Chromium Trioxide Supported onto Wet Silica Gel: Rapid Oxidation of Alcohols to Carbonyl Compounds Under Microwave Irradiation in Solventless System

In an environmentally benign system, alcohols are rapidly oxidized to carbonyl compounds using CrO 3 supported onto wet silica gel as an oxidant under microwave irradiation.     

Two stage electrostatic separator for the recycling of plastics from waste electrical and electronic equipment

The aim of study was to evaluate the effectiveness of a new facility for recycling of plastics from granular waste electrical and electronic equipment. The installation consists of two sections, the products of a first tribo-aero-electrostatic separator being subsequently treated in two free-fall electrostatic separators. The tests were performed on a mixture of polycarbonate (PC) and polyamide (PA). Analysis of the purity of the products obtained was performed using a program of image processing in MATLAB. Products of very high purity (roughly 95% for both PC and PA) were obtained at a recovery rate higher than 70%.     

A relationship between three analytical approaches to nonlinear problems

In this work, the relationship between three analytical techniques is demonstrated. The direct relationship between the variational approach (VA) and the Hamiltonian approach (HA) is illustrated for a first approximation, and subsequently the relationship between the variational approach and the harmonic balance method (HBM) is concluded. Moreover, the relationship between HA and VA is investigated for higher order solutions.     

A practical access to new pyrrolizine carboxylates via KHMDS-catalyzed carbocyclizations

Easy and effective preparation of new 1H-pyrrolizine carboxylates was achieved with high efficiency via KHMDS-induced carbocyclization of N-alkynyl proline carboxylates under substantially mild conditions. Meanwhile, some trans-diiodoallylic N-proline carboxylates were obtained from N-propargyl proline carboxylates using molecular I₂ with or without KHMDS. This method is quite feasible in terms of practical and quick access to the pyrrolizines and their derivatives over the formation of carbanions.     

Comparative analysis of refrigerant performance between LPG and R134a under subtropical climate

Journal of Thermal Analysis and Calorimetry - In this investigation, a series of experiments were conducted to explore the effects of liquefied petroleum gas (LPG) mixture of 60% propane and 40%...     

Radiation induced copolymerization reactivity of different allyl monomers with styrene

Radiation induced copolymerizations of electron donating such as allyl phenol (AP) and electron withdrawing such as allyl isothiocyanate (AITC) monomers with styrene (Sty) as a comonomer were studied in order to correlate the electronic behavior with copolymerization yield and molecular weight. The allyl monomers and comonomer were mixed in the same mol ratios under Ar atmosphere and copolymerized by using gamma radiation in various absorbed doses (55, 110, 165 kGy) obtained from a Co-60 source. Poly(AP-co-Sty), and poly(AITC-co-Sty) could have been prepared at all of the absorbed doses. The maximum copolymerization yields were calculated as a 16.35 and 6.52 percent for poly(AP-co-Sty) and poly(AITC-co-Sty), respectively. The molecular weights of poly(AP-co-Sty) copolymers are found to be higher in comparison to those of poly(AITC-co-Sty). Both results indicate that, under the same irradiation conditions, AP is more reactive on styrene than AITC is. Thus, the monomers having electron withdrawing (EW) substituents attached to allyl group may result in better copolymerization yield and molecular weight than those with electron donating (ED) substituents. Thermal stabilities of the poly(AP-co-Sty) copolymers are also higher than those of poly(AITC-co-Sty).     

Synthesis and Characterization of Novel Biodegradable Di‐ and Tri‐Block Copolymers Based on Ethylene Carbonate Polymer as Hydrophobic Segment

Synthesis of novel amphiphilic biodegradable block copolymers based on ethylene carbonate is reported in this study. Polyethylene glycol monomethyl ether (MeO‐PEO) and polyethylene glycol (PEG) of varying molar masses are used as macro‐initiator for ring‐opening polymerization of ethylene carbonate in the presence of sodium stannate trihydrate as a heterogeneous transesterification catalyst. Earlier elution of block copolymer from macro‐initiator in size exclusion chromatography (SEC) indicated the successful synthesis of the block copolymers. Ratios of both types of blocks are varied systematically. Liquid chromatography at critical conditions is used for the analysis of the non‐critical individual blocks, and if there are any critical segments that are not attached to the non‐critical block. To the best of our knowledge, this is the first report on the synthesis of ethylene carbonate‐based amphiphilic block copolymers. Chromatographic critical conditions of the ethylene carbonate polymer are also reported for the first time. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 1887–1893     

One-Pot Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones and Their Sulfur Derivatives with H2SO4 Supported on Silica Gel or Alumina

The one-pot condensation of aromatic aldehydes, β-dicarbonyl compounds, and urea or thiourea in the presence of H₂SO₄ supported on silica gel or alumina (80% m/m) in refluxing n-hexane produces 3,4-dihydropyrimidin-2(1H)-ones and their sulfur derivatives in high to excellent yields.