化学和黏土矿物钝化剂对牛粪秸秆堆肥磷形态转化的影响
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国家重点研发计划"京津冀设施农业面源和重金属污染防控技术示范"(2016YFD0801006);国家重点研发计划"黄淮海集约化奶牛养殖污染防治技术模式研究与示范"(2017YFD0801404);河北省农业关键共性技术攻关专项(18226607D);河北现代农业产业技术体系奶牛产业创新团队(HBCT2018120206);河北现代农业产业技术体系蛋肉鸡产业创新团队(HBCT2018150209)


Effects of chemical and clay mineral additives on phosphorus transformation during cow manure and corn stover composting
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    摘要:

    盲目施用粪肥导致农田土壤磷素(P)积累和产生的面源污染等环境风险已引起人们的重视。该文通过在牛粪秸秆堆肥过程中,添加质量分数2.5%的化学物质或黏土矿物2类磷素钝化剂,研究其对磷素形态转化的影响。结果显示,和对照相比,添加氧化钙、氧化镁、硫酸亚铁和明矾可明显降低堆肥产品中磷素的活性,水溶性磷(water extract phosphorus,WEP)占总磷(total phosphorus,TP)百分比分别为:38.0%、60.2%、58.8%、28.9%;添加蛭石和沸石使堆肥产品中WEP占TP百分比分别下降11.7%、17.3%。第35天堆肥样品的Hedley磷分组结果显示,添加氧化钙和氧化镁主要促进了H2O-Pi向更稳定态的NaHCO3-Pi、HCl-P(Pi和Po)、残余态-P转化;添加硫酸亚铁和明矾主要促进了H2O-Pi向更稳定态的NaOH-P(Pi和Po)、残余态-P转化。添加黏土矿物钝化剂均略微促进了不稳定态磷H2O-Pi和NaHCO3-Pi向稳定态磷HCl-Pi转化。堆肥结束时添加MgO明显提高了堆体的pH值,其他处理均对pH值影响较小。综合来看硫酸亚铁、明矾、沸石和蛭石依次为较好的磷素钝化材料。

    Abstract:

    Although livestock manure is an excellent fertilizer and its composting can become into more stable and nutritional organic fertilizer, it typically has a low N/P ratio compared with crop requirements. The overuse of manures leads to serious phosphorus (P) accumulation in soil, especially in vegetable and fruit production process that increased the potential of P loss in runoff making it became one of the major P sources to eutrophic water bodies. In order to decrease the risk of P runoff from fields with organic fertilizer input, several kinds of additives in organic fertilizer were studied in recent years. In current study, two kinds of additives, chemical substances (calcium oxide (CaO), magnesium oxide (MgO), ferrous sulfate (FeSO4·7H2O), alum (KAl(SO4)2·12H2O),) and clay mineral (vermiculite, zeolite, medical stone, bentonite), were chosen to study their potential effects on P stabilization, forms and transformation during cow manures and corn stalk composting. The addition ratio of additives was 2.5% of the dry weight of the compost material in different treatments. The evolution of total phosphorus (TP) and phosphorus speciation of compost were analyzed during the 35 days' composting process, while the solid samples were taken at various stages (the 0, 3rd, 7th, 10th, 14th, 21st, 28th, 35th day) of composting. Furthermore, the P contents and fractionation in composted products on 35th day were analyzed using Hedley P fractionation method, and were sequentially extracted by deionized water (H2O-P), NaHCO3 (NaHCO3-P), NaOH (NaOH-P), HCl (HCl-P) and H2SO4-H2O2 (Residual-P). The results showed that compared with the control treatment, the addition of CaO, MgO, FeSO4 and KAl(SO4)2 significantly decreased the percentage of water extracted phosphorus (WEP) in TP by 38.0%, 60.2%, 58.8% and 28.9% after 35 days composting, respectively. Adding the vermiculite and zeolite decreased the percentage of WEP in TP by 11.7%, 17.3%, respectively. The results of Hedley P fractionation showed that the addition of CaO and MgO mainly decreased the proportion of H2O-Pi, whereas increased the proportion of NaHCO3-Pi, HCl-Pi and HCl-Po, residual-P. The addition of FeSO4 and KAl(SO4)2 mainly decreased the proportion of H2O-Pi, whereas increased the proportion of NaOH-Pi and NaOH-Po, residual-P. For the addition of clay minerals, we all observed a slight decrease in H2O-Pi and NaHCO3-Pi, and a slight rise in HCl-Pi. The addition of MgO greatly increased the pH value, which may delay the composting process and increase ammonia volatilization, while the other additives had little effect on pH value changing. Therefore, FeSO4, KAl(SO4)2, zeolite and vermiculite had relative better performance for stabilizing P during cow manure composting.

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郜斌斌,王选,王珏,樊秉乾,常瑞雪,陈清.化学和黏土矿物钝化剂对牛粪秸秆堆肥磷形态转化的影响[J].农业工程学报,2019,35(2):242-249. DOI:10.11975/j. issn.1002-6819.2019.02.031

Gao Binbin, Wang Xuan, Wang Jue, Fan Bingqian, Chang Ruixue, Chen Qing. Effects of chemical and clay mineral additives on phosphorus transformation during cow manure and corn stover composting[J]. Transactions of the Chinese Society of Agricultural Engineering (Transactions of the CSAE),2019,35(2):242-249. DOI:10.11975/j. issn.1002-6819.2019.02.031

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  • 收稿日期:2018-04-25
  • 最后修改日期:2019-01-11
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  • 在线发布日期: 2019-01-21
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