Characteristics of water quality and bacterial communities in three water supply pipelines.

Many cities in China have implemented urban water supply pipe network renovation projects; however, at the beginning of new pipeline replacements, customers often complain about water quality problems, such as red water, odour and other water quality problems. To overcome these frequent water quality problems, this study selected a commonly used ductile cast iron (DCI) pipe, stainless steel (SS) pipe and high-density polyethylene (HDPE) pipe for laboratory simulations of the water quality regularity of new pipes, the variations in pipe inner walls, and the presence of microbial communities. Based on the research results, combined with actual water sample analysis, the stabilisation time of the interaction between the tubings inner walls and bulk water was determined, to allow pipeline cleaning and water quality maintenance. The results showed that the water quality change in the DCI was the most significant, while the SS and the HDPE pipes showed consistent changes with severe initial deterioration, then later stabilisation to meet the required standard. The DCI inner wall changed from a loose porous particle shape to a relatively dense and irregular three-dimensional shape, with the constituent elements mainly being O and Ca. The SS inner wall had a uniform structure in the early stage, but are obvious spherical balls of different sizes formed later, with the elemental composition here mainly being C and O. The HDPE inner wall was smooth and had small perforations in the early stage, while the perforation in the middle and late stages increased to become rough and scale-like at a much later stage. The proportion of Proteobacteria in effluents (72.82% to 86.87%) was significantly increased compared with the influent (48.45%), while the proportion of Proteobacteria (86.87%) in the DCI was significantly higher than in the SS (74.28%) and HDPE pipes (81.68%). Moreover, compared with the influent (23.33%), the Bacteroidetes (2.79% to 3.32%) levels in the effluents were significantly reduced, indicating that the pipe material affects the microbial abundance in water.

Effect of bacterial communities on the formation of cast iron corrosion tubercles in reclaimed water.

To understand the role bacterial communities play in corrosion scale development, the morphological and physicochemical characteristics of corrosion scales in raw and disinfected reclaimed water were systematically investigated. Corrosion tubercles were found in raw reclaimed water while thin corrosion layers formed in disinfected reclaimed water. The corrosion tubercles, composed mainly of α-FeOOH, γ-FeOOH, and CaCO3, consisted of an top surface; a shell containing more magnetite than other layers; a core in association with stalks produced by bacteria; and a corroded layer. The thin corrosion layers also had layered structures. These had a smooth top, a dense middle, and a corroded layer. They mostly consisted of the same main components as the tubercles in raw reclaimed water, but with different proportions. The profiles of the dissolved oxygen (DO) concentration, redox potential, and pH in the tubercles were different to those in the corrosion layers, which demonstrated that these parameters changed with a shift in the microbial processes in the tubercles. The bacterial communities in the tubercles were found to be dominated by Proteobacteria (56.7%), Bacteroidetes (10.0%), and Nitrospira (6.9%). The abundance of sequences affiliated to iron-reducing bacteria (IRB, mainly Geothrix) and iron-oxidizing bacteria (mainly Aquabacterium) was relatively high. The layered characteristics of the corrosion layers was due to the blocking of DO transfer by the development of the scales themselves. Bacterial communities could at least promote the layering process and formation of corrosion tubercles. Possible mechanisms might include: (1) bacterial communities mediated the pH and redox potential in the tubercles (which helped to form shell-like and core layers), (2) the metabolism of IRB and magnetic bacteria (Magnetospirillum) might contribute to the presence of Fe3O4 in the shell-like layer, while IRB contributed to green rust in the core layer, and (3) the diversity of the bacterial community resulted in the complex composition of the core layer, and gas producing bacteria (sulfate-reducing bacteria and methanogenic bacteria) played a role in the formation of the porous core layer.

The mutual co-regulation of extracellular polymeric substances and iron ions in biocorrosion of cast iron pipes.

New insights into the biocorrosion process may be gained through understanding of the interaction between extracellular polymeric substances (EPS) and iron. Herein, the effect of iron ions on the formation of biofilms and production of EPS was investigated. Additionally, the impact of EPS on the corrosion of cast iron coupons was explored. The results showed that a moderate concentration of iron ions (0.06 mg/L) promoted both biofilm formation and EPS production. The presence of EPS accelerated corrosion during the initial stage, while inhibited corrosion at the later stage. The functional groups of EPS acted as electron shuttles to enable the binding of iron ions. Binding of iron ions with EPS led to anodic dissolution and promoted corrosion, while corrosion was later inhibited through oxygen reduction and availability of phosphorus from EPS. The presence of EPS also led to changes in crystalline phases of corrosion products.

Effect of extracellular polymeric substances on corrosion of cast iron in the reclaimed wastewater.

Microorganisms were cultured in the R2A medium with inoculum from biofilm in a reclaimed wastewater distribution system and then extracellular polymeric substances (EPS) were extracted from the culture. Characterization of EPS and their effects on the corrosion of cast iron were examined. EPS extracted from different culturing stages contained different proportions of protein and polysaccharide but with similar functional groups. All types of EPS could inhibit cast iron corrosion and the EPS from the stationary stage had the highest inhibition efficiency. The inhibition efficiency was increased with addition of a small amount of EPS while decreased with excessive amount of EPS. EPS formed a protective film on the metal surface, which retarded the cathodic reduction of oxygen. Excessive amount of EPS promoted anodic dissolution through EPS-Fe binding. The CO and C(O, N) in EPS could be the anodic electrochemical sites with possible products of C(C, H).