There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality.

Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …

I and i

1.0. Introduction 4044 2.0. Biomass Chemistry and Growth Rates 4047 2.1. Lignocellulose and Starch-Based Plants 4047 2.2. Triglyceride-Producing Plants 4049 2.3. Algae 4050 2.4. Terpenes and Rubber-Producing Plants 4052 3.0. Biomass Gasification 4052 3.1. Gasification Chemistry 4052 3.2. Gasification Reactors 4054 3.3. Supercritical Gasification 4054 3.4. Solar Gasification 4055 3.5. Gas Conditioning 4055 4.0. Syn-Gas Utilization 4056 4.1. Hydrogen Production by Water−Gas Shift Reaction 4056

/pdf/synthesis-of-transportation-fuels-from-biomass-chemistry-3sckhzoqoz.pdf

Synthesis of transportation fuels from biomass: chemistry, catalysts, and engineering.

Sustainable production of renewable energy is being hotly debated globally since it is increasingly understood that first generation biofuels, primarily produced from food crops and mostly oil seeds are limited in their ability to achieve targets for biofuel production, climate change mitigation and economic growth. These concerns have increased the interest in developing second generation biofuels produced from non-food feedstocks such as microalgae, which potentially offer greatest opportunities in the longer term. This paper reviews the current status of microalgae use for biodiesel production, including their cultivation, harvesting, and processing. The microalgae species most used for biodiesel production are presented and their main advantages described in comparison with other available biodiesel feedstocks. The various aspects associated with the design of microalgae production units are described, giving an overview of the current state of development of algae cultivation systems (photo-bioreactors and open ponds). Other potential applications and products from microalgae are also presented such as for biological sequestration of CO 2 , wastewater treatment, in human health, as food additive, and for aquaculture.

/pdf/microalgae-for-biodiesel-production-and-other-applications-a-54vmwufrsu.pdf

Microalgae for biodiesel production and other applications: A review

Biomass is an important feedstock for the renewable production of fuels, chemicals, and energy. As of 2005, over 3% of the total energy consumption in the United States was supplied by biomass, and it recently surpassed hydroelectric energy as the largest domestic source of renewable energy. Similarly, the European Union received 66.1% of its renewable energy from biomass, which thus surpassed the total combined contribution from hydropower, wind power, geothermal energy, and solar power. In addition to energy, the production of chemicals from biomass is also essential; indeed, the only renewable source of liquid transportation fuels is currently obtained from biomass.

The Catalytic Valorization of Lignin for the Production of Renewable Chemicals

Biofuels produced from various lignocellulosic materials, such as wood, agricultural, or forest residues, have the potential to be a valuable substitute for, or complement to, gasoline. Many physicochemical structural and compositional factors hinder the hydrolysis of cellulose present in biomass to sugars and other organic compounds that can later be converted to fuels. The goal of pretreatment is to make the cellulose accessible to hydrolysis for conversion to fuels. Various pretreatment techniques change the physical and chemical structure of the lignocellulosic biomass and improve hydrolysis rates. During the past few years a large number of pretreatment methods have been developed, including alkali treatment, ammonia explosion, and others. Many methods have been shown to result in high sugar yields, above 90% of the theoretical yield for lignocellulosic biomasses such as woods, grasses, corn, and so on. In this review, we discuss the various pretreatment process methods and the recent literature that...

http://ucce.ucdavis.edu/files/datastore/234-1388.pdf

Methods for Pretreatment of Lignocellulosic Biomass for Efficient Hydrolysis and Biofuel Production

Chemical Conversion of Biomass Resources to Useful Chemicals and Fuels by Supercritical Water Treatment

Delignification studies on 0.5 μm sections of Douglas-fir earlywood tracheids pulped by soda, soda-anthraquinone (soda/AQ) and kraft pulping processes were performed by determining bromine concentrations in various morphological regions with SEM-EDXA technique. Soda/AQ pulping was much more selective in removing lignin from the middle lamella regions than either soda or kraft pulping. However, up to 50% delignification, more lignin was removed from the secondary wall by soda or kraft, compared to soda/AQ pulping. The kinetics of lignin removal in the various morphological regions were established. Addition of AQ and sodium sulfide resulted in an earlier transition from a slow initial to a rapid bulk delignification, particularly in the middle lamella, and in an enhanced bulk delignification in the secondary wall. Anthraquinone was also found to promote residual delignification in the secondary wall, where sodium sulfide was not effective. The opposite was observed for the bulk delignification in the middle lamella, where only sodium sulfide addition improved the rate significantly. The great differences observed in the bulk delignification rates between middle lamella and secondary wall in soda pulping as well as their response to additives suggest structural differences between middle lamella and secondary wall lignins.

Topochemistry of delignification in Douglas-fir wood with soda, soda-anthraquinone and karft pulping as determined by SEM-EDXA

Strong interactions during lignin pyrolysis in wood – A study by in situ probing of the radical chain reactions using model dimers

An effort was made to develop photocatalytic TiO2 crystallite–activated carbon (TiO2-AC) composites from tetraisopropyl titanate (TPT)-soaked activated carbon in supercritical isopropanol. It was subsequently found that TPT in supercritical isopropanol could be effectively converted to the anatase form of the TiO2 crystallites. The prepared composites, composed of activated carbon as an adsorbent and the anatase form of TiO2 as a photocatalyst, were evaluated for their adsorption capacity and subsequent photocatalytic activity against formaldehyde, one of the harmful air pollutants in the environment. As a result, the supercritically treated TiO2–AC composites, particularly at 300°C and 350°C, had much higher formaldehyde-decomposing ability compared to a noncomposite comprising a simple mixture of activated carbon and TiO2 granules. This indicates that the supercritical treatment can be effective for preparing the photocatalytic composites that have a high synergetic effect of adsorption and photocatalytic decomposition of formaldehyde for environmental cleaning.

Photocatalytic activity of TiO2 crystallite-activated carbon composites prepared in supercritical isopropanol for the decomposition of formaldehyde

https://repository.kulib.kyoto-u.ac.jp/dspace/bitstream/2433/134799/1/j.carres.2010.10.018.pdf

Shiro Saka

Papers

Chemical Conversion of Biomass Resources to Useful Chemicals and Fuels by Supercritical Water Treatment

Topochemistry of delignification in Douglas-fir wood with soda, soda-anthraquinone and karft pulping as determined by SEM-EDXA

Strong interactions during lignin pyrolysis in wood – A study by in situ probing of the radical chain reactions using model dimers

Photocatalytic activity of TiO2 crystallite-activated carbon composites prepared in supercritical isopropanol for the decomposition of formaldehyde

Thermal glycosylation and degradation reactions occurring at the reducing ends of cellulose during low-temperature pyrolysis.