To seal off dangerous lead pipes, just add electricity

Science ◽  
2019 ◽  
Author(s):  
Robert Service
Keyword(s):  
1858 ◽  
Vol 13 (40) ◽  
pp. 318-318
Keyword(s):  

BMJ ◽  
1995 ◽  
Vol 310 (6991) ◽  
pp. 1408-1409
Author(s):  
E. Millstone ◽  
J. Russell

Minerals ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1047
Author(s):  
Jill Dill Pasteris ◽  
Yeunook Bae ◽  
Daniel E. Giammar ◽  
Sydney N. Dybing ◽  
Claude H. Yoder ◽  
...  

The identification and characterization of lead-bearing and associated minerals in scales on lead pipes are essential to understanding and predicting the mobilization of lead into drinking water. Despite its long-recognized usefulness in the unambiguous identification of crystalline and amorphous solids, distinguishing between polymorphic phases, and rapid and non-destructive analysis on the micrometer spatial scale, the Raman spectroscopy (RS) technique has been applied only occasionally in the analysis of scales in lead service lines (LSLs). This article illustrates multiple applications of RS not just for the identification of phases, but also compositional and structural characterization of scale materials in harvested lead pipes and experimental pipe-loop/recirculation systems. RS is shown to be a sensitive monitor of these characteristics through analyses on cross-sections of lead pipes, raw interior pipe walls, particulates captured in filters, and scrapings from pipes. RS proves to be especially sensitive to the state of crystallinity of scale phases (important to their solubility) and to the specific chemistry of phases precipitated upon the introduction of orthophosphate to the water system. It can be used effectively alone as well as in conjunction with more standard analytical techniques. By means of fiber-optic probes, RS has potential for in situ, real-time analysis within water-filled pipes.


1936 ◽  
Vol 26 (8) ◽  
pp. 778-780 ◽  
Author(s):  
G. N. Quam ◽  
Arthur Klein
Keyword(s):  

CORROSION ◽  
10.5006/0616 ◽  
2012 ◽  
Vol 68 (11) ◽  
pp. 1037-1048 ◽  
Author(s):  
J. Hu ◽  
F. Gan ◽  
S. Triantafyllidou ◽  
C.K. Nguyen ◽  
M.A. Edwards

The effect of added cupric ions (0 mg/L to 5 mg/L Cu+2) on possible deposition corrosion of lead pipe was investigated in bench-scale experiments under flowing and stagnant water conditions. Under stagnation the presence of cupric ions in the water feeding lead pipes marginally increased lead release into the water, but under continuous recirculation it could increase lead release by orders of magnitude. Other bench-scale experiments investigated galvanic corrosion between lead and copper pipes under stagnation, confirming that water chemistry (particularly the chloride-to-sulfate mass ratio [CSMR]) is a controlling factor in either “strengthening” galvanic corrosion and increasing water lead contamination by orders of magnitude (high CSMR water) or “weakening” the galvanic effect with less but still significant contribution to water lead contamination (low CSMR water). Longitudinal water pH measurements along the length of the galvanic rigs revealed a significant pH drop close to the lead:copper junction at relatively short stagnation times in high CSMR water, which is consistent with the observations of higher lead leaching and higher galvanic current measured in that situation.


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