Corrosion inhibition of α,β-unsaturated carbonyl compounds on steel in acid medium

Corrosion inhibition of three α,β-unsaturated carbonyl compounds on N80 steel at high temperature and in concentrated acid medium was evaluated, and the inhibition mechanism was investigated. The results proved that both cinnamaldehyde and benzalacetone had an evident anticorrosion effect and could reduce the corrosion of steel effectively in acid medium, α,β-unsaturated carbonyl compounds with a benzene ring structure had good adsorption on steel surface. The experiments proved that polymerization of α,β-unsaturated carbonyl compounds on the steel surface at a high temperature and in concentrated acid medium resulted in a good corrosion inhibiting effect, which was attributed to the structures of α,β-unsaturated carbonyl compounds.

Silica sulfuric acid:A versatile reagent for oxathioacetalyzation of carbonyl compounds and deprotection of 1,3-oxathiolanes

Oxathioacetalyzation of carbonyl compounds with 2-mercaptoethanol and deprotection of the obtained 1,3-oxathiolanes is easily performed in the presence of silica sulfuric acid （SSA）. All reactions were performed under mild and completely heterogeneous reaction conditions in good to high yields.

[Hmim]_3PW_(12)O_(40):A high-efficient and green catalyst for the acetalization of carbonyl compounds

[Hmim]_3PW_(12)O_(40) was developed and used in the acetalization of carbonyl compounds in excellent yields.The ionic liquidheteropoly acid hybrid compound and reaction medium formed temperature-dependent phase-separation system with the ease of product as well as catalyst separation.The catalyst was recycled more than 10 times without any apparent loss of catalytic activity.

MICHAEL ADDITION OF NITROALKANE TO α,β-UNSATURATED CARBONYL COMPOUNDS ON KF / Al_2O_3/ PEG4000

Michael addition of nitroalkanes to α,β-unsaturated carbonyl compounds occurs in the presence of KF/AI_2O_3/PEG4000 without solvent.Yields are fair to good and work-ups are easy.

Trifluoromethylation of Carbonyl Compounds with Sodium Trifluoroacetate

In the presence of copper （I） halide as catalyst, a variety of carbonyl compounds could be trifluoromethylated with sodium trifluoroacetate to give the corresponding alcohols in moderate to high yields.

Zeolite-Catalyzed Acetalization Ⅰ. Synthesis of Some Acetals and Ketals through Reaction of Carbonyl Compounds with Ethanediol

The acetalization of a series of carbonyl compounds with ethanediolwas performed over two self-steaxned HY zeolle catalpsts' The acetal and ketaiproducts were obtained with high ytelds Espectw, the HY zeollte with highfraxnework Si/A1 ratio was proven to be suitable cataipst for the acetabotion ofunsaturated carbonyl compounds, during which the C =C double bond was notperturbed

OXIDATION OF α-METHYL OR α-METHYLENE GROUPS IN CARBONYL COMPOUNDS WITH AMMONIUM CHLOROCHROMATE

This paper reports a new method for oxidizing the α-methyl or α-methylene groups in carbonyl compounds into 1,2-dicarbonyl compounds by ammonium chlorochromate(ACC).

Addition of Per(poly)fluoroalkyl Iodides to vinyl Cyclopropane Derivatives: Synthesis of Fluoroalkyl Substituted γ,δ-Unsaturated Carbonyl Compounds

In the presence of CrC13 /Fe bimetal couple,per(poly)fluoroalkyl iodides add to vinyl cyclopropane compounds giving addition-ring-opening products in good yields.

A New HPLC Method to Determine Carbonyl Compounds in Air

In this paper, a new HPLC method was established to determine the carbonyl compounds in air. As the absorbent, 2, 4-dinitrophenylhydrazine (2, 4-DNPH) reacted with carbonyls specifically, which form the corresponding 2,4-dinitrophenylhydrazones, then analyzed by HPLC. The chromatographic conditions, the recovery rate, stability of samples, reagent blank, sampling efficiency were all studied systematically. The results showed that this established method had high sensitivity and good selectivity compared with other analytical methods, and it can determine ten carbonyl compounds in air in 26 min simultaneously.

CONVERSION OF ACETALS AND KETALS TO CARBONYL COMPOUNDS PROMOTED BY ZrCl_4-NaBH_4

In our study on the chemistry of ZrCl_4-NaBH_4,we have found that aldehydes and ketones can be regenerated from acetals and ketals at 30℃ in Et_2O in high yield The reaction mechanism was discussed.

α-C(sp^(3))-H Arylation of Cyclic Carbonyl Compounds

α-C(sp^(3))-H arylation is an important type of C-H functionalization.Various biologically significant natural products,chemi-cal intermediates,and drugs have been effectively prepared via C-H functionalization.Cyclic carbonyl compounds comprise of cyclic ketones,enones,lactones,and lactams.Theα-C(sp^(3))-H arylation of these compounds have been exhibited high efficiency in forming C(sp^(3))-C(sp^(2))bonds,played a crucial role in organic synthesis,and attracted majority of interests from organic and medicinal communities.This review focused on the most significant advances including methods,mechanism,and applications in total synthesis of natural products in the field ofα-C(sp^(3))-H arylations of cyclic carbonyl compounds in recent years.

Emissions of volatile organic compounds and carbonyl compounds from residential coal combustion in China

Emissions of volatile organic compounds （VOCs） and carbonyls from residential coal combustion of five coals with different maturities were studied in a simulated room.The coals were burned in form of honeycomb briquettes in a domestic coal stove,one of the most common fuel/stove combinations in China.Through a dilution system,VOCs and carbonyls samples were collected by canisters and silica-gel cartridges and analyzed by gas chromatography and mass spectrum （GC/MS） and high performance liquid chromatography/ultraviolet （HPLC/UV）,respectively.The results show that the bituminous coals with medium volatile matter content produce the highest emissions while the anthracite yields the lowest.Among the identified carbonyls from the coal smoke,the aromatic compounds （benzaldehyde,2,5-dimethylbenzaldehyde and p-tolualdehyde,m/o-tolualdehyde,benzene,m,p-xylene and trimethyl-benzene） were relatively abundant,which might be due to the molecular structure of the coal.For formaldehyde,aromatic carbonyls and aliphatic alkanes,their concentrations increase up to the maximum values and then decrease with increasing coal maturity.The total carbonyls and VOCs have the same tendency,which was observed for the emission factors of organic carbon （OC）,elemental carbon （EC）,particulate matter （PM） and polycyclic aromatic hydrocarbons （PAHs） detected in the series study.

Selectivity of Organosamarium(Ⅲ) Hydride in Reducing Unsaturated Carbonyl Compounds

The selectivity of organosamarium(Ⅲ) hydride in reducing unsaturated carbonyl compounds has been studied. Dimeric organosamarium hydride[(C_9H_7)_2SmH]_2·4THF·NaCl prepared by the reaction of (C_9H_7)_2SmCl·2THF with NaH in THF reacts with unsaturated carbonyl compounds to give the corresponding reduction products with a high selectivity. The carbonyl groups have been reduced while the carbon-carbon double bonds are not affected.

Real-world emission characteristics of carbonyl compounds from agricultural machines based on a portable emission measurement system

Emissions of carbonyl compounds from agricultural machines cannot be ignored.Carbonyl compounds can cause the formation of ozone(O3)and secondary organic aerosols,which can cause photochemical smog to form.In this study,20 agricultural machines were tested using portable emission measurement system(PEMS)under real-world tillage processes.The exhaust gases were sampled using 2,4-dinitrophenylhydrazine cartridges,and 15 carbonyl compounds were analyzed by high-performance liquid chromatography.Carbonyl compound emission factors for agricultural machines were 51.14–3315.62 mg/(kg-fuel),and were 2.58±2.05,0.86±1.07 and 0.29±0.20 g/(kg-fuel)for China 0,China II and China III emission standards,respectively.Carbonyl compound emission factor for sowing seeds of China 0 agricultural machines was 3.32±1.73 g/(kg-fuel).Formaldehyde,acetaldehyde and acrolein were the dominant carbonyl compounds emitted.Differences in emission standards and tillage processes impact ozone formation potential(OFP).The mean OFP was 20.15±16.15 g O3/(kg-fuel)for the China 0 emission standard.The OFP values decreased by 66.9% from China 0 to China II,and 67.4%from China II to China III.The mean OFP for sowing seeds of China 0 agricultural machines was 25.92±13.84 g O3/(kg-fuel).Between 1.75 and 24.22 times more ozone was found to be formed during sowing seeds than during other processes for China 0 and China II agricultural machines.Total carbonyl compound emissions from agricultural machines in China was 19.23 Gg in 2019.The results improve our understanding of carbonyl compound emissions from agricultural machines in China.

PEG-OSO_3H as an efficient and recyclable catalyst for the synthesis of β-amino carbonyl compounds via the Mannich reaction in PEG-H_2O

Sulfuric acid-modified polyethylene glycol 6000（PEG-OSO_3H） was applied as an efficient and recyclable catalyst for the synthesis ofβ-amino carbonyl compounds via the Mannich reaction between aldehydes,aromatic ketones and aromatic amines at room temperature using PEG400-H_2O（1：1） as environment-friendly solvents.The reactions were completed in short times and mild reaction conditions with good to excellent yields.

Engineering electrophilic atomic Ir sites on CeO_(2) colloidal spheres for selectivity control in hydrogenation of α,β-unsaturated carbonyl compounds

Selective hydrogenation of the carbonyl bond inα,β-unsaturated carbonyl compounds is rather challenging owing to the more feasible hydrogenation of ethylenic bond from both thermodynamic and kinetic aspects.Here,we demonstrate a facile emulsionbased molecule-nanoparticle self-assembly strategy for the atomic engineering of Ir species on three-dimensional CeO_(2)spheres(Ir1@CeO_(2)).When applied to the hydrogenation ofα,β-unsaturated aldehydes,Ir1@CeO_(2)catalyst remarkably exhibited~100%selectivity towards unsaturated alcohols,whereas the formation of Ir nanoparticles on CeO_(2)drastically decreased the selectivity for unsaturated alcohols.Spectroscopic studies revealed that strong metal-support interactions triggered the charge transfer from Ir to CeO_(2),leading to the partial reduction of Ce^(4+)to Ce^(3+)along with the formation new Ir^(δ+)-O_(2)--Ce^(3+)(OV)interfaces.The electrophilic atomic Ir species at the Ir^(δ+)-O_(2)--Ce^(3+)(OV)interfaces would therefore preferentially adsorb and facilitate hydrogenation of polar C=O bond to achieve exceptional selectivity.

Indoor carbonyl compounds in an academic building in Beijing, China： concentrations and influencing factors

Carbonyl compounds in indoor air are of great concern for their adverse health effects. Between February and May, 2009, concentrations of 13 carbonyl compounds were measured in an academic building in Beijing, China. Total concentration of the detected carbonyls ranged from 20.7 to 189.1 I.tg.m3, and among them acetone and formaldehyde were the most abundant, with mean concentrations of 26.4 and 22.6gg.m-3, respectively. Average indoor concentrations of other carbonyls were below I 0 gg. m^3. Principal component analysis identified a combined effect of common indoor carbonyl sources and ventilation on indoor carbonyl levels. Diurnal variations of the carbonyl compounds were investigated in one office room, and carbonyl concentrations tended to be lower in the daytime than at night, due to enhanced ventilation. Average concentrations of carbonyl compounds in the office room were generally higher in early May than in late February, indicating the influence of temperature. Carbo- nyl source emission rates from both the room and human occupants were estimated during two lectures, based on one-compartment mass balance model. The influence of human occupants on indoor carbonyl concentrations varies with environmental conditions, and may become signifi- cant in the case of a large human occupancy.

Simple and Clean Synthesis: Tin-mediated Allylation of Carbonyl Compounds in Water

Tin mediated allylation of aldehydes or ketones in distilled water gives rise to the corresponding homoallyl alcohols in high yield without assistance such as heat, supersonic and acidic media.

Carbonyl compounds in dining areas,kitchens and exhaust streams in restaurants with varying cooking methods in Kaohsiung,Taiwan

Eighteen carbonyl species in C_1-C_（10） were measured in the dining areas,kitchens and exhaust streams of six different restaurant types in Kaohsiung,southern Taiwan.Measured results in the dining areas show that Japanese barbecue（45.06 ppb） had the highest total carbonyl concentrations（sum of 18 compounds）,followed by Chinese hotpot（38.21 ppb）,Chinese stir-frying（8.99 ppb）,Western fast-food（8.22 ppb）,Chinese-Western mixed style（7.38 ppb）,and Chinese buffet（3.08 ppb）,due to their different arrangements for dining and cooking spaces and different cooking methods.On average,low carbon-containing species（C_1-C_4）,e.g.,formaldehyde,acetaldehyde,acetone and butyraldehyde were dominant and contributed 55.01%-94.52%of total carbonyls in the dining areas of all restaurants.Meanwhile,Chinese-Western mixed restaurants（45.48 ppb） had high total carbonyl concentrations in kitchens mainly because of its small kitchen and poor ventilation.However,high carbon-containing species（C_5-C_（10）） such as hexaldehyde,heptaldehyde and nonanaldehyde（16.62%-77.00%of total carbonyls） contributed comparatively with low carbon-containing compounds（23.01%-83.39%of total carbonyls） in kitchens.Furthermore,Chinese stir-frying（132.10 ppb）,Japanese barbecue（125.62 ppb）,Western fast-food（122.67 ppb）,and Chinese buffet（119.96 ppb） were the four restaurant types with the highest total carbonyl concentrations in exhaust streams,indicating that stir-frying and grilling are inclined to produce polluted gases.Health risk assessments indicate that Chinese hotpot and Japanese barbecue exceeded the limits of cancer risk（10^（-6）） and hazard index（=1）,mainly due to high concentrations of formaldehyde.The other four restaurants were below both limits.