Hydrogels are hydrophilic polymer materials that can swell but are insoluble in water. Hydrogels can be synthesized with synthetic or natural polymers, but natural polymers are preferred because they are similar to natural tissues, which can absorb a high water content, are biocompatible, and are biodegradable. The three-dimensional structure of the hydrogel affects its water insolubility and ability to maintain its shape. Cellulose hydrogels are preferred over other polymers because they are highly biocompatible, easily accessible, and affordable. Carboxymethyl cellulose sodium (CMCNa) is an example of a water-soluble cellulose derivative that can be synthesized using natural materials. A crosslinking agent is used to strengthen the properties of the hydrogel. Chemical crosslinking agent is used more often than physical crosslinking agent. In this review, article, different types of crosslinking agents are discussed based on synthetic and natural crosslinking agents. Hydrogels that utilize synthetic crosslinking agent have advantages, such as adjustable mechanical properties and easy control of the chemical composition. However, hydrogels that use natural crosslinking agent have better biocompatibility and less latent toxic effect.
In the present study, recycled natural rubber glove (rNRg) were used in an attempt to create a value-added thermoplastic elastomer material based on polypropylene/recycled natural rubber glove blends. Carbon black (CB) was also incorporated in a way to improve the mechanical properties to the blends. The blends were prepared in an internal mixer where the effects of CB loadings on processability, tensile properties, morphology and thermal stability of the blends were investigated. Results showed that the stabilization torque comparatively increases with the increment of the CB loading. Adding CB also improves the tensile strength and thermal stability to the blends. This is attributed to the better filler-matrix interaction and filler dispersion observed upon the incorporation of CB.
Purpose-The purpose of this research is to study the process conditions that give best yield and expected compositions of liquid smoke products that result during the pyrolisis process relying on predetermined variables.
Glycerin residue is waste oleochemical industry that still contain glycerin. To produce quality and maximum quantity of glycerin, then research the effect of pH acidification using phosphoric acid. Glycerin analysis includes the analysis of pH, Fatty Acid and Ester (FAE), and analysis of the levels of glycerin. The maximum yield obtained at pH acidification 2 is grading 91,60% glycerin and Fatty Acid and Ester (FAE) 3,63 meq/100 g. Glycerin obtained is used as a plasticizer in the manufacture of bioplastics. Manufacture of bioplastics using the method of pouring a solution with varying concentrations of starch banana weevil (5% w/v and 7% w/v), variations of the addition of glycerin (1 ml, 3 ml, 5 ml and 7 ml), and a variety of gelatinization temperature (60°C, 70°C, and 80°C). Analysis of bioplastics include FTIR testing, tensile strength that is supported by SEM analysis. The results obtained in the analysis of FTIR does not form a new cluster on bioplastics starch banana weevil, but only a shift in the recharge area only, it is due to the addition of O-H groups originating from water molecules that enter the polysaccharide through a mechanism gelatinitation that generates interaction hydrogen bonding strengthened. The maximum tensile strength of bioplastics produced at a concentration of starch 7% w/v, 1 ml glycerine and gelatinization temperature of 80°C is 3,430 MPa. While the tensile strength bioplastic decreased with increasing glycerin which can be shown from the results of SEM where there is a crack, indentations and lumps of starch insoluble.
Alkanolamide-modifed kaolin was added into natural rubber latex (NRL) pre-vulcanization system at 70°C and the products were formed into films by coagulant dipping method. The dipped films then were dried at 120°C for 15 and 30 min. The effect of drying time on properties of NRL films such as crosslink density, tensile strength, tensile modulus, and elongation at break was observed in this study. Results showed that longer drying time improved the properties of NRL films due to the additional formation of crosslink process in the NRL films. The longer drying time swelled the particles more in matrix as confirmed by Scanning Electron Microscopy (SEM) micrograph.
The effect of aging on mechanical properties of natural rubber latex (NRL) products filled with alkanolamide-modified cassava peel waste powder (CPWP) was studied. CPWP used as fillers was prepared by milling and sieving it until the size of 100 mesh. The powder then was dispersed in a suspension containing water and alkanolamide in order to modify the prepared powders. The dispersion system of 10 pphr (part per hundred rubber) then was added into NRL matrix followed by pre-vulcanization at 70°C for 10 minutes. The NRL compound then were casted into films by coagulant dipping method then dried at 120°C for 10 minutes. Afterwards, the films were allowed to cool at room temperature for 24 hours before being aged in a circulation of hot air for 24 hours at 70°C. The properties such as tensile strength, tensile modulus, and elongation at break were evaluated between the aged samples and the unaged samples. From this study, it showed that the aged films have increasing value of tensile strength and tensile modulus while the value of elongation at break decreases. These datas are supported by Scanning Electron Microscope (SEM) micrographs which indicate that the change of morphology in NRL films occurs before and after aging.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.