A Practical Manner To GTR Recycling in Waste HDPE/ABS

Waste high-density polyethylene (w-HDPE)/ acrylonitrile-butadiene-styrene (ABS)/ground tire rubber (GTR) have been melt blended by two-roll milling. Ternary blends of w-HDPE/ABS/GTR have been observed to be incompatible in the composition range studied which revealed in the deteriorated mechanical properties. Two main types of compatibilizers such as an olefin-maleic anhydride copolymer based one synthesized by the authors and a commercial maleic anhydride grafted polypropylene (MA-g-PP) have been chosen for enhancing compatibility between the components ergo the mechanical properties. For characterizing tensile and impact properties of the blends mechanical tests have been carried out besides the scanning electron microscopy (SEM), X-ray diffraction and Fourier transform infrared spectroscopy. The most advantageous result in industrial practice can be that the experimental additive allows to apply higher GTR concentration ergo gives the opportunity to recycle higher level of GTR.

Enhancement of the Processability and Properties of Nylon 6 by Blending with Polyketone

Polyketones (PKs) having strong hydrogen bonding properties and a chain extender are used as additives in the melt processing of nylon 6 (PA6). Their effect on the chain structure and properties of PA6 is studied to enhance the processability of PA6 in melt processing. The addition of the chain extender to PA6 increases the melt viscosity by forming branches on the backbone. The addition of PKs results in an additional increase in viscosity through the hydrogen bonding between N–H of PA6 and C=O of PK. The change in the N–H bond FT-IR peak of PA6 and the swelling data of the PA6/PK blend containing a chain extender, styrene maleic anhydride copolymer (ADR), suggest that incorporation of chain extender and PK in the melt processing of PA6 results in physical crosslinks through hydrogen bonding between the branched PA6 formed by the addition of chain extender and PK chains. This change in the chain structure of PA6 not only increases the melt strength of PA6 but also increases randomness resulting in decreased crystallinity.

Synthesis and characterization of alkyl-methacrylate-maleic anhydride copolymer for use as a biodiesel flow improver

Methacrylic acid was esterified with four alcohols: 1-decanol, 1-dodecanol, 1-tetradecanol, and 1-cetanol. Afterwards, the obtained monomers were copolymerized with maleic anhydride. The synthesized monomers and copolymers were characterized by 1H-NMR (Nuclear magnetic resonance) and Fourier transform infrared (FTIR) spectroscopy. The ability of the obtained copolymers to reduce the pour point of waste cooking oil-based biodiesel was investigated. The results showed that the polymer additive with the alkyl chain C14H29- demonstrated the best flow improvement performance. At a concentration of 1000 ppm, this polymer additive reduced the pour point of waste cooking oil-based biodiesel from 12 to 5oC.In this study,the effect of alkyl chain length, molecular weight, as well as the concentration of the additives on the pour point of biodiesel was also discussed.

Carboxylated bleached kraft pulp from maleic anhydride copolymers

Seven copolymers of maleic anhydride were hydrolyzed and impregnated into sheets of bleached softwood kraft pulps to enhance market pulp properties. Drying the impregnated pulps at 120 °C for 10 minutes, attached to the fiber surfaces up 0.16 meq of carboxyl groups per gram of dry pulp. Heating the impregnated pulps regenerates succinic anhydride moieties which can then form stable ester linkages with cellulosic hydroxyls. The pH of the impregnation solution is important. Impregnation with solutions at pH 8 gave polymer contents without repulping issues. By contrast, impregnation at pH 4 gave dried pulp sheets that were too strong to enable repulping in a paper mill. Although most of the seven copolymers were fixed to cellulose, poly(ethylene-alt-maleic anhydride) gave the highest density of carboxyl groups. The simplicity of waterborne polymers and mild drying temperatures suggests maleic anhydride copolymer treatment could be implemented in a conventional market pulp mill.

Enhancing properties of PC/PA blends via compatibilization of olefin-maleic-anhydride copolymer based additives in masterbatch form

Polymer blending has been a simple and efficient way for designing and controlling the performance of polymeric materials using easily available types. Both polycarbonate and polyamide have excellent mechanical properties and thermal stability but their disadvantages such as limited chemical or water resistance can be eliminate by tailoring them. Main difficulties in processing of PC/PA blends are the poor compatibility and high moisture adsorption capacity of the two raw materials complicating processing and also deteriorating mechanical properties of the products. Compatibilizing additives such as olefin-maleic-anhydride copolymer based compounds used in the experimental work can help to overcome the abovementioned difficulties. To determine the processing conditions of the raw materials several drying temperatures have been tested and thermal degradation has been examined by FT-IR spectroscopy. Experimental compatibilizing additives based on an olefin-maleic-anhydride copolymer have been investigated to enhance mechanical properties of the blends prepared by extrusion moulding. Mechanical, rheological, SEM and FT-IR measurements have been performed and at least one additive has been found to be efficient in improving selected properties.

The preparation of modified polyamide clay nanocomposite/recycled maleic anhydride polyamide 6 and blending with low density polyethylene for film blowing application

Generally, polyamide cannot be used as film blowing material because of its unsuitable properties. In this study, polyamide 6 clay nanocomposite (cPA) and styrene maleic anhydride copolymer (SMA) were mixed in various ratios for the preparation of modified polyamide 6 clay nanocomposite SxcPAy resins by reactive extrusion. The S1cPA14 resin was blended with recycled maleic anhydride polyamide (rPA) to form the (S1cPA14)x rPAy resins. Finally, they were mixed with LDPE in 1:9 ratio to afford (SxcPAy)1LDPE9 and ((S1cPA14)x rPAy)1LDPE9 resins, respectively, followed by film blowing and the analyses of the physicochemical properties of resins. The FTIR spectrum illustrated that the C=O symmetric and asymmetric absorption fingerprint peaks in the anhydride (-OC-O-CO-) group of SMA disappeared and the new characteristic absorption peak of-CO-N-CO- of imides was observed. The anhydride functional group of SMA underwent reactive extrusion with the terminal amino group of cPA to generate the imides structure. The thermal properties showed that the glass transition temperature and crystallinity of SxcPAy and (S1cPA14)x rPAy resins increased with increasing SMA and S1cPA14 contents. The Tg (85.4.0°C) of (S1cPA14)12 rPA1 resin were enhanced significantly, with 30°C higher than cPA. In terms of tensile mechanical properties, S1cPA14 test pieces demonstrated the highest Young’s modulus and tensile strength. After mixing with LDPE, the tensile mechanical properties of (SxcPAy)1LDPE9 and ((S1cPA14)x rPAy)1LDPE9 resins and films were both higher than that of LDPE. ((S1cPA14)12 rPA1)1LDPE9 film shown the best tensile properties and barrier performance compared with other films due to the optimal rPA content could assisted SMA as a better compatibilizer to improve the dispersion and compatibility of cPA in HDPE. It was worth noting that (SxcPAy)1LDPE9 and ((S1cPA14)x rPAy)1LDPE9 resins were formed by film blowing at the processing temperature of 140°C followed by successful preparation of the film.

The Localization Behavior of Different CNTs in PC/SAN Blends Containing a Reactive Component

Co-continuous blend systems of polycarbonate (PC), poly(styrene-co-acrylonitrile) (SAN), commercial non-functionalized multi-walled carbon nanotubes (MWCNTs) or various types of commercial and laboratory functionalized single-walled carbon nanotubes (SWCNTs), and a reactive component (RC, N-phenylmaleimide styrene maleic anhydride copolymer) were melt compounded in one step in a microcompounder. The blend system is immiscible, while the RC is miscible with SAN and contains maleic anhydride groups that have the potential to reactively couple with functional groups on the surface of the nanotubes. The influence of the RC on the localization of MWCNTs and SWCNTs (0.5 wt. %) was investigated by transmission electron microscopy (TEM) and energy-filtered TEM. In PC/SAN blends without RC, MWCNTs are localized in the PC component. In contrast, in PC/SAN-RC, the MWCNTs localize in the SAN-RC component, depending on the RC concentration. By adjusting the MWCNT/RC ratio, the localization of the MWCNTs can be tuned. The SWCNTs behave differently compared to the MWCNTs in PC/SAN-RC blends and their localization occurs either only in the PC or in both blend components, depending on the type of the SWCNTs. CNT defect concentration and surface functionalities seem to be responsible for the localization differences.