与一般的高吸收铬鞣助剂相比，端羧基超支化聚合物具有的络合活性基团更多，吸收和固定铬的效果更好，同时还可以节约铬盐，减少铬污染，实现一举两得的效果．通过“一步法”由3，5-二氨基苯甲酸合成了一种端氨基超支化聚合物，经乙醛酸改性后得到一种超支化铬鞣助剂．将其用于羊皮服装革的铬鞣实验，优化出了最佳的应用工艺条件：在铬粉加入前加入2％的铬鞣助剂，铬鞣后期提碱终点pH4．0～4．2．其结果表明，使用该助剂后，铬粉用量仅为5％时，皮革收缩温度（ T s）就能达到常规铬鞣的要求．
以二乙醇胺(DEA)和丁二酸酐为原料,甲醇为溶剂,合成一种新型羧酸型亲水单体N,N-二羟乙基-2-氨基丙酸(DMCA),优化得到DMCA的最佳条件为:冰水浴0℃,n(DEA)∶n(丁二酸酐)为1∶1.2,时间为80 min,甲醇用量为300 m L/mol(DEA),在最佳条件下DMCA的转化率为86.18%。采用红外(FTIR)、核磁(1H NMR)、X射线衍射(XRD)、热重(TG)、元素分析等手段对DMCA进行结构和性能的表征。以DMCA作为亲水扩链剂制备超支化水性聚氨酯DMCA-HWPU,其性能检测结果表明,DMCA-HWPU为非结晶性体系,其乳液呈乳白色泛蓝光,无沉淀,乳液稳定性高,并且具有很好的热稳定性。
In this study, a novel adsorption material amino terminated hyperbranched polyamide collagen fiber( CF-HBPN)was prepared by loading amino terminated hyperbranched polyamide( HBPN) which was synthesized by polycondensation of methacrylate and diethylenetriamine onto the surface of collagen fiber( CF) with glutaraldehyde as the cross-linking agent. X-ray photoelectron spectroscopy( XPS) and thermogravimetric analysis( TGA) were employed to characterize the structures of CF and CFHBPN. In addition,the adsorption property of CF-HBPN toward Cr( Ⅵ) and adsorption thermodynamic were studied as well. The experimental results indicated that the Cr( Ⅵ) 's removal rate by CF-HBPN was 3. 09 higher than that of CF under the same conditions. Langmuir single layer adsorption model was found more suitable to describe the adsorption process than Freundlich adsorption model. The adsorption process was an endothermic reaction. The adsorption efficiency was enhanced with the increase of temperature. X-ray diffraction( XRD) was employed to elucidate the difference between CF-HBPN and Cr( Ⅵ) loaded CF-HBPN[CF-HBPN-Cr( Ⅵ) ].
