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Abstract In the present study, Loblolly pine biomass residue was converted to bio-oil in a two-step process, consisting of 1) fast pyrolysis in the presence of zeolite ZSM-5 as a catalyst to produce pyrolysis oil, 2) hydrogenation of pyrolysis oil using formic acid as the hydrogen source in presence of Ru/activated carbon catalyst. Pyrolysis oils were analyzed by 13C, 31P and HSQC-NMR and the results revealed that the zeolite-induced catalytic fast pyrolysis process led to effective demethoxylation, producing more catechol and p-hydroxy-phenyl hydroxyl groups in the bio-oils, resulting in a decrease in the methoxyl group content by about 85 % and rich aromatic structures in the pyrolysis oils. The properties of pyrolysis oil with and without zeolite were in the bio-oil range. Hydrogenated pyrolysis oil showed that 79 % of the aromatic protons are eliminated and 87 % of protons are aliphatic in nature, with no oxygen attached to the α-carbon.

The ‘4 per mille Soils for Food Security and Climate’ was launched at the COP21 with an aspiration to increase global soil organic matter stocks by 4 per 1000 (or 0.4 %) per year as a compensation for the global emissions of greenhouse gases by anthropogenic sources. This paper surveyed the soil organic carbon (SOC) stock estimates and sequestration potentials from 20 regions in the world (New Zealand, Chile, South Africa, Australia, Tanzania, Indonesia, Kenya, Nigeria, India, China Taiwan, South Korea, China Mainland, United States of America, France, Canada, Belgium, England & Wales, Ireland, Scotland, and Russia). We asked whether the 4 per mille initiative is feasible for the region. The outcomes highlight region specific efforts and scopes for soil carbon sequestration. Reported soil C sequestration rates globally show that under best management practices, 4 per mille or even higher sequestration rates can be accomplished. High C sequestration rates (up to 10 per mille) can be achieved for soils with low initial SOC stock (topsoil less than 30 t C ha− 1), and at the first twenty years after implementation of best management practices. In addition, areas which have reached equilibrium will not be able to further increase their sequestration. We found that most studies on SOC sequestration only consider topsoil (up to 0.3 m depth), as it is considered to be most affected by management techniques. The 4 per mille number was based on a blanket calculation of the whole global soil profile C stock, however the potential to increase SOC is mostly on managed agricultural lands. If we consider 4 per mille in the top 1m of global agricultural soils, SOC sequestration is between 2-3 Gt C year− 1, which effectively offset 20–35% of global anthropogenic greenhouse gas emissions. As a strategy for climate change mitigation, soil carbon sequestration buys time over the next ten to twenty years while other effective sequestration and low carbon technologies become viable. The challenge for cropping farmers is to find disruptive technologies that will further improve soil condition and deliver increased soil carbon. Progress in 4 per mille requires collaboration and communication between scientists, farmers, policy makers, and marketeers.

Abstract Space–time kinetics calculations for CANDU ® 1 reactors are routinely performed using the Improved Quasistatic (IQS) method. The IQS method calculates kinetics parameters such as the effective delayed-neutron fraction and generation time using adjoint weighting. In the current implementation of IQS, the direct flux, as well as the adjoint, is calculated using a two-group cell-homogenized reactor model which is inadequate for capturing the effect of the softer energy spectrum of the delayed neutrons. Additionally, there may also be fine spatial effects that are lost because the intra-cell adjoint shape is ignored. The purpose of this work is to compare the kinetics parameters calculated using the two-group cell-homogenized model with those calculated using lattice-level fine-group heterogeneous adjoint weighting and to assess whether the differences are large enough to justify further work on incorporating lattice-level adjoint weighting into the IQS method. A second goal is to evaluate whether the use of a fine-group cell-homogenized lattice-level adjoint, such as is the current practice for Light Water Reactors (LWRs), is sufficient to capture the lattice effects in question. It is found that, for CANDU lattices, the generation time is almost unaffected by the type of adjoint used to calculate it, but that the effective delayed-neutron fraction is affected by the type of adjoint used. The effective delayed-neutron fraction calculated using the two-group cell-homogenized adjoint is 5.2% higher than the “best” effective delayed-neutron fraction value obtained using the detailed lattice-level fine-group heterogeneous adjoint. The effective delayed-neutron fraction calculated using the fine-group cell-homogenized adjoint is only 1.7% higher than the “best” effective delayed-neutron fraction value but is still not equal to it. This situation is different from that encountered in LWRs where weighting by a fine-group cell-homogenized adjoint is sufficient to calculate the correct effective delayed-neutron fraction. It is concluded that lattice-level weighting with a detailed fine-group heterogeneous adjoint is desirable for the correct calculation of the effective delayed-neutron fraction in CANDU lattices.

Most of the world’s mountain glaciers have been retreating for more than a century in response to climate change. Glacier retreat is evident on all continents, and the rate of retreat has accelerated during recent decades. Accurate, spatially explicit information on the position of glacier margins over time is useful for analyzing patterns of glacier retreat and measuring reductions in glacier surface area. This information is also essential for evaluating how mountain ecosystems are evolving due to climate warming and the attendant glacier retreat. Here, we present a non-comprehensive spatially explicit dataset showing multiple positions of glacier fronts since the Little Ice Age (LIA) maxima, including many data from the pre-satellite era. The dataset is based on multiple historical archival records including topographical maps; repeated photographs, paintings, and aerial or satellite images with a supplement of geochronology; and own field data. We provide ESRI shapefiles showing 728 past positions of 94 glacier fronts from all continents, except Antarctica, covering the period between the Little Ice Age maxima and the present. On average, the time series span the past 190 years. From 2 to 46 past positions per glacier are depicted (on average: 7.8).

La production industrielle d'huile de palme génère simultanément une quantité substantielle de fibres de grappe de fruits vides (EFB) qui pourraient être utilisées comme matière première dans une bioraffinerie à base de lignocellulose. Les sous-produits de la lignine générés par ce processus peuvent offrir des possibilités d'isolation des produits à valeur ajoutée, tels que le p-hydroxybenzoate (pBz), pour aider à compenser les coûts d'exploitation. L'analyse de la lignine EFB par spectroscopie de résonance magnétique nucléaire (RMN) a clairement révélé la présence d'acétate lié et de pBz, la saponification révélant que 1,1 % en poids de l'EFB était du pBz ; avec une teneur en lignine de 22,7 %, 4,8 % de la lignine est du pBz qui peut être obtenu comme composant pur pour être utilisé comme charge chimique. L'analyse de la lignine EFB par RMN et dérivatisation suivie d'un clivage réducteur (DFRC) a montré que le pBz acylate sélectivement le groupe γ-hydroxyle des unités S. Cette sélectivité suggère que le pBz, de manière analogue à l'acétate dans le kénaf, le p-coumarate dans les graminées et le ferrate dans un peuplier transgénique augmenté d'une féruloyl-CoA monolignol transférase (FMT), est incorporé dans la chaîne de lignine en croissance via son conjugué monolignol γ-p-hydroxybenzoylé. L'implication de tels conjugués dans la lignification des palmiers est prouvée par l'observation de nouvelles unités couplées au β-β non résinol p-hydroxybenzoylé dans les lignines. Ensemble, les données impliquent l'existence de p-hydroxybenzoyl-CoA :monolignol transférases qui sont impliquées dans la lignification chez les différents saules (Salix spp.), peupliers et peupliers faux-trembles (Populus spp., famille des Salicacées) et palmiers (famille des Arecacées) qui ont des lignines p-hydroxybenzoylées. Même sans augmenter les niveaux par la sélection ou le génie génétique, les « déchets » actuels de l'EFB d'huile de palme devraient être en mesure de générer un flux important d'acide p-hydroxybenzoïque qui offre des opportunités pour le développement de produits à valeur ajoutée dérivés de l'industrie du palmier à huile. La producción industrial de aceite de palma genera simultáneamente una cantidad sustancial de fibras de racimo de frutas vacías (EFB) que podrían utilizarse como materia prima en una biorrefinería a base de lignocelulosa. Los subproductos de lignina generados por este proceso pueden ofrecer oportunidades para el aislamiento de productos de valor agregado, como el p-hidroxibenzoato (pBz), para ayudar a compensar los costos operativos. El análisis de la lignina EFB por espectroscopía de resonancia magnética nuclear (RMN) reveló claramente la presencia de acetato unido y pBz, y la saponificación reveló que el 1,1% en peso del EFB era pBz; con un contenido de lignina del 22,7 %, el 4,8 % de la lignina es pBz que se puede obtener como un componente puro para su uso como materia prima química. El análisis de la lignina EFB por RMN y la derivatización seguida de escisión reductora (DFRC) mostró que pBz acila selectivamente el grupo γ-hidroxilo de las unidades S. Esta selectividad sugiere que pBz, análogamente con acetato en kenaf, p-cumarato en gramíneas y ferular en un álamo transgénico aumentado con una feruloil-CoA monolignol transferasa (FMT), se incorpora a la cadena de lignina en crecimiento a través de su conjugado de monolignol γ-p-hidroxibenzoilado. La participación de dichos conjugados en la lignificación de la palma se demuestra al observar nuevas unidades no acopladas a β-β-resinol p-hidroxibenzoiladas en las ligninas. Juntos, los datos implican la existencia de p-hidroxibenzoil-CoA:monolignol transferasas que participan en la lignificación en los diversos sauces (Salix spp.), álamos y álamo temblón (Populus spp., familia Salicaceae) y palmeras (familia Arecaceae) que tienen ligninas p-hidroxibenzoiladas. Incluso sin mejorar los niveles mediante mejoramiento o ingeniería genética, los 'desechos' actuales de aceite de palma EFB deberían ser capaces de generar una corriente considerable de ácido p-hidroxibenzoico que ofrezca oportunidades para el desarrollo de productos de valor agregado derivados de la industria de la palma aceitera. The industrial production of palm oil concurrently generates a substantial amount of empty fruit bunch (EFB) fibers that could be used as a feedstock in a lignocellulose-based biorefinery. Lignin byproducts generated by this process may offer opportunities for the isolation of value-added products, such as p-hydroxybenzoate (pBz), to help offset operating costs. Analysis of the EFB lignin by nuclear magnetic resonance (NMR) spectroscopy clearly revealed the presence of bound acetate and pBz, with saponification revealing that 1.1 wt% of the EFB was pBz; with a lignin content of 22.7 %, 4.8 % of the lignin is pBz that can be obtained as a pure component for use as a chemical feedstock. Analysis of EFB lignin by NMR and derivatization followed by reductive cleavage (DFRC) showed that pBz selectively acylates the γ-hydroxyl group of S units. This selectivity suggests that pBz, analogously with acetate in kenaf, p-coumarate in grasses, and ferulate in a transgenic poplar augmented with a feruloyl-CoA monolignol transferase (FMT), is incorporated into the growing lignin chain via its γ-p-hydroxybenzoylated monolignol conjugate. Involvement of such conjugates in palm lignification is proven by the observation of novel p-hydroxybenzoylated non-resinol β–β-coupled units in the lignins. Together, the data implicate the existence of p-hydroxybenzoyl-CoA:monolignol transferases that are involved in lignification in the various willows (Salix spp.), poplars and aspen (Populus spp., family Salicaceae), and palms (family Arecaceae) that have p-hydroxybenzoylated lignins. Even without enhancing the levels by breeding or genetic engineering, current palm oil EFB 'wastes' should be able to generate a sizeable stream of p-hydroxybenzoic acid that offers opportunities for the development of value-added products derived from the oil palm industry. ينتج الإنتاج الصناعي لزيت النخيل في الوقت نفسه كمية كبيرة من ألياف مجموعة الفاكهة الفارغة (EFB) التي يمكن استخدامها كمادة وسيطة في مصفاة حيوية تعتمد على اللجينوسليلوز. قد توفر المنتجات الثانوية لليجنين الناتجة عن هذه العملية فرصًا لعزل المنتجات ذات القيمة المضافة، مثل p - hydroxybenzoate (pBz)، للمساعدة في تعويض تكاليف التشغيل. كشف تحليل اللجنين EFB بواسطة مطياف الرنين المغناطيسي النووي (NMR) بوضوح عن وجود أسيتات مرتبطة و pBz، مع كشف التصبن أن 1.1 ٪ بالوزن من EFB كان pBz ؛ مع محتوى اللجنين بنسبة 22.7 ٪، 4.8 ٪ من اللجنين عبارة عن pBz يمكن الحصول عليه كمكون نقي للاستخدام كمادة وسيطة كيميائية. أظهر تحليل اللجنين EFB بواسطة NMR والاشتقاق متبوعًا بالانقسام الاختزالي (DFRC) أن pBz يعمل بشكل انتقائي على أسيتيل مجموعة γ - hydroxyl من وحدات S. تشير هذه الانتقائية إلى أن pBz، بالتناظر مع الأسيتات في الكناف، و p - comarate في الأعشاب، و ferulate في حور معدّل وراثيًا معززًا بـ feruloyl - CoA monolignol transferase (FMT)، يتم دمجه في سلسلة اللجنين المتنامية عبر γ - p - hydroxybenzoylated monolignol conjugate. ثبت تورط مثل هذه المترافقات في ترصيع النخيل من خلال ملاحظة وحدات p - hydroxybenzoylated غير الراتينول β - β المقترنة في اللجنين. معا، تشير البيانات إلى وجود p - hydroxybenzoyl - CoA: monolignol transferases التي تشارك في تبييض في الصفصاف المختلفة (Salix spp.)، الحور والحور (Populus spp.، عائلة Salicaceae)، والنخيل (عائلة Arecaceae) التي تحتوي على p - hydroxybenzoylated lignins. حتى من دون تعزيز المستويات عن طريق التكاثر أو الهندسة الوراثية، يجب أن تكون "نفايات" زيت النخيل الحالية قادرة على توليد تيار كبير من حمض p - hydroxybenzoic الذي يوفر فرصًا لتطوير منتجات ذات قيمة مضافة مشتقة من صناعة نخيل الزيت.