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Kneaders reactors are used for combined unitary processing in the polymer industry for devolatilization compounding or polymerization. Multiple feed ports are used in screw type reactors to allow adding multiple substrates into one product whereas one unitary operation has to get to a certain degree of completion before the next substrate can be added. We have found that even for identical substrates multiple feed ports can be advantageous to avoid specific working points where the product behavior is disadvantageous for efficient processing. Such processes require advanced design simulation tools to predict process behavior. We compare simulation results on pilot and the scale up.
Kneaders reactors are used for combined unitary
processing in the polymer industry for devolatilization,
compounding or polymerization. Multiple feed ports
are used in screw type reactors to allow adding
multiple substrates into one product whereas one
unitary operation has to get to a certain degree of
completion before the next substrate can be added. We
have found that even for identical substrates multiple
feed ports can be advantageous to avoid specific
working points, where the product behavior is
disadvantageous for efficient processing. Such
processes require advanced design simulation tools to
predict process behavior. We compare simulation
results on pilot and the scale up.
Shi-Qing Wang , P. E. Boukany , S. Ravindranath , Y. Y. Wang, May 2008
This presentation discusses the latest developments in
the field of nonlinear rheology of entangled polymeric
liquids resulting from nearly two dozens of publications
from the Polymer Dynamics Interface and Rheology
Group at Akron. The essential findings are that a)
entangled liquids respond to sudden startup flow
elastically and undergo cohesive failure or yielding before
subsequent flow is possible b) the flow field beyond the
yield point is dictated by the characteristics of the yielding
process that can be strongly inhomogeneous c) entangled
liquids possess finite cohesion that can be overcome after
flow cessation by internal elastic restoring forces.
Shi-Qing Wang , P. E. Boukany , S. Ravindranath , Y. Y. Wang, May 2008
This presentation discusses the latest developments in the field of nonlinear rheology of entangled polymeric liquids, resulting from nearly two dozens of publications from the Polymer Dynamics, Interface and Rheology Group at Akron. The essential findings are that a) entangled liquids respond to sudden startup flow elastically and undergo cohesive failure or yielding before subsequent flow is possible, b) the flow field beyond the yield point is dictated by the characteristics of the yielding process that can be strongly inhomogeneous, c) entangled liquids possess finite cohesion that can be overcome after flow cessation by internal elastic restoring forces.
Biopolymers are generally defined as polymers that are found in nature derived from nature or utilized as medical implants. Polymeric biomaterials which are utilized as medical implants are typically characterized for enduse performance as well as processability. While lactic acid is found in the human body polylactic acid is derived from natural resources and utilized as medical implants. This paper will utilize poly(lactic acid) as an example of a bioplastic where the morphological and isomeric structure has an influence on end-use properties such as mechanical properties biodegradability and biocompatibility.
Peel strength between layers in coextruded cast film is
found to increase with increasing post die process time.
The results suggest that adhesion is limited by the time and
temperature available for bonding after new interfacial area
is created during drawing. This contrasts with previous
work in blown film where increases in peel strength with
process time were attributed primarily to stress effects.
The results from both processes however were found to
collapse onto a single master curve by multiplying the peel
strength by the modulus of the tie resin and dividing the
process time by the relaxation time of the tie resin.
Peel strength between layers in coextruded cast film is found to increase with increasing post die process time.The results suggest that adhesion is limited by the time and temperature available for bonding after new interfacial area is created during drawing. This contrasts with previous work in blown film where increases in peel strength with process time were attributed primarily to stress effects.The results from both processes, however, were found to collapse onto a single master curve by multiplying the peel strength by the modulus of the tie resin and dividing the process time by the relaxation time of the tie resin.
Hassan Eslami , Miroslav Grmela , Mosto Bousmina, May 2008
Poly[butylenes succinate-co-adipate] (PBSA)
layered silicate nanocomposite was prepared by
melt extrusion of PBSA and organically
modified montmorillonite (OMMT).
Nanocomposites were prepared at a single clay
loading. Before taking rheological
measurements the nanocomposites were
characterized by X-ray diffraction (XRD) and
transmission electron microscopy (TEM). Stress
growth experiments were performed for both
pure polymer and nanocomposite. Flow reversal
experiments were conducted for
nanocomposites at different predetermined rest
time after cessation of forward flow. The
orientation state of silicate layers were also
investigated by cooling down the sample in the
rheometer before and after the forward flow and
then by performing X-ray in the transmission
mode.
Hassan Eslami , Miroslav Grmela , Mosto Bousmina, May 2008
Poly[butylenes succinate-co-adipate] (PBSA) layered silicate nanocomposite was prepared by melt extrusion of PBSA and organically modified montmorillonite (OMMT). Nanocomposites were prepared at a single clay loading. Before taking rheological measurements, the nanocomposites were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Stress growth experiments were performed for both pure polymer and nanocomposite. Flow reversal experiments were conducted for nanocomposites at different predetermined rest time after cessation of forward flow. The orientation state of silicate layers were also investigated by cooling down the sample in the rheometer before and after the forward flow and then by performing X-ray in the transmission mode.
Hydrotalcite anionic clays were reacted with
phosphonium ionic liquids containing different
anions. Montmorillonite cationic clays were also
reacted with the residual cation of the ILs after
modification of the anionic clay. The clays were
analyzed by FTIR thermal analysis EDX and X-ray
diffraction in order to determine the extent and type
of intercalation of the IL anions/cations at the clay
interlayers. The modified cationic and anionic clays
and their mixtures were then melt compounded with
polylactic acid and their effects on the thermal and
mechanical properties of the resulting micro- and
nano-composites were investigated.
Hydrotalcite anionic clays were reacted with phosphonium ionic liquids containing different anions. Montmorillonite cationic clays were also reacted with the residual cation of the ILs after modification of the anionic clay. The clays were analyzed by FTIR, thermal analysis, EDX and X-ray diffraction in order to determine the extent and type of intercalation of the IL anions/cations at the clay interlayers. The modified cationic and anionic clays and their mixtures were then melt compounded with polylactic acid and their effects on the thermal and mechanical properties of the resulting micro- and nano-composites were investigated.
The properties of polylactic acid (PLA) may be modified
by the addition of clays or the incorporation of ionic
liquids (IL). The effects of clays depend on degree of
polymer intercalation and the presence of clay
organomodifiers. Some ionic liquids act as plasticizers
and lubricants reducing glass transition temperature (Tg)
and melt viscosity the effects depending on the IL
structure and its polymer miscibility. This article
compares the effects of different cationic or anionic clays
and different ILs on the thermal hydrolytic and soil
degradation of PLA as measured by molecular weight
(MW) changes and relates to the structure of the additives
and their degree of dispersion/dissolution in the polymer
melt.
The properties of polylactic acid (PLA) may be modified by the addition of clays or the incorporation of ionic liquids (IL). The effects of clays depend on degree of polymer intercalation and the presence of clay organomodifiers. Some ionic liquids act as plasticizers and lubricants reducing glass transition temperature (Tg) and melt viscosity, the effects depending on the IL structure and its polymer miscibility. This article compares the effects of different cationic or anionic clays and different ILs on the thermal, hydrolytic and soil degradation of PLA as measured by molecular weight (MW) changes and relates to the structure of the additives and their degree of dispersion/dissolution in the polymer melt.
Multi wall carbon nanotubes (MWNT) range 1 3 & 5
wt% were used in the blend of poly (ether imide) and poly
(ether ether Ketone). Differential scanning calorimetry
(DSC) and dynamic mechanical thermal analysis (DMTA)
were used to investigate the changes in glass transition
temperature. The dynamic mechanical behavior of
polymer blends was found to be affected by the nanotubes
inclusion dispersion and interaction between the
compositions. At high filler inclusion nanotubes align
anisotropic during injection molding processing possibly
due to the high melt viscosity of the final composition.
Multi wall carbon nanotubes (MWNT) range 1, 3 & 5 wt% were used in the blend of poly (ether imide) and poly (ether ether Ketone). Differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) were used to investigate the changes in glass transition temperature. The dynamic mechanical behavior of polymer blends was found to be affected by the nanotubes inclusion, dispersion and interaction between the compositions. At high filler inclusion, nanotubes align anisotropic during injection molding processing possibly due to the high melt viscosity of the final composition.
B. O. Rhee , E. J. Lee , Y. J. Lee , H. P. Park , B. S. Cha, May 2008
Since the runner-valve system (RVS) was proposed
by the authors for the filling balance in multi-cavity
molds its balancing capability has been proved in many
experiments. However it is not practical to adjust the
valve manually during the molding process. Therefore
authors developed an automated RVS. A motorized
actuator with a small installation area was designed and
built. An experimental mold with 4 cavities was machined
and the actuators were installed. In order to reliably
determine the resin-arrival-time in the automated RVS a
new method based on the sigmoid function approximation
was developed and optimum sampling range was obtained
in terms of a characteristic time. The data processing
program for the approximation was designed by the
LabVIEW. This work is ongoing project so that
experiment using the automated RVS is going to be done.
B. O. Rhee , E. J. Lee , Y. J. Lee , H. P. Park , B. S. Cha, May 2008
Since the runner-valve system (RVS) was proposed by the authors for the filling balance in multi-cavity molds, its balancing capability has been proved in many experiments. However, it is not practical to adjust the valve manually during the molding process. Therefore, authors developed an automated RVS. A motorized actuator with a small installation area was designed and built. An experimental mold with 4 cavities was machined and the actuators were installed. In order to reliably determine the resin-arrival-time in the automated RVS, a new method based on the sigmoid function approximation was developed, and optimum sampling range was obtained in terms of a characteristic time. The data processing program for the approximation was designed by the LabVIEW. This work is ongoing project so that experiment using the automated RVS is going to be done.
Qingfeng Wu , Chul B. Park , Nanqiao Zhou, May 2008
Both batch and continuous foaming processes were
employed to prepare plastic foams from polypropylene
(PP) / polydimethylsiloxane (PDMS) blends. The
blends were batch foamed at different saturation
pressures using carbon dioxide (CO2) as the blowing
agent. Ultimately the blend foams exhibited better cell
morphologies and higher cell densities in comparison to
those prepared from PP alone. The increased solubility
of CO2 in PDMS made it as a CO2 reservoir to induce
more nucleation. It was also noted that the addition of
PDMS to the PP matrix generated a bi-cellular structure
i.e. very small cells in the larger cell walls. In the case
of extrusion foaming the addition of PDMS had a
pronounced effect on both the expansion ratio and the
cell density. At 5% CO2 content the maximum
expansion ratio of the blend foams increased to as much
as twenty-five-fold whereas the maximum expansion
ratio of neat PP was below 10-fold with the same die.
Qingfeng Wu , Chul B. Park , Nanqiao Zhou, May 2008
Both batch and continuous foaming processes were employed to prepare plastic foams from polypropylene (PP) / polydimethylsiloxane (PDMS) blends. The blends were batch foamed at different saturation pressures using carbon dioxide (CO2) as the blowing agent. Ultimately, the blend foams exhibited better cell morphologies and higher cell densities in comparison to those prepared from PP alone. The increased solubility of CO2 in PDMS made it as a CO2 reservoir to induce more nucleation. It was also noted that the addition of PDMS to the PP matrix generated a bi-cellular structure, i.e., very small cells in the larger cell walls. In the case of extrusion foaming, the addition of PDMS had a pronounced effect on both the expansion ratio and the cell density. At 5% CO2 content, the maximum expansion ratio of the blend foams increased to as much as twenty-five-fold whereas the maximum expansion ratio of neat PP was below 10-fold with the same die.
Chun Lee , William Podborny , Tim Schloemer, May 2008
Interlayer adhesion between tie and barrier layers in
blown and cast film plays a major role in determining the
performance of tie layer resins in barrier applications. In
general tie-layer adhesion increases and film clarity
decreases with increased maleic anhydride functionality
(MAF). The tie resin employed for this investigation
showed reduced adhesion to EVOH even with increased
MAF. Understanding such unusual behavior is an
important aspect of the structure of tie-layer resins to be
used in industrial barrier packaging applications. We
investigated structural factors of the tie resins using
rheological measurements. It was found that dynamic
shear rheological data does not provide useful information
to understand tie layer performance. However extensional
rheological data showed useful information to understand
tie resin performance. The strain-hardening behavior of
the tie-layer resin during the melt extensional process
plays a major role in determining the interfacial adhesion
between tie and EVOH layers and clarity regardless of a
given range of MAF levels.
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Any article that is cited in another manuscript or other work is required to use the correct reference style. Below is an example of the reference style for SPE articles:
Brown, H. L. and Jones, D. H. 2016, May.
"Insert title of paper here in quotes,"
ANTEC 2016 - Indianapolis, Indiana, USA May 23-25, 2016. [On-line].
Society of Plastics Engineers
Available: www.4spe.org.
Note: if there are more than three authors you may use the first author's name and et al. EG Brown, H. L. et al.