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Synthesis of polyaspartic acid–aminobenzenesulfonic acid grafted copolymer and its scale inhibition performance and dispersion capacity

机译:聚天冬氨酸-氨基苯磺酸接枝共聚物的合成及其阻垢性能和分散能力

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Polysuccinimide (abridged as PSI) was synthesized by urea and maleic anhydride.nAminobenzenesulfonic acid (ABSA) was introduced at different mole ratio to PSI to generatenpolyaspartic acid (abridged as PASP)/ABSA graft copolymer. The scale inhibition behavior of resultantnPASP/ABSA copolymer was evaluated by using static scale inhibition method. The transmittance ofnthe supernatant of the copolymer solution was measured to evaluate its dispersion ability for ferricnoxide. The corrosion inhibition performance of the copolymer for iron plates immersed in the refinedntesting water (including 0.555 g of CaCl2·2H2O, 0.493 g of MgSO4·7H2O, 50 mg PASP/ABSA graftncopolymer and 0.168 g of NaCl) was tested. It was found that PASP/ABSA copolymer was able tonefficiently inhibit CaCO3 and Ca3(PO4)2 scales and had good corrosion inhibition ability as well, and itnalso had good dispersion ability for Fe2O3. Besides, the inhibition efficiency of PASP/ABSA againstnCaCO3 and Ca3(PO4)2 scales and its dispersion capacity for Fe2O3 was highly dependent on dosage.nThe reason may lie in that PASP/ABSA copolymer simultaneously possesses carboxylic ion andnsulfonic group which can chelate Ca2þ to form stabilized and dissoluble chelates, resulting innincrease of solubility of calcium salts in water. Also it may lie in that the introduction of acidicnhydrophilic sulfonic group with a strong electrolytic capacity into PASP molecule simultaneouslynenhances the dispersion of the inhibitor molecules and hinders the formation of Ca (PO ) scale.
机译:以尿素和马来酸酐合成聚琥珀酰亚胺(简称PSI)。以不同的摩尔比引入氨基苯磺酸(ABSA),生成聚天冬氨酸(简称PASP)/ ABSA接枝共聚物。采用静态阻垢法对所得的nPASP / ABSA共聚物的阻垢性能进行了评价。测定共聚物溶液的上清液的透射率,以评价其对二氧化铁的分散能力。测试了该共聚物对浸入精制水的铁板的腐蚀抑制性能(包括0.555 g的CaCl2·2H2O,0.493 g的MgSO4·7H2O,50 mg的PASP / ABSA接枝共聚物和0.168 g的NaCl)。结果发现,PASP / ABSA共聚物能够有效抑制CaCO3和Ca3(PO4)2的结垢,并具有良好的缓蚀性能,并且对Fe2O3具有良好的分散性。此外,PASP / ABSA共聚物对nCaCO3和Ca3(PO4)2垢的抑制作用及其对Fe2O3的分散能力高度依赖于剂量。n原因可能是PASP / ABSA共聚物同时具有可与Ca2 +螯合的羧基和磺酸基。形成稳定的和可溶的螯合物,导致钙盐在水中的溶解度增加。也可能在于将具有强电解能力的酸性亲水磺酸基引入PASP分子中同时增强了抑制剂分子的分散并阻碍了Ca(PO)水垢的形成。

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