C/C复合材料SiC-SiO_2/ZrO_2-SiC复合抗氧化涂层

为了提高C/C复合材料在高温有氧环境的抗氧化性,在SiC抗氧化涂层防护的基础上,采用气相沉积法及溶胶凝胶吸附冷凝热蒸汽法在C/C复合材料表面制备出了SiC-SiO2/ZrO2-SiC复合涂层。利用扫描电镜、能谱质谱测试及X射线衍射等检测方法对涂层各层进行了分析。结果表明,溶胶吸附ZrCl4蒸汽法制备ZrO2涂层,不仅能够在高温自动修复单层SiC涂层的裂纹缺陷,还起到了在制备外层SiC涂层过程中缓冲应力的作用。这种多层复合涂层在高温下具有良好的抗氧化性,在1 800℃等离子焰动态空气氧化120 s后,计算得出该涂层失重速率仅为0.4 g/(m2·s),表明该涂层具有卓越的抗氧化性。     

C/SiC-MoSi2复合材料微结构和力学行为研究

以三维针刺碳毡作为预制体,先采用树脂单向加压浸渍-热解工艺制备出C/C多孔体,然后采用反应熔体浸渗法将Si-Mo合金浸渗到C/C多孔体中制备C/SiC-MoSi2复合材料.对C/SiC-MoSi2复合材料的物相组成、显微结构以及力学性能进行了研究.结果表明,该复合材料由C、SiC、MoSi2和Si组成;生成的SiC和M...     

C/C复合材料抗氧化耐高温SiC陶瓷涂层的研究

采用高温反应法和PVD法在SiC工业合成炉内制备了C/C复合材料耐高温抗氧化SiC陶瓷涂层.用XRD、SEM对其物相组成和显微结构进行了表征与分析,讨论了涂层的形成机理,并研究了其高温氧化性能.研究结果表明,所制备的陶瓷涂层主要由α-SiCβ-SiC组成,晶粒发育完整,涂层表面致密、无裂纹,且与碳基体结合紧密,涂层厚度约600μm,涂层抗氧化性良好,在1500℃空气中氧化10h失重约为0.3%.     

Cf/SiC 复合材料的 ZrB2-SiC/SiC 超高温陶瓷涂层研究

采用两步包埋法在Cf/SiC复合材料表面制备了Zr B_2-SiC/SiC超高温陶瓷涂层。借助SEM、XRD对涂层的微观结构及物相组成进行了分析研究,并进行了高温静态氧化和热震测试。研究表明,1500°C氧化5 h后,涂层表面覆盖有平整的玻璃相氧化层,氧化失重率为6.4%;热震测试10次后涂层的氧化失重率为14%。Zr B_2-SiC/SiC涂层能有效提高Cf/SiC复合材料的高温抗氧化性能。     

水热温度对SiC–C/C复合材料表面水热电泳沉积SiCn–MoSi2复合抗氧化涂层的影响

采用水热电泳沉积法在SiC–C/C复合材料表面制备了纳米碳化硅和二硅化钼的复相(SiCn–MoSi2)抗氧化涂层。采用X射线衍射和扫描电子显微镜等对制备涂层的晶相组成、表面及断面微观结构进行了表征。研究了水热温度对制备涂层的结构及高温抗氧化性能的影响,分析了涂层在1 600℃静态氧化行为及失效机理。结果表明:外涂层主要由MoSi2和β-SiC晶相组成。复相外涂层的致密程度、厚度及抗氧化性能随着水热温度的升高而提高。SiCn–MoSi2/SiC复合涂层具有较好的抗氧化和抗热震能力,在1 600℃氧化80 h后氧化质量损失为3.6×10–3 g/cm2。复合涂层在1 600℃的氧化失效主要是由于经过长时间氧化后SiO2玻璃膜层不能及时有效填补涂层中的缺陷,涂层中出现贯穿性的裂纹和孔洞导致的。     

水热温度对SiC-C/C复合材料表面水热电泳沉积SiCn-MoSi2复合抗氧化涂层的影响

采用水热电泳沉积法在SiC–C/C复合材料表面制备了纳米碳化硅和二硅化钼的复相(SiCn–MoSi2)抗氧化涂层。采用X射线衍射和扫描电子显微镜等对制备涂层的晶相组成、表面及断面微观结构进行了表征。研究了水热温度对制备涂层的结构及高温抗氧化性能的影响,分析了涂层在1 600℃静态氧化行为及失效机理。结果表明:外涂层主要由MoSi2和β-SiC晶相组成。复相外涂层的致密程度、厚度及抗氧化性能随着水热温度的升高而提高。SiCn–MoSi2/SiC复合涂层具有较好的抗氧化和抗热震能力,在1 600℃氧化80 h后氧化质量损失为3.6×10–3 g/cm2。复合涂层在1 600℃的氧化失效主要是由于经过长时间氧化后SiO2玻璃膜层不能及时有效填补涂层中的缺陷,涂层中出现贯穿性的裂纹和孔洞导致的。     

ZrC改性C/C复合材料的抗氧化涂层研究

为了提高C/C复合材料的高温抗氧化性能，采用含锆有机溶剂实现了对C/C复合材料的ZrC改性，通过粉末包埋法在其表面制备了SiC过渡层，通过溶胶凝胶法制备了外部的复合陶瓷氧阻挡层。设计三因素三水平的正交试验，研究了ZrC改性增重、过渡层厚度和氧阻挡层厚度三个主要因素对C/C复合材料高温抗氧化性能的影响。9个样品在1600℃马弗炉中进行了30 min的静态氧化测试，结果表明，ZrC改性增重5%、过渡层厚度为60μm和氧阻挡层厚度为80μm的样品抗氧化性能最好，质量损失率仅约5.51%。     

C/C复合材料SiC-Mo(Si,Al)_2涂层结构和抗氧化性能研究

采用高温原位反应法在C/C复合材料表面制备了SiC-Mo(Si, Al)_2防氧化复合涂层,用XRD、SEM测试表征了其物相组成和显微结构,对制备粉料中铝硅含量对涂层微观结构和抗氧化能力的影响进行了研究,分析了涂层失效原因。研究结果表明:添加Al粉使涂层制备过程粉料浸渗能力增强;Al、Si原子比为1∶10时所得到的复合涂层主要有Mo(Si, Al)_2、MoSi_2、SiC和游离Si等物相,具有较大的厚度和致密的结构,体现出良好的抗氧化性能。随着氧化的进行,SiO_2玻璃层出现的孔洞加速了涂层材料损耗,导致涂层中出现贯穿性裂纹,是涂层失效的主要原因。     

碳碳复合材料SiCCr-Al-Si复合涂层的抗氧化性能研究

随着技术的进步,复合材料成为目前新材料应用的一个重要领域,采用等离子喷涂法对SiC/Cr-Al-Si的抗氧化性能进行研究,结果发现涂刷法制备所得的SiC/Cr-Al-Si复合涂层C/C复合材料试样抗氧化性能较不带涂层和带SiC涂层的C/C复合材料试样有了很大的提高,性能得到了很大改善,且涂层间结合较好,没有开裂现象,涂层在一定时间内能对基体起到较好的保护作用,表现为试样在氧化前12h一直为增重状态。     

SiC-MoSi2复合材料的制备及其性能的研究进展

二硅化钼(MoSi2)是目前广泛应用的一种高温材料,但低温脆性和高温抗蠕变性差限制了其应用领域,通过在MoSi2中添加碳化硅(SiC)能有效改善上述性能.本文综述了近十年来SiC-MoSi2复合材料制备方法,SiC颗粒、晶须、纤维等强韧化MoSi2材料的研究进展,并对SiC-MoSi2复合材料的其它性能进行了总结.     

Biosynthesis of Epimers C2 and C2a in the Gentamicin C Complex

Gentamicin is a broad‐spectrum aminoglycoside antibiotic widely used to treat life‐threatening bacterial infections. The gentamicin C complex consists of gentamicin C1, gentamicin C1a, and epimers gentamicin C2 and gentamicin C2a. At present there is a generally accepted pathway of gentamicin biosynthesis, except for detailed understanding of the epimerization process involving gentamicins C2 and C2a. Here we have investigated the biosynthesis of these epimers. JI‐20B—an intermediate in the gentamicin biosynthetic pathway—and its epimer JI‐20Ba were generated by in‐frame deletion within genP, which encodes a phosphotransferase that catalyzes the first step of 3′,4′‐bisdehydroxylation in gentamicin biosynthesis. GenB1 and GenB2 are aminotransferases with different substrate specificities and enantioselectivities. JI‐20Ba, containing a 6′S chiral amine, a precursor of gentamicin C2a, was synthesized from G418 by GenQ/GenB1 through sequential oxidation/transamination at C‐6′. GenQ/GenB2 catalyzed the synthesis of JI‐20B, containing a 6′R chiral amine, a precursor of gentamicin C2, from G418. GenB2 catalyzed the epimerization of JI‐20Ba/JI‐20B and of gentamicins C2a/C2.     

Enhanced one-step purification of C2H4 from C2H2/C2H4/C2H6 mixtures by fluorinated Zr-MOF

The extraction of C₂H₄ from C₂H₆/C₂H₄/C₂H₂ mixtures is of great significance in the chemical industry for C₂H₄ production but the process remains challenging due to the similarity of these C₂ hydrocarbon species in their molecular size and physical properties. Here, we report the fluorination of a stable Zr-MOF, UiO-66, to fine-tune the pore dimensions and pore functionality. In particular, UiO-66-CF₃ shows notably preferential adsorption of C₂H₆ and C₂H₂ over C₂H₄, with C₂H₂/C₂H₄ and C₂H₆/C₂H₄ selectivities of 1.4 and 1.9, respectively. Theoretical calculations provide insight into the binding sites of UiO-66-CF₃ for C₂ hydrocarbon adsorption. Breakthrough experiments further confirmed the capability of the material for purification of C₂H₄ from C₂H₂/C₂H₄/C₂H₆ ternary mixtures, evidenced by the high purity C₂H₄ (99.9%+) obtained directly from outlet gas.     

生产乙炔对电石的要求及乙炔清净

目前国内外乙炔大部分仍是由电石制得。然而由于工业电石除CaC2 外还含有很多杂质 ,所以生产乙炔不仅要求电石的纯度、粒度 ,还要求水温。一般电石的块度采用 8～ 2 5mm ,发生器温度控制在 85± 5℃ ,乙炔气体中含H2 S、H3 P、NH3 等气体会使氯乙烯合成氯化催化剂活性下降。因此 ,必须对乙炔气体进行清洁。采用次氯酸钠液体的氧化性将乙炔中的杂质氧化成酸性物质而除去。     

碳四组分对碳二加氢系统的影响

论述了碳二加氢进料C4组分含量较高的原因及其对反应器的影响,提出了避免反应器飞温和出口漏炔的方法,减少乙烯损失,提高经济效益,节能降耗。     

Efficient H2 Production from Ethanol over Mo2C/C Nanotube Catalyst

Mo₂C deposited on silica is an effective catalyst for the decomposition of ethanol; the extent of the reaction approached 100% even at 623–673 K. Beside H₂ several C-containing compounds were produced, which caused the low yield of hydrogen. Preparation of Mo₂C by the reaction of MoO₃ with multiwall carbon nanotube, however, dramatically altered the product distribution. The formation of hydrogen came into prominence; about 40% of hydrogen content of ethanol decomposed at 523–723 K has been converted into H₂. Another feature of the Mo₂C/C nanotube is the relatively slow deactivation. Adding water to ethanol further enhanced the hydrogen production.     

We Need 2C but Not 2B: Developing Serotonin 2C (5‐HT2C) Receptor Agonists for the Treatment of CNS Disorders

The serotonin 2C (5‐HT_2C) receptor has been identified as a potential drug target for the treatment of a variety of central nervous system (CNS) disorders, such as obesity, substance abuse, and schizophrenia. In this Viewpoint article, recent progress in developing selective 5‐HT_2C agonists for use in treating these disorders is summarized, including the work of our group. Challenges in this field and the possible future directions are described. Homology modeling as a method to predict the binding modes of 5‐HT_2C ligands to the receptor is also discussed. Compared to known ligands, the improved pharmacological profiles of the 2‐phenylcyclopropylmethylamine‐based 5‐HT_2C agonists make them preferred candidates for further studies.     

Alkaline Hydration Of C2S and C3S

This study analyzed the behavior of two laboratory‐synthesized calcium silicates, C₃S and C₂S, after hydration in 8‐M NaOH and in water as a control. Two‐ and 28‐d mechanical strength values were determined and the products were characterized with XRD, TEM, and ²⁹Si and ²³Na MAS NMR. The results showed that hydrating C₃S in a highly alkaline medium had no significant effect on the mechanical development of the material, whereas in C₂S hydration, that medium hastened hydration substantially, impacting setting and hardening times. This finding has technological implications, given the low early‐age reactivity of dicalcium silicate under normal hydration conditions.     

Conversion of methane to benzene over Mo2C and Mo2C/ZSM-5 catalysts

The activation and dehydrogenation of CH₂ on Mo₂C and MO₂C/ZSM-5 have been investigated under non-oxidizing conditions. Unsupported Mo₂C exhibited very little activity towards methane decomposition at 973 K. The main reaction pathway was the decomposition of methane to give hydrogen and carbon with a trace amount of ethane. Mixing Mo₂C with ZSM-5 support somewhat enhanced its catalytic activity, but did not change the products of the reaction. A dramatic change in the product formation occurred on partially oxidized Mo2C/ZSM-5 catalyst; besides some hydrocarbons benzene was produced with a selectivity of 70–80% at a conversion of 5–7%. Carburization of highly dispersed MoO₃ on ZSM-5 also led to a very active catalyst: the conversion of methane at the steady state was 5–6% and the selectivity of benzene formation was 85%.This laboratory is a part of the Center for Catalysis, Surface and Material Science at the University of Szeged.