The announcement of invention
As the forcing machine of employed matrix resin in the manufacturing process of long fiber-reinforced polyolefin shaped material, general known have single shaft forcing machine and biaxial extruder.And when dipping former provided the fusion matrix resin of equivalent, the single shaft forcing machine was compared with biaxial extruder, and have following advantage: equipment price is cheap, and because screw-rod structure is uncomplicated, the cleaning when therefore changing molten resin material is extremely simple.
But in the manufacturing of long fiber-reinforced polyolefin resin molding material, when using the single shaft forcing machine as forcing machine, when in dipping former, filling plasticising and fused matrix resin, there is following problem: can not stably provide matrix resin to dipping former, easy generation filling is bad etc., the feed rate that is difficult to regulate the matrix resin that provides to dipping former.Therefore, to the resin feed rate instability that dipping former provides, resin can not spread all over out the fine rod etc. of using sometimes, easily produces fortifying fibre broken string etc., causes the productivity of long fiber-reinforced polyolefin resin molding material to descend.
Therefore, the object of the present invention is to provide and to utilize the single shaft forcing machine stably to provide and fill the manufacture method that matrix resin comes the long fiber-reinforced polyolefin resin molding material of manufacturing machine rerum natura and excellent in te pins of durability to dipping former.
The present inventor in order to achieve the above object, carried out research and thought causing described resin feed rate to descend or unsettled reason is to use additives such as powder shaped oxidation inhibitor, photostabilizer, UV light absorber, and caused that the situation of the problems referred to above is many especially when finding to state in the use low melting point additive in the additive.
On the other hand, even used the higher above-mentioned various additives of fusing point, but since liken to into the low-melting additive of the polyolefin resin of main raw material more, though, still be easy to generate matrix resin and in dipping former, fill condition of poor so resin is supplied with stable slightly raising but be also insufficient.
In addition, for weather resistance such as the thermotolerance that improves rosin products, resistance to oxidation deterioration, the method that is used in combination multiple additives is very effective, therefore if can not use low-melting additive, then the kind of selectable additive is restricted, thereby aspect effect, be subjected to remarkably influenced, and can't fully obtain necessary performance sometimes, therefore unrealistic.
Also can consider to make long fiber-reinforced polyolefin resin molding material with the matrix resin that does not contain additive, but in order to obtain the molding of excellent in te pins of durability such as resistance to oxidation deterioration, thermotolerance, weathering resistance, when long fibre enhanced polypropylene olefine resin shaped material is made molding with the dilution that does not contain fortifying fibre with acrylic resin hybrid shaping, be necessary to mix necessary additive.But, wish that because the difference of particle diameter etc. makes the easy classification of additive, existence diminishes the problem of the productivity of molding with long fibre enhanced polypropylene olefine resin shaped material, when diluting with acrylic resin and additive mixing and shaping.
Therefore, the present inventor has carried out various researchs, found that: by in advance the fusion in polyolefin resin of additives such as oxidation inhibitor, photostabilizer, UV light absorber being disperseed to make masterbatch, then it is mixed use with the polyolefin resin that becomes matrix, can in dipping former, fill the fusion matrix resin with above-mentioned single shaft forcing machine highly stablely, thereby finish the present invention.
Promptly, the manufacture method of long fiber-reinforced polyolefin resin molding material of the present invention is that polyolefine resin composition is filled in the dipping former after with single shaft forcing machine plasticising fusion, make fortifying fibre pass through this dipping former, and the long fiber-reinforced polyolefin resin bar that obtains is cut into the manufacture method of the long fiber-reinforced polyolefin resin molding material of specified length, it is characterized in that, as the said polyolefins resin combination, adopt and to contain the matrix resin that forms by polyolefin resin and by will be as the composition that fusing point is the additive masterbatch that the fusion dispersion obtains in polyolefin resin in advance of the low melting point additive below 125 ℃ that contains of the composition (except the polyolefin resin) of masterbatch.
In the present invention, the MFR of the polyolefin resin of above-mentioned masterbatch better is 5~40 (g/10min).Take this, the mixing property of additive and polyolefin resin is good, thereby can improve the content of additive in the masterbatch.And, utilize tablets press etc. can fully integrate the shape of masterbatch, size etc., make matrix resin and masterbatch be easy to mix, stably fill the fusion master batch resin to dipping former.In addition, so-called here MFR refers to the melt flow rate value stipulated among the JIS-K-7210, is illustrated under 230 ℃, load 2.16kgf per 10 minutes from the effusive amount of resin of cylindrical drum.If this MFR is high, represent that then the viscosity of resin is low.
The MFR of the polyolefin resin of above-mentioned matrix resin is preferably 20~200 (g/10min).Take this, its infiltration in fortifying fibre is good, can obtain the long fiber-reinforced polyolefin resin molding material of physical strength excellence.
The polyolefin resin of above-mentioned matrix resin and the polyolefin resin of above-mentioned masterbatch are preferably polypropylene-based resin.Polypropylene-based resin has economy and versatility, and the polyolefin resin by making above-mentioned matrix resin and the polyolefin resin of above-mentioned masterbatch be resin of the same race, makes matrix resin and masterbatch be easy to mix, and stably fills the fusion matrix resin to dipping former.
In addition, above-mentioned additive preferably is selected from least a in oxidation inhibitor, photostabilizer and the UV light absorber.By the above-mentioned additive of fusion in long fiber-reinforced polyolefin resin molding material, can improve the weather resistance such as thermotolerance, resistance to oxidation deterioration of the polyolefin resin molding that makes as the finished product.
And above-mentioned masterbatch preferably contains the additive except that the said polyolefins resin of 15~50 quality %.In addition, the additive of above-mentioned masterbatch preferably contains the above-mentioned low melting point additive of 30~100 quality %.In addition, the said polyolefins resin combination above-mentioned masterbatch that preferably to contain with respect to above-mentioned matrix resin 100 mass parts be 2~35 mass parts.
According to the present invention, when making long fiber-reinforced polyolefin resin molding material, can stably provide matrix resin to dipping former with the single shaft forcing machine, can reduce the manufacturing cost and the maintenance cost of long fiber-reinforced polyolefin resin molding material.
And, the long fiber-reinforced polyolefin resin molding material that obtains according to the present invention is the shaped material that contains additives such as oxidation inhibitor, photostabilizer, UV light absorber, when therefore adopting this shaped material to make resin forming product, except the dilution that do not contain fortifying fibre with the polyolefin resin, need not to mix above-mentioned additive.That is to say, when making resin forming product in that long fiber-reinforced polyolefin resin molding material, dilution are mixed with polyolefin resin and additive fusion, because the difference of particle diameter etc., sometimes additive classification, but if adopt the present invention, even blast blending not then, by above-mentioned long fiber-reinforced polyolefin resin molding material and dilution are mixed and are shaped with polyolefin resin, also can make the good resin forming products of weather resistance such as resistance to oxidation deterioration, thermotolerance, weathering resistance, be difficult for classification, and can not reduce the physical strength of resin forming product.
The best mode that carries out an invention
The manufacture method of long fiber-reinforced polyolefin resin molding material of the present invention is as follows: the polyolefine resin composition that becomes matrix resin is filled in the dipping former after the plasticising fusion in the single shaft forcing machine, make fortifying fibre pass through this dipping former, thereby in fortifying fibre, infiltrate polyolefine resin composition, the long fiber-reinforced polyolefin resin bar that obtains is cut into specified length.
As fortifying fibre, can use in high-melting-point fibers such as glass fibre, carbon fiber, steel fiber, aromatic polyamide fibre etc. any.These fortifying fibres by with generally well-known collecting agent with 100~10000, preferably 400~6000 ultimate fibre boundlings are made fibrous bundle and are used.In the above-mentioned fortifying fibre, consider the intensity of the long fiber-reinforced polyolefin resin molding material that obtains and price etc., preferred glass fibers.In addition, the filamentary diameter of fortifying fibre is preferably 6~30 μ m, more preferably 9~23 μ m.
The said polyolefins resin combination (hereinafter referred to as " matrix resin ") that uses as the matrix resin of fortifying fibre of the present invention is to contain the matrix resin that formed by polyolefin resin and by being preferably the composition that contains 2~35 mass parts masterbatch with respect to matrix resin 100 mass parts as the composition that fusing point is the additive masterbatch that the fusion dispersion obtains in polyolefin resin in advance of the low melting point additive below 125 ℃ that contains of masterbatch composition (except the polyolefin resin).If the content of masterbatch does not reach 2 in above-mentioned value, then be difficult to obtain the effectiveness of additive, the additive containing ratio that must increase in the masterbatch is renderd a service with acquisition, but owing to be difficult to form masterbatch, therefore not preferred.When the content of masterbatch surpassed 35 mass parts in above-mentioned value, material cost might increase, and was therefore not preferred.Wherein, the composition that more preferably contains 4~30 mass parts masterbatch with respect to matrix resin 100 mass parts.
Polyolefin resin (hereinafter referred to as " matrix polyolefin resin ") as above-mentioned matrix resin, can enumerate the homopolymer or the multipolymer of ethene, propylene, butylene, 4-methylpentene etc., with monomeric random, the block of vinyl-acetic ester, vinylformic acid, acrylate, maleic anhydride isopolarity or graft copolymer etc.Wherein, consider economy and versatility, the graftomer of homopolymer, acrylic resin and the maleic anhydride of preferred propylene.
The MFR of matrix polyolefin resin is preferably 20~200 (g/10min).If MFR less than 20 (g/10min), then the infiltration in fortifying fibre is poor, if surpass 200 (g/10min), though then infiltration property is good, but owing to molecular weight and molecular weight causes the strength degradation of resin self, the intensity difference of gained long fiber-reinforced polyolefin resin molding material, thereby not preferred.The MFR of matrix polyolefin resin is 50~150 (g/10min) more preferably.
As the masterbatch that uses in the matrix resin of the present invention, adopt by will be as the additive masterbatch that the fusion dispersion obtains in polyolefin resin in advance that fusing point is the low melting point additive below 125 ℃ that contains of masterbatch composition (except the polyolefin resin).
Polyolefin resin (hereinafter referred to as " MB polyolefin resin ") when making above-mentioned masterbatch, no particular restriction can be used the resin identical with the matrix polyolefin resin.Preferably with the congener resin of matrix polyolefin resin, matrix polyolefin resin and MB polyolefin resin be polypropylene-based resin more preferably.Polypropylene-based resin has economy and versatility, and the range of choice of processing temperature condition, MFR is wide, therefore easily extrudes when making above-mentioned masterbatch and mixes.By making matrix polyolefin resin and MB polyolefin resin is congener resin, makes matrix resin and masterbatch easily mixed, stably fills the fusion matrix resin to dipping former.Here, as polypropylene-based resin, can enumerate the multipolymer etc. of graft copolymer, propylene and ethene of homopolymer, acrylic resin and the maleic anhydride of propylene.
In addition, the MFR of MB polyolefin resin is preferably 5~40 (g/10min), more preferably 10~30 (g/10min).If the MFR less than 5 (g/10min) of above-mentioned MB polyolefin resin, then the difference with the MFR value of matrix polyolefin resin increases, masterbatch is difficult to disperse in the matrix polyolefin resin, and the additive that contains in the masterbatch is difficult to homodisperse in long fiber-reinforced polyolefin resin molding material.If MFR surpasses 40 (g/10min), practice when mixing during then masterbatch is made and close insufficiently, thereby can't improve additive level.Consequently, must increase the usage quantity of masterbatch so that contain the additive of aequum in the long fiber-reinforced polyolefin resin molding material, thus unfavorable aspect cost.In addition, extrude when mixing for making masterbatch, the thickness inequality that melt extrudes bar from the mould of making masterbatch, or it is meticulous and can't fully carry out granulation (cut-out), the size of masterbatch and formation become uneven easily, and therefore metering property is poor, and if the difference of shape inequality, shape becomes greatly, then with the miscibility variation of matrix polyolefin resin, inequality appears in additive level easily in the gained long fiber-reinforced polyolefin resin molding material.
The additive that uses in the masterbatch of the present invention refers to oxidation inhibitor, photostabilizer, UV light absorber etc., must contain fusing point in these additives below 125 ℃, more preferably fusing point below 100 ℃, preferred especially 40~80 ℃ low melting point additive (below be also referred to as " low melting point additive "), except that the low melting point additive, also can surpass 125 ℃, more preferably fusing point is the high-melting-point additive (below be also referred to as " high-melting-point additive ") more than 150 ℃ and uses with fusing point.By being used in combination multiple oxidation inhibitor, can improve the weather resistance such as resistance to oxidation deterioration of polyolefin resin molding effectively with different melting points.
The additive that uses in the masterbatch preferably contains 30~100 quality %, more preferably 30~90 quality %, the low melting point additive of 30~70 quality % more preferably.If low melting point content of additive less than 30 quality %, then be difficult to obtain with the high-melting-point additive and use the effects such as weather resistance raising that produced, the effect of additive is insufficient sometimes.
And the above-mentioned additive containing ratio of masterbatch is preferably 15~50 quality %, more preferably 20~40 quality %.If the additive containing ratio less than 15 quality % of masterbatch then because the usage quantity of masterbatch increases, and material cost might increase, if surpass 50 quality %, then are difficult to form masterbatch, and the bad stability of masterbatch, thereby not preferred.
Oxidation inhibitor (fusing point is below 125 ℃) as the low melting point additive, can enumerate 2, the 6-ditertbutylparacresol, 2,2 '-methylene-bis(4-ethyl-6-t-butyl phenol), 2,6-di-t-butyl-4-ethylphenol, Octadecane base-3-(3, the 5-di-tert-butyl-hydroxy phenyl) propionic ester, four [methylene radical-3-(3, the 5-di-tert-butyl-hydroxy phenyl) propionic ester] methane, triethylene glycol two [3-(3-tertiary butyl-4-hydroxy-5-aminomethyl phenyl) propionic ester], [3-(3 for tetramethylolmethane four, the 5-di-tert-butyl-hydroxy phenyl) propionic ester], [3-(3 for sulfo-diethylidene-two, the 5-di-tert-butyl-hydroxy phenyl) propionic ester], 2,4-dimethyl-6-(1-methyl pentadecyl) phenol, 4, two (octylsulfo methyl) ortho-cresols of 6-, ethylenebis (ethylene oxide) two [3-(tolyl between the 5-tertiary butyl-4-hydroxy) propionic esters], hexa-methylene is two, and [3-(3, the 5-di-tert-butyl-hydroxy phenyl)] propionic ester, 2,6-di-t-butyl-4-(4, two (octylsulfo)-1 of 6-, 3,5-triazine-2 base is amino) phenol, diethyl [(3, two (1, the 1-the dimethyl ethyl)-4-hydroxy phenyls of 5-) methyl] Hinered phenols antioxidant such as phosphonic acid ester; Thioether kind antioxidants such as dilauryl thiopropionate, distearyl thiodipropionate, myristyl thiodipropionate, double tridecyl thiodipropionate; Phosphorus oxidation inhibitor such as phosphorous acid two [2, two (1, the 1-the dimethyl ethyl)-6-aminomethyl phenyls of 4-] ethyl ester, four (2, the 4-di-tert-butyl-phenyl) [1, the 1-xenyl]-4,4 '-two basic bis-phosphites, three nonyl phenyl phosphites, triphenyl phosphorous acid ester; Two dodecyls-3,3 '-thiodipropionate, two tetradecyl-3,3 '-thiodipropionate, two octadecyl-3, sulfur type antioxidants such as 3 '-thiodipropionate.Wherein, with Hinered phenols antioxidant and time spent, because of effective preferred thioether kind antioxidant such as the raising of the synergistic effect of thermostability and weather resistance etc., preferred especially myristyl-3,3 '-thiodipropionate, dilauryl-3,3 '-thiodipropionate and distearyl-3,3 '-thiodipropionate.
As the UV light absorber (fusing point is below 125 ℃) of low melting point additive, can enumerate 2-(3,5-two tert-pentyls-2-hydroxy phenyl) benzotriazole, 2-(2 '-hydroxyl-5 '-uncle's octyl phenyl) benzotriazole etc.
As the photostabilizer (fusing point is below 125 ℃) of low melting point additive, can enumerate two (2,2,6,6-tetramethyl--4-piperidyl) sebates etc.
As the oxidation inhibitor (fusing point is above 125 ℃) of high-melting-point additive, can enumerate 4,4 '-thiobis (the 6-tertiary butyl-3-methylphenol), 4,4 '-butylidene two (the 6-tertiary butyl-3-methylphenol), 2,2 '-methylene-bis (4-methyl-6-tert butyl phenol), 1,1,3 '-three (2-methyl-4-hydroxyl-5-tert.-butyl phenol) butane, N, N '-hexane-1,6 '-two bases are two, and [3-(3,5-di-tert-butyl-hydroxy phenyl propionic acid amide)], 3,3 ', 3 "; 5,5 ', 5 "-six tertiary butyls-a, a ', a "-(mesitylene-2,4; 6-three bases) three p-cresol; 1,3,5-three [3; the 5-di-tert-butyl-4-hydroxyl benzyl]-1,3,5-triazines-2; 4,6 (1H, 3H; 5H)-triketone, 1,3,5-three [(the 4-tertiary butyl-3-hydroxyl-2, the 6-xylyl) methyl]-1,3,5-triazines-2,4,6 (1H, 3H, 5H)-triketone, 2 ', Hinered phenols antioxidants such as two [3-(3, the 5-di-tert-butyl-hydroxy phenyl) propionyl] the propionyl hydrazines of 3-; Phosphorus oxidation inhibitor such as three (2, the 4-di-tert-butyl-phenyl) phosphorous acid ester, two (2, the 4-di-tert-butyl-phenyl) pentaerythritol diphosphites.Wherein, the combination of preferred Hinered phenols antioxidant and Phosphorus oxidation inhibitor.
UV light absorber (fusing point is above 125 ℃) as the high-melting-point additive, can enumerate 2-(5-methyl-2-hydroxy phenyl) benzotriazole, 2-[2-hydroxyl-3, two (the α of 5-, α-Er Jiajibianji) phenyl]-2H-benzotriazole, 2-(3,5-di-t-butyl-2-hydroxy phenyl) benzotriazole, 2-(the 3-tertiary butyl-5-methyl-2-hydroxy phenyl)-5-chlorobenzotriazole, 2-(3,5-di-t-butyl-2-hydroxy phenyl)-5-chlorobenzotriazole etc.
As the photostabilizer (fusing point is above 125 ℃) of high-melting-point additive, can enumerate 2-(3, the 5-di-tert-butyl-4-hydroxyl benzyl)-2-n-butylmalonic acid two (1,2,2,6,6-pentamethyl--4-piperidyl) ester, 2,4-di-tert-butyl-phenyl-3,5-di-tert-butyl-4-hydroxybenzoic acid ester etc.
In addition, as the additive beyond oxidation inhibitor, UV light absorber, the photostabilizer, for example can enumerate fire retardant; Metal passivator; Metallic soaps such as Magnesium Stearate, calcium stearate, Zinic stearas, barium stearate, aluminum stearate, lithium stearate, zinc laurate, barium laurate, p-tert-butyl benzoic acid barium, p-tert-butyl benzoic acid zinc; Acid neutralizing agents such as hydrotalcite; Dispersion agent; Lubricant; The anti-electrostatic agent interfering; Softening agent; Releasing agent; Crystallization promotor (nucleator); Antifogging agent; Alkali earth metallic compound such as magnesium hydroxide, aluminium hydroxide; Whipping agent; Linking agent; Antiseptic-germicide; Anti-algae agent; Modifiers such as mould inhibitor; Tinting materials such as carbon black, zinc sulphide, pigment, dyestuff; Titanium oxide, talcum powder, lime carbonate, mica, clay, graphite, glass flake even-granular weighting agent; Organic filling agents such as fiber, bamboo fibers, aramid fiber; Whiskers such as potassium titanate etc. can suitably select fusing point to use at additive below 125 ℃ and the additive above 125 ℃.
Except that above-mentioned matrix resin and above-mentioned masterbatch, can also further contain the low melting point additive that do not form masterbatch and high-melting-point additive etc. in the matrix resin that the present invention uses, be preferably the resin combination that forms by above-mentioned matrix resin and above-mentioned masterbatch.
In the present invention, long fiber-reinforced polyolefin resin molding material for example can be made by operation shown in Figure 1.
At first, in the continuous fortifying fibre 1 importing dipping former 5 that never illustrated coiling body is extracted out, infiltration fortifying fibre 1 in the melts of the matrix resin with above-mentioned composition (polyolefine resin composition) that single shaft forcing machine 3 provides.Here, in single shaft forcing machine 3, provide a certain amount of matrix resin from hopper 4, the matrix resin that provides fusion therein mixes, and from molten resin supplying path 2 the fusion matrix resin is supplied with and is filled into the dipping former 5.When having a matrix resin of above-mentioned composition fusion being mixed in single shaft forcing machine 3, because the good fluidity of molten resin, so dipping former 5 can stably be supplied with molten resin and be filled in by single shaft forcing machine 3.
The fortifying fibre 1 that will infiltrate in the fusion matrix resin then, is extracted out by nozzle 6.Thereby remove the unnecessary matrix resin that is attached to fortifying fibre 1, can obtain the required long fiber-reinforced polyolefin resin bar 7 that has stable fiber containing ratio and formed the regulation cross-sectional shape.This long fiber-reinforced polyolefin resin bar 7 is cooled off in cooling tank 8, extract with extraction machine 9.The tablets press 10 that the long fiber-reinforced polyolefin resin bar 7 that extracts is had rotary cutting knife is cut into specified length, obtains long fiber-reinforced polyolefin resin molding material 11.
The long fiber-reinforced polyolefin resin molding material that makes as stated above, fortifying fibre is arranged in parallel with same length and along same direction in fact in as the polyolefin resin of matrix resin.As the shape of long fiber-reinforced polyolefin resin molding material, preferred wire rod shape or particulate state.Here, be arranged in parallel with same length and along same direction in fact that to contain major part that fortifying fibre is meant fortifying fibre be along same direction side by side and the state arranged of almost parallel, and a part of fiber can be the local bending or the state of complexing mutually.
The fiber containing ratio of long fiber-reinforced polyolefin resin molding material does not have particular restriction, is preferably 20~80 quality %, more preferably 30~75 quality %.If fiber containing ratio less than 20 quality %, then can not fully obtain reinforced effects, if surpass 80 quality %, the then easy variation of the infiltration of matrix resin by the fortifying fibre generation, in the drawing procedure of aftermentioned nozzle, easily produce burr and broken string etc., cause productivity to descend.
The mean diameter of long fiber-reinforced polyolefin resin molding material is preferably 0.3~3.5mm, more preferably 0.4~3mm.If the not enough 0.3mm of mean diameter, then the volume density of above-mentioned shaped material diminishes, and carries property supplied with so variation, surpasses 3.5mm as if mean diameter, then the dispersed variation easily of fortifying fibre when forming by injection molding.
In addition, the length of long fiber-reinforced polyolefin resin molding material does not have particular restriction, is preferably 3~25mm, more preferably 4~20mm.If curtailment 3mm when then cutting with tablets press 10 grades, easily produces the crack; and be difficult for manifesting fibre-reinforced effect, if length surpasses 25mm, then when forming by injection molding; be difficult to supply with, might cause the dispersiveness and mobile decline of fortifying fibre to forming mill.
Embodiment
Enumerate embodiment below and specify the present invention.But these embodiment only are used to specify embodiments of the present invention, are not to limit the scope of the invention.
[embodiment 1]
To adopt the raw material shown in the following table 1 and directly be that the single shaft forcing machine of 65mm is 50rpm, 280 ℃ of fusings down at screw speed with screw rod by the matrix resin of the blending example 1 of the proportioning preparation of table 2, the fusion matrix resin is offered dipping former, observe the supply stability of matrix resin.In addition, in embodiment 1, oxidation inhibitor A, B are using as masterbatch (content of oxidation inhibitor is 25 quality %) after the fusion dispersion in acrylic resin B under 200 ℃.
Resin is supplied with stability and is estimated by following three ranks.Zero: [providing certain resin to dipping former], △ from the single shaft forcing machine: [the single shaft forcing machine with zero same rotational speed under the resin feed rate few, or rare for a long time change during the resin feed rate], *: [the single shaft forcing machine does not provide resin fully].Evaluation result is as shown in table 2.
[embodiment 2]
Use the matrix resin of the blending example 2 of the proportioning preparation of using the raw material shown in the table 1 and pressing table 2, in addition all operations similarly to Example 1, the supply stability of observing matrix resin.In addition, in embodiment 2, oxidation inhibitor B, C are using as masterbatch after the fusion dispersion in acrylic resin B under 200 ℃.
[comparative example 1]
Oxidation inhibitor A, B are not made masterbatch, directly add among the acrylic resin A as matrix resin, use the matrix resin of the blending example 3 of the proportioning preparation of pressing table 2, in addition all operations similarly to Example 1, provide the fusion matrix resin to dipping former, observe the supply stability of matrix resin.
[comparative example 2]
Oxidation inhibitor B, C are not made masterbatch, directly add among the acrylic resin A as matrix resin, use the matrix resin of the blending example 4 of the proportioning preparation of pressing table 2, in addition all operations similarly to Example 2, the supply stability of observing matrix resin.
[table 1]
Raw material |
Compound title etc. |
Fusing point (℃) |
MFR (g/10min) |
Acrylic resin A (matrix resin) |
Acrylic resin (maleic anhydride modified PP) |
165 |
120 |
Acrylic resin B |
Acrylic resin |
165 |
15 |
Oxidation inhibitor A |
Myristyl-3,3 '-thiodipropionate |
52 |
- |
Oxidation inhibitor B |
Tetramethylolmethane four [3-(3,5-di-t-butyl-4-hydroxy phenyl) propionic ester] |
117 |
- |
Oxidation inhibitor C |
Three (2, the 4-di-tert-butyl-phenyl) phosphorous acid ester |
184 |
- |
[table 2]
* 1The masterbatch use that the additive containing ratio is 25 quality % is made in fusion in acrylic resin B
By The above results as can be known, will contain fusing point be the fusion in acrylic resin of the oxidation inhibitor of the oxidation inhibitor below 125 ℃ disperse among the embodiment 1 that the back uses as masterbatch and be oxidation inhibitor below 125 ℃ and the fusing point oxidation inhibitor that surpasses 125 ℃ with fusing point as oxidation inhibitor and with and the fusion in acrylic resin of these oxidation inhibitor disperseed among the embodiment 2 that the back uses as masterbatch, the single shaft forcing machine is stably supplied with the fusion matrix resin to dipping former.
On the other hand, be that oxidation inhibitor below 125 ℃ is not made masterbatch and directly added in the comparative example 1 that uses in the acrylic resin as matrix resin with fusing point, the single shaft forcing machine fails to supply with resin to dipping former.
In addition, with fusing point be oxidation inhibitor below 125 ℃ and fusing point surpass 125 ℃ oxidation inhibitor as oxidation inhibitor and with but these oxidation inhibitor are not made masterbatch and directly add in the comparative example 2 that uses in the acrylic resin as matrix resin, although the amount of low melting point additive seldom, can not stably provide resin to dipping former.
Quote of the announcement of the full content of Japanese patent application 2005-375302 specification sheets, claims, accompanying drawing and the summary of filing an application on December 27th, 2005 at this as specification sheets of the present invention.