Cross-linked Mixture Research Articles

Effects of Laccase and Transglutaminase on the Physicochemical and Functional Properties of Hybrid Lupin and Whey Protein Powder.

Plant-based protein is considered a sustainable protein source and has increased in demand recently. However, products containing plant-based proteins require further modification to achieve the desired functionalities akin to those present in animal protein products. This study aimed to investigate the effects of enzymes as cross-linking reagents on the physicochemical and functional properties of hybrid plant- and animal-based proteins in which lupin and whey proteins were chosen as representatives, respectively. They were hybridised through enzymatic cross-linking using two laccases (laccase R, derived from Rhus vernicifera and laccase T, derived from Trametes versicolor) and transglutaminase (TG). The cross-linking experiments were conducted by mixing aqueous solutions of lupin flour and whey protein concentrate powder in a ratio of 1:1 of protein content under the conditions of pH 7, 40 °C for 20 h and in the presence of laccase T, laccase R, or TG. The cross-linked mixtures were freeze-dried, and the powders obtained were assessed for their cross-linking pattern, colour, charge distribution (ζ-potential), particle size, thermal stability, morphology, solubility, foaming and emulsifying properties, and total amino acid content. The findings showed that cross-linking with laccase R significantly improved the protein solubility, emulsion stability and foaming ability of the mixture, whereas these functionalities were lower in the TG-treated mixture due to extensive cross-linking. Furthermore, the mixture treated with laccase T turned brownish in colour and showed a decrease in total amino acid content which could be due to the enzyme's oxidative cross-linking mechanism. Also, the occurrence of cross-linking in the lupin and whey mixture was indicated by changes in other investigated parameters such as particle size, ζ-potential, etc., as compared to the control samples. The obtained results suggested that enzymatic cross-linking, depending on the type of enzyme used, could impact the physicochemical and functional properties of hybrid plant- and animal-based proteins, potentially influencing their applications in food.

Mimicking the Physicochemical Properties of the Cornea: A Low-Cost Approximation Using Highly Available Biopolymers.

Corneal diseases represent a significant global health challenge, often resulting in blindness, for which penetrating keratoplasty is the clinical gold standard. However, in cases involving compromised ocular surfaces or graft failure, osteo-odonto keratoprosthesis (OOKP) emerges as a vital yet costly and complex alternative. Thus, there is an urgent need to introduce soft biomaterials that mimic the corneal tissue, considering its translation's physicochemical, biological, and economic costs. This study introduces a cross-linked mixture of economically viable biomaterials, including gelatin, chitosan, and poly-D-lysine, that mimic corneal properties. The physicochemical evaluation of certain mixtures, specifically gelatin, chitosan, and poly-D-lysine cross-linked with 0.10% glutaraldehyde, demonstrates that properties such as swelling, optical transmittance, and thermal degradation are comparable to those of native corneas. Additionally, constructs fabricated with poly-D-lysine exhibit good cytocompatibility with fibroblasts at 72 h. These findings suggest that low-cost biopolymers, particularly those incorporating poly-D-lysine, mimic specific corneal characteristics and have the potential to foster fibroblast survival. While further studies are required to reach a final corneal-mimicking solution, this study contributes to positioning low-cost reagents as possible alternatives to develop biomaterials with physicochemical properties like those of the human cornea.

Bioavailability enhancement of sildenafil citrate via hydrogel-forming microneedle strategy in combination with cyclodextrin complexation

Sildenafil citrate (SIL) as a first-line treatment for erectile dysfunction is currently reported to have poor solubility and bioavailability. Moreover, SIL undergoes first-pass metabolism when taken orally and its injection can lead to discomfort. In this study, we introduce a novel transdermal delivery system that integrates hydrogel-forming microneedles with the inclusion complex tablet reservoir. The hydrogel-forming microneedle was prepared from a mixture of polymers and crosslinkers through a crosslinking process. Importantly, the formulations showed high swelling capacity (>400 %) and exhibited adequate mechanical and penetration properties (needle height reduction < 10 %), penetrating up to five layers of Parafilm® M (assessed to reach the dermis layer). Furthermore, to improve the solubility of SIL in the reservoir, the SIL was pre-complexed with β-cyclodextrin. Molecular docking analysis showed that SIL was successfully encapsulated into the β-cyclodextrin cavity and was the most suitable conformation compared to other CD derivatives. Moreover, to maximize SIL delivery, sodium starch glycolate was also added to the reservoir formulation. As a proof of concept, in vivo studies demonstrated the effectiveness of this concept, resulting in a significant increase in AUC (area under the curve) compared to that obtained after administration of pure SIL oral suspension, inclusion complex, and Viagra® with relative bioavailability > 100 %. Therefore, the approach developed in this study could potentially increase the efficacy of SIL in treating erectile dysfunction by being non-invasive, safe, avoiding first-pass metabolism, and increasing drug bioavailability.

Cell harvesting on robust smart thermosensitive pseudo-double networks prepared by one-step procedure

In this work, pseudo-double networks (pseudo-DN) based on N-vinyl caprolactam (VCL, major component, precursor of thermosensitive chains) and hexyl methacrylate (HMA, minor component, hydrophobic) have been prepared by using single step approach. The adjective pseudo refers to the fact that through the simultaneous copolymerization of VCL and HMA with different relative reaction kinetics, in the presence of an appropriate mixture of crosslinkers, networks with complex structures that tend towards DN-type structures are obtained. Hydrogels have been prepared with HMA/VCL molar ratios from 0 to 23.2 mol %. The series of hydrogels prepared show a composition-dependent behaviour in terms of thermosensitivity, swelling at temperatures below the Volume Phase Transition Temperature (VPTT) value, mechanical properties and performance during the cell culture experiments. More precisely, hydrogels with low percentages of HMA show elastic moduli under compression tests slightly lower than 1 MPa and presented a high thermal response (high swelling below the VPTT) allowing in addition the non-aggressive detachment of cell monolayer by controlled decrease of temperature. As the percentage of HMA increases, the elastic modulus increases, obtaining improved mechanical properties (reaching values in the range 1–3 MPa), thermosensitivity decreases (low swelling below VPTT) and a progressive delay in cell proliferation is also observed, being still cytocompatible. In this sense, hydrogels with low percentages of HMA (up 2.7 mol %) allow cell proliferation and transplantation similar to the control sample.

Chitosan-TPP microcapsules for controlled drug release

Production of chitosan/sodium tripolyphosphate (CS/TPP) microcapsules via spray drying involves atomizing an emulsion containing CS, TPP, acetic acid (AcOH), and folic acid (FA) into fine droplets exposed to high-temperature, low-pressure gas flow. Solvent evaporation within the drying chamber leads to solid particle formation. Spray drying is valuable for creating solid CS/TPP microcapsules. Precise equipment parameter adjustments, like inlet temperature and gas flow rate, enable the study of microcapsule morphology, size, and properties. This adaptability allows for customization to specific pH dissolution ranges. The production method's impact on CS/TPP microcapsules was studied by modifying spray drier parameters, including inlet temperature and aspirator pressure, to enhance understanding of their behavior in solution under varied production conditions.&#x0D; In chitosan delivery systems, various approaches can encapsulate drug agents like folic acid, an analog to the cancer treatment drug methotrexate. Agents can be added to the chitosan solution pre-crosslinking, incorporated into gelation-inducing agents pre-mixing with chitosan, or included in the crosslinking mixture. Experiments were conducted to assess CS/TPP microcapsules' behavior when encapsulating agents like folic acid. Release profiles were analyzed to understand their drug delivery capabilities and potential as controlled release carriers.

Benefits of FAIMS to Improve the Proteome Coverage of Deteriorated and/or Cross-Linked TMT 10-Plex FFPE Tissue and Plasma-Derived Exosomes Samples.

The proteome characterization of complex, deteriorated, or cross-linked protein mixtures as paired clinical FFPE or exosome samples isolated from low plasma volumes (250 µL) might be a challenge. In this work, we aimed at investigating the benefits of FAIMS technology coupled to the Orbitrap Exploris 480 mass spectrometer for the TMT quantitative proteomics analyses of these complex samples in comparison to the analysis of protein extracts from cells, frozen tissue, and exosomes isolated from large volume plasma samples (3 mL). TMT experiments were performed using a two-hour gradient LC-MS/MS with or without FAIMS and two compensation voltages (CV = -45 and CV = -60). In the TMT experiments of cells, frozen tissue, or exosomes isolated from large plasma volumes (3 mL) with FAIMS, a limited increase in the number of identified and quantified proteins accompanied by a decrease in the number of peptides identified and quantified was observed. However, we demonstrated here a noticeable improvement (>100%) in the number of peptide and protein identifications and quantifications for the plasma exosomes isolated from low plasma volumes (250 µL) and FFPE tissue samples in TMT experiments with FAIMS in comparison to the LC-MS/MS analysis without FAIMS. Our results highlight the potential of mass spectrometry analyses with FAIMS to increase the depth into the proteome of complex samples derived from deteriorated, cross-linked samples and/or those where the material was scarce, such as FFPE and plasma-derived exosomes from low plasma volumes (250 µL), which might aid in the characterization of their proteome and proteoforms and in the identification of dysregulated proteins that could be used as biomarkers.

Vat Photopolymerization 3D Printing of Hydrogels with Re-Adjustable Swelling.

Vat photopolymerization typically prints highly crosslinked networks. Printing hydrogels, which are also networks but with a high swelling capacity in water and therefore with low crosslinking density, is a challenge for this technique. However, it may be of interest in medicine and in other areas, since it would allow for the preparation of this type of 3D-shaped material. In this work, an approach for printing hydrogels via vat photopolymerization that uses a mixture of stable and hydrolysable crosslinkers has been evaluated so that an initial highly crosslinked network can be printed, although after hydrolysis it becomes a network with low crosslinking. This approach has been studied with PEO/PEG-related formulations, that is, with a PEG-dimethacrylate as a stable crosslinker, a PEO-related derivative carrying β-aminoesters as a degradable crosslinker, and PEG-methyl ether acrylate and hydroxyethyl acrylate as monofunctional monomers. A wide family of formulations has been studied, maintaining the weight percentage of the crosslinkers at 15%. Resins have been studied in terms of viscosity, and the printing process has been evaluated through the generation of Jacobs working curves. It has been shown that this approach allows for the printing of pieces of different shapes and sizes via vat photopolymerization, and that these pieces can re-ajust their water content in a tailored fashion through treatments in different media (PBS or pH 10 buffer).

A microfluidic biosensor architecture for the rapid detection of COVID-19

The lack of enough diagnostic capacity to detect severe acute respiratory syndrome coronavirus 2 (SARS-COV-2) has been one of the major challenges in the control the 2019 COVID pandemic; this led to significant delay in prompt treatment of COVID-19 patients or accurately estimate disease situation. Current methods for the diagnosis of SARS-COV-2 infection on clinical specimens (e.g. nasal swabs) include polymerase chain reaction (PCR) based methods, such as real-time reverse transcription (rRT) PCR, real-time reverse transcription loop-mediated isothermal amplification (rRT-LAMP), and immunoassay based methods, such as rapid antigen test (RAT). These conventional PCR methods excel in sensitivity and specificity but require a laboratory setting and typically take up to 6 h to obtain the results whereas RAT has a low sensitivity (typically at least 3000 TCID50/ml) although with the results with 15 min. We have developed a robust micro-electro-mechanical system (MEMS) based impedance biosensor fit for rapid and accurate detection of SARS-COV-2 of clinical samples in the field with minimal training. The biosensor consisted of three regions that enabled concentrating, trapping, and sensing the virus present in low quantities with high selectivity and sensitivity in 40 min using an electrode coated with a specific SARS-COV-2 antibody cross-linker mixture. Changes in the impedance value due to the binding of the SARS-COV-2 antigen to the antibody will indicate positive or negative result. The testing results showed that the biosensor's limit of detection (LoD) for detection of inactivated SARS-COV-2 antigen in phosphate buffer saline (PBS) was as low as 50 TCID50/ml. The biosensor specificity was confirmed using the influenza virus while the selectivity was confirmed using influenza polyclonal sera. Overall, the results showed that the biosensor is able to detect SARS-COV-2 in clinical samples (swabs) in 40 min with a sensitivity of 26 TCID50/ml.

Sustainable hemp-based bioplastics with tunable properties via reversible thermal crosslinking of cellulose

Modern bioplastics and biocomposites frequently contain non-biodegradable or non-sustainable components and require complex recycling routes. Sustainable materials require integrating bio-based, cheap, widely available, recycled, or waste components. In order to incorporate these concepts, we selected hemp stalk waste, the industrial byproducts glycerol and xylan (hemicellulose), and citric acid as key components. Hemp stalks were processed into cast papers using only mechanical processes and no chemical modifications or pre-treatments. Cast papers were impregnated with a crosslinking mixture of glycerol, xylan, citric acid, and the plasticizer polyethylene glycol (PEG). Thermal crosslinking was performed as a single-step reaction by curing materials at 140 °C. All prepared bioplastics were washed in water for 48 h and extensively tested for water resistance and water absorption. A recycling route with depolymerization (for pulp recovery) in sodium hydroxide is demonstrated. A comprehensive analysis of crosslinking reaction is provided via FTIR and rheology, supplemented by structure analysis via SEM. A 7-fold reduction in water uptake was achieved compared to cast hemp paper. Obtained bioplastics, after washing in water, show elastic modulus up to 2.9 GPa, tensile strength up to 70 MPa, and elongation up to 4.3 %. As a result of component ratio variation, bioplastics achieve a high tuneability of properties ranging from brittle to ductile. Dielectric analysis indicates that bioplastics have the potential for application in electric insulation. A three-layer laminate is demonstrated as a concept for potential application as an adhesive for bio-based composites.

SPECTRAL AND PHOTOPHYSICAL CHARACTERISTICS OF ASYMMETRIC POLYMETHINE DYES IN POLYURETHANE MATRICES

Here the composite polymer sorbent hydrogels were synthesized by in situ technique via free radical polymerization of acrylamide (AAm), 2-hydroxyethyl methacrylate (2HEMA) and N,N’-methylene-bis(acrylamide) crosslinker mixture in the presence of as-prepared dispersion of nickel-aluminum layered double hydroxide (NiAl-LDH). A content of active NiAl-LDH filler in the polymer matrix was varied in a range of 30 – 70 wt.%. It was found a high filler content suppresses a molecular mobility of copolymer matrix chains and reduces a beginning of glass transition temperature of the polymer constituent. The results of thermal analysis of polymer composites demonstrate a high hydrophilicity level of polymer matrix and high solvation energy of polar functionalities by Н2О molecules that was concluded from slow moisture elimination process while the temperature grows up to 200–210 оС. Additionally, a dehydration process and changes in a structure of thermally labile filler were also observed at the same temperature interval. At higher temperatures a thermal degradation of polymer poly(AAm-co-2HEMA) matrix is carried out. When a temperature overcomes 400 оС the partially changed filler demonstrates a chemical interaction with degraded organic constituents of the composites and defined catalytic activity as well. Studying sorption activity of the composites shown that introducing NiAl-LDH into hydrophilic polymer matrix provides anion-exchange activity to the composite sorbents and, correspondingly, the ability to eliminate the anionic contaminants from aqueous media while the polymer matrix doesn’t absorb these substances at such conditions. The highest sorption capacity of 11,40 μmol/g against model contaminant – methyl orange dye was determined for composite sorbent with filler content of 70 wt. %. At the same time sorption capacity of NiAl-LDH filler in composite sorbents reduces from 25,7 to 16,6 μmol/g while a filler content grows from 30 to 70 wt.% as a result of filler particles aggregation processes during composites formation stage. To evaluate the ability of the composite sorbents to reuse the experiment of materials recycling was performed. It was stated out the using of anion-exchange technique and aqueous Na2CO3 solution as an efficient and non-hazardous eluent provides 80 % recovering efficiency of the active filler in the composites. It can be concluded the composite sorbents demonstrate a high overall efficiency and are valuable materials for practical application for decontamination of waste water.

Fabrication of graded porous structure of hydroxypropyl cellulose hydrogels via temperature-induced phase separation

A novel hydroxypropyl cellulose (gHPC) hydrogel with graded porosity has been fabricated, in which pore size, shape, and mechanical properties vary across the material. The graded porosity was achieved by cross-linking different parts of the hydrogel at temperatures below and above 42 °C, which was found to be the temperature of turbidity onset (lower critical solution temperature, LCST) for the HPC and divinylsulfone cross-linker mixture. Scanning electron microscopy imaging revealed a decreasing pore size along the cross-section of the HPC hydrogel from the top to the bottom layer. HPC hydrogels demonstrate graded mechanical properties whereby the top layer, Zone 1, cross-linked below LCST, can be compressed by about 50% before fracture, whereas the middle and bottom layers (Zone 2 and 3, respectively) cross-linked at 42 °C, can withstand 80% compression before failure. This work demonstrates a straightforward, yet novel, concept of exploiting a graded stimulus to incorporate a graded functionality into porous materials that can withstand mechanical stress and minor elastic deformations.

Investigation of the Gum Stock Behavior of Polyurethane Crosslinking Matrix by Adding Triol Diol Mixtures for the Application of Composite Solid Rocket Propellants

The addition of some advanced additives to improve the mechanical properties of polyurethane (PU) polymeric matrix, which acts as a binder system in composite solid rocket propellants (CSRPs), is a target for the energetic materials researchers. In this investigation, 45 compositions of different crosslinked PU matrices were produced to demonstrate the effect of adding crosslinking mixture (CM) on the mechanical capabilities of polyurethane gum stock. The crosslinking mixture (CM) is composed of a triol crosslinker, trimethylolpropane (TMP), and a chain extender, 1,4-butanediol&#x0D; (BD). For comparison, traditional PU samples without crosslinking additives were formulated. As a prepolymer, HTPB was used with a curing agent (HMDI). The research was carried out with different ratios of TMP to BD, different curing ratios (NCO/OH=0.7, 0.9, and 1.1), and crosslinking mixture contents in the range of 0-5 wt.%. The mechanical characteristics of all the cured formulations were measured. It was demonstrated that changing the ratio of TMP to BD has a significant impact on the mechanical performance causing a wide range of elongation and strength qualities. Increasing the wt.% of triol crosslinker in the sample enhanced the tensile strength, whereas the strain has been decreased. The addition of diol chain extender increased the strain rate of the samples. The mechanical parameters were adjusted simply by employing the crosslinking ingredients to get exceptional mechanical characteristics at each NCO/OH curing ratios. Also it was concluded that PU samples of curing ratio (NCO/OH= 0.7-0.9) with TMP:BD (1:1) showed a promising results and could be used according to the requirements of the rocket system designers.

A New Family of Renewable Thermosets: Kraft Lignin Poly-adipates.

Thermosetting polymeric materials have advantageous properties and are therefore used in numerous applications. In this study, it was hypothesized and ultimately shown that thermosets could be derived from comparably sustainable sub‐components. A two‐step procedure to produce a thermoset comprising of Kraft lignin (KL) and the cross‐linker adipic acid (AdA) was developed. The cross‐linking was activated by means of an acetylating agent comprising isopropenyl acetate (IPA) to form a cross‐linking mixture (CLM). The cross‐linking was confirmed by FTIR and solid‐state NMR spectroscopy, and the esterification reactions were further studied using model compounds. When the KL lignin was mixed with the CLM, partial esterification occurred to yield a homogeneous viscous liquid that could easily be poured into a mold, as the first step in the procedure. Without any additions, the mold was heated and the material transformed into a thermoset by reaction of the two carboxylic acid‐derivatives of AdA and KL in the second step.

Azo-Crosslinked Double-Network Hydrogels Enabling Highly Efficient Mechanoradical Generation.

Double-network (DN) hydrogels have recently been demonstrated to generate numerous radicals by the homolytic bond scission of the brittle first network under the influence of an external force. The mechanoradicals thus generated can be utilized to trigger polymerization inside the gels, resulting in significant mechanical and functional improvements to the material. Although the concentration of mechanoradicals in DN gels is much higher than that in single-network hydrogels, a further increase in the mechanoradical concentration in DN gels will widen their application. In the present work, we incorporate an azoalkane crosslinker into the first network of DN gels. Compared with the traditional crosslinker N,N'-methylenebis(acrylamide), the azoalkane crosslinker causes a decrease in the yield stress but significantly increases the mechanoradical concentration of DN gels after stretching. In the azoalkane-crosslinked DN gels, the concentration of mechanoradicals can reach a maximum of ∼220 μM, which is 5 times that of the traditional crosslinker. In addition, DN gels with the azoalkane crosslinker show a much higher energy efficiency for mechanoradical generation. Interestingly, DN gels crosslinked by a mixture of azoalkane crosslinker and traditional crosslinker also exhibit excellent radical generation performance. The increase in the mechanoradical concentration accelerates polymerization and can broaden the application range of force-responsive DN gels to biomedical devices and soft robots.

Low temperature fracture toughness of polysulfide modified BPA-epoxide primers

A mixture of amidoamine and polysulfide crosslinkers were used to toughen a BPA-epoxide primer. Viscoelastic properties, fracture toughness, impact resistance, adhesion strength, corrosion properties were investigated. Fracture toughness study was conducted at ambient and low temperatures to approximate an aircraft at altitude. At ambient temperature, the amidoamine was sufficiently flexible due to ethylene oxide soft segments. However, at low temperature, the addition of polysulfide showed improved fracture toughness. The SEM of fractured surface revealed that fracture toughness improvement at low temperature is due to the both cavitation and shear yielding of polysulfide domains and epoxide matrix which dissipate energy and increase the toughness.

Heat transfer and storage characteristics of composite phase change materials with high oriented thermal conductivity based on polymer/graphite nanosheets networks

Energy storage materials are being increasingly utilized. However, traditional solid–liquid phase change materials (PCM) have two disadvantages: low thermal conductivity and an inability to maintain stable properties. In this work, a novel anti-leakage, form-stable composite PCM with enhanced thermal conductivity was successfully proposed. This composite PCM uses a cross-linked mixture of paraffin wax and an olefin block copolymer as the base material and expanded graphite as the thermally conductive filler. The vacuum adsorption method and directional molding method were used to achieve shape stability and high thermal conductivity of the material. When the mass ratio of expanded graphite was increased from 5% to 30%, the corresponding thermal conductivity increased from 2.79 to 25.56 W∙m−1∙K−1, which was an improvement of 111 times compared to paraffin wax. When the mass ratio of expanded graphite reached 10%, the heat storage reached its maximum value of 520 J/ cm2, while the peak heat storage power reached 11.5 Wcm−2 with a 30% graphite mass fraction. Battery thermal management experiments showed that, the battery temperature rise could be effectively controlled within 17 °C. In the case of natural convection, the temperature rise reached 39 °C. The proposed composite PCM demonstrates promising potential for application in thermal management, building energy and heat storage.

Cross-Linking/Mass Spectrometry Combined with Ion Mobility on a timsTOF Pro Instrument for Structural Proteomics.

The combination of cross-linking/mass spectrometry (XL-MS) and ion mobility is still underexplored for conducting protein conformational and protein-protein interaction studies. We present a method for analyzing cross-linking mixtures on a timsTOF Pro mass spectrometer that allows separating ions based on their gas-phase mobilities. Cross-linking was performed with three urea-based MS-cleavable cross-linkers that deliver distinct fragmentation patterns for cross-linked species upon collisional activation. The discrimination of cross-linked species from non-cross-linked peptides was readily performed based on their collisional cross sections. We demonstrate the general feasibility of our combined XL-MS/ion mobility approach for three protein systems of increasing complexity: (i) bovine serum albumin (BSA), (ii) Escherichia coli ribosome, and (iii) HEK293T cell nuclear lysates. We identified a total of 623 unique cross-linking sites for BSA, 670 for the E. coli ribosome, and 1623 unique cross-links for nuclear lysates, corresponding to 1088 intra- and 535 interprotein interactions and yielding 564 distinct protein-protein interactions. Our results underline the strength of combining XL-MS with ion mobility not only for deriving three-dimensional (3D) structures of single proteins but also for performing system-wide protein interaction studies.

The Comparison of Three Metallic, Organic, and Polymeric Crosslinked HPAM Gels for Water Conformance Applications

Unwanted production of water in oil and gas reservoirs due to water coning is one of the headaches of the petroleum industry. Despite mechanical methods, some chemicals are also developed to delay or prevent this problem. Polymer gels have been proved to be a reliable and economical solution for water production. In this paper, we present a summary of tests for three different gel systems for a pre-determined reservoir condition. A metallic crosslinker (Chromium(III) Acetate), a polymeric crosslinker (Polyethylenimine), and an organic crosslinker mixture (Hexamethyleneteramine + Hydroquinone) are used for crosslinking HPAM polymer. The tests are performed for different concentrations of polymer and cross-linker. Gel strength and stability of these polymer gels are recorded over six weeks. The apparent viscosity of these gels is recoded and compared. The impact of salinity on gel strength and stability is also investigated. The results show that for the determined reservoir conditions HPAM-Chromium(III) Acetate and HPAM-Hexamethyleneteramine-Hydroquinone gels could form a stable and rigid barrier against water.

The Effect of Crosslinking Mixture Addition on the mechanical properties of PU Polymeric Matrix

Polyurethanes are prepared by extending a prepolymer chains made from a macro diol and a diisocyanate and its mechanical properties could be improved by using special additives to enhance the crosslinking process. In this study, 15 hydroxyl terminated polybutadiene (HTPB) based poly urethanes were prepared using 1, 6- hexamethylene diisocyanate (HMDI) and crosslinking mixture (CM) consists of trimethylol propane (TMP) as a triol crosslinker and butane diol (BD) as a chain extender. Five different crosslinking mixtures were used through the combination between TMP: BD = 1:0, 0:1, 1:1, 2:1 and 1:2. The research investigated the impact occurred on the mechanical behaviour of PU formulations prepared by adding certain cross-linking additives with various content from 0 % to 5 % and the curing ratio NCO/OH maintained constant at 0.7. The strength-strain relationships of all the finished samples were determined by using a LLOYD testing machine. The mechanical properties have been plotted vs. crosslinking mixture content and TMP: BD percentage which could be utilized to choose an appropriate network forming agent formulation for a particular grain technology and implementation. It was concluded that both TMP and BD have a major influence on the mechanical behaviour which allow obtaining a wide range of strength and elongation capabilities. The tensile strength increased by the excess of triol addition while the strain had a lowering effect which was compensated by the existence of diol extender. Tailoring the mechanical characteristics was easy to make by using a suitable proportions of TMP and BD to obtain outstanding mechanical properties for fixed NCO/OH, especially elastic capabilities, compared to polyurethanes formulated without any crosslinking additives.

Synthesis of the superabsobents enriched in chitosan derivatives with excellent water absorption properties

The superabsorbent polymers (SAPs) containing up to 30% w of N-succinylchitosan and N-maleoylchitosan were successfully synthesized by free radical polymerization in an aqueous solution. The structures and surfaces of the synthesized SAPs were characterized by FTIR and SEM, respectively. The influence of the parameters such as type and content of polysaccharide, cross-linker, and comonomer mixture content on the swelling rate was researched. The chitosan-derivative-based SAPs have a higher swelling rate compared to chitosan-based SAPs. Equilibrium swelling rate, Qe, of the synthesized SAPs lying in the range 102–1144 g/g decreases with the rise of polysaccharide content. It was found that N-succinylchitosan-based SAPs are characterized by higher Qe values compared to N-maleoylchitosan ones. The highest swelling rate (Qe = 1144 g/g) was achieved for N-succinylchitosan-based polymer containing 2% w of N-succinylchitosan, 0.5% w of cross-linker, and acrylamide-acrylic acid weight ratio was 1:3. Researching the swelling kinetics shows equilibrium swelling is reached during 0–30 min for all synthesized polymers, and equilibrium reaching time rises with the increase in polysaccharide content. Also, swelling is correctly described by the pseudo-second-order model and controlled by chemical absorption of water molecules. The synthesized eco friendly SAPs enriched in polysaccharide content are characterized by excellent water-absorbing properties.