Chemical precipitation for controlling nitrogen loss during composting.

Aimed at controlling the nitrogen loss during composting, the mixture of magnesium hydroxide (Mg(OH)( 2)) and phosphoric acid (H(3)PO(4)) (molar ratio 1:2) were utilized as additives to avoid increasing total salinity. In trial TA, the additives were put into absorption bottles connecting with a gas outlet of fermentor (ex situ method); in trial TB, the additives were directly added to the composting materials (in situ method). During the 26 day composting period, the temperature, pH, total organic carbon (TOC), total nitrogen (TN), ammonium nitrogen (NH(4)(+)-N), total phosphorus (TP), available phosphorus (AP) and germination index (GI) were measured. The experimental results show that the additives reduced the pH, while NH( 4)(+)-N and TN were obviously improved. NH(4)( +)-N was 11.9 g kg(-1) and 3 g kg(- 1) in amended compost trial (TB) and unamended compost trial (TA), respectively; TN increased from 26.5 g kg(-1) to 40.3 g kg(-1) in TB and increased from 26.5 g kg( -1) to 26.8 g kg(-1) in TA. Analysis of the TOC and carbon mass revealed that absorbents accelerated the degradation of organic matter. The germination index test showed the maturity of TB (102%) was better than TA (82%) in final compost. Furthermore, TP and AP were also obviously improved. X-ray diffraction analysis of precipitation showed that the precipitation in absorption bottle of TA was newberyite (MgHPO( 4) 3H(2)O), however, the crystal in the TB compost was struvite (MgNH(4)PO(4) 6H(2)O: magnesium ammonium phosphate). These results indicated that Mg(OH)(2) and H(3)PO( 4) could reduce the ammonia emission by struvite crystallization reaction. Optimal conditions for struvite precipitation should be determined for different systems.