Catalytic pyrolysis of crude glycerol over a shaped H-ZSM-5 zeolite catalyst with (partial) recycling of the product oil was studied with the incentive to improve benzene, toluene, and xylene (BTX) yields. Recycling of the polycyclic aromatic hydrocarbon (PAH) fraction, after separation from BTX by distillation and co-feeding with the crude glycerol feed, was shown to have a positive effect on the BTX yield. Further improvements were achieved by hydrogenation of the PAH fraction using a Ru/C catalyst and hydrogen gas prior to co-pyrolysis, and BTX yields up to 16 wt% on feed were obtained. The concept was also shown to be beneficial to other biomass feeds such as e.g., Kraft lignin, cellulose, and Jatropha oil.
DOCUMENT
The present invention relates to a novel process for the preparation of low molecular weight aromatic compounds such as benzene, toluene, and xylenes (BTX) from plastics. Provided is a thermo-catalytic pyrolysis process for the preparation of aromatic compounds from a feed stream comprising plastic, comprising the steps of: a) subjecting a feed stream comprising a plastic to a pyrolysis treatment at a pyrolysis temperature in the range of 600-1000°C to produce pyrolysis vapors; b) optionally cooling the pyrolysis vapors to a temperature that is below the pyrolysis temperature; c) contacting the vaporous phase with an aromatization catalyst at an aromatization temperature in the range of 450 - 700 °C, which aromatization temperature is at least 50°C lower than the pyrolysis temperature, in a catalytic conversion step to yield a conversion product comprising aromatic compounds; and d) optionally recovering the aromatic compounds from the conversion product.
LINK
For the recycling of carpet and artificial turf the latex backing is often a real stumble block. Many strategies have been developed like freezing the carpet, followed by grinding and subsequent separation of the milled particles. Once it has been separated from its backing materials, PA 6 is relatively easy to depolymerise. This produces fresh caprolactam that can be used to manufacture PA 6 with no loss in quality, and is suitable for further recycling [1]. The comparable process for PA 6,6 is not as easy, but DuPont and Polyamid 2000 have developed and patented a process that depolymerises any mixture of PA 6 and 6,6 using ammonia. The result is fresh caprolactam and 1,6 diaminohexane for manufacture of PA 6 and 6,6 respectively [2]. Obviously a lot of research has been devoted to avoiding latex as a backing like e.g. polyurethane carpet backing systems based on natural oil polyols and polymer polyols [4]. Still carboxylated styrene butadiene is the leading synthetic latex polymer used in EU-27 for carpet backing, followed by styrene-acrylics and pure acrylics. This contrasts with Eastern Europe, Russia, and Turkey where styrene-acrylics dominate, followed by PVAc and redispersible powders [3]. In addition there has been a lot of research into developing alternative backing systems where the backing can easily be removed. Examples are the use of gecko technology [5] or using click chemistry (reversible Diels Alder reactions) [6]. But the best option for recycling is of course to develop carpets based completely on monomaterials. Paper for the 14th Autex World Textile Conference May 26th-28th 2014, Bursa, Turkey.
MULTIFILE
tmoA and related genes encode the alpha-subunit of the hydroxylase component of the major group (subgroup 1 of subfamily 2) of bacterial multicomponent mono-oxygenase enzyme complexes involved in aerobic benzene, toluene, ethylbenzene and xylene (BTEX) degradation. A PCR-denaturing gradient gel electrophoresis (DGGE) method was developed to assess the diversity of tmoA-like gene sequences in environmental samples using a newly designed moderately degenerate primer set suitable for that purpose. In 35 BTEX-degrading bacterial strains isolated from a hydrocarbon polluted aquifer, tmoA-like genes were only detected in two o-xylene degraders and were identical to the touA gene of Pseudomonas stutzeri OX1. The diversity of tmoA-like genes was examined in DNA extracts from contaminated and non-contaminated subsurface samples at a site containing a BTEX-contaminated groundwater plume. Differences in DGGE patterns were observed between strongly contaminated, less contaminated and non-contaminated samples and between different depths, suggesting that the diversity of tmoA-like genes was determined by environmental conditions including the contamination level. Phylogenetic analysis of the protein sequences deduced from the amplified amplicons showed that the diversity of TmoA-analogues in the environment is larger than suggested from described TmoA-analogues from cultured isolates, which was translated in the DGGE patterns. Although different positions on the DGGE gel can correspond to closely related TmoA-proteins, relationships could be noticed between the position of tmoA-like amplicons in the DGGE profile and the phylogenetic position of the deduced protein sequence.
DOCUMENT
Concepts to protect wood from factors like ultraviolet (UV) radiation, water and wood-decaying fungi with the help of fungi exist in different variants. The idea to treat wood with the help of linseed oil and the living fungus Aureobasidium pullulans originated in 1996 during an European project assessing sustainable protection systems (Sailer et al., 2010). At that time, wood impregnated with natural oils resulted surprisingly in an evenly dark colored surface. These color changes were usually associated with irregular discoloration and staining and were further investigated. It has been shown that the fungus Aureobasidium pullulans was growing on surfaces treated with linseed oil. The fact that Aureobasium pullulans reproducibly grows on water repellent linseed surfaces in many regions around the world makes it suitable for use in a wide range of applications. Research did show that Aureobasidium pullulans produces pigments and binders on its own. This contribution documents the investigation to, identify the possibilities of biological wood surface treatment with Aureobasidium. The combination of the hydrophobizing effect of linseed oil and the surface treatment with the so-called biofinish creates an aesthetically appealing dark living surface, which significantly prolongs the life of wood outdoors and reduces maintenance costs. Since the idea has been developed into an industrially applicable process (Xyhlo biofinish, 2018). Using this concept, building components e.g. façades can be protected with a biological and functional coating thereby contribution to lessen the environmental impact of buildings.
MULTIFILE
A process for the prepn. of arom. compds. from a feed stream contg. biomass or mixts. of biomass, the process comprising: a) subjecting a feed stream contg. biomass or mixts. of biomass to a process to afford a conversion product comprising arom. compds.; b) recovering the arom. compds. from said conversion product; c) sepg. a higher mol. wt. fraction comprising polyarom. hydrocarbons (PAH) from a lower mol. wt. fraction comprising benzene, toluene and xylene (BTX) by distn.; d) reducing at least part of said higher mol. wt. fraction to obtain a reduced fraction comprising polycyclic aliphatics (PCA); and e) subjecting the higher mol. wt. fraction obtained in step c), the reduced fraction obtained in step d), or a mixt. thereof, to a process to obtain lower mol. wt. aroms. (BTX). [on SciFinder(R)]
DOCUMENT
Sustainable production of aromatics, especially benzene, toluene and xylenes (BTX), is essential considering their broad applications and the current global transition away from crude oil utilization. Aromatization of lower olefins, particularly ethene and propene, offers great potential if they are derived from more circular alternative carbon feedstocks such as biomass and waste plastics. This work aims to identify the preferred olefin feed, ethene or propene, for BTX production in a fixed-bed reactor. A commercial H-ZSM-5 (Si/Al = 23) catalyst was used as a reference catalyst, as well as a Ga-ZSM-5 catalyst, prepared by Ga ion-exchange of the H-ZSM-5 catalyst. At 773 K, 1 bar, 45 vol % olefin, 6.75 h−1, propene aromatization over the Ga-ZSM-5 catalyst exhibited higher BTX selectivity of 55 % and resulted in slower catalyst deactivation compared to ethene aromatization.
DOCUMENT
The present study examined efficacy of traditional Chinese medicine (TCM) treatment in Dutch children with asthma in areas with differing air pollution. The study results indicate that TCM treatment of children living in more polluted urban area is less successful then that of children living in cleaner air area. http://dx.doi.org/10.5402/2012/547534 https://www.linkedin.com/in/helenkopnina/
MULTIFILE
Bio-aromatics (benzene, toluene, xylenes, BTX) were prepared by the catalytic pyrolysis of six different black liquors using both in situ and ex situ approaches. A wide range of catalysts was screened and conditions were optimized in microscale reactors. Up to 7 wt % of BTX, based on the organic fraction of the black liquors, was obtained for both the in situ and ex situ pyrolysis ( T = 500-600 °C) using a Ga-modified H-ZSM-5 catalyst. The in situ catalytic pyrolysis of black liquors from hardwood paper mills afforded slightly higher yields of aromatics/BTX than softwood black liquors, a trend that could be confirmed by the results obtained in the ex situ catalytic pyrolysis. An almost full deoxygenation of the lignin and carbohydrate fraction was achieved and both organic fractions were converted to a broad range of (substituted) aromatics. The zeolite catalyst used was remarkably stable and even after 100 experiments in batch mode with intermittent oxidative catalyst regeneration, the yields and selectivity toward BTX remained similar. The ex situ pyrolysis of black liquor has potential for large-scale implementation in a paper mill without disturbing the paper production process.
MULTIFILE
Pyrolysis liquids from lignocellulosic biomass have the potential to be used as a feed for aromatics such as benzene, toluene, and xylenes (BTX) using catalytic upgrading with zeolites. We here report an experimental study on the conversion of various pyrolysis oil fractions to determine the most suitable one for BTX synthesis. For this purpose, the pyrolysis liquid was fractionated using several extraction/distillation steps to give four fractions with different chemical compositions. The fractions were analyzed in detail using nuclear magnetic resonance spectroscopy, elemental analysis, gas chromatography-mass spectroscopy, thermogravimetric analysis, Karl-Fischer titration, and gel permeation chromatography. Catalytic pyrolysis experiments were carried out using a tandem microreactor with H-ZSM-5 (23) as the catalyst. The highest BTX yield of 24% (on a carbon and dry basis) was obtained using the fractions enriched in phenolics, whereas all others gave far lower yields (4.4-9%, on a carbon and dry basis). Correlations were established between the chemical composition of the feed fraction and the BTX yield. These findings support the concept of a pyrolysis biorefinery, where the pyrolysis liquid is separated into well-defined fractions before further dedicated catalytic conversions to biobased chemicals and biofuels using tailored catalysts.
DOCUMENT
