3D Printing Conductive Composites with Poly(ionic liquid) as a Noncovalent Intermedia to Fabricate Carbon Circuits

In this study, a kind of imidazole type poly(ionic liquid) ([PEP-MIM]Cl) is synthesized, which can disperse carbon effectively. [PEP-MIM]Cl is used as an intermediate to coat carbon on the poly(acrylic acid)(PAA-co-MBA) via ion exchange to obtain conductive polymer composite (CPC). A series of characterizations are performed. Experiments show that carbon can be coated on the PAA-co-MBA uniformly, and compared with using carbon as filler, this method requires less carbon to achieve good conductive performance. The carbon layer on the polymer's surface is enriched via the swelling-shrinking properties of PAA-co-MBA according to the SEM images. Furthermore, in combination with 3D printing technology, PAA-co-MBA can be designed into different shapes to achieve various functions such as pressure-sensing element. Finally, a new type of CPC named carbon clad polymeric laminate (CCPL) is prepared by using the carbon coating method and 3D printing technology. It has the potential to replace copper clad laminate (CCL) and printed circuit board (PCB), to a certain extent. This technology expands the preparation method and application of the CPC such as flexible and wearable conductive fabrics.     

On the involvement of radical oxygen species O− in catalytic oxidation of benzene to phenol by nitrous oxide

Catalytic oxidation of benzene to phenol by nitrous oxide over Fe-MFI zeolites was studied in relation to the active oxygen species taking part in the oxidation. A linear dependence of the reaction rate on the concentration of independently identified active sites generating O⁻ radicals (α sites) was obtained within a broad range of values. The dependence is interpreted as convincing evidence of the O⁻ involvement in the catalytic (not only stoichiometric) oxidation of benzene to phenol. This conclusion is of particular importance in connection with a long discussion in the literature on a possible role of O⁻ radicals in selective oxidation catalysis over V and Mo oxides. Reliable evidence of the catalytic role of O⁻ obtained with zeolites may renew general interest in the once-suggested but not recognized role of radical oxygen in oxidation over widely used metal oxide catalysts.     

Enzymatic hydrolysis of lysine diisocyanate based polyurethanes and segmented polyurethane ureas by various proteases

This work studies the enzymatic degradation of polyurethanes (PUs) and segmented polyurethane ureas (SPUUs) derived from lysine diisocyanate (LDI) by various proteases. Thiol proteases, such as papain, bromelain, and ficin, showed high activity on PUs. Protease K and chymotrypsin also hydrolyzed the PUs. For almost all SPUUs, papain showed high activity. For example, LDI/poly(caprolactone) diol (M_w = 1250)/ethylene diamine (2/1/1) was hydrolyzed to 43% under the same conditions. The water-soluble degradation products of a polyurethane, LDI/BD (1/1), and two model compounds treated with papain were studied with NMR and GPC analysis. From the results, it was evident that the pendant methyl ester group in LDI was rapidly hydrolyzed, followed by slow hydrolysis of urethane bonds in the backbone chain.     

Synthesis,structure, and adsorption properties of a three-dimensional porous yttrium–organic coordination network

Deprotonation of 4,4′-biphenyldicarboxylic acid (H₂BPDC) with triethylamine followed by the copolymerization with Y(III) in N,N-dimethylformamide (DMF) at room temperature yields a new three-dimensional (3-D) porous metal–organic coordination network, [Y₂(BPDC)₃(DMF)₂(H₂O)₂]_n · (DMF)_n · (H₂O)_n (1). Compound 1 (C_24.50H₁₉N_1.50O₉Y) crystallizes in the triclinic P-1 space group (a = 8.220 (2), b = 13.998 (4), c = 14.212 (4) Å, α = 111.058 (5)°, β = 90.187 (5)°, γ = 94.318 (5)°, V = 1520.9 (7) ų, and Z = 2). X-ray crystallography reveals that 1 consists of a 3-D framework contained open 1-D channels with the dimension of 5 × 10 Å along the crystallographic a axis. The adsorption measurements show that compound 1 can adsorb N₂, Ar and CO₂ into its pores. The adsorption isotherms for MeOH and H₂O were also measured.     

Effect of coagulation temperature on structures and properties of poly(<Emphasis Type="Italic">p</Emphasis>-phenylene benzobisoxazole) (DHPBO) fibers during dry-jet wet-spinning process

The effect of coagulation temperature on the morphology, microstructures and mechanical properties of dihydroxy poly(p-phenylene benzobisoxazole) (DHPBO) fibers was investigated during dry-jet wet-spinning process, in which the coagulation bath concentration and drawn ratio were kept as 10 wt% of PPA in water and 1.7, respectively. The structures and mechanical properties of the as-spun DHPBO fibers were characterized by FTIR, XRD, SEM, and single fiber tensile testing. The results indicated that in PPA/H₂O coagulation system, when the coagulation temperature was 25°C, highly crystallized DHPBO as-spun fibers possessing fine crystallites, circular and smooth morphology, and excellent mechanical properties could be achieved. Supported by the National Natural Science Foundation of China (Grant No. 50673017), Shanghai Leading Academic Discipline Project (Grant No. B603) and the Program of Introducing Taleuts of Discipline to University of People’s Republic of China (“111” Program) (Grant No. 111-2-04)     

Effect of coagulation temperature on structures and properties of poly(p-phenylene benzobisoxazole) (DHPBO) fibers during dry-jet wet-spinning process

The effect of coagulation temperature on the morphology, microstructures and mechanical properties of dihydroxy poly(p-phenylene benzobisoxazole) (DHPBO) fibers was investigated during dry-jet wet- spinning process, in which the coagulation bath concentration and drawn ratio were kept as 10 wt% of PPA in water and 1.7, respectively. The structures and mechanical properties of the as-spun DHPBO fibers were characterized by FTIR, XRD, SEM, and single fiber tensile testing. The results indicated that in PPA/H2...     

摆动磁场条件下的焊接接头组织研究

为了优化不锈钢焊接工艺,提高焊接质量,进行了外加电磁场条件下的304不锈钢钨极氩弧焊(TIG),磁场施加方式分别为横向磁场和旋转磁场.焊后采用电子显微镜对焊接接头进行显微组织观察,研究了不同外加磁场类型和不同焊接速度对不锈钢焊接接头组织的作用规律.试验结果表明,外加磁场改变了熔池的流动形态,使金属液由四周向中心流动并伴有搅拌,也使焊缝熔深增大的同时,抑制柱状晶的形成,细化组织.     

钎焊温度对SiC/YG8接头微观组织的影响

在保温时间为5min、钎焊温度为940~990℃条件下,采用CuMnNi钎料钎焊SiC陶瓷与YG8硬质合金.利用金相显微镜、扫描电镜和能谱仪对接头的微观组织进行分析,研究钎焊温度对接头微观组织的影响.结果表明:在靠近SiC一侧生成一层带状反应层,主要由Cu基固溶体、硅化物、碳和碳化物组成;焊缝主要由基底Cu基固溶体以及Mn、Si、Co、Cu、Ni元素形成的化合物组成.随着钎焊温度的增加,焊缝的宽度减少,焊缝中心的Cu基固溶体基底减少,而化合物相增多.     

高强钢焊接研究现状及发展趋势

在国家低碳节能发展趋势的推动下,高强钢得到广泛应用,高强钢焊接在交通运输、海洋工程等应用中显得越来越重要.从焊接工艺、焊接接头组织、力学性能等特点对国内外高强钢焊接方面的研究成果进行了综述,得出高强钢焊接接头各个区域的组织与性能不同,在不同焊接规范下相同区域的金相组织基本相似,熔合区因组织不均匀为最薄弱环节,指出防止高强钢热影响区的脆性破坏以及提高钢的韧性是今后高强钢焊接研究的重点.