing about 35-to 40% by weight of resin solids;

The stability on storage'of' our-liquid resins is influenced by such-factors as the ratio-offormaldehyde tourea' used in the preparation of the resin, the extent of thereaction between the cationic additive and'the urea-formaldehydepartial reaction product, andthe pH of the liquid resin. The storage stability can be improved by increasing the proportion of formaldehyde above 2.5- mols of formaldehyde per mol of urea or by decreasing the extent or the'reaction between the additive and the urea-formaldehydepartial reaction'product to a point such that the liquid resin has aviscositysubstantially below about 200'centipoises at'25 C. However; such improvements in storage stability obtained-in thismanner are secured only atthe sacrifice of wet strength in the treatedpaper: Within-rather-broad limits the pH- of the liquidresin appears tohave no great effect onthe wet strength or thepaper treated therewith. Forexample; thepI-I of the resin may vary" from 5.0 to 8.5; but preferably is adjusted to a pH within the range of 6375 to- 7125 in order to provide aproduct which hasoptimum stability on storage.

What wecl'aim is:

l. A method of producing wet strength paper which comprises applying to the fibers thereof about 0.1% to 5% 'of a resinous composition comprising aurea-formaldehyde resin having intercondensedthereina water-soluble product of re-.-. actiorrof'(l.) dicyandiamidewith (2) theproduct of reaction, under acidconditions, of f ormaldehyde and anamine selectedifrom theclassconsisting" of" primary aromatic monoamines and secondary monoamines havingat least onemono valent aromatic radical attached to theamine nitrogen atom, the formaldehyde and the amine being employed in-the ratio of from about 0.5 to about 1.5 mols of formaldehyde per mol of the amine, and the dicyandiamide of (1) being :employedin an amount corresponding to'at least about 0.9 mol thereofiper mol of the amine. used informing'thezreaction productof (2). and then heatingsaidpaper at. az-temperature of at least 230-260P F. for ab.outa..1-2zminutes;to. curessaid resin.

2. A, method of. producing. wetj strengthpaper which comprises. applying. to the; fibers. thereof about.0.1%. to; 5% of; a; heat-curable. resinous. composition comprisinga thermosetting, resin obtained by effectinghreaction between (1;). a.

product of. partial. reaction undernon-acidic .co nditions between urea and formaldehydeand, (2)

a water-soluble product of reaction, under acid;

conditions, of (a) dicyandiamidewith. (b). the product of reaction, under/acid conditions of formaldehyde andan amineselected from the class-consisting of :primaryaromaticmonoamines and secondarymonoamines havingat least one;

monovalent aromatic radical attached. to l; the; amine nitrogen atom, .thezformaldehyde and; the

aminebeing employed. in theratiooftfrom; about employed in. an amount corresponding tofrom-Z,

to 30% by weight of. the ureansedin formingthe partial reaction product. of. (1) and. then. heating said paper at atemperatureof at.least 230-260? F. for about l.-2.minutes.to cure saidlresin.

3. A methodtof. producing. wet. strength, paper which comprises applying to the fibers thereof; about.0.1% to. 5% of: a:liquid,,heat-curab1e;cationic resin comprising a solution. of: a thermosetting resin obtained by effecting .reactionunder. acidconditionsbetween (1) aproduct of partial. reaction. under alkaline conditionscbetween. urea and formaldehyde and. (2). a water-soluble prod: uct of. reaction,.under..acid conditions, of (a); dicyandiamide with (b) the product of, reaction,1 under acid conditions, offormaldehyde and;v a, primary aromatic monoamine in: the ratio of; from 0.6.to.1.3.mols of formaldehydepermol of, the said amine, the dicyandiamide of; (a); being employed in an amount correspondingtofrom about 1 to about 1.3 mols thereof for each, molof the amine used. in. forming; the reactionproduct of (b), and the water-solublereaction productof (2) being. employed in ,an amount correspQnding to from. 6. to 15%. by weight .of the urea used in forming the partial. reaction. product. of (1) and. then heating said paper at:a..tempera ture of.:;at least 230 -260 F. for about;1-2.minutes. to cure said resin.

4; A-method of producing wet strength. paper,

which: comprises applying to .the fibersthereofy about 0.1% to 5% ofa-li'quid, heatcurable, catie onic resin comprising a-solution. of a thermoand formaldehyde-and- (2) a water-solubleprodnot of reaction, underacidconditions, of (a:)-di-. cyandiamide with (b) the productof reaction,

underacid conditions; of formaldehyde and an.

N-lower alkyl aniline-in the ratioof from 0.6 to

1.3 mols of formaldehyde permol of the-said-N lower alkyl aniline, the dicyandiamide of (a) being employed in an amount-corresponding to from about 1 to about l.3 mols-thereof for each mol of the N-lower alkyl aniline used in forming the reaction product of (b) and thewater-solu ble reaction product of (2) being-employed-in an" amount corresponding to from 6 to 15% by weight of the ureaused informing thepartialireaction product of (1) and then heating said paper at a temperature of at least 230-260 F. for about 1-2 minutes to cure said resin.

5. A method of producing wet strength paper which comprises applying to the fibers thereof about 0.1% to of a liquid, thermosetting, resinous composition comprising a solution of a water-soluble, heat-curable, cationic, urea-formaldehyde resin having intercondensed therein a water-soluble product of reaction, under acid conditions, of (1) dicyandiamide with (2) the product of reaction, under acid conditions, of formaldehyde and aniline in the ratio of from about 0.5 to about 1.5 mols of formaldehyde per mol of aniline, the dicyandiamide of (1) being employed in an amount corresponding to at least about 0.9 mol thereof for each mm of aniline used in forming the reaction product of (2), and the said water-soluble product of reaction being employed in an amount corresponding to from 2 to by weight of the urea used in the said urea-formaldehyde resin and then heating said paper at a temperature of at least 230-260 F. for about 1-2 minutes to cure said resin.

6. A method of producing wet strength paper which comprises applying to the fibers thereof about 0.1% to 5% of a liquid, thermosetting, resinous composition comprising a solution of a water-soluble, heat-curable, cationic urea-formaldehyde resin having intercondensed therein a water-soluble product of reaction, under acid conditions, of (1) dicyandiamide with (2) the product of reaction, under acid. conditions, of formaldehyde and N-methylaniline in the ratio of from about 0.5 to about 1.5 mols of formaldehyde per mol of N-methylaniline, the dicyandiamide of (1) being employed in an amount corresponding to at least about 0.9 mol thereof for each mol of N-methylaniline used in forming the reaction product of (2) and the said watersoluble product of reaction being employed in an amount corresponding to from 2 to 30% by weight .of the urea used in the said urea-formaldehyde resin and then heating said paper at a temperature of at least 230-260 F. for about 1-2 minutes to cure said resin.

7. A method of producing wet strength paper which comprises applying to the fibers thereof about 0.1% to 5% of a liquid, cationic, hydrophilic, thermosetting, resinous composition comprising an aqueous solution of a water-soluble,

heat-curable resin obtained by effecting reaction under acid conditions between (1) a product of partial reaction under non-acidic conditions between urea and an aqueous solution of formaldehyde in the ratio of from about 2.0 to about 2.8 mols of formaldehyde per mol of urea and (2) a water-soluble product of reaction, under acid conditions, of (a) dicyandiamide with (b) the product of reaction, at a pH not substantially exceeding about 3, of an aqueous solution of formaldehyde and aniline in the ratio of from 0.6 to 1.3 mols of formaldehyde per mol of aniline, the dicyandiamide of (a) being employed in an amount corresponding to from about 1 to about 1.3 mols thereof for each mol of aniline used in forming the reaction product of (b), and the water-soluble reaction product of (2) being employed in an amount corresponding to from 6 to 15% by weight of the urea used in forming the partial reaction product of (1) and then heating said paper at a temperature of at least 230- 260 F. for about l-2 minutes to cure said resin.

8. A method of producing wet strength paper which comprises applying to the fibers thereof about 0.1% to 5% of a liquid, cationic, hydrophilic, thermosetting, resinous composition comprising an aqueous solution of a water-soluble, heat-curable resin obtained by effecting reaction under acid conditions between (1)' a product of partial reaction under non-acidic conditions be-v tween urea and an aqueous solution of formal,- dehyde in the ratio of from about 2.0 to about 2.8 mols of formaldehyde per mol of urea and (2) a water-soluble product of reaction, under acid conditions, of (a) dicyandiamide with (b) the product of reaction, at a pH not substantially exceeding about 3, of an aqueous solution of formaldehyde and N-methylaniline in the ratio of from 0.6 to 1.3 mols of formaldehyde per mol'of N-methylaniline, the dicyandiamide of (a) being employed in an amount corresponding to fromabout 1 to about 1.3 mols thereof for each mol of N-methylaniline used in forming the reaction product of (b), and the water-soluble reaction roduct of (2) being employed in an amount corresponding to from 6 to 15% by weight of the urea used in forming the partial reaction product of (l) and then heating said paper at a temperature of at least 230-260 F. for about 1-2 minutes to cure said resin.

9. A method of producing wet strength paper which comprises applying to the fibers thereof about 0.1% to 5% of an aqueous, cationic, resinous composition which is especially adapted for treating the fibers of paper to increase the wetstrength characteristics of the paper and which i is convertible under heat to a water-insoluble condition, said composition comprising an aqueous solution of a water-soluble, thermosetting resin obtained by effecting reaction under acid conditions between (1) a product of partial reaction under alkaline conditions between urea and an aqueous solution of formaldehyde in the ratio of from 2.2 to 2.6 mols of formaldehyde per mol of urea and (2) a water-soluble product of reaction, under acid conditions, of (a) dicyandiamide with (b) the product of reaction, at a pH of less than 2, of aniline and an aqueous solution of formaldehyde in the ratio of from 0.6 to 1.3 mols of formaldehyde per mol of aniline, the dicyandiamide of (a) being employed in an amount corresponding to from about 1 to about 1.3 mols thereof per mol of aniline used in forming the reaction product of (b), the water-soluble reaction product of (2) being employed in an amount corresponding to from -6 to 15% by weight of the urea used in forming the partia1 reaction product of (1), and the said watersoluble thermosetting resin being so advanced in cure that a 35-40%, by weight, aqueous solution thereof has a viscosity at 25 C. of at least centipoises and then heating said paper at a temperature of at least 230-26 0 F. for about 1-2 minutes to cure said resin.

10. A process for the production of wet strength paper which comprises adding to an aqueous suspension of cellulosic paper stock about 0.1% to 5% of a heat-curable resinous composition comprising a thermosetting resin obtained by effecting reaction between (1) a product of partial reaction under non-acidic conditions between urea and formaldehyde and (2) a water-soluble product of reaction, under acid conditions, of (a) dicyandiamide with (b) the product of reaction, under acid conditions, of formaldehyde and an amine selected from the class consisting of primary aromatic monoamines and secondary monoamines having at least one monovalent aromatic radical attached to the amine nitrogen atom, the formaldehyde and the 21 amine being employed in the ratio of from about 0.5 to about 1.5 mols of formaldehyde per mol of the amine, the dicyandiamide of (a) being employed in an amount corresponding to at 1east about 0.9 mol thereof for each mol of the amine used in forming the reaction product of (b) and the water-soluble reaction product of (2) being employed in an amount corresponding to from 2 to 30% by weight of the urea used in forming the partial reaction product of (1), absorbing about 0.1% to 5% of said resin on said paper stock, forming the stock so treated into a waterlaid sheet, and heating the sheet at a temperature of at least 230-260 F. for about 1-2 min- 12. A process according to claim 10 in which the amount of the water-soluble reaction product of (2) is about 6% to 15% of the weight of the urea.

JAMES R. DUDLEY. JOHN A. ANTHES.

REFERENCES CITED UNITED STATES PATENTS Number Name Date 1,992,589 Tucker Feb. 26, 1935 2,009,173 Gams et a1. July 23, 1935 2,027,090 Carter Jan. '7, 1936 2,325,302 Britt July 27, 1943 2,338,602 Schur Jan. 4, 1944 2,345,543 Wohnsiedler et a1. Mar. 28, 1944 2,395,825 Hesler Mar. 5, 1946 2,407,376 Maxwell Sept. 10, 1946 FOREIGN PATENTS Number Country Date 557,558 Great Britain -1 Nov. 25, 1943 OTHER REFERENCES Paper Industry and Paper World, June 1943, pp. 263-269.

Pacific Pul and Paper Industry, April 1943, pp. 6-8.

Claims (1)

1. A METHOD OF PRODUCING WET STRENGTH PAPER WHICH COMPRISES APPLYING TO THE FIBERS THEREOF ABOUT 0.1% TO 5% OF A RESINOUS COMPOSITION COMPRISING A UREA-FORMALDEHYDE RESIN HAVING INTERCONDENSED THEREIN A WATER-SOLUBLE PRODUCT OF REACTION OF (1) DICYANDIAMIDE WITH (2) THE PRODUCT OF REACTION, UNDER ACID CONDITIONS, OF FORMALDEHYDE AND AN AMINE SELECTED FROM THE CLASS CONSISTING OF PRIMARY AROMATIC MONOAMINES AND SECONDARY MONOAMINES HAVING AT LEAST ONE MONOVALENT AROMATIC RADICAL ATTACHED TO THE AMINE NITROGEN ATOM, THE FORMALDEHYDE AND THE AMINE BEING EMPLOYED IN THE RATIO OF FROM ABOUT 0.5 TO ABOUT 1.5 MOLS OF FORMALDEHYDE PER MOL OF THE AMINE, AND THE DICYANDIAMIDE OF (1) BEING EM PLOYED IN AN AMOUNT CORRESPONDING TO AT LEAST ABOUT 0.9 MOL THEREOF PER MOL FO THE AMINE USED IN FORMING THE REACTION PRODUCT OF (2) AND THEN HEATING SAID PAPER AT A TEMPERATURE OF AT LEAST 230*-260* F. FOR ABOUT 1-2 MINUTES TO CURE SAID RESIN.