Method for producing polyacetal copolymer

Patent metadata

Field	Value
Publication number	US-9745400-B2
Application number	US-201415119567-A
Country	US
Kind code	B2
Filing date	Dec 10, 2014
Priority date	Mar 31, 2014
Publication date	Aug 29, 2017
Grant date	Aug 29, 2017

Abstract

A high-quality polyacetal produced by a process including supplying a raw material comprising trioxane, a comonomer capable of copolymerizing with trioxane and a non-volatile protonic acid to a reactor of a continuous stirring/mixing machine type; carrying out a polymerization reaction of the raw material to produce a reaction mixture; vaporizing an unreacted monomer to separate the unreacted monomer from the reaction mixture and supplying the unreacted monomer to the raw material supplying; collecting a polyacetal copolymer from the reaction mixture into a collection unit which is arranged downstream from a discharge port and is adjusted to have a gauge pressure of 0.2 kPa or more; and adding a basic compound to the collected polyacetal and then subjecting the resultant mixture to a melt-kneading treatment to deactivate the non-volatile protonic acid.

First claim

The invention claimed is:

1. A method of manufacturing a polyacetal copolymer, the method comprising: a raw material-introducing step of introducing a raw material comprising a trioxane, a comonomer copolymerizable with the trioxane and a nonvolatile protonic acid to a reaction apparatus of continuous stirring mixer-type having two parallel axes rotating in the same direction or in different directions relative to each other, a large number of paddles attached on each of the axes and a barrel located close to the outer peripheries of the paddles, wherein ends of long axes of the paddles are configured to periodically approach ends of short axes of their counterparts, and the raw material is to be introduced through an inlet provided at one end in the axial direction, and a reaction mixture and unreacted monomers are to be withdrawn through an outlet provided at the other end;
a polymerization reaction step of performing a polymerization reaction of the raw material to obtain the reaction mixture;
an unreacted-monomer re-introducing step of performing vapor separation of the unreacted monomers from the reaction mixture, and supplying the unreacted monomers to the raw material-introducing step;
a polyacetal copolymer-recovery step of recovering a polyacetal copolymer from the reaction mixture into a recovery section provided downstream of the outlet and adjusted to a gage pressure of 0.2 kPa or more; and
a deactivation step of adding a basic compound to the polyacetal copolymer recovered at the polyacetal copolymer-recovery step, and performing melt-kneading treatment to deactivate the nonvolatile protonic acid.

2. The method of manufacturing a polyacetal copolymer according to claim 1 , wherein the gage pressure is adjusted by charging an inert gas from the outlet, a location upstream of the recovery section or the vicinity thereof.

3. The method of manufacturing a polyacetal copolymer according to claim 1 , wherein the content of moisture contained in the polyacetal copolymer recovered at the polyacetal copolymer-recovery step is 0.1 parts by weight or less relative to 100 parts by weight of the polyacetal copolymer.

4. The method of manufacturing a polyacetal copolymer according to claim 1 , wherein the content of unreacted trioxane contained in the polyacetal copolymer recovered at the polyacetal copolymer-recovery step is 1.0 part by weight or less relative to 100 parts by weight of the polyacetal copolymer.

5. The method of manufacturing a polyacetal copolymer according claim 1 , wherein the nonvolatile protonic acid comprises at least one selected from the group consisting of heteropolyacids, isopolyacids, and acid salts thereof.

6. The method of manufacturing a polyacetal copolymer according to claim 5 , wherein the nonvolatile protonic acid comprises a heteropolyacid represented by the following general formula (1) or an acid salt thereof:
H x [M m ·M′ n O l ]·yH 2 O tm (1),

wherein in the general formula (1), M represents a central element selected from the group consisting of P and/or Si, and M′ represents one or more coordinating elements selected from the group consisting of W, Mo and V; and
1 is 10 to 100, and m is 1 to 10, and n is 6 to 40, and x is 1 or more, and y is 0 to 50.

7. The method of manufacturing a polyacetal copolymer according to claim 5 , the heteropolyacid or an acid salt thereof comprises at least one compound selected from the group consisting of phosphomolybdic acid, phosphotungstic acid, phosphomolybdotungstic acid, phosphomolybdovanadic acid, phosphomolybdotungstovanadic acid, phosphotungstovanadic acid, silicotungstic acid, silicomolybdic acid, silicomolybdotungstic acid, silicomolybdotungstovanadic acid and acid salts thereof.

8. The method of manufacturing a polyacetal copolymer according to claim 5 , wherein the nonvolatile protonic acid comprises an isopolyacid represented by the following general formula (2) or (3) or an acid salt thereof:
xM I 2 O·pM v 2 O 6 ·yH 2 O   (2)

xM I 2 O·pM VI 2 O 6 ·yH 2 O   (3)

wherein in the general formulas (2) and (3), M I represents hydrogen optionally replaced with a metal in some occurrences;
M V represents one or more elements selected from the group consisting of V, Nb and Ta of the V group in the periodic table;
M VI represents one or more elements selected from the group consisting of Cr, Mo, W and U of the VI group in the periodic table; and
p and x are 1 or more, and y is 0 to 50.

9. The method of manufacturing a polyacetal copolymer according to claim 5 , wherein the isopolyacid or an acid salt thereof comprises at least one compound selected from the group consisting of paratungstic acid, metatungstic acid, paramolybdic acid, metamolybdic acid, paravanadic acid, metavanadic acid and acid salts thereof.

10. The method of manufacturing a polyacetal copolymer according to claim 1 , wherein the comonomer comprises at least one selected from the group consisting of 1, 3-dioxolane, diethylene glycol formal, 1, 4-butanediol formal and ethylene oxide.

11. The method of manufacturing a polyacetal copolymer according claim 1 , wherein the basic compound comprises at least one selected from the group consisting of triazine ring-containing compounds having amino groups or substituted amino groups; carbonate, hydrogencarbonate or carboxylate salts of alkali metal elements or alkali earth metal elements and hydrates thereof.

12. The method of manufacturing a polyacetal copolymer according to claim 11 , wherein the carbonate, hydrogencarbonate or carboxylate salt of an alkali metal element or an alkali earth metal element or a hydrate thereof comprises at least one selected from the group consisting of sodium formate, sodium acetate, sodium carbonate, sodium hydrogen carbonate, disodium succinate, sodium laurate, sodium palmitate, sodium stearate and calcium stearate.

13. The method of manufacturing a polyacetal copolymer according to claim 1 , wherein the polyacetal copolymer after deactivation of the nonvolatile protonic acid at the deactivation step has
a melt index of the polyacetal copolymer of 10 g/10 min or less as measured at 190° C. with a load of 2160 g,
an amount of formaldehyde generated from the polyacetal copolymer of 100 ppm or less, and
a b value of the polyacetal copolymer of 2.0 or less as measured with a color-difference meter.

Assignees

• Polyplastics Co

Inventors

• Nakao Hiroaki
• Masuda Eiji

Classifications

• C08K3/24

  Acids; Salts thereof {(C08K3/16 takes precedence)} · CPC title

• C08G2/10

  Polymerisation of cyclic oligomers of formaldehyde · CPC title

• C08G2/06

  Catalysts (Catalysts in general B01J) · CPC title

• C08L2201/02

  Flame or fire retardant/resistant · CPC title

• C08L59/00

  Compositions of polyacetals; Compositions of derivatives of polyacetals (of polyvinyl acetals C08L29/14) · CPC title