Degradability and biocompatibility of bioglass/poly(amino acid) composites with different surface bioactivity as bone repair materials

Bioglass (BG) possesses excellent bioactivity and has been widely used in the manufacture of biomaterials. In this study, a composite with different surface bioactivity was fabricated via in situ melting polymerization by incorporating BG and poly(amino acid) (PAA) at a suitable ratio. The structure of the composite was characterized by Fourier transform infrared spectroscopy and XRD. The compressive strength of the BG/PAA composites was 139 MPa (BG:PAA = 30:70). The BG/PAA composites were degradable, and higher BG in composite showed higher weight loss after 4 weeks of incubation in simulated body fluid. In addition, the BG/PAA composite maintained adequate residual compressive strength during the degradation period. The SEM results showed the differences in surface bioactivities of the composites directly, and 30BG/PAA composite showed thicker apatite layer and higher Ca/p than 15BG/PAA. in vitro MG-63 cell culture experiments showed that the composite was noncytotoxic and thus allows cells to adhere, proliferate, and differentiate. This indicates that the composite has good biocompatibility. The implantations in the bone defects of rabbits for 4 and 12 weeks were studied. The composites had good biocompatibility and were capable of guiding new bone formation without causing any inflammation. The composite may be successfully used in the development of bone implants.     

Preparation of treelike and rodlike carboxymethylated nanocellulose and their effect on carboxymethyl cellulose films

In this work, carboxymethyl cellulose (CMC) with low substitution degree, followed by different posttreatments, was applied to prepare treelike CMC nanofibrils (CMCNFs) and rodlike CMC nanocrystals (CMCNCs), and their performance in CMC composite film was evaluated simultaneously. From transmission electron microscopy results, it was found that the treelike CMCNCFs exhibited a lager aspect ratio compared to the rodlike CMCNCs. As for reinforcing CMC film, 4 wt% was the best adding amount, at this time, the tensile strength of CMC/CMCNFs and CMC/CMCNCs composite films was increased by 72.1% and 47.3%, respectively. Moreover, adding these nanofillers to CMC also could enhance the thermal stability of composite films slightly, while the transmittance of composite films was reduced at the same time. In addition, CMC/CMCNFs film was designed as a packaging box to determine its performance. Therefore, this study could reveal the differences of properties for composites with different types of nanocellulose and provide a foundation for further application of nanocellulose.     

Removal behavior and mechanism of silver from low concentration wastewater using cellulose aerogel modified by thiosemicarbazide

Due to the low concentration of silver in water, most of the cellulose adsorbents exhibited low removal efficiency, which greatly limited their practical applications. Herein, a cellulose aerogel modified by thiosemicarbamide (CAT) was fabricated for reducing and adsorbing silver ions from low concentration wastewater. The characterization results concluded that CAT owned a three-dimensional spongy structure with many circular microspheres and a better specific surface area (19.37 m² g⁻¹), as well as the functional groups of ─C═N⁺─H and ─(C═S)─N. The static batch adsorption experiments demonstrated that CAT could reached the maximum removal percentage of 94.94% and adsorption capacity of 42.12 mg g⁻¹ under the initial concentration of Ag(I) was 15 mg L⁻¹ and the pH value was 7. Meanwhile, the adsorption of Ag(I) on CAT was second-order reaction, and the Langmuir model could better fit the adsorption process. In addition, CAT exhibited wide pH values (1–9) adaptability and excellent adsorption performance for silver through electrostatic interaction, chelation, and reduction. This study probably provides a new method as well as important experimental data and theoretical reference for the removal of silver ions and other metals.     

Engineering all-aromatic polyamide surface from hydrophilic to superhydrophobic and the accelerated strategy

Being a new kind of nanomaterials, aromatic polyamide nanofibers (ANF) have been much highlighted in recent studies. We here demonstrate an isopropyl alcohol (IPA) accelerated chemical cleavage on poly (p-phenylene terephthalamide) chopped fibers, which provides an efficient preparation method of ANF. The comprehensive study on the processes accelerated by different alcohols revealed that the preparation time of ANF in the mixed medium of dimethyl sulfoxide (DMSO)-alcohol (20:1 in volume) was shorten to 45 min and 75 min for methanol (ethanol) and isopropanol, respectively. However, the nanofibers prepared in DMSO-IPA exhibited the minimum in axial and radial dimensions, providing the finest and most uniform diameter of 16 nm. The corresponding ANF films through vacuum assisted filtration also showed the highest tensile strength of 150 MPa, in comparison with those of the ANF films prepared using other alcohols, which were about 110 MPa. Furthermore, ANF/silicon hybrid films were prepared by the ionic ring-opening reaction followed by the alkoxysilane condensation and nanoparticle fabrication. By changing the organo functional groups in the alkoxysilane, the surface of the films were adjustable in a wide contact angle range from 56° (hydrophilic) to 150° (superhydrophobic), suggesting the amendable interfacial properties potential applicable to composite fabrication with most of the resin matrix.     

Ultrahigh molecular weight polyethylene with improved crosslink density,oxidation stability,and microbial inhibition by chemical crosslinking and tea polyphenols for total joint replacements

Highly crosslinked ultrahigh molecular weight polyethylene (UHMWPE) stabilized by vitamin E (VE) is widely applied in artificial joints as the bearings. Despite the approval, there is a discord that VE lowers the crosslinking efficiency, limiting its use at high concentration. In this work, we aim to obtain highly crosslinked and oxidation resistant UHMWPE through the conjunction of tea polyphenol and chemical crosslinking. We hypothesized that highly incorporated tea polyphenol with multiple reactive sites can ameliorate crosslinking efficiency of chemical crosslinked UHMWPE in comparison to VE. Epigallocatechin gallate (EGCG) as representative tea polyphenol was incorporated into UHMWPE at high concentration (2–8 wt%), followed by chemical crosslinking with 2 wt% organic peroxide. Unlike VE/UHMWPE blends as the control, chemical crosslinking achieved an increasing trend in crosslink density of EGCG/UHMWPE blends with increasing antioxidant concentration. High concentration of EGCG also enhanced the oxidation stability of UHMWPE. Intriguingly, EGCG endowed UHMWPE with an excellent antimicrobial property, which was inefficient in VE/UHMWPE. Cell viability was hardly affected by the high loaded antioxidant and peroxide. The chemically crosslinked UHMWPE blended with EGCG is proved to be a reasonable, cost effective and realistic alternative for use in artificial joints.     

ZAlSi12Cu2Mg1微弧氧化陶瓷膜层形成过程研究

通过控制微弧氧化时间,研究了ZAlSi12Cu2Mg1在不同氧化时间下膜层的生长过程,分析了氧化过程中正向电流密度、膜层厚度的变化.结果表明微弧氧化阶段又分为氧化过渡阶段和氧化烧结阶段.氧化过渡阶段陶瓷层以向外生长为主;生成Al2O3非晶氧化物;氧化烧结阶段膜层以向内生长为主,此阶段膜层生长速率最快,生成Al2O3晶体和莫来石.氧化烧结阶段对陶瓷膜层的形成起重要作用,对氧化烧结阶段的控制可直接影响膜层的厚度以及膜层中Al2O3晶体含量.     

酸浸+等离子体刻蚀YG6微米-纳米金刚石复合涂层工具研究

金刚石涂层工具一直是金刚石膜工具应用研究的主流.制约其产业化的主要因素是涂层的附着力低和微晶金刚石涂层工具的加工精度差.通过对衬底的有效预处理和CVD沉积过程控制的研究,开发在硬质合金基体上沉积高结合强度、低粗糙度的金刚石涂层新技术,对于实现CVD金刚石涂层刀具高效、高精度切削加工具有重要意义.对旨在提高金刚石涂层附着力的预处理技术,本文探索了将酸蚀脱钴+等离子体刻蚀处理衬底法.利用优化的沉积工艺,在酸浸+等离子刻蚀处理的YG6刀片上沉积的两层金刚石复合膜表面粗糙度为0.13μm,附着力压痕测试临界载荷大于1500N.金刚石涂层工具的切削加工性能明显高于无涂层硬质合金工具.在加工ZAlSi12合金时,单层和两层金刚石涂层车刀片的切削寿命分别是无涂层车刀片切削寿命的21倍和28倍.     

反应熔渗法制备Mo(Si,Al)2-SiC复合材料的研究

通过尝试对MoSi2+C坯体中熔融渗Al制备了Mo(Si,Al)2-SiC复合材料,并对其组织及性能进行了研究.反应熔渗Al法制备Mo(Si,Al)2-SiC复合材料中,反应生成物主要为Mo(Si1-x,Alx)2和SiC相,还有少量Mo5Si3C和Al相.随着x值的增加,Mo5Si3C相和Al相逐渐减少,并消失.其组织为片状Mo(Si,Al)2组织间隙中分布着针尖状SiC颗粒;从断口形貌看,SiC颗粒非常细小,团聚在大的Mo(Si,Al)2颗粒周围.根据断口形貌,部分形成的SiC为晶须状,当x=0.4时,形成的SiC多为晶须状,并且形成的晶须状的SiC和Mo(Si,Al)2连成片.反应熔渗Al法制备复合材料抗弯强度是随着x值先增加后降低,在设计值x=0.237时取得最高值.     

连续型Δ∑调制器设计综述

Δ∑调制器作为数字转换器中重要的类型,以其较高精度及对CMOS工艺演进的更强适应性得到广泛应用.阐述了Δ∑调制器中连续型的Δ∑调制器的主要设计要点,介绍了国内外在连续型Δ∑调制器上的研究现状,并对相应设计方法进行分类总结.分析了连续Δ∑调制器的工作原理、系统结构、电路误差及模型,对其发展趋势以及面临的挑战进行了总结.结果说明合理地利用新工艺及新型积分器可以有效提高连续型Δ∑调制器的带宽及能效.     

RGB-D Hand-Held Ob ject Recognition Based on Heterogeneous Feature Fusion

Ob ject recognition has many applications in human-machine interaction and multimedia retrieval. However, due to large intra-class variability and inter-class similarity, accurate recognition relying o...