几种有机物对紫色土镉的溶出效应与吸附-解吸行为影响的研究

研究了天然有机物胡敏酸和富里酸 ,螯合剂EDTA和DTPA和四种简单有机酸对紫色土镉的溶出效应和吸附解吸行为的影响。结果表明 ,供试八种有机物均能显著促进镉从紫色土中的溶出。作用大小顺序为 :EDTA≥DTPA >柠檬酸 >胡敏酸 >草酸 >富里酸 >酒石酸≥水杨酸。有机物对土壤镉溶出和迁移的影响是其对土壤镉吸附和解吸综合作用的结果。有机物显著降低了紫色土对镉的吸附 ,其作用大小顺序与其对镉的溶出能力的相对大小顺序一致 ,同时也改变了吸附镉的解吸特性。有机物影响下 ,紫色土镉的吸附动力学模型以双常数方程拟合最佳。而吸附等温曲线以Freundlich方程拟合最好 ,吸附常数n与有机物对土壤镉的溶出率之间存在良好的相关性。     

CO2-defatted oats: Solubility,emulsification and foaming properties

Functional properties of conventional oat materials are relatively poor with respect to foam and emulsion formation and stabilization. This is largely due to the poor solubility of oat proteins and the presence of lipids in aqueous extracts of oats. In the experimental part of this study, extracts were prepared from different type oat flours (oat endosperm flour, oat fine flour, CO₂-defatted whole oat flour and CO₂-defatted oat flour) with a buffered aqueous extraction procedure at acidic (pH 4.5 and 6.5) and basic (pH 8.5 and 10.5) regions. The solubility of proteins was the highest at pH 10.5 and NaCl concentration of 2%. Among the extracts, CO₂-oat flour showed improved foaming and emulsifying properties at basic pH values. The presence of 0.1% NaCl resulted in the lowest foam volumes, but the emulsion activity and stability values being the highest. Sucrose addition resulted in increased foam and emulsion stability of suspensions. Heat treatment at 80 °C impaired foam properties, whereas the stability of emulsions increased with the increase in temperature from 20 °C to 80 °C. CO₂-extracted oats can be useful raw materials in beverages and other aqueous applications where protein functionality plays an important role.     

Effect of fermentation on sorghum protein fractions and in vitro protein digestibility

Changes in pH, titratable acidity, total soluble solids and proteins ofDabar sorghum (Sorghum bicolor (Linn) Moench.) during naturalfermentation at 37 ^°C for up to 36 h were monitored. The pH ofthe fermenting material decreased sharply with a concomitant increase in the titratable acidity. Total soluble solids increased with progressivefermentation time. The crude protein and non-protein nitrogen slightlyincreased during the last stages of fermentation. The in vitroprotein digestibility markedly increased as a result of fermentation.The globulin plus albumin fractions increased significantly (p 0.05)during the first 8 h of fermentation. Kaffirin fraction decreasedduring the first 8 h of fermentation but increased sharply as fermentationprogressed. Cross-linked kaffirins fluctuated during the fermentationprocess. Glutelin like protein, which was the minor fraction, trueglutelins, the second most abundant fraction, together with non-extractableproteins fluctuated during the fermentation process.     

Effect of cooking on cowpea protein fractions

Nine cowpea cultivars obtained from Wad Medani Research Station were used in this study. The variation in protein fraction was: albumins 4.0–12.0, globulins 65.6–79.7, prolamins 1.4–2.2, G₁-glutelins 0.9–3.0, G₂-glutelins 1.4–2.9. G₃-glutenins 9.1–14.0 and insoluble protein 0.5–3.0%. Two cowpea cultivars, H8-14 and CB-46, selected for their high albumin content, were cooked in 150 ml of boiling distilled water under reflux for 45 minutes. The protein fractions in the cooked seeds were determined. Results indicated that albumin and globulin fractions decreased significantly (p0.05) for both cultivars after cooking. This decrease was accompanied by a significant increase in G₃-glutelin fractions.     

Preparation of regenerated cellulose fiber via carbonation. I. Carbonation and dissolution in an aqueous NaOH solution

Cellulose carbonate was prepared by the reaction of cellulose pulp and CO₂ with treatment reagents, such as aqueous ZnCl₂ (20–40 wt%) solution, acetone or ethyl acetate, at −5–0°C and 30–40 bar (CO₂) for 2 hr. Among the treatment reagents, ethyl acetate was the most effective. Cellulose carbonate was dissolved in 10% sodium hydroxide solution containing zinc oxide up to 3 wt% at −5–0°C. Intrinsic viscosities of raw cellulose and cellulose carbonate were measured with an Ubbelohde viscometer using 0.5 M cupriethylenediamine hydroxide (cuen) as a solvent at 20°C according to ASTM D1795 method. The molecular weight of cellulose was rarely changed by carbonation. Solubility of cellulose carbonate was tested by optical microscopic observation, UV absorbance and viscosity measurement. Phase diagram of cellulose carbonate was obtained by combining the results of solubility evaluation. Maximum concentration of cellulose carbonate for soluble zone was increased with increasing zinc oxide content. Cellulose carbonate solution in good soluble zone was transparent and showed the lowest absorbance and the highest viscosity. The cellulose carbonate and its solution were stable in refrigerator (−5°C and atmospheric pressure).     

Synthesis and characterization of copolyester sizing agents

The effect of main chain structure of anion-containing copolyesters on the properties of copolyester sizing agents was investigated. The copolyesters were prepared by conventional two step polymerization technique from DMT, DMI, DMS, EG, and DEG. The copolyesters synthesized were characterized by atomic absorption spectroscopy,¹H-NMR Spectroscopy, GC, FTIR Spectroscopy, and DSC. The solubility decreased as the DMT content increased. The copolyesters having DMT:DMI=1:1 showed the minimum viscosity. The effect of EG content on the solution stability was not clear and the samples having high DMI content showed better solution stability. The water resistance was best when only DMI and EG were used, while it was worst when DMT:DMI was 1:0.     

用热水解法制备不同分子质量丝胶粉的溶解性差异及其成因探讨

用沸水法和高温高压热水法提取丝胶溶液,分别在90℃热水中进行二次降解处理,获得具有不同分子质量分布范围的各种热水解丝胶溶液,经冷冻干燥制成丝胶粉。对各种丝胶粉的热水溶解性差异比较和成因探讨表明,热水二次降解能够提高丝胶的水溶性,降解处理时间越长,其水溶性越大;丝胶的分子质量大小能显著影响其溶解性,而丝胶的结晶结构含量对其溶解性的影响较小。研究结果有助于对不同溶解性丝胶的有效利用。     

丝素/明胶共混膜的结构与溶解性能的初探

将丝素溶液与明胶溶液按不同共混比在不同条件下进行混合,制备成丝素/明胶共混膜。用环境扫描电镜、红外光谱仪、差示扫描量热分析系统分别测定共混膜的结构与热性能,采用烘干质量法测定共混膜的溶胀率和溶解率。结果表明:丝素与明胶的共混性好,共混膜结构改变,热稳定性好;烘干时间对共混膜的溶胀率和溶解率影响不显著,不同浓度乙醇处理对溶胀率有极显著影响,不同共混比则对溶胀率和溶解率都有极显著影响。     

木糖结晶的热力学特性研究

[目的]研究木糖结晶的溶解度及介稳区。[方法]采用激光法试验考察了木糖在纯水、乙醇-水溶液中的溶解度以及木糖在水中的超溶解度,确定木糖水溶液的结晶介稳区。[结果]木糖在纯水和不同体积配比的乙醇-水溶液中的溶解度随着溶液体系温度降低而明显减小,结晶介稳区的宽度在低温范围内比高温阶段要宽。[结论]为利用农产品废弃物木糖结晶的生产操作提供了理论依据。     

利用有限酶解技术提高鲶鱼食用肉粉溶解度的研究

[目的]筛选出有限酶解鲶鱼肉蛋白的最佳用酶种类和酶解工艺条件,为鲶鱼食用肉粉的加工提供理论依据。[方法]以鲶鱼为原料,经预处理、采肉、漂洗、斩拌、有限酶解、打浆和干燥等工序加工而成鲶鱼食用肉粉。其中选择4种酶（风味蛋白酶、枯草杆菌中性蛋白酶、碱性蛋白酶和木瓜蛋白酶）作为水解用酶,分别在各酶最佳酶解条件下对鲶鱼肉糜进行水解,以鲶鱼肉粉的溶解度为评价指标。[结果]用中性蛋白酶作为有限酶解的酶类加工出的鲶鱼食用肉粉溶解度可达90%以上,最佳酶解工艺条件为：酶用量0.55%,酶解时间60 min,料水比1∶3（g∶g）。[结论]用中性蛋白酶作为有限酶解的酶类,加工出的鲶鱼食用肉粉溶解度最高,风味最佳。