Integrated process development for the recovery of Europium and Yttrium from waste fluorescent powder

Journal of Material Cycles and Waste Management - Fluorescent powder plays an important role in the modern electronic lighting products. During the production of electronic lighting products, a...     

The Design of a New Energy-conservation Type Solar-powered Lighting System Using a High‐pressure Sodium Lamp

This study designs and applies a new energy-conservation type solar-powered lighting system using a high-pressure sodium lamp to areas not having any utility company's electricity. The proposed system uses a zero-voltage-switching (ZVS) DC/DC converter in the batteries’ charge circuit to reduce the switching loss for a higher charging efficiency. Said system also adopts the maximum power point tracking (MPPT) technique to maximize the solar panels’ photovoltaic conversion capability. When dark, the batteries in the proposed system will discharge, with a raised voltage, through a push-pull DC/DC converter; said voltage, as the input voltage of the series-parallel resonant inverter, will be regulated to dim the lamp. To enable the efficient usage of the batteries’ stored energy capacity, this control scheme of the proposed system may adjust the night-time discharge time lengths, according to season difference, and compute the usable capacity for the load, according to the batteries’ charged voltage, so as to select a suitable pre-scheduled light-dimming curve for the lamp to achieve energy conservation for the batteries and continuity in lighting when dark.     

Investigation into the genetics of fetal congenital lymphatic anomalies

Objective

Congenital lymphatic anomalies (LAs) arise due to defects in lymphatic development and often present in utero as pleural effusion, chylothorax, nuchal and soft tissue edema, ascites, or hydrops. Many LAs are caused by single nucleotide variants, which are not detected on routine prenatal testing.

Methods

Demographic data were compared between two subcohorts, those with clinically significant fetal edema (CSFE) and isolated fetal edema. A targeted variant analysis of LA genes was performed using American College of Medical Genetics criteria on whole exome sequencing (WES) data generated for 71 fetal edema cases who remained undiagnosed after standard workup.

Results

CSFE cases had poor outcomes, including preterm delivery, demise, and maternal preeclampsia. Pathogenic and likely pathogenic variants were identified in 7% (5/71) of cases, including variants in RASopathy genes, RASA1, SOS1, PTPN11, and a novel PIEZO1 variant. Variants of uncertain significance (VOUS) were identified in 45% (32/71) of cases. In CSFEs, VOUS were found in CELSR1, EPHB4, TIE1, PIEZO1, ITGA9, RASopathy genes, SOS1, SOS2, and RAF1.

Conclusions

WES identified pathogenic and likely pathogenic variants and VOUS in LA genes in 51% of fetal edema cases, supporting WES and expanded hydrops panels in cases of idiopathic fetal hydrops and fluid collections.