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Weld Lines and Mechanical Properties of

Injection Molded Polyethylene/


Polystyrene/ Copolymer Blends
B. BRAHIMI, A. AIT-KADI,* and A. AJJI**

Centre de Recherche en Sciences et Inghnierie des MacromoGcules


Dkpartement de Gknie Chimique
Facult6 des Sciences et de Gknie
Universitt.Lava1
Qukbec, Que., G I K 7P4,Canada
In this article, we investigate the effect of weld lines on the tensile mechanical
properties of unmodified and copolymer modified high density polyethylene (HDPE)
and polystyrene (PS) blends. The homopolymers were melt blended in the propor-
tion of 20 wt% HDPE and 80 wt% PS using a twin screw extruder at a temperature
of 200°C.The results show that the mechanical properties are generally lower
when weld lines are present. The decrease of the mechanical properties is much
more pronounced for the blends. The addition of small amounts of a commercial
styrene/butadiene copolymer significantly improves the strength and the elonga-
tion at break of this blend. An optimum copolymer concentration was observed at
3 wt%. This value coincides with the interphase saturation concentration of the
copolymer obtained from the analysis of the DMTA (dynamic mechanical and
thermal) properties of the blends. The copolymer was also found to induce impor-
tant changes in the morphology of the blend. The interdiffusion of the polymer
fronts in the weld region was also improved by the presence of the copolymer. It is
believed that these two aspects contribute to the enhanced properties obtained
with copolymer modified blends in presence of weld lines. An important effect of
the injection temperature on the tensile strength and the elongation at break
of welded samples with copolymer modified blends was observed. The effect of
mold temperature on these properties was less important mainly at low injection
temperatures. Only a slight effect of these two parameters was observed for the
tensile modulus in the range of mold and injection temperatures considered in
this study.

INTRODUCTION weld lines which will form when the polymer flow
fronts from the different gates meet dunng the filling
he injection molding process is one of the most
T important polymer processes by which polymeric
resins are converted into useful finished products. A
process (1-5). Weld lines are also present when the
mold cavity contains inserts around which the flow
front is divided and then recombined at the opposite
wide variety of complex geometry articles ranging from
very small parts such as precision gear wheels to side of the insert (2-5). Weld lines are characterized
relatively large parts such as exterior and interior by poor mechanical properties (3, 6-12). There are
automotive parts (e.g. bumpers) can be produced. different manners to partially solve this problem.
These parts are generally obtained at a high fre- In the case of homopolymers (either amorphous or
quency with virtually no wear of the processing semicrystalline), the mechanical properties of welded
machinery. In the case of large parts, multigated regions were found to be sensitive to the processing
mold cavities are necessary in order to avoid freezing conditions (3, 9-10, 13, 14). Malaguarnera and
of the polymer before the cavity is completely filled. In Manisali (11) have studied the effect of melt tem-
this case, the finished product will invariably contain perature, mold temperature, injection speed, and
injection pressure on the tensile properties of com-
mercial grades of polystyrene (PSI: high impact
*To whom all correspondence should be addressed. polystyrene (HIPS), and polypropylene (PP). They
“Current address: Industrial Materials Institute. 75 Bd De Mortagne.
Boucherville. Quebec. J 4 B 6Y4 Canada. found that the most important processing parame-

1202 POLYMER ENGINEERING AND SCIENCE, MID-AUGUST 1994, Vol. 34, NO. 15
Weld Lines and Mechanical Properties

ters are melt and mold temperatures. They noticed a of PE/PS blends. However, they observed that the
little effect of the injection speed and pressure on the increase of the shear rates induced a fine morphol-
tensile properties of the samples studied. For the PS, ogy. Han and co-workers (18) have studied the
a higher melt temperature induced a considerable injection molding of high density polyethylene/
increase of both the elongation and the stress at polystyrene (HDPE/PS) blends and polystyrene/
break. However, in the case of HIPS, the effect of melt polypropylene (PS/PP) blends. After optimizing the
temperature (T,) is apparent only for the elongation molding conditions for the studied systems, they
at break which substantially increases upon increas- investigated the influence of the mode of preparation
ing T., Hubbauer (6)investigated the effect of molding on the state of dispersion of a minor phase in the
pressure on acrylonitde-butadiene-styrene (ABS) blend. They concluded that the state of dispersion of
and found a slight improvement of the tensile p r e the components has a great effect on the mechani-
perties upon increasing the injection pressure. The cal properties of two-phase systems (18). More
enhancement was attributed to the material relax- recently, Paul and co-workers (15, 21) studied the
ation time, melt viscosity, and pressure along the mechanical properties of injection molded and com-
weld line. Crawford and Benham (7) examined pression molded PE/ PS/ copolymer blends. They
the creep and fatigue properties of acetal copolymer observed an important increase of the ductility and
samples both with and without weld lines. They found the impact resistance of the blends as the copolymer
that the fatigue life of a specimen with weld line was was added. However these improvements induced a
always about one fiftieth that of a sample without a decrease of the elastic modulus and the yield stress.
weld line over the whole range of stress tested. By They observed a difference in the properties of sam-
optimizing the molding conditions they found an ples molded by compression and injection, which are
improvement to one twenty-fifth of the fatigue life of a due to the crystallinity and orientation induced dur-
nonwelded sample. Using three test materials, ing molding (1 5 . 2 1). Concerning the effects of copoly-
polystyrene (PS), polycarbonate (PC), and polyoxy- mer addition to binary polymer blends, literature
methylene (POM), Criens and MoslC (8)have studied reviews can be found in recent publications (22-23).
the relationship between design and processing The literature is however less abundant in the case
parameters as well as the effect of weld lines on of weld lines with heterophase polymer systems
tensile properties of injection molded plates contain- (24-26). In this work, we investigate the effect of weld
ing circular inserts. They found that the influence of line on the tensile mechanical properties of an
melt temperature varies from one polymer to the HDPE/PS blend, as well as the effect of a copolymer
other. It was also noticed that both the processing used as a compatibilizingagent. The effect of process
parameters and the way by which the lines have been ing conditions on these propertiesfor injection molded
formed, together with the size of the obstacle in the specimens is investigated for HDPE/PS/KRO1/20/
melt flow has an influence on the weld line proper- 80/3 wt%.
ties. A recent study carried out by Tomari, et al (9).
in which they investigated the relationships between EXPERIMENTAL
the properties of welded specimen, their variation Materials
with the sample thickness and molding conditions
ofgeneral purpose injection moldings. They found The homopolymers used in this study are a high
that the higher the filling pressure, the higher was density polyethylene (HDPE, XS 84672.03) and a
the strength of the weld line. They also found that the polystyrene (PS, CS 55388 1205) provided by Dow
depth of the V-notch observed with welded specimens Chemical Canada Inc. The compatibiljzer used is a
depends on molding conditions. They could improve styrene/butadiene copolymer (K-resin, KRO 1) s u p
the weld line strength by raising the holding pres- plied by Phillips 66 Inc. Some characteristics of these
sure, even when the fflling pressure was low. Other materials are presented in Table 1.
particular techniques can be used to either eliminate Blending
weld lines in certain part geometry or to control the
structural characteristics of the weld area ( 13). The blends are prepared in the melt state using a
In the case of polymer blends, particularly immisci- twin screw extruder (Werner & F'fleiderer) at a rotat-
ble polymer blends (which is the most general case), ing speed of 250 rpm and a temperature of 200°C. In
the problem is much more complex In fact, together the case of modifled blends, the copolymer is first
with the effect of processing parameters mentioned combined with the minor phase, and then blended
earlier for homopolymers, we must take into account with the matrix.The blend composition used for this
specific features of heterophase systems such as
morphology, size of dispersed phase, and interphase
Table 1. Material Characteristics.
interactions. Morphologyand dispersed size are highly
influenced by processing conditions ( 15-20). Min and M.F.1 Den89
White (16) found t h a t t h e variation of Material (g/10 min) (g/cm 1
the blending temperature (180 to 240°C) during HDPE 6.8 0.91-0.97
extrusion, for polyethylene with different molecular PS 8.8 1.045
weights, has a slight influence on the morphology KROl 8.0 1.010

POLYMER ENGWERfNG AND SCIENCE, MID-AUGUST 1994, YO/. 34, NO. 15 1203
B. Brahimi, A. Ait-Kadi, a n d A. A j i

study is 20/80 wt% HDPE/PS. To investigate the Jeol JSM-25s I11 scanning electron microscope (SEMI.
effect of copolymer content, blends with different A gold/palladium alloy was deposited on all samples
amounts of copolymer (1, 3, 5, 10, and 20 wt% of prior to examination.
the overall composition) are prepared. The effect
of injection molding temperature and mold temper- RESULTS AND DISCUSSION
ature is studied on a selected HDPE/PS/KROl Effect of Copolymer Concentration
(20/80/3) composition.
The stress at break of nonwelded samples (an) and
Injection Molding the ratio u,/a,, a, being the stress at break of the
welded specimens, as a function of the copolymer
All samples are prepared on a NISSEI fully hydraulic content are reported in Fig. 2. In the case of unmodi-
injection molding machine, with a maximum injec- fied blends (0 wt%), this ratio is around 23%. This
tion capacity of 1 14 cm3/shot. The double gated mold indicates that the strength of the samples is greatly
used in this study is shown in Figs. la and b for
single and double filling gates respectively. All blends
are dried at 70°C during 2 h prior to injection. Table 2. Injection Molding Conditions.
The different sets of molding conditions are listed in injection
Table 2. The term “melt temperature” refers to the Mold injection Filling Holding injection Cooling
temperature of the material inside the barrel. The temperature speed pressure pressure time time
upper and lower limits of these injection parameters (“C) (%) (%) (%I (S) (S)
were fured based on the operating characteristics of 240 50 60 80 30 10 25 A
our injection molding machine and on the experimen-
200 30 50 50 65 10 25 t
tal limits. Specimens with and without weld line are 50
prepared. 70
90
Characterization
220 30 50 50 65 10 25
The tensile tests are performed according to ASTM 50 B
D638 standard on an Instron machine, using a 70
90
crosshead speed of 1 cm/min. The measurements
are carried out at room temperature (21°C). The 240 30 50 50 65 10 25
results presented are averaged over ten tensile tests. 50
70
Mechanical properties in the dynamic mode are
90 i
obtained using a Polymer Laboratories DMTA instru-
A Conditions used for the investigation of copolymer content effect.
ment. The experiments are carried out at 1 Hz for 6 Conditions used for the investigation of melt and mold temperatures.
temperatures ranging from -150 to 150°C. Micro-
graphs of tensile fractured surfaces are obtained on a

- 30
0.5
-
m
b’
z - 25
0

b’ b‘
0.4
- 20

0.3
- 15

lmml 10
0 5 10 15 20 25
Copolymer content (wt%)
(a) (b) Fig. 2. Variations of the tensile strength un and the ratio
Fig. 1 . Mold cauityfor tensile specimen: A) no weld line, B) (u,/u,) as afunction of copolymer concentrationfor HDPE/
with weld line. PS (20/ 80) blends.

1204 POLYMER ENGINEERING AND SCIENCE, MID-AUGUST 1994, Vol. 34, NO. 15
Weld Lines and Mechanical Properties

affected by the presence of weld lines. This ratio in- for 0.5%copolymer content). In other words, the pres-
creased when only few amounts of copolymer are ence of copolymer in the blend hardly affects
added to the blends. We should mention here that in the tensile modulus at least in the range of concen-
the case of nonwelded specimens, the presence of the trations considered in this study. On the other hand,
copolymer has no effect on the terlsile properties over an increase followed by a decrease of the En modu-
the entire range of copolymer concentrations consid- lus is observed upon increasing the copolymer
ered in this study. The effect of copolymer observed concentration in the 0 to 3 wt% range.
in Fig. 2 is entirely due to the effect of copolymer on Figure 4 shows the elongation at break of non-
the tensile strength of welded specimens. The most welded specimens ( E , ) and the ratio of the elongation
important increase is observed for copolymer concen- at break of welded specimens ( E , ) to that of non-
trations between 0 and 3 wt% where an optimum is welded ones. Almost, the same behavior as the one
observed. In fact, the stress ratio is increased from observed for the stress at break ratio is noticed. The
23% (for the unmodified blend) to 45% (for the 3 wt% most important increase occurs when only a small
modified ones), that is, the stress at break for amount of copolymer is added. This ratio is almost
the 3 wt% modifled blend with weld line is almost equal to 21% for the unmodified blends. It reaches
doubled compared to that of the unmodified one since 39%for the 3 wt% modified blend where a maximum
the stress at break for the nonwelded specimen is reached. For higher copolymer concentrations,
remains constant upon addition of copolymer (see a decrease followed by a progressive increase is
Fig. 2). For higher copolymer concentrations, a observed. Again, in the case of welded specimen, the
decrease followed by a monotonic increase is elongation at break of the 3 wt% copolymer modified
observed. We should point out that the copolymer blend is almost two folds that of the unmodified one.
concentrations of interest are in the low copoly- Note that we do not approach the tensile properties
mer concentrations range. The copolymer is used only ratio for the homopolymers but we certainly enhance
as a compatibilizer and not as a minor or a major the stress and the elongational ratios for the 3 wt%
component of the blend. In this aim the 3 wt% copolymer modified blend. Figure 5 shows the tensile
copolymer content gives the best results. properties for the homopolymers, the unmodified and
The ratio of the tensile modulus of welded speci- copolymer modifled blends. Except for the elongation
mens (E,) to that of nonwelded ones ( E n ) together ratio of KRO 1 , the tensile ratios for the homopolymers
with the tensile modulus ( E n )as a function of copoly- will be higher than those of the blends. Note also that
mer content are reported in Ag. 3. The results show the tensile modulus of the HDPE (semicrystalline)is
that the effect of the copolymer on the modulus ratio not affected by the presence of the weld line. More
is less important than that observed for the stress over, the fracture during tensile testing for the HDPE
ratio. The overall variation of the modulus ratio is samples occurs (50%times) away from the weld line.
inside the experimental precision of the test (except For the PS (amorphous), the copolymer (KROl), and

- t 1

-
1.8
1.2 0.4 - 6

- 1.7
1.1 0.3 - 5

- 1.6
E s
'u
ui
0.2 - 4

0.9 c 0.1 - 3

I 1 1.4

0.8 1.3 0.0 -2


0 5 10 15 20 25 0 5 10 15 20 25
Copolymer content (wt%) Copolymer content (wt%)
a. 3. Variations of the tensile moduius En and the ratio a.4. Variations of the elongation at break c, and the ratio
( E w / E n ) as afunction of copolgmer concentrationfor HDPE/ ( c w / c n ) as afunction of copolymer concentrationfor HDPE/
PS ( 20/ 80)blends. PS ( 20/ 80) blends.

POLYMER E#G##E€fUffi AND SCIENCE, MfBAUGUST 1994, V d . 34,No. 15 1205


B. Brahimi A. Ait-Kadi, and A. AJi

the blend samples, the fracture invariably takes place sponds to the copolymer concentration at which
at the weld lines. the stress ratio and the elongational ratio shown in
In a previous work on the effect of well designed Figs. 2 and 4 are maximum (in the region of interest
copolymers on the properties of HDPE and high as mentioned earlier). The increase and the decrease
impact polystyrene (HIPS) blends, it was found that of the shear modulus in the 0 to 3 wt% copolymer
the dynamic mechanical and thermal (DMTA) proper- concentration region is similar to that observed for
ties are sensitive to the presence of the copolymers in the tensile modulus in the same region (see Fig. 3).
the blends (23).The shape of the shear modulus as a DMTA can then be used to obtain the optimum
function of the copolymer concentration (mainly in copolymer concentration for the particular blend
the low temperature region) is interpreted in terms of HDPE/PS even with commercial copolymers. We
of the state of the copolymer in the blend and the should mention here, that it is not claimed that the
optimum copolymer concentration is associated with DMTA analysis will be effective for any immiscible
the interface saturation concentration of the copoly- polymer system. Several conditions such as a dif-
mer. The same analysis is performed here with the ference in the thermal expansion coefficient of the
HDPE/PS blends modified by the commercial copoly- components and a difference in their low temperature
mer (K-resin, KRO1). The results of the shear modu- modulus (both properties should be higher for
lus as a function of the copolymer concentration are the dispersed phase), are required for the analysis
reported in Fig. 6 for -100,0, and 80°C. It is clearly of the DMTA results.
seen from this Figure, and according to the interpre-
Effect of Operating Conditions
tation of the DMTA results (231,that the saturation
concentration for this particular system (HDPE/ PS/ The second objective of this study is to investigate
KRO l),is situated between 2 and 3 wt% of copolymer. the influence of processing conditions, during the
This result is of particular interest since it corre- injection molding process, on the mechanical proper-

I I El:NO-WELD
- 2.50 -
50
24 -
= ezd [;E9: WELD

40 - 2.00 -
20 -

-
30 - 1.50 - 16

12 -
20 - 1.00 -

. 8 -

10 - 0.50 -
4 -

0 -
1
0.00 - 0
2 3 1 2 3 1 2 3 1 2 3 1 2 3 1 2 3
KRO1 PS HDPE HDPEIPS HDPEIPSIKROl
20/80 20/80/3
IQg. 5. Comparison of the stress at break, the tensile modulus and the elongation at break of the homopolymers (HDPE and PSI, the
copolymer (KROl), the unrnodijied HDPE / PS ( 2 0 / 80) blend, and the modiJed HDPE / PS / KROl ( 2 0 /
80/ 3 ) blend, with or without weld line.

1206 POLYMER ENGINEERINGAND SCIENCE, MID-AUGUST 1994, Vol. 34 No. 15


Weld Lines and Mechanical Properties
9.2 I , , , , ,
. , . , . , . , . , . , . , .
HDPEIPSIKR01120/80 HDP€lQS1KR01120/0013 wt%

t 30

25

E
20 - 1
0-0
A-A :2200c1
:2 4 o o c

'b 1 5

8.01
0
t "
2 4
I ' "
6 8 10 $2 14 16
'
1
I
20 30 40 50 60 70 00 90 100
Copolymer content Iwt%)
Mold Temperature [OC)
Rg. 6. 7% dynamic storage modulus (E') as function of
copolymer content at &fferent temperatures. Rg. 7. combined effits of mo dl and melt temperatures
on the stress at break (a,,)
of welded specimens of a HDPE/
PS/KR01(20/80/ 3?6) blends.
ties of an immiscible blend. On the basis of the DMTA
and the tensile properties results of our system, a
composition of HDPE/PS/KRO1/20/80/3 wt% is
2.5 . , . , . , . ,. , . , . , .
HDP€IPSIKR01120/00/3wt%
chosen to study the effect of the mold and injection
(melt) temperatures. The following results deal only
with welded specimens. The effect of processing con-
ditions on the mechanical properties of nonwelded
specimens is not reported because the mechanical
2.0
- {/!-I
properties for this particular system were found to be
less sensitive to the processing conditions within the
considered range of parameters. i!
'u
1.5
- '1 0 - 0 : 200oc
A-A
0-0
: 220OC
:24OOC
The data of the stress at break (a,)as a function of -
1.0
mold temperature, for three different melt tempera-
tures, are shown in Fig. 7. A n appreciableincrease of
' b
-
4 /
A
the stress at break upon increasing the melt temper-
ature is observed. The most important raise is 0.5 - 0-0- P
observed when the melt temperature is increased
from 220 to 240°C. The results of Flg. 7 also show
that the effect of mold temperature is not as impor- 0.0.. ' . ' . ' ' ' . ' . ' '

tant as that of the melt temperature mainly at 200


and 220°C.
In Fig. 8,the data of the elongation at break ( E , ) as FSg. 8. Combined effectsof mo l and melt temperatures on
d
a function of mold temperature and melt temperature the elongation at break (en) of welded specimens of a HDPE/
are reported. The effect of both parameters is similar P S / K R O I (20.80/3%)blends.
to that observed for the stress at break reported in
Q. 7.
For the tensile modulus the results presented in fillmg) which depend on the transport properties
Fig. 9 show only a slight effect of the mold tempera- (thermal dasivity, viscosity) and also on the elastic
ture and an effect of melt temperature that is less properties of the material. In the case of semicrys-
important than that observed for a, and E,, (Figs.7 talline polymers, the injection parameters may affect
and 8). the crystallinity of the material and hence the
The interpretation of the effect of molding parame mechanical properties of the injected sample. In order
ters on the mechanical properties is not an obvious to have a quantitative interpretation of the effect of
task. Conclusions drawn for a given system can be molding conditions on the mechanical properties even
completely different for another system (27).The for the homopolymer systems, one should solve the
mechanical properties depend indeed on the frozen governing equations for the system. However, these
stresses (dynamic and thermal stresses due to the equations are coupled and highly nonlinear. They
nonisothermal cooling and relaxation after mold require sophisticated numerical methods even for

POLYMER ENW#EERMIO AND SCIENCE, MID-AUGUST 1994, Vol. 34, No. 15 1207
B. Brahimi, A. Ait-Kadi, and A. AJi
2.00 ’ , ’ , ‘ I ’ U ’ , . , . ,
.$
rlDPEIPSIKR0112018013wt% P
6’
d
6
J
1.75
-k
2
w

1.50

1.25
20 30 40 50 60 70 80 90 100
Mold Temperature I°C)
Fg. 9. Combined effects of mold and melt temperatures
on the tensile modulus (En)of welded specimens of a HDPE/
PS / KRO 1 ( 20/ 80/3%) blends.

f f
simple mold cavities (28-30). Moreover, to our knowl- Q
edge, there is no rheological models that can ade-
quately represent the response of a viscoelastic fluid
in all the situations experienced in injection molding
(entrance effects, elongational flows, nonisothermal
startup, and relaxation, etc.). In the case of immisci-
ble blends, the situation is even more complicated
since one must take into account minor phase
dimensions and deformation, interphase interac-
tions, surface tension which characterize these
blends. The rheological models developed for
these systems are based on emulsion models and are
only tractable in small deformation processes (linear
viscoelasticity) (31). However, the results obtained in
Figs. 7 to 10 can be qualitatively interpreted in terms
of interdiffusion of the polymer fronts. In fact, as the
melt temperature increases, the temperature of
the polymer at the meeting fronts is increased result-
ing in an enhanced interdiffusion of polymer at the
weld line due to the increase of the interdiffusion
coefficient (32, 33). The presence of the copolymer
which locates at the interface contributes to the in-
terdiffusion of the polymers at the weld line. The “V- f
notch” generally observed when weld lines are pre-
sent is less pronounced in the case of copolymer
modified blends as shown on the micrographs of Flg.
10. Moreover, it is also well known that the presence
of a copolymer in an immiscible blend reduces signifi- Ftg. 10. Scanning electron micrographs of weld line details:
cantly the dimension of the minor phase (22, 23). It A) unmodijied HDPE/PS (20/80) blend, B) modifid
can be seen from Fig. 1 1 that indeed the morphology HDPE/PS/KRO1(20/80/3)blend.
either with no weld and with weld lines is influenced
by the presence of the copolymer.
mer. It was observed that the optimum copolymer
CONCLUSION
concentration in the case of HDPE/PS/KROl system
The weakness induced by the presence of weld line corresponds to that obtained from the DMTA results
in an immiscible polymer blend can be significantly of this system. The tensile mechanical properties
improved by addition of small amounts of a copoly- (mainly the stress and the elongation at break) of

1208 POLYMER ENGINEERING AND SCIENCE, MID-AUGUST 1994, Vol. 34, NO. 15
Weld Lines and MechanicalProperfies

5 w-n 5 m

Fig. 1 1. Scanning electron micrographs offractured sections during tensile test of HDPE/ €5(20.80)blend: A) 0 WWO( no weld), B)
3 w% (no weld), C)0 w% (weld). D ) 3 WWO(weld).

blends modifled at 3 wt% of copolymer were found to 3. E.Hagerman, Plat. Eng., 67, (1973).
be sensitive to the injection temperature. The effect of 4. S. Y.Hobbs, Polyrn Eng. Sci, 14. 621 ( 1974).
mold temperature on these properties is less pro- 5. Z.Tadmore and C. G. Gogos, principles of Polymer Pro
cessing, p. 603,John Wiley, New York (1979).
nounced mainly at low injection temperatures. 6.P. Hubbauer, Plast. Eng., 37.(1973).
7. R J. Crawford and P. P. Benham. J. Mech Erg. Sci.. 16,
ACKNOWLEDGMENT 178 ( 1974).
The authors acknowledge the financial support 8. R M. Criens and H. G. MoslC, Polyrn Eng. Sci, 23. 591
provided by the Natural Sciences and Engineering (1983).
9.K. Tomari.S.Tonogai, T. Harada, H. Hamada, K. Lee,
Research Council of Canada and by the province of T. Morii, and 2. Maekawa, Polyrn Eng. S c L , 30, 931
QuCbec (Action structurante and FCAR programs). ( 1990).
We are also grateful to Dow Chemical Canada Inc. 10.R A Worth, Polyrn Erg. Sci, 20. 551 (1980).
and Phillips 66 for providing the raw materials used 11. S.C.Malguamera and A. Manisali, Polyrn Eng. Sci. 21,
in this work. 586 (1981).
12.S.C. Malguamera, A I. Manisali, and D. C. Riggs. Polyrn
REFERENCES Eng. Sci,21, 1149 (1981).
13.Scortec Inc., British Technology Group, Gulph Mills, Pa.
1. C. I. Chung. ?fans. N.Y. Acad Sci, p. 319 (1974). ( 1991).
2. U. W. Magdeburg, Kunststofle 78, 123 (1988). 14.R Pisfpati and D. G. Baird, in Polymer Processing and

POLYMER E # Q I " o AND SCENCE, MID-AUGUST 1994, V d . 34,NO. 15 1209


B. Brahimi, A. Ait-Kadi, and A. AJi
Properties, G . Astarita and L. Nicolais, eds.. Plenum 25. F. Lalande, SPE ANTEC Tech. Papers, 37,404 (1991).
Press, New York (1984). 26. M. Rahmani and B. Fisa, SPE ANTEC Tech. Papers, 37,
15. M. C. Schwarz, J. W. Barlow, and D. R. Paul, J . Appl. 400 (1991).
Polym Sci, 35,2053 (1988). 27. M. R Kamal, V. Tan, and M. E. Ryan, in Science and
16. K. Min and J. L. White, Polym Eng. Sci., 24, 1327 Technology of Polymer Processing, p. 34, N. P. Suh and N.
( 1984). H. Sung, eds., The MIT Press, Cambridge, Mass. (1977).
17. L. H. Wang and R S. Porter, J. Polym Sci, Polym Phys. 28. M. R Kamal and P. G. Lafleur. PoZym Eng. Sci. 22, 1066
Ed., 21, 1815 (1983). ( 1982).
18. C. D. Han, C . A Villamizar, a n d Y. W. Kim, J. Appl.
29. A I. Isayev and C . A. Hieber, RheoL Acta, 19. 168 (1980).
PoZyym Sci, 21, 353 (1977).
19. J. R Stell, D. R Paul, and J. W. Barlow, Polym Eng. Sci, 30. J. S. Yu, D. M. Kalyon, a n d A. H. Wagner, SPE ANTEC
16. 496 (1976). Tech Papers. 35,281 (1989).
20. U. Yilmazer, J. Appl. Polym Sci, 42, 2379 (1991). 31. J. F. Palierne, Rheol. Acta, 29, 204 (1990).
21. M. C. Schwarz, H. Keskkula, J. W. Barlow, and 32. W. W. Graessley, J. Polym Sci, PoZym Phys. Ed.. 18. 27
D. R Paul, J . AppL Polym Sci., 35. 653 (1988). ( 1980).
22. M. Xanthos, Polyym Eng. Sci, 28. 1392 (1988). 33. S. G. Kim and N. P. Suh, PoZym Eng. Sci.. 26, 1200
23. B. Brahimi. A. Ajji, A Ait-Kadi, a n d R Fayt, J. Polym (1986).
Sci, Phys. Eds., 29. 945 (1991).
24. B. Brahimi, A Ait-Kadi, and A. Ajji, SPE ANTEC Tech. Received December 10, 1992
Papers, 37. 1129 (1991).

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