非晶颗粒态玉米淀粉制备方法

系统地报道了水分散体系高温溶胀、常温碱分散体系强碱溶胀作用非晶颗粒态玉米淀粉制备方法,采用偏光显微镜对多晶态向非晶态的变化进行了确认,提出在一定条件下,高交联玉米淀粉可以由原淀粉多晶颗粒态制备成只含无定形结构的非晶颗粒态淀粉。     

高温水分散体系交联玉米淀粉的非晶化现象研究

研究了用三偏磷酸钠为交联剂制备高交联玉米淀粉的方法,采用偏光显微镜和广角X-射线衍射对交联玉米淀粉由多晶态向非晶态的渐变过程进行了详细报道,发现了随着温度的升高交联玉米淀粉逐渐非晶化现象,提出在高温条件下交联玉米淀粉存在着只含无定型结构的非晶颗粒态,并用扫描电镜对非晶颗粒态玉米淀粉的结构进行了详细研究.     

高交联木薯淀粉非晶化特性研究

研究了以三氯氧磷为交联剂的高交联木薯淀粉的制备方法,报告了高交联木薯淀粉颗粒随反应取代度增加而逐渐非晶化的现象;同时,采用偏光显微镜和广角Ｘ－射线衍射对其由多晶态向非晶态的渐变过程进行了研究,提出高交联木薯淀粉存在着不同于原淀粉多晶颗粒态的只含无定形结构的非晶颗粒态。对非晶颗粒态高交联木薯淀粉颗粒的粒度分布的进一步研究结果还表明,此时的淀粉颗粒发生了轻度有限的膨胀     

高交联马铃薯淀粉非晶化特性研究

研究了以三氯氧磷为交联剂的高交联马铃薯淀粉的制备方法,报道了高交联马铃闰随反应承代度增加而逐渐非晶化的现象,同时,采用偏光显生镜和广角Ｘ－射线衍射对其由多晶态向非晶态的渐变过程进行了研究,提出主交联马铃薯淀粉存在着不同于原淀粉多晶颗粒态的只含无定形结构的非晶颗态。对非晶颗粒态高交联马铃薯淀粉颗粒的粒度分布的进一步研究还表明,此时的淀粉颗粒发生了轻度有限的膨胀。     

环氧氯丙烷交联沸水溶胀制备非晶颗粒态淀粉

采用环氧氯丙烷高交联改性的方法处理玉米淀粉,然后对交联淀粉水浴加热至100℃制备非晶颗粒态淀粉.考察不同的交联剂用量对玉米原淀粉非晶化的影响.用偏光显微镜观测处理后淀粉颗粒结构,结合X射线衍射曲线确认淀粉由多晶态向非晶态的变化.结果表明,当交联剂环氧氯丙烷用量达到8.0%(淀粉干基)的时候,玉米淀粉可由多晶颗粒态的原淀粉制备出只含无定形结构的非晶颗粒态淀粉.     

甲醛交联高温溶胀法制备非晶颗粒态玉米淀粉

甲醛作为交联剂,高交联改性玉米淀粉后水域加热至78℃制备非晶颗粒态淀粉。考察不同的交联剂用量对原玉米淀粉非晶化的影响。用偏光显微镜观测处理后淀粉颗粒结构,结合X射线衍射曲线确认淀粉由多晶态向非晶态的变化。结果表明,当交联剂甲醛用量达到12.5%(淀粉干基)的时候,玉米淀粉可由多晶颗粒态的原淀粉制备出只含无定形结构的非晶颗粒态淀粉。     

混合酸交联高温溶胀制备非晶颗粒态淀粉

采用已二酸和醋酸酯的混合酸交联处理玉米淀粉,然后对交联淀粉水浴加热至80℃制备非晶颗粒态淀粉.本文考察了不同的交联剂用量对玉米原淀粉非晶化的影响.用偏光显微镜观测处理后淀粉颗粒结构,结合X射线衍射曲线确认淀粉由多晶态向非晶态的变化.结果表明,当交联剂用量达到13%（淀粉干基）的时候,玉米淀粉可由多晶颗粒态的原淀粉制备出只含无定形结构的非晶颗粒态淀粉.     

非晶颗粒态马铃薯淀粉的制备方法

报道了水分散体系高温溶胀、常温碱分散体系强碱溶胀作用非晶颗粒态马铃薯淀粉的制备方法 ,采用偏光显微镜对多晶态向非晶态的变化进行了确认 ,提出在一定条件下 ,高交联马铃薯淀粉 ,可以由原淀粉多晶颗粒态制备成只含无定形结构的非晶颗粒态淀粉     

高温水分散体系交联马铃薯淀粉的非晶化现象研究

研究了用三偏磷酸钠为交联剂高交联马铃薯淀粉的制备方法,采用偏光显微镜和广角X-射线衍射对交联马铃薯淀粉由多晶态向非晶态的渐变过程进行了详细报道发现了随着温度的升高交联马铃薯淀粉逐渐非晶化现象,提出在高温条件下交联马铃薯淀粉存在着只含无定型结构的非晶颗粒态,并用扫描电镜对非晶颗粒态马铃薯淀粉的结构进行了详细研究。     

以捏合机为反应器制备非晶颗粒态玉米淀粉

以捏合机为反应器,研究制备非晶颗粒态淀粉的新方法。将淀粉与水分按不同比例混合并在高温下反应,用偏光显微镜观测处理后的淀粉颗粒结构。结果表明,当淀粉与水分质量比为3∶6时,温度80℃维持30min,90%以上的原玉米淀粉多晶颗粒态转化成无定形结构的非晶颗粒态。     

Physicochemical Properties of Non‐thermally Cross‐linked Corn Starch with Phosphorus Oxychloride using Ultra High Pressure (UHP)

Corn starch (20%, w/w) was non‐thermally and conventionally cross‐linked with phosphorus oxychloride (POCl₃; 0.01, 0.05, or 0.1%, based on dry weight of starch) at 400 MPa for 5, 15 and 30 min and at 45°C for 2 h, respectively. Swelling power and solubility of both non‐thermally and conventionally cross‐linked corn starches were relatively lower than those of native corn starch. The pressure holding time did not affect the solubility and swelling power of non‐thermally cross‐linked corn starches. X‐ray diffraction patterns and relative crystallinity were not significantly altered by both conventional and non‐thermal cross‐linking. DSC thermal characteristics of both non‐thermally and conventionally cross‐linked corn starches were not significantly changed indicating that the double helical structure of amylopectin was not influenced by both conventional and non‐thermal cross‐linking reactions. Both non‐thermal and conventional cross‐linking greatly affected the Rapid Visco Analyser (RVA) pasting properties, such as increase in pasting temperature and decrease in peak viscosity compared to native starch. This result suggests that in case of cross‐linking using POCl₃, both non‐thermal and conventional methods result in similar physicochemical properties and non‐thermal cross‐linking with POCl₃ can reduce the reaction time from 2 h to 15 min. This work shows the potential and possibility of non‐thermal starch modification and provides the basic and scientific information on the physicochemical properties of non‐thermally cross‐linked corn starches with phosphorus oxychloride using UHP.     

三偏磷酸钠交联马铃薯淀粉颗粒膨胀历程及溶胀机理研究

本文利用淀粉与三偏磷酸钠的交联反应，通过控制交联反应程度，成功地控制了交联淀粉颗粒地膨胀并使其停留在不同的溶胀阶段，详细地研究了处在不同溶胀阶段交联淀粉颗粒的结构特征和变化趋势，揭示了交联淀粉颗粒由高交联非糊化到低交联溶胀糊化具体地膨胀历程及溶胀机理，即交联马铃薯淀粉是以颗粒尾端为主的不均衡膨胀。     

Combined effect of autoclaving‐cooling and cross‐linking treatments of normal corn starch on the resistant starch formation and physicochemical properties

Normal corn starch (NCS) was treated by both autoclaving‐cooling and cross‐linking to produce resistant starch (RS). The RS yield, crystalline structure, as well as other physicochemical properties of the modified starch were investigated. The yield of RS was 12.2% by four autoclaving‐cooling cycles, and it could be further increased up to 31.0% by the subsequent cross‐linking using sodium trimetaphosphate/sodium tripolyphosphate. The scanning electron microscopy images clearly illustrated that the granular structure of native starch was disrupted and a continuous network with irregular shape was formed after autoclaving‐cooling cycles. The subsequent chemical cross‐linking appeared to make the network structure more compact and dense. X‐ray diffraction patterns showed that B‐ and V‐types coexisted in all the modified corn starches, and all these modified starches exhibited very low viscosity which remained almost constant regardless of temperature changes.     

Effects of Granule Sizes on Physicochemical Properties of Cross‐linked and Acetylated Wheat Starches

Large and small wheat starch granules were used for cross‐linking and acetylation to determine effects of granule sizes on physicochemical properties of the modified starches. The native and cross‐linked starches from the small granules showed higher phosphorus contents than did those from the large granules. However, the level of phosphate substituents in the modified starches was not significantly different between the large and small granules under the same conditions. In contrast, the large granules had a higher reactivity with acetic anhydride than did the small granules. The phosphate group cross‐linked starch (CS), acetylated starch (AS) and acetylated cross‐linked starch (ACS) from the large granules had lower gelatinization temperatures and higher enthalpies than those from the small granules. The paste viscosities of the CSs from the large granules decreased rapidly, whereas those of the AS or ACS increased significantly as compared with those from the small granules. The pastes of cross‐linked starches from the small granules were more stable than those from the large granules, whereas the pastes of AS and ACS from the large and small granules had similar resistance to freeze‐thaw treatment. Scanning electron microscopy (SEM) also showed that the small granules were less damaged after modification than the large ones. Thus, the different granule sizes resulted in different physicochemical properties of starch after modification.     

三偏磷酸钠交联玉米淀粉颗粒膨胀历程及结构特征

利用淀粉与三偏磷酸钠的交联反应,通过控制交联反应程度,成功地控制了交联淀粉颗粒膨胀程度并使其停留在不同的溶胀阶段,详细研究了处在不同溶胀阶段交联淀粉颗粒的结构特征和变化趋势,揭示了三偏磷酸钠交联玉米淀粉颗粒的膨胀历程及结构特征,即随着淀粉颗粒交联程度的降低,颗粒的膨胀历程由中心脐点处爆裂膨胀方式转化为颗粒整体向外的均匀膨胀方式.     

变性淀粉对烘焙果酱品质的影响

探讨了6种蜡质玉米变性淀粉对烘焙果酱保水胜、耐烘焙性、凝胶特性、外观品质和口感的影响,结果表明,两种低交联度磷酸盐交联羟丙基化蜡质玉米变性淀粉,由于其耐烘焙性较差,不宜在烘焙果酱中应用.另外两种磷酸盐交联羟丙基化蜡质玉米变性淀粉和两种己二酸交联醋酸酯化蜡质玉米变性淀粉都能显著改善烘焙果酱的耐烘焙性和持水性,赋予产品良好的组织状态和口感,其中,高交联度磷酸盐交联羟丙基化蜡质玉米变性淀粉CR3010还具有良好的热稳定性和耐酸性能,尤其适合应用于烘焙果酱中.     

Dual Modification of Banana Starch: Partial Characterization

Banana starch was double modified by cross‐linking and substitution, using two different cross‐linking agents, i.e. phosphorus oxychloride (POCl₃) and a mixture of sodium trimetaphosphate/sodium tripolyphosphate. The morphological and physicochemical properties and the absorption capacity for heavy metals of the modified starches were assessed. Double modified starch granules (cross‐linked carboxymethyl starches CCSA and CCSB) presented changes in the surfaces. These starches had a bigger average particle size than unmodified starch due to the swelling of the granules during the chemical modification, also aggregates were formed. The double modified banana starches presented an A‐type X‐ray diffraction pattern with slightly decreased crystallinity compared with the unmodified counterparts. The double modification of banana starch decreases the temperature and enthalpy of gelatinization and the decomposition temperature. These results are related to partial disorganization during the chemical treatment. The double modified banana starch possess sorption capacity for heavy metal ions in the order Cd²⁺ >Pb²⁺>Cu²⁺>Hg²⁺. Due to their physicochemical characteristics and absorption capacity, the double modified banana starches can be used in diverse applications.     

甘肃主要杂豆淀粉理化特性分析

以甘肃产三角豌豆、白豌豆、小白芸豆、麻豌豆为材料,采用湿磨法提取淀粉,以玉米、马铃薯及绿豆淀粉为对照,对杂豆淀粉的理化特性进行分析。结果表明：参试杂豆淀粉颗粒多呈卵圆形,偏光十字较明显,多呈“X”形和斜十字形,部分淀粉颗粒呈现明显多脐点现象,平均粒径为21～29μm,其中三角豌豆淀粉的粒径最大而麻豌豆淀粉颗粒最小;淀粉颗粒的结晶类型与绿豆淀粉相同,为C型。其直链淀粉含量远高于玉米淀粉和马铃薯淀粉,且麻豌豆＞小白芸豆＞白豌豆＞三角豌豆淀粉。杂豆淀粉属限制型膨胀淀粉,起糊温度为72.6～78.8℃,且具有较好的热糊和冷糊稳定性,淀粉糊的透明度较高,但凝沉速度均极快,冻融稳定性也都较差。4种杂豆淀粉的理化特性与绿豆淀粉相近,可耐受高温处理,但不宜用于冷冻类食品的生产。