快干型芭蕉芋淀粉粘合剂的制备

介绍一种快干型芭蕉芋淀粉粘合剂，它特别适合于粘结瓦楞纸板，其制法是芭蕉芋等直链淀粉含量较代低的天然植物淀粉为原料，经氧化、糊化、交联等步骤而制得；产品结力强，产品性能稳定，贮存期长。     

聚乙烯醇改性固体淀粉胶粘剂的研制

介绍新型固体淀粉胶的制备方法。以淀粉为主要原料，经加热催化分步氧化，再加入聚乙烯醇合成树脂改善其性能，然后用硬脂酸钠作为赋型剂。制得的淀粉胶剪切强度比泡花碱高0.01MPa。     

三氯氧磷交联木薯淀粉的消化性能及酶降解程度

采用In Vitro消化模型模拟人体消化道环境 ,对不同交联度 (DC)的三氯氧磷淀粉 (DC =3.70× 10 -5至 2 .2 7×10 -2 )的消化性能进行了研究 ;同时用微生素酶对三氯氧磷交联木薯淀粉进行生物降解并测定各个样品的抗酶解淀粉 (RS)含量。三氯氧磷交联变性处理对木薯淀粉的消化速度和生物降解程度的影响随交联度的不同而不同。高交联特别是使淀粉达到完全非晶化时对淀粉的消化速度和生物降解程度影响更大。     

多孔淀粉在内墙涂料中的应用

本用多孔淀粉和淀粉吸附天然除虫菊酯后加入内墙涂料，通过对两解吸附量、释放时间的比较，说明在内墙涂料中加入杀虫剂的可行性，同时也表明多孔淀粉作为一种新型的吸附和缓释剂，有着广泛的用途。     

Formation of hydrophilic starch coatings on polyethylene films

Thin starch coatings were deposited onto polyethylene (PE) film surfaces when PE films were immersed in 1% jet cooked starch solutions and the hot solutions were allowed to cool. Normal cornstarch, waxy cornstarch, high amylose cornstarch, and solvent‐extracted normal cornstarch (to remove native lipid) were used in these experiments. Amounts of adsorbed starch varied from about 0.03–0.05 mg per cm² of PE, and these starch coatings imparted hydrophilic properties to film surfaces, as evidenced by contact angle measurements. Although starch could be removed by gently rubbing water‐wet PE surfaces, air‐dried coatings were more firmly attached, and did not separate from the PE surface when films were bent or flexed. SEM images of starch‐coated film surfaces showed that starch was deposited as particles less than 1 μm in diameter, and also as aggregates of these submicron particles. Despite the fact that some starch samples contained only very small amounts of amylose and native lipid, surface‐deposited starch in all experiments contained 90–100% amylose; and exhibited the same V_h X‐ray diffraction pattern, indicative of helical inclusion complex formation. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1781–1788, 2002; DOI 10.1002/app.10589     

玉米淀粉胶粘剂的改性研究

以玉米淀粉为主要原料 ,通过预糊化、氧化、加碱糊化进行化学改性 ,并加入稳定剂可制备固含量高、贮存稳定性好 ,具有一定初粘力和透明性的改性淀粉胶粘剂。本论文主要研究了改性玉米淀粉胶粘剂的主要成分配比及工艺条件对产品性能的影响。结果表明 :淀粉氧化前是否进行预糊化处理、氧化剂的用量、体系pH值、加碱糊化时碱液用量、稳定剂的种类和用量等对改性玉米淀粉胶粘剂性能影响较大。     

变性淀粉取代聚乙烯醇生产Al2O3刚玉陶瓷的胶粘剂研究

论述了变性淀粉取代聚乙烯醇(PVA)生产Al2O3刚玉陶瓷的意义及聚乙烯醇结构与吸附性能的关系，并且根据胶粘机理，通过分析Al203胶粒的表面特性和变性淀粉的结构，说明了变性淀粉可以取代聚乙烯醇。     

聚乙烯可降解薄膜研究进展

聚乙烯(PE)是目前应用生产薄膜最大的塑料品种之一,为了避免"白色污染",利用淀粉和无机填料改性聚乙烯制得可降解薄膜是目前最主要的两种手段。本文探讨了淀粉改性聚乙烯的工艺、机理和改性后薄膜的性能;同时讨论了不同无机填料改性聚乙烯的工艺、机理。     

压力条件下淀粉合成甲基葡萄糖苷

以淀粉、甲醇为原料 ,以酸为催化剂 ,在压力条件下合成甲基葡萄糖苷 (简称甲苷 ) ,得出最佳催化剂是浓硫酸。通过正交实验 ,考察了糖醇比、反应压力、催化剂用量及反应时间对合成甲苷的影响 ,得到合成甲苷的最佳条件为n(淀粉 )∶n(甲醇 ) =1∶30 ,压力 0 5MPa ,催化剂用量为淀粉质量的 5 % ,反应时间 12 0min ,收率达 98 9%。     

Graft polymerization of vinyl acetate onto granular starch: Comparison on the potassium persulfate and ceric ammonium nitrate initiated system

This work was undertaken to discuss in depth the vital differences in the morphological development during synthesis, and properties of starch‐g‐poly‐(vinyl acetate) copolymers using two different initiators, potassium persulfate (KPS) and ceric ammonium nitrate (CAN). KPS‐initiated system gave relatively low values of grafting ratio and grafting efficiency, indicating a great tendency for the formation of poly(vinyl acetate) homopolymer (PVAc). Yet, higher values were seen for the CAN‐initiated system. Transmission electron microscope observations indicated a relatively broad distribution of latex particles for the KPS‐initiated system. The surface potential of latex particles was about ?3.5 mV, which turned out to be insufficient to maintain stability of latex particles. On the other hand, a uniform particle size distribution was found for the CAN‐initiated system, as the surface potential of latex particles was 21.5 mV. Moreover, radicals on starch molecules were generated directly through a redox reaction with positively charged ceric ion. The hydrophobic PVAc chains were thus grafted on starch, resulting in an amphiphilic graft copolymer, which provides a sufficient stabilization degree as a role of surfactant to render a relatively uniform distribution of latex particles. The synthesized starch‐g‐poly(vinyl acetate) copolymers were further converted to starch‐g‐poly(vinyl alcohol) through saponification, which were subjected to evaluations regarding the biodegradation and cell culture capability. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3017–3027, 2006