Hydrogels Are Reinforced with Colombian Fique Nanofibers to Improve Techno-Functional Properties for Agricultural Purposes

Colombia is the world’s largest producer of fique fibers (Furcraea bedinghausii), with a net production of 30,000 tons per year. This work proposes to revalue waste from the Colombian fique agroindustry. For this purpose, cellulose nanofibers were obtained from fique and used as reinforcement material to create acrylic superabsorbent hydrogels. Unreinforced acrylic hydrogels (AHR0) and acrylic hydrogels reinforced with fique nanofibers at 3% w/w (AHR3), 5% w/w (AHR5), and 10 % w/w (AHR10) were synthesized using the solution polymerization method. The best hydrogel formulation for agricultural purposes was chosen by comparing their swelling behavior, mechanical properties, and using scanning electron microscopy (SEM). By raising the nanofiber concentration to 3% (AHR3), the best-chosen formulation, the interaction between the nanofibers and the polymer matrix increased, which favored the network stability. However, beyond AHR3, there was a higher viscosity of the reactive system, which caused a reduction in the mobility of the polymer chains, thus disfavoring the swelling capacity. The reinforced hydrogel proposed in this study (AHR3) could represent a contribution to overcoming the problems of land dryness present in Colombia, an issue that will worsen in the coming years due to the climate emergency.

Synthesis and Characterization of Poly(methyl acrylate)-grafted-Sodium Salt of Partially Carboxymethylated Tamarind Kernel Powder

Ceric ammonium nitrate (CAN)-initiated graft copolymerization of methyl acrylate (MA) onto sodium salt of partially carboxymethylated tamarind kernel powder (Na-PCMTKP, DS = 0.15) was studied in an aqueous medium by solution polymerization technique. The growth of the graft reaction was monitored gravimetrically. The role of various synthesis variables on the grafting yields was examined to achieve the maximum graft yields (%G = 278.27, %GE = 94.38, %Hp = 5.62) and the influence of the synthesis variables in the graft copolymerization has been discussed. The reactivity of methyl acrylate (MA) towards graft copolymerization was compared with that of acrylonitrile (AN) on the basis of the results obtained from the earlier studies and plausible explanation was furnished for the observed reactivity of both the monomers towards grafting. The evaluated optimized reaction conditions were utilized to study the effect of reaction medium on grafting and it was found that reaction medium plays an important role in graft copolymerization. In order to ascertain the grafting, characterization of the samples made by FTIR, TGA and SEM was conducted. The synthesized novel graft copolymer may find potential application to be used as metal adsorbents.

Antibacterial properties of poly ( N , N -dimethylaminoethyl methacrylate) obtained at different initiator concentrations in solution polymerization

The samples of poly( N , N -dimethylaminoethyl methacrylate) were synthesized by radical polymerization. The amount of monomer and solvent was constant as opposed to an amount of initiator which was changing. No clear relationship between polymerization conditions and the molecular weight of the polymer was found, probably due to the branched configuration of produced polymer. Bactericidal interactions in all samples against Gram-positive and Gram-negative bacteria have been demonstrated. However, the observed effect has various intensities, depending on the type of bacteria and the type of sample.

Water Absorption Enhancement of Sodium Poly Acrylate and Poly(2-Acrylamido-2-Methylpropane Sulphonic Acid) Based Hydrogel Mixtures

Introduction: Hydrogels are hydrophilic polymers which are cross-linked to form three-dimensional structures, which can absorb, swell and retain huge amounts of water or aqueous fluids. Objective: This paper reports the preparation and characterisation of Poly(2-Acrylamido-2-Methylpropane Sulphonic Acid) (PAMPS) hydrogel with different crosslinking intensities. Methodology: 2-Acrylamido-2-methylpropane sulfonic acid (AMPS) monomer was purchased from Alfa Aesar Company as reagent grade. It was used as received (>98% purity) without any further purification. PAMPS hydrogel was prepared by free radical crosslinking solution polymerization of AMPS in water at room temperature under a nitrogen blanket in cylindrical glass tubes. The characteristics of the obtained PAMPS hydrogel were compared with those of commercial sodium polyacrylates hydrogel. Results: It was found that decreasing the crosslinker weight improved the absorbance capacity but to a limit. The suggested reasons were discussed. The mixture showed higher absorbance rate than PAMPS, and bigger absorbance capacity than sodium polyacrylates. Conclusion: This paper investigates the effect of crosslinker ratio on the swelling capacity of PAMPS. It was found that as the crosslinking ratio decreases, the porosity of the hydrogel increases, thus improving the swelling capacity.

Optimal Control of Non-Isothermal, Batch Polymerization of Methacrylates with Specified Time, Monomer Conversion, and Average Molecular Weights

Optimal control policies are determined for the free radical polymerization of three different polymerization processes, in a non-isothermal batch reactor as follows: (1) bulk polymerization of n-butyl methacrylate; (2) solution polymerization of methyl methacrylate with monofunctional initiator; (3) solution polymerization of methyl methacrylate with bifunctional initiator. Four different optimal control objectives are realized for the above three processes. The objectives are: (i) maximization of monomer conversion in a specified operation time, (ii) minimization of operation time for a specified, final monomer conversation, (iii) maximization of monomer conversion for a specified, final number average polymer molecular weight, and (iv) maximization of monomer conversion for a specified, final weight average polymer molecular weight. The realization of these objectives is expected to be very useful for the batch production of polymers. To realize the above four different optimal control objectives, a genetic algorithms-based optimal control method is applied, and the temperature of heat exchange fluid inside reactor jacket is used as a control function. Necessary equations are provided in the above three processes to suitably transform the process model in the range of a specified variable other than time, and to evaluate the elements of Jacobian to help in the accurate solution of the process model. The results of this optimal control application reveal considerable improvements in the performance of the batch polymerization processes.

Optimal Control of Non-Isothermal, Batch Polymerization of Methacrylates with Specified Time, Monomer Conversion, and Average Molecular Weights

Optimal control policies are determined for the free radical polymerization of three different polymerization processes, in a non-isothermal batch reactor as follows: (1) bulk polymerization of n-butyl methacrylate; (2) solution polymerization of methyl methacrylate with monofunctional initiator; (3) solution polymerization of methyl methacrylate with bifunctional initiator. Four different optimal control objectives are realized for the above three processes. The objectives are: (i) maximization of monomer conversion in a specified operation time, (ii) minimization of operation time for a specified, final monomer conversation, (iii) maximization of monomer conversion for a specified, final number average polymer molecular weight, and (iv) maximization of monomer conversion for a specified, final weight average polymer molecular weight. The realization of these objectives is expected to be very useful for the batch production of polymers. To realize the above four different optimal control objectives, a genetic algorithms-based optimal control method is applied, and the temperature of heat exchange fluid inside reactor jacket is used as a control function. Necessary equations are provided in the above three processes to suitably transform the process model in the range of a specified variable other than time, and to evaluate the elements of Jacobian to help in the accurate solution of the process model. The results of this optimal control application reveal considerable improvements in the performance of the batch polymerization processes.

Investigating the Properties of Modified Drilling Mud with Barite/Polyacrylamide Nanocomposite

Summary Drilling mud plays a significant role in the drilling operation because it is influential in the quality of the drilled well and the efficiency of the drilling operation. In this paper, we aim to identify the methods to improve the effectiveness of drilling operations by analyzing and evaluating the impact of adding polyacrylamide and a barite/polyacrylamide nanocomposite, synthesized through the solution polymerization method, on the properties of drilling mud. The study added the synthesized nanocomposite to the water-based drilling mud (350 cm3 water with 10 g bentonite) and examined the properties of the drilling mud, including viscosity, fluid loss, and mudcake thickness. Overall, the results indicated that the addition of the synthesized nanocomposite caused a decrease in fluid loss and the thickness of the mudcake, while it increased the drilling mud’s viscosity.