Study on changes of plasmalemma permeability and some primary inorganic ions of Antarctic ice microalgae (Chlamydomonas sp. ICE-L) in the low-temperature stress

The changes of plasmalemma permeability and some primary inorganic ions of Antarctic ice microalgae （ Chlamydomonas sp. ICE-L） in the low-temperature stress were examined. The plasmalemma of 1CE-L could maintain the stability at the freezing condition of -6 ℃. That signifies that it could maintain the proper function of plasmalemma and stability of the intracellular environment during sea ice formation. The function of inorganic ions on low-temperature adaptation of ICE-L was investigated by using the X-ray microanalysis method. Low temperature （0 - -6 ℃ ） induces Ca^2 ＋ concentration increment of cytoplasm, but after 24 h the content decrease quickly to normal value. As a matter of fact, Ca^2 ＋ plays an important role as the second messenger in the low temperature adaptation of ICE-L. In addition, low temperature also influences on the other primary inorganic ions transfer and the cell maintains activity by keeping ratio balance among different ions. Above all, it is necessary for Antarctic ice microalgae to survive and breed by maintaining the stability of K^ ＋ content and the balance of Na^ ＋/Cl^ -.

Effects of Fe3+ and Ca2+ on sorption of phenanthrene by Humin in karst soil,Southwest China

Humin(HM) is the main organic matter component to af fect the migration and transformation of polycyclic aromatic hydrocarbons(PAHs) in soil. The study on infl uence of the morphology change of inorganic ions on the adsorption of PAHs in soil and its organic matter is still rare at microscopic scale. In this paper, yellow soil humin(YS-HM) and lime soil humin(LS-HM) were chosen as samples, then Fe^(3+) and Ca^(2+) were added into samples to facilitate the precipitation by changing the existing conditions of ions, and the mechanism by which inorganic precipitation changed adsorption capacity of karst soil was analyzed from the microscopic scale. The results showed that the adsorption capacity of HM reduced with the inorganic precipitation increasing. The precipitation of Ca^(2+)and Fe^(3+) both reduced the adsorption capacity of YS-HM and LS-HM by 61.71% and 71.83% on average, respectively. The results of scanning electron microscope-energy dispersive spectrometry(SEM-EDS) and pore analysis showed that the HM porosity decreased after formation of Ca^(2+) and Fe^(3+) precipitation. According to the value of Freundlich parameter n, it may be because the precipitation or colloid of Ca^(2+) and Fe^(3+) fi lled micropores and covers high-energy adsorption sites of the HM. This research provides theoretical support for studying the PAHs migration and bioavailability of Calcium-rich in karst soil.

Temporal variations in geochemistry of hydraulic fracturing fluid and flowback water in a tight oil reservoir

Hydraulic fracturing facilitates the development and exploitation of unconventional reservoirs.In this study,the injected hydraulic fracturing fluid(HFF)and flowback and produced water(FPW)in tight oil reservoirs of the Lucaogou Formation in the Junggar Basin are temporally sampled from day 1 to day 64.Freshwater is used for fracturing,and HFF is obtained.The chemical and isotopic parameters(including the water type,total salinity,total dissolved solids(TDS),pH,concentrations of Na^(+),Cl^(-),Ba^(+),K^(+),Fe^(2+)+Fe^(3+),and CO_(3)^(2-),dD,and δ^(18)O)are experimentally obtained,and their variations with time are systematically analyzed based on the flowback water.The results show that the water type,Na/Cl ratio,total salinity,and TDS of the FPW change periodically primarily due to the HFF mixing with formation water,thus causing δD and δ^(18)O to deviate from the meteoric water line of Xinjiang.Because of watererock interaction(WRI),the concentrations of Fe^(2+)+Fe^(3+)and CO_(3)^(2-)of the FPW increase over time,with the solution pH becoming more alkaline.Furthermore,based on the significant changes observed in the geochemistry of the FPW,three separate time intervals of flowback time are identified:Stage Ⅰ(<10 days),where the FPW is dominated by the HFF and the changes in ions and isotopes are mainly caused by the WRI;Stage Ⅱ(10-37 days),where the FPW is dominated by the addition of formation water to the HFF and the WRI is weakened;and finally,Stage Ⅲ(>37 days),where the FPW is dominated by the chemistry of the formation water.The methodology implemented in this study can provide critical support for the source identification of formation water.

Composition, source, mass closure of PM_(2.5) aerosols for four forests in eastern China

PM2.5 aerosols were collected in forests along north latitude in boreal-temperate, temperate, subtropical and tropical climatic zones in eastern China, i.e., Changbai Mountain Nature Reserve （CB）, Dongping National Forest Park in Chongming Island （CM）, Dinghu Mountain Nature Reserve （DH）, Jianfengling Nature Reserve in Hainan Island （HN）. The mass concentrations of PM2.5, organic carbon （OC）, elemental carbon （EC）, water soluble organic carbon （WSOC） as well as concentrations of ten inorganic ions （F？, Cl？, NO3？, SO42？, C2O42？, NH4＋, Na＋, K＋, Ca2＋, Mg2＋） were determined. Aerosol chemical mass closures were achieved. The 24-hr average concentrations of PM2.5 were 38.8, 89.2, 30.4, 18 μg/m3 at CB, CM, DH and HN, respectively. Organic matter and EC accounted for 21%–33% and 1.3%–2.3% of PM2.5 mass, respectively. The sum of three dominant secondary ions （SO42-, NO3-, NH4＋） accounted for 44%, 50%, 45% and 16% of local PM2.5 mass at CB, CM, DH and HN, respectively. WSOC comprised 35%–65% of OC. The sources of PM2.5 include especially important regional anthropogenic pollutions at Chinese forest areas.

Characteristics of Aerosol Pollution Under Different Visibility Conditions in Winter in a Coastal Mega-City in China

To investigate chemical profiles and formation mechanisms of aerosol particles in winter haze events,comprehensive measurements including hourly concentrations of PM2.5 and water-soluble inorganic ions and related gasphase precursors were conducted via an online monitoring system from January to March of 2016 in Shenzhen,a coastal mega-city in south China.In this study,high concentrations of PM2.5,NO2 and lower levels of O3 were observed during haze periods in comparison with clear days(Visibility>15 km).The major secondary ionic species were NH+4、NO-3 and SO2-4,which varied significantly on haze and clear days.The ratio of NO-3/SO2-4 in haze days was greater than that on clear days and tended to be larger when air pollution became more serious.At the same time,compared with previous studies,it has been found that the ratio has been increasing gradually in Shenzhen,indicating that the motor vehicle exhaust emissions have a more and more important impact on air quality in Shenzhen.Sulfur oxidation rate(SOR)and nitrogen oxidation rate(NOR)was higher during the haze period than that in clean days,indicating efficient gas to particle conversion.Further analysis shows that high concentrations of sulfate might be explained by aqueous oxidation,but gas-phase reactions might dominate nitrate formation.This study also highlights that wintertime nitrate formation can be an important contributor to aerosol particles,especially during haze periods.

Effects of parasitic plant Cistanche deserticola on chlorophyll a fluorescence and nutrient accumulation of host plant Haloxylon ammodendron in the Taklimakan Desert

The parasitic plant Cistanche deserticola attaches to Haloxylon ammodendron, a perennial shrub with high tolerance to salinity and drought. However, little was known about the parasite-host relation between the two species. Effects of the parasite on chlorophyll a fluorescence and nutrient accumulation in the host plant （H. am- modendron） were investigated in the Taklimakan Desert. Some photosynthetic parameters of both host and non-host H. ammodendron plants were measured by in vivo chlorophyll a fluorescence technology in the field. The assimilating branches of host and non-host plants were collected and nutrient and inorganic ion contents were analyzed. The results from field experiments showed that the infection of C. deserticola reduced the non-photochemical quenching of the variable chlorophyll fluorescence （NPQ） and the potential maximum quantum yield for primary photochemistry （Fv/Fm） of the host. Compared with non-host plants, the host H. ammodendron had low nutrient, low inorganic ion contents （Na~ and K~） and low K~/Na~ ratios in the assimilating branches. It suggested that C. deserticola infection reduced the nutrient acquisition and caused damage to the photoprotection through thermal dissipation of the energy of the photosystem II in the host, resulting in a decrease in the tolerance to salinity and high radiation. It was concluded that the attachment of the parasite plant （C. deserticola） had negative effects on the growth of its host.

Effect of Rare Earth Elements on Exchange Performances of Cesium Ion-Sieve

The exchange performances and the distribution coefficient of Cesium Ion-Sieve (Cs-IS) for cesium and for some rare earth elements were compared. In particula r, the effects of neodymium on the cesium ion exchange and the Cs+ selectivity v ariation on Cs-IS owing to introduction of rare earth elements into HLLW were s tudied. Though rare earth elements exhibit a small influence on the distributio n coefficient for Cs+, they impair Cs-exchange capacity of Cs-IS to some ext ent. This interruption on the selectivity to Cs+ can be significantly eliminat ed provided an appropriate ratio of liquid to solid V:m is used.

Growth of nitrate contribution to aerosol pollution during wintertime in Xi'an,northwest China:Formation mechanism and effects of NH_(3)

With the strengthened controls on SO2 emissions and extensive increases in motor vehicles'exhaust,aerosol pollution shifts from sulfate-rich to nitrate-rich in recent years in Xi'an,China.To further gain insights into the factors on nitrate formation and efficiently mitigate air pollution,highly time-resolved observations of water-soluble inorganic ions(WSIIs)in PM_(2.5) were measured in a suburban area of Xi'an,China during wintertime.Hourly concentration of total WSIIs is 39.8μg m-3 on average,accounting for 50.3%of PM_(2.5) mass.In contrast to a slight decrease in the mass fraction of SO_(4)^(2-),NO_(3)-shows a sig-nificant increase of the PM_(2.5) contribution with the aggravation of aerosol pollution.This suggests the importance of NO_(3)-formation to haze evolution.Furthermore,homogeneous reactions govern the formation of NO_(3)-,while alkali metals such as calcium and sodium play an additional role in retaining NO_(3)-in PM_(2.5) during clean periods.However,the heterogeneous hydrolysis reaction contributed more to NO_(3)-formation during the pollution periods under high relative humidity.Our investigation reveals that temperature,relative humidity,oxidant,and ammonia emissions facilitate rapid NO_(3)-formation.Using the random forest(RF)model,NO_(3)-concentrations were successfully simulated with measured variables for the training and testing datasets(R2>0.95).Among these variables,CO,NH_(3),and NO_(2) were found to be the main factors affecting the NO_(3)-concentrations.Compared with the period without vehicle re-striction,the contributions of NO_(3)-and NH4+to PM_(2.5) mass decreased by 5.3%and 3.4%in traffic re-striction periods,respectively.The vehicle restriction leads to the decreases of precursor gases of NO_(2),SO_(2),and NH_(3) by 12.8%,5.9%,and 27.6%,respectively.The results demonstrate collaborative emission reduction of NO_(x) and NH_(3) by vehicle restrictions,and using new energy vehicles(or electric vehicles)can effectively alleviate particulate matter pollution in northwest China.

Chemical characteristics of PM_(2.5) during a typical haze episode in Guangzhou

The chemical characteristics（water-soluble ions and carbonaceous species） of PM2.5 in Guangzhou were measured during a typical haze episode.Most of the chemical species in PM2.5 showed significant difference between normal and haze days.The highest contributors to PM2.5 were organic carbon（OC）,nitrate,and sulfate in haze days and were OC,sulfate,and elemental carbon（EC） in normal days.The concentrations of secondary species such as,NO3^-,SO4^2-,and NH4^＋ in haze days were 6.5,3.9,and 5.3 times higher than those in normal days,respectively,while primary species（EC,Ca^2＋,K^＋） show similar increase from normal to haze days by a factor about 2.2-2.4.OC/EC ratio ranged from 2.8 to 6.2 with an average of 4.7 and the estimation on a minimum OC/EC ratio showed that SOC（secondary organic carbon） accounted more than 36.6% for the total organic carbon in haze days.The significantly increase in the secondary species（SOC,NO3^-,SO4^2-,and NH4^＋）,especially in NO3^-,caused the worst air quality in this region.Simultaneously,the result illustrated that the serious air pollution in haze episodes was strongly correlated with the meteorological conditions.During the sampling periods,air pollution and visibility had a good relationship with the air mass transport distance;the shorter air masses transport distance,the worse air quality and visibility in Guangzhou,indicating the strong domination of local sources contributing to haze formation.High concentration of the secondary aerosol in haze episodes was likely due to the higher oxidation rates of sulfur and nitrogen species.

亲水作用色谱柱与阳离子交换树脂柱结合分离无机离子(英文)

A combination of hydrophilic interaction chromatographic(HILIC) column and a weakly acidic cation-exchange resin(WCX) column was used for simultaneous separation of inorganic anions and cations by ion chromatography(IC).Firstly,the capability of HILIC column for the separation of analyte ions was evaluated under acidic eluent conditions.The columns used were SeQuant ZIC-HILIC(ZIC-HILIC) with a sulfobetaine-zwitterion stationary phase(ZIC-HILIC) and Acclaim HILIC-10 with a diol stationary phase(HILIC-10).When using tartaric acid as the eluent,the HILIC columns indicated strong retentions for anions,based on ion-pair interaction.Especially,HILIC-10 could strongly retain anions compared with ZIC-HILIC.The selectivity for analyte anions of HILIC-10 with 5 mmol/L tartaric acid eluent was in the order of I-> NO-3 > Br-> Cl-> H2PO-4.However,since HILIC-10 could not separate analyte cations,a WCX column(TSKgel Super IC-A/C) was connected after the HILIC column in series.The combination column system of HILIC and WCX columns could successfully separate ten ions(Na+,NH+4,K+,Mg2+,Ca2+,H2PO-4,Cl-,Br-,NO-3 and I-) with elution of 4 mmol/L tartaric acid plus 8 mmol/L 18-crown-6.The relative standard deviations(RSDs) of analyte ions by the system were in the ranges of 0.02%-0.05% in retention times and 0.18%-5.3% in peak areas through three-time successive injections.The limits of detection at signal-to-noise ratio of 3 were 0.24-0.30 μmol/L for the cations and 0.31-1.2 μmol/L for the anions.This system was applied for the simultaneous determination of the cations and the anions in a vegetable juice sample with satisfactory results.

强碱阴离子交换树脂及碱性洗脱剂的离子排阻/阴离子交换色谱法同时测定NH_4^+，NO_2^-和NO_3^-(英文)

Ion-exclusion/anion-exchange chromatography(IEC/AEC) on a combination of a strongly basic anion-exchange resin in the OH——form with basic eluent has been developed.The separation mechanism is based on the ion-exclusion/penetration effect for cations and the anion-exchange effect for anions to anion-exchange resin phase.This system is useful for simultaneous separation and determination of ammonium ion(NH+4),nitrite ion(NO-2),and nitrate ion(NO-3) in water samples.The resolution of analyte ions can be manipulated by changing the concentration of base in eluent on a polystyrene-divinylbenzene based strongly basic anion-exchange resin column.In this study,several separation columns,which consisted of different particle sizes,different functional groups and different anion-exchange capacities,were compared.As the results,the separation column with the smaller anion-exchange capacity(TSKgel Super IC-Anion) showed well-resolved separation of cations and anions.In the optimization of the basic eluent,lithium hydroxide(LiOH) was used as the eluent and the optimal concentration was concluded to be 2 mmol/L,considering the resolution of analyte ions and the whole retention times.In the optimal conditions,the relative standard deviations of the peak areas and the retention times of NH+4,NO-2,and NO-3 ranged 1.28%-3.57% and 0.54%-1.55%,respectively.The limits of detection at signal-to-noise of 3 were 4.10 μmol/L for NH+4,1.87 μmol/L for NO-2 and 2.83 μmol/L for NO-3.

Year-round observation of atmospheric inorganic aerosols in urban Beijing:Size distribution,source analysis,and reduction mechanism

To investigate particle characteristics and find an effective measure to control severe particle pollution,year-round observation of size-segregated inorganic aerosols was conducted in Beijing fromJanuary to December,2016.The sampled atmospheric particles all presented bimodal size distribution at four pollution levels(clear,slight pollution,moderate pollution and severe pollution),and peak values appeared at the size range of 0.7-2.1μmand>9.0μm,respectively.As dominant particle compositions,NO_(3)^(-),SO_(4)^(2-),and NH_(4)^(+)in four pollution levels all showed significant peaks in fine mode,especially at the size range of 1.1-2.1μm.Secondary inorganic aerosols accounted for about 67.6%(36.3%(secondary sulfates)+31.3%(secondary nitrates))of the total sources of fine particles in urban Beijing.Severe pollution of fine particles was mainly caused by the air masses transported from nearby western and southern areas,which are industrial and densely populated region,respectively.Sensitivity tests further revealed that the control measures focusing on ammonium emission reduction was the most effective for particle pollution mitigation,and fine particles all showed nonlinear responses after reducing ammonium,nitrate,and sulfate concentrations,with the fitting curves of y=-120.8x-306.1x^(2)+290.2x^(3),y=-43.5x-67.8x^(2),and y=-25.8x-110.4x^(2)+7.6x^(3),respectively(y and x present fine particle mass variation(μg/m3)and concentration reduction ratio(CRR)/100(dimensionless)).Overall,our study presents useful information for understanding the characteristics of atmospheric inorganic aerosols in urban Beijing,as well as offers policy makers with effective measure for mitigating particle pollution.

Highly efficient cobalt-based amorphous catalyst for peroxymonosulfate activation toward wastewater remediation

Metallic glasses(MGs)are rising novae in the catalytic field,due to their unique amorphous structure,large residual stress,and high density of low coordination sites.However,there is still an absence of suitable MGs'catalysts for advanced oxidation processes(AOPs)with peroxymonosulfate(PMS),the most efficient and promising wastewater remediation technology.Herein,the cobalt-based MG(Co-MG)with a nominal composition of Co_(67)Fe_(4)-Mo_(1.5)Si_(16.5)B_(11)(at%)was utilized as an activator of PMS for azo dye degradation.The results demonstrated that the CoMG/PMS system had an order of magnitude higher efficiency on OrangeⅡ(OII)degradation than the Fe-MG/PMS system.For fundamental study and field application,the effect of adding inorganic anions(Cl^(-),HCO_(3)^(-),H_(2)PO_(4)^(-),SO_(4)^(2-),NO_(3)^(-)),environmental factors,and cycle experiments on the catalytic properties of Co-MG were investigated emphatically to evaluate overall degradation performance.It has demonstrated that the Co-MG with more stability,better corrosion resistance and durability contrasted to Fe-MGs.In addition,the excellent catalytic performance of Co-MG was analyzed based on the quenched experiment,electron paramagnetic resonance(EPR),and X-ray photoelectron spectroscopy(XPS)analysis.The present results provide not only a new candidate but also shed light on exploring a new kind of AOPs system based on Co-MGs for wastewater treatment.

Chemical compositions of PM_(2.5) aerosol during haze periods in the mountainous city of Yong'an, China

Haze phenomena were found to have an increasing tendency in recent years in Yong＇an, a mountainous industrial city located in the center part of Fujian Province, China. Atmospheric fine particles （PM2.5） in the urban area during haze periods in three seasons （spring, autumn and winter） from 2007 to 2008 were collected, and the mass concentrations and chemical compositions （seventeen elements, water soluble inorganic ions （WSIIs） and carbonaceous species） of PM2.5 were determined. PM2.5 mass concentrations did not show a distinct difference among the three seasons. The carbonaceous species organic carbon （OC） and elemental carbon （EC） constituted up to 19.2%-30.4% of the PM2.5 mass during sampling periods, while WSIIs made up 25.3%-52.5% of the PM2.5 mass. The major ions in PM2.5 were SO42-, NO3- and NH4~, while the major elements were Si, K, Pb, Zn, Ca and A1. The experimental results （from data based on three haze periods with a 10-day sampling length for each period） showed that the crustal element species was the most abundant component of PM2.5 in spring, and the secondary ions species （SO42-, NO3-, NH4＋, etc.） was the most abundant component in PM2.5 in autumn and winter. This indicated that dust was the primary pollution source for PM2.5 in spring and combustion and traffic emissions could be the main pollution sources for PM2.5 in autumn and winter. Generally, coal combustion and traffic emissions were considered to be the most prominent pollution sources for this city on haze days.

Chemical characteristics and source apportionment of PM_(2.5) between heavily polluted days and other days in Zhengzhou, China

PM（2.5） samples were collected in Zhengzhou during 3 years of observation, and chemical characteristics and source contribution were analyzed. Approximately 96% of the daily PM（2.5） concentrations and annual average values exceeded the Chinese National Ambient Air Quality Daily and Annual Standards, indicating serious PM（2.5） pollution. The average concentration of water-soluble inorganic ions was 2.4 times higher in heavily polluted days（daily PM32.5 concentrations ＆gt; 250 μg/mand visibility ＆lt; 3 km） than that in other days, with sulfate, nitrate, and ammonium as major ions. According to the ratio of NO-3/SO2-4,stationary sources are still the dominant source of PM（2.5） and vehicle emission could not be ignored. The ratio of secondary organic carbon to organic carbon indicated that photochemical reactivity in heavily polluted days was more intense than in other days.Crustal elements were the most abundant elements, accounting for more than 60% of 23 elements. Chemical Mass Balance results indicated that the contributions of major sources（i.e., nitrate, sulfate, biomass, carbon and refractory material, coal combustion, soil dust,vehicle, and industry） of PM（2.5） were 13%, 16%, 12%, 2%, 14%, 8%, 7%, and 8% in heavily polluted days and 20%, 18%, 9%, 2%, 27%, 14%, 15%, and 9% in other days, respectively.Extensive combustion activities were the main sources of polycyclic aromatic hydrocarbons during the episode（Jan 1-9, 2015） and the total benzo[a]pyrene equivalency concentrations in heavily polluted days present significant health threat. Because of the effect of regional transport, the pollution level of PM（2.5） in the study area was aggravated.

Ionic composition of submicron particles(PM_(1.0)) during the long-lasting haze period in January 2013 in Wuhan, central China

In January 2013, a long-lasting severe haze episode occurred in Northern and Central China; at its maximum, it covered a land area of approximately 1.4 million km2. In Wuhan, the largest city in Central China, this event was the most severe haze episode in the 21st century. Aerosol samples of submicron particles （PMI.o） were collected during the long-lasting haze episode at an urban site and a suburban site in Wuhan to investigate the ion characteristics of PMi.0 in this area. The mass concentrations of PM1.0 and its water-soluble inorganic ions （WSIIs） were almost at the same levels at two sites, which indicates that PM1.0 pollution occurs on a regional scale in Wuhao. WSIIs （Na^＋, NH4^＋, K^＋, Mg^2＋, Ca^2＋, Cl^-, NO3 and SO2-） were the dominant chemical species and constituted up to 48.4% and 47.4% of PM1.0 at WD and TH, respectively. The concentrations of PM1.0 and WSIIs on haze days were approximately two times higher than on normal days. The ion balance calculations indicate that the particles were more acidic on haze days than on normal days. The results of the back trajectory analysis imply that the high concentrations of PM1.0 and its water-soluble inorganic ions may be caused by stagnant weather conditions in Wuhan.

Advances in cyclodextrin polymers adsorbents for separation and enrichment:Classification,mechanism and applications

Over the past few decades,supramolecular chemistry has entered the field of scientific research and attracted extensive attention.Among supramolecular macrocycles,cyclodextrins(CDs)are widely applied in the field of adsorption due to their unique structure and properties.This review focuses on the important role of cyclodextrin polymers(CDPs)as adsorbents in the adsorption of different substances.It covers the category of CDPs adsorbents(including crosslinked CDPs,grafted CDPs,CD-based polyrotaxanes/pseudopolyrotaxanes,and imprinted CDPs),their adsorption mechanism and applications in the adsorption of inorganic metal ions,organic pollutants,and biomacromolecules.Finally,the challenges and future perspectives in relative research fields are discussed.

Tuned single atom coordination structures mediated by polarization force and sulfur anions for photovoltaics

Impeding high temperature sintering is challengeable for synthesis of carbon-supported single-atom catalysts (C-SACs), which requires high-cost precursor and strictly-controlled procedures. Herein, by virtue of the ultrastrong polarity of salt melts, sintering of metal atoms is effectively suppressed. Meanwhile, doping with inorganic sulfur anions not only produces sufficient anchoring sites to achieve high loading of atomically dispersed Co up to 13.85 wt.%, but also enables their electronic and geometric structures to be well tuned. When served as a cathode catalyst in dye-sensitized solar cells, the C-SAC with Co-N4-S2 moieties exhibits high activity towards the iodide reduction reaction (IRR), achieving a higher power conversion efficiency than that of conventional Pt counterpart. Density function theory (DFT) calculations revealed that the superior IRR activity was ascribed to the unique structure of Co-N4-S2 moieties with lower reaction barriers and moderate binding energy of iodine on the Co center, which was beneficial to I2 dissociation.

Chemical characteristics of haze particles in Xi＇an during Chinese Spring Festival： Impact of fireworks burning

Fireworks burning releases massive fine particles and gaseous pollutants, significantly deteriorating air quality during Chinese Lunar New Year （LNY） period. To investigate the impact of the fireworks burning on the atmospheric aerosol chemistry, 1-hr time resolution of PM2.5 samples in Xi＇an during the winter of 2016 including the LNY were collected and detected for inorganic ions, acidity and liquid water content （LWC） of the fine aerosols. PM2.5 during the LNY was 167 ± 87 μg/m^3, two times higher than the China National Ambient Air Quality Standard （75 μg/m^3）. K^＋ （28 wt.% of the total ion mass） was the most abundant ion in the LNY period, followed by SO^2-4 （25 wt.%） and C1^- （18 wt.%）. In contrast, NO^-3 （34 wt.%） was the most abundant species in the haze periods （hourly PM2.5 〉 75 μg/m^3）, followed by SO^2-4 （29.2 wt.%） and NH^＋4 （16.3 wt.%）, while SC94 （35 wt.%） was the most abundant species in the clean periods （hourly PM2.5 〈 75 μg/m^3）, followed by NO^-3 （23.1 wt.%） and NH^＋4 （11 wt.%）. Being different from the acidic nature in the non-LNY periods, aerosol in the LNY period presented an alkaline nature with a pH value of 7.8 ± 1.3. LWC during the LNY period showed a robust linear correlation with K2SO4 and KC1, suggesting that aerosol hygroscopicity was dominated by inorganic salts derived from fireworks burning. Analysis of correlations between the ratios of NO^-3/SO^2-4 and NH^＋4/SO^2-4 indicated that heterogeneous reaction of HNO3 with NH3 was an important formation pathway of particulate nitrate and ammonium during the LNY period.

Characteristics of chemical components in PM2.5 at a plateau city, South-west China

A sampling campaign including summer, autumn and winter of 2014 and spring of 2015 was accomplished to obtain the characteristic of chemical components in PM2.5 at three sites ofKunming, a plateau city in South-west China. Nine kinds of water-soluble inorganic ions （WSI）, organic and element carbon （OC and EC） in PM2.5 were analyzed by ion chromatography and thermal optical reflectance method, respectively. Results showed that the average concentrations of total WSI, OC and EC were 22.85±10.95 μg.m -3, 17.83±9.57 μg.m-3 and 5.114-4.29 μg.m-3, respectively. They totally accounted for 53.0% of PM2.5. Secondary organic and inorganic aerosols （SOA and SIA） were also assessed by the minimum ratio of OC/EC, nitrogen and sulfur oxidation ratios. The annual average concentrations of SOA and SIA totally accounted for 28.3% of the PM2.5 concentration. The low proportion suggested the primary emission was the main source of PM2.5 in Kunming. However, secondary pollution in the plateau city should also not be ignorable, due to the appropriate temperature and strong solar radiation, which can promote the atmospheric photochemical reactions.