Waste cooking oils as processing aids for eco-sustainable elastomeric compounding

2021 ◽  
pp. 147776062110289
Author(s):  
Valeria Cherubini ◽  
Francesca Romana Lamastra ◽  
Mario Bragaglia ◽  
Francesca Nanni
Keyword(s):  
Mechanical Properties ◽  
Good Practice ◽  
Tensile Tests ◽  
Rheological Characterization ◽  
Mineral Oils ◽  
Waste Oils ◽  
Waste Cooking Oils ◽  
Cooking Oils ◽  
Kinetics Of ◽  
Processing Aids

This work focuses on the replacement of mineral oils with bio-based waste cooking oils in rubber compounding. Two different waste cooking oils from potatoes and chicken frying process were analyzed by means of chemical and rheological tests to evaluate the chemical composition, the oxidative stability and the viscosity. Waste oils have been introduced in elastomeric compounds as substitute for typical processing aids (i.e. lubricants). Cure kinetics of rubber compounds was studied by rheological characterization. Mechanical properties of vulcanized samples were determined by means of tensile tests, hardness tests and dynamic mechanical analysis. The waste oils showed a rheological behavior very similar to the mineral oils conventionally employed in rubber manufacturing leading to almost the same processability of the resulting compound. The waste oils did not significantly affect the vulcanization kinetics of the rubber compound, as expected for conventional lubricants. Waste cooking oils and mineral oil show analogous influence on mechanical properties of cured compounds. At increasing oil content, the elongation at break and the tensile strength increased whereas the values of Elastic Modulus at 100% strain, the Storage Modulus and Shore A Hardness decreased with respect to the oil-free sample. These results are very promising, confirming the possibility to replace the mineral oils, in a good practice of circular economy.

A Tribochemical Boost for Cu Based Lubricant Nano-Additive

2019 ◽  
Vol 813 ◽  
pp. 292-297 ◽  
Author(s):  
Maria Sarno ◽  
Adolfo Senatore ◽  
Domenico Spina ◽  
Waleed Ahmed Abdalglil Mustafa
Keyword(s):  
Scientific Community ◽  
Fine Chemicals ◽  
Tribochemical Reaction ◽  
Industrial Plants ◽  
Wet Chemistry ◽  
Waste Oils ◽  
Cooking Process ◽  
Waste Cooking Oils ◽  
Cooking Oils ◽  
By Products

Waste cooking oils (WCOs) are widely considered in the scientific community as potential energy vector or source for bio-lubricants. This is because of the opportunity deriving from recycling and the difficulties in disposing of waste oils. Indeed, industrial plants for WCOs treatment include bio-refineries (bio-diesel, bio-lubricants, fine chemicals...) or simple recovery systems: the former ones assume triglycerides transformation into other compounds, according to the specific commercial destination; in the latter, triglycerides are preserved and the WCO is purified from by-products, formed during cooking process, in order to sell to the market. In an era scarred by CO2 and petroleum dependency, biodegradable products, offer many advantages. In this scenario, nanostructured additives, which are pointed out as the step forward in lubricant technology, can exploit WCOs’ derivatives for compatibilization or as reactive components allowing improvements in nanolubricant fluids. This paper proposes a Cu nanoparticle-based additive, properly surface functionalized and prepared through a “wet chemistry” approach, to be involved in tribochemical reaction with epoxidized vegetable oil. The idea was to promote the formation of tribofilm under contact, exploiting energy generated during the movement.

PROCESSIBILITY OF WASTE TO WEALTH GREEN POLYMER WITH POLYETHYLENE BY INJECTION MOULDING

2015 ◽  
Vol 77 (32) ◽  
Author(s):  
Nurul Syamimi M. Salim ◽  
Anika Zafiah M. Rus
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
High Density Polyethylene ◽  
Tensile Strain ◽  
Molding Machine ◽  
Melt Mixing ◽  
Surface Fracture ◽  
Waste Cooking Oils ◽  
Cooking Oils ◽  
Green Polymer

Green polymer from waste cooking oils is successfully converted into high functionality of hydroxylated green monomer. The green monomer was used crosslinker and known as Green Polymer. Green Polymer is compounded with High-Density Polyethylene (HDPE) and Low-Density Polyethylene (LDPE). These wastes to wealth green polymer are successfully compounded with HDPE and LDPE by melt-mixing used an injection molding machine known as Pro-GreP. The effect of different ratio of compounding materials on the mechanical properties of Pro-GreP was studied by tensile test. Morphological of surface fracture with magnification 100x on Pro-GreP is revealed the homogenous characteristic with high compatibility properties. Finally, the presence of biopolymer provide biodegradable properties, but it also improves the mechanical properties. It can be showed that the tensile strength and tensile strain is decreased than the neat thermoplastic and they were found to decreased with the increasing of biopolymer compounds. However, LDPE are lower in tensile strength and tensile strain than HDPE.

Effects of Retained Austenite Stability on Mechanical Properties of High Strength TRIP Steel

2012 ◽  
Vol 602-604 ◽  
pp. 287-293
Author(s):  
Zhi Feng Li ◽  
Ren Yu Fu ◽  
Qing Shan Li
Keyword(s):  
Mechanical Properties ◽  
Trip Steel ◽  
Retained Austenite ◽  
Mechanical Stability ◽  
High Strength ◽  
Tensile Tests ◽  
Transformation Kinetics ◽  
Austenite Stability ◽  
Kinetics Of ◽  
Strength And Ductility

Mechanical stability of retained austenite and its effect on mechanical properties of high strength TRIP steel were studied by means of OM, SEM, TEM, XRD, and mechanical testing after various heat treatments. Results revealed that the film-type retained austenite located between bainite laths with high carbon content showed gradual martensitic transformation with strain, demonstrating a good TRIP effect. Samples annealed at 800°C and held at 420°C showed an optimum value of strength and ductility product up to 18381.2MPa%. Transformation kinetics of the retained austenite were evaluated through tensile tests and fitted by the function y=0.86-0.86×exp(-Ax). The fitting results were good.

scholarly journals Preparation of Cellulose/Chitin Blend Materials and Influence of Their Properties on Sorption of Heavy Metals

2021 ◽  
Vol 13 (11) ◽  
pp. 6460
Author(s):  
Dao Zhou ◽  
Hongyu Wang ◽  
Shenglian Guo
Keyword(s):  
Mechanical Properties ◽  
Heavy Metals ◽  
Water System ◽  
Tensile Tests ◽  
Atomic Absorption Spectrophotometry ◽  
Scanning Electron Micrographs ◽  
Mesh Structure ◽  
Chitin Content ◽  
Sorption Ability ◽  
Kinetics Of

A series of biodegradable cellulose/chitin materials (beads and membranes) were successfully prepared by mixing cellulose with chitin in an NaOH/thiourea–water system and coagulation in a H2SO4 solution. The effects of chitin content on the materials’ mechanical properties, morphology, structure, and sorption ability for heavy metal ions (Pb2+, Cd2+, and Cu2+) were studied by tensile tests, scanning electron micrographs, Fourier transform infrared spectroscopy, and atomic absorption spectrophotometry. The results revealed that the cellulose/chitin blends exhibited relatively good mechanical properties, a homogeneous, microporous mesh structure, and the existence of strong hydrogen bonds between molecules of cellulose and chitin when the chitin content was less than 30 wt%, which indicated a good compatibility of the cellulose/chitin materials. Furthermore, in the same chitin content range, Pb2+, Cd2+, and Cu2+ can be adsorbed efficiently onto the cellulose/chitin beads at pH0 = 5, and the sorption capacity of the beads is more than that of chitin flakes. This shows that the hydrophilicity and microporous mesh structure of the blends are favorable for the kinetics of sorption. Preparation of environmentally friendly cellulose/chitin blend materials provides a simple and economical way to remove and recover heavy metals, showing a potential application of chitin as a functional material.

Elaboration and Characterization of the Properties of Refractory Cr Base Alloys

2010 ◽  
Vol 72 ◽  
pp. 46-52 ◽  
Author(s):  
Laurent Royer ◽  
Stéphane Mathieu ◽  
Christophe Liebaut ◽  
Pierre Steinmetz
Keyword(s):  
Mechanical Properties ◽  
Melting Point ◽  
Molten Glass ◽  
Energy Production ◽  
Creep Properties ◽  
Refractory Alloys ◽  
Industrial Use ◽  
Kinetics Of ◽  
Selection Of

For energy production and also for the glass industry, finding new refractory alloys which could permit to increase the process temperatures to 1200°C or more is a permanent challenge. Chromium base alloys can be good candidates, considering the melting point of Cr itself, and also its low corrosion rate in molten glass. Two families of alloys have been studied for this purpose, Cr-Mo-W and Cr-Ta-X alloys (X= Mo, Si..). A finer selection of compositions has been done, to optimize their chemical and mechanical properties. Kinetics of HT oxidation by air, of corrosion by molten glass and also creep properties of several alloys have been measured up to 1250°C. The results obtained with the best alloys (Cr-Ta base) give positive indications as regards the possibility of their industrial use.

scholarly journals Influence of Treated Distillate Aromatic Extract (TDAE) Content and Addition Time on Rubber-Filler Interactions in Silica Filled SBR/BR Blends

Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 698
Author(s):  
Selin Sökmen ◽  
Katja Oßwald ◽  
Katrin Reincke ◽  
Sybill Ilisch
Keyword(s):  
Mechanical Properties ◽  
Oil Content ◽  
Tensile Modulus ◽  
Mechanical Analysis ◽  
Styrene Butadiene Rubber ◽  
Butadiene Rubber ◽  
Binary Blends ◽  
Rubber Layer ◽  
Processing Aids ◽  
Rubber Filler

High compatibility and good rubber–filler interactions are required in order to obtain high quality products. Rubber–filler and filler–filler interactions can be influenced by various material factors, such as the presence of processing aids. Although different processing aids, especially the plasticizers, and their effects on compatibility have been investigated in the literature, their influence on rubber–filler interactions in highly active filler reinforced mixtures is not explicit and has not been investigated in depth. For this purpose, the influence of treated distillate aromatic extract (TDAE) oil content and its addition time on interactions between silica and rubber chains were investigated in this study. Rubber–filler and filler–filler interactions of uncured and cured silica-filled SBR/BR blends were characterized by using rubber layer L concept and dynamic mechanical analysis, whereas mechanical properties were studied by tensile test and Shore A hardness. Five parts per hundred rubber (phr) TDAE addition at 0, 1.5, and 3 min of mixing were characterized to investigate the influence of TDAE addition time on rubber–filler interactions. It was observed that addition time of TDAE can influence the development of bounded rubber structure and the interfacial interactions, especially at short time of mixing, less than 5 min. Oil addition with silica at 1.5 min of mixing resulted in fast rubber layer development and a small reduction in storage shear modulus of uncured blends. The influence of oil content on rubber–filler and filler–filler interactions were investigated for the binary blends without oil, with 5 and 20 phr TDAE content. The addition of 5 phr oil resulted in a slight increase in rubber layer and 0.05 MPa reduction in Payne effect of uncured blends. The storage tensile modulus of vulcanizates at small strains decreased from 13.97 to 8.28 MPa after oil addition. Twenty parts per hundred rubber (phr) oil addition to binary blends caused rubber layer L to decrease from 0.45 to 0.42. The storage tensile modulus of the vulcanizates and its reduction with higher amplitudes were incontrovertibly high among the vulcanizates with lower oil content, which were 13.57 and 4.49 MPa, respectively. When any consequential change in mechanical properties of styrene–butadiene rubber (SBR)/butadiene rubber (BR) blends could not be observed at different TDAE addition time, increasing amount of oil in blends enhanced elongation at break, and decreased Shore A hardness and tensile strength.

On the use of Ozawa/Flynn/Wall method to determine aging activation energy for elastomers

2021 ◽  
pp. 009524432110203
Author(s):  
Sudhir Bafna
Keyword(s):  
Mechanical Properties ◽  
Activation Energy ◽  
Weight Loss ◽  
Oxygen Consumption ◽  
Dwell Time ◽  
Room Temperature ◽  
Elevated Temperatures ◽  
Degradation Mechanism ◽  
Kinetics Of ◽  
Wall Method

It is often necessary to assess the effect of aging at room temperature over years/decades for hardware containing elastomeric components such as oring seals or shock isolators. In order to determine this effect, accelerated oven aging at elevated temperatures is pursued. When doing so, it is vital that the degradation mechanism still be representative of that prevalent at room temperature. This places an upper limit on the elevated oven temperature, which in turn, increases the dwell time in the oven. As a result, the oven dwell time can run into months, if not years, something that is not realistically feasible due to resource/schedule constraints in industry. Measuring activation energy (Ea) of elastomer aging by test methods such as tensile strength or elongation, compression set, modulus, oxygen consumption, etc. is expensive and time consuming. Use of kinetics of weight loss by ThermoGravimetric Analysis (TGA) using the Ozawa/Flynn/Wall method per ASTM E1641 is an attractive option (especially due to the availability of commercial instrumentation with software to make the required measurements and calculations) and is widely used. There is no fundamental scientific reason why the kinetics of weight loss at elevated temperatures should correlate to the kinetics of loss of mechanical properties over years/decades at room temperature. Ea obtained by high temperature weight loss is almost always significantly higher than that obtained by measurements of mechanical properties or oxygen consumption over extended periods at much lower temperatures. In this paper, data on five different elastomer types (butyl, nitrile, EPDM, polychloroprene and fluorocarbon) are presented to prove that point. Thus, use of Ea determined by weight loss by TGA tends to give unrealistically high values, which in turn, will lead to incorrectly high predictions of storage life at room temperature.

scholarly journals Synthesis, Properties, and Biodegradability of Thermoplastic Elastomers Made from 2-Methyl-1,3-propanediol, Glutaric Acid and Lactide

Life ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 43
Author(s):  
Lamya Zahir ◽  
Takumitsu Kida ◽  
Ryo Tanaka ◽  
Yuushou Nakayama ◽  
Takeshi Shiono ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Glutaric Acid ◽  
Triblock Copolymers ◽  
Tensile Tests ◽  
Thermoplastic Elastomers ◽  
Proteinase K ◽  
Synthesis Properties

An innovative type of biodegradable thermoplastic elastomers with improved mechanical properties from very common and potentially renewable sources, poly(L-lactide)-b-poly(2-methyl-1,3-propylene glutarate)-b-poly(L-lactide) (PLA-b-PMPG-b-PLA)s, has been developed for the first time. PLA-b-PMPG-b-PLAs were synthesized by polycondensation of 2-methyl-1,3-propanediol and glutaric acid and successive ring-opening polymerization of L-lactide, where PMPG is an amorphous central block with low glass transition temperature and PLA is hard semicrystalline terminal blocks. The copolymers showed glass transition temperature at lower than −40 °C and melting temperature at 130–152 °C. The tensile tests of these copolymers were also performed to evaluate their mechanical properties. The degradation of the copolymers and PMPG by enzymes proteinase K and lipase PS were investigated. Microbial biodegradation in seawater was also performed at 27 °C. The triblock copolymers and PMPG homopolymer were found to show 9–15% biodegradation within 28 days, representing their relatively high biodegradability in seawater. The macromolecular structure of the triblock copolymers of PLA and PMPG can be controlled to tune their mechanical and biodegradation properties, demonstrating their potential use in various applications.

Comprehensive study on mechanical properties of coated biaxial warp-knitted fabrics

2021 ◽  
pp. 073168442110204
Author(s):  
Bin Yang ◽  
Yingying Shang ◽  
Zeliang Yu ◽  
Minger Wu ◽  
Youji Tao ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Failure Modes ◽  
Least Squares Method ◽  
Tensile Tests ◽  
Tensile Creep ◽  
Base Layer ◽  
Sustained Load ◽  
Uniaxial Tensile ◽  
Membrane Structures ◽  
Knitted Fabrics

In recent years, coated fabrics have become the major material used in membrane structures. Due to the special structure of base layer and mechanical properties, coated biaxial warp-knitted fabrics are increasingly applied in pneumatic structures. In this article, the mechanical properties of coated biaxial warp-knitted fabrics are investigated comprehensively. First, off-axial tensile tests are carried out in seven in-plane directions: 0°, 15°, 30°, 45°, 60°, 75°, and 90°. Based on the stress–strain relationship, tensile strengths are obtained and failure modes are studied. The adaptability of Tsai–Hill criterion is analyzed. Then, the uniaxial tensile creep test is performed under 24-h sustained load and the creep elongation is calculated. Besides, tearing strengths in warp and weft directions are obtained by tearing tests. Finally, the biaxial tensile tests under five different load ratios of 1:1, 2:1, 1:2, 1:0, and 0:1 are carried out, and the elastic constants and Poisson’s ratio are calculated using the least squares method based on linear orthotropic assumption. Moreover, biaxial specimens under four load ratios of 3:1, 1:3, 5:1, and 1:5 are further tensile tested to verify the adaptability of linear orthotropic model. These experimental data offer a deeper and comprehensive understanding of mechanical properties of coated biaxial warp-knitted fabrics and could be conveniently adopted in structural design.

scholarly journals Influence of Hydrostatic Extrusion on the Mechanical Properties of the Model Al-Mg Alloys

2021 ◽  
Author(s):  
Aleksandra Towarek ◽  
Wojciech Jurczak ◽  
Joanna Zdunek ◽  
Mariusz Kulczyk ◽  
Jarosław Mizera
Keyword(s):  
Mechanical Properties ◽  
Plastic Deformation ◽  
Tensile Strength ◽  
Microstructural Analysis ◽  
Tensile Tests ◽  
Hydrostatic Extrusion ◽  
Microstructure Formation ◽  
Initial State ◽  
Degree Of Deformation ◽  
Al Mg Alloys

AbstractTwo model aluminium-magnesium alloys, containing 3 and 7.5 wt.% of Mg, were subjected to plastic deformation by means of hydrostatic extrusion (HE). Two degrees of deformation were imposed by two subsequent reductions of the diameter. Microstructural analysis and tensile tests of the materials in the initial state and after deformation were performed. For both materials, HE extrusion resulted in the deformation of the microstructure—formation of the un-equilibrium grain boundaries and partition of the grains. What is more, HE resulted in a significant increase of tensile strength and decrease of the elongation, mostly after the first degree of deformation.

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