JP2017031244A - Resin composition for cleaning three-dimensional molding apparatus and production method thereof, and resin filament for cleaning three-dimensional molding apparatus - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a resin composition for cleaning a three-dimensional molding apparatus, which facilitates a cleaning operation and has a high cleaning effect and high retaining property of the cleaning effect.SOLUTION: The resin composition for cleaning a three-dimensional molding apparatus of the present invention comprises a thermoplastic resin, at least one component (X) selected from the group consisting of a surfactant and a metal soap, and a filler, and the composition has a melt mass flow rate of 0.5 to 10 g/10 min. The thermoplastic resin preferably has a Vicat softening point of 90 to 170°C.SELECTED DRAWING: None

Description

  The present invention relates to a resin composition for cleaning a three-dimensional modeling apparatus, a method for producing the same, and a resin filament for cleaning a three-dimensional modeling apparatus using the same.

In recent years, development of a three-dimensional modeling apparatus capable of producing a three-dimensional modeled object without using a mold and without material loss has been progressing.
Several three-dimensional structures have been proposed depending on the material.
The present invention is directed to a resin-made three-dimensional structure.
Examples of the three-dimensional resin modeling method include an optical modeling method using a photocurable resin, a thermal melting method using a thermoplastic resin, and an inkjet method.

  In the optical modeling method, an uncured photocurable resin layer is formed on a modeling stage and then irradiated while scanning with a light beam such as a UV (ultraviolet light) laser beam. Say "pattern layer". By repeating these operations, a plurality of pattern layers are stacked to produce a three-dimensional structure.

  In the thermal melting method, a molten thermoplastic resin is discharged in a desired pattern from a movable modeling head including a nozzle on a modeling stage. Since the modeling stage is set in advance to a temperature at which the molten resin is cooled and solidified, the molten resin discharged onto the modeling stage is immediately solidified. A resin layer having a desired pattern is formed on the modeling stage by two-dimensionally scanning the movable modeling head. By repeating these operations, a plurality of pattern layers are laminated to produce a three-dimensional structure.

  In the inkjet method, after a liquid photocurable resin is ejected in a desired pattern from an inkjet head including a nozzle on a modeling stage, a pattern layer is obtained by photocuring using UV lamp light or the like. By repeating these operations, a plurality of pattern layers are stacked to produce a three-dimensional structure.

Among these, the thermal dissolution method and the ink jet method that do not require the non-pattern layer to be formed in advance are preferable.
In the thermal melting method and the ink jet method, a modeling material is discharged from a nozzle (note that the expression “spray” or “push out” may be used depending on the material or the like).
In order to manufacture a three-dimensional structure such as a precision part that requires high shape accuracy, it is important that the discharge amount from the nozzle does not deviate from a setting value calculated in advance using a computer or the like.
In this specification, “discharge amount” means a discharge amount per unit time unless otherwise specified.

Generally, in the heat melting method, acrylonitrile-butadiene-styrene (ABS) resin or the like is preferable because it is excellent in heat resistance and can be subjected to processing such as painting on a molded article relatively easily. used.
ABS resins tend to be thermally decomposed more easily than olefin resins and the like. For this reason, in the thermal melting method using ABS-based resin, if molding is repeatedly performed, foreign matter such as the resin used or its thermal decomposition product accumulates inside the metal tube and nozzle where the molten resin flows down, and the discharge amount is reduced. There is a risk of becoming stable.
For the metal tube and the nozzle, refer to FIG. 1 and its description later.
Note that the above-described problem of deposits may occur even in resins other than ABS resins.
This can also occur in an ink jet method using a nozzle.

Conventionally, as a method for removing the deposit,
Decomposing and removing method of disassembling the modeling apparatus and physically removing deposits attached to the inside of the metal tube and nozzle using a wire etc.,
Resin replacement method that uses other resin that does not easily adhere to deposits instead of resin that deposits are likely to adhere to
and,
An organic solvent cleaning method (see paragraph 0002 of Patent Document 1 and paragraph 0003 of Patent Document 2) that employs an organic solvent such as ethanol and ketone is employed.

Japanese Patent Laid-Open No. 2005-1206 JP 2007-76090 A

Although the decomposition and removal method is highly effective in removing deposits, it takes time and effort to disassemble and remove the modeling apparatus.
In the resin replacement method and the organic solvent cleaning method, it is difficult to effectively remove deposits, and the removal effect is temporary.

  An object of the present invention is to provide a resin composition for cleaning a three-dimensional modeling apparatus that has a simple cleaning operation, a high cleaning effect, and a high cleaning effect durability.

The resin composition for cleaning a three-dimensional modeling apparatus of the present invention is
A thermoplastic resin, at least one component (X) selected from the group consisting of a surfactant and a metal soap, and a filler,
The melt mass flow rate (hereinafter sometimes abbreviated as “MFR”) is 0.5 to 10 g / 10 min.

In the present specification, unless otherwise specified, the MFR of the resin composition is measured under the conditions of 190 ° C. and a load of 2.16 kg in accordance with ISO 1133.
Specifically, a sufficiently dried sample is placed in a cylinder (inner diameter 9.5 mmφ) that has been heated to a measurement temperature (190 ° C.) in advance. After the sample reaches the measurement temperature (190 ° C.), a predetermined load (2.16 kg) is applied to the piston inserted into the cylinder to remove the sample from the orifice (inner diameter 2.095 mmφ) attached to the bottom of the cylinder. Extrude. As MFR, the mass of the sample extruded in 10 minutes is determined.

  According to the present invention, it is possible to provide a resin composition for cleaning a three-dimensional modeling apparatus that has a simple cleaning operation, a high cleaning effect, and a high cleaning effect durability.

It is a principal part schematic sectional drawing of a three-dimensional modeling apparatus.

"Resin composition for cleaning 3D modeling equipment"
The three-dimensional modeling apparatus cleaning resin composition of the present invention (hereinafter sometimes abbreviated as “cleaning resin composition” or “resin composition”) is a three-dimensional resin modeling apparatus using a thermal melting method, an inkjet method, or the like. It is suitably used for cleaning.

In the three-dimensional resin molding apparatus using the thermal melting method, when molding is repeatedly performed, foreign substances such as used resin and carbides such as thermal decomposition products accumulate in the metal tube and nozzle where the molten resin flows down, and the discharge amount May become unstable.
Similarly, in the three-dimensional resin modeling apparatus using the ink jet method, foreign matter such as a used resin and a carbide such as a decomposition product thereof may accumulate inside a nozzle or the like, and the discharge amount may become unstable.
The present invention is particularly applicable to the thermal dissolution method, but can also be applied to the ink jet method.

  Although details will be described later, by operating the modeling apparatus so as to perform normal modeling using the resin composition of the present invention instead of the modeling material in a hot melting method or the like, inside the nozzle or the like of the modeling apparatus Adhering deposits can be effectively removed.

The resin composition of the present invention can be molded into an arbitrary shape and used as necessary.
In the hot melting method or the like, the filament shape is preferable as in the modeling material.

The resin composition of the present invention can drive a modeling apparatus so as to perform normal modeling using the resin composition of the present invention instead of a modeling material in a hot melting method or the like, and has a desired shape. Since it can be molded, a thermoplastic resin is included.
The resin composition of the present invention contains a component (X) having high slipperiness in order to improve the feedability of the resin composition of the present invention in the modeling apparatus. Specifically, the highly slippery component (X) is a surfactant and / or a metal soap.
The resin composition of the present invention contains a filler in order to effectively scrape deposits adhering to the inside of the nozzle of the modeling apparatus.
That is, the resin composition of the present invention includes a thermoplastic resin, at least one component (X) selected from the group consisting of a surfactant and a metal soap, and a filler.
Furthermore, the MFR of the resin composition of the present invention is in the range of 0.5 to 10 g / 10 minutes.

(Thermoplastic resin)
The thermoplastic resin used in the present invention is not particularly limited.
For example,
Olefin resins such as polyethylene and polypropylene;
(Meth) acrylic resins such as methyl (meth) acrylate:
Polystyrene, styrene-maleic anhydride copolymer, acrylonitrile-styrene (AS) resin, acrylonitrile-butadiene-styrene (ABS) resin, acrylonitrile / ethylene / propylene / diene / styrene (AES) resin, acrylic / acrylonitrile / Styrene resins such as styrene (AAS) resins, acrylonitrile-chlorinated ethylene-styrene (ACS) resins, and methacrylbutadiene styrene (MBS) resins;
Amide resins such as nylon 6 and nylon 66;
Ester resins such as polyethylene terephthalate and polybutylene terephthalate;
Carbonate resins;
Acetal resin;
Vinyl chloride resin;
and,
Examples include ether imide resins.
These can be used alone or in combination of two or more.

  In this specification, “(meth) acryl” means methacryl or acryl.

The thermoplastic resin used may be the same as or different from the resin used for modeling.
In general, an ABS-based resin or the like is preferably used in modeling by a hot melting method.
Since a sufficient amount of filler can be mixed, the deposit removal effect can be effectively obtained, the resin itself is resistant to thermal decomposition, and it is versatile and low cost. Of these thermoplastic resins, olefin resins such as polyethylene and polypropylene are preferred.

  The olefin resin is a homopolymer or copolymer of one or more monomers including at least one olefin monomer.

The olefin monomer is not particularly limited,
Ethylene, propylene, styrene, etc., α-olefins such as 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, and 4-methyl-1-pentene, and cyclobutene and cyclopentene. A cyclic olefin etc. are mentioned.
The olefin resin may be a homopolymer of one olefin monomer or a copolymer of two or more olefin monomers.
The olefin resin may be a copolymer of an olefin monomer and a monomer other than the olefin monomer.
The copolymerizable monomer other than the olefin monomer is not particularly limited, and examples thereof include conjugated dienes such as butadiene and isoprene.

As the olefin monomer, ethylene and propylene are preferable.
That is, as an olefin-based resin, an ethylene homopolymer (polyethylene), a propylene homopolymer (polypropylene), a copolymer of ethylene and an α-olefin other than ethylene, and an α-olefin other than propylene and propylene Of these, the copolymer is preferred.
Of these, ethylene homopolymer (polyethylene) and propylene homopolymer (polypropylene) are more preferred.

The thermoplastic resin is preferably softened at a temperature that facilitates molding.
Moreover, in order to remove deposits effectively, it is necessary for the resin composition to flow with a certain degree of viscosity (not to flow too much) inside the modeling apparatus.
The Vicat softening point is suitable as an index of MFR of a thermoplastic resin.
By selecting the Vicat softening point of the thermoplastic resin within a suitable range, the MFR of the thermoplastic resin can be adjusted within a suitable range. Furthermore, the MFR of the resin composition of the present invention can be adjusted within a suitable range by the MFR and the blending amount of the thermoplastic resin, and the flow state of the molten resin flowing inside the modeling apparatus can be made suitable. .
The Vicat softening point of the thermoplastic resin is not particularly limited, but is preferably 90 to 170 ° C., more preferably 100 to 130 ° C., from the viewpoint of the moldability of the resin composition and the deposit removal effect.

  In this specification, unless otherwise specified, the “softening point” is a Vicat softening point measured according to JIS-K6758 and JIS-K7206.

The MFR of the thermoplastic resin is not particularly limited.
However, the MFR of the resin composition of the present invention is determined in consideration of the types and amounts of other components so that the MFR is within the above range.
The MFR of the thermoplastic resin is preferably in the range of 0.5 to 10 g / 10 minutes, for example.

(Ingredient (X))
Component (X) is at least one component selected from the group consisting of surfactants and metal soaps.

<Surfactant>
The surfactant is not particularly limited, and examples thereof include an anionic surfactant, a nonionic surfactant, a cationic surfactant, and an amphoteric surfactant.
One or more surfactants can be used.

Examples of anionic surfactants include phosphate surfactants, sulfonate surfactants, sulfate surfactants, and fatty acid surfactants.
For example, sodium lauryl sulfate, triethanolamine lauryl sulfate, ammonium lauryl sulfate, sodium dodecylbenzene sulfonate, sodium alkyl naphthalene sulfonate, sodium dialkyl sulfosuccinate, sodium alkyl diphenyl ether disulfonate, alkoxy alkyl phosphate, alkyl Phosphate, alkyl phosphate diethanolamine salt, alkyl phosphate potassium salt, polyoxyethylene lauryl sodium ether sulfate, polyoxyethylene alkyl ether sodium sulfate, polyoxyethylene alkyl ether sulfate triethanolamine , Sodium polyoxyethylene alkylphenyl ether sulfate, Sodium alkyl sulfonate, Mixed fatty acid soda soap, Semi-cured tallow fatty acid -Da soap, semi-cured beef tallow fatty acid soap, stearic acid soda soap, oleic acid potassium soap, castor oil potassium soap, higher sodium alcohol sulfate, sodium salt of β-naphthalene sulfonic acid formalin condensate, special aromatic Examples thereof include a sulfonic acid formalin condensate and a special carboxylic acid type surfactant.

As nonionic surfactant,
Polyoxyethylene alkyl ethers such as polyoxyethylene cetyl ether and polyoxyethylene stearyl ether;
Polyoxyethylene phenyl ethers such as polyoxyethylene nonylphenyl ether;
Sorbitan fatty acid esters such as sorbitan monostearate;
Polyoxyethylene sorbitan fatty acid esters such as polyoxyethylene sorbitan monolaurate;
Glycerin fatty acid esters such as stearic acid monoglyceride;
and,
Examples include polyethylene glycol monolaurate, and polyoxyethylene fatty acid esters such as polyoxyethylene-polyoxypropylene block polymers.

As a cationic surfactant,
Hydrochlorides of primary amines such as monomethylamine, monoethylamine, and monostearylamine;
Secondary amine hydrochlorides such as dimethylamine, diethylamine, and distearylamine;
Tertiary amine hydrochlorides such as trimethylamine, triethylamine, and stearyldimethylamine;
Hydrochlorides of ethanolamines such as monoethanolamine, diethanolamine, and triethanolamine;
Hydrochlorides of polyethylenepolyamines such as ethylenediamine and diethylenetriamine;
and,
Examples thereof include hydrochlorides of amines such as pyridine, morpholine, and hydrazine.

  Examples of amphoteric surfactants include alkyldimethylamine oxide and alkylcarboxybetaine.

  Among these, anionic surfactants and nonionic surfactants are preferred, and nonionic surfactants are more preferred from the viewpoints of feedability (slidability) of the resin composition inside the modeling apparatus and versatility.

<Metal soap>
The metal soap is not particularly limited, and a metal salt of a linear aliphatic monocarboxylic acid having 12 to 18 carbon atoms is preferable.
One or more metal soaps can be used.
Examples of the linear aliphatic monocarboxylic acid having 12 to 18 carbon atoms include lauric acid, palmitic acid, stearic acid, oleic acid, and ricinoleic acid.
Examples of the metal salt include calcium salt, zinc salt, magnesium salt, barium salt, and aluminum salt.
Among the above, zinc stearate and magnesium stearate are preferable as the metal soap.
As component (X), it is preferable to use a surfactant and a metal soap in combination.

(Filler)
The filler is not particularly limited, and either an inorganic filler or an organic filler may be used. One or more fillers can be used.
Inorganic fillers include calcium carbonate, calcium sulfate, calcium sulfite, magnesium carbonate, calcium silicate, barium sulfate, talc, mica, clay, montmorillonite, smectite, kaolin, glass fiber, glass milled fiber, glass flake, and carbon fiber. , Carbon flakes, carbon beads, carbon milled fibers, silica, ceramic particles, ceramic fibers, and ceramic balloons.
Examples of the organic filler include aramid particles and aramid fibers.
Among these, inorganic fillers are preferable, and calcium carbonate and talc are preferable.

The average diameter of the filler is not particularly limited, and is preferably 0.1 to 50 μm, more preferably 1 in consideration of the cleaning effect of the deposit, ease of blending into the thermoplastic resin composition, nozzle diameter, and the like. It is -30 micrometers, Most preferably, it is 1-10 micrometers.
When cleaning the nozzle of a three-dimensional modeling apparatus by a thermal melting method, the average diameter of the filler is preferably 1 to 50 μm, taking into consideration the inner diameter (for example, about 0.3 to 0.6 mmφ) of a commonly used nozzle. More preferably, it is 1-30 micrometers, Most preferably, it is 1-10 micrometers.
When cleaning a nozzle of a three-dimensional modeling apparatus by an ink jet method, the average diameter of the filler is preferably 0.1 to 20 μm in consideration of the inner diameter (for example, about 0.1 to 0.3 mmφ) of a commonly used nozzle. More preferably, it is 0.1-10 micrometers, Most preferably, it is 0.1-2 micrometers.

The shape of the filler is not particularly limited. Moreover, the shape may be uniform as a whole or may be non-uniform.
Examples of the shape of the filler include a fiber shape, a spherical shape, an elliptical spherical shape, a cylindrical shape, a prismatic shape, a scale shape, and deformed shapes thereof.

In the present specification, unless otherwise specified, the “average diameter of filler” is an average primary diameter measured by the following method.
Using a scanning electron microscope (SEM), an enlarged image of about 1000 times to about 10,000 times is obtained for the raw material filler, or the resin composition or molded body containing the filler. About 100 fillers are randomly selected on this enlarged image, the diameter is measured for each filler, and an average value is obtained.
When the filler is fiber-like, the “diameter” is defined by the diameter of the cross section perpendicular to the fiber extending direction.
For other shapes, when the diameter of the filler varies depending on the direction, the “diameter” is defined by the maximum diameter.

(Composition composition)
The content of each component in the resin composition is not particularly limited.
The resin composition preferably contains a sufficient amount of thermoplastic resin for molding such as filament molding.
The resin composition preferably contains a sufficient amount of the component (X) to express slipperiness that makes the feedability of the resin composition of the present invention in the modeling apparatus good.
The resin composition also preferably contains a sufficient amount of filler for deposit removal.

From the viewpoint of balance between molding processability, feedability of the resin composition of the present invention in the modeling apparatus, and deposit removal effect, the content of each component in the resin composition is preferably within the following range.
The content of the thermoplastic resin in the resin composition is preferably 25 to 60% by mass, more preferably 25 to 50% by mass, and particularly preferably 25 to 45% by mass.
Content of component (X) becomes like this. Preferably it is 6-25 mass%, More preferably, it is 9-20 mass%.
As a component (X), when using a surfactant and a metal soap,
The content of the surfactant in the resin composition is preferably 1 to 10% by mass, more preferably 2 to 8% by mass,
Content of the metal soap in a resin composition becomes like this. Preferably it is 5-15 mass%, More preferably, it is 7-12 mass%.
The content of the filler in the resin composition is preferably 20 to 65% by mass, more preferably 30 to 60% by mass, and particularly preferably 40 to 60% by mass.

(Optional component)
The resin composition of this invention can contain the 1 type (s) or 2 or more types of arbitrary components other than the above as needed.

<Heat stabilizer>
The resin composition of the present invention can contain a thermal stabilizer as an optional component in order to improve thermal stability during production.
One or more heat stabilizers can be used.

As the heat stabilizer, a phosphorus stabilizer and / or a hindered phenol antioxidant is preferable, and a combination thereof is more preferable.
The addition amount of the phosphorus stabilizer and / or hindered phenol antioxidant in the resin composition of the present invention is not particularly limited.
Since the effect of improving the thermal stability is effectively obtained and does not affect the blending amount of each of the above essential components, it is preferably 0.01 to 1 part by mass with respect to 100 parts by mass of the thermoplastic resin. More preferably, it is 0.01-0.6 mass part.

As phosphorus stabilizers,
Phosphorous acid, phosphoric acid, phosphonous acid, phosphonic acid, and esters thereof;
Phosphonite compounds and
And tertiary phosphine.

  Phosphites (phosphite compounds) include triphenyl phosphite, tris (nonylphenyl) phosphite, tridecyl phosphite, distearyl pentaerythritol diphosphite, bis (2,4-di-tert-butylphenyl) ) Pentaerythritol diphosphite, bis (2,6-di-tert-butyl-4-methylphenyl) pentaerythritol diphosphite, bis {2,4-bis (1-methyl-1-phenylethyl) phenyl} penta Examples include erythritol diphosphite, phenylbisphenol A pentaerythritol diphosphite, bis (nonylphenyl) pentaerythritol diphosphite, and dicyclohexyl pentaerythritol diphosphite.

As the phosphite ester (phosphite compound), those having a cyclic structure by reacting with dihydric phenols can be used in addition to the above.
For example, 2,2′-methylenebis (4,6-di-tert-butylphenyl) (2,4-di-tert-butylphenyl) phosphite, 2,2′-methylenebis (4,6-di-tert- Butylphenyl) (2-tert-butyl-4-methylphenyl) phosphite, 2,2-methylenebis (4,6-di-tert-butylphenyl) octyl phosphite, and the like.

  Examples of phosphate esters (phosphate compounds) include triphenyl phosphate and trimethyl phosphate.

Examples of the phosphonite compound include tetrakis (di-tert-butylphenyl) -biphenylenediphosphonite and bis (di-tert-butylphenyl) -phenyl-phenylphosphonite.
The phosphonite compound can be used in combination with the phosphite compound having an aryl group in which two or more alkyl groups are substituted, and is preferable.

  Examples of the phosphonic acid ester (phosphonate compound) include dimethyl benzenephosphonate, diethyl benzenephosphonate, and dipropyl benzenephosphonate.

  Examples of the tertiary phosphine include triphenylphosphine.

  Among the phosphorus stabilizers, phosphonite compounds or phosphite compounds represented by the following general formula (XI) are preferable.

（式（XI）中、ＲおよびＲ’は炭素数６〜３０のアルキル基または炭素数６〜３０のアリール基を表し、互いに同一であっても異なっていてもよい。）

(In formula (XI), R and R ′ represent an alkyl group having 6 to 30 carbon atoms or an aryl group having 6 to 30 carbon atoms, and may be the same or different from each other.)

  As described above, tetrakis (2,4-di-tert-butylphenyl) -biphenylene diphosphonite is preferred as the phosphonite compound.

  Among the above formulas (XI), more preferred phosphite compounds are distearyl pentaerythritol diphosphite, bis (2,4-di-tert-butylphenyl) pentaerythritol diphosphite, bis (2,6-di-). tert-butyl-4-methylphenyl) pentaerythritol diphosphite, and bis {2,4-bis (1-methyl-1-phenylethyl) phenyl} pentaerythritol diphosphite.

  Examples of hindered phenol compounds include tetrakis [methylene-3- (3-tert-butyl-4-hydroxy-5-methylphenyl) propionate] methane, octadecyl-3- (3,5-di-tert-butyl-4- Hydroxyphenyl) propionate, and 3,9-bis [2- {3- (3-tert-butyl-4-hydroxy-5-methylphenyl) propionyloxy} -1,1-dimethylethyl] -2,4,8 , 10-tetraoxaspiro [5,5] undecane and the like.

The resin composition of this invention can contain other thermal stabilizers other than a phosphorus stabilizer and hindered phenolic antioxidant as needed.
The other heat stabilizer is preferably used in combination with at least one of a phosphorus stabilizer and a hindered phenol antioxidant, and particularly preferably used in combination with both.

Other heat stabilizers include lactone stabilizers represented by the reaction product of 3-hydroxy-5,7-di-tert-butyl-furan-2-one and o-xylene (details of this stabilizer). (See JP-A-7-233160).
Regarding the lactone stabilizer, Irganox HP-136 (registered trademark, manufactured by CIBA SPECIALTY CHEMICALS) and the like are commercially available.
Irganox HP-2921 (registered trademark, manufactured by CIBA SPECIALTY CHEMICALS) and the like are commercially available as stabilizers obtained by mixing the lactone-based stabilizer, phosphite compound, and hindered phenol compound.
The addition amount of the lactone stabilizer is preferably 0.0005 to 0.05 parts by mass, more preferably 0.001 to 0.03 parts by mass with respect to 100 parts by mass of the thermoplastic resin.

  Other stabilizers include sulfur-containing stabilizers such as pentaerythritol tetrakis (3-mercaptopropionate), pentaerythritol tetrakis (3-lauryl thiopropionate), and glycerol-3-stearyl thiopropionate. It is done.

  The addition amount of other stabilizers other than the phosphorus stabilizer and / or the hindered phenol antioxidant in the resin composition of the present invention is not particularly limited, and is preferably 0 with respect to 100 parts by mass of the thermoplastic resin. .0005 to 0.1 parts by mass, more preferably 0.001 to 0.08 parts by mass, and particularly preferably 0.001 to 0.05 parts by mass.

<Other optional components>
Examples of other optional components include antifoaming agents, antioxidants, UV absorbers, light stabilizers, plasticizers, lubricants, mold release agents, antistatic agents, and flame retardants.

(MFR)
The resin composition of the present invention preferably has good moldability.
In order to effectively remove deposits using the resin composition of the present invention, it is necessary for the resin composition to flow with a certain degree of viscosity (not to flow too much) inside the modeling apparatus. .
From the viewpoint of molding processability and deposit removal effect, the MFR value of the resin composition of the present invention is 0.5 to 10 g / 10 min, preferably 0.8 to 8 g / 10 min, more preferably 0.8 to 5 g / 10 min.
The MFR of the resin composition can be adjusted by the blending composition, for example, by adjusting the MFR of the thermoplastic resin and the blending amount.

“Forms and Manufacturing Methods of Resin Composition and Molded Body”
The form of the resin composition of the present invention is not particularly limited, and examples thereof include powders, granules, pellets, and mixed forms thereof.

The resin composition of this invention can be shape | molded in arbitrary shapes as needed.
The shape of the molded body is not particularly limited, and a filament shape or the like is preferable.
According to the present invention, it comprises a thermoplastic resin, at least one component (X) selected from the group consisting of a surfactant and a metal soap, and a filler, and has an MFR of 0.5 to 10 g / 10 min. A resin filament for cleaning a certain three-dimensional modeling apparatus (hereinafter sometimes abbreviated as “resin filament” or “filament”) can be provided.
The filament has a shape corresponding to the inner shape of the metal tube and nozzle through which the resin composition flows down in the three-dimensional modeling apparatus. Therefore, the resin composition can be continuously supplied to the inside of the metal pipe and the nozzle through which the resin composition flows without including air, and these can be effectively cleaned.
The filament diameter is not particularly limited, and may be equal to or smaller than the inner diameter of the metal tube and nozzle through which the resin composition flows in the three-dimensional modeling apparatus. In order to suppress the occurrence of a space where the molten resin does not flow, the filament diameter is particularly preferably equal to the inner diameter of the metal tube and nozzle through which the resin composition flows down.

The resin composition of the present invention can be produced by applying a known method.
Preferably, a plurality of raw materials including a thermoplastic resin, at least one component (X) selected from the group consisting of a surfactant and a metal soap, and a filler are melt-kneaded so that the MFR is 0.5. The resin composition of this invention which is 10 g / 10min can be manufactured.
Prior to melt-kneading, the above-mentioned plural kinds of raw materials may be dry blended in advance.
The melt kneading can be performed using, for example, a Banbury mixer, a two-roll, a three-roll, a single-screw kneading extruder, a twin-screw kneading extruder, or the like.
Melt kneading may be performed in one stage or in multiple stages.
The melt kneading temperature may be a temperature at which the thermoplastic resin is sufficiently melted and thermal degradation of the thermoplastic resin does not become a problem. For example, when an olefin resin having a Vicat softening point of about 120 ° C. is used, the melt kneading temperature is preferably about 150 to 250 ° C.

  The melt-kneaded product (when performing melt-kneading in a plurality of stages, the same applies to the melt-kneaded product obtained in the middle stage) can be pulverized, granulated, or pelletized by a known method as necessary. it can.

The resin composition obtained by melt-kneading can be pulverized using a pulverizer to form a powder. Examples of the pulverizer include a hammer mill, a jet mill, and a bead mill.
The powdery resin composition can be granulated by granulating using a granulator. Examples of the granulator include a compression granulator, an agitation granulator, and an extrusion granulator, and a compression granulator and the like are preferable.
Examples of the pelletizing method include a method of cutting a strand of a resin composition discharged from a die head of an extruder by a hot cut method. The hot cut method is a method in which a strand discharged from a die head is immediately cut at a high temperature.

As a molding method, a known resin molding method can be applied.
As a manufacturing method of the resin filament,
A method of preparing dry blends or pellets containing the above-mentioned plurality of raw materials in advance and extruding them into filaments using an extruder equipped with a discharge port for discharging the molten resin into filaments;
and,
A pellet containing a plurality of raw materials of some of the plurality of raw materials was prepared in advance, and after dry blending with the remaining one or more raw materials, a discharge port for discharging the molten resin into a filament shape was provided. Examples thereof include a method of extruding into a filament using an extruder.
The resin filament extruded from the extruder can be wound using known winding means such as a winding roll and a winding reel.

It is preferable that the filament diameter corresponds to the inner diameter of the nozzle to be cleaned.
For example, the filament diameter can be adjusted by adjusting the diameter of the discharge port of the extruder.
When the resin filament extruded from the extruder is wound while being pulled by the winding means, a resin filament having a smaller diameter than that of the resin filament immediately after being extruded from the extruder is finally produced. In this case, the filament diameter can be adjusted by the diameter of the discharge port of the extruder and the tensile stress by the winding means.

(amount of water)
The resin composition of the present invention preferably has a water content of 1000 ppm or less, and more preferably 850 ppm or less.
The lower limit of the amount of water is theoretically 0 ppm, but about 50 ppm is preferable because it is technically difficult.
Preferably, if the water content is 1000 ppm or less, foaming of the resin composition during melt kneading and molding of the raw material can be suppressed. Therefore, it is possible to stably produce a resin composition and a molded body that do not contain bubbles, have few defects, have good shape accuracy, and have good mechanical properties such as strength. Such resin compositions and molded articles are excellent in general handleability because of good mechanical properties such as strength. Further, even when the three-dimensional modeling apparatus is cleaned, it is difficult for folds and chips to occur, and the feedability in the apparatus is improved. Furthermore, when the three-dimensional modeling apparatus is cleaned, a space in which the resin composition of the present invention does not flow is prevented from being generated inside the cleaning target, and the deposit can be cleaned effectively.
In addition, as mentioned above, it is suppressed that the space where the resin composition of the present invention does not flow is generated inside the object to be cleaned, and the effect that the deposit can be effectively cleaned is particularly effective in the resin filament.

In order to adjust the water content of the resin composition of the present invention within the above range, the raw material or the raw material mixture can be dried by a known method as necessary, and then used for the production of the resin composition of the present invention.
The drying method is not particularly limited, and there is a method of drying using a known dryer. In this case, heat drying, hot air drying, reduced pressure drying, reduced pressure heating drying, and the like are possible depending on the type of dryer.
The drying conditions are not particularly limited, and may be determined according to the amount of water contained in the raw material before drying.
In the case of heat drying, for example, a drying temperature of about 70 to 80 ° C. and a drying time of about 4 to 5 hours are preferable, but the conditions can be appropriately changed.
As another drying method, there is a method of removing moisture by opening the exhaust vent after charging the plurality of raw materials into the extruder.

  In the present specification, unless otherwise specified, the “water content” is a value measured in accordance with JIS K 1133.

"3D modeling equipment"
With reference to drawings, the structure of the three-dimensional modeling apparatus by a heat melting method and the three-dimensional modeling method using the same will be described.
FIG. 1 is a schematic cross-sectional view of a main part of a three-dimensional modeling apparatus.
Here, although the case where a resin filament is used is demonstrated as an example, the form of the resin composition to be used is arbitrary.

A three-dimensional modeling apparatus 1 shown in FIG. 1 includes a modeling stage 10 that can move up and down, and a modeling head 20 that can move in a two-dimensional direction parallel to the stage surface of the modeling stage 10.
The modeling head 20 has an insertion port 21A into which a modeling resin filament is inserted from above, a metal tube 21 in which the inserted resin filament flows down in a molten state, and a nozzle 22 connected to the lower end of the metal tube 21. With.
In the figure, arrow F indicates the filament insertion direction, and arrow R indicates the resin discharge direction.
In the figure, reference numeral 22A denotes a nozzle outlet.
In the figure, reference numeral 30 denotes a resin flow path formed inside the metal tube 21 and the nozzle 22.

A heater block (heating member) 24 for heating and melting the resin composition flowing in the metal tube 21 is attached to the outer periphery of the lower portion of the metal tube 21. The heater block 24 can be connected to a known scanning member (not shown) such as a scanning arm or a scanning rail for two-dimensionally scanning the modeling head 20.
A heat sink (heat radiating member) 23 for preventing heat conduction to the filament inserted into the insertion port 21A is attached to the outer periphery of the upper portion of the metal tube 21.

In the three-dimensional modeling apparatus 1, modeling is performed as follows.
The modeling resin filament is continuously supplied into the modeling head 20 from the insertion port 21A.
The constituent resin of the resin filament for modeling is not particularly limited, and an ABS resin, a styrene resin such as high impact polystyrene (HIPS), polylactic acid, and an amide resin are preferable.
The resin filament inserted into the modeling head 20 is heated and melted by a heater provided inside the modeling head 20, flows down in the metal tube 21 in a molten state, and is discharged from the nozzle 22 onto the modeling stage 10.
The modeling stage 10 is set to a temperature at which the molten resin is cooled and solidified.
By continuously discharging the molten resin from the nozzle 22 while scanning the modeling head 20 in a two-dimensional direction parallel to the stage surface of the modeling stage 10, the first-layer resin layer 30 having a desired pattern is formed on the modeling stage 10. It is formed.
After the first-layer resin layer 30 having a desired pattern is formed, the modeling stage 10 is lowered further.
By repeating the above operation and laminating a plurality of resin layers 30 having a desired pattern, a three-dimensional structure having a desired shape is manufactured.
The pattern of each resin layer 30 is determined in advance based on a CAD model obtained by slicing a target modeled object into a plurality of horizontal layers.

When the above three-dimensional modeling is repeatedly performed, foreign matter such as used resin or a thermal decomposition product thereof may accumulate inside the metal tube 21 and the nozzle 22 where the molten resin flows down, and the discharge amount may become unstable.
The three-dimensional modeling apparatus 1 can be cleaned using the cleaning resin filament of the present invention instead of the modeling resin filament.
Specifically, the cleaning resin filament of the present invention may be continuously supplied into the modeling head 20 from the insertion port 21A, and the molten resin may be discharged from the nozzle 22 in the same manner as in modeling.
In addition, since there is no need for modeling at the time of washing, two-dimensional scanning of the modeling head 20 and vertical movement of the modeling stage 10 are not particularly required.
The timing of the cleaning is not particularly limited, and for example, the cleaning can be performed when the resin discharge amount is 50 to 60% of the normal time (no deposits are in a clean state).

  The heating and melting temperature of the resin filament for cleaning is determined according to the Vicat softening point of the thermoplastic resin contained therein. Therefore, it may be different from the heating and melting temperature at the time of modeling. The heating and melting temperature of the cleaning resin filament is, for example, about 150 to 280 ° C.

Since the cleaning resin filament of the present invention contains a thermoplastic resin, the same operation as that at the time of modeling can be performed using the cleaning resin filament instead of the modeling resin filament.
Since the cleaning resin filament of the present invention contains the component (X), the feedability in the three-dimensional modeling apparatus 1 is good.
Since the cleaning resin filament of the present invention contains a filler, the deposit can be scraped off and removed. Further, the cleaning resin filament of the present invention has an MFR in a suitable range, and flows down in the modeling apparatus with a suitable viscosity.
In the present invention, the above effects can be combined and the deposits can be effectively removed.
In the present invention, a high cleaning effect can be obtained by a single cleaning operation, and the durability of the cleaning effect is also high.

  In addition, after completion | finish of washing | cleaning, the resin resin for washing | cleaning which remained in the inside of the shaping | molding apparatus is changed by changing the resin filament for washing | cleaning to the resin filament for modeling, and discharging molten resin from the nozzle 22 for a certain period of time similarly to modeling After the object is discharged, modeling starts.

  When applied to a three-dimensional modeling apparatus using an inkjet method, the cleaning resin composition of the present invention may be melted in advance and then used for cleaning.

  As described above, in the present invention, the inside of the three-dimensional modeling apparatus 1 can be easily and effectively cleaned by the same operation as that during normal modeling without disassembling the three-dimensional modeling apparatus 1. it can.

  As described above, according to the present invention, the cleaning operation is simple, the cleaning effect is high, and the cleaning effect is durable. The three-dimensional modeling apparatus cleaning resin composition and the three-dimensional modeling using the same An apparatus cleaning resin filament can be provided.

  Hereinafter, examples and comparative examples according to the present invention will be described.

[Examples 1-18, Comparative Examples 1-3]
(Production of detergent resin filament)
In each of Examples 1 to 18 and Comparative Examples 1 to 3, cleaning resin filaments having a diameter of 0.75 mmφ were produced as follows.
All conditions not specifically stated were common conditions.
In each example, a thermoplastic resin, a surfactant, a metal soap, and a filler were dry blended with the composition shown in Tables 1 to 3.
In Comparative Example 2, the obtained mixture was directly subjected to extrusion molding. In other examples and comparative examples, the obtained mixture was heat-dried at 70 ° C. for 5 hours to remove moisture contained in each raw material, and then subjected to extrusion molding.
The above mixture was melted and extruded into a filament using an extruder, and wound up while being pulled on a take-up reel rotated at high speed.
The extrusion molding conditions were as follows.
Extruder: “FS30” manufactured by Ikekai
Discharge port diameter: 30 mmφ,
Extrusion temperature: 190 ° C
Screw rotation speed: 100 rpm.

Each code | symbol in a table | surface shows the following raw materials.
<Thermoplastic resin>
A-1: High density polyethylene (HDPE) (Vicat softening point 130 ° C., “Hi-Zex 2200J” manufactured by Prime Polymer Co., Ltd.)
A-2: High density polyethylene (HDPE) (Vicat softening point 122 ° C., “Hi-Zex 2110JH” manufactured by Prime Polymer Co., Ltd.)
A-3: High density polyethylene (HDPE) (Vicat softening point 124 ° C., “Hi-Zex 7000F” manufactured by Prime Polymer Co., Ltd.)
A-4: Polypropylene (PP) (Vicat softening point 125 ° C., “Nobrene W531D” manufactured by Sumitomo Chemical Co., Ltd.),
A-5: High density polyethylene (HDPE) (Vicat softening point 122 ° C., “Novatech HDHJ590N” manufactured by Nippon Polyethylene Co., Ltd.).
The MFR of each used thermoplastic resin is as shown in Tables 1 to 3.

<Nonionic surfactant>
B-1: Polyoxyethylene cetyl ether (“Emulgen 220” manufactured by Kao Corporation),
B-2: Sorbitan monolaurate (“Emazole L-10V” manufactured by Kao Corporation).

<Anionic surfactant>
B-3: Sodium lauryl sulfate (“Emar 10G” manufactured by Kao Corporation).

<Metal soap>
C-1: Zinc stearate
C-2: Magnesium stearate.

<Filler>
D-1: Calcium carbonate (average diameter 2.1 μm, Calfine “KS1000”),
D-2: Calcium carbonate (average diameter 4.4 μm, “NCC # 45” manufactured by Nitto Flour Industry Co., Ltd.),
D-3: Talc (average diameter 5 μm, “MICRO ACE P-3” manufactured by Nippon Talc Co., Ltd.).

[amount of water]
The water content of the cleaning resin composition obtained in each example was measured.
Using a Karl Fischer moisture meter (“CA-100” manufactured by Dia Instruments Co., Ltd.) equipped with a moisture vaporizer “VA-100 type” as an option, the moisture content was measured under the conditions of a vaporization temperature of 200 ° C. and heating for 10 minutes.
The “cleaning resin composition” referred to here is one that is melt-kneaded in an extruder.

[MFR]
MFR was measured by the method defined in this specification for the raw material thermoplastic resin used and the cleaning resin composition obtained in each example.

[Cleaning test]
Using a three-dimensional modeling apparatus (“Value 3D Magix MF-1000” manufactured by Mutoh Engineering Co., Ltd., nozzle inner diameter 0.5 mmφ), a three-dimensional modeled object was repeatedly produced by a thermal melting method.
An ABS resin filament was used as a modeling material. The heating and melting temperature was 230 ° C.
The stacking pitch was 0.4 mm.
In addition, a lamination | stacking pitch refers to the thickness of the resin layer of one layer formed in a three-dimensional modeling apparatus, and is a numerical value regarding the preparation time and preparation precision of a molded article.
The shape of the three-dimensional structure was a cube having a side length of 20 mm.

Each time a single three-dimensional structure is manufactured, the total amount of resin discharged from the nozzle (the mass of the formed object) is measured, and the amount of resin discharged per unit time (hereinafter simply referred to as “resin discharge amount”). Called).
Further, for the second and subsequent modeling, the initial ratio of the resin discharge amount was obtained.
Here, the “initial ratio of resin discharge amount” is the ratio of the resin discharge amount at a certain point in time to the initial resin discharge amount, and was obtained using the following equation. The “initial resin discharge amount” is the resin discharge amount when the first modeled object is produced in the modeling.
[Initial ratio of resin discharge amount (%)] = [Resin discharge amount at a certain point] / [Initial resin discharge amount]

When the initial ratio of the resin discharge amount reached 50 to 60%, the following cleaning test was started.
Instead of the modeling resin filament, the cleaning resin filament obtained in each example was used, and the molten cleaning resin filament was ejected from the nozzle by a length of 50 cm by the same operation as in modeling. As in the modeling, the heating and melting temperature was 230 ° C.

  After the cleaning, the ABS resin filament was used again to repeatedly produce a three-dimensional structure by the same operation as before the cleaning. As before the cleaning, the amount of resin discharged from the nozzle was measured every time one piece of the three-dimensional structure was produced, and the initial ratio of the resin discharged amount was obtained.

[Evaluation items and evaluation methods]
(1) Filament feedability:
At the time of cleaning, the feedability of the cleaning resin filament flowing down the metal tube and nozzle of the three-dimensional modeling apparatus was visually evaluated based on the following criteria.
<Criteria>
○ (good): Filament feeding was smooth.
X (defect): Filament feeding was not smooth.

(2) Detergency:
In order to evaluate the cleaning effect, the initial ratio of the resin discharge amount immediately before the cleaning and the initial ratio of the resin discharge amount at the time of the first molding after the cleaning were compared.

(3) Washing durability:
In order to evaluate the cleaning effect, the change in the initial ratio of the resin discharge amount was evaluated for the second and subsequent moldings after cleaning.

The evaluation results are shown in Tables 1 to 3.
Examples 1 to 18 include a thermoplastic resin, at least one component (X) selected from the group consisting of a surfactant and a metal soap, and a filler, and an MFR of 0.5 to 10 g / 10 min. A cleaning resin filament was prepared.
In each of these examples, the feeding property of the filament was good, and a good cleaning effect was obtained. Furthermore, the washing persistence was also good.

  In Comparative Example 1 in which a cleaning resin filament containing no filler was produced, even when cleaning was performed, the resin discharge amount was the same level as before cleaning, and the cleaning effect was not obtained.

  In Comparative Example 2, since a thermoplastic resin having a small MFR was used and a large amount of filler was blended, the MFR of the obtained resin composition was below the measurement limit, and filament-shaped molding could not be performed. Moreover, since the raw material mixture was not dried, the water content of the resin composition exceeded 1000 ppm.

  In Comparative Example 3, since a thermoplastic resin having a large MFR was used, the MFR of the obtained resin composition exceeded 10 g / 10 minutes, and effective cleaning could not be performed.

  The present invention is not limited to the above-described embodiments and examples, and can be appropriately modified without departing from the spirit of the present invention.

1 3D modeling apparatus 10 Modeling stage 20 Modeling head 21 Metal tube 21A Insert port 22 Nozzle 23 Heat sink 24 Heater block 30 Resin layer

Claims (7)

A thermoplastic resin, at least one component (X) selected from the group consisting of a surfactant and a metal soap, and a filler,
The melt mass flow rate is from 0.5 to 10 g / 10 min,
A resin composition for cleaning a three-dimensional modeling apparatus.   The resin composition for washing a three-dimensional modeling apparatus according to claim 1, wherein the thermoplastic resin has a Vicat softening point of 90 to 170 ° C.   The resin composition for washing a three-dimensional modeling apparatus according to claim 1 or 2, wherein the filler has an average diameter of 1 to 50 µm.   The resin composition for 3D modeling apparatus washing | cleaning of any one of Claims 1-3 whose water content is 1000 ppm or less. The content of the thermoplastic resin is 25 to 60% by mass,
The content of the component (X) is 6 to 25% by mass,
The filler content is 20 to 65% by mass.
The resin composition for 3D modeling apparatus washing | cleaning of any one of Claims 1-4.   A three-dimensional composition comprising a thermoplastic resin, at least one component (X) selected from the group consisting of a surfactant and a metal soap, and a filler, and having a melt mass flow rate of 0.5 to 10 g / 10 min. Resin filament for washing molding equipment. A plurality of raw materials including a thermoplastic resin, at least one component (X) selected from the group consisting of a surfactant and a metal soap, and a filler are melt-kneaded so that the melt mass flow rate is 0.5 to 0.5. Producing a resin composition for washing a three-dimensional modeling apparatus that is 10 g / 10 minutes,
A method for producing a resin composition for cleaning a three-dimensional modeling apparatus.

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