Low dielectric constant(low-k)materials are critical for advanced packaging in high-density microelectronic devices and high-frequency communication technologies.Ladder polysiloxanes,which are characterized by their u...Low dielectric constant(low-k)materials are critical for advanced packaging in high-density microelectronic devices and high-frequency communication technologies.Ladder polysiloxanes,which are characterized by their unique double-chain structure and intrinsic microporosity,offer remarkable advantages in terms of thermal stability,oxidation resistance,and dielectric performance.However,structural defects in ladder polysiloxanes,such as cage-like and irregular oligomers,and their effects on dielectric properties remain underexplored.In this study,a series of ladder-like polysiloxanes(X-TMS)with diverse side groups weresynthesized via a one-step base-catalyzed method.The influence of the benzocyclobutene(BCB)side groups on the formation of regular ladder structures was systematically investigated.Notably,BCB incorporation disrupted the structural regularity,favoring the formation of cage-like and irregular topologies,which were extensively characterized using 29silicon nuclear magnetic resonance spectroscopy(^(29)Si-NMR),Fourier transform infrared spectroscopy(FTIR),gel permeation chromatography(GPC),and X-ray diffraction(XRD).These structural defects were beneficial for improving the hydrophobicity and thermal stability.Copolymerization of X-TMS with commercial DVS-BCB resins further enhanced the mechanical properties,with the elastic modulus increasing from 3.6 GPa to 4.4 GPa and water absorption reduced from 0.33 wt%to 0.06 wt%.This study establishes a clear correlation between topological structures and material properties.These findings not only advance the understanding of the structure-property relationships in ladder polysiloxanes but also provide a novel approach for designing high-performance interlayer dielectric materials for next-generation microelectronics.展开更多
To address the poor mechanical performance and improve the tribological properties of self-lubricating polyphenylene sulfide/irradiation treated polytetrafluoroethylene(PPS/i-PTFE)blends,different aspect ratio carbon ...To address the poor mechanical performance and improve the tribological properties of self-lubricating polyphenylene sulfide/irradiation treated polytetrafluoroethylene(PPS/i-PTFE)blends,different aspect ratio carbon fibers(i.e.,PSCF:50,SCF:about 429)were introduced as reinforcement fillers.The results showed that the hybriding of PSCF and SCF at certain mass ratios exhibited simultaneous enhancement of mechanical and tribological performance for PPS/i-PTFE blend through the construction of synergistic lubrication and mechanical interlocking network.Specifically,the flexural strength and modulus of PPS/i-PTFE were increased by 125.6% and 389.3%,the friction coefficient and specific wear rate were decreased by 13.9% and 95%,respectively.It was worth noting that PPS composites possessed excellent integrated performance which were able to withstand sliding action under high PV(≥10 MPa·m/s)conditions,as assessed by a customized pin-on-disc tester.This work demonstrated that the formation of intact lubricating film combined with the enhanced thermal and mechanical properties were favorable for improving the tribological properties of PPS-based composites,which makes them suitable for advanced engineering applications.展开更多
Inter-salt shale oil reservoirs located between two salt layers are always accompanied by high temperature and high salinity. However, the present commonly used water-soluble polymers in fracturing fluids su er from p...Inter-salt shale oil reservoirs located between two salt layers are always accompanied by high temperature and high salinity. However, the present commonly used water-soluble polymers in fracturing fluids su er from poor tolerance to high temperature and high salinity. Thermoviscosifying polymers(TVP) whose aqueous solution shows viscosity increase upon increasing temperature and salt concentration have received considerable attention recently, which is promising for utilization in fracturing fluids to overcome these problems. In this work, both the salt-induced viscosifying property and mechanism of a TVP solution were investigated and the performance of TVP used as fracturing fluid based on the conditions of the Jianghan inter-salt shale oil reservoir in China was evaluated. It is found that the salt-induced viscosifying property of the TVP solution decreases with temperature and shear rate, but increases with polymer concentration. The number of intermolecular hydrophobic domains increases with the salt concentration contributing to the strengthening of a 3D network structure, which results in an increase in viscosity. In addition, the TVP fracturing fluid formulated with saturated brine exhibits excellent temperature and shear resistance, sand-suspending performance, and gel-breaking performance. Its viscosity remains above50 m Pa s after being sheared for 1 h even at a high temperature of 140 °C and the sand-suspending stability can be maintained for more than 1 week at 100 °C. Furthermore, the fracturing fluid can be easily broken down within 12h using 0.2 wt%–0.3 wt% potassium persulfate without residue.展开更多
A series of aliphatic biodegradable poly（ether-ester）s based on poly（butylene succinate）（PBS）as hard segment and poly（tetramethylene oxide）（PTMO,M_n=1 000 g/mol） as soft segment were synthesized.The composit...A series of aliphatic biodegradable poly（ether-ester）s based on poly（butylene succinate）（PBS）as hard segment and poly（tetramethylene oxide）（PTMO,M_n=1 000 g/mol） as soft segment were synthesized.The composition dependence of thermal behavior,morphology and mechanical properties was investigated by differential scanning calorimetry（DSC）,atomic force microscopy（AFM）,and tensile testing.The crystallization temperature（T_c） and melting temperature（T_m） of the PBS block within poly（ether-ester）s decrease steadily at first,but decrease sharply with PTMO content above 50 wt%.Two crystallization peaks were detected for PTMO in PBSPTMO60 sample,suggesting the occurrence of fractionated crystallization.The crystallization enthalpies（△H_c） and melting enthalpies（△H_m） of PBS block decrease at first,then increase as PTMO content increases further.AFM has demonstrated that phase-separated morphology transforms from a phase of continuous hard matrix to one of continuous soft matrix containing isolated hard domain as PTMO content is increased.Finally,the results of tensile testing show that the poly（ether-ester）s present the behavior of plastics when PTMO content is below 40 wt%,and of thermoplastic elastomers with PTMO content above 50 wt%.By varying the composition of copolymer,the aliphatic poly（ether-ester）s plastics,or especially biodegradable aliphatic poly（ether-ester）s thermoplastic elastomers can be obtained.展开更多
The effect of crystallization conditions of poly(butylene succinate)(PBS) component on the crystallization of poly(tetramethylene oxide)(PTMO) component in their segment block copolymer, with a higher PTMO content(PTM...The effect of crystallization conditions of poly(butylene succinate)(PBS) component on the crystallization of poly(tetramethylene oxide)(PTMO) component in their segment block copolymer, with a higher PTMO content(PTMO mass fraction is 67%), was investigated by DSC and temperature-dependent FTIR. It is found that the isothermal crystallization time(tIC) of PBS has an effect on the crystallization behavior of PTMO component. Perturbation correlation move-window two-dimensional(PCMW2 D) correlation analysis and generalized 2 D correlation analysis(2 DIR) were performed to explore the origin of this phenomenon. The PCMW2 D and 2 DIR results show that the correlation intensity peak observed at around 20 ℃ for PTMO is due to the PTMO chains movements forced by the PBS chains folded movements. If tIC of PBS at temperature of 20 ℃ is prolonged, more PTMO components are incorporated in the region between PBS lamellae and the peak at-7.6 ℃(belonging to less-constricted PTMO chains) changes smaller and even disappears, while the peak at-16.3 ℃ belonging to more-constricted PTMO chains gets bigger. A crystallization model was also established in this study. The results of tensile testing showed that tensile strength slightly increased and elongation at break decreased with increasing heat treatment time at 40 ℃.展开更多
In this study,the three dimensional nanoscale organization in the photoactive layers of poly(3-hexylthiophene) (P3HT) and a methanofullerene derivative (PCBM) is revealed by transmission electron tomography.After anne...In this study,the three dimensional nanoscale organization in the photoactive layers of poly(3-hexylthiophene) (P3HT) and a methanofullerene derivative (PCBM) is revealed by transmission electron tomography.After annealing treatment,either at elevated temperature or during slow solvent evaporation,nanoscale interpenetrating networks are formed with high crystalline order and favorable concentration gradients of both components through the thickness of the photoactive layer.Such a tailored morphology account...展开更多
With the aim of developing a low-cost and efficient visible-light-driven photocatalyst for radical polymerization,iron-chelating polyimide networks(Fe@MPI)was fabricated by firstly synthesizing photoactive melamine-co...With the aim of developing a low-cost and efficient visible-light-driven photocatalyst for radical polymerization,iron-chelating polyimide networks(Fe@MPI)was fabricated by firstly synthesizing photoactive melamine-containing polyimide(MPI)networks and then incorporating Fe(III)cations into the polymer networks.Fe@MPI exhibits a wide absorption spectrum ranging from 220 to 1250 nm and 3.5 times higher photocurrent intensity as compared with the pristine MPI.Based on its excellent photo-electric properties,Fe@MPI was employed as a recyclable heterogeneous catalyst,providing sufficient activity for the visible-light driven radical polymerization to synthesize poly(methyl methacrylate)with molecular weight up to 31.×10^4 g mol.Taking advantage of the heterogeneous nature of the catalyst,Fe@MPI could be facilely regenerated from the polymerization solution by filtration without an obvious loss of its activity.This research provides a novel recyclable catalyst for visible-light driven radical polymerization.展开更多
Polymer flooding has been witnessed an effective technology for enhancing oil recovery from medium-to low-permeability reservoirs;however, direct visualization of polymer solution flow in such reservoir condition is s...Polymer flooding has been witnessed an effective technology for enhancing oil recovery from medium-to low-permeability reservoirs;however, direct visualization of polymer solution flow in such reservoir condition is still lacking. In this work, a three-dimensional (3D) core-on-a-chip device with a permeability of around 200 mD was prepared and employed to visualize the pore-scale flow and displacement of a self-adaptive polymer (SAP, 8.7 × 106 g·mol−1)−whose microscopic association structure and macroscopic viscosity can reversibly change in response to shear action−versus partially hydrolyzed polyacrylamide (HPAM), by recording their flow curves, monitoring dynamic transportation process via particle imaging velocimetry, and building 3D structure of remaining oil. The results show that, in single-phase flow, all polymer solutions exhibit flow thinning and then thickening regions as flow rate increases, but the transition between two regimes occurs at a small Weissenberg number (10−3−10−1) in this medium-permeable condition. In contrast to HPAM-1 with close weight-average molecular weight (Mw), the adaptive character not only extends SAP's shear-govern region, allowing SAP to propagate piece by piece and achieve higher accessible pore volume, but it also enhances the elastic resistibility of polymer in the extension-dominated regime, increasing the microscopic displacement efficiency. These two effects result in 1.5–3 times more oil recovery factor for SAP than for HPAM-1. Regarding ultra-high-Mw HPAM-2 (25 × 106 g·mol−1), plugging and chain degradation do occur, thus producing lower oil recovery than SAP. This work provides a direct approach for in-situ assessment of polymer-based displacing system under a more authentic condition of practical reservoirs.展开更多
The kinetics of ultrasonic degradation of aqueous solution of polyacrylamide（PAM）and poly（ethyleneoxide）（PEO）as well as ultrasonic block copolymerization of aqueous solution of the mixture of PAM/PEOwere studied...The kinetics of ultrasonic degradation of aqueous solution of polyacrylamide（PAM）and poly（ethyleneoxide）（PEO）as well as ultrasonic block copolymerization of aqueous solution of the mixture of PAM/PEOwere studied respectively.The degradation reaction of PEO follows a linear relationship between（P1-P∞）-1and irradiation time,while that of PAM follows a linear relationship between（P1-P∞）-1/2and irradiation time.The structure of the copolymer was identified by IR,NMR and DTA,and the copolymer prepared is a blockone.The copolymer formed by irradiating 1% aqueous solution of PEO/PAM mixture（1:1）for a period of40min.at 18.2 kHz with a sonic intensity corresponding to 2.OA input current on the reversed main circuitamounts to 61.8%.展开更多
The tireless pursuit of supercapacitors with high energy density entails the parallel advancement of wellsuited electrode materials and elaborately engineered architectures.Polypyrrole(PPy)emerges as an exceedingly co...The tireless pursuit of supercapacitors with high energy density entails the parallel advancement of wellsuited electrode materials and elaborately engineered architectures.Polypyrrole(PPy)emerges as an exceedingly conductive polymer and a prospective pseudocapacitive materials for supercapacitors,yet the inferior cyclic stability and unpredictable polymerization patterns severely impede its real-world applicability.Here,for the first time,an innovative seed-induced in-situ polymerization assisted 3D printing strategy is proposed to fabricate PPy-reduced graphene oxide/poly(vinylidene difluoride-cohexafluoropropylene)(PVDF-HFP)(PPy-rGO/PH)electrodes with controllable polymerization behavior and exceptional areal mass loading.The preferred active sites uniformly pre-planted on the 3D-printed graphene substrates serve as reliable seeds to induce efficient polypyrrole deposition,achieving an impressive mass loading of 185.6 mg cm^(-2)(particularly 79.2 mg cm^(-2)for polypyrrole)and a superior areal capacitance of 25.2 F cm^(-2)at 2 mA cm^(-2)for a 12-layer electrode.In agreement with theses appealing features,an unprecedented areal energy density of 1.47 mW h cm^(-2)for a symmetrical device is registered,a rarely achieved value for other PPy/rGO-based supercapacitors.This work highlights a promising route to preparing high energy density energy storage modules for real-world applications.展开更多
The increasing demand for short charging time on electric vehicles has motivated realization of fast chargeable lithium-ion batteries(LIBs).However,shortening the charging time of LIBs is limited by Li^(+)intercalatio...The increasing demand for short charging time on electric vehicles has motivated realization of fast chargeable lithium-ion batteries(LIBs).However,shortening the charging time of LIBs is limited by Li^(+)intercalation process consisting of liquid-phase diffusion,de-solvation,SEI crossing,and solid-phase diffusion.Herein,we propose a new strategy to accelerate the de-solvation step through a control of interaction between polymeric binder and solvent-Li^(+)complexes.For this purpose,three alkali metal ions(Li^(+),Na^(+),and K^(+))substituted carboxymethyl cellulose(Li-,Na-,and K-CMC)are prepared to examine the effects of metal ions on their performances.The lowest activation energy of de-solvation and the highest chemical diffusion coefficient were observed for Li-CMC.Specifically,Li-CMC cell with a capacity of 3 mAh cm^(-2)could be charged to>95%in 10 min,while a value above>85%was observed after 150 cycles.Thus,the presented approach holds great promise for the realization of fast charging.展开更多
In this paper, the rigid structural thermosensitive polymer （made in lab） of NBS （N-butyl styrene）, N, N-DEAM （diethyl acrylamide） and AM （acrylamide） was prepared. The influence of viscosity for copolymer sol...In this paper, the rigid structural thermosensitive polymer （made in lab） of NBS （N-butyl styrene）, N, N-DEAM （diethyl acrylamide） and AM （acrylamide） was prepared. The influence of viscosity for copolymer solution under different reaction conditions such as temperatures and inorganic salt （monovalent salt and divalent salt） was analyzed. The experiment studies the combination of polymer situation and three different types of surfactants under certain conditions of the room temperature （25℃） and the formation temperature （76℃）. At last, the influence of the surfactant kinds and concentration on the viscosity of the polymer solution are studied. The results show that： The copolymer solution, the apparent viscosity of which decreases with the increasement of temperature, but its viscosity has suddenly increased and thereafter dropped in the transition temperature. So the temperature sensitive effect ofcopolymer is very significantly. When the concentration of inorganic salt and surfactant can be controlled in certain extent, the copolymer solution, the effect increases with the increasement of the concentration, but the viscosity of which decreases with the increasement of shear rate. Shear rate can be controlled in certain extent, shearing stability properties of the copolymer solution are proved.展开更多
As the application scenarios of aerogels expand,higher requirements are put forward for the materials used to prepare aerogels.Due to the unique chemical structure,polytetrafluoroethylene(PTFE)has excellent properties...As the application scenarios of aerogels expand,higher requirements are put forward for the materials used to prepare aerogels.Due to the unique chemical structure,polytetrafluoroethylene(PTFE)has excellent properties such as high-temperature resistance,hydrophobicity,and chemical stability.However,the PTFE aerogels are difficult to be molded due to the weak interaction between resin particles.In this work,poly(ethylene oxide)(PEO)was selected as the carrier to assist the PTFE aerogels molding.The pure PTFE aerogels were prepared by homogeneously mixing PTFE aqueous dispersion and PEO,freeze-drying,and high-temperature sintering.When the mass fraction of PTFE and PEO were appropriate,the porosity of PTFE aerogels exceeded 90%and had a hierarchical honeycomb structure.Results showed that the PTFE aerogels not only had excellent hydrophobicity but also possessed superior acoustic insulation,mechanical strength,thermal insulation,and heat resistance properties.Specifically,the water contact angle is about 140°.The noise reduction coefficient is 0.34 and the average sound absorption coefficient is greater than 88%in the frequency range of 2000-6400 Hz.Meanwhile,the thermal conductivity in the air is about 0.045 W/(m·K),and the initial thermal decomposition temperature is 450℃.More importantly,the PTFE aerogels had excellent temperature and corrosion resistance.Even after extremely thermal and chemical treatment,they remained unchanged porous structure as well as acoustic and thermal insulation properties,which exhibits great potential for application in many harsh environments.展开更多
The Janus fabrics designed for personal moisture/thermal regulation have garnered significant attention for their potential to enhance human comfort.However,the development of smart and dynamic fabrics capable of mana...The Janus fabrics designed for personal moisture/thermal regulation have garnered significant attention for their potential to enhance human comfort.However,the development of smart and dynamic fabrics capable of managing personal moisture/thermal comfort in response to changing external environments remains a challenge.Herein,a smart cellulose-based Janus fabric was designed to dynamically manage personal moisture/heat.The cotton fabric was grafted with N-isopropylacrylamide to construct a temperature-stimulated transport channel.Subsequently,hydrophobic ethyl cellulose and hydrophilic cellulose nanofiber were sprayed on the bottom and top sides of the fabric to obtain wettability gradient.The fabric exhibits anti-gravity directional liquid transportation from hydrophobic side to hydrophilic side,and can dynamically and continuously control the transportation time in a wide range of 3–66 s as the temperature increases from 10 to 40℃.This smart fabric can quickly dissipate heat at high temperatures,while at low temperatures,it can slow down the heat dissipation rate and prevent the human from becoming too cold.In addition,the fabric has UV shielding and photodynamic antibacterial properties through depositing graphitic carbon nitride nanosheets on the hydrophilic side.This smart fabric offers an innovative approach to maximizing personal comfort in environments with significant temperature variations.展开更多
Herein,we report the multi-metal atomic catalysts for solid-state dehydrogenation of MgH_(2).It aims to reveal the multi-element synergy in catalysts for solid-state hydrogen storage.The kinetic measurements and fitti...Herein,we report the multi-metal atomic catalysts for solid-state dehydrogenation of MgH_(2).It aims to reveal the multi-element synergy in catalysts for solid-state hydrogen storage.The kinetic measurements and fitting reveal two mechanisms:one shows a maximum rate at the early stage,such as V and Cr;the other needs a temperature-sensitive preparation time for its maximum rate,such as Ni.The combina-tion of two catalyst components demonstrates the best kinetics:V and Cr boost the initial dehydrogena-tion,and Ni benefits the further hydrogen transfer which alleviates the rate of decay.This work provides guidelines for the design of multi-element doped catalysts for MgH_(2) dehydrogenation.展开更多
Achieving continuous motions typically requires dynamic external stimuli for cyclic deformation,or crafted geometries with intricate modules to form a self-regulated feedback loop upon static stimulation.It is still a...Achieving continuous motions typically requires dynamic external stimuli for cyclic deformation,or crafted geometries with intricate modules to form a self-regulated feedback loop upon static stimulation.It is still a grand challenge to realize self-sustained motion in soft robots subject to unchanging environment,without complex geometry or a control module.In this work,we report soft robots based on an anisotropic cylindrical hydrogel showing self-regulated,continuous rolling motions under constant light irradiation.The robots are animated by mirror-symmetry-breaking induced by photothermal strain gradient.The self-sustained motion is attributed to the fast and reversible deformation of the gel and the autonomous refresh of the irradiated region during the rolling motion.The hydrogel robots can reach a rolling speed of 1.27 mm·s^(-1)on a horizonal surface and even climb a ramp of 18°at a speed of 0.57 mm·s^(-1)in an aqueous environment.Furthermore,the hydrogel robots can overcome an obstacle,with rolling direction controllable through irradiation angle of the light and local irradiation on selective regions.This work suggests a facile strategy to develop hydrogel robots and may provide unforeseen inspirations for the design of self-regulated soft robots by using other intelligent materials.展开更多
The full arrival of 5 G and advances in electronic integration make efficient heat dissipation crucial for stable operation and longer product lifespan. In this study, a vacuum-assisted filtration process was employed...The full arrival of 5 G and advances in electronic integration make efficient heat dissipation crucial for stable operation and longer product lifespan. In this study, a vacuum-assisted filtration process was employed to fabricate ammoniated alumina/MXene/bacterial cellulose (Al_(2)O_(3)-NH_(2)/MXene/BC) composite films that display a unique integration of properties, encompassing ultra-high thermal conductivity (λ), mechanical flexibility, and high photothermal conversion performance. By leveraging the bridging effect among spherical Al_(2)O_(3)-NH_(2) and MXene nanosheets, a densely packed “point-surface” structure was constructed in BC by using a one-step preparation process. When the mass fraction of Al_(2)O_(3)-NH_(2)/MXene (1:3, w/w) is 40 wt%, the O-BAl1M3 exhibited an in-plane λ of 20.02 W m^(-1) K^(-1), which was 436 % and 94 % higher than that of pure BC and T-BAl1M3 (prepared by a two-step method), respectively. Furthermore, constructing an intact thermal conductive network within BC notably promoted photothermal and photoelectric conversion performance. The maximum surface temperature and voltage of the O-BAl1M3 film reached 106.9 ℃ and 48.34 mV when a sample with an area of 1.56 cm^(2) was exposed under a light intensity of 200 mW cm^(-2). By applying O-BAl1M3 film, the temperature inside a self-built greenhouse model reached up to 64.8 ℃ within 1200 s under a light intensity of 100 mW cm^(-2), which validated the practical application of the composite films and offered a novel approach for creating flexible films with superior photothermal conversion capability. This work provided insights into preparing functional composite films for efficient thermal management and photothermal conversion applications.展开更多
This paper presents a comprehensive test and systematic evaluation analysis of cabin noise in the Robinson R44 RAVEN II helicopter.Initially,microphones were placed within the cabin to conduct systematic assessments o...This paper presents a comprehensive test and systematic evaluation analysis of cabin noise in the Robinson R44 RAVEN II helicopter.Initially,microphones were placed within the cabin to conduct systematic assessments of noise levels under various flight conditions,including takeoff,climbing,level flight,landing,hovering,etc.Subsequently,time–frequency analysis was conducted on the test data utilizing traditional A-weighted sound pressure levels,which was followed by quantitative comparisons across different flight conditions.Then,detailed evaluation and discussion were conducted,taking into account the subjective perceptions and communication challenges of cabin crew members.This assessment incorporated the use of aviation noise indicators,speech interference levels,and metrics related to sound quality.Finally,potential noise reduction measures and their effects were preliminarily discussed.The results indicate that helicopter cabin noise exhibited variations across different flight states or positions within the same state,ranging from 87.6 d B(A)to 92.6 dB(A).Discrepancies between A-weighted sound pressure level and psychoacoustic parameters were observed,particularly during hovering states,which indicate that there is a necessity for the combination of multiple evaluation indicators.Notably,damping measure can serve as a pivotal factor in mitigating cabin noise.展开更多
基金financially supported by the National Natural Science Foundation of China(Nos.52373316,22075298,and52373020)the Beijing Municipal Natural Science Foundation(No.2212053)。
文摘Low dielectric constant(low-k)materials are critical for advanced packaging in high-density microelectronic devices and high-frequency communication technologies.Ladder polysiloxanes,which are characterized by their unique double-chain structure and intrinsic microporosity,offer remarkable advantages in terms of thermal stability,oxidation resistance,and dielectric performance.However,structural defects in ladder polysiloxanes,such as cage-like and irregular oligomers,and their effects on dielectric properties remain underexplored.In this study,a series of ladder-like polysiloxanes(X-TMS)with diverse side groups weresynthesized via a one-step base-catalyzed method.The influence of the benzocyclobutene(BCB)side groups on the formation of regular ladder structures was systematically investigated.Notably,BCB incorporation disrupted the structural regularity,favoring the formation of cage-like and irregular topologies,which were extensively characterized using 29silicon nuclear magnetic resonance spectroscopy(^(29)Si-NMR),Fourier transform infrared spectroscopy(FTIR),gel permeation chromatography(GPC),and X-ray diffraction(XRD).These structural defects were beneficial for improving the hydrophobicity and thermal stability.Copolymerization of X-TMS with commercial DVS-BCB resins further enhanced the mechanical properties,with the elastic modulus increasing from 3.6 GPa to 4.4 GPa and water absorption reduced from 0.33 wt%to 0.06 wt%.This study establishes a clear correlation between topological structures and material properties.These findings not only advance the understanding of the structure-property relationships in ladder polysiloxanes but also provide a novel approach for designing high-performance interlayer dielectric materials for next-generation microelectronics.
基金financially supported by the National Natural Science Foundation of China(No.52103040)China Postdoctoral Science Foundation(No.2020M673217)the Fundamental Research Funds for the Central Universities(No.2023SCU12022)。
文摘To address the poor mechanical performance and improve the tribological properties of self-lubricating polyphenylene sulfide/irradiation treated polytetrafluoroethylene(PPS/i-PTFE)blends,different aspect ratio carbon fibers(i.e.,PSCF:50,SCF:about 429)were introduced as reinforcement fillers.The results showed that the hybriding of PSCF and SCF at certain mass ratios exhibited simultaneous enhancement of mechanical and tribological performance for PPS/i-PTFE blend through the construction of synergistic lubrication and mechanical interlocking network.Specifically,the flexural strength and modulus of PPS/i-PTFE were increased by 125.6% and 389.3%,the friction coefficient and specific wear rate were decreased by 13.9% and 95%,respectively.It was worth noting that PPS composites possessed excellent integrated performance which were able to withstand sliding action under high PV(≥10 MPa·m/s)conditions,as assessed by a customized pin-on-disc tester.This work demonstrated that the formation of intact lubricating film combined with the enhanced thermal and mechanical properties were favorable for improving the tribological properties of PPS-based composites,which makes them suitable for advanced engineering applications.
基金financial support from State Energy Center for Shale Oil Research and Development(Grant No.G5800-17-ZS-KFNY008)
文摘Inter-salt shale oil reservoirs located between two salt layers are always accompanied by high temperature and high salinity. However, the present commonly used water-soluble polymers in fracturing fluids su er from poor tolerance to high temperature and high salinity. Thermoviscosifying polymers(TVP) whose aqueous solution shows viscosity increase upon increasing temperature and salt concentration have received considerable attention recently, which is promising for utilization in fracturing fluids to overcome these problems. In this work, both the salt-induced viscosifying property and mechanism of a TVP solution were investigated and the performance of TVP used as fracturing fluid based on the conditions of the Jianghan inter-salt shale oil reservoir in China was evaluated. It is found that the salt-induced viscosifying property of the TVP solution decreases with temperature and shear rate, but increases with polymer concentration. The number of intermolecular hydrophobic domains increases with the salt concentration contributing to the strengthening of a 3D network structure, which results in an increase in viscosity. In addition, the TVP fracturing fluid formulated with saturated brine exhibits excellent temperature and shear resistance, sand-suspending performance, and gel-breaking performance. Its viscosity remains above50 m Pa s after being sheared for 1 h even at a high temperature of 140 °C and the sand-suspending stability can be maintained for more than 1 week at 100 °C. Furthermore, the fracturing fluid can be easily broken down within 12h using 0.2 wt%–0.3 wt% potassium persulfate without residue.
基金Funded by the National Natural Science Foundation of China(No.50873071)the Teaching and Research Award Program for Outstanding Young Professors in Higher Education Institute,MOE,China
文摘A series of aliphatic biodegradable poly（ether-ester）s based on poly（butylene succinate）（PBS）as hard segment and poly（tetramethylene oxide）（PTMO,M_n=1 000 g/mol） as soft segment were synthesized.The composition dependence of thermal behavior,morphology and mechanical properties was investigated by differential scanning calorimetry（DSC）,atomic force microscopy（AFM）,and tensile testing.The crystallization temperature（T_c） and melting temperature（T_m） of the PBS block within poly（ether-ester）s decrease steadily at first,but decrease sharply with PTMO content above 50 wt%.Two crystallization peaks were detected for PTMO in PBSPTMO60 sample,suggesting the occurrence of fractionated crystallization.The crystallization enthalpies（△H_c） and melting enthalpies（△H_m） of PBS block decrease at first,then increase as PTMO content increases further.AFM has demonstrated that phase-separated morphology transforms from a phase of continuous hard matrix to one of continuous soft matrix containing isolated hard domain as PTMO content is increased.Finally,the results of tensile testing show that the poly（ether-ester）s present the behavior of plastics when PTMO content is below 40 wt%,and of thermoplastic elastomers with PTMO content above 50 wt%.By varying the composition of copolymer,the aliphatic poly（ether-ester）s plastics,or especially biodegradable aliphatic poly（ether-ester）s thermoplastic elastomers can be obtained.
基金Funded by the Science and Technology Program of Sichuan,China(No.2016FZ0033)the Science and Technology Program of Sichuan Luzhou,China(No.2016-S-63(1/3)
文摘The effect of crystallization conditions of poly(butylene succinate)(PBS) component on the crystallization of poly(tetramethylene oxide)(PTMO) component in their segment block copolymer, with a higher PTMO content(PTMO mass fraction is 67%), was investigated by DSC and temperature-dependent FTIR. It is found that the isothermal crystallization time(tIC) of PBS has an effect on the crystallization behavior of PTMO component. Perturbation correlation move-window two-dimensional(PCMW2 D) correlation analysis and generalized 2 D correlation analysis(2 DIR) were performed to explore the origin of this phenomenon. The PCMW2 D and 2 DIR results show that the correlation intensity peak observed at around 20 ℃ for PTMO is due to the PTMO chains movements forced by the PBS chains folded movements. If tIC of PBS at temperature of 20 ℃ is prolonged, more PTMO components are incorporated in the region between PBS lamellae and the peak at-7.6 ℃(belonging to less-constricted PTMO chains) changes smaller and even disappears, while the peak at-16.3 ℃ belonging to more-constricted PTMO chains gets bigger. A crystallization model was also established in this study. The results of tensile testing showed that tensile strength slightly increased and elongation at break decreased with increasing heat treatment time at 40 ℃.
基金the research program of the Dutch Polymer Institute (DPI),project # 524.Additional financial support was provided by the Dutch Science Organization (NWO).
文摘In this study,the three dimensional nanoscale organization in the photoactive layers of poly(3-hexylthiophene) (P3HT) and a methanofullerene derivative (PCBM) is revealed by transmission electron tomography.After annealing treatment,either at elevated temperature or during slow solvent evaporation,nanoscale interpenetrating networks are formed with high crystalline order and favorable concentration gradients of both components through the thickness of the photoactive layer.Such a tailored morphology account...
文摘With the aim of developing a low-cost and efficient visible-light-driven photocatalyst for radical polymerization,iron-chelating polyimide networks(Fe@MPI)was fabricated by firstly synthesizing photoactive melamine-containing polyimide(MPI)networks and then incorporating Fe(III)cations into the polymer networks.Fe@MPI exhibits a wide absorption spectrum ranging from 220 to 1250 nm and 3.5 times higher photocurrent intensity as compared with the pristine MPI.Based on its excellent photo-electric properties,Fe@MPI was employed as a recyclable heterogeneous catalyst,providing sufficient activity for the visible-light driven radical polymerization to synthesize poly(methyl methacrylate)with molecular weight up to 31.×10^4 g mol.Taking advantage of the heterogeneous nature of the catalyst,Fe@MPI could be facilely regenerated from the polymerization solution by filtration without an obvious loss of its activity.This research provides a novel recyclable catalyst for visible-light driven radical polymerization.
基金financially supported by the National Natural Science Foundation of China(grant number U1762218).
文摘Polymer flooding has been witnessed an effective technology for enhancing oil recovery from medium-to low-permeability reservoirs;however, direct visualization of polymer solution flow in such reservoir condition is still lacking. In this work, a three-dimensional (3D) core-on-a-chip device with a permeability of around 200 mD was prepared and employed to visualize the pore-scale flow and displacement of a self-adaptive polymer (SAP, 8.7 × 106 g·mol−1)−whose microscopic association structure and macroscopic viscosity can reversibly change in response to shear action−versus partially hydrolyzed polyacrylamide (HPAM), by recording their flow curves, monitoring dynamic transportation process via particle imaging velocimetry, and building 3D structure of remaining oil. The results show that, in single-phase flow, all polymer solutions exhibit flow thinning and then thickening regions as flow rate increases, but the transition between two regimes occurs at a small Weissenberg number (10−3−10−1) in this medium-permeable condition. In contrast to HPAM-1 with close weight-average molecular weight (Mw), the adaptive character not only extends SAP's shear-govern region, allowing SAP to propagate piece by piece and achieve higher accessible pore volume, but it also enhances the elastic resistibility of polymer in the extension-dominated regime, increasing the microscopic displacement efficiency. These two effects result in 1.5–3 times more oil recovery factor for SAP than for HPAM-1. Regarding ultra-high-Mw HPAM-2 (25 × 106 g·mol−1), plugging and chain degradation do occur, thus producing lower oil recovery than SAP. This work provides a direct approach for in-situ assessment of polymer-based displacing system under a more authentic condition of practical reservoirs.
文摘The kinetics of ultrasonic degradation of aqueous solution of polyacrylamide（PAM）and poly（ethyleneoxide）（PEO）as well as ultrasonic block copolymerization of aqueous solution of the mixture of PAM/PEOwere studied respectively.The degradation reaction of PEO follows a linear relationship between（P1-P∞）-1and irradiation time,while that of PAM follows a linear relationship between（P1-P∞）-1/2and irradiation time.The structure of the copolymer was identified by IR,NMR and DTA,and the copolymer prepared is a blockone.The copolymer formed by irradiating 1% aqueous solution of PEO/PAM mixture（1:1）for a period of40min.at 18.2 kHz with a sonic intensity corresponding to 2.OA input current on the reversed main circuitamounts to 61.8%.
基金financially supported by the National Natural Science Foundation of China(No.51933007,No.52373047,No.52302106)the Sichuan Youth Science and Technology Innovation Research Team Project(No.2022JDTD0012)+2 种基金the Program for Featured Directions of Engineering Multidisciplines of Sichuan University(No.2020SCUNG203)the Natural Science Foundation of Sichuan Province(No.2023NSFSC0418)the Program for State Key Laboratory of Polymer Materials Engineering(No.sklpme2022-3-10)。
文摘The tireless pursuit of supercapacitors with high energy density entails the parallel advancement of wellsuited electrode materials and elaborately engineered architectures.Polypyrrole(PPy)emerges as an exceedingly conductive polymer and a prospective pseudocapacitive materials for supercapacitors,yet the inferior cyclic stability and unpredictable polymerization patterns severely impede its real-world applicability.Here,for the first time,an innovative seed-induced in-situ polymerization assisted 3D printing strategy is proposed to fabricate PPy-reduced graphene oxide/poly(vinylidene difluoride-cohexafluoropropylene)(PVDF-HFP)(PPy-rGO/PH)electrodes with controllable polymerization behavior and exceptional areal mass loading.The preferred active sites uniformly pre-planted on the 3D-printed graphene substrates serve as reliable seeds to induce efficient polypyrrole deposition,achieving an impressive mass loading of 185.6 mg cm^(-2)(particularly 79.2 mg cm^(-2)for polypyrrole)and a superior areal capacitance of 25.2 F cm^(-2)at 2 mA cm^(-2)for a 12-layer electrode.In agreement with theses appealing features,an unprecedented areal energy density of 1.47 mW h cm^(-2)for a symmetrical device is registered,a rarely achieved value for other PPy/rGO-based supercapacitors.This work highlights a promising route to preparing high energy density energy storage modules for real-world applications.
基金supported by Electronics and Telecommunications Research Institute(ETRI)grant funded by the Korea government(20ZB1200,Development of ICT Materials,Components and Equipment Technologies)the National Research Foundation of Korea(NRF)grant funded by the Korea government(No.2020R1A4A4079810)funding from the National Research Foundation(NRF)funded by the Ministry of Science and ICT,Rep.of Korea(Project No.2021R1C1C1008776)
文摘The increasing demand for short charging time on electric vehicles has motivated realization of fast chargeable lithium-ion batteries(LIBs).However,shortening the charging time of LIBs is limited by Li^(+)intercalation process consisting of liquid-phase diffusion,de-solvation,SEI crossing,and solid-phase diffusion.Herein,we propose a new strategy to accelerate the de-solvation step through a control of interaction between polymeric binder and solvent-Li^(+)complexes.For this purpose,three alkali metal ions(Li^(+),Na^(+),and K^(+))substituted carboxymethyl cellulose(Li-,Na-,and K-CMC)are prepared to examine the effects of metal ions on their performances.The lowest activation energy of de-solvation and the highest chemical diffusion coefficient were observed for Li-CMC.Specifically,Li-CMC cell with a capacity of 3 mAh cm^(-2)could be charged to>95%in 10 min,while a value above>85%was observed after 150 cycles.Thus,the presented approach holds great promise for the realization of fast charging.
文摘In this paper, the rigid structural thermosensitive polymer （made in lab） of NBS （N-butyl styrene）, N, N-DEAM （diethyl acrylamide） and AM （acrylamide） was prepared. The influence of viscosity for copolymer solution under different reaction conditions such as temperatures and inorganic salt （monovalent salt and divalent salt） was analyzed. The experiment studies the combination of polymer situation and three different types of surfactants under certain conditions of the room temperature （25℃） and the formation temperature （76℃）. At last, the influence of the surfactant kinds and concentration on the viscosity of the polymer solution are studied. The results show that： The copolymer solution, the apparent viscosity of which decreases with the increasement of temperature, but its viscosity has suddenly increased and thereafter dropped in the transition temperature. So the temperature sensitive effect ofcopolymer is very significantly. When the concentration of inorganic salt and surfactant can be controlled in certain extent, the copolymer solution, the effect increases with the increasement of the concentration, but the viscosity of which decreases with the increasement of shear rate. Shear rate can be controlled in certain extent, shearing stability properties of the copolymer solution are proved.
基金supported by the National Natural Science Foundation of China(No.52233003)the Department of Sichuan Province(No.2022JDJQ0023)。
文摘As the application scenarios of aerogels expand,higher requirements are put forward for the materials used to prepare aerogels.Due to the unique chemical structure,polytetrafluoroethylene(PTFE)has excellent properties such as high-temperature resistance,hydrophobicity,and chemical stability.However,the PTFE aerogels are difficult to be molded due to the weak interaction between resin particles.In this work,poly(ethylene oxide)(PEO)was selected as the carrier to assist the PTFE aerogels molding.The pure PTFE aerogels were prepared by homogeneously mixing PTFE aqueous dispersion and PEO,freeze-drying,and high-temperature sintering.When the mass fraction of PTFE and PEO were appropriate,the porosity of PTFE aerogels exceeded 90%and had a hierarchical honeycomb structure.Results showed that the PTFE aerogels not only had excellent hydrophobicity but also possessed superior acoustic insulation,mechanical strength,thermal insulation,and heat resistance properties.Specifically,the water contact angle is about 140°.The noise reduction coefficient is 0.34 and the average sound absorption coefficient is greater than 88%in the frequency range of 2000-6400 Hz.Meanwhile,the thermal conductivity in the air is about 0.045 W/(m·K),and the initial thermal decomposition temperature is 450℃.More importantly,the PTFE aerogels had excellent temperature and corrosion resistance.Even after extremely thermal and chemical treatment,they remained unchanged porous structure as well as acoustic and thermal insulation properties,which exhibits great potential for application in many harsh environments.
基金support of this work by National Key Research and Development Program of China(2019YFC19059003)the Natural Science Foundation of the Jiangsu Higher Education Institutions of China(23KJB430024)+1 种基金Jiangsu Funding Program for Excellent Postdoctoral Talent(2023ZB680)Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)are gratefully acknowledged.
文摘The Janus fabrics designed for personal moisture/thermal regulation have garnered significant attention for their potential to enhance human comfort.However,the development of smart and dynamic fabrics capable of managing personal moisture/thermal comfort in response to changing external environments remains a challenge.Herein,a smart cellulose-based Janus fabric was designed to dynamically manage personal moisture/heat.The cotton fabric was grafted with N-isopropylacrylamide to construct a temperature-stimulated transport channel.Subsequently,hydrophobic ethyl cellulose and hydrophilic cellulose nanofiber were sprayed on the bottom and top sides of the fabric to obtain wettability gradient.The fabric exhibits anti-gravity directional liquid transportation from hydrophobic side to hydrophilic side,and can dynamically and continuously control the transportation time in a wide range of 3–66 s as the temperature increases from 10 to 40℃.This smart fabric can quickly dissipate heat at high temperatures,while at low temperatures,it can slow down the heat dissipation rate and prevent the human from becoming too cold.In addition,the fabric has UV shielding and photodynamic antibacterial properties through depositing graphitic carbon nitride nanosheets on the hydrophilic side.This smart fabric offers an innovative approach to maximizing personal comfort in environments with significant temperature variations.
基金Yijing Wang acknowledges the funding support of the National Key Research and Development Program of China(No.2021YFB4000604)the National Natural Science Foundation of China(No.52271220)+6 种基金the Higher Education Discipline Innovation Project(No.B12015)“the Fundamental Research Funds for the Central Universities”Huaiyu Shao acknowledges the funding support of the Multi-Year Research Grant(MYRG)from the University of Macao(No.MYRG2022-00105-IAPME)the Joint Scientific Research Project Funding by the National Natural Science Foundation of China and the Macao Science and Technology Development Fund(No.0090/2022/AFJ)the Macao Science and Technology Development Fund(FDCT)for funding No.006/2022/ALC of the Macao Centre for Research and Development in Advanced Materials(No.2022-2024)the Natural Science Foundation of Guangdong Province(Grant No.2023A1515010765)the Shenzhen-Hong Kong-Macao Science and Technology Innovation Project(Category C).
文摘Herein,we report the multi-metal atomic catalysts for solid-state dehydrogenation of MgH_(2).It aims to reveal the multi-element synergy in catalysts for solid-state hydrogen storage.The kinetic measurements and fitting reveal two mechanisms:one shows a maximum rate at the early stage,such as V and Cr;the other needs a temperature-sensitive preparation time for its maximum rate,such as Ni.The combina-tion of two catalyst components demonstrates the best kinetics:V and Cr boost the initial dehydrogena-tion,and Ni benefits the further hydrogen transfer which alleviates the rate of decay.This work provides guidelines for the design of multi-element doped catalysts for MgH_(2) dehydrogenation.
基金supported by the National Natural Science Foundation of China(Nos.52325302 and 52173012)Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering(No.2022SZ-FR005)。
文摘Achieving continuous motions typically requires dynamic external stimuli for cyclic deformation,or crafted geometries with intricate modules to form a self-regulated feedback loop upon static stimulation.It is still a grand challenge to realize self-sustained motion in soft robots subject to unchanging environment,without complex geometry or a control module.In this work,we report soft robots based on an anisotropic cylindrical hydrogel showing self-regulated,continuous rolling motions under constant light irradiation.The robots are animated by mirror-symmetry-breaking induced by photothermal strain gradient.The self-sustained motion is attributed to the fast and reversible deformation of the gel and the autonomous refresh of the irradiated region during the rolling motion.The hydrogel robots can reach a rolling speed of 1.27 mm·s^(-1)on a horizonal surface and even climb a ramp of 18°at a speed of 0.57 mm·s^(-1)in an aqueous environment.Furthermore,the hydrogel robots can overcome an obstacle,with rolling direction controllable through irradiation angle of the light and local irradiation on selective regions.This work suggests a facile strategy to develop hydrogel robots and may provide unforeseen inspirations for the design of self-regulated soft robots by using other intelligent materials.
基金support of this work by the Project of Education Department of Shaanxi Province(No.23JK0373)the Shaanxi University of Technology Graduate Innovation Fund(No.SLGYCX2402)the Talent Start-up Fund of Shaanxi University of Technology(No.SLGRCQD2329).
文摘The full arrival of 5 G and advances in electronic integration make efficient heat dissipation crucial for stable operation and longer product lifespan. In this study, a vacuum-assisted filtration process was employed to fabricate ammoniated alumina/MXene/bacterial cellulose (Al_(2)O_(3)-NH_(2)/MXene/BC) composite films that display a unique integration of properties, encompassing ultra-high thermal conductivity (λ), mechanical flexibility, and high photothermal conversion performance. By leveraging the bridging effect among spherical Al_(2)O_(3)-NH_(2) and MXene nanosheets, a densely packed “point-surface” structure was constructed in BC by using a one-step preparation process. When the mass fraction of Al_(2)O_(3)-NH_(2)/MXene (1:3, w/w) is 40 wt%, the O-BAl1M3 exhibited an in-plane λ of 20.02 W m^(-1) K^(-1), which was 436 % and 94 % higher than that of pure BC and T-BAl1M3 (prepared by a two-step method), respectively. Furthermore, constructing an intact thermal conductive network within BC notably promoted photothermal and photoelectric conversion performance. The maximum surface temperature and voltage of the O-BAl1M3 film reached 106.9 ℃ and 48.34 mV when a sample with an area of 1.56 cm^(2) was exposed under a light intensity of 200 mW cm^(-2). By applying O-BAl1M3 film, the temperature inside a self-built greenhouse model reached up to 64.8 ℃ within 1200 s under a light intensity of 100 mW cm^(-2), which validated the practical application of the composite films and offered a novel approach for creating flexible films with superior photothermal conversion capability. This work provided insights into preparing functional composite films for efficient thermal management and photothermal conversion applications.
基金the Natural Science Foundation of Sichuan Province,China(Nos.2023NSFSC0902,2024ZYD0083)the Open Project of Key Laboratory of Aerodynamic Noise Control of China Aerodynamics Research and Development Center(No.ANCL20220202)+1 种基金the Open Project of Key Laboratory of Flight Techniques and Flight Safety,CAAC,China(No.FZ2022KF01)the Fundamental Research Funds for the Central Universities,China(No.24CAFUC01007)。
文摘This paper presents a comprehensive test and systematic evaluation analysis of cabin noise in the Robinson R44 RAVEN II helicopter.Initially,microphones were placed within the cabin to conduct systematic assessments of noise levels under various flight conditions,including takeoff,climbing,level flight,landing,hovering,etc.Subsequently,time–frequency analysis was conducted on the test data utilizing traditional A-weighted sound pressure levels,which was followed by quantitative comparisons across different flight conditions.Then,detailed evaluation and discussion were conducted,taking into account the subjective perceptions and communication challenges of cabin crew members.This assessment incorporated the use of aviation noise indicators,speech interference levels,and metrics related to sound quality.Finally,potential noise reduction measures and their effects were preliminarily discussed.The results indicate that helicopter cabin noise exhibited variations across different flight states or positions within the same state,ranging from 87.6 d B(A)to 92.6 dB(A).Discrepancies between A-weighted sound pressure level and psychoacoustic parameters were observed,particularly during hovering states,which indicate that there is a necessity for the combination of multiple evaluation indicators.Notably,damping measure can serve as a pivotal factor in mitigating cabin noise.
