JP2006348168A - Method for producing polyester resin and hollow molded product made of the polyester resin - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a polyester resin scarcely causing soil on a mold, when molded, and capable of being suitably used for a beverage-filling container, to provide a method for producing the polyester resin, and to provide a hollow molded product made of the polyester resin. <P>SOLUTION: This polyester resin comprises an aromatic dicarboxylic acid or its ester forming derivative and an aliphatic diol or its ester forming derivative, wherein the polyester resin contains a soluble boron compound in an amount of 0.1-500 ppm as boron atoms, and further contains atoms M selected from aluminum, titanium, gallium, manganese, cobalt, zinc, silicon, zirconium, tin, scandium, yttrium, lanthanum, alkali metals, alkaline earth metals, antimony, and germanium in an amount of 0.1-300 ppm as a total amount ΣM<SB>i</SB>. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention provides a polyester resin suitable for beverage filling containers, a polyester resin suitable for beverage filling container use, and a hollow molding comprising a polyester resin because of good color tone and little increase in cyclic trimer during heating. About the body.

  Polyester resins such as polyethylene terephthalate are excellent in mechanical strength, heat resistance, transparency and gas barrier properties, and are used for materials such as juice, soft drinks, carbonated beverages, and other beverage filling containers, as well as materials such as films, sheets, and fibers. Is preferably used.

  Such a polyester resin is usually produced using a dicarboxylic acid such as terephthalic acid and an aliphatic diol such as ethylene glycol as raw materials. Specifically, first, a low-order condensate (ester low polymer) is formed by an esterification reaction of an aromatic dicarboxylic acid and an aliphatic diol, and then this low-order condensate is formed in the presence of a polycondensation catalyst. It is deglycolized (liquid phase polycondensation) to increase the molecular weight. Moreover, when using as a raw material of a drink filling container, solid-phase polycondensation is usually performed to further increase the molecular weight. Further, this polyester resin is supplied to a molding machine such as an injection molding machine to form a preform for a hollow molded body, and the preform is inserted into a mold having a predetermined shape and stretch blow molded, or further subjected to heat treatment (heat Set) and molded into a hollow molded container.

  However, conventionally known polyester resins obtained by the method described above contain oligomers such as cyclic trimers, and these oligomers adhere to the inner surface of the blow mold and cause mold contamination. It is the cause. Such mold contamination causes quality deterioration such as rough surface of the resulting hollow molded container and reduced transparency.

In view of the above situation, the present inventors have intensively studied to obtain a polyester resin that hardly causes mold contamination during molding. The main cause of mold contamination during molding is that during molding of the polyester resin. It is found that a large amount of oligomers such as cyclic trimers are formed and the total amount of oligomers such as cyclic trimers contained in the polyester resin is increased, and obtained through solid phase polycondensation. It has been found that, by bringing the obtained polyester resin into contact with water, an increase in the cyclic trimer during molding can be remarkably suppressed and mold contamination can be reduced (for example, see Patent Document 1).
Japanese Patent Publication No. 7-14997

  The present invention has been made in view of the above circumstances, and provides a polyester resin that is less likely to cause mold contamination and suitable for beverage filling container applications, a method for producing the polyester resin, and a hollow molded body made of the polyester resin. With the goal.

In order to achieve the above object, a polyester resin according to the present invention is a polyester resin comprising an aromatic dicarboxylic acid or an ester-forming derivative thereof and an aliphatic diol or an ester-forming derivative thereof. An atom M containing 0.1 to 500 ppm as an atom and selected from aluminum, titanium, gallium, manganese, cobalt, zinc, silicon, zirconium, tin, scandium, yttrium, lanthanum, alkali metal, alkaline earth metal, antimony and germanium a polyester resin characterized by 0.1~300ppm containing as their total amount? M _i.
It is preferable to contain at least aluminum and titanium as the atom M. Further, the titanium content is preferably 1 to 14 ppm, and the aluminum content is particularly preferably 2 to 50 ppm.

  Here, the soluble boron compound refers to a boron compound dissolved and dispersed in a polyester resin, and excludes insoluble boron compounds such as aluminum borate described in JP-A-2003-138112, for example. . The content is defined by the boron content in the polyester resin from which insolubles have been removed by the method described below.

  The polyester resin of the present invention preferably has a cyclic trimer content of 0.50% by weight or less.

  The polyester resin production method of the present invention includes a soluble boron compound, aluminum, titanium, gallium, manganese, cobalt, zinc, silicon, zirconium, tin, scandium, yttrium, lanthanum, alkali metal, alkaline earth metal, A polyester resin production method comprising polymerizing a polyester in the presence of a compound of an element selected from antimony and germanium.

  Moreover, the hollow molded object of this invention is a hollow molded object which consists of a polyester resin manufactured by said polyester resin or said method.

  According to the present invention, it is possible to obtain a polyester resin and a hollow molded article having a good color tone and suitable for beverage filling container applications.

(Polyester resin)
The polyester resin of the present invention comprises an aromatic dicarboxylic acid or an ester-forming derivative thereof and an aliphatic diol or an ester-forming derivative thereof.

  Here, as the aromatic dicarboxylic acid, for example, terephthalic acid, isophthalic acid, phthalic acid, 2,6-naphthalenedicarboxylic acid, 2,7-naphthalenedicarboxylic acid, 1,4-naphthalenedicarboxylic acid, 4,4′- Sulfonbisbenzoic acid, 4,4′-biphenyldicarboxylic acid, 4,4′-sulfide bisbenzoic acid, 4,4′-oxybisbenzoic acid and the like can be used. These can be used alone or in combination of two or more.

  Examples of the aliphatic diol include ethylene glycol, 1,2-propanediol, 1,3-propanediol, diethylene glycol, 1,4-butanediol, 1,6-hexanediol, neopentyl glycol, and dodecamethylene glycol. , Triethylene glycol, tetraethylene glycol and the like can be used. These can be used alone or in combination of two or more.

  Further, in the present invention, aromatic dicarboxylic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, glutaric acid, adipic acid, sebacic acid, azelaic acid, decanedicarboxylic acid and other aliphatic dicarboxylic acids, cyclohexane Alicyclic dicarboxylic acids such as dicarboxylic acids can be used as raw materials. In addition to aliphatic diols, alicyclic diols such as cyclohexanedimethanol, 1,3-bis (2-hydroxyethoxy) benzene, 1,4-bis (2-hydroxyethoxy) benzene, bis [4- (2 -Hydroxyethoxy) phenyl] sulfone, 2,2-bis (4-β-hydroxyethoxyphenyl) propane, bisphenols, diols containing aromatic groups such as hydroquinone, resorcin, and the like can be used as raw materials.

  Furthermore, in the present invention, polyvalent carboxylic acids such as ethanetricarboxylic acid, propanetricarboxylic acid, pyromellitic acid, trimellitic acid, trimesic acid, 3,4,3 ′, 4′-biphenyltetracarboxylic acid, glycerin, diglycerin, (Trishydroxymethyl) methane, 1,1,1,-(trishydroxymethyl) ethane, 1,1,1,-(trishydroxymethyl) propane, pentaerythritol, dipentaerythritol, sorbitol, glucose, lactose, galactose, Polyhydric alcohols such as fructose, sucrose, 1,3,5-trishydroxyethoxyisocyanurate, glycolic acid, lactic acid, 4-hydroxy-n-butyric acid, 2-hydroxyisobutyric acid, 5-hydroxy-n-valeric acid, 3-hydroxypropionic acid, que Acid, malic acid, tartaric acid, such as p- hydroxybenzoic acid hydroxycarboxylic acids and the like can be used as a raw material.

Examples of the polyester resin of the present invention include polyethylene terephthalate, polyethylene isophthalate, polytrimethylene terephthalate, polybutylene terephthalate, poly (1,4-cyclohexanedimethylene terephthalate), polyethylene naphthalate and copolymers thereof, and poly A copolymer with glycolic acid or polylactic acid is particularly preferred.
The polyester resin of the present invention preferably contains terephthalic acid in all dicarboxylic acid units, preferably 90 mol% or more, more preferably 95 mol% or more, and ethylene glycol in all diol units, preferably 90 mol% or more, more preferably 95 mol% or more. It is preferable to include.

(Boron content)
The polyester resin of the present invention essentially contains 0.1 ppm to 500 of a soluble boron compound as a boron atom. The boron content in the polyester resin of the present invention is preferably 1 to 200 ppm as a boron atom, more preferably 2 to 100 ppm, and further preferably 3 to 40 ppm.

  In the present invention, the content of the soluble boron compound in the polyester resin is determined by dissolving the polyester resin in a hexafluoroisopropanol / chloroform solvent, separating the insoluble matter with a PTFE 0.45 μm filter, removing the solvent, It is quantified by analyzing the precipitated polyester resin by the ICP method.

When the boron content is less than the above range, the increase amount of the cyclic trimer when the polyester resin is melt-molded is increased, and mold fouling is likely to occur. On the other hand, when the boron content exceeds the above range, the color tone and other qualities of the resulting polyester resin may deteriorate.
When an insoluble boron compound such as aluminum borate is used, the dispersibility of the boron compound in the polyester resin is deteriorated, and the effect of suppressing the cyclic trimer may not be sufficiently obtained.

The polyester resin of the present invention contains aluminum, titanium, gallium, manganese, cobalt, zinc, silicon, zirconium, tin, scandium, yttrium, lanthanum, alkali metal, alkaline earth metal, antimony and germanium contained in the polyester resin. amounts to mandatory that the 0.1ppm~500ppm total amount? M _i of their atoms. The total amount ΣM _i of the elements contained in the polyester of the present invention is preferably 1 to 200 ppm, more preferably 2 to 100 ppm, and further preferably 3 to 30 ppm.
When ΣM _i is less than the above range, the productivity of the polyester resin may be lowered. On the other hand, when it exceeds the above range, quality such as color tone may be deteriorated when the polyester resin is melt-molded.

The polyester resin of the present invention preferably contains 0.1 to 200 ppm of titanium as a titanium atom. The titanium content in the polyester resin of the present invention is more preferably 0.1 to 50 ppm as a titanium atom, further preferably 1 to 14 ppm, and particularly preferably 2 to 10 ppm.
When the titanium content is less than the above range, the productivity of the polyester resin may be lowered. On the other hand, when the titanium content exceeds the above range, quality such as color tone may be deteriorated when the polyester resin is melt-molded.

The polyester resin of the present invention has an aluminum content of 0. It is preferable to contain -200 ppm. The aluminum content of the polyester of the present invention is more preferably 1 to 100 ppm, further preferably 2 to 50 ppm, and particularly preferably 3 to 30 ppm.
When the aluminum content is less than the above range, the productivity of the polyester resin may be lowered. On the other hand, when the aluminum content exceeds the above range, quality such as color tone may be deteriorated when the polyester resin is melt-molded.

The content ratio of titanium and aluminum in the polyester resin of the present invention is preferably 1000 or less, more preferably 0.01 to 100, more preferably 0.1 to 10 as the weight ratio of titanium atoms to aluminum atoms. More preferably, it is particularly preferably 0.2 to 10.
When the weight ratio of titanium atoms to aluminum atoms is out of the above range, the balance between productivity and color tone of the polyester resin may be deteriorated.

The polyester resin of the present invention preferably contains an alkali metal and an alkaline earth metal in an amount of 0.1 ppm or more as the total amount MA of those atoms. The total amount MA of alkali metal and alkaline earth metal contained in the polyester of the present invention is preferably 0.1 to 300 ppm, more preferably 1 to 200 ppm, further preferably 2 to 100 ppm, It is particularly preferably 3 to 30 ppm.
When the MA is less than the above range, the quality such as color tone may deteriorate when the polyester resin is melt-molded. On the other hand, when the MA exceeds the above range, the quality such as transparency of the resulting polyester molded product deteriorates. Sometimes.

  The antimony content of the polyester resin of the present invention is preferably 100 ppm or less, more preferably 50 ppm or less, and further preferably 10 ppm or less as antimony atoms.

  The germanium content of the polyester resin of the present invention is preferably 60 ppm or less, more preferably 30 ppm or less, and even more preferably 10 ppm or less as germanium atoms.

  The polyester resin of the present invention may contain phosphorus. The phosphorus content of the polyester of the present invention is preferably 0.1 ppm to 100 ppm as a phosphorus atom, more preferably 2 to 50 ppm, and further preferably 3 to 30 ppm.

  When the phosphorus content is less than the above range, quality such as color tone may be deteriorated when the polyester resin is melt-molded. On the other hand, when the content exceeds the above range, the productivity of the polyester resin may be lowered.

  The polyester resin of the present invention may contain nitrogen. The nitrogen content of the polyester of the present invention is preferably 0.1 to 500 ppm, more preferably 1 to 200 ppm as a nitrogen atom.

  When the nitrogen content is within the above range, the resin quality such as color tone and acetaldehyde content may be improved when the polyester resin is melt-molded.

The polyester resin of the present invention preferably contains 0.1 to 500 ppm of sulfur as a sulfur atom. The sulfur content of the polyester of the present invention is preferably 0.1 to 200 ppm as a sulfur atom, more preferably 1 to 100 ppm, further preferably 2 to 50 ppm, and more preferably 3 to 30 ppm. Particularly preferred.
If the sulfur content is less than the above range, the amount of increase in the cyclic trimer when the polyester resin is melt-molded may increase. On the other hand, if the sulfur content exceeds the above range, the color tone may be increased when the polyester resin is melt-molded. Such as quality may deteriorate.

Sulfur content contained in the polyester resin of the present invention, and boron, aluminum, titanium, gallium, manganese, cobalt, zinc, silicon, tin, scandium, yttrium, lanthanum, alkali metal, alkaline earth metal, antimony and germanium The relationship of the content of the selected element preferably satisfies the following (A) and (B).
(A) 2 ≦ (Σn _i M _i / W _i ) / (S / 32)
(B) 1 ≦ S ≦ 500 (ppm)
Here, S is indicative of the amount of sulfur atoms derived from a sulfur compound to the product polyester (ppm), M _i represents the amount of from element i for generating the polyester atom (ppm), W _i indicates the atomic weight of the element i , N _i represents the oxidation number of element i in the compound of element i, and Σn _i M _i / W _i represents the sum of n _i M _i / W _i of all elements i. The element i is an element selected from boron, aluminum, titanium, gallium, manganese, cobalt, zinc, silicon, zirconium, tin, scandium, yttrium, lanthanum, alkali metal, alkaline earth metal, antimony, and germanium.

Here, the formula (A) indicates a ratio between the total amount of positive charges derived from elements having different valences contained in the polyester resin and the amount of sulfur, and is derived from each element contained in the polyester resin. This corresponds to a ratio of the total molar amount of positive charges to the molar amount of sulfur being 2 or more.
When the formula (A) is not satisfied, the cyclic trimer concentration in the polyester resin may increase, and by-products such as diethylene glycol in the polyester resin may increase. On the other hand, when the formula (B) is not satisfied, the productivity of the polyester resin may be lowered, and the increase amount of the cyclic trimer when the polyester resin is melt-molded may be increased.

In the method for producing the polyester of the present invention, it is preferable that the following formulas (A-2) and (B-2) are satisfied.
(A-2) 3 ≦ (Σn _i M _i / W _i ) / (S / 32)
(B-2) 1 ≦ S ≦ 200 (ppm)
In the method for producing a polyester of the present invention, it is more preferable that the following formulas (A-3) and (B-3) are satisfied.
(A-3) 4 ≦ (Σn _i M _i / W _i ) / (S / 32)
(B-3) 2 ≦ S ≦ 100 (ppm)

In the polyester resin of the present invention, the cyclic trimer amount CT contained in the polyester is preferably 0.50% by weight or less, and more preferably 0.40% by weight or less. When CT is out of the above range, mold contamination is likely to occur during molding of a hollow molded article or the like.
In addition, the polyester resin of the present invention includes an amount of cyclic trimer contained in a molded product obtained by molding at 280 ° C. using an injection molding machine, and an amount of cyclic trimer contained in the polyester resin before molding. Is preferably 0.1% by weight or less, and more preferably 0.05% by weight or less. When the difference in the amount of the cyclic trimer before and after the molding is out of the above range, mold contamination is likely to occur during the molding of a hollow molded body or the like.

  In the polyester resin of the present invention, the content ratio DEG of diethylene glycol units in the polyester resin is preferably 3.0% by weight or less. The DEG of the polyester resin of the present invention is preferably 0.1 to 3.0% by weight, more preferably 0.5 to 2.0% by weight, and 0.8 to 1.8% by weight. It is particularly preferred. If the DEG is less than the above range, the moldability of the polyester resin may be deteriorated, while if it exceeds the above range, the heat resistance of the polyester resin may be reduced.

  In the polyester resin of the present invention, the amount AA of acetaldehyde contained in the polyester resin is preferably 4 ppm or less, more preferably 3 ppm or less, and further preferably 2 ppm or less. When AA is outside the above range, the taste and smell of the contents of the container molded from the obtained polyester may be adversely affected.

  The polyester resin of the present invention preferably has a color b value of 7 or less, more preferably 5 or less, and even more preferably 3 or less. When the color b value of the polyester resin is outside the above range, the yellowness of a hollow molded article such as a bottle tends to be strong.

(Production method of polyester resin)
The method for producing a polyester resin of the present invention comprises a soluble boron compound, aluminum, titanium, gallium, manganese, cobalt, zinc, silicon, zirconium, tin, scandium, yttrium, lanthanum, alkali metal, alkaline earth metal, antimony, A method for producing a polyester resin, comprising polymerizing a polyester in the presence of a compound of an element selected from germanium.

As a soluble boron compound used in the method for producing a polyester resin of the present invention,
Boranes such as borane, diborane, trimethylborane, triethylborane, tri-n-propylborane, triphenylborane;
Boric acids such as orthoboric acid and metaboric acid;
Borate salts such as ammonium borate, lithium borate, sodium borate, disodium hydrogen borate, sodium dihydrogen borate, potassium borate, rubidium borate, cesium borate;
Borate esters such as methyl borate, ethyl borate, n-propyl borate, isopropyl borate, n-butyl borate, phenyl borate, ethyl borate, glycolyl boronic acid, isopropyl pinacolyl borate;
organoboron compounds such as n-butylboronic acid, phenylboronic acid, sodium tetraphenylborate;
And boron oxide, boron bromide, boron fluoride and complexes thereof, inorganic boron compounds such as sodium tetrafluoroborate, sodium borohydride; and the like.
Among these, boric acid, sodium borate, disodium hydrogen borate, and sodium dihydrogen borate are preferable.

  Examples of the polycondensation catalyst used in addition to the boron compound in the method for producing a polyester resin of the present invention include aluminum, titanium, gallium, manganese, cobalt, zinc, silicon, zirconium, tin, scandium, yttrium, lanthanum, and alkali metal. And compounds of at least one element selected from the group consisting of alkaline earth metals, antimony, and germanium.

As an aluminum compound used in the method for producing a polyester resin of the present invention, for example,
Aluminum halide compounds such as aluminum fluoride, aluminum chloride, polyaluminum chloride, aluminum chloride hydroxide, aluminum bromide, aluminum iodide;
Inorganic acid aluminum salt compounds such as aluminum carbonate, aluminum sulfate, aluminum nitrate, aluminum phosphate, aluminum silicate, potassium aluminum sulfate, sodium aluminum sulfate;
Other inorganic aluminum compounds such as aluminum hydroxide, aluminum oxide, ammonium aluminate, sodium aluminate, lithium aluminum hydride;
Aluminum organometallic compounds such as trimethylaluminum, triethylaluminum, triisopropylaluminum, diethylaluminum chloride, methylalumoxane;
Aryloxyaluminum compounds such as triphenoxyaluminum;
Siloxyaluminum compounds such as tris (trimethylsiloxy) aluminum, tris (triphenylsiloxy) aluminum;
Organic acid aluminum salt compounds such as aluminum acetate, aluminum propionate, aluminum lactate, aluminum citrate, aluminum tartrate, aluminum acetylacetonate, aluminum organic sulfonate, and aluminum organic phosphonate;
Aluminum amide compounds such as tris (diethylamino) aluminum and aluminum tripyrrolide;
Aluminum alkoxides such as aluminum trimethoxide, aluminum triethoxide, aluminum tri-n-propoxide, aluminum triisopropoxide, aluminum tri-sec-butoxide, aluminum tri-2-ethylhexoxide;
And hydrolysates thereof.

  Among these, aluminum chloride, aluminum hydroxide, sodium aluminate, aluminum acetate, aluminum acetylacetonate, aluminum tri-sec-butoxide and the like are preferable.

  These aluminum compounds can be used alone or in combination of two or more. In addition, these aluminum compounds can be used in combination with other compounds such as diluting with a solvent such as water or alcohols, if necessary.

As a titanium compound used as necessary in the method for producing a polyester resin of the present invention, for example,
Titanium halide compounds such as titanium tetrafluoride, titanium tetrachloride, titanium tetrabromide, titanium tetraiodide, hexafluorotitanic acid;
titanic acid compounds such as α-titanic acid, β-titanic acid, ammonium titanate, sodium titanate, peroxotitanate complex, anatase;
Inorganic acid titanium salt compounds such as titanium sulfate, titanium nitrate, titanium phosphate, titanium silicate;
Titanium organometallic compounds such as tetramethyl titanium, tetraethyl titanium, tetrabenzyl titanium, tetraphenyl titanium, bis (cyclopentadienyl) titanium dichloride;
Aryloxytitanium compounds such as tetraphenoxytitanium;
Siloxy titanium compounds such as tetrakis (trimethylsiloxy) titanium, tetrakis (triphenylsiloxy) titanium;
Organic acid titanium salt compounds such as titanium acetate, titanium propionate, titanium lactate, titanium citrate, titanium tartrate, titanyl potassium oxalate, organic sulfonic acid titanium, organic phosphonic acid titanium;
Examples thereof include titanium amide compounds such as tetrakis (diethylamino) titanium and titanium tetrapyrrolide; or alkoxytitanium compounds described in detail below, and hydrolysates thereof.

  As a method for obtaining the above-mentioned titanium compound hydrolyzate, for example, a method described in European Patent EP1013692 can be used.

In addition, as said alkoxy titanium compound, for example,
Titanium tetraalkoxides such as titanium tetramethoxide, titanium tetraethoxide, titanium tetra-n-propoxide, titanium tetraisopropoxide, titanium tetra-n-butoxide, titanium tetra-2-ethylhexoxide;
Condensed titanium alkoxides such as poly (dibutyl titanate), Ti ₇ O ₄ (OC ₂ H ₅ ) ₂₀ , Ti ₁₆ O ₁₆ (OC ₂ H ₅ ) ₃₂ ;
Halogen-substituted titanium alkoxides such as chlorotitanium triisopropoxide and dichlorotitanium diethoxide;
Carboxylic acid group-substituted titanium alkoxides such as titanium acetate triisopropoxide and titanium methacrylate triisopropoxide;
Phosphonic acid group-substituted titanium alkoxides such as titanium tris (dioctylpyrophosphate) isopropoxide, titanium (monoethyl phosphate) triisopropoxide;
Sulfonic acid group-substituted titanium alkoxides such as titanium tris (dodecylbenzenesulfonate) isopropoxide;
Alkoxy titanates such as ammonium hexaethoxy titanate, sodium hexaethoxy titanate, potassium hexaethoxy titanate, sodium hexa-n-propoxy titanate;
Β-diketonate substituted titanium alkoxides such as titanium bis (2,4-pentanedionate) diisopropoxide, titanium bis (ethylacetoacetate) diisopropoxide;
Α-hydroxycarboxylic acid substituted titanium alkoxides such as titanium bis (ammonium lactate) diisopropoxide; and amino alcohol substituted titanium alkoxides such as titanium bis (triethanolamine) diisopropoxide and 2-aminoethoxytitanium triisopropoxide Etc.

  Among these, titanium tetrachloride, α-titanic acid, titanium acetate, titanium tetraisopropoxide, titanium tetra-n-butoxide, and hydrolysates thereof are preferable.

  In addition, a titanium-containing solution containing titanium, an aliphatic diol, and a trihydric or higher polyhydric alcohol described in International Patent Publication WO 2004/111105, and a particle diameter of the titanium-containing compound in the solution is mainly 0.4 nm to 5 nm. A certain titanium-containing solution can also be preferably used.

  These titanium compounds can be used alone or in combination of two or more. In addition, these titanium compounds can be used in combination with other compounds such as diluting with a solvent such as water or alcohols, if necessary.

  Examples of the gallium compound used in the method for producing a polyester resin of the present invention include fatty acid salts such as acetates, halides such as carbonates, sulfates, nitrates and chlorides, acetylacetonate salts and oxides. Preferred specific compounds include gallium chloride, gallium nitrate, gallium oxide and the like, with gallium oxide being particularly preferred.

  Examples of the manganese compound used in the method for producing a polyester resin of the present invention include fatty acid salts such as acetates, halides such as sulfates, nitrates, and chlorides, acetylacetonate salts, and oxides. Examples of the chemical compound include manganese salt of fatty acid such as manganese acetate, manganese carbonate, manganese chloride, manganese acetylacetonate salt and the like, and manganese acetate or manganese carbonate is particularly preferable.

  Examples of the cobalt compound used in the method for producing a polyester resin of the present invention include fatty acid salts such as acetates, halides such as sulfates, nitrates, and chlorides, acetylacetonate salts, and oxides. Examples of the target compound include fatty acid cobalt salts such as cobalt acetate, cobalt carbonate, cobalt chloride, and acetylacetonate salt of cobalt. Cobalt acetate or cobalt carbonate is particularly preferable.

  Examples of the zinc compound used in the method for producing a polyester resin of the present invention include fatty acid salts such as acetates, halides such as sulfates, nitrates and chlorides, acetylacetonate salts and oxides. Specific compounds include fatty acid zinc salts such as zinc acetate, zinc carbonate, zinc chloride, acetylacetonate salt of zinc, and the like, with zinc acetate or zinc carbonate being particularly preferred.

  Examples of the silicon compound used in the method for producing a polyester resin of the present invention include tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, and tetrabutoxysilane, and tetraethoxysilane is particularly preferable.

  Examples of the zirconium compound used in the method for producing a polyester resin of the present invention include fatty acid salts such as acetates, halides such as sulfates, nitrates, and chlorides, acetylacetonate salts, and oxides. Examples of the chemical compound include zirconium acetylacetonate, zirconium butoxide, zirconium carbonate, zirconium chloride, zirconium naphthenate, zirconium oxide, zirconium sulfate, zirconium nitrate, and the like, with zirconium butoxide being particularly preferred.

  Examples of the tin compound used in the method for producing a polyester resin of the present invention include fatty acid salts such as acetates, halides such as sulfates, nitrates, and chlorides, acetylacetonate salts, and oxides. Examples of the target compound include tin acetate, tin chloride, tin oxide, tin oxalate, and tin sulfate. Tin acetate is particularly preferable.

  Examples of the scandium compound used in the method for producing a polyester resin of the present invention include fatty acid salts such as acetates, halides such as sulfates, nitrates, and chlorides, acetylacetonate salts, and oxides. Examples of the target compound include scandium acetate, scandium chloride, scandium oxide, scandium oxalate, and scandium sulfate. Scandium acetate is particularly preferable.

  Examples of the yttrium compound used in the method for producing a polyester resin of the present invention include fatty acid salts such as acetates, halides such as sulfates, nitrates, and chlorides, acetylacetonate salts, and oxides. Examples of chemical compounds include yttrium acetate, yttrium chloride, yttrium oxide, yttrium oxalate, and yttrium sulfate, with yttrium acetate being particularly preferred.

  Examples of the lanthanum compound used in the method for producing a polyester resin of the present invention include fatty acid salts such as acetates, halides such as sulfates, nitrates, and chlorides, acetylacetonate salts, and oxides. Specific compounds include lanthanum acetate, lanthanum chloride, lanthanum oxide, lanthanum oxalate, and lanthanum sulfate, with lanthanum acetate being particularly preferred.

  These compounds can be used individually by 1 type or in combination of 2 or more types.

  Examples of the antimony compound used in the method for producing a polyester resin of the present invention include antimony oxide, antimony acetate, and antimony chloride.

  Examples of the germanium compound used in the method for producing a polyester resin of the present invention include germanium dioxide, germanium acetate, germanium chloride, germanium tetraethoxide and the like.

  In the method for producing a polyester resin of the present invention, the alkali metal compound used as necessary is a compound of at least one element selected from the group consisting of lithium, sodium, potassium, rubidium, and cesium.

  As a compound of at least one element selected from the group consisting of lithium, sodium, potassium, rubidium, and cesium, simple substances of these elements, hydrides, oxides, sulfides, hydroxides, organometallic compounds, alkoxides, Fatty acid salts such as acetate, carbonate, hydroxycarboxylate, amino acid salt, sulfate, organic sulfonate, phosphate, organic phosphonate, nitrate, silicate, borate, aluminate, chloride And halides, acetylacetonate salts and the like.

  Among these compounds, sodium hydroxide, potassium hydroxide, sodium carbonate, sodium methoxide, sodium acetate, sodium stearate, sodium aluminate and the like are preferable.

  In the method for producing a polyester resin of the present invention, the alkaline earth metal compound used as necessary is a compound of at least one element selected from the group consisting of beryllium, magnesium, calcium, strontium, and barium.

  As a compound of at least one element selected from the group consisting of beryllium, magnesium, calcium, strontium, and barium, simple substances of these elements, hydrides, oxides, sulfides, hydroxides, organometallic compounds, alkoxides, Fatty acid salts such as acetate, carbonate, hydroxycarboxylate, amino acid salt, sulfate, organic sulfonate, phosphate, organic phosphonate, nitrate, silicate, borate, aluminate, chloride And halides, acetylacetonate salts and the like.

  Among these compounds, magnesium acetate, magnesium carbonate, calcium acetate and the like are preferable.

  In the manufacturing method of the polyester resin of this invention, another metal compound can be used as needed.

  Iron compounds include iron chloride (II), iron chloride (III), iron lactate (II), iron nitrate (III), iron naphthenate (II), iron oxalate (II), iron oxide (III), sulfuric acid Iron (II), iron sulfate (III), tripotassium iron oxalate (III), iron (III) acetylacetonate, iron (III) fumarate, triiron tetroxide, etc., especially iron (III) acetyl Acetonate is preferred.

  Examples of the nickel compound include nickel sulfate, nickel carbonate, nickel nitrate, nickel chloride, nickel acetate, nickel acetylacetonate, nickel formate, nickel hydroxide, nickel sulfide, nickel stearate, and nickel acetate is particularly preferable.

  Copper compounds include copper acetate, copper bromide, copper carbonate, copper chloride, copper citrate, 2-ethylhexane copper, copper fluoride, copper formate, copper gluconate, copper hydroxide, copper methoxide, copper naphthenate, Examples thereof include copper nitrate, copper oxide, copper phthalate, and copper sulfide, and copper acetate is particularly preferable.

  In the manufacturing method of the polyester resin of this invention, a phosphorus compound can be used as needed. When a phosphorus compound is used, the quality such as the color tone of the polyester resin may be improved.

As the phosphorus compound used as necessary, as described above, for example,
Phosphate esters such as trimethyl phosphate, triethyl phosphate, tri-n-butyl phosphate, trioctyl phosphate, triphenyl phosphate;
Phosphites such as triphenyl phosphite, trisdodecyl phosphite, trisnonylphenyl phosphite;
Acidic phosphate esters such as methyl acid phosphate, ethyl acid phosphate, isopropyl acid phosphate, butyl acid phosphate, dibutyl phosphate, monobutyl phosphate, dioctyl phosphate;
Organic phosphonic acids and salts or esters thereof such as methylphosphonic acid, phenylphosphonic acid, 3,5-di (t-butyl) -4-hydroxybenzylphosphonic acid; and phosphorus compounds such as phosphoric acid, pyrophosphoric acid, polyphosphoric acid and Those salts are mentioned.

  Among these, tri-n-butyl phosphate, methyl acid phosphate, ethyl acid phosphate, phenylphosphonic acid, phosphoric acid, pyrophosphoric acid and the like are preferable.

  These phosphorus compounds can be used alone or in combination of two or more. In addition, these phosphorus compounds can be used in combination with other compounds such as diluting with a solvent such as water or alcohols as necessary.

  In the method for producing a polyester resin of the present invention, nitrogen compounds used as necessary are ammonia, hydroxylamine, trimethylamine, triethylamine, pyrrolidine, morpholine, 1,4,7-triazacyclononane, 1,8-diazabicyclo [ 5.4.0] -7-undecene, amine compounds such as aminoethanol, aniline and pyridine, and quaternary ammonium compounds such as tetramethylammonium hydroxide and tetraethylammonium hydroxide.

  Of these compounds, triethylamine, tetraethylammonium hydroxide and the like are preferable.

  The above alkali metal compounds, alkaline earth metal compounds and nitrogen compounds can be used singly or in combination of two or more. In addition, these compounds can be used in combination with other compounds such as diluting with a solvent such as water or alcohols, if necessary.

In the production method of the polyester resin of the present invention, as a sulfur compound used as necessary,
Sulfur alone;
Sulfide compounds such as ammonium sulfide and sodium sulfide;
Sulfinic acid compounds such as sulfurous acid, ammonium sulfite and sodium hydrogensulfite;
Sulfonic acids such as sulfuric acid, methanesulfonic acid, p-toluenesulfonic acid;
Sulfates such as sodium hydrogen sulfate, sodium sulfate, ammonium sulfate, magnesium sulfate, aluminum sulfate, lithium aluminum sulfate, sodium aluminum sulfate, potassium aluminum sulfate, ammonium aluminum sulfate;
Other inorganic sulfur compounds such as sulfur trioxide, persulfuric acid, sodium thiosulfate, sodium dithionite;
Examples include other organic sulfur compounds such as dimethyl sulfate and sodium p-toluenesulfonate.

  Among these, sulfuric acid, p-toluenesulfonic acid, sodium hydrogen sulfate, aluminum sulfate, sodium aluminum sulfate, aluminum potassium sulfate, and aluminum ammonium sulfate are preferable.

Said sulfur compound can be used individually by 1 type or in combination of 2 or more types. In addition, these compounds can be used in combination with other compounds such as diluting with a solvent such as water or alcohols, if necessary.
The sulfur compound may be a copolymerizable sulfur compound such as sodium 3,5-dicarboxybenzenesulfonate or sodium 4-carboxybenzenesulfonate, but is preferably a copolymerizable sulfur compound. Preferably not.

(Polyester production method)
The method for producing a polyester resin of the present invention is characterized in that an aromatic dicarboxylic acid or an ester-forming derivative thereof is polycondensed with an aliphatic diol or an ester-forming derivative thereof. An aromatic dicarboxylic acid or an ester-forming derivative thereof refers to an aromatic dicarboxylic acid and a salt, ester, acid anhydride or acid chloride thereof. An aliphatic diol or an ester-forming derivative thereof refers to an aliphatic diol and an alkoxide, ester or ether thereof. Hereinafter, an example of a method for producing a polyester resin will be described.

(Esterification process)
First, when producing a polyester resin, an aromatic dicarboxylic acid or an ester-forming derivative thereof and an aliphatic diol or an ester-forming derivative thereof are esterified.
Specifically, a slurry containing an aromatic dicarboxylic acid or an ester-forming derivative thereof and an aliphatic diol or an ester-forming derivative thereof is prepared.

  In such a slurry, 1.005 to 1.5 mol, preferably 1.01 to 1.2 mol of an aliphatic diol or ester thereof is formed per mol of the aromatic dicarboxylic acid or its ester-forming derivative. Sex derivatives. This slurry is continuously supplied to the esterification reaction step.

  The esterification reaction is preferably carried out using an apparatus in which two or more esterification reaction groups are connected in series under conditions where the aliphatic diol is refluxed while removing the water produced by the reaction out of the system using a rectification column. .

The esterification reaction step is usually carried out in multiple stages, and the first stage esterification reaction usually has a reaction temperature of 240 to 270 ° C, preferably 245 to 265 ° C, and a pressure of 0.02 to 0.3 MPaG ( 0.2 to 3 kg / cm ² G), preferably 0.05 to 0.2 MPaG (0.5 to ² kg / cm ² G), and the esterification reaction in the final stage is usually The reaction temperature is 250 to 280 ° C., preferably 255 to 275 ° C., and the pressure is 0 to 0.15 MPaG (0 to 1.5 kg / cm ² G), preferably 0 to 0.13 MPaG (0 to 1.3 kg / cm ² G).

  When the esterification reaction is carried out in two stages, the esterification reaction conditions of the first stage and the second stage are within the above ranges, respectively, and when carried out in three stages or more, the second stage The esterification reaction conditions up to one stage before the final stage may be any conditions between the reaction conditions of the first stage and the final stage.

For example, when the esterification reaction is carried out in three stages, the reaction temperature of the second stage esterification reaction is usually 245 to 275 ° C., preferably 250 to 270 ° C., and the pressure is usually 0 to 0.00. It may be ² MPaG (0 to ² kg / cm ² G), preferably 0.02 to 0.15 MPaG (0.2 to 1.5 kg / cm ² G).

  Although the esterification reaction rate in each of these stages is not particularly limited, it is preferable that the degree of increase in the esterification reaction rate in each stage is smoothly distributed, and further in the esterification reaction product in the final stage. Usually, it is desirable to reach 90% or more, preferably 93% or more.

By this esterification step, a low-order condensate (ester low polymer) that is an esterification reaction product of an aromatic dicarboxylic acid and an aliphatic diol is obtained, and the number-average molecular weight of this low-order condensate is about 500 to 5,000. It is.
The low-order condensate obtained in the esterification step as described above is then supplied to the polycondensation (liquid phase polycondensation) step.

(Liquid phase polycondensation process)
In the liquid phase polycondensation step, the low-order condensate obtained in the esterification step is polycondensed by heating under reduced pressure to a temperature not lower than the melting point of the polyester resin (usually 250 to 280 ° C.). This polycondensation reaction is desirably carried out while distilling off unreacted aliphatic diol out of the reaction system.

  The polycondensation reaction may be performed in one stage or may be performed in a plurality of stages. For example, when the polycondensation reaction is performed in a plurality of stages, the first stage polycondensation reaction has a reaction temperature of 250 to 290 ° C., preferably 260 to 280 ° C., and a pressure of 0.07 to 0.003 MPaG ( 500 to 20 Torr), preferably 0.03 to 0.004 MPaG (200 to 30 Torr). The final stage polycondensation reaction is performed at a reaction temperature of 265 to 300 ° C, preferably 270 to 295 ° C, pressure Is carried out under conditions of 1 to 0.01 kPaG (10 to 0.1 Torr), preferably 0.7 to 0.07 kPaG (5 to 0.5 Torr).

  When the polycondensation reaction is carried out in three or more stages, the polycondensation reaction between the second stage and the first stage before the last stage is performed between the reaction conditions of the first stage and the reaction conditions of the last stage. It is done on the condition between. For example, when the polycondensation step is performed in three stages, the second stage polycondensation reaction is usually performed at a reaction temperature of 260 to 295 ° C, preferably 270 to 285 ° C, and a pressure of 7 to 0.3 kPaG ( 50 to 2 Torr), preferably 5 to 0.7 kPaG (40 to 5 Torr).

  As a catalyst, a soluble boron compound and other compounds may be present during the polycondensation reaction. For this reason, the addition of these compounds may be performed in any step such as a raw material slurry preparation step, an esterification step, a liquid phase polycondensation step and the like. Further, the entire amount of the catalyst may be added at once, or may be added in a plurality of times.

  These compounds are preferably added by preparing a mixed catalyst previously mixed with an aliphatic diol. When preparing the mixed catalyst, a dissolution aid may be used. As the dissolution aid, water, a base compound such as sodium hydroxide, a chelate ligand compound such as hydroxycarboxylic acid, or a trihydric or higher polyhydric alcohol such as glycerin can be used. Sodium oxide or glycerin is preferably used. The titanium concentration in the mixed catalyst is preferably 0.5% by weight or more as titanium atoms.

  Further, these compounds may be added in the same step or in different steps. Preferably, a mixed catalyst in which a polycondensation catalyst is mixed with an aliphatic diol in advance is prepared and added.

  These mixed catalysts are preferably uniform and transparent solutions. That is, the HAZE value of the solution is preferably 10% or less, more preferably 5% or less, and particularly preferably 2% or less. The HAZE value of the solution can be measured using a device such as ND-1001DP manufactured by Nippon Denshoku Industries Co., Ltd., for example. When the HAZE value of the solution is within the above range, the transparency of the resulting polyester resin may be improved.

  The intrinsic viscosity [IV] of the liquid phase polycondensation polyester resin obtained in the above liquid phase polycondensation step is 0.40 to 1.0 dl / g, preferably 0.50 to 0.90 dl / g. desirable. The intrinsic viscosity achieved in each stage excluding the final stage of the liquid phase polycondensation process is not particularly limited, but it is preferable that the degree of increase in intrinsic viscosity in each stage is smoothly distributed.

  In addition, in this specification, intrinsic viscosity is computed from the solution viscosity measured at 25 degreeC in 1,1,1-trichloroethane / phenol = 1/1 (weight ratio) for the polyester resin.

  The liquid phase polycondensation polyester resin obtained in this polycondensation step is usually melt-extruded and formed into granules (chips).

  In this liquid phase polycondensation step, the COOH group concentration of the obtained liquid phase polycondensation polyester resin is preferably 60 equivalents / ton or less, more preferably 55 to 10 equivalents / ton, and even more preferably 50 to 15 equivalents / ton. To do. When the COOH group concentration in the liquid phase polycondensation polyester resin is within the above range, the transparency of the polyester resin after the solid phase polymerization becomes high.

  In the liquid phase polycondensation step, for example, by setting the molar ratio of the aliphatic diol to the aromatic dicarboxylic acid to 0.98 to 1.3, preferably 1.0 to 1.2, the liquid phase polymerization temperature is 275 to 295. When the temperature is set to 0 ° C., the COOH group concentration in the liquid phase polycondensation polyester resin can be 60 equivalents / ton or less.

(Solid phase polycondensation process)
The polyester resin obtained in this liquid phase polycondensation step can be further subjected to solid phase polycondensation if desired.
The granular polyester resin supplied to the solid phase polycondensation step is preliminarily crystallized by heating to a temperature lower than the temperature for solid phase polycondensation in advance, and then supplied to the solid phase polycondensation step Good.

  Such a precrystallization step can be performed by heating the granular polyester resin in a dry state to a temperature of usually 120 to 200 ° C., preferably 130 to 180 ° C. for 1 minute to 4 hours. Such precrystallization can also be performed by heating the granular polyester resin at a temperature of 120 to 200 ° C. for 1 minute or more in a steam atmosphere, a steam-containing inert gas atmosphere, or a steam-containing air atmosphere. .

The pre-crystallized polyester resin preferably has a crystallinity of 20 to 50%.
Note that, by this precrystallization treatment, the so-called polyester resin solid phase polycondensation reaction does not proceed, and the intrinsic viscosity of the precrystallized polyester resin is almost the same as the intrinsic viscosity of the polyester resin after liquid phase polycondensation. The difference between the intrinsic viscosity of the precrystallized polyester resin and the intrinsic viscosity of the polyester resin before being precrystallized is usually 0.06 dl / g or less.

  The solid phase polycondensation step comprises at least one stage, a temperature of 190 to 235 ° C., preferably 195 to 225 ° C., and a pressure of 120 to 0.001 kPa, preferably 98 to 0.01 kPa. , Under an inert gas atmosphere such as argon or carbon dioxide. Nitrogen gas is desirable as the inert gas used.

  The flow rate of the polyester resin and the inert gas is 0.1 to 50 Nm3 / hr with respect to 1 kg of the polyester resin in the batch type, and 0.01 to 2 Nm3 / hr with respect to 1 kg / hr of the polyester resin in the continuous type. It is.

  The inert gas used as the atmosphere for the solid phase polymerization may always be a pure inert gas, or the inert gas discharged from the solid phase polymerization step may be recycled. The inert gas discharged from the solid phase polymerization process contains condensates and decomposition products such as water, ethylene glycol, and acetaldehyde. In the case of recycling, an inert gas containing a condensate or a decomposition product may be used, or an inert gas obtained by removing and purifying the condensate or decomposition product may be used.

  The granular polyester resin obtained through such a solid-phase polycondensation step may be subjected to water treatment by, for example, the method described in JP-B-7-64920. It is carried out by contacting with water vapor, water vapor-containing inert gas, water vapor-containing air or the like.

  The intrinsic viscosity of the polyester resin thus obtained is usually 0.70 dl / g or more, preferably 0.75 to 1.0 dl / g.

  The COOH group concentration of the polyester resin thus obtained is preferably 10 to 35 equivalent / ton, more preferably 12 to 30 equivalent / ton.

The density of the polyester resin thus obtained is preferably 1.37 g / cm ³ or more, more preferably 1.38 g / cm ³ or more, and further preferably 1.39 g / cm ³ or more.

The haze having a thickness of 5 mm of the stepped square plate-like product obtained by molding the polyester resin thus obtained at 275 ° C. is preferably 20% or less, more preferably 15% or less.
The haze having a thickness of 4 mm of the stepped square plate-like product obtained by molding the polyester resin thus obtained at 275 ° C. is preferably 3% or less, more preferably 2% or less.

  The production process of the polyester resin including the esterification step and the polycondensation step as described above can be performed by any of batch type, semi-continuous type, and continuous type.

  Such a polyester resin is particularly excellent in hue, excellent in transparency, and particularly preferably used for bottles.

  The polyester resin thus produced may contain conventionally known additives such as stabilizers, mold release agents, antistatic agents, dispersants, nucleating agents, colorants such as dyes and the like. These additives may be added at any stage during the production of the polyester resin, or may be added by a master batch before molding.

  Accordingly, the additive may be contained at a uniform concentration inside the particles of the granular polyester resin, or may be concentrated and contained near the particle surface of the granular polyester resin. Some particles of the granular polyester resin may be contained at a higher concentration than other particles.

  The polyester resin obtained by the present invention can be used as a raw material for various molded products. For example, it is melt-molded and used for hollow molded products such as bottles, sheets, films, fibers, etc. Is preferred.

(Molding method)
As a method for molding a bottle, sheet, film, fiber or the like from the polyester resin obtained by the present invention, a conventionally known method can be employed.
For example, when forming a bottle, the polyester resin is extruded from a die in a molten state to form a tube-like parison, and then the parison is held in a mold having a desired shape, and then air is blown into the mold. A method for producing a hollow molded body, producing a preform from the above polyester resin by injection molding, heating the preform to a temperature suitable for stretching, and then holding the preform in a mold having a desired shape, There is a method of producing a hollow molded body by blowing and mounting on a mold.

  The bottle made of the polyester resin of the present invention is particularly excellent in hue, excellent in transparency, low in acetaldehyde content and high quality.

(Example)
EXAMPLES Hereinafter, although this invention is demonstrated further more concretely based on an Example, this invention is not limited to these Examples.
Elemental analysis Boron determination: Polyethylene terephthalate dissolved in hexafluoroisopropanol / chloroform solvent, insolubles were filtered off with a PTFE 0.45 μm filter, the solvent was removed by volatilization and reprecipitation, and dry ashing After the sample was decomposed by the method, it was dissolved in an acid, and boron contained in polyethylene terephthalate was quantified by ICP emission analysis.
Phosphorus quantification: Phosphorus element contained in polyethylene terephthalate was quantified by fluorescent X-ray analysis using polyethylene terephthalate melt-molded into a sheet.
Quantification of metal element: The sample was decomposed by a dry ashing method, dissolved in acid, and the metal element contained in polyethylene terephthalate was quantified by ICP emission analysis.
Intrinsic viscosity (IV)
After 0.5 g of polyethylene terephthalate was dissolved in 100 ml of a mixed solvent of phenol / tetrachloroethane (1/1 weight ratio) by heating, the intrinsic viscosity was calculated from the solution viscosity measured at 25 ° C. by cooling.
Determination of acetaldehyde 2.0 g of polyethylene terephthalate frozen and ground using a freezer mill was put into a vial, sealed with an internal standard substance (acetone) and water, and 1 in a dryer at 120 ± 2 ° C. Heated for hours. After cooling, the supernatant was measured by gas chromatography (Shimadzu Corporation GC-6A) and calculated as the amount of acetaldehyde contained in polyethylene terephthalate.
Determination of cyclic trimer oligomer (CT) Polyethylene terephthalate (0.1 g ) was dissolved in orthochlorophenol, reprecipitated with tetrahydrofuran and filtered to remove linear polyester, and the filtrate was subjected to liquid chromatography. The cyclic trimer oligomer contained in polyethylene terephthalate was quantified by supplying to LC7A (manufactured by Shimadzu Corporation).
Determination of diethylene glycol (DEG) 1 g of polyethylene terephthalate was weighed and hydrolyzed by heating at 280C in 3 ml of monoethanolamine. After standing to cool, the solution was neutralized with high-purity terephthalic acid. Filtered with 5C filter paper. 1 μl of the obtained filtrate was injected into a gas chromatograph to quantify the diethylene glycol content.
Determination of b value The color tone of the polyethylene terephthalate chip was measured with a 45 ° diffusion type color difference meter (SQ-300H manufactured by Nippon Denshoku Industries Co., Ltd.).
Melting treatment of polyethylene terephthalate
Polyethylene terephthalate was dried at 170 ° C. for 4 hours under a flow of dehumidified Air: 0.2 L / min. 6 g of the dried polyethylene terephthalate was put into a melt indexer (Toyo Seiki Co., Ltd. F-B01) whose temperature in the cylinder was set at 310 ° C., heated and melted in the cylinder for 7 minutes, and then subjected to an orifice with a load of 5 kg. More extruded and collected on an aluminum plate. The collected polyethylene terephthalate was quenched into a disk shape.
ΔCT
A value obtained by subtracting the amount of the cyclic trimer (wt%) contained in the raw material polyethylene terephthalate from the amount of the cyclic trimer (wt%) contained in the polyethylene terephthalate subjected to the melting treatment by the method described above was defined as ΔCT.

(Reference Example 1)
In a 1,000 ml glass beaker, 500 ml of deionized water was weighed, cooled in an ice bath, and 5 g of titanium tetrachloride was added dropwise with stirring. When the generation of hydrogen chloride ceased, it was removed from the ice bath and 25% aqueous ammonia was added dropwise with stirring at room temperature to adjust the pH of the solution to 9. A 15% aqueous acetic acid solution was added dropwise thereto while stirring at room temperature to adjust the pH of the solution to 5. The formed precipitate was separated by filtration. The washed precipitate is retained in 30 wt% ethylene glycol-containing water as a slurry having a slurry concentration of 2.0 wt% for 30 minutes, and then granulated and dried at a temperature of 90 ° C using a two-fluid nozzle spray dryer. A solid hydrolyzate (solid titanium-containing compound) was obtained.

The particle size distribution of the obtained solid titanium-containing compound was 0.5 to 20 μm, and the average particle size was 1.8 μm.
The metal titanium content in the solid titanium-containing compound measured by ICP analysis was 34.8% by weight, the carbon content was 11.6% by weight, and the weight ratio of titanium to carbon (Ti / C) was 3. Met.

(Preparation Example 1)
In a 200 ml glass flask, 102 g of ethylene glycol and 18 g of glycerin were weighed, and 3.38 g of the solid titanium-containing compound prepared in Reference Example 1 was added thereto, and dissolved by heating at 120 ° C. for 30 minutes. The titanium metal content in the titanium-containing solution measured by ICP analysis was 1.0% by weight. Moreover, the HAZE value of this solution measured using a haze meter (Nippon Denshoku Industries Co., Ltd., ND-1001DP) was 1.0%.

(Preparation Example 2)
In a 200 ml glass flask, 90 g of ethylene glycol was weighed, and 10 g of sodium aluminum sulfate 12 hydrate (special grade reagent manufactured by Wako Pure Chemical Industries, Ltd.) was added and dissolved therein.

(Preparation Example 3)
Weigh 97.9 g of ethylene glycol and 18 g of glycerin into a 200 ml glass flask, and add 4.1 g of sodium aluminate (reagent grade 1 manufactured by Wako Pure Chemical Industries, Ltd., aluminum / sodium weight ratio = 1/1). Dissolved. The aluminum concentration in the solution was 0.93 wt%.

(Preparation Example 4)
In a 100 ml glass flask, 67.2 g of ethylene glycol was weighed, and 0.8 g of 85% phosphoric acid (special grade reagent manufactured by Wako Pure Chemical Industries, Ltd.) was added and dissolved therein.

A low-order condensate of terephthalic acid and ethylene glycol was produced as follows.
High-purity terephthalic acid 12.81 kg, ethylene glycol 4.93 kg, tetraethylammonium hydroxide 20% aqueous solution 6.88 g were reacted with stirring under a nitrogen atmosphere of pressure 1.7 kg / cm ² G and 260 ° C. for 6 hours. A low-order condensate having an intrinsic viscosity of 0.28 dl / g was obtained. Water generated by this reaction was always distilled out of the system.

  Of the low-order condensate obtained above, 317 g was extracted and placed in a 500 ml glass polycondensation flask. Next, 0.38 g of the catalyst obtained in Preparation Example 1, 0.79 g of a 10 wt% ethylene glycol solution of boric acid, and 0.7 g of the ethylene glycol phosphate solution obtained in Preparation Example 4 were added. After melt mixing at 260 ° C. for 1 hour, the system was depressurized to 1 torr over 1 hour and at the same time the temperature was raised to 285 ° C. Further, polymerization was carried out while distilling ethylene glycol out of the system until the intrinsic viscosity became 0.54 dl / g. The time from the time when the melt viscosity began to rise to the end of the polymerization was measured, and the liquid phase polymerization rate was calculated therefrom. The results are shown in Table 1.

  After completion of the reaction, the reaction product was taken out in a strand form outside the reactor, immersed in water and cooled, and then cut into chips by a strand cutter.

  The polyethylene terephthalate thus obtained by liquid phase polymerization was further dried at 170 ° C. for 2 hours in a nitrogen atmosphere and crystallized, and then subjected to solid state polymerization at 215 ° C. for 16 hours in a nitrogen atmosphere. The intrinsic viscosity of the obtained solid heavy polyethylene terephthalate was measured, and the solid phase polycondensation rate was calculated therefrom. Further, the polyethylene terephthalate after the completion of the solid phase polymerization was treated in hot water at 90 ° C. for 4 hours. The results are shown in Table 1.

    In Example 1, 0.38 g of the catalyst obtained in Preparation Example 1 as a catalyst, 0.79 g of a 10 wt% ethylene glycol solution of boric acid, and 0.7 g of the ethylene glycol phosphate solution obtained in Preparation Example 4 Instead of 0.19 g of the catalyst obtained in Preparation Example 1, 0.23 g of the catalyst obtained in Preparation Example 3, 0.79 g of a 10 wt% ethylene glycol solution of boric acid, and obtained in Preparation Example 4. The same procedure as in Example 1 was conducted except that 0.7 g of ethylene glycol phosphate solution was added. The results are shown in Table 1.

    In Example 1, 0.38 g of the catalyst obtained in Preparation Example 1 as a catalyst, 0.79 g of a 10 wt% ethylene glycol solution of boric acid, and 0.7 g of the ethylene glycol phosphate solution obtained in Preparation Example 4 Instead of 0.13 g of the catalyst obtained in Preparation Example 1, 0.36 g of the catalyst obtained in Preparation Example 2 and 0.23 g of the catalyst obtained in Preparation Example 3 in advance, The same procedure as in Example 1 was performed except that 0.79 g of a 10 wt% ethylene glycol solution of acid and 0.7 g of the ethylene glycol phosphate solution obtained in Preparation Example 4 were added. The results are shown in Table 1.

(Comparative Example 1)
In Example 1, it carried out like Example 1 except not having added the 10 weight% ethylene glycol solution of boric acid. The results are shown in Table 1.
Comparing Example 1 and Comparative Example 1, it can be seen that the polyethylene terephthalate of Example 1 containing boron has a small ΔCT.

(Comparative Example 2)
In Example 2, it carried out like Example 2 except not having added the 10 weight% ethylene glycol solution of boric acid. The results are shown in Table 1.
Comparing Example 2 and Comparative Example 2, it can be seen that the polyethylene terephthalate of Example 2 containing boron has a small ΔCT.

Claims (5)

A polyester resin comprising an aromatic dicarboxylic acid or an ester-forming derivative thereof and an aliphatic diol or an ester-forming derivative thereof, containing 0.1 to 500 ppm of a soluble boron compound as a boron atom, aluminum, titanium, gallium, 0.1 to 500 ppm-containing manganese, cobalt, zinc, silicon, zirconium, tin, scandium, yttrium, lanthanum, alkali metals, alkaline earth metals, antimony, an atom M selected from germanium, as their total amount? M _i A polyester resin characterized by. The polyester resin according to claim 1, wherein the cyclic trimer content is 0.50% by weight or less. A hollow molded body made of the polyester resin according to claim 1. In a method for producing a polyester resin, from a soluble boron compound and aluminum, titanium, gallium, manganese, cobalt, zinc, silicon, zirconium, tin, scandium, yttrium, lanthanum, alkali metal, alkaline earth metal, antimony, germanium A method for producing a polyester resin, comprising polymerizing a polyester in the presence of a compound of a selected element. The hollow molded object which consists of a polyester resin manufactured by the manufacturing method of Claim 4.