4,359 research outputs found

    The Effects of Catalyst, Free Fatty Acids, and Water on Transecterification of Beef Tallow

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    Transesterification of beef tallow and methanol is affected by many factors. Catalyst, free fatty acids, and water in beef tallow, and reaction time were investigated. Sodium hydroxide (NUOH) was a more effective catalyst than sodium methoxide (NaMeOj. NaOH and NaMeO reached their maximum activities at 0.3% and 0.5%, w/w of beef tallow, respectively. The presence of water had more negative effect on transesterification than did the presence of free fatty acids (FFA). For best results, the water content of beef tallow should be kept not beyond 0.0696, w/w. FFA content of beef tallow should be kept below 0.596, w/w. The transesterification of beef tallow was very slow in the first minute. The production of beef tallow methyl esters (BTME) was complete after about 15 min. There were still some mono- and diglycerides in the BTME phase after the reaction was finished

    Biodiesel Fuel from Animal Fat. Ancillary Studies on Transesterification of Beef Tallow

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    Transesterification of beef tallow was investigated. The solubility of ethanol in beef tallow was much higher than that of methanol. At 100 °C the solubility of methanol was 19% (w/w). The solubility of ethanol in beef tallow reached 100% (w/w) at about 68 °C. For the distribution of methanol between beef tallow methyl esters (BTME) and glycerol, the percentage of total methanol in the glycerol phase was higher than that in the fatty acid methyl ester (FAME) phase in a simulated system at room temperature. At 65-80 °C, however, the percentage of total methanol in FAME (60% (w/w)) was higher than that in glycerol (40% (w/w)) in a 90:10 (w/w) blend of FAME and glycerol. This coincided with the methanol distribution in the transesterified product. The process for making beef tallow methyl esters should recover methanol using vacuum distillation, separate the ester and glycerol phases, and then wash the beef tallow methyl esters with warm water. At neutral pH, the separation of ester and glycerol and water washing was easier because it reduced emulsion formation

    What is the role of mitochondrial dysfunction in skin photoaging?

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    Skin ageing is a complex process involving both internal and external factors, which leads to a progressive loss of cutaneous function and structure. Solar radiation is the primary environmental factor implicated in the development of skin ageing and the term photoageing describes the distinct clinical, histological and structural features of chronically sun-exposed skin. The changes that accompany photoageing are undesirable for aesthetic reasons and can compromise the skin and make it more susceptible to a number of dermatological disorders. As a result, skin ageing is a now topic that is of growing interest and concern to the general population, illustrated by the increased demand for effective interventions that can prevent or ameliorate the clinical changes associated with aged skin. In this viewpoint essay we explore the role that mitochondria play in the process of skin photoageing. There is continuing evidence supporting the proposal that mitochondria dysfunction and oxidative stress are important contributing factors in the development of skin photoageing. Further skin-directed mitochondrial research is warranted to fully understand the impact of mitochondrial status and function in skin health. A greater understanding of the ageing process and the regulatory mechanisms involved could lead to the development of novel preventative andtherapeutic interventions for skin ageing

    Piperazine Enhancing Sulfuric Acid-Based New Particle Formation : Implications for the Atmospheric Fate of Piperazine

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    Piperazine (PZ), a cyclic diamine, is one of 160 detected atmospheric amines and an alternative solvent to the widely used monoethanolamine in post-combustion CO2 capture. Participating in H2SO4 (sulfuric acid, SA)-based new particle formation (NPF) could be an important removal pathway for PZ. Here, we employed quantum chemical calculations and kinetics modeling to evaluate the enhancing potential of PZ on SA-based NPF by examining the formation of PZ-SA clusters. The results indicate that PZ behaves more like a monoamine in stabilizing SA and can enhance SA-based NPF at the parts per trillion (ppt) level. The enhancing potential of PZ is less than that of the chainlike diamine putrescine and greater than that of dimethylamine, which is one of the strongest enhancing agents confirmed by ambient observations and experiments. After the initial formation of the (PZ)1(SA)1 cluster, the cluster mainly grows by gradual addition of SA or PZ monomer, followed by addition of (PZ)1(SA)1 cluster. We find that the ratio of PZ removal by NPF to that by the combination of NPF and oxidations is 0.5–0.97 at 278.15 K. As a result, we conclude that participation in the NPF pathway could significantly alter the environmental impact of PZ compared to only considering oxidation pathways.Peer reviewe

    SIGMAR1 mutation associated with autosomal recessive Silver-like syndrome

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    OBJECTIVE: To describe the genetic and clinical features of a simplex patient with distal hereditary motor neuropathy (dHMN) and lower limb spasticity (Silver-like syndrome) due to a mutation in the sigma nonopioid intracellular receptor-1 gene (SIGMAR1) and review the phenotypic spectrum of mutations in this gene. METHODS: We used whole-exome sequencing to investigate the proband. The variants of interest were investigated for segregation in the family using Sanger sequencing. Subsequently, a larger cohort of 16 unrelated dHMN patients was specifically screened for SIGMAR1 mutations. RESULTS: In the proband, we identified a homozygous missense variant (c.194T>A, p.Leu65Gln) in exon 2 of SIGMAR1 as the probable causative mutation. Pathogenicity is supported by evolutionary conservation, in silico analyses, and the strong phenotypic similarities with previously reported cases carrying coding sequence mutations in SIGMAR1. No other mutations were identified in 16 additional patients with dHMN. CONCLUSIONS: We suggest that coding sequence mutations in SIGMAR1 present clinically with a combination of dHMN and pyramidal tract signs, with or without spasticity, in the lower limbs. Preferential involvement of extensor muscles of the upper limbs may be a distinctive feature of the disease. These observations should be confirmed in future studies

    Long-term Effects of Weed Management on Earthworm Abundance in a Banana Plantation in Davao City, Southern Mindanao, Philippines

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    Earthworm densities have been regarded as reliable indicators of soil health. A long-term field experiment was conducted in two sites (15% and 25% slope) to compare the effects of manual and chemical weeding (using paraquat and glyphosate) and determine other factors that may affect earthworm populations in a banana plantation. Based on four years of field observation, no significant difference in earthworm count between manual and chemical plots (15% slope: F-ratio: 0.96, p = 0.43; 25% slope: F-ratio: 14.18, p = 0.06) were observed. The earthworm species composition was found to differ between the two sites. The 15% site tends to have a higher earthworm population compared to the 25%-slope site, likely because of the former’s higher soil organic matter content. Earthworm populations were on a declining trend in both treatments for both sites, but regression analyses show these trends to be insignificant. Rainfall, organic mulch, and weed cover were not significantly correlated with the earthworm counts. However, the declining pH in both sites could help explain the decline in earthworm populations. Pontocolex corethrurus showed significant avoidance response to normal glyphosate concentrations (8.055 × 10–3 mL per 350 g soil) (p = 0.03), but not to paraquat (1.5 × 10–3 g per 350 g soil) (p = 0.55). Experiments suggest that both weed management treatments do not pose a significant threat to earthworms under the conditions studied. The negative effect of declining pH needs further study

    HER2 testing in breast cancer: Opportunities and challenges

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    Human epidermal growth factor receptor 2 (HER2) is overexpressed in 15-25% of breast cancers, usually as a result of HER2 gene amplification. Positive HER2 status is considered to be an adverse prognostic factor. Recognition of the role of HER2 in breast cancer growth has led to the development of anti-HER2 directed therapy, with the humanized monoclonal antibody trastuzumab (Herceptin (R)) having been approved for the therapy of HER2-positive metastatic breast cancer. Clinical studies have further suggested that HER2 status can provide important information regarding success or failure of certain hormonal therapies or chemotherapies. As a result of these developments, there has been increasing demand to perform HER2 testing on current and archived breast cancer specimens. This article reviews the molecular background of HER2 function, activation and inhibition as well as current opinions concerning its role in chemosensitivity and interaction with estrogen receptor biology. The different tissue-based assays used to detect HER2 amplification and overexpression are discussed with respect to their advantages and disadvantages, when to test (at initial diagnosis or pre-treatment), where to test (locally or centralized) and the need for quality assurance to ensure accurate and valid testing results

    DAP12 Signaling Directly Augments Proproliferative Cytokine Stimulation of NK Cells during Viral Infections

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    Abstract NK cells vigorously proliferate during viral infections. During the course of murine CMV infection, this response becomes dominated by the preferential proliferation of NK cells that express the activation receptor Ly49H. The factors driving such selective NK cell proliferation have not been characterized. In this study, we demonstrate that preferential NK cell proliferation is dependent on DAP12-mediated signaling following the binding of Ly49H to its virally encoded ligand, m157. Ly49H signaling through DAP12 appears to directly augment NK cell sensitivity to low concentrations of proproliferative cytokines such as IL-15. The impact of Ly49H-mediated signaling on NK cell proliferation is masked in the presence of high concentrations of proproliferative cytokines that nonselectively drive all NK cells to proliferate
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