ABSTRACT
Human living environments and health are seriously affected by the odor produced from fermentation of livestock and poultry manure. In order to reduce the odor pollution caused by livestock and poultry manure, efficient strains were screened and two methods were tried in this study. The orthogonal test design was used to analyze the gas produced by pig manure under different conditions of temperature, time, wheat straw doping amount and calcium carbonate doping amount. Then, according to ammonia, hydrogen sulfide and comprehensive odor removal effects, the high efficiency of deodorizing strains were screened. The results showed that pig manure produced the least odor when the temperature was 20 °C, added 0% calcium carbonate, 20% wheat straw and waited for 48 h. Three strains were screened to inhibit the odor production of pig manure: Paracoccus denitrificans, Bacillus licheniformis and Saccharomyces cerevisiae, showed that their highest removal rate of ammonia and hydrogen sulfide gas could reach 96.58% and 99.74% among them; while for three strains of end-control pig manure stench: Pichia kudriavzevii, P. denitrificans and Bacillus subtilis, the highest removal rate of ammonia and hydrogen sulfide gas reached 85.91% and 90.80% among them. This research provides bacteria resources as the high-efficiency deodorizing function for the source suppression and the end treatment of the odor gas of pig manure, which has high application value for the control of odor pollution.
ABSTRACT
Hierarchically porous metal-organic frameworks (MOFs) have recently emerged as a novel crystalline hybrid material with tunable porosity. Many efforts have been made to develop hierarchically porous MOFs, yet their low-energy fabrication remains a challenge and the underlying mechanism is still unknown. In this study, the rapid fabrication of two hierarchically porous MOFs (Cu-BTC and ZIF-8) was carried out at room temperature and ambient pressure for 10 min using a novel surfactant as the template in a (Cu, Zn) hydroxy double salt (HDS) solution, where the (Cu, Zn) HDS accelerated the nucleation of crystals and the anionic surfactants served as templates to fabricate mesopores and macropores. The growth mechanism of hierarchically porous MOFs was analyzed via mesodynamics (MesoDyn) simulation, and then the synthetic mechanism of hierarchically porous MOFs at the molecular level was obtained. The as-synthesized hierarchically porous Cu-BTC showed a high uptake capacity of 646 mg g-1, which is about 25% higher as compared with microporous Cu-BTC (516 mg g-1) for the capture of toluene. This study provides a theoretical basis for the large-scale fabrication of hierarchically porous MOFs and offers a reference for the understanding of their synthetic mechanism.
ABSTRACT
Large pore sizes, high pore volumes, facile synthesis conditions, and high space-time yields are recognized as four crucial criteria in the fabrication of metal-organic frameworks (MOFs). However, these four objectives are rarely realized together. Herein, we have developed a simple and versatile method that employs 1,4-butanediamine (BTDM) as a template for rapidly fabricating four stable hierarchically porous MOFs (H-MOFs), including HKUST-1, ZIF-8, ZIF-67, and ZIF-90. The synthesis conditions are simple and facile at room temperature and ambient pressure, and the synthesis time can be shortened to 1 min. The resultant H-MOFs exhibit multimodal hierarchically porous structures with meso- and macropores interconnected with micropores, as well as high pore volumes (0.76 cm3 g-1). The maximum space-time yield for the hierarchically porous HKUST-1 reaches 7.4 × 104 kg m-3 d-1, at least one order of magnitude higher than previous reported yields. Notably, the additive BTDM not only facilitates crystal growth but also guides the formation of meso- and macropores. The synthesis route is highly versatile, as analogues (e.g., tetramethyl-1,3-diaminopropane and tetramethyldiaminomethane) can also be employed as templates to prepare diverse H-MOFs. Furthermore, the porosities of the H-MOFs are readily tuned by controlling the metal source, template amount and type of template. The as-synthesized H-MOFs act as adsorbents with significantly improved performances relative to those of microporous MOFs used for CH4 and CO2 gas storage. This strategy may aid in the large-scale industrial synthesis of desirable H-MOFs for gas storage.
