Global CO_(2) concentration change induced by“trigger-connectors”model,especially since about 24 Ma?A preliminary hypothesis

Background,aim,and scope The tectonic uplift of the Cenozoic Tibetan Plateau has produced a chain effect,which is an excellent location for Earth system science research,and its uplift process,mechanism and environmental effects are the hot spot and frontier of the current research.The“Tibetan Plateau uplift-weathering-CO_(2) concentration-global climate change”model was put forward by Raymo and Ruddiman to interpret the Late Cenozoic climate change.However,there are still some questions suspended,such as does the weathering of the Tibetan Plateau have the ability to control the global climate?How to explain the modern-like global CO_(2) concentration starting at about 24 Ma?Here,a short space was taken to present a brainstorm about the above questions on account of existing geological pieces of evidence.Materials and methods In this paper,we integrate the formation and evolution of the Yangtze River and Pearl River,the origin and development of the Asian inland aridification-monsoon system,the Cenozoic tectonic uplift process of the Tibetan Plateau,and the westerly winds to discuss and analyze the relationship between the Cenozoic CO_(2) concentration changes and the uplift of the Tibetan Plateau and why the CO_(2) concentration similar to the present was formed at about 24 Ma.Results Similar correspondence of the surface uplift history of Xizang,other global mountains,and the declining CO_(2) concentration could support the theory Tibetan Plateau weathering inf luences CO_(2) concentration.Starting from 24 Ma,the most important character was the uplift and erosion of Xizang and Himalaya,collaborating with Ocean Iron Fertilization(OIF)together as an entity to control the atmospheric CO_(2) concentration because the great Asian rivers,Asian monsoons,and westerlies connected Xizang and surrounded seas together through materials transportation.Discussion Paleogeographic reconstructions from 40 Ma to 20 Ma illustrate that the main topographic change occurred in the Andes,Cordillera orogenic belt,and Xizang.We comprise a comprehensive set of evidence from independent data,which correspond temporally with the tipping point(about 24 Ma)of the atmospheric CO_(2) and we noticed that modern-like Asia monsoon,inland aridity,Asian great rivers,and climate zone formed at about 24 Ma and also there are tectonic activities for the Andes and Rockies.We raised the possibility that the modern-like atmospheric CO_(2) concentration at about 24 Ma was caused by the above geological factors.Here the rivers,monsoon,and westerlies are termed as“connectors”.In addition,these Asian rivers originated from Xizang,the monsoon,and inner Asian aridification are strongly a function of the uplift and growth of Xizang,thus,Xizang here is named as“trigger”.The distinct character of“trigger-connectors”model is that this not only takes the monsoon,westerlies,and the global great rivers into consideration but also expands the range which inf luences atmospheric CO_(2) concentration,from local points to a vast area since about 24 Ma,such as from Tibetan Plateau to Asia,including surrounded seas,after about 24 Ma.However,because the opening of the Late Oligocene-Early Miocene Antarctic periphery straits is highly coincident with the onset of modern-like global atmospheric CO_(2) concentration,we are forced to consider that they also had a significant impact on the reduction of atmospheric CO_(2) concentrations at this time.Conclusions“Trigger-connectors”was put forward to explain the Cenozoic CO_(2) variation,especially modern-like global CO_(2) concentration since about 24 Ma.Recommendations and perspectives Here we use the“trigger-connectors”model to explain the formation of modern-like CO_(2) concentrations starting at about 24 Ma,but there are still some problems.The most important premise for the“trigger-connectors”model is the constructed Cenozoic CO_(2) concentration record is reliable,which is the foundation of our hypothesis.In the future,potential improvements should focus on topographic reconstructions of Xizang and the global mountains.Here we have concentrated on Xizang in the considered timeslices but still,pay less attention to other global orogenic belts.Collaborations with geologist experts in those regions could provide valuable feedback to evaluate their potential role of them in CO_(2) evolution.What is more,considerable progress may be achieved with the addition and consideration of more and new geological data.

一种具有识别Hg^(2+)和ClO^(-)荧光探针的设计和应用

设计合成了一种含双酯基的1,2,3-三氮唑化合物,与罗丹明B酰肼结合生成了具有“开-关”性质的荧光探针(简称L_(2)),应用光谱学表征了L_(2)的物理化学参数。L_(2)分别在DMF/Tris-HCl(1:1,v/v,pH=6.0,20μmol/L)和MeOH(20μmol/L)溶液中对Hg^(2+)和ClO^(-)显示出高选择性和灵敏性;利用荧光和紫外光谱分别测定了L_(2)对19种金属离子和14种阴离子的光学性能。实验表明,Hg^(2+)和ClO^(-)的存在使得L_(2)在585 nm和576 nm均有一个新的发射峰出现;同时伴随着荧光强度明显的增强,溶液体系发生了裸眼能识别的显色变化,表明Hg^(2+)可以将罗丹明分子的酰肼闭环结构转换为开环结构,并以1:2的比例方式生成了一种新配合物,这也被质谱、工作曲线、核磁滴定和TD-DFT计算的结果所证实;L_(2)对Hg^(2+)和ClO^(-)的检测限分别为7.45 nmol/L和0.67μmol/L。此外,生物活性测定显示L_(2)对HeLa细胞有非常低的毒性,并且可用于HeLa细胞中Hg^(2+)和ClO^(-)的细胞成像,表明L_(2)在体内可进行微测定Hg^(2+)和ClO^(-)的巨大潜力。

基于点击-去点击化学反应的Hg^(2+)荧光探针检测体系构建

基于杂化罗丹明与巯基化合物之间的点击化学反应及巯基化合物与金属汞离子的配位反应导致的去点击化学反应机理,构建香豆素杂化罗丹明探针-1,3,5-苯三硫酚-Hg^(2+)的三元荧光检测体系。在该体系中,探针能够与1,3,5-苯三硫酚中的巯基基团发生加成反应,破坏探针的共轭结构,从而导致探针的红色荧光猝灭。加入Hg^(2+)后,Hg^(2+)与1,3,5-苯三硫酚通过配位作用结合,使其从探针结构上离去,探针的共轭结构及红色荧光恢复。体系的荧光强度与Hg^(2+)在5×10^(-9)~1×10^(-8)、1×10^(-8)~1.1×10^(-7)mol/L浓度范围内呈良好的线性关系,检测限为2×10^(-9)mol/L,等倍量的常见重金属离子对Hg^(2+)的特异性识别无干扰。应用于实际饮用水样品中Hg^(2+)含量检测,回收率可达到86.7%~110.2%。

1,3-氧硫戊环为受体的Hg^(2+)荧光探针的设计、合成及性能

Hg^(2+)是毒性最强的重金属离子之一,会造成空气、土壤和水的污染,严重损害人体健康,开发有效的分析方法检测环境体系中的Hg^(2+)尤为重要。荧光探针因其灵敏度高、选择性好、响应速度快、可实时在线检测等优点,已广泛应用于Hg^(2+)检测。以Hg^(2+)促进硫代缩醛的去保护反应设计合成了一种全新的以1,3-氧硫戊环为受体的开启型Hg^(2+)荧光探针[2-(pyren-1-yl)-1,3-oxathiolane,POX],通过^(1)H NMR、^(13)C NMR和HRMS对POX结构进行表征,考察了POX在CH_(3)CH_(2)OH/H_(2)O中对Hg^(2+)的选择性、竞争性、浓度滴定、pH滴定、时间依赖性、检出限和识别机理等。研究结果表明,POX可在较宽的pH范围内对Hg^(2+)快速识别,并表现出高度的选择性和灵敏度;向POX中加入Hg^(2+)后,在386 nm处出现明显的荧光发射峰,表明POX对Hg^(2+)呈现出显著的荧光“开启”效应,其识别过程几乎不受其他金属离子干扰;荧光滴定实验表明POX在Hg^(2+)浓度为0~6.5μmol·L^(-1)范围内具有良好的线性响应(R^(2)=0.9994),检出限为0.168μmol·L^(-1),在实际水样中检测Hg^(2+)的RSD小于2.92%。由于POX合成简单、原料易得且pH适用范围较广,可作为定性和定量检测环境中Hg^(2+)的潜在工具。

氨基酸基氮掺杂荧光碳点的制备及饮料中Hg^(2+)的检测

汞离子是一种高毒性的重金属污染物,人体摄入后会带来健康危害,因此控制食品中的汞离子含量非常重要。以柠檬酸为碳源,不同的氨基酸为氮源掺杂,采用一步水热法制备高性能荧光的碳点(CDs),探究不同氨基酸基氮掺杂对碳点荧光量子产率(QY)的影响,以及这些氨基酸基氮掺杂碳点对汞离子的响应。结果显示,不同氨基酸的碳链长度和官能团对CDs的QY有一定的影响。Hg^(2+)能高效猝灭以甘氨酸(Gly)为氮源掺杂的Gly-CDs的荧光,Gly-CDs具有良好的荧光稳定性,在优化的试验条件下,用于Hg^(2+)检测的线性范围为0.00~7.00μmol/L和8.00~60.00μmol/L,检出限为0.20μmol/L。据此构建的荧光探针用于检测实际饮料样品中的Hg^(2+),回收率在90.08%~107.90%。该方法简便、快速、灵敏、适用于饮料中Hg^(2+)的测定。

Hg^(2+)光热传感实验的设计与实践

以问题导向学习(PBL)设计了基于温度信号的Hg^(2+)光热传感综合教学实验。在该教学实验中,学生首先基于机械化学,采用湿法研磨策略,制备了具有高光热转换效率的CuS纳米颗粒(CuS NPs),而后基于CuS NPs与Hg^(2+)的沉淀置换反应诱导的CuS NPs分散液的光热信号变化实现了环境水样中Hg^(2+)的检测。将Hg^(2+)光热传感的科研成果融入实验教学环节,探讨本科化学实验的创新教学设计理念,实现了以科学研究思维来指导设计大学化学创新实验,有助于系统全面地培养学生发现问题及解决问题的能力,同时将有效提升学生的基础知识综合利用与实践创新能力,促进高校本科实验教学改革。

氮掺杂碳点的制备及其在Hg^(2+)测定中的应用研究

以柠檬酸为碳源,尿素、邻菲罗啉、氨水、硫脲、精氨酸为氮源,通过水热法合成了5种氮掺杂荧光碳点。对合成的碳点进行荧光性能表征,测定了每种碳点的最佳激发和发射波长,在最佳发射波长下,利用荧光猝灭对Hg^(2+)进行检测。结果表明,以精氨酸为氮源制备的碳点对Hg^(2+)检测具有较灵敏的响应,其线性范围为0.25~1.5μmol/L。

磁性聚氨基噻唑吸附剂脱除水体Hg^(2+)性能

聚多巴胺(PDA)辅助负载聚氨基噻唑(PAT)法制备了磁性颗粒吸附剂Fe_(3)O_(4)@SiO_(2)@PDA-PAT。对吸附剂进行了XRD、VSM、TG、SEM、XPS、EDS和Zeta电位等表征分析,考察了吸附剂对Hg^(2+)的吸附性能。结果表明,Fe_(3)O_(4)@SiO_(2)@PDA-PAT具有超顺磁性,在pH小于2时Zeta电位为正,pH大于2时Zeta电位为负。在303 K和Hg^(2+)浓度为50 mg/L模拟废水中,当pH为1.3和5.0时,Hg^(2+)的平衡吸附量分别为121.9 mg/g和153.1 mg/g。在强酸(如pH 1.3)和弱酸(如pH 5.0)环境下Fe_(3)O_(4)@SiO_(2)@PDA-PAT吸附Hg^(2+)的过程均是自发过程,且符合二级动力学模型和Langmuir等温吸附模型。强酸环境下(如pH 1.3)Fe_(3)O_(4)@SiO_(2)@PDA-PAT吸附Hg^(2+)是焓驱动的放热过程,弱酸(如pH 5.0)环境下是熵驱动的吸热过程。用2 mol/L混酸(盐酸和硝酸摩尔比为1∶1)作为解吸液可使Hg^(2+)解吸率达91%以上。在303 K、pH 1.3、Hg^(2+)浓度20 mg/L条件下,当Na^(+)、K^(+)、Mg^(2+)、Ca^(2+)、Cu^(2+)、Zn^(2+)、Ni^(2+)质量浓度为Hg^(2+)的20倍时,Fe_(3)O_(4)@SiO_(2)@PDA-PAT的Hg^(2+)平衡吸附量分别下降了33.2%、32.1%、20.6%、26.7%、21.2%、29.6%、17.8%。在模拟海水下,Hg^(2+)吸附量下降40.9%。Fe_(3)O_(4)@SiO_(2)@PDA-PAT具有较好的Hg^(2+)选择性,具有净化海水脱除重金属的应用潜力。

Uniform deposition of ultra-thin TiO_(2) film on mica substrate by atmospheric pressure chemical vapor deposition: Effect of precursor concentration

The performance of pearlescent pigment significantly affected by the grain size and the roughness of deposited film. The effect of TiCl_(4) concentration on the initial deposition of TiO_(2) on mica by atmospheric pressure chemical vapor deposition(APCVD) was investigated. The precursor concentration significantly affected the deposition and morphology of TiO_(2) grains assembling the film. The deposition time for fully covering the surface of mica decreased from 120 to 10 s as the TiCl_(4) concentration increased from 0.38%to 2.44%. The grain size increased with the TiCl_(4) concentration. The AFM and TEM analysis demonstrated that the aggregation of TiO_(2) clusters at the initial stage finally result to the agglomeration of fine TiO_(2) grains at high TiCl_(4) concentrations. Following the results, it was suggested that the nucleation density and size was easy to be adjusted when the TiCl_(4) concentration is below 0.90%.

聚丙烯腈改性及其对Hg^(2+)吸附研究

Hg^(2+)是生态环境中存在的对人体健康危害最大的重金属离子之一。吸附法是一种去除Hg^(2+)最简单高效的方法。因此设计成本低廉、吸附性能好且能循环利用的吸附剂是非常重要的。采用乳液自由基聚合技术制备聚丙烯腈,然后用三乙烯四胺对聚丙烯腈进行改性,得到改性后的聚丙烯腈。以废水中Hg^(2+)为吸附对象,考察不同的实验条件下,改性后的聚丙烯腈对Hg^(2+)的吸附性能。在pH值为6,Hg^(2+)浓度为40 mg/L,即时吸附量q_(t)达到最大;吸附30 min后吸附基本达到饱和。分别用伪一级吸附和伪二级吸附方程动力学模型对实验数据进行拟合,结果表明,用伪二级动力学方程可以更好描述吸附过程,说明三乙烯四胺改性聚丙烯腈对Hg^(2+)的吸附过程受Hg^(2+)扩散和-NH_(2)与Hg^(2+)的配位反应影响,为化学吸附。

Spatial Inhomogeneity of Atmospheric CO_(2) Concentration and Its Uncertainty in CMIP6 Earth System Models

This paper provides a systematic evaluation of the ability of 12 Earth System Models(ESMs)participating in the Coupled Model Intercomparison Project Phase 6(CMIP6)to simulate the spatial inhomogeneity of the atmospheric carbon dioxide(CO_(2))concentration.The multi-model ensemble mean(MME)can reasonably simulate the increasing trend of CO_(2) concentration from 1850 to 2014,compared with the observation data from the Scripps CO_(2) Program and CMIP6 prescribed data,and improves upon the CMIP5 MME CO_(2) concentration(which is overestimated after 1950).The growth rate of CO_(2) concentration in the northern hemisphere(NH)is higher than that in the southern hemisphere(SH),with the highest growth rate in the mid-latitudes of the NH.The MME can also reasonably simulate the seasonal amplitude of CO_(2) concentration,which is larger in the NH than in the SH and grows in amplitude after the 1950s(especially in the NH).Although the results of the MME are reasonable,there is a large spread among ESMs,and the difference between the ESMs increases with time.The MME results show that regions with relatively large CO_(2) concentrations(such as northern Russia,eastern China,Southeast Asia,the eastern United States,northern South America,and southern Africa)have greater seasonal variability and also exhibit a larger inter-model spread.Compared with CMIP5,the CMIP6 MME simulates an average spatial distribution of CO_(2) concentration that is much closer to the site observations,but the CMIP6-inter-model spread is larger.The inter-model differences of the annual means and seasonal cycles of atmospheric CO_(2) concentration are both attributed to the differences in natural sources and sinks of CO_(2) between the simulations.

基于适配体的荧光生物传感器对Hg^(2+)的检测技术研究

工业迅速发展所带来的重金属污染,是目前威胁人类健康的重要环境问题之一。Hg^(2+)是一种毒性强且污染较为普遍的重金属离子,较低浓度Hg^(2+)就会对人体造成很大危害。基于核酸适配体错配结合Hg^(2+)的原理,以特异性双链核酸染料SYBR GreenⅠ为荧光指示探针,构建了新型的无标记核酸适配体荧光生物传感器,建立了一种高灵敏度、快速检测Hg^(2+)的方法,实现了Hg^(2+)高效检测。在优化条件下,传感器对Hg^(2+)的检测线性范围为10 nmol/L~1μmol/L,相关系数(r^(2))为0.99,检出限为1 nmol/L。5种干扰离子(Ca^(2+)、Fe^(2+)、Cu^(2+)、Ni^(2+)、Ag^(+))的存在不影响Hg^(2+)检测,表明该方法对Hg^(2+)检测具有较好的特异性。在自来水样的Hg^(2+)加标检测实验中,平均回收率达到95.8%,具备分析实际样品的能力。

Effects of Controlled Atmospheres with High_O_2 or High_CO_2 Concentrations on Postharvest Physiology and Storability of "Napoleon" Sweet Cherry

Sweet cherries ( Prunus avium L. cv. Napoleon) were stored in controlled atmospheres (CA) of high O(2) (70% O(2) + 0% CO(2)) or high CO(2) (5% O(2) + 10% CO(2)), in modified atmosphere package (MAP, (13% - 18%) O(2) + (2% -4%) CO(2)) and in air (control) at 1 degreesC to investigate the effects of different O(2) and CO(2) concentrations on physiological properties, quality and storability of the fruits during storage. The results indicated that compared with other treatments, CA with high O(2) concentration decreased fruit decay and ethanol content, but increased the accumulation of malondialdehyde (MDA) and stimulated browning. CA with high CO(2) concentration inhibited polyphenol oxidase (PPO) activity, reduced MDA content, maintained vitamin C content and firmness, decreased fruit decay and browning. Soluble solids contents (SSC) were not significantly affected by different atmosphere treatments. 'Napoleon' fruits stored in 5% O(2) + 10% CO(2) for as long as 80 d were of good quality, but only 40, 20 and 30 d stored in MAP, 70% O(2) + 0% CO(2) and air, re-spectively.

STRUCTURAL RESPONSE OF SOYBEAN LEAF TO ELEVATED CO_2 CONCENTRATION

The effects of CO 2 concentration on the morphological and anatomical characters of soybean (Glycine max) leaf were investigated by means of light microscopy and SEM.It was noticed that exomorphology did not show dramatic change,while stomatal density decreased with increasing CO 2 concentration.Under SEM,no epicuticular wax was observed on both abaxial and adaxial sides of the control group as well as on adaxial side of the treatment group.However,leaf surface of abaxial side was noticed to be densely covered with microasterisk epicuticular wax when they were exposed to CO 2 enriched environment.The epicuticular wax deposition was present in equal abundance on both stomatal and nonstomatal areas.Furthermore,leaf thickness increased significantly due largely to the origin of an extra layer of palisade in the treatment group.The results confirmed that CO 2 enrichment might enhance cell division and induce greater quantity of epicuticular wax.

Effects of Ca^(2+)concentrations on accumulations of mineral elements in the components of Pteroceltis tatarinowii

The bark of Pteroce/tis tatarinowii is a raw material for manufacturing XuanPaper. The effects of Ca^(2+) concentrations on the accumulation of mineral elements in the bark,leaf and root of Pteroceltis tatarinowii were studied under controlled conditions. The types ofHoagland nutrient solution with three Ca^(2+) concentrations levels (200, 400 and 600 μg·g^(-1))and a control (without Ca^(2+)) were designed to culture Pteroceltis tatarinowii. After 6 months,contents of seven mineral elements including Ca, K, Mg, Mn, Zn, Cu and Na in the root, leaf and barkwere analyzed. The results indicated that Ca accumulations content in the root, leaf and bark hadpositively relation with Ca^(2+) concentrations (200, 400, 600 μg · g^(-1)), and the order of theCa content in the three components was root>leaf>bark. Ca content in the root treated with 600 μg·g^(-1) Ca^(2+) concentrations was 5.5 times as high as that of the control, and about 1.4 times ashigh as that of the root treated in 200 and 400 μg/g Ca^(2+) concentrations respectively. On thecontrary, K and Mg contents in the root, leaf and bark were negatively related to Ca^(2+)concentrations, especially in the bark, and their accumulation trend followed the order ofleaf>root>bark. K content in the bark treated with 600 μg ·g^(-1) Ca^(2+) concentrations was 39.3%of that of the control, and was 79.0% and 91.8% of that of the bark treated with 200 μg ·g^(-1)and 400 μg ·g^(-1) Ca^(2+) concentrations respectively; Mg content in the bark treated with 600μg ·g^(-1) Ca^(2+) concentrations was 23.4% of that of the control, and was 27.1% and 35.4% ofthat of the bark treated with 200 and 400 μg·g^(-1) Ca^(2+) concentrations respectively. Comparedwith the control, the general tendency of Mn, Zn and Cu content decreased with increasing of Ca^(2+)concentrations and their contents were in the order: root>leaf>bark. Based on the results of thisstudy, the experiment has been useful for providing academic bases in improving the bark quality ofPteroceltis tatarinowii on non-limestone soil.

Effects of Doubled_CO_2 Concentration on Ultrastructure, Supramolecular Architecture and Spectral Characteristics of Chloroplasts from Wheat

Wheat ( Triticum aestivum L.) plants were grown under ambient and doubled_CO 2(plus 350 μL/L) concentration in cylindrical open_top chamber to examine their effects on the ultrastructure, supramolecular architecture, absorption spectrum and low temperature (77 K) fluorescence emission spectrum of the chloroplasts from wheat leaves. The results were briefly summarized as follows: (1) The wheat leaves possessed normally developed chloroplasts with intact grana and stroma thylakoid membranes; The grana intertwined with stroma thylakoid membranes and increased slightly in stacking degree and the width of granum, in spite of more accumulated starch grains within the chloroplasts than those in control; (2) The particle density in the stacked region of the endoplasmic fracture face (EFs) and protoplasmic fracture face (PFs) and in the unstacked region the endoplasmic fracture face (EFu) and the protoplasmic fracture face (PFu) was significantly higher than that of control. Furthermore, in some cases many more particles on EFs faces of thylakoid membranes appeared as a paracrystalline particle array; (3) The variations in the structure of chloroplasts were consistent with the absorption spectra and the low temperature (77 K) fluorescence emission spectra of the chloroplasts developed under the doubled_CO 2 concentration. Results indicate that the capability of light energy absorption of chloroplasts and regulative capability of excitation energy distribution between PSⅡ and PSⅠ were raised by doubled_CO 2 concentration. This is very favorable for final productivity of wheat.

RELATIONSHIPS OF STARCH CONCENTRATION WITH SPECIFIC LEAF WEIGHT AND MINERAL CONCENTRATIONS IN POTATO LEAVES UNDER VARIED CO_2 AND TEMPERATURE

Foliar concentrations of starch and major nutrients N, P, K, Ca, and Mg along with specific leaf weight (SLW) were determined in the potato (Solanun tuberosum L.) cvs "Denali", "Norland "'and "Russet Burbank" grown for 35 days under the CO2 concentrations of 500, 1 000, 1 500 and 2 000 mol mol-1 at both 16 and 20℃ air temperature. The starch concentration, pooled from the three cultivars, increased with increasing CO2 concentration at both 16 and 20℃,, and was consistently higher at 16℃ than at 20℃. The SLW (g m-2) was positively related to the foliar starch concentration on the basis of leaf area or dry weight. The concentrations of N, P, Ca, and Mg in leaves were negatively related to starch concentration under 14% starch on a dry weight basis. Above 14%, there was no significant relationship between nutrient and starch concentrations . The similar patterns were seen when the SLW and nutrient concentrations were expressed on a starch-free basis. In contrast, the leaf concentration of K was not closely related to the starch concentration. The results indicated that the changes in SLW and concentrations of N, P, Ca, and Mg in potato leaves only partially resulted from the changed starch concentration.

Prediction of SO_2 Concentration in Urban Atmosphere Based on B-P Neural Network

Base on the principle and method of B-P neural network,the prediction model of SO2 concentration in urban atmosphere was established by using the statistical data of a city in southwest China from 1991 to 2009,so as to forecast atmospheric SO2 concentration in a city of southwest China.The results showed that B-P neural network applied in the prediction of SO2 concentration in urban atmosphere was reasonable and efficient with high accuracy and wide adaptability,so it was worthy to be popularized.

聚(N-异丙基丙烯酰胺-共聚-烯丙基硫脲)智能微凝胶的制备及其Hg^(2+)响应性能的研究

以N-异丙基丙烯酰胺(NIPAM)和烯丙基硫脲(ATU)为共聚单体,N,N'-亚甲基双丙烯酰胺(MBA)为交联剂,2,2′-偶氮二(2-甲基丙基咪)二盐酸盐(V50)为引发剂,通过沉淀聚合法制备了一种可用于Hg^(2+)检测与去除的聚(N-异丙基丙烯酰胺-共聚-烯丙基硫脲)(PNA)智能微凝胶。利用傅里叶变换红外光谱仪(FT-IR)、X射线光电子能谱仪(XPS)和扫描电镜(SEM)对微凝胶进行了化学成分和形貌表征。利用动态光散射纳米粒度分析仪(DLS)对微凝胶的粒径分布及温度响应性进行了研究。探究了干扰离子、pH和温度对微凝胶Hg^(2+)响应性能的影响。利用原子吸收光谱仪(AAS)探究了PNA微凝胶对Hg^(2+)的吸附去除效果。结果显示,PNA微凝胶具有良好的温敏性以及对Hg^(2+)的特异响应性,响应Hg^(2+)后引起的收缩比(RD)随着ATU单体比例的增加而减小,并确定了最佳检测温度为30℃。随着Hg^(2+)浓度的增加,RD值逐渐减小,根据Hg^(2+)浓度与RD之间的对应关系拟合出相应的Hg^(2+)浓度计算公式。该PNA微凝胶最低检测浓度可达10^(-8)mol·L^(-1)。在吸附实验中,PNA微凝胶的吸附容量随着Hg^(2+)浓度的增加而增加,对10^(-4)mol·L^(-1)以下的Hg^(2+)溶液,吸附率可达80%以上,最低可使Hg^(2+)浓度降至0.0005 mg·L^(-1)。相比Zn^(2+)、Cd^(2+)和Pb^(2+),微凝胶对Hg^(2+)的吸附率是其他金属离子的7倍左右。研究结果为有害金属Hg^(2+)的检测和去除提供了新方法。

基于改进INFO-Bi-LSTM模型的SO_(2)排放质量浓度预测

针对火电机组SO_(2)排放质量浓度的影响因素众多,难以准确预测的问题,提出一种改进向量加权平均(weighted mean of vectors,INFO)算法与双向长短期记忆(bi-directional long short term memory,Bi-LSTM)神经网络相结合的预测模型(改进INFO-Bi-LSTM模型)。采用Circle混沌映射和反向学习产生高质量初始化种群,引入自适应t分布提升INFO算法跳出局部最优解和全局搜索的能力。选取改进INFO-Bi-LSTM模型和多种预测模型对炉内外联合脱硫过程中4种典型工况下的SO_(2)排放质量浓度进行预测,将预测结果进行验证对比。结果表明:改进INFO算法的寻优能力得到提升,并且改进INFO-Bi-LSTM模型精度更高,更加适用于SO_(2)排放质量浓度的预测,可为变工况下的脱硫控制提供控制理论支撑。