Thermoplastic, branched aromatic polyphosphonates, and a process for their production

• US 4,415,719 A
• Filed: 12/07/1981
• Issued: 11/15/1983
• Est. Priority Date: 06/22/1979
• Status: Expired due to Fees

• Current Assignee: Bayer AG
• Original Assignee: Bayer AG
• Inventors: Freitag, Dieter, Schmidt, Manfred, Block, Hans-Dieter, Reinking, Klaus, Bottenbruch, Ludwig, Rohr, Harry
• Primary Examiner(s): LEE, LESTER
• Application Number:
  US06/328,383
• Time in Patent Office: 708 Days
• Field of Search: 528/167-169, 528/125, 528/126, 528/128, 260/930, 524/592, 524/609, 524/610, 524/841
• US Class Current: 528/167
• CPC Class Codes: C08G 79/04 Phosphorus linked to oxygen or to oxygen and carbon

Abstract

Thermoplastic, branched aromatic polyphosphonates with average molecular weights (number average M_n) of from 11,000 to more than 200,000, obtainable by transesterifying (a) from 97 to 100 moles of at least one diaryl phosphonate, and (b) from 0 to 3 moles of at least one triaryl phosphate--the sum of the moles of (a) and (b) being 100--with (c) from 90 to 99 moles of at least one aromatic dihydroxy compound, and (d) from 0 to 3 moles of at least one aromatic trihydroxy or tetradhydroxy compound--with the proviso that at least one of the components (b) and (d) is present in a quantity of at least 0.001 mole and that, where (b) and (d) are used, the maximum limit on the moles is 3.0.

Claims

1. A process for the production of a thermoplastic branched, aromatic polyphosphonate having a number average molecular weight of above 11,000 said process comprising transesterifying components (a) and (b) with (c) and (d) wherein component (a) is from 97 to 100 moles of at least one diaryl phosphonate and component (b) is up to 3 moles of at least one triaryl phosphate with the sum of the moles of (a) and (b) being 100, component (c) is from 90 to 99 moles of at least one aromatic dihydroxy compound and component (d) is up to 3 moles of at least one aromatic trihydroxy or tetrahydroxy compound with the proviso that at least one of the components (b) and (d) is present in a quantity of at least 0.001 mole and that the combined amount of (b) and (d) is at most 3 moles;

said transesterification being conducted in the melt at 90°

C. to 340°

C. in an oxygen-free atmosphere at atmospheric pressure or lower and in the presence of from 10^-5 to 5×

10^-2 mole percent, based on 100 mole percent of aromatic dihydroxy compound, of at least one basic catalyst, with the volatile constituents produced in the course of transesterification being removed by distillation.

2. The process according to claim 1 wherein the diaryl phosphonate of component (a) is of the formula ##STR18## wherein R¹ is alkyl having 1 to 12 carbon atoms, alkenyl having 2 to 12 carbon atoms, cycloalkyl having 6 to 30 carbon atoms, cycloalkenyl having 6 to 30 carbon atoms, aryl having 6-30 carbon atoms, arylalkyl having 6-30 carbon atoms or arylalkenyl having 6-30 carbon atoms wherein each aryl moiety is unsubstituted or substituted by at least one halogen or alkyl having 1 to 4 carbon atoms;

Z is fluoro, chloro, bromo or alkyl having 1 to 4 carbon atoms and when more than one Z occurs on one aryl moiety they may be the same or different; and

m is zero or an integer of from 1 to 5.

3. The process according to claim 2 wherein R¹ is methyl or phenyl and m is zero.

4. The process according to claim 1 wherein the aromatic dihydroxy compound of component (c) is of the formula ##STR19## wherein A'"'"' is a single covalent bond, alkylene having 1 to 4 carbon atoms, cycloalkylene having 5 or 6 carbon atoms, sulphonyl, carbonyl, oxygen or sulphur;

e is zero or the number 1;

Z is fluoro, chloro, bromo or alkyl having 1 to 4 carbon atoms and when more than one Z occurs on one aryl moiety they may be the same or different;

d is zero or an integer of from 1 to 4; and

f is zero or an integer of from 1 to 3.

5. The process as claimed in claim 4 wherein d is zero;

e is the number 1; and

A'"'"' is a single covalent bond, a 2,2-propylene moiety or sulphur.

6. The process as claimed in claim 1 wherein the aromatic trihydroxy or tetrahydroxy compound is selected from the group consisting of phloroglucinol;

4,6-dimethyl-2,4,6-tri-(4-hydroxy phenyl)-2-heptene;

4,6-dimethyl-2,4,6-tri-(4-hydroxy phenyl)-heptane;

1,3,5-tri-(4-hydroxy phenyl)-benzene;

1,1,1-tri-(4-hydroxy phenyl)-ethane;

tri-(4-hydroxy phenyl)phenyl methane;

2,2-bis-[4,4-bis-(4-hydroxy phenyl)-cyclohexyl]-propane;

2,4-bis-(4-hydroxy phenyl)-isopropyl phenol;

2,6-bis-(2-hydroxy-5'"'"'-methyl benzyl)-4-methyl phenol;

2-(4-hydroxy phenyl)-2-(2,4-dihydroxy phenyl)-propane;

tetra-(4-hydroxy phenyl)-methane;

tetra-[4-(4-hydroxy phenyl isopropyl)-phenoxy]-methane;

1,4-bis-(4,4"-dihydroxy triphenyl methyl)-benzene and mixtures thereof.

7. The process according to claim 1 wherein the triaryl phosphate of component (b) is of the formula ##STR20## wherein Z is fluoro, chloro, bromo or alkyl having 1 to 4 carbon atoms and when more than one Z occurs on one aryl moiety they may be the same or different;

and

m is zero or an integer of from 1 to 5.

8. The process according to claim 1 wherein the triaryl phosphate is triphenyl phosphate.

9. A thermoplastic molding composition comprising the polyphosphonate prepared according to claim 1 or said polyphosphonate admixed with at least one antistatic agent, pigment, mould release agent, heat stabilizer, UV stabilizer, filler or reinforcing fiber.