Search Results (18)

To address the technical challenge of high polymer gel viscosity reducers losing viscosity at elevated temperatures and difficulty in controlling fluid loss, a polymer-based nano calcium carbonate composite high-temperature tackifier named GW-VIS was prepared using acrylamide (AM), 2-acrylamido-2-methylpropanesulfonic acid (AMPS), N-vinylpyrrolidone (NVP), and nano calcium carbonate as raw materials through water suspension polymerization. This polymer gel can absorb water well at room temperature and has a small solubility. After a long period of high-temperature treatment, most of it can dissolve in water, increasing the viscosity of the suspension. The structure of the samples was characterized by infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy, and their performance was evaluated. Rheological tests indicated that the 0.5% water suspension had a consistency coefficient (k = 761) significantly higher than the requirement for clay-free drilling fluids (k > 200). In thermal resistance experiments, the material maintained stable viscosity at 180 °C (reduction rate of 0%), and only decreased by 14.8% at 200 °C. Salt tolerance tests found that the viscosity reduction after hot rolling at 200 °C was only 17.31% when the NaCl concentration reached saturation. Field trials in three wells in the Liaohe oilfield verified that the clay-free drilling fluid supported formation operations successfully. The study shows that the polymer gel has the potential to maintain rheological stability at high temperatures by forming a network structure through polymer chain adsorption and entanglement, with a maximum temperature resistance of up to 200 °C, providing an efficient drilling fluid for deep oil and gas well development. It is feasible to select nano calcium carbonate to participate in the research of high-temperature resistant polymer materials. Meanwhile, the combined effect of monomers with large steric hindrance and inorganic materials can enhance the product’s temperature resistance and resistance to NaCl pollution. Full article

This study presents a sustainable approach to transform waste cooking oil (WCO) into a multifunctional 3D-printable photocurable elastomer with integrated self-healing capabilities. A linear monomer, WCO-based methacrylate fatty acid ethyl ester (WMFAEE), was synthesized via a sequential strategy of transesterification, epoxidation, and ring-opening esterification. By copolymerizing WMFAEE with hydroxypropyl acrylate (HPA), a novel photocurable elastomer was developed, which could be amenable to molding using an LCD light-curing 3D printer. The resulting WMFAEE-HPA elastomer exhibits exceptional mechanical flexibility (elongation at break: 645.09%) and autonomous room-temperature self-healing properties, achieving 57.82% recovery of elongation after 24 h at 25 °C. Furthermore, the material demonstrates weldability (19.97% retained elongation after 12 h at 80 °C) and physical reprocessability (7.75% elongation retention after initial reprocessing). Additional functionalities include pressure-sensitive adhesion (interfacial toughness: 70.06 J/m² on glass), thermally triggered shape memory behavior (fixed at −25 °C with reversible deformation/recovery at ambient conditions), and notable biodegradability (13.25% mass loss after 45-day soil burial). Molecular simulations reveal that the unique structure of the WMFAEE monomer enables a dual mechanism of autonomous self-healing at room temperature without external stimuli: chain diffusion and entanglement-driven gap closure, followed by hydrogen bond-mediated network reorganization. Furthermore, the synergy between monomer chain diffusion/entanglement and dynamic hydrogen bond reorganization allows the WMFAEE-HPA system to achieve a balance of multifunctional integration. Moreover, the integration of these multifunctional attributes highlights the potential of this WCO-derived photocurable elastomer for various possible 3D printing applications, such as flexible electronics, adaptive robotics, environmentally benign adhesives, and so on. It also establishes a paradigm for converting low-cost biowastes into high-performance smart materials through precision molecular engineering. Full article

We present an interferometric sensor for investigating macroscopic quantum mechanics on a table-top scale. The sensor consists of a pair of suspended optical cavities with finesse over 350,000 comprising 10 g fused silica mirrors. The interferometer is suspended by a four-stage, light, in-vacuum suspension with three common stages, which allows for us to suppress common-mode motion at low frequency. The seismic noise is further suppressed by an active isolation scheme, which reduces the input motion to the suspension point by up to an order of magnitude starting from 0.7 Hz. In the current room-temperature operation, we achieve a peak sensitivity of 0.5 fm/$\sqrt{\mathrm{Hz}}$ in the acoustic frequency band, limited by a combination of readout noise and suspension thermal noise. Additional improvements of the readout electronics and suspension parameters will enable us to reach the quantum radiation pressure noise. Such a sensor can eventually be utilized for demonstrating macroscopic entanglement and for testing semi-classical and quantum gravity models. Full article

Bipartite entanglement is comprehensively investigated in the mononuclear molecular complex (Et₃NH)[Ni(hfac)₂L], where HL denotes 2-(2-hydroxy-3-methoxy-5-nitrophenyl)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-3-oxide-1-oxyl and hfacH stands for hexafluoroacetylacetone. From the magnetic point of view, the molecular compound (Et₃NH)[Ni(hfac)₂L] consists of an exchange-coupled spin-1 Ni²⁺ magnetic ion and a spin-$\frac{1}{2}$ nitronyl-nitroxide radical substituted nitrophenol. The nickel-radical molecular complex affords an experimental realization of a mixed spin-($\frac{1}{2}$, 1) Heisenberg dimer with a strong antiferromagnetic exchange coupling, J/$k_B$ = 505 K, and two distinct g-factors, g_Rad = 2.005 and g_Ni = 2.275. By adopting this set of magnetic parameters, we demonstrate that the Zeeman splitting of a quantum ferrimagnetic ground-state doublet due to a weak magnetic field may substantially reinforce the strength of bipartite entanglement at low temperatures. The molecular compound (Et₃NH)[Ni(hfac)₂L] maintains sufficiently strong thermal entanglement, even at room temperature, vanishing only above 546 K. Specifically, the thermal entanglement in the nickel-radical molecular complex retains approximately 40% of the maximum value, corresponding to perfectly entangled Bell states at room temperature, which implies that this magnetic compound provides a suitable platform of a molecular qubit with potential implications for room-temperature quantum computation and quantum information processing. Full article

Many quantum device signals are proportional to the number of the participating atoms that take part in the detection devices. Among these are optical magnetometers, atomic clocks, quantum communications and atom interferometers. One way to enhance the signal-to-noise ratio is to introduce atom entanglement that increases the signal in a super-radiant-like effect. A coherent em field inside a laser cavity is suggested to achieve atoms’ correlation/entanglement. This may also play an important role in the basic quantum arena of many-body physics. An initial novel experiment to test the realization of atoms’ correlation is described here. A Cs optical magnetometer is used as a tool to test the operation of a cell-in-cavity laser and its characteristics. A vapor cell is inserted into an elongated external cavity of the pump laser in Littrow configuration. Higher atom polarization and reduced laser linewidth are obtained leading to better magnetometer sensitivity and signal-to-noise ratio. The Larmor frequency changes of the Free Induction Decay of optically pumped Cs atomic polarization in the ambient earth magnetic field at room temperature is measured. Temporal changes in the magnetic field of less than 10 pT/√Hz are measured. The first-order dependence of the magnetic field on temperature and temperature gradients is eliminated, important in many practical applications. Single and gradiometric magnetometer configurations are presented. Full article

By utilizing a generalized version of the Madelung quantum hydrodynamic framework that incorporates noise, we derive a solution using the path integral method to investigate how a quantum superposition of states evolves over time. This exploration seeks to comprehend the process through which a stable quantum state emerges when fluctuations induced by the noisy gravitational background are present. The model defines the conditions that give rise to a limited range of interactions for the quantum potential, allowing for the existence of coarse-grained classical descriptions at a macroscopic level. The theory uncovers the smallest attainable level of uncertainty in an open quantum system and examines its consistency with the localized behavior observed in large-scale classical systems. The research delves into connections and similarities alongside other theories such as decoherence and the Copenhagen foundation of quantum mechanics. Additionally, it assesses the potential consequences of wave function decay on the measurement of photon entanglement. To validate the proposed theory, an experiment involving entangled photons transmitted between detectors on the moon and Mars is discussed. Finally, the findings of the theory are applied to the creation of larger Q-bit systems at room temperatures. Full article

The coexistence of two spin components with different Larmor frequencies in colloidal CdSe and CdS quantum dots (QDs) leads to the entanglement of spin signals, complicating the analysis of dynamic processes and hampering practical applications. Here, we explored several methods, including varying the types of hole acceptors, air or anaerobic atmosphere and laser repetition rates, in order to facilitate the obtention of one single Larmor frequency in the coherent spin dynamics using time-resolved ellipticity spectroscopy at room temperature. In an air or nitrogen atmosphere, manipulating the photocharging processes by applying different types of hole acceptors, e.g., Li[Et₃BH] and 1-octanethiol (OT), can lead to pure spin components with one single Larmor frequency. For as-grown QDs, low laser repetition rates favor the generation of the higher Larmor frequency spin component individually, while the lower Larmor frequency spin component can be enhanced by increasing the laser repetition rates. We hope that the explored methods can inspire further investigations of spin dynamics and related photophysical processes in colloidal nanostructures. Full article

In situ-forming gels with self-assembling and self-healing properties are materials of high interest for various biomedical applications, especially for drug delivery systems and tissue regeneration. The main goal of this research was the development of an innovative gel carrier based on dynamic inter- and intramolecular interactions between amphiphilic polyurethane and peptide structures. The polyurethane architecture was adapted to achieve the desired amphiphilicity for self-assembly into an aqueous solution and to facilitate an array of connections with peptides through physical interactions, such as hydrophobic interactions, dipole-dipole, electrostatic, π–π stacking, or hydrogen bonds. The mechanism of the gelation process and the macromolecular conformation in water were evaluated with DLS, ATR-FTIR, and rheological measurements at room and body temperatures. The DLS measurements revealed a bimodal distribution of small (~30–40 nm) and large (~300–400 nm) hydrodynamic diameters of micelles/aggregates at 25 °C for all samples. The increase in the peptide content led to a monomodal distribution of the peaks at 37 °C (~25 nm for the sample with the highest content of peptide). The sol–gel transition occurs very quickly for all samples (within 20–30 s), but the equilibrium state of the gel structure is reached after 1 h in absence of peptide and required more time as the content of peptide increases. Moreover, this system presented self-healing properties, as was revealed by rheological measurements. In the presence of peptide, the structure recovery after each cycle of deformation is a time-dependent process, the recovery is complete after about 300 s. Thus, the addition of the peptide enhanced the polymer chain entanglement through intermolecular interactions, leading to the preparation of a well-defined gel carrier. Undoubtedly, this type of polyurethane/peptide-based carrier, displaying a sol–gel transition at a biologically relevant temperature and enhanced viscoelastic properties, is of great interest in the development of medical devices for minimally invasive procedures or precision medicine. Full article

Fused deposition modeling (FDM) 3D printing has printed thermoplastic materials layer-by-layer to form three dimensional products whereby interlayer adhesion must be well controlled to obtain high mechanical performance and product integrity. This research studied the effects of ambient temperatures and crystalline structure on the interlayer adhesion and properties of thermoplastic FDM 3D printing. Five kinds of poly(lactic acid) (PLA) filaments, both commercially available and the laboratory-made, were printed using the enclosure FDM 3D printer. The ambient temperatures were set by the temperature-controlled chamber from room temperature to 75 °C with and without a cooling fan. The interlayer adhesion was characterized by the degree of entanglement density, morphology, and fracture toughness. In addition, PLA filament with high crystallinity has induced heat resistance, which could prevent filament clogging and successfully print at higher chamber temperatures. The ambient temperature increased with increased chamber temperature and significantly increased when printed without a cooling fan, resulting in improved interlayer bonding. The crystalline structure and dynamic mechanical properties of the 3D printed products were promoted when the chamber temperature was increased without a cooling fan, especially in PLA composites and PLA containing a high content of L-isomer. However, although the additives in the PLA composite improved crystallinity and the degree of entanglement density in the 3D-printed products, they induced an anisotropic characteristic that resulted in the declination of the interlayer bonding in the transverse orientation products. The increasing of chamber temperatures over 40 °C improved the interlayer bonding in pristine PLA products, which was informed by the increased fracture toughness. Further, it can be noted that the amorphous nature of PLA promotes molecular entanglement, especially when printed at higher chamber temperatures with and without a cooling fan. Full article

This study investigated the mechanism for acetic acid pretreatment to improve cell wall integrity and thereby enhance the hardness of cooked Sagittaria sagittifolia L. slices by affecting polysaccharides in the cell wall. Distilled water immersion and 0.6% acetic acid immersion (the solid/liquid ratio is 1:10) for 15 h at room temperature could result in the conversion of pectin through different reactions during thermal processing. Combined in situ and in vitro analysis demonstrated that acetic acid pretreatment could promote the interaction of cellulose microfiber or hemicellulose with RG-Ⅰ side chains during thermal processing of S. sagittifolia L. slices, promote the entanglement between linear pectin molecules and make hemicellulose show a lower molecular weight under cooking, making it easy to firmly bind to pectin, which resulted in texture changes. The findings may help improve the texture of thermally processed vegetables and fruits and deep processing of starchy vegetables. Full article

Aqueous solutions of hydroxypropyl methylcellulose (HPMC) show inverse thermoreversible gelation, i.e., they respond to small temperature variations exhibiting sol–gel transition during heating, and reversibly gel–sol transition during cooling. According to the pertinent literature on HPMC aqueous systems, at room temperature, the loss modulus (G”) is higher than the storage modulus (G’). During the heating ramp, the viscoelastic response follows a peculiar path: initially, G” and G’ smoothly decrease, then drop to a minimum and finally increase. Eventually, G’ overcomes G”, indicating the gel formation. A recent explanation of this behaviour considers a two-step mechanism: first, phase separation occurs, then fibrils form from a polymer-rich phase and entangle, leading to a three-dimensional network. Based on this, our research focuses on the rheological analysis of the different steps of the sol–gel transition of an HPMC aqueous solution. We perform different viscoelastic tests: thermal ramps, time sweeps, and frequency sweeps at selected characteristic temperatures. We couple classical analysis of the SAOS experiments with an innovative approach based on the evaluation of the activation energy (Ea), made possible by the instrument intrinsic temperature oscillations around the target value. Results show that Ea can be a valid tool that contributes to further clarifying the peculiar microstructural evolution occurring in this kind of thermoreversible gel. Full article

Low-molecular-weight gels have great potential for use in a variety of fields, including petrochemicals, healthcare, and tissue engineering. These supramolecular gels are frequently metastable, implying that their properties are kinetically controlled to some extent. Here, we report on the in situ supramolecular gel formation by mixing 1,3-cyclohexane diamine (1) and isocyanate derivative (2) without any catalysis at room temperature in various organic solvents. A mixture of building blocks 1 and 2 in various organic solvents, dichloromethane, tetrahydrofuran, chloroform, toluene, and 1,4-dioxane, resulted in the stable formation of supramolecular gel at room temperature within 60–100 s. This gel formation was caused by the generation of urea moieties, which allows for the formation of intermolecular hydrogen-bonding interactions via reactions 1 and 2. In situ supramolecular gels demonstrated a typical entangled fiber structure with a width of 600 nm and a length of several hundred μm. In addition, the supramolecular gels were thermally reversible by heating and cooling. The viscoelastic properties of supramolecular gels in strain and frequency sweets were enhanced by increasing the concentration of a mixed 1 and 2. Furthermore, the supramolecular gels displayed a thixotropic effect, indicating a thermally reversible gel. Full article

A room-temperature strip-guided “manufacturable” Silicon-on-Insulator (SOI)/GeSn integrated-photonics quantum-gyroscope chip operating at 1550 nm is proposed and analysed. We demonstrate how the entangled photons generated in Si Spontaneous Four Wave Mixing (SFWM) can be used to improve the resolution of a Sagnac interferometric gyroscope. We propose different integrated architectures based on degenerate and non-degenerate SFWM. The chip comprises several beam splitters, two SFWM entangled photon sources, a pump filter, integrated Mach–Zehnder interferometric gyro, and an array of waveguide coupled GeSn/Ge/Si single-photon avalanche detectors. The laser pumped SWFM sources generate the signal-idler pairs, which, in turn, are used to measure the two-photon, four-photon, and higher order coincidences, resulting in an increasing of the gyro resolution by a factor of two and four, with respect to the classical approach. Full article

The gelation of cellulose in alkali solutions is quite relevant, but still a poorly understood process. Moreover, the role of certain additives, such as urea, is not consensual among the community. Therefore, in this work, an unusual set of characterization methods for cellulose solutions, such as cryo-transmission electronic microscopy (cryo-TEM), polarization transfer solid-state nuclear magnetic resonance (PTssNMR) and diffusion wave spectroscopy (DWS) were employed to study the role of urea on the dissolution and gelation processes of cellulose in aqueous alkali. Cryo-TEM reveals that the addition of urea generally reduces the presence of undissolved cellulose fibrils in solution. These results are consistent with PTssNMR data, which show the reduction and in some cases the absence of crystalline portions of cellulose in solution, suggesting a pronounced positive effect of the urea on the dissolution efficiency of cellulose. Both conventional mechanical macrorheology and microrheology (DWS) indicate a significant delay of gelation induced by urea, being absent until ca. 60 °C for a system containing 5 wt % cellulose, while a system without urea gels at a lower temperature. For higher cellulose concentrations, the samples containing urea form gels even at room temperature. It is argued that since urea facilitates cellulose dissolution, the high entanglement of the cellulose chains in solution (above the critical concentration, C*) results in a strong three-dimensional network. Full article

On-chip generation, manipulation and detection of nonclassical states of light are some of the major issues for quantum information technologies. In this context, the maturity and versatility of semiconductor platforms are important assets towards the realization of ultra-compact devices. In this paper we present our work on the design and study of an electrically injected AlGaAs photon pair source working at room temperature. The device is characterized through its performances as a function of temperature and injected current. Finally we discuss the impact of the device’s properties on the generated quantum state. These results are very promising for the demonstration of electrically injected entangled photon sources at room temperature and let us envision the use of III-V semiconductors for a widespread diffusion of quantum communication technologies. Full article