A Study on the Friction and Wear Behavior of PTFE Filled with Acid Treated Nano‐Attapulgite

Summary: A solid lubricant composite material was prepared by compression molding PTFE and acid treated nano‐attapulgite. The friction and wear tests were performed on a block‐on‐ring wear tester. Scanning electron microscopy (SEM), energy‐dispersive X‐ray spectrometer (EDS) and DSC were utilized to investigate material microstructures and examine modes of failure. Experimental results showed that there was no significant change in coefficient of friction, but the wear rate of the PTFE composite was orders of magnitude less than that of pure PTFE. Acid treated nano‐attapulgite was superior to untreated nano‐attapulgite in enhancing the wear resistance of PTFE. Moreover, the wear resistance of the composite increased monotonically with increasing treated attapulgite concentration. Investigation of transfer film and analysis of debris for PTFE and its composite showed that acid treated nano‐attapulgite filled to PTFE could facilitate formation of transfer film on the steel ring surface and inhibit breakage of PTFE molecular chain. The PTFE composite with higher heat absorption capacity exhibited improved wear resistance. Furthermore, the steel ring counterface abrasion was not found.

Effect of load on the wear rate of PTFE and its composites.     

Biodegradable,superhydrophobic walnut wood membrane for the separation of oil/water mixtures

The preparation of environmentally friendly oil/water separation materials remains a great challenge. Freeze-drying of wood after lignin removal yields wood aerogels, which can be used as substrates to prepare fluorine-free environmentally friendly superhydrophobic materials, However, they are more suitable for absorption rather than filtration applications due to their poor strength. A study using cross-sections of pristine wood chips as substrates retains the original strength of wood, but the use of the cross-sectional of wood pieces limits their thickness, strength, and size. In this paper, a degradable fluorine-free superhydrophobic film (max. water contact angle of approximately 164.2°) with self-cleaning and abrasion resistance characteristics was prepared by a one-step method using pristine and activated walnut longitudinal section films as the substrate, with tetraethyl orthosilicate as a precursor and dodecyltriethoxysilane as a modifier. The tensile strength results show that superhydrophobic films with pristine or activated wood substrates maintained the strength of pristine wood and were 2.2 times stronger than the wood aerogel substrate. In addition, after cross-laminating the two samples, the films had the ability to separate oil and water by continuous filtration with high efficiency (98.5%) and flux (approximately 1.3 × 10³ L∙m^‒2∙h^‒1). The method has potential for the large-scale fabrication of degradable superhydrophobic filtration separation membranes.     

Enhanced Hydrolysis of Cellulose to Reducing Sugars on Kaolinte Clay Activated by Mineral Acid

Catalysis Letters - Kaolinite, a natural, layered phyllosilicate, has been used as the solid catalyst for the hydrolysis of cellulose in our previous work. In the present study, kaolinite was...     

吲哚席夫碱类衍生物的合成及其抗HIV-1活性研究

设计、合成吲哚席夫碱类衍生物并研究其抗HIV-1活性。以3-吲哚甲醛衍生物为原料,在碱催化下与芳香胺发生缩合反应合成吲哚席夫碱类化合物,并采用通过 MTT 法测试了目标化合物在MT-4 细胞内的抗 HIV-1病毒株的活性。 合成了32个吲哚席夫碱类衍生物,其结构均通过1H NMR和MS加以确证。初步的生物活性结果测试表明,所合成的吲哚席夫碱类化合物对HIV-1均有优秀的抑制活性,并具有广谱的抗HIV-1活性。其中化合物31 (EC50 = 0.06 mol/L)展现出了最强的抗HIV-1活性,与阳性药物地拉韦啶 (DLV, EC50 = 0.57 mol/L)相当;同时,化合物31具有非常低的毒性,选择指数 (SI)高达2500,明显高于地拉韦啶 (DLV, SI = 1272.9)和依法韦仑 (EFV, SI = 321)。将吲哚和席夫碱两个药效团,能够得到高效、低毒的HIV-1逆转录酶抑制剂,为今后发展新型的HIV-1抑制剂提供了新思路。     

UPLC-MS/MS法测定美洛昔康中两个中间体杂质

建立UPLC-MS/MS法测定美洛昔康中杂质A和杂质B.采用ACQUITY UPLC?HSS T3 C18(2.1 mm×100 mm,1.8μm)色谱柱,流动相为0.1％甲酸水溶液-甲醇(45:55).采用电喷雾离子源(ESI),多反应监测(MRM)模式,正离子扫描;脱溶剂温度:500℃;干燥气流速:15 L/min...     

Efficient cycloaddition of CO2 and epoxides to cyclic carbonates using salen-based covalent organic framework as a heterogeneous catalyst

Journal of Porous Materials - Salen-based covalent organic framework (COF), constructed by salen skeleton, has great potential applications as the heterogeneous catalyst due to its unique...     

加压溶剂法提取雷公藤甲素及其条件优化

以雷公藤为原料,采用加压溶剂法提取雷公藤甲素,以1,2-二氯乙烷为溶剂,考察了提取时间、料液比和提取温度等因素对提取工艺的影响,并在单因素试验基础上,根据中心组合试验设计原理采用三因素三水平的响应面分析法进行工艺优化,得到提取过程优化的工艺条件为:料液比1:9.7,提取温度115℃,提取时间80min,雷公藤甲素的实际得率可达0.173‰,纯度为1.21%,与常规回流提取法相比优势明显。     

A novel Electro-Fenton-Like system using PW11O39Fe(III)(H2O) as an electrocatalyst for wastewater treatment

A novel Electro-Fenton-Like (EFL) system was developed using the Keggin-type iron-substituted heteropolytungstate anion PW₁₁O₃₉Fe(III)(H₂O)⁴⁻ to substitute for Fe³⁺ in the conventional Electro-Fenton (EF) system for treatment of water polluted with organic compounds. The EFL system overcomes the drawback of low pH in conventional EF approaches and can be directly applied to neutral water treatment without any pH adjustment. Experimental results for dimethylphthalate (DMP) revealed complete degradation in <80 min in pH 6.86 solution containing 0.1 mM DMP at a potential of −0.5 V and O₂ flow rate of 60 mL min⁻¹. Total organic carbon removal of ∼56% was achieved at 120 min. Comparison with conventional EF oxidation revealed better efficiency of the present system for DMP degradation, suggesting its potential in treatment of water and wastewater with a relaxed pH requirement. The cumulative H₂O₂ concentration generated in situ at the electrode was monitored and the observed degradation rate constants k_obs were determined for different initial DMP concentrations. The ligand exchange reaction of PW₁₁O₃₉Fe(III)(H₂O)⁴⁻ with H₂O₂ and the electron transfer resulting in hydroxyl radicals were examined using HPLC and electrochemical impedance spectroscopy. An electrocatalytic model involving inner-sphere electron transfer and a reaction mechanism for PW₁₁O₃₉Fe(III)(H₂O)⁴⁻ electrocatalytic reduction of H₂O₂ are proposed.     

对苯二酚合成过程中酚醌物质的气相色谱法分析

采用气相色谱（GC）分析方法,以氢火焰离子化检测器（FID）和30 m×0.25 mm×0.25μm KB-5毛细管色谱柱,实现了苯酚为原料合成对苯二酚合成过程中对苯二酚,对苯醌,邻苯二酚及苯酚四种物质的同步定量。该方法操作简便,能准确、快捷的测定合成过程中各物质的含量,是对先前工作新的发展。