The reversible addition-fragmentation chain transfer(RAFT) miniemulsion polymerization of vinyl acetate mediated by xanthate

The reversible addition-fragmentation chain transfer （RAFT） miniemulsion polymerization of vinyl acetate （VAc） mediated by methyl （methoxycarbonothioyl） sulfanyl acetate （MMSA） was carried out. The results showed that polymerizations initiated by AIBN and KPS proceeded in a controlled way. The RAFT miniemulsion polymerization of VAc initiated by KPS showed the shorter inhibition period, higher propagation rate coefficient and final conversion than those in experiment initiated by AIBN. When the monomer conversion reached 25%, the polydispersity index （PDI） of polymer became broad, which was related to chain transfer reaction in RAFT miniemulsion of VAc.

Synthesis of polystyrene-styrene/butadiene diblock copolymers via reversible addition-fragmentation chain transfer miniemulsion polymerization

Polystyrene-styrene/butadiene diblock copolymers were synthesized via reversible addition-fragmentation chain transfer （RAFT） miniemulsion polymerization.During the polymerization process,the molecular weight distribution was narrow and the numerical molecular weight of the copolymers increased with increasing conversion of monomers,which was close to the theoretical.FT-IR and ^1H NMR results indicated that the microstructure of the polymer was mainly 1,4-trans-butadiene with small amount of 1,2-units,and composition in the copolymers was obtained.

Evaluation of the clenbuterol imprinted monolithic column prepared by reversible addition-fragmentation chain transfer polymerization

To make more homogenous organic monolithic structure, reversible addition-fragmentation chain transfer （RAFT） process was employed in the synthesis of the clenbuterol imprinted polymer. In the synthesis, the influence of synthetic conditions on the polymer structure and separation efficiency was studied. The result demonstrated that the imprinted columns prepared with RAFT process have higher column efficiency and selectivity than the columns prepared with conventional polymerization in the present study, which may result from the higher surface area, smaller pore size and the narrower globule size distribution in their structures. The result indicated that RAFT polymerization provided better conditions for the clenbuterol imprinted monolithic polymer preparation. 2009 Xiang Chao Dong. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

Reversible addition-fragmentation chain transfer graft polymerization of acrylonitrile onto PE/PET composite fiber initiated by γ-irradiation

Reversible addition-fragmentation chain transfer(RAFT) mediated grafting of acrylonitrile onto Polyethylene/Poly(ethylene terephthalate)(PE/PET) composite fibers was performed using γ-irradiation as the initial source at ambient temperature. Different initial concentrations of 2-cyanoprop-2-yl dithiobenzonate were used as the chain transfer agent. The kinetics of graft polymerization is in accordance with the living RAFT polymerization. The successful grafting of acrylonitrile is proved by Fourier transform infrared spectroscopy analysis.The results of monofilament tensile test show that mechanical properties of the fibers change slightly after grafting. Scanning electronic microscopy images of the fibers show that the surface of RAFT grafted fibers is smoother than that of fibers grafted conventionally.

Reversed charge transfer induced by nickel in Fe-Ni/Mo_(2)C@nitrogen-doped carbon nanobox for promoted reversible oxygen electrocatalysis

The interaction between metal and support is critical in oxygen catalysis as it governs the charge transfer between these two entities,influences the electronic structures of the supported metal,affects the adsorption energies of reaction intermediates,and ultimately impacts the catalytic performance.In this study,we discovered a unique charge transfer reversal phenomenon in a metal/carbon nanohybrid system.Specifically,electrons were transferred from the metal-based species to N-doped carbon,while the carbon support reciprocally donated electrons to the metal domain upon the introduction of nickel.This led to the exceptional electrocatalytic performances of the resulting Ni-Fe/Mo_(2)C@nitrogen-doped carbon catalyst,with a half-wave potential of 0.91 V towards oxygen reduction reaction(ORR)and a low overpotential of 290 m V at 10 mA cm^(-2)towards oxygen evolution reaction(OER)under alkaline conditions.Additionally,the Fe-Ni/Mo_(2)C@carbon heterojunction catalyst demonstrated high specific capacity(794 mA h g_(Zn)~(-1))and excellent cycling stability(200 h)in a Zn-air battery.Theoretical calculations revealed that Mo_(2)C effectively inhibited charge transfer from Fe to the support,while secondary doping of Ni induced a charge transfer reversal,resulting in electron accumulation in the Fe-Ni alloy region.This local electronic structure modulation significantly reduced energy barriers in the oxygen catalysis process,enhancing the catalytic efficiency of both ORR and OER.Consequently,our findings underscore the potential of manipulating charge transfer reversal between the metal and support as a promising strategy for developing highly-active and durable bi-functional oxygen electrodes.

Mass transfer process of peanut protein extracted by bis(2-ethylhexyl)sodium sulfosuccinate reverse micelles

The liquid-liquid extraction method using reverse micelles can simultaneously extract lipid and protein of oilseeds,which have become increasingly popular in recent years.However,there are few studies on mass transfer processes and models,which are helpful to better control the extraction process of oils and proteins.In this paper,mass transfer process of peanut protein extracted by bis(2-ethylhexyl)sodium sulfosuccinate(AOT)/isooctane reverse micelles was investigated.The effects of stirring speed(0,70,140,and 210 r/min),temperature of extraction(30,35,40,45,and 50℃),peanut flour particle size(0.355,0.450,0.600,and 0.900 mm)and solidliquid ratio(0.010,0.0125,0.015,0.0175,and 0.020 g/mL)on extraction rate were examined.The results showed that extraction rate increased with temperature rising,particle size reduction as well as solid-liquid ratio increase respectively,while little effect of stirring speed(P>0.05)was observed.The apparent activation energy of extraction process was calculated as 10.02 kJ/mol and Arrhenius constant(A)was 1.91 by Arrhenius equation.There was a linear relationship between reaction rate constant and the square of the inverse of initial particle radius(1/r_(0)^(2))(P<0.05).This phenomenon and this shrinking core model were anastomosed.In brief,the extraction process was controlled by the diffusion of protein from the virgin zone interface of particle through the reacted zone and it was in line with the first order reaction.Mass transfer kinetics of peanut protein extracted by reverse micelles was established and it was verified by experimental results.The results provide an important theoretical guidance for industrial production of peanut protein separation and purification.

APST-Flow: A Reversible Network-Based Artistic Painting Style Transfer Method

In recent years,deep generative models have been successfully applied to perform artistic painting style transfer(APST).The difficulties might lie in the loss of reconstructing spatial details and the inefficiency of model convergence caused by the irreversible en-decoder methodology of the existing models.Aiming to this,this paper proposes a Flow-based architecture with both the en-decoder sharing a reversible network configuration.The proposed APST-Flow can efficiently reduce model uncertainty via a compact analysis-synthesis methodology,thereby the generalization performance and the convergence stability are improved.For the generator,a Flow-based network using Wavelet additive coupling(WAC)layers is implemented to extract multi-scale content features.Also,a style checker is used to enhance the global style consistency by minimizing the error between the reconstructed and the input images.To enhance the generated salient details,a loss of adaptive stroke edge is applied in both the global and local model training.The experimental results show that the proposed method improves PSNR by 5%,SSIM by 6.2%,and decreases Style Error by 29.4%over the existing models on the ChipPhi set.The competitive results verify that APST-Flow achieves high-quality generation with less content deviation and enhanced generalization,thereby can be further applied to more APST scenes.

Reverse Atom Transfer Radical Polymerization of (-)-Menthyl Methacrylate

The reverse atom transfer radical polymerization(RATRP) of (-)-menthyl methacrylate ((-)-MnMA) with AIBN(AIBN/CuCl2/bipyridine(bipy) or (-)sparteine((-)Sp) =1/2/4) initiating system in THF has been studied. The dependence of the specific rotation on molecular weight was investigated.

A thermal actuated switchable dry adhesive with high reversibility for transfer printing

Transfer printing based on switchable adhesive that heterogeneously integrates materials is essential to develop novel electronic systems,such as flexible electronics and micro LED displays.Here,we report a robust design of a thermal actuated switchable dry adhesive,which features a stiff sphere embedded in a thermally responsive shape memory polymer(SMP)substrate and encapsulated by an elastomeric membrane.This construct bypasses the unfavorable micro-and nano-fabrication processes and yields an adhesion switchability of over1000 by combining the peel-rate dependent effect of the elastomeric membrane and the thermal actuation of the sub-surface embedded stiff sphere.Experimental and numerical studies reveal the underlying thermal actuated mechanism and provide insights into the design and operation of the switchable adhesive.Demonstrations of this concept in stamps for transfer printing of fragile objects,such as silicon wafers,silicon chips,and inorganic micro-LED chips,onto challenging non-adhesive surfaces illustrate its potential in heterogeneous material integration applications,such as flexible electronics manufacturing and deterministic assembly.

Grafting of MIPs from PVDF Membranes via Reversible Addition-fragmentation Chain Transfer Polymerization for Selective Removal of p-Hydroxybenzoic Acid

Effective molecularly imprinted membranes（MIMs） were developed as an efficient adsorbent for the selective removal ofp-hydroxybenzoic acid（p-HB） from acetylsalicylic acid（ASA, aspirin）. The MIMs were grafted successfully from poly（vinylidene fluoride） microfiltration membranes via reversible addition-fragmentation chain transfer（RAFT） polymerization. The graft copolymerization of acrylic acid（AA） in the presence of template p-hydroxybenzoic acid led to molecularly imprinted polymer（MIP） film coated membranes. The obtained MIMs were characterized by scanning electron microscopy（SEM）, Fourier transform infrared spectrophotometer（FTIR） and Raman spectra, and batch mode adsorption studies were carried ont to investigate the specific adsorption equilibrium, kinetics and selective recognition properties of different MIMs. The kinetic properties of the MIMs could be well described by the pseudo-second-order rate equation. Selective permeation experiments were performed to evaluate the permeation selectivity of the p-HB imprinted membranes. The observed performances of the MIMs are applicable to the further purification of aspirin. Keywords Acetylsalicylic acid; Reversible addition-fragmentation chain transfer; Molecularly imprinted membrane; p-Hydroxybenzoic acid; Selective adsorption

Modeling of Mass Transfer in Cavity Limited by a Semi Permeable Membrane （Simulation of Spiral Wound Module）

The reverse osmosis process has been applied in large industrial fields （water treatment, food industry, biotechnology, and ect.）. Despite, this progress more investigation are required to optimize the reverse osmosis process. The present paper deals the modeling of mass transfer in a cavity limited by a semi-permeable membrane. Mass conservation and momentum balances are developed, dimensionless and control volume method has been applied. The velocity and concentration profiles versus the Reynolds number and Sherwood are studied. The results show that the permeability of the membrane decreases as function of the transversal （radial） component of the velocity. The axial （tangential） component of the velocity presents a good stability along the thickness of the cavity; this phenomenon can be attributed to the zero gradient of the tangential velocity. These preliminary results show that the phenomenon of the concentration polarization affects the mass transfer coefficient in a channel. Current study has considered the cavity without a promoter of the turbulence; whereas, the design of the spacer has an important role on mass transfer coefficient in the reverse osmosis module. Our next interest is the integration of the spacer in the cavity, and the study of the effect of its design on the concentration and velocity profiles and the mass transfer coefficient through the reverse osmosis membrane.

Numerical analysis of reverse dual-rotation friction stir welding process

A three-dimensional model of reverse dual-rotation friction stir welding （RDR-FSW） is developed to conduct the numerical simulation of heat generation and material flow during the process. The reverse rotation of the assisted shoulder and the tool pin is considered to model the heat generation rate. The predicted temperature difference between the advancing side and the retreating side in RDR-FSW is less than that in conventional FSW. There are two reverse flows during the RDR-FSW which is beneficial to the uniformity of the temperature profile. Due to the reverse rotation effects of the assisted shoulder, the predicted shape and size of thermal-mechanically affected zone （TMAZ） based on the iso-viscosity line are decreased greatly compared to the conventional FSW. It lays solid foundation for optimizing the process parameters in RDR-FSW.

Bulk Polymerization of Styrene Using Benzyl Dithiobenzoate as a Chain Transfer

Bulk polymerization of styrene was carried out in the presence of a reversible addition fragmentation chain transfer (RAFT) of benzyl dithiobenzoate (BDB). The comparison between reaction systems with and without BDB indicates that there is significant retardation in the reaction rate when BDB is used. The molecular weight of styrene polymer prepared with BDB shows linear relationship with the conversion of monomer, polydispersity is as narrow as 1.2, and no gel effects are observed during the polymerization with BDB, which are characteristics of a living radical polymerization. It has been found that the concentrations of BDB and azobis (isobutyronitrile) (AIBN) have opposite effects on the polymerization kinetics, and the AIBN dominates.

Thermodynamics and Irreversibility: From Some Paradoxes to the Efficiency of Effective Engines

The traditional thermodynamic theory explains the reversible phenomena quite well, except that reversible phenomena are rare or even impossible in practice. Here the purpose is to propose an explanation valid for reversible and also irreversible phenomena, irreversibility being common or realistic. It previously exposed points tricky to grasp, as the sign of the work exchange, the adiabatic expansion in vacuum (free expansion) or the transfer of heat between two bodies at the same temperature (isothermal transfer). After having slightly modified the concepts of heat transfer (each body produces heat according to its own temperature) and work (distinguishing external pressure from internal pressure), the previous points are more easily explained. At last, an engine efficiency in case of irreversible transfer is proposed. This paper is focused on the form of thermodynamics, on “explanations”;it does not question on “results” (except the irreversible free expansion of 1845...) which remain unchanged.

基于谐波通讯的无线电能与反向信号同步传输技术

针对现有无线电能与反向信号同步传输(simultaneous wireless power and reverse signal transmission,SWPRST)系统存在较大无功功率、负载电压易受信号传输发生波动或需要额外增加高频信号源等问题,提出一种基于谐波通讯的SWPRST技术,通过利用逆变器输出方波电压中的基波分量传输电能,三次谐波分量传输信号。不需要外加高频信号发射电路,实现了可靠的电能与反向信号同步传输。首先,给出基于谐波通讯的SWPRST系统结构,对其工作模式和基本原理进行分析;接着,建立系统等效数学模型,分析系统参数取值对信号与电能传输之间的互扰影响;然后,对信号的调制解调电路进行设计,分析信号检测通道参数对信号传输速率的影响;最后,搭建实验平台对理论分析进行验证,实验结果表明,该方法在有效实现了无线电能与反向信号同步传输的同时,信号无误码率传输速率可达5 kbps,同时系统具有无功小,输出负载电压几乎无波动(电压波动率0.33%)等优点。该方法采用谐波作为信号载体,为多频利用式实现电能与反向信号同步传输系统提供一种新的思路,具有较好的理论意义与实际工程应用价值。

Unlocking the potential of thin-film composite reverse osmosis membrane performance:Insights from mass transfer modeling

Thin-film composite(TFC)reverse osmosis(RO)membranes have attracted considerable attention in water treatment and desalination processes due to their specific separation advantages.Nevertheless,the trade-off effect between water flux and salt rejection poses huge challenges to further improvement in TFC RO membrane performance.Numerous research works have been dedicated to optimizing membrane fabrication and modification for addressing this issue.In the meantime,several reviews summarized these approaches.However,the existing reviews seldom analyzed these methods from a theoretical perspective and thus failed to offer effective optimization directions for the RO process from the root cause.In this review,we first propose a mass transfer model to facilitate a better understanding of the entire process of how water and solute permeate through RO membranes in detail,namely the migration process outside the membrane,the dissolution process on the membrane surface,and the diffusion process within the membrane.Thereafter,the water and salt mass transfer behaviors obtained from model deduction are comprehensively analyzed to provide potential guidelines for alleviating the trade-off effect between water flux and salt rejection in the RO process.Finally,inspired by the theoretical analysis and the accurate identification of existing bottlenecks,several promising strategies for both regulating RO membranes and optimizing operational conditions are proposed to further exploit the potential of RO membrane performance.This review is expected to guide the development of high-performance RO membranes from a mass transfer theory standpoint.

聚羧酸保坍剂分子序列结构对其性能的影响

通过普通自由基聚合合成侧链密度不同的无规序列结构聚羧酸保坍剂PCE-1、PCE-2;通过可逆加成-碎裂链转移聚合(RAFT)合成侧链在主链上分布形式分别为“外密内疏”和“外疏内密”梯度序列结构的聚羧酸保坍剂PCE-3、PCE-4。通过凝胶渗透色谱仪(GPC)测试证明PCE-3、PCE-4的分子质量与转化率呈线性关系,符合“活性”聚合特征。净浆和混凝土试验发现,各减水剂分散性能排序为PCE-4<PCE-1<PCE-2<PCE-3,即“外密内疏”的序列结构最适合发挥PCE的分散性,而“外疏内密”不适合作为PCE的结构。含蒙脱土的净浆试验表明,具有“紧密”侧链序列的PCE-1、PCE-3有着更好的抗泥效果。吸附试验表明,吸附能力排序为PCE-4<PCE-3<PCE-1≈PCE-2。

Aggregation-induced emission polymers via reversible-deactivation radical polymerization Special Collection:Distinguished Australian Researchers

Aggregation-induced emission(AIE)is a unique phenomenon whereby aggregation of molecules induces fluorescence emission as opposed to the more commonly known aggregation-caused quenching(ACQ).AIE has the potential to be utilized in the large-scale production of AIE-active polymeric materials because of their wide range of practical applications such as stimuli-responsive sensors,biological imaging agents,and drug delivery systems.This is evident from the increasing number of publications over the years since AIE was first discovered.In addition,the evergrowing interest in this field has led many researchers around the world to develop new and creative methods in the design of monomers,initiators and crosslinkers,with the goal of broadening the scope and utility of AIE polymers.One of the most promising approaches to the design and synthesis of AIE polymers is the use of the reversible-deactivation radical polymerization(RDRP)techniques,which enabled the production of well-controlled AIE materials that are often difficult to achieve by other methods.In this review,a summary of some recent works that utilize RDRP for AIE polymer design and synthesis is presented,including(i)the design of AIE-related monomers,initiators/crosslinkers;the achievements in preparation of AIE polymers using(ii)reversible addition–fragmentation chain transfer(RAFT)technique;(iii)atom transfer radical polymerization(ATRP)technique;(iv)other techniques such as Cu(0)-RDRP technique and nitroxide-mediated polymerization(NMP)technique;(v)the possible applications of these AIE polymers,and finally(vi)a summary/perspective and the future direction of AIE polymers.

基于光引发可逆加成断裂链转移自由基聚合的3D打印

针对高分子化学本科教学中“活性自由基聚合”知识点抽象,学生难以理解的教学难题,开展了光引发可逆加成断裂链转移(RAFT)自由基聚合3D打印实验。实验首先合成O-(乙基)-S-(2-丙酸乙酯基)黄原酸酯(EXEP),随后使用商用光敏树脂,进行添加/不添加EXEP条件下的3D打印。随后使用得到的打印体开展荧光功能后修饰与焊接对比实验。通过对比实验现象,深入理解活性自由基聚合机理及其对产物后功能化能力的影响,实现“活性自由基聚合”原理的“可视化”和实例化应用展示。本实验将基础理论有机融合到趣味实验中,实验耗时合理,操作简便,效果明显,符合本科教学实验基本要求,有助于提升学生综合分析能力,激发学生深入研究的兴趣,培养其创新意识及拓展延伸的能力。

接受不同抗逆转录病毒治疗方案的HIV感染者血浆中可溶性炎症标志物水平差异研究

目的探究接受不同抗逆转录病毒治疗(ART)方案的人类免疫缺陷病毒(HIV)感染者血浆中可溶性炎症标志物表达水平的差异。方法选取2019年6月至2021年6月于海南省中医院就诊的初诊HIV感染者100例,随机将患者分为非核苷类逆转录酶抑制剂(NNRTI)组和整合酶链转移抑制剂(INSTI)组,各50例。所有患者基础用药为恩曲他滨替诺福韦片,NNRTI组患者联用依非韦伦片,INSTI组患者联用拉替拉韦钾片。分别于治疗前及治疗6个月后随访,比较两组患者血生化指标、T细胞计数、病毒学指标、炎性细胞因子表达。结果治疗6个月后两组患者血生化指标、T细胞计数、病毒学指标及血浆炎性细胞因子表达水平较治疗前均有显著差异(P<0.05),且INSTI组患者各项指标改变更显著(P<0.05)。结论相比NNRTI,应用INSTI更有助于降低HIV感染者全身炎症水平,且药物抑制病毒效果显著。