集聚纺纱胶辊、胶圈的应用技术探讨

针对集聚纺纱对胶辊、胶圈的技术要求更高的特点,通过试验指出,胶辊硬度低、直径大有利于提高成纱质量.结合生产实践指出,精磨胶辊磨削量以0.2 mm为宜,表面粗糙度Ra值以0.4μm～0.5μm为宜,并适当缩短磨砺周期,牵伸胶辊与牵引胶辊应按比例控制磨削量.胶圈要新旧搭配,并且要及时清洗.     

弹力竹节牛仔布织造工艺优化

介绍了弹力竹节牛仔布的生产工艺 ,同时对KT36 8剑杆织机织造该织物的工艺进行了优化研究     

圆盘锯机性能提升途径

圆盘锯机在线材厂投入使用时不能满足生产的需要：锯切周期太长，锯片使用性能差，经过对设备进行技术改造和对设备操作规程进行优化，以及在操作上加强管理，使之关键指标大幅度提升，为圆盘锯机的使用改善提供了新的思路。     

光化学方法活化CO_2为CO的研究进展

介绍了国内外近年来用光化学方法将CO2活化为CO的研究进展。目前,CO2活化为CO的光化学法主要有气相活化法、均相活化法和非均相活化法,对这些方法的特点及反应机理进行了总结。     

数字电位器的应用技术

从应用的角度出发，介绍合理设计应用电路和合理选择数字电位器的种类与型号，来克服数字电位器普遍存在的主要缺点的方法。文章具有较强的针对性和可操作性，对数字电位器的应用实践具有指导作用。     

延迟破胶及强制裂缝闭合技术的研究及应用

采用延迟破胶技术,在压裂施工过程中加入不同浓度的胶囊破胶剂,利用它的延缓释放特性,使植物胶压裂液耐温、耐剪切稳定性增强,并且可以在不造成压裂液的流变性、滤失性和携砂性等过早丧失的前提下高浓度使用胶囊破胶剂。该技术与常规破胶技术相比,延缓释放率达50%,能更有效地清除液体残渣,减少压裂液对储层的伤害。同时由于有延缓破胶的特性,放喷采用相应的措施,可以降低支撑剂沉降速度,形成较好的沉砂剖面,提供高的裂缝导流能力,并且可以降低滤饼和压裂液残渣的伤害。     

桐梓河园满贯水电站工程泄洪消能设计

针对桐梓河园满贯水电站工程洪峰流量大、河床狭窄的不利条件,采用坝顶表孔泄洪,溢洪道尾部设置为不对称宽尾墩 连续挑坎型式,使水舌横向扩散、纵向拉开、空间碰撞,减轻对下游河床的冲刷。     

PURIFICATION AND PROPERTIES OF TRANSGLUTAMINASE FROM STREPTOVERTICILLIUM MOBARAENSE

Transglutaminase (TGase) was separated from the culture broth of an isolated strain of Streptoverticillium mobaraense. The crude enzyme was prepared by centrifugation, ultrafiltration, precipitation by alcohol, centrifugation and freeze‐drying. The yield after these processes was 65–70%. Then the enzyme was purified to homogeneity by chromatography on CM‐cellulose and Sephadex G‐75 on which the yields were about 70% and 80%, respectively; the purified folds reached 2.5–4.7 and 1.08–2.06, respectively. The molecular weight of this TGase was 39,500–40,100 Da by gel filtration chromatography. Optimum enzyme activity was observed in the pH range of 5.0–7.0, and it was maintained stable at 20–40C. The optimal temperature and pH was 52C and 6.0, respectively. At 1 mM and 5 mM metal ion or inhibitors concentration, TGase activity was strongly inhibited by Zn²⁺ and NEM, and not affected obviously by Ba²⁺, Ca²⁺, Co²⁺, Cu²⁺, Fe²⁺, Fe³⁺, Mg²⁺, Mn²⁺, Na⁺ as well as PMSF and EDTA. The effects of these additions on this TGase were compared with those of other microbial TGases.