U.S. patent application number 11/631690 was filed with the patent office on 2008-09-11 for polymer material comprising chains bearing imidazolidone functions.
Invention is credited to Philippe Cordier, Manuel Hidalgo, Ludwik Leibler, Annett Linemann, Corinne Soulie-Ziakovic, Francois-Genes Tournilhac.
Application Number | 20080221272 11/631690 |
Document ID | / |
Family ID | 34946550 |
Filed Date | 2008-09-11 |
United States Patent
Application |
20080221272 |
Kind Code |
A1 |
Tournilhac; Francois-Genes ;
et al. |
September 11, 2008 |
Polymer Material Comprising Chains Bearing Imidazolidone
Functions
Abstract
The invention concerns a polymer material consisting of
macromolecular chains bound by hydrogen bonds wherein: the
macromolecular chains consist of a polymer skeleton whereon is
fixed by at least one covalent bond a modifying agent, the
modifying agent comprising, assembled in a common molecule, one or
more associative groups capable of being bound by hydrogen bonds
and one or more reactive groups capable of forming covalent bonds
with the polymer skeleton, at least one of the associative groups
of the modifying agent is an imidazolidone heterocycle, the
macromolecular chains bear on average 1 to 10 imidazolidone groups
per chain. The average number of imidazolidone groups to be
introduced into the macromolecular chains depends both on the
average mass of said chains and the final properties desired for
the material. The inventive polymer material can be extruded,
co-extruded, injected, blown, moulded, overmoulded, calandered,
thermoformed. It can be used to produce articles such as tubes,
films, plates, extruded strings, bottles, containers. The inventive
polymer material can also be mixed with other materials such as
other polymers, thus it is used for example as impact modifier or
rheology regulator. The invention further concerns the use of said
polymer material as compatibility agent in a composition comprising
among others at least two polymers belonging to different classes
of polymers.
Inventors: |
Tournilhac; Francois-Genes;
(Paris, FR) ; Leibler; Ludwik; (Paris, FR)
; Cordier; Philippe; (Fueil-Malmaison, FR) ;
Soulie-Ziakovic; Corinne; (Paris, FR) ; Linemann;
Annett; (Sarreguemines, FR) ; Hidalgo; Manuel;
(Brignais, FR) |
Correspondence
Address: |
ARKEMA INC.;PATENT DEPARTMENT - 26TH FLOOR
2000 MARKET STREET
PHILADELPHIA
PA
19103-3222
US
|
Family ID: |
34946550 |
Appl. No.: |
11/631690 |
Filed: |
July 6, 2005 |
PCT Filed: |
July 6, 2005 |
PCT NO: |
PCT/FR05/01741 |
371 Date: |
May 14, 2007 |
Current U.S.
Class: |
525/194 ;
525/418; 525/420; 525/50 |
Current CPC
Class: |
C08G 69/48 20130101;
Y10T 428/1352 20150115; C08F 8/32 20130101; C08F 8/32 20130101;
C08F 8/34 20130101; C08F 220/14 20130101; C08F 210/02 20130101;
C08F 8/32 20130101; C08F 8/30 20130101; Y10T 428/139 20150115 |
Class at
Publication: |
525/194 ; 525/50;
525/418; 525/420 |
International
Class: |
C08F 8/30 20060101
C08F008/30; C08G 63/91 20060101 C08G063/91 |
Foreign Application Data
Date |
Code |
Application Number |
Jul 8, 2004 |
FR |
0407608 |
Claims
1. A polymer material composed of macromolecular chains linked via
hydrogen bonds, in which: the macromolecular chains are composed of
a polymer backbone to which a modifying agent is attached via at
least one covalent bond, the modifying agent comprises, combined in
the same molecule, one or more associative groups capable of
uniting via hydrogen bonds and one or more reactive groups capable
of forming covalent bonds with the polymer backbone, at least one
of the associative groups of the modifying agent is a heterocycle
of imidazolidone type, the macromolecular chains carry, on average,
1 to 10 imidazolidone groups per chain.
2. The material as claimed in claim 1, in which the modifying
agents are of the following general formula: ##STR00006## in which:
R denotes a halogen or a primary or secondary amine, alcohol,
thiol, aldehyde, ketone, carboxylic acid or derivative (acid
chloride or bromide, acid anhydride or ester), sulfonic acid or
derivative, isocyanate or epoxy group, X denotes a hydrocarbon
chain carrying one or more heteroelements, such as a linear or
branched alkyl chain composed of 1 to 30 carbon atoms, a ring or a
sequence of alkyl or aryl units linked via --C(O)O--, OC(O),
--C(O)NH--, --NHC(O)--, C(O), --O--, --S-- or --NH-- bridges.
3. The material as claimed in either of claims 1 and 2, in which
the attaching of the modifying agent brings about the appearance of
a bonding group of --NHC(O)-- or --C(O)NH-- amide type.
4. The polymer material as claimed in claim 2, in which the
modifying agent is: ##STR00007##
5. The polymer material as claimed in claim 2, in which the
modifying agent is: ##STR00008##
6. The polymer material as claimed in claim 2, in which the
modifying agent is: ##STR00009##
7. The polymer material as claimed in claim 2, in which the
modifying agent is: ##STR00010##
8. The polymer material as claimed in any one of the preceding
claims, in which the polymer backbones exhibit a number-average
weight of between 1000 and 100,000.
9. The material as claimed in any one of the preceding claims, in
which there are two different polymer backbones.
10. The material as claimed in any one of claims 1 to 8, in which
there are polymer backbones of two different types A and B carrying
a modifying agent at each of their ends forming an A/B multiblock
linear associated.
11. The material as claimed in any one of claims 1 to 8, in which
there are polymer backbones of two different types A and B, each
chain of A carries at least two modifying agents and B carries a
modifying agent at one of its ends or a modifying agent at each of
its ends.
12. The material as claimed in any one of the preceding claims, in
which the polymer backbone is PMMA.
13. The material as claimed in any one of claims 1 to 11, in which
the polymer backbone is a polyamide.
14. The material as claimed in any one of claims 1 to 11, in which
the polymer backbone is polyethylene.
15. An object, such as a pipe, film, sheet, lace, bottle or
container, manufactured with the material of any one of the
preceding claims.
16. The use of the material of any of the preceding claims as
impact modifier or rheology regulator.
17. The use of the material of any one of the preceding claims as
compatibilizing agent in a composition comprising, inter alia, at
least two polymers belonging to different polymer catagories.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to the field of polymer
materials, particularly to the field of polymer materials composed
of macromolecular chains linked via interactions of hydrogen bond
type. It also relates to the processes for the syntheses of these
materials and to their uses as additives in compositions.
[0002] The materials of the invention can be used as is or, for
example, as impact modifiers or rheology-regulating agents.
THE PRIOR ART AND THE TECHNICAL PROBLEM
[0003] One of the technical problems which the invention attempts
to solve is the compromise between the viscosity level which
polymers exhibit in the molten state and their mechanical
properties. This is because, in the thermoplastics technology, for
example, a low viscosity is required during the processing, which
can only be obtained with systems of low molecular weight, but, at
the same time, a high elongation at break, a good impact strength,
a good creep strength and good resistance to solvents are desired
for the final material, which, conversely, requires high molecular
weights.
[0004] Moreover, it is well known that the synthesis of polymers of
very high molecular weights is markedly more difficult than that of
polymers of low weights.
[0005] Another technical problem to be solved is the preparation of
polymer compositions having an improved chemical resistance and an
improved chemical stability.
[0006] Another problem which the invention attempts to solve is the
preparation of block or comb sequential copolymers by joining up
homopolymers prepared in a first step.
[0007] The Applicant company has found that these problems can be
solved by the chemical modification of polymers by introducing
therein a modifying agent comprising imidazolidone groups.
[0008] The chemical modification of polymer systems according to
the invention involves the formation of a covalent bond between the
polymer backbone and the modifying agent. The modifying agent
comprises, combined in the same molecule, one or more associative
groups capable of uniting via hydrogen bonds and one or more
reactive groups capable of forming covalent bonds with the polymer
backbone. According to the invention, at least one of the
associative groups of the modifying agent is a heterocycle of
imidazolidone type. If appropriate, the polymer backbone under
consideration can comprise a certain number of comonomers carefully
chosen in order to facilitate the grafting operation, that is to
say the attaching of the modifying agent to the polymer backbone
via at least one covalent bond.
[0009] Due to the presence of the associative groups, the modified
polymer chains are capable of uniting via cooperative hydrogen
bonds; the role of the associative groups may also be to strengthen
this associative ability if the latter preexists in the unmodified
system. One advantage of this type of association is that these
hydrogen bonds are reversible: they can be cleaved by a rise in
temperature or by the action of a selective solvent and can
subsequently be reformed.
[0010] One advantage of the chemical modifications disclosed in
this patent is the improvement in the conditions for processing and
the final properties, in particular mechanical properties, of the
modified polymers. Likewise, the use of associative groups confers
the properties of polymers of high weights on polymers of small
molecular weights which are easier to produce in a controlled
fashion.
[0011] The chemical modifications disclosed in this patent make it
possible to graft the same type of associative group to different
types of macromolecular chains.
[0012] The associative groups can be introduced into the polymers
by different routes. Mention may be made of copolymerization with a
monomer carrying the associative group or the use, during the
synthesis of the polymer, of the modifying agent as transfer agent
or terminating agent. According to the invention, the associative
groups are introduced onto preformed polymer or copolymer systems
by reaction with the modifying agent; in other words, after the
polymerization or polycondensation stage. For the polymer systems
resulting from polycondensations, such as, for example, polyesters
and polyamides, which de facto exhibit reactive chain ends, the
modifying agent can also be introduced during the synthesis as
chain-limiting agent.
[0013] One of the advantages of proceeding by modification of
existing polymers or copolymers is to be able to synthesize an
entire range of products from a single polymerization; for example,
modified polymers comprising a relatively large number of
associative groups can be obtained by varying the amount of
modifying agent or the reaction time during the grafting stage,
whereas, to achieve the same result using monomers carrying the
associative group, it is necessary to carry out a fresh
polymerization in each case.
[0014] Finally, the presence of these associative groups on
macromolecular chains belonging to different polymer categories
makes it possible to produce block copolymers, the two blocks of
which are linked via hydrogen bonds.
BRIEF DESCRIPTION OF THE INVENTION
[0015] The subject matter of the invention is thus a polymer
material composed of macromolecular chains linked via hydrogen
bonds, in which:
the macromolecular chains are composed of a polymer backbone to
which a modifying agent is attached via at least one covalent bond,
the modifying agent comprises, combined in the same molecule, one
or more associative groups capable of uniting via hydrogen bonds
and one or more reactive groups capable of forming covalent bonds
with the polymer backbone, at least one of the associative groups
of the modifying agent is a heterocycle of imidazolidone type, the
macromolecular chains carry, on average, 1 to 10 imidazolidone
groups per chain.
[0016] If appropriate, the polymer backbone under consideration can
comprise a certain number of comonomers carefully chosen in order
to facilitate the grafting operation, that is to say the attaching
of the modifying agent to the polymer backbone via at least one
covalent bond.
[0017] The average number of imidazolidone groups to be introduced
into the macromolecular chains depends both on the average weight
of these chains and on the final properties which it is desired to
confer on the material.
[0018] It is possible to use a mixture of modifying agents. For
example, different modifying agents can be attached to the same
polymer backbone, one modifying agent can be attached to polymer
backbones and another modifying agent to the other polymer
backbones, the polymer backbones can be mixtures of different
polymer backbones or any combination of these possibilities.
[0019] The polymer material of the invention can be extruded,
coextruded, injection molded, blow molded, molded, overmolded,
calendered or thermoformed. Objects, such as, for example, pipes,
films, sheets, laces, bottles or containers, can be prepared
therefrom. The polymer material of the invention can also be
blended with other materials, such as other polymers; thus, it is,
for example, used as impact modifier or rheology regulator.
[0020] The present invention also relates to the use of the
preceding polymer material as compatibilizing agent in a
composition comprising, inter alia, at least two polymers belonging
to different polymer categories.
DETAILED DESCRIPTION OF THE INVENTION
[0021] As regards the polymer backbones, they can belong to
different polymer categories. They are preferably chosen from
polyolefins, polydienes, polyvinyls, polyacrylates,
polymethacrylates, polyesters, polyamides, polyethers,
polycarbonates, polysiloxanes, polyurethanes and copolymers of the
above types. According to a preferred form, the number-average
molar mass of the polymer backbones is between 1000 and 100
000.
[0022] As regards the modifying agent, it comprises, combined in
the same molecule, one or more associative groups A capable of
uniting via hydrogen bonds and one or more reactive groups R
capable of forming covalent bonds with the polymer. The groups A
and R are connected to one another via a rigid or flexible chain
X:
A-X-R
[0023] According to the invention, at least one of the associative
groups of the modifying agent is a heterocycle of imidazolidone
type.
##STR00001##
[0024] The reactive group(s) present in the modifying agent does/do
not have to be a polymerizable chemical group but only a group
capable of forming a covalent bond with reactive groups present on
the polymer backbone. Preferably, R can be a halogen or a primary
or secondary amine, alcohol, thiol, aldehyde, ketone, carboxylic
acid or derivative (acid chloride or bromide, acid anhydride or
ester), sulfonic acid or derivative, isocyanate or epoxy group.
[0025] The rigid or flexible chain X can be a hydrocarbon chain
carrying one or more heteroelements; it can be a linear or branched
alkyl chain composed of 1 to 30 carbon atoms, a ring or a sequence
of alkyl or aryl units linked via --C(O)O--, OC(O), C(O), --O--,
--S-- or --NH-- bridges; advantageously, these groups present on
the chain X, in particular when C(O)NH amide bridges are involved,
are capable of joining together via hydrogen bonds.
[0026] Optionally, the reaction of R with the polymer backbone can
bring about the appearance of additional groups which can combine
via hydrogen bonding and in particular --C(ON)NH-- or
--NHC(O)-amide bridges.
[0027] According to a preferred form of the invention, the
modifying agent corresponds to one of the following molecules:
##STR00002##
[0028] Surprisingly, the chemical modification of polymers by
grafting imidazolidone associative groups results in a considerable
variation in the physical properties of these polymers. In
particular, the presence of the associative groups is reflected by
a rise in the elastic modulus of the modified polymers, this being
the case within a broad temperature range. Thus, in the case of
modified PMMA, an improvement in the elastic modulus is found up to
a temperature of approximately 170.degree. C., whereas, in the
systems described previously, the improvement in the mechanical
properties is substantial only at low temperature (below 80.degree.
C. [Yamauchi K. et al., Macromolecules, 37, 3519 (2004)] or below
140.degree. C. [Colombani O. Doctoral thesis, Universite de Paris
VI (2003)] according to the system under consideration). This
characteristic makes it possible to envisage the strengthening of
systems, such as PMMA, which already have a high thermomechanical
strength, while retaining other properties, such as transparency,
high-temperature flow or ease of processing. In addition, the
polymer systems modified by associative groups of imidazolidone
type exhibit an improved resistance to solvents.
[0029] The blending of two different polymer backbones carrying
imidazolidone functional groups makes it possible to form "block
copolymers". These diblocks exhibit a microphase separation.
Diblock-Type Linear Association:
##STR00003##
[0031] "Multiblock"-type linear association: A and B different
polymer backbones
[0032] .+-.: group comprising the imidazolidone functional group.
Different polymer backbones A and B carry a modifying agent at each
of their ends. An A/B multiblock linear association is thus
obtained.
##STR00004##
[0033] "Branched" association of "grafted copolymer" type: A and B
two different polymer backbones.
[0034] .+-.: group comprising the imidazolidone functional
group
[0035] A and B different polymer backbones, each chain of A carries
at least two modifying agents and B carries a modifying agent at
one of its ends or a modifying agent at each of its ends.
##STR00005##
EXAMPLE 1
Synthesis of N-aminoethyl-2-imidazolidone (AEIO)
[0036] 154.5 g (1.5 mol) of diethylenetriamine (DETA) and 154.5 g
(8.58 mol) of water are introduced into a 500 ml three-necked flask
equipped with a water-cooled reflux condenser and a magnetic
stirrer. Nitrogen sweeps through the reaction mixture.
[0037] The evolution of heat brought about by the water/DETA mixing
makes it possible to preheat the reaction medium. 45 g (0.75 mol)
of urea are then added. The temperature is increased until reflux
is obtained (.about.130.degree. C.). The reaction is carried out
for 10 hours.
[0038] After reaction, without changing the temperature but
removing the reflux system, the water and the DETA are allowed to
evaporate as much as possible. The residual DETA is evaporated by
simple distillation under a slight vacuum (10 mmHg) at
.about.75.degree. C.
[0039] The mixture is then distilled by fractional distillation
under vacuum at .about.0.08-0.09 mmHg. The first fraction is not
collected. For the second fraction, the column top temperature is
then 105.degree. C.
[0040] A white crystalline solid, AEIO, is obtained with a melting
point M.p. of 41.degree. C. and a molecular weight of 129 g. The
yield after distillation is .eta.=75% with respect to the urea.
EXAMPLE 2
Grafting of AEIO to MMA-Based Copolymer
[0041] 3 g of HT10 copolymer (acrylic copolymer comprising 90% of
methyl methacrylate, M.sub.n=40 000 g/mol, .about.30 anhydride
functional groups per chain) and 290 mg (2.25 mmol) of AEIO
synthesized according to example 1 are introduced at 220.degree. C.
into a Daca twin-screw extruder equipped with recirculation. The
blending time is 5 min and gives the grafted copolymer
HT10-g-UD.
[0042] For each copolymer, 3 bands are recorded by FTIR relating to
the C=0 double bonds (between 1850 and 1600 cm.sup.-1):
TABLE-US-00001 Functional Functional HT10 group HT10-g-UD group
1803 cm.sup.-1 Anhydride 1730 cm.sup.-1 Ester 1760 cm.sup.-1
Anhydride 1674 cm.sup.-1 Imidazolidone 1732 cm.sup.-1 Ester 1650
cm.sup.-1 Amide
[0043] The grafting is testified to by the complete disappearance
of the anhydride bands and the appearance of bands characteristic
of the imidazolidone unit.
[0044] For the modified copolymer, a significant reduction in the
solubility in chloroform and an increase in the glass transition
temperature are recorded.
Tg(HT10)=121.degree. C. and Tg(HT10-g-UD)=129.degree. C.
[0045] By DMA, the difference between the Tg values of the two
copolymers is also encountered with regard to the softening point.
Furthermore, from 190.degree. C., the elastic modulus of HT10-g-UD
falls and ends up by being coincident with that of HT10.
EXAMPLE 3
Grafting of AEIO to MMA-Based Copolymer
[0046] 3 g of HT121 copolymer (acrylic copolymer comprising 96% of
methyl methacrylate, M.sub.n=40 000 g/mol, .about.3 anhydride
functional groups per chain) and 29 mg (0.225 mmol) of AEIO
synthesized according to example 1 are introduced at 220.degree. C.
into a Daca twin-screw extruder equipped with recirculation. The
blending time is 5 min and gives the grafted copolymer
HT121-g-UD.
[0047] For each copolymer, 3 bands are recorded by FTIR relating to
the C.dbd.O double bonds (between 1850 and 1600 cm.sup.-1):
TABLE-US-00002 Functional Functional HT121 group HT121-g-UD group
1803 cm.sup.-1 Anhydride 1730 cm.sup.-1 Ester 1760 cm.sup.-1
Anhydride 1674 cm.sup.-1 Imidazolidone 1732 cm.sup.-1 Ester 1650
cm.sup.-1 Amide
[0048] The grafting is testified to by the complete disappearance
of the anhydride bands and the appearance of bands characteristic
of the imidazolidone unit.
[0049] For the copolymer, an increase in the glass transition
temperature is recorded.
Tg(HT121)=123.degree. C. and Tg(HT121-g-UD)=129.degree. C.
EXAMPLE 4
Grafting of AEIO to Ethylene-Based Copolymer
[0050] 3 g of Lotader 3210 copolymer (M.sub.n=13 500 g/mol, 2.8
anhydride groups per chain), comprising 0.21 mmol of anhydride
functional groups, and 27 mg (0.21 mmol) of AEIO synthesized
according to Example 1 are introduced at 140.degree. C. into a Daca
twin-screw extruder equipped with recirculation. The blending time
is 10 min and gives the grafted copolymer Lotader 3210-g-UD.
[0051] Three bands relating to the C.dbd.O double bonds (between
1850 and 1600 cm.sup.-1) are recorded by FTIR for each
copolymer:
TABLE-US-00003 Lotader Functional Lotader Functional 3210 group
3210-g-UD group 1854 cm.sup.-1 Anhydride 1843 cm.sup.-1 Anhydride
1780 cm.sup.-1 Anhydride 1777 cm.sup.-1 Anhydride 1735 cm.sup.-1
Ester 1734 cm.sup.-1 Ester 1710 cm.sup.-1 Acid 1709 cm.sup.-1 Acid
1680 cm.sup.-1 Imidazolidone 1650 cm.sup.-1 Amide
[0052] The infrared spectrum of Lotader 3210 shows that a high
proportion of the maleic anhydride groups are hydrolyzed and will
not participate in the grafting. In Lotader 3210-g-UD, a fall in
the intensity of the anhydride peaks is observed to the advantage
of the acid peak and of the new amide and imidazolidone peaks.
However, the grafting is not 100%.
[0053] The melting point of the copolymers is identical
(105.degree. C.), as is the degree of crystallinity (28%). By DMA,
after melting, the elastic modulus of the Lotader 3210-g-UD
copolymer exhibits a secondary plateau at approximately 0.15 MPa,
whereas the Lotader 3210 copolymer does not have it.
EXAMPLE 5
Grafting of AEIO to Polyamide
[0054] AEIO is grafted under similar conditions to a polyamide of
low molecular weight M.sub.w=1500 g/mol comprising COOH endings. In
comparison with a polyamide of the same family of molecular weight
M.sub.w=15 000 g/mol (Platamid), the modified polyamide, PADU,
exhibits an increase in the elastic modulus at ambient temperature
and up to a temperature of approximately 65.degree. C. and a
greater flow at high temperature.
EXAMPLE 6
Grafting of AEIO to PMMA with 5% of Acid Functional Groups
[0055] A copolymer of methyl methacrylate and of methacrylic acid
(4.5% by number) HT121 (M.sub.n=40 000 g/mol) is extruded in a DSM
twin-screw miniextruder with recirculation at 220.degree. C. for 30
min. The appearance of two absorption bands by FTIR (in solution in
chloroform) characteristic of the C.dbd.O bonds of anhydrides is
observed at 1755 and 1805 cm.sup.-1.
[0056] 15 g of this product are subsequently blended in the same
extruder with 1 g of AEIO at 220.degree. C. for 5 min. The FTIR
study (CHCl.sub.3) of the product obtained shows partial grafting:
the band of the C.dbd.O bond of the amide formed appears at
approximately 1670 cm.sup.-1 but the bands corresponding to the
C.dbd.O bonds of the anhydride only decrease very slightly.
[0057] The HT121 and grafted HT121 samples are prepared by
compressing in the form of disks. These disks are placed in an Ares
parallel plate rheometer at 175.degree. C. and a frequency sweep
test is carried out (from 10 Hz to 0.32 MHz) with a constant strain
of 1%.
TABLE-US-00004 HT121 Grafted HT121 Complex viscosity at 10 Hz (Pa
s) 7267 7329 Complex viscosity at 0.00032 Hz (Pa s) 2.5E+06 1.7E+07
Frequency where G' = G'' (Hz) 0.0257 <0.00032 Relaxation time
(s) 6.2 >500
[0058] The viscosity at the frequencies above 0.2 Hz is the same
for both samples. On the other hand, the viscosity at low
frequencies is significantly enhanced by the grafting. A very
marked increase in the relaxation time of the chains is also
observed for the grafted HTl21; this time is too long to be
measurable in the frequency sweep mode used.
[0059] By DMA, above the glass transition temperature, a slower
decrease in the elastic modulus is observed for grafted HT121 (E'
of the order of 50 MPa at 150.degree. C.).
EXAMPLE 7
Grafting of AEIO to PMMA with Anhydride Functional Groups
[0060] A copolymer of methyl methacrylate and of methacrylic acid
(7.5% by number) (M.sub.n=30 000 g/mol) comprising 3.3% of
anhydride functional groups is chosen. It is recorded as 72565.15 g
of this polymer are blended with 0.64 g of AEIO in a DSM twin-screw
miniextruder equipped with recirculation for 5 minutes at
220.degree. C. FTIR spectroscopy (CHCl.sub.3) reveals the decrease
in the bands characteristic of the anhydrides at 1755 and 1805
cm.sup.-1 and the appearance of the band at approximately 1670
cm.sup.-1 attributed to the amide formed during the grafting.
[0061] An increase in the glass transition temperature Tg due to
the grafting is observed:
Tg(72565)=130.8.degree. C. Tg(grafted 72565)=133.7.degree. C.
[0062] A DMA bending creep test is carried out for 72565 and
grafted 72565; for each compound, the test temperature is lower
than the Tg by 10.degree. C. A stress of 10 MPa is applied for 2
hours and then the recovery is observed over a period of 2 hours.
FIG. 2 represents the strain and constant stress profiles measured
as a function of the time. 72565 has a strain level of 9.2% after 2
hours, in comparison to 7.2% for grafted 72565. The grafting also
significantly improves the recovery; after recovering for 2 hours,
grafted 72565 has a residual strain of 3.8% (i.e., virtually half
of the strain brought about by the creep), in comparison with 6.0%
for 72565, which thus recovered only a third of the strain
introduced by the creep.
[0063] Frequency sweeps are carried out at 175.degree. C. in a
rheometer with parallel plate geometry. The viscosity at high
frequencies is not significantly modified but it increases quite
sizably at low frequencies.
TABLE-US-00005 72565 Grafted 72565 Complex viscosity at 10 Hz (Pa
s) 1.0E+04 1.6E+04 Complex viscosity at 0.00046 Hz (Pa s) 2.4E+06
8.4E+06 Frequency where G' = G'' (Hz) 0.03 0.0033 Relaxation time
(s) 5.3 48.2
EXAMPLE 8
Grafting in Solution of AEIO to PMMA with Anhydride Functional
Groups
[0064] 40 g of PMMA 72565, 3.5 g of AEIO (in excess) and 600 ml of
anhydrous chloroform are introduced into a one-liter round-bottomed
flask equipped with a reflux heating system.
[0065] FTIR (CHCl.sub.3) reveals the disappearance of the bands at
1755 and 1805 cm.sup.-1 attributed to the anhydrides and the
appearance of an amide band at 1670 cm.sup.-1.
[0066] The DSC study also shows a significant rise in the Tg:
Tg(72565)=130.8.degree. C. Tg(grafted 72565_solution)=138.3.degree.
C.
EXAMPLE 8a
Extrusion Grafting of AEIO to a PMMA of M.sub.n=10 000 g/mol with
Anhydride Functional Groups
[0067] 10 g of PMMA-3 (with a number-average weight equal to 10 000
g/mol comprising 8 mol % of anhydride functional groups) are
extruded at 220.degree. C. in a DSM twin-screw extruder, in the
absence or in the presence of one equivalent of AEIO. The extruded
polymer is injection molded in the form of bars with a cross
section of 1.5.times.4 mm. Thermomechanical analysis reveals
differences between the samples of modified polymer (graft, graft2)
and the unmodified samples (neat, neat2, neat3). Thus, the glass
transition temperature Tg is 120.degree. C. and 136.degree. C.
respectively in the unmodified and modified polymer samples. In
three point bending (with a distance of 10.2 mm between points), a
rise of +15% in the modulus and of +80% in the strain at break are
observed at 30.degree. C. in the modified samples.
[0068] Furthermore, an improvement in the creep strength is
observed: for this experiment, bars with a length of 18 mm and with
a cross section of 1.5.times.4 mm are subjected to a stress of 1
MPa in single cantilever geometry; the temperature is set at
10.degree. C. above Tg. Thus, at 126.degree. C. in the modified
sample, the rate of strain after 2 hours is 0.16% per hour,
whereas, under the same conditions and at a temperature of
110.degree. C., it is 0.35% per hour in the sample of unmodified
polymer. After removing the stress and while maintaining the
temperature for a further 3 hours, the strain decreases down to 29%
of its initial value in the sample of modified polymer, whereas it
remains at 60% of its initial value in the sample of unmodified
polymer.
EXAMPLE 9
Grafting of AEIO to a Polyamide
[0069] 3 g of a polyamide PA (Platamid) of low weight (M.sub.n=3000
g/mol), terminated by acid groups, are introduced, with 0.256 g of
AEIO and a drop of orthophosphoric acid, into a Daca twin-screw
miniextruder with recirculation. The blend is stirred at
230.degree. C. for 2 minutes, 20 minutes and 1 hour.
[0070] An FTIR analysis shows that the band corresponding to the
C.dbd.O double bonds of carboxylic acid at approximately 1710
cm.sup.-1 decreases with time.
TABLE-US-00006 Grafting time Level of the band at 1710 cm.sup.-1 0'
0.06 2' 0.032 20' 0.026 60' 0.023
[0071] Analyses using an Ares parallel plate rheometer at
150.degree. C., under a constant strain of 1%, show an increase in
the viscous modulus over the entire frequency range (from 10 Hz to
0.32 MHz) as a function of the grafting time (the elastic moduli
are too low to be measured with accuracy).
TABLE-US-00007 PA PA + UDETA PA + UDETA PA + UDETA Grafting time 0'
2' 20' 60' G'' at 15 Hz 1104 641 1140 1676 (Pa)
[0072] For reaction times of greater than 20 minutes, an increase
in the viscous modulus is observed for the PA+AEIO blends in
comparison with the pure ungrafted PA.
* * * * *