粉煤灰合成钙长石多孔陶瓷的结构与性能

以高钙粉煤灰为主要原料,通过添加造孔剂,采用高温固相烧结法合成出钙长石多孔陶瓷。考察了烧成制度和造孔剂含量对多孔陶瓷显气孔率及抗折强度的影响。利用X射线衍射仪和扫描电子显微镜表征了多孔陶瓷的物相组成和微观结构。结果表明:提高烧成温度和延长保温时间会降低多孔陶瓷的显气孔率,增强其抗折强度;增加造孔剂含量会导致显气孔率升高,但过量添加反而造成显气孔率下降。当烧成温度为1 140℃、保温时间为90 min、造孔剂含量为35%(质量分数)时,多孔陶瓷具有较高的显气孔率和抗折强度(分别达到58.05%和9.41 MPa)。多孔陶瓷的主晶相为钙长石,孔径分布为数微米到150μm。     

无机盐/石英基复合相变储能材料多孔陶瓷基体的制备

以石英为骨料,钾长石为高温粘结剂,木炭为造孔剂制备无机盐/石英基复合相变储能材料用的微米孔石英多孔陶瓷基体,采用正交实验法系统研究了骨料颗粒粒度、造孔剂粒度、造孔剂含量、高温粘结剂含量及烧成温度对石英多孔陶瓷的显气孔率和抗折强度的影响.研究结果表明,影响石英多孔陶瓷抗折强度的最主要因素是长石含量,其次是骨料粒度和造孔剂粒度;影响石英多孔陶瓷显气孔率的主要因素是造孔剂含量.制备微米孔石英多孔陶瓷的优化配方和工艺是:石英、木炭和长石均过325目筛,三者质量比为7:2:1,烧成温度为1270f,保温时间为1h.该陶瓷具有以下优良的性能:显气孔率为55.12％,体积密度为1.14 g,/cm3,抗折强度为3.14 MPa,抗压强度为7.12 MPa,平均孔径为13.87 μm且孔径分布范围较窄,96％的气孔孔径在9～21 μm之间.     

氧化铝纤维对多孔陶瓷载体性能的影响

通过添加适量的塑性剂和造孔剂,采用挤压成型的方式制成了氧化铝纤维增强多孔陶瓷.探讨了不同烧结温度和不同纤维含量对于多孔陶瓷性能的影响.随着烧结温度的提高和纤维含量的增加,样品的线收缩率不断减小,而气孔率和抗折强度先增加后减小.在900℃烧结后,纤维含量4％时,材料最大抗折强度最高并达到4.19Mpa,比基体材料提高了35％.氧化铝纤维的加入有效地解决了多孔陶瓷开裂的问题.     

以硅藻土为硅源制备硅酸钙多孔陶瓷

以硅藻土和碳酸钙为主要原料、淀粉为造孔剂、PVA为粘结剂,通过反应烧结制备了硅酸钙多孔陶瓷。研究了配比和烧结温度对样品体积收缩率、抗压强度和物相组成的影响。同时,也研究了造孔剂含量对气孔率和强度的影响。结果表明,收缩率随烧结温度的升高而增大,造孔剂含量与气孔率成正比、与抗压强度成反比。当碳酸钙含量为20 wt%,造孔剂含量为15 wt%时,在1250?C烧结可制备出气孔率为48.79%、抗压强度为12.2 MPa的多孔陶瓷。     

SiC/莫来石复相多孔陶瓷气孔率和强度的影响因素

以煅烧高岭土、Al(OH)3粉末、SiC粉末为主要原料,以石墨为造孔剂制备了SiC/莫来石复相多孔陶瓷,研究了造孔剂含量、碳化硅颗粒粒径以及烧结温度对SiC/莫来石复相多孔陶瓷抗弯强度和气孔率的影响,并分别用XRD和SEM分析晶相组成和断面显微结构.结果表明:当SiC粒径为60 μm,造孔剂含量为15％时,在1400℃下保温3h制备的样品综合性能最佳,其孔隙率为30.3％,抗折强度达到58.0 MPa.     

高铝粉煤灰制备陶瓷膜支撑体的性能研究

粉煤灰是电厂燃烧煤之后的固体废弃物,粉煤灰的高附加值应用是国家重点扶持的一个方向。采用高铝粉煤灰制备多孔陶瓷支撑体可以代替氧化铝多孔陶瓷在污水处理、固液分离等方面的应用,可以大大减少成本。以高铝粉煤灰为原料,分别使用淀粉和碱式碳酸镁作为造孔剂,羧甲基纤维素钠(CMC)为粘结剂,采用模压法成型,分别在1200~1500℃烧结下制备5组不同含量的多孔陶瓷样品,并测试其孔隙率、收缩率、气通量、水通量、抗折强度等性能。实验结果表明,烧结温度和造孔剂的种类和含量对多孔陶瓷的性能影响显著。碱式碳酸镁造孔作用明显优于淀粉,且随着造孔剂含量的增高,孔隙率、气通量、水通量逐渐升高,抗折强度略有降低。随着烧结温度的提高,气通量、水通量先升高后降低,在1350℃时达到最大值4854.24m~3/(m~2·h·bar)、48.61m~3/(m~2·h·bar)。综合考虑,造孔剂为20%碱式碳酸镁在1350℃温度下烧结2~3 h,作为多孔陶瓷支撑体性能最佳。     

高温烟气过滤用多孔陶瓷材料的研制

以氧化铝纤维和玻璃粉为主体材料,活性炭粉为造孔剂,通过半干压成型工艺制备了高温烟气过滤陶瓷.详细研究了玻璃粉含量、造孔剂含量以及烧成温度对材料过滤阻力、抗折强度、显气孔率等性能的影响,并对原料配方和烧成制度进行了优化,最优配方为:氧化铝70wt%、玻璃粉30wt%、外加造孔剂25wt%、羧甲基纤维素钠8wt%,最佳的烧成温度为1100 ℃,制得的高温烟气过滤陶瓷抗折强度8.9 MPa,过滤阻力95 Pa,显气孔率达59%.     

不同铝源对SiC/堇青石复相多孔陶瓷的制备及性能影响

以碳化硅、氮化铝、层析氧化铝、氢氧化铝、氟化铝、滑石为主要原料,石墨为造孔剂通过原位反应烧结技术制备碳化硅/堇青石复相多孔陶瓷.研究了含铝化合物种类、烧结温度、石墨含量对SiC/堇青石复相多孔陶瓷相组成、微观结构、气孔率和抗折强度的影响,同时对S0组在1200℃烧结温度下制得的SiC/堇青石复合多孔陶瓷的孔径分布进行了测试分析.结果表明:以AlN为铝源在1200℃下烧结,石墨含量在15％时,堇青石结合SiC多孔陶瓷的抗弯强度和气孔率两项综合性能达到最优,气孔率为31.99％,相应的弯曲强度86.20 MPa.S0组的平均孔径大小在3.0191 μm.     

添加造孔剂法制备多孔陶瓷及其强度与孔径控制

采用添加造孔剂法制备了多孔陶瓷.系统地研究了造孔剂种类、粘结剂含量、球磨时间、烧结制度对多孔陶瓷强度及开口孔隙率的影响,以及钠长石含量对多孔陶瓷孔径分布的影响.结果表明,不同造孔剂对多孔陶瓷强度的影响不同.并且在球磨时间为12h之前,随着球磨时间的延长,多孔陶瓷的强度呈增加趋势.而随着钠长石含量的增加,多孔陶瓷的孔径呈减小的趋势.     

碳化硅/堇青石复相多孔陶瓷的制备及性能研究

采用碳化硅、烧高岭土、氢氧化铝、滑石为主要原料,石墨为造孔剂制备了碳化硅/堇青石复相多孔陶瓷.研究了烧结温度和烧结助剂二氧化铈对碳化硅/堇青石复相多孔陶瓷气孔率和强度的影响,并分别用XRD和SEM分析晶相组成和断面显微结构表明:制备出的SiC多孔陶瓷的主相是SiC,结合相是堇青石与方石英,多孔陶瓷具有相互连通的开孔结构;在1350℃烧结,并保温3h,当造孔剂含量为15％时,碳化硅/堇青石复合多孔陶瓷性能最佳,其气孔率31.80％,相应的弯曲强度为63.74 MPa.在1200℃下,添加不同含量的CeO2,对烧结样品的相组成有影响,能够降低生成堇青石的温度,在CeO2含量为3％的样品中,堇青石的峰最明显,但是过量的氧化铈会抑制了堇青石的生成;随着CeO2加入量的增加,其气孔率和弯曲强度也会随之变化,1200℃下,在CeO2加入量为4％时其弯曲强度最优.但随着CeO2的含量的增加,其气孔率逐渐下降.     

梯度多孔载Ag羟基磷灰石陶瓷的制备和性能研究

本文采用添加造孔剂法制备孔隙呈现梯度分布的多孔载Ag羟基磷灰石(Ag-HA)陶瓷.研究了造孔剂分布、烧结温度和载Ag含量对梯度多孔Ag-HA陶瓷孔隙度的影响.分析了烧结产物的物相组成和微观形貌,测量了烧结后梯度多孔Ag-HA陶瓷的压缩性能和抗菌性能.研究结果表明:随着中间层造孔剂含量增加,梯度多孔Ag-HA陶瓷的孔隙度...     

Recycling of waste red mud for fabrication of SiC/mullite composite porous ceramics

SiC/mullite composite porous ceramics were fabricated from recycled solid red mud (RM) waste. The porous ceramics were formed using a graphite pore forming agent, RM, Al(OH)₃ and SiC in the presence of catalysts. The influence of firing temperature and the pore-forming agent content on the mechanical performance, porosity and the microstructure of the porous SiC ceramics were investigated. Optimal preparation condition were determined by some testing. The results indicated that the flexural strength of specimens increased as a function of firing temperature and a reduction in graphite content, which concomitantly decreased porosity. The ceramic prepared under optimal conditions having 15?wt% graphite and sintered at 1350?°C, demonstrated excellent performance. Under optimal preparation conditions the flexural strength and porosity of the ceramic were 49.4?MPa and 31.4%, respectively. Scanning electron microscopy observation result showed that rod-shape mullite grains endowed the samples with high flexural strength and porosity. X-ray diffraction analysis indicated that the main crystallization phases of the porous ceramics were 6H-SiC, mullite, cristobalite and alumina. This work demonstrates that RM can be sucessfully reused as a new raw material for SiC/mullite composite porous ceramics.     

造孔剂和增强剂对工业固废基多孔陶瓷性能的影响

以镁渣,粉煤灰为原料,添加造孔剂(电石渣、碳粉)和增强剂(高岭土、膨润土)制备多孔陶瓷,并研究造孔剂和增强剂种类和含量对多孔陶瓷性能的影响.结果表明,添加造孔剂后,多孔陶瓷的烧失率、吸水率和气孔率升高,体积密度和强度降低.同等含量时,碳粉具有较好的造孔效果;多孔陶瓷的烧失率、吸水率和气孔率最高可分别达到30％,38％和53％,体积密度最小达到1.4 g/cm3;添加增强剂后,多孔陶瓷的强度大为提高,但其吸水率、气孔率降低,体积密度增加.高岭土的含量不大于10％时,其粘结增强效果明显优于同等含量膨润土的;多孔陶瓷的压缩强度可至28 MPa.     

Fabrication and characterization of porous CaSiO3 ceramics

Porous CaSiO₃ ceramics were prepared via a solid-state reaction method using CaCO₃ and SiO₂ as raw materials and active carbon as a pore-forming agent. The results indicated that porous CaSiO₃ ceramics could be obtained under a low sintering temperature of 1320?°C. The addition of active carbon significantly affected the volume density, microstructure, pore size distribution and mechanical strength of porous CaSiO₃ ceramics. With the increase of active carbon content, the volume density decreased, meanwhile the pore size and porosity increased gradually. Besides, the three-point bending tests demonstrated that the mechanical strength was decreased with increasing active carbon content. However, all the porous ceramics still exhibited high mechanical strength. These results implied that the increase of active carbon content not only enlarged the pore size and enhanced the porosity, but also kept a remarkable mechanical strength of porous CaSiO₃ ceramics. Therefore, these rationally designed CaSiO₃ porous ceramics will be a highly potential material in various applications due to its high mechanical strength, low sintering temperature and narrow pore size distribution.     

稀土La2O3添加对氧化铝多孔陶瓷性能的影响

以煅烧α-Al2O3为原料,稀土氧化镧(La2O3)为添加剂,羧甲基纤维素为成型粘结剂,通过混料、困料、研磨、模压成型、高温烧结等工序制备了氧化铝多孔陶瓷,研究了烧结温度及La2O3添加量对氧化铝多孔陶瓷的线收缩率、体积密度、孔隙率、抗折强度和微观形貌的影响。结果表明:在相同烧结温度下,随稀土添加量的增加,多孔陶瓷的体积密度、线收缩率与抗折强度均降低,而孔隙率则逐渐增加。微观形貌与X衍射分析表明,稀土La2O3的加入,抑制了氧化铝颗粒间的烧结,并在高温下与氧化铝反应生成了片状晶体LaAl11O18,片状晶LaAl11O18阻碍了氧化铝晶粒的长大,进而抑制了坯体的收缩,最终使得氧化铝多孔陶瓷具有较高的孔隙率。     

Preparation of calcium hexaluminate porous ceramics by gel-casting method with polymethyl methacrylate as pore-forming agent

Calcium hexaluminate (CA₆) porous ceramics were prepared by gel-casting method, with α-Al₂O₃ and CaCO₃ as raw materials and polymethyl methacrylate (PMMA) microspheres as pore-forming agent. The effects of the amount of pore-forming agent PMMA microspheres on the phase composition, bulk density, apparent porosity, flexural strength, microstructure, thermal shock stability and thermal conductivity of CA₆ porous ceramics were systematically studied. The pores of CA₆ porous ceramics are mainly formed by the burning loss of PMMA microspheres and the decomposition of organic matter. Adding an appropriate amount of PMMA microspheres as pore-forming agent has a positive effect on the thermal shock stability of CA₆ porous ceramics. When the amount of pore-forming agent is 15 wt%, the volume density of CA₆ porous ceramics is 1.33 g/cm³, the porosity is 63%, the flexural strength is 13.9 MPa, the thermal shock times can reach 9 times, and the thermal conductivity is 0.293 W/(m·K), which can meet the application in refractory, ceramics or high temperature cement industries.     

钛酸钾晶须耐碱多孔陶瓷的制备及表征

The preparation and characterization of alkaline resistant porous ceramics from potassium titanate whiskers are studied. K2Ti4O9 whiskers in the whisker preforms （mixtures of K2Ti6O13 and K2Ti4O9） were completely converted to K2Ti6O13 at 960℃. The alkaline resistance as well as the change in bending strength, porosity and permeability of the ceramics was investigated by altering the composition of the preforms in which the content of K2Ti6O13 whiskers was higher than 50% （molar fraction）. The alkaline resistance of the porous K2Ti6O13 ceramics is found much higher than that of Al2O3 in caustic NaOH solutions, and further study indicates that the K2Ti6O13 ceramics can be stably used in solutions of pH〉2.0. The bending strength increases initially with the content of the raw K2Ti6O13 in the preforms up to 66% （molar fraction） and then decreases, contrary to the behaviors of porosity and permeability. The values of bending strength, porosity and permeability of the ceramics prepared from the preform of 80% （molar fraction） raw K2Ti6O13 whiskers are respectively 56MPa, 29.4% and 330L·m^-2〈h^-1 , which are comparable to those of the porous Al2O3 ceramics.     

脱硝催化剂用堇青石多孔陶瓷的制备与性能研究

以偏高岭土、氧化铝和滑石为原料,利用压制成型制备出堇青石多孔陶瓷并采用浸渍涂覆法制备锰基低温脱硝催化剂.通过气孔率、抗折强度、热膨胀系数、SEM、BET等测试探究了碳粉和淀粉两种造孔剂及添加量、不同酸处理时间等因素对堇青石性能的影响并考察了不同浸渍次数的催化剂在80~200 ℃间的脱硝性能.结果表明:造孔剂为碳粉且添加量为4%时,得到的堇青石具有良好的性能,此时气孔率达31.12%,热膨胀系数为3.10×10-6/K,抗折强度为21.41 MPa;适当的酸处理有助于堇青石表面孔结构的丰富且能大幅提升其比表面积,最佳处理时间为2 h;当浸渍次数为4次时,整体式催化剂的性能最佳,牢固度可达90.18%,140 ℃时的脱硝率可达74.5%以上.     

烧结助剂含量对多孔Si3N4/BN复合陶瓷力学性能和介电性能的影响

以Si3N4和BN为原料,叔丁醇为溶剂,SiO2、Y2O3和Al2O3为烧结助剂,采用凝胶注模成型工艺制备具有高强度、低介电常数多孔Si3N4/BN复合陶瓷。研究了Y2O3和Al2O3含量对多孔陶瓷气孔率、孔径分布、物相组成、显微结构、抗弯强度和介电常数的影响。结果表明:通过调节Y2O3和Al2O3含量,多孔Si3N4/BN复合陶瓷的气孔率由55%增加到68%,气孔尺寸呈单峰分布,平均孔径为0.89～1.02μm;抗弯强度和相对介电常数随Y2O3和Al2O3含量的增加而单调增大,抗弯强度和相对介电常数的变化范围分别为29.9～60.9 MPa和2.30～2.85;通过调节Y2O3和Al2O3含量调控气孔率,能够获得介电性能和力学性能可调的高性能透波材料。     

用粉煤灰和菱镁矿低温制备堇青石质多孔材料

在粉煤灰中添加不同比例菱镁矿,于1 200、1 250℃和1 300℃烧成温度下制备出堇青石质多孔耐火材料。研究表明：菱镁矿在烧成过程中于700℃分解产生CO2,起到造孔剂和发泡剂的作用,分解生成的MgO将与粉煤灰中的Al2O3、SiO2反应生成堇青石;随着菱镁矿添加量的增加,粉煤灰中Al2O3和SiO2与MgO的反应更完全,主要生成堇青石和少量镁橄榄石;当菱镁矿添加量过多时,新生成的MgO与粉煤灰中SiO2反应,产生液相过多,造成部分气孔封闭,使得烧成后试样的显气孔率随菱镁矿添加量的增加呈先增加后减小的趋势。优化烧成工艺条件为1250℃并保温3h,当菱镁矿添加量为15%（质量分数）时,制备出显气孔率达48%、孔径为20～40μm、体积密度为1.27g/cm3、抗压强度为38MPa、抗折强度为29MPa的堇青石质多孔材料。