160Gd(n,2n)159Gd和158Gd(n,p)158Eu反应截面测量

报道了在13.5—14.6MeV中子能区用活化法测得的¹⁶⁰Gd(n,2n)¹⁵⁹Gd和¹⁵⁸Gd(n,p)¹⁵⁸Eu的 反应截面值. 中子注量用⁹³Nb(n, 2n)⁹²m Nb反应截面得到. 由(13.5±0.2)MeV,(14.1±0.1)MeV和(14.6±0.2)MeV中子引起的¹⁶⁰Gd(n, 2n) ¹⁵⁹Gd反应截面值分别为(1940±83)mb, (2324±92)mb和(1983±77)mb, ¹⁵⁸Gd(n, p) ¹⁵⁸Eu反应截面值分别为(1.9±0.1)mb, (2.1±0.1)mb和(3.5±0.1)mb. 单能中子由T(d, n)⁴He反应获得.文中还列举了已收集到的数据以作比较.     

13.5－14.6MeV中子能区锡的同位素的(n,2n)反应截面的测量

报道了在13.5－14.6MeV中子能区用活化法测得的112Sn(n,2n)111Sn,118Sn(n,2n)117Sn 和 124Sn(n,2n)123mSn的反应截面值. 中子注量用93Nb(n, 2n)92mNb或27Al(n,α)24Na反应截面得到.单能中子由T(d, n)4He反应获得. 同时还列举了已收集到的文献值以作比较.     

14MeV中子引起的185Re(n,2n)184g,mRe和191Ir(n,2n)190Ir的核反应截面测量

利用活化方法测量了1?4MeV中子引起的¹⁸⁵Re(n,2n)^184gRe,¹⁸⁵Re(n,2n)^184mRe和¹⁹¹Ir(n,2n)¹⁹⁰Ir核反应的截面.中子能量E_n=(14.7±0.2)MeV时的实验结果分别为:(1817±85)mb,(390±18)mb和(2038±82)mb.并利用HFTT程序计算了中子能量在7—18MeV范围内的截面值,给出了其中两个核反应的激发函数曲线.     

63Cu(n,α)60Co反应截面测量

本文报告了E_n=13.6—14.8MeV中子能区用活化法以²⁷Al(n,α)²⁴Na截面为中子注量标准得的⁶³Cu(n,α)⁶⁰Co的反应截面.在中子能量为13.64,13.79,14.03,14.33,14.60和14.80MeV的截面值分别为58.3±3.1,56.3±2.4,53.4±2.0,50.8±1.9,48.4±1.7和47.4±1.7mb.在文中还列举了一些作者的数据以作比较.中子能量是用铌锆截面比法测定的.     

14MeV钕的同位素反应截面的测量

报道了在13.5—14.6MeV中子能区用活化法以⁹³Nb(n,2n)^92mNb反应截面为中子注量标准测得的¹⁵⁰Nd(n,2n)¹⁴⁹Nd,¹⁴⁸Nd(n,2n)¹⁴⁷Nd和¹⁴²Nd(n,2n)¹⁴¹Nd的反应截面值.由13.5±0.2,14.1±0.1和14.6±0.2MeV中子引起的¹⁵⁰Nd(n,2n)¹⁴⁹Nd反应截面值分别为2037±85,1737±68,1657±65mb,¹⁴⁸Nd(n,2n)¹⁴⁷Nd反应截面值分别为1394±58,1416±54,1956±76mb,^{142Nd(n,2n)141Nd反应截面值分别为1501±59,1623±62,1764±111mb.单能中子由T(d,n)4He反应获得.文中还收集了已发表的数据以作比较.}     

13.5—14.6MeV中子能区镓的同位素反应截面的测量

报道了在13.5—14.6MeV中子能区用活化法以⁹³Nb(n,2n)^92mNb反应截面为中子注量标准测得的⁶⁹Ga(n,2n)⁶⁸Ga,⁶⁹Ga(n,p)^69mZn,⁷¹Ga(n,p)^71mZn和⁷¹Ga(n,n′α)⁶⁷Cu的反应截面值.由(13.5±0.2),(14.1±0.1)和(14.6±0.2)MeV中子引起的⁶⁹Ga(n,2n)68Ga反应截面值分别为(794±31),(869±35)和(986±39)mb,⁷¹Ga(n,n′α)⁶⁷Cu反应截面值分别为(1.3±0.1),(1.7±0.1)和(2.5±0.1)mb.在中子能量为(14.1±0.1)MeV能量点,⁶⁹Ga(n,p)^69mZn反应截面值为(21.5±1.0)mb,⁷¹Ga(n,p)^71mZn反应截面值为(12.4±0.7)mb.单能中子由T(d,n)⁴He反应获得.文中还列举了尽可能收集到的数据以作比较.     

用基态特征γ射线计算同质异能态反应截面的公式及其应用

根据人工放射性的生长与衰变规律, 推导出一个在特殊情况下用基态特征γ射线计算同质异能态反应截面的公式, 并据此公式用活化法以⁹³Nb(n,2n)^92mNb反应截面为中子注量标准对¹²⁸Te(n,2n)^127mTe反应截面进行了测量. 由能量为(14.1±0.2)和(14.6±0.3)MeV的中子引发的¹²⁸Te(n,2n)^127mTe反应截面值分别为(737±69)和(853±82)mb. 单能中子用T(d,n)⁴He反应获得, 其能量用铌锆截面比法测定. 为减小热中子的(n, γ)反应的影响, 在辐照过程中对样品进行了包镉处理.     

13.5-14.6MeV能区中子引起的铂同位素核反应截面测量

用活化法以93Nb(n，2n)92mNb和27Al(n，a)24Na反应截面为中子注量标准，对198Pt(n，2n)197m+gPt，198Pt(n， 2n)197mPt， 192Pt(n，2n)191Pt，194Pt(n，p)194Ir，195Pt(n，p)195mIr和 196Pt(n，p)196mIr反应截面进行了测量，由(13.5±0.2)，(14.1±0.1)和(14.6±0.2)MeV中子引起的198Pt(n，2n)197m+gPt反应截面分别为(2038±159)，(1919±73)和(1836±68)mb，198Pt(n，2n)197mPt反应截面为(974±37)，(1055±39)和(1042±39)mb；由(14.1±0.1)，(14.4±0.2)和(14.6±0.2)MeV中子引起的192Pt(n，2n)191Pt反应截面为(1680±103)，(1810±67)和(2047±97)mb；由(14.1±0.1) 和(14.4±0.2)MeV中子引起的194Pt(n，p)194Ir反应截面为(3.8±0.4)和(5.4±0.5)mb；由(14.1±0.1)，(14.4±0.2)MeV和(14.6±0.2)MeV中子引起的195Pt(n，p)195mIr反应截面为(1.0±0.2)，(1.6±0.2)和(1.8±0.2)mb；由(13.5±0.2)和(14.4±0.2)MeV中子引起的196Pt(n，p)196mIr反应截面分别为(1.13±0.07)和(1.18±0.06)mb. 本工作的数据和其他一些作者的数据进行了比较.     

93Nb(n,2n)92mNb反应截面测量

用活化法以^27Al(n,α)^24Na反应截面为中子注量标准，对14MeV能区中子引起的^93Nb(n,2n)^92mNb反应截面进行了测量。中子能量由硅探测器法测定。     

181Hf(n,γ)182Hf反应截面测量

在中国原子能科学研究院重水研究堆上用活化法对反应堆中子引起的181Hf (n,γ)182Hf反应截面进行了测量. 反应堆中样品照射位置的热中子与超热中子的通量比值约为10. 照射后样品中的182Hf/180Hf和 181Hf/180Hf的原子数比值是用热电离质谱测量的. 本工作以180Hf (n,γ)181Hf反应截面(14.80±0.60 b)为标准，测得的反应堆中子引起的181Hf (n,γ)182Hf反应截面值为80.0±5.6 b.     

(n,2n)反应同质异能态截面比

在统计理论及考虑角动量守恒的激子模型的基础上,运用Monte Carlo方法计算(n,20)反应同质异能态截面比. 以⁵⁹Co(n,2n)⁵⁸Co、⁹³Nb(n,2n)⁹²Nb和¹⁸¹Ta(n,2n)¹⁸⁰Ta的3个反应道为例,计算从其阈能到20MeV能区的同质异能态截面比,并和已有实验数据做了比较,结果符合较好. 这表明本文提供的方法是计算(n,2n)反应同质异能态截面比的一种有效方法.     

(p,n)和(p,2n)反应激发函数的系统学研究

从普朗克(Planck)黑体辐射公式和实验测量数据出发,采用唯象的方法提出了包含两个可调参量,入射质子能量从阈能到150MeV,靶核质量数在44相似文献   

Conservation Laws of K(m, n) and mK(m, n) Equations

Based on the rank analysis method, algorithmization idea, and symbolic computation, in this paper we have presented a method to construct the conservation laws for nonlinear evolution equations. The polynomial conservation laws for K (n 2, n) equations and mnK(m, n) equations are found by using of this approach and some new results have been obtained.     

Conservation Laws of K（m,n） and mK（m,n） Equations

Based on the rank analysis method, algorithmization idea, and symbolic computation, in this paper we have presented a method to construct the conservation laws for nonlinear evolution equations. The polynomial conservation laws for K (n 2,n) equations and mK (m,n) equations are found by using of this approach and some new results have been obtained.     

替代反应法测量锕系核(n,f)和(n,xn)截面

对于某些中子反应截面,在直接测量上存在困难。为了获得那些对核能发展极其重要的核数据,人们提出替代反应法,即利用带电粒子代替中子进行反应,从而实现中子反应截面间接测量的方法。现有替代反应一般采用非弹激发、转移等周边反应,涉及的角动量远比中子反应的大,需要理论修正,这造成了一定的困难。有鉴于此,提出利用轻带电离子的俘获反应作为替代反应,其复合核自旋与中子反应的相当,有效避免了自旋修正的困难。根据这个思路,采用236U的（α,f）和（α,2n）反应作为替代反应,成功提取了239Pu的（n,f）和（n,2n）反应截面,与ENDFB7评价库数据在误差范围内符合较好,表明了替代反应法的优越性,可以在核数据测量中推广应用。There are always difficulties in the direct measurement of reactions induced by neutron, in order to obtain the neutron induced nuclear reaction data which are extremely important for nuclear power development, the surrogate reaction method, which uses charged particles instead of neutron, was proposed. The existing surrogate reaction method generally chooses peripheral reaction as the surrogate reaction, such as inelastic scattering excitation or transfer reaction. As a result, the angular momentum involved is always far larger than the neutron induced reaction, which causes difficulties in the theoretical calculation. Because of this, we proposed to use light-ion capture reaction as the surrogate reaction, the compound nuclei spin is similar with that of the neutron induced reaction, so that the difficulties in spin correction can be effectively avoided. Based on this idea, the 239Pu(n, f) and (n, 2n) reaction cross sections were successfully extracted using 236U(α,f) and (α,2n) reactions as the surrogate reaction. The results coincide well with the data of ENDFB7 within the error range, which shows that the surrogate reaction method has its own superiority, and it can be applied in the measurement of nuclear data.     

（n,2n）反应实验研究中的中子准直器设计

用3He球形4中子探测器,通过直接反应法可以对核素的（n,2n）反应截面进行测量。在此类实验中,要求对中子束进行很好的准直。好的准直器设计要求能够提高样品处的中子注量率的均匀性,同时保证中子束流边缘处的下降幅度,能够降低低能中子所占份额。本工作采用FLUKA和MCNPX对圆柱形准直器、单锥形准直器及三种不同斜率的双锥形准直器对中子注量率的均匀性和低能中子所占份额进行了对比研究,结果表明,低斜率的双锥形准直器可以满足实验对这两方面的要求。同时,在有样品和无样品两种条件下,对探测系统经由这五种不同准直器准直后的中子束流的响应做了对比,结果显示,经过低斜率的双锥形准直器准直的中子束流,探测系统在有样品时表现为较高的计数率,在无样品时表现为较低的本底。除此之外,对准直器出口处的斜率对准直效果的影响也做了比较。最终中子准直器选用为这种低斜率的双锥形准直器,材料选用为紫铜、不锈钢、聚乙烯和铅。准直孔开口处直径为2.64 cm,长度为137 cm,经准直后样品处的中子束斑直径为3.2 cm。     

Measurement of 85Rb（n, 2n） 84Rb reaction cross-section from 12 MeV up to 19.8 MeV

The cross-section data of the 85Rb(n,2 n)84Rb reaction have been measured with the neutron energies of 12 MeV to 19.8 MeV using the activation technique and the relative method.The 85Rb samples were irradiated on the surface of a two-ring orientation assembly with neutrons produced from the 3H(d,n)4He reaction at the 5SDH-21.7-MV Tandem accelerator in China.Theoretical model calculations were performed with the TALYS-1.9 code.The present data were compared with previously obtained experimental data and the available evaluated data.     

Additivity and non-additivity of dissociation energies in intermolecular interactions. Theoretical studies on (H2)n,n = 2-8, (CO2)n,n = 2-6 and (HF)n,n = 2-8

CCSD(T) and MP2 results using the aug-cc-pV5Z basis set are reported for chain, cyclic and other structures of the clusters (H₂)_n, n?=?2-8, (CO₂)_n, n?=?2-6 and (HF)_n, n?=?2-8. In chain-like structures of (H₂)_n and (CO₂)_n, with the bonding type of the dimer maintained, the dissociation energy D_e of the dimer doubles for the trimer, triples for the tetramer, and so on. Due to these systems being dominated by short-range forces, interactions are essentially restricted to neighbouring monomers. For other types of (H₂)_n and (CO₂)_n structures, the multipliers relative to the dimerisation energy can be much higher. Dissociation energies for the hexamers in S₆ symmetry of both H₂ (379?cm^?1) and CO₂ (4925?cm^?1) are over ten times the respective dimerisation energies. For the chain-like trimer of HF, however, D_e is in excess of double the dimer value. Mainly due to longer-range dipolar forces, the interactions reach beyond the neighbouring monomers. The interaction energy between HF monomers in chains follows an approximate R^?2 (R being the F–F distance) relationship, The calculated dissociation energies of the HF octamer are 15,985?cm^?1 (factor of 10.4) for the chain, and 21,003?cm^?1 (factor of 13.7) for the C_6h cyclic structure.     

(HgSe)_n(n=1～6)团簇结构和性质的密度泛函研究

本工作采用LANL2DZ赝势基组、B3LYP方法对(HgSe)n(n=1~6)团簇进行了结构优化、自然键原子轨道和频率计算,得到(HgSe)n(n=1~6)团簇基态的平衡几何结构、电子状态、垂直电离势、垂直电子亲和势、偶极矩、三个基本热力学函数等相关性质,并系统分析了该团簇的几何构型、原子净电荷布局、前沿分子轨道特征.结果表明:基态稳定结构(HgSe)2为平面四边形,(HgSe)n(n=3~6)为笼状结构,且稳定顺序为(HgSe)5(HgSe)4(HgSe)6(HgSe)2HgSe(HgSe)3,极性顺序为:(HgSe)4HgSe(HgSe)3(HgSe)5(HgSe)6(HgSe)2,(HgSe)6和(HgSe)2分子空间结构的对称性较好.(HgSe)n(n=1~6)团簇各体系都有较好的电子供体及受体等活性部位,随着n增大轨道离域现象明显,利于电子的转移,导电性增强.