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鹽度對疏水改性聚丙烯酰胺吸附行為的影響

Effect of salinity on the adsorption behavior of hydrophobically modified polyacrylamide

  • 摘要: 選擇性絮凝分選是微細粒礦物高效分選的重要手段之一。為了強化絮凝劑在親水、疏水礦物表面的絮凝選擇性,將疏水基團十六烷基二甲基烯丙基氯化銨(C16DMAAC)引入聚丙烯酰胺(PAM)分子鏈中合成了疏水改性聚丙烯酰胺(HMPAM),采用耗散型石英晶體微天平(QCM-D)研究了不同濃度K+和Ca2+對分散劑六偏磷酸鈉(SHMP)和HMPAM在親水和疏水化表面原位吸附行為的影響,并使用激光粒度分析儀分析了不同鹽度下SHMP和HMPAM對硅微粉及疏水改性硅微粉粒徑分布的影響。結果表明,不同鹽度環境下HMPAM均呈現了較好的絮凝選擇性。背景溶液分別為10 mmol?L?1、100 mmol?L?1 KCl及1 mmol?L?1 CaCl2時,QCM-D結果表明SHMP在疏水化表面均未形成吸附層,隨后HMPAM在疏水化表面發生吸附,且隨著鹽度的增加,HMPAM的吸附量增大且吸附層的耗散性降低;背景溶液為10 mmol?L?1 CaCl2時,SHMP也未抑制HMPAM在疏水化表面的吸附,形成了諧振頻率變化(Δf)為?18.3 Hz的吸附層。相比,100 mmol?L?1 KCl時1 mmol?L?1 SHMP在SiO2表面形成薄而致密的吸附層,隨后抑制了HMPAM的吸附;10 mmol?L?1 CaCl2中SHMP在SiO2表面形成耗散的吸附層,隨后10 mmol?L?1 CaCl2沖洗過程中沉積了較為致密的吸附層,也抑制了HMPAM吸附。不同鹽度下SHMP和HMPAM對硅微粉及疏水化硅微粉粒徑分布的影響與QCMD試驗結果相一致。本研究是選擇性絮凝分選中絮凝劑選擇與研發的重要研究基礎。

     

    Abstract: Selective flocculation separation is one of the most efficient methods for fine mineral separation. To enhance the flocculation selectivity on the surfaces of hydrophilic and hydrophobic minerals, a hydrophobic group such as cetyldimethyl allyl ammonium chloride (C16DMAAC) was introduced within the molecular chain of polyacrylamide (PAM) to synthesize hydrophobically modified polyacrylamide (HMPAM). The effects of different K+ and Ca2+ concentrations on the in situ adsorption behavior of dispersants such as sodium hexametaphosphate (SHMP) and HMPAM and their effect on hydrophilic and hydrophobic surfaces were studied using dissipative quartz crystal microbalance (QCM-D). The effects of SHMP and HMPAM on the particle size distribution of silicon powder and hydrophobically modified silicon powder with different salinity were analyzed using a laser particle size analyzer. Results indicated that HMPAM exhibited good flocculation selectivity at varying salinity concentrations. When the background solutions were 10 mmol?L?1, 100 mmol?L?1 KCl, and 1 mmol?L?1 CaCl2, the QCM-D results indicated that no adsorption layer of SHMP was formed on the hydrophobic surface; moreover, the HMPAM was adsorbed on the hydrophobic surface in sequence. With an increase in salinity, the adsorption of HMPAM increased, and the dissipation of the adsorption layer decreased. Moreover, in the background solution of 10 mmol?L?1 CaCl2, SHMP did not inhibit the adsorption of HMPAM on hydrophobic surfaces, and an adsorption layer with the change of resonant frequency (Δf) of ?18.3 Hz was formed. Conversely, a thin and dense adsorption layer of SHMP was generated on the surface of SiO2 in 100 mmol?L?1 KCl, which inhibited the adsorption of HMPAM. In 10 mmol?L?1 CaCl2, a dissipative adsorption layer of SHMP was detected on the surface of SiO2. Furthermore, a relatively dense adsorption layer was deposited after the injection of 10 mmol?L?1 CaCl2 solution, which also inhibited the adsorption of HMPAM. The results of floc size measurements revealed that the position and shape of the floc size distribution peak of the silica powder did not change with the effect of SHMP and HMPAM in the background solutions of 100 mmol?L?1 KCl and 10 mmol?L?1 CaCl2, thus indicating that the SHMP inhibited the flocculation of silica powder by HMPAM. The floc size of the hydrophobically modified silica powder increased with the effect of SHMP and HMPAM. Summarily, the effects of SHMP and HMPAM on the particle size distribution of silicon micro powder and hydrophobic silicon micro powder under different salinity were consistent with the results of QCM-D measurements. This study is an important research basis for selecting and developing flocculants for selective flocculation separation.

     

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