Crystals (Nov 2020)

Synthesis and Visualization of a Novel Fluorescent-Tagged Polymeric Antiscalant during Gypsum Crystallization in Combination with Bisphosphonate Fluorophore

  • Maxim Oshchepkov,
  • Vladimir Golovesov,
  • Anastasia Ryabova,
  • Svetlana Frolova,
  • Sergey Tkachenko,
  • Semen Kamagurov,
  • Galina Rudakova,
  • Konstantin Popov

DOI
https://doi.org/10.3390/cryst10110992
Journal volume & issue
Vol. 10, no. 11
p. 992

Abstract

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An attempt to reveal the mechanisms of scale inhibition with the use of two different fluorescent-tagged antiscalants at once is undertaken. To reach the goal, a novel 1,8-naphthalimide-tagged polyacrylate (PAA-F2) is synthesized and tested separately and jointly with 1,8-naphthalimide-tagged bisphosphonate (HEDP-F) as a gypsum scale inhibitor within the frames of NACE Standard TM0374-2007. Here, it is found that at a dosage of 10 mg·dm−3 it provides a much higher inhibition efficiency (96%) than HEDP-F (32%). A PAA-F2 and HEDP-F blend (1:1 mass) has an intermediate efficacy (66%) and exhibits no synergism relative to its individual components. The visualization of PAA-F2 revealed a paradoxical effect: an antiscalant causes modification of the CaSO4·2H2O crystals habit, but does not interact with them, forming particles of its own solid complex [Ca-PAA-F2]. This paradox is interpreted in terms of the “nano/microdust” concept, prioritizing the bulk heterogeneous nucleation step, while an ability of the scale inhibitor to block the nucleus growth at the next steps is proven to be of secondary importance. At the same time, HEDP-F does not change the gypsum crystals morphology, although this antiscalant is completely located on the surface of the scale phase. The PAA-F2 and HEDP-F blend revealed an accumulation of both antiscalants in their own [Ca-PAA-F2/Ca-HEDP-F] phase with some traces of HEDP-F and PAA-F2 on the CaSO4·2H2O crystals surface. Thus, the visualization of two different antiscalants separately and jointly applied to gypsum deposition demonstrates differences in phosphonic and polymeric inhibitors location, and a lack of causal relationship between antiscalant efficiency and scale particle habit modification. Finally, it is shown that the confocal microscopy of several fluorescent antiscalant blends is capable of providing unique information on their interrelationships during scale deposition.

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