The industrial production of dimethyl carbonate from methanol and carbon dioxide

This work discusses the design of a dimethyl carbonate (DMC) production plant based on methanol and CO2 as feed materials, which are a cheap and environment-friendly feedstock. DMC is a good alternative for methyl-tert-butyl ether (MTBE) as a fuel oxygenating agent, due to its low toxicity and fast biodegradability. Based on the MTBE demand of a general gasoline plant, the annual production capacity of the process design is stipulated to be 86 kt DMC, with a purity of 99 wt%. Three routes are proposed to form DMC: 1) direct synthesis from methanol and CO2, 2) reaction of CO2 and ammonia to urea, which can be converted to DMC with methanol, 3) reaction of ethylene oxide with CO2 to a cyclic carbonate, which can be converted to DMC by transesterification with methanol. From a black box cost analysis based on raw material prices, it is concluded that the ethylene oxide route is the least profitable. Because of higher single-pass conversions found in literature, smaller recycles and easier separations, it is concluded that the urea route would be the most feasible. The required process functions for the urea route have been determined in the conceptual design phase. A detailed design of the most important process operations is made and an overall technical and economic evaluation of the process has been carried out. In the first step of this DMC synthesis, urea is produced from carbon dioxide and ammonia with the ACES21 process. After separation and purification steps, urea is fed to a reactor with methanol (150 °C, 20 bar), where methyl carbamate (MC), an intermediate of DMC production, and ammonia are formed in the absence of a catalyst. Subsequently, MC and methanol are converted to DMC and ammonia (190 °C, 40 bar) over a ZnO-Al2O3 catalyst in a fixed-bed reactor. Methanol and DMC form an azeotrope; extractive distillation with methyl isobutyl ketone (MIBK) as entrainer is used to separate the azeotropic mixture. The reactor model for the reaction towards DMC based on kinetic rate expressions, showed that a long residence time (>10 h) and a relatively high MeOH:MC molar feed ratio of 6 are required to achieve reasonable single-pass conversions (15 %). This resulted however in an unrealistically large reactor volume and a large methanol load on the process. A feasibility study was done in order to improve the performance of the process. It was calculated that with a MeOH:MC ratio of 2 and a single-pass conversion of MC of 30 % the process would become technically feasible; the reactor volume decreased from 5,000 m3 to 600 m3 and the energy consumption of the process was decreased from 238 MW to 50 MW. A Pinch analysis showed that maximally 6 MW could be saved with heat integration, which corresponds to approximately 2 M$/y savings on energy costs. To produce 86 kt/y of DMC, the required amounts of raw materials are 80 kt/y of methanol and 58 kt/y of CO2, which results in an overall DMC yield from methanol of 38$. Economic feasibility depends on the DMC selling price. A price range between 800 and 1,100 $/t was assumed. For 800$/t it is not possible to repay the capital investment within an assumed lifetime of 10 years and the process would therefore not be profitable. The break-even point is at 845 $/t. For a selling price of 1,100$/t the gross profit becomes 22 M$/y, with a payback period of 3 years and a return on investment of 20 %

Endosymbiosis: Lessons in Conflict Resolution

Endosymbiotic bacteria live within a host species. There are many and diverse examples of such relationships, the study of which provides important lessons for ecology and evolutio

The FOAM study : Is Hysterosalpingo foam sonography (HyFoSy) a cost-effective alternative for hysterosalpingography (HSG) in assessing tubal patency in subfertile women? Study protocol for a randomized controlled trial

This is an investigator initiated trial, VU medical center Amsterdam is the sponsor, contact information: prof. CJM de Groot, Department of Obstetrics and Gynaecology, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands, Tel: + 31-204444444. This study is funded by ZonMw, a Dutch organization for Health Research and Development, project number 837001504. ZonMW gives financial support for the whole project. IQ Medical Ventures provides the ExEm FOAM® kits. The funding bodies have no role in the design of the study; collection, analysis, and interpretation of data; and in writing the manuscript.Peer reviewedPublisher PD

Can hysterosalpingo-foam sonography replace hysterosalpingography as first-choice tubal patency test? A randomized non-inferiority trial

Funding Information: The FOAM study was an investigator-initiated study funded by ZonMw, The Netherlands organization for Health Research and Development (project number 837001504). ZonMw funded the whole project. IQ Medical Ventures provided the ExEm-foamVR kits free of charge. The funders had no role in study design, collection, analysis and interpretation of the data. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication.Peer reviewedPublisher PD

Decreased 3D observer variation with matched CT-MRI, for target delineation in Nasopharynx cancer

Contains fulltext : 88137.pdf (publisher's version ) (Open Access)PURPOSE: To determine the variation in target delineation of nasopharyngeal carcinoma and the impact of measures to minimize this variation. MATERIALS AND METHODS: For ten nasopharyngeal cancer patients, ten observers each delineated the Clinical Target Volume (CTV) and the CTV elective. After 3D analysis of the delineated volumes, a second delineation was performed. This implied improved delineation instructions, a combined delineation on CT and co-registered MRI, forced use of sagittal reconstructions, and an on-line anatomical atlas. RESULTS: Both for the CTV and the CTV elective delineations, the 3D SD decreased from Phase 1 to Phase 2, from 4.4 to 3.3 mm for the CTV and from 5.9 to 4.9 mm for the elective. There was an increase agreement, where the observers intended to delineate the same structure, from 36 to 64 surface % (p = 0.003) for the CTV and from 17 to 59% (p = 0.004) for the elective. The largest variations were at the caudal border of the delineations but these were smaller when an observer utilized the sagittal window. Hence, the use of sagittal side windows was enforced in the second phase and resulted in a decreased standard deviation for this area from 7.7 to 3.3 mm (p = 0.001) for the CTV and 7.9 to 5.6 mm (p = 0.03) for the CTV elective. DISCUSSION: Attempts to decrease the variation need to be tailored to the specific causes of the variation. Use of delineation instructions multimodality imaging, the use of sagittal windows and an on-line atlas result in a higher agreement on the intended target

Integrative analysis of neuroblastoma by single-cell RNA sequencing identifies the NECTIN2-TIGIT axis as a target for immunotherapy

Pediatric patients with high-risk neuroblastoma have poor survival rates and urgently need more effective treatment options with less side effects. As novel and improved immunotherapies may fill this need, we dissected the immunoregulatory interactions in neuroblastoma by single-cell RNA-sequencing of 25 tumors (10 pre- and 15 post-chemotherapy, including 5 pairs) to identify strategies for optimizing immunotherapy efficacy. Neuroblastomas were infiltrated by NK, T and B cells, and immunosuppressive myeloid populations. NK cells showed reduced cytotoxicity and T cells had a dysfunctional profile. Interaction analysis revealed a vast immunoregulatory network and identified NECTIN2-TIGIT as a crucial immune checkpoint. Combined blockade of TIGIT and PD-L1 significantly reduced neuroblastoma growth, with complete responses in vivo. Moreover, addition of TIGIT blockade to standard relapse treatment in a chemotherapy-resistant Th-ALKF1174L/MYCN 129/SvJ syngeneic model significantly improved survival. Concluding, our integrative analysis of neuroblastoma’s vast immunoregulatory network provides novel targets and a rationale for immunotherapeutic combination strategies

Macrophage Glucose-6-Phosphate Dehydrogenase Stimulates Proinflammatory Responses with Oxidative Stress

Glucose-6-phosphate dehydrogenase (G6PD) is a key enzyme that regulates cellular redox potential. In this study, we demonstrate that macrophage G6PD plays an important role in the modulation of proinflammatory responses and oxidative stress. The G6PD levels in macrophages in the adipose tissue of obese animals were elevated, and G6PD mRNA levels positively correlated with those of proinflammatory genes. Lipopolysaccharide (LPS) and free fatty acids, which initiate proinflammatory signals, stimulated macrophage G6PD. Overexpression of macrophage G6PD potentiated the expression of proinflammatory and prooxidative genes responsible for the aggravation of insulin sensitivity in adipocytes. In contrast, when macrophage G6PD was inhibited or suppressed via chemical inhibitors or small interfering RNA (siRNA), respectively, basal and LPS-induced proinflammatory gene expression was attenuated. Furthermore, macrophage G6PD increased activation of the p38 mitogen-activated protein kinase (MAPK) and NF-??B pathways, which may lead to a vicious cycle of oxidative stress and proinflammatory cascade. Together, these data suggest that an abnormal increase of G6PD in macrophages promotes oxidative stress and inflammatory responses in the adipose tissue of obese animals.open5

Physics searches at the LHC

With the LHC up and running, the focus of experimental and theoretical high energy physics will soon turn to an interpretation of LHC data in terms of the physics of electroweak symmetry breaking and the TeV scale. We present here a broad review of models for new TeV-scale physics and their LHC signatures. In addition, we discuss possible new physics signatures and describe how they can be linked to specific models of physics beyond the Standard Model. Finally, we illustrate how the LHC era could culminate in a detailed understanding of the underlying principles of TeV-scale physics.Comment: 184 pages, 55 figures, 14 tables, hundreds of references; scientific feedback is welcome and encouraged. v2: text, references and Overview Table added; feedback still welcom