CAJ | 학술논문

为了降低厨余垃圾堆肥过程中 NH3和 H2S 恶臭气体的排放，该研究通过向堆肥物料中添加H3PO4+Mg(OH)2、Ca(H2PO4)2、FeCl3和β环糊精4种不同的氮素控制材料，同时以不添加控制材料的处理作为对照，研究控制材料添加对NH3和H2S排放的影响。结果表明控制材料的添加降低了堆肥体系的pH值，明显降低了堆肥物料的损失率；从电导率（electric conductivity）和发芽率指数（germination index）来看，5个处理的堆肥产品均达到腐熟的要求；4种控制材料的添加均不同程度减少了NH3和H2S的排放，但是减排机理不尽相同。总体来看FeCl3对NH3和H2S的控制效果最好，与对照相比，NH3和H2S的累积排放量分别降低了64.2%和52.0%。该研究结果为厨余垃圾堆肥过程中恶臭物质控制材料的筛选提供参考。
위료강저주여랄급퇴비과정중 NH3화 H2S 악취기체적배방，해연구통과향퇴비물료중첨가H3PO4+Mg(OH)2、Ca(H2PO4)2、FeCl3화β배호정4충불동적담소공제재료，동시이불첨가공제재료적처리작위대조，연구공제재료첨가대NH3화H2S배방적영향。결과표명공제재료적첨가강저료퇴비체계적pH치，명현강저료퇴비물료적손실솔；종전도솔（electric conductivity）화발아솔지수（germination index）래간，5개처리적퇴비산품균체도부숙적요구；4충공제재료적첨가균불동정도감소료NH3화H2S적배방，단시감배궤리불진상동。총체래간FeCl3대NH3화H2S적공제효과최호，여대조상비，NH3화H2S적루적배방량분별강저료64.2%화52.0%。해연구결과위주여랄급퇴비과정중악취물질공제재료적사선제공삼고。
In order to reduce odor emissions such as NH3 and H2S, this study designed experiments to investigate the effects of H3PO4+Mg(OH)2, Ca(H2PO4)2, FeCl3, andβcyclodextrin on producing and releasing NH3 and H2S during kitchen waste composting. The composting treatment without adding chemical materials was used as control. The kitchen waste consisted of 53%vegetation waste, 24%fruit wall, 19%meat, and 4%leaves. For all treatments, cornstalks as an additive using the wet weight ration of 1:5.7 were added to the kitchen waste composting. All treatments were analyzed using 60 L heat insulated composting vessels with forced aeration systems. The vessels were controlled by the C-LGX program, which enables aeration to be controlled automatically by time or inside temperature. Aeration consisted of pumping ambient air into the reactor continuously at a rate of 0.2 L/(kg·min) dry matter. The TKN and TOC were determined according to the Chinese national standard (NY 525-2002). The pH, EC, and GI were determined in water extracts (20 g of dry weight compost were extracted with 200 ml of distilled water, stirred for 1 h, and then centrifuged at 4000 rpm). pH value was measured with a pH meter, electrical conductivity (EC) was measured by a DDS-12A conductivity meter. The moisture content was determined by drying the samples at 105℃, until the weight was unvarying. The boric acid titration method was used to determine ammonia emission. The H2S content was analyzed daily using a portable biogas analyzer. Composting gas samples were extracted using a suction pump (built-in biogas analyzer, gas flow:550 mL/min), and then transferred to the inlet port of the biogas analyzer via a Teflon hose that contained a filter element (2.0μm PTFE) installed in the middle of the pipe. The measurement was taken for about 90 seconds, and the measured value of H2S was read directly from the screen. The results showed that adding nitrogen control material reduced the pH of the composting systems, and the loss rate of the composting materials obviously decreased compared with CK. The analysis of phytotoxicity indexes of EC and GI showed that all treatments reached the compost maturity requirements. Four kinds of control materials could all decrease NH3 and H2S emissions, but the reduction mechanism are not the same. Compared with treatment CK, the cumulative emissions of NH3 were reduced by 49.5%, 38.5%, 64.2%, and 62.7%, and the cumulative emissions of H2S were reduced by 39.2%, 5.9%, 52.0%and 47.8%for the treatments of P+M, CaP, FC, and CD, respectively. After integrating the reduction of NH3 and H2S emission and the phytotoxicity of compost, FeCl3 was the best nitrogen and sulfur conservation material during kitchen waste composting in this work. This study can provide a reference for the screening of odor control materials in a kitchen waste composting process.