共查询到20条相似文献,搜索用时 15 毫秒
1.
2.
3.
阴离子交换高效液相色谱法同时分离和分析三种氨基羧酸 总被引:3,自引:1,他引:2
建立了利用阴离子交换高效液相色谱同时分离分析甘氨酸、亚氨基二乙酸和氨三乙酸的方法。色谱柱为Sax强阴离子交换柱,用0.01 mol/L磷酸二氢钾缓冲液(pH=2.2)为流动相,紫外检测器波长为210 nm,对样品进行分析,并用外标法对这三种氨基羧酸进行定量。结果表明甘氨酸、亚氨基二乙酸和氨三乙酸分别在0.1024~2.0484 g/L、0.1006~2.0119 g/L、0.0050~0.3009g/L范围内线性关系良好(r>0.9995)。此法具有灵敏度高,线性相关系数和重现性好,流动相成本较低等特点。 相似文献
4.
5.
黄酮类化合物是在植物中分布非常广泛的一类天然产物,具有多种生物活性。大孔吸附树脂纯化是一项不需复杂设备、操作条件温和的新型分离技术。综述了大孔吸附树脂分离纯化黄酮类化合物的研究进展。 相似文献
6.
7.
研究大孔吸附树脂分离纯化番石榴叶总皂苷的工艺条件.番石榴叶用70%乙醇回流提取后,上D101型大孔树脂,水洗后分别用30%,50%,70%乙醇洗脱,以番石榴叶总皂苷的洗脱率为指标,考察大孔树脂分离纯化番石榴叶总皂苷的吸附性能和洗脱参数.番石榴叶总皂苷主要富集于30%、50%乙醇洗脱液部分,大孔吸附树脂的吸附容量为17.53 mg·g-1,洗脱率达70.42%,而50%乙醇洗脱时总皂苷纯度可达55.68%,优选洗脱条件为用水洗去水溶性杂质,50%乙醇洗脱总皂苷. 相似文献
8.
大孔树脂分离纯化核桃青皮总黄酮的研究 总被引:3,自引:0,他引:3
以总黄酮回收率为考察指标,研究了大孔树脂分离纯化核桃青皮总黄酮的工艺。结果表明:D101型树脂对核桃青皮总黄酮有较好的吸附分离性能,是分离纯化核桃青皮总黄酮的适宜大孔树脂;最佳工艺条件为:上柱总黄酮与干树脂质量比为1:12,上样液质量浓度可在3.0875~6.175 g/L 范围内,pH值为5, 6BV(1BV=23.7 mL)的水洗后用5BV的70%乙醇洗脱。经D101处理后的核桃青皮总黄酮回收率在60%,纯度可达80%以上。该工艺简便,能有效分离纯化核桃青皮黄酮类化合物。 相似文献
9.
10.
大孔吸附树脂分离纯化银杏叶总黄酮的研究 总被引:2,自引:0,他引:2
利用4种大孔吸附树脂分离纯化银杏叶总黄酮.结果表明,HPD100型大孔吸附树脂最适合分离纯化银杏叶总黄酮,该树脂的静态饱和吸附量(以干树脂计)为63.8 mg·g-1,静态洗脱率为91.2%,动态饱和吸附-洗脱量为14.0 mg·g-1,洗脱剂为70%乙醇,洗脱剂用量为4倍树脂体积,树脂可重复使用7个周期. 相似文献
11.
12.
《分离科学与技术》2012,47(6):809-813
In this study, batch and column mode tests were performed to evaluate the efficiency of boron removal from geothermal water containing 10-11 mg B/L using Lewatit MK 51 which is a macroporous weak base anion exchange resin with polyhydroxyl groups showing a very high selectivity and capacity for boron. The optimum resin amount for boron removal from geothermal water was determined as 4.0 g resin/L-geothermal water. It was found that the sorption kinetics was influenced by particle size of the resin and temperature. The stirring rate had almost no effect on kinetic performance of the resin. According to the results of column-mode study performed, breakthrough and total capacities of the resin were obtained as 2.75 and 4.98 mg/mL-resin, respectively. 相似文献
13.
以栾树叶多酚提取物为原料,比较了7种大孔树脂对栾树叶多酚的静态吸附与解吸效果,结果表明AB-8树脂性能最佳,其24h静态吸附量为13.74mg/g,解吸率为98.35%,3h内达到吸附平衡与解吸平衡。AB-8树脂动态吸附较佳条件为上样液质量浓度为4g/L,上样液pH值为6,在此条件下吸附率为88.21%,动态洗脱较佳条件为洗脱剂乙醇体积分数为60%,洗脱速度为1mL/min,解吸率达到89.91%,在该条件下栾树叶总多酚经AB-8树脂纯化后,质量分数由50.36%增加到72.37%,回收率为86.83%。 相似文献
14.
通过大孔吸附树脂对申嗪霉素发酵滤液静态吸附和解吸试验,从6种大孔吸附树脂中筛选出分离纯化申嗪霉素最优的树脂,考察了该树脂对申嗪霉素的静态、动态吸附与解吸性能并对吸附与洗脱的最佳条件进行了研究。结果表明:AB-8树脂对申嗪霉素有很好的吸附和解吸性能,其最优的动态吸附工艺条件为:上样液浓度3 000μg/mL,上样量4 BV,上样流速2 BV/h;最优的解吸条件为:洗脱剂为80%乙醇溶液,洗脱液用量3 BV,洗脱流速1 BV/h。在此优化条件下,申嗪霉素的吸附率、解吸率、收率、纯度的平均值分别达到(90.33±0.14)%、(90.87±0.12)%、(82.1±0.1)%和(90.74±0.14)%(n=5)。 相似文献
15.
16.
以茶条槭叶为原料碱水解提取没食子酸,通过静态吸附和解吸实验对7种大孔吸附树脂进行筛选,采用筛选出来的XDA-8树脂进行纯化工艺研究。结果表明:XDA-8树脂是7种树脂中最合适的纯化树脂,最佳纯化工艺为,上样液pH=3,上样流速3 mL/min,洗脱剂最适宜的浓度、pH和用量分别为80%乙醇,pH≤1和3 BV(倍柱体积)。经XDA-8大孔吸附树脂纯化后所得产物没食子酸含量为25.878%较提取液中没食子酸含量12.483%有所提高,但纯化效果不显著。 相似文献
17.
Sinapic acid present in the waste stream of yellow mustard protein isolation was purified by strong base Dowex (1 × 8, Cl?) ion exchange chromatography. The ratio of loading volume to resin bed volume was 19:1. Approximately 80 % of sinapic acid was adsorbed. The column was washed with two bed volumes of water to remove remaining undesirable components. Approximately 75 % of sinapic acid adsorbed by the resins in the column was eluted by ten bed volumes of a solution containing 0.9 M acetic acid and methanol (4:6, v/v). Up to 15 adsorption and regeneration cycles resulted in only a slight, 3–5 %, reduction in ion exchange capacity, indicating that this is a viable approach to the recovery and purification of sinapic acid. The recovery of this valuable nutraceutical ingredient improves the economic viability of an integrated extraction process for this Canadian oilseed crop. 相似文献
18.
19.
《分离科学与技术》2012,47(16):2526-2530
Zizyphi Spinosi Semen is well known as a kind of herb for the treatment of insomnia and anxiety. However, due to the lack of purified compounds for functional tests, limited data proves pharmacological activities of each jujubasaponin monomer. In this study, we developed a novel method for the preparative separation and purification of jujuboside A, A1, B, and B1, simultaneously, from Zizyphi Spinosi Semen. Macroporous resin and reversed-phase flash chromatography was successfully used and gave a good resolution of each jujubasaponins monomer. Jujuboside A, A1, B, and B1 with a purity of over 98% were yielded. 相似文献
20.
串联阴阳离子交换色谱分离牛初乳中乳铁蛋白与IgG 总被引:1,自引:0,他引:1
脱脂牛初乳用浓度为6 mol/L的盐酸调节其pH至4.0,以5 000 r/m in离心分离20 m in除去酪蛋白制得乳清,缓慢滴加浓度为1 mol/L的氢氧化钠回调pH至6.8;处理后的乳清经截留相对分子质量为50 000的组分并超滤稀释后,再经过阴阳离子交换串联色谱,乳铁蛋白(Lf)吸附于CM Sepharose Fast F low,免疫球蛋白G(Immunoglobu lin G,IgG)吸附于DEAE Sepharose Fast F low;阳离子交换柱用c(NaC l)=0.27 mol/L、0.85 mol/L的水溶液阶跃洗脱,得到色谱纯度为96.6%的Lf产品,阴离子交换柱用c(NaC l)=17 mmol/L、51 mmol/L的水溶液阶跃洗脱,得到色谱纯度为95%的IgG产品。 相似文献