Pulp composition

Abstract

To provide a novel pulp composition that can be used to produce a pulp molded product with an improved strength.SOLUTION: There is provided a pulp composition, comprising: pulp; wax; and a paper strength agent, wherein the paper strength agent is at least one selected from the group consisting of a polyacrylamide-based paper strength agent, a polysaccharide-based paper strength agent, and a polyamide-based paper strength agent, an amount of the wax is 0.2 wt.% or more and 10.0 wt.% or less with respect to the pulp, and the pulp composition satisfies at least one of the following (1) to (3): (1) an amount of the polyacrylamide-based paper strength agent is 0.1 wt.% or more and 1.1 wt.% or less relative to the pulp; (2) an amount of the polysaccharide-based paper strength agent is 0.6 wt.% or more and 5.0 wt.% or less relative to the pulp; and (3) an amount of the polyamide-based paper strength agent is 0.3 wt.% or more and 0.9 wt.% or less relative to the pulp.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present disclosure relates to oil-proofing agents for waxes and pulp. [Background technology]

[0002] Patent Document 1 discloses a colored paperboard having two or more paper layers in which a dye, a water-resistant agent, and a water-repellent agent are internally added to the surface layer. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Japanese Patent Application Laid-Open No. 2013-129948 Summary of the Invention [Problem to be solved by the invention]

[0004] Patent Document 1 does not consider the type or amount of paper strength agent used, nor does it describe or suggest the strength of molded pulp products.

[0005] An object of the present disclosure is to provide a novel pulp composition that can be used to produce molded pulp products with improved strength. [Means for solving the problem]

[0006] The present disclosure includes the following aspects: [Section 1] A pulp composition comprising pulp, wax, and a paper strength agent, The paper strength agent is at least one selected from the group consisting of polyacrylamide-based paper strength agents, polysaccharide-based paper strength agents, and polyamide-based paper strength agents, The amount of the wax is 0.2% by weight or more and 10.0% by weight or less with respect to the pulp, The following (1) to (3): (1) The amount of the polyacrylamide-based paper strength agent is 0.1% by weight or more and 1.1% by weight or less relative to the pulp; (2) The amount of the polysaccharide-based paper strength agent is 0.6% by weight or more and 5.0% by weight or less relative to the pulp; (3) The amount of the polyamide-based paper strength agent is 0.3% by weight or more and 0.9% by weight or less relative to the pulp; A pulp composition that satisfies at least one of the above. [Section 2] Item 2. The pulp composition according to Item 1, wherein the amount of the polyacrylamide-based paper strength agent is 0.1% by weight or more and 1.1% by weight or less relative to the pulp. [Section 3] Item 3. The pulp composition according to Item 1 or 2, wherein the amount of the polysaccharide-based paper strength agent is 0.6% by weight or more and 5% by weight or less relative to the pulp. [Section 4] 4. The pulp composition according to any one of items 1 to 3, wherein the amount of the polyamide-based paper strength agent is 0.3% by weight or more and 0.9% by weight or less based on the weight of the pulp. [Section 5] Item 5. The pulp composition according to any one of Items 1 to 4, wherein the wax is a petroleum wax. [Section 6] Item 6. The pulp composition according to any one of Items 1 to 5, wherein the wax is at least one selected from the group consisting of paraffin wax and microcrystalline wax. [Section 7] Item 7. The pulp composition according to any one of Items 1 to 6, wherein the wax is paraffin wax. [Section 8] Item 8. The pulp composition according to any one of Items 1 to 7, comprising at least one selected from the group consisting of benzalkonium chloride, formic acid, acetic acid, and rosin. [Section 9] Item 9. The pulp composition according to any one of items 1 to 8, which does not contain a dye. [Section 10] The wax is paraffin wax, and Item 10. The pulp composition according to any one of items 1 to 9, comprising at least one selected from the group consisting of benzalkonium chloride, formic acid, acetic acid, and rosin. [Section 11] Item 11. A molded pulp product formed from the pulp composition according to any one of Items 1 to 10. [Section 12] Item 12. The molded pulp product according to Item 11, further comprising a wax and a further strength agent attached to the surface. [Section 13] Item 13. The molded pulp product according to Item 11 or 12, which is for use in contact with food. [Section 14] A method for producing a pulp composition according to any one of items 1 to 10, a wax addition step of adding the wax to the pulp; and a paper strength agent adding step of adding the paper strength agent to the pulp; A method for producing a pulp composition, comprising: [Effects of the Invention]

[0007] According to the present disclosure, a molded pulp product with improved strength can be produced. DETAILED DESCRIPTION OF THE INVENTION

[0008] The pulp composition of the present disclosure contains a repellent component, and a molded pulp product formed from the pulp composition can have not only excellent strength but also excellent liquid repellency. The pulp composition of the present disclosure can also have excellent pulp moldability. Furthermore, the pulp product obtained from the pulp composition of the present disclosure can have excellent redisintegrability (recyclability).

[0009] <Repellent> The repellent agent in the present disclosure can be adhered to a substrate (particularly a pulp substrate) to impart liquid repellency, such as water resistance, oil resistance, water repellency, oil repellency, and / or stain resistance, to the substrate, and can also function as a water resistance agent, oil resistance agent, water repellent agent, oil repellent agent, and / or stain resistance agent.

[0010] The repellent of the present disclosure may contain wax as an active ingredient (wax will be described in detail separately under [Wax]). Wax may be used as a repellent by itself, or may be used as a repellent in combination with other ingredients as described below.

[0011] The repellent agent of the present disclosure may not contain any compound selected from the group consisting of a compound having a fluoroalkyl group having 8 or more carbon atoms, a compound having a perfluoroalkyl group having 8 or more carbon atoms, a compound having a fluoroalkyl group having 4 or more carbon atoms, a compound having a perfluoroalkyl group having 4 or more carbon atoms, a compound having a perfluoroalkyl group, a compound having a fluoroalkyl group, and a compound having a fluorine atom. The repellent agent of the present disclosure can impart liquid repellency to a substrate even if it does not contain these fluorine compounds.

[0012] The volumetric abundance ratio of particles of 100 μm or larger in the repellent of the present disclosure, as measured by laser diffraction scattering, may be 0.1% or larger, 0.3% or larger, 0.5% or larger, 1% or larger, 1.5% or larger, 3% or larger, 4% or larger, 5% or larger, or 10% or larger, or may be 50% or smaller, 30% or smaller, 20% or smaller, 15% or smaller, 10% or smaller, 5% or smaller, 3% or smaller, or 1.5% or smaller. The method for achieving the volumetric abundance ratio of particles of 1 μm or larger, as measured by laser diffraction scattering, within the above range is not limited, and may be, for example, by using a grinder, homogenizer, or the like to micronize the particles in the raw material and / or dispersion.

[0013] The volume median diameter of the repellent agent of the present disclosure, as measured by a laser diffraction scattering method, may be 0.01 μm or more, 0.05 μm or more, 0.1 μm or more, 0.2 μm or more, 0.3 μm or more, 0.4 μm or more, 0.5 μm or more, or 0.6 μm or more, or may be 10 μm or less, 5 μm or less, 3 μm or less, 1 μm or less, 0.9 μm or less, 0.8 μm or less, 0.7 μm or less, 0.6 μm or less, 0.5 μm or less, 0.4 μm or less, 0.3 μm or less, or 0.2 μm or less, preferably 1 μm or less. In the present disclosure, the volume median diameter refers to the median diameter (D50) in the volume-based particle size distribution measured by a laser diffraction scattering method.

[0014] The ionic charge density in the repellent of the present disclosure may be -1000 μeq / g or more, -800 μeq / g or more, -600 μeq / g or more, -500 μeq / g or more, -400 μeq / g or more, -250 μeq / g or more, -100 μeq / g or more, -50 μeq / g or more, -25 μeq / g or more, 0 μeq / g or more, 1 μeq / g or more, 25 μeq / g or more, 50 μeq / g or more, 100 μeq / g or more, 200 μeq / g or more, preferably -600 μeq / g or more, for example -400 μeq / g or more. The ionic charge density may be 5000 μeq / g or less, 2500 μeq / g or less, 1000 μeq / g or less, 750 μeq / g or less, 500 μeq / g or less, 400 μeq / g or less, 350 μeq / g or less, 300 μeq / g or less, 200 μeq / g or less, 100 μeq / g or less, or 50 μeq / g or less, preferably 1000 μeq / g or less, more preferably 500 μeq / g or less, for example 300 μeq / g or less. In particular, the ionic charge density of the repellent of the present disclosure is preferably -600 μeq / g or more and 100 μeq / g or less. The ionic charge density of the repellent of the present disclosure can be measured, for example, by the following method.

[0015] A sample liquid with a solid content of 0.1 g / L is used with a 1 / 1000 N potassium polyvinyl sulfonate solution to measure the anion demand with a particle charge meter (BTG MUTEK PCD-04), and the ionic charge density (cationic charge density) is calculated using the following formula (1). Alternatively, the cation demand is measured in the same way using a polydiallyldimethylammonium chloride solution instead of potassium polyvinyl sulfonate, and the ionic charge density (anionic charge density) is calculated using the following formula (1). Ionic charge density (μeq / g) = A / B (1) A: Cation demand or anion demand (μeq / L) B: Sample liquid concentration (g / L)

[0016] 〔wax〕 The repellent of the present disclosure may contain wax. The wax may be an organic substance that is solid at room temperature and becomes liquid when heated, and may be, for example, a hydrocarbon compound or a compound having a hydrocarbon group (e.g., an alkyl group) having 6 to 40 carbon atoms.

[0017] The waxes of the present disclosure can be adhered to a substrate (particularly a pulp substrate) to impart liquid repellency, such as water resistance, oil resistance, water repellency, oil repellency, and / or stain resistance, to the substrate.

[0018] The wax may be a compound having a monovalent hydrocarbon group having 1 to 40 carbon atoms, which may have a substituent, or a monovalent polysiloxane group. From the viewpoint of improving liquid repellency, the wax may have a hydrocarbon group having 6 to 40 carbon atoms (for example, an alkyl group).

[0019] [Wax characteristics, etc.] Possible properties of the wax are listed below.

[0020] The wax may be in a particulate (powder) form. The average particle size of the wax may be 0.01 μm or more, 0.05 μm or more, 0.1 μm or more, 0.2 μm or more, 0.3 μm or more, 0.4 μm or more, 0.5 μm or more, or 0.6 μm or more, or 10 μm or less, 5 μm or less, 3 μm or less, 1 μm or less, 0.9 μm or less, 0.8 μm or less, 0.7 μm or less, 0.6 μm or less, 0.5 μm or less, 0.4 μm or less, 0.3 μm or less, or 0.2 μm or less, preferably 1 μm or less. The above particle size is the primary particle size. A particle size within the above range can provide excellent particle stability and good liquid repellency. The average particle size can be measured using a microscope (scanning electron microscope). Specifically, a wax particle sample is observed under a microscope at an arbitrary magnification. Next, if the particle shape is spherical, the diameter is considered to be the particle size, and if it is non-spherical, the average of the longest and shortest diameters is considered to be the particle size. By measuring the particle size of all particles present within the field of view, then moving the field of view and measuring the particle size again, the particle size is measured at 100 or more points, and the average value is considered to be the average particle size.

[0021] The HD (n-hexadecane) contact angle of the wax may be 10° or more, 20° or more, 25° or more, 30° or more, 35° or more, 40° or more, 45° or more, 50° or more, 55° or more, 60° or more, or 65° or more, preferably 25° or more, more preferably 30° or more, and may be 100° or less, 90° or less, or 75° or less. When the wax has an HD contact angle equal to or greater than the lower limit, it can impart good liquid repellency (especially oil repellency) to the substrate. The HD contact angle is the static contact angle of the wax with a spin-coated film, and is obtained by dropping 2 μL of HD onto the spin-coated film and measuring the contact angle 1 second after the drop lands.

[0022] The water contact angle of the wax may be 35° or more, 40° or more, 45° or more, 50° or more, 55° or more, 65° or more, 75° or more, 85° or more, 90° or more, or 100° or more, and may be 160° or less, 140° or less, 130° or less, 120° or less, 110° or less, 100° or less, or 90° or less. When the wax has a water contact angle equal to or greater than the above lower limit, it can impart good liquid repellency (particularly water repellency) to the substrate. The water contact angle is the static contact angle of the wax with respect to a spin-coated film, and is obtained by dropping 2 μL of water onto the spin-coated film and measuring the contact angle 1 second after the drop lands.

[0023] The wax may be a low molecular weight (for example, a molecular weight of 1000 or less, or 500 or less) or a polymer. When the wax is a polymer, its weight average molecular weight may be 1000 or more, 3000 or more, 5000 or more, 7500 or more, 10000 or more, 30000 or more, 100000 or more, 300000 or more, or 500000 or more, or may be 10000000 or less, 75000000 or less, 50000000 or less, 3000000 or less, 1000000 or less, 750000 or less, 500000 or less, 300000 or less, 1 ... or less, 50000 or less, 300000 or less, 100000 or less, 75000 or less, 50000 or less, 300000 or less, 100000 or less, 75000 or less, 50000 or less, 30000 or less, 100000 or less, 75000 or less, 50000 or less, 30000 or less, 100000 or less, 75000 or less, 50000 or less, 30000 or less, 100000 or less, 75000 or less, 50

[0024] The melting point of the wax may be 30° C. or higher, 40° C. or higher, 60° C. or higher, 80° C. or higher, 100° C. or higher, or 120° C. or higher, preferably 40° C. or higher, 50° C. or higher, 60° C. or higher, 70° C. or higher, or 80° C. or higher, and may be 250° C. or lower, 225° C. or lower, 200° C. or lower, 150° C. or lower, 130° C. or lower, 120° C. or lower, 110° C. or lower, 100° C. or lower, 80° C. or lower, or 50° C. or lower, for example, 150° C. or lower, or 100° C. or lower. The melting point of the wax may be measured in accordance with JIS K 2235-1991.

[0025] [Wax structure, etc.] The wax in the present disclosure does not necessarily have any group selected from the group consisting of a fluoroalkyl group having 8 or more carbon atoms, a perfluoroalkyl group having 8 or more carbon atoms, a fluoroalkyl group having 4 or more carbon atoms, a perfluoroalkyl group having 4 or more carbon atoms, a perfluoroalkyl group, a fluoroalkyl group, and a fluorine atom. Even if the wax does not contain these fluorine-containing groups, it can still impart liquid repellency to the substrate.

[0026] The wax may be a hydrocarbon compound, or a compound having a monovalent hydrocarbon group having from 1 to 40 carbon atoms, which may have a substituent, or a monovalent polysiloxane group. From the viewpoint of improving liquid repellency, the wax may be a hydrocarbon compound or a compound having a hydrocarbon group (e.g., an alkyl group) having from 6 to 40 carbon atoms.

[0027] (Optionally substituted monovalent hydrocarbon group) The wax may have a monovalent hydrocarbon group which may have a substituent.

[0028] The hydrocarbon group may be a monovalent hydrocarbon group having from 1 to 40 carbon atoms. The hydrocarbon group may be an aromatic hydrocarbon group or an aliphatic hydrocarbon group, and is preferably an aliphatic hydrocarbon group, particularly a saturated aliphatic hydrocarbon group (alkyl group). The hydrocarbon group may be branched, cyclic, or linear, and is more preferably linear.

[0029] The number of carbon atoms in the hydrocarbon group may be 1 or more, 3 or more, 6 or more, 8 or more, 10 or more, 12 or more, 14 or more, 16 or more, 18 or more, 20 or more, or 22 or more, preferably 6 or more, 10 or more, 12 or more, or 16 or more, and may be 40 or less, 35 or less, 30 or less, 25 or less, 20 or less, 15 or less, or 10 or less, preferably 30 or less, 25 or less, or 20 or less.

[0030] The hydrocarbon group may have a substituent, but is preferably unsubstituted. Examples of the substituent include -OR', -N(R')2, -COOR', and a halogen atom (wherein R' is, independently in each occurrence, a hydrogen atom or a hydrocarbon group having 1 to 30, 1 to 20, 1 to 10, or 1 to 4 carbon atoms). The substituent may or may not have an active hydrogen. The number of substituents may be 6 or less, 5 or less, 4 or less, 3 or less, 2 or less, 1 or less, or 0. In the substituted hydrocarbon group, the amount of carbon atoms relative to the amount of carbon atoms and heteroatoms may be 70 mol% or more, 80 mol% or more, 90 mol% or more, 95 mol% or more, or 99 mol% or more, preferably 75 mol% or more, and may be 95 mol% or less, 90 mol% or less, 85 mol% or less, or 80 mol% or less. For example, the hydrocarbon group may have 1 to 3 (for example, 1) -OR' (particularly -OH) as a substituent (for example, other than at the terminal).

[0031] (monovalent polysiloxane group) The wax may have monovalent polysiloxane groups, which, like the (monovalent) hydrocarbon groups, may impart liquid repellency to the substrate.

[0032] The polysiloxane group has the formula: -[-Si(R s )2-O-] a - [In the formula, R s is independently in each occurrence a hydrocarbon group or a reactive group having 1 to 40 carbon atoms; a is an integer between 5 and 10,000. It may be expressed as:

[0033] R s is a hydrocarbon group having 1 to 40 carbon atoms or a reactive group.

[0034] Examples of hydrocarbon groups having 1 to 40 carbon atoms include hydrocarbon groups having 1 to 5 carbon atoms and hydrocarbon groups having 6 to 40 carbon atoms.

[0035] Examples of hydrocarbon groups having 1 to 5 carbon atoms include hydrocarbon groups having 1 to 5 carbon atoms such as a methyl group, an ethyl group, a propyl group, a butyl group, and a pentyl group (particularly aliphatic hydrocarbon groups, particularly alkyl groups such as a methyl group or an ethyl group, particularly a methyl group).

[0036] The hydrocarbon group having 6 to 40 carbon atoms may be an aromatic hydrocarbon group or an aliphatic hydrocarbon group, preferably an aliphatic hydrocarbon group, and particularly preferably a saturated aliphatic hydrocarbon group (alkyl group). The hydrocarbon group may be cyclic, linear, or branched, preferably linear. The number of carbon atoms in the hydrocarbon group may be 6 or more, 8 or more, 10 or more, 12 or more, 14 or more, 16 or more, or 18 or more, preferably 10 or more, more preferably 12 or more, and may be 40 or less, 35 or less, 30 or less, 25 or less, 20 or less, 15 or less, or 10 or less, preferably 30 or less, more preferably 25 or less.

[0037] Examples of reactive groups include groups having functional groups (e.g., hydroxyl, amino, mercapto, epoxy, carboxyl, halogen-substituted alkyl, vinyl, (meth)acrylic, (meth)acryloyloxy, and (meth)acrylamide groups, and hydrogen atoms directly bonded to silicon atoms). These functional groups may be directly bonded to the silicon atom or to an organic group directly bonded to the silicon atom. The organic group may be a hydrocarbon group, such as an alkylene group or a divalent aromatic group. The hydrocarbon group may have from 2 to 12 carbon atoms, and alkylene groups preferably have from 2 to 10 carbon atoms. Divalent aromatic groups preferably have from 6 to 12 carbon atoms. The reactive group may be a group selected from the group consisting of a hydroxyl group, an epoxy ring, a carboxyl group, a (meth)acrylic group, and an amino group, and may be, for example, at least one selected from the group consisting of an epoxy ring, a hydroxyl group, a (meth)acrylic group, and a carboxyl group.

[0038] a may be 3 or more, 5 or more, 10 or more, 30 or more, 50 or more, 100 or more, 500 or more, 1000 or more, 2000 or more, or 3000 or more, and is preferably 10 or more, and may be 10,000 or less, 7,500 or less, 5,000 or less, 3,000 or less, 1,500 or less, 1,000 or less, 500 or less, 300 or less, 200 or less, 100 or less, or 50 or less, and is preferably 500 or less.

[0039] In the polysiloxane group, R is a hydrocarbon group having 1 to 5 carbon atoms. s The quantity of R s It may be 20 mol% or more, 40 mol% or more, 60 mol% or more, or 80 mol% or more, preferably 50 mol% or more, and may be 100 mol% or less, 90 mol% or less, 80 mol% or less, or 70 mol% or less, based on the total of R s Based on the total number of groups, 50 mol % or more may be methyl groups or ethyl groups (particularly methyl groups).

[0040] In the polysiloxane group, R is a hydrocarbon group having 6 to 40 carbon atoms. s The quantity of Rs and may be 100 mol % or less, 90 mol % or less, 80 mol % or less, or 70 mol % or less, based on the total of

[0041] In the polysiloxane group, the reactive group R s The quantity of R s and may be 5 mol % or more, 10 mol % or more, 20 mol % or more, or 30 mol % or more, and may be 50 mol % or less, 40 mol % or less, 30 mol % or less, or 20 mol % or less, based on the total of

[0042] R s The groups may be introduced randomly or in blocks, but are preferably introduced randomly.

[0043] The terminal structure of the polysiloxane group is not limited, but may be, for example, -OR s , -Si(R s )3, etc. The R s Examples of the reactive group are as described above, and may be, for example, at least one selected from the group consisting of an epoxy ring, a hydroxy group, a (meth)acrylic group, and a carboxyl group.

[0044] The polysiloxane group may have a linker, and the raw material compound and the polysiloxane group may be bonded via a linker. Such a linker may be, but is not limited to, a hydrocarbon group having 1 to 40 (e.g., 1 to 20) carbon atoms which may be interrupted by an oxygen atom, for example, a (poly)oxyalkylene group having 1 to 40 (e.g., 1 to 20) carbon atoms.

[0045] Examples of polysiloxane groups include: -[-Si(R s )2-O-] a -Si(R s )3 -L s1 -[-Si(R s )2-O-] a -Si(Rs )3 -L s1 -OL s1 -[-Si(R s )2-O-] a -R s -L s1 -[-Si(R s )2-O-] a -Si(R s )3 -L s1 -OL s1 -[-Si(R s )2-O-] a -R s -L s1 -[-Si(R s )2-O-] a -Si(R s ) 3、 -L s1 -[-Si(R s )2-O-] a -R s [In the formula, R s is independently in each occurrence a hydrocarbon group or a reactive group having 1 to 40 carbon atoms, and the terminal R s has one or more reactive groups, R s 50 mol % or more of the total groups are methyl groups, L s1 is a hydrocarbon group having 1 to 20 carbon atoms, a is between 5 and 10,000. JPEG2025124868000001.jpg2169 [In the formula, a represents an integer of 0 to 150, b represents an integer of 1 to 150, (a+b) is 5 to 200, and n is an integer of 0 to 36.] etc.

[0046] [Example of wax] The wax may be a hydrocarbon compound or a compound having a hydrocarbon group. Examples and preferred ranges of the hydrocarbon group are as described above. For example, the hydrocarbon group may have 6 to 40 carbon atoms.

[0047] Examples of waxes include hydrocarbon waxes (paraffin, polyolefin, etc.), non-hydrocarbon waxes, and polymer waxes (vinyl polymers, silicone wax, etc.). Examples of waxes include: Petroleum waxes such as paraffin wax, microcrystalline wax, montan wax, ozokerite wax, ceresin wax, and petrolatum wax; Examples of suitable waxes include synthetic waxes such as Fischer-Tropsch wax, polyethylene wax, polypropylene wax, acrylic polymer wax, polytetrafluoroethylene wax, and silicone wax.

[0048] The wax may be a hydrocarbon compound and may not have any functional groups.

[0049] [Amount of wax] The amount of wax in the repellent may be 0.01% by weight or more, 0.5% by weight or more, 1% by weight or more, 3% by weight or more, 5% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, 50% by weight or more, 70% by weight or more, or 80% by weight or more, and may be 95% by weight or less, 90% by weight or less, 80% by weight or less, 70% by weight or less, 60% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, 5% by weight or less, or 3% by weight or less. Wax alone may be used as the repellent.

[0050] [Dispersant] The repellent of the present disclosure may contain a dispersant. The dispersant may be at least one selected from an organic dispersant and an inorganic dispersant. The dispersant may be at least one selected from an anionic dispersant, a nonionic dispersant, a cationic dispersant, an amphoteric dispersant, and an inorganic dispersant.

[0051] As the dispersant, an organic dispersant and an inorganic dispersant may be used individually, or a combination of an organic dispersant and an inorganic dispersant may be used.

[0052] An organic dispersant may be used as the dispersant. The organic dispersant can be classified into a nonionic dispersant, an anionic dispersant, a cationic dispersant, and an amphoteric dispersant, and the organic dispersant may refer to a surfactant.

[0053] The dispersant may be fluorine-free.

[0054] [Nonionic dispersant] The dispersant may include a nonionic dispersant, which may be a nonionic surfactant.

[0055] The nonionic dispersant may be a low molecular weight or a high molecular weight dispersant, and may have a molecular weight of 100 or more, 500 or more, 1000 or more, 2000 or more, 4000 or more, or 6000 or more, and may be 100,000 or less, 10,000 or less, 7,500 or less, 5,000 or less, 25,000 or less, 750 or less, or 250 or less.

[0056] Examples of nonionic dispersants include ethers, esters, ester ethers, alkanolamides, polyols and amine oxides.

[0057] An example of an ether is a compound having an oxyalkylene group (preferably a polyoxyethylene group).

[0058] An example of the ester is an ester of an alcohol and a fatty acid. An example of the alcohol is a mono- to trideca-hydric (particularly di- to deca-hydric) alcohol (e.g., aliphatic alcohol) having 1 to 50 carbon atoms (particularly 10 to 30 carbon atoms). An example of the fatty acid is a saturated or unsaturated fatty acid having 2 to 50 carbon atoms, particularly 5 to 30 carbon atoms.

[0059] An example of an ester ether is a compound in which an alkylene oxide (particularly ethylene oxide) is added to an ester of an alcohol and a fatty acid. An example of an alcohol is a mono- to trideca-hydric (particularly di- to deca-hydric) alcohol (e.g., aliphatic alcohol) having 1 to 50 carbon atoms (particularly 3 to 30 carbon atoms). An example of a fatty acid is a saturated or unsaturated fatty acid having 2 to 50 carbon atoms, particularly 5 to 30 carbon atoms.

[0060] An example of an alkanolamide is formed from a fatty acid and an alkanolamine. The alkanolamide may be a monoalkanolamide or a dialkanolamine. An example of a fatty acid is a saturated or unsaturated fatty acid having 2 to 50 carbon atoms, particularly 5 to 30 carbon atoms. The alkanolamine may be an alkanol having 2 to 50 carbon atoms, particularly 5 to 30 carbon atoms, and having 1 to 3 amino groups and 1 to 5 hydroxyl groups.

[0061] The polyol may be a di- to penta-hydric alcohol having 10 to 30 carbon atoms. The amine oxide may be an oxide (having, for example, 5 to 50 carbon atoms) of an amine (secondary amine or preferably tertiary amine).

[0062] The nonionic dispersant is preferably a nonionic dispersant having an oxyalkylene group (preferably a polyoxyethylene group). The number of carbon atoms in the alkylene group in the oxyalkylene group is preferably 2 to 10. The number of oxyalkylene groups in the molecule of the nonionic dispersant is generally preferably 2 to 100.

[0063] The nonionic dispersant is selected from the group consisting of ethers, esters, ester ethers, alkanolamides, polyols and amine oxides, and is preferably a nonionic dispersant having an oxyalkylene group.

[0064] The nonionic dispersant may be an alkylene oxide adduct of a linear and / or branched aliphatic (saturated and / or unsaturated) group, a polyalkylene glycol ester of a linear and / or branched fatty acid (saturated and / or unsaturated), a sorbitan ester of a linear and / or branched fatty acid (saturated and / or unsaturated), a glycerin ester of a linear and / or branched fatty acid (saturated and / or unsaturated), a polyglycerin ester of a linear and / or branched fatty acid (saturated and / or unsaturated), a sucrose ester of a linear and / or branched fatty acid (saturated and / or unsaturated), a polyoxyethylene (POE) / polyoxypropylene (POP) copolymer (random copolymer or block copolymer), an alkylene oxide adduct of acetylene glycol, or the like. Among these, those in which the structure of the alkylene oxide adduct moiety and the polyalkylene glycol moiety is polyoxyethylene (POE), polyoxypropylene (POP), or a POE / POP copolymer (which may be a random copolymer or a block copolymer) are preferred. Additionally, the nonionic dispersant may be free of aromatic groups.

[0065] The nonionic dispersant has the formula: R 1 O-(CH2CH2O) p -(R 2 O) q -R 3 [In the formula, R 1 is an alkyl group having 1 to 22 carbon atoms, or an alkenyl group or acyl group having 2 to 22 carbon atoms, R 2 are independently the same or different and are alkylene groups having 3 or more carbon atoms (e.g., 3 to 10), R 3 is a hydrogen atom, an alkyl group having 1 to 22 carbon atoms, or an alkenyl group having 2 to 22 carbon atoms, p is a number greater than or equal to 2, q is a number of 0 or 1 or more. The compound may be a compound represented by the formula:

[0066] R 1R preferably has 8 to 20 carbon atoms, particularly 10 to 18 carbon atoms. 1 Preferred specific examples include an octyl group, a nonyl group, a trimethylnonyl group, a lauryl group, a tridecyl group, an oleyl group, and a stearyl group. R 2 Examples of the alkyl group include a propylene group and a butylene group. In the nonionic dispersant, p may be a number of 3 or more (for example, 5 to 200). q may be a number of 2 or more (for example, 5 to 200). That is, -(R 2 O) q - may form a polyoxyalkylene chain. The nonionic dispersant may be a polyoxyethylene alkylene alkyl ether containing a hydrophilic polyoxyethylene chain and a hydrophobic oxyalkylene chain (particularly a polyoxyalkylene chain) at the center. Examples of the hydrophobic oxyalkylene chain include an oxypropylene chain, an oxybutylene chain, and a styrene chain, with the oxypropylene chain being preferred.

[0067] Specific examples of nonionic dispersants include ethylene oxide and hexylphenol, isooctatylphenol, hexadecanol, oleic acid, alkanes (C 12 -C 16 ) Thiol, Sorbitan Mono Fatty Acid (C7-C 19 ) or alkyl (C 12 -C 18 ) amines, etc., sorbitan fatty acid esters, glycerin fatty acid esters, polyglycerin fatty acid esters, sucrose fatty acid esters, propylene glycol fatty acid esters, polyoxyethylene alkyl ethers, polyoxyethylene polyoxypropylene alkyl ethers, polyoxyethylene glycerin fatty acid esters, polyoxyethylene sorbitan fatty acid esters, lecithin derivatives, etc. Examples of nonionic dispersants include polyoxyethylene alkyl ethers, polyoxyethylene polyoxypropylene alkyl ethers, polyoxyethylene polyoxybutylene alkyl ethers, polyoxyethylene polyoxypropylene glycol, polyethyleneimine ethoxylate, etc.

[0068] The proportion of the polyoxyethylene block can be 5 to 80% by weight, for example 30 to 75% by weight, particularly 40 to 70% by weight, based on the molecular weight of the nonionic dispersant (copolymer). The average molecular weight of the nonionic dispersant is generally 300 to 5,000, for example, 500 to 3,000. The nonionic dispersant may be a single type or a mixture of two or more types. The nonionic dispersant may be a mixture of a compound having an HLB (hydrophilic-hydrophobic balance) of less than 15 (particularly 5 or less) and a compound having an HLB of 15 or more. Specifically, it is preferable to select from polyoxyethylene alkyl ethers, polyoxyethylene polyoxypropylene alkyl ethers, polyoxyethylene, and polyoxypropylenes having an HLB value of 1 to 18, and sorbitan fatty acid esters, glycerin fatty acid esters, polyglycerin fatty acid esters, sucrose fatty acid esters, propylene glycol fatty acid esters, polyoxyethylene glycerin fatty acid esters, and polyoxyethylene sorbitan fatty acid esters having an HLB value of less than 7.

[0069] [Cationic dispersant] The dispersant may include a cationic dispersant. The cationic dispersant may be a cationic surfactant. The cationic dispersant may be a compound having no amide group.

[0070] The cationic dispersant may be a low molecular weight type (e.g., a molecular weight of 2000 or less, particularly 10,000 or less) or a high molecular weight type (e.g., a molecular weight of 2000 or more). The molecular weight of the cationic dispersant may be 100 or more, 500 or more, 1,000 or more, 2,000 or more, 4,000 or more, or 6,000 or more, and may be 1,000,000 or less, 750,000 or less, 500,000 or less, 250,000 or less, 100,000 or less, 50,000 or less, 10,000 or less, 7,500 or less, 5,000 or less, 25,000 or less, 750 or less, or 250 or less.

[0071] The cationic dispersant may be aliphatic or aromatic, and examples thereof include ammonium salts (e.g., quaternary ammonium salts). The cationic dispersant may be an oxyethylene adduct ammonium salt. Specific examples include amine salt-type dispersants such as alkylamine salts, amino alcohol fatty acid derivatives, polyamine fatty acid derivatives, and imidazolines; quaternary ammonium salt-type dispersants such as alkyltrimethylammonium salts, dialkyldimethylammonium salts, alkyldimethylbenzylammonium salts, pyridinium salts, alkylisoquinolinium salts, benzalkonium chloride, and benzethonium chloride; and polymeric cationic dispersants such as polyquaternium-1 to -47. Examples of cationic dispersants include alkylamine salts and quaternary ammonium salts.

[0072] Low molecular weight cationic dispersants are R 21 -N + (-R 22 )(-R 23 )(-R 24 )X - [In the formula, R 21 , R 22 , R 23 and R 24 is hydrogen or a hydrocarbon group having 1 to 40 carbon atoms, X is an anionic group. R 21 , R 22 , R 23 and -R 24 Specific examples of X include alkyl groups (e.g., methyl, butyl, stearyl, and palmityl groups) and aromatic groups (e.g., benzyl and phenyl groups). Specific examples of X include halogens (e.g., chlorine) and acids (e.g., hydrochloric acid and acetic acid). Examples of cationic dispersants include monoalkyltrimethylammonium salts (alkyl having 4 to 40 carbon atoms) and benzalkonium chloride.

[0073] Specifically, the low molecular weight cationic dispersant is represented by the formula: R 1 p -N +R 2 q X - [In the formula, R 1 is C12 or higher (e.g., C 12 ~C 50 ) is a linear and / or branched aliphatic (saturated and / or unsaturated) group of R 2 is H or a C1-4 alkyl group, a benzyl group, or a polyoxyethylene group (the number of oxyethylene groups is, for example, 1 (particularly 2, especially 3) to 50) (CH3 and C2H5 are particularly preferred), X is a halogen atom (e.g., chlorine), or a C1-C4 fatty acid salt, or a C1-C4 sulfonate; p is 1 or 2, q is 2 or 3, and p+q=4. R 1 may have 12 to 50 carbon atoms, for example, 12 to 30 carbon atoms.

[0074] Low molecular weight cationic dispersants include dodecyltrimethylammonium acetate, trimethyltetradecylammonium chloride, hexadecyltrimethylammonium bromide, trimethyloctadecylammonium chloride, (dodecylmethylbenzyl)trimethylammonium chloride, benzyldodecyldimethylammonium chloride, methyldodecyldi(hydropolyoxyethylene)ammonium chloride, benzyldodecyldi(hydropolyoxyethylene)ammonium chloride, N-[2-(diethylamino)ethyl]oleamide hydrochloride, and the like.

[0075] The polymeric cationic dispersant may be any of various polymers (e.g., polyquaternium-1 to 47) having cationic groups (e.g., ammonium groups, quaternary ammonium groups). Examples of polymeric cationic dispersants include cationic natural products (particularly cationic sugars) such as cationic starch, cationic cellulose (e.g., O-(2-hydroxy-3-(trimethylammonio)propylhydroxyethylcellulose chloride), cationic guar gum, cationic xanthan gum, and chitosan; and polymers of cationic group-containing monomers such as aziridine, vinylimidazole, aminoalkyl methacrylate, N,N,N',N'-tetramethyl-2-butene-1,4-diamine, quaternized dimethylammonium ethyl methacrylate, diallyldimethylammonium chloride, dimethylaminopropylamine, and quaternized vinylimidazole.

[0076] [Anionic dispersant] The dispersant may include an anionic dispersant. The anionic dispersant may be an anionic surfactant. The dispersant may be free of an anionic dispersant.

[0077] The anionic dispersant may be a low molecular weight or a high molecular weight dispersant, and may have a molecular weight of 100 or more, 500 or more, 1000 or more, 2000 or more, 4000 or more, or 6000 or more, and may have a molecular weight of 100,000 or less, 10,000 or less, 7,500 or less, 5,000 or less, 25,000 or less, 750 or less, or 250 or less.

[0078] Examples of anionic dispersants include alkyl ether sulfates, alkyl sulfates, alkenyl ether sulfates, alkenyl sulfates, olefin sulfonates, alkanesulfonates, saturated or unsaturated fatty acid salts, alkyl or alkenyl ether carboxylates, α-sulfonic acid salts, N-acylamino acid dispersants, phosphate mono- or diester dispersants, and sulfosuccinates. An example of an anionic dispersant is a carboxylate (e.g., a fatty acid salt).

[0079] [Amphoteric dispersant] The dispersant may comprise an amphoteric dispersant, which may be an amphoteric surfactant.

[0080] The amphoteric dispersant may be a low molecular weight or a high molecular weight dispersant, and may have a molecular weight of 100 or more, 500 or more, 1000 or more, 2000 or more, 4000 or more, or 6000 or more, and may be 100,000 or less, 10,000 or less, 7,500 or less, 5,000 or less, 25,000 or less, 750 or less, or 250 or less.

[0081] Examples of amphoteric dispersants include alanines, imidazolinium betaines, amido betaines, and acetic acid betaine, and specific examples include lauryl betaine, stearyl betaine, lauryl carboxymethyl hydroxyethyl imidazolinium betaine, lauryl dimethylamino acetic acid betaine, and fatty acid amidopropyl dimethylamino acetic acid betaine.

[0082] [Inorganic dispersant] The dispersant may include an inorganic dispersant.

[0083] The average primary particle size of the inorganic dispersant may be 5 nm or more, 30 nm or more, 100 nm or more, 1 μm or more, 10 μm or more, or 25 μm or more, and may be 100 μm or less, 50 μm or less, 10 μm or less, 1 μm or less, 500 nm or less, or 300 nm or less. The average primary particle size can be measured, for example, by observation with a microscope (scanning electron microscope or transmission electron microscope). The inorganic dispersant may be hydrophilic particles.

[0084] Examples of inorganic dispersants include polyvalent metal phosphates such as tricalcium phosphate, magnesium phosphate, aluminum phosphate, zinc phosphate, and hydroxyapatite; carbonates such as calcium carbonate and magnesium carbonate; silicates such as calcium metasilicate; sulfates such as calcium sulfate and barium sulfate; and hydroxides such as calcium hydroxide, magnesium hydroxide, and aluminum hydroxide.

[0085] [Amount of dispersant] The amount of dispersant may be, relative to 100 parts by weight of wax, 0.01 parts by weight or more, 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 50 parts by weight or more, 75 parts by weight or more, or 100 parts by weight or more, and may be 500 parts by weight or less, 300 parts by weight or less, 200 parts by weight or less, 100 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, 5 parts by weight or less, 3 parts by weight or less, or 1 part by weight or less.

[0086] [Liquid medium] The repellent agent of the present disclosure may include a liquid medium. The liquid medium may be water, an organic solvent, or a mixture of water and an organic solvent. The repellent agent may be a dispersion or a solution. The repellent agent of the present disclosure may include at least water.

[0087] Examples of organic solvents include esters (e.g., esters having 2 to 40 carbon atoms, specifically, ethyl acetate and butyl acetate), ketones (e.g., ketones having 2 to 40 carbon atoms, specifically, methyl ethyl ketone and diisobutyl ketone), alcohols (e.g., alcohols having 1 to 40 carbon atoms, specifically, isopropyl alcohol), aromatic solvents (e.g., toluene and xylene), and petroleum solvents (e.g., alkanes having 5 to 10 carbon atoms, specifically, naphtha and kerosene). The organic solvent is preferably a water-soluble organic solvent. The water-soluble organic solvent may contain a compound having at least one hydroxy group (e.g., alcohol, polyol such as glycol-based solvent, ether form of polyol (e.g., monoether form), etc.). These may be used alone or in combination of two or more.

[0088] [Amount of liquid medium] The amount of the liquid medium may be 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 20 parts by weight or more, 30 parts by weight or more, 40 parts by weight or more, 50 parts by weight or more, 100 parts by weight or more, 200 parts by weight or more, 300 parts by weight or more, 500 parts by weight or more, or 1000 parts by weight or more, and may be 3000 parts by weight or less, 2000 parts by weight or less, 1000 parts by weight or less, 500 parts by weight or less, 200 parts by weight or less, 175 parts by weight or less, 150 parts by weight or less, 125 parts by weight or less, 100 parts by weight or less, 80 parts by weight or less, 60 parts by weight or less, 40 parts by weight or less, 20 parts by weight or less, or 10 parts by weight or less, relative to 1 part by weight of the wax.

[0089] The amount of water may be 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 20 parts by weight or more, 30 parts by weight or more, 40 parts by weight or more, 50 parts by weight or more, 100 parts by weight or more, 200 parts by weight or more, 300 parts by weight or more, 500 parts by weight or more, or 1000 parts by weight or more, and may be 3000 parts by weight or less, 2000 parts by weight or less, 1000 parts by weight or less, 500 parts by weight or less, 200 parts by weight or less, 175 parts by weight or less, 150 parts by weight or less, 125 parts by weight or less, 100 parts by weight or less, 80 parts by weight or less, 60 parts by weight or less, 40 parts by weight or less, 20 parts by weight or less, or 10 parts by weight or less, per part by weight of wax.

[0090] The amount of organic solvent may be 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 20 parts by weight or more, 30 parts by weight or more, 40 parts by weight or more, 50 parts by weight or more, 100 parts by weight or more, 200 parts by weight or more, 300 parts by weight or more, 500 parts by weight or more, or 1000 parts by weight or more, and may be 3000 parts by weight or less, 2000 parts by weight or less, 1000 parts by weight or less, 500 parts by weight or less, 200 parts by weight or less, 175 parts by weight or less, 150 parts by weight or less, 125 parts by weight or less, 100 parts by weight or less, 80 parts by weight or less, 60 parts by weight or less, 40 parts by weight or less, 20 parts by weight or less, or 10 parts by weight or less, relative to 1 part by weight of wax.

[0091] 〔silicone〕 The repellent agent of the present disclosure may contain silicone (polyorganosiloxane). By containing silicone, it is possible to achieve good texture and durability in addition to good liquid repellency.

[0092] As the silicone, known silicones can be used, and examples of silicones include polydimethylsiloxane and modified silicones (amino-modified, epoxy-modified silicone, carboxy-modified silicone, methylhydrogen silicone, etc.). The silicone may be a silicone wax having wax-like properties. These may be used alone or in combination of two or more.

[0093] The weight average molecular weight of the silicone may be 1,000 or more, 10,000 or more, or 50,000 or more, and may be 500,000 or less, 2,500,000 or less, 100,000 or less, or 50,000 or less.

[0094] [Silicone amount] The amount of silicone may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 50 parts by weight or more, 75 parts by weight or more, or 100 parts by weight or more, and may be 500 parts by weight or less, 300 parts by weight or less, 200 parts by weight or less, 100 parts by weight or less, 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less, relative to 100 parts by weight of the wax.

[0095] [Organic acid] The repellent of the present disclosure may contain an organic acid. Known organic acids can be used. Preferred organic acids include carboxylic acids, sulfonic acids, sulfinic acids, etc., with carboxylic acids being particularly preferred. Examples of the carboxylic acid include formic acid, acetic acid, propionic acid, butyric acid, oxalic acid, succinic acid, glutaric acid, adipic acid, malic acid, citric acid, etc., with formic acid or acetic acid being particularly preferred. In the present disclosure, one type of organic acid may be used, or two or more types may be used in combination. For example, formic acid and acetic acid may be used in combination.

[0096] [Amount of organic acid] The amount of organic acid may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 50 parts by weight or more, 75 parts by weight or more, or 100 parts by weight or more, and may be 500 parts by weight or less, 300 parts by weight or less, 200 parts by weight or less, 100 parts by weight or less, 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less, per 100 parts by weight of wax. The amount of organic acid may be adjusted so that the pH of the repellent is 3 to 10, for example, 5 to 9, particularly 6 to 8. The repellent may be acidic (pH 7 or less, for example, 6 or less).

[0097] [Inorganic acid] The repellent of the present disclosure may contain an inorganic acid. Known inorganic acids can be used. Examples of inorganic acids include hydrogen chloride, hydrogen bromide, hydrogen iodide, nitric acid, boric acid, sulfuric acid, and phosphoric acid. In the present disclosure, one type of inorganic acid may be used, or two or more types may be used in combination. Addition of an inorganic acid can improve the stability of the aqueous dispersion.

[0098] [Amount of inorganic acid] The amount of inorganic acid may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 50 parts by weight or more, 75 parts by weight or more, or 100 parts by weight or more, and may be 500 parts by weight or less, 300 parts by weight or less, 200 parts by weight or less, 100 parts by weight or less, 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less, per 100 parts by weight of wax. The amount of inorganic acid may be adjusted so that the pH of the repellent is 3 to 10, for example, 5 to 9, particularly 6 to 8. The repellent may be acidic (pH 7 or less, for example, 6 or less).

[0099] [Curing agent] The repellent of the present disclosure may include a curing agent (an active hydrogen reactive compound or an active hydrogen containing compound).

[0100] The curing agent (crosslinking agent) in the repellent agent can cure the agent well. The curing agent may be an active hydrogen-reactive compound or an active hydrogen-containing compound that reacts with active hydrogen or an active hydrogen-reactive group. Examples of active hydrogen-reactive compounds are isocyanate compounds, epoxy compounds, chloromethyl group-containing compounds, carboxyl group-containing compounds, and hydrazide compounds. Examples of active hydrogen-containing compounds are hydroxyl group-containing compounds, amino group-containing compounds, carboxyl group-containing compounds, ketone group-containing compounds, hydrazide compounds, and melamine compounds.

[0101] The curing agent may contain an isocyanate compound. The isocyanate compound may be a polyisocyanate compound. A polyisocyanate compound is a compound having two or more isocyanate groups in one molecule. The polyisocyanate compound functions as a crosslinking agent. Examples of polyisocyanate compounds include aliphatic polyisocyanates, alicyclic polyisocyanates, araliphatic polyisocyanates, aromatic polyisocyanates, and derivatives of these polyisocyanates. The isocyanate compound may be a blocked isocyanate compound (for example, a blocked polyisocyanate compound). A blocked isocyanate compound is a compound in which the isocyanate group of an isocyanate compound is masked with a blocking agent to inhibit reaction.

[0102] Examples of aliphatic polyisocyanates are trimethylene diisocyanate, tetramethylene diisocyanate, hexamethylene diisocyanate, pentamethylene diisocyanate, 1,2-propylene diisocyanate, 1,2-butylene diisocyanate, 2,3-butylene diisocyanate, 1,3-butylene diisocyanate, 2,4,4- or 2,2,4-trimethylhexamethylene diisocyanate, 2,6-diisocyanate, Aliphatic diisocyanates such as cyanatomethyl caproate, and aliphatic triisocyanates such as lysine ester triisocyanate, 1,4,8-triisocyanatooctane, 1,6,11-triisocyanatoundecane, 1,8-diisocyanato-4-isocyanatomethyloctane, 1,3,6-triisocyanatohexane, and 2,5,7-trimethyl-1,8-diisocyanato-5-isocyanatomethyloctane. These may be used alone or in combination of two or more.

[0103] Examples of alicyclic polyisocyanates include alicyclic diisocyanates and alicyclic triisocyanates. Specific examples of alicyclic polyisocyanates include 1,3-cyclopentene diisocyanate, 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate (isophorone diisocyanate), and 1,3,5-triisocyanatocyclohexane. These may be used alone or in combination of two or more.

[0104] Examples of araliphatic polyisocyanates include araliphatic diisocyanates and araliphatic triisocyanates. Specific examples of araliphatic polyisocyanates include 1,3- or 1,4-xylylene diisocyanate or a mixture thereof, 1,3- or 1,4-bis(1-isocyanato-1-methylethyl)benzene (tetramethylxylylene diisocyanate) or a mixture thereof, and 1,3,5-triisocyanatomethylbenzene. These may be used alone or in combination of two or more.

[0105] Examples of aromatic polyisocyanates include aromatic diisocyanates, aromatic triisocyanates, and aromatic tetraisocyanates. Specific examples of aromatic polyisocyanates include m-phenylene diisocyanate, p-phenylene diisocyanate, 4,4'-diphenyl diisocyanate, 1,5-naphthalene diisocyanate, 2,4'- or 4,4'-diphenylmethane diisocyanate or a mixture thereof, 2,4- or 2,6-tolylene diisocyanate or a mixture thereof, triphenylmethane-4,4',4''-triisocyanate, and 4,4'-diphenylmethane-2,2',5,5'-tetraisocyanate. These may be used alone or in combination of two or more.

[0106] Examples of the polyisocyanate derivatives include various derivatives of the above-mentioned polyisocyanate compounds, such as dimers, trimers, biurets, allophanates, carbodiimides, uretdiones, uretimines, isocyanurates, and iminooxadiazinediones. These may be used alone or in combination of two or more.

[0107] These polyisocyanates can be used alone or in combination of two or more. As the polyisocyanate compound, it is preferable to use a blocked polyisocyanate compound (blocked isocyanate), which is a compound in which the isocyanate group of a polyisocyanate compound is blocked with a blocking agent.The use of a blocked polyisocyanate compound is preferable for reasons such as its relative stability in solution and its usability in the same solution as the repellent.

[0108] The blocking agent blocks free isocyanate groups. When the blocked polyisocyanate compound is heated to, for example, 100°C or higher, e.g., 130°C or higher, the isocyanate groups are regenerated and can easily react with hydroxyl groups. Examples of blocking agents include phenolic compounds, lactam compounds, aliphatic alcohol compounds, and oxime compounds. The polyisocyanate compounds can be used alone or in combination.

[0109] The epoxy compound is a compound having an epoxy group. Examples of the epoxy compound include epoxy compounds having a polyoxyalkylene group, such as polyglycerol polyglycidyl ether and polypropylene glycol diglycidyl ether; and sorbitol polyglycidyl ether. The chloromethyl group-containing compound is a compound having a chloromethyl group. Examples of the chloromethyl group-containing compound include chloromethyl polystyrene. The carboxyl group-containing compound is a compound having a carboxyl group. Examples of the carboxyl group-containing compound include (poly)acrylic acid and (poly)methacrylic acid.

[0110] Specific examples of the ketone group-containing compound include (poly)diacetone acrylamide and diacetone alcohol. Specific examples of the hydrazide compound include hydrazine, carbohydrazide, and adipic acid hydrazide. Specific examples of the melamine compound include melamine resins and methyl etherified melamine resins.

[0111] [Amount of hardener] The amount of curing agent may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 50 parts by weight or more, 75 parts by weight or more, or 100 parts by weight or more, and may be 500 parts by weight or less, 300 parts by weight or less, 200 parts by weight or less, 100 parts by weight or less, 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less, relative to 100 parts by weight of the wax.

[0112] [Other ingredients] The repellent may contain other components in addition to the above components. Examples of the other components include polysaccharides, paper strength agents, flocculants, retention aids, coagulants, binder resins, anti-slip agents, sizing agents, paper strength agents, fillers, antistatic agents, preservatives, ultraviolet absorbers, antibacterial agents, deodorizers, fragrances, etc. These may be used alone or in combination of two or more. In addition to the above ingredients, other ingredients may include other water and / or oil repellents, dispersants, texture adjusters, softeners, flame retardants, paint fixatives, wrinkle inhibitors, drying speed adjusters, crosslinking agents, film-forming aids, compatibilizers, antifreeze agents, viscosity adjusters, UV absorbers, antioxidants, pH adjusters, insect repellents, defoamers, shrinkage inhibitors, anti-wrinkle agents after washing, shape retention agents, drape retention agents, ironing improvers, whitening agents, whitening agents, fabric softening clay, dye transfer inhibitors such as polyvinylpyrrolidone, polymer dispersants, stain release agents, scum dispersants, fluorescent whitening agents such as 4,4-bis(2-sulfostyryl)biphenyl disodium (Ciba Specialty Chemicals' Tinopal CBS-X), dye fixatives, and anti-fading agents such as 1,4-bis(3-aminopropyl)piperazine. The following may be blended: stain removers, enzymes such as cellulase, amylase, protease, lipase, and keratinase as fiber surface modifiers; foam inhibitors; and agents capable of imparting silk texture and functionality such as moisture absorption and release. These include silk protein powder, surface-modified products, or emulsified dispersions thereof (e.g., K-50, K-30, K-10, A-705, S-702, L-710, FP series (Idemitsu Petrochemicals), hydrolyzed silk liquid (Jomo), Silkgen G Soluble S (Ichimaru Falcos)). Stain inhibitors (e.g., nonionic polymeric compounds consisting of alkylene terephthalate and / or alkylene isophthalate units and polyoxyalkylene units (e.g., FR627 manufactured by GOO Chemical Industry Co., Ltd., SRC-1 manufactured by Clariant Japan, etc.) can also be blended. These may be used alone or in combination of two or more.

[0113] [Amount of other ingredients] The amount of each of the other components or the total amount thereof may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 50 parts by weight or more, 75 parts by weight or more, or 100 parts by weight or more, relative to 100 parts by weight of the wax, and may be 500 parts by weight or less, 300 parts by weight or less, 200 parts by weight or less, 100 parts by weight or less, 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less.

[0114] <Pulp composition> The pulp composition of the present disclosure comprises pulp and a repellent component. The pulp composition of the present disclosure is obtained by treating pulp with a repellent.

[0115] 〔pulp〕 The pulp composition contains pulp, and the pulp is treated with a repellent as a pulp base material. The pulp base material may be in the form of pulp alone, pulp slurry, pulp product, etc. Examples of the pulp base material include pulp such as bleached or unbleached chemical pulp such as kraft pulp or sulfite pulp, bleached or unbleached high-yield pulp such as groundwood pulp, mechanical pulp or thermomechanical pulp, pulp slurries containing the above pulp, and pulp products such as paper, paper containers, and molded paper products made from recycled paper pulp such as recycled newspaper, recycled magazine paper, recycled corrugated cardboard, and deinked recycled paper. Specific examples of pulp products include food packaging materials, food containers, gypsum board base paper, coated base paper, medium-quality paper, general liners and corrugating media, neutral white roll paper, neutral liners, rust-proof liners and metal interleaving paper, kraft paper, neutral printing and writing paper, neutral coated base paper, neutral PPC paper, neutral thermal paper, neutral pressure-sensitive base paper, neutral inkjet paper and neutral information paper, molded paper (molded containers), etc. Suitable examples of pulp products include food packaging materials and food containers, and particularly pulp molded products for food contact applications.

[0116] The amount of pulp in the pulp composition may be 0.1% by weight or more, 0.5% by weight or more, 1% by weight or more, 3% by weight or more, 5% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, 50% by weight or more, 75% by weight or more, or 90% by weight or more, and may be 99% by weight or less, 75% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, 5% by weight or less, 4% by weight or less, or 3% by weight or less. Typically, when the pulp composition is prepared by internal addition, the amount of pulp in the pulp composition is 30% by weight or less, and when the pulp composition is prepared by external addition, the amount of pulp in the pulp composition may be 75% by weight or more.

[0117] [Liquid medium] The pulp composition may include a liquid medium, which may be water, an organic solvent, or a mixture of water and an organic solvent, typically an aqueous medium, particularly water, and may include a liquid medium derived from a repellent agent.

[0118] [Amount of liquid medium] The amount of the liquid medium in the pulp composition may be 0.1% by weight or more, 0.5% by weight or more, 1% by weight or more, 3% by weight or more, 5% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, 50% by weight or more, 75% by weight or more, 90% by weight or more, or 95% by weight or more, and may be 99% by weight or less, 75% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, 5% by weight or less, 4% by weight or less, or 3% by weight or less. Typically, when the pulp composition is prepared by internal addition, the amount of the liquid medium in the pulp composition is 50% by weight or more, particularly 90% by weight or more, and when the pulp composition is prepared by external addition, the amount of the liquid medium in the pulp composition is 30% by weight or less, particularly 10% by weight or less.

[0119] [Repellent] The pulp composition may contain wax in a repellent, which will be described in detail separately in the section <Repellent>.

[0120] [Amount of repellent] The amount of repellent added to the pulp (also referred to as the pulp base material) may be adjusted to a desired amount of wax. The amount of wax may be 0.1% by weight or more, 0.3% by weight or more, 0.5% by weight or more, 0.75% by weight or more, 1.0% by weight or more, 2.0% by weight or more, or 3.0% by weight or more, or 10% by weight or less, 7.5% by weight or less, 5.0% by weight or less, 4.0% by weight or less, 3.0% by weight or less, 2.0% by weight or less, 1.0% by weight or less, 0.75% by weight or less, or 0.5% by weight or less, preferably 5.0% by weight or less, more preferably 3.0% by weight or less.

[0121] In the external addition treatment, the amount of wax contained in the coating layer is 0.01 g / m 2 More than 0.03g / m 2 More than 0.05g / m 2 More than 0.1g / m 2 More than 0.3g / m 2 More than 0.5g / m 2 or more, or 1.0 g / m 2 or more, and 5.0 g / m 2 Below 4.0g / m 2 Below 3.0g / m 2 Below 2.0g / m 2 Below 1.0g / m 2 Below 0.5g / m 2 Below 0.3g / m 2 or less, or 0.1 g / m 2 It may be the following:

[0122] [Paper strength agent] The pulp composition may include a strength agent. Examples of strength agents include: Polyacrylamide-based paper strength agents such as cationic polyacrylamide, anionic polyacrylamide, and amphoteric polyacrylamide; polysaccharide-based paper strength agents such as starch, enzyme-modified starch, thermochemically modified starch, oxidized starch, esterified starch, etherified starch (e.g., hydroxyethylated starch), aldehyde starch, cationized starch, starch, xanthan gum, karaya gum, welan gum, guar gum, pectin, tamarind gum, carrageenan, chitosan, gum arabic, locust bean gum, cellulose, alginic acid, agar, dextran, cellulose, carboxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, chitin nanofiber, cellulose nanofiber, and pullulan, and modified polysaccharides thereof (e.g., modified polysaccharides into which hydroxyl groups or cationic groups have been introduced); Polyamide-based paper strength agents such as polyamide resins, polyamine resins, polyamide-polyamine resins, polyamide-epichlorohydrin resins, polyamide-polyamine-epichlorohydrin resins, polyamide-polyurea-formaldehyde resins, and epoxidized polyamide resins; Urea / melamine-based paper strength agents such as urea resin, melamine resin, urea-formaldehyde resin, and melamine-formaldehyde resin; polyvinyl alcohol-based paper strength agents such as polyvinyl alcohol, fully saponified polyvinyl alcohol, partially saponified polyvinyl alcohol, carboxyl-modified polyvinyl alcohol, silanol-modified polyvinyl alcohol, cation-modified polyvinyl alcohol, and terminal alkyl-modified polyvinyl alcohol; Examples of the paper strength agent include styrene-butadiene copolymer, polyvinyl acetate, vinyl chloride-vinyl acetate copolymer, polyvinyl chloride, polyvinylidene chloride, polyacrylic acid ester, fatty acid diamide, polyethyleneimine resin, ketone aldehyde resin, etc. The paper strength agent in the present disclosure is preferably a polyacrylamide-based paper strength agent, a polysaccharide-based paper strength agent, or a polyamide-based paper strength agent.

[0123] [Amount of paper strength agent] The total amount of the strength agent may be 0.1% by weight or more, 0.3% by weight or more, 0.5% by weight or more, 0.75% by weight or more, 1.0% by weight or more, 2.0% by weight or more, or 3.0% by weight or more, and may be 10% by weight or less, 7.5% by weight or less, 5.0% by weight or less, 4.0% by weight or less, 3.0% by weight or less, 2.0% by weight or less, 1.0% by weight or less, 0.75% by weight or less, or 0.5% by weight or less, and is preferably 5.0% by weight or less, based on the pulp.

[0124] The amount of the polyacrylamide-based paper strength agent may be 0.1% by weight or more, 0.2% by weight or more, 0.4% by weight or more, 0.6% by weight or more, 0.8% by weight or more, or 1.0%, and is preferably 0.3% by weight or more, and may be 1.1% by weight or less, 0.9% by weight or less, 0.7% by weight or less, 0.5% by weight or less, or 0.3% by weight or less, based on the pulp.

[0125] The amount of the polysaccharide strength agent may be 0.6% by weight or more, 1.0% by weight or more, 1.5% by weight or more, 2.0% by weight or more, 2.5% by weight or more, 3.0% by weight or more, 3.5% by weight or more, 4.0% by weight or more, or 4.5% by weight or more, and is preferably 2.0% by weight or more, and may be 5% by weight or less, 4.7% by weight or less, 4.2% by weight or less, 3.7% by weight or less, 3.2% by weight or less, 2.7% by weight or less, 2.2% by weight or less, or 1.7% by weight or less, based on the pulp.

[0126] The amount of the polyamide-based paper strength agent may be 0.3% by weight or more, 0.4% by weight or more, 0.5% by weight or more, 0.6% by weight or more, 0.7% by weight or more, or 0.8% by weight or more, and may be 0.9% by weight or less, 0.8% by weight or less, 0.7% by weight or less, 0.6% by weight or less, 0.5% by weight or less, or 0.4% by weight or less, based on the weight of the pulp.

[0127] [Sizing agent] The pulp composition may contain a sizing agent. Examples of the sizing agent include cationic sizing agents, anionic sizing agents, neutral sizing agents, and amphoteric sizing agents, such as rosin-based sizing agents (e.g., acidic rosin-based sizing agents and neutral rosin-based sizing agents), alkyl ketene dimers, and alkenyl succinic anhydrides.

[0128] [Amount of sizing agent] The amount of sizing agent may be 0.1% by weight or more, 0.2% by weight or more, 0.3% by weight or more, 0.5% by weight or more, 0.75% by weight or more, 1.0% by weight or more, 2.0% by weight or more, or 3.0% by weight or more, and may be 10% by weight or less, 7.5% by weight or less, 5.0% by weight or less, 4.0% by weight or less, 3.0% by weight or less, 2.0% by weight or less, 1.0% by weight or less, 0.75% by weight or less, or 0.5% by weight or less, based on the pulp.

[0129] [Other additives] In addition to the above, the pulp composition may contain additives used in the production of pulp products, such as fixing agents (aluminum sulfate, etc.), organic acids (formic acid, acetic acid, etc.), flocculants, retention aids, dyes, fluorescent dyes, slime control agents, and defoamers. The pulp composition contains components derived from the repellent, but each of the components that can be contained in the repellent described above may also be added to the pulp composition as an additive. The pulp composition does not have to contain a colorant (e.g., a dye).

[0130] The amount of each of the above additives may be 0.1% by weight or more, 1% by weight or more, 3% by weight or more, or 5% by weight or more, and may be 30% by weight or less, 20% by weight or less, 10% by weight or less, or 5% by weight or less, based on the weight of the pulp.

[0131] <Manufacturing method of pulp products> The method for producing a pulp product according to the present disclosure may include a step of treating a pulp base material with a repellent (wax addition step). A pulp composition is obtained by treating the pulp base material with a repellent. The pulp composition may be produced by a wax addition step of adding wax to the pulp, and a strength agent addition step of adding a strength agent to the pulp. The wax addition step and the strength agent addition step may be carried out separately or simultaneously. The obtained pulp composition may be subjected to treatment steps such as drying, heating, and molding, as necessary, to produce a pulp product.

[0132] The types and compositions of the pulp substrate and repellent agent are described in the "pulp composition" section above. The repellent agent of the present disclosure can be applied to the substrate as a treatment agent (particularly a surface treatment agent) by a conventionally known method. The treatment method may involve dispersing and diluting the repellent agent of the present disclosure in an organic solvent or water, as necessary, and applying it to the interior and / or surface of the pulp substrate by a known method such as dip coating, spray coating, or foam coating, followed by drying. After drying, a pulp product is obtained with the solid components of the repellent agent attached. If necessary, the repellent agent may be applied together with an appropriate crosslinking agent and cured. The concentration of the repellent agent in the treatment agent to be contacted with the pulp substrate may be varied depending on the application, but may be 0.01 to 10% by weight, for example, 0.05 to 5% by weight.

[0133] The repellent agent can be applied to the pulp substrate by any of the known methods for treating a pulp substrate with a liquid. The pulp substrate may be immersed in the repellent agent, the pulp substrate and the repellent agent may be mixed, or the solution may be applied or sprayed onto the pulp substrate. The treated pulp substrate is preferably dried and cured by heating to develop liquid repellency. The heating temperature may be, for example, 100°C to 200°C, 100°C to 170°C, or 100°C to 120°C. In the present disclosure, the heating time may be 5 seconds to 60 minutes, for example, 30 seconds to 3 minutes.

[0134] The pulp base material can be treated by an internal treatment method in which a repellent is added to pulp (e.g., pulp slurry) before papermaking, or an external treatment method in which a repellent is applied to pulp (e.g., pulp product) after papermaking. Examples of internal treatment methods include mixing and immersion, and may include a step of adding a repellent to pulp slurry and stirring and mixing. Examples of external treatment methods include spraying and application, and specific examples include pond-type two-roll size presses, gate-roll type, and rod-metering size presses. The treatment may be an external treatment or an internal treatment. For example, when the pulp base material is paper, the repellent may be coated on the paper, or the solution may be attached or sprayed on the paper, or the repellent may be mixed with the pulp slurry before papermaking.

[0135] The treatment method may be an internal addition treatment in which a repellent is added to the pulp slurry before papermaking. The internal addition treatment may include, but is not limited to, one or more of the following steps: adding the repellent to the pulp slurry and stirring and mixing it; suction-dehydrating the pulp composition prepared in the above step through a mesh of a predetermined shape to deposit the pulp composition and form a molded pulp product intermediate; and molding and drying the molded pulp product intermediate in a heated mold to obtain a molded pulp product. The treated paper may be briefly dried at room temperature or at an elevated temperature, and then optionally subjected to a heat treatment depending on the paper's properties. The heat treatment temperature may be 150°C or higher, 180°C or higher, or 210°C or higher, or 300°C or lower, 250°C or lower, or 200°C or lower, and particularly preferably 80°C to 180°C. Heat treatment within this temperature range can exhibit excellent oil resistance, water resistance, etc. The internally treated pulp substrate may be treated with a repellent by external addition, and an additional wax and an additional paper strength agent may be attached to the surface. Examples of the additional wax and the additional paper strength agent are as described above, but are not limited thereto.

[0136] The treatment method may be an external addition treatment in which a repellent agent is applied to the pulp base material after papermaking. Size presses for external addition treatment can also be classified as follows based on the application method. One application method is the so-called pond-type two-roll size press, in which a coating liquid (size liquid) is supplied to the nip formed by passing paper between two rubber rolls, creating a coating liquid pool called a pond, and the paper is passed through this coating liquid pool to apply the sizing liquid to both sides of the paper. Other application methods include the gate roll type, in which the sizing liquid is applied using a surface transfer method, and the rod metering size press. In the pond-type two-roll size press, the sizing liquid easily penetrates into the paper, while in the surface transfer type, the sizing liquid components tend to remain on the paper surface. In the surface transfer type, the coating layer tends to remain on the paper surface compared to the pond-type two-roll size press, and the coating layer formed on the surface is larger than in the pond-type two-roll size press. In the present disclosure, performance can be imparted to paper even when the former pond-type two-roll size press is used. Papers treated in this way can exhibit excellent oil and water resistance etc., after simple drying at room temperature or at elevated temperatures, optionally followed by a heat treatment which, depending on the properties of the paper, can range from 300°C, for example up to 200°C, especially from 80°C to 180°C.

[0137] <Strength of pulp molded products> [Dry strength] The dry strength of the pulp molded product of the present invention is not particularly limited, but is evaluated by the specific tensile strength in a dry state measured in accordance with JIS P 8113: 2006. The specific dry tensile strength is obtained by dividing the dry tensile strength by the density.

[0138] The dry strength (specific dry tensile strength) of the pulp molded product of the present invention is preferably 20.0 Nm / g or more, 25.0 Nm / g or more, 30.0 Nm / g or more, more preferably 35.0 Nm / g or more, and even more preferably 40.0 Nm / g or more. There is no particular upper limit, but from the viewpoint of ease of production, it is 200 Nm / g or less, more preferably 100 Nm / g or less, and even more preferably 50 Nm / g or less.

[0139] Adding wax to a pulp base material reduces the dry strength of the resulting pulp product. While not limited to the method of addition, the internal addition method, in which wax is added to the pulp slurry before papermaking, and the external addition method, in which wax is applied to the paper after papermaking, result in a greater decrease in dry strength with the internal addition method. In the present disclosure, it has been discovered that by employing a specific composition, it is possible to suppress the decrease in dry strength even when wax is used.

[0140] [Wet strength] The wet strength of the pulp molded product of the present invention is not particularly limited, but is evaluated by the specific wet tensile strength measured in accordance with JIS P 8135: 0998. The specific wet tensile strength is obtained by dividing the wet tensile strength by the density.

[0141] The wet strength (specific wet tensile strength) of the pulp molded product of the present invention may be 3.0 Nm / g or more, 6.0 Nm / g or more, 8.0 Nm / g or more, 10.0 Nm / g or more, 12.0 Nm / g or more, or 14.0 Nm / g or more, preferably 3.0 Nm / g or more, more preferably 4.0 Nm / g or more, even more preferably 5.0 Nm / g or more, and even more preferably 8.0 Nm / g or more. There is no particular upper limit, but from the viewpoint of ease of production, it may be 20 Nm / g or less, 18 Nm / g or less, 16 Nm / g or less, or 15 Nm / g or less, preferably 16 Nm / g or less, for example 14 Nm / g or less.

[0142] Adding wax to a pulp base material reduces the wet strength of the resulting pulp product. While not limited to the addition method, the internal treatment method, in which an oil-proofing agent is added to the pulp slurry before papermaking, and the external treatment method, in which an oil-proofing agent is applied to the paper after papermaking, result in a greater reduction in wet strength than the internal treatment method. The present disclosure has discovered that by employing a specific composition, it is possible to suppress the reduction in wet strength even when wax is used. [Example]

[0143] The present disclosure will be described in detail below with reference to examples, but the present disclosure is not limited to these examples.

[0144] <Test Method> The test procedure is as follows:

[0145] [Dry tensile strength] The tensile strength was measured by a method in accordance with JIS P 8113.

[0146] [Wet tensile strength] The wet strength was measured according to a method in accordance with JIS P 8135.

[0147] [Oil resistance] 100 mL of corn oil at 50°C was poured onto the pulp molding, and after leaving it at room temperature for 30 minutes, the corn oil was removed from the pulp molding and the degree of staining of the pulp molding was evaluated. The following evaluation values ​​were set depending on the degree of staining. 5: No stains inside. 4: Stain on the inside. No stain on the back. 3: Stain on the inside. Slight bleeding on the back. 2: Stain on the inside, with less than 50% of the area bleeding to the back. 1: Staining on the inside, with bleeding to the back covering 50% to less than 100% of the area. 0: Seeped through to the entire back side.

[0148] [Moldability] The occurrence of poor dehydration and poor adhesion during molding of the pulp molded product was evaluated according to the following criteria. ○: Poor dehydration and molding ×: Poor dehydration and molding

[0149] [Redisintegrability] Ten grams of each molded pulp product was torn into 3-4 cm square pieces and immersed in tap water at 20°C. The pulp molded products were diluted to a concentration of 1.5% and then disintegrated using a disintegrator at 3,000 rpm for 20 minutes. The degree of disintegration of the resulting pulp slurry pieces was evaluated according to the following criteria. ○: Paper pieces completely disintegrated into fibers ×: Pieces of paper still remain undissolved

[0150] [Example 1] To a 550cc (Canadian freeness) sample, 2000g of a 0.5% by weight aqueous dispersion of a mixture of 70 parts of beaten bleached hardwood kraft pulp and 30 parts of bleached softwood kraft pulp was added with stirring, and then a wax emulsion (repellent) containing 2g of paraffin wax, 0.05g of benzalkonium chloride, 0.04g of an abietic acid derivative (rosin-based sizing agent), 0.04g of formic acid, 0.04g of acetic acid, and 7.83g of water was added in an amount equivalent to the amount of wax per pulp. A polyacrylamide-based paper strength agent (product name: T-FC109, manufactured by Seiko PMC) was added at a ratio of 0.1% to pulp and the mixture was stirred for 1 minute. Aluminum sulfate was then added at a ratio of 0.04% to pulp in terms of aluminum oxide and the mixture was stirred for 1 minute. Alkyl ketene dimer (AKD) (Hercon (registered trademark) 79 manufactured by Solenis) was then added at a ratio of 0.45% to pulp and the mixture was stirred for 1 minute.

[0151] The pulp composition obtained above was placed in a metal tank. A metal mold with numerous suction holes was placed at the bottom of the tank, with a mesh-like structure placed on top. A vacuum pump was used to suck and dehydrate the pulp composition through the mold and mesh-like structure from the side of the mold opposite the mesh-like structure, depositing the solids (pulp, etc.) contained in the pulp composition on the mesh-like structure to obtain a molded pulp intermediate. The obtained molded pulp intermediate was then dried by applying pressure from above and below using a male-female metal mold heated to 60 to 200°C. This produced a molded pulp product with a weight of 500 gsm, molded into the shape of a container. The content ratio of each component relative to the pulp in the obtained molded pulp product, as well as the tensile strength index, oil resistance, moldability, and remacerability were evaluated. The tensile strength index was evaluated based on at least one of dry tensile strength and wet tensile strength (the same applies below).

[0152] [Example 2] Except for adding a polyacrylamide-based strength agent at a ratio of 0.5% to the pulp, the experiment was carried out in the same manner as in Example 1. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0153] [Example 3] Except for adding a polyacrylamide-based strength agent at a ratio of 1.1% to the pulp, the experiment was carried out in the same manner as in Example 1. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0154] [Example 4] The experiment was carried out in the same manner as in Example 2, except that the wax emulsion was added in a ratio of 0.20% of the pulp in terms of wax amount. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated. The results are shown in Table 1.

[0155] [Example 5] The experiment was carried out in the same manner as in Example 2, except that the wax emulsion was added in a ratio of 10.0% of the pulp in terms of wax amount. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0156] [Example 6] The experiment was carried out in the same manner as in Example 1, except that a polysaccharide-based strength agent (product name: CATOSIZE380H, manufactured by Ingredion) was added at a ratio of 0.6% to the pulp instead of the polyacrylamide-based strength agent. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated. The results are shown in Table 1.

[0157] [Example 7] The experiment was carried out in the same manner as in Example 6, except that the polysaccharide-based paper strength agent was added at a ratio of 1.5% to the pulp. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0158] [Example 8] The experiment was carried out in the same manner as in Example 6, except that the polysaccharide-based paper strength agent was added at a ratio of 5.0% to the pulp. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0159] [Example 9] The experiment was carried out in the same manner as in Example 1, except that a polyamide-based strength agent (product name: WS4020, manufactured by Seiko PMC) was added in a ratio of 0.3% to the pulp instead of the polyacrylamide-based strength agent. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated. The results are shown in Table 2.

[0160] [Example 10] The experiment was carried out in the same manner as in Example 9, except that the polyamide-based paper strength agent was added at a ratio of 0.6% to the pulp. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 2.

[0161] [Example 11] The experiment was carried out in the same manner as in Example 9, except that the polyamide-based paper strength agent was added at a ratio of 0.9% to the pulp. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 2.

[0162] [Comparative Example 1] Except for not adding wax emulsion or polyacrylamide-based paper strength agent, the experiment was conducted in the same manner as in Example 1. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0163] Comparative Example 2 Except for not adding a polyacrylamide-based paper strength agent, the experiment was conducted in the same manner as in Example 1. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0164] Comparative Example 3 Except for adding a polyacrylamide-based strength agent at a ratio of 0.02% to the pulp, the experiment was carried out in the same manner as in Example 1. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0165] Comparative Example 4 Except for adding a polyacrylamide-based strength agent at a ratio of 1.85% to the pulp, the experiment was carried out in the same manner as in Example 1. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0166] Comparative Example 5 The experiment was carried out in the same manner as in Comparative Example 2, except that the wax emulsion was added in a ratio of 0.20% of the pulp in terms of wax amount. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated. The results are shown in Table 1.

[0167] Comparative Example 6 The experiment was carried out in the same manner as in Comparative Example 2, except that the wax emulsion was added in a ratio of 10.0% of the pulp in terms of wax amount. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated. The results are shown in Table 1.

[0168] Comparative Example 7 The experiment was carried out in the same manner as in Example 6, except that the polysaccharide-based paper strength agent was added at a ratio of 8.0% to the pulp. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 1.

[0169] [Comparative Example 8] The experiment was carried out in the same manner as in Example 6, except that the wax emulsion was added externally to the surface of the molded pulp product after molding, rather than internally. The content ratio of each component relative to the pulp in the obtained molded pulp product, as well as the tensile strength index, oil resistance, moldability, and remacerability were evaluated, and the results are shown in Table 1.

[0170] Comparative Example 9 The experiment was carried out in the same manner as in Example 9, except that the polyamide-based paper strength agent was added at a ratio of 1.2% to the pulp. The content ratio of each component relative to the pulp in the obtained pulp molded product, as well as the tensile strength index, oil resistance, moldability, and repulverization properties were evaluated, and the results are shown in Table 2.

[0171] TIFF2025124868000002.tif25371

[0172] TIFF2025124868000003.tif84133

Claims

1. A pulp composition comprising pulp, wax, and a paper strength agent, The paper strength agent is at least one selected from the group consisting of polyacrylamide-based paper strength agents, polysaccharide-based paper strength agents, and polyamide-based paper strength agents, The amount of the wax is 0.2% by weight or more and 10.0% by weight or less based on the pulp, The following (1) to (3): (1) The amount of the polyacrylamide-based paper strength agent is 0.1% by weight or more and 1.1% by weight or less relative to the pulp; (2) The amount of the polysaccharide-based paper strength agent is 0.6% by weight or more and 5.0% by weight or less relative to the pulp; (3) The amount of the polyamide-based paper strength agent is 0.3% by weight or more and 0.9% by weight or less relative to the pulp; A pulp composition that satisfies at least one of the above.

2. The pulp composition according to claim 1, wherein the amount of the polyacrylamide-based paper strength agent is 0.1% by weight or more and 1.1% by weight or less, based on the pulp.

3. The pulp composition according to claim 1, wherein the amount of the polysaccharide-based paper strength agent is 0.6% by weight or more and 5% by weight or less relative to the pulp.

4. The pulp composition according to claim 1, wherein the amount of the polyamide-based paper strength agent is 0.3% by weight or more and 0.9% by weight or less relative to the pulp.

5. 10. The pulp composition of claim 1, wherein the wax is a petroleum wax.

6. 2. The pulp composition according to claim 1, wherein the wax is at least one selected from the group consisting of paraffin wax and microcrystalline wax.

7. The pulp composition of claim 1 wherein the wax is paraffin wax.

8. The pulp composition of claim 1, further comprising at least one selected from the group consisting of benzalkonium chloride, formic acid, acetic acid, and rosin.

9. The pulp composition of claim 1 which is dye-free.

10. The wax is paraffin wax, and The pulp composition of claim 1, further comprising at least one selected from the group consisting of benzalkonium chloride, formic acid, acetic acid, and rosin.

11. A molded pulp product formed from the pulp composition according to any one of claims 1 to 10.

12. The molded pulp product according to claim 11, having an additional wax and an additional strength agent attached to the surface thereof.

13. The molded pulp product according to claim 11, which is for use in contact with food.

14. A method for producing a pulp composition according to any one of claims 1 to 10, a wax addition step of adding the wax to the pulp; and a paper strength agent adding step of adding the paper strength agent to the pulp; A method for producing a pulp composition, comprising:

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