scholarly journals Effect of Soil Burial on Tensile Properties of Polypropylene/Plasticized Cassava Starch Blends

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Henry C. Obasi ◽  
Isaac O. Igwe ◽  
Innocent C. Madufor

Polypropylene (PP)/plasticized cassava starch (PCS) blended with and without compatibilizer (polypropylene-graft-maleic anhydride (PP-g-MA)) via melt blending were prepared for soil burial which lasted for 90 days. Plasticized starch loadings of 0, 10, 20, 30, 40, and 50 wt.% were used, while pp-g-ma was used at 10 wt.% based on starch weight. The PP/PCS and PP/PCS/PP-G-MA blends were evaluated for their tensile properties. It was observed that the tensile strength, elongation at break, and young’s modulus decreased with increases in soil burial time as well as starch content for PP/PCS blends. Similar treads for the tensile properties were observed for PP/PCS/PP-g-MA, but with higher properties as compared to uncompatibilized blends. However, the tensile properties for both PP/PCS and PP/PCS/PP-g-Ma decrease with increases in starch loading and also as the burial period progressed.

2013 ◽  
Vol 747 ◽  
pp. 645-648 ◽  
Author(s):  
Koay Seong Chun ◽  
Salmah Husseinsyah ◽  
Hakimah Osman

Polypropylene/Cocoa Pod Husk (PP/CPH) biocomposites with different maleated polypropylene (MAPP) content were prepared via melt blending process using Brabender Plastrograph mixer. The tensile strength and tensile modulus of PP/CPH biocomposites increased with increasing of MAPP content. The PP/CPH biocomposites with 5 phr of MAPP showed the optimum improvement on tensile properties. However, the increased of MAPP content reduced the elongation at break of PP/CPH biocomposites. At 5 phr of MAPP content, PP/CPH biocomposites showed lowest elongation at break. Scanning electron microscope confirms the PP/CPH biocomposites with MAPP have better filler-matrix interaction and adhesion due to the effect of MAPP.


2018 ◽  
Vol 34 ◽  
pp. 01030 ◽  
Author(s):  
Indra Surya ◽  
Syahrul Fauzi Siregar ◽  
Hanafi Ismail

Effects of alkanolamide (ALK) addition on cure characteristics, swelling behaviour and tensile properties of silica-filled natural rubber (NR)/chloroprene rubber (CR) blends were investigated. The ALK was synthesized from Refined Bleached Deodorized Palm Stearin (RBDPS) and diethanolamine, and incorporated into the silica-filled NR/CR blends as a non-toxic rubber additive. The ALK loadings were 0.0, 1.0, 3.0, 5.0 and 7.0 phr. It was found that the ALK exhibited shorter scorch and cure times and higher elongation at break of the silica-filled NR/CR blends. The ALK also exhibited higher torque differences, tensile modulus and tensile strength at a 1.0 phr of ALK loading and then decreased with further increases in the ALK loading. The swelling measurement proved that the 1.0 phr loading of ALK caused the highest degree in crosslink density of the silica-filled NR/CR blends.


2012 ◽  
Vol 32 (6-7) ◽  
pp. 435-444 ◽  
Author(s):  
Hsin-Tzu Liao ◽  
Chin-San Wu

Abstract Melt blending of polylactide (PLA), poly(ε-caprolactone) (PCL), and wood flour (WF) was performed in an effort to overcome the major drawbacks (brittleness and high price) of PLA. In addition, the acrylic acid (AA)-grafted PLA70PCL30 (PLA70PCL30-g-AA) was used as the alternative for the preparation of ternary blends to improve the compatibility and the dispersability of WF within the PLA70PCL30 matrix. As expected, PCL improved the elongation at break and the toughness of PLA but decreased the tensile strength and modulus. Because the hydrophilic WF is dispersed physically in the hydrophobic PLA70PCL30 matrix, as the result of Fourier transform infrared analysis, the mechanical properties of PLA70PCL30 became noticeably worse when it was blended with WF. This problem was successfully conquered by using PLA70PCL30-g-AA to replace PLA70PCL30 due to the formation of an ester carbonyl group between PLA70PCL30-g-AA and WF. Furthermore, the PLA70PCL30-g-AA/WF blend provided a plateau tensile strength at break when the WF content was up to 50 wt%. PLA70PCL30/WF exhibited a tensile strength at break of approximately 3–25 MPa more than PLA70PCL30-g-AA/WF. By using p-cresol and tyrosinase, the enzymatic biodegradable test showed that PLA70PCL30-g-AA is somewhat more biodegradable than PLA70PCL30 because the former has better water absorption. After 16 weeks, the weight loss of the PLA70PCL30/WF (50 wt%) composite was >80%. PLA70PCL30-g-AA/WF exhibited a weight loss of approximately 1–12 wt% more than PLA70PCL30-g-AA/WF. It was also found that the addition of WF to PLA70PCL30 or PLA70PCL30-g-AA decreased the crystallinity of PLA and PCL in PLA70PCL30 or PLA70PCL30-g-AA and then increased their biodegradable property.


2013 ◽  
Vol 681 ◽  
pp. 256-259
Author(s):  
Xiu Qi Liu ◽  
He Qin Xing ◽  
Li Li Zhao ◽  
Dan Wang

In our study, a new kind of foam composite was prepared by melt blending with PVC as the matrix and carbon black (CB) as the filler, the standard-spline was made in the dumbbell system prototype. Tensile strength and elongation at break were measured at 25°C。When the CB was added greater than 2.0%, with the increase of CB added, the determination of sample mechanical index began to decline, when the CB content was greater than 9%, tensile strength and elongation at break of the composites remained basically unchanged.


2017 ◽  
Vol 26 (5) ◽  
pp. 096369351702600 ◽  
Author(s):  
Wenjing Xia ◽  
Nianqing Zhu ◽  
Zhongbin Ni ◽  
Mingqing Chen

Biodegradable composites from poly (butylene succinate-co-butylene adipate) (PBSA) and Taihu Lake (Wuxi, China) blue algae were prepared by melt blending. The property and structure of biocomposites were investigated. By adding extra amount of water to blue algae, the formulated blue algae acted as a plastic in the composites during blending, and exhibited a reinforcing effect on the PBSA matrix. With increasing blue algae content, the thermal stability of the composites decreased; the tensile strength at break and elongation at break of the composites reduced, but the Young's modulus of the composites increased. However, the composite with 30% blue algae loading still exhibited good mechanical performance (tensile strength at break of 21.3 MPa, elongation at break of 180%). The fabrication of value-added PBSA/algae composites appeared as an effective approach to reduce the secondary environmental pollution of Taihu blue algae.


2013 ◽  
Vol 411-414 ◽  
pp. 2993-2996
Author(s):  
Yu Pu Deng ◽  
Lin Xue Du ◽  
Xi Hong Li ◽  
Xia Liu ◽  
Hai Jiao Liu

The novel packaging was synthesised by coating polyvinyl chloride (PVC) film with Polyvinylamine/Polyvinyl alcohol (PVAm/PVA) mixture which can effectively inhibit the migration of DOP in this paper. The effect of PVAm/PVA mixture on inhibiting DOP migration was detected via extraction tests. The results showed that the novel packaging significantly reduced the migration rate of DOP compared with the control (PVC film). After 24h extracted by hexane 40% PVAm in mixture being coated on PVC had the lowest migration rate (6.20%) among the samples, while 7.60% is the migration rate of control sample. Tensile properties analysis indicated the elongation at break and tensile strength of samples coating PVAm/PVA higher than control sample. The thermogravimetric analysis demonstrated that the PVAm/PVA mixed solution can deduce thermogravimetric rate. Therefore, coating PVC with PVAm/PVA mixture is an effective approach to suppress the migration of DOP.


2017 ◽  
Vol 751 ◽  
pp. 230-235 ◽  
Author(s):  
Suchipha Wannaphatchaiyong ◽  
Prapaporn Boonme ◽  
Wiwat Pichayakorn

This study aimed to develop gelatin (GEL) and gelatin/Alpha starch (GEL/αSt) dissolving films as drug delivery by casting method. Because these films were brittle and lack of elasticity, therefore, glycerin (GLY), propylene glycol (PG) or polyethylene glycol 400 (PEG) in various amounts (5-30 part per hundred of gelatin; phg) was used as plasticizer. It was found that all types and amounts of plasticizer could be blended into gelatin solution and the transparent GEL films were formed, except the GEL/PEG films presented in opaque characteristics. However, 30 phg GLY blended film was too softy. Increasing amount of plasticizer caused a decrease in tensile strength and increase in elongation at break (EAB) of films. These GEL films swelled, dissolved and eroded in 2 hours. The αSt was also blended, and the effects of αSt amounts (5-30 phg) and plasticizer types (at 25 phg) on GEL film properties were studied. The αSt dispersions mixed well in gelatin solution and gave homogenous films. The swelling and erosion of GEL/αSt films in water were faster than those of GEL films. Increasing αSt amount prolonged the swelling time and decreased the degradation rate of GEL/αSt films. The tensile strength of GEL/αSt/GLY films slightly increased when the αSt amount increased but those of PEG and PG blended films were not different. The EAB of all plasticizer blended films decreased when the amount of αSt increased. Either lidociane or lidociane hydrochloride was mixed in GEL/αSt/GLY dissolving films to use as local anesthetic. The morphology, Fourier Transform Infrared Spectroscopy confirmed their compatibilities in these films, but Differential Scanning Calorimeter showed some changes that should be further evaluated.


2017 ◽  
Vol 50 (6) ◽  
pp. 491-500 ◽  
Author(s):  
Sajjad Daneshpayeh ◽  
Amir Tarighat ◽  
Faramarz Ashenai Ghasemi ◽  
Mohammad Sadegh Bagheri

The object of this work is to study and predict the tensile properties (tensile strength, elastic modulus, and elongation at break) of ternary nanocomposites based on epoxy/glass fiber/nanosilica using the fuzzy logic (FL). Two factors in three levels including glass fiber at 0, 5, and 10 wt% and nanosilica at 0, 0.5, and 1 wt% were chosen for adding to an epoxy matrix. From FL surfaces, it was found that the glass fiber content had a main role in the tensile properties of nanocomposites. The high levels of glass fiber content led to a significant increase in the elastic modulus and generally, the presence of glass fiber decreased the tensile strength and elongation at break. Also, addition of the nanosilica content resulted in an increased elastic modulus but decreased the elongation at break of nanocomposites. Finally, an FL model was obtained for each tensile property.


2015 ◽  
Vol 754-755 ◽  
pp. 161-165
Author(s):  
Nurul Fatin Syazwani binti Arshad ◽  
Salmah Husseinsyah ◽  
Lim Bee Ying

This research focused on the utilization of kapok husk (KH) as filler in low linear density polyethylene (LLDPE). The effect of filler content on tensile properties and morphology of LLDPE/KH eco-composites were investigated. The eco-composites were prepared by using Brabender Plasticiser EC Plus at temperature 160 °C and rotor speed 50 rpm. The results indicated that the tensile strength and elongation at break decreased with KH content increased. However, the modulus of elasticity increased with increasing of KH content. The morphology study of eco-composites exhibit poor interfacial adhesion between KH and LLDPE.


2008 ◽  
Vol 2008 ◽  
pp. 1-9 ◽  
Author(s):  
Joe-Lahai Sormana ◽  
Santanu Chattopadhyay ◽  
J. Carson Meredith

Nanocomposites based on segmented poly(urethane urea) were prepared by reacting a poly(diisocyanate) with diamine-modified Laponite-RD nanoparticles that served as a chain extender. The nanocomposites were prepared at a constantNH2to NCO mole ratio of 0.95, while varying the fraction of diamine-modified Laponite relative to the free diamine chain extender. Compared to neat poly(urethane urea), all nanocomposites showed increased tensile strength and elongation at break. As Laponite loading increased, tensile properties passed through a maximum at a particle concentration of 1 mass%, at which a 300% increase in tensile strength and 40% increase in elongation at break were observed. A maximum in urea and urethane hard-domain melting endotherms was also observed at this Laponite loading. Optimal mechanical and thermal properties coincided with a minimum in the size of the inorganic Laponite phase. Nanocomposites containing diamine-modified Laponite had higher tensile strengths than those with nonreactive monoamine-modified Laponite or diamine-modified Cloisite.


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