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Pleistocene lakes and paleohydrologic environments of the Tecopa basin, California: Constraints on the drainage integration of the Amargosa River 期刊论文
GEOLOGICAL SOCIETY OF AMERICA BULLETIN, 2020, 132 (7-8) : 1537-1565
作者:  Reheis, Marith C.;  Caskey, John;  Bright, Jordon;  Paces, James B.;  Mahan, Shannon A.;  Wan, Elmira
收藏  |  浏览/下载:10/0  |  提交时间:2020/08/18
Physico-chemical characterization of urban aerosols from specific combustion sources in West Africa at Abidjan in Cote d'Ivoire and Cotonou in Benin in the frame of the DACCIWA program 期刊论文
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2020, 20 (9) : 5327-5354
作者:  Adon, Aka Jacques;  Liousse, Catherine;  Doumbia, Elhadji Thierno;  Baeza-Squiban, Armelle;  Cachier, Helene;  Leon, Jean-Francois;  Yoboue, Veronique;  Akpo, Aristique Barthel;  Galy-Lacaux, Corinne;  Guinot, Benjamin;  Zouiten, Cyril;  Xu, Hongmei;  Gardrat, Eric;  Keita, Sekou
收藏  |  浏览/下载:7/0  |  提交时间:2020/07/02
Characterising the levels and sources of the historical metal contamination in the atmosphere of Montreal (Canada) from 1973 to 2013 by coupling chemistry and Lead and Osmium isotope ratios 期刊论文
ATMOSPHERIC RESEARCH, 2020, 235
作者:  Bagur, M.;  Widory, D.
收藏  |  浏览/下载:0/0  |  提交时间:2020/07/02
An engineered PET depolymerase to break down and recycle plastic bottles 期刊论文
NATURE, 2020, 580 (7802) : 216-+
作者:  Zhao, Evan Wenbo;  Liu, Tao;  Jonsson, Erlendur;  Lee, Jeongjae;  Temprano, Israel;  Jethwa, Rajesh B.;  Wang, Anqi;  Smith, Holly;  Carretero-Gonzalez, Javier;  Song, Qilei;  Grey, Clare P.
收藏  |  浏览/下载:86/0  |  提交时间:2020/07/03

Present estimates suggest that of the 359 million tons of plastics produced annually worldwide(1), 150-200 million tons accumulate in landfill or in the natural environment(2). Poly(ethylene terephthalate) (PET) is the most abundant polyester plastic, with almost 70 million tons manufactured annually worldwide for use in textiles and packaging(3). The main recycling process for PET, via thermomechanical means, results in a loss of mechanical properties(4). Consequently, de novo synthesis is preferred and PET waste continues to accumulate. With a high ratio of aromatic terephthalate units-which reduce chain mobility-PET is a polyester that is extremely difficult to hydrolyse(5). Several PET hydrolase enzymes have been reported, but show limited productivity(6,7). Here we describe an improved PET hydrolase that ultimately achieves, over 10 hours, a minimum of 90 per cent PET depolymerization into monomers, with a productivity of 16.7 grams of terephthalate per litre per hour (200 grams per kilogram of PET suspension, with an enzyme concentration of 3 milligrams per gram of PET). This highly efficient, optimized enzyme outperforms all PET hydrolases reported so far, including an enzyme(8,9) from the bacterium Ideonella sakaiensis strain 201-F6 (even assisted by a secondary enzyme(10)) and related improved variants(11-14) that have attracted recent interest. We also show that biologically recycled PET exhibiting the same properties as petrochemical PET can be produced from enzymatically depolymerized PET waste, before being processed into bottles, thereby contributing towards the concept of a circular PET economy.


Computer-aided engineering produces improvements to an enzyme that breaks down poly(ethylene terephthalate) (PET) into its constituent monomers, which are used to synthesize PET of near-petrochemical grade that can be further processed into bottles.


  
Investigation of the global methane budget over 1980-2017 using GFDL-AM4.1 期刊论文
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2020, 20 (2) : 805-827
作者:  He, Jian;  Naik, Vaishali;  Horowitz, Larry W.;  Dlugokencky, Ed;  Thoning, Kirk
收藏  |  浏览/下载:7/0  |  提交时间:2020/07/02
Gram-scale bottom-up flash graphene synthesis 期刊论文
NATURE, 2020, 577 (7792) : 647-651
作者:  Long, Haizhen;  Zhang, Liwei;  Lv, Mengjie;  Wen, Zengqi;  Zhang, Wenhao;  Chen, Xiulan;  Zhang, Peitao;  Li, Tongqing;  Chang, Luyuan;  Jin, Caiwei;  Wu, Guozhao;  Wang, Xi;  Yang, Fuquan;  Pei, Jianfeng;  Chen, Ping;  Margueron, Raphael;  Deng, Haiteng;  Zhu, Mingzhao;  Li, Guohong
收藏  |  浏览/下载:14/0  |  提交时间:2020/07/03

Most bulk-scale graphene is produced by a top-down approach, exfoliating graphite, which often requires large amounts of solvent with high-energy mixing, shearing, sonication or electrochemical treatment(1-3). Although chemical oxidation of graphite to graphene oxide promotes exfoliation, it requires harsh oxidants and leaves the graphene with a defective perforated structure after the subsequent reduction step(3,4). Bottom-up synthesis of high-quality graphene is often restricted to ultrasmall amounts if performed by chemical vapour deposition or advanced synthetic organic methods, or it provides a defect-ridden structure if carried out in bulk solution(4-6). Here we show that flash Joule heating of inexpensive carbon sources-such as coal, petroleum coke, biochar, carbon black, discarded food, rubber tyres and mixed plastic waste-can afford gram-scale quantities of graphene in less than one second. The product, named flash graphene (FG) after the process used to produce it, shows turbostratic arrangement (that is, little order) between the stacked graphene layers. FG synthesis uses no furnace and no solvents or reactive gases. Yields depend on the carbon content of the source  when using a high-carbon source, such as carbon black, anthracitic coal or calcined coke, yields can range from 80 to 90 per cent with carbon purity greater than 99 per cent. No purification steps are necessary. Raman spectroscopy analysis shows a low-intensity or absent D band for FG, indicating that FG has among the lowest defect concentrations reported so far for graphene, and confirms the turbostratic stacking of FG, which is clearly distinguished from turbostratic graphite. The disordered orientation of FG layers facilitates its rapid exfoliation upon mixing during composite formation. The electric energy cost for FG synthesis is only about 7.2 kilojoules per gram, which could render FG suitable for use in bulk composites of plastic, metals, plywood, concrete and other building materials.


Flash Joule heating of inexpensive carbon sources is used to produce gram-scale quantities of high-quality graphene in under a second, without the need for a furnace, solvents or reactive gases.


  
Redox-switchable carboranes for uranium capture and release 期刊论文
NATURE, 2020, 577 (7792) : 652-+
作者:  Marques, Joao C.;  Li, Meng;  Schaak, Diane;  Robson, Drew N.;  Li, Jennifer M.
收藏  |  浏览/下载:31/0  |  提交时间:2020/07/03

The uranyl ion (UO22+  U(vi) oxidation state) is the most common form of uranium found in terrestrial and aquatic environments and is a central component in nuclear fuel processing and waste remediation efforts. Uranyl capture from either seawater or nuclear waste has been well studied and typically relies on extremely strong chelating/binding affinities to UO22+ using chelating polymers(1,2), porous inorganic(3-5) or carbon-based(6,7) materials, as well as homogeneous(8) compounds. By contrast, the controlled release of uranyl after capture is less established and can be difficult, expensive or destructive to the initial material(2,9). Here we show how harnessing the redox-switchable chelating and donating properties of an ortho-substituted closo-carborane (1,2-(Ph2PO)(2)-1,2-C2B10H10) cluster molecule can lead to the controlled chemical or electrochemical capture and release of UO22+ in monophasic (organic) or biphasic (organic/aqueous) model solvent systems. This is achieved by taking advantage of the increase in the ligand bite angle when the closo-carborane is reduced to the nido-carborane, resulting in C-C bond rupture and cage opening. The use of electrochemical methods for uranyl capture and release may complement existing sorbent and processing systems.


Redox-switchable chelation is demonstrated for a carborane cluster molecule, leading to controlled chemical or electrochemical capture and release of uranyl in monophasic or biphasic model solvent systems.


  
The impact of sea-salt aerosols on particulate inorganic nitrogen deposition in the western Taiwan Strait region, China 期刊论文
ATMOSPHERIC RESEARCH, 2019, 228: 68-76
作者:  Wu, Shui-Ping;  Dai, Lu-Hong;  Zhu, Heng;  Zhang, Ning;  Yan, Jin-Pei;  Schwab, James J.;  Yuan, Chung-Shin
收藏  |  浏览/下载:10/0  |  提交时间:2019/11/27
Sea-salt aerosol  Size distribution  Inorganic nitrogen  Nitrogen deposition flux  
Contributions of Nordic anthropogenic emissions on air pollution and premature mortality over the Nordic region and the Arctic 期刊论文
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2019, 19 (20) : 12975-12992
作者:  Im, Ulas;  Christensen, Jesper H.;  Nielsen, Ole-Kenneth;  Sand, Maria;  Makkonen, Risto;  Geels, Camilla;  Anderson, Camilla;  Kukkonen, Jaakko;  Lopez-Aparicio, Susana;  Brandt, Jorgen
收藏  |  浏览/下载:9/0  |  提交时间:2019/11/27
Nepal emission inventory - Part I: Technologies and combustion sources (NEEMI-Tech) for 2001-2016 期刊论文
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2019, 19 (20) : 12953-12973
作者:  Sadavarte, Pankaj;  Rupakheti, Maheswar;  Bhave, Prakash;  Shakya, Kiran;  Lawrence, Mark
收藏  |  浏览/下载:9/0  |  提交时间:2019/11/27