Low Polymer Concentrations Research Articles

Combined Effect of End-of-Life Rubber and a Hydrophobic Polymer on Coastal Saturated Sand: A Multiaspect Investigation

Nowadays, mass production of tires and construction operations adjacent to saturated soils have become a concern for engineers. The present study aimed to explore the potential of the combined effect of a waterproof polymer and rubber powder, confining pressure, and cyclic stress ratio on the static and dynamic properties of sand-rubber-polymer mixtures using a scanning electron microscope (SEM), attenuated total reflectance (ATR) analysis, unconfined compressive strength (UCS), and cyclic triaxial tests. The findings indicated that with the inclusion of 4% rubber, rough polymer chains are extended due to creating C─ CH3 bonds, uniform distribution of rubber particles between rigid materials, and interlocking rubbers in hydrocarbon chains. These chains increase adhesion with sand particles and prevent rubber flexibility, increasing UCS and shear modulus. In contrast, with the inclusion of 8% rubber, due to several mechanisms, including poor adhesion between particles because of the high surface area of the mixture and low polymer content (i.e., 2%), the dominance of weak rubber–polymer and rubber–rubber bonds over polymer–polymer and sand–polymer bonds, emerging free rubber particles (free CH2 groups), and creating the aromatic and double bond structures due to the nature of rubber flexibility, the trend is reversed.

Ultrasoft edge-labelled hydrogel sensors reveal internal tissue stress patterns in invasive engineered tumors

Measuring internal mechanical stresses within 3D tissues can provide important insights into drivers of morphogenesis and disease progression. Cell-sized hydrogel microspheres have recently emerged as a powerful technique to probe tissue mechanobiology, as they can be sufficiently soft as to deform within remodelling tissues, and optically imaged to measure internal stresses. However, measuring stresses at resolutions of ∼10 Pa requires ultrasoft, low-polymer content hydrogel formulations that are challenging to label with sufficiently fluorescent materials to support repeated measurements, particularly in optically dense tissues over 100 μm thick, as required in cancer tumor models. Here, we leverage thermodynamic partitioning of hydrogel components to create “edge-labelled” ultrasoft hydrogel microdroplets, in a single polymerization step. Bright and stable fluorescent nanoparticles preferentially polymerize at the hydrogel droplet interface, and can be used to repeatedly track sensor surfaces over long-term experiments, even when embedded deep in light-scattering tissues. We utilize these edge-labelled microspherical stress gauges (eMSGs) in inducible breast cancer tumor models of invasion, and demonstrate distinctive internal stress patterns that arise from cell-matrix interactions at different stages of breast cancer progression. Our studies demonstrate a long-term macroscale compaction of the tumor during matrix encapsulation, but only a short-term increase in local stress as non-invasive tumors rapidly make small internal reorganizations that reduce the mechanical stress to baseline levels. In contrast, once invasion programs are initiated, internal stress throughout the tumor is negligible. These findings suggest that internal tumor stresses may initially prime the cells to invade, but are lost once invasion occurs. Together, this work demonstrates that mapping internal mechanical stress in tumors may have utility in advancing cancer prognostic strategies, and that eMSGs can have broad utility in understanding dynamic mechanical processes of disease and development.

Towards low polymer content transparent composites via novel integration engineering

Abstract The high polymer and low wood content of current transparent wood has limitation in the mechanical strength and hence obstruct green sustainable transition of the building industry. In this study, a novel method for manufacturing transparent wood was reported by minimizing the usage of polyethylene glycol using partial impregnation followed by a densification approach. The delignified wood was firstly partially impregnated by polyethylene glycol, and subsequently compressed to eliminate pores for the compressed transparent wood, providing the strong hydrogen bonds and dense structures for transparent wood. The wood content of the novel compressed transparent wood was dramatically increased to 64%, compared with the uncompressed transparent wood of 25%. Additionally, the obtained compressed transparent wood demonstrated satisfactory optical transmittance, suitable thermal energy storage, and superior mechanical strengths owing to the formation of densely packed microstructures. This novel, sustainable, and low-cost transparent wood was easy to be manufactured while having increased mechanical and energy-saving characteristics compared to those available in the existing market.

A triple crosslinked micelle-hydrogel lacrimal implant for localized and prolonged therapy of glaucoma

Glaucoma is a chronic disease that requires lifelong treatment, whereas, discomfort caused by frequent medication may affect the quality of life. Moreover, the therapeutic efficacy of traditional local administration was unsatisfactory due to the rapid ocular clearance mechanism and the ocular barrier. Herein, a triple crosslinked micelle-hydrogel lacrimal implant with low polymer content was fabricated for localized and prolonged therapy of glaucoma. Latanoprost and timolol were simultaneously entrapped in the PEG-PLA micelles with high encapsulation efficiency and further loaded into the triple crosslinked hydrogel, facilitating a double sustained release of drugs. Subsequently, the implant was constructed by a unique molecular orientation fixation technology, which enables the implant to be fixed in the lacrimal duct. The triple crosslinked micelle-hydrogel lacrimal implant manifested a distinguished physicochemical characterization to sustain the release of latanoprost and timolol. In vitro release experiment demonstrated the duration of two drugs was extended for up to 28 days. The in vivo test of elevated intraocular pressure (IOP) in a rabbit model revealed that the IOP-lowering effects were sustained longer than 28 days as expected. The relative pharmacological availability (PA) of lacrimal implants was 5.7 times greater than that of the eye drops. The results of the studies on ocular irritation and histological examination demonstrated the good safety of the lacrimal implant. In conclusion, the triple crosslinked micelle-hydrogel lacrimal implant could effectively lower the IOP with splendid compatibility, demonstrating the promising prospect in the long-term noninvasive treatment of glaucoma.

Block Copolymer Adsorption on the Surface of Multi-Walled Carbon Nanotubes for Dispersion in N,N Dimethyl Formamide

This research aims to characterize the adsorption morphology of block copolymer dispersants of the styrene-block-4-vinylpyridine family (S4VP) on the surface of multi-walled carbon nanotubes (MWCNT) in a polar organic solvent, N,N-dimethyl formamide (DMF). Good, unagglomerated dispersion is important in several applications such as fabricating CNT nanocomposites in a polymer film for electronic or optical devices. Small-angle neutron scattering (SANS) measurements, using the contrast variation (CV) method, are used to evaluate the density and extension of the polymer chains adsorbed on the nanotube surface, which can yield insight into the means of successful dispersion. The results show that the block copolymers adsorb onto the MWCNT surface as a continuous coverage of low polymer concentration. Poly(styrene) (PS) blocks adsorb more tightly, forming a 20 Å layer containing about 6 wt.% PS, whereas poly(4-vinylpyridine) (P4VP) blocks emanate into the solvent, forming a thicker shell (totaling 110 Å in radius) but of very dilute (<1 wt.%) polymer concentration. This indicates strong chain extension. Increasing the PS molecular weight increases the thickness of the adsorbed layer but decreases the overall polymer concentration within it. These results are relevant for the ability of dispersed CNTs to form a strong interface with matrix polymers in composites, due to the extension of the 4VP chains allowing for entanglement with matrix chains. The sparse polymer coverage of the CNT surface may provide sufficient space to form CNT-CNT contacts in processed films and composites, which are important for electrical or thermal conductivity.

Adjusting Degree of Modification and Composition of gelAGE-Based Hydrogels Improves Long-Term Survival and Function of Primary Human Fibroblasts and Endothelial Cells in 3D Cultures.

This study aimed to develop a suitable hydrogel-based 3D platform to support long-term culture of primary endothelial cells (ECs) and fibroblasts. Two hydrogel systems based on allyl-modified gelatin (gelAGE), G1MM and G2LH, were cross-linked via thiol-ene click reaction with a four-arm thiolated polyethylene glycol (PEG-4-SH). Compared to G1MM, the G2LH hydrogel was characterized by the lower polymer content and cross-linking density with a softer matrix and homogeneous and open porosity. Cell viability in both hydrogels was comparable, although the G2LH-based platform supported better F-actin organization, cell-cell interactions, and collagen and fibronectin production. In co-cultures, early morphogenesis leading to tubular-like structures was observed within 2 weeks. Migration of fibroblasts out of spheroids embedded in the G2LH hydrogels started after 5 days of incubation. Taken together, the results demonstrated that the G2LH hydrogel fulfilled the demands of both ECs and fibroblasts to enable long-term culture and matrix remodeling.

Antibiotic-loaded hydroxyapatite scaffolds fabricated from Nile tilapia bones for orthopaedics

This work aimed to develop new antibiotic-coated/ antibiotic-loaded hydroxyapatite (HAp) scaffolds for orthopaedic trauma, specifically to treat the infection after fixation of skeletal fracture. The HAp scaffolds were fabricated from the Nile tilapia (Oreochromis niloticus) bones and fully characterized. The HAp scaffolds were coated with 12 formulations of poly (lactic-co-glycolic acid) (PLGA) or poly (lactic acid) (PLA), blended with vancomycin. The vancomycin release, surface morphology, antibacterial properties, and the cytocompatibility of the scaffolds were conducted.The HAp powder contains elements identical to those found in human bones. This HAp powder is suitable as a starting material to build scaffolds. After the scaffold fabrication, The ratio of HAp to β-TCP changed, and the phase transformation of β-TCP to α-TCP was observed. All antibiotic-coated/ antibiotic-loaded HAp scaffolds can release vancomycin into the phosphate-buffered saline (PBS) solution. PLGA-coated scaffolds obtained faster drug release profiles than PLA-coated scaffolds. The low polymer concentration in the coating solutions (20%w/v) gave a faster drug release profile than the high polymer concentration (40%w/v). All groups showed a trace of surface erosion after being submerged in PBS for 14 days. Most of the extracts can inhibit Staphylococcus aureus (S. aureus) and methicillin-resistant S. aureus (MRSA). The extracts not only caused no cytotoxicity to Saos-2 bone cells but also can increase cell growth. This study demonstrates that it is possible to use these antibiotic-coated/ antibiotic-loaded scaffolds in the clinic as an antibiotic bead replacement.

Organic Photodiodes with Thermally Reliable Dark Current and Excellent Detectivity Enabled by Low Donor Concentration.

Reducing the dark current (Jd) under reverse bias while maintaining a high external quantum efficiency (EQE) is essential for the practical application of organic photodiodes (OPDs). However, the high Jd of OPDs is generally difficult to reduce because its origin in organic photodiodes is still not well understood and is strongly temperature dependent. To address the issues related to high Jd in typical OPDs, we investigate fullerene-based OPDs with various donor concentrations. It is surprising that OPDs with a low donor concentration in the active layer can achieve a very low Jd of 1.68 × 10-7 mA cm-2 at a reverse bias of -2 V, which is almost temperature-independent owing to the low polymer content. More importantly, the fullerene-based OPDs with a low donor concentration of 5 wt % can still achieve an external quantum efficiency (EQE) as high as 40%, resulting in a promisingly high detectivity of above 1013 Jones at 300-800 nm compared to the OPDs with a standard donor/acceptor ratio. The presented optimized OPD device can also be used for real-time heart rate detection, indicating its potential for practical photon-sensing applications.

From Free-Radical to Radical-Free: A Paradigm Shift in Light-Mediated Biofabrication.

In recent years, the development of novel photocrosslinking strategies and photoactivatable materials has stimulated widespread use of light-mediated biofabrication techniques. However, despite great progress toward more efficient and biocompatible photochemical strategies, current photoresins still rely on photoinitiators (PIs) producing radical-initiating species to trigger the so-called free-radical crosslinking/polymerization. In the context of bioprinting, where cells are encapsulated in the bioink, the presence of radicals raises concerns of potential cytotoxicity. In this work, a universal, radical-free (RF) photocrosslinking strategy to be used for light-based technologies is presented. Leveraging RF uncaging mechanisms and Michael addition, cell-laden constructs are photocrosslinked by means of one- and two-photon excitation with high biocompatibility. A hydrophilic coumarin-based group is used to cage a universal RF photocrosslinker based on 4-arm-PEG-thiol (PEG4SH). Upon light exposure, thiols are uncaged and react with an alkene counterpart to form a hydrogel. RF photocrosslinker is shown to be highly stable, enabling potential for off-the-shelf products. While PI-based systems cause a strong upregulation of reactive oxygen species (ROS)-associated genes, ROS are not detected in RF photoresins. Finally, optimized RF photoresin is successfully exploited for high resolution two-photon stereolithography (2P-SL) using remarkably low polymer concentration (<1.5%), paving the way for a shift toward radical-free light-based bioprinting.

Study of crosslinker size on the rheological properties of borate crosslinked guar gum

Borate crosslinked guar gum gels have played a vital role in stimulating oil and gas wells for many years; however, the high dosage of guar gum in the existing fracturing fluid will increase the cost and cause more damage to the reservoir and ultimately affect the effect of stimulation. In this study, borate esters are modified onto polyethyleneimine (PEI) of different molecular weights, affording organic borate crosslinkers of different sizes. By analyzing the effect of crosslinker size on gel rheology, sand-carrying properties, and microstructure, it is observed that the crosslinking efficiency is most significantly enhanced when the crosslinker size is similar to the diameter of the guar gum molecules. This makes it possible for the gel to maintain good performance at low polymer concentrations and meet the performance requirements of fracturing, which provides new ideas for developing the next generation of economical, clean, and green fracturing fluids.

Tetra-arm poly(ethylene glycol) gels with highly concentrated sulfolane-based electrolytes exhibiting high Li-ion transference numbers.

We demonstrate that tetra-arm poly(ethylene glycol) gels containing highly concentrated sulfolane-based electrolytes exhibit high Li+ transference numbers. The low polymer concentration and homogeneous polymer network in the gel electrolyte are useful in achieving both mechanical reliability and high Li+ transport ability.

A natural polymer-based hydrogel with shape controllability and high toughness and its application to efficient osteochondral regeneration.

Hydrogels prepared from sustainable natural polymers have broad prospects in the biological field. However, their poor mechanical properties and challenges in achieving shape control have limited their application. Herein, a novel preforming dual-effect post-enhancing method is proposed to address these issues. The method utilizes the hydrogen bonding of agar to obtain a shape-controllable preformed hydrogel at low polymer concentrations using casting, injection, or 3D printing techniques. Subsequently, the preformed hydrogel was subjected to a permeation process to form a post-enhanced multi-network (PEMN) hydrogel with hierarchical chain entanglements to ensure its high toughness, which exhibits tensile and compressive strengths of up to 0.51 MPa and 1.26 MPa with solely physically crosslinking networks. The excellent biocompatibility of the PEMN hydrogel prepared without the need for additional initiator agents under mild conditions was confirmed by both in vitro and in vivo experiments. Furthermore, the adaptability for irregular defects, suitable toughness, adhesive properties, and degradability of PEMN hydrogels are beneficial to provide mechanical support, induce endogenous cell mineralization, and accelerate the regeneration of cartilage and subchondral bone with more than 40% bone regeneration in 12 weeks. Our work has provided a novel solution to simultaneously achieve shape controllability and high toughness based on natural polymers among the already well-explored strategies for osteochondral regeneration.

Crosslinker structure modulates bulk mechanical properties and dictates hMSC behavior on hyaluronic acid hydrogels.

Synthetic hydrogels are attractive platforms due in part to their highly tunable mechanics, which impact cell behavior and secretory profile. These mechanics are often controlled by altering the number of crosslinks or the total polymer concentration in the gel, leading to structure-property relationships that inherently couple network connectivity to the overall modulus. In contrast, the native extracellular matrix (ECM) contains structured biopolymers that enable stiff gels even at low polymer content, facilitating 3D cell culture and permeability of soluble factors. To mimic the hierarchical order of natural ECM, this work describes a synthetic hydrogel system in which mechanics are tuned using the structure of sequence-defined peptoid crosslinkers, while fixing network connectivity. Peptoid crosslinkers with different secondary structures are investigated: 1) a helical, molecularly stiff peptoid, 2) a non-helical, less stiff peptoid, and 3) an unstructured, relatively flexible peptoid. Bulk hydrogel storage modulus increases when crosslinkers of higher chain stiffness are used. In-vitro studies assess the viability, proliferation, cell morphology, and immunomodulatory activity of human mesenchymal stem cells (hMSCs) on each hydrogel substrate. Matrix mechanics regulate the morphology of hMSCs on the developed substrates, and all of the hydrogels studied upregulate IDO production over culture on TCP. Softer substrates further this upregulation to a plateau. Overall, this system offers a biomimetic strategy for decoupling hydrogel storage modulus from network connectivity, enabling systematic study of biomaterial properties on hMSC behavior and enhancement of cellular functionality for therapeutic applications. STATEMENT OF SIGNIFICANCE: Various strategies to tune hydrogel mechanics have been developed to control human mesenchymal stem cell (hMSC) behavior and regulate their immunomodulatory potential. However, these strategies typically couple mechanics to network connectivity, which in turn changes other hydrogel properties such as permeability that may have unintended effects on hMSC behavior. This work presents a strategy to tune hydrogel mechanics using crosslinkers with different secondary structure and molecular rigidity. This strategy successfully decouples hydrogel moduli from crosslinker stoichiometry and mimics the hierarchical nature of the native extracellular matrix. The moduli of the developed hydrogels led to significant impacts on hMSC morphology and proliferation, and increased immunomodulatory potential, indicating that molecular rigidity is a promising avenue to control engineered ECM mechanics for therapeutic applications.

Preparation of Highly Durable Reverse-Mode Polymer-Stabilized Liquid Crystal Films with Polymer Walls.

Reverse-mode polymer-stabilized liquid crystal (PSLC) films have wide applications in smart windows for cars as well as buildings and dimming glasses due to their low haze, low energy consumption, and better safety in case of emergency power off. However, PSLC films usually have poor stability of electro-optical properties due to their low polymer content (ca. 5 wt %), and it still remains a challenging task to improve the stability and processability by increasing the polymer content in PSLC as the driving voltage might dramatically increase. In this work, a reverse-mode PSLC film with polymer walls was prepared, which showed excellent stability of electro-optical properties even after 150 000 cycles. The film was prepared through polymerization with a photomask, in which the monomers concentrated on specific areas to form patterned polymer walls. In this way, the polymer content could be increased dramatically and the anchoring effect would not be too strong, thus avoiding a sharp increase in the driving voltage. As a result, the desired reverse-mode film with high stability, relatively low driving voltage, and high contrast ratio was obtained. The effects of monomer compositions, curing temperature, UV light intensity, and the pattern of the photomask on the microstructures, as well as electro-optical performances of the films were carefully studied. This work provides a new idea for the preparation of reverse-mode electrically switchable light-transmittance controllable films with excellent stability and good electro-optical performance, which would broaden their application in smart cars, building windows, and dimming glasses for light management and potential energy saving.

Investigation of Cell Aggregation on the Printing Performance in Inkjet-Based Bioprinting of Cell-Laden Bioink.

During 3D bioprinting, when the gravitational force exceeds the buoyant force, cell sedimentation will be induced, resulting in local cell concentration change and cell aggregation which affect the printing performance. This paper aims at studying and quantifying cell aggregation and its effects on the droplet formation process during inkjet-based bioprinting and cell distribution after inkjet-based bioprinting. The major conclusions of this study are as follows: (1) Cell aggregation is a significant challenge during inkjet-based bioprinting by observing the percentage of individual cells after different printing times. In addition, as polymer concentration increases, the cell aggregation is suppressed. (2) As printing time and cell aggregation increase, the ligament length and droplet velocity generally decrease first and then increase due to the initial increase and subsequent decrease of the viscous effect. (3) As the printing time increases, both the maximum number of cells within one microsphere and the mean cell number have a significant increase, especially for low polymer concentrations such as 0.5% (w/v). In addition, the increased rate is the highest using the lowest polymer concentration of 0.5% (w/v) because of its highest cell sedimentation velocity.

Improving Alkali Polymer Flooding Economics by Capitalizing on Polymer Solution Property Evolution at High pH

Summary Alkali polymer (AP) flooding is a promising enhanced oil recovery (EOR) method to increase oil recovery from reactive oils. It is essential to carefully select the alkali and polymer type and concentration to optimize incremental oil recovery. In addition to the conventional laboratory tests for polymer flooding, the effects of the high pH on the polymer and its evolving properties over time need to be investigated. Consideration of near-wellbore and reservoir effects is key in designing the process. We are showing how understanding and taking advantage of the polymer performance in a high pH environment allow for cost reduction and increase in injectivity and incremental oil recovery for AP projects. The polymer performance was evaluated for AP flooding of the Matzen field (Austria). Evaluations included changes in polymer rheology during aging at high pH conditions, phase behavior tests, and single-/two-phase corefloods with aged and nonaged polymer solutions. In addition, adsorption of the aged polymer and interfacial tension (IFT) were measured. The aging was studied in anaerobic conditions at reservoir temperature and through an accelerated method at elevated temperatures. The accelerated method developed earlier for neutral pH range provides a possibility to run aging at elevated temperatures in a short time frame and transfer the data to reservoir temperature to give information on the long-term performance. The transfer takes place through a conversion factor derived from the first-order kinetics of acrylamide hydrolysis in pH 6–8. In the present work, the applicability of the accelerated method is evaluated for elevated pH by determining the degree of polymer hydrolysis over time via nuclear magnetic resonance and linking it to viscosity performance at various temperatures. The AP conditions in the Matzen AP flooding project (pH &amp;gt; 10) lead to an increased initial rate of polymer hydrolysis of the tested hydrolyzed polyacrylamide (HPAM) by a factor of 100 compared to hydrolysis at a neutral pH level. This resulted in a rapid increase in a polymer solution viscosity of 160% compared with initial conditions within days at a reservoir temperature of 49°C, after which the viscosity leveled off. Accelerated aging experiments at higher temperatures predict long-term stability of the increased viscosity level for several years. Single-phase injection test in a representative core confirmed the performance of the aged solution compared to a nonaged solution at the same polymer concentration. The retention of polymers is reduced in AP conditions compared with traditional neutral pH conditions, 19 vs. 48 µg/g in the static adsorption test, respectively. Two-phase coreflood tests showed increased polymer viscosity at reservoir conditions. The displacement efficiency of the aged and nonaged polymer solution was similar, confirming the potential for cost savings using lower polymer concentration. This is leading to an improved injectivity and makes use of the increased polymer viscosity down in the reservoir through hydrolysis. The current work combines multiple aspects that should be considered in the proper planning of AP projects—not only improvements in polymer viscosity performance due to water softening but also long-term effects due to increased pH. Additionally, these aspects are combined with changes in adsorption properties. The results show that the design of AP projects will benefit from the holistic approach and understanding the changes in polymer rheology with time. The costs of AP projects can be reduced owing to the lower required polymer concentrations for the same displacement efficiency and reduced retention of polymer. An efficient design of AP projects takes good injectivity of nonaged polymers and the aging of the polymer solutions in alkali into account. Overall, we aim to reduce the polymer concentration—which is a key cost driver—compared with a nonaged application. We show that for AP effects, these effects should be evaluated to improve the economics.

ДОСЛІДЖЕННЯ КОМПЛЕКСОУТВОРЕННЯ ПОЛІЕТИЛЕНІМІНУ З ЙОНАМИ МІДІ (ІІ), НІКЕЛЮ (ІІ), КОБАЛЬТУ (ІІ)

There is described the influence of polyethylenimine globule structure on complexation with copper (II), nickel (II) and cobalt (II) ions. There are determined the values of the coordination number with the change of the pH of the solution for the complexes of ethylenediamine, diethylenetriamine and polyethylenimine with metal ions. It is investigated that the complexation of these metal ions with low molecular weight amines passes through three stages and with PEI through two stages. It is shown that the content of free nitrogen atoms in PEI, which do not react with metal ions, increases with increasing concentration of PEI in solution. The number of monomer units associated with metal ions depends on the size of the globule of the macromolecule, as well as the reaction process. The complexation reaction in solution is determined by the diffusion of metal ions into the polymer globule. If the reaction takes place in a diffusion field at a low polymer concentration, the rate of complexation is proportional to the concentration of macromolecules and the concentration of metal ions in solution.

Chitosan Micro-Membranes with Integrated Gold Nanoparticles as an LSPR-Based Sensing Platform.

Currently, there is an increasing need to develop highly sensitive plasmonic sensors able to provide good biocompatibility, flexibility, and optical stability to detect low levels of analytes in biological media. In this study, gold nanoparticles (Au NPs) were dispersed into chitosan membranes by spin coating. It has been demonstrated that these membranes are particularly stable and can be successfully employed as versatile plasmonic platforms for molecular sensing. The optical response of the chitosan/Au NPs interfaces and their capability to sense the medium's refractive index (RI) changes, either in a liquid or gas media, were investigated by high-resolution localized surface plasmon resonance (HR-LSPR) spectroscopy, as a proof of concept for biosensing applications. The results revealed that the lowest polymer concentration (chitosan (0.5%)/Au-NPs membrane) presented the most suitable plasmonic response. An LSPR band redshift was observed as the RI of the surrounding media was incremented, resulting in a sensitivity value of 28 ± 1 nm/RIU. Furthermore, the plasmonic membrane showed an outstanding performance when tested in gaseous atmospheres, being capable of distinguishing inert gases with only a 10-5 RI unit difference. The potential of chitosan/Au-NPs membranes was confirmed for application in LSPR-based sensing applications, despite the fact that further materials optimization should be performed to enhance sensitivity.

Enhanced Retention and Synergistic Plugging Effect of Multi-Complexed Gel on Water-Swellable Rubber

For the management of fractured large pores in high-water-bearing reservoirs, the general approach is to use transfer dissection and sealing. Conventional regulators have a limited regulating radius and can only produce blocking in the near-well zone, which is not ideal. Deep dissection technology can expand the radius of action and substantially improve the blocking effect. The existing deep-dissection agent system has problems such as high cost and poor effect, which affect its large-scale application. In this paper, to address these problems, a gel-type dissection modifier cross-linking agent was synthesized and optimized in the laboratory using low-concentration polymer, and the factors affecting the final gel formation effect were experimentally studied. The final polymer concentration was chosen to be 1500 mg/L~3000 mg/L, the poly-crossing ratio was 30:1, the pH was controlled at 7–9, and the temperature was controlled at 30–60 °C; the rubber was formed with good shear resistance and thermal stability, and had good adaptability to the high-mineralization environment. The optimal injection concentration of water-expanded rubber particles for this system was confirmed to be 3000 mg/L. Cryo-electron microscopy was used to observe the morphology of polymer gel formation and the adhesion of nucleated water-expanded particles to the gel, to clarify the mechanism of enhanced retention and sealing of nucleated water-expanded rubber particles by the multiple complex gel system, and finally to verify the sealing performance of the composite sealing system and determine the use effect by indoor simulation experiments with a two-dimensional flat plate model. This study is of great significance for the efficient development of high-water-bearing late reservoirs and further improvement of crude oil recovery.

Influence of temperature on the compression behavior of pharmaceutical excipients

Tableting on an industrial scale is characterized by an increase in temperature, which is dependent on numerous factors. The aim of this study was to examine the glass transition temperature of frequently used polymers as a critical parameter on tablet properties. Tablets were produced in a tablet press equipped with a temperature-controlled die at four different temperatures ranging from 22 to 70 °C. While pure polymers were characterized for their temperature-dependent compressibility behavior using Heckel analysis, tableting was performed from binary blends containing lactose as a filler and the polymer to be examined (ratio 9:1). Tablets were characterized in terms of tabletability, compactibility and their correlation with the glass transition temperature. The decrease in mean yield pressure upon temperature rise could clearly be correlated to the glass transition temperature of a given polymer, whereby polymers with low glass transition temperatures proved to be more responsive to temperature changes. Tablet properties were equally affected by the applied temperature despite the low polymer content. Thus, polymers with higher glass transition temperatures should be preferred in a full-production scale to avoid an alteration of tablet characteristics, whereas polymers with lower glass transition temperatures could be advantageous if a change of material properties is desired.