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231224s2013 xx |||||o 00| ||eng c |
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|a 10.2166/wst.2013.540
|2 doi
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|a pubmed24n0779.xml
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Yu, Rongtai
|e verfasserin
|4 aut
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|a Ammonium removal from wastewater via struvite pyrolysate recycling with Mg(OH)2 addition
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|c 2013
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 13.03.2014
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|a Date Revised 07.12.2022
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|a published: Print
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|a Citation Status MEDLINE
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|a Magnesium ammonium phosphate (MAP) pyrolysate recycling technology was investigated with Mg(OH)2-mediated pyrolysis. The results revealed that the removal ratio of ammonium was stable at about 75%, and could be increased to 79% after additional acidolysis. The phosphate concentration in the supernate was low at 2 mg/L. The optimum conditions for ammonia release were a 1:1 molar ratio of Mg(OH)2:NH4(+), a heating temperature of 110 °C and a heating time of 3 h. With continual additions of Mg(OH)2 to release ammonia, magnesium phosphate (Mg3(PO4)2) was suggested as a possible derivative. However, with Mg(OH)2-mediated pyrolysis, the growth and nucleation of MAP was inhibited during MAP pyrolysate recycling
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Ammonium Compounds
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|a Magnesium Compounds
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|a Phosphates
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|a Waste Water
|2 NLM
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|a Water Pollutants, Chemical
|2 NLM
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|a Struvite
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|a AW3EJL1462
|2 NLM
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|a Magnesium Hydroxide
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|a NBZ3QY004S
|2 NLM
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| 700 |
1 |
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|a Cheng, Subin
|e verfasserin
|4 aut
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|a Ren, Hongqiang
|e verfasserin
|4 aut
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|a Wang, Yanru
|e verfasserin
|4 aut
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|a Ding, Lili
|e verfasserin
|4 aut
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|a Geng, Jinju
|e verfasserin
|4 aut
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|a Xu, Ke
|e verfasserin
|4 aut
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| 700 |
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|a Zhang, Yan
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Water science and technology : a journal of the International Association on Water Pollution Research
|d 1986
|g 68(2013), 12 vom: 19., Seite 2661-7
|w (DE-627)NLM098149431
|x 0273-1223
|7 nnns
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| 773 |
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|g volume:68
|g year:2013
|g number:12
|g day:19
|g pages:2661-7
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|u http://dx.doi.org/10.2166/wst.2013.540
|3 Volltext
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