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低濃度聚丙烯酰胺含量的檢測及溶液離子的影響

Rapid detection of low-concentration polyacrylamide and study on the influence of ions in solution

  • 摘要: 處理后選礦廢水中殘余的聚丙烯酰胺(PAM)影響回水水質及其回用,本文為建立一種低檢出限的低濃度PAM快速檢測方法,在190~300 nm波長范圍內建立了4種類型及分子量不同PAM的紫外吸收光譜,研究了不同濃度K+和Ca2+對PAM濃度檢測的影響,并通過原子力顯微鏡(AFM)分析了PAM分子構象的變化. 結果表明,4種類型的PAM峰值吸光度均在波長194 nm處測得,PAM濃度與吸光度之間具有強線性關系(R2>0.98),檢出限均低于0.1 mg·L?1,但PAM類型影響其濃度與吸光度的線性關系. 隨著K+和Ca2+濃度的增加,PAM溶液吸光度特征峰的強度逐漸降低并降速減緩,最大吸收波長不斷紅移,分別沉積在二氧化硅和金基底的APAM-3與CPAM-12的表面形貌粗糙度分別隨K+和Ca2+濃度的增加而增大,說明PAM分子鏈在溶液中的構象逐漸變卷曲,使紫外光譜特征吸收峰的峰值降低,10、100 mmol·L?1 K+與1、10 mmol·L?1 Ca2+對PAM構象變化的影響程度基本相同. 本研究實現聚丙烯酰胺的快速定量檢測,對開展選礦水處理中聚丙烯酰胺的遷移規律研究具有重要意義.

     

    Abstract: The residual polyacrylamide (PAM) in treated mineral processing wastewater affects the quality of recycled water and its potential for reuse. Continuous circulation and accumulation of cations in mineral processing wastewater can also influence the chemical properties and flocculating performance of PAM. In this study, a rapid detection method for low detection limit and concentration of PAM was proposed. The ultraviolet absorption spectra of four types and different molecular weights of PAM were collected in the wavelength range of 190–300 nm. The sensitivity and detection limits of this ultraviolet spectral method of PAM were verified. The effects of different K+ and Ca2+ concentrations on the detection of PAM concentration were examined. Change in the PAM molecular conformation was analyzed using atomic force microscopy. The findings demonstrated that for the four polymers, the highest absorbance was recorded at 194 nm. There was a strong linear relationship between PAM concentration and absorbance (R2>0.98). The limit of detection was lower than 0.1 mg·L?1. This method showed high detection sensitivity. However, the linear relationship between concentration and absorbance was affected by the type of PAM used. With increasing K+ and Ca2+ concentrations, the intensity of the absorbance characteristic peak of the PAM solution was reduced. The maximum absorption wavelength was continuously red-shifted. In addition, when the K+ and Ca2+ concentrations were greater than 50 and 5 mmol·L?1, respectively. The intensity of the characteristic absorbance peak gradually decreased. In deionized water, the surface roughness (Rq) values of APAM-3 and CPAM-12 deposited on SiO2 and Au substrates were 24.3 and 38.1 nm, respectively. When the K+ and Ca2+ concentrations increased from 10 and 1 mmol·L?1 to 100 and 10 mmol·L?1, Rq increased from 80.4 and 120.0 nm to 124.0 and 145.0 nm, respectively. In the morphology map, the molecular chains of PAM transformed from linear dendrites to point blocky structures. It was demonstrated that the conformation of PAM chains in solution gradually became curled, resulting in a decrease in the peak intensity of the characteristic UV absorption spectrum. The effect of 10 and 100 mmol·L?1 K+ and 1 and 10 mmol·L?1 Ca2+ on the conformational change of PAM was essentially the same degree. The effects of typical monovalent and bivalent cations (K+ and Ca2+) on the molecular conformation of PAM were in alignment with the findings of their UV absorption spectra. In this study, the rapid and accurate quantitative detection of PAM is critical for exploring its migration behavior in mineral processing water treatment.

     

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