Patent Application
20220194118
The present invention relates to a water-based ballpoint pen provided with a writing ball that includes a hard phase component and a binder phase component.
Cemented alloys, ceramics and the like are widely known as materials configuring the balls of ballpoint pens, such as in Japanese Utility Model Application Laid-Open (JP-U) No. S52-106235 and Japanese Patent Application Laid-Open (JP-A) Nos. 2002-19366 and 2015-51571. Improvements in ink adhesion and the writing sensation of balls fabricated of cemented alloys have been considered in Japanese Patent Application Publication (JP-B) No. S50-31049 and JP-A No. 2002-19366.
Moreover, JP-A No. 2003-155435 discloses an ink of a water-based ballpoint pen including colored resin particles. In particular, JP-A No. 2017-214540 discloses a use of a microsphere coloring agent.
Furthermore, JP-A No. 2006-142511 discloses an improvement of writing characteristics with an ink that uses a thermochromic pigment and a ball containing cobalt and nickel.
When a water-based ballpoint pen using an ink composition containing relatively large-diameter resin particles, with an average particle diameter of 0.3 μm or more, is left in a state in which the ballpoint pen tip is exposed to outside air, it is often the case that the ink does not easily emerge from the tip when writing is resumed. It has been observed that this is because moisture contained in ink adhered to the tip end of the ballpoint pen tip evaporates, as a result of which the resin particles in the ink lose consistent dispersibility, and loose agglomerations of the resin particles are formed. This effect is more likely to occur when the average particle diameter of the resin particles in the ink is relatively large and when there is a high proportion of the resin particles in the composition.
Attempts have previously been made to solve this problem in initial writing performance by adjusting the ink composition, such as in JP-A No. 2016-132749. However, attempts have not yet been made to improve initial the writing performance without altering the ink composition.
In consideration of the problem described above, an object of aspects of the present disclosure is to improve the initial writing performance of a water-based ballpoint pen after the water-based ballpoint pen has been left in a state in which a ballpoint pen tip is exposed to outside air, the water-based ballpoint pen using an ink composition containing relatively large-diameter resin particles with an average particle diameter of 0.3 μm or more, without altering the composition of the ink.
In order to solve the problem described above, a first aspect of the present disclosure is a water-based ballpoint pen containing an aqueous ink composition blended with resin particles having an average particle diameter of 0.3 μm or more, the water-based ballpoint pen comprising a ballpoint pen tip having a writing ball formed from a mixture including: a hard phase component including tungsten carbide; a binder phase component including cobalt and nickel; and chromium.
An upper limit of the average particle diameter of the resin particles is not particularly limited, but is preferably less than 5 μm so as not to impair the flowability of the ink and the dispersibility of the resin particles.
In a water-based ballpoint pen according to a second aspect of the present disclosure, in addition to the characteristics of the first aspect described above, the aqueous ink composition contains from 5 to 30 mass % of the resin particles.
In a water-based ballpoint pen according to a third aspect of the present disclosure, in addition to the characteristics of the first aspect or second aspect described above, the resin particles include a coloring agent.
According to the aspects of the present disclosure with the configurations described above, in a water-based ballpoint pen that uses an ink composition containing relatively large-diameter resin particles with an average particle diameter of at least 0.3 μm, the initial writing performance of the water-based ballpoint pen, after the water-based ballpoint pen has been left in a state in which the ballpoint pen tip is exposed to outside air, is improved without the composition of the ink being altered.
An exemplary embodiment of the present disclosure is described below with reference to the drawings. Note that reference symbols marked on the drawings that are the same in plural drawings have the same technical meaning even if not mentioned in the descriptions of the drawings below. An upper side of each drawing is referred to as a tip end side and a lower side of each drawing is referred to as a rear end side.
When the holder 21 is assembled, the writing ball 30 is inserted into the ball house 22 from the tip side thereof. Then, by the upper portion of the writing ball 30 being pressed in the direction toward the rear end, the ball seat 24 is deformed in accordance with an exterior shape of the writing ball 30. Thereafter, a swaging process using taper-shaped rollers is applied to the tip end of the taper portion 27, providing the swaged portion 23. Thus, the holder 21 is formed.
The holder 21 is formed of stainless steel with a Vickers hardness of around 200 to 420. The holder 21 may be formed using an alternative metal such as nickel silver or brass or a resin or the like as the material thereof, with a desirable Vickers hardness (Hv) being from 170 to 450.
In the present exemplary embodiment, the holder 21 is formed by a process of cutting from a solid wire material. However, the process of cutting from a wire material is not limiting. For example, the holder 21 may be formed by plastic machining of a hollow pipe material.
The writing ball 30 according to the present exemplary embodiment is formed of a mixture including a hard phase component comprising tungsten carbide (WC), a binder phase component comprising cobalt (Co) and nickel (Ni), and also chromium (Cr). The metallic elements referred to herein may be used in their elemental forms or as compounds. The mixture may also include another metallic element such as, for example, molybdenum (Mo).
The hard phase component is preferably 80 mass % or more as a proportion of the whole of the writing ball 30.
Powder materials of the hard phase component, the binder phase components and chromium mentioned above and, if other components are to be included, powder materials of the other components are pulverized and mixed. This mixture is formed into a substantially spherical shape, and then sintered and formed into a spherical body. The spherical body obtained thus far is rolled together with diamond powder between two grindstones that are retained at a certain spacing. Thus, a ball surface 31 is finished to a mirror surface and the writing ball 30 is formed. The Vickers hardness (Hv) of the ball surface 31 is from 1,600 to 2,000.
Resin particles having an average particle diameter of at least 0.3 μm are blended in the aqueous ink composition 40 according to the present exemplary embodiment. Microscopic spherical bodies (microspheres or microcapsules) containing a dye or pigment as a coloring agent may be used as the resin particles. A hollow resin may also be used as the resin particles. A preferable content amount of the resin particles is from 5 to 30 mass % of the whole of the ink composition. An upper limit of the average particle diameter of the resin particles is not particularly limited as long as flowability of the ink and dispersibility of the resin particles are not impaired. However, the average particle diameter is preferably 5 μm or less.
Writing balls were fabricated with following compositions.
Ball 1 was a writing ball fabricated by the method described above from a mixture with a following composition.
WC (hard phase component): 91 mass %
Co (binder phase component): 5 mass %
Ni (binder phase component): 2 mass %
Cr3C2: 2 mass %
Ball 2 was a writing ball fabricated by the method described above from a mixture with a following composition.
WC (hard phase component): 89 mass %
Co (binder phase component): 3 mass %
Ni (binder phase component): 5 mass %
Cr3C2: 3 mass %
Ball 3 was a writing ball fabricated by the method described above from a mixture with a following composition.
WC (hard phase component): 86 mass %
Co (binder phase component): 10 mass %
Ni (binder phase component): 1 mass %
Cr3C2: 3 mass %
Ball 4 was a writing ball fabricated by the method described above from a mixture with a following composition.
WC (hard phase component): 85 mass %
Co (binder phase component): 10 mass %
Cr3C2: 5 mass %
Ball 5 was a writing ball fabricated by the method described above from a mixture with a following composition.
WC (hard phase component): 91 mass %
Ni (binder phase component): 6 mass %
Cr3C2: 3 mass %
Inks 1 to 3 were prepared as follows.
While 12.5 mass parts of ethyl acetate serving as an organic solvent was heated at 60° C., 3.5 mass parts of an oil-soluble black dye serving as a water-insoluble dye (OIL BLACK 860, from Orient Chemical Industries Co., Ltd.) was added to the ethyl acetate and thoroughly dissolved. Then, 8 mass parts of a modified isocyanurate of hexamethylene diisocyanate serving as a prepolymer (TLA-100, from Asahi Kasei Chemicals Corporation) was added. Thus, an oil phase solution was prepared.
While 200 mass parts of distilled water was heated at 60° C., 15 mass parts of polyvinyl alcohol serving as a dispersion agent (PVA-205, from Kuraray Co., Ltd.) was dissolved therein. Thus, a water phase solution was prepared.
The oil phase solution was added to the water phase solution heated to 60° C., and polymerization was completed by emulsion mixing in a homogenizer. Microspheres containing the coloring agent were recovered from the obtained dispersion by centrifugal processing. The average particle diameter was 1.5 μm. The average particle diameter was measured using a particle size analyzer (HRA9320-X100, from Nikkiso Co., Ltd.), taking a D50 value calculated by reference to volume with a refractive index of 1.81 (the same applies to Ink 2 and Ink 3, which are described below).
Then, an ink composition with following components was used for Ink 1.
The microspheres: 15 mass parts
Xanthan gum (thickening agent, KESLAN S, from Sansho Co., Ltd.): 0.18 mass parts
Phosphate ester (PLYSURF A219B, from DKS Co., Ltd.): 0.5 mass parts
Preservative (BIODEN 421, from Daiwa Chemical Industries Co., Ltd.): 0.2 mass parts
Benzotriazole (corrosion inhibitor): 0.3 mass parts
Aminomethylpropanol (pH adjuster): 0.1 mass parts
Propylene glycol (solvent): 15 mass parts
Deionized water: 68.72 mass parts
One mass part of ETAC (from Yamada Chemical Co., Ltd.) serving as a leuco dye, 2 mass parts of bisphenol A serving as a developing agent, and 24 mass parts of myristyl myristate serving as a thermochromism temperature adjuster were heated to 100° C. and fused, providing a homogeneous composition.
The 27 mass parts of the obtained composition was heated uniformly at 100° C. in a solution. As capsule wall agents, 10 mass parts of isocyanate and 10 mass parts of polyol were added to the heated solution and mixed by agitation. Then, 60 mass parts of a 12% aqueous solution of polyvinyl alcohol serving as a protective colloid was added and emulsified at 25° C., preparing a dispersion. Then, 5 mass parts of 5% polyamine was added and treated at 85° C. for 45 minutes, providing core-shell type microcapsules containing the coloring agent. The average particle diameter was 2.1 μm.
An ink composition with following components was used for Ink 2.
The thermochromic microcapsule dye: 15 mass parts
Xanthan gum (thickening agent, KESLAN S, from Sansho Co., Ltd.): 0.3 mass parts
Phosphate ester (PLYSURF A219B, from DKS Co., Ltd.): 0.3 mass parts
Preservative (BIODEN 421, from Daiwa Chemical Industries Co., Ltd.): 0.2 mass parts
Benzotriazole (corrosion inhibitor): 0.3 mass parts
Triethanolamine (pH adjuster): 0.1 mass parts
Glycerol (solvent): 10 mass parts
Deionized water: 73.8 mass parts
An ink composition with following components was used for Ink 3.
Pigment (FUJI RED 2510, from Fuji Pigment Co., Ltd.): 8 mass parts
Pigment dispersion agent (JONCRYL 60, from BASF Japan Ltd.): 6 mass parts
Hollow resin particles (ROPAQUE OP-84J, from The Dow Chemical Company, solids 42.5%, average particle diameter 0.55 μm): 10 mass parts
Xanthan gum (thickening agent, KESLAN S, from Sansho Co., Ltd.): 0.3 mass parts
Phosphate ester (PLYSURF A219B, from DKS Co., Ltd.): 0.3 mass parts
Preservative (BIODEN 421, from Daiwa Chemical Industries Co., Ltd.): 0.2 mass parts
Benzotriazole (corrosion inhibitor): 0.3 mass parts
Triethanolamine (pH adjuster): 0.5 mass parts
Glycerol (solvent): 10 mass parts
Deionized water: 64.4 mass parts
The water-based ballpoint pens as illustrated in the exemplary embodiment were prepared using Ball 1 to Ball 5 and Ink 1 to Ink 3 described above.
A water-based ballpoint pen according to Example 1 employed Ball 1 as the writing ball. Three refills were prepared containing, respectively, Ink 1 to Ink 3.
A water-based ballpoint pen according to Example 2 employed Ball 2 as the writing ball. Three refills were prepared containing, respectively, Ink 1 to Ink 3.
A water-based ballpoint pen according to Example 3 employed Ball 3 as the writing ball. Three refills were prepared containing, respectively, Ink 1 to Ink 3.
A water-based ballpoint pen according to Comparative Example 1 employed Ball 4 as the writing ball. Three refills were prepared containing, respectively, Ink 1 to Ink 3.
A water-based ballpoint pen according to Comparative Example 2 employed Ball 5 as the writing ball. Three refills were prepared containing, respectively, Ink 1 to Ink 3.
The water-based ballpoint pens according to Examples 1 to 3 and Comparative Examples 1 and 2 described above were left in an uncapped state for 60 minutes in an environment with temperature 25° C. and humidity 50%. Then, they wrote straight lines on ordinary photocopier paper and initial writing performances were evaluated by following evaluation standards.
A: No blurring was seen at all in the line from the start of writing.
B: Blurring of the line was observed from the start of writing.
The results according to these evaluation standards were as in Table 1 below.
The water-based ballpoint pens according to Examples 1 to 3 using, respectively, the writing balls of Ball 1 to Ball 3 were excellent in initial writing performance with no blurring of lines at the start of writing, whichever of Ink 1 to Ink 3 was used.
In contrast, with the water-based ballpoint pen according to Comparative Example 1 using Ball 4 that did not contain nickel, blurring of the line at the start of writing was seen whichever of Ink 1 to Ink 3 was used. With the water-based ballpoint pen according to Comparative Example 2 using Ball 5 that did not contain cobalt, blurring of the line at the start of writing was seen whichever of Ink 1 to Ink 3 was used.
As shown above, when both cobalt and nickel are blended as components of a writing ball in addition to tungsten carbide and chromium, initial writing performance may be improved regardless of types of resin particles.
The present invention is applicable to ballpoint pens containing aqueous inks in which resin particles are blended.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2019-091401 | May 2019 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2020/010542 | 3/11/2020 | WO | 00 |
