JP2000226473A - Resin additive - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain a resin additive which can inhibit the degradation of a resin under thermal melting and the decrease in impact strength of the resin by treating the surfaces of inorganic particles with catechin, then with a phenone compound, and with a coupling agent. SOLUTION: This resin additive is obtained by treating the surfaces of inorganic particles with 0.5-6.0 wt.% catechin, then with 0.4-4.2 wt.% phenone compound (e.g. benzophenone), and with 0.4-4.2 wt.% silane coupling agent (e.g. γ-methacryloyloxypropyltrimethoxysilane). The additive in an amount of 0.5-3.5 wt.% is compounded into a polycarbonate resin, a thermoplastic polyester resin or a blend with other resins. Catechin, a polyphenol compound, is a polyoxy derivative of 3-oxyflavan and is represented by the formula. Examples of the particles are silicates (e.g. silica, talc, and mica), alumina, aluminates, silicate glass, fly ash, and carbon.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

TECHNICAL FIELD The present invention relates to a polycarbonate resin (PC), polybutylene terephthalate (PBT),
Polyethylene terephthalate (PET) or a blend thereof, or a thermoplastic resin in which one or more of these resins are blended with another resin causes thermal decomposition when heated and melted in various molding processes. , Mechanical properties are degraded. The present invention relates to a resin additive that prevents thermal decomposition at this time and does not significantly reduce impact strength.

[0002]

SUMMARY OF THE INVENTION Resin materials, especially PC,
The molecular weight of each of the PBT and PET resins was drastically reduced during heat melting, and the molecular weight was significantly reduced due to the heat applied in each molding step and the shear stress during kneading.
Therefore, it is difficult to recycle the spool and runner generated during molding, as well as to recycle the product. According to the study of the present inventors, the addition of inorganic particles surface-treated with catechin to the above-mentioned resin could suppress the decrease in the molecular weight of the resin upon heating and melting, but IZOT There was a problem that the impact strength was reduced. The present invention heats and melts the resin by treating the surface of the inorganic particles by contacting the surface with a catechin solution, and then treating the surface with a phenone compound, and further treating with a coupling agent to perform a multilayer surface treatment. It is an object of the present invention to provide a resin additive which simultaneously prevents deterioration at the time of deterioration and prevents reduction in IZOT impact strength.

[0003]

Means for Solving the Problems The present inventors have prepared a resin additive obtained by subjecting inorganic particles to a surface treatment with catechin, further treating the surface with a phenone compound, and further treating the surface with a coupling agent. The present inventors have found that by adding the compound to a thermoplastic resin, it is possible to suppress a decrease in the molecular weight of the resin upon heating and melting, and to prevent a decrease in IZOT impact strength, thereby completing the present invention.

[0004] The inorganic particles used in the present invention are not particularly limited, and may be any inorganic particles that can be effectively used for the purpose of the present invention.
Examples thereof include silica salts such as anhydrous silica, silica gel or talc, clay, mica, aluminum silicate and kaolinite, and salts thereof such as alumina and aluminate. In addition, an inorganic substance in a glass state as an inorganic material, that is, glass can also be used in the present invention, and various types such as oxide glass, particularly silicate glass, glass fiber powder, glass beads, glass balloon, and fly ash are used. it can. Further, carbon or carbon fiber powder can also be used as the inorganic particles. Of these, silica powder and the like are particularly preferably used because they are naturally produced and therefore have high economic efficiency. The particle size and shape of the inorganic particles to be used are not particularly limited, and are appropriately selected and used depending on the type and purpose of use.

[0005] The catechin used in the present invention is a polyoxy derivative of 3-oxyflavan, a polyhydric phenol compound, and is widely contained in plants in nature. Catechin is said to have heterogeneous forms of various molecular structures,
Since each is a natural compound, there are many catechins having different structures. The catechin used in the present invention is not particularly limited, and may be any catechin that can be effectively used for the purpose of the present invention. Catechin is also called astringent. At present, catechin is used as an anticancer agent for pharmaceutical use, and as a color fixing and mordant for nylon for industrial use. Catechin is very soluble in water and lower alcohols and can be used as a highly concentrated solution.

About four types of representative catechins are shown in the following formulas (a) to (d), respectively. Further, since catechin is a compound widely contained in plants in the natural world, it is easily presumed that the chemical structure partially differs. In the present invention, such catechins as polyhydric phenols can be used as synonyms without distinction.

[0007]

Embedded image The treatment of the inorganic particles with catechin is carried out by adding the inorganic particles to a solution of catechin and stirring the mixture to adsorb the catechin, then filtering and drying the treated inorganic particles. In this case, the amount of catechin used is desirably treated with a solution containing 0.5 to 6.0% by weight (wt%) of catechin based on the inorganic particles to be treated. If the amount of catechin is less than 0.5 wt%, there is no thermal stabilizing effect of the resin, and if it is more than 6.0 wt%, the effect does not change, and further use is meaningless. As the solvent used in the treatment with catechin, water, lower alcohols, tetrahydrofuran, toluene, benzene, acetone, acetonitrile, various ketones, esters and the like are used, and preferably, water and lower alcohols are used. The concentration of the catechin solution used in the present invention is not particularly limited as long as it is not more than the saturated concentration of catechin at the temperature at which it is adsorbed on the surface of the inorganic particles, and any concentration can be used. Further, the temperature at which catechin is adsorbed on the inorganic particles is not particularly limited, but is usually carried out at room temperature. Further, two or more catechins can be used.

[0008] The catechin-treated inorganic particles (abbreviated as Particle 1) are further subjected to the following surface treatment with a phenone compound.

The phenone compound used in the present invention is:
Benzophenone or a derivative thereof, benzophenone itself being advantageous, but benzophenone-2-
Of course, it may be a derivative of benzophenone such as carboxylic acid or benzophenone-4,4 dicarboxylic acid. Since the phenone compound has the same function as the coupling agent, it may be used in the same amount as the coupling agent, and its use range is from 0.4 to catechin-treated inorganic particles.
4.2 wt% is preferred. If the amount of the phenone compound is too small, there is no effect, and if the amount is too large, the resin acts as a plasticizer, and the mechanical strength of the resin is undesirably reduced.

In the treatment of the particles 1 with the phenone compound, for example, a phenone compound corresponding to 0.4 to 4.2 wt% of the particles 1 is dissolved in an organic solvent such as toluene or xylene, and the particles 1 are added thereto. After stirring, the treated particles 1 are separated by filtration and dried to obtain particles 1 treated with the phenone compound.
(Abbreviated as “particle 2”). In this case, the order of adding the phenone compound and the particle 1 to the organic solvent may be either one. There is no particular limitation on the treatment conditions with the phenone compound, and the treatment temperature,
The treatment time, the type and amount of the solvent used, and the like are appropriately selected and performed according to the type and amount of the inorganic particles and the phenone compound used. Two or more phenone compounds can be used. The particles 2 thus obtained are further subjected to the following treatment with a coupling agent.

As the coupling agent, a silane coupling agent is preferably used in the present invention, and among them, those having a terminal group such as an epoxy group, a vinyl group or an amino group are preferably used. Specific examples of these silane-based coupling agents include, for example, vinyltriethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-aminopropyltriethoxysilane, and trifluorofluorosilane. Although propylmethyldimethoxysilane and the like can be mentioned, particularly preferred silane coupling agents include γ-methacryloxypropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, trifluoropropylmethyldimethoxysilane and the like. be able to. The coupling agent is used in an amount of 0.4 to 4.2% by weight, more preferably 0.8 to 2.5% by weight, based on the weight of the catechin-treated inorganic particles. If the amount of the surface treatment with the coupling agent is small, the effect is ineffective. If the amount is too large, the coupling agent plays a role of a plasticizer in the resin, and the mechanical properties of the resin are deteriorated.

The treatment of the particles 2 with the coupling agent can be carried out by various methods. For example, the particles 2 may be used in the production of the particles 2 to be treated with the coupling agent in water or an organic solvent such as toluene or xylene. After adding a coupling agent corresponding to 0.4 to 4.2 wt% of the obtained particles 1, the particles 2 to be treated with the coupling agent are added thereto, and the mixture is sufficiently stirred and mixed to adsorb the coupling agent. Then, the treated particles 2 are filtered and dried to obtain particles 2 (the resin additive of the present invention) treated with a coupling agent. In this case, the order of adding the coupling agent and the particles 2 to the solvent may be either one. The processing conditions with the coupling agent are not particularly limited, and the processing temperature, the processing time, the type and amount of the solvent to be used, the type of the inorganic particles used, the type of the coupling agent, and the amount used thereof, etc. Is appropriately selected according to the conditions. Two or more coupling agents can be used in combination. In addition, as a treatment method using a coupling agent, there is a method in which a coupling agent or a solution of the coupling agent is directly sprayed on the particles 2.
In this case, it is more effective to leave the sprayed particles 2 in a closed container at room temperature to about 40 ° C. for several days to about one month after spraying. Further, a method of simultaneously melting and kneading the particles 2 with the coupling agent and the resin may be used, but the present invention is not limited to these methods, and any method may be used. The processing order of the inorganic particles when producing the resin additive of the present invention,
Usually, catechin treatment is first performed, then treatment with a phenone compound is performed, and finally treatment with a coupling agent is performed. However, the treatment order is not limited to this, and the treatment may be performed in any order.

The resin to which the resin additive of the present invention is added is not particularly limited, but a polycarbonate resin or a thermoplastic polyester, especially polyethylene terephthalate, polybutylene terephthalate, etc., is convenient. Further blends of these, and one of these
One or a combination of a plurality of resins and another resin such as PC / ABS, PBT / ABS, PC / PB
Blend resins such as T, PC / PET and PC / polystyrene are preferably used.

Incidentally, the resin additive of the present invention is generally used by adding 0.5 to 3.5 wt% to the resin.

The inorganic particles surface-treated with catechin have tannic acid molecules firmly attached to the surface. On the other hand, when the resin is thermally decomposed, radical molecules are generated. Decomposition of the resin can be suppressed by changing the radical molecules into stable molecules. Catechin has many hydroxyl groups, and these hydroxyl groups supplement radicals generated by decomposition of the resin. However, it is considered that many hydroxyl groups are arranged outside the catechin firmly attached to the surface of the inorganic particles, and as a result, the catechin-treated inorganic particles are considered to have little wettability with the matrix resin. Therefore, the resin and the inorganic particles do not bond strongly. Therefore, the IZOT impact strength is greatly reduced from the original value of the original resin. By firmly bonding the inorganic particles surface-treated with the catechin and phenone compound to the matrix resin with a coupling agent, it is thought that two things will be possible, namely, stabilization of the resin and suppression of a decrease in IZOT impact strength. It is. On the other hand, when the phenone compound is present between the catechin layer and the coupling agent layer, a large IZOT impact strength can be obtained by dispersing the stress applied to the resin, that is, serving as a so-called cushion. However, the present invention is not limited by such a reason.

The catechin-treated inorganic particles thus obtained suppress the decrease in the molecular weight of the thermoplastic resin upon heating and melting, and the inorganic particles treated with the phenone compound and the coupling agent further form As described above, it is a resin additive that can suppress not only a decrease in the molecular weight of the resin but also a decrease in the IZOT impact strength.

[0017]

The present invention will be described in more detail with reference to the following Examples and Comparative Examples.

Example 1 200 ml of pure water was placed in a 300 ml beaker, and 3 g of catechin (catechin, manufactured by Fuji Chemical Industry Co., Ltd.) was dissolved therein. Add silica powder (Unimin Specialty Minera
IMSIL A-25 manufactured by ls Inc .; average particle size 3.2 μm
m) was charged in an amount of 100 g. In this case, the amount of tannic acid corresponds to 3% by weight based on the surface-treated silica particles. This was stirred for 10 minutes with a glass rod. Further, the mixture was subjected to suction filtration using a Buchner funnel and dried (D-30 manufactured by Daiwa Kagaku Co., Ltd.).
) And dried at 60 ° C for 24 hours. 2 g of benzophenone (reagent grade, manufactured by Wako Pure Chemical Industries, Ltd.) was dissolved in 200 ml of xylene, KN3 was added, the mixture was stirred for 10 minutes with a glass rod, filtered through a Buchner funnel, and dried at 60 ° C. for 1 hour in the same manner. It was confirmed that the odor disappeared. This is called KNB3. Next, 2 g of a silane coupling agent (KBM503, manufactured by Shin-Etsu Chemical Co., Ltd.) was further added to 200 ml of xylene in exactly the same manner, and KNB3 was added in a slightly dissolved solution. After stirring with a glass rod for 10 minutes, the mixture was similarly filtered through a Buchner funnel, and dried in a drier at 60 ° C. for 1 hour to confirm that there was no odor of xylene. This was converted to a PC resin (manufactured by Teijin Chemicals Limited, Panlite L-1250, Mn: 24700, Mw: 60).
800, Mw / Mn; 2.46, IZOT impact strength; 6
(6 kgfcm / cm) and 10 kg, and mixed in a paper bag. As a result, powder and pellets were separated at the bottom of the bag to some extent, but they could be mixed almost in a state of dusting. This resin is injected into an injection molding machine (Toshiba Machine I
(S-170 type), the entire amount was put into the hopper, and the nozzle temperature was 2
80 ° C, injection pressure 995kgf / cm2, holding pressure 595kg
f / cm2, injection time, 1.61 sec, dwell time 2
Each test piece was manufactured by molding using a mold capable of coexisting various test pieces in 1.4 sec. JIS K7110 for IZOT impact test specimen, JIS K for tensile strength test specimen
7113, the bending strength test piece conforms to JIS K 7203, and furthermore, 2.5 mm × 127 mm × 254 mm
Were molded using a mold that can simultaneously mold the flat plate. The molded product at this time is shown in FIG.

Attempting to recycle 100% of the PC material under the same molding conditions, all the molded test pieces were pulverized using a pulverizer (FNSK-15D 1.5 kW, Nissui Chemicals, Inc.). The pulverized resin is dried again at 110 ° C. for 4 hours using a dehumidifying dryer (DR-30Z type manufactured by Kawata Corporation) and a temperature controller (DN2-20-3 type manufactured by Kato Riki Seisakusho Co., Ltd.). Then, injection molding was repeated four times under the same conditions. The IZOT impact test piece was manufactured by Toyo Seiki Seisakusho Co., Ltd. JISLD type IZO.
Using a T test machine, the V notch was made with the company's B3515 type. The impact strength was found to be 53 kgfcm / cm. Further, a part of the test piece was collected and placed in a stoppered Erlenmeyer flask together with a tetrahydrofuran (THF) solvent.
After adjusting to a concentration of 05 wt%, the composite system was left standing in a room for 24 hours to dissolve. The silica particles were filtered and removed with a microfilter (GL Chromato Disc 13N, non-aqueous, manufactured by Kurashiki Boseki Co., Ltd.) to obtain a PC molecular weight measurement sample. The average molecular weight is measured in advance using standard polystyrene (PRESSURE CHEMICALC).
o. Standard PS, Mw / Mn = 1.0
6) was dissolved in a THF solvent at the same concentration as that of the sample, and the relative conversion was determined from the calibration curve of the molecular weight and the column discharge time. The results are shown in Table 1.

COMPARATIVE EXAMPLE 1 IZOT impact strength was measured under the same conditions as in Example 1 except that injection molding was performed using a PC in which nothing was inserted. Table 1 shows the results
Described together.

Comparative Example 2 IZOT impact strength and molecular weight were measured in the same manner as in Example 1 except that the catechin treatment was performed. The results are shown in Table 1.

Example 2 About 5 kg of KN3 treated with 3% by weight of catechin was prepared in the same manner as in Example 1 for silica particles. 0.4 g of benzophenone in 100 g at a time.
0.7, 1.5, 2.0, 3.0, and 4.0 wt% were added, and the coupling agent was fixed at 2 wt% for treatment. For convenience, this is called KNBS0.4, KNBS0.7,
KNSB1.5, KNBS2.0, KNBS3.0, K
NBS 4.0. This is performed in the same manner as in the first embodiment.
The results of measuring the ZOT impact strength are also shown in Table 1. Those treated with the silane coupling agent in this manner have a small decrease in IZOT impact strength.

Comparative Example 3 0.2% and 4.5% by weight which were not obtained in Example 2
Except for the case where benzophenone was added, the same treatment was performed, and the IZOT impact strength was measured. Thus, when the amount of benzophenone is small, the IZOT impact strength is relatively small, and even when it is large, the effect is not so much obtained.

Example 3 In Example 1, PC was replaced with PBT resin (Polyplastics Co., Ltd.).
Juranex 3200), PET (Kuraray Co., Ltd. 1030), PC / ABS alloy (Ube Sycon Co., Ltd. Uberoy CX10A), PBT / ABS
(Novaroy-B, B150 manufactured by Daicel Chemical Industries, Ltd.)
Except that the procedure was changed to 0), the procedure was the same as in Example 1. The results are also shown in Table 1.

COMPARATIVE EXAMPLE 4 Each of the resins used in Example 3 was repeated without any addition in the same manner as in Example 1, and the IZOT impact strength was measured. The results are also shown in Table 1. Thus, it can be clearly seen that the non-added one has a reduced IZOT impact strength.

[0026]

[Table 1]

[0027]

As shown in the above Examples and Comparative Examples, those obtained by merely treating the surface of the inorganic particles with catechin suppress the decrease in the molecular weight of the thermoplastic resin upon heating and melting, but the treatment with the coupling agent. The reduction of the IZOT impact strength can be suppressed by repeating the above, and the reduction of the IZOT impact strength can be further reduced by adding a phenone compound between them. Therefore, the resin additive of the present invention suppresses a decrease in the molecular weight of a thermoplastic resin such as PC, PBT, or PET during heating and melting, and at the same time, suppresses the IZOT.
This has the effect of reducing the reduction in impact strength.

[Brief description of the drawings]

FIG. 1 is an injection-molded product used in Examples of the present invention, which is a co-produced product of various test pieces.

[Explanation of symbols]

 (A) Drop weight test board (b) Tensile test piece (c) Heat deformation temperature test piece (d) IZOT impact strength test piece (e) Compression test piece (f) Flexural strength test piece (g) Color sample board (h) ) Resin pool (i) Inlet for molten resin

────────────────────────────────────────────────── ───

[Procedure amendment]

[Submission date] November 2, 1999 (1999.11.
2)

[Procedure amendment 1]

[Document name to be amended] Statement

[Correction target item name] 0002

[Correction method] Change

[Correction contents]

[0002]

SUMMARY OF THE INVENTION Resin materials, especially PC,
The molecular weight of each of the PBT and PET resins was drastically reduced during heat melting, and the molecular weight was significantly reduced due to the heat applied in each molding step and the shear stress during kneading.
Therefore, it is difficult to recycle the spool and runner generated during molding, as well as to recycle the product. According to the study of the present inventors, the addition of the inorganic particles surface-treated with catechin to the above-mentioned resin could suppress the decrease in the molecular weight of the resin upon heating and melting. There was a problem that the D impact strength was reduced. The present invention heats and melts the resin by treating the surface of the inorganic particles by contacting the surface with a catechin solution, and then treating the surface with a phenone compound, and further treating with a coupling agent to perform a multilayer surface treatment. and to provide at the same time fulfill resin additive deterioration preventing deterioration prevention and IZO D impact strength when.

[Procedure amendment 2]

[Document name to be amended] Statement

[Correction target item name] 0003

[Correction method] Change

[Correction contents]

[0003]

Means for Solving the Problems The present inventors have prepared a resin additive obtained by subjecting inorganic particles to a surface treatment with catechin, further treating the surface with a phenone compound, and further treating the surface with a coupling agent. heating of the resin by adding to the thermoplastic resin, to suppress the decrease in molecular weight when melted and thereby completing the present invention found that it is possible to prevent a reduction of IZO D impact strength.

[Procedure amendment 3]

[Document name to be amended] Statement

[Correction target item name] 0015

[Correction method] Change

[Correction contents]

The inorganic particles surface-treated with catechin have tannic acid molecules firmly attached to the surface. On the other hand, when the resin is thermally decomposed, radical molecules are generated. Decomposition of the resin can be suppressed by changing the radical molecules into stable molecules. Catechin has many hydroxyl groups, and these hydroxyl groups supplement radicals generated by decomposition of the resin. However, it is considered that many hydroxyl groups are arranged outside the catechin firmly attached to the surface of the inorganic particles, and as a result, the catechin-treated inorganic particles are considered to have little wettability with the matrix resin. Therefore, the resin and the inorganic particles do not bond strongly. Therefore IZO D impact strength will be significantly reduced than the original resin original value. By this is strongly bonded with the matrix resin by catechin and phenone compound coupling agent surface-treated inorganic particles by, when it is possible for two of suppressing a decrease in stabilization and IZO D impact strength of the resin Seem. On the other hand, by phenone compound is between catechin layer and the coupling agent layer, to disperse stress applied to the resin by the role of the so-called cushion, it is possible to obtain a large IZO D impact strength. However, the present invention is not limited by such a reason.

[Procedure amendment 4]

[Document name to be amended] Statement

[Correction target item name] 0016

[Correction method] Change

[Correction contents]

The catechin-treated inorganic particles thus obtained suppress the decrease in the molecular weight of the thermoplastic resin upon heating and melting, and the inorganic particles treated with the phenone compound and the coupling agent further form not only to suppress the decrease in the molecular weight of the resin as described above, a resin additive which can inhibit also decrease the IZO D impact strength.

[Procedure amendment 5]

[Document name to be amended] Statement

[Correction target item name] 0018

[Correction method] Change

[Correction contents]

[0018] take the pure water 200ml in Example 1 300ml beaker, which in the catechin (Fuji Chemical Industry Co., Ltd., Japanese Pharmacopoeia catechin) 3g
Dissolved. Add silica powder (Unimin Specialty Mine)
IMSIL A-25 manufactured by rals Inc .; average particle size 3.2 μm
m) was charged in an amount of 100 g. In this case, the amount of tannic acid corresponds to 3% by weight based on the surface-treated silica particles. This was stirred for 10 minutes with a glass rod. Further, the mixture was subjected to suction filtration using a Buchner funnel and dried (D-30 manufactured by Daiwa Kagaku Co., Ltd.).
) And dried at 60 ° C for 24 hours. 2 g of benzophenone (reagent grade, manufactured by Wako Pure Chemical Industries, Ltd.) was dissolved in 200 ml of xylene, KN3 was added, the mixture was stirred for 10 minutes with a glass rod, filtered through a Buchner funnel, and dried at 60 ° C. for 1 hour in the same manner. It was confirmed that the odor disappeared. This is called KNB3. Next, 2 g of a silane coupling agent (KBM503 manufactured by Shin-Etsu Chemical Co., Ltd.) was further added to 200 ml of xylene in the same manner, and KNB3 was added to a slightly dissolved solution. After stirring with a glass rod for 10 minutes, the mixture was similarly filtered through a Buchner funnel, and dried in a drier at 60 ° C. for 1 hour to confirm that there was no odor of xylene. This was converted to a PC resin (manufactured by Teijin Chemicals Limited, Panlite L-1250, Mn: 24700, Mw: 60).
800, Mw / Mn; 2.46, IZO D impact strength; 6
6 kgfcm / cm) 10 kg and mixing in a paper bag, powder and pellets separated at the bottom of the bag to some extent, but could be mixed almost in a state of dusting the pellets. This resin is injected into an injection molding machine (Toshiba Machine I
(S-170 type), the entire amount was put into the hopper, and the nozzle temperature was 2
80 ° C, injection pressure 995kgf / cm ² , holding pressure 595kg
f / cm ² , injection time, 1.61 sec, dwell time 2
Various test specimens were molded in 1.4 sec using a mold capable of coexisting various test specimens. JIS K7110 for IZO D impact test specimen, JIS K for tensile strength test specimen
7113, the bending strength test piece conforms to JIS K 7203, and furthermore, 2.5 mm × 127 mm × 254 mm
Were molded using a mold that can simultaneously mold the flat plate. The molded product at this time is shown in FIG.

[Procedure amendment 6]

[Document name to be amended] Statement

[Correction target item name] 0019

[Correction method] Change

[Correction contents]

Attempting to recycle 100% of the PC material under the same molding conditions, all the molded test pieces were pulverized using a pulverizer (FNSK-15D 1.5 kW, Nissui Chemicals, Inc.). The pulverized resin is dried again at 110 ° C. for 4 hours using a dehumidifying dryer (DR-30Z type manufactured by Kawata Corporation) and a temperature controller (DN2-20-3 type manufactured by Kato Riki Seisakusho Co., Ltd.). Then, injection molding was repeated four times under the same conditions. IZO D impact test piece was manufactured by Toyo Seiki Seisakusho Co., Ltd. JISLD type IZO.
Using a D tester, the V-notch was made with the company's B3515 type. The impact strength was found to be 53 kgfcm / cm. Further, a part of the test piece was collected and placed in a stoppered Erlenmeyer flask together with a tetrahydrofuran (THF) solvent.
After adjusting to a concentration of 05 wt%, the composite system was left standing in a room for 24 hours to dissolve. The silica particles were filtered and removed with a microfilter (GL Chromato Disc 13N, non-aqueous, manufactured by Kurashiki Boseki Co., Ltd.) to obtain a PC molecular weight measurement sample. The average molecular weight is measured in advance using standard polystyrene (PRESSURE CHEMICALC).
o. Standard PS, Mw / Mn = 1.0
6) was dissolved in a THF solvent at the same concentration as that of the sample, and the relative conversion was determined from the calibration curve of the molecular weight and the column discharge time. The results are shown in Table 1.

[Procedure amendment 7]

[Document name to be amended] Statement

[Correction target item name] 0020

[Correction method] Change

[Correction contents]

[0020] was measured IZO D impact strength than injection molded using the comparative Example 1 do not put the PC same condition as in Example 1. Table 1 shows the results
Described together.

[Procedure amendment 8]

[Document name to be amended] Statement

[Correction target item name] 0021

[Correction method] Change

[Correction contents]

[0021] In Comparative Example 2 Example 1, except that instead merely subjected to catechin treatment was measured IZO D impact strength and molecular weight in the same manner as in Example 1. The results are shown in Table 1.

[Procedure amendment 9]

[Document name to be amended] Statement

[Correction target item name] 0022

[Correction method] Change

[Correction contents]

Example 2 About 5 kg of KN3 treated with 3% by weight of catechin was prepared in the same manner as in Example 1 for silica particles. 0.4 g of benzophenone in 100 g at a time.
0.7, 1.5, 2.0, 3.0, and 4.0 wt% were added, and the coupling agent was fixed at 2 wt% for treatment. For convenience, this is called KNBS0.4, KNBS0.7,
KN BS 1.5, KNBS2.0, KNBS3.0, K
NBS 4.0. This is performed in the same manner as in the first embodiment.
The results of measurement of the ZO D impact strength described together in Table 1. Thus those silane coupling agent treatment decreased the IZO D impact strength is small.

[Procedure amendment 10]

[Document name to be amended] Statement

[Correction target item name] 0023

[Correction method] Change

[Correction contents]

Comparative Example 3 0.2% and 4.5% by weight which were not obtained in Example 2
Benzophenone was subjected to exactly the same process except plus, was measured IZO D impact strength, were as shown in Table 1. IZO D impact strength when the amount of the thus benzophenone is small can not be obtained so effective be relatively small, and many.

[Procedure amendment 11]

[Document name to be amended] Statement

[Correction target item name] 0025

[Correction method] Change

[Correction contents]

[0025] The respective resins used in Comparative Example 4 Example 3, nothing was measured IZO D impact strength repeatedly molded in the same manner as in Example 1 was not added. The results are also shown in Table 1. Thus, additive-free ones seen often is IZO D impact strength is lowered.

[Procedure amendment 12]

[Document name to be amended] Statement

[Correction target item name] 0026

[Correction method] Change

[Correction contents]

[0026]

[Table 1]

[Procedure amendment 13]

[Document name to be amended] Statement

[Correction target item name] 0027

[Correction method] Change

[Correction contents]

[0027]

As shown in the above Examples and Comparative Examples, those obtained by merely treating the surface of the inorganic particles with catechin suppress the decrease in the molecular weight of the thermoplastic resin upon heating and melting, but the treatment with the coupling agent. the by performing overlapping, reduction of IZO D impact strength can be suppressed, further by placing phenone compound therebetween can be further reduced deterioration of IZO D impact strength. Therefore, the resin additive of the present invention suppresses a decrease in the molecular weight of thermoplastic resins such as PC, PBT, and PET at the time of heating and melting, and at the same time, suppresses IZO D
This has the effect of reducing the reduction in impact strength.

[Procedure amendment 14]

[Document name to be amended] Statement

[Correction target item name] Brief description of drawings

[Correction method] Change

[Correction contents]

[Brief description of the drawings]

FIG. 1 is an injection-molded product used in Examples of the present invention, which is a co-produced product of various test pieces.

[Explanation of symbols] (a) Drop weight test plate (b) Tensile test piece (c) Heat deformation temperature test piece (d) IZO D impact strength test piece (e) Compression test piece (f) Flexural strength test piece (g ) Color sample board (h) Resin pool (i) Inlet for molten resin ────────────────────

[Procedure amendment]

[Submission date] February 2, 2000 (200.2.2)

[Procedure amendment 1]

[Document name to be amended] Statement

[Correction target item name] Claim 4

[Correction method] Change

[Correction contents]

Continued on the front page (51) Int.Cl. ⁷ Identification code FI Theme coat II (Reference) C09C 3/08 C09C 3/08 F term (Reference) 4J002 CF001 CG001 EE027 EL086 EX008 FB086 FB087 FB098 FD066 FD067 FD068 4J037 AA17 AA18 AA24A AA30 CB08 CB11 CB23 FF13 FF17 FF21

Claims (6)

[Claims] 1. A resin additive, wherein the surface of inorganic particles is treated with catechin, then treated with a phenone compound, and further treated with a coupling agent. 2. Inorganic particles surface-treated with catechin are surface-treated with a phenone compound corresponding to 0.4 to 4.2% by weight of the inorganic particles, and 0.4 to 4.2% by weight of inorganic particles surface-treated with catechin. The resin additive according to claim 1, which has been surface-treated with a coupling agent corresponding to 4.2 wt%. 3. The resin additive according to claim 1, wherein the coupling agent is a silane coupling agent. 4. The resin additive according to claim 1, wherein the inorganic particles are silica, alumina, a salt thereof, or glass. 5. The resin additive according to claim 1, wherein the resin to be added is a thermoplastic carbonate resin or a thermoplastic resin containing the carbonate resin. 6. The resin additive according to claim 1, wherein the resin to be added is a thermoplastic polyester resin or a thermoplastic resin containing this resin.