Properties of Calcium Phosphate Cements With Different Tetracalcium Phosphate and Dicalcium Phosphate Anhydrous Molar Ratios

Calcium phosphate cements (CPCs) were prepared using mixtures of tetracalcium phosphate (TTCP) and dicalcium phosphate anhydrous (DCPA), with TTCP/DCPA molar ratios of 1/1, 1/2, or 1/3, with the powder and water as the liquid. Diametral tensile strength (DTS), porosity, and phase composition (powder x-ray diffraction) were determined after the set specimens have been immersed in a physiological-like solution (PLS) for 1 d, 5 d, and 10 d. Cement dissolution rates in an acidified PLS were measured using a dual constant composition method. Setting times ((30 ± 1) min) were the same for all cements. DTS decreased with decreasing TTCP/DCPA ratio and, in some cases, also decreased with PLS immersion time. Porosity and hydroxyapatite (HA) formation increased with PLS immersion time. Cements with TTCP/DCPA ratios of 1/2 and 1/3, which formed calcium-deficient HA, dissolved more rapidly than the cement with a ratio of 1/1. In conclusion, cements may be prepared with a range of TTCP/DCPA ratios, and those with lower ratio had lower strengths but dissolved more rapidly in acidified PLS.     

PVA/P(AA-AM)复合水凝胶的制备及性能

采用水溶液聚合方法合成了不同组成的丙烯酸-丙烯酰胺共聚物(P(AA-AM))。将聚乙烯醇(PVA)与所合成的P(AA-AM)共混,以戊二醛为交联剂,制备出了不同结构的PVA/P(AA-AM)复合水凝胶。采用扫描电镜观察了凝胶形貌,研究了复合水凝胶的结构与性能关系。结果表明,复合水凝胶溶胀性能与所用交联剂加量有关,复合水凝胶的溶胀度随着交联剂加量增加先增大后减小,在交联剂加量为0.5%时水凝胶溶胀度达到最大值。复合凝胶中的聚合物组成对溶胀度影响显著,随着P(AA-AM)含量提高,水凝胶的溶胀度逐渐增大。适当结构的复合水凝胶具有pH敏感性,敏感程度随着凝胶中P(AA-AM)含量的增加而增强。     

Calcium phosphate metabolism and bone mineral density with nocturnal hemodialysis

An elevated calcium x phosphate product (Ca x P) is an independent risk factor for vascular calcification and cardiovascular death in dialysis patients. More physiological dialysis in patients undergoing nocturnal hemodialysis (NHD) has been shown to produce biochemical advantages compared with conventional hemodialysis (CHD) including superior phosphate (P) control. Benefits of dialysate with greater calcium (Ca) concentration are also reported in NHD to prevent Ca depletion and subsequent hyperparathyroidism, but there are concerns that a higher dialysate Ca concentration may contribute to raised serum Ca levels and greater Ca x P and vascular disease. The NHD program at our unit has been established for 4 years, and we retrospectively analyzed Ca and P metabolism in patients undergoing NHD (8-9 h/night, 6 nights/week). Our cohort consists of 11 patients, mean age 49.3 years, who had been on NHD for a minimum of 12 months, mean 34.3 months. Commencement was with low-flux (LF) NHD and 1.5 mmol/L Ca dialysate concentration, with conversion to high-flux (HF) dialyzers after a period (mean duration 18.7 months). We compared predialysis serum albumin, intact parathyroid hormone, P, total corrected Ca, and Ca x P at baseline on CHD, after conversion to LF NHD and during HF NHD. We also prospectively measured bone mineral density (BMD) on all patients entering the NHD program. Bone densitometry (DEXA) scans were performed at baseline (on CHD) and yearly after commencement of NHD. With the introduction of HF dialyzers, the Ca dialysate concentration was concurrently raised to 1.75 mmol/L after demonstration on DEXA scans of worsening osteopenia. Analysis of BMD, for all parameters, revealed a decrease over the first 12 to 24 months (N = 11). When the dialysate Ca bath was increased, the median T and Z scores subsequently increased (data at 3 years, N = 6). The mean predialysis P levels were significantly lower on LF NHD vs. CHD (1.51 vs. 1.77 mmol/L, p = 0.014), while on HF NHD P was lower again (1.33 mmol/L, p = 0.001 vs. CHD). Predialysis Ca levels decreased with conversion from CHD to LF NHD (2.58 vs. 2.47 mmol/L, p = 0.018) using a 1.5 mmol/L dialysate Ca concentration. The mean Ca x P on CHD was 4.56 compared with a significant reduction of 3.74 on LF NHD (p = 0.006) and 3.28 on HF NHD (p = 0.001 vs. CHD), despite the higher dialysate Ca in the latter. We conclude that an elevated dialysate Ca concentration is required to prevent osteopenia. With concerns that prolonged higher Ca levels contribute to increased cardiovascular mortality, the optimal Ca dialysate bath is still unknown. Better P control on NHD, however, reduces the overall Ca x P, despite the increased Ca concentration, therefore reducing the risk of vascular calcification.     

喷涂距离和喷涂功率对羟基磷灰石涂层的影响

本文以Ｔｉ－６Ａｌ－４Ｖ合金为基体材料,采用等离子喷涂方法,在不同喷涂距离和喷涂功率下制备羟基磷灰石（ＨＡ）涂层,研究喷涂距离和喷涂功率这两个重要的喷涂参数对涂层结构和组成的影响．使用扫描电子显微镜（ＳＥＭ）观察了羟基磷灰石涂层的形貌．涂层的相组成由Ｘ射线衍射谱仪（ＸＲＤ）分析而得．并使用Ｘ射线荧光谱仪（ＸＲＦ）测定了涂层的Ｃａ／Ｐ摩尔比．研究结果表明,喷涂距离对羟基磷灰石涂层的形貌、相组成以及Ｃａ／Ｐ摩尔比有着明显的影响．随着喷涂距离的增大,羟基磷灰石粉末的熔化状态得到改善,涂层的显微结构较为致密．然而,喷涂距离的增大使得涂层的非晶化更加严重,涂层中非晶相含量增大．在实验范围内,喷涂功率对涂层结构和相组成的影响不明显．Ｃａ／Ｐ比测定显示,等离子喷涂羟基磷灰石涂层均为缺磷涂层,Ｃａ／Ｐ比随喷涂距离的增大而降低,随喷涂功率的增大而增大．     

二氧化硅纳米颗粒的反应离子刻蚀及其在硅纳米针尖制备中的应用

系统地研究了硅衬底上二氧化硅纳米颗粒的反应离子刻蚀（R IE）过程,并在此基础上制备了可用于场发射的硅纳米针尖阵列.首先,采用改进的蒸发法在硅衬底上实现二氧化硅纳米颗粒的单层密排结构,再采用典型的刻蚀二氧化硅的RIE技术同时刻蚀硅衬底和二氧化硅纳米颗粒,在对纳米颗粒尺寸随刻蚀进行而改变的电镜照片分析的基础上,获得了相应的二氧化硅纳米颗粒刻蚀模型,计算得到横向和纵向的刻蚀速率;当刻蚀后的二氧化硅纳米颗粒从衬底上脱落后,进一步对硅衬底的刻蚀可以得到锐利的硅纳米针尖阵列,初步的实验结果表明,所制备的硅纳米针尖具有较好的场发射特性.     

粉末冶金低合金钢的制备和性能研究进展

分别从粉末制备、成形工艺、烧结工艺及其组织控制等方面较系统地介绍了国内外粉末冶金低合金钢的制备情况,并展望了其将来的研究方向和前景.     

Biocompatibility of Surface-Modified Biphasic Calcium Phosphate/Poly-L-Lactide Biocomposite in vitro and in vivo

The biocompatibility of surface-modified biphasic calcium phosphate (mBCP)/poly-L-Lactide (PLLA) biocomposite was investigated through a series of experiments in vitro and in vivo. Acute toxicity and short term systemic toxicity experiments revealed no toxicity of the materials. Hemolysis assay indicated the good blood compatibility of the composite. In cytotoxicity assay, L929 mouse fibroblasts could well differentiate and proliferate. Animal experiments in vivo were performed by implanting the materials i...     

TC4钛合金微弧氧化因素对生物陶瓷膜中Ca,P相对含量的影响

为了提高钛合金陶瓷膜的生物相容性,采用微弧氧化技术在TC4钛合金表面制备了一层富含Ca,P的生物活性陶瓷膜。采用SEM,EDS,XRD研究了电流密度、溶液中Ca,P摩尔比、添加剂EDTA.2Na浓度对膜层中Ca,P相对含量(原子分数)及Ca,P摩尔比的影响及微弧氧化生物陶瓷膜层的形貌及组成。结果表明:随着电流密度的增大,膜层中的Ca,P相对含量增加,Ca,P摩尔比也逐渐增加;增大溶液中Ca,P摩尔比,膜层中Ca相对含量有所增加,Ca,P摩尔比也逐渐增加;当加入添加剂EDTA.2Na时,膜层中的Ca相对含量显著增加,从而使膜层中Ca,P摩尔比显著增加;氧化膜由致密的内膜层和多孔的外膜层构成,主要由Ca,P,O,Ti,V元素组成,其相成分主要为金红石和板钛矿型TiO2,并含有一定量的非晶相Ca,P化合物。     

不同Ti／Ba摩尔比的钛酸钡纳米晶粉体的Sol—gel法制备与表征

采用Ｓｏｌ－ｇｅｌ法制备了不同Ｔｉ／Ｂａ摩尔比的ＢａｙＴｉｘＯ３（ｘ／ｙ＝０．９９０,１．０００,１．０１０,１．０２０,１．０４５）纳米晶粉体。应用热分析、Ｘ射线粉末衍射、激光和透射电镜等技术对干凝胶热分解历程和粉体性能进行了研究,发现随Ｔｉ／Ｂａ摩尔比的增加,粉体的平均晶粒尺寸、晶体结构和粉体粒度分布各呈现规律性变化。本文并对这些规律性变化进行了初步讨论     

Al2O3纳米粒子增强锌铝基耐蚀涂层的制备及性能研究

为解决锌铝基耐蚀涂层在高速、强摩擦等特殊服役条件下的使用问题,将Al2O3纳米粒子添加到锌铝基耐蚀涂层中进行改性,以提高涂层的硬度和耐蚀性.研究了Al2O3纳米粒子及其添加量对涂层硬度、摩擦系数、附着强度、耐冲击性能和耐腐蚀性能的影响,并对涂层的微观组织和成分进行了分析.结果表明,添加Al2O3纳米粒子可显著提高锌铝基耐蚀涂层的硬度和耐蚀性能,降低摩擦系数,且对涂层的附着强度和耐冲击性能无负面影响.Al2O3纳米粒子在涂层中的均匀分散是获得涂层优异综合性能的必要条件.     

氧化石墨烯/壳聚糖层层自组装复合膜的制备及其在环保领域中的应用

利用层层自组装技术将氧化石墨烯与壳聚糖进行自组装,制备出一种新型的氧化石墨烯/壳聚糖复合膜,并利用原位合成的方法引入纳米银粒子。采用紫外可见光谱(UV-Vis)、红外光谱(FTIR)、X射线衍射(XRD)和原子吸收等分析方法对复合膜的自组装行为和催化性能进行了研究。实验结果表明,氧化石墨烯与壳聚糖可通过层层自组装技术制备出新型复合膜,这种复合膜可包裹纳米银粒子,膜内纳米银粒子对4-硝基苯酚的催化活性较高,并且可实现循环使用。此外,在稳定性实验中,复合膜不会释放纳米银粒子或银离子,避免了给水体带来二次污染。因此,这种材料在水处理等环保领域中可能具有巨大的潜在实用价值。     

Zr_2P_2WO_(12)/Fe-Ni复合材料的制备及其热膨胀性能研究

使用水热法成功制备Zr_2P_2WO_(12)粉末,采用真空热压烧结方法制备接近致密的Zr_2P_2WO_(12)/Fe-Ni复合材料。使用X射线衍射、扫描电镜及热膨胀测试仪对制备的Zr_2P_2WO_(12)及其Fe-Ni复合材料进行性能测试和表征,使用维氏硬度计测试复合材料的硬度,使用排水法表征复合材料的密度。结果表明:水热法制备的Zr_2P_2WO_(12)粉为高纯度的单相Zr_2P_2WO_(12),颗粒规则,晶粒尺寸约为50nm;随Zr_2P_2WO_(12)含量的增加,Zr_2P_2WO_(12)/Fe-Ni复合材料的硬度增加,而密度和致密度则降低,在25~800℃区间内平均热膨胀系数从13.5×10~(-6)/℃降低到8.6×10~(-6)/℃。     

Evaluating and Modeling the Mechanical Properties of the Prepared PLGA/nano-BCP Composite Scaffolds for Bone Tissue Engineering

In this paper, preparation of nano-biphasic calcium phosphate (nBCP), mechanical behavior and load-bearing of poly (lactide-co-glycolide) (PLGA) and PLGA/nBCP are presented. The nBCP with composition of 63/37 (w/w) HA/β-TCP (hydroxyapatite/β-tricalcium phosphate) was produced by heating of bovine bone at 700℃. Composite scaffolds were made by using PLGA matrix and 10-50 wt% nBCP powders as reinforcement material. All scaffolds were prepared by thermally induced solid-liquid phase separation (TIPS) at -60℃ under 4 Pa (0.04 mbar) vacuum. The results of elastic modulus testing were adjusted with Ishai-Cohen and Narkis models for rigid polymeric matrix and compared to each other. PLGA/nBCP scaffolds with 30 wt% nBCP showed the highest value of yield strength among the scaffolds. In addition, it was found that by increasing the nBCP in scaffolds to 50 wt%, the modulus of elasticity was highly enhanced. However, the optimum value of yield strength was obtained at 30 wt% nBCP, and the agglomeration of reinforcing particles at higher percentages caused a reduction in yield strength. It is clear that the elastic modulus of matrix has the significant role in elastic modulus of scaffolds, as also the size of the filler particles in the matrix.     

基于类等势场的粉末高温合金盘件预成形设计

根据能量最小原理和最小阻力原理,利用塑性变形过程中坯料的流动规律与静电场等势线分布类似这一特性,提出一种能够进行预成形设计的新方法——类等势场法,并采用该方法对粉末高温合金盘件进行预成形设计,从中优选出6组预成形形状,利用MSC/Super Form商用有限元软件对上述预制坯的等温成形过程进行了数值模拟,得到了6组粉末高温合金盘件在预锻到终锻过程中的应力率参数和应变率梯度.通过对盘件轮毂、辐板和轮缘3个部位6个典型单元体应力率参数g的比较与分析,以及整体盘件应变率梯度的比较,并参考预锻变形量和终锻变形量,认为选择3号预锻模为最佳方案.     

GF/P(3HB-co-4HB)-PLA生物基复合材料的制备与性能

为了提高聚（3-羟基丁酸酯-co-4 羟基丁酸酯）-聚乳酸（P（3HB-co-4HB）-PLA）生物基共混材料的力学性能和尺寸稳定性,扩大应用领域,以P（3HB-co-4HB）和PLA共混物为基体,盐酸或偶联剂表面处理的玻璃纤维（GF）为增强材料,采用熔融共混法制备GF/P（3HB-co-4HB）-PLA复合材料。通过傅里叶变换红外光谱仪（FTIR）、扫描电子显微镜（SEM）、热失重分析仪（TGA）和万能电子拉力机等研究了GF表面处理方法对复合材料力学性能、热性能、尺寸稳定性及断面形态的影响。研究结果表明：表面改性GF的加入可显著提高P（3HB-co-4HB）-PLA共混材料的综合性能。经偶联剂表面接枝的GF可均匀分散在P（3HB-co-4HB）-PLA基体中并形成较强的界面结合。添加质量分数20%的偶联剂改性GF使复合材料的拉伸强度、弯曲强度、缺口冲击强度和硬度分别提高了29.38%、20.32%、41.38%和15.31%;初始热分解温度（IDT）和维卡软化温度（VST）分别提高了6.64 ℃和10.7 ℃;室温和60 ℃放置60 d后复合材料试样长度方向的尺寸稳定性分别提高了32.47%和33.70%。     

聚合物浸渍裂解法制备C/C-ZrC复合材料及其性能

本文以低密度C/C复合材料为坯体,有机锆聚合物为前驱体,采用聚合物浸渍裂解法(PIP)制备C/C-ZrC复合材料,并对其微观结构、力学性能、烧蚀性能以及烧蚀机理进行了研究。结果表明ZrC在材料内分布均匀,密度为2.05g·cm~(-3)的C/C-ZrC复合材料其弯曲强度为89.70MPa,呈脆性断裂。经氢-氧焰烧蚀150s后其线烧蚀率为-2.2×10~(-3)mm·s~(-1),质量烧蚀率为-1.0×10-3g·s~(-1),远低于密度为1.86g·cm~(-3)的C/C复合材料(线烧蚀率:4.4×10~(-3) mm·s~(-1),质量烧蚀率:7.5×10~(-4)g·s~(-1));在烧蚀的过程中,ZrC表现出优先氧化,同时生成的ZrO_2阻挡层能有效阻挡热量的传递和氧气的渗透,提高了材料的抗烧蚀性能。     

溶胶-凝胶法有机-无机精细复合材料P(VDF/TeFE)-SiO_2的制备与显微结构

用溶胶－凝胶法制备了有机－无机精细复合材料Ｐ（ＶＤＦ／ＴｅＦＥ）－ＳｉＯ２。利用水解－聚合反应由正硅酸乙脂（ＴＥＯＳ）合成ＳｉＯ２溶胶，乙醇作溶剂，盐酸作催化剂。将Ｐ（ＶＤＦ／ＴｅＦＥ）溶于丙酮，并与ＳｉＯ２溶胶均匀混合。凝胶后经干燥和热处理得到有机－无机精细复合材料Ｐ（ＶＤＦ／ＴｅＦＥ）－ＳｉＯ２。用红外光谱分析、扫描电镜分析、差示扫描热分析和热失重分析对有机－无机精细复合材料Ｐ（ＶＤＦ／ＴｅＦＥ）－ＳｉＯ２进行了显微结构表征。     

起始物对Li+、Ca2+混合型低硅X型分子筛(LSX)制备及吸附性能的影响

采用Li-LSX, Ca-LSX为起始物进行离子交换分别制备了Li⁺、Ca²⁺混合型LSX, 通过ICP-AES, ⁷Li MAS NMR, ²³Na MAS NMR及静态吸附等检测方法, 考察了起始物不同对离子交换限度, 离子定位与产品吸附性能的影响. 实验结果表明, 以Ca-LSX为起始物进行Li交换得到的Li-Ca-LSX最大交换率为31.5%, 此时吸附性能最优, 氮氧吸附量分别为36.4和5.0mL/g, 选择性系数为12.4, 且节约了Li的用量. 借助NMR结果发现, 对吸附性能有直接影响的Li⁺, 除公认SIII位置外, 尚有少量SI’亦有较显著作用.     

SiO2/TiO2复合气凝胶的孔道结构研究

为了在常压干燥下制备高比表面积且具有多级孔道结构的SiO2/TiO2复合气凝胶,以正硅酸乙酯、钛酸丁酯为原料,利用低聚体聚合将分相平行引入到溶胶凝胶过程中,获得SiO2/TiO2醇凝胶,并通过溶剂替换技术实现气凝胶的常压干燥制备.不同硅钛比气凝胶的内部结构研究表明:合成的气凝胶是由纳米SiO2和TiO2颗粒分散复合而成的介孔块体,其中Ti—O—Ti、Si—O—Si和Ti—O—Si键相互交织.气凝胶的结构变化是分相与溶胶凝胶过程相互竞争的结果.Si含量能显著改善气凝胶的结构,当n(Ti)∶n(Si)为3∶1时,比表面积高达712.2 m2/g,平均孔径为3.36 nm;当n(Ti)∶n(Si)为1.5∶1时,复合气凝胶具有明显双连续孔道,比表面积高,同时孔状结构清晰.     

Preparation and characterization of P3HT:CuInSe2:TiO2 thin film for hybrid solar cell applications

Improved efficiency of hybrid Al/Ca/P3HT:CISe:TiO₂/PEDOT:PSS/ITO thin film solar cells was obtained by optimizing P3HT/CISe ratio. This study also investigated the effects of TiO₂ content in the P3HT:CISe active layer, and altering annealing temperature conditions. The optimum TiO₂ content and annealing temperature for solar cell efficiency is 25 wt.% and 150 °C, respectively. The optimal results for the open circuit voltages (V_OC), short-circuit current density (J_SC), fill factor (FF), and efficiency (η) of the prepared hybrid thin film solar cell were V_OC = 0.335 V, J_SC = 8.07 mA/cm², FF = 52.75, and η = 1.425.