Glycoxylated Starch Additive for Pulp Products

Abstract

A glyoxylate starch may be formed by dispersing a starch in a liquid to form a starch slurry. The starch may be one or more of a cationic starch, nonionic starch, and an anionic starch. 2-chloracetamide is added to the starch slurry mixture to form a first reaction mixture. The temperature of the first reaction mixture may then be raised, and then cooled to form a modified starch, and glyoxal may be added to the modified starch solution to form a second reaction mixture that may then be stirred to produce a glyoxylate starch.

Claims

1. An aqueous glyoxylate starch, comprising: starch, a modifying agent, and glyoxal, wherein a weight ratio of water to starch of aqueous glyoxylate starch is from about 99.9:0.1 to about 1,000:500, and, wherein a weight ratio of the modifying agent to the starch of aqueous glyoxylate starch is from about 1:1 to about 1:1,000.

2. The aqueous glyoxylate starch of claim 1, wherein: the starch is selected from the group consisting of cationic starch, anionic starch, and nonionic starch,

3. The aqueous glyoxylate starch of claim 1, wherein: the modifying agent comprises a chloroacetamide.

4. The aqueous synthesized glyoxylate starch of claim 1 wherein: about 0.1 wt % to about 50 wt % of the aqueous glyoxylate starch is starch.

5. The aqueous synthesized glyoxylated starch of claim 1 wherein: the modifying agent comprises about 0.1 wt % to about 500 wt % of the aqueous glyoxylate starch.

6. The aqueous synthesized glyoxylate starch of claim 1 wherein: the aqueous synthesized glyoxylate starch is synthesized utilizing a chemical reaction between the starch and glyoxal.

7. The aqueous synthesized glyoxylate starch of claim 1, wherein: the chemical reaction occurs at a reaction temperature of from about 1 C. to about 300 C.

8. The aqueous synthesized glyoxylate starch of claim 1, wherein: a reaction time of the chemical reaction between starch and glyoxal to form the glyoxylate starch compound is from about 0.01 minutes to about 10,000 minutes.

9. The aqueous synthesized glyoxylate starch of claim 8, wherein: a reaction time of the chemical reaction between starch and glyoxal to form the glyoxylate starch compound is from about 1.0 minutes to about 10,000 minutes.

10. The aqueous glyoxylate starch of claim 1 wherein: the aqueous glyoxylate starch is biodegradable.

11. The aqueous synthesized glyoxylate starch of claim 1, wherein: a weight ratio of water to starch of aqueous glyoxylate starch is from about 99.9:1 to about 1,000:500.

12. The aqueous synthesized glyoxylate starch of claim 8, wherein: the chemical reaction occurs at a reaction temperature of from about room temperature to about 300 C.

13. The aqueous synthesized glyoxylate starch of claim 1, wherein: said aqueous synthesized glyoxylate starch is capable of being used as a strength additive for at least one product selected from the group consisting of pulp fiber products, and textiles.

14. The aqueous synthesized glyoxylate starch of claim 13, wherein: said aqueous synthesized glyoxylate starch is capable of being used as a wet and dry strength additive for pulp fiber products, including paper, wipes, tissues, towels, napkins, paperboard, paper-based food containers, paper-based cups, double re-creped (DRC) items, and textiles.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0011] In the drawings:

[0012] FIG. 1 is a flow chart showing a method of synthesizing a glyoxylate starch composition according to one aspect of the present disclosure;

[0013] FIG. 1A is a flow diagram showing starch being reacted with chloroacetamide;

[0014] FIG. 1B is a flow diagram showing modified starch being reacted with glyoxal to produce glyoxate starch;

[0015] FIG. 2 is a flow chart showing a method of synthesizing a glyoxylate starch composition according to another aspect of the present disclosure;

[0016] FIG. 3 is a graph depicting wet strength of pulp paper sheet (62 gsm) with synthesized glyoxylate starch embodiment and commercial paper wet and dry strength additive (PAE) as well as a glycoxylate PAE additive;

[0017] FIG. 4 is a graph depicting dry strength of pulp paper sheet (62 gsm) with synthesized glyoxylate starch embodiment and commercial paper wet and dry strength additive (PAE) as well as a glycoxylate PAE additive;

[0018] FIG. 5 is a graph depicting wet strength of tissue towel (30 gsm) with synthesized glyoxylate starch embodiment and commercial paper wet and dry strength additive (PAE) as well as a glycoxylate PAE additive; and

[0019] FIG. 6 is a graph depicting dry strength of tissue towel (30 gsm) with synthesized glyoxylate starch embodiment and commercial paper wet and dry strength additive (PAE) as well as a glycoxylate PAE additive.

DETAILED DESCRIPTION OF EMBODIMENTS

[0020] For purposes of description herein the terms upper, lower, right, left, rear, front, vertical, horizontal, and derivatives thereof are not limiting, and it is to be understood that the disclosure may assume various alternative orientations and step sequences, except where expressly specified to the contrary. It is also to be understood that the specific devices and processes illustrated in the attached drawings, and described in the following specification are simply exemplary embodiments of the inventive concepts defined in the appended claims. Hence, specific dimensions and other physical characteristics relating to the embodiments disclosed herein are not to be considered as limiting, unless the claims expressly state otherwise.

[0021] Processes or methods according to the present disclosure are shown in FIGS. 1, 1A, 1B, and 2. As discussed in more detail below, a method/process according to an aspect of the present disclosure may involve two steps. First, starch may be reacted with chloroacetamide as shown in FIG. 1A. Second, the modified starch may then be reacted with glyoxal to produce glyoxate starch as shown in FIG. 1B.

[0022] FIG. 1 depicts steps in an aspect 1A of the present disclosure where the starch is initially dissolved in isopropyl alcohol. Step 2A generally includes dispersing a carbohydrate that may consist of one or more of a cationic starch, a nonionic starch, and an anionic starch in water to form a starch slurry, which may be at a first temperature. The first temperature may be about room temperature (e.g. about 40 C.). At step 4A, a (NaOH) solution (e.g. 15% concentrate, or other suitable concentrate) is combined with the starch slurry formed during step 2A while maintaining a pH of about 10 to form a mixture. It will be understood that in the processes described herein, the pH does not necessarily need to be exactly 10 in order to achieve the desired reaction. For example, a pH in the range of about 9.5 to about 10.5, or a pH in the range of about 9.0 to about 11.0, or a pH outside these ranges may be utilized. Also, it will be understood that virtually any suitable agent (e.g. magnesium hydroxide) or combination of agents may be utilized to provide a suitable pH, and NaOH is merely an example of one suitable compound. At step 6A, the mixture formed at step 4A may be stirred for a first period of time (e.g. about 10 minutes or other suitable time) until the mixture is well mixed.

[0023] At step 8A, 2-chloroacetamide is added into the starch slurry formed at step 6A (preferably while stirring) to allow reaction of the 2-chloroacetamide with the starch to form a first reaction mixture. At step 10A, the first reaction mixture that was formed at step 8A is then stirred for a second period of time (e.g. about 5 hours or other suitable period of time) at a second temperature. The second temperature may be room temperature or other suitable temperature (e.g. about 40 C.) as required to facilitate the reaction. At step 12A, the temperature of the first reaction mixture may be raised to a third temperature (e.g., about 90 C. or other suitable temperature) for a third period of time. The third period of time may be about 10 minutes or other suitable period of time. At step 14A, the first reaction mixture may then be cooled by ambient cooling or other suitable cooling methodology to approximately room temperature (e.g. about 20 C.), and then may be filtered to remove the solvent, to thereby form a modified starch that may consist of one or more of modified cationic starch, a modified nonionic starch, and a modified anionic starch.

[0024] At step 16A, a modified starch is dissolved in hot water (e.g. about 70 C. to about 90 C. or 100 C. or other suitable temperature) to form a modified starch solution. At step 18A, glyoxal is added to the modified starch solution while the modified starch solution is hot (e.g. about 40 C. or 70 C. to about 90 C. or other suitable temperature) to form a second reaction mixture. As shown at step 20A, the second reaction mixture may then be stirred at a suitable temperature (e.g., about 40 C. to 60 C. to about 90 C. or other suitable temperature) for a sufficient time (e.g., about 30 minutes to about 120 minutes or other suitable time period) to form at least one of glyoxylate starch, glyoxylate nonionic starch, and glyoxylate anionic starch.

[0025] With reference to FIG. 2, in a process 1B, glyoxylate is prepared with water only. Specifically, at step 2B, carbohydrate consisting of one or more of cationic starch, nonionic starch (native starch) and anionic starch is dispersed in water at a first temperature to form a starch slurry. At step 4B, NaOH (e.g. about 15% concentrate) solution is combined with the starch slurry formed at step 2B to form a mixture and to maintain a pH of about 8. It will be understood that in the processes described herein, the pH does not necessarily need to be exactly 8 in order to achieve the desired reaction. For example, a pH in the range of about 7.5 to about 8.5, or a pH in the range of about 7.0 to about 9.0, or a pH outside these ranges may be utilized. At step 6B, the mixture is stirred for a first period of time (e.g. about 10 minutes) until the mixture is well-mixed. At step 8B, 2-chloroacetamide is added into the starch slurry (preferably while stirring) to allow reaction with starch to thereby form a first reaction mixture. At step 10B, the first reaction mixture is then stirred for a second period of time (e.g. about 1.5 hours) at a second temperature (e.g. room temperature, or about 20 C., to about 40 C. to 50 C.). The temperature of the first reaction mixture is then raised to a third temperature (e.g. about 80 C. to 115 C., about 95 C. to about 100 C. for third period of time) (e.g. about 10 minutes). At step 14B, the first reaction mixture is cooled by ambient cooling to room temperature (e.g. about 20 C.) to thereby form a modified starch solution including one or more of modified cationic starch, modified nonionic starch, and modified anionic starch. At step 18B, glyoxal is added to the modified starch solution while the modified starch solution is at room temperature (e.g. about 20 C.). At step 20B, the second reaction mixture is stirred at a suitable temperature (e.g. about 20 C. to about 40 C.) for a sufficient time (e.g. about 30 minutes to about 120 minutes) to form at least one of glyoxylate cationic starch, glyoxylate nonionic starch, and glyoxylate anionic starch.

[0026] Glyoxylate starch-based paper strength agents (glyoxylate starch solutions) may be prepared and used as follows. In an experiment, starch (cationic, anionic and nonionic-native starch) was modified with chloroacetamide through a chemical reaction in: a) an aqueous media, b) a solvent media (alcohol) separately (solvent media based modified starch may be separated by filtration to remove the solvent and then dissolved with hot water), and c) glyoxylate with glyoxal. Glyoxal was added to the modified starch solution to form glyoxylate starch through a chemical reaction. The glyoxal/modified starch mixture solution was stirred for a required period of time at a selected temperature to promote reaction between amine groups of modified starch and aldehyde groups of glyoxal to thereby produce a glyoxylate functional group that contains starch. Example 1:1 liter of modified starch solution was prepared by using 50 g modified starch and 950 g hot water. Example 2:1 liter of glyoxylate starch solution was prepared by using 50 g modified starch, 240 g glyoxal, and 830 g water.

[0027] According to another aspect of the present disclosure, hand sheet paper may also be formed. In an experiment, about 0.5% glyoxylate starch solution (based on OD pulp) was mixed with pulp slurry (0.3% consistency) and stirred for about 1 minute before making a hand sheet paper sample. The hand sheet paper was prepared with a hand sheet molding machine. The hand sheet paper samples were dried at 105 C. in an air oven.

[0028] Analysis of hand sheet paper samples properties: The dried hand sheet paper samples were characterized in terms of strength properties such as dry and wet tensile strength, measured in Newtons. These were determined according to TAPPI Standard Methods Tensile properties of paper and paperboard (using constant rate of elongation apparatus) ref: T 494 om-06.

[0029] With further reference to FIG. 3, test results show that starches according to an aspect of the present disclosure may confer significantly increased wet tensile strength of pulp paper sheet (62 gsm) compared to unmodified starch (i.e. starch that has not been modified as described herein). The unmodified starch is designated Control in FIG. 3. The wet tensile strength of commercially available PAE and glycoxylate PAE treatments are also shown in FIG. 3.

[0030] With further reference to FIG. 4, test results also show that pulp paper sheet (62 gsm) treated with synthesized glyoxylate starch according to an aspect of the present disclosure has increased dry tensile strength relative to a control paper that has not been treated with glyoxylate starch. The dry tensile strength of commercially available PAE and glycoxylate PAE treatments are also shown in FIG. 4.

[0031] With further reference to FIG. 5, test results for tissue sheet (30 gsm) treated with synthesized glyoxylate starch according to an aspect of the present disclosure is significantly greater than the wet tensile strength of untreated control tissue sheet. Finally, with further reference to FIG. 6, test results for tissue sheet (30 gsm) treated with synthesized glyoxylate starch according to an aspect of the present disclosure is significantly greater than the dry tensile strength of untreated control tissue sheets. The wet and dry tensile strength of commercially available PAE and glycoxylate PAE treatments are also shown in FIGS. 5 and 6.

[0032] A glyoxylate starch according to the present disclosure may be utilized to provide a bio-based carbohydrate strength agent for paper and/or other products, and may significantly increase wet and/or dry strength of pulp products while also being biodegradable. The test results described above show that a glyoxylate starch according to an aspect of the present disclosure provides increased tensile strength (wet and/or dry) in treated pulp paper sheet products, providing tensile strength that is comparable to paper treated with commercially available strength additives.

[0033] It will be understood that any described processes or steps within described processes may be combined with other disclosed processes or steps to form structures within the scope of the present device. The sequence of the process or method steps described herein are not limited to the sequences described herein unless a different sequence is not possible. The exemplary structures and processes disclosed herein are for illustrative purposes and are not to be construed as limiting.

[0034] It is also to be understood that variations and modifications can be made on the aforementioned structures and methods without departing from the concepts of the present device, and further it is to be understood that such concepts are intended to be covered by the following claims unless these claims by their language expressly state otherwise.

[0035] The above description is considered that of the illustrated embodiments only. Modifications of the device will occur to those skilled in the art and to those who make or use the device. Therefore, it is understood that the embodiments shown in the drawings and described above are merely for illustrative purposes and not intended to limit the scope of the device, which is defined by the following claims as interpreted according to the principles of patent law, including the Doctrine of Equivalents.