scholarly journals RECENT ADVANCEMENTS IN RUBBER NANOCOMPOSITES

2014 ◽  
Vol 87 (3) ◽  
pp. 417-442 ◽  
Author(s):  
Maurizio Galimberti ◽  
Valeria Cipolletti ◽  
Sara Musto ◽  
Serena Cioppa ◽  
Giulia Peli ◽  
...  
Keyword(s):  
Interlayer Space ◽  
Interfacial Area ◽  
Melt Blending ◽  
Hybrid Filler ◽  
Initial Modulus ◽  
Organically Modified ◽  
The Matrix ◽  
Rubber Nanocomposites ◽  
Matrix Modulus ◽  
Low Crystalline

ABSTRACT Nanocomposites were prepared via melt blending, based on organically modified clays (OC), carbon nanotubes (CNT), and graphitic nanofillers made by a few layers of graphene (nanoG). In particular, nanocomposites based on a hybrid filler system, with a nanostructured filler such as carbon black (CB), are examined. It is shown that low crystalline order in the interlayer space of a layered nanofiller (such as OC and nanoG) leads to easier delamination. Nanofillers give rise to filler networking at low concentration, particularly in the presence of CB. Hybrid filler systems lead to nanocomposites' having initial moduli that are much higher than those calculated through the sum of the initial modulus of composites containing either only CB or only the nanofiller. Nanofillers enhance the matrix modulus by a multiplication factor that depends only on the nanofiller type and content, regardless of whether the matrix is a neat or a CB-filled polymer. Furthermore, the filler–polymer interfacial area is shown to be a parameter able to correlate the mechanical behavior of both nano-CNT and nanostructured (CB) fillers. By plotting values of the composite initial modulus versus the filler–polymer interfacial area, points due to CB, CNT, and the hybrid CB-CNT system lie on the same curve.

Effect of carbon nanotubes decorated with silver nanoparticles as hybrid filler on properties of natural rubber nanocomposites

2018 ◽  
Vol 136 (13) ◽  
pp. 47281 ◽  
Author(s):  
Apinya Krainoi ◽  
Claudia Kummerlöwe ◽  
Norbert Vennemann ◽  
Yeampon Nakaramontri ◽  
Skulrat Pichaiyut ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Silver Nanoparticles ◽  
Natural Rubber ◽  
Hybrid Filler ◽  
Rubber Nanocomposites

Characterization of Layered Double Hydroxide Modified with Sodium Dodecyl Sulfate and its Dispersion in Polyethylene

2013 ◽  
Vol 591 ◽  
pp. 138-141
Author(s):  
Zhi Dong Han ◽  
Xin Ke Zhang ◽  
Yue Wang ◽  
Zheng Quan Jiang ◽  
Peng Wang
Keyword(s):  
Sodium Dodecyl Sulfate ◽  
Layered Double Hydroxide ◽  
Sodium Dodecyl ◽  
Melt Blending ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Dodecyl Sulfate ◽  
The Matrix ◽  
Mixing Method ◽  
Double Hydroxide

Mg-Al layered double hydroxide (LDH) was modified with sodium dodecyl sulfate (SDS) by regeneration method. The structure of modified LDH (SDS-LDH) was investigated by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The composites of SDS-LDH and polyethylene (PE) were prepared by melt blending and solution mixing method with maleated PE (PEgMA) as compatibilizer. The structure of the composites and the dispersion of SDS-LDH in the matrix were investigated by XRD and transmission electron microscopy (TEM), respectively. The results reveal that SDS was successfully intercalated into the interlayer space of LDH. SDS-LDH was hardly exfoliated in PE/PEgMA by melt blending. The nanocomposites of PE/(PEgMA/SDS-LDH) were successfully prepared by melt blending PE with SDS-LDH/PEgMA master-batch obtained by solution mixing. Homogeneous dispersion of SDS-LDH in the matrix was observed by TEM.

Studies on the Mechanical Properties of Foam CB-PVC Composite

2013 ◽  
Vol 681 ◽  
pp. 256-259
Author(s):  
Xiu Qi Liu ◽  
He Qin Xing ◽  
Li Li Zhao ◽  
Dan Wang
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Mechanical Index ◽  
Melt Blending ◽  
Elongation At Break ◽  
Foam Composite ◽  
The Matrix ◽  
System Prototype ◽  
Made In

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.

Optimisation of the ceramic-like body for ceramifiable EVA-based composites

2017 ◽  
Vol 24 (4) ◽  
pp. 599-607 ◽  
Author(s):  
Xinhao Gong ◽  
Tingwei Wang
Keyword(s):  
Ceramic Body ◽  
Ethylene Vinyl Acetate ◽  
Melt Blending ◽  
Red Phosphorus ◽  
X Ray Diffraction ◽  
Modified Montmorillonite ◽  
Organically Modified Montmorillonite ◽  
Organically Modified ◽  
Dense Ceramic ◽  
Acetate Copolymer

AbstractVarious ceramifiable ethylene-vinyl acetate copolymer (EVA) composites were prepared by melt blending with two kinds of glass frits, organically modified montmorillonite (OMMT) and whitened and capsulised red phosphorus (WCRP). The influence of different filler components and firing temperatures on the ceramifiable properties of the composites was studied. The dripping behaviour of the composites was analyzed by a vertical burning test. The microstructure of the residues was characterised by X-ray diffraction (XRD) and scanning electron microscopy. The results showed that the optimised EVA composite was free of melt dripping during burning with the addition of OMMT. A dimensionally stable and dense ceramic residue was also obtained, especially with the addition of WCRP. It was suggested that new phases were formed at firing temperatures, and WCRP could promote the formation of ceramic body which was not fused during firing at 900°C as evidenced by XRD.

The synthesis of organically modified layered double hydroxide and its effect on the structure and physical properties of low-density polyethylene/ethylene–vinyl acetate blends

2019 ◽  
Vol 27 (5) ◽  
pp. 287-298
Author(s):  
Xincheng Guo ◽  
Mengqi Tang ◽  
Na Wang ◽  
Lingtong Li ◽  
Yifan Wu ◽  
...  
Keyword(s):  
Vinyl Acetate ◽  
Layered Double Hydroxide ◽  
Organic Anion ◽  
Ethylene Vinyl Acetate ◽  
Degree Of Crystallinity ◽  
Low Density Polyethylene ◽  
Low Density ◽  
Organically Modified ◽  
The Matrix ◽  
Double Hydroxide

Organically modified layered double hydroxide (OM-LDH) was synthesized via anion exchange reaction and potassium monolauryl phosphate (MAPK) was used as an intercalator. The OM-LDH nanofillers were embedded into low-density polyethylene/ethylene–vinyl acetate (LDPE/EVA) via melt blending process which provided LDPE/EVA/OM-LDH nanocomposites. The structure and properties of the fabricated samples were characterized through Fourier transform infrared spectroscopy, X-ray diffraction techniques, scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry, and tensile testing. The results showed that the organic anion was intercalated into the interlayer region of LDH and enlarged the interlayer distance. The TGA results of the nanocomposites showed significantly improved thermal stability at a higher temperature when containing 6 wt% OM-LDH due to the good dispersion of OM-LDH in the matrix. The DSC data indicated that the degree of crystallinity was increased obviously due to the incorporation of OM-LDH in the matrix. The formation of organic side chains on the OM-LDH surface also contributed to an improvement in the interfacial adhesion, resulting in enhanced tensile strength and elongation at break compared with LDH.

scholarly journals Controlled Release of Agrochemicals Intercalated into Montmorillonite Interlayer Space

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Harrison Wanyika
Keyword(s):  
Fourier Transform ◽  
Controlled Release ◽  
Interlayer Space ◽  
Rotary Evaporation ◽  
Surface Areas ◽  
Space Reduction ◽  
Immersion Technique ◽  
The Matrix ◽  
The Fourier Transform ◽  
Mmt Clay

Periodic application of agrochemicals has led to high cost of production and serious environmental pollution. In this study, the ability of montmorillonite (MMT) clay to act as a controlled release carrier for model agrochemical molecules has been investigated. Urea was loaded into MMT by a simple immersion technique while loading of metalaxyl was achieved by a rotary evaporation method. The successful incorporation of the agrochemicals into the interlayer space of MMT was confirmed by several techniques, such as, significant expansion of the interlayer space, reduction of Barrett-Joyner-Halenda (BJH) pore volumes and Brunauer-Emmett-Teller (BET) surface areas, and appearance of urea and metalaxyl characteristic bands on the Fourier-transform infrared spectra of the urea loaded montmorillonite (UMMT) and metalaxyl loaded montmorillonite (RMMT) complexes. Controlled release of the trapped molecules from the matrix was done in water and in the soil. The results reveal slow and sustained release behaviour for UMMT for a period of 10 days in soil. For a period of 30 days, MMT delayed the release of metalaxyl in soil by more than 6 times. It is evident that MMT could be used to improve the efficiency of urea and metalaxyl delivery in the soil.

scholarly journals Translation of a Coated Rigid Spherical Inclusion in an Elastic Matrix: Exact Solution, and Implications for Mechanobiology

2019 ◽  
Vol 86 (5) ◽  
Author(s):  
Xin Chen ◽  
Moxiao Li ◽  
Shaobao Liu ◽  
Fusheng Liu ◽  
Guy M. Genin ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Exact Solution ◽  
Analytical Solution ◽  
Spherical Inclusion ◽  
Matrix Material ◽  
Elastic Matrix ◽  
Protein Ligands ◽  
First Case ◽  
The Matrix ◽  
Matrix Modulus

The displacement of relatively rigid beads within a relatively compliant, elastic matrix can be used to measure the mechanical properties of the matrix. For example, in mechanobiological studies, magnetic or reflective beads can be displaced with a known external force to estimate the matrix modulus. Although such beads are generally rigid compared to the matrix, the material surrounding the beads typically differs from the matrix in one or two ways. The first case, as is common in mechanobiological experimentation, is the situation in which the bead must be coated with materials such as protein ligands that enable adhesion to the matrix. These layers typically differ in stiffness relative to the matrix material. The second case, common for uncoated beads, is the situation in which the beads disrupt the structure of the hydrogel or polymer, leading to a region of enhanced or reduced stiffness in the neighborhood of the bead. To address both cases, we developed the first analytical solution of the problem of translation of a coated, rigid spherical inclusion displaced within an isotropic elastic matrix by a remotely applied force. The solution is applicable to cases of arbitrary coating stiffness and size of the coating. We conclude by discussing applications of the solution to mechanobiology.

Tuning of HDPE Properties for 3D Printing

2018 ◽  
Vol 773 ◽  
pp. 67-71 ◽  
Author(s):  
Paweesinee Chatkunakasem ◽  
Panisa Luangjuntawong ◽  
Aphiwat Pongwisuthiruchte ◽  
Chuanchom Aumnate ◽  
Pranut Potiyaraj
Keyword(s):  
3D Printing ◽  
Melt Flow Index ◽  
Flow Index ◽  
Melt Blending ◽  
X Ray Diffraction ◽  
Screw Extruder ◽  
Scanning Calorimetry ◽  
Crystalline Polymers ◽  
Twin Screw ◽  
Low Crystalline

The objective of this study is to improve high density polyethylene (HDPE) properties for 3D printing by addition of graphene and low density polyethylene (LDPE). Graphene was prepared by modified Hummer’s method. The prepared graphene was characterized by the infrared spectroscopy and the X-ray diffraction analysis (XRD). Graphene/HDPE and LDPE/HDPE composites were successfully prepared through the melt-blending technique using a twin-screw extruder. The melt flow index (MFI) and differential scanning calorimetry (DSC) were employed to characterize neat HDPE and the modified HDPE. FTIR and XRD results show that graphite was successfully changed into graphene completely and MFI of graphene/HDPE and LDPE/HDPE decreased as the amount of graphene and LDPE in the composite blends increased. DSC results show that the addition of low crystalline polymers can reduce a crystallization temperature and crystallinity content.

Sign in / Sign up

Export Citation Format

Share Document