A110－1－H／A110－1型氨合成催化剂在双筐并流合成塔中的使用

在双筐并流氨合成塔中使用了Ａ１１０－１－Ｈ／Ａ１１０－１型氨合成催化剂，使用寿命达１７４０天，累计产氨４３８３７８ｔ．该催化剂组合具有低温活性好、易还原、高催化活性、高抗毒能力、良好的热稳定性与破碎强度等优点．     

江西于都琉璃釉资源评价

本文从资源概况、琉璃釉工艺特征和应用效果等方面对江西于都发现的天然黄绿色琉璃釉资源进行了初步评价。     

黄磷尾气净化脱除磷化氢、硫化氢中试试验

采用自制的催化剂JC-4,设计出碱洗-催化氧化工艺对黄磷尾气进行深度净化处理。中试试验结果表明:常压、100℃、尾气流量为36~50 m3/h、氧气体积分数为1.2%~1.5%时,PH3的脱除率接近100%,出口质量浓度低于1.0 mg/m3;碱洗单元可以除去90%的H2S,经过催化氧化单元可以进一步脱除H2S,净化效率接近100%,出口质量浓度低于1.0 mg/m3;催化剂经100~200 h需要再生,400 h后需要活化,再生和活化处理后的催化剂性能良好。     

超高相对分子质量聚乙烯注射成型技术

分析了超高相对分子质量聚乙烯(PE-UHMW)的流变性能和独特的口模流动特性以及PE-UHMW注射成型所存在的难点,据此研制出PE-UHMW专用注塑机(螺杆直径45 mm,长径比20),介绍了该机的性能和特点。初步讨论了PE-UHMW注射成型的配方及工艺参数如成型温度、注射压力和注射速度等对注射成型制品表观质量的影响。采用该机,以一模双腔模具成功地制得不同相对分子质量(相对分子质量从2．5×106到4×106以上)的试样, 其力学性能测试结果优良;同时还探讨了PE-UHMW注射成型制品的应用和市场前景。     

加氢法与生物法联合脱除催化柴油有机硫探索实验

由于存在空间位阻,二苯并噻吩(DBT)及其烷基化衍生物(Cx-DBT)中的硫原子很难与加氢催化剂接触.因此,作为柴油脱硫的主要工艺,加氢催化对于柴油中的主要有机硫化物DBT和Cx-DBT的脱除率比较低,难以实现深度脱硫.针对硫质量分数为3 358 μg/g的催化柴油,采用加氢脱硫与生物脱硫相结合的办法进行处理后,催化柴油的硫质量分数降低到20μg/g以下,使用气相色谱-原子发射仪对柴油脱硫前后的硫分布进行检测,发现2种工艺的结合能有效地脱除催化柴油组分中绝大多数的DBT和Cx-DBT,显示出良好的应用前景.     

Compatibilization of polymer blends from poly(styrene‐co‐acrylonitrile) and polycarbonate by oxazoline modification of poly(styrene‐co‐acrylonitrile) in the melt

A good way of achieving compatibility in polymer blends of poly(styrene‐co‐acrylonitrile) (S/AN) and bisphenol A polycarbonate (PC) is the chemical modification of S/AN in the melt. A catalyzed reaction of the nitrile groups with a substituted 2‐amino alcohol or 2‐amino phenol resulted in a conversion of nitrile groups of 55–75% in 60 min. The introduced heterocyclic structures were ethyl hydroxymethyl oxazoline (EHMOXA) and benzoxazole (BenzOXA), respectively. The use of dibutyltin oxide as a catalyst led to the highest efficiency. The modified polymer was characterized by Fourier transform infrared and NMR spectroscopy, elemental analysis, and reactions with organic acids and anhydrides. The modified S/AN showed good technical compatibility (single glass‐transition temperature) with PC in blends made from solution and from the melt. All blends were characterized with oscillating rheometry and differential scanning calorimetry. Rheological measurements showed that EHMOXA–S/AN reacted with PC and had crosslinked structures, whereas BenzOXA–S/AN showed compatibilization without any (crosslinking) reaction. The melt blends of BenzOXA–S/AN and PC showed a downward shift in the complex viscosity due to the influence of the BenzOXA group. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2322–2332, 2003     

管式气体分散式反应器制备纳米碳酸钙

以石灰石为原料，利用管式气体分散式反应器新工艺制备出了粒径30～70nm的碳酸钙粉体。采用X射线衍射（XRD）、扫描电镜（SEM）、粒度分布仪及红外光谱仪（Fr-IR）等测试手段，对产品的物相、形貌和粒度分布进行了表征。X射线衍射表明产物为六方晶系方解石型碳酸钙并且产品结晶性能良好；扫描电镜及粒度分析表明粒度大小均匀、分散性良好；红外光谱表明改性后硬脂酸钠已吸附在碳酸钙表面，碳酸钙颗粒基本呈单分散状态。管式气体分散式反应器制备纳米碳酸钙粉体的优点是工艺简单，操作容易，原料易得，生产的产品粒径小，粒度分布窄，易于工业化生产。     

Structural material from waste plastic

In efforts to contribute to community development, particularly in the context of Egyptian communities, waste plastics materials were successfully recycled without the difficult task of separation and reused to economically produce new structural material. Recycling was performed by mixing molten waste plastics with sand to produce these new materials. Samples with different percentages of plastics and different particle sizes of sand were used in the process. Materials showed acceptable density and high compressive strength, which was shown to be at a maximum with contents of about 30–40% waste plastic. Furthermore, certain types of sand having different colors were used to produce attractive materials, suitable for decorative uses. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2543–2547, 2004     

淀粉分子磁化修饰及其再生膜材料制备

以高直链淀粉（HS）为原料，通过“还原胺化-点击化学法”在其还原性端的潜在醛基上进行磁化分子修饰，得到具有磁性的变性淀粉（MMS），并在外磁场作用下制备再生淀粉膜。具体包括在HS分子唯一的潜在醛基上引入炔基，对四氧化三铁粒子（MNP）进行硅烷包覆得到叠氮化磁体粒子（azide-MNPs），两者经点击化学反应得到分子链末端带磁的变性淀粉。借助XRD、FTIR、NMR和MALDI-TOF MS对产物进行结构表征，结果表明，磁体粒子精准接枝到高直链淀粉分子还原末端，得到目标产物MMS。再生淀粉膜性能测试结果表明，在外磁场诱导条件下MMS逐渐趋于分子有序排列，制得的再生淀粉膜较纯CMS淀粉膜断裂伸长提升49.5%，断裂强度提升88.3%，短程有序程度提高。该文为基于外加磁场下的淀粉再生膜结构设计和力学性能调控提供了新思路。     

Preparation,characterization, and some physical properties of polypropylene/poly(methyl acrylate)‐grafted glass wool composites

Polypropylene/poly(methyl acrylate)‐grafted glass wool (PMA‐g‐GW) mixes were prepared. The polymerization process was carried out using potassium persulfate (PPS) and PPS/acetone sodium bisulfite (ASBS) as a redox‐pair initiation system at 60 and 70°C. The effect of using PPS or PPS/ASBS on the grafting percent and conversion percent reveals that the conversion percent values on using PPS as an initiator are higher than those of PPS/ASBS, while in the case of grafting, the inverse is true, that is, using PPS as an initiator gives grafting percent values lower than those that can be obtained using PPS/ASBS. The dielectric properties, thermal diffusivity, specific heat capacity, and thermal conductivity of PP loaded with modified glass wool as a function of different types and concentrations of initiators—used in the grafting polymerization process, namely, PPS and the redox initiating system—were also studied. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 723–732, 2003