共查询到18条相似文献,搜索用时 93 毫秒
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本文对新型两亲单体,2-丙烯酰胺基十六烷磺酸(AMC_(16)S),及其两亲聚合物PAMC_(16)S在空气-水界面上形成单层膜的特点进行了研究。AMC_(16)S可通过在亚相中添加Ca~(2+)或Cd~(2+)等多价阳离子在界面上原位生成不溶性磺酸盐的方法获得满意的成膜行为。PAMC_(16)S不溶于水,可直接成膜。发现,PAMC_(16)S的成膜行为与亚相的性质明显相关。纯水亚相下PAMC_(16)S的极限单体链节面积较大,如亚相含有Ca~(2+)或Cd~(2+),极限面积明显缩小,说明烷基碳氢链的排列趋向紧密。 相似文献
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2-丙烯酰胺基烷磺酸的溶解行为和胶体化学性质明显随烷基长短而异,由于手性碳原子的存在,与其相邻亚甲基的质子峰在HNMR谱上清楚地发生分裂,研究了2-丙烯酰胺基十六烷磺酸(AMC16S)在水/二氧六环混合溶剂中的聚合动力学和胶体化化学性质,发现聚合速度和所得聚合物分子量均均在水/二氧六环体积比为1~1/2时出现最小值,临界胶束浓度随混合溶剂中二氧六环含量的增加而增加,当水/二氧六环体积比为1/2~1 相似文献
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用自组装技术在金(纯金和经阳极氧化的金)表面上获得了新型两亲聚合物PAMC_(16)S的有序膜。用接触角测试,XPS谱和电化学分析等方法对自组装膜进行了表征。根据膜表面的润湿性,金表面的自组装膜是疏水的,亲水的磺酸基团连于金表面,而疏水的碳氢链从表面伸展出。XPS实验结果支持金表面上单层膜的疏水结构。聚合物单层膜复盖的金电极起到含有针孔缺陷的阻膈型电极的作用。单层膜在法拉第反应中显示很强的吸附稳定性,说明聚合物LB膜在潜在应用中有其特有的特点。 相似文献
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水溶性聚合物和两亲聚合物:聚(丙烯酰胺-co-丙烯酸钠)-g-聚(β-胺基丙酸)接枝共聚物 总被引:1,自引:0,他引:1
合成了端丙烯酰胺基聚(β-胺基两酸)大分子单体,用端基滴定法和1H—NMR法测定了大分子单体的分子量,用13C—NMR和氢氧化钠水解法测定了支化度.在水溶液中用硫酸亚铁/异丙苯过氧化氢氧化还原引发体系引发丙烯酸胺、丙烯酸钠与聚(β-胺基丙酸)大分子单体的共聚反应,合成了聚(丙烯酰胺-co-丙烯酸钠)-g-聚(β-胺基丙酸)接枝共聚物.用1H—NMR和滴定法测定了接枝共聚物的组成.溶液性质的数据表明,与部分水解聚丙烯酰胶相比,聚(β-胺基丙酸)含量较高的接枝共聚物具有较好的耐盐性和优异的贮存稳定性. 相似文献
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水溶性聚合物和两亲聚合物:聚(丙烯酰胺-co-丙烯酸钠)-g-聚(β-胺基丙酸)接枝共聚物 总被引:2,自引:0,他引:2
合成了端丙烯酰胺基聚(β-胺基丙酸)大分子单体,用端基滴定法和1H-NMR法测定了大分子单体的分子量,用^1^3C-MNR和氢氧化钠水解法测定了支化度,在水溶液中用硫酸亚铁/异丙苯过氧化氢氧化还原引发体系引发丙烯酰胺,丙烯酸钠与聚(β-胺基丙酸)大分子单体的共聚反应,合成了聚(丙烯酰胺-co-丙烯酸钠)-g-聚(β-胺基丙酸)用1H-NMR和滴定法测定了接枝共聚物的组成。溶液性质的数据表明,与部分 相似文献
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应用薄层色谱法对工业品2 丙烯酰胺基 2 甲基丙烷磺酸(简称AMPS)进行了分析,以硅胶GF254作为吸附剂,从几种溶剂系统中优选了V(苯)∶V(甲醇)=2∶1溶液作为展开剂,用254nm紫外分析仪检测展开后的样品斑点。实验表明:AMPS的Rf为036,而其主要杂质丙烯酰胺(AM)的Rf为0.64;AMPS的最小检出限为5μg,展开时间约为25min。方法简便、快速、重现性好,有利于在生产过程中快速分析AMPS及其所含杂质,从而指导对AMPS的纯化处理。 相似文献
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Charles L. Mccormick Luis C. Salazar 《Journal of polymer science. Part A, Polymer chemistry》1993,31(5):1099-1104
The new monomer 2-acrylamido-2-methylpropanetrimethylammonium chloride (AMP-TAC, M2) has been synthesized. Free radical copolymerization with acrylamide (AM, M1) in feed ratios varying from 10 to 50 mol % AMPTAC gave the cationic ATAM series. Copolymer compositions were determined from 13C-NMR. The reactivity ratio product r1r2 was found to be 0.62. Molecular weights varied from 1.4 to 16.5 × 106 g/mol for the copolymers. Turbidimetric studies showed aqueous solutions of the copolymers to be phase stable in the presence of CaCl2 and Na2CO3 up to 100°C. Solution behavior was independent of pH in the range of 3 to 11, and temperature in the range of 25 to 60°C. Intrinsic viscosities of the cationic copolymers decreased with the addition of electrolytes; however, some samples showed curvature in plots of intrinsic viscosity versus the inverse square root of ionic strength. © 1993 John Wiley & Sons, Inc. 相似文献
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水溶液中丙烯酸/乙酸乙烯酯无规共聚物的存在不仅降低了Na2SO4和CaCl2生成CaSO4的沉淀量和结晶速度,而且可显减小CaSO4粒子的大小,改变其形状和晶形,降低结晶的完善程度。 相似文献
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E. Sauvage N. Plucktaveesak R.H. Colby D.A. Amos B. Antalek K.M. Schroeder J.S. Tan 《Journal of polymer science. Part A, Polymer chemistry》2004,42(19):3584-3597
The dilute solution behavior of several alternating copolymers of maleic acid has been characterized by static and dynamic light scattering, intrinsic viscosity, and pulsed-gradient spin-echo NMR spectroscopy. The copolymer of maleic acid–sodium salt and isobutylene (IBMA-Na, Mw ∼350 kg/mol) dissolves readily in concentrated aqueous salt solutions. Changes in chain dimensions with ionic strength and pH are similar to those of the lesser salt solution-soluble poly(acrylic acid-sodium salt). The hydrophobically modified (with n-butyl, n-hexyl, n-octyl, and phenethyl amines) copolymers of maleic acid–sodium salts and isobutylene (IBMA-NHR-Na) show no sign of large intermolecular aggregation in 0.1 N sodium acetate (NaAc). However, the sizes of the copolymers are relatively small compared to that of the ionized parent copolymer (IBMA-Na, Mw ∼350 kg/mol), suggesting intramolecular aggregation of the alkyl side-chain groups along the polymer backbone. The copolymer modified with the longer chain n-decyl, on the other hand, forms stable large intermolecular aggregates containing 33 chains/aggregate. The copolymers of maleic acid–sodium salt and styrene (SMA-Na) appear to have no signs of aggregation, despite being a hydrophobic polyelectrolyte. The copolymer of maleic acid–sodium salt and di-isobutylene (DIBMA-Na) has a similar salting-out concentration as SMA-Na. The radius of gyration measurements by static light scattering suggest that at least some fraction of the DIBMA-Na chains form large intermolecular aggregates. The copolymers of maleic acid–sodium salt with n-alkenes (n-CmMA-Na) in 0.1 N NaAc form small intermolecular aggregates (three to five chains/aggregate). In contrast to these static light scattering results, PGSE NMR diffusion measurements for the above aggregated systems indicate only one diffusion coefficient consistent with the motion of single isolated chains. A plausible explanation for this discrepancy is that the population of the aggregates is too small to be sufficiently detected in the PGSE NMR experiment. Furthermore, it is likely that the aggregate has a larger relaxation rate than the nonaggregate, and therefore has a comparatively reduced signal in the PGSE NMR experiment. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 3584–3597, 2004 相似文献
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O/CO气氛下稻秆添加磷酸二氢铵对固钾及灰熔融特性的研究 《燃料化学学报》2015,43(8):955-960
研究了21%O2/79%CO2气氛下,磷酸二氢铵对稻秆不同温度下的固钾能力及对灰熔融性的影响。利用电感耦合等离子体发射光谱(ICP-AES)、X射线衍射(XRD)以及扫描电子显微镜(SEM)等检测手段,对稻秆燃烧灰中K元素含量、产物物相以及微观形貌进行分析。固定床燃烧固钾实验表明,添加NH4H2PO4能够有效提高稻秆固钾率,900℃下稻秆自身固钾率为14.65%,添加NH4H2PO4后固钾率为68.79%,可以有效抑制生物质燃烧过程中碱金属以气态形式析出,并缓解了灰结渣现象。700℃燃烧条件下NH4H2PO4和钾反应的主要产物为KPO3;900℃下反应的主要产物为高熔点物质K2CaP2O7,从微观形貌可以看出NH4H2PO4能够抑制灰颗粒的烧结,添加NH4H2PO4能有效提升稻秆灰熔点。 相似文献