Stromal lenticule addition keratoplasty with corneal crosslinking for corneal ectasia secondary to FS-LASIK:a case series

●AIM:To explore the clinical efficacy and safety of stromal lenticule addition keratoplasty(SLAK)with corneal crosslinking(CXL)on patients with corneal ectasia secondary to femtosecond laser-assisted in situ keratomileusis(FS-LASIK).●METHODS:A series of 5 patients undertaking SLAK with CXL for the treatment of corneal ectasia secondary to FS-LASIK were followed for 4-9mo.The lenticules were collected from patients undertaking small incision lenticule extraction(SMILE)for the correction of myopia.Adding a stromal lenticule was aimed at improving the corneal thickness for the safe application of crosslinking and compensating for the thin cornea to improve its mechanical strength.●RESULTS:All surgeries were conducted successfully with no significant complications.Their best corrected visual acuity(BCVA)ranged from 0.05 to 0.8-2 before surgery.The pre-operational total corneal thickness ranged from 345-404μm and maximum keratometry(Kmax)ranged from 50.8 to 86.3.After the combination surgery,both the corneal keratometry(range 55.9 to 92.8)and total corneal thickness(range 413-482μm)significantly increased.Four out of 5 patients had improvement of corneal biomechanical parameters(reflected by stiffness parameter A1 in Corvis ST).However,3 patients showed decreased BCVA after surgery due to the development of irregular astigmatism and transient haze.Despite the onset of corneal edema right after SLAK,the corneal topography and thickness generally stabilized after 3mo.●CONCLUSION:SLAK with CXL is a potentially beneficial and safe therapy for advanced corneal ectasia.Future work needs to address the poor predictability of corneal refractometry and compare the outcomes of different surgical modes.

Crosslinking Mechanism of Soy Protein-based Adhesives based on Glyoxal and a Compound of Protein Model

The crosslinking mechanism of glyoxal and asparagine was analyzed,and the relationship between the mechanism and practical performances of soy protein-based adhesives was also discussed.It is shown that when pH=1 and 3,glyoxal reacted with asparagine in the form of major cyclic ether compounds.When pH=5,glyoxal reacted with asparagine in two structural forms of sodium glycollate and cyclic ether compounds.However,amidogens of asparagine were easy to develop protonation under acid conditions.Supplemented by the instability of cyclic ether compounds,the reaction activity and reaction degree between glyoxal and asparagine were relatively small.Under alkaline conditions,glyoxal mainly reacted with asparagine in the form of sodium glycollate.With the increase of pH,the polycondensation was more sufficient and the produced polycondensation products were more stable.The reaction mechanism between glyoxal and asparagine had strong correspondence to the practical performances of the adhesives.Glyoxal solution could develop crosslinking reactions with soy protein under both acid and alkaline conditions.Bonding strength and water resistance of the prepared soy protein-based adhesives were increased significantly.When pH>7,glyoxal had relatively high reaction activity and reaction intensity with soy protein,and the prepared adhesives had high crosslinking density and cohesion strength,showing relatively high bonding strength,water resistance and thermal stability.

Novel polyimide binder for achieving high-rate capability and long-term cycling stability of LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2) cathode via constructing polar and micro-branched crosslinking network structure

LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)material,as the promising cathode candidate for next-generation highenergy lithium-ion batteries,has gained considerable attention for extremely high theoretical capacity and low cost.Nevertheless,the intrinsic drawbacks of NCM811 such as unstable structure and inevitable interface side reaction result in severe capacity decay and thermal runaway.Herein,a novel polyimide(denoted as PI-Om DT)constructed with the highly polar and micro-branched crosslinking network is reported as a binder material for NCM811 cathode.The micro-branched crosslinking network is achieved by using 1,3,5-Tris(4-aminophenoxy)benzene(TAPOB)as a crosslinker via condensation reaction,which endows excellent mechanical properties and large free volume.Meanwhile,the massive polar carboxyl(-COOH)groups provide strong adhesion sites to active NCM811 particles.These functions of PIOm DT binder collaboratively benefit to forming the mechanically robust and homogeneous coating layer with rapid Li+diffusion on the surface of NCM811,significantly stabilizing the cathode structure,suppressing the detrimental interface side reaction and guaranteeing the shorter ion-diffusion and electron-transfer paths,consequently enhancing electrochemical performance.As compared to the NCM811 with PVDF binder,the NCM811 using PI-Om DT binder delivers a superior high-rate capacity(121.07 vs.145.38 m Ah g^(-1))at 5 C rate and maintains a higher capacity retention(80.38%vs.91.6%)after100 cycles at 2.5–4.3 V.Particularly,at the high-voltage conditions up to 4.5 and 4.7 V,the NCM811 with PI-Om DT binder still maintains the remarkable capacity retention of 88.86%and 72.5%after 100 cycles,respectively,paving the way for addressing the high-voltage operating stability of the NCM811 cathode.Moreover,the full-charged NCM811 cathode with PI-Om DT binder exhibits a significantly enhanced thermal stability,improving the safety performance of batteries.This work opens a new avenue for developing high-energy NCM811 based lithium-ion batteries with long cycle-life and superior safety performance using a novel and effective binder.

Evaluation of different crosslinking methods in altering the properties of extrusion-printed chitosan-basedmulti-material hydrogel composites

Three-dimensional printing technologies exhibit tremendous potential in the advancing fields of tissue engineering and regenerative medicine due to the precise spatial control over depositing the biomaterial.Despite their widespread utilization and numerous advantages,the development of suitable novel biomaterials for extrusion-based 3D printing of scaffolds that support cell attachment,proliferation,and vascularization remains a challenge.Multi-material composite hydrogels present incredible potential in this field.Thus,in this work,a multi-material composite hydrogel with a promising formulation of chitosan/gelatin functionalized with egg white was developed,which provides good printability and shape fidelity.In addition,a series of comparative analyses of different crosslinking agents and processes based on tripolyphosphate(TPP),genipin(GP),and glutaraldehyde(GTA)were investigated and compared to select the ideal crosslinking strategy to enhance the physicochemical and biological properties of the fabricated scaffolds.All of the results indicate that the composite hydrogel and the resulting scaffolds utilizing TPP crosslinking have great potential in tissue engineering,especially for supporting neo-vessel growth into the scaffold and promoting angiogenesis within engineered tissues.

Carcinoma-associated fibroblast-derived lysyl oxidase-rich extracellular vesicles mediate collagen crosslinking and promote epithelial-mesenchymal transition via p-FAK/ p-paxillin/YAP signaling

Carcinoma-associated fibroblasts(CAFs)are the main cellular components of the tumor microenvironment and promote cancer progression by modifying the extracellular matrix(ECM).The tumor-associated ECM is characterized by collagen crosslinking catalyzed by lysyl oxidase(LOX).Small extracellular vesicles(sEVs)mediate cell-cell communication.However,the interactions between sEVs and the ECM remain unclear.Here,we demonstrated that sEVs released from oral squamous cell carcinoma(OSCC)-derived CAFs induce collagen crosslinking,thereby promoting epithelial-mesenchymal transition(EMT).CAF sEVs preferably bound to the ECM rather than being taken up by fibroblasts and induced collagen crosslinking,and a LOX inhibitor or blocking antibody suppressed this effect.Active LOX(αLOX),but not the LOX precursor,was enriched in CAF sEVs and interacted with periostin,fibronectin,and bone morphogenetic protein-1 on the surface of sEVs.CAF sEV-associated integrinα2β1 mediated the binding of CAF sEVs to collagen I,and blocking integrinα2β1 inhibited collagen crosslinking by interfering with CAF sEV binding to collagen I.CAF sEV-induced collagen crosslinking promoted the EMT of OSCC through FAK/paxillin/YAP pathway.Taken together,these findings reveal a novel role of CAF sEVs in tumor ECM remodeling,suggesting a critical mechanism for CAF-induced EMT of cancer cells.

基于淀粉微球交联剂的低浓度羟丙基胍胶压裂液性能研究

目的针对低渗透油藏,需要降低压裂液稠化剂用量,减少对储层的伤害,并确保压裂液具备延迟交联、携砂等性能和耐温耐剪切性能。方法利用反相乳液聚合法合成淀粉微球,通过硅配体和硼羟基修饰淀粉微球表面,制备了一种交联性能优良、伤害性低的微球型硅硼交联剂(KBSM)。结果KBSM交联剂能够实现多活性位点交联,增强交联密度,从而降低羟丙基胍胶(HPG)的用量,具有延迟交联特性。其延迟交联时间在2~6 min内可调。质量分数为0.2%的HPG交联冻胶在120℃、170 s-1剪切120 min后的黏度为80 mPa·s。交联冻胶中砂质量分数(以下简称携砂比)为40%时,陶粒沉降速度为0.1167 cm/min。加入质量分数为0.25%的过硫酸铵破胶剂可使交联冻胶在90℃下、120 min内完全破胶,且残渣质量浓度为214 mg/L。同时,破胶液的岩心损害率为26.55%。结论基于淀粉微球交联剂的低含量羟丙基胍胶压裂液对于降低低渗储层伤害有一定的指导意义。

AM-AMPS共聚吸水树脂的制备与性能研究

用丙烯酰胺(AM)和2-丙烯酰胺基-2-甲基丙磺酸(AMPS)两种单体采用溶液共聚方法,用过硫酸铵和亚硫酸氢钠作引发剂,N,N-亚甲基双丙烯酰胺作交联剂,制备了AM-AMPS共聚物吸水树脂。考察了AM/AMPS比例、引发剂用量、交联剂、pH、反应温度、反应时间等工艺条件对吸水倍率的影响。结果表明,AM/AMPS质量比为1/2~1/1,引发剂用量为0.3%,交联剂为0.06%~0.1%,pH值为7,反应温度在35~40℃,反应时间在2~4h时,制备的树脂有良好的吸水性。采用傅里叶变换红外光谱仪、热重分析仪和凝胶渗透色谱仪对产物进行了测试表征。

高压XLPE电缆缓冲层缺陷研究现状综述

高压交联聚乙烯电缆因缓冲层缺陷引发的故障频发,已严重威胁到电力系统的安全运行。本文首先介绍了缓冲层的基本结构和作用,并在此基础上梳理了目前国内外对于缓冲层失效的相关研究;其次从缓冲层的材料特征和内部结构等角度结合电场仿真来分析缺陷发生的主要原因;之后对缓冲层缺陷中出现的白色粉末绝缘性能和理化特征进行总结,并提出其形成机理;最后对缓冲层缺陷的检测手段进行汇总,提出使用计算机断层成像技术对电缆缓冲层缺陷进行检测以弥补现有检测手段的不足,并建议对铝护套及缓冲层的材料或结构进行优化,以预防缓冲层缺陷的生成。

一种壳聚糖改性产物的制备工艺及其产品吸附性能的研究

以壳聚糖(CTS)为母体,加入冰醋酸溶解得到CTS溶液,以无水乙醇为致孔剂,制备多孔壳聚糖微球,将制得的CTS微球与环氧氯丙烷(ECH)交联,制备出羟丙基壳聚糖微球(HPCTS),对产物进行红外光谱和电镜扫描性能表征。通过红外光谱图分析可以看出,ECH与CTS进行了交联反应。比较CTS和HPCTS的电镜扫描图片,发现HPCTS表面因为交联反应而形成大量多孔结构,增加了大量可供吸附重金属离子的空穴,使得HPCTS比交联前的表面积有了大幅提高。通过单因素实验,研究了制备HPCTS的工艺参数,在较优工艺参数下制备的产物交联度可达75.23%,产品具有良好的可再生性。

低浓度胍胶压裂液有机硼交联剂BOA的合成及其性能评价

针对胍胶压裂液体系胍胶使用浓度偏高、破胶后残渣含量较高的问题,开展低浓度胍胶压裂液体系有机硼交联剂的合成和性能评价研究。以硼酸、正丁醇、乙二醇及二乙烯三胺为原料合成有机硼交联剂并对其反应物加量进行优化,确定出有机硼交联剂BOA合成中反应物的优选质量分数分别为二乙烯三胺34.5%、硼酸14.3%、乙二醇38.7%和正丁醇6.9%。对交联剂进行性能评价,结果表明:有机硼交联剂BOA与0.2%胍胶交联形成的胍胶压裂液的黏度可达84 mPa·s;有机硼交联剂BOA与0.2%胍胶交联形成的胍胶压裂液具有良好的抗温抗剪切性,在100 s^(-1)下逐渐升温至90℃、剪切60 min时及在60℃、100 s^(-1)下剪切90 min时胍胶压裂液的黏度均维持在90 mPa·s,且具有滤失低(滤失系数为2.0×10^(-4)m/min^(1/2))、携砂性能好(悬砂沉降速度为0.045 mm/s)、破胶速度快(在90 min内可完全破胶)、破胶液黏度<5 mPa·s、残渣含量较低(151 mg/L)的优势,可满足压裂液现场施工要求。

开环易位烯烃聚合物的动态交联改性研究进展

开环易位聚合(ROMP)为烯烃聚合物的制备提供了一种精确而高效的方法,可制备不同拓扑结构的功能性热塑性烯烃聚合物材料。热塑性烯烃聚合物尽管可以在高温下熔融再加工,但其较低的力学性能和耐热性能限制了其在极端条件下的使用寿命。通过固化交联改性则可以大大改善材料的力学性能等,但也为废旧材料的回收再利用带来了困难。为克服上述局限,构建含有动态键的烯烃聚合物交联网络引起了广泛关注,该类聚合物在提升力学等性能的同时也赋予了其可重复加工的能力。本文聚焦于通过开环易位聚合合成不同拓扑结构的烯烃聚合物,并利用不同类型动态键对其进行动态交联改性的最新研究进展。并对该领域的发展现状和未来研究方向进行了总结。

基于共混和层层自组装方法协同交联剂对琼胶/海藻酸钠复合膜性能的影响

以琼胶和海藻酸钠为成膜基质,通过共混和层层自组装两种方法制备了琼胶/海藻酸钠共混膜和双层膜,并引入交联剂柠檬酸和阿魏酸,通过测定复合膜的机械强度、耐水性、热稳定性、傅里叶变换红外光谱(Fourier transform infrared spectrometer,FT-IR)和微观结构等指标,探究了不同制膜方式结合交联剂对复合膜性能的影响。结果表明,与共混膜相比,双层膜表现出更优异的机械性能和耐水性,添加交联剂后,膜的水蒸气透过率(P<0.05)显著降低,拉伸强度、热稳定性和不透明度提高。其中柠檬酸交联的双层膜综合性能最佳,即拉伸强度51.57 MPa,断裂伸长率26.02%,水溶性24.42%,溶胀率101.67%。FT-IR分析表明柠檬酸通过与琼胶和海藻酸钠发生酯化反应形成CO进行共价交联,而阿魏酸通过与成膜基质形成氢键进行非共价交联。扫描电镜分析表明琼胶和海藻酸钠的相容性良好,各膜表面均平整、光滑,而添加交联剂后,膜截面褶皱减少,膜结构更加紧密。由此表明,层层自组装技术和交联剂的结合使用可以制备出综合性能更好的复合膜。

过氧化物酶在食品分子及其胶体体系修饰中的应用进展

过氧化物酶是一类大量存在于自然界及生物体内的氧化还原酶。其家族成员众多,但都可以催化以过氧化氢(H_(2)O_(2))作为底物的氧化反应。现有研究表明可以通过利用过氧化物酶的氧化特性,来提高功能食品的质量属性和营养特性。而辣根过氧化物酶作为过氧化物酶家族的一员,近些年来被大量研究。尤其是在食品研究开发中,有很多研究通过使用辣根过氧化物酶去催化蛋白质或淀粉等食品分子来改善食品本身的性质或获得更合适的食品胶体,因此值得更深层次的挖掘其应用价值及市场。本文在介绍过氧化物酶的结构、催化机制及影响其催化的关键因素基础上,分析了过氧化物酶催化对食品分子结构和性质的影响,综述了近年来过氧化物酶在食品分子及其胶体体系修饰中的一些应用,以期为今后过氧化物酶的研究提供一定的理论参考和新思路。

The flow behavior of droplet adsorption on a liquid-liquid interface accompanied by cross-linking reaction and phase separation in a microchannel

The adsorption process of droplets on the liquid-liquid interface and phase separation process can regulate the spatial distribution of the fluid system,which are crucial for chemical engineering.However,the cross-linking reaction,which is widely used in the field of polymers,can change the physical properties of the fluids and affect the flow behavior accordingly.A configuration of microchannels is designed to conveniently generate uniform droplets in one phase of the parallel flow.The flow behavior of the adsorption process of sodium alginate droplets on the liquid-liquid interface is investigated,and the subsequent process of phase separation is studied.In the process of droplet adsorption,the crosslinking reaction occurs synchronously,which makes the droplet viscosity and the elasticity modules of the droplet surface increase,thus affecting the dynamics of the adsorption process and the equilibrium shape of the droplet.The variation of the adsorption length with time is divided into three stages,which all conform to power law relationship.The exponents of the second and third stages deviate from the results of the Tanner's law.The flow pattern maps of droplet adsorption and phase separation are drawn,and the operating ranges of complete adsorption and complete separation are provided.This study provides a theoretical basis for further studying the flow behavior of droplets with cross-linking reaction in a microchannel.

玉米淀粉-糠醛共缩聚树脂塑料的制备

以来自农林的廉价植物提取物——玉米淀粉和糠醛为原料,合成一款生物基塑料淀粉-糠醇-甲醛共缩聚塑料(SFFP)。通过电喷雾电离质谱(ESI-MS)和X射线衍射(XRD)测试,表明淀粉、糠醛和甲醛在酸性条件下进行了共缩聚反应。该生物基SFFP塑料的抗压强度与酚醛(PF)塑料相近。在300℃、氮气处理条件下的重量损失为18%,与PF塑料相比,SFFP具有较好的热降解性。此外,与PF塑料相比,SFFP具有更好的疏水性,且其可再生原材料含量高达87%,具有一定的应用价值。

水驱油藏聚乙烯亚胺交联聚合物凝胶体系研究进展

聚乙烯亚胺(PEI)是一种低毒性环保材料,它与聚合物交联的凝胶体系具有适用温度范围广、成胶时间可控、成胶后强度大、高温稳定时间长、几乎不受储层岩石矿物影响等优点。本文回顾了以PEI作为交联剂的各类凝胶体系的研究动态,阐明了PEI与各类聚合物的交联反应机理及其凝胶体系特点,分析了各类因素对凝胶性能的影响,并列举了改善凝胶性能的方法和成功的矿场应用实例,重点分析了提高凝胶体系交联活性的方法研究。最后,提出聚丙烯酰胺(PAM)/PEI凝胶体系作为环保型调驱体系在中低温油藏深部调控方面具有非常大的应用前景,应继续深入研究提高PAM/PEI凝胶体系交联效率的方法及其作用机理,以降低聚合物与交联剂用量,为这一体系的推广应用提供理论依据与实验基础。

卡宾在聚合物交联反应中的研究进展

归纳分析了三氟甲基类卡宾化合物、重氮酯类卡宾化合物、N-杂化卡宾化合物等稳定结构的卡宾前驱体的结构、性能特点,并重点介绍了其在聚合物改性领域的应用研究进展。

不同交联方法构建的胶原基支架及其性能表征

分别采用1-乙基-(3-二甲氨基丙基)碳酰二亚胺(EDC)和N-羟基琥珀酰亚胺(NHS)交联法、甲基丙烯酸酐(MA)修饰光聚合交联法和苯基-2,4,6-三甲基苯甲酰基磷酸锂(LAP)光交联法制备了3种胶原基支架材料,并对其微观结构、理化性能和生物学性能进行了评价。结果表明:这3种交联法制备的胶原基支架材料的孔洞结构具有显著差异,其孔径范围均为50~250μm,符合组织修复材料对孔径的需求。此外,通过MA复合光交联所得的胶原基支架材料(Col-MA),其抗压强度可达2.17 MPa,满足组织工程理想支架材料对力学性能的基本要求。生物相容性实验结果表明,这3种支架材料均能够为细胞生长提供合适的空间以及供应足够的营养物质。

交联剂改善羧基化石墨烯量子点荧光性能

1-(3-二甲氨基丙基)-3-乙基碳二亚胺盐酸盐(EDC)作为一种水溶性交联剂,目前广泛应用于纳米材料研究中。然而,其对石墨烯量子点(GQDs)的光学性质影响很少被关注。本工作以羧基化石墨烯量子点(CGQDs)为对象,研究EDC交联剂对C-GQDs光学性质的影响,改善了C-GQDs的荧光强度。实验中采用一步水相法得到C-GQDs与EDC复合物(C-GQDs/EDC)。实验结果表明,与EDC反应后,C-GQDs荧光显著增强约23倍。此外,也验证了溶液浓度、光辐照和反应时间等因素对荧光的影响。分析表明,C-GQDs的发光是本征态、表面态和缺陷态能级跃迁的多过程作用结果,而原C-GQDs中丰富的缺陷能级导致了发光性能的减弱。机理分析认为,EDC与羧基间发生的活化反应起到了表面缺陷钝化作用,提高了C-GQDs的表面态激子复合效率。该工作有效改善了C-GQDs发光强度低的问题,扩展了其在发光领域的应用前景,并为GQDs光学性质调控提供了参考方案。

Ti_(3)C_(2)系MXene原位制备方法的研究及其二维膜的结构调控

作为具有代表性的二维纳米材料之一,MXene通过层层堆叠可以构建具有分子筛分通道的新型二维分离膜。利用氟化锂/盐酸原位生成氢氟酸的方法,系统地研究了刻蚀液浓度对碳化钛(Ti_(3)C_(2))系MXene纳米片结构的影响,并利用热处理探究了MXene二维膜的结构演变。结果表明,当刻蚀剂中F^(-)的摩尔质量是Al^(3+)的7倍及以上时,能获得较好的单层MXene,且纳米片层之间的层间距随着刻蚀剂中F^(-)浓度的提高而增大;利用热自交联反应,可以在增强纳米片层与片层之间作用力的同时,改变纳米片的层间距。