Co-composting of fresh tobacco leaves and soil: an exploration on the utilization of fresh tobacco waste in farmland

Author(s):  
Huihui Di ◽  
Rui Wang ◽  
Xiaohong Ren ◽  
Jianqiang Deng ◽  
Xiaohua Deng ◽  
...  
Keyword(s):  
2022 ◽  
Vol 2160 (1) ◽  
pp. 012052
Author(s):  
Jun Wang ◽  
Bixia Jiang ◽  
Lan Liu ◽  
Lin Cao ◽  
Qinghua Yuan ◽  
...  

Abstract A large amount of industrial and agricultural wastes are generated in the tobacco industry, such as tobacco steams, tobacco stalks, and tobacco leaves. How to increase the economic added value of industrial and agricultural wastes is an important issue. It is a promising value-added way that these biological wastes are recycled into carbon materials with excellent electrochemical properties. Herein, biochar were prepared from tobacco waste biomass (mainly tobacco stems, tobacco stalks and tobacco leaves) through one-step carbonization. The as-obtained biochar exhibited high specific capacitance of 305.92 F·g−1 (tobacco stems), 328.07 F·g−1 (tobacco stalks), and 272.48 F·g−1 (tobacco leaves) at 1 A·g−1, when tested in a three-electrode system with 6 M KOH electrolyte. This study highlights the possibility of reusing tobacco waste to produce low-cost, green and high-performance carbon-based electrode materials for sustainable electrochemical energy storage systems.


Author(s):  
S. Edith Taylor ◽  
Patrick Echlin ◽  
May McKoon ◽  
Thomas L. Hayes

Low temperature x-ray microanalysis (LTXM) of solid biological materials has been documented for Lemna minor L. root tips. This discussion will be limited to a demonstration of LTXM for measuring relative elemental distributions of P,S,Cl and K species within whole cells of tobacco leaves.Mature Wisconsin-38 tobacco was grown in the greenhouse at the University of California, Berkeley and picked daily from the mid-stalk position (leaf #9). The tissue was excised from the right of the mid rib and rapidly frozen in liquid nitrogen slush. It was then placed into an Amray biochamber and maintained at 103K. Fracture faces of the tissue were prepared and carbon-coated in the biochamber. The prepared sample was transferred from the biochamber to the Amray 1000A SEM equipped with a cold stage to maintain low temperatures at 103K. Analyses were performed using a tungsten source with accelerating voltages of 17.5 to 20 KV and beam currents from 1-2nA.


2013 ◽  
Vol 38 (2) ◽  
pp. 374-379 ◽  
Author(s):  
Zhi-Li PAN ◽  
Meng QI ◽  
Chun-Yang WEI ◽  
Feng LI ◽  
Shi-Xiang ZHANG ◽  
...  

2018 ◽  
Author(s):  
Benedict M. Long ◽  
Wei Yih Hee ◽  
Robert E. Sharwood ◽  
Benjamin D. Rae ◽  
Sarah Kaines ◽  
...  
Keyword(s):  

BIO-PROTOCOL ◽  
2013 ◽  
Vol 3 (5) ◽  
Author(s):  
Shunhua Ding ◽  
Xiaogang Wen ◽  
Congming Lu
Keyword(s):  

2021 ◽  
Vol 13 (8) ◽  
pp. 4481
Author(s):  
Marija Banožić ◽  
Antun Jozinović ◽  
Jovana Grgić ◽  
Borislav Miličević ◽  
Stela Jokić

Three fractions of tobacco waste (scrap, dust and midrib) were subjected to a high voltage electric discharge (HVED) assisted extraction procedure under different experimental conditions: solvent:solid ratio (300, 500, 700 mL/g), frequency (40, 70, 100 Hz) and treatment time (15, 30, 45 min), in order to study the influence of these conditions on the content of chlorogenic acid. The content of chlorogenic acid ranged from 1.54 to 3.66 mg/100 g for scrap, from 1.90 to 2.97 mg/100 g for dust, and from 2.30 to 3.38 mg/100 g for midrib extract, showing a strong dependence on the applied process parameters. The temperature change and the change in pH and electrical conductivity of the extracts after high voltage discharge treatment were also observed. The studied process parameters showed a statistically significant effect on the chemical and physical properties of the extracts from tobacco waste as well as on the content of chlorogenic acid, indicating the potential of HVED assisted processes in the separation of chlorogenic acid from tobacco industry waste. Multiple regression analysis was used to fit the results for the chlorogenic acid to a second order polynomial equation and the optimum conditions were determined.


1949 ◽  
Vol 180 (1) ◽  
pp. 37-45 ◽  
Author(s):  
Hubert.Bradford. Vickery ◽  
Marjorie D. Abrahams
Keyword(s):  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yaarit Kutsher ◽  
Michal Fisler ◽  
Adi Faigenboim ◽  
Moshe Reuveni

AbstractIt is widely known that during the reproductive stage (flowering), plants do not root well. Most protocols of shoot regeneration in plants utilize juvenile tissue. Adding these two realities together encouraged us to study the role of florigen in shoot regeneration. Mature tobacco tissue that expresses the endogenous tobacco florigen mRNA regenerates poorly, while juvenile tissue that does not express the florigen regenerates shoots well. Inhibition of Nitric Oxide (NO) synthesis reduced shoot regeneration as well as promoted flowering and increased tobacco florigen level. In contrast, the addition of NO (by way of NO donor) to the tissue increased regeneration, delayed flowering, reduced tobacco florigen mRNA. Ectopic expression of florigen genes in tobacco or tomato decreased regeneration capacity significantly. Overexpression pear PcFT2 gene increased regeneration capacity. During regeneration, florigen mRNA was not changed. We conclude that florigen presence in mature tobacco leaves reduces roots and shoots regeneration and is the possible reason for the age-related decrease in regeneration capacity.


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